| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | KEGG_ko | KEGG_Pathway | BRITE | Description |
|---|---|---|---|---|---|---|---|---|---|
| HEJOHAOE_00001 | 1.17e-33 | arsC | 1.20.4.1 | - | T | ko:K03741 | - | ko00000,ko01000 | low molecular weight |
| HEJOHAOE_00003 | 0.0 | clpC | - | - | O | ko:K03696 | ko01100,map01100 | ko00000,ko03110 | Belongs to the ClpA ClpB family |
| HEJOHAOE_00004 | 4.16e-92 | mcsB | 2.7.14.1 | - | E | ko:K19405 | - | ko00000,ko01000 | Catalyzes the specific phosphorylation of arginine residues in proteins |
| HEJOHAOE_00005 | 5.99e-13 | - | - | - | S | ko:K19411 | - | ko00000 | UvrB/uvrC motif |
| HEJOHAOE_00006 | 3.22e-51 | ctsR | - | - | K | ko:K03708 | - | ko00000,ko03000 | Belongs to the CtsR family |
| HEJOHAOE_00010 | 5.28e-47 | - | - | - | K | - | - | - | Probable zinc-ribbon domain |
| HEJOHAOE_00011 | 7.57e-25 | sigH | - | - | K | ko:K03091 | - | ko00000,ko03021 | RNA polymerase sigma factor, sigma-70 family |
| HEJOHAOE_00012 | 4.36e-212 | comM | - | - | O | ko:K07391 | - | ko00000 | chelatase subunit ChlI |
| HEJOHAOE_00013 | 2.27e-25 | - | - | - | C | - | - | - | Hydrid cluster protein-associated redox disulfide domain |
| HEJOHAOE_00014 | 1.81e-41 | trmK | 2.1.1.217 | - | S | ko:K06967 | - | ko00000,ko01000,ko03016 | SAM-dependent methyltransferase |
| HEJOHAOE_00015 | 3.44e-34 | - | 3.5.4.16 | - | S | ko:K22391 | ko00790,ko01100,map00790,map01100 | ko00000,ko00001,ko00002,ko01000 | NGG1p interacting factor 3 |
| HEJOHAOE_00016 | 9.79e-84 | trmB | 2.1.1.33 | - | J | ko:K03439 | - | ko00000,ko01000,ko03016 | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
| HEJOHAOE_00017 | 1.9e-36 | - | - | - | S | - | - | - | Tetratricopeptide repeat |
| HEJOHAOE_00018 | 3e-137 | - | - | - | K | - | - | - | response regulator receiver |
| HEJOHAOE_00019 | 4.27e-116 | - | - | - | T | - | - | - | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain |
| HEJOHAOE_00020 | 2.87e-125 | prmC | - | - | S | - | - | - | Protein of unknown function (DUF1385) |
| HEJOHAOE_00021 | 2.03e-66 | prmC | 2.1.1.297 | - | J | ko:K02493 | - | ko00000,ko01000,ko03012 | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif |
| HEJOHAOE_00022 | 2.33e-196 | recA | - | - | L | ko:K03553 | ko03440,map03440 | ko00000,ko00001,ko00002,ko03400 | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage |
| HEJOHAOE_00023 | 7.92e-68 | recX | - | - | S | ko:K03565 | - | ko00000,ko03400 | Modulates RecA activity |
| HEJOHAOE_00024 | 3.02e-190 | rimO | 2.8.4.4 | - | J | ko:K14441 | - | ko00000,ko01000,ko03009 | Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 |
| HEJOHAOE_00025 | 5.96e-38 | pgsA | 2.7.8.5 | - | I | ko:K00995 | ko00564,ko01100,map00564,map01100 | ko00000,ko00001,ko01000 | Belongs to the CDP-alcohol phosphatidyltransferase class-I family |
| HEJOHAOE_00026 | 1.36e-90 | cysE | 2.3.1.30 | - | E | ko:K00640 | ko00270,ko00920,ko01100,ko01110,ko01120,ko01200,ko01230,ko05111,map00270,map00920,map01100,map01110,map01120,map01200,map01230,map05111 | ko00000,ko00001,ko00002,ko01000 | serine O-acetyltransferase |
| HEJOHAOE_00027 | 4.49e-254 | cysS | 6.1.1.16 | - | J | ko:K01883 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Belongs to the class-I aminoacyl-tRNA synthetase family |
| HEJOHAOE_00028 | 1.05e-73 | pdaB | - | - | G | - | - | - | Polysaccharide deacetylase |
| HEJOHAOE_00030 | 3.24e-08 | - | - | - | K | - | - | - | Helix-turn-helix XRE-family like proteins |
| HEJOHAOE_00032 | 1.77e-33 | - | - | - | S | - | - | - | PFAM ErfK YbiS YcfS YnhG family protein |
| HEJOHAOE_00034 | 3.72e-65 | - | - | - | M | - | - | - | Glycosyl hydrolases family 25 |
| HEJOHAOE_00035 | 6.27e-37 | luxS | 4.4.1.21 | - | H | ko:K07173 | ko00270,ko01100,ko01230,ko02024,ko02026,ko05111,map00270,map01100,map01230,map02024,map02026,map05111 | ko00000,ko00001,ko00002,ko01000 | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) |
| HEJOHAOE_00036 | 5.89e-34 | - | - | - | D | ko:K21471 | - | ko00000,ko01000,ko01002,ko01011 | Peptidase, M23 |
| HEJOHAOE_00037 | 6.9e-23 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00042 | 2.57e-93 | trmL | 2.1.1.207 | - | J | ko:K03216 | - | ko00000,ko01000,ko03016 | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily |
| HEJOHAOE_00043 | 4.38e-245 | pgk | 2.7.2.3, 5.3.1.1 | - | G | ko:K00927,ko:K01803 | ko00010,ko00051,ko00562,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00010,map00051,map00562,map00710,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000,ko04147 | Phosphoglycerate kinase |
| HEJOHAOE_00044 | 1.79e-133 | tpiA | 5.3.1.1 | - | G | ko:K01803 | ko00010,ko00051,ko00562,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00010,map00051,map00562,map00710,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000,ko04147 | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) |
| HEJOHAOE_00045 | 1.41e-291 | gpmI | 5.4.2.12 | - | G | ko:K15633 | ko00010,ko00260,ko00680,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00010,map00260,map00680,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate |
| HEJOHAOE_00046 | 1.66e-243 | - | - | - | V | ko:K06147 | - | ko00000,ko02000 | ABC transporter |
| HEJOHAOE_00047 | 3.14e-234 | - | - | - | V | ko:K06147,ko:K11085 | ko02010,map02010 | ko00000,ko00001,ko01000,ko02000 | ABC transporter |
| HEJOHAOE_00048 | 8.13e-56 | rplQ | - | - | J | ko:K02879 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L17 |
| HEJOHAOE_00049 | 6.18e-185 | rpoA | 2.7.7.6 | - | K | ko:K03040 | ko00230,ko00240,ko01100,ko03020,map00230,map00240,map01100,map03020 | br01611,ko00000,ko00001,ko00002,ko01000,ko03021,ko03400 | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates |
| HEJOHAOE_00050 | 1.04e-95 | rpsD | - | - | J | ko:K02986 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit |
| HEJOHAOE_00051 | 6.28e-70 | rpsK | - | - | J | ko:K02948 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome |
| HEJOHAOE_00052 | 3.22e-73 | rpsM | - | - | J | ko:K02952 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits |
| HEJOHAOE_00053 | 9.35e-15 | rpmJ | - | - | J | - | - | - | Belongs to the bacterial ribosomal protein bL36 family |
| HEJOHAOE_00054 | 1.51e-33 | infA | - | - | J | ko:K02518 | - | ko00000,ko03012 | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex |
| HEJOHAOE_00055 | 5.45e-15 | - | - | - | J | - | - | - | COG2163 Ribosomal protein L14E L6E L27E |
| HEJOHAOE_00056 | 3.4e-142 | map | 3.4.11.18 | - | E | ko:K01265 | - | ko00000,ko01000,ko01002 | Methionine aminopeptidase |
| HEJOHAOE_00057 | 5.88e-100 | adk | 2.7.4.3 | - | F | ko:K00939 | ko00230,ko00730,ko01100,ko01110,ko01130,map00230,map00730,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000,ko04147 | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism |
| HEJOHAOE_00058 | 6.93e-208 | secY | - | - | U | ko:K03076 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently |
| HEJOHAOE_00059 | 2.41e-66 | rplO | - | - | J | ko:K02876 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds to the 23S rRNA |
| HEJOHAOE_00060 | 8.27e-24 | rpmD | - | - | J | ko:K02907 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | ribosomal protein |
| HEJOHAOE_00061 | 1.6e-89 | rpsE | - | - | J | ko:K02988 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body |
| HEJOHAOE_00062 | 2.82e-52 | rplR | - | - | J | ko:K02881 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance |
| HEJOHAOE_00063 | 8.87e-97 | rplF | - | - | J | ko:K02933 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center |
| HEJOHAOE_00064 | 2.44e-75 | rpsH | - | - | J | ko:K02994 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit |
| HEJOHAOE_00065 | 7.72e-35 | rpsN | - | - | J | ko:K02954 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site |
| HEJOHAOE_00066 | 2.45e-109 | rplE | - | - | J | ko:K02931 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits |
| HEJOHAOE_00067 | 4.2e-59 | rplX | - | - | J | ko:K02895 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit |
| HEJOHAOE_00068 | 4.07e-76 | rplN | - | - | J | ko:K02874 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome |
| HEJOHAOE_00069 | 6.8e-42 | rpsQ | - | - | J | ko:K02961 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA |
| HEJOHAOE_00070 | 1.12e-21 | rpmC | - | - | J | ko:K02904 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the universal ribosomal protein uL29 family |
| HEJOHAOE_00071 | 1.13e-86 | rplP | - | - | J | ko:K02878 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs |
| HEJOHAOE_00072 | 6.3e-113 | rpsC | - | - | J | ko:K02982 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation |
| HEJOHAOE_00073 | 2.1e-53 | rplV | - | - | J | ko:K02890 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome |
| HEJOHAOE_00074 | 9.8e-56 | rpsS | - | - | J | ko:K02965 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA |
| HEJOHAOE_00075 | 7.61e-167 | rplB | - | - | J | ko:K02886 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity |
| HEJOHAOE_00076 | 1.3e-24 | rplW | - | - | J | ko:K02892 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome |
| HEJOHAOE_00077 | 1.13e-114 | rplD | - | - | J | ko:K02926 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Forms part of the polypeptide exit tunnel |
| HEJOHAOE_00078 | 2.86e-114 | rplC | - | - | J | ko:K02906 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit |
| HEJOHAOE_00079 | 5.19e-61 | rpsJ | - | - | J | ko:K02946 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Involved in the binding of tRNA to the ribosomes |
| HEJOHAOE_00080 | 6.32e-37 | btuR | 2.5.1.17 | - | H | ko:K19221 | ko00860,ko01100,map00860,map01100 | ko00000,ko00001,ko00002,ko01000 | ATP corrinoid adenosyltransferase |
| HEJOHAOE_00081 | 2.35e-143 | - | - | - | P | - | - | - | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family |
| HEJOHAOE_00082 | 2.91e-133 | - | - | - | S | - | - | - | Uncharacterized protein conserved in bacteria (DUF2179) |
| HEJOHAOE_00084 | 6.89e-65 | - | - | - | S | - | - | - | Baseplate J-like protein |
| HEJOHAOE_00094 | 2.5e-141 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00096 | 1.26e-81 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00097 | 2.44e-107 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00098 | 8.33e-199 | - | - | - | S | - | - | - | Phage terminase, large subunit, PBSX family |
| HEJOHAOE_00099 | 1.18e-17 | - | - | - | S | - | - | - | Terminase small subunit |
| HEJOHAOE_00100 | 4.5e-34 | trxA | - | - | O | ko:K03671 | ko04621,ko05418,map04621,map05418 | ko00000,ko00001,ko03110 | Thioredoxin |
| HEJOHAOE_00101 | 1.66e-38 | - | - | - | S | - | - | - | Ferredoxin thioredoxin reductase catalytic beta chain |
| HEJOHAOE_00102 | 4.66e-160 | pdxB | 1.1.1.399, 1.1.1.95 | - | EH | ko:K00058 | ko00260,ko00680,ko01100,ko01120,ko01130,ko01200,ko01230,map00260,map00680,map01100,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000,ko04147 | D-isomer specific 2-hydroxyacid dehydrogenase |
| HEJOHAOE_00103 | 1.96e-210 | serC | 2.6.1.52 | - | E | ko:K00831 | ko00260,ko00680,ko00750,ko01100,ko01120,ko01130,ko01200,ko01230,map00260,map00680,map00750,map01100,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine |
| HEJOHAOE_00104 | 1.41e-157 | pyrF | 4.1.1.23 | - | F | ko:K01591 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the OMP decarboxylase family. Type 2 subfamily |
| HEJOHAOE_00107 | 5.4e-78 | smpB | - | - | O | ko:K03664 | - | ko00000 | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA |
| HEJOHAOE_00109 | 1.31e-91 | - | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| HEJOHAOE_00112 | 1.44e-20 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00114 | 1.01e-266 | ade | 3.5.4.2 | - | F | ko:K01486 | ko00230,ko01100,map00230,map01100 | ko00000,ko00001,ko01000 | Adenine deaminase C-terminal domain |
| HEJOHAOE_00115 | 3.02e-218 | - | - | - | G | - | - | - | Alpha amylase, catalytic domain |
| HEJOHAOE_00116 | 1.09e-06 | - | - | - | G | - | - | - | Alpha-amylase domain |
| HEJOHAOE_00117 | 9.61e-209 | yrvN | - | - | L | ko:K07478 | - | ko00000 | ATPase, AAA family |
| HEJOHAOE_00118 | 1.12e-06 | - | - | - | M | - | - | - | NLP P60 protein |
| HEJOHAOE_00119 | 1.47e-112 | - | - | - | M | - | - | - | Aminoglycoside phosphotransferase |
| HEJOHAOE_00120 | 0.000259 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00121 | 2.44e-37 | - | - | - | S | ko:K07088 | - | ko00000 | Transporter, auxin efflux carrier (AEC) family protein |
| HEJOHAOE_00125 | 3.01e-59 | ruvC | 3.1.22.4 | - | L | ko:K01159 | ko03440,map03440 | ko00000,ko00001,ko01000,ko03400 | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group |
| HEJOHAOE_00126 | 8.57e-45 | ruvA | 3.6.4.12 | - | L | ko:K03550 | ko03440,map03440 | ko00000,ko00001,ko01000,ko03400 | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB |
| HEJOHAOE_00127 | 2.52e-199 | ruvB | 3.6.4.12 | - | L | ko:K03551 | ko03440,map03440 | ko00000,ko00001,ko01000,ko03400 | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing |
| HEJOHAOE_00128 | 7.01e-213 | glmM | 5.4.2.10 | - | G | ko:K03431 | ko00520,ko01100,ko01130,map00520,map01100,map01130 | ko00000,ko00001,ko01000 | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate |
| HEJOHAOE_00129 | 5.32e-171 | rlmI | 2.1.1.191 | - | J | ko:K06969 | - | ko00000,ko01000,ko03009 | Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA |
| HEJOHAOE_00130 | 1.09e-138 | - | - | - | P | ko:K16786,ko:K16787 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates |
| HEJOHAOE_00131 | 2.68e-135 | cbiO | - | - | P | ko:K16787 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates |
| HEJOHAOE_00132 | 1.22e-100 | ecfT | - | - | P | ko:K16783,ko:K16785 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | transmembrane transporter activity |
| HEJOHAOE_00133 | 1.77e-125 | truA | 5.4.99.12 | - | J | ko:K06173 | - | ko00000,ko01000,ko03016 | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs |
| HEJOHAOE_00136 | 0.000739 | pgsA | 2.7.8.41, 2.7.8.5 | - | I | ko:K00995,ko:K08744 | ko00564,ko01100,map00564,map01100 | ko00000,ko00001,ko01000 | CDP-alcohol phosphatidyltransferase |
| HEJOHAOE_00137 | 0.0 | - | - | - | O | ko:K03697 | - | ko00000,ko03110 | ATPase family associated with various cellular activities (AAA) |
| HEJOHAOE_00138 | 3.11e-120 | - | - | - | P | ko:K10119 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | sugar transport system permease |
| HEJOHAOE_00139 | 2.6e-123 | msmF | - | - | G | ko:K10118,ko:K15771 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| HEJOHAOE_00140 | 6.91e-201 | amyE | - | - | G | ko:K10117 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Bacterial extracellular solute-binding protein |
| HEJOHAOE_00141 | 1.32e-11 | - | - | - | S | - | - | - | Protein of unknown function, DUF624 |
| HEJOHAOE_00142 | 3.48e-252 | pgcA | 5.4.2.2, 5.4.2.8 | - | G | ko:K01835,ko:K01840 | ko00010,ko00030,ko00051,ko00052,ko00230,ko00500,ko00520,ko00521,ko01100,ko01110,ko01120,ko01130,map00010,map00030,map00051,map00052,map00230,map00500,map00520,map00521,map01100,map01110,map01120,map01130 | ko00000,ko00001,ko00002,ko01000 | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain |
| HEJOHAOE_00143 | 4.28e-84 | - | 3.5.1.28 | - | MT | ko:K01448 | ko01503,map01503 | ko00000,ko00001,ko00002,ko01000,ko01011,ko03036 | N-acetylmuramoyl-L-alanine amidase |
| HEJOHAOE_00144 | 4.35e-77 | - | - | - | C | - | - | - | LUD domain |
| HEJOHAOE_00146 | 1.27e-139 | rsmF | - | - | J | - | - | - | NOL1 NOP2 sun family |
| HEJOHAOE_00147 | 7.37e-125 | ksgA | 2.1.1.182 | - | J | ko:K02528 | - | ko00000,ko01000,ko03009 | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits |
| HEJOHAOE_00149 | 0.0 | - | 3.6.3.8 | - | P | ko:K01537 | - | ko00000,ko01000 | TIGRFAM ATPase, P-type (transporting), HAD superfamily, subfamily IC |
| HEJOHAOE_00150 | 4.7e-30 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00151 | 1.45e-45 | - | - | - | DJ | ko:K06218 | - | ko00000,ko02048 | addiction module toxin, RelE StbE family |
| HEJOHAOE_00152 | 4.83e-83 | ppa | 3.6.1.1 | - | C | ko:K01507 | ko00190,map00190 | ko00000,ko00001,ko01000 | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions |
| HEJOHAOE_00154 | 4.45e-113 | yfiH | - | - | S | ko:K05810 | - | ko00000,ko01000 | Belongs to the multicopper oxidase YfiH RL5 family |
| HEJOHAOE_00156 | 1.45e-138 | rluC | 5.4.99.24 | - | J | ko:K06179 | - | ko00000,ko01000,ko03009 | Responsible for synthesis of pseudouridine from uracil |
| HEJOHAOE_00157 | 3.6e-100 | - | - | - | M | - | - | - | LysM domain |
| HEJOHAOE_00158 | 2.5e-244 | spoIVA | - | - | DZ | ko:K06398 | - | ko00000 | ATPase. Has a role at an early stage in the morphogenesis of the spore coat |
| HEJOHAOE_00160 | 7.21e-200 | gcdB | 4.1.1.3 | - | C | ko:K01572 | ko00620,ko01100,map00620,map01100 | ko00000,ko00001,ko01000,ko02000 | Na+-transporting oxaloacetate decarboxylase beta subunit |
| HEJOHAOE_00161 | 1.15e-10 | - | - | - | M | - | - | - | Chain length determinant protein |
| HEJOHAOE_00162 | 1.3e-37 | capB | - | - | D | - | - | - | ATPase MipZ |
| HEJOHAOE_00163 | 1.57e-200 | - | - | - | EK | - | - | - | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs |
| HEJOHAOE_00164 | 3.42e-133 | secD | - | - | U | ko:K03072,ko:K12257 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA |
| HEJOHAOE_00165 | 3.61e-105 | secF | - | - | U | ko:K03074 | ko03060,ko03070,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA |
| HEJOHAOE_00166 | 1.91e-89 | adcA | - | - | P | ko:K09815 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Belongs to the bacterial solute-binding protein 9 family |
| HEJOHAOE_00167 | 5.97e-87 | - | - | - | P | ko:K09817 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | AAA domain, putative AbiEii toxin, Type IV TA system |
| HEJOHAOE_00168 | 2.07e-109 | - | - | - | P | ko:K09816 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ABC 3 transport family |
| HEJOHAOE_00170 | 9.12e-72 | - | - | - | K | - | - | - | Protein of unknown function (DUF421) |
| HEJOHAOE_00171 | 3.88e-178 | - | - | - | EG | ko:K06295 | - | ko00000 | spore germination protein |
| HEJOHAOE_00174 | 1.68e-142 | hprK | - | - | F | ko:K06023 | - | ko00000,ko01000 | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion |
| HEJOHAOE_00175 | 4.3e-103 | murB | 1.3.1.98 | - | M | ko:K00075 | ko00520,ko00550,ko01100,map00520,map00550,map01100 | ko00000,ko00001,ko01000,ko01011 | Cell wall formation |
| HEJOHAOE_00176 | 5.22e-93 | yvcJ | - | - | S | ko:K06958 | - | ko00000,ko03019 | Displays ATPase and GTPase activities |
| HEJOHAOE_00177 | 1.28e-64 | whiA | - | - | K | ko:K09762 | - | ko00000 | May be required for sporulation |
| HEJOHAOE_00178 | 6.96e-05 | xseB | 3.1.11.6 | - | L | ko:K03602 | ko03430,map03430 | ko00000,ko00001,ko01000,ko03400 | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides |
| HEJOHAOE_00179 | 9.67e-85 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29 | - | H | ko:K13789 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000,ko01006 | Belongs to the FPP GGPP synthase family |
| HEJOHAOE_00180 | 3.38e-199 | dxs | 2.2.1.7 | - | H | ko:K01662 | ko00730,ko00900,ko01100,ko01110,ko01130,map00730,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) |
| HEJOHAOE_00181 | 5.86e-125 | rrmJ | 2.1.1.226, 2.1.1.227 | - | J | ko:K06442 | - | ko00000,ko01000,ko03009 | Ribosomal RNA large subunit methyltransferase J |
| HEJOHAOE_00182 | 3.65e-43 | nadK | 2.7.1.23 | - | H | ko:K00858 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko01000 | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP |
| HEJOHAOE_00183 | 4.01e-40 | argR | - | - | K | ko:K03402 | - | ko00000,ko03000 | Regulates arginine biosynthesis genes |
| HEJOHAOE_00184 | 2.75e-155 | recN | - | - | L | ko:K03631 | - | ko00000,ko03400 | May be involved in recombinational repair of damaged DNA |
| HEJOHAOE_00185 | 5.74e-29 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00186 | 4.02e-18 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00187 | 3.87e-49 | - | - | - | S | - | - | - | Domain of unknown function (DUF4160) |
| HEJOHAOE_00188 | 1.97e-231 | recJ | - | - | L | ko:K07462 | ko03410,ko03430,ko03440,map03410,map03430,map03440 | ko00000,ko00001,ko01000,ko03400 | exonuclease |
| HEJOHAOE_00189 | 0.0 | relA | 2.7.6.5 | - | KT | ko:K00951 | ko00230,map00230 | ko00000,ko00001,ko01000 | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance |
| HEJOHAOE_00190 | 3.2e-55 | dtd | - | - | J | ko:K07560 | - | ko00000,ko01000,ko03016 | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality |
| HEJOHAOE_00191 | 8.81e-49 | - | - | - | S | - | - | - | Metallo-beta-lactamase domain protein |
| HEJOHAOE_00192 | 1.15e-181 | hemZ | - | - | C | - | - | - | Coproporphyrinogen dehydrogenase |
| HEJOHAOE_00194 | 1.98e-75 | spoVB | - | - | S | ko:K06409 | - | ko00000,ko02000 | Polysaccharide biosynthesis protein |
| HEJOHAOE_00195 | 8.92e-97 | mazG | 3.6.1.66 | - | S | ko:K02428,ko:K02499 | ko00230,map00230 | ko00000,ko00001,ko01000,ko03036 | MazG family |
| HEJOHAOE_00196 | 3.3e-36 | hup | - | - | L | ko:K03530 | - | ko00000,ko03032,ko03036,ko03400 | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions |
| HEJOHAOE_00197 | 1.62e-33 | hslR | - | - | J | - | - | - | S4 domain protein |
| HEJOHAOE_00198 | 6.29e-18 | yabP | - | - | S | - | - | - | Sporulation protein YabP |
| HEJOHAOE_00200 | 1.93e-05 | - | - | - | D | - | - | - | PFAM Septum formation initiator |
| HEJOHAOE_00201 | 1.09e-34 | yugI | - | - | J | ko:K07570,ko:K07571 | - | ko00000 | S1 RNA binding domain |
| HEJOHAOE_00202 | 2.35e-42 | hpf | - | - | J | ko:K05808 | - | ko00000,ko03009 | Sigma 54 modulation/S30EA ribosomal protein C terminus |
| HEJOHAOE_00203 | 5.83e-108 | ypsC | - | - | L | ko:K07444 | - | ko00000,ko01000 | Belongs to the methyltransferase superfamily |
| HEJOHAOE_00204 | 7.19e-136 | trkA | - | - | P | ko:K03499 | - | ko00000,ko02000 | TrkA-N domain |
| HEJOHAOE_00205 | 8.3e-189 | trkH | - | - | P | ko:K03498 | - | ko00000,ko02000 | Psort location CytoplasmicMembrane, score 10.00 |
| HEJOHAOE_00206 | 1.44e-64 | alr | 5.1.1.1 | - | M | ko:K01775 | ko00473,ko01100,ko01502,map00473,map01100,map01502 | ko00000,ko00001,ko01000,ko01011 | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids |
| HEJOHAOE_00207 | 1.67e-55 | - | - | - | S | - | - | - | COG COG0110 Acetyltransferase (isoleucine patch superfamily) |
| HEJOHAOE_00208 | 0.0 | nifJ | 1.2.7.1 | - | C | ko:K03737 | ko00010,ko00020,ko00620,ko00650,ko00720,ko01100,ko01120,ko01130,ko01200,map00010,map00020,map00620,map00650,map00720,map01100,map01120,map01130,map01200 | br01601,ko00000,ko00001,ko00002,ko01000 | Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin |
| HEJOHAOE_00209 | 0.000269 | lytR | - | - | IK | - | - | - | Cell envelope-related transcriptional attenuator domain |
| HEJOHAOE_00210 | 4.43e-130 | spoVAD | - | - | I | ko:K06406 | - | ko00000 | Stage V sporulation protein AD |
| HEJOHAOE_00211 | 1.44e-30 | - | - | - | V | ko:K18346 | ko01502,ko02020,map01502,map02020 | ko00000,ko00001,ko00002,ko01504 | PFAM VanW family protein |
| HEJOHAOE_00212 | 2.16e-93 | - | 2.4.1.315 | GT28 | M | ko:K03429 | ko00561,ko01100,map00561,map01100 | ko00000,ko00001,ko01000,ko01003 | UDP-N-acetylglucosamine LPS N-acetylglucosamine transferase |
| HEJOHAOE_00213 | 4.63e-20 | - | - | - | O | ko:K13963 | ko05146,map05146 | ko00000,ko00001 | Belongs to the serpin family |
| HEJOHAOE_00214 | 8.8e-116 | - | - | - | K | - | - | - | WYL domain |
| HEJOHAOE_00215 | 8.95e-30 | bglC | - | - | K | - | - | - | AraC-type DNA-binding domain-containing proteins |
| HEJOHAOE_00217 | 2.91e-281 | gltX | 6.1.1.17, 6.1.1.24 | - | J | ko:K01885,ko:K09698 | ko00860,ko00970,ko01100,ko01110,ko01120,map00860,map00970,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000,ko01007,ko02048,ko03016 | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) |
| HEJOHAOE_00218 | 0.0 | glnS | 6.1.1.18 | - | J | ko:K01886 | ko00970,ko01100,map00970,map01100 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | tRNA synthetases class I (E and Q), anti-codon binding domain |
| HEJOHAOE_00219 | 3.59e-92 | fabG5 | 1.1.1.100 | - | IQ | ko:K00059 | ko00061,ko00333,ko00780,ko01040,ko01100,ko01130,ko01212,map00061,map00333,map00780,map01040,map01100,map01130,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | Oxidoreductase, short chain dehydrogenase reductase family protein |
| HEJOHAOE_00220 | 2.03e-205 | murE | 6.3.2.13 | - | M | ko:K01928 | ko00300,ko00550,map00300,map00550 | ko00000,ko00001,ko01000,ko01011 | acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan |
| HEJOHAOE_00221 | 5.49e-73 | - | - | - | G | ko:K15770 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Bacterial extracellular solute-binding protein |
| HEJOHAOE_00222 | 1.7e-175 | - | - | - | G | ko:K15771 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| HEJOHAOE_00223 | 2.29e-118 | - | - | - | P | ko:K15772 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | PFAM binding-protein-dependent transport systems inner membrane component |
| HEJOHAOE_00224 | 8.43e-108 | - | 3.2.1.1 | GH13 | G | ko:K01176 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | alpha-amylase |
| HEJOHAOE_00225 | 5.61e-87 | rpsL | - | - | J | ko:K02950 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit |
| HEJOHAOE_00226 | 1.9e-94 | rpsG | - | - | J | ko:K02992 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA |
| HEJOHAOE_00227 | 0.0 | fusA | - | - | J | ko:K02355 | - | ko00000,ko03012,ko03029 | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome |
| HEJOHAOE_00228 | 8.41e-264 | tuf | - | - | J | ko:K02358 | - | ko00000,ko03012,ko03029,ko04147 | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis |
