ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
MBJNBCEJ_00001 | 2.5e-106 | L | Integrase | |||
MBJNBCEJ_00002 | 6.2e-74 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
MBJNBCEJ_00003 | 5.1e-15 | prpH | 3.1.3.16 | K | 3.5.2 Transcription regulation | |
MBJNBCEJ_00004 | 6.1e-73 | prpH | 3.1.3.16 | K | 3.5.2 Transcription regulation | |
MBJNBCEJ_00005 | 1.5e-204 | V | MATE efflux family protein | |||
MBJNBCEJ_00006 | 4.4e-28 | T | diguanylate cyclase activity | |||
MBJNBCEJ_00007 | 6.6e-209 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
MBJNBCEJ_00008 | 2.3e-88 | carB | 6.3.5.5 | F | Psort location Cytoplasmic, score 8.87 | |
MBJNBCEJ_00009 | 0.0 | carB | 6.3.5.5 | F | Psort location Cytoplasmic, score 8.87 | |
MBJNBCEJ_00010 | 1.3e-36 | V | (ABC) transporter | |||
MBJNBCEJ_00011 | 3.7e-102 | ybaJ | Q | Methyltransferase domain | ||
MBJNBCEJ_00012 | 5.6e-81 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MBJNBCEJ_00013 | 1e-69 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MBJNBCEJ_00014 | 2.5e-80 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MBJNBCEJ_00015 | 7.2e-121 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
MBJNBCEJ_00016 | 4.5e-58 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
MBJNBCEJ_00017 | 1e-64 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
MBJNBCEJ_00018 | 7.8e-54 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00019 | 8e-79 | |||||
MBJNBCEJ_00020 | 5.4e-109 | msrA | 1.8.4.11, 1.8.4.12 | O | 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 | |
MBJNBCEJ_00021 | 1.4e-65 | S | ASCH domain | |||
MBJNBCEJ_00022 | 3.9e-262 | S | Uncharacterised protein family (UPF0236) | |||
MBJNBCEJ_00023 | 6.3e-08 | XK27_05370 | 5.3.1.24 | E | phosphoribosylanthranilate isomerase activity | |
MBJNBCEJ_00025 | 2.5e-247 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
MBJNBCEJ_00026 | 1e-140 | S | Protein of unknown function (DUF3100) | |||
MBJNBCEJ_00027 | 7.4e-83 | S | An automated process has identified a potential problem with this gene model | |||
MBJNBCEJ_00028 | 1.2e-177 | hsdR | 3.1.21.3 | V | Type I restriction enzyme R protein N terminus (HSDR_N) | |
MBJNBCEJ_00029 | 6.8e-77 | GM | NmrA-like family | |||
MBJNBCEJ_00030 | 6.6e-21 | S | Domain of unknown function (DUF4343) | |||
MBJNBCEJ_00032 | 1.3e-129 | T | Diguanylate cyclase, GGDEF domain | |||
MBJNBCEJ_00033 | 1.8e-72 | S | Sel1-like repeats. | |||
MBJNBCEJ_00034 | 2.9e-194 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
MBJNBCEJ_00035 | 2.4e-209 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
MBJNBCEJ_00036 | 5.1e-201 | xerS | L | Belongs to the 'phage' integrase family | ||
MBJNBCEJ_00038 | 9.8e-60 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
MBJNBCEJ_00039 | 6e-91 | C | Nitroreductase family | |||
MBJNBCEJ_00040 | 4.7e-13 | XK27_06780 | V | ABC transporter permease | ||
MBJNBCEJ_00041 | 1.4e-115 | 3.1.3.73 | G | phosphoglycerate mutase | ||
MBJNBCEJ_00042 | 1.1e-84 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
MBJNBCEJ_00043 | 1.1e-83 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
MBJNBCEJ_00044 | 3.3e-86 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MBJNBCEJ_00045 | 6.1e-120 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MBJNBCEJ_00046 | 4.9e-165 | EG | EamA-like transporter family | |||
MBJNBCEJ_00047 | 7.5e-173 | |||||
MBJNBCEJ_00048 | 6.3e-157 | degV | S | EDD domain protein, DegV family | ||
MBJNBCEJ_00049 | 3.7e-307 | FbpA | K | Fibronectin-binding protein | ||
MBJNBCEJ_00050 | 2.9e-246 | XK27_08635 | S | UPF0210 protein | ||
MBJNBCEJ_00051 | 5.6e-43 | gcvR | T | Belongs to the UPF0237 family | ||
MBJNBCEJ_00052 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
MBJNBCEJ_00053 | 3.3e-197 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
MBJNBCEJ_00054 | 1e-170 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MBJNBCEJ_00055 | 9.3e-72 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
MBJNBCEJ_00056 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
MBJNBCEJ_00057 | 5.4e-59 | |||||
MBJNBCEJ_00058 | 4.4e-67 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
MBJNBCEJ_00059 | 2e-106 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
MBJNBCEJ_00060 | 3.3e-219 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
MBJNBCEJ_00061 | 1e-57 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
MBJNBCEJ_00062 | 3.2e-106 | ypsA | S | Belongs to the UPF0398 family | ||
MBJNBCEJ_00063 | 2e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
MBJNBCEJ_00064 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
MBJNBCEJ_00065 | 0.0 | dap2 | 3.4.19.1 | E | Prolyl oligopeptidase family | |
MBJNBCEJ_00066 | 2.4e-189 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MBJNBCEJ_00067 | 1.9e-54 | I | acetylesterase activity | |||
MBJNBCEJ_00068 | 2.1e-70 | I | Psort location Cytoplasmic, score | |||
MBJNBCEJ_00069 | 6.8e-150 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MBJNBCEJ_00070 | 3.6e-114 | nth | 4.2.99.18 | L | 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 | |
MBJNBCEJ_00071 | 9.7e-115 | dnaD | L | DnaD domain protein | ||
MBJNBCEJ_00072 | 1.1e-258 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
MBJNBCEJ_00073 | 1.2e-59 | ypmB | S | Protein conserved in bacteria | ||
MBJNBCEJ_00074 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
MBJNBCEJ_00075 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
MBJNBCEJ_00076 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
MBJNBCEJ_00077 | 3.7e-168 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
MBJNBCEJ_00078 | 7.7e-177 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
MBJNBCEJ_00079 | 4.2e-203 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
MBJNBCEJ_00080 | 3.7e-193 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
MBJNBCEJ_00081 | 1.4e-170 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
MBJNBCEJ_00082 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
MBJNBCEJ_00083 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
MBJNBCEJ_00084 | 1.3e-103 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
MBJNBCEJ_00085 | 7.6e-31 | yfiC | V | ABC transporter | ||
MBJNBCEJ_00086 | 2.1e-185 | yfiC | V | ABC transporter | ||
MBJNBCEJ_00087 | 2.8e-52 | V | abc transporter atp-binding protein | |||
MBJNBCEJ_00088 | 1e-41 | V | ABC transporter, ATP-binding protein | |||
MBJNBCEJ_00089 | 8.3e-48 | lmrA | V | (ABC) transporter | ||
MBJNBCEJ_00090 | 5.7e-15 | K | Winged helix DNA-binding domain | |||
MBJNBCEJ_00091 | 5e-153 | supH | G | Sucrose-6F-phosphate phosphohydrolase | ||
MBJNBCEJ_00092 | 9e-104 | |||||
MBJNBCEJ_00093 | 2.5e-189 | 2.7.7.65 | T | diguanylate cyclase | ||
MBJNBCEJ_00094 | 4e-209 | yliE | T | Putative diguanylate phosphodiesterase | ||
MBJNBCEJ_00095 | 5e-71 | yliE | T | Putative diguanylate phosphodiesterase | ||
MBJNBCEJ_00097 | 8.4e-103 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
MBJNBCEJ_00098 | 7.8e-135 | cbiQ | P | Cobalt transport protein | ||
MBJNBCEJ_00099 | 3.8e-148 | P | ABC transporter | |||
MBJNBCEJ_00100 | 7.2e-141 | cbiO2 | P | ABC transporter | ||
MBJNBCEJ_00101 | 1.5e-101 | S | C4-dicarboxylate anaerobic carrier | |||
MBJNBCEJ_00102 | 6.6e-104 | I | NUDIX domain | |||
MBJNBCEJ_00103 | 7.6e-129 | S | Glycosyl hydrolases family 18 | |||
MBJNBCEJ_00104 | 3e-47 | S | Glycosyl hydrolases family 18 | |||
MBJNBCEJ_00105 | 7e-121 | 3.6.1.13 | L | NUDIX domain | ||
MBJNBCEJ_00107 | 3.2e-65 | lsa | S | ABC transporter | ||
MBJNBCEJ_00108 | 8.4e-16 | lsa | S | ABC transporter | ||
MBJNBCEJ_00109 | 3.3e-32 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
MBJNBCEJ_00110 | 2.4e-21 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
MBJNBCEJ_00111 | 4.1e-303 | phoR | 2.7.13.3 | T | Histidine kinase | |
MBJNBCEJ_00112 | 1.4e-124 | T | Transcriptional regulatory protein, C terminal | |||
MBJNBCEJ_00113 | 2e-112 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
MBJNBCEJ_00114 | 3.2e-141 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
MBJNBCEJ_00115 | 2.8e-157 | pstA | P | Phosphate transport system permease protein PstA | ||
MBJNBCEJ_00116 | 4.3e-161 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
MBJNBCEJ_00117 | 1.7e-154 | pstS | P | Phosphate | ||
MBJNBCEJ_00120 | 2.5e-129 | yliE | T | Putative diguanylate phosphodiesterase | ||
MBJNBCEJ_00121 | 2e-36 | |||||
MBJNBCEJ_00122 | 1.2e-74 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00123 | 7.6e-92 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00139 | 1.1e-185 | asnB | 6.3.5.4 | E | Aluminium induced protein | |
MBJNBCEJ_00140 | 1.2e-79 | asnB | 6.3.5.4 | E | Aluminium induced protein | |
MBJNBCEJ_00141 | 1.2e-160 | spoU | 2.1.1.185 | J | Methyltransferase | |
MBJNBCEJ_00143 | 1.8e-74 | |||||
MBJNBCEJ_00145 | 5.3e-164 | adhE | 1.1.1.1, 1.2.1.10 | C | Aldehyde dehydrogenase family | |
MBJNBCEJ_00146 | 1.3e-50 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
MBJNBCEJ_00147 | 3e-142 | G | polysaccharide deacetylase | |||
MBJNBCEJ_00148 | 3.8e-10 | G | polysaccharide deacetylase | |||
MBJNBCEJ_00149 | 3.8e-229 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_00153 | 6.8e-49 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
MBJNBCEJ_00155 | 2.6e-123 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
MBJNBCEJ_00156 | 1.4e-125 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
MBJNBCEJ_00157 | 6.7e-139 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
MBJNBCEJ_00158 | 1.4e-158 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
MBJNBCEJ_00159 | 3.1e-259 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
MBJNBCEJ_00160 | 1.9e-77 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
MBJNBCEJ_00161 | 1e-68 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
MBJNBCEJ_00162 | 3.9e-226 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
MBJNBCEJ_00163 | 6.3e-123 | IQ | reductase | |||
MBJNBCEJ_00164 | 7.4e-180 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
MBJNBCEJ_00165 | 1e-32 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
MBJNBCEJ_00166 | 8.9e-173 | fabH | 2.3.1.180 | I | 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 | |
MBJNBCEJ_00167 | 1.2e-183 | K | AI-2E family transporter | |||
MBJNBCEJ_00168 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
MBJNBCEJ_00169 | 2.2e-224 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_00170 | 7.5e-152 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_00171 | 2.4e-47 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_00172 | 1.3e-24 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_00173 | 4e-12 | |||||
MBJNBCEJ_00174 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
MBJNBCEJ_00175 | 2.3e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
MBJNBCEJ_00176 | 1.1e-74 | dtd | J | 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 | ||
MBJNBCEJ_00177 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
MBJNBCEJ_00178 | 4.2e-175 | prmA | J | Ribosomal protein L11 methyltransferase | ||
MBJNBCEJ_00179 | 1.1e-89 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
MBJNBCEJ_00180 | 2.2e-225 | yjjP | S | Putative threonine/serine exporter | ||
MBJNBCEJ_00181 | 4.8e-221 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
MBJNBCEJ_00182 | 2.8e-216 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
MBJNBCEJ_00183 | 1.3e-196 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
MBJNBCEJ_00184 | 3e-190 | sptS | 2.7.13.3 | T | Histidine kinase | |
MBJNBCEJ_00185 | 1.4e-27 | sptS | 2.7.13.3 | T | Histidine kinase | |
MBJNBCEJ_00186 | 7.4e-118 | K | response regulator | |||
MBJNBCEJ_00187 | 1.2e-109 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
MBJNBCEJ_00188 | 1e-159 | cas2 | 2.7.7.7 | L | CRISPR-associated protein (Cas_Cas2CT1978) | |
MBJNBCEJ_00189 | 1.2e-174 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
MBJNBCEJ_00190 | 6.9e-118 | casE | S | CRISPR_assoc | ||
MBJNBCEJ_00191 | 1.6e-131 | casD | S | CRISPR-associated protein (Cas_Cas5) | ||
MBJNBCEJ_00192 | 1.3e-180 | casC | L | CT1975-like protein | ||
MBJNBCEJ_00193 | 2.4e-107 | casB | S | CRISPR-associated protein Cse2 (CRISPR_cse2) | ||
MBJNBCEJ_00194 | 0.0 | casA | L | the current gene model (or a revised gene model) may contain a frame shift | ||
MBJNBCEJ_00195 | 0.0 | cas3 | L | CRISPR-associated helicase cas3 | ||
MBJNBCEJ_00197 | 5e-18 | |||||
MBJNBCEJ_00199 | 4.5e-204 | argH | 2.3.1.1, 4.3.2.1 | E | argininosuccinate lyase | |
MBJNBCEJ_00201 | 7e-71 | |||||
MBJNBCEJ_00202 | 0.0 | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | |||
MBJNBCEJ_00203 | 5.2e-16 | |||||
MBJNBCEJ_00204 | 3.4e-26 | |||||
MBJNBCEJ_00205 | 1.3e-111 | K | DNA-binding transcription factor activity | |||
MBJNBCEJ_00206 | 4.7e-171 | K | LysR substrate binding domain | |||
MBJNBCEJ_00207 | 0.0 | S | Bacterial membrane protein YfhO | |||
MBJNBCEJ_00208 | 3.9e-229 | S | Tetratricopeptide repeat protein | |||
MBJNBCEJ_00209 | 2.6e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
MBJNBCEJ_00210 | 7.4e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
MBJNBCEJ_00211 | 3.2e-212 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
MBJNBCEJ_00212 | 5e-108 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
MBJNBCEJ_00214 | 3.9e-117 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
MBJNBCEJ_00215 | 9.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
MBJNBCEJ_00216 | 3.4e-106 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
MBJNBCEJ_00217 | 6e-129 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
MBJNBCEJ_00218 | 8.9e-62 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
MBJNBCEJ_00219 | 5.4e-164 | xerD | D | recombinase XerD | ||
MBJNBCEJ_00220 | 4e-164 | cvfB | S | S1 domain | ||
MBJNBCEJ_00221 | 1e-88 | I | Acyltransferase family | |||
MBJNBCEJ_00223 | 5.9e-39 | ssuB | P | anion transmembrane transporter activity | ||
MBJNBCEJ_00224 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
MBJNBCEJ_00225 | 2e-180 | pfkA | 2.7.1.11, 2.7.1.90 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
MBJNBCEJ_00226 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
MBJNBCEJ_00227 | 4.3e-29 | S | Protein of unknown function (DUF2929) | |||
MBJNBCEJ_00228 | 7.6e-89 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
MBJNBCEJ_00229 | 4.4e-55 | gmuR | K | UbiC transcription regulator-associated domain protein | ||
MBJNBCEJ_00230 | 1.9e-15 | gmuR | K | UTRA | ||
MBJNBCEJ_00231 | 3.2e-98 | ywlG | S | Belongs to the UPF0340 family | ||
MBJNBCEJ_00233 | 3.7e-63 | |||||
MBJNBCEJ_00234 | 0.0 | L | SNF2 family N-terminal domain | |||
MBJNBCEJ_00235 | 6.9e-308 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
MBJNBCEJ_00236 | 1e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
MBJNBCEJ_00237 | 4.5e-138 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
MBJNBCEJ_00238 | 3.7e-176 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
MBJNBCEJ_00239 | 0.0 | oatA | I | Acyltransferase | ||
MBJNBCEJ_00240 | 8.1e-235 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
MBJNBCEJ_00241 | 0.0 | uvrC | L | 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 | ||
MBJNBCEJ_00242 | 3.2e-183 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
MBJNBCEJ_00243 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
MBJNBCEJ_00244 | 2.5e-175 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MBJNBCEJ_00245 | 2.1e-207 | S | Amidohydrolase | |||
MBJNBCEJ_00246 | 3.1e-223 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
MBJNBCEJ_00247 | 1e-76 | argR | K | Regulates arginine biosynthesis genes | ||
MBJNBCEJ_00248 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
MBJNBCEJ_00249 | 2.8e-168 | K | LysR substrate binding domain | |||
MBJNBCEJ_00250 | 2.3e-237 | EK | Aminotransferase, class I | |||
MBJNBCEJ_00251 | 1.3e-66 | E | Methionine synthase | |||
MBJNBCEJ_00252 | 2.1e-227 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_00255 | 1.8e-74 | |||||
MBJNBCEJ_00256 | 9.1e-261 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
MBJNBCEJ_00257 | 6.3e-51 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
MBJNBCEJ_00258 | 6.4e-265 | frdC | 1.3.5.4 | C | FAD binding domain | |
MBJNBCEJ_00259 | 3.4e-113 | metI | P | ABC transporter permease | ||
