ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
AHGDMNCB_00001 | 2.4e-133 | cysA | V | ABC transporter, ATP-binding protein | ||
AHGDMNCB_00003 | 1.5e-288 | pipD | E | Dipeptidase | ||
AHGDMNCB_00004 | 1.1e-162 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
AHGDMNCB_00005 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
AHGDMNCB_00006 | 1.9e-124 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
AHGDMNCB_00007 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
AHGDMNCB_00008 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
AHGDMNCB_00009 | 6.9e-130 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
AHGDMNCB_00010 | 5.7e-172 | oppB | P | ABC transporter permease | ||
AHGDMNCB_00011 | 1.1e-39 | oppF | P | Belongs to the ABC transporter superfamily | ||
AHGDMNCB_00012 | 6.6e-119 | yvyE | 3.4.13.9 | S | YigZ family | |
AHGDMNCB_00013 | 1.3e-210 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
AHGDMNCB_00014 | 4.3e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
AHGDMNCB_00015 | 8.5e-196 | 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 | ||
AHGDMNCB_00016 | 1.1e-95 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
AHGDMNCB_00017 | 2.5e-20 | ymfM | S | Helix-turn-helix domain | ||
AHGDMNCB_00019 | 5.1e-111 | papP | P | ABC transporter, permease protein | ||
AHGDMNCB_00020 | 2.8e-117 | P | ABC transporter permease | |||
AHGDMNCB_00021 | 9.7e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHGDMNCB_00022 | 2.9e-162 | cjaA | ET | ABC transporter substrate-binding protein | ||
AHGDMNCB_00023 | 1.3e-198 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
AHGDMNCB_00024 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHGDMNCB_00025 | 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 | ||
AHGDMNCB_00026 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
AHGDMNCB_00027 | 1.9e-158 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
AHGDMNCB_00028 | 5.7e-25 | |||||
AHGDMNCB_00029 | 4e-247 | mco | Q | Multicopper oxidase | ||
AHGDMNCB_00030 | 6.9e-36 | mco | Q | Multicopper oxidase | ||
AHGDMNCB_00031 | 4.7e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
AHGDMNCB_00032 | 0.0 | oppA | E | ABC transporter | ||
AHGDMNCB_00033 | 6.2e-232 | Q | Imidazolonepropionase and related amidohydrolases | |||
AHGDMNCB_00034 | 4.3e-223 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
AHGDMNCB_00035 | 2.7e-159 | repB | EP | Plasmid replication protein | ||
AHGDMNCB_00036 | 1e-19 | |||||
AHGDMNCB_00037 | 5.5e-188 | L | Belongs to the 'phage' integrase family | |||
AHGDMNCB_00038 | 4.4e-163 | L | An automated process has identified a potential problem with this gene model | |||
AHGDMNCB_00039 | 1.7e-66 | qmcA | O | prohibitin homologues | ||
AHGDMNCB_00040 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AHGDMNCB_00041 | 1.4e-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 | |
AHGDMNCB_00042 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
AHGDMNCB_00043 | 4.6e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
AHGDMNCB_00044 | 3e-251 | dnaB | L | Replication initiation and membrane attachment | ||
AHGDMNCB_00045 | 6.2e-168 | dnaI | L | Primosomal protein DnaI | ||
AHGDMNCB_00046 | 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) | |
AHGDMNCB_00047 | 2.1e-85 | |||||
AHGDMNCB_00048 | 9.5e-175 | S | Domain of unknown function (DUF389) | |||
AHGDMNCB_00049 | 2.9e-62 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
AHGDMNCB_00050 | 1.1e-47 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
AHGDMNCB_00051 | 4e-20 | 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) | |
AHGDMNCB_00052 | 2.4e-121 | msmX | P | Belongs to the ABC transporter superfamily | ||
