| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | KEGG_ko | KEGG_Pathway | BRITE | Description |
|---|---|---|---|---|---|---|---|---|---|
| CBIAAGLN_00001 | 9.45e-250 | larC | 4.99.1.12 | - | S | ko:K09121 | - | ko00000,ko01000 | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes |
| CBIAAGLN_00002 | 9.23e-101 | - | - | - | L | ko:K06864 | - | ko00000 | tRNA processing |
| CBIAAGLN_00003 | 5.15e-167 | - | - | - | S | ko:K06898 | - | ko00000 | AIR carboxylase |
| CBIAAGLN_00004 | 4.54e-261 | - | - | - | S | - | - | - | Glycosyl hydrolase-like 10 |
| CBIAAGLN_00005 | 3.45e-158 | - | 1.15.1.1 | - | P | ko:K04564 | ko04013,ko04068,ko04146,ko04211,ko04212,ko04213,ko05016,map04013,map04068,map04146,map04211,map04212,map04213,map05016 | ko00000,ko00001,ko01000 | Iron/manganese superoxide dismutases, alpha-hairpin domain |
| CBIAAGLN_00006 | 2.58e-268 | - | - | - | IM | - | - | - | Cytidylyltransferase-like |
| CBIAAGLN_00007 | 3.67e-299 | murJ | - | - | S | ko:K03980 | - | ko00000,ko01011,ko02000 | Involved in peptidoglycan biosynthesis. Transports lipid-linked peptidoglycan precursors from the inner to the outer leaflet of the cytoplasmic membrane |
| CBIAAGLN_00008 | 2.85e-80 | - | 3.6.4.12 | - | L | ko:K03657 | ko03420,ko03430,map03420,map03430 | ko00000,ko00001,ko01000,ko03400 | UvrD-like helicase C-terminal domain |
| CBIAAGLN_00010 | 0.0 | - | - | - | S | ko:K03307 | - | ko00000 | Sodium:solute symporter family |
| CBIAAGLN_00011 | 6.25e-284 | - | 2.7.1.6 | - | G | ko:K00849 | ko00052,ko00520,ko01100,map00052,map00520,map01100 | ko00000,ko00001,ko00002,ko01000,ko04147 | Galactokinase galactose-binding signature |
| CBIAAGLN_00012 | 0.0 | - | - | - | M | - | - | - | Bacterial sugar transferase |
| CBIAAGLN_00014 | 2.69e-116 | - | - | - | NU | - | - | - | Prepilin-type N-terminal cleavage methylation domain |
| CBIAAGLN_00015 | 6.67e-308 | - | 3.2.1.51 | GH29 | G | ko:K01206 | ko00511,map00511 | ko00000,ko00001,ko01000,ko04147 | PFAM coagulation factor 5 8 type domain protein |
| CBIAAGLN_00016 | 1.96e-73 | - | 3.2.1.51 | GH29 | G | ko:K01206 | ko00511,map00511 | ko00000,ko00001,ko01000,ko04147 | PFAM coagulation factor 5 8 type domain protein |
| CBIAAGLN_00017 | 9.86e-168 | - | - | - | M | - | - | - | Peptidase family M23 |
| CBIAAGLN_00018 | 2.56e-145 | 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) |
| CBIAAGLN_00019 | 7.54e-201 | - | 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 |
| CBIAAGLN_00023 | 1.88e-308 | - | - | - | S | - | - | - | PFAM CBS domain containing protein |
| CBIAAGLN_00024 | 3.68e-312 | tlyC | - | - | S | ko:K03699 | - | ko00000,ko02042 | PFAM CBS domain containing protein |
| CBIAAGLN_00025 | 1.95e-112 | 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 |
| CBIAAGLN_00027 | 6.32e-118 | - | - | - | F | - | - | - | Bacteriocin-protection, YdeI or OmpD-Associated |
| CBIAAGLN_00028 | 0.0 | - | 2.6.1.62 | - | H | ko:K00833 | ko00780,ko01100,map00780,map01100 | ko00000,ko00001,ko00002,ko01000,ko01007 | Aminotransferase class-III |
| CBIAAGLN_00029 | 8.85e-233 | - | 2.8.1.6 | - | H | ko:K01012 | ko00780,ko01100,map00780,map01100 | ko00000,ko00001,ko00002,ko01000 | Biotin and Thiamin Synthesis associated domain |
| CBIAAGLN_00030 | 3.34e-153 | - | - | - | P | - | - | - | Sulfatase |
| CBIAAGLN_00031 | 2.63e-208 | - | 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 | Polyprenyl synthetase |
| CBIAAGLN_00032 | 9.55e-242 | 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 | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate |
| CBIAAGLN_00034 | 3.08e-53 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00035 | 1.44e-110 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00036 | 9.11e-165 | - | 4.3.1.17 | - | E | ko:K01752 | ko00260,ko00270,ko01100,ko01110,ko01130,ko01200,ko01230,map00260,map00270,map01100,map01110,map01130,map01200,map01230 | ko00000,ko00001,ko01000 | Serine dehydratase alpha chain |
| CBIAAGLN_00037 | 2.61e-117 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00038 | 0.0 | sepA | - | - | Q | - | - | - | COG2015, Alkyl sulfatase and related hydrolases |
| CBIAAGLN_00039 | 5.22e-112 | - | - | - | F | ko:K08311 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03019 | NUDIX domain |
| CBIAAGLN_00040 | 3.77e-173 | - | - | - | E | ko:K07588 | - | ko00000,ko01000 | ArgK protein |
| CBIAAGLN_00042 | 1.11e-125 | - | 3.2.1.52 | GH20 | G | ko:K12373 | ko00511,ko00513,ko00520,ko00531,ko00603,ko00604,ko01100,ko04142,map00511,map00513,map00520,map00531,map00603,map00604,map01100,map04142 | ko00000,ko00001,ko00002,ko01000,ko03110 | Glycoside hydrolase, family 20, catalytic core |
| CBIAAGLN_00043 | 4.03e-174 | - | - | - | D | - | - | - | Phage-related minor tail protein |
| CBIAAGLN_00045 | 3.98e-316 | dnaX | 2.7.7.7 | - | L | ko:K02343 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity |
| CBIAAGLN_00046 | 1.39e-83 | dnaX | 2.7.7.7 | - | L | ko:K02343 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity |
| CBIAAGLN_00047 | 1.13e-60 | - | - | - | L | ko:K09747 | - | ko00000 | YbaB/EbfC DNA-binding family |
| CBIAAGLN_00048 | 4.77e-73 | - | - | - | NU | ko:K02669 | - | ko00000,ko02035,ko02044 | Type II/IV secretion system protein |
| CBIAAGLN_00049 | 3.33e-143 | - | - | - | NU | ko:K02669 | - | ko00000,ko02035,ko02044 | Type II/IV secretion system protein |
| CBIAAGLN_00050 | 6.22e-244 | ppiD | 5.2.1.8 | - | O | ko:K03769,ko:K03770,ko:K03771,ko:K07533 | - | ko00000,ko01000,ko03110 | peptidyl-prolyl cis-trans isomerase activity |
| CBIAAGLN_00052 | 0.0 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00053 | 1.5e-74 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00054 | 2.8e-189 | - | 3.6.1.66 | - | S | ko:K02428 | ko00230,map00230 | ko00000,ko00001,ko01000 | MazG nucleotide pyrophosphohydrolase domain |
| CBIAAGLN_00055 | 3.85e-66 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00056 | 5.84e-172 | - | - | - | S | - | - | - | competence protein |
| CBIAAGLN_00057 | 3.93e-99 | - | - | - | S | ko:K07107 | - | ko00000,ko01000 | Thioesterase-like superfamily |
| CBIAAGLN_00059 | 1.08e-255 | - | 3.1.6.1 | - | P | ko:K01130 | ko00140,ko00600,map00140,map00600 | ko00000,ko00001,ko01000 | Sulfatase |
| CBIAAGLN_00060 | 1.91e-164 | - | - | - | L | ko:K03424 | - | ko00000,ko01000 | TatD related DNase |
| CBIAAGLN_00061 | 0.0 | - | - | - | P | ko:K03455 | - | ko00000 | TrkA-N domain |
| CBIAAGLN_00062 | 8.91e-69 | - | - | - | S | ko:K07098 | - | ko00000 | Calcineurin-like phosphoesterase superfamily domain |
| CBIAAGLN_00063 | 3.17e-124 | - | - | - | S | ko:K07098 | - | ko00000 | Calcineurin-like phosphoesterase superfamily domain |
| CBIAAGLN_00064 | 8.75e-77 | - | - | - | E | ko:K19689 | - | ko00000,ko01000,ko01002 | Thermophilic metalloprotease (M29) |
| CBIAAGLN_00065 | 8.33e-157 | - | 3.5.1.28 | - | M | ko:K01447 | - | ko00000,ko01000 | PFAM N-acetylmuramoyl-L-alanine amidase family 2 |
| CBIAAGLN_00066 | 0.0 | - | 4.2.1.3 | - | C | ko:K01681 | ko00020,ko00630,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01210,ko01230,map00020,map00630,map00720,map01100,map01110,map01120,map01130,map01200,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | Aconitase C-terminal domain |
| CBIAAGLN_00067 | 5.08e-291 | - | 4.2.1.3 | - | C | ko:K01681 | ko00020,ko00630,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01210,ko01230,map00020,map00630,map00720,map01100,map01110,map01120,map01130,map01200,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | Aconitase C-terminal domain |
| CBIAAGLN_00072 | 9.4e-189 | - | 3.5.1.104 | - | G | ko:K22278 | - | ko00000,ko01000 | Polysaccharide deacetylase |
| CBIAAGLN_00073 | 4.48e-173 | - | - | - | T | - | - | - | Outer membrane lipoprotein-sorting protein |
| CBIAAGLN_00074 | 3.39e-182 | panB | 2.1.2.11 | - | H | ko:K00606 | ko00770,ko01100,ko01110,map00770,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha-ketoisovalerate to form ketopantoate |
| CBIAAGLN_00075 | 5.76e-108 | - | 2.7.6.3 | - | H | ko:K00950 | ko00790,ko01100,map00790,map01100 | ko00000,ko00001,ko00002,ko01000 | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) |
| CBIAAGLN_00076 | 4.14e-175 | 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 | Dihydrodipicolinate reductase, N-terminus |
| CBIAAGLN_00077 | 1.02e-203 | dapA | 4.3.3.7 | - | EM | ko:K01714 | ko00261,ko00300,ko01100,ko01110,ko01120,ko01130,ko01230,map00261,map00300,map01100,map01110,map01120,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Dihydrodipicolinate synthetase family |
| CBIAAGLN_00082 | 5.69e-09 | - | - | - | D | ko:K03466 | - | ko00000,ko03036 | Ftsk_gamma |
| CBIAAGLN_00083 | 4.69e-79 | rsfS | - | - | S | ko:K09710 | - | ko00000,ko03009 | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation |
| CBIAAGLN_00085 | 4.72e-305 | 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 |
| CBIAAGLN_00086 | 1.39e-18 | algB | - | - | T | ko:K11384 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | COG2204 Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains |
| CBIAAGLN_00087 | 0.0 | mutS | - | - | L | ko:K03555 | ko03430,map03430 | ko00000,ko00001,ko03400 | that it carries out the mismatch recognition step. This protein has a weak ATPase activity |
| CBIAAGLN_00088 | 7.28e-138 | - | 2.7.7.7 | - | L | ko:K02342 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | Exonuclease |
| CBIAAGLN_00091 | 1.24e-296 | - | - | - | MU | ko:K12340 | ko01501,ko01503,ko02020,ko03070,ko04626,ko05133,map01501,map01503,map02020,map03070,map04626,map05133 | ko00000,ko00001,ko00002,ko01504,ko02000,ko02044 | efflux transmembrane transporter activity |
| CBIAAGLN_00095 | 1.11e-204 | - | 2.7.7.24 | - | M | ko:K00973 | ko00521,ko00523,ko00525,ko01130,map00521,map00523,map00525,map01130 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis |
| CBIAAGLN_00096 | 6.96e-267 | - | 4.2.1.46 | - | M | ko:K01710 | ko00521,ko00523,ko00525,ko01055,ko01130,map00521,map00523,map00525,map01055,map01130 | ko00000,ko00001,ko00002,ko01000 | Male sterility protein |
| CBIAAGLN_00097 | 2.66e-227 | - | 2.7.1.11 | - | G | 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 | Phosphofructokinase |
| CBIAAGLN_00098 | 2.61e-181 | - | - | - | L | ko:K10800 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | uracil-dna glycosylase |
| CBIAAGLN_00099 | 1.39e-197 | - | 3.6.4.12 | - | L | ko:K02314 | ko03030,ko04112,map03030,map04112 | ko00000,ko00001,ko01000,ko03032 | DnaB-like helicase C terminal domain |
| CBIAAGLN_00100 | 1.18e-271 | - | - | - | L | ko:K04763 | - | ko00000,ko03036 | Belongs to the 'phage' integrase family |
| CBIAAGLN_00102 | 3.16e-206 | - | - | - | V | ko:K01992 | - | ko00000,ko00002,ko02000 | ABC-2 family transporter protein |
| CBIAAGLN_00103 | 6.71e-112 | - | - | - | V | ko:K01992 | - | ko00000,ko00002,ko02000 | ABC-2 family transporter protein |
| CBIAAGLN_00105 | 0.0 | - | - | - | L | ko:K02621 | - | ko00000,ko01000,ko02048,ko03032,ko03036 | DNA Topoisomerase IV |
| CBIAAGLN_00106 | 3.4e-35 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00107 | 1.01e-12 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00108 | 6.82e-223 | - | 1.2.4.1 | - | C | ko:K00161 | ko00010,ko00020,ko00620,ko01100,ko01110,ko01120,ko01130,ko01200,ko04066,ko04922,ko05230,map00010,map00020,map00620,map01100,map01110,map01120,map01130,map01200,map04066,map04922,map05230 | br01601,ko00000,ko00001,ko00002,ko01000 | Dehydrogenase E1 component |
| CBIAAGLN_00109 | 5.69e-194 | - | - | - | K | - | - | - | bacterial-type RNA polymerase transcription factor activity, metal ion regulated sequence-specific DNA binding |
| CBIAAGLN_00111 | 0.0 | - | - | - | J | ko:K02355 | - | ko00000,ko03012,ko03029 | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome |
| CBIAAGLN_00112 | 3.67e-65 | - | - | - | J | ko:K02946 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein S10p/S20e |
| CBIAAGLN_00113 | 2.13e-141 | rplC | - | - | J | ko:K02906 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit |
| CBIAAGLN_00114 | 9.43e-132 | rplD | - | - | J | ko:K02926 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L4/L1 family |
| CBIAAGLN_00115 | 1.02e-14 | rplW | - | - | J | ko:K02892 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome |
| CBIAAGLN_00118 | 1.36e-207 | ispE | 2.7.1.148 | - | I | ko:K00919 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | GHMP kinases N terminal domain |
| CBIAAGLN_00122 | 2.77e-213 | - | - | - | S | ko:K07263 | - | ko00000,ko01000,ko01002 | Insulinase (Peptidase family M16) |
| CBIAAGLN_00123 | 9.27e-77 | 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) |
| CBIAAGLN_00124 | 3.9e-149 | - | - | - | K | - | - | - | Psort location Cytoplasmic, score |
| CBIAAGLN_00125 | 1.46e-39 | metF | 1.5.1.20 | - | C | ko:K00297 | ko00670,ko00720,ko01100,ko01120,ko01200,ko01523,map00670,map00720,map01100,map01120,map01200,map01523 | ko00000,ko00001,ko00002,ko01000 | reductase |
| CBIAAGLN_00126 | 4.13e-77 | metF | 1.5.1.20 | - | E | ko:K00297 | ko00670,ko00720,ko01100,ko01120,ko01200,ko01523,map00670,map00720,map01100,map01120,map01200,map01523 | ko00000,ko00001,ko00002,ko01000 | 5,10-methylenetetrahydrofolate reductase |
| CBIAAGLN_00127 | 4.95e-73 | metE | 2.1.1.14 | - | E | ko:K00549 | ko00270,ko00450,ko01100,ko01110,ko01230,map00270,map00450,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation |
| CBIAAGLN_00128 | 0.0 | pmp21 | - | - | T | - | - | - | pathogenesis |
| CBIAAGLN_00129 | 1.54e-177 | - | 2.4.1.25 | GH77 | G | ko:K00705 | ko00500,ko01100,map00500,map01100 | ko00000,ko00001,ko01000 | 4-alpha-glucanotransferase |
| CBIAAGLN_00130 | 2.45e-11 | - | - | - | L | ko:K07462 | ko03410,ko03430,ko03440,map03410,map03430,map03440 | ko00000,ko00001,ko01000,ko03400 | DHHA1 domain |
| CBIAAGLN_00131 | 0.0 | - | - | - | L | ko:K07462 | ko03410,ko03430,ko03440,map03410,map03430,map03440 | ko00000,ko00001,ko01000,ko03400 | DHHA1 domain |
| CBIAAGLN_00132 | 1.93e-21 | - | 2.3.3.13 | - | E | ko:K01649 | ko00290,ko00620,ko01100,ko01110,ko01210,ko01230,map00290,map00620,map01100,map01110,map01210,map01230 | br01601,ko00000,ko00001,ko00002,ko01000 | HMGL-like |
| CBIAAGLN_00136 | 7.07e-81 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00137 | 0.0 | - | - | - | EGP | - | - | - | Sugar (and other) transporter |
| CBIAAGLN_00138 | 3.82e-72 | - | - | - | S | - | - | - | ankyrin repeats |
| CBIAAGLN_00139 | 2.08e-87 | - | - | - | S | - | - | - | ankyrin repeats |
| CBIAAGLN_00140 | 5.47e-289 | - | - | - | G | - | - | - | cellulose 1,4-beta-cellobiosidase activity |
| CBIAAGLN_00141 | 2.87e-112 | feoB | - | - | P | ko:K04759 | - | ko00000,ko02000 | transporter of a GTP-driven Fe(2 ) uptake system |
| CBIAAGLN_00143 | 3.94e-243 | - | - | - | S | - | - | - | PFAM Sel1 domain protein repeat-containing protein |
| CBIAAGLN_00144 | 1.41e-54 | tatA | - | - | U | ko:K03116 | ko03060,ko03070,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system |
| CBIAAGLN_00145 | 0.0 | - | - | - | J | ko:K07576 | - | ko00000 | Beta-Casp domain |
| CBIAAGLN_00146 | 4.57e-76 | - | 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 acetyltransferase, N-terminal |
| CBIAAGLN_00147 | 1.43e-222 | - | - | - | E | - | - | - | lipolytic protein G-D-S-L family |
| CBIAAGLN_00150 | 1.13e-131 | - | - | - | M | - | - | - | Polysaccharide biosynthesis/export protein |
| CBIAAGLN_00151 | 1.39e-122 | - | - | - | D | - | - | - | Chain length determinant protein |
| CBIAAGLN_00152 | 0.0 | - | - | - | D | - | - | - | Chain length determinant protein |
| CBIAAGLN_00153 | 1.83e-216 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00154 | 1.02e-107 | - | - | - | C | - | - | - | Transmembrane exosortase (Exosortase_EpsH) |
| CBIAAGLN_00155 | 4.58e-220 | prs | 2.7.6.1 | - | EF | ko:K00948 | ko00030,ko00230,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00030,map00230,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000 | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) |
| CBIAAGLN_00156 | 1.24e-131 | ctc | - | - | J | ko:K02897 | ko03010,map03010 | ko00000,ko00001,ko00002,ko03011 | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance |
| CBIAAGLN_00158 | 0.0 | - | - | - | NU | - | - | - | Type IV pilus assembly protein PilM; |
| CBIAAGLN_00159 | 2.69e-167 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00162 | 3.65e-220 | - | - | - | K | - | - | - | Transcriptional regulator |
| CBIAAGLN_00163 | 2.19e-178 | - | - | - | C | - | - | - | aldo keto reductase |
| CBIAAGLN_00164 | 5.7e-208 | fatB | - | - | P | ko:K02016 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | iron ion transport |
| CBIAAGLN_00165 | 8.62e-91 | yclP | 3.6.3.34 | - | P | ko:K02013 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | ABC transporter, ATP-binding protein |
| CBIAAGLN_00166 | 5.06e-54 | yclP | 3.6.3.34 | - | P | ko:K02013 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | ABC transporter, ATP-binding protein |
| CBIAAGLN_00167 | 2.17e-222 | fatC | - | - | P | ko:K02015 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | iron ion homeostasis |
| CBIAAGLN_00168 | 1.71e-171 | yclN | - | - | P | ko:K02015 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | iron ion homeostasis |
| CBIAAGLN_00169 | 8.61e-09 | - | - | - | M | ko:K13730 | ko05100,map05100 | ko00000,ko00001 | leucine-rich repeat-containing protein typical subtype |
| CBIAAGLN_00170 | 0.0 | - | - | - | O | ko:K08303 | ko05120,map05120 | ko00000,ko00001,ko01000,ko01002 | Collagenase |
| CBIAAGLN_00171 | 2.12e-29 | - | 6.3.2.12, 6.3.2.17 | - | H | ko:K11754 | ko00790,ko01100,map00790,map01100 | ko00000,ko00001,ko00002,ko01000 | Mur ligase middle domain |
