| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | KEGG_ko | KEGG_Pathway | BRITE | Description |
|---|---|---|---|---|---|---|---|---|---|
| HNJENPFB_00001 | 2.58e-140 | 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 |
| HNJENPFB_00002 | 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 |
| HNJENPFB_00003 | 9.44e-44 | - | 2.3.1.1 | - | K | ko:K22477 | ko00220,ko01210,ko01230,map00220,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | GCN5 family acetyltransferase |
| HNJENPFB_00004 | 1.12e-166 | 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 |
| HNJENPFB_00005 | 1.77e-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 |
| HNJENPFB_00007 | 1.1e-62 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00008 | 3.41e-98 | - | - | - | S | ko:K01992 | - | ko00000,ko00002,ko02000 | ABC-2 type transporter |
| HNJENPFB_00009 | 2.15e-85 | - | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | AAA domain, putative AbiEii toxin, Type IV TA system |
| HNJENPFB_00010 | 8.89e-38 | - | - | - | K | - | - | - | sequence-specific DNA binding |
| HNJENPFB_00013 | 2.74e-130 | mrp | - | - | D | - | - | - | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP |
| HNJENPFB_00015 | 4.39e-144 | prmA | - | - | J | ko:K02687 | - | ko00000,ko01000,ko03009 | Ribosomal protein L11 methyltransferase |
| HNJENPFB_00016 | 3.22e-190 | 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 |
| HNJENPFB_00017 | 0.0 | dnaK | - | - | O | ko:K04043 | ko03018,ko04212,ko05152,map03018,map04212,map05152 | ko00000,ko00001,ko03019,ko03029,ko03110,ko04147 | Heat shock 70 kDa protein |
| HNJENPFB_00018 | 9.3e-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 |
| HNJENPFB_00019 | 4.53e-83 | 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 |
| HNJENPFB_00021 | 1.63e-113 | fic | - | - | D | ko:K04095 | - | ko00000,ko03036 | Fic/DOC family |
| HNJENPFB_00022 | 1.73e-86 | 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 |
| HNJENPFB_00023 | 5.68e-204 | 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 | PFAM Phosphoadenosine phosphosulfate reductase |
| HNJENPFB_00024 | 1.12e-51 | - | 1.8.99.2 | - | C | ko:K00395 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko00002,ko01000 | 4 iron, 4 sulfur cluster binding |
| HNJENPFB_00025 | 1.3e-313 | aprA | 1.8.99.2 | - | C | ko:K00394 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko00002,ko01000 | Fumarate reductase flavoprotein C-term |
| HNJENPFB_00026 | 1.1e-109 | trxB | 1.8.1.9 | - | C | ko:K00384 | ko00450,map00450 | ko00000,ko00001,ko01000 | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family |
| HNJENPFB_00027 | 5.86e-76 | - | 3.13.1.6 | - | S | ko:K21140 | ko04122,map04122 | ko00000,ko00001,ko01000 | Mov34 MPN PAD-1 family |
| HNJENPFB_00028 | 5.77e-178 | - | 2.7.7.80 | - | H | ko:K21029 | ko04122,map04122 | ko00000,ko00001,ko01000 | PFAM UBA THIF-type NAD FAD binding protein |
| HNJENPFB_00029 | 4.36e-35 | thiS | - | - | H | ko:K03154 | ko04122,map04122 | ko00000,ko00001 | TIGRFAM thiamine biosynthesis protein ThiS |
| HNJENPFB_00030 | 8.64e-41 | - | - | - | O | ko:K03671 | ko04621,ko05418,map04621,map05418 | ko00000,ko00001,ko03110 | Thioredoxin-like domain |
| HNJENPFB_00031 | 4.73e-47 | - | - | - | O | - | - | - | Belongs to the sulfur carrier protein TusA family |
| HNJENPFB_00032 | 6.23e-172 | - | - | - | C | - | - | - | PFAM nitrite and sulphite reductase 4Fe-4S |
| HNJENPFB_00033 | 3.32e-225 | - | 2.5.1.49 | - | E | ko:K01740 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko01000 | Cys/Met metabolism PLP-dependent enzyme |
| HNJENPFB_00034 | 6.35e-36 | - | - | - | K | - | - | - | transcriptional regulator, Rrf2 family |
| HNJENPFB_00035 | 2.7e-57 | hemL | 5.4.3.8 | - | H | ko:K01845 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000,ko01007 | PFAM Aminotransferase class-III |
| HNJENPFB_00036 | 4.08e-23 | engA | - | - | S | - | - | - | 50S ribosome-binding GTPase |
| HNJENPFB_00037 | 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 |
| HNJENPFB_00038 | 6.87e-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 |
| HNJENPFB_00039 | 7.56e-150 | 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 |
| HNJENPFB_00040 | 2.17e-215 | 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 |
| HNJENPFB_00041 | 1.73e-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 | Peptidase C26 |
| HNJENPFB_00042 | 1.97e-139 | 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) |
| HNJENPFB_00043 | 6.55e-76 | - | - | - | K | - | - | - | Transcriptional regulator, DeoR family |
| HNJENPFB_00044 | 6.21e-219 | - | - | - | C | ko:K18471 | ko00640,map00640 | ko00000,ko00001,ko01000 | Aldo/keto reductase family |
| HNJENPFB_00045 | 6.79e-159 | - | - | - | G | - | - | - | Phosphomethylpyrimidine kinase |
| HNJENPFB_00046 | 1.1e-191 | - | - | - | G | - | - | - | Fructose-bisphosphate aldolase class-II |
| HNJENPFB_00047 | 6.03e-216 | - | - | - | E | - | - | - | Glucose dehydrogenase C-terminus |
| HNJENPFB_00048 | 2.41e-276 | - | - | - | G | ko:K08369 | - | ko00000,ko02000 | PFAM Sugar (and other) transporter |
| HNJENPFB_00050 | 1.69e-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 |
| HNJENPFB_00051 | 7.86e-134 | 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 |
| HNJENPFB_00057 | 4.33e-30 | - | - | - | T | - | - | - | protein histidine kinase activity |
| HNJENPFB_00058 | 1.56e-69 | 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 |
| HNJENPFB_00059 | 1.72e-79 | engB | - | - | D | ko:K03978 | - | ko00000,ko03036 | Necessary for normal cell division and for the maintenance of normal septation |
| HNJENPFB_00060 | 2.22e-300 | 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 |
| HNJENPFB_00061 | 9.46e-203 | 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 |
| HNJENPFB_00062 | 4.72e-107 | clpP | 3.4.21.92 | - | O | 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 |
| HNJENPFB_00063 | 2.55e-95 | 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 |
| HNJENPFB_00064 | 4.77e-43 | - | - | - | - | - | - | - | - |
| HNJENPFB_00065 | 1.25e-85 | 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 |
| HNJENPFB_00066 | 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 |
| HNJENPFB_00068 | 9.12e-42 | - | - | - | S | - | - | - | YjbR |
| HNJENPFB_00070 | 1.22e-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 |
| HNJENPFB_00071 | 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) |
| HNJENPFB_00072 | 3.53e-221 | - | - | - | S | ko:K03308 | - | ko00000 | Sodium:neurotransmitter symporter family |
| HNJENPFB_00074 | 4.69e-27 | - | - | - | E | - | - | - | Transglutaminase/protease-like homologues |
| HNJENPFB_00075 | 1.79e-11 | - | - | - | E | - | - | - | protein (some members contain a von Willebrand factor type A (vWA) domain |
| HNJENPFB_00076 | 1.36e-118 | - | - | - | S | ko:K03924 | - | ko00000,ko01000 | associated with various cellular activities |
| HNJENPFB_00077 | 1.41e-124 | - | - | - | E | - | - | - | haloacid dehalogenase-like hydrolase |
| HNJENPFB_00079 | 6.18e-202 | - | 6.1.1.13 | - | Q | ko:K03367,ko:K04784 | ko00473,ko01053,ko01503,ko02020,ko05150,map00473,map01053,map01503,map02020,map05150 | ko00000,ko00001,ko00002,ko01000,ko01004,ko01008,ko01504 | AMP-binding enzyme |
| HNJENPFB_00080 | 2.29e-52 | - | - | - | T | - | - | - | His Kinase A (phosphoacceptor) domain |
| HNJENPFB_00081 | 8.1e-78 | - | - | - | T | - | - | - | Transcriptional regulatory protein, C terminal |
| HNJENPFB_00082 | 4.77e-69 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00083 | 7.49e-15 | - | - | - | S | - | - | - | Protein of unknown function (DUF3006) |
| HNJENPFB_00084 | 7.64e-83 | - | - | - | S | ko:K02238 | - | ko00000,ko00002,ko02044 | PFAM Metallo-beta-lactamase superfamily |
| HNJENPFB_00085 | 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 |
| HNJENPFB_00086 | 1.65e-138 | 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 |
| HNJENPFB_00087 | 2.44e-194 | putP | - | - | E | ko:K03307,ko:K11928 | - | ko00000,ko02000 | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family |
| HNJENPFB_00088 | 8.09e-47 | trkA | - | - | P | ko:K03499 | - | ko00000,ko02000 | Psort location Cytoplasmic, score 8.87 |
| HNJENPFB_00089 | 1.06e-189 | trkH | - | - | P | ko:K03498 | - | ko00000,ko02000 | potassium uptake protein TrkH |
| HNJENPFB_00090 | 1.96e-82 | spoIIP | - | - | M | ko:K06385 | - | ko00000 | stage II sporulation protein P |
| HNJENPFB_00091 | 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 |
| HNJENPFB_00092 | 1.27e-278 | 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 |
| HNJENPFB_00093 | 1.19e-258 | 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 |
| HNJENPFB_00094 | 6.6e-279 | 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 |
| HNJENPFB_00095 | 5.47e-206 | 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 |
| HNJENPFB_00096 | 3.27e-123 | - | - | - | O | - | - | - | Holliday junction DNA helicase ruvB N-terminus |
| HNJENPFB_00099 | 7.89e-67 | - | - | - | S | - | - | - | Baseplate J-like protein |
| HNJENPFB_00107 | 4.05e-99 | - | - | - | S | - | - | - | metal-dependent phosphohydrolase, HD sub domain |
| HNJENPFB_00108 | 6.06e-295 | 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 |
| HNJENPFB_00109 | 2.33e-82 | spoIIIAA | - | - | S | ko:K06390 | - | ko00000 | stage III sporulation protein AA |
| HNJENPFB_00111 | 1.35e-23 | spoIIIAC | - | - | S | ko:K06392 | - | ko00000 | stage III sporulation protein AC |
| HNJENPFB_00112 | 6.87e-19 | spoIIIAD | - | - | S | ko:K06393 | - | ko00000 | Stage III sporulation protein AD |
| HNJENPFB_00113 | 1.34e-72 | - | - | - | KT | - | - | - | response regulator |
| HNJENPFB_00114 | 1.34e-139 | - | - | - | T | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00115 | 2.52e-147 | - | - | - | M | - | - | - | Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase |
| HNJENPFB_00116 | 1.54e-231 | trpS | 6.1.1.2 | - | J | ko:K01867 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Tryptophanyl-tRNA synthetase |
| HNJENPFB_00117 | 6.39e-32 | plsD | 2.3.1.51 | - | I | ko:K00655 | ko00561,ko00564,ko01100,ko01110,map00561,map00564,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko01004 | Acyltransferase |
| HNJENPFB_00118 | 3.98e-26 | - | - | - | IQ | ko:K02078 | - | ko00000,ko00001 | Phosphopantetheine attachment site |
| HNJENPFB_00119 | 9.07e-173 | - | - | - | G | ko:K15771 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| HNJENPFB_00120 | 5.61e-69 | - | - | - | G | ko:K15770 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Bacterial extracellular solute-binding protein |
| HNJENPFB_00121 | 5.21e-206 | 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 |
| HNJENPFB_00122 | 1.28e-05 | - | - | - | - | - | - | - | - |
| HNJENPFB_00123 | 1.31e-215 | - | 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 | Psort location Cytoplasmic, score |
| HNJENPFB_00124 | 3.89e-275 | - | - | - | G | - | - | - | Alpha amylase, catalytic domain |
| HNJENPFB_00125 | 1.88e-67 | ribU | - | - | U | - | - | - | 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 |
| HNJENPFB_00126 | 1.11e-69 | - | - | - | L | - | - | - | DNA alkylation repair enzyme |
| HNJENPFB_00127 | 1.14e-96 | - | - | - | M | ko:K07271 | - | ko00000,ko01000 | LicD family |
| HNJENPFB_00128 | 2.75e-118 | - | - | - | M | - | - | - | group 2 family protein |
| HNJENPFB_00131 | 3.33e-104 | - | - | - | M | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00133 | 3.85e-143 | rluC | 5.4.99.23, 5.4.99.24 | - | J | ko:K06179,ko:K06180 | - | ko00000,ko01000,ko03009 | Responsible for synthesis of pseudouridine from uracil |
| HNJENPFB_00134 | 1.8e-112 | yfiH | - | - | S | ko:K05810 | - | ko00000,ko01000 | Belongs to the multicopper oxidase YfiH RL5 family |
| HNJENPFB_00136 | 2.48e-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 |
| HNJENPFB_00138 | 5.47e-101 | - | - | - | V | - | - | - | MatE |
| HNJENPFB_00139 | 1.05e-22 | - | - | - | T | - | - | - | STAS domain |
| HNJENPFB_00140 | 1.07e-22 | - | - | - | T | - | - | - | PFAM Histidine kinase-, DNA gyrase B-, and HSP90-like |
| HNJENPFB_00142 | 4.44e-25 | plsC | 2.3.1.51 | - | I | ko:K00655 | ko00561,ko00564,ko01100,ko01110,map00561,map00564,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko01004 | acyltransferase |
| HNJENPFB_00143 | 1.31e-81 | cmk | 2.5.1.19, 2.7.4.25, 6.3.2.1 | - | F | ko:K00800,ko:K00945,ko:K03977,ko:K13799 | ko00240,ko00400,ko00410,ko00770,ko01100,ko01110,ko01130,ko01230,map00240,map00400,map00410,map00770,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000,ko03009 | Belongs to the cytidylate kinase family. Type 1 subfamily |
| HNJENPFB_00144 | 5.1e-172 | - | - | - | S | ko:K07007 | - | ko00000 | HI0933-like protein |
| HNJENPFB_00145 | 3.16e-127 | - | - | - | K | - | - | - | transcriptional regulator RpiR family |
| HNJENPFB_00146 | 1.66e-96 | 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 |
| HNJENPFB_00147 | 5.26e-17 | - | - | - | K | - | - | - | Glycosyl hydrolases family 39 |
| HNJENPFB_00148 | 8.05e-61 | - | - | - | I | - | - | - | Carboxylesterase family |