AHGDMNCB_00053 | 8.4e-276 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
AHGDMNCB_00055 | 5.9e-219 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
AHGDMNCB_00056 | 1.6e-185 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
AHGDMNCB_00057 | 1.6e-70 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
AHGDMNCB_00059 | 1.7e-22 | |||||
AHGDMNCB_00065 | 1.8e-11 | |||||
AHGDMNCB_00066 | 6.6e-08 | |||||
AHGDMNCB_00068 | 3.2e-110 | glnP | P | ABC transporter permease | ||
AHGDMNCB_00069 | 1.5e-247 | helD | 3.6.4.12 | L | DNA helicase | |
AHGDMNCB_00070 | 2.3e-54 | K | Helix-turn-helix XRE-family like proteins | |||
AHGDMNCB_00071 | 8.6e-21 | |||||
AHGDMNCB_00072 | 9.6e-152 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
AHGDMNCB_00073 | 1.7e-292 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
AHGDMNCB_00074 | 6.3e-145 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHGDMNCB_00075 | 1.8e-178 | yvdE | K | helix_turn _helix lactose operon repressor | ||
AHGDMNCB_00076 | 3.7e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHGDMNCB_00077 | 9.1e-77 | S | PAS domain | |||
AHGDMNCB_00078 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
AHGDMNCB_00079 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
AHGDMNCB_00080 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AHGDMNCB_00081 | 1.4e-116 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
AHGDMNCB_00082 | 4.7e-210 | msmX | P | Belongs to the ABC transporter superfamily | ||
AHGDMNCB_00083 | 1.3e-213 | malE | G | Bacterial extracellular solute-binding protein | ||
AHGDMNCB_00084 | 3.3e-250 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
AHGDMNCB_00085 | 9.7e-147 | malG | P | ABC transporter permease | ||
AHGDMNCB_00086 | 2e-08 | |||||
AHGDMNCB_00088 | 1.4e-89 | ymdB | S | Macro domain protein | ||
AHGDMNCB_00089 | 7.4e-212 | mdtG | EGP | Major facilitator Superfamily | ||
AHGDMNCB_00090 | 2.6e-175 | |||||
AHGDMNCB_00091 | 2.8e-47 | lysM | M | LysM domain | ||
AHGDMNCB_00092 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
AHGDMNCB_00093 | 2.2e-250 | dtpT | U | amino acid peptide transporter | ||
AHGDMNCB_00094 | 7.3e-19 | S | Sugar efflux transporter for intercellular exchange | |||
AHGDMNCB_00095 | 3e-78 | XK27_02470 | K | LytTr DNA-binding domain | ||
AHGDMNCB_00096 | 6e-124 | liaI | S | membrane | ||
AHGDMNCB_00097 | 4e-16 | |||||
AHGDMNCB_00098 | 9e-207 | S | Putative peptidoglycan binding domain | |||
AHGDMNCB_00099 | 1.9e-160 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
AHGDMNCB_00100 | 9e-121 | |||||
AHGDMNCB_00101 | 3.4e-143 | S | Belongs to the UPF0246 family | |||
AHGDMNCB_00102 | 4.9e-142 | aroD | S | Alpha/beta hydrolase family | ||
AHGDMNCB_00103 | 1e-110 | G | phosphoglycerate mutase | |||
AHGDMNCB_00104 | 2.7e-91 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
AHGDMNCB_00105 | 7.3e-176 | hrtB | V | ABC transporter permease | ||
AHGDMNCB_00106 | 1.5e-102 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
AHGDMNCB_00107 | 2.8e-276 | pipD | E | Dipeptidase | ||
AHGDMNCB_00108 | 8e-38 | |||||
AHGDMNCB_00109 | 6.3e-111 | K | WHG domain | |||
AHGDMNCB_00110 | 2.4e-95 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
AHGDMNCB_00111 | 2e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
AHGDMNCB_00112 | 3e-150 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
AHGDMNCB_00113 | 2.5e-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 | |
AHGDMNCB_00114 | 3e-53 | cvpA | S | Colicin V production protein | ||
AHGDMNCB_00115 | 1.2e-129 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
AHGDMNCB_00116 | 5.6e-147 | noc | K | Belongs to the ParB family | ||
AHGDMNCB_00117 | 3.4e-138 | soj | D | Sporulation initiation inhibitor | ||
AHGDMNCB_00118 | 1.9e-153 | spo0J | K | Belongs to the ParB family | ||