MBJNBCEJ_00260 | 5.3e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
MBJNBCEJ_00261 | 3.2e-121 | metQ2 | P | Belongs to the nlpA lipoprotein family | ||
MBJNBCEJ_00262 | 0.0 | aha1 | P | E1-E2 ATPase | ||
MBJNBCEJ_00263 | 1.9e-38 | aha1 | P | E1-E2 ATPase | ||
MBJNBCEJ_00264 | 9e-89 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
MBJNBCEJ_00265 | 1.8e-189 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
MBJNBCEJ_00266 | 2.9e-122 | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
MBJNBCEJ_00267 | 5.4e-65 | |||||
MBJNBCEJ_00268 | 0.0 | E | ABC transporter, substratebinding protein | |||
MBJNBCEJ_00270 | 2.8e-125 | pnb | C | nitroreductase | ||
MBJNBCEJ_00272 | 3.3e-191 | I | Protein of unknown function (DUF2974) | |||
MBJNBCEJ_00273 | 4.4e-44 | S | Protein of unknown function (DUF2974) | |||
MBJNBCEJ_00274 | 1.8e-107 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
MBJNBCEJ_00275 | 3.8e-232 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
MBJNBCEJ_00276 | 1.1e-194 | tig | D | 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 | ||
MBJNBCEJ_00277 | 6.1e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
MBJNBCEJ_00278 | 4.5e-149 | |||||
MBJNBCEJ_00279 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
MBJNBCEJ_00280 | 6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
MBJNBCEJ_00281 | 1.6e-33 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
MBJNBCEJ_00282 | 1.6e-180 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
MBJNBCEJ_00283 | 0.0 | comEC | S | Competence protein ComEC | ||
MBJNBCEJ_00284 | 6.4e-70 | comEA | L | Competence protein ComEA | ||
MBJNBCEJ_00285 | 2.3e-190 | ylbL | T | Belongs to the peptidase S16 family | ||
MBJNBCEJ_00286 | 9.8e-83 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
MBJNBCEJ_00287 | 1.6e-97 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
MBJNBCEJ_00288 | 1.1e-53 | ylbG | S | UPF0298 protein | ||
MBJNBCEJ_00289 | 7.1e-212 | ftsW | D | Belongs to the SEDS family | ||
MBJNBCEJ_00290 | 0.0 | typA | T | GTP-binding protein TypA | ||
MBJNBCEJ_00291 | 4.7e-102 | def | 3.5.1.31, 3.5.1.88 | J | 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 | |
MBJNBCEJ_00292 | 2.7e-35 | ykzG | S | Belongs to the UPF0356 family | ||
MBJNBCEJ_00293 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
MBJNBCEJ_00294 | 5.1e-251 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
MBJNBCEJ_00295 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
MBJNBCEJ_00296 | 1e-103 | S | Repeat protein | |||
MBJNBCEJ_00297 | 2e-123 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
MBJNBCEJ_00298 | 2.1e-221 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
MBJNBCEJ_00299 | 3.2e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
MBJNBCEJ_00300 | 2.8e-213 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
MBJNBCEJ_00301 | 3.1e-127 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
MBJNBCEJ_00302 | 5.4e-19 | |||||
MBJNBCEJ_00303 | 1.1e-101 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
MBJNBCEJ_00304 | 1.5e-32 | cspA | K | 'Cold-shock' DNA-binding domain | ||
MBJNBCEJ_00305 | 0.0 | ileS | 6.1.1.5 | J | 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) | |
MBJNBCEJ_00306 | 8.5e-145 | ylmH | S | S4 domain protein | ||
MBJNBCEJ_00307 | 7.6e-46 | yggT | S | YGGT family | ||
MBJNBCEJ_00308 | 1.1e-64 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
MBJNBCEJ_00309 | 8.6e-206 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
MBJNBCEJ_00310 | 2.2e-241 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
MBJNBCEJ_00311 | 1.1e-147 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
MBJNBCEJ_00312 | 1.2e-208 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
MBJNBCEJ_00313 | 5.6e-261 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
MBJNBCEJ_00314 | 2.7e-177 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
MBJNBCEJ_00315 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
MBJNBCEJ_00316 | 4.8e-55 | ftsL | D | Cell division protein FtsL | ||
MBJNBCEJ_00317 | 1.1e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
MBJNBCEJ_00318 | 4.1e-77 | mraZ | K | Belongs to the MraZ family | ||
MBJNBCEJ_00319 | 5.7e-55 | S | Protein of unknown function (DUF3397) | |||
MBJNBCEJ_00321 | 1.4e-95 | mreD | ||||
MBJNBCEJ_00322 | 1.8e-137 | mreC | M | Involved in formation and maintenance of cell shape | ||
MBJNBCEJ_00323 | 2.6e-175 | mreB | D | cell shape determining protein MreB | ||
MBJNBCEJ_00324 | 2.7e-114 | radC | L | DNA repair protein | ||
MBJNBCEJ_00325 | 6.8e-127 | S | Haloacid dehalogenase-like hydrolase | |||
MBJNBCEJ_00326 | 1.2e-233 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
MBJNBCEJ_00327 | 0.0 | valS | 6.1.1.9 | J | 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 | |
MBJNBCEJ_00328 | 7.8e-129 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
MBJNBCEJ_00329 | 4.2e-228 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
MBJNBCEJ_00330 | 1.4e-217 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
MBJNBCEJ_00331 | 3.4e-300 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
MBJNBCEJ_00332 | 1.2e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
MBJNBCEJ_00333 | 3.5e-82 | yueI | S | Protein of unknown function (DUF1694) | ||
MBJNBCEJ_00334 | 3.6e-241 | rarA | L | recombination factor protein RarA | ||
MBJNBCEJ_00335 | 1.3e-42 | |||||
MBJNBCEJ_00336 | 3e-78 | usp6 | T | universal stress protein | ||
MBJNBCEJ_00337 | 2.7e-219 | rodA | D | Belongs to the SEDS family | ||
MBJNBCEJ_00338 | 1.7e-34 | S | Protein of unknown function (DUF2969) | |||
MBJNBCEJ_00339 | 7.4e-48 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
MBJNBCEJ_00340 | 6.1e-177 | mbl | D | Cell shape determining protein MreB Mrl | ||
MBJNBCEJ_00341 | 5.1e-32 | ywzB | S | Protein of unknown function (DUF1146) | ||
MBJNBCEJ_00342 | 1.6e-73 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
MBJNBCEJ_00343 | 1.3e-247 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
MBJNBCEJ_00344 | 2.4e-170 | atpG | C | 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 | ||
MBJNBCEJ_00345 | 2.9e-279 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
MBJNBCEJ_00346 | 3.9e-93 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
MBJNBCEJ_00347 | 4.2e-57 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
MBJNBCEJ_00348 | 3.1e-28 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
MBJNBCEJ_00349 | 4.2e-127 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
MBJNBCEJ_00350 | 6.8e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
MBJNBCEJ_00351 | 5.4e-189 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
MBJNBCEJ_00352 | 3e-156 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
MBJNBCEJ_00353 | 2.1e-194 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
MBJNBCEJ_00354 | 1.4e-112 | tdk | 2.7.1.21 | F | thymidine kinase | |
MBJNBCEJ_00355 | 7.9e-260 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain | |
MBJNBCEJ_00356 | 4.3e-34 | |||||
MBJNBCEJ_00357 | 7.6e-191 | ampC | V | Beta-lactamase | ||
MBJNBCEJ_00360 | 9.4e-178 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00361 | 1.4e-23 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00362 | 6.2e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
MBJNBCEJ_00363 | 3.1e-107 | vanZ | V | VanZ like family | ||
MBJNBCEJ_00364 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
MBJNBCEJ_00365 | 2e-275 | T | PhoQ Sensor | |||
MBJNBCEJ_00366 | 6.1e-134 | K | Transcriptional regulatory protein, C terminal | |||
MBJNBCEJ_00368 | 1.5e-47 | |||||
MBJNBCEJ_00369 | 6.6e-88 | lysA2 | M | Glycosyl hydrolases family 25 | ||
MBJNBCEJ_00370 | 1.7e-10 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
MBJNBCEJ_00372 | 1.3e-30 | |||||
MBJNBCEJ_00375 | 2.5e-36 | S | peptidoglycan catabolic process | |||
MBJNBCEJ_00376 | 1.7e-24 | S | Uncharacterised protein conserved in bacteria (DUF2313) | |||
MBJNBCEJ_00377 | 7.3e-105 | xkdT | S | Baseplate J-like protein | ||
MBJNBCEJ_00378 | 3.6e-23 | S | Protein of unknown function (DUF2634) | |||
MBJNBCEJ_00379 | 9e-27 | S | Protein of unknown function (DUF2577) | |||
MBJNBCEJ_00380 | 3.8e-61 | yqbQ | G | PFAM Phage late control gene D protein (GPD) | ||
MBJNBCEJ_00381 | 2.6e-30 | ygaU | GH23 | S | protein containing LysM domain | |
MBJNBCEJ_00382 | 1.2e-97 | S | phage tail tape measure protein | |||
MBJNBCEJ_00383 | 4.3e-31 | xkdN | S | Phage XkdN-like tail assembly chaperone protein, TAC | ||
MBJNBCEJ_00384 | 2e-45 | S | Protein of unknown function (DUF2001) | |||
MBJNBCEJ_00385 | 7.2e-112 | S | Phage tail sheath protein | |||
MBJNBCEJ_00387 | 4.2e-10 | |||||
MBJNBCEJ_00388 | 4e-26 | S | Bacteriophage HK97-gp10, putative tail-component | |||
MBJNBCEJ_00389 | 7.5e-32 | |||||
MBJNBCEJ_00390 | 2.2e-21 | |||||
MBJNBCEJ_00391 | 7.2e-103 | |||||
MBJNBCEJ_00392 | 5.2e-37 | S | Phage minor structural protein GP20 | |||
MBJNBCEJ_00393 | 5.9e-90 | S | Phage Mu protein F like protein | |||
MBJNBCEJ_00394 | 1.4e-177 | S | Phage portal protein, SPP1 Gp6-like | |||
MBJNBCEJ_00395 | 4.3e-156 | S | Terminase-like family | |||
MBJNBCEJ_00396 | 4e-40 | L | Terminase small subunit | |||
MBJNBCEJ_00397 | 1.8e-81 | |||||
MBJNBCEJ_00402 | 2.2e-09 | |||||
MBJNBCEJ_00403 | 3.2e-54 | S | VRR-NUC domain | |||
MBJNBCEJ_00404 | 0.0 | S | Phage plasmid primase, P4 | |||
MBJNBCEJ_00405 | 8.3e-80 | S | Protein of unknown function (DUF669) | |||
MBJNBCEJ_00406 | 2.1e-117 | res | L | Helicase C-terminal domain protein | ||
MBJNBCEJ_00407 | 1.8e-130 | S | AAA domain | |||
MBJNBCEJ_00412 | 4.4e-37 | ansR | 3.4.21.88 | K | sequence-specific DNA binding | |
MBJNBCEJ_00413 | 9.5e-11 | E | Zn peptidase | |||
MBJNBCEJ_00414 | 3.4e-24 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
MBJNBCEJ_00415 | 2.1e-189 | S | Phage integrase family | |||
MBJNBCEJ_00416 | 5.3e-104 | S | Protein of unknown function (DUF3644) | |||
MBJNBCEJ_00418 | 2.6e-222 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
MBJNBCEJ_00419 | 2.8e-185 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
MBJNBCEJ_00420 | 1.9e-11 | comGF | U | Putative Competence protein ComGF | ||
MBJNBCEJ_00422 | 2.3e-75 | |||||
MBJNBCEJ_00423 | 6.5e-51 | comGC | U | competence protein ComGC | ||
MBJNBCEJ_00424 | 4.9e-158 | comGB | NU | type II secretion system | ||
MBJNBCEJ_00425 | 4.4e-180 | comGA | NU | Type II IV secretion system protein | ||
MBJNBCEJ_00426 | 1.4e-130 | yebC | K | Transcriptional regulatory protein | ||
MBJNBCEJ_00427 | 2e-94 | S | VanZ like family | |||
MBJNBCEJ_00428 | 1.2e-163 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
MBJNBCEJ_00429 | 8.9e-158 | rssA | S | Phospholipase, patatin family | ||
MBJNBCEJ_00430 | 2.2e-101 | msrA | 1.8.4.11, 1.8.4.12 | O | 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 | |
MBJNBCEJ_00431 | 0.0 | E | Amino acid permease | |||
MBJNBCEJ_00432 | 7.2e-68 | GM | epimerase | |||
MBJNBCEJ_00433 | 6.3e-84 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
MBJNBCEJ_00434 | 1.2e-65 | |||||
MBJNBCEJ_00435 | 1.5e-25 | |||||
MBJNBCEJ_00436 | 5e-265 | T | Diguanylate cyclase, GGDEF domain | |||
MBJNBCEJ_00437 | 6.1e-197 | yliE | T | EAL domain | ||
MBJNBCEJ_00438 | 2.5e-49 | |||||
MBJNBCEJ_00439 | 5.2e-33 | |||||
MBJNBCEJ_00440 | 5e-60 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
MBJNBCEJ_00441 | 4.2e-65 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
MBJNBCEJ_00442 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
MBJNBCEJ_00443 | 6.5e-55 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
MBJNBCEJ_00444 | 1.4e-77 | atkY | K | Copper transport repressor CopY TcrY | ||
MBJNBCEJ_00445 | 2e-55 | V | peptidase activity | |||
MBJNBCEJ_00446 | 6.8e-150 | S | hydrolase | |||
MBJNBCEJ_00447 | 5.3e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
MBJNBCEJ_00448 | 2.5e-63 | ybbR | S | YbbR-like protein | ||
MBJNBCEJ_00449 | 4.4e-73 | ybbR | S | YbbR-like protein | ||
MBJNBCEJ_00450 | 4.1e-150 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
MBJNBCEJ_00451 | 2.4e-206 | potD | P | ABC transporter | ||
MBJNBCEJ_00452 | 5.6e-128 | potC | P | ABC transporter permease | ||
MBJNBCEJ_00453 | 1.1e-144 | potB | P | ABC transporter permease | ||
MBJNBCEJ_00454 | 1.4e-203 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
MBJNBCEJ_00455 | 2.9e-162 | murB | 1.3.1.98 | M | Cell wall formation | |
MBJNBCEJ_00456 | 1.2e-97 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
MBJNBCEJ_00457 | 4.2e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
MBJNBCEJ_00458 | 9.7e-183 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
MBJNBCEJ_00459 | 1.5e-134 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
MBJNBCEJ_00460 | 2.6e-158 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
MBJNBCEJ_00461 | 8e-105 | |||||
MBJNBCEJ_00462 | 8.6e-50 | 3.2.2.20 | K | acetyltransferase | ||
MBJNBCEJ_00463 | 8.3e-26 | 3.2.2.20 | K | acetyltransferase | ||
MBJNBCEJ_00464 | 2.9e-142 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
MBJNBCEJ_00465 | 3e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
MBJNBCEJ_00466 | 3.8e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
MBJNBCEJ_00467 | 1.8e-212 | cggR | K | Putative sugar-binding domain | ||
MBJNBCEJ_00469 | 5.3e-136 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_00470 | 3.8e-144 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
MBJNBCEJ_00471 | 1.6e-10 | ABC-SBP | S | ABC transporter | ||
MBJNBCEJ_00472 | 1.2e-54 | ABC-SBP | S | ABC transporter | ||
MBJNBCEJ_00474 | 6.1e-213 | |||||
MBJNBCEJ_00475 | 1.1e-37 | |||||
MBJNBCEJ_00476 | 5.5e-101 | clpP | 3.4.21.92 | O | 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 | |
MBJNBCEJ_00477 | 3.4e-169 | whiA | K | May be required for sporulation | ||
MBJNBCEJ_00478 | 5e-190 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
MBJNBCEJ_00479 | 2.4e-164 | rapZ | S | Displays ATPase and GTPase activities | ||
MBJNBCEJ_00480 | 3e-81 | dmpA | 3.4.11.19 | EQ | Peptidase family S58 | |
MBJNBCEJ_00482 | 4.4e-146 | E | D-aminopeptidase | |||
MBJNBCEJ_00483 | 7.4e-92 | S | Short repeat of unknown function (DUF308) | |||
MBJNBCEJ_00484 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
MBJNBCEJ_00485 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
MBJNBCEJ_00486 | 4.9e-176 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
MBJNBCEJ_00487 | 6.5e-190 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
MBJNBCEJ_00488 | 2.9e-156 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
MBJNBCEJ_00489 | 1.2e-174 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
MBJNBCEJ_00490 | 9.1e-31 | |||||
MBJNBCEJ_00491 | 5.9e-188 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
MBJNBCEJ_00492 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
MBJNBCEJ_00493 | 1.6e-97 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
MBJNBCEJ_00494 | 1.9e-121 | comFC | S | Competence protein | ||
MBJNBCEJ_00495 | 2.7e-246 | comFA | L | Helicase C-terminal domain protein | ||
MBJNBCEJ_00496 | 4.7e-117 | yvyE | 3.4.13.9 | S | YigZ family | |
MBJNBCEJ_00497 | 3.1e-215 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
MBJNBCEJ_00498 | 5.1e-221 | rny | S | Endoribonuclease that initiates mRNA decay | ||
MBJNBCEJ_00499 | 4.6e-197 | recA | L | 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 | ||
MBJNBCEJ_00500 | 2.7e-97 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
MBJNBCEJ_00501 | 5.1e-106 | ymfM | S | Helix-turn-helix domain | ||
MBJNBCEJ_00502 | 1.2e-132 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
MBJNBCEJ_00503 | 3.9e-237 | S | Peptidase M16 | |||
MBJNBCEJ_00504 | 3.5e-230 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
MBJNBCEJ_00505 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
MBJNBCEJ_00506 | 1.9e-68 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
MBJNBCEJ_00507 | 8.7e-104 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
MBJNBCEJ_00508 | 2.1e-181 | yubA | S | AI-2E family transporter | ||
MBJNBCEJ_00509 | 3.5e-64 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
MBJNBCEJ_00515 | 7e-76 | S | Virulence-associated protein E | |||
MBJNBCEJ_00516 | 9.8e-22 | S | Primase alpha helix C-terminal domain protein | |||
MBJNBCEJ_00518 | 1.9e-18 | |||||
MBJNBCEJ_00520 | 1.5e-07 | K | Helix-turn-helix domain | |||
MBJNBCEJ_00521 | 1.3e-93 | sip | L | Belongs to the 'phage' integrase family | ||