| HNJENPFB_00149 | 9.02e-20 | - | - | - | N | - | - | - | Leucine rich repeats (6 copies) |
| HNJENPFB_00150 | 2.06e-32 | - | - | - | K | ko:K10914 | ko02020,ko02024,ko02025,ko02026,ko05111,map02020,map02024,map02025,map02026,map05111 | ko00000,ko00001,ko03000 | PFAM Bacterial regulatory proteins, crp family |
| HNJENPFB_00151 | 4.93e-252 | 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 |
| HNJENPFB_00152 | 2.94e-94 | 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 |
| HNJENPFB_00153 | 1.08e-10 | - | - | - | DJ | - | - | - | PFAM plasmid |
| HNJENPFB_00154 | 2.06e-45 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HNJENPFB_00156 | 9.5e-45 | - | - | - | KT | - | - | - | LytTr DNA-binding domain |
| HNJENPFB_00157 | 1.13e-83 | - | - | - | T | - | - | - | GHKL domain |
| HNJENPFB_00158 | 4.72e-29 | - | - | - | N | - | - | - | CHAP domain |
| HNJENPFB_00160 | 1.6e-155 | 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 |
| HNJENPFB_00161 | 2.39e-102 | bcsP | - | - | S | ko:K07080 | - | ko00000 | TRAP transporter solute receptor, TAXI family |
| HNJENPFB_00162 | 5.75e-213 | gltS | - | - | P | ko:K03312 | - | ko00000,ko02000 | Catalyzes the sodium-dependent transport of glutamate |
| HNJENPFB_00164 | 4.28e-139 | 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 |
| HNJENPFB_00165 | 8.37e-44 | - | - | - | 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 |
| HNJENPFB_00167 | 6.69e-273 | hydG | 4.1.99.19 | - | C | ko:K03150 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko01000 | biosynthesis protein ThiH |
| HNJENPFB_00169 | 4.29e-216 | 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 |
| HNJENPFB_00171 | 2.41e-39 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00172 | 6.34e-69 | - | - | - | E | - | - | - | IrrE N-terminal-like domain |
| HNJENPFB_00173 | 5.1e-21 | - | - | - | - | - | - | - | - |
| HNJENPFB_00175 | 6.9e-62 | - | - | - | T | - | - | - | PemK-like, MazF-like toxin of type II toxin-antitoxin system |
| HNJENPFB_00176 | 1.84e-23 | - | - | - | K | - | - | - | Helix-turn-helix domain |
| HNJENPFB_00177 | 3.48e-59 | 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 |
| HNJENPFB_00178 | 1.37e-290 | 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 |
| HNJENPFB_00179 | 9.29e-81 | recO | - | - | L | ko:K03584 | ko03440,map03440 | ko00000,ko00001,ko03400 | Involved in DNA repair and RecF pathway recombination |
| HNJENPFB_00181 | 7.14e-133 | 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 |
| HNJENPFB_00183 | 5.08e-51 | - | - | - | F | - | - | - | Belongs to the Nudix hydrolase family |
| HNJENPFB_00184 | 2.32e-60 | - | - | - | S | - | - | - | DHHW protein |
| HNJENPFB_00185 | 3.35e-134 | iscS | 2.8.1.7 | - | E | ko:K04487 | ko00730,ko01100,ko04122,map00730,map01100,map04122 | ko00000,ko00001,ko01000,ko02048,ko03016,ko03029 | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes |
| HNJENPFB_00186 | 4.07e-146 | 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) |
| HNJENPFB_00187 | 2.85e-77 | 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 |
| HNJENPFB_00188 | 7.19e-39 | yhbY | - | - | J | ko:K07574 | - | ko00000,ko03009 | RNA-binding protein, YhbY family |
| HNJENPFB_00189 | 3.91e-47 | nadD | 2.7.7.18 | - | H | ko:K00969 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) |
| HNJENPFB_00190 | 1.63e-68 | nadD | 2.7.7.18 | - | H | ko:K00969 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | HD superfamily hydrolase involved in NAD metabolism |
| HNJENPFB_00191 | 3.87e-07 | - | - | - | O | ko:K13963 | ko05146,map05146 | ko00000,ko00001 | Belongs to the serpin family |
| HNJENPFB_00192 | 3.1e-278 | 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) |
| HNJENPFB_00193 | 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 |
| HNJENPFB_00194 | 1.26e-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 |
| HNJENPFB_00195 | 1.55e-218 | - | 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 |
| HNJENPFB_00199 | 8.11e-60 | nnrE | 5.1.99.6 | - | G | ko:K17759 | - | ko00000,ko01000 | Catalyzes the epimerization of the S- and R-forms of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration. This is a prerequisite for the S- specific NAD(P)H-hydrate dehydratase to allow the repair of both epimers of NAD(P)HX |
| HNJENPFB_00200 | 9.3e-46 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HNJENPFB_00201 | 8.08e-88 | - | - | - | M | - | - | - | Psort location CytoplasmicMembrane, score 9.99 |
| HNJENPFB_00203 | 2.82e-79 | yfbR | 3.1.3.89 | - | S | ko:K07023,ko:K08722 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko01000 | PFAM metal-dependent phosphohydrolase HD sub domain |
| HNJENPFB_00204 | 3.75e-243 | - | - | - | S | - | - | - | Bacterial membrane protein YfhO |
| HNJENPFB_00206 | 7.42e-16 | - | - | - | EG | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00207 | 1.17e-72 | - | - | - | S | - | - | - | IA, variant 3 |
| HNJENPFB_00208 | 1.22e-206 | - | - | - | E | ko:K03310 | - | ko00000 | amino acid carrier protein |
| HNJENPFB_00209 | 1.23e-101 | - | - | - | S | ko:K07023 | - | ko00000 | HD domain |
| HNJENPFB_00210 | 6.48e-174 | hgdC | - | - | I | - | - | - | CoA-substrate-specific enzyme activase |
| HNJENPFB_00211 | 3.05e-203 | - | - | - | I | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00212 | 2.28e-88 | - | - | - | - | - | - | - | - |
| HNJENPFB_00213 | 1.45e-57 | htrA | 3.4.21.107 | - | O | ko:K04771,ko:K08372 | ko01503,ko02020,map01503,map02020 | ko00000,ko00001,ko00002,ko01000,ko01002,ko03110 | smart pdz dhr glgf |
| HNJENPFB_00214 | 4.04e-196 | 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 |
| HNJENPFB_00215 | 7.5e-36 | 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 |
| HNJENPFB_00216 | 4.26e-297 | 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) |
| HNJENPFB_00217 | 3.49e-22 | 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) |
| HNJENPFB_00218 | 2.17e-244 | 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) |
| HNJENPFB_00219 | 2.27e-131 | - | - | - | T | - | - | - | ATPase histidine kinase DNA gyrase B HSP90 domain protein |
| HNJENPFB_00220 | 3.51e-47 | - | - | - | S | ko:K18475 | - | ko00000,ko01000,ko02035 | N-methylation of lysine residues in flagellin K00599 |
| HNJENPFB_00221 | 5.16e-17 | - | - | - | - | - | - | - | - |
| HNJENPFB_00223 | 1.65e-27 | rpsT | - | - | J | ko:K02968 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds directly to 16S ribosomal RNA |
| HNJENPFB_00224 | 7.45e-131 | cobB | - | - | K | ko:K12410 | - | ko00000,ko01000 | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form |
| HNJENPFB_00225 | 2.51e-47 | 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 |
| HNJENPFB_00227 | 1.16e-172 | galE | 5.1.3.2 | - | M | ko:K01784 | ko00052,ko00520,ko01100,map00052,map00520,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the NAD(P)-dependent epimerase dehydratase family |
| HNJENPFB_00228 | 2.21e-104 | 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 |
| HNJENPFB_00229 | 5.55e-179 | tsaD | 2.3.1.234 | - | O | ko:K01409,ko:K03070 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko01000,ko02044,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 |
| HNJENPFB_00230 | 6.48e-106 | 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 |
| HNJENPFB_00231 | 6.04e-25 | - | - | - | S | ko:K14761 | - | ko00000,ko03009 | S4 domain |
| HNJENPFB_00232 | 2.86e-122 | recF | - | - | L | ko:K03629 | 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 |
| HNJENPFB_00233 | 4.52e-31 | - | - | - | S | - | - | - | Domain of unknown function (DUF370) |
| HNJENPFB_00235 | 1.62e-61 | ydhO | 3.4.14.13 | - | M | ko:K20742,ko:K21471 | - | ko00000,ko01000,ko01002,ko01011 | Peptidoglycan-binding domain 1 protein |
| HNJENPFB_00236 | 8.61e-53 | - | 3.1.3.3 | - | KT | ko:K07315 | - | ko00000,ko01000,ko03021 | Sigma factor PP2C-like phosphatases |
| HNJENPFB_00237 | 1.48e-73 | fliY1 | - | - | ET | ko:K02030 | - | ko00000,ko00002,ko02000 | ABC transporter, substrate-binding protein, family 3 |
| HNJENPFB_00238 | 2.93e-85 | tcyB | - | - | P | ko:K02029 | - | ko00000,ko00002,ko02000 | ABC transporter, permease protein |
| HNJENPFB_00239 | 2.89e-112 | glnQ | 3.6.3.21 | - | E | ko:K02028 | - | ko00000,ko00002,ko01000,ko02000 | ABC transporter |
| HNJENPFB_00241 | 1.22e-08 | cobW | - | - | S | - | - | - | CobW P47K family protein |
| HNJENPFB_00242 | 2.42e-226 | 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 |
| HNJENPFB_00243 | 8.38e-182 | yybT | - | - | T | - | - | - | domain protein |
| HNJENPFB_00244 | 1.8e-64 | rplI | - | - | J | ko:K02939 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | binds to the 23S rRNA |
| HNJENPFB_00245 | 2.54e-233 | 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 |
| HNJENPFB_00246 | 3e-39 | 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) |
| HNJENPFB_00247 | 5.86e-87 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00248 | 6.14e-58 | - | - | - | M | - | - | - | GtrA-like protein |
| HNJENPFB_00249 | 6.57e-96 | 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 |
| HNJENPFB_00250 | 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 |
| HNJENPFB_00251 | 3.51e-120 | - | 3.2.1.1 | GH13 | G | ko:K01176 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | Alpha amylase catalytic |
| HNJENPFB_00252 | 1.51e-19 | malG | - | - | P | ko:K15772 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ABC transporter (Permease |
| HNJENPFB_00253 | 1.61e-60 | - | - | - | S | ko:K01992 | - | ko00000,ko00002,ko02000 | ABC-2 family transporter protein |
| HNJENPFB_00254 | 2.88e-128 | - | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | ABC-type multidrug transport system ATPase component |
| HNJENPFB_00255 | 9.36e-48 | spoVAE | - | - | S | ko:K06407 | - | ko00000 | SpoVAC/SpoVAEB sporulation membrane protein |
| HNJENPFB_00256 | 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 |
| HNJENPFB_00258 | 1.25e-64 | 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( ) |
| HNJENPFB_00259 | 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 |
| HNJENPFB_00260 | 1.4e-27 | - | - | - | S | - | - | - | membrane |
| HNJENPFB_00261 | 9.66e-09 | yetF | - | - | S | - | - | - | membrane |
| HNJENPFB_00263 | 1.91e-172 | - | - | - | M | - | - | - | MBOAT, membrane-bound O-acyltransferase family |
| HNJENPFB_00264 | 1.57e-32 | - | - | - | E | - | - | - | lipolytic protein G-D-S-L family |
| HNJENPFB_00265 | 1.03e-31 | - | - | - | E | - | - | - | lipolytic protein G-D-S-L family |
| HNJENPFB_00268 | 4.23e-126 | pfkB | 2.7.1.56 | - | G | ko:K00882 | ko00051,map00051 | ko00000,ko00001,ko01000 | Phosphomethylpyrimidine kinase |
| HNJENPFB_00269 | 1.17e-88 | fruR | - | - | K | ko:K03436 | - | ko00000,ko03000 | DeoR C terminal sensor domain |
| HNJENPFB_00270 | 1.86e-43 | - | - | - | K | - | - | - | COG COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases |
| HNJENPFB_00271 | 7.42e-313 | 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 |
| HNJENPFB_00272 | 6.7e-61 | yjeE | 2.7.1.221 | - | S | ko:K06925,ko:K07102 | ko00520,ko01100,map00520,map01100 | ko00000,ko00001,ko01000,ko03016 | Threonylcarbamoyl adenosine biosynthesis protein TsaE |
| HNJENPFB_00273 | 2.1e-75 | yeaZ | - | - | O | ko:K14742 | - | ko00000,ko03016 | Universal bacterial protein YeaZ |
| HNJENPFB_00274 | 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 |
| HNJENPFB_00275 | 2.28e-248 | 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 |
| HNJENPFB_00276 | 2.54e-53 | 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 |
| HNJENPFB_00277 | 1.87e-97 | nrnA | 3.1.13.3, 3.1.3.7 | - | S | ko:K06881 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko01000,ko03400 | domain protein |
| HNJENPFB_00278 | 2.4e-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 |
| HNJENPFB_00279 | 1.61e-140 | map | 3.4.11.18 | - | E | ko:K01265 | - | ko00000,ko01000,ko01002 | Methionine aminopeptidase |
| HNJENPFB_00280 | 4.03e-16 | - | - | - | J | - | - | - | COG2163 Ribosomal protein L14E L6E L27E |
| HNJENPFB_00281 | 1.32e-38 | 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 |
| HNJENPFB_00282 | 5.8e-18 | rpmJ | - | - | J | ko:K02919 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bL36 family |
| HNJENPFB_00283 | 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 |
| HNJENPFB_00284 | 3.7e-73 | 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 |
| HNJENPFB_00285 | 3.43e-101 | 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 |
| HNJENPFB_00286 | 3.47e-45 | - | - | - | D | - | - | - | Transglutaminase-like superfamily |
| HNJENPFB_00287 | 1.63e-39 | - | - | - | D | - | - | - | protein involved in cytokinesis, contains TGc (transglutaminase protease-like) domain |
| HNJENPFB_00288 | 2.42e-72 | - | - | - | M | - | - | - | Sulfatase |
| HNJENPFB_00289 | 8.53e-34 | acpP | - | - | IQ | ko:K02078 | - | ko00000,ko00001 | Carrier of the growing fatty acid chain in fatty acid biosynthesis |
| HNJENPFB_00290 | 6.86e-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) |
| HNJENPFB_00291 | 4e-57 | 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 |
