ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HBMJOCDF_00001 | 1.2e-138 | glvR | K | Helix-turn-helix domain, rpiR family | ||
HBMJOCDF_00002 | 6e-80 | |||||
HBMJOCDF_00003 | 2.9e-87 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
HBMJOCDF_00004 | 2.1e-39 | |||||
HBMJOCDF_00005 | 3.9e-119 | C | nitroreductase | |||
HBMJOCDF_00006 | 1.7e-249 | yhdP | S | Transporter associated domain | ||
HBMJOCDF_00007 | 3.4e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HBMJOCDF_00008 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
HBMJOCDF_00009 | 2.9e-88 | L | PFAM transposase, IS4 family protein | |||
HBMJOCDF_00010 | 1.2e-49 | L | PFAM transposase, IS4 family protein | |||
HBMJOCDF_00011 | 5.6e-186 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
HBMJOCDF_00012 | 1.7e-129 | manY | G | PTS system | ||
HBMJOCDF_00013 | 1e-173 | manN | G | system, mannose fructose sorbose family IID component | ||
HBMJOCDF_00014 | 9.9e-64 | manO | S | Domain of unknown function (DUF956) | ||
HBMJOCDF_00015 | 1.8e-159 | K | Transcriptional regulator | |||
HBMJOCDF_00016 | 4.4e-83 | maa | S | transferase hexapeptide repeat | ||
HBMJOCDF_00017 | 8e-244 | cycA | E | Amino acid permease | ||
HBMJOCDF_00018 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HBMJOCDF_00019 | 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 | |
HBMJOCDF_00020 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
HBMJOCDF_00021 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
HBMJOCDF_00022 | 2.1e-79 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
HBMJOCDF_00023 | 1.8e-220 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
HBMJOCDF_00024 | 8.1e-134 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
HBMJOCDF_00025 | 1.6e-32 | |||||
HBMJOCDF_00026 | 4.2e-71 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
HBMJOCDF_00027 | 2.3e-156 | K | Helix-turn-helix XRE-family like proteins | |||
HBMJOCDF_00028 | 4.3e-10 | KLT | Protein kinase domain | |||
HBMJOCDF_00029 | 8.7e-298 | V | ABC transporter transmembrane region | |||
HBMJOCDF_00030 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
HBMJOCDF_00031 | 0.0 | S | TerB-C domain | |||
HBMJOCDF_00032 | 1.2e-252 | P | P-loop Domain of unknown function (DUF2791) | |||
HBMJOCDF_00033 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
HBMJOCDF_00034 | 1.9e-59 | |||||
HBMJOCDF_00035 | 2.2e-68 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
HBMJOCDF_00036 | 3.7e-60 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
HBMJOCDF_00037 | 3.8e-200 | amtB | P | ammonium transporter | ||
HBMJOCDF_00039 | 5.1e-61 | psiE | S | Phosphate-starvation-inducible E | ||
HBMJOCDF_00040 | 3.8e-113 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
HBMJOCDF_00041 | 1.5e-70 | S | Iron-sulphur cluster biosynthesis | |||
HBMJOCDF_00043 | 4.6e-31 | |||||
HBMJOCDF_00044 | 1.1e-172 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
HBMJOCDF_00045 | 6.2e-12 | |||||
HBMJOCDF_00046 | 2.2e-87 | 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 | ||
HBMJOCDF_00047 | 6.6e-29 | 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 | ||
HBMJOCDF_00049 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
HBMJOCDF_00050 | 3.1e-212 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
HBMJOCDF_00051 | 6.1e-185 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
HBMJOCDF_00052 | 2.1e-120 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
HBMJOCDF_00053 | 4.4e-144 | K | SIS domain | |||
HBMJOCDF_00054 | 2.3e-228 | slpX | S | SLAP domain | ||
HBMJOCDF_00055 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
HBMJOCDF_00056 | 7.7e-12 | |||||
HBMJOCDF_00057 | 1.1e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
HBMJOCDF_00060 | 1.6e-299 | oppA2 | E | ABC transporter, substratebinding protein | ||
HBMJOCDF_00061 | 4.3e-179 | |||||
HBMJOCDF_00062 | 2.9e-125 | gntR1 | K | UTRA | ||
HBMJOCDF_00063 | 5.1e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
HBMJOCDF_00064 | 7.3e-135 | 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 |
HBMJOCDF_00065 | 3.4e-205 | csaB | M | Glycosyl transferases group 1 | ||
HBMJOCDF_00066 | 2.4e-286 | 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 | |
HBMJOCDF_00067 | 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 | |
HBMJOCDF_00068 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
HBMJOCDF_00069 | 7e-225 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
HBMJOCDF_00070 | 4.9e-260 | epsU | S | Polysaccharide biosynthesis protein | ||
HBMJOCDF_00071 | 3.5e-134 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
HBMJOCDF_00072 | 2.8e-84 | ydcK | S | Belongs to the SprT family | ||
HBMJOCDF_00074 | 2.5e-86 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
HBMJOCDF_00075 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
HBMJOCDF_00076 | 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 | |
HBMJOCDF_00077 | 5.8e-203 | camS | S | sex pheromone | ||
HBMJOCDF_00078 | 1.5e-49 | 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) | |
HBMJOCDF_00079 | 5.2e-270 | 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) | |
HBMJOCDF_00080 | 4.1e-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) | |
HBMJOCDF_00081 | 2.7e-171 | yegS | 2.7.1.107 | G | Lipid kinase | |
HBMJOCDF_00082 | 7.2e-18 | |||||
HBMJOCDF_00083 | 2.9e-66 | K | transcriptional regulator | |||
HBMJOCDF_00084 | 1.2e-105 | ybhL | S | Belongs to the BI1 family | ||
HBMJOCDF_00085 | 4.5e-50 | |||||
HBMJOCDF_00086 | 1.3e-230 | nhaC | C | Na H antiporter NhaC | ||
HBMJOCDF_00087 | 1.6e-199 | pbpX | V | Beta-lactamase | ||
HBMJOCDF_00088 | 5.8e-255 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HBMJOCDF_00089 | 1.1e-94 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
HBMJOCDF_00094 | 9.5e-259 | emrY | EGP | Major facilitator Superfamily | ||
HBMJOCDF_00095 | 2.3e-90 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
HBMJOCDF_00096 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
HBMJOCDF_00097 | 9e-161 | V | ABC transporter transmembrane region | |||
HBMJOCDF_00098 | 7e-68 | V | ABC transporter transmembrane region | |||
HBMJOCDF_00099 | 3.8e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
HBMJOCDF_00100 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
HBMJOCDF_00101 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
HBMJOCDF_00102 | 5.8e-76 | S | Peptidase propeptide and YPEB domain | |||
HBMJOCDF_00103 | 5.2e-187 | T | GHKL domain | |||
HBMJOCDF_00104 | 3.1e-130 | T | Transcriptional regulatory protein, C terminal | |||
HBMJOCDF_00105 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
HBMJOCDF_00106 | 2.9e-277 | V | ABC transporter transmembrane region | |||
HBMJOCDF_00107 | 1.1e-56 | S | Protein of unknown function (DUF3290) | |||
HBMJOCDF_00108 | 3e-116 | yviA | S | Protein of unknown function (DUF421) | ||
HBMJOCDF_00109 | 5.8e-157 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
HBMJOCDF_00110 | 1e-181 | dnaQ | 2.7.7.7 | L | EXOIII | |
HBMJOCDF_00111 | 1.9e-158 | endA | F | DNA RNA non-specific endonuclease | ||
HBMJOCDF_00112 | 1.6e-282 | pipD | E | Dipeptidase | ||
HBMJOCDF_00113 | 9.3e-203 | malK | P | ATPases associated with a variety of cellular activities | ||
HBMJOCDF_00114 | 1.6e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
HBMJOCDF_00115 | 6.1e-146 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
HBMJOCDF_00116 | 3.5e-257 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