| HEJOHAOE_00229 | 1.1e-210 | - | - | - | S | - | - | - | Protein of unknown function (DUF1015) |
| HEJOHAOE_00230 | 1.44e-36 | - | - | - | S | ko:K07005 | - | ko00000 | Pyridoxamine 5'-phosphate oxidase |
| HEJOHAOE_00231 | 1.11e-10 | ansA | 3.5.1.1 | - | EJ | ko:K01424 | ko00250,ko00460,ko01100,ko01110,map00250,map00460,map01100,map01110 | ko00000,ko00001,ko01000 | L-asparaginase |
| HEJOHAOE_00232 | 6.96e-156 | napA | - | - | P | - | - | - | Transporter, CPA2 family |
| HEJOHAOE_00233 | 1.32e-06 | - | - | - | K | - | - | - | Transcriptional regulator |
| HEJOHAOE_00234 | 1.71e-285 | glgB | 2.4.1.18 | CBM48,GH13 | G | ko:K00700 | ko00500,ko01100,ko01110,map00500,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko04147 | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
| HEJOHAOE_00235 | 2.11e-36 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00236 | 5.97e-18 | - | - | - | M | ko:K07001 | - | ko00000 | esterase of the alpha-beta hydrolase superfamily |
| HEJOHAOE_00237 | 1.47e-40 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00238 | 8.88e-17 | - | - | - | S | - | - | - | Bacterial protein of unknown function (DUF951) |
| HEJOHAOE_00239 | 6.51e-177 | prfA | - | - | J | ko:K02835 | - | ko00000,ko03012 | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA |
| HEJOHAOE_00240 | 7.1e-135 | sua | 2.7.7.87 | - | J | ko:K07566 | - | ko00000,ko01000,ko03009,ko03016 | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine |
| HEJOHAOE_00241 | 5.86e-51 | coaE | 2.7.1.24 | - | H | ko:K00859 | ko00770,ko01100,map00770,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A |
| HEJOHAOE_00242 | 1.84e-11 | slt | - | GH23 | M | ko:K08309 | - | ko00000,ko01000,ko01011 | PFAM Lytic transglycosylase catalytic |
| HEJOHAOE_00243 | 2.3e-229 | apeA | - | - | E | - | - | - | M18 family aminopeptidase |
| HEJOHAOE_00245 | 3.08e-22 | trxA | - | - | O | ko:K03671 | ko04621,ko05418,map04621,map05418 | ko00000,ko00001,ko03110 | Belongs to the thioredoxin family |
| HEJOHAOE_00246 | 1.06e-73 | trxB | 1.8.1.9 | - | C | ko:K00384 | ko00450,map00450 | ko00000,ko00001,ko01000 | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family |
| HEJOHAOE_00247 | 3.95e-74 | - | - | - | EG | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00248 | 1.05e-69 | - | - | - | G | - | - | - | IA, variant 3 |
| HEJOHAOE_00249 | 5.94e-206 | - | - | - | E | ko:K03310 | - | ko00000 | amino acid carrier protein |
| HEJOHAOE_00250 | 1.16e-97 | - | - | - | S | ko:K07023 | - | ko00000 | HD domain |
| HEJOHAOE_00251 | 0.0 | ilvD | 4.2.1.9 | - | H | ko:K01687 | ko00290,ko00770,ko01100,ko01110,ko01130,ko01210,ko01230,map00290,map00770,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Belongs to the IlvD Edd family |
| HEJOHAOE_00252 | 0.0 | fusA2 | - | - | J | ko:K02355 | - | ko00000,ko03012,ko03029 | translation elongation |
| HEJOHAOE_00253 | 3.87e-48 | - | - | - | S | - | - | - | L,D-transpeptidase catalytic domain |
| HEJOHAOE_00254 | 5.21e-75 | KatE | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00255 | 1.45e-77 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00257 | 0.000646 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00259 | 1.94e-27 | - | - | - | K | - | - | - | COG COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases |
| HEJOHAOE_00260 | 3.47e-79 | mntP | - | - | P | - | - | - | Probably functions as a manganese efflux pump |
| HEJOHAOE_00261 | 2.55e-139 | ldh | 1.1.1.27 | - | C | ko:K00016 | ko00010,ko00270,ko00620,ko00640,ko01100,ko01110,ko01120,ko01130,ko04922,map00010,map00270,map00620,map00640,map01100,map01110,map01120,map01130,map04922 | ko00000,ko00001,ko01000,ko04147 | Belongs to the LDH MDH superfamily. LDH family |
| HEJOHAOE_00262 | 1.53e-63 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00266 | 4.36e-151 | - | - | - | K | - | - | - | WYL domain |
| HEJOHAOE_00269 | 2.15e-208 | - | - | - | L | - | - | - | Phage integrase family |
| HEJOHAOE_00270 | 5.63e-89 | - | - | - | S | ko:K07126 | - | ko00000 | FOG TPR repeat, SEL1 subfamily |
| HEJOHAOE_00271 | 4.14e-30 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00272 | 9.67e-32 | - | - | - | S | - | - | - | Helix-turn-helix domain |
| HEJOHAOE_00273 | 6.64e-30 | - | - | - | K | - | - | - | Helix-turn-helix domain |
| HEJOHAOE_00274 | 1.46e-62 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00275 | 8.6e-07 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00276 | 6.23e-144 | - | - | - | L | - | - | - | Belongs to the N(4) N(6)-methyltransferase family |
| HEJOHAOE_00277 | 1.76e-41 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00278 | 4e-161 | - | 2.1.1.72 | - | L | ko:K07318 | - | ko00000,ko01000,ko02048 | D12 class N6 adenine-specific DNA methyltransferase |
| HEJOHAOE_00279 | 2.03e-61 | - | - | - | L | - | - | - | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures |
| HEJOHAOE_00281 | 7.7e-143 | - | 3.6.4.12 | - | L | ko:K03657 | ko03420,ko03430,map03420,map03430 | ko00000,ko00001,ko01000,ko03400 | AAA domain |
| HEJOHAOE_00282 | 6.34e-71 | - | - | - | L | - | - | - | AAA domain, putative AbiEii toxin, Type IV TA system |
| HEJOHAOE_00283 | 6.17e-162 | - | - | - | L | - | - | - | AAA domain, putative AbiEii toxin, Type IV TA system |
| HEJOHAOE_00284 | 3.56e-83 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00285 | 5.48e-24 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00286 | 8.82e-56 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00287 | 8.29e-19 | - | - | - | L | - | - | - | Phage integrase, N-terminal SAM-like domain |
| HEJOHAOE_00289 | 2.79e-121 | - | - | - | D | - | - | - | FtsK/SpoIIIE family |
| HEJOHAOE_00290 | 1.59e-83 | - | - | - | S | - | - | - | Putative viral replication protein |
| HEJOHAOE_00293 | 0.0 | - | - | - | L | - | - | - | helicase domain protein |
| HEJOHAOE_00294 | 1.96e-75 | - | - | - | S | - | - | - | Domain of unknown function (DUF4391) |
| HEJOHAOE_00295 | 2.17e-29 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00296 | 1.24e-242 | mod | 2.1.1.72 | - | L | ko:K00571,ko:K07316 | - | ko00000,ko01000,ko02048 | DNA methylase |
| HEJOHAOE_00297 | 1.23e-37 | - | - | - | S | - | - | - | 23S rRNA-intervening sequence protein |
| HEJOHAOE_00298 | 0.0 | - | 3.1.21.5 | - | L | ko:K01156 | - | ko00000,ko01000,ko02048 | Type III restriction |
| HEJOHAOE_00300 | 4.42e-249 | glyA | 2.1.2.1 | - | E | ko:K00600 | ko00260,ko00460,ko00630,ko00670,ko00680,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,ko01523,map00260,map00460,map00630,map00670,map00680,map01100,map01110,map01120,map01130,map01200,map01230,map01523 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism |
| HEJOHAOE_00301 | 9.93e-116 | dus | - | - | J | ko:K05540 | - | ko00000,ko01000,ko03016 | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines |
| HEJOHAOE_00303 | 6.36e-40 | - | - | - | S | - | - | - | YjbR |
| HEJOHAOE_00304 | 4.93e-185 | pfkA | 2.7.1.11, 2.7.1.90 | - | H | ko:K21071 | ko00010,ko00030,ko00051,ko00052,ko00680,ko01100,ko01110,ko01120,ko01130,map00010,map00030,map00051,map00052,map00680,map01100,map01110,map01120,map01130 | ko00000,ko00001,ko01000 | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis |
| HEJOHAOE_00305 | 0.0 | ppk | 2.7.4.1 | - | H | ko:K00937 | ko00190,ko03018,map00190,map03018 | ko00000,ko00001,ko01000,ko03019 | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) |
| HEJOHAOE_00306 | 8.7e-222 | - | - | - | S | ko:K03308 | - | ko00000 | Sodium:neurotransmitter symporter family |
| HEJOHAOE_00307 | 0.0 | metG | 6.1.1.10 | - | J | ko:K01874 | ko00450,ko00970,map00450,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation |
| HEJOHAOE_00308 | 5.81e-99 | tatD | - | - | L | ko:K03424 | - | ko00000,ko01000 | Hydrolase, TatD family |
| HEJOHAOE_00310 | 6.07e-70 | - | 3.4.22.70 | - | M | ko:K07284 | - | ko00000,ko01000,ko01002,ko01011 | Sortase family |
| HEJOHAOE_00312 | 1.51e-16 | - | - | - | M | - | - | - | biosynthesis protein |
| HEJOHAOE_00313 | 7.7e-42 | ywqD | - | - | D | - | - | - | Capsular exopolysaccharide family |
| HEJOHAOE_00314 | 1.31e-88 | - | 2.7.8.6 | - | M | ko:K00996 | - | ko00000,ko01000,ko01005 | sugar transferase |
| HEJOHAOE_00315 | 5.37e-133 | rfbF | 2.7.7.33 | - | JM | ko:K00978 | ko00500,ko00520,ko01100,map00500,map00520,map01100 | ko00000,ko00001,ko01000 | COG1208 Nucleoside-diphosphate-sugar pyrophosphorylase involved in lipopolysaccharide biosynthesis translation initiation factor 2B, gamma epsilon subunits (eIF-2Bgamma eIF-2Bepsilon) |
| HEJOHAOE_00316 | 2.38e-197 | - | - | - | M | - | - | - | Male sterility protein |
| HEJOHAOE_00317 | 8.63e-111 | - | - | - | GM | - | - | - | NAD dependent epimerase/dehydratase family |
| HEJOHAOE_00318 | 2.14e-99 | - | - | - | M | - | - | - | dTDP-4-dehydrorhamnose 3,5-epimerase |
| HEJOHAOE_00319 | 9.74e-62 | - | - | - | M | - | - | - | COG1442 Lipopolysaccharide biosynthesis proteins, LPS glycosyltransferases |
| HEJOHAOE_00320 | 1.05e-31 | - | - | - | M | - | - | - | Glycosyl transferase 4-like domain |
| HEJOHAOE_00321 | 3.16e-44 | - | 2.3.1.79 | - | M | ko:K00661 | - | ko00000,ko01000 | Hexapeptide repeat of succinyl-transferase |
| HEJOHAOE_00322 | 1.39e-37 | - | - | - | S | - | - | - | Polysaccharide pyruvyl transferase |
| HEJOHAOE_00323 | 1.83e-100 | - | - | - | C | - | - | - | coenzyme F420-reducing hydrogenase beta subunit |
| HEJOHAOE_00324 | 3.22e-14 | - | - | - | M | - | - | - | Glycosyl transferases group 1 |
| HEJOHAOE_00325 | 7.71e-109 | - | - | - | C | - | - | - | Coenzyme F420 hydrogenase/dehydrogenase, beta subunit N-term |
| HEJOHAOE_00326 | 1.35e-132 | rsmH | 2.1.1.199 | - | J | ko:K03438 | - | ko00000,ko01000,ko03009 | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA |
| HEJOHAOE_00327 | 3.73e-27 | mraZ | - | - | K | ko:K03925 | - | ko00000 | Belongs to the MraZ family |
| HEJOHAOE_00328 | 4.65e-131 | accA | 2.1.3.15, 6.4.1.2 | - | I | ko:K01962 | ko00061,ko00620,ko00640,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01212,map00061,map00620,map00640,map00720,map01100,map01110,map01120,map01130,map01200,map01212 | ko00000,ko00001,ko00002,ko01000 | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA |
| HEJOHAOE_00329 | 1.4e-124 | accD | 2.1.3.15, 6.4.1.2 | - | I | ko:K01963 | ko00061,ko00620,ko00640,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01212,map00061,map00620,map00640,map00720,map01100,map01110,map01120,map01130,map01200,map01212 | ko00000,ko00001,ko00002,ko01000 | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA |
| HEJOHAOE_00330 | 1.72e-216 | accC | 6.3.4.14, 6.4.1.2 | - | I | ko:K01961 | ko00061,ko00620,ko00640,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01212,map00061,map00620,map00640,map00720,map01100,map01110,map01120,map01130,map01200,map01212 | ko00000,ko00001,ko00002,ko01000 | acetyl-CoA carboxylase, biotin carboxylase |
| HEJOHAOE_00331 | 8.1e-48 | fabZ | 4.2.1.59 | - | I | ko:K02372 | ko00061,ko00780,ko01100,ko01212,map00061,map00780,map01100,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs |
| HEJOHAOE_00332 | 6.32e-28 | accB | - | - | I | ko:K02160 | ko00061,ko00620,ko00640,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01212,map00061,map00620,map00640,map00720,map01100,map01110,map01120,map01130,map01200,map01212 | ko00000,ko00001,ko00002 | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA |
| HEJOHAOE_00333 | 6.28e-187 | fabF | 2.3.1.179, 2.3.1.41 | - | I | ko:K00647,ko:K09458 | ko00061,ko00780,ko01100,ko01212,map00061,map00780,map01100,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP |
| HEJOHAOE_00334 | 5.43e-80 | fabG | 1.1.1.100 | - | IQ | ko:K00059 | ko00061,ko00333,ko00780,ko01040,ko01100,ko01130,ko01212,map00061,map00333,map00780,map01040,map01100,map01130,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | reductase |
| HEJOHAOE_00335 | 1.53e-126 | fabD | 2.3.1.39 | - | I | ko:K00645 | ko00061,ko00333,ko01100,ko01130,ko01212,map00061,map00333,map01100,map01130,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | malonyl CoA-acyl carrier protein transacylase |
| HEJOHAOE_00336 | 1.45e-136 | fabK | 1.3.1.9 | - | S | ko:K02371 | ko00061,ko01100,ko01212,map00061,map01100,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | Nitronate monooxygenase |
| HEJOHAOE_00338 | 6.83e-193 | - | 2.4.1.129, 3.4.16.4 | GT51 | M | ko:K05366 | ko00550,ko01100,ko01501,map00550,map01100,map01501 | ko00000,ko00001,ko01000,ko01003,ko01011 | penicillin-binding protein |
| HEJOHAOE_00339 | 2.23e-181 | hom | 1.1.1.3 | - | E | ko:K00003 | ko00260,ko00270,ko00300,ko01100,ko01110,ko01120,ko01130,ko01230,map00260,map00270,map00300,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | homoserine dehydrogenase |
| HEJOHAOE_00340 | 2.7e-222 | lysC | 2.7.2.4 | - | E | ko:K00928 | ko00260,ko00261,ko00270,ko00300,ko01100,ko01110,ko01120,ko01130,ko01210,ko01230,map00260,map00261,map00270,map00300,map01100,map01110,map01120,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Belongs to the aspartokinase family |
| HEJOHAOE_00341 | 1.07e-13 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00342 | 7.33e-88 | nrdG | 1.97.1.4 | - | H | ko:K04068 | - | ko00000,ko01000 | queuosine metabolic process |
| HEJOHAOE_00343 | 0.0 | nrdD | 1.1.98.6 | - | F | ko:K21636 | ko00230,ko00240,ko01100,map00230,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Ribonucleoside-triphosphate reductase |
| HEJOHAOE_00344 | 9.28e-44 | - | - | - | K | - | - | - | COG COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases |
| HEJOHAOE_00345 | 4.16e-87 | fruR | - | - | GK | ko:K03436 | - | ko00000,ko03000 | DeoR C terminal sensor domain |
| HEJOHAOE_00346 | 2.79e-118 | pfkB | 2.7.1.56 | - | H | ko:K00882 | ko00051,map00051 | ko00000,ko00001,ko01000 | Belongs to the carbohydrate kinase PfkB family. LacC subfamily |
| HEJOHAOE_00347 | 1.37e-260 | - | 2.7.1.202 | - | G | ko:K02768,ko:K02769,ko:K02770 | ko00051,ko01100,ko01120,ko02060,map00051,map01100,map01120,map02060 | ko00000,ko00001,ko00002,ko01000,ko02000 | TIGRFAM PTS system, fructose subfamily, IIC |
| HEJOHAOE_00348 | 1.1e-32 | ptsH | - | - | G | ko:K11189 | - | ko00000,ko02000 | phosphoenolpyruvate-dependent sugar phosphotransferase system |
| HEJOHAOE_00349 | 1.43e-237 | ptsP | 2.7.3.9, 2.7.9.2 | - | G | ko:K01007,ko:K08483 | ko00620,ko00680,ko00720,ko01100,ko01120,ko01200,ko02060,map00620,map00680,map00720,map01100,map01120,map01200,map02060 | ko00000,ko00001,ko00002,ko01000,ko02000 | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) |
| HEJOHAOE_00350 | 2.7e-93 | queH | 1.17.99.6 | - | C | ko:K09765 | - | ko00000,ko01000,ko03016 | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) |
| HEJOHAOE_00351 | 3.14e-46 | - | 3.1.3.18 | - | S | ko:K01091 | ko00630,ko01100,ko01110,ko01130,map00630,map01100,map01110,map01130 | ko00000,ko00001,ko01000 | haloacid dehalogenase-like hydrolase |
| HEJOHAOE_00352 | 3.31e-20 | - | 3.5.1.9 | - | S | ko:K07130 | ko00380,ko00630,ko01100,map00380,map00630,map01100 | ko00000,ko00001,ko00002,ko01000 | Putative cyclase |
| HEJOHAOE_00354 | 2.38e-309 | glyQS | 6.1.1.14 | - | J | ko:K01880 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Catalyzes the attachment of glycine to tRNA(Gly) |
| HEJOHAOE_00355 | 1.06e-205 | dapL | 2.6.1.83 | - | H | ko:K10206 | ko00300,ko01100,ko01110,ko01130,ko01230,map00300,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | Involved in the synthesis of meso-diaminopimelate (m-DAP or DL-DAP), required for both lysine and peptidoglycan biosynthesis. Catalyzes the direct conversion of tetrahydrodipicolinate to LL-diaminopimelate |
| HEJOHAOE_00356 | 2.35e-295 | pyrG | 6.3.4.2 | - | F | ko:K01937 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates |
| HEJOHAOE_00357 | 0.0 | carB | 6.3.5.5 | - | F | ko:K01955 | ko00240,ko00250,ko01100,map00240,map00250,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan |
| HEJOHAOE_00358 | 9.3e-185 | carA | 6.3.5.5 | - | F | ko:K01956 | ko00240,ko00250,ko01100,map00240,map00250,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the CarA family |
| HEJOHAOE_00359 | 5.84e-33 | - | - | - | K | ko:K22010 | - | ko00000,ko00002,ko02022 | ANTAR domain protein |
| HEJOHAOE_00360 | 2.19e-32 | - | - | - | C | - | - | - | ATP synthesis coupled proton transport |
| HEJOHAOE_00361 | 4.51e-62 | coaD | 2.7.7.3 | - | H | ko:K00954 | ko00770,ko01100,map00770,map01100 | ko00000,ko00001,ko00002,ko01000 | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate |
| HEJOHAOE_00362 | 6.67e-69 | rsmD | 2.1.1.171 | - | L | ko:K08316 | - | ko00000,ko01000,ko03009 | RNA methyltransferase, RsmD family |
| HEJOHAOE_00363 | 2.85e-272 | uvrC | - | - | L | ko:K03703 | ko03420,map03420 | ko00000,ko00001,ko03400 | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision |
| HEJOHAOE_00364 | 8.8e-48 | ptsH | - | - | G | ko:K11184,ko:K11189 | - | ko00000,ko02000 | phosphocarrier, HPr family |
| HEJOHAOE_00365 | 4.05e-125 | trmD | 2.1.1.228 | - | J | ko:K00554 | - | ko00000,ko01000,ko03016 | Belongs to the RNA methyltransferase TrmD family |
| HEJOHAOE_00366 | 3.28e-57 | rimM | - | - | J | ko:K02860 | - | ko00000,ko03009 | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes |
| HEJOHAOE_00367 | 1.04e-297 | mutS2 | - | - | L | ko:K07456 | ko03430,map03430 | ko00000,ko00001,ko03400 | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity |
| HEJOHAOE_00368 | 9.29e-81 | recO | - | - | L | ko:K03584 | ko03440,map03440 | ko00000,ko00001,ko03400 | Involved in DNA repair and RecF pathway recombination |
| HEJOHAOE_00370 | 4.69e-146 | era | - | - | S | ko:K03595 | - | ko00000,ko03009,ko03029 | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism |
| HEJOHAOE_00371 | 2.93e-11 | dgkA | 2.7.1.107, 2.7.1.66 | - | M | ko:K00887,ko:K00901 | ko00550,ko00561,ko00564,ko01100,ko01110,ko04070,ko04072,ko05231,map00550,map00561,map00564,map01100,map01110,map04070,map04072,map05231 | ko00000,ko00001,ko01000 | Diacylglycerol kinase |
| HEJOHAOE_00372 | 6.79e-82 | ybeY | 3.5.4.5 | - | S | ko:K01489,ko:K07042 | ko00240,ko00983,ko01100,map00240,map00983,map01100 | ko00000,ko00001,ko01000,ko03009 | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA |
| HEJOHAOE_00373 | 1.52e-183 | phoH | - | - | T | ko:K06217 | - | ko00000 | PhoH-like protein |
| HEJOHAOE_00374 | 1.36e-18 | - | - | - | S | ko:K09787 | - | ko00000 | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein |
| HEJOHAOE_00375 | 5.02e-219 | ffh | 3.6.5.4 | - | U | ko:K03106 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko01000,ko02044 | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY |
| HEJOHAOE_00376 | 7.63e-30 | rpsP | - | - | J | ko:K02959 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011,ko03029 | Belongs to the bacterial ribosomal protein bS16 family |
| HEJOHAOE_00377 | 2.07e-28 | ylqC | - | - | S | ko:K06960 | - | ko00000 | Belongs to the UPF0109 family |
| HEJOHAOE_00378 | 6.67e-158 | tklB | 2.2.1.1 | - | G | ko:K00615 | ko00030,ko00710,ko01051,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00030,map00710,map01051,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Transketolase, pyrimidine binding domain |
| HEJOHAOE_00379 | 2.45e-137 | tktA | 2.2.1.1 | - | G | ko:K00615 | ko00030,ko00710,ko01051,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00030,map00710,map01051,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Transketolase, thiamine diphosphate binding domain |
| HEJOHAOE_00380 | 1.31e-83 | coaX | 2.7.1.33 | - | H | ko:K03525 | ko00770,ko01100,map00770,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis |
| HEJOHAOE_00381 | 2.97e-36 | - | - | - | S | - | - | - | Pfam:DUF3816 |
| HEJOHAOE_00382 | 5.31e-72 | birA | 6.3.4.15 | - | H | ko:K03524 | ko00780,ko01100,map00780,map01100 | ko00000,ko00001,ko01000,ko03000 | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor |
| HEJOHAOE_00383 | 2.73e-11 | - | 2.7.1.176 | - | S | ko:K16214 | - | ko00000,ko01000,ko02048 | Zeta toxin |
| HEJOHAOE_00384 | 3.93e-27 | - | 2.7.1.176 | - | S | ko:K16214 | - | ko00000,ko01000,ko02048 | Zeta toxin |
| HEJOHAOE_00386 | 0.0 | purL | 6.3.5.3 | - | F | ko:K01952 | ko00230,ko01100,ko01110,ko01130,map00230,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | phosphoribosylformylglycinamidine synthase |
| HEJOHAOE_00387 | 9.24e-40 | - | - | - | S | - | - | - | Polysaccharide biosynthesis protein |
| HEJOHAOE_00389 | 8.06e-79 | rpe | 5.1.3.1 | - | G | ko:K01783 | ko00030,ko00040,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00030,map00040,map00710,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Belongs to the ribulose-phosphate 3-epimerase family |
| HEJOHAOE_00390 | 2.28e-50 | - | - | - | P | - | - | - | Heavy metal translocating P-type atpase |
| HEJOHAOE_00391 | 1.36e-102 | yacO | 2.1.1.185 | - | J | ko:K03218 | - | ko00000,ko01000,ko03009 | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family |
| HEJOHAOE_00393 | 1.9e-05 | mutT | 3.6.1.55 | - | L | ko:K03574 | - | ko00000,ko01000,ko03400 | Belongs to the NUDIX hydrolase family |
| HEJOHAOE_00394 | 8.68e-55 | - | - | - | S | - | - | - | DHHW protein |
| HEJOHAOE_00395 | 1.35e-203 | - | - | - | EK | ko:K05825 | ko00300,ko01100,ko01130,ko01210,map00300,map01100,map01130,map01210 | ko00000,ko00001,ko01000 | Aminotransferase, class I |
| HEJOHAOE_00396 | 1.18e-182 | trpS | 6.1.1.2 | - | J | ko:K01867 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Tryptophanyl-tRNA synthetase |
| HEJOHAOE_00397 | 3.22e-45 | - | 2.4.1.109 | GT39 | M | ko:K00728 | ko00514,ko00515,ko01100,map00514,map00515,map01100 | ko00000,ko00001,ko01000,ko01003 | PFAM glycosyl transferase family 39 |
| HEJOHAOE_00398 | 1.21e-174 | - | - | - | V | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00399 | 3.72e-121 | - | - | - | S | - | - | - | protein conserved in bacteria |
| HEJOHAOE_00400 | 1.2e-175 | uraA | - | - | F | ko:K02824 | - | ko00000,ko02000 | Psort location CytoplasmicMembrane, score 10.00 |
| HEJOHAOE_00401 | 1.26e-249 | ilvB | 2.2.1.6 | - | H | ko:K01652 | ko00290,ko00650,ko00660,ko00770,ko01100,ko01110,ko01130,ko01210,ko01230,map00290,map00650,map00660,map00770,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | acetolactate synthase large subunit |
| HEJOHAOE_00402 | 2.04e-53 | mtnN | 3.2.2.9 | - | F | ko:K01243 | ko00270,ko01100,ko01230,map00270,map01100,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively |
| HEJOHAOE_00403 | 3.28e-62 | rsmE | 2.1.1.193 | - | J | ko:K09761 | - | ko00000,ko01000,ko03009 | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit |
| HEJOHAOE_00404 | 1.21e-42 | cinA | 3.5.1.42 | - | S | ko:K03742,ko:K03743 | ko00760,map00760 | ko00000,ko00001,ko01000 | Belongs to the CinA family |
| HEJOHAOE_00405 | 8.98e-213 | malQ | 2.4.1.25 | GH77 | G | ko:K00705 | ko00500,ko01100,map00500,map01100 | ko00000,ko00001,ko01000 | 4-alpha-glucanotransferase |
| HEJOHAOE_00406 | 0.0 | glgP | 2.4.1.1 | GT35 | G | ko:K00688 | ko00500,ko01100,ko01110,ko02026,ko04217,ko04910,ko04922,ko04931,map00500,map01100,map01110,map02026,map04217,map04910,map04922,map04931 | ko00000,ko00001,ko01000 | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
| HEJOHAOE_00407 | 6.36e-131 | metF | 1.5.1.20 | - | E | ko:K00297 | ko00670,ko00720,ko01100,ko01120,ko01200,ko01523,map00670,map00720,map01100,map01120,map01200,map01523 | ko00000,ko00001,ko00002,ko01000 | 5,10-methylenetetrahydrofolate reductase |
| HEJOHAOE_00408 | 2.97e-64 | metH2 | 2.1.1.13 | - | E | ko:K00548 | ko00270,ko00450,ko00670,ko01100,ko01110,ko01230,map00270,map00450,map00670,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | NOG21937 non supervised orthologous group |
| HEJOHAOE_00409 | 0.0 | metH | 2.1.1.13 | - | E | ko:K00548 | ko00270,ko00450,ko00670,ko01100,ko01110,ko01230,map00270,map00450,map00670,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Psort location Cytoplasmic, score |
| HEJOHAOE_00410 | 1.45e-13 | - | - | - | S | - | - | - | COG NOG18757 non supervised orthologous group |
| HEJOHAOE_00411 | 1.82e-202 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00412 | 1.22e-150 | - | - | - | C | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00413 | 2.82e-30 | - | - | - | K | ko:K07729 | - | ko00000,ko03000 | Cro/C1-type HTH DNA-binding domain |
| HEJOHAOE_00415 | 3.41e-27 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00416 | 5.8e-14 | - | - | - | S | - | - | - | YgiT-type zinc finger domain protein |
| HEJOHAOE_00417 | 8.64e-26 | - | - | - | S | - | - | - | Domain of unknown function (DUF4258) |
| HEJOHAOE_00419 | 1.5e-62 | rimP | - | - | S | ko:K09748 | - | ko00000,ko03009 | Required for maturation of 30S ribosomal subunits |
| HEJOHAOE_00420 | 3.93e-153 | nusA | - | - | K | ko:K02600 | - | ko00000,ko03009,ko03021 | Participates in both transcription termination and antitermination |
| HEJOHAOE_00421 | 9.52e-35 | ylxR | - | - | K | ko:K02600,ko:K07742 | - | ko00000,ko03009,ko03021 | Nucleic-acid-binding protein implicated in transcription termination |
| HEJOHAOE_00422 | 1.54e-13 | ylxQ | - | - | J | - | - | - | ribosomal protein |
| HEJOHAOE_00423 | 0.0 | infB | - | - | J | ko:K02519 | - | ko00000,ko03012,ko03029 | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex |
| HEJOHAOE_00424 | 8.87e-54 | rbfA | - | - | J | ko:K02834 | - | ko00000,ko03009 | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA |
| HEJOHAOE_00425 | 6.57e-98 | nrnA | 3.1.13.3, 3.1.3.7 | - | S | ko:K06881 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko01000,ko03400 | domain protein |
| HEJOHAOE_00426 | 1.24e-102 | truB | 5.4.99.25 | - | J | ko:K03177,ko:K03483 | - | ko00000,ko01000,ko03000,ko03016 | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs |
| HEJOHAOE_00428 | 1.58e-129 | mrp | - | - | D | - | - | - | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP |
| HEJOHAOE_00431 | 2.53e-37 | - | - | - | K | - | - | - | sequence-specific DNA binding |
| HEJOHAOE_00432 | 2.55e-91 | - | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | AAA domain, putative AbiEii toxin, Type IV TA system |
| HEJOHAOE_00433 | 2.02e-92 | - | - | - | S | ko:K01992 | - | ko00000,ko00002,ko02000 | ABC-2 type transporter |
| HEJOHAOE_00434 | 7.68e-68 | - | - | - | S | - | - | - | Protein of unknown function (DUF1624) |
| HEJOHAOE_00435 | 6.77e-254 | - | - | - | L | - | - | - | Domain of unknown function (DUF4368) |
| HEJOHAOE_00438 | 0.0 | mcrB | - | - | V | ko:K07452 | - | ko00000,ko01000,ko02048 | ATPase family associated with various cellular activities (AAA) |
| HEJOHAOE_00439 | 2.56e-171 | mcrC | - | - | V | ko:K19147 | - | ko00000,ko02048 | Psort location Cytoplasmic, score |
| HEJOHAOE_00440 | 9.97e-124 | - | - | - | L | - | - | - | Reverse transcriptase (RNA-dependent DNA polymerase) |
| HEJOHAOE_00442 | 5.33e-12 | - | - | - | KT | - | - | - | Sensory domain found in PocR |
| HEJOHAOE_00443 | 3.85e-59 | - | - | - | T | - | - | - | Transcriptional regulatory protein, C terminal |
| HEJOHAOE_00444 | 4.03e-50 | - | - | - | S | - | - | - | Domain in cystathionine beta-synthase and other proteins. |
| HEJOHAOE_00446 | 6.17e-85 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00447 | 2.09e-19 | mprF | - | - | S | ko:K07027 | - | ko00000,ko02000 | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms |
| HEJOHAOE_00448 | 0.0 | hcp | 1.7.99.1 | - | C | ko:K05601 | ko00910,map00910 | ko00000,ko00001,ko01000 | Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O |
| HEJOHAOE_00449 | 3.35e-06 | - | - | - | L | - | - | - | Staphylococcal nuclease homologues |
| HEJOHAOE_00450 | 1.66e-63 | - | - | - | S | ko:K01992 | - | ko00000,ko00002,ko02000 | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00451 | 2.26e-130 | - | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | ABC transporter |
| HEJOHAOE_00452 | 7.81e-93 | - | - | - | S | ko:K11068 | - | ko00000,ko02042 | protein, hemolysin III |
| HEJOHAOE_00453 | 1.74e-221 | - | - | - | P | ko:K03324 | - | ko00000,ko02000 | Na Pi-cotransporter |
| HEJOHAOE_00454 | 5.49e-118 | phoR | 2.7.13.3 | - | T | ko:K07636 | ko02020,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko02022 | Histidine kinase |
| HEJOHAOE_00455 | 9.62e-87 | - | - | - | KT | ko:K07658 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | Psort location Cytoplasmic, score 9.98 |
| HEJOHAOE_00456 | 2.96e-53 | phoU | - | - | P | ko:K02039 | - | ko00000 | Plays a role in the regulation of phosphate uptake |
| HEJOHAOE_00457 | 2.61e-146 | pstB | 3.6.3.27 | - | P | ko:K02036 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system |
| HEJOHAOE_00458 | 2.69e-124 | pstA | - | - | P | ko:K02038 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | phosphate transport system permease |
| HEJOHAOE_00459 | 1.97e-134 | pstC | - | - | P | ko:K02037 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | probably responsible for the translocation of the substrate across the membrane |
| HEJOHAOE_00460 | 6.84e-88 | pstS | - | - | P | ko:K02040 | ko02010,ko02020,ko05152,map02010,map02020,map05152 | ko00000,ko00001,ko00002,ko02000 | PBP superfamily domain |
| HEJOHAOE_00461 | 1.09e-295 | trpB | 4.2.1.20 | - | E | ko:K06001 | ko00260,ko00400,ko01100,ko01110,ko01130,ko01230,map00260,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine |
| HEJOHAOE_00463 | 9.48e-223 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | - | J | ko:K01876,ko:K02434 | ko00970,ko01100,map00970,map01100 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) |
| HEJOHAOE_00464 | 1.87e-245 | gatA | 6.3.5.6, 6.3.5.7 | - | J | ko:K02433 | ko00970,ko01100,map00970,map01100 | ko00000,ko00001,ko01000,ko03029 | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) |
| HEJOHAOE_00465 | 4.68e-08 | gatC | 6.3.5.6, 6.3.5.7 | - | J | ko:K02435 | ko00970,ko01100,map00970,map01100 | ko00000,ko00001,ko01000,ko03029 | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) |
| HEJOHAOE_00466 | 1.86e-315 | aspS | 6.1.1.12 | - | J | ko:K01876 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) |
| HEJOHAOE_00467 | 1.05e-162 | - | - | - | V | ko:K02004 | - | ko00000,ko00002,ko02000 | Permease |
| HEJOHAOE_00468 | 4.23e-116 | - | - | - | V | ko:K02003 | - | ko00000,ko00002,ko02000 | ABC-type antimicrobial peptide transport system, ATPase component |
| HEJOHAOE_00469 | 8.79e-107 | udgA | 3.2.2.27 | - | L | ko:K21929 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | Uracil-DNA glycosylase |
| HEJOHAOE_00470 | 4.62e-96 | - | 2.3.1.8 | - | Q | ko:K15024 | ko00430,ko00620,ko00640,ko00720,ko01100,ko01120,ko01200,map00430,map00620,map00640,map00720,map01100,map01120,map01200 | ko00000,ko00001,ko00002,ko01000 | Involved in 1,2-propanediol (1,2-PD) degradation by catalyzing the conversion of propanoyl-CoA to propanoyl-phosphate |
| HEJOHAOE_00471 | 3.07e-20 | - | - | - | S | - | - | - | esterase |
| HEJOHAOE_00472 | 2.05e-11 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00474 | 7.1e-87 | - | - | - | O | - | - | - | restriction endodeoxyribonuclease activity |
| HEJOHAOE_00475 | 0.0 | pckA | 4.1.1.49 | - | H | ko:K01610 | ko00010,ko00020,ko00620,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,map00010,map00020,map00620,map00710,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA |
| HEJOHAOE_00476 | 1.03e-42 | rplL | - | - | J | ko:K02935 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation |
| HEJOHAOE_00477 | 2.2e-44 | rplJ | - | - | J | ko:K02864 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors |
| HEJOHAOE_00478 | 8.24e-136 | rplA | - | - | J | ko:K02863 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release |
| HEJOHAOE_00479 | 2.78e-83 | rplK | - | - | J | ko:K02867 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors |
| HEJOHAOE_00480 | 1.65e-84 | nusG | - | - | K | ko:K02601 | - | ko00000,ko03009,ko03021 | Participates in transcription elongation, termination and antitermination |
| HEJOHAOE_00481 | 0.000225 | secE | - | - | U | ko:K03073 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation |
| HEJOHAOE_00482 | 6.59e-26 | rpmG | - | - | J | ko:K02913 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bL33 family |
| HEJOHAOE_00483 | 1.68e-55 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00484 | 3.74e-87 | murI | 5.1.1.3 | - | M | ko:K01776 | ko00471,ko01100,map00471,map01100 | ko00000,ko00001,ko01000,ko01011 | Provides the (R)-glutamate required for cell wall biosynthesis |
| HEJOHAOE_00485 | 4.73e-12 | - | - | - | S | - | - | - | Domain of unknown function (DUF1934) |
| HEJOHAOE_00486 | 7.23e-278 | argS | 6.1.1.19 | - | J | ko:K01887 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Arginyl tRNA synthetase N terminal dom |
| HEJOHAOE_00488 | 1.16e-36 | xseA | 3.1.11.6 | - | L | ko:K03601 | ko03430,map03430 | ko00000,ko00001,ko01000,ko03400 | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides |
| HEJOHAOE_00489 | 0.0 | dnaE | 2.7.7.7 | - | L | ko:K02337 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | DNA polymerase |
| HEJOHAOE_00490 | 1.46e-135 | - | - | - | S | ko:K01989 | - | ko00000,ko00002,ko02000 | ABC transporter |
| HEJOHAOE_00491 | 1.07e-131 | - | - | - | S | ko:K05832 | - | ko00000,ko00002,ko02000 | Belongs to the binding-protein-dependent transport system permease family |
| HEJOHAOE_00492 | 4.81e-134 | - | - | - | S | ko:K05833 | - | ko00000,ko00002,ko02000 | Abc transporter |
| HEJOHAOE_00493 | 1.38e-55 | - | - | - | M | - | - | - | GtrA-like protein |
| HEJOHAOE_00494 | 3.15e-192 | - | 3.2.1.1 | GH13 | G | ko:K01176 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | Starch-binding module 26 |
| HEJOHAOE_00496 | 1.09e-59 | - | - | - | G | - | - | - | Belongs to the glycosyl hydrolase 13 family |
| HEJOHAOE_00497 | 7.44e-126 | hisF | - | - | E | ko:K02500 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit |
| HEJOHAOE_00498 | 1.23e-98 | hisH | - | - | E | ko:K02501 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR |
| HEJOHAOE_00499 | 2.23e-127 | - | - | - | K | - | - | - | transcriptional regulator RpiR family |
| HEJOHAOE_00500 | 8.88e-173 | - | - | - | S | ko:K07007 | - | ko00000 | HI0933-like protein |
| HEJOHAOE_00501 | 8.2e-67 | cmk | 2.7.4.25 | - | F | ko:K00945 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the cytidylate kinase family. Type 1 subfamily |
| HEJOHAOE_00502 | 6.61e-22 | plsC | 2.3.1.51 | - | I | ko:K00655 | ko00561,ko00564,ko01100,ko01110,map00561,map00564,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko01004 | Acyltransferase |
| HEJOHAOE_00503 | 9.78e-280 | ispH | 1.17.7.4, 2.7.4.25 | - | J | ko:K00945,ko:K02945,ko:K03527 | ko00240,ko00900,ko01100,ko01110,ko01130,ko03010,map00240,map00900,map01100,map01110,map01130,map03010 | br01610,ko00000,ko00001,ko00002,ko01000,ko03011 | Ribosomal protein S1 |
| HEJOHAOE_00505 | 8.62e-129 | yebC | - | - | K | - | - | - | Transcriptional regulatory protein |
| HEJOHAOE_00506 | 2.26e-118 | yicC | - | - | S | ko:K03316 | - | ko00000 | Domain of unknown function (DUF1732) |
| HEJOHAOE_00507 | 3.99e-25 | NPD7_560 | - | - | S | ko:K09777 | - | ko00000 | Belongs to the UPF0296 family |
| HEJOHAOE_00508 | 1.22e-50 | gmk | 2.7.4.8 | - | F | ko:K00942 | ko00230,ko01100,map00230,map01100 | ko00000,ko00001,ko00002,ko01000 | Essential for recycling GMP and indirectly, cGMP |
| HEJOHAOE_00510 | 0.0 | priA | - | - | L | ko:K04066 | ko03440,map03440 | ko00000,ko00001,ko01000,ko03400 | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA |
| HEJOHAOE_00511 | 7.72e-61 | def | 3.5.1.88 | - | J | ko:K01462 | - | ko00000,ko01000 | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions |
| HEJOHAOE_00512 | 3.52e-96 | fmt | 2.1.2.9 | - | J | ko:K00604 | ko00670,ko00970,map00670,map00970 | ko00000,ko00001,ko01000 | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus |
| HEJOHAOE_00513 | 1.85e-74 | yugP | - | - | S | ko:K06973 | - | ko00000 | zinc metallopeptidase |
| HEJOHAOE_00514 | 4.6e-109 | sun | 2.1.1.176 | - | J | ko:K03500 | - | ko00000,ko01000,ko03009 | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA |
| HEJOHAOE_00515 | 1.47e-154 | rlmN | 2.1.1.192 | - | J | ko:K06941 | - | ko00000,ko01000,ko03009 | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs |
| HEJOHAOE_00516 | 3.5e-41 | - | 3.1.3.16 | - | T | ko:K20074 | - | ko00000,ko01000,ko01009 | Serine/threonine phosphatases, family 2C, catalytic domain |
| HEJOHAOE_00517 | 8.34e-218 | prkC | 2.7.11.1 | - | KLT | ko:K12132 | - | ko00000,ko01000,ko01001 | serine threonine protein kinase |
| HEJOHAOE_00518 | 2.06e-114 | rsgA | 3.1.3.100 | - | S | ko:K06949 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko01000,ko03009 | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit |
| HEJOHAOE_00519 | 8.17e-24 | thiN | 2.7.6.2 | - | H | ko:K00949 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko01000 | thiamine pyrophosphokinase |
| HEJOHAOE_00521 | 9.68e-106 | - | 2.7.11.1 | - | KLT | ko:K12132 | - | ko00000,ko01000,ko01001 | PASTA domain protein |
| HEJOHAOE_00522 | 6.1e-40 | groS | - | - | O | ko:K04078 | - | ko00000,ko03029,ko03110 | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter |
| HEJOHAOE_00523 | 2.67e-297 | groL | - | - | O | ko:K04077 | ko03018,ko04212,ko04940,ko05134,ko05152,map03018,map04212,map04940,map05134,map05152 | ko00000,ko00001,ko03019,ko03029,ko03110,ko04147 | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions |
| HEJOHAOE_00524 | 1.15e-18 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00525 | 4.47e-24 | - | - | - | U | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00526 | 1.39e-54 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00527 | 6.08e-36 | - | - | - | S | - | - | - | EDD domain protein, DegV family |
| HEJOHAOE_00528 | 5.56e-35 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00529 | 2.16e-130 | gpsA | 1.1.1.94 | - | I | ko:K00057 | ko00564,ko01110,map00564,map01110 | ko00000,ko00001,ko01000 | Glycerol-3-phosphate dehydrogenase |
| HEJOHAOE_00530 | 1.01e-281 | leuA | 2.3.3.13 | - | E | ko:K01649 | ko00290,ko00620,ko01100,ko01110,ko01210,ko01230,map00290,map00620,map01100,map01110,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) |
| HEJOHAOE_00531 | 5.17e-197 | - | - | - | S | - | - | - | Domain of unknown function (DUF4143) |
| HEJOHAOE_00532 | 5.28e-28 | - | - | - | S | - | - | - | Small, acid-soluble spore proteins, alpha/beta type |
| HEJOHAOE_00533 | 1.14e-26 | - | 2.7.7.49 | - | L | ko:K00986 | - | ko00000,ko01000 | DNA polymerase |
| HEJOHAOE_00535 | 8.11e-196 | - | - | - | L | - | - | - | Phage integrase, N-terminal SAM-like domain |
| HEJOHAOE_00536 | 2.23e-50 | - | 3.1.21.3 | - | V | ko:K01154 | - | ko00000,ko01000,ko02048 | Type I restriction modification DNA specificity domain |
| HEJOHAOE_00537 | 5.74e-96 | - | 3.1.21.3 | - | V | ko:K01154 | - | ko00000,ko01000,ko02048 | Type I restriction |
| HEJOHAOE_00538 | 2.91e-279 | hsdM | 2.1.1.72 | - | V | ko:K03427 | - | ko00000,ko01000,ko02048 | HsdM N-terminal domain |
| HEJOHAOE_00539 | 0.0 | - | 3.1.21.3 | - | L | ko:K01153 | - | ko00000,ko01000,ko02048 | Subunit R is required for both nuclease and ATPase activities, but not for modification |
| HEJOHAOE_00540 | 3.26e-67 | mcrC | - | - | V | ko:K19147 | - | ko00000,ko02048 | McrBC 5-methylcytosine restriction system component |
| HEJOHAOE_00542 | 2.12e-130 | - | - | - | L | - | - | - | Transposase |
| HEJOHAOE_00543 | 1.7e-229 | recQ | 3.6.4.12 | - | L | ko:K03654 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03400 | ATP-dependent DNA helicase RecQ |
| HEJOHAOE_00544 | 2.25e-222 | - | - | - | K | - | - | - | Putative DNA-binding domain |
| HEJOHAOE_00545 | 2.31e-23 | - | - | - | S | - | - | - | Small, acid-soluble spore proteins, alpha/beta type |
| HEJOHAOE_00546 | 4.54e-85 | - | - | - | S | ko:K01421 | - | ko00000 | Psort location Cellwall, score |
| HEJOHAOE_00547 | 2.37e-316 | - | - | - | S | ko:K07003 | - | ko00000 | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00548 | 2.1e-59 | - | - | - | K | - | - | - | Bacterial regulatory proteins, tetR family |
| HEJOHAOE_00549 | 1.34e-18 | - | - | - | H | - | - | - | 4'-phosphopantetheinyl transferase superfamily |
| HEJOHAOE_00550 | 9.24e-83 | comEB | 3.5.4.12 | - | F | ko:K01493 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000,ko02044 | MafB19-like deaminase |
| HEJOHAOE_00552 | 3.69e-57 | spmA | - | - | S | ko:K06373 | - | ko00000 | membrane protein required for spore maturation |
| HEJOHAOE_00553 | 7.4e-43 | spmB | - | - | S | ko:K06374 | - | ko00000 | PFAM nucleoside recognition domain protein |
| HEJOHAOE_00554 | 9.06e-106 | cas3 | - | - | L | ko:K07012 | - | ko00000,ko01000,ko02048 | DEAD-like helicases superfamily |
| HEJOHAOE_00556 | 7.04e-210 | ychF | - | - | J | ko:K06942 | - | ko00000,ko03009 | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner |
| HEJOHAOE_00557 | 4.59e-18 | - | - | - | S | - | - | - | PFAM thioesterase superfamily |
| HEJOHAOE_00558 | 2.91e-39 | nt5e | 3.1.3.18 | - | S | ko:K01091 | ko00630,ko01100,ko01110,ko01130,map00630,map01100,map01110,map01130 | ko00000,ko00001,ko01000 | HAD-hyrolase-like |
| HEJOHAOE_00560 | 6.25e-70 | rsuA | 5.4.99.19 | - | J | ko:K06183 | - | ko00000,ko01000,ko03009 | Belongs to the pseudouridine synthase RsuA family |
| HEJOHAOE_00561 | 7.65e-205 | msmX | - | - | E | ko:K10112 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| HEJOHAOE_00562 | 6.44e-216 | - | - | - | KT | ko:K02647 | - | ko00000,ko03000 | Psort location Cytoplasmic, score |
| HEJOHAOE_00563 | 3.68e-97 | ftsE | - | - | D | ko:K09812 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000,ko03036 | cell division ATP-binding protein FtsE |
| HEJOHAOE_00564 | 2.89e-89 | ftsX | - | - | D | ko:K09811,ko:K09812 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000,ko03036 | cell division |
| HEJOHAOE_00565 | 2.69e-53 | - | - | - | D | ko:K21471 | - | ko00000,ko01000,ko01002,ko01011 | Peptidase, M23 |
| HEJOHAOE_00567 | 8.5e-50 | greA | - | - | K | ko:K03624,ko:K06140 | - | ko00000,ko03000,ko03021 | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides |
| HEJOHAOE_00568 | 0.0 | lysS | 6.1.1.6 | - | J | ko:K04567 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Belongs to the class-II aminoacyl-tRNA synthetase family |
| HEJOHAOE_00569 | 1.23e-296 | - | - | - | V | - | - | - | MATE efflux family protein |
| HEJOHAOE_00571 | 0.0 | gyrA | 5.99.1.3 | - | L | ko:K02469 | - | ko00000,ko01000,ko03032,ko03400 | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner |
| HEJOHAOE_00572 | 3.11e-30 | yneP | - | - | S | ko:K07107 | - | ko00000,ko01000 | Acyl-ACP thioesterase |
| HEJOHAOE_00573 | 0.0 | gyrB | 5.99.1.3 | - | L | ko:K02470 | - | ko00000,ko01000,ko03032,ko03400 | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner |
| HEJOHAOE_00575 | 1.93e-32 | - | - | - | S | - | - | - | Domain of unknown function (DUF370) |
| HEJOHAOE_00576 | 2.25e-113 | recF | - | - | L | ko:K03629,ko:K07459 | ko03440,map03440 | ko00000,ko00001,ko03400 | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP |
| HEJOHAOE_00577 | 2.99e-25 | - | - | - | S | ko:K14761 | - | ko00000,ko03009 | S4 domain |
| HEJOHAOE_00578 | 2.03e-135 | dnaN | 2.7.7.7 | - | L | ko:K02338 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria |
| HEJOHAOE_00579 | 7.82e-191 | dnaA | - | - | L | ko:K02313 | ko02020,ko04112,map02020,map04112 | ko00000,ko00001,ko03032,ko03036 | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids |
| HEJOHAOE_00580 | 9.02e-18 | rpmH | - | - | J | ko:K02914 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bL34 family |
| HEJOHAOE_00581 | 2.79e-12 | rnpA | 3.1.26.5 | - | J | ko:K03536 | - | ko00000,ko01000,ko03016 | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme |
| HEJOHAOE_00582 | 6.83e-26 | - | - | - | S | ko:K08998 | - | ko00000 | Could be involved in insertion of integral membrane proteins into the membrane |
| HEJOHAOE_00583 | 2.73e-15 | - | - | - | M | ko:K03217 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044,ko03029 | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase |
| HEJOHAOE_00584 | 1.91e-92 | jag | - | - | S | ko:K06346 | - | ko00000 | R3H domain protein |
| HEJOHAOE_00585 | 1.36e-196 | mnmE | - | - | S | ko:K03650 | - | ko00000,ko01000,ko03016 | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 |
| HEJOHAOE_00586 | 0.0 | gidA | - | - | D | ko:K03495 | - | ko00000,ko03016,ko03036 | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 |
| HEJOHAOE_00587 | 1.81e-81 | rsmG | 2.1.1.170 | - | J | ko:K03501 | - | ko00000,ko01000,ko03009,ko03036 | Specifically methylates the N7 position of a guanine in 16S rRNA |
| HEJOHAOE_00588 | 4.63e-95 | noc | - | - | K | ko:K03497 | - | ko00000,ko03000,ko03036,ko04812 | Belongs to the ParB family |
| HEJOHAOE_00589 | 1.06e-123 | soj | - | - | D | ko:K03496 | - | ko00000,ko03036,ko04812 | CobQ CobB MinD ParA nucleotide binding domain |
| HEJOHAOE_00590 | 3.93e-106 | spo0J | - | - | K | ko:K03497 | - | ko00000,ko03000,ko03036,ko04812 | Belongs to the ParB family |
| HEJOHAOE_00591 | 1.01e-266 | serS | 6.1.1.11 | - | J | ko:K01875 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) |
| HEJOHAOE_00592 | 1.89e-23 | - | - | - | S | - | - | - | Domain of unknown function (DUF4234) |
| HEJOHAOE_00593 | 6.95e-30 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00595 | 4.52e-223 | - | 6.2.1.1 | - | I | ko:K01895 | ko00010,ko00620,ko00640,ko00680,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,map00010,map00620,map00640,map00680,map00720,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000,ko01004 | AMP-dependent synthetase and ligase |
| HEJOHAOE_00596 | 9.75e-124 | ddl | 6.3.2.4 | - | F | ko:K01921 | ko00473,ko00550,ko01100,ko01502,map00473,map00550,map01100,map01502 | ko00000,ko00001,ko01000,ko01011 | Belongs to the D-alanine--D-alanine ligase family |
| HEJOHAOE_00597 | 6.73e-145 | murF | 6.3.2.10 | - | M | ko:K01929 | ko00300,ko00550,ko01100,ko01502,map00300,map00550,map01100,map01502 | ko00000,ko00001,ko01000,ko01011 | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein |
| HEJOHAOE_00598 | 1.71e-214 | trpE | 4.1.3.27 | - | EH | ko:K01657 | ko00400,ko00405,ko01100,ko01110,ko01130,ko01230,ko02024,ko02025,map00400,map00405,map01100,map01110,map01130,map01230,map02024,map02025 | ko00000,ko00001,ko00002,ko01000 | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia |
| HEJOHAOE_00599 | 3.48e-90 | trpG | 4.1.3.27 | - | EH | ko:K01658 | ko00400,ko00405,ko01100,ko01110,ko01130,ko01230,ko02024,ko02025,map00400,map00405,map01100,map01110,map01130,map01230,map02024,map02025 | ko00000,ko00001,ko00002,ko01000 | Glutamine amidotransferase of anthranilate synthase |
| HEJOHAOE_00600 | 3e-134 | trpD | 2.4.2.18, 4.1.3.27 | - | F | ko:K00766,ko:K13497 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) |
| HEJOHAOE_00601 | 1.6e-105 | trpC | 4.1.1.48 | - | E | ko:K01609 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Belongs to the TrpC family |
| HEJOHAOE_00602 | 6.75e-242 | trpB | 4.2.1.20 | - | E | ko:K01696 | ko00260,ko00400,ko01100,ko01110,ko01130,ko01230,map00260,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine |
| HEJOHAOE_00603 | 2.22e-123 | trpA | 4.2.1.20 | - | E | ko:K01695 | ko00260,ko00400,ko01100,ko01110,ko01130,ko01230,map00260,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate |
| HEJOHAOE_00604 | 3.03e-130 | cobB | - | - | K | ko:K12410 | - | ko00000,ko01000 | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form |
| HEJOHAOE_00605 | 1.37e-25 | rpsT | - | - | J | ko:K02968 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds directly to 16S ribosomal RNA |
| HEJOHAOE_00607 | 4.71e-17 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00608 | 1.11e-49 | - | - | - | S | ko:K18475 | - | ko00000,ko01000,ko02035 | N-methylation of lysine residues in flagellin K00599 |
| HEJOHAOE_00609 | 4.03e-136 | - | - | - | T | - | - | - | ATPase histidine kinase DNA gyrase B HSP90 domain protein |
| HEJOHAOE_00610 | 4.07e-126 | - | - | - | K | ko:K07775 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | response regulator receiver |
| HEJOHAOE_00611 | 7.13e-144 | - | 4.2.1.2 | - | C | ko:K01677 | ko00020,ko00620,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,map00020,map00620,map00720,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | Hydrolyase, tartrate alpha subunit fumarate domain protein, Fe-S type |
| HEJOHAOE_00612 | 2.29e-94 | fumB | 4.2.1.2 | - | C | ko:K01678 | ko00020,ko00620,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,map00020,map00620,map00720,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | Hydrolyase, tartrate beta subunit fumarate domain protein, Fe-S type |
| HEJOHAOE_00613 | 2.11e-43 | - | - | - | S | - | - | - | GtrA-like protein |
| HEJOHAOE_00614 | 1.83e-130 | - | - | GT2 | M | ko:K20534 | - | ko00000,ko01000,ko01005,ko02000 | Glycosyltransferase like family 2 |
| HEJOHAOE_00615 | 1.67e-30 | ftsW | - | - | D | ko:K03588 | ko04112,map04112 | ko00000,ko00001,ko02000,ko03036 | Belongs to the SEDS family |
| HEJOHAOE_00616 | 6.72e-152 | - | - | - | M | ko:K05364 | ko00550,map00550 | ko00000,ko00001,ko01011 | penicillin binding |
| HEJOHAOE_00617 | 0.0 | secA | - | - | U | ko:K03070 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane |
| HEJOHAOE_00618 | 2.04e-28 | - | - | - | S | - | - | - | Domain of unknown function (DUF3783) |
| HEJOHAOE_00619 | 0.0 | lepA | - | - | M | ko:K03596 | ko05134,map05134 | ko00000,ko00001 | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner |
| HEJOHAOE_00620 | 8.4e-53 | - | - | - | S | - | - | - | TIGRFAM C_GCAxxG_C_C family |
| HEJOHAOE_00621 | 0.0 | asnB | 6.3.5.4 | - | E | ko:K01953 | ko00250,ko01100,ko01110,map00250,map01100,map01110 | ko00000,ko00001,ko01000,ko01002 | Asparagine synthase |
| HEJOHAOE_00622 | 1.45e-264 | - | 3.6.4.12 | - | K | ko:K03655 | ko03440,map03440 | ko00000,ko00001,ko01000,ko03400 | Putative DNA-binding domain |
| HEJOHAOE_00623 | 5.44e-105 | - | 3.4.19.11 | - | EM | ko:K01308 | - | ko00000,ko01000,ko01002 | Carboxypeptidase |
| HEJOHAOE_00624 | 2.84e-84 | nudF | 3.6.1.13 | - | L | ko:K01515 | ko00230,map00230 | ko00000,ko00001,ko01000 | Psort location Cytoplasmic, score |
| HEJOHAOE_00625 | 1.64e-90 | ribF | 2.7.1.26, 2.7.7.2 | - | H | ko:K11753 | ko00740,ko01100,ko01110,map00740,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Belongs to the ribF family |
| HEJOHAOE_00626 | 5.44e-58 | - | - | - | V | - | - | - | Abi-like protein |
| HEJOHAOE_00627 | 6.37e-79 | - | - | - | S | - | - | - | Domain of unknown function (DUF4037) |
| HEJOHAOE_00628 | 1.37e-106 | - | - | - | V | ko:K03327 | - | ko00000,ko02000 | MatE |
| HEJOHAOE_00629 | 1.6e-65 | yvdD | 3.2.2.10 | - | S | ko:K06966 | ko00230,ko00240,map00230,map00240 | ko00000,ko00001,ko01000 | Belongs to the LOG family |
| HEJOHAOE_00630 | 9.26e-17 | - | - | - | S | - | - | - | Psort location |
| HEJOHAOE_00632 | 1.78e-40 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00634 | 7.73e-30 | - | 3.4.21.89 | - | U | ko:K13280 | ko03060,map03060 | ko00000,ko00001,ko01000,ko01002 | Peptidase S24-like |
| HEJOHAOE_00635 | 4.81e-180 | - | - | - | V | - | - | - | ATPase associated with various cellular activities |
| HEJOHAOE_00642 | 1.46e-73 | - | - | - | Q | - | - | - | haloacid dehalogenase |
| HEJOHAOE_00643 | 3.4e-276 | - | - | - | G | - | - | - | Alpha amylase, catalytic domain |
| HEJOHAOE_00644 | 7.28e-211 | - | 2.3.3.1 | - | C | ko:K01647 | ko00020,ko00630,ko01100,ko01110,ko01120,ko01130,ko01200,ko01210,ko01230,map00020,map00630,map01100,map01110,map01120,map01130,map01200,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | Citrate synthase, C-terminal domain |