| CBIAAGLN_00172 | 7.68e-226 | - | 1.5.1.20 | - | E | ko:K00297 | ko00670,ko00720,ko01100,ko01120,ko01200,ko01523,map00670,map00720,map01100,map01120,map01200,map01523 | ko00000,ko00001,ko00002,ko01000 | Methylenetetrahydrofolate reductase |
| CBIAAGLN_00173 | 3.01e-150 | - | 1.14.11.27 | - | P | ko:K10277 | - | ko00000,ko01000,ko03036 | peptidyl-arginine hydroxylation |
| CBIAAGLN_00174 | 0.0 | - | - | - | M | ko:K07277 | - | ko00000,ko02000,ko03029 | Surface antigen |
| CBIAAGLN_00176 | 3.58e-56 | - | - | - | S | - | - | - | Protein of unknown function (DUF5131) |
| CBIAAGLN_00178 | 4.72e-274 | - | 2.1.1.37 | - | L | ko:K00558 | ko00270,ko01100,ko05206,map00270,map01100,map05206 | ko00000,ko00001,ko00002,ko01000,ko02048,ko03032,ko03036 | Belongs to the class I-like SAM-binding methyltransferase superfamily. C5-methyltransferase family |
| CBIAAGLN_00180 | 0.0 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00182 | 1.39e-27 | - | 3.2.1.52 | GH20 | G | ko:K12373 | ko00511,ko00513,ko00520,ko00531,ko00603,ko00604,ko01100,ko04142,map00511,map00513,map00520,map00531,map00603,map00604,map01100,map04142 | ko00000,ko00001,ko00002,ko01000,ko03110 | PFAM Glycoside hydrolase, family 20, catalytic core |
| CBIAAGLN_00183 | 4.65e-41 | - | 3.2.1.52 | GH20 | G | ko:K12373 | ko00511,ko00513,ko00520,ko00531,ko00603,ko00604,ko01100,ko04142,map00511,map00513,map00520,map00531,map00603,map00604,map01100,map04142 | ko00000,ko00001,ko00002,ko01000,ko03110 | PFAM Glycoside hydrolase, family 20, catalytic core |
| CBIAAGLN_00184 | 3.64e-305 | 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 |
| CBIAAGLN_00185 | 1.68e-252 | argC | 1.2.1.38 | - | E | ko:K00145 | ko00220,ko01100,ko01110,ko01130,ko01210,ko01230,map00220,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Semialdehyde dehydrogenase, NAD binding domain |
| CBIAAGLN_00188 | 5.84e-173 | - | - | - | K | - | - | - | Transcriptional regulator |
| CBIAAGLN_00189 | 2.75e-313 | - | - | - | P | - | - | - | Dimerisation domain of Zinc Transporter |
| CBIAAGLN_00190 | 5.52e-188 | - | - | - | P | ko:K03455 | - | ko00000 | TrkA-N domain |
| CBIAAGLN_00191 | 9.37e-10 | - | 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 |
| CBIAAGLN_00192 | 1.4e-190 | - | 2.7.13.3 | - | Q | ko:K07777 | ko02020,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko02022 | Transposase |
| CBIAAGLN_00193 | 2.23e-165 | - | 4.3.99.3 | - | O | ko:K10026 | ko00790,ko01100,map00790,map01100 | ko00000,ko00001,ko01000,ko03016 | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds |
| CBIAAGLN_00194 | 1.14e-301 | - | - | - | K | ko:K03628 | ko03018,map03018 | ko00000,ko00001,ko03019,ko03021 | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template |
| CBIAAGLN_00195 | 2.13e-60 | - | - | - | S | - | - | - | Protein of unknown function (DUF2851) |
| CBIAAGLN_00196 | 3.06e-62 | - | 3.2.1.51 | GH95 | G | ko:K15923 | ko00511,map00511 | ko00000,ko00001,ko01000 | Glycosyl hydrolase family 65, N-terminal domain |
| CBIAAGLN_00197 | 0.0 | - | 3.2.1.51 | GH95 | G | ko:K15923 | ko00511,map00511 | ko00000,ko00001,ko01000 | Glycosyl hydrolase family 65, N-terminal domain |
| CBIAAGLN_00199 | 3.37e-281 | tig | - | - | O | 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 |
| CBIAAGLN_00200 | 2.05e-125 | - | 3.4.21.92 | - | OU | ko:K01358 | ko04112,ko04212,map04112,map04212 | ko00000,ko00001,ko01000,ko01002 | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins |
| CBIAAGLN_00202 | 1.69e-76 | rplN | - | - | J | ko:K02874 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome |
| CBIAAGLN_00203 | 2.19e-56 | rpsQ | - | - | J | ko:K02961 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA |
| CBIAAGLN_00204 | 5.78e-35 | - | - | - | J | ko:K02904 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal L29 protein |
| CBIAAGLN_00205 | 3.42e-97 | - | - | - | J | ko:K02878 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs |
| CBIAAGLN_00206 | 4.27e-155 | rpsC | - | - | J | ko:K02982 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation |
| CBIAAGLN_00207 | 4.97e-70 | - | - | - | J | ko:K02890 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | its binding is stimulated by other ribosomal proteins, e.g. L4, L17, and L20. It is important during the early stages of 50S assembly. It makes multiple contacts with different domains of the 23S rRNA in the assembled 50S subunit and ribosome |
| CBIAAGLN_00208 | 9.77e-82 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00209 | 9.56e-51 | - | - | - | J | ko:K02959 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011,ko03029 | Ribosomal protein S16 |
| CBIAAGLN_00212 | 6.5e-215 | - | - | - | L | ko:K03733 | - | ko00000,ko03036 | Phage integrase, N-terminal SAM-like domain |
| CBIAAGLN_00213 | 1.08e-184 | - | - | - | DTZ | - | - | - | EF-hand, calcium binding motif |
| CBIAAGLN_00214 | 8.01e-66 | - | - | - | U | ko:K03210 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | Preprotein translocase subunit |
| CBIAAGLN_00215 | 7.63e-115 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00216 | 0.0 | - | - | - | O | - | - | - | Trypsin |
| CBIAAGLN_00220 | 1.53e-209 | lpxG | - | - | S | ko:K07098 | - | ko00000 | Calcineurin-like phosphoesterase |
| CBIAAGLN_00221 | 4.53e-244 | - | - | - | H | - | - | - | PFAM glycosyl transferase family 8 |
| CBIAAGLN_00222 | 8.86e-192 | - | - | - | S | - | - | - | Glycosyltransferase like family 2 |
| CBIAAGLN_00224 | 2.07e-123 | - | - | - | M | ko:K03642 | - | ko00000 | Lytic transglycolase |
| CBIAAGLN_00225 | 0.0 | - | 3.1.3.5 | - | F | ko:K01081 | ko00230,ko00240,ko00760,ko01100,ko01110,map00230,map00240,map00760,map01100,map01110 | ko00000,ko00001,ko01000 | Calcineurin-like phosphoesterase |
| CBIAAGLN_00227 | 8.56e-45 | acpP | - | - | IQ | ko:K02078 | - | ko00000,ko00001 | Phosphopantetheine attachment site |
| CBIAAGLN_00228 | 9.76e-172 | coaX | 2.7.1.33 | - | K | ko:K03525 | ko00770,ko01100,map00770,map01100 | ko00000,ko00001,ko00002,ko01000 | Type III pantothenate kinase |
| CBIAAGLN_00229 | 8.52e-267 | - | - | - | M | - | - | - | Monogalactosyldiacylglycerol (MGDG) synthase |
| CBIAAGLN_00232 | 1.56e-29 | - | - | GT2 | M | ko:K03820 | - | ko00000,ko01000 | Carbon-nitrogen hydrolase |
| CBIAAGLN_00233 | 2.56e-155 | - | - | GT2 | M | ko:K03820 | - | ko00000,ko01000 | Carbon-nitrogen hydrolase |
| CBIAAGLN_00234 | 5.22e-175 | - | - | - | S | - | - | - | Phosphodiester glycosidase |
| CBIAAGLN_00235 | 9e-133 | - | 2.7.7.13 | - | JM | ko:K00966 | ko00051,ko00520,ko01100,ko01110,map00051,map00520,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Nucleotidyl transferase |
| CBIAAGLN_00236 | 5.77e-75 | - | 2.7.7.13 | - | JM | ko:K00966 | ko00051,ko00520,ko01100,ko01110,map00051,map00520,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Nucleotidyl transferase |
| CBIAAGLN_00238 | 5.29e-70 | xerD1 | - | - | L | ko:K04763 | - | ko00000,ko03036 | Belongs to the 'phage' integrase family |
| CBIAAGLN_00239 | 2.82e-207 | MA20_36650 | - | - | EG | - | - | - | spore germination |
| CBIAAGLN_00241 | 2.33e-248 | - | - | - | O | - | - | - | Cytochrome C assembly protein |
| CBIAAGLN_00243 | 0.0 | - | 1.11.1.6 | - | P | ko:K03781 | ko00380,ko00630,ko01110,ko01130,ko01200,ko04011,ko04016,ko04068,ko04146,ko04211,ko04212,ko04213,ko05014,map00380,map00630,map01110,map01130,map01200,map04011,map04016,map04068,map04146,map04211,map04212,map04213,map05014 | ko00000,ko00001,ko00002,ko01000 | Catalase |
| CBIAAGLN_00245 | 4.15e-103 | yciA | - | - | I | ko:K10806 | ko01040,map01040 | ko00000,ko00001,ko01000,ko01004 | acyl-coa hydrolase |
| CBIAAGLN_00246 | 7.09e-316 | hsrA | - | - | EGP | - | - | - | Major facilitator Superfamily |
| CBIAAGLN_00247 | 1.68e-242 | - | - | - | I | - | - | - | transferase activity, transferring acyl groups other than amino-acyl groups |
| CBIAAGLN_00248 | 1.22e-189 | - | - | - | G | - | - | - | Glycosyl hydrolases family 18 |
| CBIAAGLN_00249 | 1.07e-37 | - | - | - | G | - | - | - | Glycosyl hydrolases family 18 |
| CBIAAGLN_00250 | 4.47e-315 | - | - | - | S | ko:K07126,ko:K13582 | ko04112,map04112 | ko00000,ko00001 | beta-lactamase activity |
| CBIAAGLN_00251 | 1.56e-59 | - | 2.3.1.79 | - | S | ko:K00661 | - | ko00000,ko01000 | Maltose acetyltransferase |
| CBIAAGLN_00252 | 2.46e-215 | - | - | - | D | ko:K19234,ko:K19236 | ko01503,map01503 | ko00000,ko00001,ko01002,ko01011 | ErfK ybiS ycfS ynhG family protein |
| CBIAAGLN_00253 | 0.0 | - | - | - | S | - | - | - | Terminase |
| CBIAAGLN_00255 | 7.45e-49 | XK27_09985 | - | - | S | - | - | - | Protein of unknown function (DUF1232) |
| CBIAAGLN_00256 | 1.43e-194 | - | - | - | S | ko:K07051 | - | ko00000 | TatD related DNase |
| CBIAAGLN_00257 | 2.56e-55 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00258 | 4.83e-163 | - | - | - | - | ko:K00241 | ko00020,ko00190,ko00650,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,map00020,map00190,map00650,map00720,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002 | - |
| CBIAAGLN_00260 | 6.94e-284 | - | - | - | P | - | - | - | Citrate transporter |
| CBIAAGLN_00263 | 2.47e-250 | - | - | - | E | - | - | - | Aminotransferase class-V |
| CBIAAGLN_00264 | 5.45e-234 | - | - | - | S | - | - | - | Conserved hypothetical protein 698 |
| CBIAAGLN_00265 | 4.81e-133 | - | - | - | K | - | - | - | LysR substrate binding domain |
| CBIAAGLN_00273 | 2.53e-170 | - | 5.99.1.2 | - | L | ko:K03169 | - | ko00000,ko01000,ko03032 | Bacterial DNA topoisomeraes I ATP-binding domain |
| CBIAAGLN_00277 | 0.0 | - | 1.4.1.4 | - | E | ko:K00262 | ko00220,ko00250,ko00910,ko01100,map00220,map00250,map00910,map01100 | ko00000,ko00001,ko01000 | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase |
| CBIAAGLN_00280 | 1.5e-147 | - | - | - | L | - | - | - | Transposase IS200 like |
| CBIAAGLN_00282 | 3.37e-61 | - | - | GT9 | M | ko:K02843,ko:K02849 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01003,ko01005 | ADP-heptose-lipopolysaccharide heptosyltransferase activity |
| CBIAAGLN_00283 | 2.26e-245 | - | 5.1.3.20 | - | M | ko:K03274 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01005 | 3-beta hydroxysteroid dehydrogenase/isomerase family |
| CBIAAGLN_00284 | 1.11e-287 | - | - | - | M | - | - | - | Glycosyltransferase like family 2 |
| CBIAAGLN_00286 | 5.12e-71 | - | - | - | O | ko:K03671 | ko04621,ko05418,map04621,map05418 | ko00000,ko00001,ko03110 | Thioredoxin-like domain |
| CBIAAGLN_00287 | 7.46e-294 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00294 | 2.12e-162 | - | - | - | V | ko:K02003 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| CBIAAGLN_00295 | 9.3e-175 | - | - | - | M | ko:K02005 | - | ko00000 | HlyD family secretion protein |
| CBIAAGLN_00297 | 2.48e-253 | - | - | - | S | ko:K03698 | - | ko00000,ko01000,ko03019 | Metal dependent phosphohydrolases with conserved 'HD' motif. |
| CBIAAGLN_00298 | 1.34e-161 | - | - | - | P | ko:K07089 | - | ko00000 | Psort location CytoplasmicMembrane, score 10.00 |
| CBIAAGLN_00301 | 0.0 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00302 | 4.26e-176 | - | 2.3.1.39 | - | I | ko:K00645 | ko00061,ko00333,ko01100,ko01130,ko01212,map00061,map00333,map01100,map01130,map01212 | ko00000,ko00001,ko00002,ko01000,ko01004 | Acyl transferase domain |
| CBIAAGLN_00303 | 4.19e-87 | rplQ | - | - | J | ko:K02879 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L17 |
| CBIAAGLN_00304 | 2.95e-262 | rpoA | 2.7.7.6 | - | K | ko:K03040 | ko00230,ko00240,ko01100,ko03020,map00230,map00240,map01100,map03020 | br01611,ko00000,ko00001,ko00002,ko01000,ko03021,ko03400 | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates |
| CBIAAGLN_00305 | 8.46e-65 | - | - | - | L | - | - | - | Cupin 2, conserved barrel domain protein |
| CBIAAGLN_00306 | 1.95e-127 | - | - | - | S | - | - | - | Cobalamin adenosyltransferase |
| CBIAAGLN_00309 | 4.76e-92 | - | - | - | P | ko:K02051 | - | ko00000,ko00002,ko02000 | NMT1/THI5 like |
| CBIAAGLN_00310 | 3.64e-98 | - | - | - | P | ko:K02049 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| CBIAAGLN_00311 | 1.25e-59 | - | - | - | P | ko:K02049 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| CBIAAGLN_00312 | 3.86e-193 | - | - | - | P | ko:K02050 | - | ko00000,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| CBIAAGLN_00313 | 2.68e-186 | lpxD | 2.3.1.191 | - | M | ko:K02536 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01005 | Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell |
| CBIAAGLN_00315 | 2.79e-54 | rpsN | - | - | J | ko:K02954 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site |
| CBIAAGLN_00316 | 1.7e-58 | - | - | - | S | - | - | - | Zinc ribbon domain |
| CBIAAGLN_00317 | 6.4e-24 | - | - | - | S | - | - | - | PFAM CBS domain containing protein |
| CBIAAGLN_00318 | 3.87e-268 | - | - | - | S | - | - | - | PFAM CBS domain containing protein |
| CBIAAGLN_00319 | 5.62e-199 | atpD | 3.6.3.14 | - | C | ko:K02112 | ko00190,ko00195,ko01100,map00190,map00195,map01100 | ko00000,ko00001,ko00002,ko00194,ko01000 | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits |
| CBIAAGLN_00320 | 1.51e-199 | atpG | - | - | C | ko:K02115 | ko00190,ko00195,ko01100,map00190,map00195,map01100 | ko00000,ko00001,ko00002,ko00194 | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex |
| CBIAAGLN_00321 | 2.4e-233 | atpA | 3.6.3.14 | - | C | ko:K02111 | ko00190,ko00195,ko01100,map00190,map00195,map01100 | ko00000,ko00001,ko00002,ko00194,ko01000 | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit |
| CBIAAGLN_00322 | 4.44e-305 | - | 3.2.1.23 | - | G | ko:K01190 | ko00052,ko00511,ko00600,ko01100,map00052,map00511,map00600,map01100 | ko00000,ko00001,ko01000 | Beta galactosidase small chain |
| CBIAAGLN_00323 | 2.66e-06 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00325 | 1.22e-90 | MA20_42350 | 2.7.8.12 | - | M | ko:K09809 | - | ko00000,ko01000 | Glycosyl transferase, family 2 |
| CBIAAGLN_00326 | 2.43e-88 | MA20_42350 | 2.7.8.12 | - | M | ko:K09809 | - | ko00000,ko01000 | Glycosyl transferase, family 2 |
| CBIAAGLN_00327 | 1.09e-274 | - | 1.8.1.2 | - | P | ko:K00380 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko00002,ko01000 | FAD binding domain |
| CBIAAGLN_00328 | 4.42e-107 | fabH | 2.3.1.180 | - | I | ko:K00648 | ko00061,ko01100,ko01212,map00061,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. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids |
| CBIAAGLN_00329 | 1.35e-150 | - | - | - | NU | - | - | - | Prokaryotic N-terminal methylation motif |
| CBIAAGLN_00330 | 6.87e-256 | - | 2.5.1.54 | - | E | ko:K01626 | ko00400,ko01100,ko01110,ko01130,ko01230,ko02024,map00400,map01100,map01110,map01130,map01230,map02024 | ko00000,ko00001,ko00002,ko01000 | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) |
| CBIAAGLN_00331 | 4.03e-111 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00332 | 1.62e-64 | - | - | - | S | ko:K07088 | - | ko00000 | Membrane transport protein |
| CBIAAGLN_00334 | 1.11e-261 | - | - | - | S | - | - | - | COGs COG4299 conserved |
| CBIAAGLN_00335 | 1.22e-120 | sprT | - | - | K | - | - | - | SprT-like family |
| CBIAAGLN_00336 | 3.17e-66 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00337 | 4.08e-240 | - | - | - | P | ko:K02038 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| CBIAAGLN_00338 | 2.81e-184 | - | 3.6.3.27 | - | P | ko:K02036 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system |
| CBIAAGLN_00339 | 4.41e-96 | phoU | - | - | P | ko:K02039 | - | ko00000 | negative regulation of phosphate transmembrane transport |
| CBIAAGLN_00340 | 5.76e-14 | phoU | - | - | P | ko:K02039 | - | ko00000 | negative regulation of phosphate transmembrane transport |
| CBIAAGLN_00344 | 2.79e-20 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00346 | 3.83e-176 | - | - | - | OU | ko:K04773 | - | ko00000,ko01000,ko01002 | Peptidase family S49 |
| CBIAAGLN_00347 | 0.0 | - | - | - | S | - | - | - | Phage portal protein, lambda family |
| CBIAAGLN_00349 | 2.43e-73 | - | 3.2.1.18 | GH33 | G | ko:K01186 | ko00511,ko00600,ko04142,map00511,map00600,map04142 | ko00000,ko00001,ko01000,ko02042 | exo-alpha-(2->6)-sialidase activity |
| CBIAAGLN_00350 | 5.11e-210 | - | - | - | K | - | - | - | Periplasmic binding protein-like domain |
| CBIAAGLN_00351 | 9.92e-317 | - | 3.2.1.18 | GH33 | G | ko:K01186 | ko00511,ko00600,ko04142,map00511,map00600,map04142 | ko00000,ko00001,ko01000,ko02042 | BNR/Asp-box repeat |
| CBIAAGLN_00352 | 6.76e-306 | - | 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 |
| CBIAAGLN_00353 | 2.43e-137 | - | - | - | K | ko:K03088 | - | ko00000,ko03021 | ECF sigma factor |
| CBIAAGLN_00356 | 3.25e-16 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00357 | 1.08e-29 | - | - | - | K | - | - | - | Helix-turn-helix XRE-family like proteins |
| CBIAAGLN_00359 | 2.09e-70 | - | - | - | L | - | - | - | PFAM Integrase catalytic region |
| CBIAAGLN_00360 | 5.19e-14 | - | - | - | S | - | - | - | Helix-turn-helix domain |
| CBIAAGLN_00363 | 6.89e-173 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00364 | 0.0 | - | 3.6.4.13 | - | L | ko:K05592 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03009,ko03019 | DbpA RNA binding domain |
| CBIAAGLN_00365 | 3.98e-38 | metY | 2.5.1.49 | - | E | ko:K01740 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko01000 | Cys/Met metabolism PLP-dependent enzyme |
| CBIAAGLN_00366 | 3.42e-05 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00367 | 0.0 | - | - | - | O | ko:K07391 | - | ko00000 | Magnesium chelatase, subunit ChlI C-terminal |