HBMJOCDF_00117 | 1.1e-239 | G | Bacterial extracellular solute-binding protein | |||
HBMJOCDF_00118 | 1.8e-154 | corA | P | CorA-like Mg2+ transporter protein | ||
HBMJOCDF_00119 | 7.4e-148 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
HBMJOCDF_00120 | 2.3e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
HBMJOCDF_00121 | 0.0 | ydgH | S | MMPL family | ||
HBMJOCDF_00122 | 1.4e-94 | |||||
HBMJOCDF_00123 | 3e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
HBMJOCDF_00124 | 9e-98 | |||||
HBMJOCDF_00125 | 4.9e-108 | K | LysR substrate binding domain | |||
HBMJOCDF_00126 | 1e-20 | |||||
HBMJOCDF_00127 | 2.3e-215 | S | Sterol carrier protein domain | |||
HBMJOCDF_00128 | 9.2e-95 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
HBMJOCDF_00129 | 2e-105 | argF | 2.1.3.3, 2.7.2.2 | E | Belongs to the carbamate kinase family | |
HBMJOCDF_00130 | 4.3e-66 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
HBMJOCDF_00131 | 8.8e-234 | arcA | 3.5.3.6 | E | Arginine | |
HBMJOCDF_00132 | 1e-135 | lysR5 | K | LysR substrate binding domain | ||
HBMJOCDF_00133 | 0.0 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
HBMJOCDF_00134 | 1e-48 | S | Metal binding domain of Ada | |||
HBMJOCDF_00135 | 4.2e-92 | S | SNARE associated Golgi protein | |||
HBMJOCDF_00136 | 5.3e-189 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
HBMJOCDF_00137 | 1.2e-149 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
HBMJOCDF_00138 | 9.2e-172 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HBMJOCDF_00139 | 3.8e-153 | 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 | |
HBMJOCDF_00140 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
HBMJOCDF_00141 | 5.2e-110 | yjbK | S | CYTH | ||
HBMJOCDF_00142 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
HBMJOCDF_00143 | 5.8e-160 | coiA | 3.6.4.12 | S | Competence protein | |
HBMJOCDF_00144 | 8.5e-139 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
HBMJOCDF_00145 | 3.9e-66 | 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 | |
HBMJOCDF_00146 | 0.0 | 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) | |
HBMJOCDF_00147 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
HBMJOCDF_00148 | 5.3e-26 | |||||
HBMJOCDF_00149 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
HBMJOCDF_00150 | 8.7e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
HBMJOCDF_00151 | 9.4e-305 | 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 | ||
HBMJOCDF_00152 | 7.6e-139 | hlyX | S | Transporter associated domain | ||
HBMJOCDF_00153 | 2.7e-74 | |||||
HBMJOCDF_00154 | 1.6e-85 | |||||
HBMJOCDF_00155 | 5.6e-144 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
HBMJOCDF_00156 | 1.7e-262 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HBMJOCDF_00157 | 1.4e-118 | D | Alpha beta | |||
HBMJOCDF_00158 | 1.8e-38 | D | Alpha beta | |||
HBMJOCDF_00159 | 6e-38 | L | Transposase and inactivated derivatives, IS30 family | |||
HBMJOCDF_00160 | 2.8e-33 | scrR | K | Periplasmic binding protein domain | ||
HBMJOCDF_00161 | 2e-37 | scrR | K | Periplasmic binding protein domain | ||
HBMJOCDF_00162 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HBMJOCDF_00163 | 1.3e-36 | |||||
HBMJOCDF_00164 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
HBMJOCDF_00165 | 2.1e-141 | ykuT | M | mechanosensitive ion channel | ||
HBMJOCDF_00167 | 2.5e-14 | |||||
HBMJOCDF_00168 | 1.9e-113 | K | sequence-specific DNA binding | |||
HBMJOCDF_00170 | 5.6e-112 | 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 | |
HBMJOCDF_00171 | 6.6e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HBMJOCDF_00172 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
HBMJOCDF_00173 | 9.7e-59 | 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 | ||
HBMJOCDF_00174 | 1e-53 | trxA | O | Belongs to the thioredoxin family | ||
HBMJOCDF_00175 | 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 | ||
HBMJOCDF_00176 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
HBMJOCDF_00177 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HBMJOCDF_00178 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
HBMJOCDF_00179 | 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 | |
HBMJOCDF_00180 | 4.7e-228 | 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 | |
HBMJOCDF_00181 | 1.4e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
HBMJOCDF_00182 | 6.2e-210 | 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 | |
HBMJOCDF_00183 | 9.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
HBMJOCDF_00184 | 9.6e-41 | yajC | U | Preprotein translocase | ||
HBMJOCDF_00185 | 1.5e-186 | 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 | |
HBMJOCDF_00186 | 1.7e-102 | 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 | |
HBMJOCDF_00187 | 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 | ||
HBMJOCDF_00188 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
HBMJOCDF_00189 | 2.6e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HBMJOCDF_00190 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HBMJOCDF_00191 | 3.5e-75 | |||||
HBMJOCDF_00192 | 2.3e-181 | M | CHAP domain | |||
HBMJOCDF_00193 | 0.0 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
HBMJOCDF_00194 | 3.7e-295 | scrB | 3.2.1.26 | GH32 | G | invertase |
HBMJOCDF_00195 | 1.1e-183 | scrR | K | helix_turn _helix lactose operon repressor | ||
HBMJOCDF_00196 | 1.8e-223 | S | SLAP domain | |||
HBMJOCDF_00197 | 5.7e-83 | S | Aminoacyl-tRNA editing domain | |||
HBMJOCDF_00198 | 2.2e-163 | 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 | ||
HBMJOCDF_00199 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
HBMJOCDF_00200 | 7.7e-135 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HBMJOCDF_00201 | 4.5e-58 | yodB | K | Transcriptional regulator, HxlR family | ||
HBMJOCDF_00203 | 1.2e-107 | papP | P | ABC transporter, permease protein | ||
HBMJOCDF_00204 | 5.9e-115 | P | ABC transporter permease | |||
HBMJOCDF_00205 | 1.5e-127 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HBMJOCDF_00206 | 1.6e-157 | cjaA | ET | ABC transporter substrate-binding protein | ||
HBMJOCDF_00207 | 7.1e-200 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HBMJOCDF_00208 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HBMJOCDF_00209 | 4.9e-63 | 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 | ||
HBMJOCDF_00210 | 1.4e-167 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
HBMJOCDF_00211 | 3.5e-136 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
HBMJOCDF_00212 | 1.9e-25 | |||||
HBMJOCDF_00213 | 0.0 | mco | Q | Multicopper oxidase | ||
HBMJOCDF_00214 | 1.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HBMJOCDF_00215 | 0.0 | oppA | E | ABC transporter | ||
HBMJOCDF_00216 | 4e-231 | Q | Imidazolonepropionase and related amidohydrolases | |||
HBMJOCDF_00217 | 2.7e-246 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
HBMJOCDF_00218 | 1e-137 | S | Protein of unknown function (DUF3100) | |||
HBMJOCDF_00219 | 5.7e-46 | S | An automated process has identified a potential problem with this gene model | |||
HBMJOCDF_00220 | 2.6e-51 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |||
HBMJOCDF_00221 | 1.1e-112 | S | SLAP domain | |||
HBMJOCDF_00222 | 8.4e-89 | |||||
HBMJOCDF_00223 | 2.9e-09 | isdH | M | Iron Transport-associated domain | ||
HBMJOCDF_00224 | 3.1e-122 | M | Iron Transport-associated domain | |||
HBMJOCDF_00225 | 4.3e-158 | isdE | P | Periplasmic binding protein | ||