| HNJENPFB_00292 | 3.3e-186 | aroF | 2.5.1.54 | - | E | ko:K03856 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | synthase |
| HNJENPFB_00293 | 4.69e-95 | lgt | - | - | M | ko:K13292 | - | ko00000,ko01000 | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins |
| HNJENPFB_00294 | 5.33e-169 | ymfH | - | - | S | - | - | - | Belongs to the peptidase M16 family |
| HNJENPFB_00295 | 6.19e-122 | - | - | - | S | - | - | - | Peptidase M16 inactive domain protein |
| HNJENPFB_00297 | 1.34e-200 | addB | 3.6.4.12 | - | L | ko:K16899 | - | ko00000,ko01000,ko03400 | ATP-dependent helicase deoxyribonuclease subunit B |
| HNJENPFB_00298 | 3.59e-68 | 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 |
| HNJENPFB_00299 | 3.1e-32 | - | - | - | C | - | - | - | ATP synthesis coupled proton transport |
| HNJENPFB_00300 | 6.15e-31 | mraZ | - | - | K | ko:K03925 | - | ko00000 | Belongs to the MraZ family |
| HNJENPFB_00301 | 8.68e-136 | 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 |
| HNJENPFB_00304 | 4.47e-51 | - | - | - | KT | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00305 | 9.84e-115 | 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 |
| HNJENPFB_00306 | 4.18e-08 | - | - | - | D | ko:K03569 | - | ko00000,ko02048,ko03036,ko04812 | Cell shape determining protein, MreB Mrl family |
| HNJENPFB_00307 | 1.6e-53 | mreC | - | - | M | ko:K03570 | - | ko00000,ko03036 | Cell shape-determining protein MreC |
| HNJENPFB_00309 | 6.02e-175 | mrdA | 3.4.16.4 | - | M | ko:K05515 | ko00550,ko01501,map00550,map01501 | ko00000,ko00001,ko01000,ko01011 | Penicillin-binding Protein |
| HNJENPFB_00310 | 1.12e-82 | - | - | - | T | ko:K07694 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | Response regulator receiver domain protein |
| HNJENPFB_00311 | 9.18e-46 | - | - | - | T | - | - | - | Psort location |
| HNJENPFB_00312 | 2.12e-51 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00313 | 2.32e-218 | 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) |
| HNJENPFB_00314 | 5.97e-109 | gabR | - | - | K | ko:K00375 | - | ko00000,ko03000 | transaminase activity |
| HNJENPFB_00315 | 8.45e-91 | - | - | - | L | - | - | - | ATPase domain of DNA mismatch repair MUTS family |
| HNJENPFB_00317 | 2.52e-28 | bglC | - | - | K | - | - | - | AraC-type DNA-binding domain-containing proteins |
| HNJENPFB_00318 | 3.26e-63 | - | 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 |
| HNJENPFB_00319 | 3.06e-108 | tagH | 3.6.3.40 | - | GM | ko:K01990,ko:K09691,ko:K09693 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00320 | 8.95e-08 | tagG | - | - | U | ko:K09692 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Transport permease protein |
| HNJENPFB_00321 | 3.19e-216 | - | - | - | KT | ko:K02647 | - | ko00000,ko03000 | Psort location Cytoplasmic, score |
| HNJENPFB_00322 | 2.11e-101 | ftsE | - | - | D | ko:K09812 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000,ko03036 | cell division ATP-binding protein FtsE |
| HNJENPFB_00323 | 1.26e-90 | ftsX | - | - | D | ko:K09811,ko:K09812 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000,ko03036 | cell division |
| HNJENPFB_00324 | 2.12e-42 | - | - | - | V | ko:K02004 | - | ko00000,ko00002,ko02000 | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00325 | 2.59e-74 | - | - | - | T | - | - | - | response regulator receiver |
| HNJENPFB_00326 | 1.76e-76 | - | - | - | T | - | - | - | His Kinase A (phosphoacceptor) domain |
| HNJENPFB_00327 | 3.31e-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 |
| HNJENPFB_00328 | 2.11e-138 | 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 |
| HNJENPFB_00329 | 3.23e-84 | 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 |
| HNJENPFB_00330 | 3e-47 | - | - | - | S | - | - | - | ECF transporter, substrate-specific component |
| HNJENPFB_00331 | 7.86e-15 | spoIIIAG | - | - | S | ko:K06396 | - | ko00000 | stage III sporulation protein AG |
| HNJENPFB_00332 | 3.88e-08 | spoIIIAH | - | - | S | ko:K06397 | - | ko00000 | Stage III sporulation protein |
| HNJENPFB_00333 | 3.21e-41 | - | - | - | K | - | - | - | helix_turn_helix multiple antibiotic resistance protein |
| HNJENPFB_00334 | 1.65e-102 | - | - | - | F | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00335 | 2.47e-31 | 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 |
| HNJENPFB_00336 | 3.08e-68 | - | - | - | V | ko:K01992,ko:K11051 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ABC-2 type transporter |
| HNJENPFB_00337 | 1.4e-201 | - | - | - | E | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00338 | 9.78e-147 | - | - | - | K | - | - | - | Psort location Cytoplasmic, score 9.98 |
| HNJENPFB_00339 | 4.29e-41 | - | - | - | C | - | - | - | Nitroreductase family |
| HNJENPFB_00340 | 9.88e-56 | isplu5A | - | - | L | ko:K07491 | - | ko00000 | COG1943 Transposase and inactivated derivatives |
| HNJENPFB_00342 | 8.07e-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) |
| HNJENPFB_00343 | 2.04e-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) |
| HNJENPFB_00344 | 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 |
| HNJENPFB_00345 | 1.89e-175 | 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 |
| HNJENPFB_00346 | 2.4e-127 | - | 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 |
| HNJENPFB_00347 | 1.07e-98 | pheT | 6.1.1.20 | - | J | ko:K01890 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | B3/4 domain |
| HNJENPFB_00348 | 5.55e-37 | yrzL | - | - | S | - | - | - | Belongs to the UPF0297 family |
| HNJENPFB_00349 | 8.58e-36 | - | - | - | - | - | - | - | - |
| HNJENPFB_00350 | 5.59e-223 | copA | 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 |
| HNJENPFB_00351 | 2.18e-45 | - | - | - | S | ko:K02238 | - | ko00000,ko00002,ko02044 | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00352 | 5.13e-28 | 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 |
| HNJENPFB_00353 | 1.69e-62 | rnmV | 3.1.26.8 | - | L | ko:K05985 | - | ko00000,ko01000 | Ribonuclease M5 |
| HNJENPFB_00354 | 3.48e-115 | 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 |
| HNJENPFB_00355 | 7.13e-192 | 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 |
| HNJENPFB_00356 | 3.68e-156 | 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 |
| HNJENPFB_00357 | 5.79e-232 | malQ | 2.4.1.25 | GH77 | G | ko:K00705 | ko00500,ko01100,map00500,map01100 | ko00000,ko00001,ko01000 | Psort location Cytoplasmic, score |
| HNJENPFB_00358 | 2.64e-44 | cinA | 3.5.1.42 | - | S | ko:K03742,ko:K03743 | ko00760,map00760 | ko00000,ko00001,ko01000 | Belongs to the CinA family |
| HNJENPFB_00359 | 6.72e-55 | - | - | - | - | - | - | - | - |
| HNJENPFB_00360 | 2.09e-111 | 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 |
| HNJENPFB_00361 | 3.37e-12 | - | - | - | S | - | - | - | Domain of unknown function (DUF1934) |
| HNJENPFB_00362 | 9.7e-19 | birA | 6.3.4.15 | - | HK | ko:K03524 | ko00780,ko01100,map00780,map01100 | ko00000,ko00001,ko01000,ko03000 | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor |
| HNJENPFB_00363 | 0.0 | purL | 6.3.5.3 | - | F | ko:K01952 | ko00230,ko01100,ko01110,ko01130,map00230,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | phosphoribosylformylglycinamidine synthase |
| HNJENPFB_00364 | 6e-38 | ndoA | - | - | L | ko:K07171 | - | ko00000,ko01000,ko02048 | Toxic component of a toxin-antitoxin (TA) module |
| HNJENPFB_00365 | 5.8e-55 | - | - | - | K | - | - | - | Helix-turn-helix |
| HNJENPFB_00366 | 2.06e-82 | cobC | 3.1.3.73 | - | G | ko:K02226 | ko00860,ko01100,map00860,map01100 | ko00000,ko00001,ko00002,ko01000 | Psort location Cytoplasmic, score |
| HNJENPFB_00367 | 8.97e-200 | 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 |
| HNJENPFB_00371 | 3.31e-38 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HNJENPFB_00372 | 5.68e-169 | 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 |
| HNJENPFB_00373 | 3.5e-113 | ftsW | - | - | D | ko:K03588 | ko04112,map04112 | ko00000,ko00001,ko02000,ko03036 | Belongs to the SEDS family |
| HNJENPFB_00374 | 7.77e-177 | 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) |
| HNJENPFB_00376 | 1.48e-109 | - | - | - | V | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00378 | 0.000436 | - | - | - | S | ko:K06402 | - | ko00000,ko01000,ko01002 | Belongs to the peptidase M50B family |
| HNJENPFB_00379 | 1.22e-37 | - | - | - | C | - | - | - | Elongator protein 3, MiaB family, Radical SAM |
| HNJENPFB_00380 | 9.37e-27 | - | - | - | C | - | - | - | Domain of unknown function (DUF1858) |
| HNJENPFB_00383 | 5.54e-215 | comM | - | - | O | ko:K06400,ko:K07391 | - | ko00000 | Magnesium chelatase, subunit ChlI C-terminal |
| HNJENPFB_00384 | 6.17e-179 | yhbU_1 | - | - | O | ko:K08303 | ko05120,map05120 | ko00000,ko00001,ko01000,ko01002 | Peptidase U32 |
| HNJENPFB_00385 | 9.99e-107 | mltG | - | - | S | ko:K07082 | - | ko00000 | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation |
| HNJENPFB_00387 | 1.23e-73 | ybaK | - | - | S | ko:K03976 | - | ko00000,ko01000,ko03016 | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily |
| HNJENPFB_00388 | 2.32e-134 | czcA | - | - | V | ko:K03296 | - | ko00000 | Psort location CytoplasmicMembrane, score 10.00 |
| HNJENPFB_00389 | 2.75e-132 | - | - | GT2 | M | ko:K20534 | - | ko00000,ko01000,ko01005,ko02000 | Glycosyltransferase like family 2 |
| HNJENPFB_00390 | 4.87e-86 | 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 |
| HNJENPFB_00391 | 4.65e-75 | - | - | - | S | - | - | - | peptidase M50 |
| HNJENPFB_00392 | 3.37e-34 | rpmB | - | - | J | ko:K02902 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bL28 family |
| HNJENPFB_00394 | 3.33e-15 | - | - | - | P | - | - | - | YARHG |
| HNJENPFB_00395 | 6.24e-193 | - | - | - | M | - | - | - | Domain of unknown function (DUF1727) |
| HNJENPFB_00396 | 2.75e-67 | - | - | - | S | ko:K07009 | - | ko00000 | glutamine amidotransferase |
| HNJENPFB_00398 | 3.89e-64 | - | - | - | E | - | - | - | branched-chain amino acid permease (Azaleucine resistance) |
| HNJENPFB_00399 | 1.65e-38 | - | - | - | S | - | - | - | Branched-chain amino acid transport protein (AzlD) |
| HNJENPFB_00400 | 2.58e-103 | 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 |
| HNJENPFB_00403 | 7.19e-86 | rsmG | 2.1.1.170 | - | J | ko:K03501 | - | ko00000,ko01000,ko03009,ko03036 | Specifically methylates the N7 position of a guanine in 16S rRNA |
| HNJENPFB_00404 | 1.72e-298 | 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 |
| HNJENPFB_00408 | 2.37e-187 | - | - | - | V | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00410 | 3.03e-244 | 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) |
| HNJENPFB_00411 | 1.42e-51 | yloV | - | - | S | ko:K07030 | - | ko00000 | DAK2 domain fusion protein YloV |
| HNJENPFB_00412 | 4.75e-197 | 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 |
| HNJENPFB_00413 | 9.68e-91 | jag | - | - | S | ko:K06346 | - | ko00000 | R3H domain protein |
| HNJENPFB_00414 | 8.32e-67 | yidC | - | - | U | ko:K03217 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044,ko03029 | Membrane protein insertase, YidC Oxa1 family |
| HNJENPFB_00416 | 1.4e-69 | - | - | - | G | - | - | - | Fibronectin type 3 domain |
| HNJENPFB_00417 | 1.63e-41 | nt5e | 3.1.3.18 | - | S | ko:K01091 | ko00630,ko01100,ko01110,ko01130,map00630,map01100,map01110,map01130 | ko00000,ko00001,ko01000 | HAD-hyrolase-like |
| HNJENPFB_00418 | 2.17e-23 | - | - | - | S | - | - | - | Thioesterase family |
| HNJENPFB_00419 | 5.77e-209 | ychF | - | - | J | ko:K06942 | - | ko00000,ko03009 | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner |
| HNJENPFB_00421 | 2.59e-78 | - | - | - | C | - | - | - | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family |
| HNJENPFB_00422 | 5.64e-216 | gldA | 1.1.1.6 | - | C | ko:K00005 | ko00561,ko00640,ko01100,map00561,map00640,map01100 | ko00000,ko00001,ko01000 | Iron-containing alcohol dehydrogenase |
| HNJENPFB_00423 | 1.06e-31 | - | - | - | S | - | - | - | Acyltransferase family |
| HNJENPFB_00424 | 6.33e-44 | nnrE | - | - | K | - | - | - | Acetyltransferase (GNAT) domain |
| HNJENPFB_00425 | 9.95e-109 | - | - | - | V | - | - | - | Psort location CytoplasmicMembrane, score 9.99 |
| HNJENPFB_00426 | 8.08e-37 | 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 |
| HNJENPFB_00427 | 1.5e-210 | 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 |
| HNJENPFB_00428 | 5.15e-144 | 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 |
| HNJENPFB_00430 | 1.26e-254 | megL | 2.5.1.48, 4.4.1.11 | - | E | ko:K01739,ko:K01761 | ko00270,ko00450,ko00920,ko01100,ko01110,ko01130,ko01230,map00270,map00450,map00920,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Cys Met metabolism |
| HNJENPFB_00433 | 2.53e-234 | - | - | - | L | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00434 | 6e-136 | - | - | - | S | - | - | - | Proteasome subunit |
| HNJENPFB_00435 | 3.27e-68 | - | - | - | - | - | - | - | - |
| HNJENPFB_00436 | 1.04e-96 | - | - | - | L | - | - | - | Psort location Cytoplasmic, score 8.96 |
| HNJENPFB_00437 | 9.77e-29 | ylxM | - | - | 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 |