MBJNBCEJ_00522 | 1.1e-197 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
MBJNBCEJ_00523 | 1.1e-147 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
MBJNBCEJ_00524 | 6.3e-22 | |||||
MBJNBCEJ_00525 | 8.2e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MBJNBCEJ_00526 | 3.9e-150 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
MBJNBCEJ_00527 | 3.1e-113 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
MBJNBCEJ_00528 | 3.3e-109 | yjbK | S | CYTH | ||
MBJNBCEJ_00529 | 3.4e-112 | yjbH | Q | Thioredoxin | ||
MBJNBCEJ_00530 | 4.4e-163 | coiA | 3.6.4.12 | S | Competence protein | |
MBJNBCEJ_00531 | 5.2e-136 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
MBJNBCEJ_00532 | 5e-69 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
MBJNBCEJ_00533 | 2.1e-302 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
MBJNBCEJ_00534 | 1.2e-39 | ptsH | G | phosphocarrier protein HPR | ||
MBJNBCEJ_00535 | 5.8e-10 | |||||
MBJNBCEJ_00536 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
MBJNBCEJ_00537 | 1.1e-43 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
MBJNBCEJ_00538 | 5e-26 | mco | Q | Multicopper oxidase | ||
MBJNBCEJ_00539 | 6.2e-205 | mco | Q | Multicopper oxidase | ||
MBJNBCEJ_00540 | 2.5e-26 | |||||
MBJNBCEJ_00541 | 1.6e-304 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
MBJNBCEJ_00542 | 1.2e-157 | hlyX | S | Transporter associated domain | ||
MBJNBCEJ_00543 | 1.7e-73 | |||||
MBJNBCEJ_00544 | 4.5e-85 | |||||
MBJNBCEJ_00545 | 1.7e-145 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
MBJNBCEJ_00546 | 1.1e-245 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
MBJNBCEJ_00547 | 6.2e-182 | D | Alpha beta | |||
MBJNBCEJ_00548 | 2.8e-18 | |||||
MBJNBCEJ_00549 | 3e-170 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
MBJNBCEJ_00550 | 4.5e-166 | yihY | S | Belongs to the UPF0761 family | ||
MBJNBCEJ_00551 | 3.6e-162 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
MBJNBCEJ_00552 | 2.9e-78 | fld | C | Flavodoxin | ||
MBJNBCEJ_00553 | 3.3e-51 | gtcA | S | Teichoic acid glycosylation protein | ||
MBJNBCEJ_00554 | 1.2e-211 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
MBJNBCEJ_00555 | 1.4e-24 | |||||
MBJNBCEJ_00556 | 4.1e-270 | E | Amino acid permease | |||
MBJNBCEJ_00558 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
MBJNBCEJ_00559 | 1.1e-228 | ynbB | 4.4.1.1 | P | aluminum resistance | |
MBJNBCEJ_00560 | 1e-232 | pyrP | F | Permease | ||
MBJNBCEJ_00561 | 4.7e-183 | pfoS | S | Phosphotransferase system, EIIC | ||
MBJNBCEJ_00563 | 1.2e-244 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
MBJNBCEJ_00564 | 2.9e-208 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
MBJNBCEJ_00565 | 2.3e-122 | lytC | 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
MBJNBCEJ_00566 | 6.4e-227 | potE | E | amino acid | ||
MBJNBCEJ_00567 | 9.8e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
MBJNBCEJ_00568 | 2.1e-249 | yhdP | S | Transporter associated domain | ||
MBJNBCEJ_00569 | 2.9e-21 | 3.4.22.70 | M | Sortase family | ||
MBJNBCEJ_00571 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
MBJNBCEJ_00572 | 1.2e-129 | gntR | K | UbiC transcription regulator-associated domain protein | ||
MBJNBCEJ_00573 | 1.6e-174 | rihB | 3.2.2.1 | F | Nucleoside | |
MBJNBCEJ_00574 | 5.5e-124 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
MBJNBCEJ_00575 | 2e-120 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
MBJNBCEJ_00576 | 1.5e-161 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
MBJNBCEJ_00577 | 5.9e-88 | |||||
MBJNBCEJ_00578 | 7.4e-10 | S | Protein of unknown function (DUF2974) | |||
MBJNBCEJ_00579 | 1.1e-269 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
MBJNBCEJ_00580 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
MBJNBCEJ_00581 | 9.7e-283 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
MBJNBCEJ_00582 | 9.6e-155 | glnH | ET | Bacterial periplasmic substrate-binding proteins | ||
MBJNBCEJ_00583 | 4.4e-110 | glnP | P | ABC transporter permease | ||
MBJNBCEJ_00584 | 5.5e-110 | gluC | P | ABC transporter permease | ||
MBJNBCEJ_00585 | 6.4e-151 | glnH | ET | ABC transporter substrate-binding protein | ||
MBJNBCEJ_00586 | 2.8e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MBJNBCEJ_00587 | 2.5e-118 | udk | 2.7.1.48 | F | Zeta toxin | |
MBJNBCEJ_00588 | 3.7e-111 | udk | 2.7.1.48 | F | Zeta toxin | |
MBJNBCEJ_00590 | 7e-101 | S | ABC-type cobalt transport system, permease component | |||
MBJNBCEJ_00591 | 7.8e-210 | pepA | E | M42 glutamyl aminopeptidase | ||
MBJNBCEJ_00592 | 2.2e-281 | pipD | E | Dipeptidase | ||
MBJNBCEJ_00593 | 1.3e-142 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
MBJNBCEJ_00594 | 5e-120 | ybhL | S | Belongs to the BI1 family | ||
MBJNBCEJ_00595 | 3.3e-217 | mdtG | EGP | Major facilitator Superfamily | ||
MBJNBCEJ_00596 | 2.6e-56 | |||||
MBJNBCEJ_00598 | 6.1e-49 | kgtP | EGP | Sugar (and other) transporter | ||
MBJNBCEJ_00599 | 5.3e-100 | kgtP | EGP | Sugar (and other) transporter | ||
MBJNBCEJ_00600 | 2.2e-309 | ybiT | S | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_00601 | 5.5e-167 | mleP3 | S | Membrane transport protein | ||
MBJNBCEJ_00602 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
MBJNBCEJ_00603 | 5.7e-36 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
MBJNBCEJ_00604 | 1.1e-32 | mtlD | 1.1.1.17 | G | mannitol metabolic process | |
MBJNBCEJ_00606 | 2.1e-52 | mtlR | K | transcriptional antiterminator | ||
MBJNBCEJ_00607 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
MBJNBCEJ_00608 | 1.2e-85 | K | AsnC family | |||
MBJNBCEJ_00609 | 3.8e-52 | ypaA | S | membrane | ||
MBJNBCEJ_00610 | 1.2e-26 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
MBJNBCEJ_00612 | 1.3e-30 | yliE | T | Putative diguanylate phosphodiesterase | ||
MBJNBCEJ_00613 | 5.3e-76 | T | Gaf domain | |||
MBJNBCEJ_00614 | 2.5e-94 | nudC | 1.3.7.1, 3.6.1.22 | L | NUDIX domain | |
MBJNBCEJ_00615 | 5.3e-124 | alkD | L | DNA alkylation repair enzyme | ||
MBJNBCEJ_00616 | 6.9e-240 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
MBJNBCEJ_00617 | 2.8e-100 | flp | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | |
MBJNBCEJ_00618 | 8.3e-47 | D | Di-iron-containing protein involved in the repair of iron-sulfur clusters | |||
MBJNBCEJ_00619 | 4.3e-33 | copZ | P | Heavy-metal-associated domain | ||
MBJNBCEJ_00620 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
MBJNBCEJ_00621 | 1.6e-56 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
MBJNBCEJ_00622 | 4.4e-120 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
MBJNBCEJ_00623 | 2.2e-159 | L | Mrr N-terminal domain | |||
MBJNBCEJ_00624 | 4.8e-257 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
MBJNBCEJ_00625 | 1.4e-117 | S | Protein of unknown function (DUF1211) | |||
MBJNBCEJ_00626 | 9.8e-169 | yegS | 2.7.1.107 | G | Lipid kinase | |
MBJNBCEJ_00627 | 3.2e-275 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | 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) | |
MBJNBCEJ_00628 | 2.1e-266 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
MBJNBCEJ_00629 | 1.8e-47 | gatC | 6.3.5.6, 6.3.5.7 | J | 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) | |
MBJNBCEJ_00630 | 9.2e-193 | camS | S | sex pheromone | ||
MBJNBCEJ_00631 | 0.0 | ligA | 6.5.1.2 | L | 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 | |
MBJNBCEJ_00632 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
MBJNBCEJ_00633 | 1.3e-114 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
MBJNBCEJ_00634 | 4.1e-102 | S | ECF transporter, substrate-specific component | |||
MBJNBCEJ_00636 | 1.8e-89 | ydcK | S | Belongs to the SprT family | ||
MBJNBCEJ_00637 | 2.7e-111 | V | ABC transporter | |||
MBJNBCEJ_00640 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
MBJNBCEJ_00641 | 3.3e-152 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
MBJNBCEJ_00642 | 3.1e-135 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
MBJNBCEJ_00643 | 1e-204 | csaB | M | Glycosyl transferases group 1 | ||
MBJNBCEJ_00644 | 1.4e-133 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
MBJNBCEJ_00645 | 1.5e-261 | epsU | S | Polysaccharide biosynthesis protein | ||
MBJNBCEJ_00646 | 9.1e-225 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
MBJNBCEJ_00647 | 3.9e-125 | gntR1 | K | UTRA | ||
MBJNBCEJ_00648 | 1e-198 | |||||
MBJNBCEJ_00649 | 2.9e-215 | |||||
MBJNBCEJ_00650 | 1.4e-56 | oppA2 | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00653 | 8.8e-166 | pfoS | S | Phosphotransferase system, EIIC | ||
MBJNBCEJ_00654 | 8.5e-226 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
MBJNBCEJ_00657 | 2.5e-91 | S | Phosphatidylethanolamine-binding protein | |||
MBJNBCEJ_00658 | 9.3e-48 | EGP | Major facilitator Superfamily | |||
MBJNBCEJ_00659 | 1.9e-52 | EGP | Major facilitator Superfamily | |||
MBJNBCEJ_00660 | 1.6e-119 | XK27_07525 | 3.6.1.55 | F | NUDIX domain | |
MBJNBCEJ_00661 | 1.2e-12 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00662 | 6.9e-187 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00663 | 1.6e-45 | |||||
MBJNBCEJ_00664 | 3.5e-23 | |||||
MBJNBCEJ_00665 | 3.9e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
MBJNBCEJ_00666 | 4.2e-77 | rplM | J | 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 | ||
MBJNBCEJ_00667 | 6e-151 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
MBJNBCEJ_00668 | 2.1e-143 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
MBJNBCEJ_00669 | 4.4e-163 | ecfA | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
MBJNBCEJ_00670 | 7.4e-155 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
MBJNBCEJ_00671 | 1.3e-61 | rplQ | J | Ribosomal protein L17 | ||
MBJNBCEJ_00672 | 5.6e-172 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MBJNBCEJ_00673 | 1.4e-63 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
MBJNBCEJ_00674 | 4.2e-56 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
MBJNBCEJ_00675 | 8.4e-34 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
MBJNBCEJ_00676 | 5.9e-120 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
MBJNBCEJ_00677 | 1.1e-237 | secY | U | 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 | ||
MBJNBCEJ_00678 | 1.8e-72 | rplO | J | Binds to the 23S rRNA | ||
MBJNBCEJ_00679 | 1.3e-24 | rpmD | J | Ribosomal protein L30 | ||
MBJNBCEJ_00680 | 1.3e-85 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
MBJNBCEJ_00681 | 5.7e-56 | rplR | J | 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 | ||
MBJNBCEJ_00682 | 2.8e-91 | rplF | J | 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 | ||
MBJNBCEJ_00683 | 7.2e-68 | rpsH | J | 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 | ||
MBJNBCEJ_00684 | 9.3e-95 | rplE | J | 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 | ||
MBJNBCEJ_00685 | 4.5e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
MBJNBCEJ_00686 | 1.6e-58 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
MBJNBCEJ_00687 | 3.8e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
MBJNBCEJ_00688 | 3.7e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
MBJNBCEJ_00689 | 1.9e-77 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
MBJNBCEJ_00690 | 9.4e-121 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
MBJNBCEJ_00691 | 8.9e-54 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
MBJNBCEJ_00692 | 4.5e-45 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
MBJNBCEJ_00693 | 2.8e-154 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
MBJNBCEJ_00694 | 8.3e-45 | rplW | J | 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 | ||
MBJNBCEJ_00695 | 1.6e-106 | rplD | J | Forms part of the polypeptide exit tunnel | ||
MBJNBCEJ_00696 | 1.8e-110 | rplC | J | 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 | ||
MBJNBCEJ_00697 | 1.2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
MBJNBCEJ_00698 | 0.0 | fusA | J | 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 | ||
MBJNBCEJ_00699 | 3.5e-82 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
MBJNBCEJ_00700 | 1e-69 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
MBJNBCEJ_00703 | 9e-08 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
MBJNBCEJ_00704 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MBJNBCEJ_00705 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MBJNBCEJ_00708 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
MBJNBCEJ_00709 | 1.3e-81 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
MBJNBCEJ_00713 | 1.1e-107 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
MBJNBCEJ_00714 | 1.1e-217 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
MBJNBCEJ_00715 | 4.1e-22 | metY | 2.5.1.49 | E | o-acetylhomoserine | |
MBJNBCEJ_00717 | 6.6e-139 | T | diguanylate cyclase activity | |||
MBJNBCEJ_00719 | 2.5e-278 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
MBJNBCEJ_00720 | 1.1e-197 | dus | J | 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 | ||
MBJNBCEJ_00721 | 1.3e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
MBJNBCEJ_00722 | 5e-301 | E | ABC transporter, substratebinding protein | |||
MBJNBCEJ_00723 | 5.3e-164 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
MBJNBCEJ_00724 | 0.0 | ftsH | O | 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 | ||
MBJNBCEJ_00725 | 2.7e-249 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
MBJNBCEJ_00726 | 7.5e-61 | yabR | J | S1 RNA binding domain | ||
MBJNBCEJ_00727 | 1.5e-59 | divIC | D | Septum formation initiator | ||
MBJNBCEJ_00728 | 3.2e-34 | yabO | J | S4 domain protein | ||
MBJNBCEJ_00729 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
MBJNBCEJ_00730 | 1.1e-103 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
MBJNBCEJ_00731 | 2e-126 | S | (CBS) domain | |||
MBJNBCEJ_00732 | 2.6e-216 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
MBJNBCEJ_00733 | 9.4e-71 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
MBJNBCEJ_00734 | 8.2e-239 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
MBJNBCEJ_00735 | 2.7e-260 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
MBJNBCEJ_00736 | 1.6e-41 | rpmE2 | J | Ribosomal protein L31 | ||
MBJNBCEJ_00737 | 1.9e-239 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
MBJNBCEJ_00738 | 0.0 | pyrG | 6.3.4.2 | F | 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 | |
MBJNBCEJ_00739 | 1.1e-64 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
MBJNBCEJ_00740 | 2.5e-65 | S | Domain of unknown function (DUF1934) | |||
MBJNBCEJ_00741 | 2.8e-254 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
MBJNBCEJ_00742 | 6.7e-176 | prs | 2.7.6.1 | F | 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) | |
MBJNBCEJ_00743 | 6.8e-43 | |||||
MBJNBCEJ_00744 | 4e-251 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
MBJNBCEJ_00745 | 1.6e-149 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
MBJNBCEJ_00746 | 6.4e-38 | veg | S | Biofilm formation stimulator VEG | ||
MBJNBCEJ_00747 | 6.8e-159 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
MBJNBCEJ_00748 | 2.1e-97 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
MBJNBCEJ_00749 | 3.3e-149 | tatD | L | hydrolase, TatD family | ||
MBJNBCEJ_00750 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
MBJNBCEJ_00751 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
MBJNBCEJ_00752 | 1.2e-103 | S | TPM domain | |||
MBJNBCEJ_00753 | 1.8e-89 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
MBJNBCEJ_00754 | 3.3e-194 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MBJNBCEJ_00756 | 1.1e-118 | |||||
MBJNBCEJ_00757 | 5e-75 | KLT | Protein kinase domain | |||
MBJNBCEJ_00758 | 1.4e-37 | S | Aromatic-ring-opening dioxygenase LigAB, LigA subunit | |||
MBJNBCEJ_00759 | 1.5e-129 | V | ATPases associated with a variety of cellular activities | |||
MBJNBCEJ_00760 | 5e-137 | V | ABC-2 type transporter | |||
MBJNBCEJ_00761 | 2.9e-116 | E | peptidase | |||
MBJNBCEJ_00763 | 4.1e-41 | S | Enterocin A Immunity | |||
MBJNBCEJ_00764 | 7.6e-252 | L | Putative transposase DNA-binding domain | |||
MBJNBCEJ_00765 | 7.5e-146 | 2.7.7.1, 3.6.1.55, 3.6.1.67 | F | NUDIX domain | ||
MBJNBCEJ_00766 | 2e-42 | L | Membrane | |||
MBJNBCEJ_00767 | 1.1e-106 | |||||
MBJNBCEJ_00768 | 1.3e-107 | pncA | Q | Isochorismatase family | ||