AHGDMNCB_00119 | 9.6e-45 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
AHGDMNCB_00120 | 3.6e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
AHGDMNCB_00121 | 5.3e-107 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
AHGDMNCB_00122 | 1.1e-303 | V | ABC transporter, ATP-binding protein | |||
AHGDMNCB_00123 | 0.0 | V | ABC transporter | |||
AHGDMNCB_00125 | 1.3e-205 | L | Probable transposase | |||
AHGDMNCB_00126 | 3.9e-39 | S | HicB family | |||
AHGDMNCB_00127 | 9.6e-121 | K | response regulator | |||
AHGDMNCB_00128 | 4.6e-208 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
AHGDMNCB_00129 | 5.5e-305 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
AHGDMNCB_00130 | 6.3e-139 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
AHGDMNCB_00131 | 3.1e-53 | S | Enterocin A Immunity | |||
AHGDMNCB_00132 | 2.5e-33 | |||||
AHGDMNCB_00133 | 9.5e-26 | |||||
AHGDMNCB_00134 | 1e-24 | |||||
AHGDMNCB_00135 | 3.2e-272 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
AHGDMNCB_00136 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
AHGDMNCB_00137 | 3.5e-255 | S | Archaea bacterial proteins of unknown function | |||
AHGDMNCB_00139 | 5.2e-224 | 2.7.13.3 | T | GHKL domain | ||
AHGDMNCB_00140 | 6.1e-127 | K | LytTr DNA-binding domain | |||
AHGDMNCB_00141 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
AHGDMNCB_00142 | 9e-107 | M | Transport protein ComB | |||
AHGDMNCB_00143 | 2.6e-135 | blpT | ||||
AHGDMNCB_00147 | 3.8e-31 | |||||
AHGDMNCB_00148 | 3.6e-22 | |||||
AHGDMNCB_00149 | 1.7e-80 | |||||
AHGDMNCB_00150 | 8.2e-31 | yozG | K | Transcriptional regulator | ||
AHGDMNCB_00151 | 4.8e-25 | |||||
AHGDMNCB_00152 | 4.4e-68 | |||||
AHGDMNCB_00153 | 3.6e-08 | |||||
AHGDMNCB_00154 | 4.9e-29 | |||||
AHGDMNCB_00155 | 3.6e-67 | 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) | |
AHGDMNCB_00156 | 7.2e-172 | yegS | 2.7.1.107 | G | Lipid kinase | |
AHGDMNCB_00157 | 4.3e-108 | ybhL | S | Belongs to the BI1 family | ||
AHGDMNCB_00158 | 2.6e-57 | |||||
AHGDMNCB_00159 | 1.5e-149 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
AHGDMNCB_00160 | 2.8e-244 | nhaC | C | Na H antiporter NhaC | ||
AHGDMNCB_00161 | 3.2e-200 | pbpX | V | Beta-lactamase | ||
AHGDMNCB_00162 | 5.8e-255 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHGDMNCB_00163 | 1.1e-94 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
AHGDMNCB_00168 | 5.9e-261 | emrY | EGP | Major facilitator Superfamily | ||
AHGDMNCB_00169 | 2e-91 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
AHGDMNCB_00170 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
AHGDMNCB_00171 | 1.4e-14 | S | Domain of unknown function (DUF4417) | |||
AHGDMNCB_00172 | 1.3e-19 | |||||
AHGDMNCB_00173 | 1.9e-20 | |||||
AHGDMNCB_00174 | 1.1e-14 | K | Helix-turn-helix XRE-family like proteins | |||
AHGDMNCB_00175 | 4.8e-27 | E | Zn peptidase | |||
AHGDMNCB_00176 | 5.8e-85 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
AHGDMNCB_00177 | 1.7e-159 | S | reductase | |||
AHGDMNCB_00178 | 9.3e-35 | |||||
AHGDMNCB_00179 | 1.5e-291 | K | Putative DNA-binding domain | |||
AHGDMNCB_00180 | 1e-22 | pyrP | F | Permease | ||
AHGDMNCB_00182 | 0.0 | S | PglZ domain | |||
AHGDMNCB_00183 | 8.3e-193 | K | Periplasmic binding protein-like domain | |||
AHGDMNCB_00184 | 1.7e-105 | K | Transcriptional regulator, AbiEi antitoxin | |||
AHGDMNCB_00185 | 6.9e-26 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
AHGDMNCB_00186 | 5.1e-20 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
AHGDMNCB_00187 | 5.3e-189 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
AHGDMNCB_00188 | 2e-185 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
AHGDMNCB_00189 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