| CBIAAGLN_00368 | 0.0 | - | - | - | S | - | - | - | Tetratricopeptide repeat |
| CBIAAGLN_00369 | 6.23e-97 | - | - | - | U | ko:K03559 | - | ko00000,ko02000 | Biopolymer transport protein ExbD/TolR |
| CBIAAGLN_00370 | 1.74e-46 | - | - | - | U | ko:K03561 | - | ko00000,ko02000 | MotA/TolQ/ExbB proton channel family |
| CBIAAGLN_00371 | 1.82e-75 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00372 | 8.29e-299 | - | - | - | V | ko:K03327 | - | ko00000,ko02000 | drug transmembrane transporter activity |
| CBIAAGLN_00373 | 7.86e-105 | - | - | - | P | - | - | - | Cation transport protein |
| CBIAAGLN_00374 | 3.11e-204 | - | - | - | P | ko:K01138 | - | ko00000,ko01000 | PA14 domain |
| CBIAAGLN_00375 | 5.08e-149 | - | - | - | L | - | - | - | Membrane |
| CBIAAGLN_00377 | 1.15e-194 | - | - | - | T | - | - | - | pathogenesis |
| CBIAAGLN_00378 | 2.25e-91 | - | - | - | O | - | - | - | response to oxidative stress |
| CBIAAGLN_00379 | 1.16e-286 | - | 2.3.1.31 | - | E | ko:K00641 | ko00270,ko01100,ko01130,map00270,map01100,map01130 | ko00000,ko00001,ko01000 | alpha/beta hydrolase fold |
| CBIAAGLN_00382 | 4.98e-09 | - | - | - | S | ko:K06903 | - | ko00000 | GPW Gp25 family protein |
| CBIAAGLN_00383 | 2.67e-26 | - | - | - | S | ko:K06906 | - | ko00000 | Phage P2 GpU |
| CBIAAGLN_00384 | 4.23e-31 | - | - | - | S | - | - | - | Baseplate assembly protein |
| CBIAAGLN_00385 | 4.82e-66 | - | - | - | S | ko:K06905 | - | ko00000 | COG3500 Phage protein D |
| CBIAAGLN_00387 | 2.05e-28 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00388 | 6.63e-173 | trmD | 2.1.1.228 | - | J | ko:K00554 | - | ko00000,ko01000,ko03016 | tRNA (Guanine-1)-methyltransferase |
| CBIAAGLN_00389 | 1.8e-237 | 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 |
| CBIAAGLN_00390 | 0.0 | - | - | - | E | - | - | - | 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 |
| CBIAAGLN_00396 | 9.13e-61 | - | - | - | M | - | - | - | Glycosyl transferase, family 2 |
| CBIAAGLN_00397 | 9.37e-27 | - | - | - | H | - | - | - | PFAM glycosyl transferase family 8 |
| CBIAAGLN_00398 | 6.25e-190 | - | - | - | H | - | - | - | PFAM glycosyl transferase family 8 |
| CBIAAGLN_00402 | 3.45e-121 | - | - | - | K | - | - | - | ParB domain protein nuclease |
| CBIAAGLN_00403 | 0.0 | - | - | - | S | - | - | - | Phosphoadenosine phosphosulfate reductase |
| CBIAAGLN_00405 | 2.07e-88 | cbiX | 4.99.1.3 | - | S | ko:K03795 | ko00860,ko01100,ko01120,map00860,map01100,map01120 | ko00000,ko00001,ko01000 | sirohydrochlorin cobaltochelatase activity |
| CBIAAGLN_00406 | 5.88e-163 | rpsB | - | - | J | ko:K02967 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein S2 |
| CBIAAGLN_00407 | 2.17e-173 | tsf | - | - | J | ko:K02357 | - | ko00000,ko03012,ko03029 | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome |
| CBIAAGLN_00408 | 1.88e-225 | glnA | 6.3.1.2 | - | S | ko:K01915 | ko00220,ko00250,ko00630,ko00910,ko01100,ko01120,ko01230,ko02020,ko04217,ko04724,ko04727,map00220,map00250,map00630,map00910,map01100,map01120,map01230,map02020,map04217,map04724,map04727 | ko00000,ko00001,ko01000,ko04147 | glutamine synthetase |
| CBIAAGLN_00409 | 2.11e-217 | glnA | 6.3.1.2 | - | S | ko:K01915 | ko00220,ko00250,ko00630,ko00910,ko01100,ko01120,ko01230,ko02020,ko04217,ko04724,ko04727,map00220,map00250,map00630,map00910,map01100,map01120,map01230,map02020,map04217,map04724,map04727 | ko00000,ko00001,ko01000,ko04147 | glutamine synthetase |
| CBIAAGLN_00410 | 3.59e-38 | epsH | - | GT2 | S | ko:K19425 | - | ko00000,ko01000,ko01003 | Glycosyltransferase like family 2 |
| CBIAAGLN_00411 | 7.58e-176 | - | - | - | M | - | - | - | Glycosyl transferase, family 2 |
| CBIAAGLN_00412 | 6.69e-99 | - | - | - | M | - | - | - | PFAM glycosyl transferase family 2 |
| CBIAAGLN_00414 | 3.46e-73 | - | - | - | P | - | - | - | Sulfatase |
| CBIAAGLN_00415 | 2.08e-260 | 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 | Arginosuccinate synthase |
| CBIAAGLN_00420 | 3.38e-97 | - | - | - | S | - | - | - | polysaccharide biosynthetic process |
| CBIAAGLN_00421 | 2.74e-94 | - | - | - | S | - | - | - | polysaccharide biosynthetic process |
| CBIAAGLN_00422 | 2.37e-225 | - | - | - | C | - | - | - | Nitroreductase family |
| CBIAAGLN_00428 | 5.3e-191 | - | - | - | S | - | - | - | Domain of unknown function (DUF362) |
| CBIAAGLN_00429 | 1.37e-131 | - | - | - | J | - | - | - | Putative rRNA methylase |
| CBIAAGLN_00430 | 7.18e-110 | - | 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 |
| CBIAAGLN_00432 | 1.8e-219 | - | - | - | M | ko:K07276 | - | ko00000 | Mitochondrial fission ELM1 |
| CBIAAGLN_00433 | 2.08e-184 | - | 1.17.99.6 | - | C | ko:K18979 | - | ko00000,ko01000,ko03016 | Domain of unknown function (DUF1730) |
| CBIAAGLN_00434 | 1.25e-265 | - | 4.1.1.15 | - | E | ko:K01580 | ko00250,ko00410,ko00430,ko00650,ko01100,ko01110,ko01120,ko02024,ko04727,ko04940,map00250,map00410,map00430,map00650,map01100,map01110,map01120,map02024,map04727,map04940 | ko00000,ko00001,ko00002,ko01000 | Pyridoxal-dependent decarboxylase conserved domain |
| CBIAAGLN_00435 | 4.01e-240 | - | - | - | E | - | - | - | UDP-4-amino-4-deoxy-L-arabinose aminotransferase |
| CBIAAGLN_00437 | 3.33e-296 | - | - | - | S | ko:K07148 | - | ko00000 | Protein of unknown function (DUF418) |
| CBIAAGLN_00438 | 1.11e-20 | - | - | - | J | ko:K02986 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein S4/S9 N-terminal domain |
| CBIAAGLN_00439 | 2.61e-185 | - | - | - | E | - | - | - | haloacid dehalogenase-like hydrolase |
| CBIAAGLN_00442 | 6.3e-257 | - | - | - | S | ko:K11744 | - | ko00000 | AI-2E family transporter |
| CBIAAGLN_00443 | 3.48e-75 | gph | 3.1.3.18, 3.6.1.1 | - | S | ko:K01091,ko:K06019 | ko00190,ko00630,ko01100,ko01110,ko01130,map00190,map00630,map01100,map01110,map01130 | ko00000,ko00001,ko01000 | glycolate biosynthetic process |
| CBIAAGLN_00444 | 1.88e-32 | - | - | - | E | - | - | - | Amino acid permease |
| CBIAAGLN_00445 | 8.4e-129 | pqqE | - | - | C | ko:K06139 | - | ko00000 | SMART Elongator protein 3 MiaB NifB |
| CBIAAGLN_00446 | 8.96e-268 | pqqE | - | - | C | ko:K06139 | - | ko00000 | SMART Elongator protein 3 MiaB NifB |
| CBIAAGLN_00449 | 0.0 | - | - | - | P | - | - | - | E1-E2 ATPase |
| CBIAAGLN_00450 | 1.35e-46 | - | - | - | K | - | - | - | Helix-turn-helix diphteria tox regulatory element |
| CBIAAGLN_00451 | 0.0 | - | 5.99.1.3 | - | L | ko:K02469 | - | ko00000,ko01000,ko03032,ko03400 | DNA Topoisomerase IV |
| CBIAAGLN_00452 | 1.87e-147 | - | - | - | C | - | - | - | lactate oxidation |
| CBIAAGLN_00462 | 8.74e-34 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00463 | 7.39e-22 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00464 | 1.01e-223 | - | - | - | I | - | - | - | PFAM Prenyltransferase squalene oxidase |
| CBIAAGLN_00465 | 1.81e-59 | - | 3.2.1.23 | - | M | ko:K12308 | ko00052,map00052 | ko00000,ko00001,ko01000 | Belongs to the glycosyl hydrolase 43 family |
| CBIAAGLN_00466 | 1.19e-203 | - | 3.2.1.23 | - | M | ko:K12308 | ko00052,map00052 | ko00000,ko00001,ko01000 | Belongs to the glycosyl hydrolase 43 family |
| CBIAAGLN_00468 | 1.5e-37 | thiL | 2.7.4.16 | - | H | ko:K00946 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 |
| CBIAAGLN_00469 | 0.0 | - | - | - | I | - | - | - | Acetyltransferase (GNAT) domain |
| CBIAAGLN_00470 | 4.48e-38 | - | - | - | I | - | - | - | Acetyltransferase (GNAT) domain |
| CBIAAGLN_00474 | 3.62e-235 | - | - | - | P | - | - | - | Sulfatase |
| CBIAAGLN_00475 | 3.8e-123 | - | - | - | P | ko:K02051 | - | ko00000,ko00002,ko02000 | NMT1/THI5 like |
| CBIAAGLN_00476 | 2.03e-180 | - | - | - | P | ko:K02049 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| CBIAAGLN_00477 | 3.23e-174 | - | - | - | P | ko:K02050 | - | ko00000,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| CBIAAGLN_00478 | 1.03e-143 | poxB | 1.2.3.3, 1.2.5.1 | - | EH | ko:K00156,ko:K00158 | ko00620,ko01100,map00620,map01100 | ko00000,ko00001,ko01000 | Thiamine pyrophosphate enzyme, central domain |
| CBIAAGLN_00479 | 3.48e-80 | 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) |
| CBIAAGLN_00480 | 1.19e-227 | 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) |
| CBIAAGLN_00481 | 7.15e-16 | - | - | - | M | - | - | - | NPCBM/NEW2 domain |
| CBIAAGLN_00482 | 0.0 | - | - | - | M | ko:K04744 | - | ko00000,ko02000 | involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane |
| CBIAAGLN_00483 | 1.04e-26 | - | 2.7.1.11, 2.7.1.90 | - | G | ko:K21071 | ko00010,ko00030,ko00051,ko00052,ko00680,ko01100,ko01110,ko01120,ko01130,map00010,map00030,map00051,map00052,map00680,map01100,map01110,map01120,map01130 | ko00000,ko00001,ko01000 | Phosphofructokinase |
| CBIAAGLN_00484 | 1.96e-219 | - | - | - | L | - | - | - | Membrane |
| CBIAAGLN_00485 | 3.87e-60 | zupT | - | - | P | ko:K07238 | - | ko00000,ko02000 | transporter |
| CBIAAGLN_00486 | 9.71e-91 | zupT | - | - | P | ko:K07238 | - | ko00000,ko02000 | transporter |
| CBIAAGLN_00487 | 6.14e-57 | - | - | - | CO | - | - | - | Protein of unknown function, DUF255 |
| CBIAAGLN_00488 | 9.23e-62 | - | - | - | V | - | - | - | Type II restriction enzyme, methylase subunits |
| CBIAAGLN_00489 | 7.39e-87 | - | - | - | V | - | - | - | DNA modification |
| CBIAAGLN_00490 | 2.62e-16 | - | - | - | V | - | - | - | Type II restriction enzyme, methylase |
| CBIAAGLN_00492 | 2.62e-146 | - | - | - | E | ko:K02035,ko:K15580 | ko01501,ko02010,ko02024,map01501,map02010,map02024 | ko00000,ko00001,ko00002,ko02000 | transmembrane transport |
| CBIAAGLN_00493 | 3.61e-288 | - | - | - | E | ko:K02035,ko:K15580 | ko01501,ko02010,ko02024,map01501,map02010,map02024 | ko00000,ko00001,ko00002,ko02000 | transmembrane transport |
| CBIAAGLN_00495 | 9.04e-317 | nuoN | 1.6.5.3 | - | C | ko:K00343 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient |
| CBIAAGLN_00496 | 1.76e-235 | - | 1.6.5.3 | - | C | ko:K00342 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | Proton-conducting membrane transporter |
| CBIAAGLN_00497 | 8.61e-54 | himA | - | - | L | ko:K03530,ko:K04764,ko:K05788 | - | ko00000,ko03032,ko03036,ko03400 | regulation of translation |
| CBIAAGLN_00498 | 4.01e-71 | - | - | - | S | - | - | - | Phage terminase large subunit (GpA) |
| CBIAAGLN_00503 | 1.55e-49 | - | - | - | G | - | - | - | Major Facilitator Superfamily |
| CBIAAGLN_00504 | 1.61e-79 | - | - | - | M | - | - | - | PFAM YD repeat-containing protein |
| CBIAAGLN_00507 | 1.1e-86 | - | - | - | D | ko:K03466 | - | ko00000,ko03036 | Ftsk_gamma |
| CBIAAGLN_00509 | 2.76e-147 | - | - | - | J | - | - | - | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins |
| CBIAAGLN_00511 | 1.55e-27 | - | 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 |
| CBIAAGLN_00512 | 6.98e-80 | - | - | - | FG | ko:K02503 | - | ko00000,ko04147 | HIT domain |
| CBIAAGLN_00513 | 7.11e-31 | - | - | - | S | ko:K07040 | - | ko00000 | Uncharacterized ACR, COG1399 |
| CBIAAGLN_00514 | 3.93e-57 | - | - | - | S | ko:K07040 | - | ko00000 | Uncharacterized ACR, COG1399 |
| CBIAAGLN_00515 | 2.17e-35 | rpmF | - | - | J | ko:K02911 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011,ko03029 | Belongs to the bacterial ribosomal protein bL32 family |
| CBIAAGLN_00516 | 3.74e-224 | 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 |
| CBIAAGLN_00518 | 0.0 | murB | - | - | M | - | - | - | UDP-N-acetylenolpyruvoylglucosamine reductase, C-terminal domain |
| CBIAAGLN_00519 | 3.05e-69 | - | - | - | S | ko:K07126 | - | ko00000 | beta-lactamase activity |
| CBIAAGLN_00520 | 0.0 | - | - | - | S | ko:K07126 | - | ko00000 | beta-lactamase activity |
| CBIAAGLN_00521 | 8.85e-15 | - | 2.8.1.7, 4.4.1.16 | - | E | ko:K11717 | ko00450,ko01100,map00450,map01100 | ko00000,ko00001,ko01000 | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine |
| CBIAAGLN_00522 | 0.0 | - | - | - | S | - | - | - | acetyltransferases and hydrolases with the alpha beta hydrolase fold |
| CBIAAGLN_00523 | 3.89e-90 | - | - | - | S | ko:K01128 | - | ko00000,ko01000 | acid phosphatase activity |
| CBIAAGLN_00527 | 1.28e-180 | - | - | - | S | - | - | - | Uncharacterized protein conserved in bacteria (DUF2219) |
| CBIAAGLN_00530 | 7.65e-63 | - | 3.6.4.12 | - | L | ko:K03654 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03400 | RecQ zinc-binding |
| CBIAAGLN_00532 | 4.24e-264 | - | - | - | M | - | - | - | Glycosyl transferases group 1 |
| CBIAAGLN_00534 | 1.1e-41 | - | - | - | S | - | - | - | NAD-specific glutamate dehydrogenase |
| CBIAAGLN_00535 | 2.96e-265 | - | - | - | M | - | - | - | Glycosyl transferase 4-like domain |
| CBIAAGLN_00537 | 4.02e-31 | - | - | - | K | - | - | - | bacterial-type RNA polymerase transcription factor activity, metal ion regulated sequence-specific DNA binding |
| CBIAAGLN_00538 | 2.03e-26 | - | - | - | K | - | - | - | bacterial-type RNA polymerase transcription factor activity, metal ion regulated sequence-specific DNA binding |
| CBIAAGLN_00539 | 3e-229 | - | - | - | C | - | - | - | Aldo/keto reductase family |
| CBIAAGLN_00543 | 3.66e-113 | hisI | 3.5.4.19 | - | E | ko:K01496 | ko00340,ko01100,ko01110,ko01230,map00340,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | Phosphoribosyl-AMP cyclohydrolase |
| CBIAAGLN_00544 | 1.27e-223 | - | 2.7.7.7 | - | L | ko:K02341 | ko00230,ko00240,ko01100,ko03030,ko03430,ko03440,map00230,map00240,map01100,map03030,map03430,map03440 | ko00000,ko00001,ko00002,ko01000,ko03032,ko03400 | DNA polymerase III, delta subunit |
| CBIAAGLN_00545 | 4e-12 | - | 3.2.2.28 | - | L | ko:K03649 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | G/U mismatch-specific uracil-DNA glycosylase activity |
| CBIAAGLN_00546 | 6.82e-74 | rplR | - | - | J | ko:K02881 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance |
| CBIAAGLN_00547 | 1.95e-86 | rplF | - | - | J | ko:K02933 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center |
| CBIAAGLN_00548 | 3.89e-81 | rpsH | - | - | J | ko:K02994 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit |
| CBIAAGLN_00549 | 5.36e-138 | rplE | - | - | J | ko:K02931 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits |
| CBIAAGLN_00550 | 1.53e-47 | rplX | - | - | J | ko:K02895 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal proteins 50S L24/mitochondrial 39S L24 |
| CBIAAGLN_00551 | 3.97e-26 | supH | - | - | Q | - | - | - | phosphatase activity |
| CBIAAGLN_00553 | 5.49e-85 | nuoA | 1.6.5.3 | - | C | ko:K00330 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient |
| CBIAAGLN_00557 | 0.0 | - | 3.2.1.52 | GH20 | G | ko:K12373 | ko00511,ko00513,ko00520,ko00531,ko00603,ko00604,ko01100,ko04142,map00511,map00513,map00520,map00531,map00603,map00604,map01100,map04142 | ko00000,ko00001,ko00002,ko01000,ko03110 | Glycoside hydrolase, family 20, catalytic core |
| CBIAAGLN_00559 | 1.22e-178 | proC | 1.5.1.2 | - | E | ko:K00286 | ko00330,ko01100,ko01110,ko01130,ko01230,map00330,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Pyrroline-5-carboxylate reductase dimerisation |
| CBIAAGLN_00562 | 3.8e-60 | - | - | - | C | ko:K19265 | - | ko00000,ko01000 | Aldo/keto reductase family |
| CBIAAGLN_00563 | 2.31e-205 | hppA | 3.6.1.1 | - | C | ko:K15987 | ko00190,map00190 | ko00000,ko00001,ko01000 | Sodium pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for Na( ) movement across the membrane |
| CBIAAGLN_00565 | 6.15e-26 | - | 1.8.1.4 | - | C | ko:K00382 | ko00010,ko00020,ko00260,ko00280,ko00620,ko00630,ko00640,ko01100,ko01110,ko01120,ko01130,ko01200,map00010,map00020,map00260,map00280,map00620,map00630,map00640,map01100,map01110,map01120,map01130,map01200 | br01601,ko00000,ko00001,ko00002,ko01000,ko04147 | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain |
| CBIAAGLN_00566 | 1.74e-274 | - | 1.8.1.4 | - | C | ko:K00382 | ko00010,ko00020,ko00260,ko00280,ko00620,ko00630,ko00640,ko01100,ko01110,ko01120,ko01130,ko01200,map00010,map00020,map00260,map00280,map00620,map00630,map00640,map01100,map01110,map01120,map01130,map01200 | br01601,ko00000,ko00001,ko00002,ko01000,ko04147 | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain |
| CBIAAGLN_00567 | 3.05e-171 | - | 3.5.4.28, 3.5.4.31 | - | F | ko:K12960 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko01000 | Amidohydrolase family |
| CBIAAGLN_00568 | 4.1e-160 | hyl | 2.3.1.48, 3.2.1.169, 3.2.1.35 | GH84 | G | ko:K01197,ko:K15719 | ko00531,ko01100,ko04931,map00531,map01100,map04931 | ko00000,ko00001,ko00002,ko00536,ko00537,ko01000,ko02042 | beta-N-acetylhexosaminidase activity |
| CBIAAGLN_00570 | 4.25e-232 | - | 5.1.3.2 | - | M | ko:K01784 | ko00052,ko00520,ko01100,map00052,map00520,map01100 | ko00000,ko00001,ko00002,ko01000 | NmrA-like family |
| CBIAAGLN_00571 | 2.33e-62 | - | - | - | V | ko:K18095 | ko01501,ko02020,map01501,map02020 | ko00000,ko00001,ko00002,ko01504,ko02000 | AcrB/AcrD/AcrF family |
| CBIAAGLN_00572 | 0.0 | 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 |
| CBIAAGLN_00573 | 2.37e-221 | - | - | - | S | ko:K02238 | - | ko00000,ko00002,ko02044 | Competence protein |
| CBIAAGLN_00574 | 6.64e-81 | - | - | - | IQ | - | - | - | Enoyl-(Acyl carrier protein) reductase |
| CBIAAGLN_00575 | 7.11e-12 | - | - | - | IQ | - | - | - | Enoyl-(Acyl carrier protein) reductase |
| CBIAAGLN_00580 | 5.99e-267 | - | - | - | K | - | - | - | Periplasmic binding protein-like domain |
| CBIAAGLN_00581 | 1.32e-161 | 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 |
| CBIAAGLN_00583 | 2.65e-81 | - | - | - | P | ko:K03499 | - | ko00000,ko02000 | TrkA-N domain |
| CBIAAGLN_00584 | 3.03e-167 | - | 3.6.4.13 | - | L | ko:K03578 | - | ko00000,ko01000 | Oligonucleotide/oligosaccharide-binding (OB)-fold |