| HNJENPFB_00438 | 2.43e-221 | 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 |
| HNJENPFB_00439 | 1.49e-197 | - | - | - | S | - | - | - | phage terminase, large subunit, PBSX family |
| HNJENPFB_00440 | 1.5e-115 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00441 | 1.48e-92 | 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 |
| HNJENPFB_00443 | 7.39e-39 | - | - | - | M | - | - | - | heme binding |
| HNJENPFB_00444 | 9.96e-18 | 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) |
| HNJENPFB_00445 | 5.33e-190 | 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 |
| HNJENPFB_00446 | 1.03e-104 | 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 |
| HNJENPFB_00447 | 6.63e-94 | pdaB | 3.5.1.104 | - | G | ko:K22278 | - | ko00000,ko01000 | Polysaccharide deacetylase |
| HNJENPFB_00448 | 6.37e-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 |
| HNJENPFB_00449 | 5.21e-99 | 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 |
| HNJENPFB_00450 | 1.23e-21 | 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 |
| HNJENPFB_00451 | 7.48e-38 | - | - | GH23 | M | ko:K08309 | - | ko00000,ko01000,ko01011 | Transglycosylase SLT domain |
| HNJENPFB_00452 | 3.26e-229 | apeA | - | - | E | - | - | - | M18 family aminopeptidase |
| HNJENPFB_00454 | 5.9e-25 | phoU | - | - | P | ko:K02039 | - | ko00000 | Plays a role in the regulation of phosphate uptake |
| HNJENPFB_00455 | 1.48e-89 | phoB | - | - | K | ko:K07658 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | response regulator receiver |
| HNJENPFB_00456 | 2.24e-122 | phoR | 2.7.13.3 | - | T | ko:K07636 | ko02020,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko02022 | Histidine kinase |
| HNJENPFB_00457 | 4.06e-257 | ileS | 6.1.1.5 | - | J | ko:K01870 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) |
| HNJENPFB_00458 | 3.32e-21 | - | - | - | D | ko:K04074 | - | ko00000,ko03036 | DivIVA domain protein |
| HNJENPFB_00459 | 7.44e-61 | - | - | - | S | - | - | - | S4 domain protein |
| HNJENPFB_00460 | 2.54e-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) |
| HNJENPFB_00461 | 2e-143 | 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 |
| HNJENPFB_00462 | 5.83e-251 | - | 2.7.13.3 | - | T | ko:K18350 | ko01502,ko02020,map01502,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko01504,ko02022 | Histidine kinase- DNA gyrase B |
| HNJENPFB_00463 | 5.69e-171 | - | - | - | T | ko:K18349 | ko01502,ko02020,map01502,map02020 | ko00000,ko00001,ko00002,ko01504,ko02022 | Psort location Cytoplasmic, score 9.98 |
| HNJENPFB_00464 | 3.4e-43 | - | - | - | K | - | - | - | Cro/C1-type HTH DNA-binding domain |
| HNJENPFB_00465 | 1.4e-279 | 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 |
| HNJENPFB_00467 | 9.68e-14 | - | - | - | T | - | - | - | His Kinase A (phosphoacceptor) domain |
| HNJENPFB_00468 | 4.4e-24 | - | - | - | S | - | - | - | Ferredoxin thioredoxin reductase catalytic beta chain |
| HNJENPFB_00470 | 5.15e-96 | - | - | - | J | ko:K19055 | - | ko00000,ko01000,ko03016 | YbaK proline--tRNA ligase associated domain protein |
| HNJENPFB_00471 | 2.3e-180 | 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 |
| HNJENPFB_00472 | 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 |
| HNJENPFB_00473 | 1.33e-139 | - | - | - | 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 |
| HNJENPFB_00475 | 1.2e-71 | - | 3.4.16.4 | - | V | ko:K07258 | ko00550,ko01100,map00550,map01100 | ko00000,ko00001,ko01000,ko01002,ko01011 | L,D-transpeptidase catalytic domain |
| HNJENPFB_00476 | 1.21e-77 | KatE | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00477 | 6.67e-40 | - | - | - | S | - | - | - | Dolichyl-phosphate-mannose-protein mannosyltransferase |
| HNJENPFB_00478 | 2.34e-107 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00479 | 5.12e-102 | - | - | - | T | - | - | - | domain protein |
| HNJENPFB_00482 | 1.87e-52 | bioY | - | - | S | ko:K03523 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | BioY family |
| HNJENPFB_00483 | 5.06e-150 | 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 | Fructose-1,6-bisphosphate aldolase, class II |
| HNJENPFB_00484 | 4.4e-25 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00485 | 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 |
| HNJENPFB_00486 | 2.49e-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 |
| HNJENPFB_00488 | 7.48e-53 | - | - | - | - | - | - | - | - |
| HNJENPFB_00489 | 8.34e-19 | - | - | - | - | - | - | - | - |
| HNJENPFB_00490 | 9.85e-49 | - | - | - | S | - | - | - | Bacteriophage Gp15 protein |
| HNJENPFB_00492 | 9.59e-15 | - | - | - | S | - | - | - | SigmaK-factor processing regulatory protein BofA |
| HNJENPFB_00493 | 7.81e-22 | secG | - | - | U | ko:K03075 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | P-P-bond-hydrolysis-driven protein transmembrane transporter activity |
| HNJENPFB_00494 | 0.0 | - | 5.99.1.3 | - | L | ko:K02469 | - | ko00000,ko01000,ko03032,ko03400 | PFAM DNA gyrase topoisomerase IV, subunit A |
| HNJENPFB_00495 | 4.45e-07 | - | - | - | I | - | - | - | Carboxyl transferase domain |
| HNJENPFB_00496 | 1.93e-15 | gcdC | - | - | I | - | - | - | Biotin-requiring enzyme |
| HNJENPFB_00497 | 1.33e-275 | oadA | 4.1.1.3 | - | C | ko:K01571 | ko00620,ko01100,map00620,map01100 | ko00000,ko00001,ko01000,ko02000 | Pyruvate carboxylase, C-terminal domain subunit K01960 |
| HNJENPFB_00498 | 3.59e-73 | 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 |
| HNJENPFB_00499 | 1.6e-107 | - | - | - | S | - | - | - | Protein of unknown function (DUF1275) |
| HNJENPFB_00500 | 1.13e-264 | yhgF | - | - | K | ko:K06959 | - | ko00000 | Tex-like protein N-terminal domain |
| HNJENPFB_00501 | 3.74e-96 | - | - | - | S | ko:K06889 | - | ko00000 | thiolester hydrolase activity |
| HNJENPFB_00502 | 5.83e-296 | sufB | - | - | O | ko:K07033,ko:K09014 | - | ko00000 | FeS assembly protein SufB |
| HNJENPFB_00503 | 3.03e-92 | sufD | - | - | O | ko:K07033,ko:K09015 | - | ko00000 | Uncharacterized protein family (UPF0051) |
| HNJENPFB_00504 | 1.36e-113 | - | - | - | S | - | - | - | Elongator protein 3, MiaB family, Radical SAM |
| HNJENPFB_00505 | 1.61e-101 | - | - | - | S | ko:K09125 | - | ko00000 | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage |
| HNJENPFB_00507 | 4.54e-51 | glnB | - | - | K | ko:K04751,ko:K04752 | ko02020,map02020 | ko00000,ko00001 | Nitrogen regulatory protein P-II |
| HNJENPFB_00508 | 3.7e-219 | amt | - | - | U | ko:K03320 | - | ko00000,ko02000 | Ammonium Transporter Family |
| HNJENPFB_00509 | 2.28e-93 | rny | - | - | D | ko:K18682 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03019 | Endoribonuclease that initiates mRNA decay |
| HNJENPFB_00510 | 2.6e-103 | - | 2.4.1.315 | GT28 | M | ko:K03429 | ko00561,ko01100,map00561,map01100 | ko00000,ko00001,ko01000,ko01003 | Monogalactosyldiacylglycerol synthase |
| HNJENPFB_00513 | 2.64e-79 | yigZ | 2.1.1.45, 3.4.13.9 | - | S | ko:K00560,ko:K01271 | ko00240,ko00670,ko01100,ko01523,map00240,map00670,map01100,map01523 | ko00000,ko00001,ko00002,ko01000,ko01002 | Uncharacterized protein family UPF0029 |
| HNJENPFB_00514 | 6.21e-39 | rpmE | - | - | J | ko:K02909 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L31 |
| HNJENPFB_00515 | 1.26e-20 | qmcA | - | - | O | - | - | - | SPFH domain Band 7 family |
| HNJENPFB_00516 | 2.96e-77 | - | - | - | S | - | - | - | Putative ABC-transporter type IV |
| HNJENPFB_00517 | 3.34e-75 | 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) |
| HNJENPFB_00518 | 3.9e-154 | ypsC | - | - | L | ko:K07444 | - | ko00000,ko01000 | Belongs to the methyltransferase superfamily |
| HNJENPFB_00519 | 7.44e-65 | hpf | - | - | J | ko:K05808 | - | ko00000,ko03009 | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase |
| HNJENPFB_00520 | 1.24e-12 | yabR | - | - | J | ko:K07570,ko:K07571 | - | ko00000 | S1 RNA binding domain |
| HNJENPFB_00521 | 1.3e-140 | - | - | - | K | - | - | - | LysR substrate binding domain |
| HNJENPFB_00522 | 3.17e-09 | cotJC | - | - | P | ko:K06334,ko:K07217 | - | ko00000 | catalase activity |
| HNJENPFB_00523 | 1.87e-12 | cotJB | - | - | S | ko:K06333 | - | ko00000 | COG NOG18028 non supervised orthologous group |
| HNJENPFB_00524 | 1.59e-08 | - | - | - | S | - | - | - | Spore coat associated protein JA (CotJA) |
| HNJENPFB_00526 | 3.79e-55 | hisE | 3.6.1.31 | - | E | ko:K01523 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Phosphoribosyl-ATP |
| HNJENPFB_00527 | 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 |
| HNJENPFB_00528 | 2.74e-59 | 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 |
| HNJENPFB_00529 | 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 |
| HNJENPFB_00530 | 8.37e-119 | 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 |
| HNJENPFB_00531 | 1.45e-13 | - | - | - | S | - | - | - | COG NOG18757 non supervised orthologous group |
| HNJENPFB_00532 | 3.46e-18 | - | - | - | V | - | - | - | MatE |
| HNJENPFB_00533 | 3.92e-22 | rnfE | - | - | C | ko:K03613 | - | ko00000 | Part of a membrane complex involved in electron transport |
| HNJENPFB_00534 | 5.15e-134 | rnfG | - | - | C | ko:K03612 | - | ko00000 | Part of a membrane complex involved in electron transport |
| HNJENPFB_00536 | 1.29e-110 | - | - | - | S | ko:K01421 | - | ko00000 | Psort location Cellwall, score |
| HNJENPFB_00537 | 9.75e-178 | 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) |
| HNJENPFB_00538 | 8.23e-215 | 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) |
| HNJENPFB_00539 | 3.77e-76 | stp | 3.1.3.16 | - | T | ko:K20074 | - | ko00000,ko01000,ko01009 | Serine/threonine phosphatases, family 2C, catalytic domain |
| HNJENPFB_00540 | 2.05e-156 | 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 |
| HNJENPFB_00541 | 1.48e-84 | aml1 | - | - | G | - | - | - | Alpha-amylase |
| HNJENPFB_00542 | 8.12e-06 | - | - | - | K | - | - | - | Acetyltransferase (GNAT) domain |
| HNJENPFB_00543 | 2.77e-11 | - | - | - | S | - | - | - | Helix-turn-helix domain |
| HNJENPFB_00544 | 7.01e-55 | - | - | - | S | - | - | - | PFAM Haloacid dehalogenase domain protein hydrolase |
| HNJENPFB_00545 | 1.37e-38 | 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 |
| HNJENPFB_00546 | 9.02e-18 | rpmH | - | - | J | ko:K02914 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bL34 family |
| HNJENPFB_00547 | 4.13e-199 | 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 |
| HNJENPFB_00548 | 1.44e-313 | 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 |
| HNJENPFB_00549 | 0.0 | - | - | - | O | ko:K03697 | - | ko00000,ko03110 | ATPase family associated with various cellular activities (AAA) |
| HNJENPFB_00552 | 4.2e-19 | spo0J | - | - | K | ko:K03497 | - | ko00000,ko03000,ko03036,ko04812 | Belongs to the ParB family |
| HNJENPFB_00553 | 9.33e-265 | 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) |
| HNJENPFB_00554 | 5.76e-25 | - | - | - | S | - | - | - | Domain of unknown function (DUF4234) |
| HNJENPFB_00555 | 5.48e-29 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00556 | 1.2e-73 | - | - | - | J | ko:K02945 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | S1 RNA binding domain protein |
| HNJENPFB_00557 | 3.06e-130 | rmuC | - | - | S | ko:K09760 | - | ko00000 | RmuC domain protein |
| HNJENPFB_00560 | 1.09e-203 | sigA | - | - | K | ko:K03086 | - | ko00000,ko03021 | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth |
| HNJENPFB_00561 | 9.72e-22 | - | - | - | S | - | - | - | Zincin-like metallopeptidase |
| HNJENPFB_00562 | 5.79e-21 | lyc2 | 3.2.1.17 | - | M | ko:K01185,ko:K07273 | - | ko00000,ko01000 | family 25 |
| HNJENPFB_00563 | 3.32e-219 | 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 |
| HNJENPFB_00564 | 7.94e-75 | - | - | - | M | - | - | - | Acetyltransferase (GNAT) domain |
| HNJENPFB_00565 | 1.13e-49 | - | - | - | S | - | - | - | Cupin domain protein |
| HNJENPFB_00566 | 3.29e-81 | - | 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 |
| HNJENPFB_00567 | 5.11e-65 | - | - | - | S | ko:K09768 | - | ko00000 | Belongs to the UPF0178 family |
| HNJENPFB_00568 | 5.17e-33 | - | - | - | G | - | - | - | Glycosyl hydrolase family 3 N-terminal domain protein |
| HNJENPFB_00570 | 1.01e-52 | greA | - | - | K | ko:K03624 | - | ko00000,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 |
| HNJENPFB_00572 | 4.06e-79 | yugP | - | - | S | ko:K06973 | - | ko00000 | Putative neutral zinc metallopeptidase |
| HNJENPFB_00573 | 1.72e-111 | 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 |
| HNJENPFB_00574 | 1.2e-63 | 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 |
| HNJENPFB_00575 | 4.02e-32 | 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) |
| HNJENPFB_00576 | 2.63e-89 | - | - | - | M | - | - | - | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family |
| HNJENPFB_00577 | 9.68e-92 | ylmE | - | - | S | ko:K06997 | - | ko00000 | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis |
| HNJENPFB_00579 | 7.16e-126 | - | - | - | CO | - | - | - | Redoxin family |