HBMJOCDF_00226 | 3.8e-58 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
HBMJOCDF_00227 | 1.4e-79 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
HBMJOCDF_00228 | 6.7e-139 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
HBMJOCDF_00229 | 6.7e-44 | 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 | ||
HBMJOCDF_00230 | 3.4e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
HBMJOCDF_00231 | 1.3e-38 | S | RelB antitoxin | |||
HBMJOCDF_00232 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
HBMJOCDF_00233 | 0.0 | S | membrane | |||
HBMJOCDF_00234 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
HBMJOCDF_00235 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HBMJOCDF_00236 | 2.7e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
HBMJOCDF_00237 | 4e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
HBMJOCDF_00238 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
HBMJOCDF_00239 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
HBMJOCDF_00240 | 1.1e-167 | 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) | |
HBMJOCDF_00241 | 2.9e-224 | ynbB | 4.4.1.1 | P | aluminum resistance | |
HBMJOCDF_00242 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HBMJOCDF_00243 | 3e-170 | |||||
HBMJOCDF_00244 | 1.2e-145 | |||||
HBMJOCDF_00245 | 3e-217 | lmrB | EGP | Major facilitator Superfamily | ||
HBMJOCDF_00246 | 5e-30 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
HBMJOCDF_00247 | 8.9e-27 | ptcC1 | 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 | ||
HBMJOCDF_00248 | 1.4e-100 | S | Metal-independent alpha-mannosidase (GH125) | |||
HBMJOCDF_00249 | 0.0 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
HBMJOCDF_00250 | 9.5e-274 | mdlA | V | ABC transporter | ||
HBMJOCDF_00251 | 5.4e-264 | mdlB | V | ABC transporter | ||
HBMJOCDF_00252 | 2.8e-241 | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain | |
HBMJOCDF_00253 | 2.4e-154 | U | Binding-protein-dependent transport system inner membrane component | |||
HBMJOCDF_00254 | 1.4e-43 | lplC | U | Binding-protein-dependent transport system inner membrane component | ||
HBMJOCDF_00255 | 2.3e-107 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HBMJOCDF_00258 | 8.7e-218 | 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 | |
HBMJOCDF_00259 | 2.4e-246 | qacA | EGP | Major facilitator Superfamily | ||
HBMJOCDF_00260 | 0.0 | sacX | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
HBMJOCDF_00261 | 3.1e-151 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
HBMJOCDF_00262 | 1.4e-183 | yfeW | 3.4.16.4 | V | Beta-lactamase | |
HBMJOCDF_00263 | 3.1e-187 | S | Bacterial protein of unknown function (DUF871) | |||
HBMJOCDF_00264 | 4.5e-144 | ybbH_2 | K | rpiR family | ||
HBMJOCDF_00265 | 1.5e-272 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
HBMJOCDF_00266 | 2.5e-173 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
HBMJOCDF_00267 | 2.4e-311 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
HBMJOCDF_00268 | 4.1e-269 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
HBMJOCDF_00269 | 2.2e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
HBMJOCDF_00270 | 6.1e-177 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
HBMJOCDF_00271 | 3.6e-160 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
HBMJOCDF_00272 | 1.2e-230 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
HBMJOCDF_00273 | 1.6e-43 | 1.3.5.4 | C | FAD binding domain | ||
HBMJOCDF_00274 | 1.6e-85 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HBMJOCDF_00275 | 2.6e-169 | K | LysR substrate binding domain | |||
HBMJOCDF_00276 | 6.4e-122 | 3.6.1.27 | I | Acid phosphatase homologues | ||
HBMJOCDF_00277 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HBMJOCDF_00278 | 6.8e-298 | ytgP | S | Polysaccharide biosynthesis protein | ||
HBMJOCDF_00279 | 4.3e-47 | pspC | KT | PspC domain | ||
HBMJOCDF_00281 | 1.6e-233 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HBMJOCDF_00282 | 6.9e-153 | 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 | |
HBMJOCDF_00283 | 7.9e-99 | M | ErfK YbiS YcfS YnhG | |||
HBMJOCDF_00284 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
HBMJOCDF_00285 | 6e-171 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
HBMJOCDF_00286 | 3e-90 | S | PFAM Archaeal ATPase | |||
HBMJOCDF_00287 | 5.1e-91 | S | PFAM Archaeal ATPase | |||
HBMJOCDF_00288 | 7.7e-26 | |||||
HBMJOCDF_00289 | 4.3e-76 | menA | 2.5.1.74 | H | UbiA prenyltransferase family | |
HBMJOCDF_00290 | 4.2e-53 | K | LytTr DNA-binding domain | |||
HBMJOCDF_00291 | 7.7e-39 | S | Protein of unknown function (DUF3021) | |||
HBMJOCDF_00292 | 8.3e-168 | V | ABC transporter | |||
HBMJOCDF_00293 | 8e-92 | S | domain protein | |||
HBMJOCDF_00294 | 9.4e-51 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HBMJOCDF_00295 | 1.3e-26 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HBMJOCDF_00296 | 8.4e-251 | ade | 3.5.4.2 | F | Adenine deaminase C-terminal domain | |
HBMJOCDF_00297 | 1.1e-144 | potD2 | P | ABC transporter | ||
HBMJOCDF_00298 | 1.4e-136 | potA11 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
HBMJOCDF_00299 | 2.2e-108 | potC3 | E | Binding-protein-dependent transport system inner membrane component | ||
HBMJOCDF_00300 | 3.8e-103 | potB | E | Binding-protein-dependent transport system inner membrane component | ||
HBMJOCDF_00301 | 4e-98 | rihB | 3.2.2.1 | F | Nucleoside | |
HBMJOCDF_00302 | 3.2e-72 | 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 | ||
HBMJOCDF_00303 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
HBMJOCDF_00304 | 3e-57 | 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 | ||
HBMJOCDF_00305 | 2.3e-152 | 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 | |
HBMJOCDF_00306 | 8.6e-199 | tnpB | L | Putative transposase DNA-binding domain | ||
HBMJOCDF_00307 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
HBMJOCDF_00308 | 4.4e-200 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
HBMJOCDF_00309 | 4.4e-123 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HBMJOCDF_00310 | 4.3e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
HBMJOCDF_00311 | 5.3e-59 | 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 | ||
HBMJOCDF_00312 | 4.6e-216 | ylbM | S | Belongs to the UPF0348 family | ||
HBMJOCDF_00313 | 4.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
HBMJOCDF_00314 | 1.2e-126 | K | response regulator | |||
HBMJOCDF_00315 | 1.3e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
HBMJOCDF_00316 | 9.5e-79 | S | CAAX protease self-immunity | |||
HBMJOCDF_00317 | 3.4e-78 | M | LysM domain protein | |||
HBMJOCDF_00318 | 2.5e-160 | D | nuclear chromosome segregation | |||
HBMJOCDF_00319 | 1.2e-105 | G | Phosphoglycerate mutase family | |||
HBMJOCDF_00320 | 1.7e-88 | G | Histidine phosphatase superfamily (branch 1) | |||
HBMJOCDF_00321 | 6.6e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
HBMJOCDF_00322 | 3.3e-113 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
HBMJOCDF_00323 | 2.3e-164 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
HBMJOCDF_00324 | 1.6e-294 | L | Nuclease-related domain | |||
HBMJOCDF_00325 | 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 | |
HBMJOCDF_00326 | 8.3e-106 | S | Repeat protein | |||
HBMJOCDF_00327 | 3.9e-127 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
HBMJOCDF_00328 | 5.1e-220 | 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 | |