| CBIAAGLN_00585 | 9.84e-255 | - | 3.6.4.13 | - | L | ko:K03578 | - | ko00000,ko01000 | Oligonucleotide/oligosaccharide-binding (OB)-fold |
| CBIAAGLN_00586 | 1.09e-59 | - | - | - | S | ko:K08998 | - | ko00000 | Haemolytic |
| CBIAAGLN_00587 | 4.03e-75 | - | 3.1.26.5 | - | J | ko:K03536 | - | ko00000,ko01000,ko03016 | Ribonuclease P |
| CBIAAGLN_00588 | 1.1e-34 | - | - | - | J | ko:K02914 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L34 |
| CBIAAGLN_00589 | 5.08e-261 | glnA | 6.3.1.2 | - | S | ko:K01915 | ko00220,ko00250,ko00630,ko00910,ko01100,ko01120,ko01230,ko02020,ko04217,ko04724,ko04727,map00220,map00250,map00630,map00910,map01100,map01120,map01230,map02020,map04217,map04724,map04727 | ko00000,ko00001,ko01000,ko04147 | glutamine synthetase |
| CBIAAGLN_00592 | 8.25e-273 | - | - | - | S | - | - | - | Phosphotransferase enzyme family |
| CBIAAGLN_00593 | 1.33e-168 | - | - | - | JM | - | - | - | Nucleotidyl transferase |
| CBIAAGLN_00595 | 3.95e-17 | pgk | 2.7.2.3 | - | G | ko:K00927 | ko00010,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00010,map00710,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000,ko04147 | Phosphoglycerate kinase |
| CBIAAGLN_00596 | 1.71e-244 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00597 | 1.09e-204 | - | 3.2.1.20 | GH31 | G | ko:K01187 | ko00052,ko00500,ko01100,map00052,map00500,map01100 | ko00000,ko00001,ko01000 | myo-inosose-2 dehydratase activity |
| CBIAAGLN_00599 | 5.99e-157 | - | - | - | CO | - | - | - | Thioredoxin-like |
| CBIAAGLN_00600 | 2.38e-236 | - | - | - | CO | - | - | - | Thioredoxin-like |
| CBIAAGLN_00601 | 4.62e-155 | - | 3.2.1.23 | - | G | ko:K01190 | ko00052,ko00511,ko00600,ko01100,map00052,map00511,map00600,map01100 | ko00000,ko00001,ko01000 | Domain of unknown function (DUF4982) |
| CBIAAGLN_00602 | 1.87e-215 | 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 |
| CBIAAGLN_00604 | 7.97e-108 | - | 2.2.1.6 | - | E | ko:K01653 | ko00290,ko00650,ko00660,ko00770,ko01100,ko01110,ko01130,ko01210,ko01230,map00290,map00650,map00660,map00770,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | ACT domain |
| CBIAAGLN_00605 | 5.04e-148 | - | - | - | O | - | - | - | Trypsin |
| CBIAAGLN_00611 | 3.37e-224 | - | - | - | M | - | - | - | D-alanyl-D-alanine carboxypeptidase |
| CBIAAGLN_00612 | 1.35e-21 | - | - | - | U | ko:K03561 | - | ko00000,ko02000 | MotA/TolQ/ExbB proton channel family |
| CBIAAGLN_00613 | 2.07e-149 | nth | 4.2.99.18 | - | L | ko:K10773 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate |
| CBIAAGLN_00614 | 1.39e-157 | - | - | - | S | - | - | - | 3D domain |
| CBIAAGLN_00615 | 2.83e-303 | - | - | - | M | ko:K07267 | - | ko00000,ko02000 | wide pore channel activity |
| CBIAAGLN_00616 | 1.71e-170 | - | - | - | O | - | - | - | Trypsin-like peptidase domain |
| CBIAAGLN_00617 | 4.43e-272 | - | - | - | O | - | - | - | Domain present in PSD-95, Dlg, and ZO-1/2. |
| CBIAAGLN_00618 | 1.84e-272 | cobD | 2.6.1.9, 2.7.7.74, 4.1.1.81 | - | M | ko:K00817,ko:K04720,ko:K07281 | ko00340,ko00350,ko00360,ko00400,ko00401,ko00562,ko00860,ko00960,ko01100,ko01110,ko01130,ko01230,map00340,map00350,map00360,map00400,map00401,map00562,map00860,map00960,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | nucleotidyl transferase |
| CBIAAGLN_00621 | 1.04e-154 | - | - | - | J | ko:K05541 | - | 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 |
| CBIAAGLN_00622 | 2.79e-171 | - | 1.17.7.4 | - | IM | ko:K03527 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | LytB protein |
| CBIAAGLN_00623 | 5.02e-89 | - | 1.17.7.4 | - | IM | ko:K03527 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | LytB protein |
| CBIAAGLN_00624 | 5.47e-243 | 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 |
| CBIAAGLN_00625 | 0.0 | - | - | - | V | - | - | - | ABC-2 type transporter |
| CBIAAGLN_00632 | 7.29e-60 | csoR | - | - | S | ko:K21600 | - | ko00000,ko03000 | negative regulation of transcription, DNA-templated |
| CBIAAGLN_00633 | 4.53e-22 | - | - | - | S | - | - | - | Acetyltransferase (GNAT) domain |
| CBIAAGLN_00634 | 4.52e-307 | - | - | - | C | - | - | - | Sulfatase-modifying factor enzyme 1 |
| CBIAAGLN_00635 | 4.37e-115 | - | 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 | KR domain |
| CBIAAGLN_00636 | 7.4e-178 | 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 |
| CBIAAGLN_00637 | 8.98e-138 | - | 4.2.99.20 | - | I | ko:K08680 | ko00130,ko01100,ko01110,map00130,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Alpha/beta hydrolase family |
| CBIAAGLN_00638 | 1.46e-75 | - | - | - | S | ko:K09954 | - | ko00000 | Putative quorum-sensing-regulated virulence factor |
| CBIAAGLN_00640 | 1.45e-50 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00641 | 4.19e-133 | - | - | - | S | - | - | - | Protein of unknown function (DUF2589) |
| CBIAAGLN_00642 | 2.2e-131 | - | - | - | E | ko:K02035,ko:K15580 | ko01501,ko02010,ko02024,map01501,map02010,map02024 | ko00000,ko00001,ko00002,ko02000 | transmembrane transport |
| CBIAAGLN_00643 | 1.95e-267 | - | - | - | S | - | - | - | tRNA-splicing ligase RtcB |
| CBIAAGLN_00646 | 4.87e-31 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00647 | 7.64e-193 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00648 | 9.46e-20 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00649 | 6.77e-129 | - | - | - | C | - | - | - | Na+/H+ antiporter family |
| CBIAAGLN_00650 | 1.64e-97 | - | - | - | S | - | - | - | Responsible for the incorporation of O-acetyl groups into the enterobacterial common antigen (ECA) trisaccharide repeat units |
| CBIAAGLN_00651 | 1.85e-304 | - | 1.1.1.42 | - | C | ko:K00031 | ko00020,ko00480,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko01210,ko01230,ko04146,map00020,map00480,map00720,map01100,map01110,map01120,map01130,map01200,map01210,map01230,map04146 | br01601,ko00000,ko00001,ko00002,ko01000 | Isocitrate/isopropylmalate dehydrogenase |
| CBIAAGLN_00652 | 4.2e-14 | - | - | - | S | - | - | - | Protein of unknown function (DUF4230) |
| CBIAAGLN_00653 | 0.0 | - | 3.2.1.20 | GH31 | G | ko:K01187 | ko00052,ko00500,ko01100,map00052,map00500,map01100 | ko00000,ko00001,ko01000 | Glycosyl hydrolases family 31 |
| CBIAAGLN_00658 | 3.14e-65 | - | 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 |
| CBIAAGLN_00660 | 9.05e-85 | acpS | 2.7.8.7 | - | I | ko:K00997 | ko00770,map00770 | ko00000,ko00001,ko01000 | 4'-phosphopantetheinyl transferase superfamily |
| CBIAAGLN_00661 | 2.6e-130 | pdxJ | 2.6.99.2 | - | H | ko:K03474 | ko00750,ko01100,map00750,map01100 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate |
| CBIAAGLN_00662 | 9.28e-53 | - | 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 |
| CBIAAGLN_00663 | 1.35e-142 | - | 2.7.8.5 | - | I | ko:K00995 | ko00564,ko01100,map00564,map01100 | ko00000,ko00001,ko01000 | CDP-alcohol phosphatidyltransferase |
| CBIAAGLN_00664 | 9.88e-113 | - | - | - | L | - | - | - | SNF2 family N-terminal domain |
| CBIAAGLN_00665 | 1.88e-44 | - | - | - | M | ko:K06077 | - | ko00000 | Glycine zipper 2TM domain |
| CBIAAGLN_00666 | 3.37e-26 | - | - | - | M | ko:K06077 | - | ko00000 | Glycine zipper 2TM domain |
| CBIAAGLN_00667 | 2.8e-230 | - | 5.1.3.3 | - | G | ko:K01785 | ko00010,ko00052,ko01100,ko01110,ko01120,ko01130,map00010,map00052,map01100,map01110,map01120,map01130 | ko00000,ko00001,ko00002,ko01000 | Converts alpha-aldose to the beta-anomer |
| CBIAAGLN_00668 | 4.74e-67 | - | - | - | P | ko:K02039 | - | ko00000 | PhoU domain |
| CBIAAGLN_00670 | 0.0 | - | - | - | E | - | - | - | Aminotransferase class I and II |
| CBIAAGLN_00671 | 4.64e-70 | - | 1.97.1.4 | - | C | ko:K04069 | - | ko00000,ko01000 | 4Fe-4S single cluster domain |
| CBIAAGLN_00672 | 1.09e-49 | - | 1.97.1.4 | - | C | ko:K04069 | - | ko00000,ko01000 | 4Fe-4S single cluster domain |
| CBIAAGLN_00673 | 7.39e-256 | - | 2.3.1.241 | - | M | ko:K02517 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01005 | Glycosyltransferase family 9 (heptosyltransferase) |
| CBIAAGLN_00676 | 0.0 | - | 4.1.1.3 | - | C | ko:K01572 | ko00620,ko01100,map00620,map01100 | ko00000,ko00001,ko01000,ko02000 | Na+-transporting oxaloacetate decarboxylase beta subunit |
| CBIAAGLN_00677 | 6.41e-180 | - | - | - | S | - | - | - | Integral membrane protein (intg_mem_TP0381) |
| CBIAAGLN_00679 | 0.0 | gidA | - | - | D | ko:K03495 | - | ko00000,ko03016,ko03036 | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 |
| CBIAAGLN_00681 | 2.36e-116 | ybeY | - | - | S | ko:K07042 | - | ko00000,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 |
| CBIAAGLN_00682 | 3.04e-278 | - | - | - | S | ko:K07037 | - | ko00000 | 7TM receptor with intracellular HD hydrolase |
| CBIAAGLN_00686 | 5.03e-121 | - | - | - | T | - | - | - | Bacterial regulatory protein, Fis family |
| CBIAAGLN_00687 | 8.89e-171 | - | - | - | O | - | - | - | C-terminal four TMM region of protein-O-mannosyltransferase |
| CBIAAGLN_00689 | 2.27e-148 | - | - | - | MU | ko:K18139 | ko01501,ko02024,map01501,map02024 | ko00000,ko00001,ko00002,ko01504,ko02000 | Outer membrane efflux protein |
| CBIAAGLN_00691 | 1.21e-58 | - | - | - | V | ko:K03296 | - | ko00000 | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family |
| CBIAAGLN_00693 | 7.19e-45 | - | - | - | T | - | - | - | PAS domain |
| CBIAAGLN_00694 | 9.17e-135 | - | - | - | T | - | - | - | PAS domain |
| CBIAAGLN_00695 | 3.12e-93 | - | - | - | S | ko:K07107 | - | ko00000,ko01000 | Thioesterase superfamily |
| CBIAAGLN_00698 | 8.84e-245 | - | - | - | S | - | - | - | Glycosyltransferase like family 2 |
| CBIAAGLN_00699 | 3.85e-18 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00700 | 4.95e-70 | - | - | - | S | - | - | - | Flavodoxin-like fold |
| CBIAAGLN_00701 | 7.97e-113 | - | - | - | K | ko:K13640 | - | ko00000,ko03000 | bacterial-type RNA polymerase transcription factor activity, metal ion regulated sequence-specific DNA binding |
| CBIAAGLN_00702 | 1.11e-100 | - | - | - | G | - | - | - | single-species biofilm formation |
| CBIAAGLN_00703 | 8.62e-50 | - | 3.2.1.1 | GH13 | G | ko:K01176 | ko00500,ko01100,ko04973,map00500,map01100,map04973 | ko00000,ko00001,ko01000 | Alpha amylase, catalytic domain |
| CBIAAGLN_00705 | 3.18e-214 | - | - | - | S | - | - | - | Phosphotransferase enzyme family |
| CBIAAGLN_00706 | 9.44e-22 | - | - | - | S | ko:K07071 | - | ko00000 | Domain of unknown function (DUF1731) |
| CBIAAGLN_00707 | 1.03e-121 | - | - | - | M | ko:K03098 | - | ko00000,ko04147 | Lipocalin-like domain |
| CBIAAGLN_00708 | 1.35e-236 | - | 1.1.1.86 | - | E | ko:K00053 | ko00290,ko00770,ko01100,ko01110,ko01130,ko01210,ko01230,map00290,map00770,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate |
| CBIAAGLN_00709 | 7.94e-149 | - | 1.11.1.5 | - | P | ko:K00428 | - | ko00000,ko01000 | Di-haem cytochrome c peroxidase |
| CBIAAGLN_00710 | 1.13e-40 | feoA | - | - | P | ko:K04758 | - | ko00000,ko02000 | iron ion homeostasis |
| CBIAAGLN_00711 | 4.02e-48 | feoA | - | - | P | ko:K04758 | - | ko00000,ko02000 | iron ion homeostasis |
| CBIAAGLN_00712 | 2.97e-85 | - | 2.1.1.72 | - | H | ko:K07318 | - | ko00000,ko01000,ko02048 | PFAM D12 class N6 adenine-specific DNA methyltransferase |
| CBIAAGLN_00713 | 9.67e-114 | - | 2.1.1.72 | - | H | ko:K07318 | - | ko00000,ko01000,ko02048 | PFAM D12 class N6 adenine-specific DNA methyltransferase |
| CBIAAGLN_00715 | 7.05e-55 | - | 3.5.4.12 | - | F | ko:K01493 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000,ko02044 | Cytidine and deoxycytidylate deaminase zinc-binding region |
| CBIAAGLN_00716 | 0.0 | - | - | - | EGIP | - | - | - | Phosphate acyltransferases |
| CBIAAGLN_00717 | 2.25e-248 | - | 2.1.1.191 | - | J | ko:K06969 | - | ko00000,ko01000,ko03009 | S-adenosylmethionine-dependent methyltransferase |
| CBIAAGLN_00718 | 4.7e-57 | - | - | - | S | ko:K06960 | - | ko00000 | KH domain |
| CBIAAGLN_00719 | 1.23e-78 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00720 | 1.42e-46 | - | 2.7.13.3 | - | T | ko:K07646 | ko02020,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko02022 | Osmosensitive K+ channel His kinase sensor domain |
| CBIAAGLN_00721 | 6.99e-165 | - | - | - | T | ko:K07667 | ko02020,ko02024,map02020,map02024 | ko00000,ko00001,ko00002,ko02022 | Transcriptional regulatory protein, C terminal |
| CBIAAGLN_00723 | 1.5e-44 | - | 2.7.7.6 | - | K | ko:K03060 | ko00230,ko00240,ko01100,ko03020,map00230,map00240,map01100,map03020 | br01611,ko00000,ko00001,ko00002,ko01000,ko03021,ko03400 | RNA polymerase activity |
| CBIAAGLN_00724 | 1.43e-135 | - | 5.4.99.20 | - | J | ko:K06181 | - | ko00000,ko01000,ko03009 | RNA pseudouridylate synthase |
| CBIAAGLN_00725 | 2.63e-207 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00726 | 0.0 | - | - | - | V | ko:K11085 | ko02010,map02010 | ko00000,ko00001,ko01000,ko02000 | ABC transporter transmembrane region |
| CBIAAGLN_00727 | 2.07e-106 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | - | EH | ko:K01665,ko:K03342,ko:K13503,ko:K13950 | ko00400,ko00790,ko01100,ko01110,ko01130,ko01230,map00400,map00790,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | 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 |
| CBIAAGLN_00728 | 8.01e-23 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | - | EH | ko:K01665,ko:K03342,ko:K13503,ko:K13950 | ko00400,ko00790,ko01100,ko01110,ko01130,ko01230,map00400,map00790,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | 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 |
| CBIAAGLN_00729 | 5.97e-145 | - | 4.1.3.38 | - | E | ko:K02619 | ko00790,map00790 | ko00000,ko00001,ko01000 | branched-chain-amino-acid transaminase activity |
| CBIAAGLN_00730 | 0.0 | - | - | - | S | - | - | - | Phage terminase large subunit (GpA) |
| CBIAAGLN_00732 | 2.95e-165 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00734 | 7.25e-55 | - | - | - | S | - | - | - | Bacteriophage head to tail connecting protein |
| CBIAAGLN_00735 | 4.41e-86 | mnmE | - | - | J | 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 |
| CBIAAGLN_00736 | 3.95e-13 | - | - | - | S | - | - | - | Mac 1 |
| CBIAAGLN_00737 | 3.14e-121 | - | - | - | S | - | - | - | UPF0126 domain |
| CBIAAGLN_00738 | 1.13e-222 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00739 | 1.45e-199 | - | - | - | P | - | - | - | Domain of unknown function (DUF4976) |
| CBIAAGLN_00740 | 6.24e-267 | - | - | - | E | - | - | - | FAD dependent oxidoreductase |
| CBIAAGLN_00741 | 1.42e-27 | leuB | 1.1.1.85 | - | CE | 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 |
| CBIAAGLN_00742 | 1.35e-19 | - | - | - | C | ko:K02108 | ko00190,ko00195,ko01100,map00190,map00195,map01100 | ko00000,ko00001,ko00002,ko00194,ko03110 | ATP synthase A chain |
| CBIAAGLN_00743 | 2.57e-07 | - | - | - | S | - | - | - | ATP synthase subunit C |
| CBIAAGLN_00744 | 1.03e-76 | atpF | - | - | C | ko:K02109 | ko00190,ko00195,ko01100,map00190,map00195,map01100 | ko00000,ko00001,ko00002,ko00194 | ATP synthase B/B' CF(0) |
| CBIAAGLN_00745 | 6.46e-86 | - | - | - | C | ko:K02113 | ko00190,ko00195,ko01100,map00190,map00195,map01100 | ko00000,ko00001,ko00002,ko00194 | ATP synthase delta (OSCP) subunit |
| CBIAAGLN_00746 | 2.43e-42 | atpA | 3.6.3.14 | - | C | ko:K02111 | ko00190,ko00195,ko01100,map00190,map00195,map01100 | ko00000,ko00001,ko00002,ko00194,ko01000 | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit |
| CBIAAGLN_00747 | 0.0 | infB | - | - | J | ko:K02519 | - | ko00000,ko03012,ko03029 | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex |
| CBIAAGLN_00750 | 3.09e-122 | - | 3.6.1.55 | - | F | ko:K03574 | - | ko00000,ko01000,ko03400 | NUDIX domain |
| CBIAAGLN_00752 | 3.09e-203 | - | 4.2.3.4 | - | E | ko:K01735 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | 3-dehydroquinate synthase |
| CBIAAGLN_00754 | 1.17e-106 | - | - | - | E | - | - | - | ATPases associated with a variety of cellular activities |
| CBIAAGLN_00756 | 1.05e-20 | - | 2.1.1.13 | - | E | ko:K00548 | ko00270,ko00450,ko00670,ko01100,ko01110,ko01230,map00270,map00450,map00670,map01100,map01110,map01230 | ko00000,ko00001,ko00002,ko01000 | B12 binding domain |
| CBIAAGLN_00761 | 1.46e-15 | - | 3.2.1.22 | - | G | ko:K07407 | ko00052,ko00561,ko00600,ko00603,map00052,map00561,map00600,map00603 | ko00000,ko00001,ko01000 | Glycosyl hydrolase family 36 N-terminal domain |
| CBIAAGLN_00762 | 0.0 | - | - | - | S | - | - | - | Carbohydrate esterase, sialic acid-specific acetylesterase |
| CBIAAGLN_00763 | 4.09e-90 | - | - | - | E | - | - | - | GDSL-like Lipase/Acylhydrolase family |
| CBIAAGLN_00764 | 4.41e-177 | - | - | - | E | - | - | - | GDSL-like Lipase/Acylhydrolase family |
| CBIAAGLN_00766 | 7.75e-100 | - | - | - | M | - | - | - | Bacterial membrane protein, YfhO |
| CBIAAGLN_00768 | 1.2e-85 | - | - | - | S | ko:K09793 | - | ko00000 | Protein of unknown function (DUF456) |
| CBIAAGLN_00769 | 1.8e-203 | - | 3.5.2.6 | - | V | ko:K17836 | ko00311,ko01130,ko01501,map00311,map01130,map01501 | ko00000,ko00001,ko00002,ko01000,ko01504 | Beta-lactamase enzyme family |
| CBIAAGLN_00770 | 4.72e-42 | - | - | - | V | ko:K18095 | ko01501,ko02020,map01501,map02020 | ko00000,ko00001,ko00002,ko01504,ko02000 | AcrB/AcrD/AcrF family |
| CBIAAGLN_00775 | 2.62e-222 | - | - | - | P | ko:K03281 | - | ko00000 | Voltage gated chloride channel |
| CBIAAGLN_00776 | 2.95e-149 | - | - | GT2 | S | ko:K19427 | - | ko00000,ko01000 | PFAM glycosyl transferase family 2 |
| CBIAAGLN_00777 | 1.02e-64 | - | - | GT2 | S | ko:K19427 | - | ko00000,ko01000 | PFAM glycosyl transferase family 2 |
| CBIAAGLN_00782 | 1.14e-72 | - | - | - | S | - | - | - | Glycosyl hydrolase 108 |