| HNJENPFB_00580 | 6.3e-116 | - | - | - | C | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00581 | 4.39e-56 | - | - | - | C | - | - | - | FeS-containing Cyanobacterial-specific oxidoreductase |
| HNJENPFB_00582 | 2.33e-230 | der | - | - | S | ko:K03977 | - | ko00000,ko03009 | GTPase that plays an essential role in the late steps of ribosome biogenesis |
| HNJENPFB_00583 | 4.33e-96 | 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) |
| HNJENPFB_00584 | 7e-63 | yphJ | 4.1.1.44 | - | S | ko:K01607 | ko00362,ko01100,ko01120,ko01220,map00362,map01100,map01120,map01220 | ko00000,ko00001,ko01000 | peroxiredoxin activity |
| HNJENPFB_00586 | 1.04e-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 |
| HNJENPFB_00587 | 2.01e-55 | 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 |
| HNJENPFB_00588 | 3.64e-35 | - | - | - | L | ko:K02315,ko:K07452 | - | ko00000,ko01000,ko02048,ko03032 | DNA-dependent DNA replication |
| HNJENPFB_00593 | 1.69e-222 | - | 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 |
| HNJENPFB_00594 | 6.39e-94 | 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) |
| HNJENPFB_00596 | 1.01e-158 | 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 |
| HNJENPFB_00598 | 1.28e-185 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HNJENPFB_00599 | 7.67e-111 | rbr | - | - | C | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00601 | 2.02e-234 | - | - | - | U | - | - | - | Relaxase/Mobilisation nuclease domain |
| HNJENPFB_00602 | 3.82e-164 | - | - | - | S | - | - | - | Protein of unknown function (DUF3801) |
| HNJENPFB_00603 | 1.07e-33 | - | - | - | - | - | - | - | - |
| HNJENPFB_00604 | 4.3e-121 | - | - | - | P | ko:K07238 | - | ko00000,ko02000 | ZIP Zinc transporter |
| HNJENPFB_00605 | 6.1e-52 | sbcC | - | - | L | ko:K03546 | - | ko00000,ko03400 | Putative exonuclease SbcCD, C subunit |
| HNJENPFB_00606 | 1.38e-73 | 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 |
| HNJENPFB_00607 | 5.05e-72 | hpt | 2.4.2.8, 6.3.4.19 | - | F | ko:K00760,ko:K04075,ko:K15780 | ko00230,ko00983,ko01100,ko01110,map00230,map00983,map01100,map01110 | ko00000,ko00001,ko01000,ko03016 | Belongs to the purine pyrimidine phosphoribosyltransferase family |
| HNJENPFB_00608 | 1.03e-12 | 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 |
| HNJENPFB_00609 | 6e-32 | - | - | - | H | - | - | - | Psort location Cytoplasmic, score 7.50 |
| HNJENPFB_00610 | 2.1e-91 | - | - | - | V | ko:K03327 | - | ko00000,ko02000 | Mate efflux family protein |
| HNJENPFB_00611 | 4.42e-44 | - | - | - | - | - | - | - | - |
| HNJENPFB_00612 | 3.33e-159 | 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) |
| HNJENPFB_00613 | 3.84e-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 |
| HNJENPFB_00614 | 1.11e-162 | 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 |
| HNJENPFB_00615 | 5.7e-28 | - | - | - | - | - | - | - | - |
| HNJENPFB_00616 | 2.72e-68 | - | 3.5.1.28 | - | M | ko:K01449 | - | ko00000,ko01000 | cell wall hydrolase |
| HNJENPFB_00617 | 9.17e-49 | yybJ | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| HNJENPFB_00618 | 1.52e-32 | - | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| HNJENPFB_00620 | 2.74e-38 | - | - | - | - | - | - | - | - |
| HNJENPFB_00621 | 5.69e-11 | 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 |
| HNJENPFB_00623 | 8.14e-307 | 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 |
| HNJENPFB_00624 | 3.13e-24 | 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 |
| HNJENPFB_00625 | 1.02e-06 | 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, catalytic domain |
| HNJENPFB_00626 | 2.23e-116 | - | - | - | V | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00627 | 9.13e-55 | - | - | - | G | - | - | - | IA, variant 3 |
| HNJENPFB_00628 | 1.16e-64 | - | - | - | S | - | - | - | Conserved protein domain typically associated with flavoprotein oxygenases DIM6 NTAB family |
| HNJENPFB_00630 | 9.92e-187 | - | 3.6.3.3, 3.6.3.5 | - | P | ko:K01534 | - | ko00000,ko01000 | ATPase, P-type (transporting), HAD superfamily, subfamily IC |
| HNJENPFB_00631 | 5.09e-56 | yicC | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00632 | 1.12e-27 | NPD7_560 | - | - | S | ko:K09777 | - | ko00000 | Belongs to the UPF0296 family |
| HNJENPFB_00633 | 5.6e-61 | gmk | 2.7.4.8 | - | F | ko:K00942 | ko00230,ko01100,map00230,map01100 | ko00000,ko00001,ko00002,ko01000 | Essential for recycling GMP and indirectly, cGMP |
| HNJENPFB_00635 | 7.98e-13 | - | - | - | - | - | - | - | - |
| HNJENPFB_00636 | 2.71e-90 | nrdG | 1.97.1.4 | - | C | ko:K04068 | - | ko00000,ko01000 | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine |
| HNJENPFB_00637 | 1.12e-164 | nrdD | 1.1.98.6 | - | F | ko:K21636 | ko00230,ko00240,ko01100,map00230,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Anaerobic ribonucleoside-triphosphate reductase |
| HNJENPFB_00639 | 2.62e-64 | - | - | - | T | - | - | - | ATPase histidine kinase DNA gyrase B HSP90 domain protein |
| HNJENPFB_00643 | 1.4e-169 | - | 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 |
| HNJENPFB_00644 | 2.55e-95 | 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 |
| HNJENPFB_00645 | 1.38e-84 | tmk | 2.7.4.9 | - | F | ko:K00943 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis |
| HNJENPFB_00646 | 1.83e-171 | spoIIE | 3.1.3.16 | - | KT | ko:K06382 | - | ko00000,ko01000 | stage II sporulation protein E |
| HNJENPFB_00648 | 4.49e-82 | mcsB | 2.7.14.1 | - | E | ko:K19405 | - | ko00000,ko01000 | Catalyzes the specific phosphorylation of arginine residues in proteins |
| HNJENPFB_00649 | 2.93e-26 | - | - | - | K | - | - | - | COG COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases |
| HNJENPFB_00650 | 3.71e-38 | vanW | - | - | V | ko:K18346 | ko01502,ko02020,map01502,map02020 | ko00000,ko00001,ko00002,ko01504 | VanW like protein |
| HNJENPFB_00651 | 2.14e-138 | spoVAD | - | - | I | ko:K06406 | - | ko00000 | Stage V sporulation protein AD |
| HNJENPFB_00652 | 3.65e-120 | - | - | - | L | - | - | - | AAA domain |
| HNJENPFB_00653 | 2.24e-283 | - | - | - | D | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00655 | 2.14e-113 | - | - | - | S | ko:K07137 | - | ko00000 | 'oxidoreductase |
| HNJENPFB_00656 | 8.41e-19 | - | - | - | S | - | - | - | Protein of unknown function (DUF1292) |
| HNJENPFB_00657 | 5.67e-37 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HNJENPFB_00659 | 4.34e-06 | - | - | - | M | ko:K07001 | - | ko00000 | esterase of the alpha-beta hydrolase superfamily |
| HNJENPFB_00660 | 1.26e-08 | - | - | - | S | ko:K07001 | - | ko00000 | esterase of the alpha-beta hydrolase superfamily |
| HNJENPFB_00662 | 6.8e-86 | - | 2.3.1.79 | - | S | ko:K00661 | - | ko00000,ko01000 | Maltose acetyltransferase |
| HNJENPFB_00663 | 6.64e-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 |
| HNJENPFB_00664 | 2.44e-180 | - | 3.2.1.1 | GH13 | G | ko:K01176 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | Starch-binding module 26 |
| HNJENPFB_00665 | 1.87e-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 |
| HNJENPFB_00666 | 4.13e-59 | - | - | - | O | ko:K08303 | ko05120,map05120 | ko00000,ko00001,ko01000,ko01002 | Evidence 5 No homology to any previously reported sequences |
| HNJENPFB_00668 | 6.2e-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 |
| HNJENPFB_00669 | 1.84e-141 | fabK | 1.3.1.9 | - | S | ko:K02371 | ko00061,ko01100,ko01212,map00061,map01100,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | Nitronate monooxygenase |
| HNJENPFB_00670 | 1.87e-58 | - | - | - | K | - | - | - | Transcriptional regulator |
| HNJENPFB_00671 | 2.03e-100 | - | - | - | S | ko:K06901 | - | ko00000,ko02000 | Permease family |
| HNJENPFB_00672 | 6.68e-81 | 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 |
| HNJENPFB_00673 | 1.77e-212 | 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 |
| HNJENPFB_00674 | 4.75e-76 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00675 | 5.7e-100 | alkA | 4.2.99.18 | - | L | ko:K03660 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | 8-oxoguanine DNA glycosylase |
| HNJENPFB_00676 | 1.19e-33 | - | - | - | S | - | - | - | protein, YerC YecD |
| HNJENPFB_00677 | 5.68e-91 | - | - | - | Q | - | - | - | Methyltransferase domain protein |
| HNJENPFB_00678 | 8.56e-117 | 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 |
| HNJENPFB_00679 | 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 |
| HNJENPFB_00680 | 1.5e-07 | 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 |
| HNJENPFB_00681 | 1.3e-100 | pstS | - | - | P | ko:K02040 | ko02010,ko02020,ko05152,map02010,map02020,map05152 | ko00000,ko00001,ko00002,ko02000 | phosphate binding protein |
| HNJENPFB_00682 | 7.04e-128 | typA | - | - | T | ko:K06207 | - | ko00000 | GTP-binding protein TypA |
| HNJENPFB_00683 | 1.68e-12 | - | - | - | L | - | - | - | exonuclease |
| HNJENPFB_00686 | 3.58e-78 | whiA | - | - | K | ko:K09762 | - | ko00000 | WhiA C-terminal HTH domain |
| HNJENPFB_00687 | 3.66e-05 | xseB | 3.1.11.6 | - | L | ko:K03602 | ko03430,map03430 | ko00000,ko00001,ko01000,ko03400 | exodeoxyribonuclease VII activity |
| HNJENPFB_00688 | 7.46e-115 | 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 |
| HNJENPFB_00690 | 6.65e-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 |
| HNJENPFB_00691 | 5.98e-34 | hslR | - | - | J | - | - | - | S4 domain protein |
| HNJENPFB_00692 | 7.15e-15 | yabP | - | - | S | - | - | - | TIGRFAM sporulation protein YabP |
| HNJENPFB_00693 | 8.82e-10 | - | - | - | D | ko:K13052 | - | ko00000,ko03036 | Septum formation initiator |
| HNJENPFB_00694 | 3.43e-144 | 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 |
| HNJENPFB_00695 | 2.03e-100 | - | - | - | S | ko:K07099 | - | ko00000 | Ser Thr phosphatase family protein |
| HNJENPFB_00696 | 2.48e-49 | - | - | - | K | - | - | - | LytTr DNA-binding domain |
| HNJENPFB_00698 | 9.23e-135 | - | - | - | E | - | - | - | cysteine desulfurase family protein |
| HNJENPFB_00700 | 5.05e-87 | 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 |
| HNJENPFB_00701 | 3.85e-98 | 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 |
| HNJENPFB_00702 | 1.88e-250 | 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 |
| HNJENPFB_00703 | 3.91e-27 | spoIVB | 3.4.21.116 | - | M | ko:K06399 | - | ko00000,ko01000,ko01002 | Stage IV sporulation protein B |
| HNJENPFB_00704 | 1.21e-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 |
| HNJENPFB_00705 | 7.59e-136 | 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 |
| HNJENPFB_00707 | 1.72e-197 | rimO | 2.8.4.4 | - | J | ko:K14441 | - | ko00000,ko01000,ko03009 | Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 |
| HNJENPFB_00708 | 4.23e-18 | recX | - | - | S | ko:K03565 | - | ko00000,ko03400 | regulation of DNA repair |
| HNJENPFB_00709 | 1.34e-96 | - | - | - | G | - | - | - | Phosphoglycerate mutase family |
| HNJENPFB_00711 | 7.13e-26 | - | - | - | S | ko:K11068 | - | ko00000,ko02042 | protein, hemolysin III |
| HNJENPFB_00712 | 1.04e-226 | - | - | - | P | ko:K03324 | - | ko00000,ko02000 | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00713 | 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 |
| HNJENPFB_00718 | 1.95e-38 | yabE | - | - | S | - | - | - | G5 domain |
| HNJENPFB_00719 | 2.08e-141 | - | - | - | V | ko:K06147 | - | ko00000,ko02000 | ABC transporter |
| HNJENPFB_00720 | 1.16e-07 | - | - | - | S | - | - | - | Protein of unknown function, DUF624 |
| HNJENPFB_00723 | 3.08e-37 | ntpK | - | - | C | ko:K02124 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | ATP synthase subunit C |
| HNJENPFB_00724 | 1.96e-61 | ntpI | - | - | C | ko:K02123 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | Belongs to the V-ATPase 116 kDa subunit family |
| HNJENPFB_00725 | 3.24e-99 | - | - | - | C | - | - | - | Iron only hydrogenase large subunit, C-terminal domain |
| HNJENPFB_00726 | 2.11e-43 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_00728 | 9.11e-51 | 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 |
| HNJENPFB_00731 | 3.38e-12 | - | - | - | - | - | - | - | - |
| HNJENPFB_00733 | 2.67e-46 | yfcE1 | - | - | S | ko:K07095 | - | ko00000 | Phosphoesterase |
| HNJENPFB_00734 | 8.41e-15 | - | - | - | V | ko:K02004 | - | ko00000,ko00002,ko02000 | COG COG0577 ABC-type antimicrobial peptide transport system, permease component |
| HNJENPFB_00735 | 4.67e-136 | thiF | - | - | H | ko:K22132 | - | ko00000,ko03016 | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 |
| HNJENPFB_00736 | 3.38e-67 | cysA | 3.6.3.25 | - | E | ko:K02045,ko:K02052 | ko00920,ko02010,ko02024,map00920,map02010,map02024 | ko00000,ko00001,ko00002,ko01000,ko02000 | ATPases associated with a variety of cellular activities |
| HNJENPFB_00737 | 3.93e-32 | gph | 3.1.3.18 | - | C | ko:K01091 | ko00630,ko01100,ko01110,ko01130,map00630,map01100,map01110,map01130 | ko00000,ko00001,ko01000 | TIGRFAM HAD-superfamily hydrolase, subfamily IA, variant 3 |
| HNJENPFB_00738 | 5.97e-94 | 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) |
| HNJENPFB_00739 | 6.3e-119 | 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) |