MBJNBCEJ_00769 | 7.8e-54 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00770 | 1.2e-131 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00771 | 1.2e-285 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
MBJNBCEJ_00772 | 2.6e-80 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
MBJNBCEJ_00773 | 1.1e-92 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MBJNBCEJ_00774 | 3.8e-47 | Q | phosphatase activity | |||
MBJNBCEJ_00775 | 4.6e-188 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
MBJNBCEJ_00776 | 2.1e-76 | K | DNA-binding transcription factor activity | |||
MBJNBCEJ_00777 | 2.8e-07 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Maltose acetyltransferase | |
MBJNBCEJ_00778 | 8.6e-78 | ywhH | S | Aminoacyl-tRNA editing domain | ||
MBJNBCEJ_00779 | 9.2e-175 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
MBJNBCEJ_00780 | 8.6e-156 | mmuP | E | amino acid | ||
MBJNBCEJ_00781 | 5.8e-20 | mmuP | E | amino acid | ||
MBJNBCEJ_00782 | 1.2e-166 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
MBJNBCEJ_00783 | 2.4e-250 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
MBJNBCEJ_00784 | 7.4e-130 | 2.4.2.3 | F | Phosphorylase superfamily | ||
MBJNBCEJ_00786 | 4.8e-42 | tcyB | E | ABC transporter | ||
MBJNBCEJ_00787 | 1.8e-72 | tcyB | E | ABC transporter | ||
MBJNBCEJ_00788 | 2.4e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MBJNBCEJ_00789 | 3.8e-132 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
MBJNBCEJ_00792 | 1.1e-15 | S | Psort location Cytoplasmic, score | |||
MBJNBCEJ_00794 | 1.6e-242 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
MBJNBCEJ_00795 | 1.4e-142 | K | Transcriptional regulator | |||
MBJNBCEJ_00796 | 3.2e-284 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MBJNBCEJ_00797 | 5.7e-169 | KLT | Protein kinase domain | |||
MBJNBCEJ_00798 | 1.9e-233 | KLT | Protein kinase domain | |||
MBJNBCEJ_00799 | 5.8e-64 | S | HicB family | |||
MBJNBCEJ_00800 | 3.4e-39 | S | HicA toxin of bacterial toxin-antitoxin, | |||
MBJNBCEJ_00801 | 2.4e-300 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
MBJNBCEJ_00802 | 3.1e-204 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
MBJNBCEJ_00803 | 1.3e-99 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
MBJNBCEJ_00804 | 2.1e-225 | pbuX | F | xanthine permease | ||
MBJNBCEJ_00805 | 2.1e-61 | |||||
MBJNBCEJ_00806 | 1.7e-96 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
MBJNBCEJ_00807 | 8e-145 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
MBJNBCEJ_00808 | 3.1e-189 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
MBJNBCEJ_00809 | 4.1e-250 | purA | 6.3.4.4 | F | 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 | |
MBJNBCEJ_00810 | 2.1e-79 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
MBJNBCEJ_00811 | 2.1e-73 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
MBJNBCEJ_00812 | 6.5e-259 | pepC | 3.4.22.40 | E | Papain family cysteine protease | |
MBJNBCEJ_00813 | 5.1e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
MBJNBCEJ_00814 | 2.8e-179 | oppF | P | Belongs to the ABC transporter superfamily | ||
MBJNBCEJ_00815 | 3.9e-198 | oppD | P | Belongs to the ABC transporter superfamily | ||
MBJNBCEJ_00816 | 7.8e-183 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
MBJNBCEJ_00817 | 2.6e-145 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
MBJNBCEJ_00818 | 3e-301 | oppA | E | ABC transporter | ||
MBJNBCEJ_00819 | 1.4e-97 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00820 | 3.5e-123 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00821 | 1.9e-30 | oppA | E | transmembrane transport | ||
MBJNBCEJ_00822 | 9.4e-292 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00823 | 2.3e-173 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00824 | 9.1e-62 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00825 | 4e-19 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00826 | 3.1e-121 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
MBJNBCEJ_00827 | 1.6e-243 | N | Uncharacterized conserved protein (DUF2075) | |||
MBJNBCEJ_00829 | 1.8e-242 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
MBJNBCEJ_00832 | 2.7e-160 | cjaA | ET | ABC transporter substrate-binding protein | ||
MBJNBCEJ_00833 | 1.5e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MBJNBCEJ_00834 | 4e-79 | P | ABC transporter permease | |||
MBJNBCEJ_00835 | 6e-112 | papP | P | ABC transporter, permease protein | ||
MBJNBCEJ_00836 | 1.4e-98 | 3.6.1.55, 3.6.1.67 | F | NUDIX domain | ||
MBJNBCEJ_00837 | 5.5e-95 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_00838 | 1.5e-52 | S | Responsible for the incorporation of O-acetyl groups into the enterobacterial common antigen (ECA) trisaccharide repeat units | |||
MBJNBCEJ_00839 | 0.0 | XK27_08315 | M | Sulfatase | ||
MBJNBCEJ_00840 | 2.9e-108 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
MBJNBCEJ_00841 | 1.7e-206 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MBJNBCEJ_00842 | 3.9e-130 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
MBJNBCEJ_00843 | 2e-132 | |||||
MBJNBCEJ_00844 | 9.2e-99 | S | Oxidoreductase | |||
MBJNBCEJ_00845 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
MBJNBCEJ_00846 | 2.7e-275 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
MBJNBCEJ_00847 | 6.3e-192 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
MBJNBCEJ_00848 | 4e-34 | S | Protein of unknown function (DUF2922) | |||
MBJNBCEJ_00849 | 3.4e-29 | |||||
MBJNBCEJ_00850 | 6.2e-86 | |||||
MBJNBCEJ_00851 | 1.7e-72 | |||||
MBJNBCEJ_00852 | 0.0 | kup | P | Transport of potassium into the cell | ||
MBJNBCEJ_00853 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
MBJNBCEJ_00854 | 5e-62 | Z012_07300 | O | Glutaredoxin-related protein | ||
MBJNBCEJ_00855 | 1.4e-228 | yttB | EGP | Major facilitator Superfamily | ||
MBJNBCEJ_00856 | 3.7e-49 | XK27_04775 | S | PAS domain | ||
MBJNBCEJ_00857 | 9.4e-33 | S | Iron-sulfur cluster assembly protein | |||
MBJNBCEJ_00858 | 3.9e-141 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
MBJNBCEJ_00859 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
MBJNBCEJ_00860 | 7.6e-249 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
MBJNBCEJ_00861 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
MBJNBCEJ_00862 | 1.7e-273 | S | Calcineurin-like phosphoesterase | |||
MBJNBCEJ_00863 | 1.5e-83 | |||||
MBJNBCEJ_00864 | 7.1e-28 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00865 | 3.9e-207 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_00866 | 1.1e-147 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
MBJNBCEJ_00867 | 7.5e-125 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
MBJNBCEJ_00868 | 3.3e-138 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
MBJNBCEJ_00869 | 2.3e-157 | phnD | P | Phosphonate ABC transporter | ||
MBJNBCEJ_00870 | 2.5e-83 | uspA | T | universal stress protein | ||
MBJNBCEJ_00871 | 1.7e-148 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
MBJNBCEJ_00872 | 1.1e-83 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
MBJNBCEJ_00873 | 3e-89 | ntd | 2.4.2.6 | F | Nucleoside | |
MBJNBCEJ_00874 | 1.5e-222 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
MBJNBCEJ_00875 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
MBJNBCEJ_00876 | 1.3e-143 | malG | P | ABC transporter permease | ||
MBJNBCEJ_00877 | 1.5e-101 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
MBJNBCEJ_00878 | 2.5e-52 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
MBJNBCEJ_00879 | 2.8e-17 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
MBJNBCEJ_00880 | 2.4e-169 | I | alpha/beta hydrolase fold | |||
MBJNBCEJ_00881 | 4.5e-130 | yibF | S | overlaps another CDS with the same product name | ||
MBJNBCEJ_00882 | 9.9e-184 | yibE | S | overlaps another CDS with the same product name | ||
MBJNBCEJ_00883 | 1.8e-44 | |||||
MBJNBCEJ_00884 | 7.6e-205 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
MBJNBCEJ_00885 | 5.3e-200 | S | Cysteine-rich secretory protein family | |||
MBJNBCEJ_00886 | 7.2e-118 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
MBJNBCEJ_00887 | 1.7e-143 | |||||
MBJNBCEJ_00888 | 2.4e-124 | luxT | K | Bacterial regulatory proteins, tetR family | ||
MBJNBCEJ_00889 | 4.3e-186 | prs | 2.7.6.1 | F | 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) | |
MBJNBCEJ_00890 | 1.1e-124 | S | Alpha/beta hydrolase family | |||
MBJNBCEJ_00891 | 5.7e-160 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
MBJNBCEJ_00892 | 6.3e-163 | ypuA | S | Protein of unknown function (DUF1002) | ||
MBJNBCEJ_00893 | 5.9e-127 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
MBJNBCEJ_00894 | 5.6e-180 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
MBJNBCEJ_00895 | 5.5e-283 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
MBJNBCEJ_00896 | 2.3e-81 | |||||
MBJNBCEJ_00897 | 4.2e-132 | cobB | K | SIR2 family | ||
MBJNBCEJ_00898 | 3.7e-66 | yeaO | S | Protein of unknown function, DUF488 | ||
MBJNBCEJ_00899 | 9.4e-123 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
MBJNBCEJ_00900 | 1.9e-273 | glnP | P | ABC transporter permease | ||
MBJNBCEJ_00901 | 3.5e-140 | glnQ | E | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_00902 | 5e-114 | CBM50 | M | NlpC P60 family protein | ||
MBJNBCEJ_00903 | 2.2e-173 | L | HNH nucleases | |||
MBJNBCEJ_00904 | 2.8e-16 | |||||
MBJNBCEJ_00905 | 5e-207 | ybiR | P | Citrate transporter | ||
MBJNBCEJ_00906 | 1.6e-94 | lemA | S | LemA family | ||
MBJNBCEJ_00907 | 3.9e-54 | htpX | O | Belongs to the peptidase M48B family | ||
MBJNBCEJ_00908 | 5e-74 | htpX | O | Belongs to the peptidase M48B family | ||
MBJNBCEJ_00909 | 1.2e-152 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
MBJNBCEJ_00910 | 1.3e-221 | S | ATP diphosphatase activity | |||
MBJNBCEJ_00912 | 2.5e-138 | S | ABC-2 family transporter protein | |||
MBJNBCEJ_00913 | 1.6e-108 | S | ABC-2 family transporter protein | |||
MBJNBCEJ_00914 | 9.5e-172 | natA1 | S | ABC transporter | ||
MBJNBCEJ_00915 | 2.2e-151 | K | helix_turn_helix, arabinose operon control protein | |||
MBJNBCEJ_00916 | 4.6e-269 | emrY | EGP | Major facilitator Superfamily | ||
MBJNBCEJ_00917 | 1.4e-251 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_00918 | 1.6e-112 | P | Cobalt transport protein | |||
MBJNBCEJ_00919 | 1.8e-18 | L | transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00920 | 1.3e-33 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00921 | 2.7e-61 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
MBJNBCEJ_00925 | 2.8e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
MBJNBCEJ_00926 | 7.2e-162 | htrA | 3.4.21.107 | O | serine protease | |
MBJNBCEJ_00927 | 8.8e-150 | vicX | 3.1.26.11 | S | domain protein | |
MBJNBCEJ_00928 | 4.4e-141 | yycI | S | YycH protein | ||
MBJNBCEJ_00929 | 5e-242 | yycH | S | YycH protein | ||
MBJNBCEJ_00930 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
MBJNBCEJ_00931 | 2.6e-132 | K | response regulator | |||
MBJNBCEJ_00933 | 5.5e-149 | arbV | 2.3.1.51 | I | Acyl-transferase | |
MBJNBCEJ_00934 | 3.2e-155 | arbx | M | Glycosyl transferase family 8 | ||
MBJNBCEJ_00935 | 1.6e-116 | arbY | M | Glycosyl transferase family 8 | ||
MBJNBCEJ_00936 | 2.5e-166 | arbZ | I | Phosphate acyltransferases | ||
MBJNBCEJ_00937 | 0.0 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | C | FAD binding domain | |
MBJNBCEJ_00938 | 1.6e-171 | K | Transcriptional regulator, LysR family | |||
MBJNBCEJ_00939 | 1.7e-148 | ydiN | EGP | Major Facilitator Superfamily | ||
MBJNBCEJ_00940 | 2.9e-96 | S | Membrane | |||
MBJNBCEJ_00941 | 1.3e-221 | naiP | EGP | Major facilitator Superfamily | ||
MBJNBCEJ_00942 | 2.4e-167 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
MBJNBCEJ_00943 | 7.3e-172 | glk | 2.7.1.2 | G | Glucokinase | |
MBJNBCEJ_00945 | 2.9e-103 | |||||
MBJNBCEJ_00946 | 6.6e-220 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
MBJNBCEJ_00947 | 1.5e-161 | cpsY | K | Transcriptional regulator, LysR family | ||
MBJNBCEJ_00948 | 1.2e-129 | |||||
MBJNBCEJ_00949 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
MBJNBCEJ_00950 | 6.5e-282 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MBJNBCEJ_00951 | 3.4e-102 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MBJNBCEJ_00952 | 1.2e-62 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MBJNBCEJ_00953 | 3.4e-14 | mmgC | 1.3.8.1 | I | Acyl-CoA dehydrogenase, C-terminal domain | |
MBJNBCEJ_00954 | 3.4e-157 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00955 | 6.7e-18 | L | transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00956 | 1.7e-150 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
MBJNBCEJ_00957 | 4.2e-91 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
MBJNBCEJ_00958 | 5.5e-137 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
MBJNBCEJ_00959 | 4.2e-74 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
MBJNBCEJ_00960 | 2.4e-259 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | ||
MBJNBCEJ_00961 | 6e-188 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MBJNBCEJ_00962 | 1.1e-54 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00963 | 1e-41 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
MBJNBCEJ_00964 | 1.3e-99 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | cob(I)alamin adenosyltransferase | |
MBJNBCEJ_00965 | 4.7e-94 | S | ECF transporter, substrate-specific component | |||
MBJNBCEJ_00966 | 3.2e-14 | S | Domain of unknown function (DUF4430) | |||
MBJNBCEJ_00967 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
MBJNBCEJ_00968 | 6.7e-164 | yvgN | C | Aldo keto reductase | ||
MBJNBCEJ_00969 | 4.2e-172 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
MBJNBCEJ_00970 | 2e-80 | |||||
MBJNBCEJ_00971 | 1.8e-161 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
MBJNBCEJ_00972 | 8.7e-59 | S | glycolate biosynthetic process | |||
MBJNBCEJ_00973 | 1.3e-18 | L | haloacid dehalogenase-like hydrolase | |||
MBJNBCEJ_00974 | 3.4e-137 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
MBJNBCEJ_00975 | 1.3e-198 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_00976 | 2e-89 | S | biotin transmembrane transporter activity | |||
MBJNBCEJ_00977 | 1.3e-42 | |||||
MBJNBCEJ_00978 | 1.1e-119 | |||||
MBJNBCEJ_00979 | 8.1e-13 | |||||
MBJNBCEJ_00980 | 4.7e-125 | gpmB | G | Phosphoglycerate mutase family | ||
MBJNBCEJ_00981 | 1.2e-103 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
MBJNBCEJ_00982 | 1.1e-103 | T | EAL domain | |||
MBJNBCEJ_00983 | 1.7e-145 | yitS | S | EDD domain protein, DegV family | ||
MBJNBCEJ_00984 | 5.5e-92 | racA | K | Domain of unknown function (DUF1836) | ||
MBJNBCEJ_00985 | 1.3e-179 | yfdH | GT2 | M | Glycosyltransferase like family 2 | |
MBJNBCEJ_00986 | 0.0 | S | Bacterial membrane protein, YfhO | |||
MBJNBCEJ_00987 | 5.7e-167 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
MBJNBCEJ_00988 | 4.2e-135 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
MBJNBCEJ_00989 | 3.9e-84 | K | DNA-templated transcription, initiation | |||
MBJNBCEJ_00991 | 3.9e-139 | |||||
MBJNBCEJ_00992 | 3.5e-18 | yliE | T | EAL domain | ||
MBJNBCEJ_00993 | 3.7e-28 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
MBJNBCEJ_00994 | 8.1e-190 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
MBJNBCEJ_00995 | 6.9e-25 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | beta-glucosidase activity |
MBJNBCEJ_00997 | 6.9e-25 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | beta-glucosidase activity |
MBJNBCEJ_00999 | 2.7e-181 | L | Transposase | |||
MBJNBCEJ_01001 | 1.8e-74 | |||||
MBJNBCEJ_01003 | 1.3e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
MBJNBCEJ_01004 | 3e-56 | qorB | 1.6.5.2 | GM | NmrA-like family | |
MBJNBCEJ_01006 | 1.4e-72 | K | Transcriptional regulator | |||
MBJNBCEJ_01007 | 2.3e-84 | S | YcxB-like protein | |||
MBJNBCEJ_01008 | 4.1e-98 | T | integral membrane protein | |||
MBJNBCEJ_01009 | 0.0 | L | Helicase C-terminal domain protein | |||
MBJNBCEJ_01010 | 2.9e-91 | S | ECF-type riboflavin transporter, S component | |||
MBJNBCEJ_01011 | 2e-152 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
MBJNBCEJ_01013 | 1.2e-14 | L | Transposase | |||
MBJNBCEJ_01014 | 4.5e-93 | L | Psort location Cytoplasmic, score 8.87 | |||
MBJNBCEJ_01015 | 9.5e-29 | K | Acetyltransferase (GNAT) domain | |||