AHGDMNCB_00190 | 2.5e-186 | lacR | K | Transcriptional regulator | ||
AHGDMNCB_00191 | 0.0 | lacS | G | Transporter | ||
AHGDMNCB_00192 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
AHGDMNCB_00193 | 2.8e-282 | thrC | 4.2.3.1 | E | Threonine synthase | |
AHGDMNCB_00194 | 4.3e-220 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AHGDMNCB_00195 | 6.6e-159 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
AHGDMNCB_00196 | 2.6e-115 | |||||
AHGDMNCB_00197 | 3e-159 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AHGDMNCB_00199 | 1.9e-10 | 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 | |
AHGDMNCB_00200 | 4.8e-123 | L | Belongs to the 'phage' integrase family | |||
AHGDMNCB_00204 | 7.5e-104 | 3.4.21.88 | K | Peptidase S24-like | ||
AHGDMNCB_00205 | 5e-14 | S | sequence-specific DNA binding | |||
AHGDMNCB_00212 | 3.2e-270 | |||||
AHGDMNCB_00213 | 1.5e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
AHGDMNCB_00214 | 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 | |
AHGDMNCB_00215 | 3.9e-25 | |||||
AHGDMNCB_00216 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
AHGDMNCB_00217 | 2e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
AHGDMNCB_00218 | 1.9e-220 | ecsB | U | ABC transporter | ||
AHGDMNCB_00219 | 1.6e-125 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
AHGDMNCB_00220 | 2.9e-13 | S | Protein of unknown function (DUF805) | |||
AHGDMNCB_00221 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
AHGDMNCB_00222 | 6.3e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHGDMNCB_00223 | 1.4e-248 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
AHGDMNCB_00224 | 5.9e-129 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
AHGDMNCB_00225 | 2.4e-184 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AHGDMNCB_00226 | 1.3e-84 | yueI | S | Protein of unknown function (DUF1694) | ||
AHGDMNCB_00227 | 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 | ||
AHGDMNCB_00228 | 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 | ||
AHGDMNCB_00229 | 1.5e-214 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
AHGDMNCB_00230 | 3.9e-226 | 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 | |
AHGDMNCB_00232 | 6.3e-111 | |||||
AHGDMNCB_00234 | 1.4e-94 | |||||
AHGDMNCB_00236 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
AHGDMNCB_00237 | 1.1e-164 | |||||
AHGDMNCB_00238 | 1.4e-104 | K | Helix-turn-helix domain | |||
AHGDMNCB_00239 | 5.9e-32 | K | Helix-turn-helix domain | |||
AHGDMNCB_00240 | 4.4e-16 | 1.3.5.4 | C | FAD binding domain | ||
AHGDMNCB_00241 | 2.2e-63 | S | Phage derived protein Gp49-like (DUF891) | |||
AHGDMNCB_00242 | 6e-42 | K | Helix-turn-helix XRE-family like proteins | |||
AHGDMNCB_00243 | 4.2e-68 | |||||
AHGDMNCB_00244 | 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 | |
AHGDMNCB_00245 | 2.7e-241 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHGDMNCB_00246 | 2e-32 | |||||
AHGDMNCB_00247 | 1.4e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
AHGDMNCB_00248 | 1.7e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AHGDMNCB_00249 | 3.3e-166 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
AHGDMNCB_00250 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
AHGDMNCB_00251 | 6.6e-139 | stp | 3.1.3.16 | T | phosphatase | |
AHGDMNCB_00252 | 6.1e-244 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
AHGDMNCB_00253 | 1.9e-172 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
AHGDMNCB_00254 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
AHGDMNCB_00255 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
AHGDMNCB_00256 | 1.8e-110 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
AHGDMNCB_00257 | 7.6e-242 | yfnA | E | Amino Acid | ||