| HNJENPFB_00740 | 8.46e-254 | 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 |
| HNJENPFB_00741 | 3.94e-40 | FcbC | - | - | S | ko:K07107 | - | ko00000,ko01000 | acyl-CoA thioester hydrolase |
| HNJENPFB_00742 | 1.91e-254 | 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 |
| HNJENPFB_00743 | 5.07e-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 |
| HNJENPFB_00745 | 4.12e-24 | - | - | - | K | - | - | - | Helix-turn-helix domain |
| HNJENPFB_00747 | 5.57e-74 | - | - | - | K | - | - | - | membrane |
| HNJENPFB_00750 | 1.18e-160 | 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 |
| HNJENPFB_00751 | 7.99e-145 | trpS | 6.1.1.2 | - | J | ko:K01867 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Tryptophanyl-tRNA synthetase |
| HNJENPFB_00752 | 7.7e-49 | - | - | - | D | - | - | - | protein involved in cytokinesis, contains TGc (transglutaminase protease-like) domain |
| HNJENPFB_00753 | 8.35e-65 | metH2 | 2.1.1.13 | - | E | ko:K00548 | ko00270,ko00450,ko00670,ko01100,ko01110,ko01230,map00270,map00450,map00670,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Vitamin B12 dependent methionine synthase, activation domain |
| HNJENPFB_00754 | 1.67e-144 | 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 |
| HNJENPFB_00756 | 2.64e-50 | rfbF | 2.7.7.33 | - | JM | ko:K00978 | ko00500,ko00520,ko01100,map00500,map00520,map01100 | ko00000,ko00001,ko01000 | Nucleotidyl transferase |
| HNJENPFB_00757 | 4.96e-196 | rfbG | 4.2.1.45 | - | M | ko:K01709 | ko00520,map00520 | ko00000,ko00001,ko01000 | CDP-glucose 4,6-dehydratase |
| HNJENPFB_00759 | 1.91e-97 | - | - | - | P | - | - | - | Voltage gated chloride channel |
| HNJENPFB_00760 | 1.6e-35 | - | - | - | V | - | - | - | MATE efflux family protein |
| HNJENPFB_00762 | 4.86e-205 | tetP | - | - | J | - | - | - | elongation factor G |
| HNJENPFB_00763 | 2.09e-12 | - | - | - | K | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00765 | 4.15e-23 | - | - | - | M | - | - | - | Sortase family |
| HNJENPFB_00766 | 3.04e-92 | 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 |
| HNJENPFB_00767 | 1.65e-27 | - | - | - | S | - | - | - | Domain of unknown function (DUF3783) |
| HNJENPFB_00768 | 4.9e-41 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00769 | 1.03e-57 | kdpE | - | - | K | ko:K07667 | ko02020,ko02024,map02020,map02024 | ko00000,ko00001,ko00002,ko02022 | COG COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain |
| HNJENPFB_00770 | 2.01e-57 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00771 | 4e-17 | - | - | - | - | - | - | - | - |
| HNJENPFB_00772 | 1.31e-58 | - | 3.4.22.70 | - | S | ko:K08600 | - | ko00000,ko01000,ko01002,ko01011 | Sortase family |
| HNJENPFB_00773 | 4.61e-19 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00774 | 1.07e-48 | smf | - | - | LU | ko:K04096 | - | ko00000 | DNA mediated transformation |
| HNJENPFB_00776 | 9.67e-55 | nusA | - | - | K | ko:K02600 | - | ko00000,ko03009,ko03021 | Participates in both transcription termination and antitermination |
| HNJENPFB_00777 | 1.11e-38 | ylxR | - | - | K | ko:K07742 | - | ko00000 | Nucleic-acid-binding protein implicated in transcription termination |
| HNJENPFB_00778 | 7.21e-17 | ylxRQ | - | - | J | ko:K07590,ko:K07742 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | ncRNA processing |
| HNJENPFB_00779 | 4.46e-46 | 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 |
| HNJENPFB_00780 | 5.84e-06 | - | - | - | S | - | - | - | Short repeat of unknown function (DUF308) |
| HNJENPFB_00781 | 3.75e-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 |
| HNJENPFB_00782 | 3.23e-27 | - | - | - | L | ko:K07460 | - | ko00000 | Belongs to the UPF0102 family |
| HNJENPFB_00783 | 9.23e-92 | rnhB | 3.1.26.4 | - | L | ko:K03470 | ko03030,map03030 | ko00000,ko00001,ko01000,ko03032 | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids |
| HNJENPFB_00784 | 3.93e-14 | ylqF | - | - | S | ko:K14540 | - | ko00000,ko03009 | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity |
| HNJENPFB_00785 | 9.21e-66 | 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 |
| HNJENPFB_00786 | 2.54e-25 | - | - | - | S | - | - | - | Coenzyme PQQ synthesis protein D (PqqD) |
| HNJENPFB_00787 | 1.52e-23 | - | - | - | U | - | - | - | Psort location Cytoplasmic, score 8.87 |
| HNJENPFB_00788 | 1.04e-38 | - | - | - | V | ko:K06147 | - | ko00000,ko02000 | overlaps another CDS with the same product name |
| HNJENPFB_00789 | 5.5e-30 | - | 3.4.21.89 | - | U | ko:K13280 | ko03060,map03060 | ko00000,ko00001,ko01000,ko01002 | Peptidase S24-like |
| HNJENPFB_00792 | 1.46e-242 | 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 |
| HNJENPFB_00793 | 9.16e-54 | 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 |
| HNJENPFB_00794 | 5.66e-27 | spoIIAA | - | - | T | ko:K06378 | - | ko00000 | Belongs to the anti-sigma-factor antagonist family |
| HNJENPFB_00795 | 3.06e-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 |
| HNJENPFB_00796 | 1.3e-38 | - | - | - | S | ko:K07005 | - | ko00000 | Pyridoxamine 5'-phosphate oxidase |
| HNJENPFB_00797 | 7.97e-142 | - | - | - | S | - | - | - | Protein of unknown function (DUF1015) |
| HNJENPFB_00798 | 1.03e-300 | - | - | - | S | ko:K07133 | - | ko00000 | Domain of unknown function (DUF4143) |
| HNJENPFB_00799 | 4.4e-13 | - | - | - | U | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00800 | 2.72e-96 | - | - | - | V | ko:K02004 | - | ko00000,ko00002,ko02000 | Psort location CytoplasmicMembrane, score 9.99 |
| HNJENPFB_00801 | 6.62e-26 | - | - | - | S | - | - | - | Protein of unknown function (DUF2953) |
| HNJENPFB_00802 | 6.11e-47 | ytfJ | - | - | S | - | - | - | Sporulation protein YtfJ |
| HNJENPFB_00803 | 4.32e-222 | 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 |
| HNJENPFB_00804 | 1.46e-11 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00805 | 9.29e-24 | pdxK | 2.7.1.35 | - | H | ko:K00868 | ko00750,ko01100,map00750,map01100 | ko00000,ko00001,ko01000 | Phosphomethylpyrimidine kinase |
| HNJENPFB_00806 | 7.67e-34 | - | - | - | S | - | - | - | ECF-type riboflavin transporter, S component |
| HNJENPFB_00807 | 1.3e-79 | - | - | - | O | - | - | - | 4Fe-4S single cluster domain |
| HNJENPFB_00808 | 2.64e-115 | 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 |
| HNJENPFB_00809 | 5.98e-37 | speA | 4.1.1.19 | - | E | ko:K01585 | ko00330,ko01100,map00330,map01100 | ko00000,ko00001,ko00002,ko01000 | Orn/Lys/Arg decarboxylase, major domain |
| HNJENPFB_00810 | 3.31e-125 | cutR | - | - | K | - | - | - | Transcriptional regulatory protein, C terminal |
| HNJENPFB_00811 | 1.63e-170 | - | - | - | T | - | - | - | ATPase histidine kinase DNA gyrase B HSP90 domain protein |
| HNJENPFB_00813 | 5.59e-177 | spoIVA | - | - | DZ | ko:K06398 | - | ko00000 | ATPase. Has a role at an early stage in the morphogenesis of the spore coat |
| HNJENPFB_00814 | 1.93e-66 | 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 |
| HNJENPFB_00815 | 2.69e-117 | pyrP | - | - | F | ko:K02824 | - | ko00000,ko02000 | Permease |
| HNJENPFB_00816 | 7.81e-201 | - | - | - | EK | - | - | - | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs |
| HNJENPFB_00819 | 5.68e-45 | groS | - | - | O | ko:K04078 | - | ko00000,ko03029,ko03110 | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter |
| HNJENPFB_00821 | 7.58e-281 | 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 |
| HNJENPFB_00822 | 4.1e-253 | - | - | - | S | ko:K03308 | - | ko00000 | Sodium:neurotransmitter symporter family |
| HNJENPFB_00823 | 5.65e-32 | trpC | 4.1.1.48 | - | E | ko:K01609 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Indole-3-glycerol phosphate synthase |
| HNJENPFB_00824 | 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 |
| HNJENPFB_00825 | 1.33e-43 | potB | - | - | P | ko:K11071 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ABC-type spermidine putrescine transport system, permease component I |
| HNJENPFB_00826 | 9.17e-85 | potC | - | - | E | ko:K11070 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| HNJENPFB_00827 | 2.1e-170 | - | - | - | S | ko:K03308 | - | ko00000 | Sodium:neurotransmitter symporter family |
| HNJENPFB_00829 | 1.23e-115 | eriC | - | - | P | ko:K03281 | - | ko00000 | Chloride channel |
| HNJENPFB_00831 | 1.5e-62 | rimP | - | - | S | ko:K09748 | - | ko00000,ko03009 | Required for maturation of 30S ribosomal subunits |
| HNJENPFB_00835 | 1.29e-109 | 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 |
| HNJENPFB_00838 | 3.28e-14 | mscS | - | - | M | ko:K03442 | - | ko00000,ko02000 | Mechanosensitive ion channel |
| HNJENPFB_00840 | 6.11e-30 | - | - | - | QT | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00842 | 1.63e-235 | - | - | - | Q | - | - | - | Alkyl sulfatase dimerisation |
| HNJENPFB_00844 | 4.47e-23 | thiN | 2.7.6.2 | - | H | ko:K00949 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko01000 | thiamine pyrophosphokinase |
| HNJENPFB_00845 | 2.09e-109 | 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 |
| HNJENPFB_00846 | 1.66e-15 | - | - | - | S | - | - | - | PHP domain protein |
| HNJENPFB_00847 | 6.24e-134 | nadC | 2.4.2.19 | - | H | ko:K00767 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | Belongs to the NadC ModD family |
| HNJENPFB_00848 | 3.42e-43 | 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 |
| HNJENPFB_00849 | 9.08e-36 | 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 |
| HNJENPFB_00850 | 1.06e-140 | rluD | 5.4.99.23 | - | J | ko:K06180 | - | ko00000,ko01000,ko03009 | Responsible for synthesis of pseudouridine from uracil |
| HNJENPFB_00851 | 1.07e-160 | map | 3.4.11.18 | - | E | ko:K01265 | - | ko00000,ko01000,ko01002 | Methionine aminopeptidase |
| HNJENPFB_00852 | 3.22e-139 | purF_1 | 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 |
| HNJENPFB_00853 | 3.53e-98 | - | 3.4.11.9 | - | E | ko:K01262 | - | ko00000,ko01000,ko01002 | Xaa-Pro aminopeptidase |
| HNJENPFB_00854 | 8.22e-120 | 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 |
| HNJENPFB_00855 | 1.49e-131 | - | - | - | S | - | - | - | Uncharacterized protein conserved in bacteria (DUF2179) |
| HNJENPFB_00857 | 1.64e-62 | maf | - | - | D | ko:K06287 | - | ko00000 | Maf-like protein |
| HNJENPFB_00858 | 2.06e-161 | 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 |
| HNJENPFB_00859 | 5.16e-74 | - | - | - | S | - | - | - | Protein of unknown function (DUF3793) |
| HNJENPFB_00860 | 6.64e-57 | - | - | - | K | - | - | - | helix_turn_helix, arabinose operon control protein |
| HNJENPFB_00862 | 1.25e-126 | - | - | - | G | ko:K10118 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| HNJENPFB_00863 | 3.03e-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 |
| HNJENPFB_00864 | 8.78e-73 | 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 |
| HNJENPFB_00865 | 7.02e-95 | cotJC | - | - | P | ko:K06334 | - | ko00000 | PFAM Manganese containing catalase |
| HNJENPFB_00866 | 3.06e-98 | wecE | 2.6.1.59 | - | E | ko:K02805 | - | ko00000,ko01000,ko01007 | Belongs to the DegT DnrJ EryC1 family |
| HNJENPFB_00867 | 1.66e-91 | - | - | - | S | - | - | - | Transporter, auxin efflux carrier (AEC) family protein |
| HNJENPFB_00870 | 6.48e-121 | - | - | - | S | - | - | - | NADPH-dependent FMN reductase |
| HNJENPFB_00871 | 1.6e-21 | - | - | - | S | - | - | - | Mor transcription activator family |
| HNJENPFB_00872 | 9.49e-36 | - | - | - | S | - | - | - | Protein of unknown function (DUF1018) |
| HNJENPFB_00874 | 6.61e-41 | comF | - | - | S | ko:K02242 | - | ko00000,ko00002,ko02044 | ComF family |
| HNJENPFB_00875 | 5.09e-153 | recD2 | 3.1.11.5 | - | L | ko:K03581 | ko03440,map03440 | ko00000,ko00001,ko01000,ko03400 | Helix-hairpin-helix containing domain |
| HNJENPFB_00877 | 5.75e-98 | sigK | - | - | K | ko:K03091 | - | ko00000,ko03021 | Sigma-70 region 2 |
| HNJENPFB_00878 | 1.03e-31 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_00879 | 3.12e-124 | 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 |
| HNJENPFB_00880 | 1.02e-143 | 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) |
| HNJENPFB_00882 | 1.82e-51 | - | - | - | M | - | - | - | Glycosyl transferase family 8 |
| HNJENPFB_00883 | 3.3e-14 | - | - | - | M | - | - | - | dTDP-4-dehydrorhamnose 3,5-epimerase |
| HNJENPFB_00884 | 5.14e-153 | 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 |
| HNJENPFB_00885 | 1.52e-121 | 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 |
| HNJENPFB_00887 | 4.66e-58 | - | - | - | L | - | - | - | Mu transposase, C-terminal |
| HNJENPFB_00888 | 3.08e-62 | ade | 3.5.4.2 | - | F | ko:K01486 | ko00230,ko01100,map00230,map01100 | ko00000,ko00001,ko01000 | Adenine deaminase C-terminal domain |
| HNJENPFB_00889 | 8.12e-24 | - | - | - | - | - | - | - | - |
| HNJENPFB_00890 | 3.68e-38 | - | - | - | K | - | - | - | MarR family |
| HNJENPFB_00894 | 2.13e-124 | - | - | - | L | - | - | - | AAA domain |
| HNJENPFB_00895 | 9.78e-72 | - | - | - | M | - | - | - | plasmid recombination |
| HNJENPFB_00897 | 2.37e-152 | - | - | - | S | ko:K06158 | - | ko00000,ko03012 | ABC transporter |
| HNJENPFB_00898 | 9.46e-58 | minD | - | - | D | ko:K03609 | - | ko00000,ko03036,ko04812 | Belongs to the ParA family |