MBJNBCEJ_01016 | 9.4e-11 | K | Acetyltransferase (GNAT) domain | |||
MBJNBCEJ_01017 | 7.6e-240 | lysA2 | M | Glycosyl hydrolases family 25 | ||
MBJNBCEJ_01018 | 3.3e-10 | |||||
MBJNBCEJ_01019 | 2.3e-131 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
MBJNBCEJ_01020 | 2e-112 | ybbL | S | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_01022 | 1e-20 | |||||
MBJNBCEJ_01023 | 5.7e-129 | KLT | Protein kinase domain | |||
MBJNBCEJ_01024 | 0.0 | KLT | Protein kinase domain | |||
MBJNBCEJ_01025 | 8.6e-304 | msbA2 | 3.6.3.44 | V | ABC transporter | |
MBJNBCEJ_01026 | 5.4e-25 | |||||
MBJNBCEJ_01028 | 1.2e-191 | 2.7.13.3 | T | GHKL domain | ||
MBJNBCEJ_01029 | 6.8e-139 | K | LytTr DNA-binding domain | |||
MBJNBCEJ_01030 | 1.4e-114 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MBJNBCEJ_01031 | 3.3e-73 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MBJNBCEJ_01033 | 5.8e-121 | yhiD | S | MgtC family | ||
MBJNBCEJ_01035 | 1.1e-68 | |||||
MBJNBCEJ_01036 | 0.0 | V | ATPases associated with a variety of cellular activities | |||
MBJNBCEJ_01037 | 7.5e-227 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
MBJNBCEJ_01038 | 9.8e-250 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
MBJNBCEJ_01039 | 1.5e-74 | rplI | J | Binds to the 23S rRNA | ||
MBJNBCEJ_01040 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
MBJNBCEJ_01041 | 3.3e-36 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
MBJNBCEJ_01042 | 1.4e-88 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
MBJNBCEJ_01043 | 5.1e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
MBJNBCEJ_01044 | 0.0 | gyrA | 5.99.1.3 | L | 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 | |
MBJNBCEJ_01045 | 0.0 | gyrB | 5.99.1.3 | L | 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 | |
MBJNBCEJ_01046 | 2.2e-210 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
MBJNBCEJ_01047 | 6.5e-37 | yaaA | S | S4 domain protein YaaA | ||
MBJNBCEJ_01048 | 5.3e-201 | dnaN | 2.7.7.7 | L | 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 | |
MBJNBCEJ_01049 | 3e-243 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
MBJNBCEJ_01050 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
MBJNBCEJ_01051 | 1.4e-62 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
MBJNBCEJ_01052 | 2.6e-147 | yidC | U | 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 | ||
MBJNBCEJ_01053 | 4e-251 | mnmE | S | 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 | ||
MBJNBCEJ_01054 | 0.0 | gidA | D | 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 | ||
MBJNBCEJ_01055 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
MBJNBCEJ_01056 | 2.8e-268 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
MBJNBCEJ_01057 | 1.4e-74 | |||||
MBJNBCEJ_01058 | 3.5e-67 | |||||
MBJNBCEJ_01059 | 1.4e-139 | |||||
MBJNBCEJ_01060 | 1.5e-94 | |||||
MBJNBCEJ_01061 | 9.1e-110 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
MBJNBCEJ_01062 | 1.1e-103 | |||||
MBJNBCEJ_01063 | 1e-114 | |||||
MBJNBCEJ_01064 | 4.4e-92 | |||||
MBJNBCEJ_01065 | 2.3e-70 | |||||
MBJNBCEJ_01066 | 5.1e-17 | lmrA | 3.6.3.44 | V | ABC transporter | |
MBJNBCEJ_01067 | 4.1e-281 | clcA | P | chloride | ||
MBJNBCEJ_01068 | 3.7e-230 | pbuG | S | permease | ||
MBJNBCEJ_01069 | 2.7e-137 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MBJNBCEJ_01070 | 2.2e-268 | glnP | P | ABC transporter | ||
MBJNBCEJ_01071 | 1.4e-127 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
MBJNBCEJ_01072 | 2.6e-123 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
MBJNBCEJ_01073 | 8.4e-38 | |||||
MBJNBCEJ_01074 | 3.4e-166 | 3.2.1.17 | M | peptidoglycan-binding domain-containing protein | ||
MBJNBCEJ_01076 | 1.2e-13 | L | PFAM Integrase catalytic region | |||
MBJNBCEJ_01078 | 1.3e-125 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
MBJNBCEJ_01079 | 2.4e-158 | yeaE | S | Aldo/keto reductase family | ||
MBJNBCEJ_01080 | 2.5e-21 | EGP | Major facilitator Superfamily | |||
MBJNBCEJ_01081 | 2.2e-171 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
MBJNBCEJ_01082 | 6.8e-204 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
MBJNBCEJ_01083 | 2.1e-285 | xylG | 3.6.3.17 | S | ABC transporter | |
MBJNBCEJ_01084 | 2.3e-193 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
MBJNBCEJ_01085 | 5e-196 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
MBJNBCEJ_01086 | 1e-70 | S | Domain of unknown function (DUF4352) | |||
MBJNBCEJ_01087 | 7.3e-189 | KLT | Protein tyrosine kinase | |||
MBJNBCEJ_01088 | 1.1e-66 | S | Psort location Cytoplasmic, score | |||
MBJNBCEJ_01090 | 2.7e-194 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
MBJNBCEJ_01091 | 2.6e-200 | S | DUF218 domain | |||
MBJNBCEJ_01092 | 2.2e-122 | S | CAAX protease self-immunity | |||
MBJNBCEJ_01093 | 9.3e-201 | napA | P | Sodium/hydrogen exchanger family | ||
MBJNBCEJ_01094 | 0.0 | cadA | P | P-type ATPase | ||
MBJNBCEJ_01095 | 1.2e-85 | ykuL | S | (CBS) domain | ||
MBJNBCEJ_01096 | 3.7e-66 | L | An automated process has identified a potential problem with this gene model | |||
MBJNBCEJ_01097 | 3.8e-229 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_01098 | 4.6e-227 | ywhK | S | Membrane | ||
MBJNBCEJ_01099 | 7.4e-49 | |||||
MBJNBCEJ_01101 | 4.4e-296 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
MBJNBCEJ_01102 | 2.2e-240 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
MBJNBCEJ_01103 | 2e-36 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
MBJNBCEJ_01104 | 7.3e-247 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
MBJNBCEJ_01105 | 3.8e-66 | S | Iron-sulphur cluster biosynthesis | |||
MBJNBCEJ_01106 | 0.0 | yhcA | V | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_01107 | 5.5e-115 | K | Bacterial regulatory proteins, tetR family | |||
MBJNBCEJ_01108 | 1.8e-74 | |||||
MBJNBCEJ_01117 | 7.9e-29 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
MBJNBCEJ_01118 | 5.1e-13 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
MBJNBCEJ_01119 | 1.1e-11 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
MBJNBCEJ_01120 | 1e-193 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
MBJNBCEJ_01121 | 1.4e-78 | ribH | 2.5.1.78 | H | 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 | |
MBJNBCEJ_01122 | 3.5e-142 | K | LysR family | |||
MBJNBCEJ_01123 | 2.2e-36 | P | Sodium:sulfate symporter transmembrane region | |||
MBJNBCEJ_01124 | 1.8e-74 | |||||
MBJNBCEJ_01126 | 4e-240 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
MBJNBCEJ_01127 | 7.4e-166 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
MBJNBCEJ_01128 | 7.5e-149 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MBJNBCEJ_01129 | 3.3e-138 | puuD | S | peptidase C26 | ||
MBJNBCEJ_01130 | 5.3e-159 | yicL | EG | EamA-like transporter family | ||
MBJNBCEJ_01131 | 5.7e-49 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
MBJNBCEJ_01132 | 9e-31 | tnp2 | L | PFAM Transposase, IS204 IS1001 IS1096 IS1165 | ||
MBJNBCEJ_01133 | 1.9e-132 | L | Transposase | |||
MBJNBCEJ_01134 | 1.4e-167 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
MBJNBCEJ_01135 | 3.2e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
MBJNBCEJ_01136 | 4.2e-183 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
MBJNBCEJ_01137 | 3.2e-247 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
MBJNBCEJ_01138 | 6.4e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
MBJNBCEJ_01139 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
MBJNBCEJ_01140 | 1.6e-66 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
MBJNBCEJ_01141 | 7e-25 | 5.99.1.2 | T | diguanylate cyclase | ||
MBJNBCEJ_01142 | 2.1e-72 | 5.99.1.2 | T | diguanylate cyclase | ||
MBJNBCEJ_01143 | 1.3e-08 | T | diguanylate cyclase | |||
MBJNBCEJ_01144 | 0.0 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
MBJNBCEJ_01145 | 8.6e-37 | |||||
MBJNBCEJ_01146 | 1.4e-129 | cobQ | S | glutamine amidotransferase | ||
MBJNBCEJ_01147 | 2.5e-27 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
MBJNBCEJ_01148 | 2.4e-144 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
MBJNBCEJ_01149 | 4e-144 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
MBJNBCEJ_01150 | 0.0 | KLT | serine threonine protein kinase | |||
MBJNBCEJ_01151 | 7.2e-289 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MBJNBCEJ_01152 | 2e-146 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
MBJNBCEJ_01153 | 4.4e-91 | ymdB | S | Macro domain protein | ||
MBJNBCEJ_01154 | 2.4e-34 | |||||
MBJNBCEJ_01155 | 2.4e-151 | |||||
MBJNBCEJ_01158 | 2.5e-264 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
MBJNBCEJ_01159 | 1e-257 | P | Sodium:sulfate symporter transmembrane region | |||
MBJNBCEJ_01161 | 4.4e-255 | pipD | M | Peptidase family C69 | ||
MBJNBCEJ_01162 | 8.7e-173 | citR | K | Putative sugar-binding domain | ||
MBJNBCEJ_01163 | 6.3e-36 | lysM | M | LysM domain | ||
MBJNBCEJ_01164 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
MBJNBCEJ_01165 | 2.9e-34 | drgA | C | Nitroreductase family | ||
MBJNBCEJ_01166 | 5.9e-227 | S | Putative peptidoglycan binding domain | |||
MBJNBCEJ_01167 | 6e-117 | |||||
MBJNBCEJ_01168 | 4.2e-138 | S | Belongs to the UPF0246 family | |||
MBJNBCEJ_01169 | 2.1e-64 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
MBJNBCEJ_01170 | 7.6e-120 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
MBJNBCEJ_01171 | 2.1e-88 | ygfC | K | transcriptional regulator (TetR family) | ||
MBJNBCEJ_01172 | 7.7e-186 | hrtB | V | ABC transporter permease | ||
MBJNBCEJ_01173 | 4.4e-118 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
MBJNBCEJ_01174 | 8e-171 | K | WYL domain | |||
MBJNBCEJ_01175 | 1.3e-66 | S | pyridoxamine 5-phosphate | |||
MBJNBCEJ_01176 | 5.9e-11 | K | LytTr DNA-binding domain | |||
MBJNBCEJ_01177 | 1.3e-87 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
MBJNBCEJ_01178 | 1.1e-139 | |||||
MBJNBCEJ_01180 | 2e-107 | |||||
MBJNBCEJ_01181 | 1.8e-116 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
MBJNBCEJ_01182 | 1.1e-16 | |||||
MBJNBCEJ_01183 | 1.6e-276 | pipD | E | Dipeptidase | ||
MBJNBCEJ_01184 | 1.5e-97 | K | WHG domain | |||
MBJNBCEJ_01185 | 9.9e-97 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
MBJNBCEJ_01186 | 5e-96 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
MBJNBCEJ_01187 | 3e-142 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
MBJNBCEJ_01188 | 2e-188 | apbE | 2.7.1.180 | H | 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 | |
MBJNBCEJ_01189 | 5.3e-87 | cvpA | S | Colicin V production protein | ||
MBJNBCEJ_01190 | 7.4e-132 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
MBJNBCEJ_01191 | 3.3e-144 | noc | K | Belongs to the ParB family | ||
MBJNBCEJ_01192 | 2.6e-138 | soj | D | Sporulation initiation inhibitor | ||
MBJNBCEJ_01193 | 7.8e-155 | spo0J | K | Belongs to the ParB family | ||
MBJNBCEJ_01194 | 2.5e-45 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
MBJNBCEJ_01195 | 6.1e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
MBJNBCEJ_01196 | 3.1e-136 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
MBJNBCEJ_01197 | 0.0 | V | ABC transporter, ATP-binding protein | |||
MBJNBCEJ_01198 | 0.0 | ndvA | V | ABC transporter | ||
MBJNBCEJ_01199 | 1e-122 | K | response regulator | |||
MBJNBCEJ_01200 | 1.6e-219 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
MBJNBCEJ_01201 | 6.4e-298 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
MBJNBCEJ_01202 | 1.4e-144 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
MBJNBCEJ_01203 | 9.8e-135 | fruR | K | DeoR C terminal sensor domain | ||
MBJNBCEJ_01204 | 4.5e-166 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
MBJNBCEJ_01205 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
MBJNBCEJ_01206 | 1.6e-143 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | G | Sucrose-6F-phosphate phosphohydrolase | ||
MBJNBCEJ_01207 | 8.6e-119 | fhuC | P | ABC transporter | ||
MBJNBCEJ_01208 | 8e-135 | znuB | U | ABC 3 transport family | ||
MBJNBCEJ_01209 | 8.3e-49 | KT | response to antibiotic | |||
MBJNBCEJ_01210 | 1.7e-100 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
MBJNBCEJ_01211 | 0.0 | pepF | E | oligoendopeptidase F | ||
MBJNBCEJ_01212 | 4.2e-250 | L | Putative transposase DNA-binding domain | |||
MBJNBCEJ_01213 | 1.1e-206 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MBJNBCEJ_01214 | 2.7e-16 | |||||
MBJNBCEJ_01215 | 9.5e-294 | S | ABC transporter, ATP-binding protein | |||
MBJNBCEJ_01216 | 2.8e-137 | thrE | S | Putative threonine/serine exporter | ||
MBJNBCEJ_01217 | 1.4e-84 | S | Threonine/Serine exporter, ThrE | |||
MBJNBCEJ_01218 | 4.1e-76 | |||||
MBJNBCEJ_01219 | 2.2e-111 | |||||
MBJNBCEJ_01220 | 2.9e-290 | S | O-antigen ligase like membrane protein | |||
MBJNBCEJ_01221 | 7.2e-45 | |||||
MBJNBCEJ_01222 | 1.9e-95 | gmk2 | 2.7.4.8 | F | Guanylate kinase homologues. | |
MBJNBCEJ_01223 | 5.6e-83 | M | NlpC P60 family | |||
MBJNBCEJ_01224 | 1.4e-200 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MBJNBCEJ_01225 | 1.9e-75 | M | NlpC/P60 family | |||
MBJNBCEJ_01226 | 1.5e-106 | M | NlpC P60 family protein | |||
MBJNBCEJ_01227 | 1.2e-123 | M | NlpC P60 family protein | |||
MBJNBCEJ_01228 | 1.8e-115 | M | NlpC P60 family protein | |||
MBJNBCEJ_01229 | 3e-224 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
MBJNBCEJ_01230 | 2.1e-175 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MBJNBCEJ_01231 | 2.2e-109 | epsB | M | biosynthesis protein | ||
MBJNBCEJ_01232 | 9.8e-114 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
MBJNBCEJ_01233 | 7.5e-146 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
MBJNBCEJ_01234 | 5.8e-123 | rfbP | M | Bacterial sugar transferase | ||
MBJNBCEJ_01235 | 5.2e-86 | cpsF | M | Oligosaccharide biosynthesis protein Alg14 like | ||
MBJNBCEJ_01236 | 1.2e-83 | pssE | S | Glycosyltransferase family 28 C-terminal domain | ||
MBJNBCEJ_01237 | 1.8e-88 | M | Domain of unknown function (DUF4422) | |||
MBJNBCEJ_01238 | 2e-17 | |||||
MBJNBCEJ_01239 | 3e-188 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
MBJNBCEJ_01240 | 1.4e-60 | cps2I | M | Spore coat protein | ||
MBJNBCEJ_01241 | 1.1e-41 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01242 | 1.1e-27 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01243 | 4.7e-70 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01244 | 1.8e-116 | S | Membrane protein involved in the export of O-antigen and teichoic acid | |||
MBJNBCEJ_01245 | 4.7e-35 | gpsA | 1.1.1.94 | I | Rossmann-like domain | |
MBJNBCEJ_01246 | 2.6e-41 | S | Core-2/I-Branching enzyme | |||
MBJNBCEJ_01247 | 8.7e-201 | GT4 | M | Glycosyl transferases group 1 | ||
MBJNBCEJ_01248 | 1.3e-102 | L | Transposase and inactivated derivatives | |||
MBJNBCEJ_01249 | 3.3e-39 | L | Transposase and inactivated derivatives | |||
MBJNBCEJ_01250 | 0.0 | mcrB | V | AAA domain (dynein-related subfamily) | ||
MBJNBCEJ_01251 | 8.2e-119 | mcrC | V | McrBC 5-methylcytosine restriction system component | ||
MBJNBCEJ_01252 | 7.4e-13 | K | Bacterial regulatory proteins, tetR family | |||
MBJNBCEJ_01253 | 2e-96 | L | nuclease | |||
MBJNBCEJ_01254 | 3.8e-154 | F | DNA/RNA non-specific endonuclease | |||
MBJNBCEJ_01255 | 3.3e-11 | |||||
MBJNBCEJ_01256 | 4.8e-175 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
MBJNBCEJ_01257 | 2.7e-59 | K | Bacterial regulatory proteins, tetR family | |||
MBJNBCEJ_01258 | 5.4e-197 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
MBJNBCEJ_01260 | 8.5e-39 | higA | K | Helix-turn-helix XRE-family like proteins | ||
MBJNBCEJ_01261 | 4.1e-26 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
MBJNBCEJ_01262 | 8.8e-35 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
MBJNBCEJ_01263 | 5.4e-96 | S | ABC transporter, ATP-binding protein | |||
MBJNBCEJ_01264 | 2.8e-153 | XK27_00670 | S | ABC transporter | ||
MBJNBCEJ_01266 | 4.9e-27 | |||||
MBJNBCEJ_01267 | 6.1e-93 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_01268 | 9.8e-11 | N | phage tail tape measure protein | |||
MBJNBCEJ_01269 | 1.1e-57 | C | Coenzyme F420-dependent N5N10-methylene tetrahydromethanopterin reductase | |||
MBJNBCEJ_01270 | 4.5e-40 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | |||
MBJNBCEJ_01271 | 5e-182 | gpsA | 1.1.1.94 | I | Rossmann-like domain | |
MBJNBCEJ_01272 | 2.7e-58 | K | sequence-specific DNA binding | |||
MBJNBCEJ_01273 | 8.5e-86 | |||||