| HEJOHAOE_00645 | 1.35e-136 | - | - | - | K | - | - | - | Putative zinc ribbon domain |
| HEJOHAOE_00646 | 3.06e-38 | spoVAC | - | - | S | ko:K06405 | - | ko00000 | stage V sporulation protein AC |
| HEJOHAOE_00647 | 3.78e-135 | - | 2.8.1.7 | - | E | ko:K04487 | ko00730,ko01100,ko04122,map00730,map01100,map04122 | ko00000,ko00001,ko01000,ko02048,ko03016,ko03029 | Master enzyme that delivers sulfur to a number of partners involved in Fe-S cluster assembly, tRNA modification or cofactor biosynthesis. Catalyzes the removal of elemental sulfur atoms from cysteine to produce alanine. Functions as a sulfur delivery protein for Fe-S cluster synthesis onto IscU, an Fe-S scaffold assembly protein, as well as other S acceptor proteins |
| HEJOHAOE_00648 | 1.23e-164 | - | - | - | S | - | - | - | Bacterial membrane protein YfhO |
| HEJOHAOE_00649 | 6.59e-48 | spoVAE | - | - | S | ko:K06407 | - | ko00000 | SpoVAC/SpoVAEB sporulation membrane protein |
| HEJOHAOE_00650 | 3.32e-127 | - | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | ABC-type multidrug transport system ATPase component |
| HEJOHAOE_00651 | 9.02e-23 | - | - | - | S | ko:K01992 | - | ko00000,ko00002,ko02000 | ABC-2 family transporter protein |
| HEJOHAOE_00652 | 1.18e-92 | - | - | - | N | - | - | - | ABC-type uncharacterized transport system |
| HEJOHAOE_00654 | 7.57e-38 | - | - | - | KT | - | - | - | LytTr DNA-binding domain |
| HEJOHAOE_00655 | 1.4e-114 | upp | 2.4.2.9 | - | F | ko:K00761 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko01000 | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate |
| HEJOHAOE_00656 | 5.66e-56 | lexA | 3.4.21.88 | - | K | ko:K01356 | - | ko00000,ko00002,ko01000,ko01002,ko03400 | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair |
| HEJOHAOE_00657 | 2.51e-47 | - | 3.6.1.55 | - | L | ko:K03574 | - | ko00000,ko01000,ko03400 | Nudix hydrolase |
| HEJOHAOE_00660 | 2.76e-52 | hrcA | - | - | K | ko:K03705 | - | ko00000,ko03000 | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons |
| HEJOHAOE_00661 | 1.63e-45 | grpE | - | - | O | ko:K03687 | - | ko00000,ko03029,ko03110 | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ |
| HEJOHAOE_00662 | 0.0 | dnaK | - | - | O | ko:K04043 | ko03018,ko04212,ko05152,map03018,map04212,map05152 | ko00000,ko00001,ko03019,ko03029,ko03110,ko04147 | Heat shock 70 kDa protein |
| HEJOHAOE_00663 | 1.67e-185 | dnaJ | - | - | O | ko:K03686,ko:K05516 | - | ko00000,ko03029,ko03036,ko03110 | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins |
| HEJOHAOE_00664 | 2.95e-136 | prmA | - | - | J | ko:K02687 | - | ko00000,ko01000,ko03009 | Ribosomal protein L11 methyltransferase |
| HEJOHAOE_00665 | 1.23e-106 | - | - | - | V | ko:K02003 | - | ko00000,ko00002,ko02000 | ABC transporter |
| HEJOHAOE_00666 | 3.93e-103 | - | - | - | V | ko:K02004 | - | ko00000,ko00002,ko02000 | FtsX-like permease family |
| HEJOHAOE_00667 | 1.28e-61 | - | - | - | T | - | - | - | Transcriptional regulator |
| HEJOHAOE_00668 | 1.64e-58 | - | - | - | T | - | - | - | Histidine kinase- DNA gyrase B |
| HEJOHAOE_00669 | 1.75e-164 | - | 3.2.1.1 | GH13 | G | ko:K01176 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | Alpha-amylase domain |
| HEJOHAOE_00670 | 5.33e-61 | - | - | - | S | - | - | - | Flavin reductase like domain |
| HEJOHAOE_00671 | 7.98e-71 | - | - | - | S | ko:K18843 | - | ko00000,ko02048 | HicB family |
| HEJOHAOE_00672 | 2.34e-240 | argG | 6.3.4.5 | - | E | ko:K01940 | ko00220,ko00250,ko01100,ko01110,ko01130,ko01230,ko05418,map00220,map00250,map01100,map01110,map01130,map01230,map05418 | ko00000,ko00001,ko00002,ko01000,ko04147 | Belongs to the argininosuccinate synthase family. Type 1 subfamily |
| HEJOHAOE_00673 | 2.3e-230 | argH | 2.3.1.1, 4.3.2.1 | - | E | ko:K01755,ko:K14681 | ko00220,ko00250,ko01100,ko01110,ko01130,ko01210,ko01230,map00220,map00250,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000,ko04147 | argininosuccinate lyase |
| HEJOHAOE_00674 | 2.73e-181 | argC | 1.2.1.38 | - | E | ko:K00145 | ko00220,ko01100,ko01110,ko01130,ko01210,ko01230,map00220,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde |
| HEJOHAOE_00675 | 1.5e-181 | argJ | 2.3.1.1, 2.3.1.35 | - | E | ko:K00620 | ko00220,ko01100,ko01110,ko01130,ko01210,ko01230,map00220,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate |
| HEJOHAOE_00676 | 8.82e-150 | argB | 2.7.2.8 | - | E | ko:K00930 | ko00220,ko01100,ko01110,ko01130,ko01210,ko01230,map00220,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Belongs to the acetylglutamate kinase family. ArgB subfamily |
| HEJOHAOE_00677 | 7.66e-32 | - | 2.3.1.1 | - | K | ko:K22477 | ko00220,ko01210,ko01230,map00220,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Acetyltransferase, gnat family |
| HEJOHAOE_00678 | 4.19e-167 | argD | 2.6.1.11, 2.6.1.17 | - | E | ko:K00821 | ko00220,ko00300,ko01100,ko01110,ko01120,ko01130,ko01210,ko01230,map00220,map00300,map01100,map01110,map01120,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | acetylornithine aminotransferase |
| HEJOHAOE_00679 | 2.52e-167 | argF | 2.1.3.3 | - | E | ko:K00611 | ko00220,ko01100,ko01110,ko01130,ko01230,map00220,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline |
| HEJOHAOE_00681 | 1.35e-16 | - | - | - | S | - | - | - | CpXC protein |
| HEJOHAOE_00683 | 1.14e-70 | ogt | 2.1.1.63 | - | L | ko:K00567,ko:K13531 | - | ko00000,ko01000,ko03400 | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated |
| HEJOHAOE_00684 | 1.94e-07 | - | - | - | T | - | - | - | PFAM Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase |
| HEJOHAOE_00685 | 8.6e-06 | - | - | - | T | - | - | - | Bacterial transcriptional activator domain |
| HEJOHAOE_00686 | 0.0 | - | 6.1.1.13 | - | Q | ko:K03367 | ko00473,ko01503,ko02020,ko05150,map00473,map01503,map02020,map05150 | ko00000,ko00001,ko00002,ko01000,ko01504 | TIGRFAM amino acid adenylation domain |
| HEJOHAOE_00687 | 3.88e-101 | - | - | - | V | - | - | - | MatE |
| HEJOHAOE_00688 | 5.85e-22 | - | - | - | T | - | - | - | STAS domain |
| HEJOHAOE_00689 | 1.07e-22 | - | - | - | T | - | - | - | PFAM Histidine kinase-, DNA gyrase B-, and HSP90-like |
| HEJOHAOE_00690 | 2.02e-102 | - | - | - | E | - | - | - | branched-chain amino acid permease (azaleucine resistance) |
| HEJOHAOE_00691 | 1.44e-37 | - | - | - | S | - | - | - | Branched-chain amino acid transport protein (AzlD) |
| HEJOHAOE_00692 | 3.51e-95 | sbcD | - | - | L | ko:K03547 | - | ko00000,ko03400 | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity |
| HEJOHAOE_00693 | 3.25e-86 | sbcC | - | - | L | ko:K03546 | - | ko00000,ko03400 | Putative exonuclease SbcCD, C subunit |
| HEJOHAOE_00694 | 8.17e-120 | - | - | - | P | ko:K07238 | - | ko00000,ko02000 | ZIP Zinc transporter |
| HEJOHAOE_00695 | 3.74e-34 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00696 | 0.0 | copA_1 | - | - | P | ko:K12950 | - | ko00000,ko01000 | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00697 | 4.89e-29 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00698 | 2.31e-34 | - | - | - | K | - | - | - | transcriptional regulator |
| HEJOHAOE_00699 | 3.31e-86 | - | - | - | V | - | - | - | Polysaccharide biosynthesis C-terminal domain |
| HEJOHAOE_00700 | 3.3e-33 | - | - | - | K | - | - | - | Acetyltransferase (GNAT) domain |
| HEJOHAOE_00701 | 1.33e-93 | atpD | - | - | C | ko:K02120 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Produces ATP from ADP in the presence of a proton gradient across the membrane |
| HEJOHAOE_00702 | 1.07e-288 | atpB | - | - | C | ko:K02118 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit |
| HEJOHAOE_00703 | 7.06e-317 | ntpA | 3.6.3.14, 3.6.3.15 | - | C | ko:K02117 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit |
| HEJOHAOE_00704 | 1.72e-31 | atpF | - | - | C | ko:K02122 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Produces ATP from ADP in the presence of a proton gradient across the membrane |
| HEJOHAOE_00707 | 5.39e-38 | ntpK | - | - | C | ko:K02124 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | ATP synthase subunit C |
| HEJOHAOE_00708 | 8.74e-144 | ntpI | - | - | C | ko:K02123 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Belongs to the V-ATPase 116 kDa subunit family |
| HEJOHAOE_00710 | 1.63e-159 | - | - | - | S | - | - | - | Fic/DOC family |
| HEJOHAOE_00711 | 9.76e-65 | ybaK | - | - | S | ko:K03976 | - | ko00000,ko01000,ko03016 | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily |
| HEJOHAOE_00712 | 6.83e-284 | czcA | - | - | V | ko:K03296 | - | ko00000 | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family |
| HEJOHAOE_00713 | 1.35e-17 | - | - | - | K | - | - | - | Bacterial regulatory proteins, tetR family |
| HEJOHAOE_00714 | 2.51e-73 | yfkJ | 3.1.3.48 | - | T | ko:K01104 | - | ko00000,ko01000 | Low molecular weight phosphatase family |
| HEJOHAOE_00718 | 1.18e-87 | PflX | 1.97.1.4 | - | C | ko:K04070 | - | ko00000,ko01000 | Radical SAM superfamily |
| HEJOHAOE_00720 | 1.28e-179 | pulA | 3.2.1.41 | CBM48,GH13 | G | ko:K01200 | ko00500,ko01100,ko01110,map00500,map01100,map01110 | ko00000,ko00001,ko01000 | Belongs to the glycosyl hydrolase 13 family |
| HEJOHAOE_00724 | 7.99e-19 | - | - | - | S | - | - | - | COG NOG17973 non supervised orthologous group |
| HEJOHAOE_00725 | 2.8e-176 | nadB | 1.4.3.16 | - | H | ko:K00278 | ko00250,ko00760,ko01100,map00250,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the oxidation of L-aspartate to iminoaspartate |
| HEJOHAOE_00726 | 1.26e-133 | nadC | 2.4.2.19 | - | H | ko:K00767 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the NadC ModD family |
| HEJOHAOE_00727 | 2.39e-50 | - | 3.1.3.97 | - | S | ko:K07053 | - | ko00000,ko01000 | DNA polymerase alpha chain like domain |
| HEJOHAOE_00728 | 1.83e-84 | femX | 2.3.2.10, 2.3.2.16 | - | V | ko:K05363,ko:K11693 | ko00550,ko01100,map00550,map01100 | ko00000,ko00001,ko01000,ko01011 | Methicillin resistance |
| HEJOHAOE_00730 | 1.78e-75 | - | - | - | T | - | - | - | ATPase histidine kinase DNA gyrase B HSP90 domain protein |
| HEJOHAOE_00731 | 5.96e-87 | - | - | - | T | - | - | - | response regulator receiver |
| HEJOHAOE_00733 | 1.29e-272 | bioA | 2.6.1.113, 2.6.1.55, 2.6.1.62, 2.6.1.77 | - | H | ko:K00833,ko:K03851,ko:K12256,ko:K15372 | ko00330,ko00410,ko00430,ko00780,ko01100,map00330,map00410,map00430,map00780,map01100 | ko00000,ko00001,ko00002,ko01000,ko01007 | Aminotransferase class-III |
| HEJOHAOE_00734 | 6.03e-157 | - | - | - | C | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00735 | 2.63e-138 | - | - | - | P | ko:K02049 | - | ko00000,ko00002,ko02000 | ABC-type nitrate sulfonate bicarbonate transport system, ATPase component |
| HEJOHAOE_00736 | 2.22e-120 | - | - | - | P | ko:K02050 | - | ko00000,ko00002,ko02000 | binding-protein-dependent transport |
| HEJOHAOE_00737 | 1.24e-108 | - | - | - | P | ko:K02050 | - | ko00000,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| HEJOHAOE_00738 | 2.35e-176 | - | - | - | P | ko:K02051 | - | ko00000,ko00002,ko02000 | ABC-type nitrate sulfonate bicarbonate transport |
| HEJOHAOE_00739 | 1.6e-291 | hydA_1 | 3.5.2.2 | - | F | ko:K01464 | ko00240,ko00410,ko00770,ko00983,ko01100,map00240,map00410,map00770,map00983,map01100 | ko00000,ko00001,ko00002,ko01000,ko04147 | Amidohydrolase family |
| HEJOHAOE_00740 | 1.08e-230 | preA | 1.3.1.1 | - | C | ko:K17723 | ko00240,ko00410,ko00770,ko01100,map00240,map00410,map00770,map01100 | ko00000,ko00001,ko00002,ko01000 | dihydroorotate dehydrogenase |
| HEJOHAOE_00741 | 2.72e-267 | - | 3.5.1.6, 3.5.1.87, 3.5.3.9 | - | E | ko:K02083,ko:K06016 | ko00230,ko00240,ko01100,ko01120,map00230,map00240,map01100,map01120 | ko00000,ko00001,ko00002,ko01000,ko01002 | Peptidase family M28 |
| HEJOHAOE_00742 | 1.45e-52 | - | - | - | F | - | - | - | Cytidylate kinase-like family |
| HEJOHAOE_00743 | 2.58e-79 | - | - | - | QT | - | - | - | Transcriptional regulator, PucR family |
| HEJOHAOE_00745 | 1.92e-71 | xpt | 2.4.2.22 | - | F | ko:K03816 | ko00230,ko01100,ko01110,map00230,map01100,map01110 | ko00000,ko00001,ko01000 | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis |
| HEJOHAOE_00746 | 4.9e-194 | putP | - | - | E | ko:K03307,ko:K11928 | - | ko00000,ko02000 | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family |
| HEJOHAOE_00747 | 4.32e-137 | alr | 5.1.1.1, 5.1.1.18 | - | M | ko:K01775,ko:K18348 | ko00473,ko01100,ko01502,ko02020,map00473,map01100,map01502,map02020 | ko00000,ko00001,ko00002,ko01000,ko01011,ko01504 | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids |
| HEJOHAOE_00748 | 0.0 | polA | 2.7.7.7 | - | L | ko:K02335 | ko00230,ko00240,ko01100,ko03030,ko03410,ko03420,ko03440,map00230,map00240,map01100,map03030,map03410,map03420,map03440 | ko00000,ko00001,ko01000,ko03032,ko03400 | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity |
| HEJOHAOE_00749 | 2.45e-26 | - | 3.1.3.48, 5.3.1.6 | - | T | ko:K01104,ko:K01808 | ko00030,ko00051,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00030,map00051,map00710,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Low molecular weight phosphatase family |
| HEJOHAOE_00750 | 5.37e-40 | rimI | 2.3.1.128 | - | K | ko:K03789 | - | ko00000,ko01000,ko03009 | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 |
| HEJOHAOE_00751 | 6.23e-178 | tsaD | 2.3.1.234 | - | O | ko:K01409 | - | ko00000,ko01000,ko03016 | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction |
| HEJOHAOE_00752 | 5.39e-100 | ppiB | 5.2.1.8 | - | O | ko:K03768 | - | ko00000,ko01000,ko03110 | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides |
| HEJOHAOE_00753 | 3.31e-172 | galE | 5.1.3.2 | - | M | ko:K01784 | ko00052,ko00520,ko01100,map00052,map00520,map01100 | ko00000,ko00001,ko00002,ko01000 | UDP-glucose 4-epimerase |
| HEJOHAOE_00755 | 1.67e-229 | spoVD | 3.4.16.4 | - | M | ko:K03587,ko:K08384 | ko00550,ko01501,map00550,map01501 | ko00000,ko00001,ko01000,ko01011,ko03036 | Penicillin-binding Protein |
| HEJOHAOE_00756 | 1.69e-120 | mraY | 2.7.8.13 | - | M | ko:K01000 | ko00550,ko01100,ko01502,map00550,map01100,map01502 | ko00000,ko00001,ko01000,ko01011 | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan |
| HEJOHAOE_00757 | 4.02e-123 | ftsW | - | - | D | ko:K03588 | ko04112,map04112 | ko00000,ko00001,ko02000,ko03036 | Belongs to the SEDS family |
| HEJOHAOE_00758 | 7.36e-175 | murG | 2.4.1.227 | GT28 | M | ko:K02563 | ko00550,ko01100,ko01502,ko04112,map00550,map01100,map01502,map04112 | ko00000,ko00001,ko01000,ko01011 | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
| HEJOHAOE_00759 | 1.04e-184 | murA2 | 2.5.1.7 | - | M | ko:K00790 | ko00520,ko00550,ko01100,map00520,map00550,map01100 | ko00000,ko00001,ko01000,ko01011 | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine |
| HEJOHAOE_00760 | 8.75e-15 | - | - | - | D | ko:K03589 | ko04112,map04112 | ko00000,ko00001,ko03036 | Cell division protein FtsQ |
| HEJOHAOE_00761 | 2.96e-158 | ftsZ | - | - | D | ko:K03531 | ko04112,map04112 | ko00000,ko00001,ko02048,ko03036,ko04812 | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity |
| HEJOHAOE_00762 | 9.52e-97 | bcsP | - | - | S | ko:K07080 | - | ko00000 | TRAP transporter solute receptor, TAXI family |
| HEJOHAOE_00763 | 4.05e-213 | gltS | - | - | P | ko:K03312 | - | ko00000,ko02000 | Catalyzes the sodium-dependent transport of glutamate |
| HEJOHAOE_00765 | 3.4e-170 | cbh | 3.5.1.24 | - | M | ko:K01442 | ko00120,ko00121,ko01100,map00120,map00121,map01100 | ko00000,ko00001,ko01000 | Linear amide C-N hydrolase, choloylglycine hydrolase family protein |
| HEJOHAOE_00766 | 1.9e-117 | eriC | - | - | P | ko:K03281 | - | ko00000 | Chloride channel |
| HEJOHAOE_00768 | 6.02e-240 | - | - | - | C | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00769 | 1.18e-42 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00773 | 5.03e-52 | - | - | - | K | - | - | - | Bacterial regulatory proteins, tetR family |
| HEJOHAOE_00774 | 1.86e-52 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00775 | 0.0 | - | - | - | L | ko:K06400 | - | ko00000 | Psort location Cytoplasmic, score |
| HEJOHAOE_00777 | 4.14e-74 | - | - | - | L | ko:K07171 | - | ko00000,ko01000,ko02048 | Toxic component of a toxin-antitoxin (TA) module |
| HEJOHAOE_00778 | 8.45e-74 | - | - | - | K | ko:K03088 | - | ko00000,ko03021 | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00779 | 5.91e-199 | - | - | - | S | ko:K07098 | - | ko00000 | Calcineurin-like phosphoesterase superfamily domain |
| HEJOHAOE_00780 | 0.0 | - | - | - | V | ko:K02004 | - | ko00000,ko00002,ko02000 | FtsX-like permease family |
| HEJOHAOE_00781 | 3.81e-159 | - | - | - | V | ko:K02003 | - | ko00000,ko00002,ko02000 | ABC transporter |
| HEJOHAOE_00782 | 3.59e-283 | - | - | - | T | - | - | - | Histidine kinase |
| HEJOHAOE_00783 | 7.45e-167 | - | - | - | T | - | - | - | response regulator receiver |
| HEJOHAOE_00784 | 1.38e-37 | - | - | - | D | - | - | - | Filamentation induced by cAMP protein fic |
| HEJOHAOE_00785 | 4.12e-79 | - | - | - | K | - | - | - | Helix-turn-helix domain |
| HEJOHAOE_00786 | 0.0 | - | - | - | M | - | - | - | Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) |
| HEJOHAOE_00787 | 3.05e-187 | srtB | 3.4.22.70 | - | S | ko:K08600 | - | ko00000,ko01000,ko01002,ko01011 | Sortase family |
| HEJOHAOE_00788 | 5.98e-104 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00789 | 0.0 | - | - | - | U | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00790 | 2.08e-96 | - | - | - | U | - | - | - | PrgI family protein |
| HEJOHAOE_00791 | 4.62e-188 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00792 | 3.03e-76 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00793 | 1.66e-215 | - | - | - | U | ko:K03205 | ko03070,map03070 | ko00000,ko00001,ko00002,ko02044 | Psort location Cytoplasmic, score |
| HEJOHAOE_00794 | 3.31e-111 | gabR | - | - | K | ko:K00375 | - | ko00000,ko03000 | transaminase activity |
| HEJOHAOE_00795 | 2.08e-69 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00796 | 2.3e-50 | - | 3.4.16.4 | - | V | ko:K01286 | - | ko00000,ko01000 | beta-lactamase |
| HEJOHAOE_00797 | 1.82e-312 | pcrA | 3.6.4.12 | - | L | ko:K03657 | ko03420,ko03430,map03420,map03430 | ko00000,ko00001,ko01000,ko03400 | ATP-dependent DNA helicase |
| HEJOHAOE_00801 | 3.52e-87 | dnaC | - | - | L | ko:K02315 | - | ko00000,ko03032 | DNA replication protein |
| HEJOHAOE_00802 | 1.31e-79 | dnaD | - | - | L | - | - | - | DnaD domain protein |
| HEJOHAOE_00803 | 1.07e-24 | - | - | - | S | - | - | - | TSCPD domain |
| HEJOHAOE_00804 | 8.68e-208 | - | 5.4.2.12 | - | G | ko:K15635 | ko00010,ko00260,ko00680,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00010,map00260,map00680,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | phosphoglycerate mutase |
| HEJOHAOE_00805 | 1.63e-194 | prfB | - | - | J | ko:K02836 | - | ko00000,ko03012 | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA |
| HEJOHAOE_00806 | 7.47e-24 | - | - | - | S | - | - | - | Prokaryotic RING finger family 1 |
| HEJOHAOE_00807 | 4.78e-129 | galU | 2.7.7.9 | - | M | ko:K00963 | ko00040,ko00052,ko00500,ko00520,ko01100,ko01130,map00040,map00052,map00500,map00520,map01100,map01130 | ko00000,ko00001,ko00002,ko01000 | UTP-glucose-1-phosphate uridylyltransferase |
| HEJOHAOE_00808 | 1.75e-38 | hisK | 3.1.3.15 | - | E | ko:K04486 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | PHP domain |
| HEJOHAOE_00809 | 7.43e-29 | - | - | - | T | ko:K07166 | - | ko00000 | Belongs to the UPF0237 family |
| HEJOHAOE_00810 | 5.68e-256 | - | - | - | S | ko:K09157 | - | ko00000 | Uncharacterised ACR (DUF711) |
| HEJOHAOE_00812 | 2.04e-81 | ntpC | - | - | C | ko:K02119 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | subunit (C |
| HEJOHAOE_00813 | 2.41e-197 | ntpI | - | - | U | ko:K02123 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Belongs to the V-ATPase 116 kDa subunit family |
| HEJOHAOE_00814 | 3.57e-17 | ntpK | - | - | C | ko:K02124 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | ATP synthase subunit C |
| HEJOHAOE_00815 | 3.26e-50 | - | - | - | C | ko:K02122 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Archaeal vacuolar-type H -ATPase subunit F |
| HEJOHAOE_00817 | 0.0 | ntpA | 3.6.3.14, 3.6.3.15 | - | C | ko:K02117 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit |
| HEJOHAOE_00818 | 8.62e-278 | atpB | - | - | C | ko:K02118 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit |
| HEJOHAOE_00819 | 1.48e-87 | atpD | - | - | C | ko:K02120 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Produces ATP from ADP in the presence of a proton gradient across the membrane |
| HEJOHAOE_00822 | 2.44e-63 | yphJ | 4.1.1.44 | - | S | ko:K01607 | ko00362,ko01100,ko01120,ko01220,map00362,map01100,map01120,map01220 | ko00000,ko00001,ko01000 | peroxiredoxin activity |
| HEJOHAOE_00823 | 2.39e-305 | dxs1 | 2.2.1.7 | - | H | ko:K01662 | ko00730,ko00900,ko01100,ko01110,ko01130,map00730,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) |
| HEJOHAOE_00828 | 6.7e-112 | - | - | - | S | - | - | - | CYTH |
| HEJOHAOE_00829 | 1.88e-228 | ilvE | 2.6.1.42, 4.1.3.38 | - | E | ko:K00826,ko:K02619 | ko00270,ko00280,ko00290,ko00770,ko00790,ko01100,ko01110,ko01130,ko01210,ko01230,map00270,map00280,map00290,map00770,map00790,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | Branched-chain amino acid aminotransferase |
| HEJOHAOE_00830 | 2.05e-30 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00834 | 6.02e-32 | mec | 3.13.1.6 | - | S | ko:K21140 | ko04122,map04122 | ko00000,ko00001,ko01000 | proteolysis |
| HEJOHAOE_00835 | 9.3e-107 | trxB | 1.8.1.9 | - | C | ko:K00384 | ko00450,map00450 | ko00000,ko00001,ko01000 | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family |
| HEJOHAOE_00836 | 2.62e-313 | aprA | 1.8.99.2 | - | C | ko:K00394 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko00002,ko01000 | Fumarate reductase flavoprotein C-term |
| HEJOHAOE_00837 | 2.96e-47 | - | 1.8.99.2 | - | C | ko:K00395 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko00002,ko01000 | 4Fe-4S binding domain |
| HEJOHAOE_00838 | 1.05e-199 | cysD | 1.8.4.10, 1.8.4.8, 2.7.7.4 | - | EH | ko:K00390,ko:K00957 | ko00230,ko00261,ko00450,ko00920,ko01100,ko01120,ko01130,map00230,map00261,map00450,map00920,map01100,map01120,map01130 | ko00000,ko00001,ko00002,ko01000 | sulfate reduction |
| HEJOHAOE_00839 | 6.38e-306 | cysN | 2.7.1.25, 2.7.7.4 | - | H | ko:K00955,ko:K00956 | ko00230,ko00261,ko00450,ko00920,ko01100,ko01120,ko01130,map00230,map00261,map00450,map00920,map01100,map01120,map01130 | ko00000,ko00001,ko00002,ko01000 | Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. CysN NodQ subfamily |
| HEJOHAOE_00840 | 7.22e-05 | - | - | - | S | - | - | - | TM2 domain |
| HEJOHAOE_00842 | 1.22e-58 | - | - | - | S | - | - | - | Acyltransferase family |
| HEJOHAOE_00843 | 4.34e-283 | - | - | - | M | - | - | - | COG0463 Glycosyltransferases involved in cell wall biogenesis |
| HEJOHAOE_00844 | 1.11e-92 | - | - | - | S | - | - | - | Protein of unknown function (DUF436) |
| HEJOHAOE_00845 | 1.75e-59 | - | - | - | K | - | - | - | Acetyltransferase (GNAT) domain |
| HEJOHAOE_00846 | 0.0 | tetP | - | - | J | - | - | - | Psort location Cytoplasmic, score 9.98 |
| HEJOHAOE_00847 | 1.25e-11 | - | - | - | K | - | - | - | DNA-binding helix-turn-helix protein |
| HEJOHAOE_00849 | 1.2e-12 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00853 | 5.95e-49 | def2 | 3.5.1.88 | - | J | ko:K01462 | - | ko00000,ko01000 | Removes the formyl group from the N-terminal Met of newly synthesized proteins |
| HEJOHAOE_00854 | 1.27e-05 | - | - | - | S | - | - | - | Putative zinc-finger |
| HEJOHAOE_00855 | 3.01e-43 | - | - | - | K | ko:K03088 | - | ko00000,ko03021 | Sigma-70, region 4 |
| HEJOHAOE_00857 | 2.28e-69 | - | - | - | K | - | - | - | helix_turn_helix, mercury resistance |
| HEJOHAOE_00859 | 3.38e-69 | - | - | - | S | - | - | - | esterase of the alpha-beta hydrolase superfamily |
| HEJOHAOE_00860 | 6.4e-09 | - | - | - | K | - | - | - | Bacterial regulatory proteins, tetR family |
| HEJOHAOE_00861 | 1.28e-84 | - | - | - | S | - | - | - | NADPH-dependent FMN reductase |
| HEJOHAOE_00862 | 1.8e-61 | - | 4.2.1.59 | - | I | ko:K02372 | ko00061,ko00780,ko01100,ko01212,map00061,map00780,map01100,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | K02372 3R-hydroxymyristoyl ACP dehydrase |
| HEJOHAOE_00863 | 4.32e-107 | - | 1.1.1.100 | - | IQ | ko:K00059 | ko00061,ko00333,ko00780,ko01040,ko01100,ko01130,ko01212,map00061,map00333,map00780,map01040,map01100,map01130,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | reductase |
| HEJOHAOE_00864 | 1.81e-264 | - | 2.3.1.179 | - | I | ko:K09458 | ko00061,ko00780,ko01100,ko01212,map00061,map00780,map01100,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP |
| HEJOHAOE_00865 | 3.98e-26 | - | - | - | IQ | ko:K02078 | - | ko00000,ko00001 | Phosphopantetheine attachment site |
| HEJOHAOE_00866 | 1.89e-09 | - | - | - | I | ko:K07003 | - | ko00000 | Phosphate acyltransferases |
| HEJOHAOE_00867 | 2.66e-232 | trpS | 6.1.1.2 | - | J | ko:K01867 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Tryptophanyl-tRNA synthetase |
| HEJOHAOE_00868 | 4.39e-148 | - | - | - | M | - | - | - | Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase |
| HEJOHAOE_00869 | 1.27e-142 | - | - | - | T | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00870 | 5.04e-78 | - | - | - | T | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_00871 | 0.0 | - | - | - | Q | - | - | - | Alkyl sulfatase dimerisation |
| HEJOHAOE_00877 | 2.98e-68 | nnrD | 4.2.1.136, 5.1.99.6 | - | G | ko:K17758,ko:K17759 | - | ko00000,ko01000 | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration |
| HEJOHAOE_00878 | 7.46e-71 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00880 | 2.72e-57 | ndoA | - | - | L | ko:K07171 | - | ko00000,ko01000,ko02048 | Toxic component of a toxin-antitoxin (TA) module |
| HEJOHAOE_00881 | 1.23e-54 | - | - | - | K | - | - | - | Helix-turn-helix |
| HEJOHAOE_00882 | 1.25e-83 | cobC | 3.1.3.73 | - | G | ko:K02226 | ko00860,ko01100,map00860,map01100 | ko00000,ko00001,ko00002,ko01000 | Psort location Cytoplasmic, score |
| HEJOHAOE_00883 | 2.99e-198 | leuB | 1.1.1.85 | - | C | ko:K00052 | ko00290,ko00660,ko01100,ko01110,ko01210,ko01230,map00290,map00660,map01100,map01110,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate |
| HEJOHAOE_00884 | 2.66e-23 | ywqE | 3.1.3.48 | - | GM | ko:K01104 | - | ko00000,ko01000 | biosynthesis protein |
| HEJOHAOE_00885 | 2.66e-52 | - | - | - | S | - | - | - | conserved protein, contains double-stranded beta-helix domain |
| HEJOHAOE_00886 | 3.62e-87 | nifU | - | - | C | ko:K04488 | - | ko00000 | NifU-like N terminal domain |
| HEJOHAOE_00887 | 4.86e-206 | iscS | 2.8.1.7 | - | E | ko:K04487 | ko00730,ko01100,ko04122,map00730,map01100,map04122 | ko00000,ko00001,ko01000,ko02048,ko03016,ko03029 | Catalyzes the removal of elemental sulfur atoms from cysteine to produce alanine |
| HEJOHAOE_00888 | 1.17e-68 | rnhA | 3.1.26.4 | - | L | ko:K03469 | ko03030,map03030 | ko00000,ko00001,ko01000,ko03032 | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids |
| HEJOHAOE_00889 | 1.08e-300 | rnj | - | - | S | ko:K12574 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03019 | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay |
| HEJOHAOE_00890 | 3.36e-181 | yybT | - | - | T | - | - | - | domain protein |
| HEJOHAOE_00891 | 2.97e-63 | rplI | - | - | J | ko:K02939 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | binds to the 23S rRNA |
| HEJOHAOE_00892 | 8.8e-210 | dnaB | 3.6.4.12 | - | L | ko:K02314 | ko03030,ko04112,map03030,map04112 | ko00000,ko00001,ko01000,ko03032 | Participates in initiation and elongation during chromosome replication |
| HEJOHAOE_00893 | 4.43e-63 | tilS | 6.3.4.19 | - | D | ko:K04075 | - | ko00000,ko01000,ko03016 | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine |
| HEJOHAOE_00894 | 8.27e-66 | hpt | 2.4.2.8 | - | F | ko:K00760 | ko00230,ko00983,ko01100,ko01110,map00230,map00983,map01100,map01110 | ko00000,ko00001,ko01000 | Belongs to the purine pyrimidine phosphoribosyltransferase family |
| HEJOHAOE_00895 | 1.9e-275 | ftsH | - | - | O | ko:K03798 | - | ko00000,ko00002,ko01000,ko01002,ko03110 | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins |
| HEJOHAOE_00896 | 0.0 | uvrA | - | - | L | ko:K03701 | ko03420,map03420 | ko00000,ko00001,ko03400 | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate |
| HEJOHAOE_00897 | 8.18e-06 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00899 | 1.3e-13 | - | - | - | NU | - | - | - | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase |
| HEJOHAOE_00900 | 2.91e-188 | - | - | - | V | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00902 | 3.57e-07 | - | - | - | K | - | - | - | Sigma-70, region 4 |
| HEJOHAOE_00905 | 0.0 | thrS | 6.1.1.3 | - | J | ko:K01868 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) |
| HEJOHAOE_00906 | 4.04e-27 | vanY | 3.4.17.14 | - | M | ko:K07260 | ko00550,ko01100,ko01502,ko02020,map00550,map01100,map01502,map02020 | ko00000,ko00001,ko00002,ko01000,ko01002,ko01011,ko01504 | D-alanyl-D-alanine carboxypeptidase |
| HEJOHAOE_00907 | 6.21e-39 | rpmE | - | - | J | ko:K02909 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L31 |
| HEJOHAOE_00908 | 1.4e-74 | yvyE | - | - | S | - | - | - | YigZ family |
| HEJOHAOE_00909 | 1.15e-171 | dnaG | - | - | L | ko:K02316 | ko03030,map03030 | ko00000,ko00001,ko01000,ko03032 | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication |
| HEJOHAOE_00910 | 5.64e-10 | - | - | - | T | ko:K07720 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | helix_turn_helix, arabinose operon control protein |
| HEJOHAOE_00911 | 4.49e-33 | - | - | - | P | - | - | - | Heavy-metal-associated domain |
| HEJOHAOE_00913 | 0.0 | feoB | - | - | P | ko:K04759 | - | ko00000,ko02000 | transporter of a GTP-driven Fe(2 ) uptake system |
| HEJOHAOE_00914 | 6.78e-37 | feoA | - | - | P | ko:K04758 | - | ko00000,ko02000 | FeoA |
| HEJOHAOE_00915 | 2.22e-29 | - | - | - | P | ko:K04758 | - | ko00000,ko02000 | FeoA |
| HEJOHAOE_00916 | 2.51e-37 | mntR_1 | - | - | K | - | - | - | Involved in manganese homeostasis. Might activate the transcription of the mntABCD operon |
| HEJOHAOE_00917 | 6.7e-94 | - | - | - | S | ko:K06889 | - | ko00000 | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00918 | 0.0 | yhgF | - | - | K | ko:K06959 | - | ko00000 | Tex-like protein N-terminal domain |
| HEJOHAOE_00919 | 2.83e-103 | fnt | - | - | P | ko:K21993 | - | ko00000,ko02000 | Formate nitrite |
| HEJOHAOE_00920 | 3.38e-43 | - | - | - | S | ko:K16789 | - | ko00000,ko02000 | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_00921 | 1.59e-08 | - | - | - | S | - | - | - | Spore coat associated protein JA (CotJA) |
| HEJOHAOE_00922 | 5.33e-12 | cotJB | - | - | S | ko:K06333 | - | ko00000 | COG NOG18028 non supervised orthologous group |
| HEJOHAOE_00923 | 3.17e-09 | cotJC | - | - | P | ko:K06334,ko:K07217 | - | ko00000 | catalase activity |
| HEJOHAOE_00924 | 1.3e-140 | - | - | - | K | - | - | - | LysR substrate binding domain |
| HEJOHAOE_00925 | 5.78e-277 | - | - | - | P | ko:K03308 | - | ko00000 | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family |
| HEJOHAOE_00926 | 0.000265 | - | - | - | K | - | - | - | Acetyltransferase (GNAT) family |
| HEJOHAOE_00927 | 6.58e-112 | cysE | 2.3.1.30 | - | E | ko:K00640 | ko00270,ko00920,ko01100,ko01110,ko01120,ko01200,ko01230,ko05111,map00270,map00920,map01100,map01110,map01120,map01200,map01230,map05111 | ko00000,ko00001,ko00002,ko01000 | Psort location Cytoplasmic, score |
| HEJOHAOE_00928 | 1.21e-50 | maf | - | - | D | ko:K06287 | - | ko00000 | septum formation protein Maf |
| HEJOHAOE_00929 | 1.24e-143 | - | - | - | S | - | - | - | CobW P47K family protein |
| HEJOHAOE_00931 | 2.74e-110 | glnQ | 3.6.3.21 | - | E | ko:K02028 | - | ko00000,ko00002,ko01000,ko02000 | ABC transporter |
| HEJOHAOE_00932 | 3.2e-82 | tcyB | - | - | P | ko:K02029 | - | ko00000,ko00002,ko02000 | ABC transporter, permease protein |
| HEJOHAOE_00933 | 1.05e-73 | fliY1 | - | - | ET | ko:K02030 | - | ko00000,ko00002,ko02000 | ABC transporter, substrate-binding protein, family 3 |
| HEJOHAOE_00934 | 3.28e-94 | - | - | - | L | ko:K06400 | - | ko00000 | Resolvase, N terminal domain |
| HEJOHAOE_00935 | 1.66e-72 | cotJC | - | - | P | ko:K06334 | - | ko00000 | Manganese containing catalase |
| HEJOHAOE_00936 | 6.09e-05 | - | - | - | M | ko:K07271 | - | ko00000,ko01000 | LicD family |
| HEJOHAOE_00937 | 1.32e-222 | - | 1.1.1.22 | - | M | ko:K00012 | ko00040,ko00053,ko00520,ko01100,map00040,map00053,map00520,map01100 | ko00000,ko00001,ko00002,ko01000 | UDP-glucose/GDP-mannose dehydrogenase family, NAD binding domain |
| HEJOHAOE_00938 | 4.36e-137 | - | - | - | S | - | - | - | membrane protein involved in the export of O-antigen and teichoic acid |
| HEJOHAOE_00940 | 5.6e-63 | - | - | - | S | - | - | - | Polysaccharide pyruvyl transferase |
| HEJOHAOE_00941 | 1.92e-52 | rfaG | - | - | M | - | - | - | Glycosyltransferase like family 2 |
| HEJOHAOE_00942 | 6.66e-13 | - | - | - | S | - | - | - | Bacterial transferase hexapeptide repeat protein |
| HEJOHAOE_00943 | 3.77e-221 | mnaA | 5.1.3.14 | - | M | ko:K01791 | ko00520,ko01100,ko05111,map00520,map01100,map05111 | ko00000,ko00001,ko00002,ko01000,ko01005 | UDP-N-acetylglucosamine 2-epimerase |
| HEJOHAOE_00944 | 2.14e-57 | - | - | - | GM | - | - | - | Glycosyltransferase like family 2 |
| HEJOHAOE_00946 | 4.01e-52 | - | - | - | S | - | - | - | Hexapeptide repeat of succinyl-transferase |
| HEJOHAOE_00947 | 7.29e-137 | - | - | - | M | - | - | - | Glycosyl transferases group 1 |
| HEJOHAOE_00948 | 8.05e-05 | - | - | - | S | - | - | - | Bacterial transferase hexapeptide (six repeats) |
| HEJOHAOE_00949 | 1.07e-147 | glgC | 2.7.7.27 | - | H | ko:K00975 | ko00500,ko00520,ko01100,ko01110,ko02026,map00500,map00520,map01100,map01110,map02026 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans |
| HEJOHAOE_00950 | 1.12e-280 | glgB | 2.4.1.18 | CBM48,GH13 | G | ko:K00700 | ko00500,ko01100,ko01110,map00500,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko04147 | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
| HEJOHAOE_00951 | 2.59e-218 | gap | 1.2.1.12 | - | C | ko:K00134 | ko00010,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,ko04066,ko05010,map00010,map00710,map01100,map01110,map01120,map01130,map01200,map01230,map04066,map05010 | ko00000,ko00001,ko00002,ko01000,ko04131,ko04147 | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family |
| HEJOHAOE_00952 | 3.28e-232 | rny | - | - | D | ko:K18682 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03019 | Endoribonuclease that initiates mRNA decay |
| HEJOHAOE_00953 | 4.3e-218 | amt | - | - | U | ko:K03320 | - | ko00000,ko02000 | Ammonium Transporter Family |
| HEJOHAOE_00954 | 5.1e-50 | glnB | - | - | K | ko:K04751,ko:K04752 | ko02020,map02020 | ko00000,ko00001 | Belongs to the P(II) protein family |
| HEJOHAOE_00955 | 1.15e-27 | FcbC | - | - | S | ko:K07107 | - | ko00000,ko01000 | acyl-CoA thioester hydrolase, YbgC YbaW family |
| HEJOHAOE_00956 | 4.81e-249 | - | - | - | IQ | - | - | - | AMP-binding enzyme C-terminal domain |
| HEJOHAOE_00957 | 3.46e-170 | - | 2.3.1.179 | - | I | ko:K09458 | ko00061,ko00780,ko01100,ko01212,map00061,map00780,map01100,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP |
| HEJOHAOE_00958 | 8.51e-19 | - | - | - | K | ko:K11921 | - | ko00000,ko03000 | LysR substrate binding domain |
| HEJOHAOE_00959 | 2.06e-257 | adh | - | - | C | - | - | - | belongs to the iron- containing alcohol dehydrogenase family |
| HEJOHAOE_00960 | 2.95e-21 | - | - | - | L | ko:K07473 | - | ko00000,ko02048 | Addiction module antitoxin, RelB DinJ family |
| HEJOHAOE_00961 | 3.08e-35 | yoeB | - | - | S | ko:K19158 | - | ko00000,ko01000,ko02048 | YoeB-like toxin of bacterial type II toxin-antitoxin system |
| HEJOHAOE_00962 | 2.26e-121 | - | - | - | S | - | - | - | NADPH-dependent FMN reductase |
| HEJOHAOE_00963 | 9.6e-197 | malS | 3.2.1.1 | GH13 | G | ko:K01176 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | PFAM Alpha amylase, catalytic |
| HEJOHAOE_00964 | 3.18e-95 | - | - | - | P | - | - | - | Voltage gated chloride channel |
| HEJOHAOE_00965 | 9.62e-186 | - | - | - | V | - | - | - | CytoplasmicMembrane, score |
| HEJOHAOE_00967 | 9.03e-186 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00968 | 2.36e-110 | rbr | - | - | C | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00969 | 2.89e-188 | sbp | - | - | P | ko:K02048 | ko00920,ko02010,map00920,map02010 | ko00000,ko00001,ko00002,ko02000 | Extracellular solute-binding protein |
| HEJOHAOE_00970 | 2.32e-150 | cysT | - | - | P | ko:K02046,ko:K15496 | ko00920,ko02010,map00920,map02010 | ko00000,ko00001,ko00002,ko02000 | Sulfate ABC transporter, permease protein CysT |
| HEJOHAOE_00971 | 3.03e-147 | cysW | - | - | P | ko:K02047 | ko00920,ko02010,map00920,map02010 | ko00000,ko00001,ko00002,ko02000 | ATPase-coupled sulfate transmembrane transporter activity |
| HEJOHAOE_00972 | 7.89e-180 | cysA | 3.6.3.25 | - | P | ko:K02045 | ko00920,ko02010,map00920,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | ATPase activity |
| HEJOHAOE_00973 | 1.85e-44 | - | - | - | S | - | - | - | zeta toxin |
| HEJOHAOE_00974 | 1.71e-138 | thiF | - | - | H | ko:K22132 | - | ko00000,ko03016 | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 |
| HEJOHAOE_00975 | 7.23e-46 | hemA | 1.2.1.70 | - | H | ko:K02492 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) |
| HEJOHAOE_00976 | 1.84e-44 | cysG | 1.3.1.76, 4.99.1.4 | - | H | ko:K02304 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000 | Putative NAD(P)-binding |
| HEJOHAOE_00977 | 2.09e-54 | hemC | 2.5.1.61 | - | H | ko:K01749 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000 | Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps |
| HEJOHAOE_00978 | 6.31e-156 | cobA | 1.3.1.76, 2.1.1.107, 4.2.1.75, 4.99.1.4 | - | H | ko:K02302,ko:K02303,ko:K13542 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000 | Belongs to the precorrin methyltransferase family |
| HEJOHAOE_00979 | 5.9e-169 | hemB | 4.2.1.24 | - | H | ko:K01698 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000,ko04147 | Belongs to the ALAD family |
| HEJOHAOE_00980 | 3.32e-200 | hemL | 5.4.3.8 | - | H | ko:K01845 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000,ko01007 | Aminotransferase |
| HEJOHAOE_00981 | 1.34e-06 | - | - | - | K | - | - | - | Transcriptional regulator |
| HEJOHAOE_00982 | 2.33e-45 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_00983 | 6.12e-14 | - | - | - | - | - | - | - | - |
| HEJOHAOE_00985 | 6.25e-83 | rpsI | - | - | J | ko:K02996 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the universal ribosomal protein uS9 family |
| HEJOHAOE_00986 | 2.41e-63 | rplM | - | - | J | ko:K02871 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly |
| HEJOHAOE_00987 | 4.4e-31 | - | - | - | T | - | - | - | protein histidine kinase activity |
| HEJOHAOE_00993 | 9.42e-133 | glcK | 2.7.1.2 | - | GK | ko:K00845 | ko00010,ko00052,ko00500,ko00520,ko00521,ko00524,ko01100,ko01110,ko01120,ko01130,ko01200,map00010,map00052,map00500,map00520,map00521,map00524,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | ROK family |
| HEJOHAOE_00994 | 4.84e-284 | guaB | 1.1.1.205 | - | F | ko:K00088 | ko00230,ko00983,ko01100,ko01110,map00230,map00983,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko04147 | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth |
| HEJOHAOE_00995 | 5.66e-174 | hydF | - | - | S | - | - | - | Ferrous iron transport protein B |
| HEJOHAOE_00996 | 9.19e-274 | hydG | 4.1.99.19 | - | C | ko:K03150 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko01000 | biosynthesis protein ThiH |
| HEJOHAOE_00997 | 9.92e-155 | hydE | 2.8.1.6 | - | C | ko:K01012 | ko00780,ko01100,map00780,map01100 | ko00000,ko00001,ko00002,ko01000 | radical SAM domain protein |
| HEJOHAOE_00999 | 2.94e-93 | - | - | - | K | - | - | - | Catalyzes the reduction of ribonucleotides to deoxyribonucleotides. May function to provide a pool of deoxyribonucleotide precursors for DNA repair during oxygen limitation and or for immediate growth after restoration of oxygen |
| HEJOHAOE_01000 | 7.3e-146 | - | - | - | S | - | - | - | SPFH domain-Band 7 family |
| HEJOHAOE_01001 | 4.17e-31 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01002 | 0.0 | aspS | 6.1.1.12 | - | J | ko:K01876 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) |
| HEJOHAOE_01003 | 2.81e-199 | hisS | 6.1.1.21 | - | J | ko:K01892 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | histidyl-tRNA synthetase |
| HEJOHAOE_01004 | 4.36e-85 | mgsA | 4.2.3.3 | - | G | ko:K01734 | ko00640,ko01120,map00640,map01120 | ko00000,ko00001,ko01000 | methylglyoxal synthase |
| HEJOHAOE_01005 | 1.04e-37 | minD | - | - | D | ko:K03609 | - | ko00000,ko03036,ko04812 | Belongs to the ParA family |
| HEJOHAOE_01006 | 1.34e-176 | mrdA | 3.4.16.4 | - | M | ko:K05515 | ko00550,ko01501,map00550,map01501 | ko00000,ko00001,ko01000,ko01011 | Penicillin-binding Protein |
| HEJOHAOE_01008 | 7.32e-29 | mreC | - | - | M | ko:K03570 | - | ko00000,ko03036 | Involved in formation and maintenance of cell shape |
| HEJOHAOE_01009 | 8.8e-185 | - | - | - | D | ko:K03569 | - | ko00000,ko02048,ko03036,ko04812 | Cell shape determining protein, MreB Mrl family |
| HEJOHAOE_01010 | 2.1e-59 | dut | 3.6.1.23 | - | F | ko:K01520 | ko00240,ko00983,ko01100,map00240,map00983,map01100 | ko00000,ko00001,ko00002,ko01000,ko03400 | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA |
| HEJOHAOE_01011 | 3.6e-140 | ydcP | - | - | O | ko:K08303 | ko05120,map05120 | ko00000,ko00001,ko01000,ko01002 | Peptidase U32 |
| HEJOHAOE_01013 | 2.57e-212 | apu | 2.4.1.25, 3.2.1.133, 3.2.1.135, 3.2.1.20, 3.2.1.54 | GH13,GH31,GH77 | G | ko:K00705,ko:K01187,ko:K01208 | ko00052,ko00500,ko01100,map00052,map00500,map01100 | ko00000,ko00001,ko01000 | Alpha amylase, catalytic domain protein |
| HEJOHAOE_01014 | 1.11e-222 | - | - | - | KT | - | - | - | response regulator |
| HEJOHAOE_01018 | 0.0 | pnp | 2.7.7.8 | - | J | ko:K00962 | ko00230,ko00240,ko03018,map00230,map00240,map03018 | ko00000,ko00001,ko00002,ko01000,ko03016,ko03019 | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction |
| HEJOHAOE_01019 | 2.88e-38 | rpsO | - | - | J | ko:K02956 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome |
| HEJOHAOE_01020 | 5.59e-10 | - | - | - | K | - | - | - | Helix-turn-helix |
| HEJOHAOE_01022 | 3.81e-280 | guaA | 6.3.5.2 | - | F | ko:K01951 | ko00230,ko00983,ko01100,map00230,map00983,map01100 | ko00000,ko00001,ko00002,ko01000,ko01002 | Catalyzes the synthesis of GMP from XMP |
| HEJOHAOE_01023 | 2.94e-259 | purA | 6.3.4.4 | - | F | ko:K01939 | ko00230,ko00250,ko01100,map00230,map00250,map01100 | ko00000,ko00001,ko00002,ko01000 | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP |
| HEJOHAOE_01024 | 3.81e-278 | purB | 4.3.2.2 | - | F | ko:K01756 | ko00230,ko00250,ko01100,ko01110,ko01130,map00230,map00250,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily |
| HEJOHAOE_01025 | 6.33e-248 | purF | 2.4.2.14 | - | F | ko:K00764 | ko00230,ko00250,ko01100,ko01110,ko01130,map00230,map00250,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000,ko01002 | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine |
| HEJOHAOE_01026 | 1.72e-134 | purC | 4.3.2.2, 6.3.2.6 | - | F | ko:K01756,ko:K01923 | ko00230,ko00250,ko01100,ko01110,ko01130,map00230,map00250,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Belongs to the SAICAR synthetase family |
| HEJOHAOE_01030 | 1.86e-146 | pyrB | 2.1.3.2 | - | F | ko:K00609 | ko00240,ko00250,ko01100,map00240,map00250,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the ATCase OTCase family |
| HEJOHAOE_01031 | 2.05e-05 | - | - | - | S | - | - | - | Short repeat of unknown function (DUF308) |
| HEJOHAOE_01032 | 8.29e-190 | addA | 3.6.4.12 | - | L | ko:K16898 | - | ko00000,ko01000,ko03400 | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation |
| HEJOHAOE_01033 | 4.07e-255 | addB | 3.6.4.12 | - | L | ko:K16899 | - | ko00000,ko01000,ko03400 | ATP-dependent helicase deoxyribonuclease subunit B |
| HEJOHAOE_01034 | 1.85e-60 | spoIIR | - | - | S | ko:K06387 | - | ko00000 | stage II sporulation protein R |
| HEJOHAOE_01035 | 8.79e-54 | ispE | 2.7.1.148 | - | F | ko:K00919 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol |
| HEJOHAOE_01036 | 1.09e-210 | aspC | - | - | E | ko:K10907 | - | ko00000,ko01000,ko01007 | Aminotransferase |
| HEJOHAOE_01037 | 1.84e-36 | alaR | - | - | K | - | - | - | AsnC family transcriptional regulator |
| HEJOHAOE_01039 | 2.66e-281 | nadE | 6.3.5.1 | - | H | ko:K01950 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source |
| HEJOHAOE_01040 | 4.58e-51 | - | - | - | M | - | - | - | O-Antigen ligase |
| HEJOHAOE_01041 | 2.43e-76 | - | - | - | M | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01042 | 3.9e-30 | - | - | - | S | - | - | - | Belongs to the UPF0473 family |
| HEJOHAOE_01043 | 3.06e-11 | - | - | - | E | - | - | - | Transglutaminase-like superfamily |
| HEJOHAOE_01044 | 7.09e-65 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01045 | 1.62e-211 | - | - | - | M | ko:K19294 | - | ko00000 | membrane protein involved in D-alanine export |
| HEJOHAOE_01046 | 1.91e-125 | - | - | - | S | - | - | - | SGNH hydrolase-like domain, acetyltransferase AlgX |
| HEJOHAOE_01047 | 9.55e-58 | - | - | - | S | - | - | - | Domain of unknown function (DUF348) |
| HEJOHAOE_01048 | 4.37e-147 | - | - | - | S | - | - | - | Macro domain |
| HEJOHAOE_01049 | 6.58e-107 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01050 | 1.77e-39 | - | - | - | S | - | - | - | Dolichyl-phosphate-mannose-protein mannosyltransferase |
| HEJOHAOE_01052 | 7.36e-283 | fbp | 3.1.3.11 | - | G | ko:K04041 | ko00010,ko00030,ko00051,ko00680,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,map00010,map00030,map00051,map00680,map00710,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | D-fructose-1,6-bisphosphate 1-phosphohydrolase class 3 |
| HEJOHAOE_01053 | 1.19e-287 | htpG | - | - | O | ko:K04079 | ko04141,ko04151,ko04217,ko04612,ko04621,ko04626,ko04657,ko04659,ko04914,ko04915,ko05200,ko05215,ko05418,map04141,map04151,map04217,map04612,map04621,map04626,map04657,map04659,map04914,map04915,map05200,map05215,map05418 | ko00000,ko00001,ko01009,ko03029,ko03051,ko03110,ko04131,ko04147 | Hsp90 protein |
| HEJOHAOE_01054 | 6.91e-91 | - | - | - | M | - | - | - | Belongs to the LTA synthase family |
| HEJOHAOE_01055 | 2.61e-32 | - | - | - | D | - | - | - | Transglutaminase-like superfamily |
| HEJOHAOE_01056 | 2.9e-61 | pyrK | - | - | C | ko:K02823 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001 | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( |
| HEJOHAOE_01057 | 5.64e-174 | pyrD | 1.3.1.14 | - | F | ko:K17828 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily |
| HEJOHAOE_01058 | 2.12e-51 | - | - | - | S | - | - | - | Protein of unknown function (DUF421) |
| HEJOHAOE_01059 | 3.69e-270 | - | 3.2.1.20 | GH31 | G | ko:K01187 | ko00052,ko00500,ko01100,map00052,map00500,map01100 | ko00000,ko00001,ko01000 | Galactose mutarotase-like |
| HEJOHAOE_01060 | 2.06e-33 | - | - | - | K | - | - | - | Helix-turn-helix XRE-family like proteins |
| HEJOHAOE_01061 | 7.31e-247 | - | 5.4.2.2 | - | G | ko:K01835 | ko00010,ko00030,ko00052,ko00230,ko00500,ko00520,ko00521,ko01100,ko01110,ko01120,ko01130,map00010,map00030,map00052,map00230,map00500,map00520,map00521,map01100,map01110,map01120,map01130 | ko00000,ko00001,ko00002,ko01000 | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II |
| HEJOHAOE_01062 | 1.19e-38 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_01063 | 8.41e-19 | - | - | - | S | - | - | - | Protein of unknown function (DUF1292) |
| HEJOHAOE_01065 | 3.13e-203 | - | - | - | S | ko:K06158 | - | ko00000,ko03012 | ABC transporter |
| HEJOHAOE_01067 | 1.3e-136 | xerC | - | - | L | ko:K03733,ko:K04763 | - | ko00000,ko03036 | Phage integrase, N-terminal SAM-like domain |
| HEJOHAOE_01068 | 1.16e-255 | gdhA | 1.4.1.3, 1.4.1.4 | - | C | ko:K00261,ko:K00262 | ko00220,ko00250,ko00471,ko00910,ko01100,ko01200,ko04217,ko04964,map00220,map00250,map00471,map00910,map01100,map01200,map04217,map04964 | ko00000,ko00001,ko00002,ko01000,ko04147 | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase |
| HEJOHAOE_01074 | 0.000411 | pncP | - | - | S | ko:K07052 | - | ko00000 | CAAX amino terminal protease family protein |
| HEJOHAOE_01076 | 7.04e-32 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01080 | 1.91e-41 | - | - | - | K | - | - | - | Domain of unknown function (DUF4364) |
| HEJOHAOE_01081 | 3.57e-17 | - | - | - | S | - | - | - | SigmaK-factor processing regulatory protein BofA |
| HEJOHAOE_01082 | 5.5e-22 | secG | - | - | U | ko:K03075 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | P-P-bond-hydrolysis-driven protein transmembrane transporter activity |
| HEJOHAOE_01083 | 0.0 | - | 5.99.1.3 | - | L | ko:K02469 | - | ko00000,ko01000,ko03032,ko03400 | PFAM DNA gyrase topoisomerase IV, subunit A |
| HEJOHAOE_01084 | 0.0 | - | 5.99.1.3 | - | L | ko:K02470 | - | ko00000,ko01000,ko03032,ko03400 | DNA topoisomerase |
| HEJOHAOE_01085 | 0.0 | uvrB | - | - | L | ko:K03702 | ko03420,map03420 | ko00000,ko00001,ko03400 | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage |
| HEJOHAOE_01086 | 4.03e-55 | radC | - | - | L | ko:K03630 | - | ko00000 | Belongs to the UPF0758 family |
| HEJOHAOE_01087 | 1.52e-139 | pyrE | 2.4.2.10 | - | F | ko:K00762 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) |
| HEJOHAOE_01088 | 9.17e-172 | dinB | 2.7.7.7 | - | L | ko:K02346 | - | ko00000,ko01000,ko03400 | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII |
| HEJOHAOE_01089 | 1.64e-19 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01090 | 8.16e-140 | - | - | - | L | - | - | - | Elongator protein 3, MiaB family, Radical SAM |
| HEJOHAOE_01093 | 2.29e-06 | - | - | - | S | - | - | - | Protein of unknown function, DUF624 |
| HEJOHAOE_01095 | 2.98e-88 | proC | 1.5.1.2 | - | E | ko:K00286 | ko00330,ko01100,ko01110,ko01130,ko01230,map00330,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline |
| HEJOHAOE_01096 | 1.19e-07 | - | - | - | N | - | - | - | Bacterial Ig-like domain 2 |
| HEJOHAOE_01097 | 5.02e-05 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score 9.99 |
| HEJOHAOE_01098 | 3.13e-60 | - | - | - | O | ko:K03686 | - | ko00000,ko03029,ko03110 | DnaJ domain protein |
| HEJOHAOE_01099 | 3.56e-11 | - | - | - | S | - | - | - | COG NOG23778 non supervised orthologous group |
| HEJOHAOE_01100 | 2.97e-155 | nfnA | 1.18.1.2, 1.19.1.1 | - | C | ko:K00528,ko:K16951 | ko00920,ko01120,map00920,map01120 | ko00000,ko00001,ko01000 | domain protein |
| HEJOHAOE_01101 | 1.73e-255 | gltA | 1.4.1.13, 1.4.1.14 | - | C | ko:K00266 | ko00250,ko00910,ko01100,ko01110,ko01120,ko01130,ko01230,map00250,map00910,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko01000 | glutamate synthase |
| HEJOHAOE_01102 | 0.0 | rpoB | 2.7.7.6 | - | K | ko:K03043 | ko00230,ko00240,ko01100,ko03020,map00230,map00240,map01100,map03020 | br01611,ko00000,ko00001,ko00002,ko01000,ko03021,ko03400 | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates |
| HEJOHAOE_01103 | 0.0 | rpoC | 2.7.7.6 | - | K | ko:K03046 | ko00230,ko00240,ko01100,ko03020,map00230,map00240,map01100,map03020 | br01611,ko00000,ko00001,ko00002,ko01000,ko03021,ko03400 | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates |
| HEJOHAOE_01104 | 2.77e-15 | - | - | - | N | - | - | - | M6 family metalloprotease domain protein |
| HEJOHAOE_01105 | 4.93e-94 | thyX | 2.1.1.148 | - | H | ko:K03465 | ko00240,ko00670,ko01100,map00240,map00670,map01100 | ko00000,ko00001,ko01000 | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor, and NADPH and FADH(2) as the reductant |
| HEJOHAOE_01106 | 4.74e-84 | tmk | 2.1.1.45, 2.7.4.9, 4.1.1.19 | - | F | ko:K00560,ko:K00943,ko:K01585 | ko00240,ko00330,ko00670,ko01100,ko01523,map00240,map00330,map00670,map01100,map01523 | ko00000,ko00001,ko00002,ko01000 | dTDP biosynthetic process |
| HEJOHAOE_01107 | 3.05e-61 | - | - | - | S | ko:K01163 | - | ko00000 | Conserved protein |
| HEJOHAOE_01108 | 2.07e-05 | - | - | - | S | ko:K01163 | - | ko00000 | Psort location Cytoplasmic, score 8.96 |
| HEJOHAOE_01109 | 4.37e-51 | thiJ | 3.5.1.124 | - | S | ko:K03152 | - | ko00000,ko01000,ko01002 | DJ-1 family |
| HEJOHAOE_01110 | 3.5e-65 | ygfA | 6.3.3.2 | - | H | ko:K01934 | ko00670,ko01100,map00670,map01100 | ko00000,ko00001,ko01000 | 5-formyltetrahydrofolate cyclo-ligase family |
| HEJOHAOE_01111 | 4.75e-107 | mltG | - | - | S | ko:K07082 | - | ko00000 | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation |
| HEJOHAOE_01112 | 4.23e-154 | yhbU_1 | - | - | O | ko:K08303 | ko05120,map05120 | ko00000,ko00001,ko01000,ko01002 | Peptidase U32 |
| HEJOHAOE_01113 | 0.0 | alaS | 6.1.1.7 | - | J | ko:K01872 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain |
| HEJOHAOE_01116 | 1.06e-31 | - | - | - | N | - | - | - | CHAP domain |
| HEJOHAOE_01117 | 2.49e-82 | - | - | - | T | - | - | - | GHKL domain |
| HEJOHAOE_01118 | 2.13e-18 | - | - | - | T | - | - | - | LytTr DNA-binding domain |
| HEJOHAOE_01120 | 2.27e-09 | hprA | 1.1.1.29 | - | C | ko:K00018 | ko00260,ko00630,ko00680,ko01100,ko01110,ko01120,ko01130,ko01200,map00260,map00630,map00680,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | Dehydrogenase |
| HEJOHAOE_01123 | 2.49e-41 | - | - | - | L | - | - | - | Protein of unknown function (DUF5131) |
| HEJOHAOE_01124 | 6.12e-234 | recQ | 3.6.4.12 | - | L | ko:K03654 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03400 | ATP-dependent DNA helicase RecQ |
| HEJOHAOE_01125 | 8.41e-56 | - | - | - | I | - | - | - | Protein of unknown function (DUF2974) |
| HEJOHAOE_01126 | 2.71e-150 | xth | 3.1.11.2 | - | L | ko:K01142 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | exodeoxyribonuclease III |
| HEJOHAOE_01127 | 1.87e-29 | rubR2 | - | - | C | - | - | - | rubredoxin |
| HEJOHAOE_01128 | 6.24e-94 | rbr3A | - | - | C | - | - | - | Rubrerythrin |
| HEJOHAOE_01129 | 4.82e-41 | fur | - | - | P | ko:K03711,ko:K09825 | - | ko00000,ko03000 | belongs to the Fur family |
| HEJOHAOE_01130 | 1.4e-24 | - | - | - | G | ko:K11931 | ko02026,map02026 | ko00000,ko00001,ko01000 | Hypothetical glycosyl hydrolase family 13 |
| HEJOHAOE_01131 | 3.28e-45 | - | - | - | M | - | - | - | O-Antigen ligase |
| HEJOHAOE_01132 | 1.33e-09 | gph | 3.1.3.18 | - | G | ko:K01091 | ko00630,ko01100,ko01110,ko01130,map00630,map01100,map01110,map01130 | ko00000,ko00001,ko01000 | Phosphoglycolate phosphatase |
| HEJOHAOE_01133 | 2.11e-85 | - | - | - | G | - | - | - | Fibronectin type 3 domain |
| HEJOHAOE_01134 | 4.55e-56 | - | - | - | G | - | - | - | Fibronectin type 3 domain |
| HEJOHAOE_01135 | 3.45e-93 | - | 2.7.1.35 | - | H | ko:K00868 | ko00750,ko01100,map00750,map01100 | ko00000,ko00001,ko01000 | Phosphomethylpyrimidine kinase |
| HEJOHAOE_01136 | 3.07e-33 | - | - | - | S | - | - | - | ECF-type riboflavin transporter, S component |
| HEJOHAOE_01137 | 3.71e-79 | - | - | - | O | - | - | - | 4Fe-4S single cluster domain |
| HEJOHAOE_01139 | 1.48e-11 | - | - | - | I | - | - | - | PFAM Prenyltransferase squalene oxidase |
| HEJOHAOE_01140 | 1.15e-56 | - | - | - | L | - | - | - | DNA integration |
| HEJOHAOE_01144 | 2.72e-64 | - | - | - | S | - | - | - | Replication initiation factor |
| HEJOHAOE_01146 | 3.33e-31 | - | - | - | D | - | - | - | COG COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins |
| HEJOHAOE_01150 | 2.41e-48 | - | - | - | O | - | - | - | DnaJ molecular chaperone homology domain |
| HEJOHAOE_01151 | 3.44e-66 | - | - | - | M | - | - | - | Acetyltransferase (GNAT) family |
| HEJOHAOE_01152 | 9.15e-47 | - | - | - | S | - | - | - | Cupin |
| HEJOHAOE_01154 | 3.5e-30 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01155 | 7.77e-38 | - | - | - | S | - | - | - | Acetyltransferase GNAT family |
| HEJOHAOE_01157 | 9.76e-75 | wbbJ | 2.3.1.18, 2.3.1.79 | - | S | ko:K00633,ko:K00661 | - | ko00000,ko01000 | Bacterial transferase hexapeptide (six repeats) |
| HEJOHAOE_01158 | 2.32e-188 | hflX | - | - | S | ko:K03665 | - | ko00000,ko03009 | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis |
| HEJOHAOE_01159 | 6.1e-35 | - | 3.6.1.27 | - | I | ko:K19302 | ko00550,map00550 | ko00000,ko00001,ko01000,ko01011 | Acid phosphatase homologues |
| HEJOHAOE_01161 | 4.01e-104 | glmU | 2.3.1.157, 2.7.7.23 | - | M | ko:K04042 | ko00520,ko01100,ko01130,map00520,map01100,map01130 | ko00000,ko00001,ko00002,ko01000 | glucosamine-1-phosphate N-acetyltransferase activity |
| HEJOHAOE_01162 | 5.53e-290 | - | - | - | S | ko:K07137 | - | ko00000 | 'oxidoreductase |
| HEJOHAOE_01163 | 1.24e-136 | dnaX | 2.7.7.7 | - | L | ko:K02343 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity |
| HEJOHAOE_01164 | 1.51e-47 | yaaK | - | - | S | ko:K09747 | - | ko00000 | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection |
| HEJOHAOE_01165 | 4.67e-92 | recR | - | - | L | ko:K06187 | ko03440,map03440 | ko00000,ko00001,ko03400 | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO |
| HEJOHAOE_01166 | 4.85e-05 | - | - | - | N | - | - | - | domain, Protein |
| HEJOHAOE_01167 | 1.35e-36 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01168 | 1.36e-39 | - | - | - | T | - | - | - | Psort location |
| HEJOHAOE_01169 | 1.42e-72 | - | - | - | K | ko:K07694 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | helix_turn_helix, Lux Regulon |
| HEJOHAOE_01172 | 8.75e-57 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01174 | 7.2e-86 | - | - | - | C | - | - | - | Nitroreductase family |
| HEJOHAOE_01175 | 3.8e-64 | - | - | - | C | - | - | - | Nitroreductase family |
| HEJOHAOE_01176 | 2.5e-15 | - | - | - | S | ko:K07088 | - | ko00000 | Membrane transport protein |
| HEJOHAOE_01177 | 3.48e-17 | - | - | - | S | - | - | - | Domain of Unknown Function (DUF1540) |
| HEJOHAOE_01178 | 3.16e-27 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01182 | 1.08e-193 | - | - | - | M | - | - | - | Domain of unknown function (DUF1727) |
| HEJOHAOE_01183 | 2.22e-66 | - | - | - | S | ko:K07009 | - | ko00000 | glutamine amidotransferase |
| HEJOHAOE_01184 | 4.37e-285 | recD2 | 3.1.11.5 | - | L | ko:K03581 | ko03440,map03440 | ko00000,ko00001,ko01000,ko03400 | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity |
| HEJOHAOE_01185 | 4.81e-41 | comF | - | - | S | ko:K02242 | - | ko00000,ko00002,ko02044 | ComF family |
| HEJOHAOE_01186 | 2.56e-81 | mreB | - | - | D | ko:K03569 | - | ko00000,ko02048,ko03036,ko04812 | Cell shape determining protein, MreB Mrl family |
| HEJOHAOE_01188 | 2.4e-86 | - | 3.2.1.1 | GH13 | G | ko:K01176 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | Belongs to the glycosyl hydrolase 13 family |
| HEJOHAOE_01189 | 8.43e-150 | potA | 3.6.3.31 | - | P | ko:K11072 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system |
| HEJOHAOE_01190 | 3.97e-75 | potB | - | - | P | ko:K11071 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ABC-type spermidine putrescine transport system, permease component I |
| HEJOHAOE_01191 | 9.46e-78 | potC | - | - | E | ko:K11070 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| HEJOHAOE_01192 | 8.47e-100 | potD | - | - | E | ko:K11069 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Bacterial extracellular solute-binding protein |
| HEJOHAOE_01193 | 3.26e-87 | tagG | - | - | GM | ko:K09692 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ABC-2 type transporter |
| HEJOHAOE_01194 | 4.34e-108 | tagH | 3.6.3.40 | - | GM | ko:K01990,ko:K09691,ko:K09693 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01195 | 1.81e-62 | - | 4.1.1.35, 4.2.1.46 | - | GM | ko:K01710,ko:K08678 | ko00520,ko00521,ko00523,ko00525,ko01055,ko01100,ko01130,map00520,map00521,map00523,map00525,map01055,map01100,map01130 | ko00000,ko00001,ko00002,ko01000 | epimerase dehydratase |
| HEJOHAOE_01196 | 2.08e-30 | - | - | - | M | ko:K07271 | - | ko00000,ko01000 | LICD family |
| HEJOHAOE_01200 | 3.37e-34 | rpmB | - | - | J | ko:K02902 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bL28 family |
| HEJOHAOE_01201 | 3.07e-73 | - | - | - | S | - | - | - | peptidase M50 |
| HEJOHAOE_01202 | 2.44e-81 | scpA | - | - | D | ko:K05896 | - | ko00000,ko03036 | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves |
| HEJOHAOE_01203 | 2.53e-68 | scpB | - | - | D | ko:K06024 | - | ko00000,ko03036 | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves |
| HEJOHAOE_01204 | 1.35e-25 | - | - | - | S | - | - | - | Protein of unknown function (DUF2953) |
| HEJOHAOE_01205 | 1.3e-48 | ytfJ | - | - | S | - | - | - | Sporulation protein YtfJ |
| HEJOHAOE_01206 | 1.5e-75 | - | 3.4.16.4 | - | M | ko:K01286,ko:K07258 | ko00550,ko01100,map00550,map01100 | ko00000,ko00001,ko01000,ko01002,ko01011 | Belongs to the peptidase S11 family |
| HEJOHAOE_01207 | 5.87e-95 | rluB | 5.4.99.19, 5.4.99.22 | - | J | ko:K06178,ko:K06183 | - | ko00000,ko01000,ko03009 | Belongs to the pseudouridine synthase RsuA family |
| HEJOHAOE_01208 | 1.47e-117 | mdcD | 2.1.3.10, 4.1.1.87 | - | I | ko:K13932,ko:K13933,ko:K20510,ko:K20511 | - | ko00000,ko01000,ko02000 | CoA carboxylase activity |
| HEJOHAOE_01209 | 0.000279 | - | - | - | C | - | - | - | Conserved carboxylase domain |
| HEJOHAOE_01210 | 9.36e-276 | oadA | 4.1.1.3 | - | C | ko:K01571 | ko00620,ko01100,map00620,map01100 | ko00000,ko00001,ko01000,ko02000 | Pyruvate carboxylase, C-terminal domain subunit K01960 |
| HEJOHAOE_01212 | 4.22e-32 | - | - | - | G | - | - | - | Fibronectin type 3 domain |
| HEJOHAOE_01214 | 2.84e-93 | - | - | - | J | ko:K19055 | - | ko00000,ko01000,ko03016 | YbaK proline--tRNA ligase associated domain protein |
| HEJOHAOE_01215 | 2.34e-21 | - | - | - | - | ko:K01992 | - | ko00000,ko00002,ko02000 | - |
| HEJOHAOE_01216 | 1.3e-95 | ytrB | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | ABC-type multidrug transport system, ATPase component |
| HEJOHAOE_01217 | 4.84e-37 | - | - | - | K | ko:K07979 | - | ko00000,ko03000 | helix_turn_helix gluconate operon transcriptional repressor |
| HEJOHAOE_01218 | 7.84e-138 | sigG | - | - | K | ko:K03091 | - | ko00000,ko03021 | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released |
| HEJOHAOE_01219 | 1.07e-29 | - | - | - | S | - | - | - | protein, YerC YecD |
| HEJOHAOE_01220 | 1.32e-72 | - | - | - | H | - | - | - | Methyltransferase domain |
| HEJOHAOE_01221 | 4.79e-107 | hslO | - | - | O | ko:K04083 | - | ko00000,ko03110 | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress |
| HEJOHAOE_01222 | 0.000157 | - | - | - | S | ko:K07003 | - | ko00000 | growth of symbiont in host cell |
| HEJOHAOE_01224 | 4.88e-68 | rluD_2 | 5.4.99.23 | - | J | ko:K06180 | - | ko00000,ko01000,ko03009 | Responsible for synthesis of pseudouridine from uracil |
| HEJOHAOE_01225 | 1.55e-17 | - | - | - | S | - | - | - | Protein of unknown function (DUF1294) |
| HEJOHAOE_01226 | 1.45e-109 | - | - | - | S | - | - | - | Glycosyl hydrolase-like 10 |
| HEJOHAOE_01227 | 6.22e-168 | yqeV | 2.8.4.5 | - | J | ko:K18707 | - | ko00000,ko01000,ko03016 | tRNA methylthiotransferase YqeV |
| HEJOHAOE_01229 | 1.54e-54 | hisE | 3.6.1.31 | - | E | ko:K01523 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Phosphoribosyl-ATP |
| HEJOHAOE_01230 | 1.36e-60 | hisI | 3.5.4.19, 3.6.1.31 | - | E | ko:K01496,ko:K11755 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP |
| HEJOHAOE_01231 | 6.61e-95 | hisA | 5.3.1.16 | - | E | ko:K01814 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase |
| HEJOHAOE_01232 | 3.76e-87 | hisB | 4.2.1.19 | - | E | ko:K01693 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Imidazoleglycerol-phosphate dehydratase |
| HEJOHAOE_01233 | 9.01e-116 | hisC | 2.6.1.9 | - | E | ko:K00817 | ko00340,ko00350,ko00360,ko00400,ko00401,ko00960,ko01100,ko01110,ko01130,ko01230,map00340,map00350,map00360,map00400,map00401,map00960,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily |
| HEJOHAOE_01234 | 4.35e-213 | hisD | 1.1.1.23 | - | E | ko:K00013 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine |
| HEJOHAOE_01235 | 2.56e-108 | hisG | 2.4.2.17 | - | E | ko:K00765,ko:K02502 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity |
| HEJOHAOE_01236 | 5.96e-135 | hisZ | 2.4.2.17, 6.1.1.21 | - | E | ko:K00765,ko:K01892,ko:K02502 | ko00340,ko00970,ko01100,ko01110,ko01230,map00340,map00970,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Histidyl-tRNA synthetase |
| HEJOHAOE_01237 | 1.18e-60 | yhhT | - | - | S | - | - | - | AI-2E family transporter |
| HEJOHAOE_01238 | 0.0 | polC | 2.7.7.7 | - | L | ko:K02342,ko:K03763 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity |
| HEJOHAOE_01239 | 2.81e-183 | ispG | 1.17.7.1, 1.17.7.3 | - | I | ko:K03526 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate |
| HEJOHAOE_01240 | 1.64e-59 | rseP | - | - | M | ko:K11749 | ko02024,ko04112,map02024,map04112 | ko00000,ko00001,ko01000,ko01002 | Metalloprotease |
| HEJOHAOE_01241 | 9.1e-132 | dxr | 1.1.1.267 | - | I | ko:K00099 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) |
| HEJOHAOE_01242 | 2.35e-37 | cdsA | 2.7.7.41 | - | I | ko:K00981 | ko00564,ko01100,ko01110,ko04070,map00564,map01100,map01110,map04070 | ko00000,ko00001,ko00002,ko01000 | Psort location CytoplasmicMembrane, score 10.00 |
| HEJOHAOE_01243 | 3.91e-108 | uppS | 2.5.1.31 | - | H | ko:K00806 | ko00900,ko01110,map00900,map01110 | ko00000,ko00001,ko01000,ko01006 | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids |
| HEJOHAOE_01244 | 1.5e-66 | frr | - | - | J | ko:K02838 | - | ko00000,ko03012 | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another |
| HEJOHAOE_01245 | 3.27e-137 | pyrH | 2.7.4.22 | - | F | ko:K09903 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko01000 | Catalyzes the reversible phosphorylation of UMP to UDP |
| HEJOHAOE_01248 | 0.0 | mfd | - | - | L | ko:K03723 | ko03420,map03420 | ko00000,ko00001,ko01000,ko03400 | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site |
| HEJOHAOE_01249 | 8.81e-86 | pth | 3.1.1.29 | - | J | ko:K01056 | - | ko00000,ko01000,ko03012 | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis |
| HEJOHAOE_01250 | 2.4e-67 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01251 | 7.06e-171 | prs | 2.7.6.1 | - | F | ko:K00948 | ko00030,ko00230,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00030,map00230,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) |
| HEJOHAOE_01252 | 5.82e-65 | glmU | 2.3.1.157, 2.7.7.23 | - | M | ko:K04042 | ko00520,ko01100,ko01130,map00520,map01100,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain |
| HEJOHAOE_01253 | 0.0 | ppdK | 2.7.9.1 | - | G | ko:K01006 | ko00620,ko00710,ko00720,ko01100,ko01120,ko01200,map00620,map00710,map00720,map01100,map01120,map01200 | ko00000,ko00001,ko00002,ko01000 | Belongs to the PEP-utilizing enzyme family |
| HEJOHAOE_01255 | 0.000641 | lanR | - | - | K | ko:K07729 | - | ko00000,ko03000 | Transcriptional |
| HEJOHAOE_01257 | 6.28e-67 | sigF | - | - | K | ko:K03091 | - | ko00000,ko03021 | Belongs to the sigma-70 factor family |
| HEJOHAOE_01258 | 7.22e-57 | spoIIAB | 2.7.11.1 | - | T | ko:K06379 | - | ko00000,ko01000 | Binds to sigma F and blocks its ability to form an RNA polymerase holoenzyme (E-sigma F). Phosphorylates SpoIIAA on a serine residue. This phosphorylation may enable SpoIIAA to act as an anti-anti-sigma factor that counteracts SpoIIAB and thus releases sigma F from inhibition |
| HEJOHAOE_01259 | 7.14e-24 | spoIIAA | - | - | T | ko:K06378 | - | ko00000 | Belongs to the anti-sigma-factor antagonist family |
| HEJOHAOE_01260 | 8e-133 | folC | 6.3.2.12, 6.3.2.17 | - | H | ko:K11754 | ko00790,ko01100,map00790,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the folylpolyglutamate synthase family |
| HEJOHAOE_01261 | 7.84e-130 | rsmI | 2.1.1.198 | - | H | ko:K07056 | - | ko00000,ko01000,ko03009 | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA |
| HEJOHAOE_01262 | 4.19e-52 | - | - | - | S | - | - | - | Methyltransferase small domain |
| HEJOHAOE_01263 | 3.55e-11 | - | - | - | C | - | - | - | 4Fe-4S binding domain |
| HEJOHAOE_01264 | 9.79e-149 | yaaT | - | - | S | - | - | - | PSP1 C-terminal domain protein |
| HEJOHAOE_01265 | 1.36e-05 | holB | 2.7.7.7 | - | L | ko:K02341 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | the delta' subunit seems to interact with the gamma subunit to transfer the beta subunit on the DNA |
| HEJOHAOE_01266 | 2.28e-24 | yfcE1 | - | - | S | ko:K07095 | - | ko00000 | TIGRFAM phosphodiesterase, MJ0936 |
| HEJOHAOE_01268 | 4.75e-12 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01270 | 7.04e-193 | proA | 1.2.1.41 | - | E | ko:K00147 | ko00330,ko00332,ko01100,ko01110,ko01130,ko01230,map00330,map00332,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Aldehyde dehydrogenase family |
| HEJOHAOE_01271 | 6.75e-118 | proB | 2.7.2.11 | - | E | ko:K00931 | ko00330,ko00332,ko01100,ko01130,ko01230,map00330,map00332,map01100,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate |
| HEJOHAOE_01272 | 2.21e-46 | metAA | 2.3.1.46 | - | E | ko:K00651 | ko00270,ko00920,ko01100,ko01110,ko01230,map00270,map00920,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine |
| HEJOHAOE_01273 | 1.72e-23 | lspA | 3.4.23.36 | - | MU | ko:K03101 | ko03060,map03060 | ko00000,ko00001,ko01000,ko01002 | This protein specifically catalyzes the removal of signal peptides from prolipoproteins |
| HEJOHAOE_01274 | 1.37e-129 | rluD | 5.4.99.23 | - | J | ko:K06180 | - | ko00000,ko01000,ko03009 | Responsible for synthesis of pseudouridine from uracil |
| HEJOHAOE_01275 | 1.41e-59 | rplS | - | - | J | ko:K02884 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site |
| HEJOHAOE_01276 | 6.03e-31 | lepB | 3.4.21.89 | - | U | ko:K03100 | ko02024,ko03060,map02024,map03060 | ko00000,ko00001,ko01000,ko01002 | Belongs to the peptidase S26 family |
| HEJOHAOE_01278 | 9.85e-08 | lepB | 3.4.21.89 | - | U | ko:K03100 | ko02024,ko03060,map02024,map03060 | ko00000,ko00001,ko01000,ko01002 | Belongs to the peptidase S26 family |
| HEJOHAOE_01279 | 4.69e-143 | ylqF | - | - | S | ko:K14540 | - | ko00000,ko03009 | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity |
| HEJOHAOE_01280 | 6.05e-71 | rnhB | 3.1.26.4 | - | L | ko:K03470 | ko03030,map03030 | ko00000,ko00001,ko01000,ko03032 | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids |
| HEJOHAOE_01281 | 1.16e-18 | - | - | - | L | ko:K07460 | - | ko00000 | Belongs to the UPF0102 family |
| HEJOHAOE_01282 | 2.62e-54 | dp2 | 3.4.13.19 | - | E | ko:K01273 | - | ko00000,ko00537,ko01000,ko01002,ko04147 | Dipeptidase |
| HEJOHAOE_01283 | 6.12e-229 | thrC | 4.2.3.1 | - | E | ko:K01733 | ko00260,ko00750,ko01100,ko01110,ko01120,ko01230,map00260,map00750,map01100,map01110,map01120,map01230 | ko00000,ko00001,ko00002,ko01000 | Threonine synthase |
| HEJOHAOE_01284 | 7.86e-92 | - | - | - | S | ko:K07099 | - | ko00000 | Ser Thr phosphatase family protein |
| HEJOHAOE_01285 | 4.3e-158 | tig | - | - | D | ko:K03545 | - | ko00000 | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase |
| HEJOHAOE_01286 | 1.53e-107 | clpP | 3.4.21.92 | - | OU | ko:K01358 | ko04112,ko04212,map04112,map04212 | ko00000,ko00001,ko01000,ko01002 | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins |
| HEJOHAOE_01287 | 3.19e-198 | clpX | - | - | O | ko:K03544 | ko04112,map04112 | ko00000,ko00001,ko03110 | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP |
| HEJOHAOE_01288 | 7.25e-299 | lon | 3.4.21.53 | - | O | ko:K01338 | ko04112,map04112 | ko00000,ko00001,ko01000,ko01002 | ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner |
| HEJOHAOE_01289 | 1.96e-59 | engB | - | - | D | ko:K03978 | - | ko00000,ko03036 | Necessary for normal cell division and for the maintenance of normal septation |
| HEJOHAOE_01290 | 1.25e-209 | lysA | 4.1.1.20 | - | E | ko:K01586 | ko00300,ko01100,ko01110,ko01120,ko01130,ko01230,map00300,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine |
| HEJOHAOE_01291 | 5.89e-110 | - | - | - | S | - | - | - | Protein of unknown function (DUF1275) |
| HEJOHAOE_01292 | 1.56e-21 | - | - | - | K | - | - | - | Bacterial regulatory proteins, tetR family |
| HEJOHAOE_01293 | 1.29e-119 | - | - | - | CO | - | - | - | Redoxin |
| HEJOHAOE_01294 | 9.33e-166 | - | - | - | C | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01295 | 1.64e-125 | cutR | - | - | K | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01296 | 2.19e-167 | - | 2.7.13.3 | - | T | ko:K07645 | ko02020,ko02024,map02020,map02024 | ko00000,ko00001,ko00002,ko01000,ko01001,ko02022 | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain |
| HEJOHAOE_01297 | 2.1e-128 | - | - | - | K | - | - | - | Bacterial regulatory proteins, tetR family |
| HEJOHAOE_01300 | 1.53e-27 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01301 | 2.77e-65 | - | 3.5.1.28 | - | M | ko:K01449 | - | ko00000,ko01000 | cell wall hydrolase |
| HEJOHAOE_01304 | 3.22e-154 | - | - | - | K | - | - | - | Putative DNA-binding domain |
| HEJOHAOE_01305 | 3.01e-38 | - | - | - | K | - | - | - | sequence-specific DNA binding |
| HEJOHAOE_01306 | 5.3e-71 | rpiB | 5.3.1.6 | - | G | ko:K01808 | ko00030,ko00051,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00030,map00051,map00710,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Ribose 5-phosphate isomerase |
| HEJOHAOE_01307 | 5.43e-59 | yeaZ | - | - | O | ko:K14742 | - | ko00000,ko03016 | Glycoprotease family |
| HEJOHAOE_01308 | 5.49e-60 | yjeE | 2.7.1.221 | - | S | ko:K06925,ko:K07102 | ko00520,ko01100,map00520,map01100 | ko00000,ko00001,ko01000,ko03016 | Threonylcarbamoyl adenosine biosynthesis protein TsaE |
| HEJOHAOE_01309 | 1e-310 | fhs | 6.3.4.3 | - | H | ko:K01938 | ko00670,ko00720,ko01100,ko01120,ko01200,map00670,map00720,map01100,map01120,map01200 | ko00000,ko00001,ko00002,ko01000 | Belongs to the formate--tetrahydrofolate ligase family |
| HEJOHAOE_01310 | 1.86e-114 | rodA | - | - | D | ko:K05837 | - | ko00000,ko03036 | Belongs to the SEDS family |
| HEJOHAOE_01311 | 2.05e-17 | - | - | - | S | - | - | - | YbbR-like protein |
| HEJOHAOE_01312 | 2.49e-62 | dacA | 2.7.7.85 | - | S | ko:K18672 | - | ko00000,ko01000 | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria |
| HEJOHAOE_01313 | 3.99e-136 | - | - | - | E | - | - | - | cysteine desulfurase family protein |
| HEJOHAOE_01315 | 2.67e-105 | dapB | 1.17.1.8 | - | E | ko:K00215 | ko00261,ko00300,ko01100,ko01110,ko01120,ko01130,ko01230,map00261,map00300,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate |
| HEJOHAOE_01316 | 3.5e-128 | dapA | 4.3.3.7 | - | E | ko:K01714 | ko00261,ko00300,ko01100,ko01110,ko01120,ko01130,ko01230,map00261,map00300,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) |
| HEJOHAOE_01317 | 1.06e-202 | asd | 1.2.1.11 | - | E | ko:K00133 | ko00260,ko00261,ko00270,ko00300,ko01100,ko01110,ko01120,ko01130,ko01210,ko01230,map00260,map00261,map00270,map00300,map01100,map01110,map01120,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Belongs to the aspartate-semialdehyde dehydrogenase family |
| HEJOHAOE_01318 | 6.65e-179 | queA | 2.4.99.17 | - | H | ko:K07568 | - | ko00000,ko01000,ko03016 | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) |
| HEJOHAOE_01319 | 2.36e-214 | tgt | 2.4.2.29 | - | J | ko:K00773 | - | ko00000,ko01000,ko03016 | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) |
| HEJOHAOE_01320 | 1.46e-15 | yajC | - | - | U | ko:K03210 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | protein transport |
| HEJOHAOE_01322 | 1.69e-07 | - | 2.7.11.1 | - | T | ko:K08269,ko:K13412 | ko04136,ko04138,ko04139,ko04140,ko04150,ko04212,ko04626,ko05145,map04136,map04138,map04139,map04140,map04150,map04212,map04626,map05145 | ko00000,ko00001,ko01000,ko01001,ko03029,ko04131 | protein serine/threonine kinase activity |
| HEJOHAOE_01323 | 4.11e-192 | - | 2.6.1.59 | - | E | ko:K02805 | - | ko00000,ko01000,ko01007 | Belongs to the DegT DnrJ EryC1 family |
| HEJOHAOE_01324 | 1.37e-31 | spoIIID | - | - | K | ko:K06283 | - | ko00000,ko03000 | Stage III sporulation protein D |
| HEJOHAOE_01325 | 2.19e-47 | - | - | - | D | - | - | - | protein involved in cytokinesis, contains TGc (transglutaminase protease-like) domain |
| HEJOHAOE_01327 | 2.72e-46 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_01328 | 1.41e-63 | - | - | - | G | - | - | - | YjeF-related protein N-terminus |
| HEJOHAOE_01329 | 2.65e-11 | - | 3.2.1.37 | GH43 | G | ko:K01198 | ko00520,ko01100,map00520,map01100 | ko00000,ko00001,ko01000 | PFAM glycoside hydrolase family 39 |
| HEJOHAOE_01330 | 4.11e-122 | - | - | - | M | ko:K21472 | - | ko00000,ko01000,ko01002,ko01011 | Peptidase, M23 |
| HEJOHAOE_01331 | 3.36e-173 | algI | - | - | M | ko:K19294 | - | ko00000 | MBOAT, membrane-bound O-acyltransferase family |
| HEJOHAOE_01332 | 1.57e-68 | - | - | - | S | - | - | - | DHHW protein |
| HEJOHAOE_01334 | 4.2e-113 | - | - | - | V | - | - | - | MatE |
| HEJOHAOE_01335 | 0.0 | mshQ | - | - | U | ko:K12287 | - | ko00000,ko02044 | domain, Protein |
| HEJOHAOE_01336 | 5.87e-158 | - | 4.1.3.39 | - | E | ko:K01666 | ko00360,ko00362,ko00621,ko00622,ko01100,ko01120,ko01220,map00360,map00362,map00621,map00622,map01100,map01120,map01220 | br01602,ko00000,ko00001,ko00002,ko01000 | HMGL-like |