HBMJOCDF_00329 | 5.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
HBMJOCDF_00330 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
HBMJOCDF_00331 | 1.2e-126 | 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 | |
HBMJOCDF_00332 | 6.7e-37 | |||||
HBMJOCDF_00333 | 2.8e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
HBMJOCDF_00334 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
HBMJOCDF_00335 | 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) | |
HBMJOCDF_00336 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
HBMJOCDF_00337 | 3.7e-148 | ylmH | S | S4 domain protein | ||
HBMJOCDF_00338 | 1.7e-45 | yggT | S | YGGT family | ||
HBMJOCDF_00339 | 7.3e-74 | 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 | ||
HBMJOCDF_00340 | 1.7e-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 | ||
HBMJOCDF_00341 | 1.3e-246 | 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 | ||
HBMJOCDF_00342 | 4.5e-152 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
HBMJOCDF_00343 | 3.7e-207 | 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) |
HBMJOCDF_00344 | 5e-262 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HBMJOCDF_00345 | 1.5e-175 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HBMJOCDF_00346 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
HBMJOCDF_00347 | 7e-54 | ftsL | D | Cell division protein FtsL | ||
HBMJOCDF_00348 | 7.2e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HBMJOCDF_00349 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
HBMJOCDF_00350 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
HBMJOCDF_00352 | 2.7e-94 | mreD | ||||
HBMJOCDF_00353 | 2e-147 | mreC | M | Involved in formation and maintenance of cell shape | ||
HBMJOCDF_00354 | 2.4e-176 | mreB | D | cell shape determining protein MreB | ||
HBMJOCDF_00355 | 2.3e-108 | radC | L | DNA repair protein | ||
HBMJOCDF_00356 | 5.7e-126 | S | Haloacid dehalogenase-like hydrolase | |||
HBMJOCDF_00357 | 1.5e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HBMJOCDF_00358 | 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 | |
HBMJOCDF_00359 | 2.5e-52 | |||||
HBMJOCDF_00360 | 1.1e-132 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
HBMJOCDF_00361 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
HBMJOCDF_00363 | 6.5e-44 | |||||
HBMJOCDF_00364 | 1.5e-94 | S | Protein of unknown function (DUF3990) | |||
HBMJOCDF_00365 | 5.2e-170 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
HBMJOCDF_00366 | 2.1e-65 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
HBMJOCDF_00367 | 5.5e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HBMJOCDF_00368 | 3.2e-119 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HBMJOCDF_00369 | 1.7e-184 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HBMJOCDF_00370 | 2e-225 | 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 | |
HBMJOCDF_00371 | 7.3e-214 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
HBMJOCDF_00372 | 2.1e-294 | 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 | ||
HBMJOCDF_00373 | 1.4e-110 | 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 | ||
HBMJOCDF_00374 | 1.3e-84 | yueI | S | Protein of unknown function (DUF1694) | ||
HBMJOCDF_00375 | 2.2e-238 | rarA | L | recombination factor protein RarA | ||
HBMJOCDF_00376 | 8.4e-39 | |||||
HBMJOCDF_00377 | 1.8e-78 | usp6 | T | universal stress protein | ||
HBMJOCDF_00378 | 4.7e-216 | rodA | D | Belongs to the SEDS family | ||
HBMJOCDF_00379 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
HBMJOCDF_00380 | 1e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
HBMJOCDF_00381 | 1.2e-177 | mbl | D | Cell shape determining protein MreB Mrl | ||
HBMJOCDF_00382 | 2e-30 | ywzB | S | Protein of unknown function (DUF1146) | ||
HBMJOCDF_00383 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HBMJOCDF_00384 | 3.3e-240 | 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 | |
HBMJOCDF_00385 | 2e-172 | 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 | ||
HBMJOCDF_00386 | 2.8e-282 | 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 | |
HBMJOCDF_00387 | 2.8e-91 | 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 | ||
HBMJOCDF_00388 | 3.4e-46 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HBMJOCDF_00389 | 3.5e-27 | 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 | ||
HBMJOCDF_00390 | 3.8e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HBMJOCDF_00391 | 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 | |
HBMJOCDF_00392 | 3.7e-190 | 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 | |
HBMJOCDF_00393 | 7.3e-155 | 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 | |
HBMJOCDF_00394 | 3.1e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HBMJOCDF_00395 | 1.3e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
HBMJOCDF_00396 | 1.7e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
HBMJOCDF_00399 | 3.9e-195 | ampC | V | Beta-lactamase | ||
HBMJOCDF_00400 | 2.4e-216 | EGP | Major facilitator Superfamily | |||
HBMJOCDF_00401 | 9.2e-253 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HBMJOCDF_00402 | 3.8e-105 | vanZ | V | VanZ like family | ||
HBMJOCDF_00403 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HBMJOCDF_00404 | 7.2e-267 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
HBMJOCDF_00405 | 7.5e-132 | K | Transcriptional regulatory protein, C terminal | |||
HBMJOCDF_00406 | 7.7e-67 | S | SdpI/YhfL protein family | |||
HBMJOCDF_00407 | 7.2e-191 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
HBMJOCDF_00408 | 9.9e-227 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
HBMJOCDF_00409 | 1.3e-88 | M | Protein of unknown function (DUF3737) | |||
HBMJOCDF_00411 | 6.3e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HBMJOCDF_00412 | 3.5e-188 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
HBMJOCDF_00413 | 1.6e-21 | |||||
HBMJOCDF_00414 | 9.4e-76 | comGF | U | Putative Competence protein ComGF | ||
HBMJOCDF_00415 | 8.6e-41 | |||||
HBMJOCDF_00416 | 7.4e-71 | |||||
HBMJOCDF_00417 | 3.1e-43 | comGC | U | competence protein ComGC | ||
HBMJOCDF_00418 | 1.7e-171 | comGB | NU | type II secretion system | ||
HBMJOCDF_00419 | 1.7e-179 | comGA | NU | Type II IV secretion system protein | ||
HBMJOCDF_00420 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
HBMJOCDF_00421 | 2.9e-93 | S | VanZ like family | |||
HBMJOCDF_00422 | 5.1e-108 | ylbE | GM | NAD(P)H-binding | ||
HBMJOCDF_00423 | 9.8e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
HBMJOCDF_00425 | 2.8e-304 | E | Amino acid permease | |||
HBMJOCDF_00426 | 6.9e-178 | D | Alpha beta | |||
HBMJOCDF_00427 | 9.1e-302 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
HBMJOCDF_00428 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
HBMJOCDF_00429 | 8.3e-143 | licT | K | CAT RNA binding domain | ||
HBMJOCDF_00430 | 3.8e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HBMJOCDF_00431 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HBMJOCDF_00432 | 1.6e-118 | |||||
HBMJOCDF_00433 | 1.8e-75 | K | Penicillinase repressor | |||
HBMJOCDF_00434 | 1.4e-147 | S | hydrolase | |||
HBMJOCDF_00435 | 3.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HBMJOCDF_00436 | 2e-172 | ybbR | S | YbbR-like protein | ||
HBMJOCDF_00437 | 6.4e-151 | 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 | |
HBMJOCDF_00438 | 7.3e-208 | potD | P | ABC transporter | ||
HBMJOCDF_00439 | 4.8e-127 | potC | P | ABC transporter permease | ||