MBJNBCEJ_01274 | 2.9e-71 | F | DNA/RNA non-specific endonuclease | |||
MBJNBCEJ_01276 | 2.6e-174 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MBJNBCEJ_01277 | 1.6e-132 | S | Core-2/I-Branching enzyme | |||
MBJNBCEJ_01278 | 2.2e-119 | rfbP | 2.7.8.6 | M | Bacterial sugar transferase | |
MBJNBCEJ_01279 | 7.7e-151 | cps1D | M | Domain of unknown function (DUF4422) | ||
MBJNBCEJ_01280 | 2.5e-219 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
MBJNBCEJ_01281 | 2.4e-172 | glfT1 | 1.1.1.133 | S | Glycosyltransferase like family 2 | |
MBJNBCEJ_01282 | 1.5e-184 | M | Glycosyl transferases group 1 | |||
MBJNBCEJ_01283 | 5.1e-198 | wbbI | M | transferase activity, transferring glycosyl groups | ||
MBJNBCEJ_01284 | 2.1e-263 | epsIIL | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
MBJNBCEJ_01285 | 6e-179 | M | LicD family | |||
MBJNBCEJ_01286 | 3.4e-85 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
MBJNBCEJ_01287 | 4.7e-222 | |||||
MBJNBCEJ_01289 | 5.6e-41 | I | Acyltransferase family | |||
MBJNBCEJ_01290 | 2.1e-18 | S | Peptidase_C39 like family | |||
MBJNBCEJ_01291 | 6.2e-09 | S | Peptidase_C39 like family | |||
MBJNBCEJ_01292 | 1.1e-49 | S | Bacterial membrane protein, YfhO | |||
MBJNBCEJ_01293 | 2.5e-27 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
MBJNBCEJ_01294 | 1.9e-74 | S | VanZ like family | |||
MBJNBCEJ_01295 | 9.4e-74 | mesH | S | Teichoic acid glycosylation protein | ||
MBJNBCEJ_01296 | 2.2e-128 | S | VanZ like family | |||
MBJNBCEJ_01297 | 2.6e-58 | sidC | L | DNA recombination | ||
MBJNBCEJ_01298 | 6.9e-84 | sidC | L | DNA recombination | ||
MBJNBCEJ_01299 | 1.3e-10 | sidC | L | DNA recombination | ||
MBJNBCEJ_01300 | 0.0 | 3.1.4.46, 3.2.1.99 | GH43 | N | domain, Protein | |
MBJNBCEJ_01302 | 2.5e-39 | |||||
MBJNBCEJ_01303 | 3.4e-134 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
MBJNBCEJ_01304 | 2e-123 | pgm3 | G | Phosphoglycerate mutase family | ||
MBJNBCEJ_01305 | 4.5e-115 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
MBJNBCEJ_01306 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
MBJNBCEJ_01307 | 1.6e-25 | glnQ | 3.6.3.21 | E | ABC transporter | |
MBJNBCEJ_01308 | 5.5e-49 | aatB | ET | ABC transporter substrate-binding protein | ||
MBJNBCEJ_01309 | 4.7e-85 | aatB | ET | ABC transporter substrate-binding protein | ||
MBJNBCEJ_01310 | 1.8e-11 | liaI | S | membrane | ||
MBJNBCEJ_01311 | 2.6e-74 | XK27_02470 | K | LytTr DNA-binding domain | ||
MBJNBCEJ_01312 | 5.7e-103 | E | GDSL-like Lipase/Acylhydrolase | |||
MBJNBCEJ_01313 | 1e-170 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
MBJNBCEJ_01314 | 1.4e-98 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
MBJNBCEJ_01315 | 6.2e-76 | ymfM | S | Helix-turn-helix domain | ||
MBJNBCEJ_01316 | 1.1e-180 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
MBJNBCEJ_01317 | 1.2e-197 | |||||
MBJNBCEJ_01318 | 1.4e-14 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
MBJNBCEJ_01319 | 2.7e-109 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_01320 | 3.3e-289 | V | ABC transporter transmembrane region | |||
MBJNBCEJ_01321 | 7.8e-09 | S | PAS domain | |||
MBJNBCEJ_01322 | 3.5e-44 | GK | ROK family | |||
MBJNBCEJ_01325 | 1.6e-157 | dkg | S | reductase | ||
MBJNBCEJ_01326 | 3e-124 | endA | F | DNA RNA non-specific endonuclease | ||
MBJNBCEJ_01327 | 2.6e-42 | E | dipeptidase activity | |||
MBJNBCEJ_01328 | 5.7e-106 | |||||
MBJNBCEJ_01329 | 5.4e-86 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
MBJNBCEJ_01330 | 4.6e-176 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
MBJNBCEJ_01331 | 6.7e-154 | corA | P | CorA-like Mg2+ transporter protein | ||
MBJNBCEJ_01332 | 1.7e-157 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
MBJNBCEJ_01333 | 5.5e-26 | |||||
MBJNBCEJ_01334 | 2.3e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
MBJNBCEJ_01335 | 0.0 | ydgH | S | MMPL family | ||
MBJNBCEJ_01336 | 1.2e-173 | |||||
MBJNBCEJ_01337 | 1.7e-81 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_01338 | 1.1e-107 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_01339 | 1.2e-128 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
MBJNBCEJ_01340 | 8.6e-95 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
MBJNBCEJ_01341 | 5.2e-156 | hipB | K | Helix-turn-helix | ||
MBJNBCEJ_01342 | 7.7e-154 | I | alpha/beta hydrolase fold | |||
MBJNBCEJ_01343 | 4.4e-106 | yjbF | S | SNARE associated Golgi protein | ||
MBJNBCEJ_01344 | 6.1e-93 | J | Acetyltransferase (GNAT) domain | |||
MBJNBCEJ_01345 | 5.9e-236 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
MBJNBCEJ_01346 | 6.5e-99 | K | Sigma-70 region 2 | |||
MBJNBCEJ_01347 | 2.4e-153 | S | Protein of unknown function (DUF3298) | |||
MBJNBCEJ_01348 | 1.8e-74 | |||||
MBJNBCEJ_01352 | 7.8e-202 | S | amidohydrolase | |||
MBJNBCEJ_01353 | 1e-13 | XK27_07210 | 6.1.1.6 | S | B3 4 domain | |
MBJNBCEJ_01354 | 2.3e-124 | E | Arginine ornithine antiporter | |||
MBJNBCEJ_01355 | 4.2e-82 | E | amino acid | |||
MBJNBCEJ_01382 | 2.6e-219 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
MBJNBCEJ_01383 | 2.2e-201 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
MBJNBCEJ_01384 | 3.3e-178 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
MBJNBCEJ_01385 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
MBJNBCEJ_01386 | 2.9e-29 | secG | U | Preprotein translocase | ||
MBJNBCEJ_01387 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
MBJNBCEJ_01388 | 8e-79 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
MBJNBCEJ_01391 | 1.9e-215 | S | FtsX-like permease family | |||
MBJNBCEJ_01392 | 1.8e-119 | V | ABC transporter, ATP-binding protein | |||
MBJNBCEJ_01394 | 8.1e-232 | isp2 | L | Transposase | ||
MBJNBCEJ_01395 | 6e-91 | yjcF | S | Acetyltransferase (GNAT) domain | ||
MBJNBCEJ_01396 | 5.9e-143 | sufC | O | FeS assembly ATPase SufC | ||
MBJNBCEJ_01397 | 4e-220 | sufD | O | FeS assembly protein SufD | ||
MBJNBCEJ_01398 | 1.3e-224 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
MBJNBCEJ_01399 | 3.3e-74 | nifU | C | SUF system FeS assembly protein, NifU family | ||
MBJNBCEJ_01400 | 1.4e-275 | sufB | O | assembly protein SufB | ||
MBJNBCEJ_01401 | 9.2e-73 | cydD | V | abc transporter atp-binding protein | ||
MBJNBCEJ_01403 | 1.8e-74 | |||||
MBJNBCEJ_01405 | 4.1e-248 | nhaC | C | Na H antiporter NhaC | ||
MBJNBCEJ_01406 | 4e-74 | L | Putative transposase DNA-binding domain | |||
MBJNBCEJ_01408 | 4.7e-227 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_01409 | 3.8e-102 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01410 | 6.1e-112 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01411 | 3.6e-188 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
MBJNBCEJ_01412 | 1.2e-138 | manY | G | PTS system | ||
MBJNBCEJ_01413 | 3.9e-170 | manN | G | system, mannose fructose sorbose family IID component | ||
MBJNBCEJ_01414 | 1.6e-63 | manO | S | Domain of unknown function (DUF956) | ||
MBJNBCEJ_01416 | 8.6e-246 | cycA | E | Amino acid permease | ||
MBJNBCEJ_01417 | 2.5e-163 | 3.5.2.6 | M | NlpC/P60 family | ||
MBJNBCEJ_01419 | 1.6e-07 | K | Helix-turn-helix domain | |||
MBJNBCEJ_01420 | 5.3e-189 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
MBJNBCEJ_01421 | 0.0 | recQ1 | L | Helicase conserved C-terminal domain | ||
MBJNBCEJ_01422 | 2.4e-47 | |||||
MBJNBCEJ_01423 | 7.8e-19 | K | sequence-specific DNA binding | |||
MBJNBCEJ_01425 | 1.7e-221 | oxlT | P | Major Facilitator Superfamily | ||
MBJNBCEJ_01426 | 3.7e-21 | malS | 3.2.1.1 | GH13 | G | Glycogen debranching enzyme, glucanotransferase domain |
MBJNBCEJ_01427 | 4.6e-99 | malS | 3.2.1.1 | GH13 | G | Glycogen debranching enzyme, glucanotransferase domain |
MBJNBCEJ_01428 | 4.9e-72 | malS | 3.2.1.1 | GH13 | G | Glycogen debranching enzyme, glucanotransferase domain |
MBJNBCEJ_01430 | 1.4e-161 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_01431 | 1.1e-207 | G | Major Facilitator Superfamily | |||
MBJNBCEJ_01432 | 2.9e-38 | L | COG2963 Transposase and inactivated derivatives | |||
MBJNBCEJ_01433 | 2.9e-205 | G | Major Facilitator Superfamily | |||
MBJNBCEJ_01434 | 6.4e-31 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_01435 | 1e-276 | E | Amino acid permease | |||
MBJNBCEJ_01436 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
MBJNBCEJ_01437 | 6.2e-81 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
MBJNBCEJ_01438 | 6.5e-127 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
MBJNBCEJ_01439 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
MBJNBCEJ_01440 | 2.1e-199 | pfkA | 2.7.1.11, 2.7.1.90 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
MBJNBCEJ_01441 | 7.8e-79 | 2.7.1.199, 2.7.1.211 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
MBJNBCEJ_01442 | 1.4e-159 | scrB | 3.2.1.26 | GH32 | G | invertase |
MBJNBCEJ_01443 | 3.2e-138 | scrR | K | Transcriptional regulator, LacI family | ||
MBJNBCEJ_01444 | 7.7e-25 | |||||
MBJNBCEJ_01445 | 1.5e-106 | yiiE | S | Protein of unknown function (DUF1211) | ||
MBJNBCEJ_01446 | 7.2e-100 | K | Acetyltransferase (GNAT) domain | |||
MBJNBCEJ_01450 | 1.2e-282 | thrC | 4.2.3.1 | E | Threonine synthase | |
MBJNBCEJ_01451 | 7.2e-158 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
MBJNBCEJ_01456 | 2.7e-83 | M | LysM domain protein | |||
MBJNBCEJ_01457 | 9.5e-145 | D | nuclear chromosome segregation | |||
MBJNBCEJ_01458 | 8e-252 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
MBJNBCEJ_01459 | 1.4e-165 | cycA | E | Amino acid permease | ||
MBJNBCEJ_01460 | 1.7e-47 | cycA | E | Amino acid permease | ||
MBJNBCEJ_01461 | 1.4e-275 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
MBJNBCEJ_01462 | 2.6e-135 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
MBJNBCEJ_01463 | 1e-18 | 3.5.2.6 | V | Beta-lactamase | ||
MBJNBCEJ_01464 | 7.5e-08 | 3.5.2.6 | V | Beta-lactamase | ||
MBJNBCEJ_01465 | 4.8e-196 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
MBJNBCEJ_01466 | 1.7e-93 | wecD | K | Acetyltransferase (GNAT) family | ||
MBJNBCEJ_01467 | 1e-107 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
MBJNBCEJ_01468 | 8.5e-115 | S | membrane transporter protein | |||
MBJNBCEJ_01469 | 4.7e-128 | pgm3 | G | Belongs to the phosphoglycerate mutase family | ||
MBJNBCEJ_01470 | 2.6e-28 | |||||
MBJNBCEJ_01471 | 5.2e-29 | |||||
MBJNBCEJ_01472 | 2.2e-125 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
MBJNBCEJ_01473 | 2.1e-79 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
MBJNBCEJ_01474 | 7e-183 | S | AAA domain | |||
MBJNBCEJ_01475 | 8.1e-57 | 5.2.1.8 | O | Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD | ||
MBJNBCEJ_01476 | 3.2e-51 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MBJNBCEJ_01477 | 2.1e-32 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MBJNBCEJ_01479 | 1.9e-43 | V | AAA domain (dynein-related subfamily) | |||
MBJNBCEJ_01480 | 2.1e-44 | S | LlaJI restriction endonuclease | |||
MBJNBCEJ_01481 | 5.6e-266 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
MBJNBCEJ_01482 | 5.4e-49 | |||||
MBJNBCEJ_01483 | 1.7e-99 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
MBJNBCEJ_01484 | 6.6e-254 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
MBJNBCEJ_01485 | 9e-186 | arbY | M | Glycosyl transferase family 8 | ||
MBJNBCEJ_01486 | 7.8e-64 | yliE | T | domain protein | ||
MBJNBCEJ_01487 | 2.1e-149 | yliE | T | Putative diguanylate phosphodiesterase | ||
MBJNBCEJ_01488 | 1.8e-74 | |||||
MBJNBCEJ_01495 | 1e-60 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
MBJNBCEJ_01496 | 1.2e-168 | ytrB | V | ABC transporter | ||
MBJNBCEJ_01497 | 0.0 | S | ABC-type transport system involved in multi-copper enzyme maturation permease component | |||
MBJNBCEJ_01498 | 4.4e-36 | cycA | E | Amino acid permease | ||
MBJNBCEJ_01499 | 7.6e-160 | salL | 2.5.1.63, 2.5.1.94 | K | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
MBJNBCEJ_01500 | 1.3e-99 | S | UPF0397 protein | |||
MBJNBCEJ_01501 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_01502 | 4.4e-144 | cbiQ | P | cobalt transport | ||
MBJNBCEJ_01503 | 6.7e-262 | adhE | 1.1.1.1, 1.2.1.10 | C | Aldehyde dehydrogenase family | |
MBJNBCEJ_01504 | 3.7e-85 | S | ECF-type riboflavin transporter, S component | |||
MBJNBCEJ_01505 | 4.8e-11 | 5.99.1.2 | T | diguanylate cyclase | ||
MBJNBCEJ_01506 | 1.5e-109 | T | EAL domain | |||
MBJNBCEJ_01507 | 9.7e-29 | 5.99.1.2 | T | diguanylate cyclase | ||
MBJNBCEJ_01508 | 7.1e-71 | 2.7.13.3 | T | diguanylate cyclase | ||
MBJNBCEJ_01509 | 2.7e-213 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
MBJNBCEJ_01510 | 3.2e-212 | EGP | Transmembrane secretion effector | |||
MBJNBCEJ_01511 | 8.6e-201 | |||||
MBJNBCEJ_01512 | 8.5e-159 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
MBJNBCEJ_01513 | 9.4e-26 | 6.3.4.18, 6.3.5.5 | F | 5-(carboxyamino)imidazole ribonucleotide synthase activity | ||
MBJNBCEJ_01514 | 9.7e-180 | 6.3.4.18, 6.3.5.5 | F | 5-(carboxyamino)imidazole ribonucleotide synthase activity | ||
MBJNBCEJ_01515 | 4.8e-232 | 6.3.2.4 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | ||
MBJNBCEJ_01516 | 1.1e-92 | 3.6.1.13 | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
MBJNBCEJ_01517 | 4.2e-264 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_01518 | 8.7e-60 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
MBJNBCEJ_01519 | 1.7e-120 | skfE | V | ATPases associated with a variety of cellular activities | ||
MBJNBCEJ_01521 | 3.3e-291 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
MBJNBCEJ_01522 | 7.2e-181 | yeiH | S | Conserved hypothetical protein 698 | ||
MBJNBCEJ_01523 | 6e-160 | K | LysR substrate binding domain | |||
MBJNBCEJ_01524 | 2.7e-105 | 3.6.1.67 | F | NUDIX domain | ||
MBJNBCEJ_01525 | 1.1e-275 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MBJNBCEJ_01526 | 9.4e-77 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
MBJNBCEJ_01527 | 5.5e-138 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
MBJNBCEJ_01528 | 2.4e-101 | yvrI | K | sigma factor activity | ||
MBJNBCEJ_01529 | 1.8e-33 | |||||
MBJNBCEJ_01530 | 1.4e-112 | 4.2.99.20 | S | Alpha/beta hydrolase family | ||
MBJNBCEJ_01531 | 9.1e-95 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
MBJNBCEJ_01532 | 2.9e-96 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
MBJNBCEJ_01533 | 8.4e-63 | dxs | 2.2.1.7 | HI | 1-deoxy-D-xylulose-5-phosphate synthase | |
MBJNBCEJ_01534 | 1e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
MBJNBCEJ_01535 | 1.8e-23 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
MBJNBCEJ_01536 | 5.2e-101 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
MBJNBCEJ_01537 | 6.9e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
MBJNBCEJ_01538 | 2e-121 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
MBJNBCEJ_01539 | 2.9e-190 | S | Glycosyl transferase family 2 | |||
MBJNBCEJ_01540 | 1.6e-230 | amtB | P | ammonium transporter | ||
MBJNBCEJ_01541 | 8.5e-69 | |||||
MBJNBCEJ_01542 | 5.9e-206 | L | Putative transposase DNA-binding domain | |||
MBJNBCEJ_01543 | 1.1e-81 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
MBJNBCEJ_01544 | 1.8e-49 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
MBJNBCEJ_01545 | 1.4e-84 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_01546 | 1.6e-145 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_01547 | 4.6e-14 | P | nitric oxide dioxygenase activity | |||
MBJNBCEJ_01548 | 3.3e-83 | apbE | 2.7.1.180 | H | 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 | |
MBJNBCEJ_01550 | 3.8e-11 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
MBJNBCEJ_01551 | 3e-19 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
MBJNBCEJ_01552 | 1.6e-39 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
MBJNBCEJ_01553 | 4.2e-214 | pbpX1 | V | Beta-lactamase | ||
MBJNBCEJ_01554 | 4.6e-205 | pbpX1 | V | Beta-lactamase | ||
MBJNBCEJ_01555 | 1.9e-14 | L | Helix-turn-helix domain | |||
MBJNBCEJ_01556 | 1.2e-45 | |||||
MBJNBCEJ_01557 | 9.1e-173 | |||||
MBJNBCEJ_01558 | 1.8e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
MBJNBCEJ_01559 | 7.2e-112 | rsmC | 2.1.1.172 | J | Methyltransferase | |
MBJNBCEJ_01560 | 2.2e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
MBJNBCEJ_01561 | 7.1e-288 | dnaX | 2.7.7.7 | L | 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 | |
MBJNBCEJ_01562 | 3.5e-52 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