| CBIAAGLN_00783 | 1.8e-32 | - | - | - | K | - | - | - | DNA-binding transcription factor activity |
| CBIAAGLN_00784 | 4.83e-228 | - | - | - | J | - | - | - | Belongs to the universal ribosomal protein uS2 family |
| CBIAAGLN_00786 | 7.91e-186 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00787 | 7.21e-183 | - | - | - | S | ko:K09778 | - | ko00000 | Domain of unknown function (DUF374) |
| CBIAAGLN_00790 | 1.55e-194 | - | - | - | M | - | - | - | Glycosyl transferase family group 2 |
| CBIAAGLN_00792 | 1.89e-157 | - | 6.3.2.5 | - | H | ko:K21977 | ko00770,map00770 | ko00000,ko00001,ko00002,ko01000 | DNA / pantothenate metabolism flavoprotein |
| CBIAAGLN_00793 | 4.92e-66 | tmpC | - | - | S | ko:K07335 | - | ko00000 | basic membrane |
| CBIAAGLN_00795 | 8.94e-262 | - | 3.4.11.9 | - | E | ko:K01262 | - | ko00000,ko01000,ko01002 | Aminopeptidase P, N-terminal domain |
| CBIAAGLN_00796 | 4.53e-115 | nudF | 3.6.1.13 | - | L | ko:K01515 | ko00230,map00230 | ko00000,ko00001,ko01000 | nUDIX hydrolase |
| CBIAAGLN_00799 | 2.23e-89 | - | 2.3.1.1 | - | E | ko:K14682 | ko00220,ko01100,ko01110,ko01130,ko01210,ko01230,map00220,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Acetyltransferase (GNAT) family |
| CBIAAGLN_00801 | 5.02e-50 | - | 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 III |
| CBIAAGLN_00802 | 3.9e-144 | - | - | - | M | - | - | - | NLP P60 protein |
| CBIAAGLN_00803 | 1.07e-88 | ftsA | - | - | D | ko:K03590 | ko04112,map04112 | ko00000,ko00001,ko03036,ko04812 | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring |
| CBIAAGLN_00806 | 2.23e-100 | - | - | - | M | - | - | - | Glycosyl transferase family 2 |
| CBIAAGLN_00808 | 2.14e-309 | - | - | - | EGIP | - | - | - | Phosphate acyltransferases |
| CBIAAGLN_00811 | 5.41e-150 | - | - | - | O | - | - | - | Glycoprotease family |
| CBIAAGLN_00812 | 1.54e-289 | 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 |
| CBIAAGLN_00816 | 1.45e-283 | msrA | 1.8.4.11, 1.8.4.12 | - | O | ko:K12267 | - | ko00000,ko01000 | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine |
| CBIAAGLN_00818 | 3.89e-157 | - | - | - | S | - | - | - | Metallo-beta-lactamase superfamily |
| CBIAAGLN_00819 | 6.66e-236 | - | 3.5.2.3 | - | F | ko:K01465 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Amidohydrolase |
| CBIAAGLN_00822 | 3.1e-203 | - | - | - | T | - | - | - | Chase2 domain |
| CBIAAGLN_00823 | 6.81e-163 | - | 2.7.1.221 | - | S | ko:K07102 | ko00520,ko01100,map00520,map01100 | ko00000,ko00001,ko01000 | Phosphotransferase enzyme family |
| CBIAAGLN_00824 | 8.68e-76 | - | - | - | S | - | - | - | Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME) |
| CBIAAGLN_00825 | 7.57e-114 | - | - | - | CO | - | - | - | cell redox homeostasis |
| CBIAAGLN_00828 | 8.3e-160 | - | - | - | T | - | - | - | Transcriptional regulatory protein, C terminal |
| CBIAAGLN_00835 | 2.15e-54 | - | 3.2.2.27 | - | L | ko:K21929 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | Uracil DNA glycosylase superfamily |
| CBIAAGLN_00836 | 1.37e-176 | - | 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 |
| CBIAAGLN_00838 | 4.83e-82 | - | - | - | L | ko:K07460 | - | ko00000 | Uncharacterised protein family UPF0102 |
| CBIAAGLN_00839 | 2.36e-62 | - | 3.1.26.4 | - | L | ko:K03470 | ko03030,map03030 | ko00000,ko00001,ko01000,ko03032 | Ribonuclease HII |
| CBIAAGLN_00841 | 7.42e-125 | - | 2.4.2.8 | - | F | ko:K00760 | ko00230,ko00983,ko01100,ko01110,map00230,map00983,map01100,map01110 | ko00000,ko00001,ko01000 | Phosphoribosyl transferase domain |
| CBIAAGLN_00842 | 0.0 | - | - | - | T | - | - | - | Histidine kinase |
| CBIAAGLN_00850 | 4.56e-255 | - | 2.6.1.66 | - | E | ko:K00835 | ko00290,ko01100,ko01110,ko01130,map00290,map01100,map01110,map01130 | ko00000,ko00001,ko01000,ko01007 | Aminotransferase class I and II |
| CBIAAGLN_00855 | 6.59e-115 | - | - | - | T | - | - | - | pathogenesis |
| CBIAAGLN_00856 | 0.0 | legA | 3.5.1.2 | - | G | ko:K01425 | ko00220,ko00250,ko00471,ko01100,ko04724,ko04727,ko04964,ko05206,ko05230,map00220,map00250,map00471,map01100,map04724,map04727,map04964,map05206,map05230 | ko00000,ko00001,ko01000 | response to abiotic stimulus |
| CBIAAGLN_00857 | 1.8e-71 | - | - | - | V | - | - | - | Abi-like protein |
| CBIAAGLN_00860 | 6.87e-181 | - | 6.3.5.1 | - | H | ko:K01950 | ko00760,ko01100,map00760,map01100 | ko00000,ko00001,ko00002,ko01000 | NAD synthase |
| CBIAAGLN_00861 | 0.0 | - | - | - | I | - | - | - | Acyltransferase family |
| CBIAAGLN_00862 | 8.43e-155 | - | 1.5.1.34 | - | C | ko:K10679 | ko00633,ko01120,map00633,map01120 | ko00000,ko00001,ko01000 | Nitroreductase family |
| CBIAAGLN_00863 | 6.84e-218 | - | 2.6.1.9 | - | E | ko:K00817 | ko00340,ko00350,ko00360,ko00400,ko00401,ko00960,ko01100,ko01110,ko01130,ko01230,map00340,map00350,map00360,map00400,map00401,map00960,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000,ko01007 | Aminotransferase class I and II |
| CBIAAGLN_00864 | 8.16e-202 | - | - | - | O | - | - | - | stress-induced mitochondrial fusion |
| CBIAAGLN_00866 | 0.0 | - | - | - | P | - | - | - | Cation transport protein |
| CBIAAGLN_00870 | 1.44e-68 | - | - | - | V | - | - | - | ATPases associated with a variety of cellular activities |
| CBIAAGLN_00873 | 1.48e-120 | - | - | - | M | ko:K06142 | - | ko00000 | Outer membrane protein (OmpH-like) |
| CBIAAGLN_00874 | 2.31e-194 | panC | 6.3.2.1 | - | H | ko:K01918 | ko00410,ko00770,ko01100,ko01110,map00410,map00770,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate |
| CBIAAGLN_00875 | 3.49e-80 | - | 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 |
| CBIAAGLN_00878 | 4.64e-228 | - | - | - | P | ko:K07239 | - | ko00000 | AcrB/AcrD/AcrF family |
| CBIAAGLN_00879 | 3.44e-146 | - | - | - | K | - | - | - | Bacterial regulatory proteins, tetR family |
| CBIAAGLN_00880 | 1.25e-89 | - | - | - | S | ko:K06925 | - | ko00000,ko03016 | Threonylcarbamoyl adenosine biosynthesis protein TsaE |
| CBIAAGLN_00881 | 3.73e-200 | - | - | - | S | ko:K06889 | - | ko00000 | alpha beta |
| CBIAAGLN_00883 | 9.17e-70 | - | - | - | M | - | - | - | Polymer-forming cytoskeletal |
| CBIAAGLN_00884 | 1.47e-119 | frr | - | - | J | ko:K02838 | - | ko00000,ko03012 | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another |
| CBIAAGLN_00885 | 8.16e-124 | pyrH | 2.7.4.22 | - | F | ko:K09903 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko01000 | Amino acid kinase family |
| CBIAAGLN_00886 | 3.58e-271 | - | - | - | M | - | - | - | 4-amino-4-deoxy-L-arabinose transferase activity |
| CBIAAGLN_00887 | 8.09e-36 | - | - | - | M | - | - | - | 4-amino-4-deoxy-L-arabinose transferase activity |
| CBIAAGLN_00888 | 1.67e-50 | 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) |
| CBIAAGLN_00889 | 5.09e-210 | - | 1.8.1.9 | - | O | ko:K00384 | ko00450,map00450 | ko00000,ko00001,ko01000 | Pyridine nucleotide-disulphide oxidoreductase |
| CBIAAGLN_00891 | 0.0 | yidC | - | - | U | ko:K03217 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044,ko03029 | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins. Aids folding of multispanning membrane proteins |
| CBIAAGLN_00892 | 3.5e-73 | - | 3.4.16.4 | - | M | ko:K03587 | ko00550,ko01501,map00550,map01501 | ko00000,ko00001,ko01000,ko01011,ko03036 | Penicillin-binding Protein dimerisation domain |
| CBIAAGLN_00893 | 1.2e-62 | - | 3.4.16.4 | - | M | ko:K03587 | ko00550,ko01501,map00550,map01501 | ko00000,ko00001,ko01000,ko01011,ko03036 | Penicillin-binding Protein dimerisation domain |
| CBIAAGLN_00895 | 3.2e-131 | - | - | - | M | - | - | - | PFAM YD repeat-containing protein |
| CBIAAGLN_00898 | 1.25e-36 | - | - | - | E | - | - | - | GDSL-like Lipase/Acylhydrolase |
| CBIAAGLN_00902 | 9.92e-230 | - | 4.1.1.35 | - | M | ko:K08678 | ko00520,ko01100,map00520,map01100 | ko00000,ko00001,ko00002,ko01000 | 3-beta hydroxysteroid dehydrogenase/isomerase family |
| CBIAAGLN_00903 | 5.65e-133 | - | - | - | T | - | - | - | His Kinase A (phosphoacceptor) domain |
| CBIAAGLN_00904 | 1.08e-256 | - | - | - | S | - | - | - | Sodium:neurotransmitter symporter family |
| CBIAAGLN_00905 | 1.61e-117 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00907 | 6.17e-81 | - | - | - | S | - | - | - | Protein of unknown function DUF58 |
| CBIAAGLN_00911 | 8.5e-185 | - | 3.6.3.12 | - | P | ko:K01547 | ko02020,map02020 | ko00000,ko00001,ko01000 | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit is responsible for energy coupling to the transport system |
| CBIAAGLN_00913 | 9.22e-49 | - | - | - | S | - | - | - | Protein of unknown function (DUF3313) |
| CBIAAGLN_00914 | 6.74e-124 | lgt | - | - | M | ko:K13292 | - | ko00000,ko01000 | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins |
| CBIAAGLN_00915 | 1.19e-67 | lgt | - | - | M | ko:K13292 | - | ko00000,ko01000 | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins |
| CBIAAGLN_00916 | 1.2e-18 | lgt | - | - | M | ko:K13292 | - | ko00000,ko01000 | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins |
| CBIAAGLN_00917 | 2.43e-116 | - | - | - | G | - | - | - | M42 glutamyl aminopeptidase |
| CBIAAGLN_00921 | 1.92e-238 | - | 3.5.1.28 | - | M | ko:K01448 | ko01503,map01503 | ko00000,ko00001,ko00002,ko01000,ko01011,ko03036 | Ami_3 |
| CBIAAGLN_00922 | 2.87e-69 | 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 |
| CBIAAGLN_00925 | 1.3e-97 | - | 3.5.4.25, 4.1.99.12 | - | H | ko:K14652 | ko00740,ko00790,ko01100,ko01110,map00740,map00790,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | GTP cyclohydrolase II |
| CBIAAGLN_00926 | 1.48e-104 | ribH | 2.5.1.78 | - | H | ko:K00794 | ko00740,ko01100,ko01110,map00740,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin |
| CBIAAGLN_00930 | 7.26e-74 | - | - | - | P | - | - | - | Rhodanese-like domain |
| CBIAAGLN_00931 | 5.57e-86 | - | - | - | S | - | - | - | Protein of unknown function (DUF1573) |
| CBIAAGLN_00932 | 0.0 | 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 C-terminal |
| CBIAAGLN_00934 | 3.92e-158 | - | - | - | EP | ko:K15583 | ko01501,ko02010,ko02024,map01501,map02010,map02024 | ko00000,ko00001,ko00002,ko02000 | Oligopeptide/dipeptide transporter, C-terminal region |
| CBIAAGLN_00935 | 4.51e-148 | cat | 2.3.1.28 | - | V | ko:K19271 | - | br01600,ko00000,ko01000,ko01504 | Chloramphenicol acetyltransferase |
| CBIAAGLN_00936 | 2.89e-48 | - | - | - | V | ko:K02004 | - | ko00000,ko00002,ko02000 | MacB-like periplasmic core domain |
| CBIAAGLN_00937 | 4.44e-27 | - | - | - | E | ko:K07032 | - | ko00000 | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily |
| CBIAAGLN_00939 | 1.61e-26 | - | - | - | C | - | - | - | Cytochrome c |
| CBIAAGLN_00940 | 1.59e-61 | rbr | - | - | C | - | - | - | Rubrerythrin |
| CBIAAGLN_00944 | 8.27e-208 | - | 2.3.1.12 | - | C | ko:K00627 | ko00010,ko00020,ko00620,ko01100,ko01110,ko01120,ko01130,ko01200,map00010,map00020,map00620,map01100,map01110,map01120,map01130,map01200 | br01601,ko00000,ko00001,ko00002,ko01000 | 2-oxoacid dehydrogenases acyltransferase (catalytic domain) |
| CBIAAGLN_00946 | 2.31e-143 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00947 | 1.25e-204 | gpsA | 1.1.1.94 | - | C | ko:K00057 | ko00564,ko01110,map00564,map01110 | ko00000,ko00001,ko01000 | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus |
| CBIAAGLN_00948 | 6.16e-152 | - | 2.3.1.15 | - | I | ko:K08591 | ko00561,ko00564,ko01100,ko01110,map00561,map00564,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko01004 | Glycerol-3-phosphate acyltransferase |
| CBIAAGLN_00949 | 4.7e-50 | - | - | - | S | - | - | - | metallopeptidase activity |
| CBIAAGLN_00950 | 4.54e-284 | - | 5.4.99.22 | - | M | ko:K06178 | - | ko00000,ko01000,ko03009 | translation initiation factor activity |
| CBIAAGLN_00952 | 4.84e-125 | - | 4.1.1.36 | - | H | ko:K01598 | ko00770,ko01100,map00770,map01100 | ko00000,ko00001,ko00002,ko01000 | Flavoprotein |
| CBIAAGLN_00957 | 1.07e-173 | rpoB | 2.7.7.6 | - | K | ko:K03043 | ko00230,ko00240,ko01100,ko03020,map00230,map00240,map01100,map03020 | br01611,ko00000,ko00001,ko00002,ko01000,ko03021,ko03400 | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates |
| CBIAAGLN_00958 | 6.97e-42 | rpoB | 2.7.7.6 | - | K | ko:K03043 | ko00230,ko00240,ko01100,ko03020,map00230,map00240,map01100,map03020 | br01611,ko00000,ko00001,ko00002,ko01000,ko03021,ko03400 | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates |
| CBIAAGLN_00959 | 1.2e-65 | - | - | - | D | ko:K03569 | - | ko00000,ko02048,ko03036,ko04812 | Actin |
| CBIAAGLN_00962 | 3.69e-157 | - | 3.2.1.18 | GH33 | G | ko:K01186 | ko00511,ko00600,ko04142,map00511,map00600,map04142 | ko00000,ko00001,ko01000,ko02042 | N-terminal domain of BNR-repeat neuraminidase |
| CBIAAGLN_00963 | 4.55e-121 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00964 | 4.36e-90 | - | - | - | S | - | - | - | Peptidase family M28 |
| CBIAAGLN_00965 | 3.21e-214 | - | 3.2.1.51 | GH95 | G | ko:K15923 | ko00511,map00511 | ko00000,ko00001,ko01000 | Glycosyl hydrolase family 65, N-terminal domain |
| CBIAAGLN_00966 | 6.39e-71 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00967 | 1.92e-37 | xseA | 3.1.11.6 | - | L | ko:K03601 | ko03430,map03430 | ko00000,ko00001,ko01000,ko03400 | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides |
| CBIAAGLN_00968 | 6.35e-185 | xseA | 3.1.11.6 | - | L | ko:K03601 | ko03430,map03430 | ko00000,ko00001,ko01000,ko03400 | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides |
| CBIAAGLN_00969 | 1.11e-258 | 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 |
| CBIAAGLN_00971 | 1.41e-266 | - | - | - | S | ko:K06889 | - | ko00000 | X-Pro dipeptidyl-peptidase (S15 family) |
| CBIAAGLN_00972 | 1.28e-114 | - | - | - | S | - | - | - | Aldo/keto reductase family |
| CBIAAGLN_00975 | 2.54e-201 | - | - | - | S | - | - | - | SigmaW regulon antibacterial |
| CBIAAGLN_00977 | 1.14e-168 | 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 |
| CBIAAGLN_00978 | 2.98e-45 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00980 | 9.66e-27 | - | - | - | IQ | - | - | - | Short chain dehydrogenase |
| CBIAAGLN_00981 | 1.84e-106 | - | - | - | IQ | - | - | - | Short chain dehydrogenase |
| CBIAAGLN_00982 | 3.53e-57 | - | - | - | C | - | - | - | Carboxymuconolactone decarboxylase family |
| CBIAAGLN_00984 | 2.72e-18 | - | - | - | - | - | - | - | - |
| CBIAAGLN_00985 | 3.15e-95 | - | - | - | P | ko:K07221 | - | ko00000,ko02000 | Phosphate-selective porin O and P |
| CBIAAGLN_00987 | 0.0 | lacZ_17 | 3.2.1.23 | - | G | ko:K01190 | ko00052,ko00511,ko00600,ko01100,map00052,map00511,map00600,map01100 | ko00000,ko00001,ko01000 | beta-galactosidase activity |
| CBIAAGLN_00989 | 3.05e-48 | - | - | - | P | ko:K04759 | - | ko00000,ko02000 | Ferrous iron transport protein B C terminus |
| CBIAAGLN_00990 | 2.3e-194 | - | - | - | P | ko:K04759 | - | ko00000,ko02000 | Ferrous iron transport protein B C terminus |
| CBIAAGLN_00992 | 6.15e-191 | map | 3.4.11.18 | - | J | ko:K01265 | - | ko00000,ko01000,ko01002 | Metallopeptidase family M24 |
| CBIAAGLN_00996 | 5.56e-47 | - | - | - | CO | - | - | - | Redoxin |
| CBIAAGLN_00997 | 6.46e-83 | - | - | - | K | ko:K07343 | - | ko00000 | positive regulation of type IV pilus biogenesis |
| CBIAAGLN_01000 | 1.22e-121 | - | - | - | O | ko:K03695 | ko04213,map04213 | ko00000,ko00001,ko03110 | C-terminal, D2-small domain, of ClpB protein |
| CBIAAGLN_01005 | 1.58e-177 | - | - | - | P | ko:K14445 | - | ko00000,ko02000 | Citrate transporter |
| CBIAAGLN_01006 | 2.85e-136 | - | - | - | V | ko:K03296 | - | ko00000 | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family |
| CBIAAGLN_01007 | 6.67e-67 | - | - | - | NU | ko:K02453 | ko03070,ko05111,map03070,map05111 | ko00000,ko00001,ko00002,ko02044 | Bacterial type II and III secretion system protein |
| CBIAAGLN_01008 | 1.15e-151 | - | - | - | NU | ko:K02453 | ko03070,ko05111,map03070,map05111 | ko00000,ko00001,ko00002,ko02044 | Bacterial type II and III secretion system protein |
| CBIAAGLN_01010 | 5.75e-23 | - | 1.2.1.88, 1.5.5.2 | - | CE | ko:K13821 | ko00250,ko00330,ko01100,ko01110,ko01130,map00250,map00330,map01100,map01110,map01130 | ko00000,ko00001,ko01000,ko03000 | Proline dehydrogenase |
| CBIAAGLN_01011 | 6.39e-115 | - | - | - | J | ko:K02945 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | thus facilitating recognition of the initiation point. It is needed to translate mRNA with a short Shine-Dalgarno (SD) purine-rich sequence |
| CBIAAGLN_01012 | 1.66e-87 | - | - | - | K | ko:K03709 | - | ko00000,ko03000 | iron dependent repressor |
| CBIAAGLN_01013 | 1.1e-159 | - | - | - | K | - | - | - | Bacterial regulatory proteins, tetR family |
| CBIAAGLN_01014 | 1.1e-162 | - | - | - | CO | - | - | - | Thioredoxin-like |
| CBIAAGLN_01015 | 1.04e-272 | - | - | - | S | ko:K11941 | - | ko00000,ko01000 | transferase activity, transferring acyl groups other than amino-acyl groups |
| CBIAAGLN_01017 | 4.85e-257 | - | 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 |
| CBIAAGLN_01020 | 3.23e-121 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01021 | 5.45e-17 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01022 | 1.54e-105 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01023 | 2.43e-81 | pyrD | 1.3.5.2 | - | F | ko:K00254 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Dihydroorotate dehydrogenase |
| CBIAAGLN_01027 | 3.82e-229 | - | - | - | E | - | - | - | PFAM lipolytic protein G-D-S-L family |
| CBIAAGLN_01028 | 0.0 | - | - | - | G | - | - | - | Trehalase |