HBMJOCDF_00440 | 1.3e-129 | potB | P | ABC transporter permease | ||
HBMJOCDF_00441 | 1.8e-206 | 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 | |
HBMJOCDF_00442 | 2e-163 | murB | 1.3.1.98 | M | Cell wall formation | |
HBMJOCDF_00443 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
HBMJOCDF_00444 | 7e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
HBMJOCDF_00445 | 4.1e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HBMJOCDF_00446 | 9.7e-137 | 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 | |
HBMJOCDF_00447 | 3.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
HBMJOCDF_00448 | 1.2e-94 | |||||
HBMJOCDF_00449 | 6e-199 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HBMJOCDF_00450 | 1.7e-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) | |
HBMJOCDF_00451 | 1e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
HBMJOCDF_00452 | 6.5e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HBMJOCDF_00453 | 3.3e-189 | cggR | K | Putative sugar-binding domain | ||
HBMJOCDF_00455 | 7.8e-288 | |||||
HBMJOCDF_00456 | 4.6e-274 | ycaM | E | amino acid | ||
HBMJOCDF_00457 | 7.3e-141 | S | Cysteine-rich secretory protein family | |||
HBMJOCDF_00458 | 9.9e-33 | S | Protein of unknown function (DUF3021) | |||
HBMJOCDF_00459 | 1.3e-44 | K | LytTr DNA-binding domain | |||
HBMJOCDF_00460 | 2.8e-93 | cylB | V | ABC-2 type transporter | ||
HBMJOCDF_00461 | 1.8e-116 | cylA | V | ABC transporter | ||
HBMJOCDF_00462 | 3.2e-77 | K | MerR HTH family regulatory protein | |||
HBMJOCDF_00463 | 5.4e-262 | lmrB | EGP | Major facilitator Superfamily | ||
HBMJOCDF_00464 | 3.1e-93 | S | Domain of unknown function (DUF4811) | |||
HBMJOCDF_00465 | 9.6e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
HBMJOCDF_00466 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
HBMJOCDF_00467 | 0.0 | S | SH3-like domain | |||
HBMJOCDF_00468 | 2.3e-99 | 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 | |
HBMJOCDF_00469 | 2.1e-171 | whiA | K | May be required for sporulation | ||
HBMJOCDF_00470 | 1.5e-194 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
HBMJOCDF_00471 | 2.6e-163 | rapZ | S | Displays ATPase and GTPase activities | ||
HBMJOCDF_00472 | 1.4e-90 | S | Short repeat of unknown function (DUF308) | |||
HBMJOCDF_00473 | 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 | ||
HBMJOCDF_00474 | 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 | ||
HBMJOCDF_00475 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
HBMJOCDF_00477 | 3.9e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HBMJOCDF_00478 | 6.3e-185 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
HBMJOCDF_00479 | 3.2e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HBMJOCDF_00480 | 5.8e-180 | 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 | ||
HBMJOCDF_00481 | 5.1e-17 | |||||
HBMJOCDF_00482 | 1.3e-187 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HBMJOCDF_00483 | 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 | ||
HBMJOCDF_00484 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HBMJOCDF_00485 | 9.4e-132 | comFC | S | Competence protein | ||
HBMJOCDF_00486 | 4.7e-246 | comFA | L | Helicase C-terminal domain protein | ||
HBMJOCDF_00487 | 5.1e-119 | yvyE | 3.4.13.9 | S | YigZ family | |
HBMJOCDF_00488 | 1.3e-210 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
HBMJOCDF_00489 | 7.4e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
HBMJOCDF_00490 | 4.2e-195 | 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 | ||
HBMJOCDF_00491 | 1.1e-95 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HBMJOCDF_00492 | 5.2e-97 | ymfM | S | Helix-turn-helix domain | ||
HBMJOCDF_00493 | 2.3e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
HBMJOCDF_00494 | 1.8e-234 | S | Peptidase M16 | |||
HBMJOCDF_00495 | 2.6e-222 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
HBMJOCDF_00496 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
HBMJOCDF_00497 | 4.9e-69 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
HBMJOCDF_00498 | 4.2e-106 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HBMJOCDF_00499 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
HBMJOCDF_00500 | 1.9e-65 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
HBMJOCDF_00501 | 1.4e-200 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
HBMJOCDF_00502 | 0.0 | L | PLD-like domain | |||
HBMJOCDF_00503 | 9.6e-103 | pgm3 | 5.4.2.11 | G | Histidine phosphatase superfamily (branch 1) | |
HBMJOCDF_00504 | 8.8e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
HBMJOCDF_00505 | 2.6e-280 | thrC | 4.2.3.1 | E | Threonine synthase | |
HBMJOCDF_00506 | 6.6e-221 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
HBMJOCDF_00507 | 2.8e-157 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
HBMJOCDF_00508 | 2.5e-118 | |||||
HBMJOCDF_00509 | 4.6e-160 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
HBMJOCDF_00511 | 2.3e-08 | 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 | |
HBMJOCDF_00512 | 2.5e-122 | L | Belongs to the 'phage' integrase family | |||
HBMJOCDF_00513 | 1.6e-180 | V | Abi-like protein | |||
HBMJOCDF_00516 | 2.5e-30 | S | Hypothetical protein (DUF2513) | |||
HBMJOCDF_00517 | 6.2e-74 | 3.4.21.88 | K | Peptidase S24-like | ||
HBMJOCDF_00518 | 2.3e-10 | K | Helix-turn-helix XRE-family like proteins | |||
HBMJOCDF_00526 | 1.1e-20 | L | Psort location Cytoplasmic, score | |||
HBMJOCDF_00529 | 1.3e-09 | |||||
HBMJOCDF_00530 | 1.1e-24 | S | HNH endonuclease | |||
HBMJOCDF_00535 | 1e-83 | ps308 | K | AntA/AntB antirepressor | ||
HBMJOCDF_00541 | 1.1e-08 | |||||
HBMJOCDF_00542 | 4e-145 | yfeO | P | Voltage gated chloride channel | ||
HBMJOCDF_00543 | 4.2e-80 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
HBMJOCDF_00544 | 2.8e-85 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
HBMJOCDF_00545 | 2.8e-52 | |||||
HBMJOCDF_00546 | 3.8e-42 | |||||
HBMJOCDF_00547 | 2.4e-231 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
HBMJOCDF_00548 | 7.3e-297 | ybeC | E | amino acid | ||
HBMJOCDF_00549 | 2.6e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HBMJOCDF_00550 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
HBMJOCDF_00551 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
HBMJOCDF_00552 | 1.5e-261 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HBMJOCDF_00553 | 1.9e-251 | 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 | |
HBMJOCDF_00554 | 1.7e-60 | 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 | |
HBMJOCDF_00555 | 1e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HBMJOCDF_00556 | 3.4e-129 | S | (CBS) domain | |||
HBMJOCDF_00557 | 1.5e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HBMJOCDF_00558 | 5.1e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HBMJOCDF_00559 | 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 | ||
HBMJOCDF_00560 | 1.6e-33 | yabO | J | S4 domain protein | ||
HBMJOCDF_00561 | 6.8e-60 | divIC | D | Septum formation initiator | ||
HBMJOCDF_00562 | 1.8e-62 | yabR | J | S1 RNA binding domain | ||
HBMJOCDF_00563 | 1.5e-241 | 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 | |
HBMJOCDF_00564 | 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 | ||
HBMJOCDF_00565 | 9.7e-166 | 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 | ||
HBMJOCDF_00566 | 2e-194 | 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 | ||
HBMJOCDF_00567 | 1.7e-298 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HBMJOCDF_00568 | 5.3e-15 | O | Belongs to the peptidase S8 family | |||