AHGDMNCB_00258 | 8e-182 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHGDMNCB_00259 | 2e-149 | yxeH | S | hydrolase | ||
AHGDMNCB_00260 | 2.9e-156 | S | reductase | |||
AHGDMNCB_00261 | 1e-44 | 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 | ||
AHGDMNCB_00262 | 4.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
AHGDMNCB_00263 | 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 | ||
AHGDMNCB_00264 | 1.3e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
AHGDMNCB_00265 | 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 | ||
AHGDMNCB_00266 | 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 | ||
AHGDMNCB_00267 | 1.1e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
AHGDMNCB_00268 | 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 | ||
AHGDMNCB_00269 | 2.7e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
AHGDMNCB_00270 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
AHGDMNCB_00271 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
AHGDMNCB_00272 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
AHGDMNCB_00273 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
AHGDMNCB_00274 | 3.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
AHGDMNCB_00275 | 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 | ||
AHGDMNCB_00276 | 6.8e-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 | ||
AHGDMNCB_00277 | 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 | ||
AHGDMNCB_00278 | 9.5e-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 | ||
AHGDMNCB_00279 | 3.6e-55 | 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 | ||
AHGDMNCB_00280 | 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 | ||
AHGDMNCB_00281 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
AHGDMNCB_00282 | 2.6e-71 | rplO | J | Binds to the 23S rRNA | ||
AHGDMNCB_00283 | 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 | ||
AHGDMNCB_00284 | 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 | |
AHGDMNCB_00285 | 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 | ||
AHGDMNCB_00286 | 7.8e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
AHGDMNCB_00287 | 4.2e-56 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
AHGDMNCB_00288 | 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 | ||
AHGDMNCB_00289 | 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 | |
AHGDMNCB_00290 | 1.4e-60 | rplQ | J | Ribosomal protein L17 | ||
AHGDMNCB_00291 | 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 | ||
AHGDMNCB_00292 | 5.4e-158 | 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 | |
AHGDMNCB_00293 | 2.6e-138 | 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 | ||
AHGDMNCB_00294 | 7.8e-151 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
AHGDMNCB_00295 | 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 | ||
AHGDMNCB_00296 | 1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
AHGDMNCB_00297 | 6.7e-53 | |||||
AHGDMNCB_00298 | 1.1e-21 | |||||
AHGDMNCB_00299 | 5.8e-69 | 5.4.2.11 | G | Phosphoglycerate mutase family | ||
AHGDMNCB_00300 | 7.7e-20 | 2.3.1.183 | M | FR47-like protein | ||
AHGDMNCB_00301 | 5e-142 | M | Belongs to the glycosyl hydrolase 28 family | |||
AHGDMNCB_00302 | 7e-80 | K | Acetyltransferase (GNAT) domain | |||
AHGDMNCB_00303 | 5.7e-106 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
AHGDMNCB_00304 | 1.9e-118 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
AHGDMNCB_00305 | 6.4e-134 | S | membrane transporter protein | |||
AHGDMNCB_00306 | 7.5e-126 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
AHGDMNCB_00307 | 5.1e-162 | czcD | P | cation diffusion facilitator family transporter | ||
AHGDMNCB_00308 | 1.4e-23 | |||||
AHGDMNCB_00309 | 1.5e-126 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AHGDMNCB_00310 | 1.1e-183 | S | AAA domain | |||