| CBIAAGLN_01029 | 1.4e-151 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01032 | 1.97e-207 | - | 2.5.1.32, 2.5.1.99 | - | I | ko:K02291 | ko00906,ko01062,ko01100,ko01110,map00906,map01062,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko01006 | Squalene/phytoene synthase |
| CBIAAGLN_01040 | 1.73e-45 | - | - | - | S | - | - | - | inositol 2-dehydrogenase activity |
| CBIAAGLN_01041 | 3.52e-280 | argS | 6.1.1.19 | - | J | ko:K01887 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Arginyl tRNA synthetase N terminal dom |
| CBIAAGLN_01045 | 1.28e-53 | - | 3.6.4.12 | - | L | ko:K03654 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03400 | RQC |
| CBIAAGLN_01047 | 1.56e-169 | - | - | - | S | - | - | - | Metallo-beta-lactamase superfamily |
| CBIAAGLN_01048 | 2.25e-137 | - | - | - | K | ko:K03088 | - | ko00000,ko03021 | DNA-templated transcription, initiation |
| CBIAAGLN_01050 | 1.1e-28 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| CBIAAGLN_01051 | 1.8e-25 | - | - | - | S | - | - | - | Psort location Cytoplasmic, score |
| CBIAAGLN_01052 | 2.52e-23 | - | - | - | L | - | - | - | Protein of unknown function (DUF3849) |
| CBIAAGLN_01053 | 1.23e-39 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01054 | 3.79e-149 | - | - | - | S | - | - | - | Lysin motif |
| CBIAAGLN_01055 | 5.95e-96 | dtd | - | - | J | ko:K07560 | - | ko00000,ko01000,ko03016 | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality |
| CBIAAGLN_01058 | 1.04e-102 | - | - | - | S | - | - | - | Peptidase family M28 |
| CBIAAGLN_01063 | 6.01e-61 | nuoK | 1.6.5.3 | - | C | ko:K00340 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient |
| CBIAAGLN_01064 | 6.57e-59 | - | - | - | S | ko:K06973 | - | ko00000 | Putative neutral zinc metallopeptidase |
| CBIAAGLN_01065 | 4.85e-80 | - | - | - | S | - | - | - | peptidase |
| CBIAAGLN_01066 | 3.17e-56 | - | - | - | S | - | - | - | pathogenesis |
| CBIAAGLN_01069 | 5.01e-46 | - | - | - | 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 |
| CBIAAGLN_01070 | 1.04e-98 | - | 2.1.1.177 | - | J | ko:K00783 | - | ko00000,ko01000,ko03009 | Predicted SPOUT methyltransferase |
| CBIAAGLN_01071 | 4.8e-86 | rpsI | - | - | J | ko:K02996 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein S9/S16 |
| CBIAAGLN_01072 | 1.07e-52 | 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 |
| CBIAAGLN_01073 | 2.16e-270 | - | - | - | G | - | - | - | alpha-galactosidase |
| CBIAAGLN_01074 | 5.26e-78 | - | - | - | G | - | - | - | alpha-galactosidase |
| CBIAAGLN_01078 | 6.18e-108 | - | 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 |
| CBIAAGLN_01079 | 5.27e-71 | - | 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-bisphosphate aldolase class-II |
| CBIAAGLN_01080 | 9.24e-212 | - | - | - | T | ko:K06207 | - | ko00000 | Elongation factor G C-terminus |
| CBIAAGLN_01083 | 9.89e-66 | tagD | 2.7.7.39 | - | H | ko:K00980 | ko00564,map00564 | ko00000,ko00001,ko01000 | Glycerol-3-phosphate cytidylyltransferase |
| CBIAAGLN_01084 | 1.24e-45 | - | - | - | M | ko:K07271 | - | ko00000,ko01000 | LicD family |
| CBIAAGLN_01085 | 1.17e-49 | - | - | - | S | - | - | - | protein trimerization |
| CBIAAGLN_01086 | 1.14e-160 | - | - | - | L | ko:K03701 | ko03420,map03420 | ko00000,ko00001,ko03400 | ATPases associated with a variety of cellular activities |
| CBIAAGLN_01088 | 9.16e-111 | aglS | - | - | U | ko:K03559 | - | ko00000,ko02000 | biopolymer transport protein |
| CBIAAGLN_01089 | 1.24e-98 | exbD2 | - | - | U | ko:K03559 | - | ko00000,ko02000 | biopolymer transport protein |
| CBIAAGLN_01090 | 1.97e-127 | - | 3.4.11.10, 3.4.11.6 | - | DZ | ko:K19701 | - | ko00000,ko01000,ko01002 | aminopeptidase activity |
| CBIAAGLN_01091 | 4.1e-209 | ycaD | - | - | EGP | ko:K08219 | - | ko00000,ko02000 | Major facilitator Superfamily |
| CBIAAGLN_01094 | 2.97e-266 | - | - | - | K | - | - | - | sequence-specific DNA binding |
| CBIAAGLN_01095 | 4.27e-90 | - | - | - | J | ko:K08301 | - | ko00000,ko01000,ko03009,ko03019 | Ribonuclease E/G family |
| CBIAAGLN_01097 | 2.67e-111 | - | - | - | KT | ko:K07705 | ko02020,map02020 | ko00000,ko00001,ko00002,ko02022 | phosphorelay signal transduction system |
| CBIAAGLN_01098 | 2.59e-174 | - | - | - | S | - | - | - | Protein of unknown function (DUF2589) |
| CBIAAGLN_01099 | 1.04e-49 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01100 | 1.45e-55 | rpmB | - | - | J | ko:K02902 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal L28 family |
| CBIAAGLN_01102 | 0.0 | - | - | - | C | - | - | - | Di-haem oxidoreductase, putative peroxidase |
| CBIAAGLN_01104 | 2.35e-92 | - | 3.1.13.5 | - | J | ko:K03684 | - | ko00000,ko01000,ko03016 | 3'-5' exonuclease |
| CBIAAGLN_01107 | 2.54e-214 | - | - | - | G | - | - | - | Alpha-N-acetylglucosaminidase (NAGLU) C-terminal domain |
| CBIAAGLN_01111 | 3.91e-227 | - | - | - | NU | ko:K02653 | - | ko00000,ko02035,ko02044 | Type II secretion system (T2SS), protein F |
| CBIAAGLN_01114 | 2.9e-54 | - | - | - | P | ko:K02014 | - | ko00000,ko02000 | TonB dependent receptor |
| CBIAAGLN_01115 | 2.4e-120 | - | - | - | V | ko:K02003 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| CBIAAGLN_01117 | 1.32e-127 | - | 2.1.3.15, 6.4.1.3 | - | I | ko:K01966 | ko00280,ko00630,ko00640,ko01100,ko01120,ko01130,ko01200,map00280,map00630,map00640,map01100,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | Carboxyl transferase domain |
| CBIAAGLN_01119 | 3.52e-53 | - | - | - | I | - | - | - | PFAM biotin lipoyl attachment domain-containing protein |
| CBIAAGLN_01121 | 4.37e-135 | - | - | - | T | - | - | - | histone H2A K63-linked ubiquitination |
| CBIAAGLN_01123 | 6.15e-176 | - | - | - | O | ko:K04083 | - | ko00000,ko03110 | Hsp33 protein |
| CBIAAGLN_01125 | 2.37e-142 | wbyL | - | GT2 | M | ko:K13002 | - | ko00000,ko01000,ko01003,ko01005 | transferase activity, transferring glycosyl groups |
| CBIAAGLN_01126 | 1.17e-20 | wbyL | - | GT2 | M | ko:K13002 | - | ko00000,ko01000,ko01003,ko01005 | transferase activity, transferring glycosyl groups |
| CBIAAGLN_01127 | 6.21e-39 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01132 | 3.95e-275 | - | 3.1.5.1 | - | F | ko:K01129 | ko00230,map00230 | ko00000,ko00001,ko01000 | Phosphohydrolase-associated domain |
| CBIAAGLN_01133 | 8.88e-32 | - | 2.7.13.3 | - | T | ko:K07646 | ko02020,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko02022 | Osmosensitive K+ channel His kinase sensor domain |
| CBIAAGLN_01134 | 7.92e-84 | - | 2.7.13.3 | - | T | ko:K07646 | ko02020,map02020 | ko00000,ko00001,ko00002,ko01000,ko01001,ko02022 | Osmosensitive K+ channel His kinase sensor domain |
| CBIAAGLN_01135 | 4.93e-66 | - | - | - | S | - | - | - | PFAM glycosyl transferase family 2 |
| CBIAAGLN_01136 | 1.6e-127 | - | 3.5.1.124 | - | S | ko:K03152 | - | ko00000,ko01000,ko01002 | DJ-1/PfpI family |
| CBIAAGLN_01137 | 7.91e-96 | - | - | - | C | - | - | - | e3 binding domain |
| CBIAAGLN_01139 | 4.06e-78 | - | - | - | - | ko:K11891,ko:K16091 | ko02025,ko03070,map02025,map03070 | ko00000,ko00001,ko00002,ko02000,ko02044 | - |
| CBIAAGLN_01141 | 9.9e-121 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01142 | 1.44e-85 | - | - | - | H | ko:K22132 | - | ko00000,ko03016 | ThiF family |
| CBIAAGLN_01144 | 3.34e-36 | - | - | - | G | - | - | - | Polysaccharide deacetylase |
| CBIAAGLN_01148 | 6.42e-101 | rplO | - | - | J | ko:K02876 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal proteins 50S-L15, 50S-L18e, 60S-L27A |
| CBIAAGLN_01149 | 2.47e-37 | rpsE | - | - | J | ko:K02988 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body |
| CBIAAGLN_01150 | 1.12e-290 | hyaC | - | - | C | ko:K03620 | ko02020,map02020 | ko00000,ko00001 | Prokaryotic cytochrome b561 |
| CBIAAGLN_01153 | 4.32e-53 | - | 1.1.1.40 | - | C | ko:K00029 | ko00620,ko00710,ko01100,ko01120,ko01200,map00620,map00710,map01100,map01120,map01200 | ko00000,ko00001,ko00002,ko01000 | Malic enzyme, NAD binding domain |
| CBIAAGLN_01157 | 3.95e-169 | - | 2.1.1.144, 2.1.1.197 | - | FG | ko:K00598,ko:K02169 | ko00780,ko01100,map00780,map01100 | ko00000,ko00001,ko00002,ko01000 | trans-aconitate 2-methyltransferase activity |
| CBIAAGLN_01158 | 4.42e-95 | - | - | - | S | - | - | - | Alpha-2-macroglobulin family |
| CBIAAGLN_01159 | 7.18e-177 | - | - | - | S | - | - | - | Alpha-2-macroglobulin family |
| CBIAAGLN_01160 | 0.0 | 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) |
| CBIAAGLN_01161 | 5.46e-189 | - | 4.1.1.23 | - | F | ko:K01591 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Orotidine 5'-phosphate decarboxylase / HUMPS family |
| CBIAAGLN_01163 | 4.65e-136 | - | - | - | S | - | - | - | Converts alpha-N-acetylneuranimic acid (Neu5Ac) to the beta-anomer, accelerating the equilibrium between the alpha- and beta-anomers. Probably facilitates sialidase-negative bacteria to compete sucessfully for limited amounts of extracellular Neu5Ac, which is likely taken up in the beta-anomer. In addition, the rapid removal of sialic acid from solution might be advantageous to the bacterium to damp down host responses |
| CBIAAGLN_01165 | 1.49e-51 | - | - | - | S | ko:K06908 | - | ko00000 | Phage tail tube protein FII |
| CBIAAGLN_01166 | 2.15e-101 | - | - | - | S | ko:K06907 | - | ko00000 | COG3497 Phage tail sheath protein FI |
| CBIAAGLN_01168 | 1.22e-110 | ybaK | - | - | S | ko:K03976 | - | ko00000,ko01000,ko03016 | Cys-tRNA(Pro) hydrolase activity |
| CBIAAGLN_01169 | 1.09e-76 | proS | 6.1.1.15 | - | J | ko:K01881 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Prolyl-tRNA synthetase, C-terminal |
| CBIAAGLN_01173 | 4.4e-85 | kefA | - | - | M | ko:K05802,ko:K22051 | - | ko00000,ko02000 | cellular water homeostasis |
| CBIAAGLN_01174 | 3.42e-61 | kefA | - | - | M | ko:K05802,ko:K22051 | - | ko00000,ko02000 | cellular water homeostasis |
| CBIAAGLN_01175 | 3.87e-66 | kefA | - | - | M | ko:K05802,ko:K22051 | - | ko00000,ko02000 | cellular water homeostasis |
| CBIAAGLN_01176 | 1.4e-80 | - | - | - | M | - | - | - | polygalacturonase activity |
| CBIAAGLN_01183 | 1.64e-240 | - | - | - | C | - | - | - | PFAM 4Fe-4S ferredoxin iron-sulfur binding domain protein |
| CBIAAGLN_01186 | 1.59e-223 | - | 3.6.1.11, 3.6.1.40 | - | FP | ko:K01524 | ko00230,map00230 | ko00000,ko00001,ko01000 | Ppx/GppA phosphatase family |
| CBIAAGLN_01188 | 8.4e-49 | - | 2.1.1.191 | - | J | ko:K06969 | - | ko00000,ko01000,ko03009 | S-adenosylmethionine-dependent methyltransferase |
| CBIAAGLN_01193 | 2.61e-279 | rnr | - | - | K | ko:K12573 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03016,ko03019 | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs |
| CBIAAGLN_01194 | 1.01e-54 | - | - | - | - | ko:K07403 | - | ko00000 | - |
| CBIAAGLN_01196 | 1.77e-293 | - | - | - | V | ko:K03327 | - | ko00000,ko02000 | MatE |
| CBIAAGLN_01197 | 5.35e-114 | menB | 4.1.3.36 | - | H | ko:K01661 | ko00130,ko01100,ko01110,map00130,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Enoyl-CoA hydratase/isomerase |
| CBIAAGLN_01206 | 2.72e-89 | - | - | - | O | - | - | - | Thioredoxin-like domain |
| CBIAAGLN_01210 | 1.1e-140 | - | - | - | E | - | - | - | serine-type peptidase activity |
| CBIAAGLN_01214 | 1.08e-122 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01217 | 4.61e-222 | - | 4.1.3.3 | - | EM | ko:K01639 | ko00520,map00520 | ko00000,ko00001,ko01000 | Dihydrodipicolinate synthetase family |
| CBIAAGLN_01218 | 3.8e-43 | nrdD | 1.1.98.6 | - | F | ko:K21636 | ko00230,ko00240,ko01100,map00230,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | CTP reductase activity |
| CBIAAGLN_01219 | 1.99e-126 | - | 1.1.98.6 | - | F | ko:K21636 | ko00230,ko00240,ko01100,map00230,map00240,map01100 | ko00000,ko00001,ko00002,ko01000 | Anaerobic ribonucleoside-triphosphate reductase |
| CBIAAGLN_01220 | 3.25e-67 | mtrC | - | - | M | ko:K03585 | ko01501,ko01503,map01501,map01503 | ko00000,ko00001,ko00002,ko01504,ko02000,ko03036 | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family |
| CBIAAGLN_01221 | 2.8e-18 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01222 | 0.0 | - | - | - | H | - | - | - | Flavin containing amine oxidoreductase |
| CBIAAGLN_01224 | 3.3e-306 | - | 2.1.1.182 | - | IJ | ko:K02528 | - | ko00000,ko01000,ko03009 | Ribosomal RNA adenine dimethylases |
| CBIAAGLN_01226 | 2.13e-56 | - | 6.3.3.3 | - | H | ko:K01935 | ko00780,ko01100,map00780,map01100 | ko00000,ko00001,ko00002,ko01000 | AAA domain |
| CBIAAGLN_01227 | 6.87e-23 | 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 |
| CBIAAGLN_01230 | 1.98e-203 | - | - | - | EP | ko:K13894 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Binding-protein-dependent transport system inner membrane component |
| CBIAAGLN_01233 | 9.21e-53 | cfr9IM | 2.1.1.113, 2.1.1.72 | - | L | ko:K00571,ko:K00590,ko:K07319 | - | ko00000,ko01000,ko02048 | Belongs to the N(4) N(6)-methyltransferase family |
| CBIAAGLN_01234 | 2.21e-233 | - | - | - | S | - | - | - | AAA domain, putative AbiEii toxin, Type IV TA system |
| CBIAAGLN_01238 | 6.33e-121 | - | 3.1.13.3, 3.1.3.7 | - | S | ko:K06881 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko01000,ko03400 | DHHA1 domain |
| CBIAAGLN_01239 | 1.55e-169 | truB | 5.4.99.25 | - | J | ko:K03177 | - | ko00000,ko01000,ko03016 | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs |
| CBIAAGLN_01240 | 1.35e-107 | - | - | - | S | - | - | - | Threonine/Serine exporter, ThrE |
| CBIAAGLN_01241 | 2.75e-170 | - | - | - | S | - | - | - | Putative threonine/serine exporter |
| CBIAAGLN_01243 | 7.8e-76 | - | 5.4.99.2 | - | I | ko:K01847 | ko00280,ko00630,ko00640,ko00720,ko01100,ko01120,ko01200,map00280,map00630,map00640,map00720,map01100,map01120,map01200 | ko00000,ko00001,ko00002,ko01000 | Methylmalonyl-CoA mutase |
| CBIAAGLN_01246 | 0.0 | - | - | - | U | - | - | - | Involved in the tonB-independent uptake of proteins |
| CBIAAGLN_01247 | 3.27e-181 | - | 2.4.1.18 | CBM48,GH13 | G | ko:K00700 | ko00500,ko01100,ko01110,map00500,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko04147 | Alpha amylase, C-terminal all-beta domain |
| CBIAAGLN_01248 | 1.33e-34 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01249 | 2.41e-74 | - | - | - | K | - | - | - | Acetyltransferase (GNAT) domain |
| CBIAAGLN_01250 | 4.88e-35 | - | - | - | K | - | - | - | Acetyltransferase (GNAT) domain |
| CBIAAGLN_01255 | 3.75e-307 | - | - | - | S | - | - | - | Sulfatase-modifying factor enzyme 1 |
| CBIAAGLN_01256 | 2.56e-69 | - | - | - | S | - | - | - | Glycosyl hydrolase 108 |
| CBIAAGLN_01257 | 6.26e-101 | - | - | - | K | ko:K07726 | - | ko00000,ko03000 | sequence-specific DNA binding |
| CBIAAGLN_01260 | 4.46e-43 | kdsB | 2.7.7.38 | - | M | ko:K00979 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01005 | Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria |
| CBIAAGLN_01265 | 1.15e-99 | - | - | - | S | ko:K15977 | - | ko00000 | DoxX |
| CBIAAGLN_01266 | 1.85e-276 | - | 6.3.2.45 | - | M | ko:K02558 | - | ko00000,ko01000 | Mur ligase family, catalytic domain |
| CBIAAGLN_01267 | 2.6e-33 | 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 |
| CBIAAGLN_01268 | 7.48e-217 | - | - | - | S | - | - | - | Aspartyl protease |
| CBIAAGLN_01269 | 1.63e-29 | - | 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | M | ko:K02527 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01003,ko01005 | 3-Deoxy-D-manno-octulosonic-acid transferase (kdotransferase) |
| CBIAAGLN_01270 | 2.6e-95 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01271 | 3.13e-92 | - | - | - | S | - | - | - | Protein of unknown function (DUF1194) |
| CBIAAGLN_01272 | 2.13e-77 | - | - | - | S | - | - | - | Protein of unknown function (DUF1194) |
| CBIAAGLN_01277 | 1.59e-268 | - | - | - | NU | ko:K02652 | - | ko00000,ko02035,ko02044 | Type II secretion system (T2SS), protein E, N-terminal domain |
| CBIAAGLN_01278 | 1.15e-184 | - | - | - | T | - | - | - | Calcineurin-like phosphoesterase superfamily domain |
| CBIAAGLN_01279 | 1.09e-52 | - | - | - | S | - | - | - | Tetratricopeptide repeat |
| CBIAAGLN_01280 | 5.27e-170 | BT0174 | - | - | C | ko:K04488 | - | ko00000 | iron-sulfur transferase activity |
| CBIAAGLN_01281 | 1.1e-100 | purL | 6.3.5.3 | - | F | ko:K01952 | ko00230,ko01100,ko01110,ko01130,map00230,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate |
| CBIAAGLN_01282 | 7.2e-175 | - | 6.3.5.3 | - | F | ko:K01952 | ko00230,ko01100,ko01110,ko01130,map00230,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | CobB/CobQ-like glutamine amidotransferase domain |
| CBIAAGLN_01288 | 3.62e-135 | - | - | - | S | - | - | - | RDD family |
| CBIAAGLN_01289 | 9.23e-47 | - | - | - | M | ko:K09808 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | MacB-like periplasmic core domain |
| CBIAAGLN_01290 | 2.3e-31 | - | 1.6.5.3 | - | C | ko:K00335 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | NADH-ubiquinone oxidoreductase-F iron-sulfur binding region |
| CBIAAGLN_01291 | 2.88e-142 | - | 1.6.5.3 | - | C | ko:K00334 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | Thioredoxin-like [2Fe-2S] ferredoxin |
| CBIAAGLN_01292 | 5.4e-20 | nuoD | 1.6.5.3 | - | C | ko:K00333 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient |
| CBIAAGLN_01293 | 3.16e-258 | 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 |
| CBIAAGLN_01294 | 3.09e-63 | - | 5.2.1.8 | - | O | ko:K03771 | - | ko00000,ko01000,ko03110 | SurA N-terminal domain |
| CBIAAGLN_01296 | 8.38e-189 | - | 3.6.3.34 | - | P | ko:K02013 | ko02010,map02010 | ko00000,ko00001,ko00002,ko01000,ko02000 | ATPases associated with a variety of cellular activities |
| CBIAAGLN_01298 | 1.68e-106 | - | 5.3.1.28 | - | G | ko:K03271 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01005 | SIS domain |