| HNJENPFB_00899 | 4.36e-85 | mgsA | 4.2.3.3 | - | G | ko:K01734 | ko00640,ko01120,map00640,map01120 | ko00000,ko00001,ko01000 | methylglyoxal synthase |
| HNJENPFB_00900 | 1.27e-18 | gatB | 6.3.5.6, 6.3.5.7 | - | J | ko:K02434 | 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) |
| HNJENPFB_00902 | 6.3e-77 | 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 |
| HNJENPFB_00903 | 1.5e-68 | - | - | - | C | - | - | - | 4Fe-4S binding domain |
| HNJENPFB_00904 | 4.76e-126 | - | - | - | CO | - | - | - | Redoxin |
| HNJENPFB_00905 | 8.97e-140 | - | - | - | GM | ko:K09691 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| HNJENPFB_00906 | 1.37e-84 | 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 |
| HNJENPFB_00907 | 3.09e-104 | 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 |
| HNJENPFB_00908 | 2.27e-52 | - | - | - | S | ko:K09747 | - | ko00000 | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection |
| HNJENPFB_00909 | 1.05e-191 | ddl | 6.3.2.35, 6.3.2.4 | - | M | ko:K01921,ko:K18856 | ko00473,ko00550,ko01100,ko01502,ko02020,map00473,map00550,map01100,map01502,map02020 | ko00000,ko00001,ko00002,ko01000,ko01011,ko01504 | Belongs to the D-alanine--D-alanine ligase family |
| HNJENPFB_00910 | 5.11e-41 | argH | 4.3.2.1 | - | E | ko:K01755 | ko00220,ko00250,ko01100,ko01110,ko01130,ko01230,map00220,map00250,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000,ko04147 | argininosuccinate lyase |
| HNJENPFB_00911 | 2.21e-145 | 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 |
| HNJENPFB_00913 | 4.3e-201 | 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 |
| HNJENPFB_00914 | 3.69e-29 | 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 |
| HNJENPFB_00915 | 3.54e-27 | - | - | - | S | - | - | - | Belongs to the UPF0342 family |
| HNJENPFB_00917 | 7.48e-100 | - | - | - | M | - | - | - | dTDP-4-dehydrorhamnose 3,5-epimerase |
| HNJENPFB_00920 | 7.63e-162 | - | 2.7.13.3 | - | T | ko:K18345 | ko01502,ko02020,map01502,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko01504,ko02022 | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain |
| HNJENPFB_00921 | 8.06e-39 | fabF | 2.3.1.179 | - | IQ | 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 |
| HNJENPFB_00922 | 5.98e-32 | 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 |
| HNJENPFB_00923 | 4.19e-59 | 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 |
| HNJENPFB_00924 | 1.98e-34 | - | - | - | S | - | - | - | PFAM ErfK YbiS YcfS YnhG family protein |
| HNJENPFB_00925 | 7.23e-24 | yunB | - | - | S | - | - | - | sporulation protein YunB |
| HNJENPFB_00926 | 3.6e-52 | 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 |
| HNJENPFB_00927 | 1.04e-43 | - | - | - | G | - | - | - | Aamy_C |
| HNJENPFB_00929 | 8.52e-55 | def2 | 3.5.1.88 | - | J | ko:K01462 | - | ko00000,ko01000 | Removes the formyl group from the N-terminal Met of newly synthesized proteins |
| HNJENPFB_00931 | 5.06e-54 | rsuA | 5.4.99.19 | - | J | ko:K06183 | - | ko00000,ko01000,ko03009 | Belongs to the pseudouridine synthase RsuA family |
| HNJENPFB_00932 | 7.31e-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 |
| HNJENPFB_00933 | 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 |
| HNJENPFB_00935 | 7.7e-09 | degV | - | - | S | - | - | - | protein conserved in bacteria |
| HNJENPFB_00936 | 1.21e-31 | - | - | - | - | - | - | - | - |
| HNJENPFB_00937 | 1.55e-111 | - | - | - | V | ko:K02003 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| HNJENPFB_00938 | 4.54e-47 | dnaE | 2.7.7.7 | - | L | ko:K02337,ko:K14162 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | DNA polymerase III alpha subunit |
| HNJENPFB_00939 | 7.69e-199 | metY | 2.5.1.49 | - | H | ko:K01740 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko01000 | Cys/Met metabolism PLP-dependent enzyme |
| HNJENPFB_00941 | 1.13e-117 | - | - | - | K | - | - | - | WYL domain |
| HNJENPFB_00943 | 2.23e-84 | 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 |
| HNJENPFB_00944 | 4.02e-40 | - | - | - | K | - | - | - | CarD-like/TRCF domain |
| HNJENPFB_00945 | 2.99e-50 | - | - | - | C | - | - | - | Metallo-beta-lactamase domain protein |
| HNJENPFB_00946 | 1.34e-21 | ntpC | - | - | C | ko:K02119 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002 | subunit (C |
| HNJENPFB_00947 | 3.86e-43 | mprF | - | - | M | ko:K07027 | - | ko00000,ko02000 | lysyltransferase activity |
| HNJENPFB_00948 | 9.39e-23 | - | - | - | S | - | - | - | Proteins of 100 residues with WXG |
| HNJENPFB_00951 | 1.12e-70 | - | - | - | S | - | - | - | small multi-drug export protein |
| HNJENPFB_00952 | 3.72e-24 | - | - | - | S | - | - | - | VanZ like family |
| HNJENPFB_00953 | 7.14e-187 | - | - | - | S | - | - | - | Phage terminase, large subunit, PBSX family |
| HNJENPFB_00955 | 1.4e-131 | - | - | - | M | - | - | - | Glycosyl transferase family 2 |
| HNJENPFB_00956 | 6.49e-103 | 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 |
| HNJENPFB_00957 | 7.27e-78 | - | - | - | M | - | - | - | Glycosyl hydrolases family 25 |
| HNJENPFB_00959 | 9.3e-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 |
| HNJENPFB_00960 | 1.56e-58 | - | 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 |
| HNJENPFB_00962 | 6.11e-50 | yebC | - | - | K | - | - | - | Transcriptional regulatory protein |
| HNJENPFB_00965 | 4.41e-66 | yajL | 3.5.1.124 | - | S | ko:K03152 | - | ko00000,ko01000,ko01002 | DJ-1 family |
| HNJENPFB_00966 | 1.52e-63 | ygfA | 6.3.3.2 | - | H | ko:K01934 | ko00670,ko01100,map00670,map01100 | ko00000,ko00001,ko01000 | 5-formyltetrahydrofolate cyclo-ligase family |
| HNJENPFB_00967 | 3.93e-05 | spr | 3.4.17.13 | CBM50 | M | ko:K13694,ko:K19224,ko:K21471 | - | ko00000,ko01000,ko01002,ko01011 | NlpC p60 family |
| HNJENPFB_00968 | 1.62e-126 | soj | - | - | D | ko:K03496 | - | ko00000,ko03036,ko04812 | Cobyrinic acid ac-diamide synthase |
| HNJENPFB_00970 | 1.6e-41 | - | - | - | S | - | - | - | Sortase family |
| HNJENPFB_00971 | 3.89e-165 | 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 |
| HNJENPFB_00974 | 5.57e-112 | sbp | - | - | P | ko:K02048 | ko00920,ko02010,map00920,map02010 | ko00000,ko00001,ko00002,ko02000 | Extracellular solute-binding protein |
| HNJENPFB_00975 | 8.75e-87 | amt | - | - | EP | ko:K03320 | - | ko00000,ko02000 | Ammonium Transporter Family |
| HNJENPFB_00976 | 5.01e-82 | - | - | - | G | - | - | - | PFAM Polysaccharide deacetylase |
| HNJENPFB_00977 | 5.39e-19 | - | - | - | M | - | - | - | O-Antigen ligase |
| HNJENPFB_00978 | 4.94e-37 | - | - | - | S | ko:K07040 | - | ko00000 | metal-binding, possibly nucleic acid-binding protein |
| HNJENPFB_00979 | 2.48e-20 | rpmF | - | - | J | ko:K02911 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011,ko03029 | Belongs to the bacterial ribosomal protein bL32 family |
| HNJENPFB_00980 | 1.18e-59 | 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 |
| HNJENPFB_00981 | 2.5e-24 | - | - | - | K | - | - | - | Helix-turn-helix |
| HNJENPFB_00982 | 4.49e-16 | yqgF | - | - | L | ko:K07447 | - | ko00000,ko01000 | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA |
| HNJENPFB_00983 | 1.04e-191 | 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 |
| HNJENPFB_00984 | 1.26e-59 | rplQ | - | - | J | ko:K02879,ko:K16193 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L17 |
| HNJENPFB_00986 | 2.21e-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 |
| HNJENPFB_00988 | 1.4e-100 | 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 |
| HNJENPFB_00989 | 7.28e-48 | - | - | - | M | ko:K07273 | - | ko00000 | lysozyme activity |
| HNJENPFB_00990 | 0.000833 | - | - | - | K | - | - | - | Helix-turn-helix XRE-family like proteins |
| HNJENPFB_00991 | 1.96e-163 | 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) |
| HNJENPFB_00993 | 4.11e-113 | clpC | - | - | O | ko:K03696 | ko01100,map01100 | ko00000,ko03110 | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE |
| HNJENPFB_00994 | 6.68e-128 | 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 |
| HNJENPFB_00995 | 7.33e-20 | - | - | - | - | - | - | - | - |
| HNJENPFB_00996 | 4.88e-56 | Lrp | - | - | K | - | - | - | Transcriptional regulator, AsnC family |
| HNJENPFB_00997 | 1.15e-44 | ywqD | 2.7.10.2 | - | D | ko:K00903 | - | ko00000,ko01000,ko01001 | NUBPL iron-transfer P-loop NTPase |
| HNJENPFB_00998 | 1.73e-13 | - | - | - | M | - | - | - | Bacterial sugar transferase |
| HNJENPFB_00999 | 2.77e-141 | 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 |
| HNJENPFB_01001 | 5.67e-25 | nrdR | - | - | K | ko:K07738 | - | ko00000,ko03000 | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes |
| HNJENPFB_01002 | 7.64e-82 | - | - | - | C | - | - | - | Flavodoxin |
| HNJENPFB_01003 | 7.01e-31 | - | - | - | S | - | - | - | Cupin domain |
| HNJENPFB_01004 | 2.21e-65 | - | - | - | S | - | - | - | Methyltransferase small domain |
| HNJENPFB_01005 | 7.3e-164 | - | - | - | U | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_01006 | 3.46e-107 | - | - | - | P | ko:K16785 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | PFAM Cobalt transport protein |
| HNJENPFB_01007 | 8.98e-37 | - | - | - | I | - | - | - | Domain of unknown function (DUF4430) |
| HNJENPFB_01008 | 7.54e-129 | - | - | - | V | ko:K01990 | - | ko00000,ko00002,ko02000 | ABC transporter |
| HNJENPFB_01009 | 1.02e-85 | ttcA | - | - | D | - | - | - | Belongs to the TtcA family |
| HNJENPFB_01010 | 1.95e-21 | - | - | - | K | - | - | - | Helix-turn-helix XRE-family like proteins |
| HNJENPFB_01013 | 5.34e-193 | - | - | - | L | - | - | - | Protein of unknown function (DUF3991) |
| HNJENPFB_01016 | 3.18e-50 | - | - | - | S | ko:K19157 | - | ko00000,ko01000,ko02048 | Bacterial toxin of type II toxin-antitoxin system, YafQ |
| HNJENPFB_01017 | 5.4e-48 | - | - | - | L | ko:K07473 | - | ko00000,ko02048 | RelB antitoxin |
| HNJENPFB_01018 | 2.35e-39 | 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 |
| HNJENPFB_01020 | 4.31e-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 |
| HNJENPFB_01022 | 9.26e-10 | - | - | - | S | - | - | - | Protein of unknown function, DUF624 |
| HNJENPFB_01024 | 1.67e-41 | spoIIIAE | - | - | S | ko:K06394 | - | ko00000 | stage III sporulation protein AE |
| HNJENPFB_01026 | 1.66e-50 | btuR | 2.5.1.17 | - | H | ko:K19221 | ko00860,ko01100,map00860,map01100 | ko00000,ko00001,ko00002,ko01000 | ATP:corrinoid adenosyltransferase BtuR/CobO/CobP |
| HNJENPFB_01027 | 3.99e-72 | dnaD | - | - | L | - | - | - | DnaD domain protein |
| HNJENPFB_01028 | 1.15e-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 |
| HNJENPFB_01029 | 6.41e-40 | 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 |
| HNJENPFB_01030 | 1.27e-62 | - | - | - | - | - | - | - | - |
| HNJENPFB_01031 | 3.79e-89 | - | - | - | U | ko:K03205 | ko03070,map03070 | ko00000,ko00001,ko00002,ko02044 | Psort location Cytoplasmic, score |
| HNJENPFB_01032 | 6.66e-30 | - | - | - | S | - | - | - | Maff2 family |
| HNJENPFB_01033 | 1.04e-71 | - | - | - | S | - | - | - | dinuclear metal center protein, YbgI |
| HNJENPFB_01034 | 6.33e-12 | - | - | - | M | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_01035 | 1.67e-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 |
| HNJENPFB_01037 | 3.26e-23 | - | 3.2.1.4 | GH5,GH9 | G | ko:K01179 | ko00500,ko01100,map00500,map01100 | ko00000,ko00001,ko01000 | M42 glutamyl aminopeptidase |
| HNJENPFB_01039 | 1.28e-19 | mbl | - | - | D | ko:K03569 | - | ko00000,ko02048,ko03036,ko04812 | Cell shape determining protein, MreB Mrl family |
| HNJENPFB_01040 | 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 |
| HNJENPFB_01041 | 1.21e-31 | hisS | 6.1.1.21 | - | J | ko:K01892 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | histidyl-tRNA synthetase |
| HNJENPFB_01043 | 9.93e-45 | - | 3.5.1.9 | - | S | ko:K07130 | ko00380,ko00630,ko01100,map00380,map00630,map01100 | ko00000,ko00001,ko00002,ko01000 | Putative cyclase |
| HNJENPFB_01044 | 1.85e-109 | - | - | - | GM | - | - | - | Methyltransferase FkbM domain |
| HNJENPFB_01045 | 0.000118 | purM | 6.3.3.1 | - | F | ko:K01933 | ko00230,ko01100,ko01110,ko01130,map00230,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | Phosphoribosylformylglycinamidine cyclo-ligase |
| HNJENPFB_01046 | 6.53e-96 | purN | 2.1.2.2 | - | F | ko:K11175 | 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 |
| HNJENPFB_01047 | 3.52e-92 | - | - | - | K | - | - | - | response regulator receiver |
| HNJENPFB_01049 | 1.01e-83 | 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 |
| HNJENPFB_01051 | 2.18e-21 | - | 3.6.1.27 | - | I | ko:K19302 | ko00550,map00550 | ko00000,ko00001,ko01000,ko01011 | Psort location CytoplasmicMembrane, score |
| HNJENPFB_01053 | 7.35e-107 | 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 |
| HNJENPFB_01055 | 1.48e-124 | 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 |
| HNJENPFB_01057 | 3.44e-44 | spsC | 2.6.1.102 | - | E | ko:K13010 | ko00520,map00520 | ko00000,ko00001,ko01000,ko01005,ko01007 | Belongs to the DegT DnrJ EryC1 family |