AHGDMNCB_00311 | 4.7e-43 | |||||
AHGDMNCB_00312 | 4.3e-266 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHGDMNCB_00313 | 1.9e-52 | |||||
AHGDMNCB_00314 | 1.8e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
AHGDMNCB_00315 | 1.3e-254 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
AHGDMNCB_00320 | 2.4e-30 | M | Prophage endopeptidase tail | |||
AHGDMNCB_00324 | 1.5e-09 | M | translation initiation factor activity | |||
AHGDMNCB_00325 | 6.3e-20 | atl | 3.2.1.96, 3.5.1.28 | GH73 | UW | LPXTG-motif cell wall anchor domain protein |
AHGDMNCB_00326 | 1.4e-77 | K | MerR HTH family regulatory protein | |||
AHGDMNCB_00327 | 3.5e-143 | S | Cysteine-rich secretory protein family | |||
AHGDMNCB_00328 | 4.6e-274 | ycaM | E | amino acid | ||
AHGDMNCB_00329 | 9.8e-291 | |||||
AHGDMNCB_00331 | 1.5e-189 | cggR | K | Putative sugar-binding domain | ||
AHGDMNCB_00332 | 6.5e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
AHGDMNCB_00333 | 1e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
AHGDMNCB_00334 | 2.9e-142 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
AHGDMNCB_00335 | 1.2e-94 | |||||
AHGDMNCB_00336 | 8.1e-157 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHGDMNCB_00337 | 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 | |
AHGDMNCB_00338 | 6.3e-182 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
AHGDMNCB_00339 | 1.4e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
AHGDMNCB_00340 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
AHGDMNCB_00341 | 1.8e-164 | murB | 1.3.1.98 | M | Cell wall formation | |
AHGDMNCB_00342 | 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 | |
AHGDMNCB_00343 | 1.4e-131 | potB | P | ABC transporter permease | ||
AHGDMNCB_00344 | 4.8e-127 | potC | P | ABC transporter permease | ||
AHGDMNCB_00345 | 4.7e-207 | potD | P | ABC transporter | ||
AHGDMNCB_00346 | 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 | |
AHGDMNCB_00347 | 2.4e-234 | L | Transposase | |||
AHGDMNCB_00349 | 2.2e-145 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
AHGDMNCB_00350 | 6.5e-202 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
AHGDMNCB_00351 | 1.8e-283 | secA2 | 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 | ||
AHGDMNCB_00352 | 3.8e-45 | asp3 | S | Accessory Sec secretory system ASP3 | ||
AHGDMNCB_00353 | 1.9e-156 | asp2 | 3.4.11.5 | S | Accessory Sec system GspB-transporter | |
AHGDMNCB_00354 | 1.7e-117 | asp1 | S | Accessory Sec system protein Asp1 | ||
AHGDMNCB_00355 | 9.3e-77 | O | OsmC-like protein | |||
AHGDMNCB_00356 | 3e-81 | |||||
AHGDMNCB_00357 | 3.2e-104 | S | Domain of unknown function DUF1829 | |||
AHGDMNCB_00358 | 5.5e-158 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
AHGDMNCB_00359 | 8.1e-64 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
AHGDMNCB_00363 | 1e-25 | S | Phage tail tube protein | |||
AHGDMNCB_00364 | 8.3e-13 | S | Protein of unknown function (DUF806) | |||
AHGDMNCB_00365 | 5.5e-28 | S | Bacteriophage HK97-gp10, putative tail-component | |||
AHGDMNCB_00366 | 6.5e-08 | S | Phage head-tail joining protein | |||
AHGDMNCB_00367 | 4.7e-14 | S | Phage gp6-like head-tail connector protein | |||
AHGDMNCB_00369 | 5.6e-239 | 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) | |
AHGDMNCB_00370 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
AHGDMNCB_00371 | 9.8e-103 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
AHGDMNCB_00372 | 2.1e-38 | |||||
AHGDMNCB_00373 | 2.6e-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 | |
AHGDMNCB_00374 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
AHGDMNCB_00375 | 2.2e-57 | XK27_04120 | S | Putative amino acid metabolism | ||