HBMJOCDF_00569 | 0.0 | O | Belongs to the peptidase S8 family | |||
HBMJOCDF_00570 | 3.4e-175 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
HBMJOCDF_00571 | 4.2e-93 | dhaL | 2.7.1.121 | S | Dak2 | |
HBMJOCDF_00572 | 2.5e-54 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
HBMJOCDF_00573 | 4.9e-120 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HBMJOCDF_00574 | 1.9e-16 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HBMJOCDF_00575 | 8.4e-71 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HBMJOCDF_00576 | 4.1e-14 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
HBMJOCDF_00577 | 3.9e-139 | 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 | |
HBMJOCDF_00578 | 5e-145 | 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 | |
HBMJOCDF_00579 | 1e-154 | pstA | P | Phosphate transport system permease protein PstA | ||
HBMJOCDF_00580 | 4.3e-162 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HBMJOCDF_00581 | 1.8e-156 | pstS | P | Phosphate | ||
HBMJOCDF_00582 | 3.2e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HBMJOCDF_00583 | 1.2e-68 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HBMJOCDF_00584 | 3.1e-101 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HBMJOCDF_00585 | 3.6e-24 | 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 | ||
HBMJOCDF_00586 | 0.0 | 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) | |
HBMJOCDF_00587 | 8.4e-287 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
HBMJOCDF_00588 | 2.3e-26 | |||||
HBMJOCDF_00589 | 4.2e-95 | sigH | K | Belongs to the sigma-70 factor family | ||
HBMJOCDF_00590 | 6.6e-139 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HBMJOCDF_00591 | 2.9e-73 | 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) | ||
HBMJOCDF_00592 | 3.4e-277 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HBMJOCDF_00593 | 2.1e-290 | 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) | |
HBMJOCDF_00594 | 2.7e-255 | 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 | ||
HBMJOCDF_00595 | 1.8e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
HBMJOCDF_00596 | 8e-38 | |||||
HBMJOCDF_00597 | 3.7e-111 | K | WHG domain | |||
HBMJOCDF_00598 | 6.4e-96 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
HBMJOCDF_00599 | 2.9e-96 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
HBMJOCDF_00600 | 1.5e-149 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
HBMJOCDF_00601 | 7.2e-180 | 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 | |
HBMJOCDF_00602 | 3e-53 | cvpA | S | Colicin V production protein | ||
HBMJOCDF_00603 | 1.6e-129 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HBMJOCDF_00604 | 1.9e-147 | noc | K | Belongs to the ParB family | ||
HBMJOCDF_00605 | 3.4e-138 | soj | D | Sporulation initiation inhibitor | ||
HBMJOCDF_00606 | 1.7e-154 | spo0J | K | Belongs to the ParB family | ||
HBMJOCDF_00607 | 9.6e-45 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
HBMJOCDF_00608 | 3.6e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HBMJOCDF_00609 | 3.8e-137 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
HBMJOCDF_00610 | 1.3e-302 | L | Transposase | |||
HBMJOCDF_00611 | 2.7e-216 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
HBMJOCDF_00612 | 4.6e-211 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
HBMJOCDF_00613 | 2.5e-214 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
HBMJOCDF_00614 | 2.1e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
HBMJOCDF_00615 | 1.8e-162 | yihY | S | Belongs to the UPF0761 family | ||
HBMJOCDF_00616 | 6.5e-164 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
HBMJOCDF_00617 | 4.8e-86 | gtcA | S | Teichoic acid glycosylation protein | ||
HBMJOCDF_00618 | 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) | |
HBMJOCDF_00619 | 1.8e-167 | dnaI | L | Primosomal protein DnaI | ||
HBMJOCDF_00620 | 1.2e-249 | dnaB | L | Replication initiation and membrane attachment | ||
HBMJOCDF_00621 | 3.9e-81 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HBMJOCDF_00622 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
HBMJOCDF_00623 | 9.4e-155 | 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 | |
HBMJOCDF_00624 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HBMJOCDF_00625 | 3.8e-30 | |||||
HBMJOCDF_00626 | 5.8e-164 | msmX | P | Belongs to the ABC transporter superfamily | ||
HBMJOCDF_00627 | 2.7e-164 | lacR | K | Transcriptional regulator | ||
HBMJOCDF_00628 | 0.0 | lacS | G | Transporter | ||
HBMJOCDF_00629 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
HBMJOCDF_00630 | 8.1e-126 | S | PAS domain | |||
HBMJOCDF_00631 | 1.6e-11 | |||||
HBMJOCDF_00632 | 2.7e-57 | |||||
HBMJOCDF_00633 | 6.6e-56 | |||||
HBMJOCDF_00634 | 4e-08 | |||||
HBMJOCDF_00635 | 1.1e-68 | S | Domain of unknown function (DUF1934) | |||
HBMJOCDF_00636 | 1.5e-46 | 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 | ||
HBMJOCDF_00637 | 3.4e-310 | 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 | |
HBMJOCDF_00638 | 1.4e-245 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HBMJOCDF_00639 | 2.1e-80 | K | acetyltransferase | |||
HBMJOCDF_00640 | 1.3e-47 | adk | 2.7.4.3 | F | AAA domain | |
HBMJOCDF_00641 | 4.4e-285 | pipD | E | Dipeptidase | ||
HBMJOCDF_00642 | 2.2e-148 | msmR | K | AraC-like ligand binding domain | ||
HBMJOCDF_00643 | 1.4e-226 | pbuX | F | xanthine permease | ||
HBMJOCDF_00644 | 3.1e-104 | 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 | |
HBMJOCDF_00645 | 2.1e-42 | K | Helix-turn-helix | |||
HBMJOCDF_00646 | 3e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HBMJOCDF_00648 | 4.9e-99 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
HBMJOCDF_00649 | 5.6e-226 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
HBMJOCDF_00650 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HBMJOCDF_00651 | 1.7e-29 | secG | U | Preprotein translocase | ||
HBMJOCDF_00652 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
HBMJOCDF_00653 | 5.1e-78 | 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 | ||
HBMJOCDF_00654 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
HBMJOCDF_00655 | 7e-146 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
HBMJOCDF_00656 | 4.5e-188 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HBMJOCDF_00657 | 2.4e-161 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
HBMJOCDF_00658 | 4.4e-106 | K | Transcriptional regulator, AbiEi antitoxin | |||
HBMJOCDF_00659 | 1.1e-189 | K | Periplasmic binding protein-like domain | |||
HBMJOCDF_00660 | 0.0 | S | PglZ domain | |||
HBMJOCDF_00661 | 4.7e-276 | 1.3.5.4 | C | FMN_bind | ||
HBMJOCDF_00662 | 2.7e-226 | P | Sodium:sulfate symporter transmembrane region | |||
HBMJOCDF_00663 | 8.3e-109 | K | LysR family | |||
HBMJOCDF_00664 | 1.4e-272 | 1.3.5.4 | C | FMN_bind | ||
HBMJOCDF_00665 | 2.6e-86 | K | LysR family | |||
HBMJOCDF_00666 | 2.5e-164 | S | Protein of unknown function (DUF2974) | |||
HBMJOCDF_00667 | 4.7e-109 | glnP | P | ABC transporter permease | ||
HBMJOCDF_00668 | 9.7e-91 | gluC | P | ABC transporter permease | ||
HBMJOCDF_00669 | 1.3e-148 | glnH | ET | ABC transporter substrate-binding protein | ||
HBMJOCDF_00670 | 1.9e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HBMJOCDF_00671 | 1.8e-113 | udk | 2.7.1.48 | F | Zeta toxin | |
HBMJOCDF_00672 | 3e-254 | G | MFS/sugar transport protein | |||