| HNJENPFB_01058 | 2.98e-97 | - | - | - | S | - | - | - | Protein of unknown function (DUF2974) |
| HNJENPFB_01059 | 2.03e-109 | yvcJ | - | - | S | ko:K06958 | - | ko00000,ko03019 | Displays ATPase and GTPase activities |
| HNJENPFB_01060 | 1.24e-36 | murB | 1.3.1.98 | - | M | ko:K00075 | ko00520,ko00550,ko01100,map00520,map00550,map01100 | ko00000,ko00001,ko01000,ko01011 | Cell wall formation |
| HNJENPFB_01061 | 4.66e-169 | proA | 1.2.1.41 | - | E | ko:K00147 | ko00330,ko00332,ko01100,ko01110,ko01130,ko01230,map00330,map00332,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate |
| HNJENPFB_01062 | 4.8e-17 | 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 |
| HNJENPFB_01065 | 1.68e-107 | tepA | 3.4.21.92 | - | OU | ko:K01358 | ko04112,ko04212,map04112,map04212 | ko00000,ko00001,ko01000,ko01002 | Psort location Cytoplasmic, score |
| HNJENPFB_01066 | 9.13e-50 | - | - | - | P | ko:K09817 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | ATPases associated with a variety of cellular activities |
| HNJENPFB_01072 | 2.11e-102 | - | - | - | K | - | - | - | Putative DNA-binding domain |
| HNJENPFB_01073 | 2.84e-133 | 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 |
| HNJENPFB_01074 | 6.28e-167 | feoB2 | - | - | P | ko:K04759 | - | ko00000,ko02000 | transporter of a GTP-driven Fe(2 ) uptake system |
| HNJENPFB_01075 | 3.08e-126 | - | - | - | T | ko:K07775 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | response regulator, receiver |
| HNJENPFB_01077 | 5.96e-139 | abiGI | - | - | K | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_01078 | 5.27e-25 | rpsU | - | - | J | ko:K02970 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Belongs to the bacterial ribosomal protein bS21 family |
| HNJENPFB_01079 | 5.26e-77 | 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 |
| HNJENPFB_01081 | 3.88e-124 | 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 |
| HNJENPFB_01083 | 4.71e-103 | napA | - | - | P | - | - | - | Transporter, CPA2 family |
| HNJENPFB_01084 | 5.25e-140 | - | - | - | L | - | - | - | Phage integrase family |
| HNJENPFB_01085 | 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 |
| HNJENPFB_01086 | 4.62e-10 | - | - | - | S | - | - | - | YcxB-like protein |
| HNJENPFB_01088 | 4.79e-128 | ytqA | - | - | S | ko:K07139 | - | ko00000 | radical SAM protein, TIGR01212 family |
| HNJENPFB_01089 | 3.8e-78 | - | - | - | S | ko:K07025 | - | ko00000 | HAD-hyrolase-like |
| HNJENPFB_01091 | 2.05e-69 | - | - | - | S | ko:K07007 | - | ko00000 | Flavoprotein family |
| HNJENPFB_01092 | 6.14e-76 | 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 |
| HNJENPFB_01093 | 9.05e-141 | - | - | - | L | - | - | - | Psort location Cytoplasmic, score 8.96 |
| HNJENPFB_01094 | 2.73e-55 | - | - | - | - | - | - | - | - |
| HNJENPFB_01095 | 1.54e-35 | 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 |
| HNJENPFB_01096 | 1.76e-82 | spoVFB | - | - | H | ko:K06411 | - | ko00000 | Flavoprotein |
| HNJENPFB_01097 | 0.000333 | recJ | - | - | L | ko:K07462 | ko03410,ko03430,ko03440,map03410,map03430,map03440 | ko00000,ko00001,ko01000,ko03400 | exonuclease |
| HNJENPFB_01098 | 2.08e-185 | 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 |
| HNJENPFB_01100 | 3.22e-97 | glgX | 3.2.1.68 | CBM48,GH13 | G | ko:K01214 | ko00500,ko01100,ko01110,map00500,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Belongs to the glycosyl hydrolase 13 family |
| HNJENPFB_01101 | 3.82e-65 | - | - | - | V | - | - | - | MatE |
| HNJENPFB_01102 | 1.36e-60 | - | - | - | V | - | - | - | MatE |
| HNJENPFB_01103 | 5.77e-29 | ysxB | - | - | J | ko:K07584 | - | ko00000 | Cysteine protease Prp |
| HNJENPFB_01104 | 3.45e-43 | rplU | - | - | J | ko:K02888 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This protein binds to 23S rRNA in the presence of protein L20 |
| HNJENPFB_01105 | 3.49e-72 | folD | 1.5.1.5, 3.5.4.9 | - | E | 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 |
| HNJENPFB_01106 | 1.72e-115 | - | - | - | V | ko:K02003 | - | ko00000,ko00002,ko02000 | ABC-type antimicrobial peptide transport system, ATPase component |
| HNJENPFB_01107 | 2.73e-133 | - | 3.6.3.8 | - | P | ko:K01537 | - | ko00000,ko01000 | ATPase, P-type (transporting), HAD superfamily, subfamily IC |
| HNJENPFB_01108 | 6.99e-10 | - | - | - | K | - | - | - | Acetyltransferase (GNAT) domain |
| HNJENPFB_01109 | 6.74e-81 | 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 | Bacterial transferase hexapeptide (six repeats) |
| HNJENPFB_01111 | 1.44e-62 | 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) |
| HNJENPFB_01112 | 1.01e-26 | - | - | - | O | ko:K03671 | ko04621,ko05418,map04621,map05418 | ko00000,ko00001,ko03110 | Belongs to the thioredoxin family |
| HNJENPFB_01113 | 1.28e-40 | nfo | 3.1.21.2 | - | L | ko:K01151 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin |
| HNJENPFB_01114 | 5.81e-16 | - | - | - | S | ko:K07088 | - | ko00000 | Membrane transport protein |
| HNJENPFB_01115 | 9.88e-158 | - | 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 |
| HNJENPFB_01116 | 5.21e-21 | - | - | - | S | - | - | - | Protein of unknown function (DUF3801) |
| HNJENPFB_01117 | 9.12e-45 | - | 3.4.22.70 | - | M | ko:K07284 | - | ko00000,ko01000,ko01002,ko01011 | Sortase family |
| HNJENPFB_01118 | 1.25e-08 | - | - | - | K | - | - | - | Helix-turn-helix domain |
| HNJENPFB_01119 | 0.000143 | yvgK | - | - | P | ko:K07219 | - | ko00000 | COG1910 Periplasmic molybdate-binding protein domain |
| HNJENPFB_01120 | 0.000313 | - | - | - | S | - | - | - | Helix-turn-helix domain |
| HNJENPFB_01121 | 1.6e-23 | - | - | - | K | ko:K03497 | - | ko00000,ko03000,ko03036,ko04812 | ParB-like nuclease domain |
| HNJENPFB_01123 | 3.27e-160 | fusA2 | - | - | J | ko:K02355 | - | ko00000,ko03012,ko03029 | translation elongation |
| HNJENPFB_01124 | 1.17e-130 | pheS | 6.1.1.20 | - | J | ko:K01889 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | tRNA synthetases class II core domain (F) |
| HNJENPFB_01125 | 4.08e-27 | - | - | - | S | - | - | - | Protein of unknown function (DUF3801) |
| HNJENPFB_01126 | 1.94e-74 | - | - | - | S | - | - | - | Acetyltransferase (GNAT) domain |
| HNJENPFB_01128 | 1.32e-45 | addA | 3.6.4.12 | - | L | ko:K16898 | - | ko00000,ko01000,ko03400 | PD-(D/E)XK nuclease superfamily |
| HNJENPFB_01130 | 6.21e-93 | - | - | - | Q | - | - | - | HAD-superfamily phosphatase, subfamily IIIC |
| HNJENPFB_01131 | 2.38e-22 | 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 |
| HNJENPFB_01132 | 3.62e-48 | 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) |
| HNJENPFB_01133 | 1.88e-80 | - | - | - | K | - | - | - | Transcriptional regulatory protein, C terminal |
| HNJENPFB_01134 | 3.02e-72 | csm1 | - | - | S | ko:K07016 | - | ko00000,ko02048 | CRISPR-associated protein, Csm1 family |
| HNJENPFB_01135 | 7.05e-52 | spoVAC | - | - | S | ko:K06405 | - | ko00000 | stage V sporulation protein AC |
| HNJENPFB_01136 | 5.47e-82 | - | - | - | K | - | - | - | Putative zinc ribbon domain |
| HNJENPFB_01137 | 2.32e-118 | - | - | - | S | ko:K09157 | - | ko00000 | Uncharacterised ACR (DUF711) |
| HNJENPFB_01138 | 2.19e-33 | - | - | - | T | ko:K07166 | - | ko00000 | Belongs to the UPF0237 family |
| HNJENPFB_01139 | 4.58e-122 | 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 |
| HNJENPFB_01140 | 1.09e-143 | 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 |
| HNJENPFB_01142 | 1.62e-42 | - | - | - | S | ko:K09157 | - | ko00000 | UPF0210 protein |
| HNJENPFB_01144 | 4.4e-18 | 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 |
| HNJENPFB_01145 | 2.16e-126 | 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 |
| HNJENPFB_01146 | 9.36e-53 | - | 3.4.21.92 | - | OU | ko:K01358 | ko04112,ko04212,map04112,map04212 | ko00000,ko00001,ko01000,ko01002 | Belongs to the peptidase S14 family |
| HNJENPFB_01147 | 5.89e-34 | rpmI | - | - | J | ko:K02916 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L35 |
| HNJENPFB_01148 | 6.37e-97 | 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 |
| HNJENPFB_01149 | 1.35e-140 | BT0173 | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_01150 | 4.66e-12 | - | - | - | - | - | - | - | - |
| HNJENPFB_01151 | 2.03e-35 | - | - | - | - | - | - | - | - |
| HNJENPFB_01152 | 1.09e-37 | - | - | - | I | - | - | - | Pkd domain containing protein |
| HNJENPFB_01153 | 5.34e-18 | ysdA | - | - | L | - | - | - | Membrane |
| HNJENPFB_01155 | 3.9e-09 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_01156 | 8.87e-49 | hinT | - | - | FG | ko:K02503 | - | ko00000,ko04147 | Psort location Cytoplasmic, score |
| HNJENPFB_01157 | 2.34e-06 | 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 |
| HNJENPFB_01158 | 2.2e-16 | - | - | - | S | - | - | - | Sugar-transfer associated ATP-grasp |
| HNJENPFB_01159 | 7.06e-19 | - | - | - | M | - | - | - | O-Antigen ligase |
| HNJENPFB_01161 | 1.52e-71 | cytX | - | - | F | - | - | - | COG COG1457 Purine-cytosine permease and related proteins |
| HNJENPFB_01162 | 5.82e-83 | - | - | - | S | ko:K06921 | - | ko00000 | ATPase domain predominantly from Archaea |
| HNJENPFB_01163 | 3.53e-116 | 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 |
| HNJENPFB_01164 | 8.03e-32 | - | - | - | P | ko:K04758 | - | ko00000,ko02000 | FeoA |
| HNJENPFB_01165 | 1.24e-43 | - | - | - | K | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_01166 | 8.8e-48 | ptsH | - | - | G | ko:K11184,ko:K11189 | - | ko00000,ko02000 | phosphocarrier, HPr family |
| HNJENPFB_01167 | 3.46e-90 | trmD | 2.1.1.228 | - | J | ko:K00554 | - | ko00000,ko01000,ko03016 | Belongs to the RNA methyltransferase TrmD family |
| HNJENPFB_01169 | 3.56e-68 | iscU | - | - | C | ko:K04488 | - | ko00000 | SUF system FeS assembly protein, NifU family |
| HNJENPFB_01170 | 8.31e-63 | greA | - | - | K | ko:K03624 | - | ko00000,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 |
| HNJENPFB_01171 | 1.44e-75 | - | - | - | U | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_01174 | 1.51e-20 | - | - | - | K | - | - | - | Acetyltransferase (GNAT) domain |
| HNJENPFB_01175 | 3.59e-59 | - | - | - | O | ko:K03686 | - | ko00000,ko03029,ko03110 | DnaJ domain protein |
| HNJENPFB_01176 | 1.65e-44 | rluB | 5.4.99.19, 5.4.99.22 | - | J | ko:K06178,ko:K06183 | - | ko00000,ko01000,ko03009 | Belongs to the pseudouridine synthase RsuA family |
| HNJENPFB_01177 | 3.53e-15 | scfA | - | - | S | - | - | - | RSAM-modified six-cysteine peptide |
| HNJENPFB_01178 | 1.88e-46 | - | - | - | D | ko:K21471 | - | ko00000,ko01000,ko01002,ko01011 | Peptidase, M23 |
| HNJENPFB_01180 | 3.7e-30 | - | 3.1.3.48 | - | GM | ko:K01104 | - | ko00000,ko01000 | capsular polysaccharide biosynthesis protein |
| HNJENPFB_01181 | 2.41e-73 | 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 |
| HNJENPFB_01182 | 2.8e-148 | yaaT | - | - | S | - | - | - | PSP1 C-terminal domain protein |
| HNJENPFB_01183 | 9.36e-74 | pcrA | 3.6.4.12 | - | L | ko:K03657 | ko03420,ko03430,map03420,map03430 | ko00000,ko00001,ko01000,ko03400 | ATP-dependent DNA helicase |
| HNJENPFB_01184 | 4.03e-18 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| HNJENPFB_01185 | 1.97e-15 | - | - | - | S | - | - | - | Phage terminase, large subunit, PBSX family |
| HNJENPFB_01187 | 9.67e-63 | 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 |
| HNJENPFB_01188 | 1.93e-100 | FbpA | - | - | K | - | - | - | Fibronectin-binding protein |
| HNJENPFB_01189 | 1.59e-27 | trmB | 2.1.1.33 | - | J | ko:K03439 | - | ko00000,ko01000,ko03016 | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
| HNJENPFB_01190 | 3.64e-44 | yihY | - | - | H | ko:K07058 | - | ko00000 | Belongs to the UPF0761 family |
| HNJENPFB_01193 | 1.67e-71 | - | 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 |
| HNJENPFB_01194 | 8.01e-26 | - | - | - | OU | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_01195 | 1.42e-132 | 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 |
| HNJENPFB_01197 | 4.07e-148 | thiD | 2.7.1.49, 2.7.4.7 | - | H | ko:K00941 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko00002,ko01000 | Carbohydrate kinase |
| HNJENPFB_01198 | 6.98e-182 | - | - | - | S | - | - | - | Psort location CytoplasmicMembrane, score |
| HNJENPFB_01200 | 3.88e-24 | sigH | - | - | K | ko:K03091 | - | ko00000,ko03021 | Belongs to the sigma-70 factor family |
| HNJENPFB_01201 | 3e-48 | - | - | - | K | - | - | - | Probable zinc-ribbon domain |
| HNJENPFB_01202 | 1.03e-05 | - | - | - | G | ko:K08174 | - | ko00000,ko02000 | Major facilitator superfamily |
| HNJENPFB_01205 | 5.28e-31 | - | 3.1.3.18 | - | F | ko:K01091 | ko00630,ko01100,ko01110,ko01130,map00630,map01100,map01110,map01130 | ko00000,ko00001,ko01000 | Psort location Cytoplasmic, score |
| HNJENPFB_01206 | 6.93e-77 | asnB | 6.3.5.4 | - | E | ko:K01953 | ko00250,ko01100,ko01110,map00250,map01100,map01110 | ko00000,ko00001,ko01000,ko01002 | Asparagine synthase |
| HNJENPFB_01207 | 2.38e-58 | - | 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 |
| HNJENPFB_01210 | 3.07e-70 | - | - | - | - | - | - | - | - |
eggNOG-mapper v2.1.12 (Database: eggNOG v5.0.2, Mar. 2021 release)