MBJNBCEJ_01563 | 1.5e-106 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
MBJNBCEJ_01564 | 1.4e-34 | S | Protein of unknown function (DUF2508) | |||
MBJNBCEJ_01565 | 2.4e-113 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
MBJNBCEJ_01566 | 2.4e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
MBJNBCEJ_01567 | 1e-159 | holB | 2.7.7.7 | L | DNA polymerase III | |
MBJNBCEJ_01568 | 9.9e-55 | yabA | L | Involved in initiation control of chromosome replication | ||
MBJNBCEJ_01569 | 8.6e-159 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
MBJNBCEJ_01570 | 3.1e-141 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
MBJNBCEJ_01571 | 3.4e-89 | folT | S | ECF transporter, substrate-specific component | ||
MBJNBCEJ_01572 | 2e-89 | folT | S | ECF transporter, substrate-specific component | ||
MBJNBCEJ_01573 | 3.6e-126 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
MBJNBCEJ_01574 | 7.7e-94 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
MBJNBCEJ_01575 | 7.6e-194 | tsaD | 2.3.1.234 | J | 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 | |
MBJNBCEJ_01576 | 6.8e-302 | uup | S | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_01577 | 1e-122 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
MBJNBCEJ_01578 | 8.8e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
MBJNBCEJ_01579 | 1.8e-290 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
MBJNBCEJ_01580 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
MBJNBCEJ_01581 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
MBJNBCEJ_01582 | 6.4e-105 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
MBJNBCEJ_01583 | 1.6e-185 | ruvB | 3.6.4.12 | L | 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 | |
MBJNBCEJ_01584 | 3e-34 | yajC | U | Preprotein translocase | ||
MBJNBCEJ_01585 | 7.9e-282 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
MBJNBCEJ_01586 | 6.4e-207 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
MBJNBCEJ_01587 | 4.1e-178 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
MBJNBCEJ_01588 | 7.5e-226 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
MBJNBCEJ_01589 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
MBJNBCEJ_01590 | 5.7e-42 | yrzL | S | Belongs to the UPF0297 family | ||
MBJNBCEJ_01591 | 3.9e-72 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
MBJNBCEJ_01592 | 1e-40 | yrzB | S | Belongs to the UPF0473 family | ||
MBJNBCEJ_01593 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
MBJNBCEJ_01594 | 1e-53 | trxA | O | Belongs to the thioredoxin family | ||
MBJNBCEJ_01595 | 1.7e-66 | yslB | S | Protein of unknown function (DUF2507) | ||
MBJNBCEJ_01596 | 2.3e-113 | rdgB | 3.6.1.66, 5.1.1.3 | F | 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 | |
MBJNBCEJ_01597 | 2.7e-149 | ykuT | M | mechanosensitive ion channel | ||
MBJNBCEJ_01598 | 5.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
MBJNBCEJ_01599 | 1.7e-39 | |||||
MBJNBCEJ_01600 | 1.4e-27 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
MBJNBCEJ_01602 | 1.8e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
MBJNBCEJ_01603 | 4.9e-182 | ccpA | K | catabolite control protein A | ||
MBJNBCEJ_01604 | 5.6e-58 | |||||
MBJNBCEJ_01605 | 5.6e-280 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
MBJNBCEJ_01606 | 2.8e-83 | yutD | S | Protein of unknown function (DUF1027) | ||
MBJNBCEJ_01607 | 3.1e-144 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
MBJNBCEJ_01608 | 3.5e-106 | S | Protein of unknown function (DUF1461) | |||
MBJNBCEJ_01609 | 6.6e-119 | dedA | S | SNARE-like domain protein | ||
MBJNBCEJ_01610 | 1e-184 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
MBJNBCEJ_01611 | 1.8e-74 | |||||
MBJNBCEJ_01619 | 1.1e-217 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
MBJNBCEJ_01620 | 3.8e-260 | mdr | EGP | Sugar (and other) transporter | ||
MBJNBCEJ_01621 | 1.3e-119 | 3.6.1.27 | I | Acid phosphatase homologues | ||
MBJNBCEJ_01622 | 5.8e-160 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_01623 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MBJNBCEJ_01624 | 2.2e-293 | ytgP | S | Polysaccharide biosynthesis protein | ||
MBJNBCEJ_01625 | 3.8e-85 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
MBJNBCEJ_01626 | 1.4e-158 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
MBJNBCEJ_01627 | 7.5e-57 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
MBJNBCEJ_01628 | 7.6e-67 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
MBJNBCEJ_01629 | 9.5e-153 | |||||
MBJNBCEJ_01630 | 9.5e-247 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
MBJNBCEJ_01631 | 2e-74 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
MBJNBCEJ_01633 | 1.6e-230 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
MBJNBCEJ_01634 | 4e-75 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
MBJNBCEJ_01635 | 6.5e-66 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
MBJNBCEJ_01636 | 7.5e-230 | M | ErfK YbiS YcfS YnhG | |||
MBJNBCEJ_01638 | 2.6e-48 | L | Putative transposase DNA-binding domain | |||
MBJNBCEJ_01639 | 7e-55 | L | Putative transposase DNA-binding domain | |||
MBJNBCEJ_01640 | 2.5e-57 | |||||
MBJNBCEJ_01641 | 1e-57 | 3.4.22.70 | M | Sortase family | ||
MBJNBCEJ_01642 | 4.7e-96 | M | ErfK YbiS YcfS YnhG | |||
MBJNBCEJ_01643 | 3.9e-170 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
MBJNBCEJ_01644 | 5.3e-161 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MBJNBCEJ_01645 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
MBJNBCEJ_01646 | 8.1e-55 | yheA | S | Belongs to the UPF0342 family | ||
MBJNBCEJ_01647 | 3.9e-226 | yhaO | L | Ser Thr phosphatase family protein | ||
MBJNBCEJ_01648 | 0.0 | L | AAA domain | |||
MBJNBCEJ_01649 | 1.1e-178 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
MBJNBCEJ_01650 | 4.7e-66 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | shikimate kinase activity | |
MBJNBCEJ_01651 | 9.8e-52 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
MBJNBCEJ_01652 | 1.1e-156 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
MBJNBCEJ_01653 | 2.3e-113 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
MBJNBCEJ_01654 | 1.2e-132 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
MBJNBCEJ_01655 | 5.2e-170 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
MBJNBCEJ_01656 | 1.8e-54 | |||||
MBJNBCEJ_01657 | 1.5e-79 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
MBJNBCEJ_01658 | 4.5e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_01659 | 1.1e-217 | ecsB | U | ABC transporter | ||
MBJNBCEJ_01660 | 5.2e-124 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
MBJNBCEJ_01661 | 1.2e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
MBJNBCEJ_01662 | 3.4e-120 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
MBJNBCEJ_01663 | 4.4e-255 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
MBJNBCEJ_01664 | 2e-112 | K | Helix-turn-helix domain | |||
MBJNBCEJ_01665 | 3.8e-65 | L | MobA MobL family protein | |||
MBJNBCEJ_01666 | 2.7e-199 | L | Transposase and inactivated derivatives, IS30 family | |||
MBJNBCEJ_01667 | 1.1e-42 | EGP | Major facilitator Superfamily | |||
MBJNBCEJ_01668 | 2.7e-112 | EGP | Major facilitator Superfamily | |||
MBJNBCEJ_01669 | 4.2e-40 | EGP | Major facilitator Superfamily | |||
MBJNBCEJ_01670 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
MBJNBCEJ_01671 | 1.7e-156 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
MBJNBCEJ_01672 | 2.5e-101 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
MBJNBCEJ_01673 | 2.7e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
MBJNBCEJ_01674 | 3.4e-247 | dnaB | L | Replication initiation and membrane attachment | ||
MBJNBCEJ_01675 | 1.3e-168 | dnaI | L | Primosomal protein DnaI | ||
MBJNBCEJ_01676 | 0.0 | thrS | 6.1.1.3 | J | 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) | |
MBJNBCEJ_01677 | 2.9e-42 | |||||
MBJNBCEJ_01678 | 2.3e-32 | |||||
MBJNBCEJ_01679 | 1.3e-273 | S | Archaea bacterial proteins of unknown function | |||
MBJNBCEJ_01680 | 5.4e-113 | guaB2 | L | Resolvase, N terminal domain | ||
MBJNBCEJ_01681 | 3.9e-237 | L | Putative transposase DNA-binding domain | |||
MBJNBCEJ_01682 | 2.6e-86 | infC | J | 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 | ||
MBJNBCEJ_01683 | 1.8e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
MBJNBCEJ_01684 | 1.1e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
MBJNBCEJ_01685 | 2.3e-212 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
MBJNBCEJ_01686 | 8.4e-119 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
MBJNBCEJ_01687 | 1.9e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
MBJNBCEJ_01688 | 1.2e-58 | rsfS | J | 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 | ||
MBJNBCEJ_01689 | 1.9e-214 | ylbM | S | Belongs to the UPF0348 family | ||
MBJNBCEJ_01690 | 8.4e-102 | yceD | S | Uncharacterized ACR, COG1399 | ||
MBJNBCEJ_01691 | 2.9e-128 | K | response regulator | |||
MBJNBCEJ_01692 | 3e-290 | arlS | 2.7.13.3 | T | Histidine kinase | |
MBJNBCEJ_01693 | 4.9e-155 | yidC | U | 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 | ||
MBJNBCEJ_01694 | 2e-45 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
MBJNBCEJ_01695 | 1.2e-135 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
MBJNBCEJ_01696 | 2e-61 | yodB | K | Transcriptional regulator, HxlR family | ||
MBJNBCEJ_01697 | 2.1e-199 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
MBJNBCEJ_01698 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
MBJNBCEJ_01699 | 2e-80 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
MBJNBCEJ_01700 | 0.0 | S | membrane | |||
MBJNBCEJ_01701 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
MBJNBCEJ_01702 | 7.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
MBJNBCEJ_01703 | 4.7e-105 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
MBJNBCEJ_01704 | 7.7e-115 | gluP | 3.4.21.105 | S | Rhomboid family | |
MBJNBCEJ_01705 | 9.5e-33 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
MBJNBCEJ_01706 | 2.6e-70 | yqhL | P | Rhodanese-like protein | ||
MBJNBCEJ_01707 | 3.4e-169 | miaA | 2.5.1.75 | F | 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) | |
MBJNBCEJ_01708 | 1.2e-138 | ynbB | 4.4.1.1 | P | aluminum resistance | |
MBJNBCEJ_01709 | 2.8e-257 | glnA | 6.3.1.2 | E | glutamine synthetase | |
MBJNBCEJ_01710 | 8.8e-218 | EGP | Major facilitator Superfamily | |||
MBJNBCEJ_01711 | 4.5e-64 | S | Domain of unknown function DUF1828 | |||
MBJNBCEJ_01712 | 6.8e-27 | L | Transposase | |||
MBJNBCEJ_01713 | 3.8e-229 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_01714 | 1.9e-83 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01715 | 7.7e-58 | |||||
MBJNBCEJ_01716 | 8.5e-187 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
MBJNBCEJ_01717 | 8e-205 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
MBJNBCEJ_01718 | 4.7e-232 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
MBJNBCEJ_01719 | 3e-24 | L | Transposase | |||
MBJNBCEJ_01720 | 6.1e-74 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01721 | 4.7e-171 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
MBJNBCEJ_01722 | 5e-150 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
MBJNBCEJ_01724 | 1.3e-216 | EGP | Major facilitator Superfamily | |||
MBJNBCEJ_01725 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
MBJNBCEJ_01727 | 0.0 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
MBJNBCEJ_01728 | 1.3e-308 | S | SH3-like domain | |||
MBJNBCEJ_01729 | 1e-234 | |||||
MBJNBCEJ_01730 | 5.4e-98 | P | nitrite transmembrane transporter activity | |||
MBJNBCEJ_01731 | 4.2e-119 | EGP | Major Facilitator Superfamily | |||
MBJNBCEJ_01732 | 4.8e-41 | XK27_05520 | S | Uncharacterized protein conserved in bacteria (DUF2087) | ||
MBJNBCEJ_01733 | 1.1e-83 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
MBJNBCEJ_01734 | 1.6e-210 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
MBJNBCEJ_01735 | 4.4e-252 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
MBJNBCEJ_01736 | 1.6e-134 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
MBJNBCEJ_01737 | 2.8e-38 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
MBJNBCEJ_01738 | 5.2e-127 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
MBJNBCEJ_01739 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
MBJNBCEJ_01740 | 6.6e-284 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
MBJNBCEJ_01741 | 4.6e-199 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
MBJNBCEJ_01742 | 1.4e-109 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
MBJNBCEJ_01743 | 4.3e-294 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
MBJNBCEJ_01744 | 3.1e-242 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
MBJNBCEJ_01745 | 2.6e-60 | livF | E | ABC transporter | ||
MBJNBCEJ_01746 | 4e-90 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
MBJNBCEJ_01747 | 3.9e-65 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
MBJNBCEJ_01748 | 9.9e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
MBJNBCEJ_01749 | 2.1e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
MBJNBCEJ_01750 | 1.1e-195 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
MBJNBCEJ_01751 | 2.4e-101 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
MBJNBCEJ_01752 | 8.1e-73 | yqhY | S | Asp23 family, cell envelope-related function | ||
MBJNBCEJ_01753 | 1.8e-66 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
MBJNBCEJ_01754 | 3.7e-154 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
MBJNBCEJ_01755 | 8e-252 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
MBJNBCEJ_01756 | 1.7e-32 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
MBJNBCEJ_01757 | 5.4e-161 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
MBJNBCEJ_01758 | 7.8e-154 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
MBJNBCEJ_01759 | 1.4e-306 | recN | L | May be involved in recombinational repair of damaged DNA | ||
MBJNBCEJ_01760 | 1.6e-46 | oppA | E | transmembrane transport | ||
MBJNBCEJ_01761 | 2.9e-14 | oppA | E | ABC transporter, substratebinding protein | ||
MBJNBCEJ_01762 | 3.2e-33 | oppA | E | transmembrane transport | ||
MBJNBCEJ_01763 | 2.6e-49 | |||||
MBJNBCEJ_01764 | 1.1e-110 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
MBJNBCEJ_01765 | 2.4e-33 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
MBJNBCEJ_01766 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
MBJNBCEJ_01767 | 1.1e-172 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
MBJNBCEJ_01768 | 1.6e-244 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
MBJNBCEJ_01769 | 4.3e-138 | stp | 3.1.3.16 | T | phosphatase | |
MBJNBCEJ_01770 | 0.0 | KLT | serine threonine protein kinase | |||
MBJNBCEJ_01771 | 1.1e-164 | rsgA | 3.1.3.100 | S | 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 | |
MBJNBCEJ_01772 | 1.4e-127 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
MBJNBCEJ_01774 | 1.8e-30 | D | nuclear chromosome segregation | |||
MBJNBCEJ_01777 | 3e-279 | V | ABC transporter transmembrane region | |||
MBJNBCEJ_01778 | 3.2e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
MBJNBCEJ_01779 | 8.8e-57 | asp | S | Asp23 family, cell envelope-related function | ||
MBJNBCEJ_01780 | 1.6e-278 | yloV | S | DAK2 domain fusion protein YloV | ||
MBJNBCEJ_01781 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
MBJNBCEJ_01782 | 7.5e-183 | plsX | 2.3.1.15 | I | 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 | |
MBJNBCEJ_01783 | 5.7e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
MBJNBCEJ_01784 | 1.4e-189 | oppD | P | Belongs to the ABC transporter superfamily | ||
MBJNBCEJ_01785 | 6.5e-145 | oppF | P | Belongs to the ABC transporter superfamily | ||
MBJNBCEJ_01786 | 1.3e-176 | oppB | P | ABC transporter permease | ||
MBJNBCEJ_01787 | 1.3e-157 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
MBJNBCEJ_01788 | 0.0 | oppA1 | E | ABC transporter substrate-binding protein | ||
MBJNBCEJ_01789 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
MBJNBCEJ_01790 | 3.1e-127 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
MBJNBCEJ_01791 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
MBJNBCEJ_01792 | 7.5e-154 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
MBJNBCEJ_01794 | 1.7e-15 | pipD | E | Dipeptidase | ||
MBJNBCEJ_01795 | 1.1e-07 | pipD | E | Dipeptidase | ||