| HEJOHAOE_01337 | 1.39e-190 | pyrC | 3.5.2.3 | - | F | ko:K01465 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily |
| HEJOHAOE_01339 | 2.54e-125 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01340 | 1.1e-05 | - | - | - | S | - | - | - | Putative ABC-transporter type IV |
| HEJOHAOE_01341 | 3.69e-61 | rnmV | 3.1.26.8 | - | L | ko:K05985 | - | ko00000,ko01000 | Ribonuclease M5 |
| HEJOHAOE_01342 | 2.67e-20 | holA | 2.7.7.7 | - | L | ko:K02340 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | DNA polymerase III delta subunit |
| HEJOHAOE_01343 | 2.67e-57 | - | - | - | S | ko:K02238 | - | ko00000,ko00002,ko02044 | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01345 | 1.05e-83 | - | 2.4.2.7 | - | F | ko:K00759 | ko00230,ko01100,map00230,map01100 | ko00000,ko00001,ko01000,ko04147 | Psort location Cytoplasmic, score |
| HEJOHAOE_01346 | 1.17e-46 | hinT | - | - | FG | ko:K02503 | - | ko00000,ko04147 | Hit family |
| HEJOHAOE_01347 | 2.61e-62 | plsY | 2.3.1.15 | - | I | ko:K08591 | ko00561,ko00564,ko01100,ko01110,map00561,map00564,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko01004 | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP |
| HEJOHAOE_01348 | 5.73e-231 | der | - | - | S | ko:K03977 | - | ko00000,ko03009 | GTPase that plays an essential role in the late steps of ribosome biogenesis |
| HEJOHAOE_01349 | 5.24e-170 | - | - | - | C | - | - | - | FeS-containing Cyanobacterial-specific oxidoreductase |
| HEJOHAOE_01350 | 2.8e-12 | rpmF | - | - | J | ko:K02911 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011,ko03029 | Belongs to the bacterial ribosomal protein bL32 family |
| HEJOHAOE_01351 | 4.63e-18 | - | - | - | S | ko:K07040 | - | ko00000 | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_01352 | 1.43e-115 | - | - | - | S | - | - | - | Elongator protein 3, MiaB family, Radical SAM |
| HEJOHAOE_01353 | 2.29e-101 | - | - | - | S | ko:K09125 | - | ko00000 | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage |
| HEJOHAOE_01355 | 8.07e-15 | - | - | - | KT | - | - | - | BlaR1 peptidase M56 |
| HEJOHAOE_01357 | 6.67e-132 | rmuC | - | - | S | ko:K09760 | - | ko00000 | RmuC domain protein |
| HEJOHAOE_01358 | 8.65e-106 | - | - | - | J | ko:K02945 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | S1 RNA binding domain protein |
| HEJOHAOE_01359 | 2.11e-57 | - | - | - | O | - | - | - | Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD |
| HEJOHAOE_01362 | 2.76e-21 | - | - | - | K | - | - | - | Helix-turn-helix XRE-family like proteins |
| HEJOHAOE_01363 | 2.35e-190 | ttcA | - | - | D | - | - | - | Belongs to the TtcA family |
| HEJOHAOE_01364 | 1.62e-51 | - | 3.1.3.3 | - | KT | ko:K07315 | - | ko00000,ko01000,ko03021 | Sigma factor PP2C-like phosphatases |
| HEJOHAOE_01365 | 4.93e-54 | - | - | - | M | - | - | - | Papain family cysteine protease |
| HEJOHAOE_01366 | 2.35e-108 | gpr | 3.4.24.78 | - | C | ko:K06012 | - | ko00000,ko01000,ko01002 | Initiates the rapid degradation of small, acid-soluble proteins during spore germination |
| HEJOHAOE_01367 | 1.55e-33 | spoIIP | - | - | M | ko:K06385 | - | ko00000 | PFAM Stage II sporulation P family protein |
| HEJOHAOE_01368 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | - | C | ko:K04072 | ko00010,ko00071,ko00350,ko00620,ko00625,ko00626,ko00650,ko01100,ko01110,ko01120,ko01130,ko01220,map00010,map00071,map00350,map00620,map00625,map00626,map00650,map01100,map01110,map01120,map01130,map01220 | ko00000,ko00001,ko01000 | belongs to the iron- containing alcohol dehydrogenase family |
| HEJOHAOE_01370 | 3.15e-74 | - | - | - | S | - | - | - | Belongs to the UPF0348 family |
| HEJOHAOE_01371 | 4.04e-186 | ackA | 2.7.2.1 | - | H | ko:K00925 | ko00430,ko00620,ko00640,ko00680,ko00720,ko01100,ko01120,ko01200,map00430,map00620,map00640,map00680,map00720,map01100,map01120,map01200 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction |
| HEJOHAOE_01372 | 6.17e-28 | yuzA | - | - | S | ko:K09779 | - | ko00000 | Conserved protein |
| HEJOHAOE_01374 | 1.3e-85 | - | - | - | S | ko:K07088 | - | ko00000 | Membrane transport protein |
| HEJOHAOE_01375 | 1.39e-130 | - | - | - | L | - | - | - | ATPase domain of DNA mismatch repair MUTS family |
| HEJOHAOE_01376 | 0.0 | leuS | 6.1.1.4 | - | J | ko:K01869 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Belongs to the class-I aminoacyl-tRNA synthetase family |
| HEJOHAOE_01377 | 1.03e-22 | rpsU | - | - | J | ko:K02970 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bS21 family |
| HEJOHAOE_01378 | 4.13e-75 | aroQ | 4.2.1.10 | - | E | ko:K03786 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes a trans-dehydration via an enolate intermediate |
| HEJOHAOE_01379 | 2.48e-83 | yqhT | 3.4.11.9 | - | E | ko:K01262 | - | ko00000,ko01000,ko01002 | Xaa-Pro dipeptidase |
| HEJOHAOE_01380 | 3.91e-118 | efp | - | - | J | ko:K02356 | - | ko00000,ko03012 | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase |
| HEJOHAOE_01381 | 8.65e-29 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01382 | 7.23e-24 | yunB | - | - | S | - | - | - | sporulation protein YunB |
| HEJOHAOE_01383 | 8.56e-234 | miaB | 2.8.4.3 | - | J | ko:K06168 | - | ko00000,ko01000,ko03016 | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine |
| HEJOHAOE_01384 | 6.2e-28 | - | - | - | S | - | - | - | Belongs to the UPF0342 family |
| HEJOHAOE_01385 | 0.0 | mutS | - | - | L | ko:K03555 | ko03430,map03430 | ko00000,ko00001,ko03400 | that it carries out the mismatch recognition step. This protein has a weak ATPase activity |
| HEJOHAOE_01386 | 7.38e-212 | mutL | - | - | L | ko:K03572 | ko03430,map03430 | ko00000,ko00001,ko03400 | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex |
| HEJOHAOE_01387 | 9.25e-103 | miaA | 2.5.1.75 | - | J | ko:K00791 | ko00908,ko01100,ko01110,map00908,map01100,map01110 | ko00000,ko00001,ko01000,ko01006,ko03016 | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) |
| HEJOHAOE_01388 | 2.11e-94 | - | - | - | M | - | - | - | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family |
| HEJOHAOE_01389 | 1.68e-92 | ylmE | - | - | S | ko:K06997 | - | ko00000 | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis |
| HEJOHAOE_01390 | 2.35e-62 | sepF | - | - | D | ko:K09772 | - | ko00000,ko03036 | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA |
| HEJOHAOE_01391 | 3.26e-62 | - | - | - | S | - | - | - | S4 domain protein |
| HEJOHAOE_01392 | 9.12e-20 | - | - | - | D | ko:K04074 | - | ko00000,ko03036 | DivIVA domain protein |
| HEJOHAOE_01394 | 1.18e-154 | mnmA | 2.8.1.13 | - | J | ko:K00566 | ko04122,map04122 | ko00000,ko00001,ko01000,ko03016 | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 |
| HEJOHAOE_01395 | 1.09e-155 | nadA | 2.5.1.72 | - | H | ko:K03517 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate |
| HEJOHAOE_01397 | 2.11e-58 | - | 3.4.22.70 | - | S | ko:K08600 | - | ko00000,ko01000,ko01002,ko01011 | Sortase family |
| HEJOHAOE_01398 | 1.39e-48 | - | - | - | K | - | - | - | Cell envelope-like function transcriptional attenuator common domain protein |
| HEJOHAOE_01399 | 2.54e-37 | - | - | - | K | - | - | - | Cell envelope-related transcriptional attenuator |
| HEJOHAOE_01400 | 5.55e-77 | yfbR | 3.1.3.89 | - | S | ko:K07023,ko:K08722 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko01000 | HD containing hydrolase-like enzyme |
| HEJOHAOE_01401 | 1.07e-239 | - | - | - | S | - | - | - | Bacterial membrane protein YfhO |
| HEJOHAOE_01402 | 1.44e-70 | ytjP | 3.5.1.18 | - | E | ko:K01439 | ko00300,ko01100,ko01120,ko01230,map00300,map01100,map01120,map01230 | ko00000,ko00001,ko00002,ko01000 | Dipeptidase |
| HEJOHAOE_01404 | 8.22e-101 | - | - | - | M | - | - | - | Succinoglycan biosynthesis protein exoa |
| HEJOHAOE_01405 | 3.93e-82 | licD3 | - | - | M | ko:K07271 | - | ko00000,ko01000 | LicD family |
| HEJOHAOE_01406 | 1.76e-27 | - | - | - | L | - | - | - | Psort location Cytoplasmic, score 8.96 |
| HEJOHAOE_01407 | 3.66e-62 | ribU | - | - | S | - | - | - | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins |
| HEJOHAOE_01408 | 6.64e-23 | - | - | - | T | - | - | - | Pfam:DUF3816 |
| HEJOHAOE_01409 | 1.63e-227 | glgA | 2.4.1.21 | GT5 | G | ko:K00703 | ko00500,ko01100,ko01110,ko02026,map00500,map01100,map01110,map02026 | ko00000,ko00001,ko00002,ko01000,ko01003 | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
| HEJOHAOE_01410 | 2.9e-98 | glgD | 2.7.7.27 | - | G | ko:K00975 | ko00500,ko00520,ko01100,ko01110,ko02026,map00500,map00520,map01100,map01110,map02026 | ko00000,ko00001,ko00002,ko01000 | Glucose-1-phosphate adenylyltransferase, GlgD subunit |
| HEJOHAOE_01411 | 1.39e-21 | glgC | 2.7.7.27 | - | H | ko:K00975 | ko00500,ko00520,ko01100,ko01110,ko02026,map00500,map00520,map01100,map01110,map02026 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans |
| HEJOHAOE_01412 | 5.49e-10 | - | - | - | M | - | - | - | NLP P60 protein |
| HEJOHAOE_01413 | 1.48e-150 | - | - | - | S | ko:K06923 | - | ko00000 | ATPase (AAA superfamily) |
| HEJOHAOE_01414 | 1.47e-110 | - | - | - | GM | - | - | - | methyltransferase FkbM family |
| HEJOHAOE_01416 | 2.51e-138 | pflA | 1.97.1.4 | - | C | ko:K04069 | - | ko00000,ko01000 | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine |
| HEJOHAOE_01417 | 0.0 | pflB | 2.3.1.54 | - | C | ko:K00656 | ko00620,ko00640,ko00650,ko01100,ko01120,map00620,map00640,map00650,map01100,map01120 | ko00000,ko00001,ko01000 | Psort location Cytoplasmic, score |
| HEJOHAOE_01418 | 7.79e-59 | - | - | - | H | - | - | - | HD domain |
| HEJOHAOE_01419 | 4.68e-97 | alkA | 4.2.99.18 | - | L | ko:K03660 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | 8-oxoguanine DNA glycosylase |
| HEJOHAOE_01420 | 1.13e-297 | glmS | 2.6.1.16 | - | M | ko:K00820 | ko00250,ko00520,ko01100,ko01130,ko04931,map00250,map00520,map01100,map01130,map04931 | ko00000,ko00001,ko01000,ko01002 | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source |
| HEJOHAOE_01421 | 5.37e-244 | capD | - | - | GM | - | - | - | Polysaccharide biosynthesis protein |
| HEJOHAOE_01422 | 1.6e-44 | - | - | - | M | ko:K07098 | - | ko00000 | Calcineurin-like phosphoesterase superfamily domain |
| HEJOHAOE_01424 | 1.07e-69 | srtB | 3.4.22.70 | - | S | ko:K08600 | - | ko00000,ko01000,ko01002,ko01011 | Sortase family |
| HEJOHAOE_01425 | 1.35e-76 | thiI | 2.8.1.4 | - | H | ko:K03151 | ko00730,ko01100,ko04122,map00730,map01100,map04122 | ko00000,ko00001,ko01000,ko03016 | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS |
| HEJOHAOE_01426 | 1.6e-06 | - | - | - | K | - | - | - | Helix-turn-helix |
| HEJOHAOE_01430 | 4.71e-49 | - | - | - | S | ko:K07025 | - | ko00000 | HAD family hydrolase |
| HEJOHAOE_01431 | 2.95e-98 | nth | 4.2.99.18 | - | L | ko:K10773 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate |
| HEJOHAOE_01432 | 1.14e-42 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01436 | 1.65e-198 | mgtE | - | - | P | ko:K06213 | - | ko00000,ko02000 | Acts as a magnesium transporter |
| HEJOHAOE_01437 | 3.86e-67 | - | 3.4.21.107 | - | O | ko:K04771 | ko01503,ko02020,map01503,map02020 | ko00000,ko00001,ko00002,ko01000,ko01002,ko03110 | Trypsin-like serine proteases typically periplasmic contain C-terminal PDZ domain |
| HEJOHAOE_01438 | 6.48e-186 | fba | 4.1.2.13 | - | G | ko:K01624 | ko00010,ko00030,ko00051,ko00680,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00010,map00030,map00051,map00680,map00710,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_01439 | 1.32e-52 | bioY | - | - | S | ko:K03523 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | BioY family |
| HEJOHAOE_01441 | 0.0 | - | - | - | L | - | - | - | AAA domain |
| HEJOHAOE_01442 | 2.14e-54 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HEJOHAOE_01443 | 4.66e-12 | yabN | 3.6.1.66 | - | K | ko:K02428,ko:K02499 | ko00230,map00230 | ko00000,ko00001,ko01000,ko03036 | COG3956 Protein containing tetrapyrrole methyltransferase domain and MazG-like |
| HEJOHAOE_01444 | 3.68e-258 | - | - | - | S | ko:K06921 | - | ko00000 | ATPase domain predominantly from Archaea |
| HEJOHAOE_01445 | 2.49e-195 | cytX | - | - | F | - | - | - | COG COG1457 Purine-cytosine permease and related proteins |
| HEJOHAOE_01446 | 2.73e-146 | thiD | 2.7.1.49, 2.7.4.7 | - | H | ko:K00941 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko00002,ko01000 | Carbohydrate kinase |
| HEJOHAOE_01447 | 2.17e-41 | - | - | - | S | - | - | - | Hydrolase |
| HEJOHAOE_01448 | 5.09e-105 | thiE | 2.5.1.3 | - | H | ko:K00788 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko00002,ko01000 | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) |
| HEJOHAOE_01449 | 1.4e-159 | thiM | 2.7.1.50 | - | H | ko:K00878 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) |
| HEJOHAOE_01451 | 3.99e-296 | - | - | - | P | ko:K03498 | - | ko00000,ko02000 | Potassium uptake protein |
| HEJOHAOE_01452 | 3.26e-143 | ktrA | - | - | P | ko:K03499 | - | ko00000,ko02000 | domain protein |
| HEJOHAOE_01453 | 2.44e-44 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01454 | 0.0 | kdpD | 2.7.13.3 | - | T | ko:K07646 | ko02020,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko02022 | ATPase histidine kinase DNA gyrase B HSP90 domain protein |
| HEJOHAOE_01455 | 5.88e-164 | kdpE | - | - | KT | ko:K07667 | ko02020,ko02024,map02020,map02024 | ko00000,ko00001,ko00002,ko02022 | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain |
| HEJOHAOE_01456 | 9.37e-174 | - | - | - | L | - | - | - | Radical SAM domain protein |
| HEJOHAOE_01457 | 8.45e-162 | spoIIE | 3.1.3.16 | - | KT | ko:K06382 | - | ko00000,ko01000 | stage II sporulation protein E |
| HEJOHAOE_01460 | 9.59e-22 | - | - | - | NU | - | - | - | CotH kinase protein |
| HEJOHAOE_01461 | 8.91e-125 | pyk | 2.7.1.40 | - | G | ko:K00873 | ko00010,ko00230,ko00620,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,ko04922,ko04930,ko05165,ko05203,ko05230,map00010,map00230,map00620,map01100,map01110,map01120,map01130,map01200,map01230,map04922,map04930,map05165,map05203,map05230 | ko00000,ko00001,ko00002,ko01000,ko04131,ko04147 | Belongs to the pyruvate kinase family |
| HEJOHAOE_01462 | 2.06e-18 | aroK | 2.7.1.71 | - | E | ko:K00891 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate |
| HEJOHAOE_01463 | 1.05e-126 | pheA | 4.2.1.51, 5.4.99.5 | - | E | ko:K04518,ko:K14170 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Prephenate dehydratase |
| HEJOHAOE_01464 | 1.36e-153 | aroC | 4.2.3.5 | - | E | ko:K01736 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system |
| HEJOHAOE_01465 | 1.1e-148 | aroA | 2.5.1.19 | - | E | ko:K00800 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate |
| HEJOHAOE_01466 | 2.84e-122 | aroB | 4.2.3.4 | - | E | ko:K01735 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) |
| HEJOHAOE_01467 | 3.23e-120 | tyrA | 1.3.1.12 | - | E | ko:K04517 | ko00400,ko00401,ko01100,ko01110,ko01130,ko01230,map00400,map00401,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | prephenate dehydrogenase |
| HEJOHAOE_01468 | 1.64e-186 | aroF | 2.5.1.54 | - | E | ko:K03856 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | synthase |
| HEJOHAOE_01469 | 2.51e-27 | aroK | 2.7.1.71 | - | F | ko:K00891 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate |
| HEJOHAOE_01470 | 1.7e-98 | aroE | 1.1.1.25 | - | E | ko:K00014 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) |
| HEJOHAOE_01471 | 6.74e-15 | acpP | - | - | IQ | ko:K02078 | - | ko00000,ko00001 | Carrier of the growing fatty acid chain in fatty acid biosynthesis |
| HEJOHAOE_01472 | 7.18e-259 | proS | 6.1.1.15 | - | J | ko:K01881 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro) |
| HEJOHAOE_01473 | 4.89e-27 | - | - | - | S | ko:K07137 | - | ko00000 | 'oxidoreductase |
| HEJOHAOE_01474 | 5.68e-146 | - | - | - | G | - | - | - | hydrolase activity, hydrolyzing O-glycosyl compounds |
| HEJOHAOE_01475 | 1.13e-212 | - | 1.1.1.38 | - | C | ko:K00027 | ko00620,ko01200,ko02020,map00620,map01200,map02020 | ko00000,ko00001,ko01000 | Malic enzyme, NAD binding domain |
| HEJOHAOE_01476 | 2.15e-159 | ArtM | - | - | E | ko:K02029,ko:K02030 | - | ko00000,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| HEJOHAOE_01477 | 3.39e-122 | glnQ | 3.6.3.21 | - | E | ko:K02028 | - | ko00000,ko00002,ko01000,ko02000 | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01478 | 1.81e-131 | cca | 2.7.7.19, 2.7.7.72 | - | J | ko:K00970,ko:K00974 | ko03013,ko03018,map03013,map03018 | ko00000,ko00001,ko01000,ko03016,ko03019 | tRNA nucleotidyltransferase poly(A) polymerase |
| HEJOHAOE_01479 | 7.19e-216 | - | - | - | P | ko:K12952 | - | ko00000,ko01000 | E1-E2 ATPase |
| HEJOHAOE_01480 | 5.68e-71 | spoIVB | 3.4.21.116 | - | M | ko:K06399 | - | ko00000,ko01000,ko01002 | Stage IV sporulation protein B |
| HEJOHAOE_01481 | 2.43e-108 | spo0A | - | - | NT | ko:K03413,ko:K07699 | ko02020,ko02024,ko02030,map02020,map02024,map02030 | ko00000,ko00001,ko00002,ko02022,ko02035 | May play the central regulatory role in sporulation. It may be an element of the effector pathway responsible for the activation of sporulation genes in response to nutritional stress. Spo0A may act in concert with spo0H (a sigma factor) to control the expression of some genes that are critical to the sporulation process |
| HEJOHAOE_01482 | 7.67e-226 | purD | 6.3.2.6, 6.3.4.13 | - | F | ko:K01945,ko:K13713 | ko00230,ko01100,ko01110,ko01130,map00230,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Belongs to the GARS family |
| HEJOHAOE_01483 | 2.33e-239 | purH2 | 2.1.2.3, 3.5.4.10 | - | F | ko:K00602 | ko00230,ko00670,ko01100,ko01110,ko01130,ko01523,map00230,map00670,map01100,map01110,map01130,map01523 | ko00000,ko00001,ko00002,ko01000,ko04147 | AICARFT IMPCHase bienzyme |
| HEJOHAOE_01484 | 4.78e-129 | - | - | - | F | - | - | - | IMP cyclohydrolase-like protein |
| HEJOHAOE_01485 | 4.52e-94 | purN | 2.1.2.2, 6.3.2.6, 6.3.4.13 | - | F | ko:K11175,ko:K13713 | ko00230,ko00670,ko01100,ko01110,ko01130,map00230,map00670,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate |
| HEJOHAOE_01486 | 2.18e-25 | - | - | - | M | - | - | - | Dolichyl-phosphate-mannose-protein mannosyltransferase |
| HEJOHAOE_01487 | 4.66e-144 | - | - | - | M | - | - | - | Glycosyl transferase family 2 |
| HEJOHAOE_01488 | 7.26e-166 | pfkA | 2.7.1.11 | - | H | ko:K00850 | ko00010,ko00030,ko00051,ko00052,ko00680,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,ko03018,ko04152,ko05230,map00010,map00030,map00051,map00052,map00680,map01100,map01110,map01120,map01130,map01200,map01230,map03018,map04152,map05230 | ko00000,ko00001,ko00002,ko01000,ko01009,ko03019 | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis |
| HEJOHAOE_01490 | 3.57e-54 | mscS | - | - | M | ko:K03442 | - | ko00000,ko02000 | Mechanosensitive ion channel |
| HEJOHAOE_01492 | 2.13e-108 | sigE | - | - | K | ko:K03091 | - | ko00000,ko03021 | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released |
| HEJOHAOE_01493 | 8.27e-45 | - | - | - | S | - | - | - | Sporulation factor SpoIIGA |
| HEJOHAOE_01494 | 8.43e-99 | - | - | - | S | - | - | - | DegV family |
| HEJOHAOE_01495 | 6.22e-15 | - | - | - | S | - | - | - | TIGRFAM Sporulation protein YlmC YmxH |
| HEJOHAOE_01497 | 1.35e-145 | rpsB | - | - | J | ko:K02967 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the universal ribosomal protein uS2 family |
| HEJOHAOE_01498 | 3.71e-140 | tsf | - | - | J | ko:K02357 | - | ko00000,ko03012,ko03029 | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome |
| HEJOHAOE_01499 | 3.77e-18 | - | - | - | E | - | - | - | haloacid dehalogenase-like hydrolase |
| HEJOHAOE_01501 | 1.08e-05 | dinG | 3.6.4.12 | - | L | ko:K03722 | - | ko00000,ko01000,ko03400 | helicase involved in DNA repair and perhaps also replication |
| HEJOHAOE_01502 | 0.0 | typA | - | - | T | ko:K06207 | - | ko00000 | GTP-binding protein TypA |
| HEJOHAOE_01503 | 0.0 | acnA | 4.2.1.3 | - | C | ko:K01681 | ko00020,ko00630,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01210,ko01230,map00020,map00630,map00720,map01100,map01110,map01120,map01130,map01200,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | aconitate hydratase |
| HEJOHAOE_01504 | 9.29e-246 | icd | 1.1.1.42 | - | C | ko:K00031 | ko00020,ko00480,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01210,ko01230,ko04146,map00020,map00480,map00720,map01100,map01110,map01120,map01130,map01200,map01210,map01230,map04146 | br01601,ko00000,ko00001,ko00002,ko01000 | Belongs to the isocitrate and isopropylmalate dehydrogenases family |
| HEJOHAOE_01505 | 1.07e-86 | rex | - | - | K | ko:K01926 | - | ko00000,ko03000 | Modulates transcription in response to changes in cellular NADH NAD( ) redox state |
| HEJOHAOE_01506 | 1.27e-165 | pulA | 3.2.1.41 | CBM48,GH13 | G | ko:K01200 | ko00500,ko01100,ko01110,map00500,map01100,map01110 | ko00000,ko00001,ko01000 | Belongs to the glycosyl hydrolase 13 family |
| HEJOHAOE_01507 | 1.32e-170 | - | 3.2.1.41 | CBM48,GH13 | G | ko:K01200 | ko00500,ko01100,ko01110,map00500,map01100,map01110 | ko00000,ko00001,ko01000 | Belongs to the glycosyl hydrolase 13 family |
| HEJOHAOE_01508 | 6.36e-180 | eno | 4.2.1.11 | - | G | ko:K01689 | ko00010,ko00680,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,ko03018,ko04066,map00010,map00680,map01100,map01110,map01120,map01130,map01200,map01230,map03018,map04066 | ko00000,ko00001,ko00002,ko01000,ko03019,ko04147 | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis |
| HEJOHAOE_01509 | 2.82e-07 | - | - | - | S | - | - | - | peptidoglycan catabolic process |
| HEJOHAOE_01510 | 5.25e-24 | - | - | - | S | - | - | - | Zincin-like metallopeptidase |
| HEJOHAOE_01511 | 1.19e-179 | purM | 6.3.3.1 | - | F | ko:K01933 | ko00230,ko01100,ko01110,ko01130,map00230,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Phosphoribosylformylglycinamidine cyclo-ligase |
| HEJOHAOE_01512 | 1.5e-166 | purF | 2.4.2.14 | - | F | ko:K00764 | ko00230,ko00250,ko01100,ko01110,ko01130,map00230,map00250,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000,ko01002 | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine |
| HEJOHAOE_01513 | 3.56e-74 | purE | 5.4.99.18 | - | F | ko:K01588 | ko00230,ko01100,ko01110,ko01130,map00230,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) |
| HEJOHAOE_01514 | 4.16e-77 | - | - | - | S | - | - | - | Putative ABC-transporter type IV |
| HEJOHAOE_01515 | 2.87e-65 | qmcA | - | - | O | - | - | - | prohibitin homologues |
| HEJOHAOE_01516 | 2.09e-136 | - | - | - | L | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01523 | 2.32e-10 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01524 | 7.91e-45 | - | - | - | L | - | - | - | Helicase C-terminal domain protein |
| HEJOHAOE_01526 | 1.71e-05 | dnaN | 2.7.7.7 | - | L | ko:K02338 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria |
| HEJOHAOE_01529 | 1.21e-89 | - | - | - | S | ko:K09769 | - | ko00000 | metallophosphoesterase |
| HEJOHAOE_01530 | 1.29e-17 | yqfD | - | - | S | ko:K06438 | - | ko00000 | Putative stage IV sporulation protein YqfD |
| HEJOHAOE_01532 | 5.02e-24 | ylbJ | - | - | S | - | - | - | Sporulation integral membrane protein YlbJ |
| HEJOHAOE_01533 | 8.03e-265 | asnB | 6.3.5.4 | - | E | ko:K01953 | ko00250,ko01100,ko01110,map00250,map01100,map01110 | ko00000,ko00001,ko01000,ko01002 | asparagine synthase |
| HEJOHAOE_01534 | 1.27e-19 | - | - | - | I | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01535 | 1.89e-54 | mscL | - | - | M | ko:K03282 | - | ko00000,ko02000 | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell |
| HEJOHAOE_01536 | 9.15e-226 | tyrS | 6.1.1.1 | - | J | ko:K01866 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) |
| HEJOHAOE_01537 | 3.03e-21 | - | - | - | S | - | - | - | Metallo-beta-lactamase superfamily |
| HEJOHAOE_01538 | 1.69e-311 | - | - | - | C | - | - | - | UPF0313 protein |
| HEJOHAOE_01539 | 1.97e-223 | spoIIIE | - | - | D | ko:K03466 | - | ko00000,ko03036 | Belongs to the FtsK SpoIIIE SftA family |
| HEJOHAOE_01540 | 4.2e-92 | uppP | 3.6.1.27 | - | V | ko:K06153 | ko00550,map00550 | ko00000,ko00001,ko01000,ko01011 | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin |
| HEJOHAOE_01541 | 1.14e-58 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01542 | 7.49e-15 | - | - | - | S | - | - | - | Protein of unknown function (DUF3006) |
| HEJOHAOE_01543 | 1.12e-80 | - | - | - | S | ko:K02238 | - | ko00000,ko00002,ko02044 | PFAM Metallo-beta-lactamase superfamily |
| HEJOHAOE_01544 | 0.0 | - | - | - | V | ko:K06147 | - | ko00000,ko02000 | overlaps another CDS with the same product name |
| HEJOHAOE_01545 | 2.09e-267 | - | - | - | V | ko:K06147 | - | ko00000,ko02000 | Abc transporter |
| HEJOHAOE_01546 | 5.95e-37 | - | - | - | K | - | - | - | MarR family |
| HEJOHAOE_01548 | 2.44e-57 | yihY | - | - | H | ko:K07058 | - | ko00000 | Belongs to the UPF0761 family |
| HEJOHAOE_01549 | 8.04e-83 | - | - | - | S | ko:K07124 | - | ko00000 | Belongs to the short-chain dehydrogenases reductases (SDR) family |
| HEJOHAOE_01550 | 2.27e-50 | - | - | - | Q | - | - | - | O-methyltransferase |
| HEJOHAOE_01551 | 2.27e-22 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01552 | 3.66e-136 | rumA | 2.1.1.190 | - | J | ko:K03215 | - | ko00000,ko01000,ko03009 | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family |
| HEJOHAOE_01553 | 3.66e-224 | murC | 6.3.2.8 | - | M | ko:K01924 | ko00471,ko00550,ko01100,map00471,map00550,map01100 | ko00000,ko00001,ko01000,ko01011 | Belongs to the MurCDEF family |
| HEJOHAOE_01554 | 7.43e-101 | - | 3.4.21.107 | - | O | ko:K04771 | ko01503,ko02020,map01503,map02020 | ko00000,ko00001,ko00002,ko01000,ko01002,ko03110 | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain |
| HEJOHAOE_01555 | 5.03e-55 | - | - | - | F | - | - | - | AAA domain |
| HEJOHAOE_01557 | 6.89e-38 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01558 | 1.92e-255 | pgi | 5.3.1.9 | - | G | ko:K01810 | ko00010,ko00030,ko00500,ko00520,ko01100,ko01110,ko01120,ko01130,ko01200,map00010,map00030,map00500,map00520,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000,ko04147 | Belongs to the GPI family |
| HEJOHAOE_01559 | 1.67e-146 | dacF | 3.4.16.4 | - | M | ko:K07258 | ko00550,ko01100,map00550,map01100 | ko00000,ko00001,ko01000,ko01002,ko01011 | Belongs to the peptidase S11 family |
| HEJOHAOE_01560 | 3.69e-74 | ispF | 2.7.7.60, 4.6.1.12 | - | H | ko:K01770,ko:K12506 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) |
| HEJOHAOE_01561 | 2.93e-55 | ispD | 2.7.7.60 | - | I | ko:K00991 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) |
| HEJOHAOE_01562 | 3.39e-245 | - | - | - | E | - | - | - | Cys/Met metabolism PLP-dependent enzyme |
| HEJOHAOE_01565 | 3.9e-28 | - | - | - | K | - | - | - | Helix-turn-helix XRE-family like proteins |
| HEJOHAOE_01566 | 3.45e-24 | - | - | - | K | - | - | - | transcriptional regulator |
| HEJOHAOE_01567 | 2.94e-79 | spoVFB | - | - | H | ko:K06411 | - | ko00000 | Together with DpaA, catalyzes the conversion of dihydrodipicolinate to dipicolinate (DPA) |
| HEJOHAOE_01568 | 6.65e-55 | spoVFA | - | - | EH | ko:K06410 | - | ko00000 | Dipicolinate synthase subunit A N-terminal domain |
| HEJOHAOE_01570 | 7.21e-170 | - | - | - | IQ | - | - | - | Enoyl-(Acyl carrier protein) reductase |
| HEJOHAOE_01571 | 3e-136 | - | - | - | GM | ko:K09691 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| HEJOHAOE_01572 | 1.23e-94 | - | - | - | GM | ko:K09690 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ABC-2 type transporter |
| HEJOHAOE_01573 | 1.33e-80 | - | 5.2.1.8 | - | O | ko:K01802 | - | ko00000,ko01000 | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides |
| HEJOHAOE_01574 | 3.79e-66 | - | - | - | S | ko:K09768 | - | ko00000 | Belongs to the UPF0178 family |
| HEJOHAOE_01575 | 4.9e-129 | - | 3.2.1.52 | - | G | ko:K01207 | ko00520,ko00531,ko01100,ko01501,map00520,map00531,map01100,map01501 | ko00000,ko00001,ko00002,ko01000 | Hydrolase Family 3 |
| HEJOHAOE_01576 | 0.000206 | - | - | - | M | - | - | - | Carboxypeptidase regulatory-like domain |
| HEJOHAOE_01577 | 1.28e-43 | - | - | - | K | ko:K07736 | - | ko00000,ko03000 | CarD-like/TRCF domain |
| HEJOHAOE_01578 | 5.85e-193 | - | - | - | C | - | - | - | Metallo-beta-lactamase superfamily |
| HEJOHAOE_01583 | 4.92e-308 | gltD | 1.4.1.13, 1.4.1.14 | - | C | ko:K00266 | ko00250,ko00910,ko01100,ko01110,ko01120,ko01130,ko01230,map00250,map00910,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko01000 | glutamate synthase |
| HEJOHAOE_01584 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | - | E | ko:K00265,ko:K00284 | ko00250,ko00630,ko00910,ko01100,ko01110,ko01120,ko01130,ko01230,map00250,map00630,map00910,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko01000 | glutamate synthase |
| HEJOHAOE_01585 | 0.0 | glnA | 6.3.1.2 | - | S | ko:K01915 | ko00220,ko00250,ko00630,ko00910,ko01100,ko01120,ko01230,ko02020,ko04217,ko04724,ko04727,map00220,map00250,map00630,map00910,map01100,map01120,map01230,map02020,map04217,map04724,map04727 | ko00000,ko00001,ko01000,ko04147 | Glutamine synthetase type III N terminal |
| HEJOHAOE_01586 | 4.04e-266 | amt | - | - | EP | ko:K03320 | - | ko00000,ko02000 | Ammonium Transporter Family |
| HEJOHAOE_01587 | 1.15e-11 | - | - | - | L | - | - | - | RelB antitoxin |
| HEJOHAOE_01588 | 2.15e-25 | - | - | - | S | ko:K19157 | - | ko00000,ko01000,ko02048 | Bacterial toxin of type II toxin-antitoxin system, YafQ |
| HEJOHAOE_01589 | 1.23e-36 | rpsR | - | - | J | ko:K02963 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit |
| HEJOHAOE_01590 | 2.12e-29 | ssb | - | - | L | ko:K03111 | ko03030,ko03430,ko03440,map03030,map03430,map03440 | ko00000,ko00001,ko03029,ko03032,ko03400 | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism |
| HEJOHAOE_01591 | 2.95e-42 | rpsF | - | - | J | ko:K02990 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011,ko03029 | Binds together with S18 to 16S ribosomal RNA |
| HEJOHAOE_01592 | 2.29e-72 | trpF | 5.3.1.24 | - | E | ko:K01817 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | N-(5'phosphoribosyl)anthranilate (PRA) isomerase |
| HEJOHAOE_01593 | 8.34e-154 | cysK | 2.5.1.47 | - | E | ko:K01738 | ko00270,ko00920,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00270,map00920,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Belongs to the cysteine synthase cystathionine beta- synthase family |
| HEJOHAOE_01594 | 2.78e-246 | metY | 2.5.1.49 | - | E | ko:K01740 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko01000 | O-acetylhomoserine |
| HEJOHAOE_01595 | 1.8e-59 | - | - | - | K | - | - | - | Transcriptional regulator |
| HEJOHAOE_01596 | 7.04e-184 | - | - | - | S | ko:K06901 | - | ko00000,ko02000 | Permease family |
| HEJOHAOE_01597 | 1.87e-88 | sigK | - | - | K | ko:K03091 | - | ko00000,ko03021 | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released |
| HEJOHAOE_01601 | 6.03e-32 | - | - | - | S | - | - | - | Ion channel |
| HEJOHAOE_01602 | 3.85e-13 | - | - | - | S | - | - | - | Virulence protein RhuM family |
| HEJOHAOE_01604 | 8.63e-273 | pncB | 6.3.4.21 | - | H | ko:K00763 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko01000 | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP |
| HEJOHAOE_01605 | 3.01e-212 | - | 3.2.1.1, 5.4.99.16 | GH13 | G | ko:K01176,ko:K05343 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | Alpha-amylase domain |
| HEJOHAOE_01607 | 1.61e-19 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01608 | 3.06e-48 | smf | - | - | LU | ko:K04096 | - | ko00000 | DNA mediated transformation |
| HEJOHAOE_01610 | 0.0 | valS | 6.1.1.9 | - | J | ko:K01873 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner |
| HEJOHAOE_01611 | 7.55e-67 | - | - | - | K | - | - | - | transcriptional regulator DeoR family |
| HEJOHAOE_01612 | 2.5e-24 | - | - | - | K | - | - | - | Helix-turn-helix |
| HEJOHAOE_01614 | 1.72e-51 | yrrK | - | - | L | ko:K07447 | - | ko00000,ko01000 | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA |
| HEJOHAOE_01615 | 1.84e-43 | xseA | 3.1.11.6 | - | L | ko:K03601 | ko03430,map03430 | ko00000,ko00001,ko01000,ko03400 | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides |
| HEJOHAOE_01616 | 9.36e-108 | gcp1 | 2.3.1.234 | - | O | ko:K01409 | - | ko00000,ko01000,ko03016 | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction |
| HEJOHAOE_01617 | 1.1e-22 | nusB | - | - | K | ko:K03625 | - | ko00000,ko03009,ko03021 | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons |
| HEJOHAOE_01618 | 2.19e-38 | - | - | - | M | ko:K07271 | - | ko00000,ko01000 | LicD family |
| HEJOHAOE_01619 | 4.98e-154 | - | 4.1.1.35, 4.2.1.46 | - | GM | ko:K01710,ko:K08678 | ko00520,ko00521,ko00523,ko00525,ko01055,ko01100,ko01130,map00520,map00521,map00523,map00525,map01055,map01100,map01130 | ko00000,ko00001,ko00002,ko01000 | epimerase dehydratase |
| HEJOHAOE_01620 | 1.34e-155 | - | 2.7.7.60 | - | I | ko:K00991 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase |
| HEJOHAOE_01621 | 8.58e-23 | - | - | - | S | ko:K07052 | - | ko00000 | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01622 | 7.96e-51 | tadA | 3.5.4.33 | - | FJ | ko:K11991 | - | ko00000,ko01000,ko03016 | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) |
| HEJOHAOE_01623 | 7.81e-205 | ynbB | - | - | P | - | - | - | Cystathionine beta-lyase family protein involved in aluminum resistance |
| HEJOHAOE_01625 | 1.82e-107 | - | 3.2.1.4 | GH5,GH9 | G | ko:K01179 | ko00500,ko01100,map00500,map01100 | ko00000,ko00001,ko01000 | M42 glutamyl aminopeptidase |
| HEJOHAOE_01626 | 1.21e-33 | cel | 3.2.1.4 | GH5,GH9 | G | ko:K01179 | ko00500,ko01100,map00500,map01100 | ko00000,ko00001,ko01000 | aminopeptidase activity |
| HEJOHAOE_01627 | 1.69e-53 | murD | 6.3.2.9 | - | M | ko:K01925 | ko00471,ko00550,ko01100,map00471,map00550,map01100 | ko00000,ko00001,ko01000,ko01011 | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) |
| HEJOHAOE_01628 | 1.02e-33 | ziaR | - | - | K | ko:K21903 | - | ko00000,ko03000 | regulatory protein, arsR |
| HEJOHAOE_01629 | 3.72e-202 | murA | 2.5.1.7 | - | M | ko:K00790 | ko00520,ko00550,ko01100,map00520,map00550,map01100 | ko00000,ko00001,ko01000,ko01011 | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine |
| HEJOHAOE_01630 | 7.73e-56 | yycJ | - | - | S | - | - | - | Metallo-beta-lactamase domain protein |
| HEJOHAOE_01631 | 1.21e-56 | rlmH | 2.1.1.177 | - | J | ko:K00783 | - | ko00000,ko01000,ko03009 | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA |
| HEJOHAOE_01632 | 1.49e-221 | FbpA | - | - | K | - | - | - | Fibronectin-binding protein |
| HEJOHAOE_01633 | 2.43e-83 | - | - | - | Q | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01634 | 3.94e-24 | - | - | - | O | - | - | - | regulation of methylation-dependent chromatin silencing |
| HEJOHAOE_01635 | 4.1e-269 | - | - | - | KL | - | - | - | Recombinase zinc beta ribbon domain |
| HEJOHAOE_01637 | 7.01e-31 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01638 | 4.37e-17 | repA | - | - | S | - | - | - | Replication initiator protein A |
| HEJOHAOE_01639 | 5.26e-49 | topA | 5.99.1.2 | - | L | ko:K03168 | - | ko00000,ko01000,ko03032,ko03400 | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone |
| HEJOHAOE_01640 | 2.25e-212 | trmFO | 2.1.1.74 | - | J | ko:K04094 | - | ko00000,ko01000,ko03016,ko03036 | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs |
| HEJOHAOE_01641 | 3.85e-135 | plsX | 2.3.1.15 | - | I | ko:K03621 | ko00561,ko00564,ko01100,ko01110,map00561,map00564,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko01004 | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA |
| HEJOHAOE_01642 | 2.82e-108 | rnc | 3.1.26.3 | - | J | ko:K03685 | ko03008,ko05205,map03008,map05205 | ko00000,ko00001,ko01000,ko03009,ko03019,ko03036 | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism |
| HEJOHAOE_01643 | 2.68e-92 | - | - | - | BK | - | - | - | Radical SAM domain protein |
| HEJOHAOE_01644 | 0.0 | smc | - | - | D | ko:K03529 | - | ko00000,ko03036 | Required for chromosome condensation and partitioning |
| HEJOHAOE_01645 | 6.1e-158 | ftsY | - | - | U | ko:K03110 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) |
| HEJOHAOE_01646 | 2.6e-63 | rdgB | 3.6.1.66 | - | F | ko:K02428 | ko00230,map00230 | ko00000,ko00001,ko01000 | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions |
| HEJOHAOE_01647 | 4.68e-33 | yhbY | - | - | J | ko:K07574 | - | ko00000,ko03009 | RNA-binding protein, YhbY family |
| HEJOHAOE_01648 | 5.49e-31 | nadD | 2.7.7.18 | - | F | ko:K00969 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | Cytidylyltransferase-like |
| HEJOHAOE_01649 | 5.14e-39 | yqeK | - | - | H | - | - | - | Metal dependent phosphohydrolases with conserved 'HD' motif. |
| HEJOHAOE_01650 | 3.55e-295 | prfC | - | - | J | ko:K02837 | - | ko00000,ko03012 | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP |
| HEJOHAOE_01651 | 2.32e-112 | speA | 4.1.1.19 | - | E | ko:K01585 | ko00330,ko01100,map00330,map01100 | ko00000,ko00001,ko00002,ko01000 | Orn Lys Arg decarboxylase major |
| HEJOHAOE_01652 | 1.28e-10 | scfA | - | - | S | - | - | - | Six-cysteine peptide SCIFF |
| HEJOHAOE_01653 | 8.74e-279 | scfB | - | - | C | ko:K06871 | - | ko00000 | Radical SAM |
| HEJOHAOE_01654 | 3.28e-110 | - | 3.1.26.11 | - | S | ko:K00784 | ko03013,map03013 | ko00000,ko00001,ko01000,ko03016 | Psort location Cytoplasmic, score 8.96 |
| HEJOHAOE_01655 | 1.12e-211 | feoB2 | - | - | P | ko:K04759 | - | ko00000,ko02000 | transporter of a GTP-driven Fe(2 ) uptake system |
| HEJOHAOE_01656 | 1.27e-12 | - | - | - | P | ko:K04758 | - | ko00000,ko02000 | Fe2 transport system protein A |
| HEJOHAOE_01657 | 6.42e-116 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01658 | 1.58e-151 | - | - | - | S | ko:K07090 | - | ko00000 | membrane transporter protein |
| HEJOHAOE_01659 | 1.46e-11 | - | - | - | N | - | - | - | dockerin type I repeat-containing domain protein |
| HEJOHAOE_01661 | 5.17e-37 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01662 | 7.44e-57 | - | - | - | KLT | - | - | - | Protein kinase domain |
| HEJOHAOE_01663 | 4.87e-10 | - | - | - | K | - | - | - | Transcriptional |
| HEJOHAOE_01665 | 7.37e-45 | dprA | - | - | L | ko:K04096 | - | ko00000 | TIGRFAM DNA protecting protein DprA |
| HEJOHAOE_01666 | 8.42e-81 | spoU | - | - | J | ko:K03437 | - | ko00000,ko03016 | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family |
| HEJOHAOE_01667 | 2.22e-66 | rplT | - | - | J | ko:K02887 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit |
| HEJOHAOE_01668 | 5.89e-34 | rpmI | - | - | J | ko:K02916 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L35 |
| HEJOHAOE_01669 | 2.09e-76 | infC | - | - | J | ko:K02520 | - | ko00000,ko03012,ko03029 | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins |
| HEJOHAOE_01670 | 7.44e-08 | spoIIIAH | - | - | S | ko:K06397 | - | ko00000 | Stage III sporulation protein |
| HEJOHAOE_01671 | 3.55e-12 | spoIIIAG | - | - | S | ko:K06396 | - | ko00000 | Stage III sporulation protein AG |
| HEJOHAOE_01673 | 3.2e-52 | spoIIIAE | - | - | S | ko:K06394 | - | ko00000 | stage III sporulation protein AE |
| HEJOHAOE_01674 | 4.86e-19 | spoIIIAD | - | - | S | ko:K06393 | - | ko00000 | Stage III sporulation protein AD |
| HEJOHAOE_01675 | 7.04e-19 | spoIIIAC | - | - | S | ko:K06392 | - | ko00000 | stage III sporulation protein AC |
| HEJOHAOE_01677 | 4.11e-83 | spoIIIAA | - | - | S | ko:K06390 | - | ko00000 | stage III sporulation protein AA |
| HEJOHAOE_01678 | 7.71e-36 | - | - | - | S | - | - | - | TIGRFAM Addiction module toxin, Txe YoeB |
| HEJOHAOE_01679 | 2.52e-19 | - | - | - | L | ko:K07473 | - | ko00000,ko02048 | RelB antitoxin |
| HEJOHAOE_01681 | 1.66e-112 | - | - | - | S | ko:K03924 | - | ko00000,ko01000 | associated with various cellular activities |
| HEJOHAOE_01682 | 3.17e-09 | - | - | - | S | - | - | - | conserved protein (some members contain a von Willebrand factor type A (vWA) domain) |
| HEJOHAOE_01683 | 1.15e-29 | - | - | - | E | - | - | - | Transglutaminase/protease-like homologues |
| HEJOHAOE_01685 | 8.12e-39 | - | - | - | K | - | - | - | LytTr DNA-binding |
| HEJOHAOE_01687 | 9.31e-105 | - | - | - | V | ko:K01990,ko:K11050 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| HEJOHAOE_01688 | 1.09e-68 | - | - | - | V | ko:K01992,ko:K11051 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ABC-2 type transporter |
| HEJOHAOE_01689 | 1.4e-201 | - | - | - | E | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01690 | 4.61e-07 | - | - | - | S | - | - | - | Protein of unknown function (DUF2798) |
| HEJOHAOE_01691 | 9.23e-75 | - | - | - | T | - | - | - | Transcriptional regulatory protein, C terminal |
| HEJOHAOE_01692 | 1.77e-25 | - | - | - | T | - | - | - | Histidine kinase |
| HEJOHAOE_01693 | 2.96e-202 | - | - | - | Q | - | - | - | Belongs to the ATP-dependent AMP-binding enzyme family |
| HEJOHAOE_01694 | 1.44e-112 | - | 4.1.1.20 | - | E | ko:K01586 | ko00300,ko01100,ko01110,ko01120,ko01130,ko01230,map00300,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Pyridoxal-dependent decarboxylase, C-terminal sheet domain |
| HEJOHAOE_01695 | 1.86e-30 | - | - | - | IQ | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01696 | 1.13e-184 | - | - | - | M | - | - | - | MBOAT, membrane-bound O-acyltransferase family |
| HEJOHAOE_01697 | 1.16e-75 | - | - | - | E | - | - | - | lipolytic protein G-D-S-L family |
| HEJOHAOE_01699 | 4.86e-76 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01700 | 1.84e-30 | mrnC | - | - | J | ko:K11145 | - | ko00000,ko01000,ko03009 | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) |
| HEJOHAOE_01701 | 8.88e-234 | obg | - | - | S | ko:K03979 | - | ko00000,ko01000,ko03009 | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control |
| HEJOHAOE_01702 | 1.83e-51 | rpmA | - | - | J | ko:K02899 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bL27 family |
| HEJOHAOE_01703 | 4.99e-28 | - | - | - | J | ko:K07584 | - | ko00000 | Cysteine protease Prp |
| HEJOHAOE_01704 | 7.46e-31 | rplU | - | - | J | ko:K02888 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This protein binds to 23S rRNA in the presence of protein L20 |
| HEJOHAOE_01705 | 7.8e-136 | folD | 1.5.1.5, 3.5.4.9 | - | F | ko:K01491 | ko00670,ko00720,ko01100,ko01120,ko01200,map00670,map00720,map01100,map01120,map01200 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate |
| HEJOHAOE_01706 | 9.64e-88 | lgt | - | - | M | ko:K13292 | - | ko00000,ko01000 | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins |
| HEJOHAOE_01707 | 1.07e-169 | ymfH | - | - | L | ko:K07263 | - | ko00000,ko01000,ko01002 | Peptidase, M16 |
| HEJOHAOE_01708 | 2.61e-68 | - | - | - | S | - | - | - | Peptidase M16 |
| HEJOHAOE_01709 | 1.83e-300 | hgdC2 | - | - | I | - | - | - | CoA-substrate-specific enzyme activase |
| HEJOHAOE_01710 | 1.51e-203 | - | - | - | I | - | - | - | Psort location Cytoplasmic, score |
| HEJOHAOE_01711 | 1.49e-86 | - | - | - | K | - | - | - | Psort location CytoplasmicMembrane, score |
| HEJOHAOE_01713 | 1.11e-33 | yabE | - | - | S | - | - | - | G5 domain protein |
| HEJOHAOE_01714 | 2.41e-19 | - | - | - | K | - | - | - | PFAM helix-turn-helix- domain containing protein, AraC type |
| HEJOHAOE_01715 | 1.37e-20 | - | - | - | K | - | - | - | COG COG2207 AraC-type DNA-binding domain-containing proteins |
| HEJOHAOE_01716 | 1.78e-49 | - | - | - | I | - | - | - | Carboxylesterase family |
| HEJOHAOE_01717 | 7.05e-06 | - | - | - | N | - | - | - | domain, Protein |
| HEJOHAOE_01718 | 4.61e-31 | - | - | - | K | ko:K10914 | ko02020,ko02024,ko02025,ko02026,ko05111,map02020,map02024,map02025,map02026,map05111 | ko00000,ko00001,ko03000 | PFAM Bacterial regulatory proteins, crp family |
| HEJOHAOE_01719 | 2e-251 | leuC | 4.2.1.33, 4.2.1.35, 4.2.1.85 | - | E | ko:K01703,ko:K20452 | ko00290,ko00660,ko00760,ko00966,ko01100,ko01110,ko01120,ko01210,ko01230,map00290,map00660,map00760,map00966,map01100,map01110,map01120,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate |
| HEJOHAOE_01720 | 5.46e-90 | leuD | 4.2.1.33, 4.2.1.35, 4.2.1.85 | - | E | ko:K01704,ko:K20453 | ko00290,ko00660,ko00760,ko01100,ko01110,ko01120,ko01210,ko01230,map00290,map00660,map00760,map01100,map01110,map01120,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate |
| HEJOHAOE_01722 | 8.95e-05 | ompC | 2.4.1.10, 3.5.1.28 | GH68 | MN | ko:K00692,ko:K01448,ko:K13730 | ko00500,ko01100,ko01503,ko02020,ko05100,map00500,map01100,map01503,map02020,map05100 | ko00000,ko00001,ko00002,ko01000,ko01003,ko01011,ko03036 | Fibronectin type 3 domain |
| HEJOHAOE_01723 | 4.02e-220 | ilvC | 1.1.1.86 | - | H | ko:K00053 | ko00290,ko00770,ko01100,ko01110,ko01130,ko01210,ko01230,map00290,map00770,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate |
| HEJOHAOE_01724 | 5.83e-71 | ilvN | 2.2.1.6 | - | E | ko:K01653 | ko00290,ko00650,ko00660,ko00770,ko01100,ko01110,ko01130,ko01210,ko01230,map00290,map00650,map00660,map00770,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Acetolactate synthase small |
| HEJOHAOE_01725 | 3.44e-280 | ilvI | 2.2.1.6 | - | H | ko:K01652 | ko00290,ko00650,ko00660,ko00770,ko01100,ko01110,ko01130,ko01210,ko01230,map00290,map00650,map00660,map00770,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | acetolactate synthase large subunit |
| HEJOHAOE_01726 | 3.98e-186 | - | 3.6.3.3, 3.6.3.5 | - | P | ko:K01534 | - | ko00000,ko01000 | ATPase, P-type (transporting), HAD superfamily, subfamily IC |
| HEJOHAOE_01729 | 9.87e-124 | ytqA | - | - | S | ko:K07139 | - | ko00000 | Radical_SAM C-terminal domain |
| HEJOHAOE_01731 | 9.71e-65 | - | - | - | C | - | - | - | Protein conserved in bacteria |
| HEJOHAOE_01732 | 0.0 | - | - | - | C | - | - | - | Elongator protein 3, MiaB family, Radical SAM |
| HEJOHAOE_01735 | 5.36e-220 | - | 3.2.1.133, 3.2.1.135, 3.2.1.54, 3.5.4.33 | GH13 | G | ko:K01208,ko:K11991 | ko00500,ko01100,map00500,map01100 | ko00000,ko00001,ko01000,ko03016 | Alpha amylase, catalytic domain protein |
| HEJOHAOE_01736 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | ko:K01214 | ko00500,ko01100,ko01110,map00500,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Alpha amylase, catalytic domain |
| HEJOHAOE_01737 | 2.71e-51 | dltR | - | - | T | - | - | - | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain |
| HEJOHAOE_01738 | 4.91e-08 | - | - | - | M | - | - | - | Leucine-rich repeat (LRR) protein |
| HEJOHAOE_01739 | 5.38e-77 | - | - | - | I | - | - | - | Domain of unknown function (DUF4430) |
| HEJOHAOE_01740 | 1.66e-107 | - | - | - | P | ko:K16785 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | PFAM Cobalt transport protein |
| HEJOHAOE_01741 | 0.0 | - | - | - | G | ko:K16785,ko:K16786,ko:K16787 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | AAA domain, putative AbiEii toxin, Type IV TA system |
| HEJOHAOE_01742 | 6.05e-122 | dacF1 | 3.4.16.4 | - | M | ko:K01286,ko:K07258 | ko00550,ko01100,map00550,map01100 | ko00000,ko00001,ko01000,ko01002,ko01011 | Belongs to the peptidase S11 family |
| HEJOHAOE_01743 | 2.51e-236 | recG | 3.6.4.12 | - | L | ko:K03655 | ko03440,map03440 | ko00000,ko00001,ko01000,ko03400 | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) |
| HEJOHAOE_01744 | 1.52e-93 | yloV | - | - | S | ko:K07030 | - | ko00000 | DAK2 domain fusion protein YloV |
| HEJOHAOE_01745 | 8.76e-35 | yrzL | - | - | S | - | - | - | Belongs to the UPF0297 family |
| HEJOHAOE_01746 | 8.58e-36 | - | - | - | - | - | - | - | - |
| HEJOHAOE_01747 | 3.32e-29 | - | - | - | S | ko:K19157 | - | ko00000,ko01000,ko02048 | addiction module toxin, RelE StbE family |
| HEJOHAOE_01748 | 3.33e-20 | - | - | - | L | ko:K07473 | - | ko00000,ko02048 | RelB antitoxin |
| HEJOHAOE_01749 | 0.0 | actP | 3.6.3.4, 3.6.3.54 | - | P | ko:K01533,ko:K17686 | ko01524,ko04016,map01524,map04016 | ko00000,ko00001,ko01000 | ATPase, P-type (transporting), HAD superfamily, subfamily IC |
| HEJOHAOE_01750 | 1.21e-47 | csoR | - | - | S | ko:K21600 | - | ko00000,ko03000 | Metal-sensitive transcriptional repressor |
| HEJOHAOE_01752 | 3.48e-294 | ligA | 6.5.1.2 | - | L | ko:K01972 | ko03030,ko03410,ko03420,ko03430,map03030,map03410,map03420,map03430 | ko00000,ko00001,ko01000,ko03032,ko03400 | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA |
| HEJOHAOE_01753 | 4.05e-99 | - | - | - | S | - | - | - | metal-dependent phosphohydrolase, HD sub domain |
| HEJOHAOE_01755 | 2.72e-153 | - | - | - | H | ko:K07137 | - | ko00000 | 5-formyltetrahydrofolate cyclo-ligase activity |
| HEJOHAOE_01756 | 1.41e-88 | - | - | - | S | ko:K07007 | - | ko00000 | HI0933 family |
| HEJOHAOE_01757 | 6.08e-70 | - | - | - | S | - | - | - | small multi-drug export protein |
| HEJOHAOE_01758 | 2.98e-23 | - | - | - | S | - | - | - | VanZ like family |
| HEJOHAOE_01759 | 7.03e-227 | - | 2.5.1.49 | - | E | ko:K01740 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko01000 | Cys/Met metabolism PLP-dependent enzyme |
| HEJOHAOE_01760 | 2.53e-171 | - | - | - | C | - | - | - | PFAM nitrite and sulphite reductase 4Fe-4S |
| HEJOHAOE_01761 | 4.73e-47 | - | - | - | O | - | - | - | Belongs to the sulfur carrier protein TusA family |
| HEJOHAOE_01762 | 4.99e-40 | - | - | - | O | ko:K03671 | ko04621,ko05418,map04621,map05418 | ko00000,ko00001,ko03110 | Thioredoxin-like domain |
| HEJOHAOE_01763 | 1.16e-30 | thiS | - | - | H | ko:K03154 | ko04122,map04122 | ko00000,ko00001 | TIGRFAM thiamine biosynthesis protein ThiS |
| HEJOHAOE_01764 | 1.65e-177 | - | 2.7.7.80 | - | H | ko:K21029 | ko04122,map04122 | ko00000,ko00001,ko01000 | PFAM UBA THIF-type NAD FAD binding protein |
| HEJOHAOE_01765 | 0.0 | pheT | 6.1.1.20 | - | J | ko:K01890 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | B3/4 domain |
| HEJOHAOE_01766 | 2.03e-169 | pheS | 6.1.1.20 | - | J | ko:K01889 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily |
| HEJOHAOE_01769 | 3.11e-67 | - | - | - | C | - | - | - | Flavodoxin |
| HEJOHAOE_01770 | 5.24e-90 | - | - | - | S | - | - | - | conserved protein, contains double-stranded beta-helix domain |
| HEJOHAOE_01771 | 1.54e-81 | - | - | - | C | - | - | - | Flavodoxin |
| HEJOHAOE_01772 | 8.4e-17 | nrdR | - | - | K | ko:K07738 | - | ko00000,ko03000 | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes |
| HEJOHAOE_01773 | 4.89e-82 | metK | 2.5.1.6 | - | H | ko:K00789 | ko00270,ko01100,ko01110,ko01230,map00270,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme |
| HEJOHAOE_01774 | 9.08e-67 | - | 3.5.99.10 | - | J | ko:K09022 | - | ko00000,ko01000 | endoribonuclease L-PSP |
| HEJOHAOE_01775 | 9.37e-211 | ilvA | 4.3.1.19 | - | E | ko:K01754 | ko00260,ko00290,ko01100,ko01110,ko01130,ko01200,ko01230,map00260,map00290,map01100,map01110,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA |
| HEJOHAOE_01776 | 1.06e-66 | - | - | - | C | - | - | - | Flavodoxin |
| HEJOHAOE_01777 | 4.71e-19 | map_1 | 3.4.11.18 | - | E | ko:K01265 | - | ko00000,ko01000,ko01002 | methionine aminopeptidase, type I |
| HEJOHAOE_01778 | 1.87e-25 | - | 3.5.1.28 | - | M | ko:K01448 | ko01503,map01503 | ko00000,ko00001,ko00002,ko01000,ko01011,ko03036 | N-acetylmuramoyl-L-alanine amidase |
| HEJOHAOE_01779 | 3.93e-227 | radA | - | - | O | ko:K04485 | - | ko00000,ko03400 | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function |
| HEJOHAOE_01781 | 1.2e-299 | - | - | - | S | ko:K07133 | - | ko00000 | Domain of unknown function (DUF4143) |
eggNOG-mapper v2.1.12 (Database: eggNOG v5.0.2, Mar. 2021 release)