AHGDMNCB_00376 | 4.6e-221 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
AHGDMNCB_00377 | 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 | |
AHGDMNCB_00378 | 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 | ||
AHGDMNCB_00379 | 3.3e-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 | ||
AHGDMNCB_00380 | 5.7e-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 | ||
AHGDMNCB_00381 | 1.4e-297 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
AHGDMNCB_00383 | 1.6e-08 | |||||
AHGDMNCB_00384 | 1.6e-08 | |||||
AHGDMNCB_00386 | 1.3e-81 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
AHGDMNCB_00387 | 3.5e-39 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
AHGDMNCB_00388 | 8.1e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
AHGDMNCB_00389 | 1e-242 | cpdA | S | Calcineurin-like phosphoesterase | ||
AHGDMNCB_00390 | 7.6e-79 | |||||
AHGDMNCB_00391 | 1.9e-115 | rdgB | 3.6.1.66, 5.1.1.3 | F | Ham1 family | |
AHGDMNCB_00392 | 3.4e-33 | |||||
AHGDMNCB_00393 | 3.6e-63 | |||||
AHGDMNCB_00402 | 2.1e-15 | S | Domain of unknown function (DUF3173) | |||
AHGDMNCB_00403 | 6e-85 | |||||
AHGDMNCB_00404 | 6.6e-147 | |||||
AHGDMNCB_00405 | 9.7e-18 | lmrB | EGP | Major facilitator Superfamily | ||
AHGDMNCB_00406 | 5.7e-128 | lmrB | EGP | Major facilitator Superfamily | ||
AHGDMNCB_00407 | 6.7e-29 | EGP | the major facilitator superfamily | |||
AHGDMNCB_00408 | 2.4e-206 | msmX | P | Belongs to the ABC transporter superfamily | ||
AHGDMNCB_00409 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
AHGDMNCB_00410 | 1.6e-182 | cah5 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
AHGDMNCB_00411 | 7.1e-250 | G | Bacterial extracellular solute-binding protein | |||
AHGDMNCB_00412 | 1.6e-152 | P | ABC-type sugar transport systems, permease components | |||
AHGDMNCB_00413 | 7.8e-163 | malG | U | Binding-protein-dependent transport system inner membrane component | ||
AHGDMNCB_00414 | 3.4e-82 | |||||
AHGDMNCB_00415 | 1.8e-275 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHGDMNCB_00416 | 2.4e-83 | S | Putative inner membrane protein (DUF1819) | |||
AHGDMNCB_00417 | 1.7e-89 | S | Domain of unknown function (DUF1788) | |||
AHGDMNCB_00418 | 1.6e-222 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
AHGDMNCB_00419 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
AHGDMNCB_00420 | 2.9e-93 | S | VanZ like family | |||
AHGDMNCB_00421 | 3.2e-110 | ylbE | GM | NAD(P)H-binding | ||
AHGDMNCB_00422 | 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 | ||
AHGDMNCB_00424 | 7.4e-305 | E | Amino acid permease | |||
AHGDMNCB_00425 | 1.4e-173 | D | Alpha beta | |||
AHGDMNCB_00426 | 2.1e-276 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
AHGDMNCB_00427 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
AHGDMNCB_00428 | 1.5e-191 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AHGDMNCB_00429 | 5.7e-288 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
AHGDMNCB_00430 | 1e-40 | S | Protein of unknown function (DUF975) | |||
AHGDMNCB_00431 | 2.7e-137 | lysA2 | M | Glycosyl hydrolases family 25 | ||
AHGDMNCB_00432 | 2.1e-291 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHGDMNCB_00433 | 1.9e-36 | |||||
AHGDMNCB_00434 | 0.0 | XK27_06780 | V | ABC transporter permease | ||
AHGDMNCB_00435 | 5.1e-125 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
AHGDMNCB_00436 | 7.4e-239 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
AHGDMNCB_00437 | 2.6e-166 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHGDMNCB_00438 | 0.0 | clpE | O | AAA domain (Cdc48 subfamily) | ||
AHGDMNCB_00439 | 1.6e-118 | V | ABC transporter transmembrane region | |||
AHGDMNCB_00440 | 1.6e-114 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHGDMNCB_00441 | 1.3e-233 | cycA | E | Amino acid permease | ||