HBMJOCDF_00673 | 8.4e-102 | S | ABC-type cobalt transport system, permease component | |||
HBMJOCDF_00674 | 0.0 | V | ABC transporter transmembrane region | |||
HBMJOCDF_00675 | 3.6e-310 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
HBMJOCDF_00676 | 1.4e-80 | K | Transcriptional regulator, MarR family | |||
HBMJOCDF_00677 | 1.5e-186 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
HBMJOCDF_00678 | 5.3e-136 | glvR | K | Helix-turn-helix domain, rpiR family | ||
HBMJOCDF_00679 | 2.7e-268 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
HBMJOCDF_00680 | 6.7e-87 | S | hydrolase | |||
HBMJOCDF_00681 | 2.5e-59 | S | Enterocin A Immunity | |||
HBMJOCDF_00682 | 3.1e-136 | glcR | K | DeoR C terminal sensor domain | ||
HBMJOCDF_00683 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
HBMJOCDF_00684 | 7.6e-160 | rssA | S | Phospholipase, patatin family | ||
HBMJOCDF_00685 | 5.4e-147 | S | hydrolase | |||
HBMJOCDF_00686 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
HBMJOCDF_00687 | 9.3e-136 | UW | LPXTG-motif cell wall anchor domain protein | |||
HBMJOCDF_00688 | 9.3e-196 | UW | LPXTG-motif cell wall anchor domain protein | |||
HBMJOCDF_00689 | 9.6e-45 | UW | LPXTG-motif cell wall anchor domain protein | |||
HBMJOCDF_00690 | 2.3e-23 | UW | LPXTG-motif cell wall anchor domain protein | |||
HBMJOCDF_00691 | 5.3e-237 | 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) | |
HBMJOCDF_00692 | 2.4e-98 | J | Acetyltransferase (GNAT) domain | |||
HBMJOCDF_00693 | 1.8e-110 | yjbF | S | SNARE associated Golgi protein | ||
HBMJOCDF_00694 | 1.2e-151 | I | alpha/beta hydrolase fold | |||
HBMJOCDF_00695 | 1.5e-155 | hipB | K | Helix-turn-helix | ||
HBMJOCDF_00696 | 2.6e-83 | F | Nucleoside 2-deoxyribosyltransferase | |||
HBMJOCDF_00697 | 1.9e-253 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
HBMJOCDF_00698 | 1.9e-149 | |||||
HBMJOCDF_00699 | 7e-43 | yfdE | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
HBMJOCDF_00700 | 3.2e-170 | frc | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
HBMJOCDF_00701 | 8.1e-286 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
HBMJOCDF_00702 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
HBMJOCDF_00703 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
HBMJOCDF_00704 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
HBMJOCDF_00705 | 2.8e-230 | potE | E | amino acid | ||
HBMJOCDF_00706 | 1.1e-130 | M | Glycosyl hydrolases family 25 | |||
HBMJOCDF_00707 | 8.1e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
HBMJOCDF_00708 | 1.8e-248 | 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 | ||
HBMJOCDF_00710 | 5.9e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
HBMJOCDF_00711 | 8.9e-133 | L | Phage integrase family | |||
HBMJOCDF_00712 | 5.1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HBMJOCDF_00713 | 5.9e-79 | 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 | ||
HBMJOCDF_00714 | 8.4e-145 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
HBMJOCDF_00715 | 7.2e-136 | 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 | ||
HBMJOCDF_00716 | 4.6e-157 | 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 | |
HBMJOCDF_00717 | 3.7e-154 | 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 | ||
HBMJOCDF_00718 | 1.4e-60 | rplQ | J | Ribosomal protein L17 | ||
HBMJOCDF_00719 | 1.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HBMJOCDF_00720 | 3e-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 | ||
HBMJOCDF_00721 | 3.6e-55 | 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 | ||
HBMJOCDF_00722 | 7.8e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HBMJOCDF_00723 | 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 | ||
HBMJOCDF_00724 | 3.5e-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 | |
HBMJOCDF_00725 | 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 | ||
HBMJOCDF_00726 | 2.6e-71 | rplO | J | Binds to the 23S rRNA | ||
HBMJOCDF_00727 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
HBMJOCDF_00728 | 4.1e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HBMJOCDF_00729 | 1.1e-54 | 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 | ||
HBMJOCDF_00730 | 3.3e-92 | 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 | ||
HBMJOCDF_00731 | 3.2e-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 | ||
HBMJOCDF_00732 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
HBMJOCDF_00733 | 5.5e-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 | ||
HBMJOCDF_00734 | 3.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HBMJOCDF_00735 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HBMJOCDF_00736 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HBMJOCDF_00737 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HBMJOCDF_00738 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HBMJOCDF_00739 | 2.7e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HBMJOCDF_00740 | 4e-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 | ||
HBMJOCDF_00741 | 1.1e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HBMJOCDF_00742 | 7.3e-155 | 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 | ||
HBMJOCDF_00743 | 3.1e-47 | 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 | ||
HBMJOCDF_00744 | 1.7e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HBMJOCDF_00745 | 9e-113 | 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 | ||
HBMJOCDF_00746 | 3.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HBMJOCDF_00747 | 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 | ||
HBMJOCDF_00748 | 2.7e-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 | ||
HBMJOCDF_00749 | 7.8e-70 | 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 | ||
HBMJOCDF_00750 | 3.6e-120 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
HBMJOCDF_00751 | 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 | |
HBMJOCDF_00752 | 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 | |
HBMJOCDF_00753 | 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 | ||
HBMJOCDF_00754 | 1.3e-81 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
HBMJOCDF_00756 | 1.6e-08 | |||||
HBMJOCDF_00757 | 1.2e-49 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
HBMJOCDF_00758 | 7e-135 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
HBMJOCDF_00759 | 1.3e-68 | GM | NAD(P)H-binding | |||
HBMJOCDF_00760 | 8.9e-34 | S | Domain of unknown function (DUF4440) | |||
HBMJOCDF_00761 | 6.6e-90 | K | LysR substrate binding domain | |||
HBMJOCDF_00763 | 3.3e-45 | K | Tetracycline repressor, C-terminal all-alpha domain | |||
HBMJOCDF_00764 | 3.2e-79 | S | X-Pro dipeptidyl-peptidase (S15 family) | |||
HBMJOCDF_00765 | 7.7e-10 | C | Flavodoxin | |||
HBMJOCDF_00766 | 6.4e-148 | glnH | ET | ABC transporter | ||
HBMJOCDF_00767 | 1.9e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HBMJOCDF_00768 | 1.5e-242 | steT | E | amino acid | ||
HBMJOCDF_00769 | 2.2e-238 | steT | E | amino acid | ||
HBMJOCDF_00770 | 6.1e-151 | |||||
HBMJOCDF_00771 | 5.9e-174 | S | Aldo keto reductase | |||
HBMJOCDF_00772 | 2.7e-310 | ybiT | S | ABC transporter, ATP-binding protein | ||
HBMJOCDF_00773 | 1.7e-209 | pepA | E | M42 glutamyl aminopeptidase | ||
HBMJOCDF_00774 | 1.6e-45 | |||||
HBMJOCDF_00775 | 2.4e-136 | |||||
HBMJOCDF_00776 | 1.1e-217 | mdtG | EGP | Major facilitator Superfamily | ||
HBMJOCDF_00777 | 9.2e-262 | emrY | EGP | Major facilitator Superfamily | ||
HBMJOCDF_00778 | 4.7e-91 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HBMJOCDF_00779 | 2.9e-238 | pyrP | F | Permease | ||