MBJNBCEJ_01796 | 1.5e-73 | pipD | E | Dipeptidase | ||
MBJNBCEJ_01797 | 8.6e-54 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
MBJNBCEJ_01798 | 2.6e-245 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
MBJNBCEJ_01799 | 3.8e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
MBJNBCEJ_01800 | 1.5e-91 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
MBJNBCEJ_01801 | 1.4e-138 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
MBJNBCEJ_01802 | 1.8e-09 | CP_1020 | S | Psort location Cytoplasmic, score 8.87 | ||
MBJNBCEJ_01803 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
MBJNBCEJ_01804 | 5.5e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
MBJNBCEJ_01805 | 0.0 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
MBJNBCEJ_01806 | 0.0 | S | TerB-C domain | |||
MBJNBCEJ_01807 | 3.4e-247 | P | P-loop Domain of unknown function (DUF2791) | |||
MBJNBCEJ_01808 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
MBJNBCEJ_01809 | 3.4e-97 | |||||
MBJNBCEJ_01810 | 9.6e-145 | glnH | ET | ABC transporter substrate-binding protein | ||
MBJNBCEJ_01811 | 6e-149 | glcU | U | ribose uptake protein RbsU | ||
MBJNBCEJ_01812 | 3.5e-114 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
MBJNBCEJ_01813 | 8.9e-34 | ynzC | S | UPF0291 protein | ||
MBJNBCEJ_01814 | 2.3e-31 | yneF | S | Uncharacterised protein family (UPF0154) | ||
MBJNBCEJ_01815 | 0.0 | mdlA | V | ABC transporter | ||
MBJNBCEJ_01816 | 0.0 | mdlB | V | ABC transporter | ||
MBJNBCEJ_01817 | 2.6e-71 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
MBJNBCEJ_01818 | 3.6e-213 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
MBJNBCEJ_01819 | 1.3e-251 | yclM | 2.7.2.4 | E | Belongs to the aspartokinase family | |
MBJNBCEJ_01820 | 4.8e-182 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
MBJNBCEJ_01821 | 1.4e-115 | plsC | 2.3.1.51 | I | Acyltransferase | |
MBJNBCEJ_01822 | 7.1e-189 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
MBJNBCEJ_01823 | 1.1e-136 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
MBJNBCEJ_01824 | 5.4e-184 | tsf | J | 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 | ||
MBJNBCEJ_01825 | 4.9e-131 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
MBJNBCEJ_01826 | 2.9e-91 | frr | J | 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 | ||
MBJNBCEJ_01827 | 7.6e-124 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
MBJNBCEJ_01828 | 1.1e-144 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
MBJNBCEJ_01829 | 4.3e-228 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
MBJNBCEJ_01830 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
MBJNBCEJ_01831 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
MBJNBCEJ_01832 | 1.9e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
MBJNBCEJ_01833 | 6.8e-194 | nusA | K | Participates in both transcription termination and antitermination | ||
MBJNBCEJ_01834 | 4.3e-43 | ylxR | K | Protein of unknown function (DUF448) | ||
MBJNBCEJ_01835 | 4.8e-42 | rplGA | J | ribosomal protein | ||
MBJNBCEJ_01836 | 0.0 | infB | J | 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 | ||
MBJNBCEJ_01837 | 5.5e-59 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
MBJNBCEJ_01838 | 1.8e-167 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
MBJNBCEJ_01839 | 8.4e-54 | cysE | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | |
MBJNBCEJ_01840 | 7e-220 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
MBJNBCEJ_01841 | 3.9e-170 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
MBJNBCEJ_01842 | 2e-22 | |||||
MBJNBCEJ_01843 | 7.4e-32 | S | Uncharacterised protein family (UPF0236) | |||
MBJNBCEJ_01844 | 4.3e-88 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
MBJNBCEJ_01845 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
MBJNBCEJ_01846 | 3e-24 | L | Transposase | |||
MBJNBCEJ_01847 | 2e-118 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01848 | 3.6e-40 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01849 | 9.9e-100 | sip | L | Belongs to the 'phage' integrase family | ||
MBJNBCEJ_01850 | 6.8e-178 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
MBJNBCEJ_01851 | 8.7e-190 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
MBJNBCEJ_01852 | 5.7e-80 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
MBJNBCEJ_01853 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
MBJNBCEJ_01854 | 1.7e-170 | dnaJ | O | 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 | ||
MBJNBCEJ_01855 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
MBJNBCEJ_01856 | 2.1e-123 | srtA | 3.4.22.70 | M | sortase family | |
MBJNBCEJ_01857 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
MBJNBCEJ_01858 | 9.1e-95 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
MBJNBCEJ_01859 | 2.5e-49 | K | DNA-binding transcription factor activity | |||
MBJNBCEJ_01860 | 5.9e-155 | czcD | P | cation diffusion facilitator family transporter | ||
MBJNBCEJ_01861 | 5.3e-200 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
MBJNBCEJ_01862 | 1.2e-184 | S | AI-2E family transporter | |||
MBJNBCEJ_01863 | 6.8e-14 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MBJNBCEJ_01864 | 1.2e-103 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MBJNBCEJ_01865 | 7.3e-164 | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
MBJNBCEJ_01866 | 3.6e-180 | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
MBJNBCEJ_01867 | 2.4e-161 | lysR5 | K | LysR substrate binding domain | ||
MBJNBCEJ_01868 | 1.1e-259 | glnPH2 | P | ABC transporter permease | ||
MBJNBCEJ_01869 | 2.8e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MBJNBCEJ_01870 | 1.6e-103 | S | Protein of unknown function (DUF4230) | |||
MBJNBCEJ_01871 | 2.6e-155 | yjgN | S | Bacterial protein of unknown function (DUF898) | ||
MBJNBCEJ_01872 | 2.6e-53 | S | Protein of unknown function (DUF2752) | |||
MBJNBCEJ_01873 | 1.7e-243 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
MBJNBCEJ_01874 | 9.8e-152 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
MBJNBCEJ_01875 | 1.6e-100 | 3.6.1.27 | I | Acid phosphatase homologues | ||
MBJNBCEJ_01876 | 1.2e-157 | |||||
MBJNBCEJ_01877 | 4.1e-164 | lysR7 | K | LysR substrate binding domain | ||
MBJNBCEJ_01878 | 5.3e-309 | yfiB1 | V | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_01879 | 0.0 | XK27_10035 | V | ABC transporter | ||
MBJNBCEJ_01881 | 1.2e-09 | yliE | T | Putative diguanylate phosphodiesterase | ||
MBJNBCEJ_01882 | 3e-09 | yliE | T | EAL domain | ||
MBJNBCEJ_01883 | 1.8e-07 | yliE | T | Putative diguanylate phosphodiesterase | ||
MBJNBCEJ_01884 | 4.3e-169 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
MBJNBCEJ_01885 | 4.1e-220 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
MBJNBCEJ_01886 | 4.8e-117 | hlyIII | S | protein, hemolysin III | ||
MBJNBCEJ_01887 | 3.3e-155 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
MBJNBCEJ_01888 | 5.5e-36 | yozE | S | Belongs to the UPF0346 family | ||
MBJNBCEJ_01889 | 7.4e-163 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
MBJNBCEJ_01890 | 4.4e-138 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
MBJNBCEJ_01891 | 2e-152 | dprA | LU | DNA protecting protein DprA | ||
MBJNBCEJ_01892 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
MBJNBCEJ_01893 | 6.8e-248 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
MBJNBCEJ_01894 | 1.8e-164 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
MBJNBCEJ_01895 | 4e-90 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
MBJNBCEJ_01896 | 2.4e-243 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
MBJNBCEJ_01897 | 4e-175 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
MBJNBCEJ_01900 | 3.4e-252 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
MBJNBCEJ_01901 | 9.4e-225 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
MBJNBCEJ_01904 | 1.1e-161 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
MBJNBCEJ_01906 | 1.5e-155 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
MBJNBCEJ_01907 | 2e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
MBJNBCEJ_01908 | 1.3e-171 | phoH | T | phosphate starvation-inducible protein PhoH | ||
MBJNBCEJ_01909 | 6.7e-98 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
MBJNBCEJ_01910 | 2.9e-75 | cdd | 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
MBJNBCEJ_01911 | 2.8e-168 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
MBJNBCEJ_01912 | 6.8e-136 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
MBJNBCEJ_01913 | 6.7e-178 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
MBJNBCEJ_01914 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
MBJNBCEJ_01915 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
MBJNBCEJ_01916 | 4.4e-200 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
MBJNBCEJ_01917 | 6.2e-202 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
MBJNBCEJ_01918 | 1.1e-203 | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | |||
MBJNBCEJ_01919 | 4e-30 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
MBJNBCEJ_01920 | 2.4e-37 | celA | 3.2.1.86 | GT1 | G | beta-glucosidase activity |
MBJNBCEJ_01921 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
MBJNBCEJ_01922 | 5.2e-93 | mdt(A) | EGP | Major facilitator Superfamily | ||
MBJNBCEJ_01923 | 3.2e-21 | U | Relaxase/Mobilisation nuclease domain | |||
MBJNBCEJ_01924 | 1.4e-98 | repA | S | Replication initiator protein A | ||
MBJNBCEJ_01925 | 2.6e-26 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01926 | 1.6e-227 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_01927 | 9.7e-203 | S | Protein of unknown function DUF262 | |||
MBJNBCEJ_01928 | 3.3e-306 | N | Uncharacterized conserved protein (DUF2075) | |||
MBJNBCEJ_01929 | 1.6e-77 | 1.3.5.4 | C | FAD binding domain | ||
MBJNBCEJ_01930 | 6.5e-104 | 1.3.5.4 | C | FAD binding domain | ||
MBJNBCEJ_01931 | 2.2e-90 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
MBJNBCEJ_01932 | 8.9e-26 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
MBJNBCEJ_01933 | 1.4e-137 | S | Peptidase family M23 | |||
MBJNBCEJ_01934 | 3.1e-80 | mutT | 3.6.1.55 | F | NUDIX domain | |
MBJNBCEJ_01935 | 2.3e-122 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
MBJNBCEJ_01936 | 1.8e-150 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
MBJNBCEJ_01937 | 4.1e-138 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
MBJNBCEJ_01938 | 4.4e-88 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
MBJNBCEJ_01939 | 7.3e-23 | |||||
MBJNBCEJ_01940 | 5.2e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
MBJNBCEJ_01941 | 9.8e-160 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
MBJNBCEJ_01942 | 3.9e-53 | S | Alpha beta hydrolase | |||
MBJNBCEJ_01943 | 3.8e-21 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
MBJNBCEJ_01944 | 2.5e-39 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
MBJNBCEJ_01945 | 8.8e-78 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01946 | 5.6e-27 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01947 | 7.7e-106 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01948 | 3.8e-229 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_01949 | 1.5e-26 | L | DDE superfamily endonuclease | |||
MBJNBCEJ_01950 | 0.0 | lacS | G | Transporter | ||
MBJNBCEJ_01951 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
MBJNBCEJ_01952 | 6.6e-26 | K | purine nucleotide biosynthetic process | |||
MBJNBCEJ_01953 | 6.3e-108 | galR | K | Transcriptional regulator | ||
MBJNBCEJ_01954 | 7.3e-233 | isp2 | L | Transposase | ||
MBJNBCEJ_01955 | 1.4e-258 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
MBJNBCEJ_01956 | 2.9e-198 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
MBJNBCEJ_01957 | 3.5e-104 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
MBJNBCEJ_01958 | 3.7e-31 | |||||
MBJNBCEJ_01959 | 4.6e-23 | |||||
MBJNBCEJ_01960 | 8.8e-70 | K | GNAT family | |||
MBJNBCEJ_01961 | 0.0 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
MBJNBCEJ_01962 | 4e-228 | 4.4.1.8 | E | Aminotransferase, class I | ||
MBJNBCEJ_01963 | 1.3e-165 | htpX | O | Peptidase family M48 | ||
MBJNBCEJ_01964 | 6.4e-77 | 1.6.5.2 | GM | NmrA-like family | ||
MBJNBCEJ_01965 | 3.6e-10 | 1.6.5.2 | GM | NAD(P)H-binding | ||
MBJNBCEJ_01966 | 3e-78 | K | Transcriptional regulator | |||
MBJNBCEJ_01967 | 1.2e-169 | E | ABC transporter, ATP-binding protein | |||
MBJNBCEJ_01968 | 7.2e-278 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
MBJNBCEJ_01969 | 1.2e-266 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
MBJNBCEJ_01970 | 8e-117 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
MBJNBCEJ_01971 | 2.1e-137 | prsW | S | Involved in the degradation of specific anti-sigma factors | ||
MBJNBCEJ_01972 | 5.6e-112 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
MBJNBCEJ_01973 | 1.3e-25 | |||||
MBJNBCEJ_01974 | 4.2e-138 | |||||
MBJNBCEJ_01975 | 1.3e-174 | |||||
MBJNBCEJ_01976 | 7.8e-266 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
MBJNBCEJ_01977 | 7.8e-157 | 3.4.17.13 | V | LD-carboxypeptidase | ||
MBJNBCEJ_01979 | 2.8e-12 | D | Filamentation induced by cAMP protein fic | |||
MBJNBCEJ_01980 | 1.3e-08 | D | Filamentation induced by cAMP protein fic | |||
MBJNBCEJ_01981 | 9.8e-77 | 1.3.5.4 | C | FMN_bind | ||
MBJNBCEJ_01982 | 3.5e-108 | pat | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
MBJNBCEJ_01983 | 2.8e-131 | ydcF | S | Gram-negative-bacterium-type cell wall biogenesis | ||
MBJNBCEJ_01984 | 4.1e-99 | yyaQ | S | YjbR | ||
MBJNBCEJ_01985 | 4.4e-146 | ligA | 2.7.7.7, 6.5.1.2 | L | EXOIII | |
MBJNBCEJ_01986 | 1.9e-167 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_01987 | 1.5e-50 | L | COG3547 Transposase and inactivated derivatives | |||
MBJNBCEJ_01988 | 1.3e-131 | C | FAD binding domain | |||
MBJNBCEJ_01990 | 2e-132 | gph | 3.1.3.18 | S | HAD-hyrolase-like | |
MBJNBCEJ_01991 | 2.6e-42 | yjdJ | S | GCN5-related N-acetyl-transferase | ||
MBJNBCEJ_01993 | 8.4e-63 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
MBJNBCEJ_01994 | 2.6e-162 | rnhA | 3.1.26.4 | L | Resolvase, N-terminal | |
MBJNBCEJ_01995 | 2e-18 | P | Rhodanese Homology Domain | |||
MBJNBCEJ_01996 | 0.0 | V | ABC transporter transmembrane region | |||
MBJNBCEJ_01997 | 3.4e-308 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
MBJNBCEJ_01998 | 3.4e-77 | K | Transcriptional regulator, MarR family | |||
MBJNBCEJ_01999 | 9.1e-164 | 1.1.1.399, 1.1.1.95 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
MBJNBCEJ_02000 | 2.9e-78 | V | Psort location CytoplasmicMembrane, score | |||
MBJNBCEJ_02001 | 4.1e-167 | V | Psort location CytoplasmicMembrane, score 10.00 | |||
MBJNBCEJ_02002 | 5.9e-46 | V | (ABC) transporter | |||
MBJNBCEJ_02003 | 1.4e-113 | ylbE | GM | NAD(P)H-binding | ||
MBJNBCEJ_02004 | 2.6e-85 | S | Hydrolases of the alpha beta superfamily | |||
MBJNBCEJ_02005 | 3.1e-57 | |||||
MBJNBCEJ_02006 | 0.0 | yacH | D | Putative exonuclease SbcCD, C subunit | ||
MBJNBCEJ_02009 | 1.1e-19 | S | Protein of unknown function N-terminus (DUF3323) | |||
MBJNBCEJ_02010 | 1e-47 | GM | epimerase | |||
MBJNBCEJ_02011 | 6e-71 | K | Transcriptional regulator | |||
MBJNBCEJ_02012 | 3.9e-119 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
MBJNBCEJ_02013 | 2.5e-80 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MBJNBCEJ_02014 | 1e-69 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MBJNBCEJ_02015 | 5.6e-81 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MBJNBCEJ_02016 | 3.7e-102 | ybaJ | Q | Methyltransferase domain | ||
MBJNBCEJ_02017 | 1.3e-36 | V | (ABC) transporter | |||
MBJNBCEJ_02018 | 0.0 | carB | 6.3.5.5 | F | Psort location Cytoplasmic, score 8.87 | |
MBJNBCEJ_02019 | 2.3e-88 | carB | 6.3.5.5 | F | Psort location Cytoplasmic, score 8.87 | |
MBJNBCEJ_02020 | 6.6e-209 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
MBJNBCEJ_02021 | 8.6e-37 | T | diguanylate cyclase activity | |||
MBJNBCEJ_02023 | 1.3e-117 | V | MATE efflux family protein | |||
MBJNBCEJ_02024 | 6.1e-74 | V | MATE efflux family protein | |||
MBJNBCEJ_02025 | 6.1e-73 | prpH | 3.1.3.16 | K | 3.5.2 Transcription regulation | |
MBJNBCEJ_02026 | 5.1e-15 | prpH | 3.1.3.16 | K | 3.5.2 Transcription regulation | |
MBJNBCEJ_02027 | 6.2e-74 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
MBJNBCEJ_02028 | 1.8e-104 | L | Integrase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)