| CBIAAGLN_01299 | 4.5e-166 | - | 2.7.1.167, 2.7.7.70 | - | M | ko:K03272 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01005 | pfkB family carbohydrate kinase |
| CBIAAGLN_01300 | 2.16e-135 | - | - | - | L | ko:K03631 | - | ko00000,ko03400 | RecF/RecN/SMC N terminal domain |
| CBIAAGLN_01303 | 1.8e-124 | nuoI | 1.6.5.3 | - | C | ko:K00338 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient |
| CBIAAGLN_01304 | 2.02e-131 | nuoH | 1.6.5.3 | - | C | ko:K00337 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone |
| CBIAAGLN_01306 | 4.57e-181 | - | - | - | CH | - | - | - | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain |
| CBIAAGLN_01310 | 5.17e-52 | - | - | - | L | - | - | - | UvrD/REP helicase N-terminal domain |
| CBIAAGLN_01312 | 1.42e-244 | tdh | 1.1.1.103 | - | E | ko:K00060 | ko00260,map00260 | ko00000,ko00001,ko01000 | Alcohol dehydrogenase GroES-like domain |
| CBIAAGLN_01313 | 8.99e-53 | - | 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 |
| CBIAAGLN_01314 | 4.01e-249 | - | 3.2.1.23 | - | G | ko:K01190 | ko00052,ko00511,ko00600,ko01100,map00052,map00511,map00600,map01100 | ko00000,ko00001,ko01000 | Beta galactosidase small chain |
| CBIAAGLN_01315 | 5.25e-124 | - | 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 | Pyridoxal-phosphate dependent enzyme |
| CBIAAGLN_01316 | 2.6e-164 | - | 1.8.4.10, 1.8.4.8 | - | EH | ko:K00390 | ko00920,ko01100,ko01120,map00920,map01100,map01120 | ko00000,ko00001,ko00002,ko01000 | Phosphoadenosine phosphosulfate reductase family |
| CBIAAGLN_01319 | 2.24e-67 | - | - | - | L | - | - | - | Conserved hypothetical protein 95 |
| CBIAAGLN_01321 | 4.16e-85 | - | - | - | J | ko:K02950 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein S12/S23 |
| CBIAAGLN_01322 | 2.91e-104 | - | - | - | J | ko:K02992 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein S7p/S5e |
| CBIAAGLN_01323 | 1.17e-207 | - | - | - | G | - | - | - | Glycosyl hydrolases family 18 |
| CBIAAGLN_01324 | 4.33e-194 | - | - | - | V | - | - | - | Beta-lactamase |
| CBIAAGLN_01325 | 7.91e-47 | - | - | - | MU | - | - | - | Outer membrane efflux protein |
| CBIAAGLN_01326 | 6.64e-260 | dnaJ | - | - | O | ko:K03686 | - | ko00000,ko03029,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 |
| CBIAAGLN_01328 | 4.77e-08 | - | - | - | OU | - | - | - | serine-type endopeptidase activity |
| CBIAAGLN_01329 | 1.58e-79 | - | - | - | OU | - | - | - | Phage prohead protease, HK97 family |
| CBIAAGLN_01330 | 2.69e-156 | - | 2.7.7.19 | - | J | ko:K00970 | ko03018,map03018 | ko00000,ko00001,ko01000,ko03019 | Poly A polymerase head domain |
| CBIAAGLN_01332 | 5.59e-73 | - | 4.1.1.19 | - | E | ko:K01585 | ko00330,ko01100,map00330,map01100 | ko00000,ko00001,ko00002,ko01000 | Pyridoxal-dependent decarboxylase, pyridoxal binding domain |
| CBIAAGLN_01333 | 2.65e-196 | - | 4.1.1.19 | - | E | ko:K01585 | ko00330,ko01100,map00330,map01100 | ko00000,ko00001,ko00002,ko01000 | Pyridoxal-dependent decarboxylase, pyridoxal binding domain |
| CBIAAGLN_01334 | 7.51e-13 | - | - | - | L | - | - | - | Belongs to the 'phage' integrase family |
| CBIAAGLN_01335 | 7.61e-223 | - | - | - | P | - | - | - | Domain of unknown function |
| CBIAAGLN_01336 | 5.89e-98 | - | - | - | S | ko:K15977 | - | ko00000 | DoxX |
| CBIAAGLN_01337 | 3.97e-104 | - | 4.2.1.129, 5.4.99.17 | - | I | ko:K06045 | ko00909,ko01110,map00909,map01110 | ko00000,ko00001,ko01000 | PFAM Prenyltransferase squalene oxidase |
| CBIAAGLN_01341 | 1.56e-60 | - | - | - | J | ko:K02990 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011,ko03029 | Ribosomal protein S6 |
| CBIAAGLN_01342 | 9.36e-123 | - | 1.1.1.262 | - | H | ko:K00097 | ko00750,ko01100,map00750,map01100 | ko00000,ko00001,ko00002,ko01000 | Pyridoxal phosphate biosynthetic protein PdxA |
| CBIAAGLN_01346 | 3.95e-274 | - | - | - | M | - | - | - | Glycosyl transferase 4-like domain |
| CBIAAGLN_01347 | 3.01e-49 | rpsO | - | - | J | ko:K02956 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal_S15 |
| CBIAAGLN_01348 | 5.6e-248 | - | - | - | L | - | - | - | SNF2 family N-terminal domain |
| CBIAAGLN_01351 | 3.67e-228 | - | 2.7.4.1 | - | P | ko:K00937 | ko00190,ko03018,map00190,map03018 | ko00000,ko00001,ko01000,ko03019 | Polyphosphate kinase middle domain |
| CBIAAGLN_01352 | 1.36e-61 | - | - | - | H | - | - | - | PFAM glycosyl transferase family 8 |
| CBIAAGLN_01353 | 5.02e-237 | - | 3.1.1.1 | - | S | ko:K03928 | - | ko00000,ko01000 | thiolester hydrolase activity |
| CBIAAGLN_01354 | 2.74e-33 | - | - | - | S | - | - | - | Responsible for the incorporation of O-acetyl groups into the enterobacterial common antigen (ECA) trisaccharide repeat units |
| CBIAAGLN_01357 | 3.14e-213 | - | 2.7.7.41 | - | S | ko:K00981 | ko00564,ko01100,ko01110,ko04070,map00564,map01100,map01110,map04070 | ko00000,ko00001,ko00002,ko01000 | Cytidylyltransferase family |
| CBIAAGLN_01359 | 6.35e-132 | panZ | - | - | K | - | - | - | -acetyltransferase |
| CBIAAGLN_01361 | 2.14e-21 | - | - | - | K | ko:K03826 | - | ko00000,ko01000 | acetyltransferase |
| CBIAAGLN_01362 | 9.05e-20 | - | - | - | K | ko:K03826 | - | ko00000,ko01000 | acetyltransferase |
| CBIAAGLN_01363 | 6.25e-48 | - | - | - | K | ko:K03436 | - | ko00000,ko03000 | DeoR C terminal sensor domain |
| CBIAAGLN_01369 | 4.89e-39 | - | - | - | M | ko:K03585 | ko01501,ko01503,map01501,map01503 | ko00000,ko00001,ko00002,ko01504,ko02000,ko03036 | Biotin-lipoyl like |
| CBIAAGLN_01370 | 1.88e-250 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01372 | 3.59e-132 | - | - | - | Q | - | - | - | methyltransferase activity |
| CBIAAGLN_01373 | 7.74e-184 | - | - | - | N | - | - | - | ABC-type uncharacterized transport system |
| CBIAAGLN_01375 | 2.03e-53 | - | - | - | M | - | - | - | Glycosyl transferase family 2 |
| CBIAAGLN_01376 | 1.03e-202 | - | - | - | S | - | - | - | Glycosyltransferase like family 2 |
| CBIAAGLN_01377 | 2.08e-264 | - | - | - | H | - | - | - | Elongator protein 3, MiaB family, Radical SAM |
| CBIAAGLN_01378 | 1.87e-229 | - | - | - | S | - | - | - | Tetratricopeptide repeat |
| CBIAAGLN_01379 | 8.03e-26 | - | - | - | S | - | - | - | Tetratricopeptide repeat |
| CBIAAGLN_01380 | 4.75e-251 | hemL | 5.4.3.8 | - | H | ko:K01845 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000,ko01007 | Aminotransferase class-III |
| CBIAAGLN_01381 | 4.86e-80 | - | - | - | P | ko:K03455 | - | ko00000 | TrkA-N domain |
| CBIAAGLN_01382 | 5.22e-60 | - | - | - | D | ko:K03496 | - | ko00000,ko03036,ko04812 | AAA domain |
| CBIAAGLN_01385 | 1.69e-129 | - | - | - | U | ko:K05595 | - | ko00000,ko02000 | MarC family integral membrane protein |
| CBIAAGLN_01389 | 1.74e-27 | - | 1.3.5.1, 1.3.5.4 | - | C | ko:K00239 | ko00020,ko00190,ko00650,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,ko05134,map00020,map00190,map00650,map00720,map01100,map01110,map01120,map01130,map01200,map05134 | ko00000,ko00001,ko00002,ko01000 | Fumarate reductase flavoprotein C-term |
| CBIAAGLN_01390 | 4.42e-105 | - | 1.3.5.1, 1.3.5.4 | - | C | ko:K00240 | ko00020,ko00190,ko00650,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,map00020,map00190,map00650,map00720,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | 2Fe-2S iron-sulfur cluster binding domain |
| CBIAAGLN_01391 | 2.67e-55 | - | 1.3.5.1, 1.3.5.4 | - | C | ko:K00240 | ko00020,ko00190,ko00650,ko00720,ko01100,ko01110,ko01120,ko01130,ko01200,map00020,map00190,map00650,map00720,map01100,map01110,map01120,map01130,map01200 | ko00000,ko00001,ko00002,ko01000 | 2Fe-2S iron-sulfur cluster binding domain |
| CBIAAGLN_01393 | 7.87e-217 | - | - | - | S | - | - | - | Polyphosphate kinase 2 (PPK2) |
| CBIAAGLN_01394 | 2.8e-85 | - | - | - | M | - | - | - | Glycosyl transferase, family 2 |
| CBIAAGLN_01397 | 7.76e-280 | - | - | - | M | - | - | - | transferase activity, transferring glycosyl groups |
| CBIAAGLN_01399 | 1.07e-192 | ahcY | 3.3.1.1 | - | H | ko:K01251 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko00002,ko01000,ko01009,ko04147 | May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine |
| CBIAAGLN_01400 | 3.38e-52 | ahcY | 3.3.1.1 | - | H | ko:K01251 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko00002,ko01000,ko01009,ko04147 | May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine |
| CBIAAGLN_01402 | 2.59e-75 | - | - | - | J | ko:K02909 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Ribosomal protein L31 |
| CBIAAGLN_01403 | 2.09e-178 | secY | - | - | U | ko:K03076 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently |
| CBIAAGLN_01404 | 3.46e-238 | hemA | 1.2.1.70 | - | H | ko:K02492 | ko00860,ko01100,ko01110,ko01120,map00860,map01100,map01110,map01120 | ko00000,ko00001,ko00002,ko01000 | Glutamyl-tRNAGlu reductase, N-terminal domain |
| CBIAAGLN_01405 | 2.34e-48 | - | - | - | S | - | - | - | Cytochrome C assembly protein |
| CBIAAGLN_01407 | 2.63e-84 | - | - | - | M | - | - | - | Lysin motif |
| CBIAAGLN_01408 | 2.45e-62 | - | - | - | L | ko:K03424 | - | ko00000,ko01000 | TatD related DNase |
| CBIAAGLN_01409 | 1.18e-242 | - | - | - | J | - | - | - | PFAM Endoribonuclease L-PSP |
| CBIAAGLN_01410 | 2.58e-93 | rplK | - | - | J | ko:K02867 | ko03010,map03010 | br01610,ko00000,ko00001,ko00002,ko03011 | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors |
| CBIAAGLN_01411 | 7.6e-49 | nusG | - | - | K | ko:K02601 | - | ko00000,ko03009,ko03021 | In Spt5p, this domain may confer affinity for Spt4p. It possesses a RNP-like fold. |
| CBIAAGLN_01412 | 1.97e-230 | - | - | - | M | - | - | - | Glycosyl transferases group 1 |
| CBIAAGLN_01414 | 8.41e-147 | - | 2.7.7.15 | - | H | ko:K00968 | ko00440,ko00564,ko01100,ko05231,map00440,map00564,map01100,map05231 | ko00000,ko00001,ko00002,ko01000 | Oxidoreductase family, NAD-binding Rossmann fold |
| CBIAAGLN_01415 | 2.64e-132 | - | 2.7.7.15 | - | H | ko:K00968 | ko00440,ko00564,ko01100,ko05231,map00440,map00564,map01100,map05231 | ko00000,ko00001,ko00002,ko01000 | Oxidoreductase family, NAD-binding Rossmann fold |
| CBIAAGLN_01418 | 5.33e-95 | folD | 1.5.1.5, 3.5.4.9 | - | H | 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 |
| CBIAAGLN_01420 | 1.66e-127 | - | - | - | C | ko:K00184 | - | ko00000 | 4Fe-4S dicluster domain |
| CBIAAGLN_01423 | 3.68e-130 | tadA | 3.5.4.33 | - | FJ | ko:K11991 | - | ko00000,ko01000,ko03016 | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) |
| CBIAAGLN_01426 | 4.12e-100 | - | 5.1.99.1 | - | E | ko:K05606 | ko00280,ko00630,ko00640,ko00720,ko01100,ko01120,ko01200,map00280,map00630,map00640,map00720,map01100,map01120,map01200 | ko00000,ko00001,ko00002,ko01000 | Glyoxalase-like domain |
| CBIAAGLN_01427 | 8.46e-15 | - | - | - | U | ko:K03561 | - | ko00000,ko02000 | MotA/TolQ/ExbB proton channel family |
| CBIAAGLN_01428 | 1.05e-92 | - | - | - | U | ko:K03559 | - | ko00000,ko02000 | Biopolymer transport protein ExbD/TolR |
| CBIAAGLN_01429 | 8.02e-130 | - | 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 |
| CBIAAGLN_01430 | 4.75e-101 | - | - | - | S | ko:K06889 | - | ko00000 | X-Pro dipeptidyl-peptidase (S15 family) |
| CBIAAGLN_01433 | 3.7e-43 | fucI | 5.3.1.25, 5.3.1.3 | - | G | ko:K01818 | ko00051,ko01120,map00051,map01120 | ko00000,ko00001,ko01000 | Converts the aldose L-fucose into the corresponding ketose L-fuculose |
| CBIAAGLN_01436 | 1.98e-117 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01437 | 1.93e-56 | - | - | - | V | ko:K02003 | - | ko00000,ko00002,ko02000 | ATPases associated with a variety of cellular activities |
| CBIAAGLN_01439 | 9.06e-187 | 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 |
| CBIAAGLN_01440 | 1.46e-74 | - | 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 |
| CBIAAGLN_01441 | 3.2e-140 | - | - | - | M | - | - | - | Glycosyl transferases group 1 |
| CBIAAGLN_01445 | 6.02e-99 | aspS | 6.1.1.12 | - | J | ko:K01876 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016,ko03029 | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) |
| CBIAAGLN_01447 | 2.29e-11 | - | - | - | S | ko:K03924 | - | ko00000,ko01000 | ATPase family associated with various cellular activities (AAA) |
| CBIAAGLN_01448 | 3.26e-133 | - | - | - | S | - | - | - | Protein of unknown function DUF58 |
| CBIAAGLN_01449 | 3.53e-22 | - | - | - | L | ko:K02622 | - | ko00000,ko01000,ko02048,ko03032,ko03036 | TopoisomeraseII |
| CBIAAGLN_01450 | 5.21e-165 | - | 2.5.1.31 | - | I | ko:K00806 | ko00900,ko01110,map00900,map01110 | ko00000,ko00001,ko01000,ko01006 | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids |
| CBIAAGLN_01452 | 7.76e-211 | - | 2.7.1.180 | - | H | ko:K03734 | - | ko00000,ko01000 | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein |
| CBIAAGLN_01454 | 5.77e-208 | - | 2.1.1.45 | - | F | ko:K00560 | ko00240,ko00670,ko01100,ko01523,map00240,map00670,map01100,map01523 | ko00000,ko00001,ko00002,ko01000 | Thymidylate synthase |
| CBIAAGLN_01455 | 1.2e-18 | - | - | - | C | - | - | - | Zinc-binding dehydrogenase |
| CBIAAGLN_01456 | 1.45e-92 | - | - | - | L | ko:K07447 | - | ko00000,ko01000 | Likely ribonuclease with RNase H fold. |
| CBIAAGLN_01457 | 4.16e-23 | - | - | - | L | - | - | - | AAA domain |
| CBIAAGLN_01458 | 6.66e-64 | - | - | - | C | - | - | - | Psort location Cytoplasmic, score |
| CBIAAGLN_01463 | 1.07e-128 | dxr | 1.1.1.267 | - | I | ko:K00099 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | 1-deoxy-D-xylulose 5-phosphate reductoisomerase C-terminal |
| CBIAAGLN_01465 | 1.46e-99 | menG | 2.1.1.163, 2.1.1.201 | - | Q | ko:K03183 | ko00130,ko01100,ko01110,map00130,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | ubiE/COQ5 methyltransferase family |
| CBIAAGLN_01466 | 2.17e-08 | - | - | - | M | - | - | - | major outer membrane lipoprotein |
| CBIAAGLN_01468 | 3.67e-190 | - | 2.7.7.9 | - | G | ko:K00963 | ko00040,ko00052,ko00500,ko00520,ko01100,ko01130,map00040,map00052,map00500,map00520,map01100,map01130 | ko00000,ko00001,ko00002,ko01000 | UTP--glucose-1-phosphate uridylyltransferase |
| CBIAAGLN_01469 | 7.96e-36 | - | 2.7.7.9 | - | G | ko:K00963 | ko00040,ko00052,ko00500,ko00520,ko01100,ko01130,map00040,map00052,map00500,map00520,map01100,map01130 | ko00000,ko00001,ko00002,ko01000 | UTP--glucose-1-phosphate uridylyltransferase |
| CBIAAGLN_01470 | 2.73e-66 | - | 2.7.1.26, 2.7.7.2 | - | H | ko:K11753 | ko00740,ko01100,ko01110,map00740,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Riboflavin kinase |
| CBIAAGLN_01471 | 9e-65 | panD | 4.1.1.11 | - | H | ko:K01579 | ko00410,ko00770,ko01100,ko01110,map00410,map00770,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine |
| CBIAAGLN_01472 | 2.06e-114 | - | 1.6.5.3 | - | C | ko:K00336 | ko00190,ko01100,map00190,map01100 | ko00000,ko00001,ko00002,ko01000 | NADH-ubiquinone oxidoreductase-G iron-sulfur binding region |
| CBIAAGLN_01473 | 4.21e-125 | - | - | - | I | - | - | - | Prenyltransferase and squalene oxidase repeat |
| CBIAAGLN_01474 | 3.65e-42 | - | - | - | T | - | - | - | STAS domain |
| CBIAAGLN_01477 | 2.51e-56 | gumC | - | - | DM | ko:K16554 | ko05111,map05111 | ko00000,ko00001,ko02000 | PFAM lipopolysaccharide biosynthesis protein |
| CBIAAGLN_01478 | 2.51e-160 | - | 3.1.3.48 | - | GM | ko:K01104 | - | ko00000,ko01000 | protein tyrosine phosphatase activity |
| CBIAAGLN_01480 | 2.21e-91 | - | 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 |
| CBIAAGLN_01481 | 1.65e-271 | - | - | - | E | - | - | - | PFAM major facilitator superfamily MFS_1 |
| CBIAAGLN_01482 | 1.09e-193 | - | 3.2.1.23 | - | G | ko:K12308 | ko00052,map00052 | ko00000,ko00001,ko01000 | Glycosyl hydrolases family 35 |
| CBIAAGLN_01483 | 5.24e-188 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01484 | 2.95e-81 | - | - | - | NU | ko:K02457,ko:K08084 | ko03070,ko05111,map03070,map05111 | ko00000,ko00001,ko00002,ko02044 | protein transport across the cell outer membrane |
| CBIAAGLN_01486 | 8.47e-122 | adk | 2.7.4.3 | - | F | ko:K00939 | ko00230,ko00730,ko01100,ko01110,ko01130,map00230,map00730,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000,ko04147 | adenylate kinase activity |
| CBIAAGLN_01487 | 9.16e-53 | - | 3.6.3.21 | - | E | ko:K02028 | - | ko00000,ko00002,ko01000,ko02000 | AAA domain, putative AbiEii toxin, Type IV TA system |
| CBIAAGLN_01488 | 7.81e-45 | 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 |
| CBIAAGLN_01489 | 1.33e-27 | ptsH | - | - | G | ko:K11184,ko:K11189 | - | ko00000,ko02000 | phosphocarrier, HPr family |
| CBIAAGLN_01491 | 2.63e-81 | - | 3.2.1.23 | - | G | ko:K01190 | ko00052,ko00511,ko00600,ko01100,map00052,map00511,map00600,map01100 | ko00000,ko00001,ko01000 | Psort location Cytoplasmic, score 8.87 |
| CBIAAGLN_01492 | 3.4e-167 | - | 4.1.99.17 | - | H | ko:K03147 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko00002,ko01000 | ThiC-associated domain |
| CBIAAGLN_01493 | 4.66e-266 | - | - | - | M | - | - | - | Sulfatase |
| CBIAAGLN_01494 | 3.2e-70 | - | - | - | K | - | - | - | HxlR-like helix-turn-helix |
| CBIAAGLN_01495 | 9.11e-139 | - | - | - | G | - | - | - | Domain of unknown function (DUF4091) |
| CBIAAGLN_01496 | 4.34e-153 | tsaD | 2.3.1.234 | - | O | ko:K01409 | - | ko00000,ko01000,ko03016 | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction |
| CBIAAGLN_01498 | 7.57e-08 | - | - | - | S | - | - | - | Swim zinc finger domain protein |
| CBIAAGLN_01501 | 6.36e-99 | - | - | - | L | - | - | - | UvrD/REP helicase N-terminal domain |
| CBIAAGLN_01503 | 8.12e-107 | mnmA | 2.8.1.13 | - | J | ko:K00566 | ko04122,map04122 | ko00000,ko00001,ko01000,ko03016 | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 |