HBMJOCDF_00780 | 2.9e-287 | K | Putative DNA-binding domain | |||
HBMJOCDF_00781 | 2e-29 | |||||
HBMJOCDF_00782 | 7.8e-157 | S | reductase | |||
HBMJOCDF_00783 | 5.8e-85 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
HBMJOCDF_00784 | 2.8e-79 | 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 | |
HBMJOCDF_00785 | 2.2e-226 | 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 | |
HBMJOCDF_00786 | 8.7e-86 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
HBMJOCDF_00787 | 3.2e-139 | 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 | |
HBMJOCDF_00789 | 8.3e-138 | L | An automated process has identified a potential problem with this gene model | |||
HBMJOCDF_00790 | 2.8e-48 | S | Peptidase propeptide and YPEB domain | |||
HBMJOCDF_00791 | 6.5e-169 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
HBMJOCDF_00792 | 7.2e-183 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HBMJOCDF_00793 | 4.3e-52 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
HBMJOCDF_00794 | 2e-155 | crtI | 1.3.99.23, 5.2.1.13 | Q | HI0933-like protein | |
HBMJOCDF_00795 | 5e-125 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
HBMJOCDF_00796 | 2.8e-140 | sufC | O | FeS assembly ATPase SufC | ||
HBMJOCDF_00797 | 3.5e-174 | sufD | O | FeS assembly protein SufD | ||
HBMJOCDF_00798 | 5.3e-178 | 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 | |
HBMJOCDF_00799 | 2.4e-59 | nifU | C | SUF system FeS assembly protein, NifU family | ||
HBMJOCDF_00800 | 2e-266 | sufB | O | assembly protein SufB | ||
HBMJOCDF_00801 | 2.4e-45 | yitW | S | Iron-sulfur cluster assembly protein | ||
HBMJOCDF_00802 | 2.9e-247 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HBMJOCDF_00803 | 5.2e-184 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
HBMJOCDF_00804 | 2.3e-116 | dedA | S | SNARE-like domain protein | ||
HBMJOCDF_00805 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
HBMJOCDF_00806 | 6.9e-144 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
HBMJOCDF_00807 | 8.3e-105 | yutD | S | Protein of unknown function (DUF1027) | ||
HBMJOCDF_00808 | 5.8e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
HBMJOCDF_00809 | 4.3e-55 | |||||
HBMJOCDF_00810 | 2.3e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
HBMJOCDF_00811 | 3.2e-181 | ccpA | K | catabolite control protein A | ||
HBMJOCDF_00812 | 9.1e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HBMJOCDF_00813 | 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 | ||
HBMJOCDF_00814 | 3.5e-32 | ykzG | S | Belongs to the UPF0356 family | ||
HBMJOCDF_00815 | 4e-101 | 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 | |
HBMJOCDF_00816 | 0.0 | typA | T | GTP-binding protein TypA | ||
HBMJOCDF_00817 | 1.3e-210 | ftsW | D | Belongs to the SEDS family | ||
HBMJOCDF_00818 | 5.1e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
HBMJOCDF_00819 | 4.5e-97 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
HBMJOCDF_00820 | 3.6e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HBMJOCDF_00821 | 5.3e-187 | ylbL | T | Belongs to the peptidase S16 family | ||
HBMJOCDF_00822 | 3.1e-79 | comEA | L | Competence protein ComEA | ||
HBMJOCDF_00823 | 0.0 | comEC | S | Competence protein ComEC | ||
HBMJOCDF_00824 | 2.6e-175 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
HBMJOCDF_00825 | 2.6e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
HBMJOCDF_00826 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HBMJOCDF_00827 | 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 | ||
HBMJOCDF_00828 | 3.4e-100 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
HBMJOCDF_00829 | 3.2e-105 | K | response regulator | |||
HBMJOCDF_00830 | 1.1e-103 | sptS | 2.7.13.3 | T | Histidine kinase | |
HBMJOCDF_00831 | 2.6e-103 | sptS | 2.7.13.3 | T | Histidine kinase | |
HBMJOCDF_00832 | 7.2e-209 | EGP | Major facilitator Superfamily | |||
HBMJOCDF_00833 | 2.3e-69 | O | OsmC-like protein | |||
HBMJOCDF_00834 | 2.2e-85 | S | Protein of unknown function (DUF805) | |||
HBMJOCDF_00835 | 2.2e-78 | |||||
HBMJOCDF_00836 | 5.1e-281 | |||||
HBMJOCDF_00837 | 7.2e-15 | S | Fic/DOC family | |||
HBMJOCDF_00838 | 6.3e-212 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
HBMJOCDF_00839 | 5e-235 | G | Bacterial extracellular solute-binding protein | |||
HBMJOCDF_00840 | 7.7e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
HBMJOCDF_00841 | 3.5e-166 | 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 | |
HBMJOCDF_00842 | 1e-125 | 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 | |
HBMJOCDF_00843 | 0.0 | kup | P | Transport of potassium into the cell | ||
HBMJOCDF_00844 | 9.1e-175 | rihB | 3.2.2.1 | F | Nucleoside | |
HBMJOCDF_00845 | 2.8e-134 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
HBMJOCDF_00846 | 6.8e-40 | S | hydrolase | |||
HBMJOCDF_00847 | 5.6e-179 | S | PFAM Archaeal ATPase | |||
HBMJOCDF_00848 | 1.8e-193 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
HBMJOCDF_00849 | 7.4e-128 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
HBMJOCDF_00850 | 1.6e-140 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HBMJOCDF_00851 | 2.9e-78 | G | Phosphoglycerate mutase family | |||
HBMJOCDF_00852 | 8.9e-10 | G | Phosphoglycerate mutase family | |||
HBMJOCDF_00853 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
HBMJOCDF_00854 | 6.5e-151 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HBMJOCDF_00855 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HBMJOCDF_00856 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
HBMJOCDF_00857 | 5.9e-230 | yhaO | L | Ser Thr phosphatase family protein | ||
HBMJOCDF_00858 | 0.0 | L | AAA domain | |||
HBMJOCDF_00859 | 1.9e-186 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HBMJOCDF_00860 | 2.9e-23 | |||||
HBMJOCDF_00861 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
HBMJOCDF_00862 | 3.1e-265 | |||||
HBMJOCDF_00863 | 1.9e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
HBMJOCDF_00864 | 1.5e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
HBMJOCDF_00865 | 3.9e-25 | |||||
HBMJOCDF_00866 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
HBMJOCDF_00867 | 1.7e-134 | ecsA | V | ABC transporter, ATP-binding protein | ||
HBMJOCDF_00868 | 2.9e-221 | ecsB | U | ABC transporter | ||
HBMJOCDF_00869 | 3.3e-126 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
HBMJOCDF_00871 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
HBMJOCDF_00872 | 1.7e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HBMJOCDF_00873 | 2.1e-185 | |||||
HBMJOCDF_00874 | 1e-248 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HBMJOCDF_00875 | 1.5e-234 | mepA | V | MATE efflux family protein | ||
HBMJOCDF_00876 | 1.3e-171 | S | SLAP domain | |||
HBMJOCDF_00877 | 7.4e-74 | L | Putative transposase DNA-binding domain | |||
HBMJOCDF_00878 | 1.7e-84 | L | Putative transposase DNA-binding domain | |||
HBMJOCDF_00879 | 1.4e-83 | L | Resolvase, N-terminal | |||
HBMJOCDF_00880 | 1.2e-157 | M | Peptidase family M1 domain | |||
HBMJOCDF_00881 | 2.7e-193 | S | Bacteriocin helveticin-J | |||
HBMJOCDF_00882 | 1.6e-18 | |||||
HBMJOCDF_00883 | 2.4e-50 | L | RelB antitoxin | |||
HBMJOCDF_00884 | 9.1e-140 | qmcA | O | prohibitin homologues | ||
HBMJOCDF_00885 | 2.6e-104 | darA | C | Flavodoxin | ||
HBMJOCDF_00886 | 5.5e-138 | purD | 6.3.4.13 | F | Belongs to the GARS family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)