| CBIAAGLN_01506 | 4.12e-144 | - | 3.2.2.27 | - | L | ko:K21929 | ko03410,map03410 | ko00000,ko00001,ko01000,ko03400 | Uracil DNA glycosylase superfamily |
| CBIAAGLN_01507 | 7.83e-72 | sun | 2.1.1.176, 2.1.1.178 | - | J | ko:K03500,ko:K11392 | - | ko00000,ko01000,ko03009 | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA |
| CBIAAGLN_01508 | 6.72e-118 | - | - | - | S | ko:K07095 | - | ko00000 | Calcineurin-like phosphoesterase superfamily domain |
| CBIAAGLN_01509 | 2.63e-104 | ispG | 1.17.7.1, 1.17.7.3 | - | I | ko:K03526 | ko00900,ko01100,ko01110,ko01130,map00900,map01100,map01110,map01130 | ko00000,ko00001,ko00002,ko01000 | GcpE protein |
| CBIAAGLN_01510 | 9.4e-148 | - | - | - | IQ | - | - | - | RmlD substrate binding domain |
| CBIAAGLN_01512 | 2.23e-67 | lpxG | - | - | S | ko:K07098 | - | ko00000 | Calcineurin-like phosphoesterase |
| CBIAAGLN_01517 | 1.6e-66 | - | - | - | EGP | - | - | - | Major facilitator Superfamily |
| CBIAAGLN_01518 | 2.3e-104 | - | - | - | EGP | - | - | - | Major facilitator Superfamily |
| CBIAAGLN_01519 | 2e-63 | - | 3.5.3.12 | - | E | ko:K10536 | ko00330,ko01100,map00330,map01100 | ko00000,ko00001,ko01000 | Porphyromonas-type peptidyl-arginine deiminase |
| CBIAAGLN_01520 | 6.22e-16 | - | - | - | H | ko:K07137 | - | ko00000 | 5-formyltetrahydrofolate cyclo-ligase activity |
| CBIAAGLN_01526 | 2.47e-64 | - | - | - | O | ko:K09014 | - | ko00000 | Uncharacterized protein family (UPF0051) |
| CBIAAGLN_01527 | 8.47e-24 | - | - | - | D | - | - | - | nuclear chromosome segregation |
| CBIAAGLN_01531 | 2.89e-123 | - | 2.1.1.63 | - | L | ko:K00567 | - | ko00000,ko01000,ko03400 | 6-O-methylguanine DNA methyltransferase, DNA binding domain |
| CBIAAGLN_01533 | 2.11e-228 | - | - | - | NU | - | - | - | Prokaryotic N-terminal methylation motif |
| CBIAAGLN_01535 | 4.24e-58 | - | - | - | M | - | - | - | Peptidase M60-like family |
| CBIAAGLN_01536 | 1.27e-38 | - | - | - | S | - | - | - | haloacid dehalogenase-like hydrolase |
| CBIAAGLN_01537 | 2.89e-20 | - | 2.1.1.226, 2.1.1.227 | - | J | ko:K06442 | - | ko00000,ko01000,ko03009 | FtsJ-like methyltransferase |
| CBIAAGLN_01541 | 1.56e-40 | - | - | - | S | - | - | - | metal-dependent phosphohydrolase, HD sub domain |
| CBIAAGLN_01542 | 7.55e-36 | - | - | - | KT | - | - | - | Belongs to the MT-A70-like family |
| CBIAAGLN_01544 | 1.54e-72 | - | 4.2.1.51, 5.4.99.5 | - | E | ko:K14170 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Chorismate mutase type II |
| CBIAAGLN_01545 | 2.06e-89 | - | 4.2.1.51, 5.4.99.5 | - | E | ko:K14170 | ko00400,ko01100,ko01110,ko01130,ko01230,map00400,map01100,map01110,map01130,map01230 | ko00000,ko00001,ko00002,ko01000 | Chorismate mutase type II |
| CBIAAGLN_01547 | 9.48e-185 | - | 2.4.1.129, 3.4.16.4 | GT51 | M | ko:K05366 | ko00550,ko01100,ko01501,map00550,map01100,map01501 | ko00000,ko00001,ko01000,ko01003,ko01011 | Transglycosylase |
| CBIAAGLN_01548 | 8.21e-22 | - | - | - | S | - | - | - | Haloacid dehalogenase-like hydrolase |
| CBIAAGLN_01549 | 1.66e-76 | - | - | - | S | - | - | - | Haloacid dehalogenase-like hydrolase |
| CBIAAGLN_01553 | 8.41e-202 | - | - | - | S | - | - | - | DisA bacterial checkpoint controller nucleotide-binding |
| CBIAAGLN_01555 | 1.36e-171 | - | 2.8.1.10 | - | H | ko:K03149 | ko00730,ko01100,map00730,map01100 | ko00000,ko00001,ko01000 | Thiazole biosynthesis protein ThiG |
| CBIAAGLN_01556 | 2.38e-25 | - | - | - | E | - | - | - | Amino acid permease |
| CBIAAGLN_01557 | 4.78e-198 | - | 5.1.1.1 | - | M | ko:K01775 | ko00473,ko01100,ko01502,map00473,map01100,map01502 | ko00000,ko00001,ko01000,ko01011 | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids |
| CBIAAGLN_01559 | 3.01e-242 | - | - | - | S | - | - | - | Glycosyltransferase family 10 (fucosyltransferase) C-term |
| CBIAAGLN_01560 | 5.85e-58 | - | 3.4.24.70 | - | E | ko:K01414 | - | ko00000,ko01000,ko01002 | Peptidase family M3 |
| CBIAAGLN_01563 | 5.6e-129 | - | 1.1.1.205 | - | F | ko:K00088 | ko00230,ko00983,ko01100,ko01110,map00230,map00983,map01100,map01110 | ko00000,ko00001,ko00002,ko01000,ko04147 | IMP dehydrogenase / GMP reductase domain |
| CBIAAGLN_01564 | 5.44e-204 | - | - | - | M | - | - | - | Mechanosensitive ion channel |
| CBIAAGLN_01567 | 5.35e-181 | - | - | - | IQ | - | - | - | KR domain |
| CBIAAGLN_01569 | 2.42e-154 | - | 1.5.1.34 | - | C | ko:K10679 | ko00633,ko01120,map00633,map01120 | ko00000,ko00001,ko01000 | Nitroreductase family |
| CBIAAGLN_01570 | 9.02e-56 | - | 5.4.99.23 | - | J | ko:K06180 | - | ko00000,ko01000,ko03009 | RNA pseudouridylate synthase |
| CBIAAGLN_01573 | 7.03e-181 | - | 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 |
| CBIAAGLN_01575 | 7.69e-28 | - | 2.1.1.185 | - | J | ko:K03218 | - | ko00000,ko01000,ko03009 | SpoU rRNA Methylase family |
| CBIAAGLN_01576 | 7.56e-205 | - | 3.1.1.53 | - | L | ko:K03547,ko:K05970 | - | ko00000,ko01000,ko03400 | 3'-5' exonuclease activity |
| CBIAAGLN_01579 | 1.02e-128 | - | 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 | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate |
| CBIAAGLN_01581 | 4.8e-110 | - | 3.4.16.4 | - | M | ko:K07258 | ko00550,ko01100,map00550,map01100 | ko00000,ko00001,ko01000,ko01002,ko01011 | D-alanyl-D-alanine carboxypeptidase |
| CBIAAGLN_01583 | 2.81e-178 | pgk | 2.7.2.3 | - | G | ko:K00927 | ko00010,ko00710,ko01100,ko01110,ko01120,ko01130,ko01200,ko01230,map00010,map00710,map01100,map01110,map01120,map01130,map01200,map01230 | ko00000,ko00001,ko00002,ko01000,ko04147 | Phosphoglycerate kinase |
| CBIAAGLN_01584 | 5.06e-76 | - | - | - | O | - | - | - | Cytochrome C assembly protein |
| CBIAAGLN_01586 | 1.83e-93 | der | - | - | S | ko:K03977 | - | ko00000,ko03009 | KH-domain-like of EngA bacterial GTPase enzymes, C-terminal |
| CBIAAGLN_01589 | 5.16e-151 | rsmH | 2.1.1.199 | - | M | ko:K03438 | - | ko00000,ko01000,ko03009 | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA |
| CBIAAGLN_01590 | 1.16e-144 | - | 3.3.1.1 | - | H | ko:K01251 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko00002,ko01000,ko01009,ko04147 | adenosylhomocysteinase activity |
| CBIAAGLN_01591 | 8.57e-174 | - | 2.5.1.49 | - | E | ko:K01740 | ko00270,ko01100,map00270,map01100 | ko00000,ko00001,ko01000 | Cys/Met metabolism PLP-dependent enzyme |
| CBIAAGLN_01593 | 7.91e-147 | - | - | - | S | - | - | - | Oxidoreductase family, NAD-binding Rossmann fold |
| CBIAAGLN_01595 | 2.37e-26 | - | - | - | P | ko:K03297,ko:K11741 | - | ko00000,ko02000 | Multidrug Resistance protein |
| CBIAAGLN_01596 | 4.49e-99 | - | - | - | S | ko:K06158 | - | ko00000,ko03012 | ABC transporter |
| CBIAAGLN_01597 | 1.6e-48 | - | - | - | S | ko:K06158 | - | ko00000,ko03012 | ABC transporter |
| CBIAAGLN_01599 | 9.9e-78 | ybhL | - | - | S | ko:K06890 | - | ko00000 | Inhibitor of apoptosis-promoting Bax1 |
| CBIAAGLN_01600 | 8.26e-09 | - | - | - | S | ko:K07043 | - | ko00000 | Protein of unknown function DUF45 |
| CBIAAGLN_01602 | 1.35e-49 | - | 1.1.1.18, 1.1.1.369 | - | S | ko:K00010 | ko00521,ko00562,ko01100,ko01120,ko01130,map00521,map00562,map01100,map01120,map01130 | ko00000,ko00001,ko01000 | Oxidoreductase family, C-terminal alpha/beta domain |
| CBIAAGLN_01603 | 9.4e-100 | - | 1.1.1.18, 1.1.1.369 | - | S | ko:K00010 | ko00521,ko00562,ko01100,ko01120,ko01130,map00521,map00562,map01100,map01120,map01130 | ko00000,ko00001,ko01000 | Oxidoreductase family, C-terminal alpha/beta domain |
| CBIAAGLN_01608 | 1.73e-123 | paiA | - | - | K | - | - | - | acetyltransferase |
| CBIAAGLN_01610 | 4.2e-145 | - | 3.2.1.51 | GH29 | G | ko:K01206 | ko00511,map00511 | ko00000,ko00001,ko01000,ko04147 | Alpha-L-fucosidase |
| CBIAAGLN_01612 | 9.97e-154 | folE2 | 3.5.4.16 | - | S | ko:K09007 | ko00790,ko01100,map00790,map01100 | ko00000,ko00001,ko00002,ko01000 | Type I GTP cyclohydrolase folE2 |
| CBIAAGLN_01613 | 2.54e-132 | - | - | - | S | - | - | - | CAAX protease self-immunity |
| CBIAAGLN_01616 | 3.23e-240 | - | - | - | CH | - | - | - | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain |
| CBIAAGLN_01618 | 4.28e-09 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01619 | 1.58e-13 | - | 3.1.3.16 | - | T | ko:K20074 | - | ko00000,ko01000,ko01009 | Serine/threonine phosphatases, family 2C, catalytic domain |
| CBIAAGLN_01620 | 6.88e-181 | carB | 6.3.5.5 | - | EF | ko:K01955 | ko00240,ko00250,ko01100,map00240,map00250,map01100 | ko00000,ko00001,ko00002,ko01000 | Carbamoyl-phosphate synthetase large chain, oligomerisation domain |
| CBIAAGLN_01621 | 5.08e-255 | - | 3.2.1.22 | - | G | ko:K07407 | ko00052,ko00561,ko00600,ko00603,map00052,map00561,map00600,map00603 | ko00000,ko00001,ko01000 | Alpha galactosidase A |
| CBIAAGLN_01622 | 2.08e-83 | - | - | - | I | - | - | - | alpha/beta hydrolase fold |
| CBIAAGLN_01626 | 5.01e-62 | - | - | - | S | - | - | - | Protein of unknown function (DUF1232) |
| CBIAAGLN_01627 | 5.24e-91 | - | - | - | I | ko:K06889,ko:K09914 | - | ko00000 | PFAM Prenyltransferase squalene oxidase |
| CBIAAGLN_01628 | 3.17e-147 | - | - | - | KQ | - | - | - | Hypothetical methyltransferase |
| CBIAAGLN_01629 | 5.41e-39 | - | - | - | KQ | - | - | - | Hypothetical methyltransferase |
| CBIAAGLN_01630 | 4.71e-183 | - | 3.4.24.3 | - | NU | ko:K01387 | - | ko00000,ko01000,ko01002,ko02042 | translation initiation factor activity |
| CBIAAGLN_01636 | 4.28e-91 | - | 3.2.1.52 | GH20 | G | ko:K01207,ko:K12373 | ko00511,ko00513,ko00520,ko00531,ko00603,ko00604,ko01100,ko01501,ko04142,map00511,map00513,map00520,map00531,map00603,map00604,map01100,map01501,map04142 | ko00000,ko00001,ko00002,ko01000,ko03110 | Glycoside hydrolase, family 20, catalytic core |
| CBIAAGLN_01638 | 1.51e-179 | - | - | - | O | ko:K03696 | ko01100,map01100 | ko00000,ko03110 | C-terminal, D2-small domain, of ClpB protein |
| CBIAAGLN_01639 | 3.3e-45 | - | 1.10.3.14 | - | C | ko:K00425 | ko00190,ko01100,ko02020,map00190,map01100,map02020 | ko00000,ko00001,ko00002,ko01000 | Cytochrome bd terminal oxidase subunit I |
| CBIAAGLN_01645 | 4.01e-111 | - | - | - | K | ko:K03088 | - | ko00000,ko03021 | ECF sigma factor |
| CBIAAGLN_01646 | 4.59e-83 | - | 3.2.1.18 | GH33 | G | ko:K01186 | ko00511,ko00600,ko04142,map00511,map00600,map04142 | ko00000,ko00001,ko01000,ko02042 | N-terminal domain of BNR-repeat neuraminidase |
| CBIAAGLN_01647 | 2.17e-229 | - | - | - | D | ko:K03593 | - | ko00000,ko03029,ko03036 | Iron-sulfur cluster assembly protein |
| CBIAAGLN_01648 | 7.82e-65 | - | - | - | M | ko:K03282 | - | ko00000,ko02000 | Large-conductance mechanosensitive channel, MscL |
| CBIAAGLN_01649 | 1.06e-152 | 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 |
| CBIAAGLN_01651 | 2.71e-188 | - | - | - | KLT | - | - | - | Protein tyrosine kinase |
| CBIAAGLN_01660 | 2.72e-35 | - | - | - | E | ko:K15580 | ko01501,ko02010,ko02024,map01501,map02010,map02024 | ko00000,ko00001,ko00002,ko02000 | Bacterial extracellular solute-binding proteins, family 5 Middle |
| CBIAAGLN_01666 | 9.36e-215 | - | - | - | G | - | - | - | pfkB family carbohydrate kinase |
| CBIAAGLN_01669 | 2.11e-155 | kdpB | 3.6.3.12 | - | P | ko:K01547 | ko02020,map02020 | ko00000,ko00001,ko01000 | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit is responsible for energy coupling to the transport system |
| CBIAAGLN_01670 | 1.75e-101 | - | - | - | S | ko:K07126 | - | ko00000 | beta-lactamase activity |
| CBIAAGLN_01671 | 2.78e-162 | - | 2.7.7.4 | - | EH | ko:K00957 | ko00230,ko00261,ko00450,ko00920,ko01100,ko01120,ko01130,map00230,map00261,map00450,map00920,map01100,map01120,map01130 | ko00000,ko00001,ko00002,ko01000 | Phosphoadenosine phosphosulfate reductase family |
| CBIAAGLN_01674 | 4.88e-07 | pyrB | 2.1.3.2 | - | F | ko:K00609 | ko00240,ko00250,ko01100,map00240,map00250,map01100 | ko00000,ko00001,ko00002,ko01000 | Aspartate/ornithine carbamoyltransferase, carbamoyl-P binding domain |
| CBIAAGLN_01675 | 6.71e-79 | - | 2.4.2.9 | - | F | ko:K02825 | ko00240,ko01100,map00240,map01100 | ko00000,ko00001,ko01000,ko03000 | Phosphoribosyl transferase domain |
| CBIAAGLN_01676 | 5.49e-215 | - | - | - | M | - | - | - | pathogenesis |
| CBIAAGLN_01677 | 8.66e-68 | hprK | - | - | T | 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) |
| CBIAAGLN_01678 | 7.64e-52 | - | - | - | G | ko:K11189 | - | ko00000,ko02000 | PTS HPr component phosphorylation site |
| CBIAAGLN_01680 | 4.06e-107 | - | - | - | U | ko:K03110 | ko02024,ko03060,ko03070,map02024,map03060,map03070 | ko00000,ko00001,ko00002,ko02044 | SRP54-type protein, GTPase domain |
| CBIAAGLN_01681 | 6.21e-49 | - | - | - | 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 |
| CBIAAGLN_01682 | 5.9e-105 | thrS | 6.1.1.3 | - | J | ko:K01868 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) |
| CBIAAGLN_01685 | 5.91e-13 | galK | 2.7.1.6 | - | G | ko:K00849 | ko00052,ko00520,ko01100,map00052,map00520,map01100 | ko00000,ko00001,ko00002,ko01000,ko04147 | Belongs to the GHMP kinase family |
| CBIAAGLN_01686 | 5.48e-44 | - | - | - | S | - | - | - | ACT domain protein |
| CBIAAGLN_01687 | 9.29e-132 | - | - | - | J | ko:K02356 | - | ko00000,ko03012 | Elongation factor P (EF-P) OB domain |
| CBIAAGLN_01691 | 5.9e-68 | - | - | - | Q | ko:K02066 | ko02010,map02010 | ko00000,ko00001,ko00002,ko02000 | Permease MlaE |
| CBIAAGLN_01694 | 6.17e-236 | - | 5.4.99.23 | - | J | ko:K06180 | - | ko00000,ko01000,ko03009 | Responsible for synthesis of pseudouridine from uracil |
| CBIAAGLN_01696 | 1.55e-34 | argB | 2.7.2.8 | - | E | ko:K00930 | ko00220,ko01100,ko01110,ko01130,ko01210,ko01230,map00220,map01100,map01110,map01130,map01210,map01230 | ko00000,ko00001,ko00002,ko01000 | Amino acid kinase family |
| CBIAAGLN_01697 | 1.8e-40 | - | - | - | P | ko:K03284 | - | ko00000,ko02000 | CorA-like Mg2+ transporter protein |
| CBIAAGLN_01700 | 7.26e-152 | - | 1.11.1.15 | - | O | ko:K03386 | ko04214,map04214 | ko00000,ko00001,ko01000,ko04147 | C-terminal domain of 1-Cys peroxiredoxin |
| CBIAAGLN_01708 | 2.17e-86 | - | - | - | S | - | - | - | Acetyltransferase (GNAT) family |
| CBIAAGLN_01709 | 8.83e-55 | - | - | - | C | - | - | - | Nitroreductase family |
| CBIAAGLN_01712 | 1.38e-193 | - | - | - | U | ko:K03321 | - | ko00000,ko02000 | Sulfate permease family |
| CBIAAGLN_01717 | 5.77e-67 | pheT | 6.1.1.20 | - | J | ko:K01890 | ko00970,map00970 | ko00000,ko00001,ko00002,ko01000,ko01007,ko03016 | B3/4 domain |
| CBIAAGLN_01718 | 2.15e-50 | - | - | - | S | - | - | - | Alpha/beta hydrolase family |
| CBIAAGLN_01723 | 2.2e-26 | - | 3.1.1.29 | - | J | ko:K01056 | - | ko00000,ko01000,ko03012 | Peptidyl-tRNA hydrolase |
| CBIAAGLN_01724 | 1.03e-138 | mntP | - | - | P | - | - | - | manganese ion transmembrane transporter activity |
| CBIAAGLN_01725 | 5.79e-131 | 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 |
| CBIAAGLN_01727 | 2.86e-74 | - | - | - | C | ko:K04651 | - | ko00000,ko03110 | Hydrogenase/urease nickel incorporation, metallochaperone, hypA |
| CBIAAGLN_01728 | 6.47e-38 | - | - | - | C | ko:K03605 | - | ko00000,ko01000,ko01002 | Hydrogenase maturation protease |
| CBIAAGLN_01729 | 8.9e-101 | - | - | - | L | - | - | - | DNA restriction-modification system |
| CBIAAGLN_01730 | 5.3e-91 | lpxK | 2.7.1.130 | - | M | ko:K00912 | ko00540,ko01100,map00540,map01100 | ko00000,ko00001,ko00002,ko01000,ko01005 | Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) |
| CBIAAGLN_01733 | 3.34e-97 | - | - | - | S | - | - | - | PFAM Sel1 domain protein repeat-containing protein |
| CBIAAGLN_01737 | 1.81e-217 | kbl | 2.3.1.29 | - | E | ko:K00639 | ko00260,map00260 | ko00000,ko00001,ko01000,ko01007 | Aminotransferase class I and II |
| CBIAAGLN_01738 | 2.3e-157 | 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 |
| CBIAAGLN_01739 | 6.23e-46 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01740 | 2.71e-41 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01742 | 5.86e-149 | carA | 6.3.5.5 | - | F | ko:K01956 | ko00240,ko00250,ko01100,map00240,map00250,map01100 | ko00000,ko00001,ko00002,ko01000 | Carbamoyl-phosphate synthase small chain, CPSase domain |
| CBIAAGLN_01743 | 5.39e-111 | - | - | - | S | ko:K08999 | - | ko00000 | Bifunctional nuclease |
| CBIAAGLN_01746 | 9.83e-155 | - | - | - | S | ko:K03748 | - | ko00000 | DUF218 domain |
| CBIAAGLN_01747 | 7.38e-108 | - | 3.6.4.12 | - | L | ko:K02314 | ko03030,ko04112,map03030,map04112 | ko00000,ko00001,ko01000,ko03032 | DnaB-like helicase C terminal domain |
| CBIAAGLN_01751 | 9.28e-154 | - | 1.1.1.169 | - | H | ko:K00077 | ko00770,ko01100,ko01110,map00770,map01100,map01110 | ko00000,ko00001,ko00002,ko01000 | Ketopantoate reductase PanE/ApbA C terminal |
| CBIAAGLN_01752 | 2.25e-34 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01753 | 2.14e-55 | lsgC | - | - | M | - | - | - | transferase activity, transferring glycosyl groups |
| CBIAAGLN_01754 | 4.36e-198 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01756 | 6.26e-29 | - | - | - | S | - | - | - | very-long-chain-acyl-CoA dehydrogenase activity |
| CBIAAGLN_01760 | 3.03e-87 | - | - | - | S | - | - | - | L,D-transpeptidase catalytic domain |
| CBIAAGLN_01763 | 1.5e-13 | - | 1.10.3.14 | - | C | ko:K00426 | ko00190,ko01100,ko02020,map00190,map01100,map02020 | ko00000,ko00001,ko00002,ko01000 | Cytochrome bd terminal oxidase subunit II |
| CBIAAGLN_01766 | 5.5e-168 | - | - | - | C | - | - | - | 4 iron, 4 sulfur cluster binding |
| CBIAAGLN_01771 | 6.53e-70 | - | - | - | - | - | - | - | - |
| CBIAAGLN_01772 | 2.4e-173 | - | - | - | S | - | - | - | peptidoglycan biosynthetic process |
eggNOG-mapper v2.1.12 (Database: eggNOG v5.0.2, Mar. 2021 release)