AHGDMNCB_00442 | 2.5e-245 | yifK | E | Amino acid permease | ||
AHGDMNCB_00443 | 1.8e-138 | puuD | S | peptidase C26 | ||
AHGDMNCB_00444 | 2.2e-228 | steT_1 | E | amino acid | ||
AHGDMNCB_00445 | 1.4e-189 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
AHGDMNCB_00446 | 3.9e-206 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
AHGDMNCB_00449 | 7e-189 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
AHGDMNCB_00450 | 6.4e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
AHGDMNCB_00451 | 6.9e-245 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
AHGDMNCB_00452 | 2.8e-36 | hicA | S | HicA toxin of bacterial toxin-antitoxin, | ||
AHGDMNCB_00453 | 1.3e-54 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
AHGDMNCB_00454 | 4.7e-25 | S | Protein conserved in bacteria | |||
AHGDMNCB_00455 | 3.9e-57 | |||||
AHGDMNCB_00456 | 7.7e-88 | |||||
AHGDMNCB_00457 | 2.3e-262 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
AHGDMNCB_00458 | 2.2e-185 | XK27_05540 | S | DUF218 domain | ||
AHGDMNCB_00459 | 2.7e-109 | |||||
AHGDMNCB_00460 | 2.5e-107 | |||||
AHGDMNCB_00461 | 2.5e-118 | yicL | EG | EamA-like transporter family | ||
AHGDMNCB_00462 | 1.6e-166 | EG | EamA-like transporter family | |||
AHGDMNCB_00463 | 1.6e-166 | EG | EamA-like transporter family | |||
AHGDMNCB_00464 | 3.2e-38 | |||||
AHGDMNCB_00467 | 4.8e-82 | M | NlpC/P60 family | |||
AHGDMNCB_00468 | 2.1e-131 | cobQ | S | glutamine amidotransferase | ||
AHGDMNCB_00470 | 1.5e-68 | L | RelB antitoxin | |||
AHGDMNCB_00471 | 6.5e-44 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
AHGDMNCB_00472 | 5.9e-47 | yoeB | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | ||
AHGDMNCB_00475 | 1.5e-133 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
AHGDMNCB_00476 | 7.9e-67 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AHGDMNCB_00477 | 9.2e-65 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AHGDMNCB_00478 | 1.2e-12 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AHGDMNCB_00479 | 4.9e-33 | S | phage tail | |||
AHGDMNCB_00480 | 2.2e-165 | S | Phage minor structural protein | |||
AHGDMNCB_00483 | 1.1e-31 | E | GDSL-like Lipase/Acylhydrolase | |||
AHGDMNCB_00484 | 2.9e-08 | |||||
AHGDMNCB_00487 | 1.2e-107 | M | hydrolase, family 25 | |||
AHGDMNCB_00488 | 8.4e-208 | M | Glycosyl hydrolases family 25 | |||
AHGDMNCB_00489 | 3.9e-159 | cinI | S | Serine hydrolase (FSH1) | ||
AHGDMNCB_00490 | 1.3e-302 | S | Predicted membrane protein (DUF2207) | |||
AHGDMNCB_00491 | 1.6e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
AHGDMNCB_00494 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
AHGDMNCB_00495 | 5.1e-36 | |||||
AHGDMNCB_00496 | 2e-213 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHGDMNCB_00497 | 4.9e-182 | ccpA | K | catabolite control protein A | ||
AHGDMNCB_00498 | 4e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AHGDMNCB_00499 | 4.3e-55 | |||||
AHGDMNCB_00500 | 1.2e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
AHGDMNCB_00501 | 6.5e-102 | yutD | S | Protein of unknown function (DUF1027) | ||
AHGDMNCB_00502 | 2.6e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
AHGDMNCB_00503 | 8.3e-100 | S | Protein of unknown function (DUF1461) | |||
AHGDMNCB_00504 | 2.3e-116 | dedA | S | SNARE-like domain protein | ||
AHGDMNCB_00505 | 8e-185 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
AHGDMNCB_00506 | 1.6e-85 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
AHGDMNCB_00507 | 2.2e-122 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
AHGDMNCB_00508 | 9.6e-89 | M | Protein of unknown function (DUF3737) | |||
AHGDMNCB_00510 | 6.1e-52 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHGDMNCB_00511 | 4.6e-149 | ybbH_2 | K | rpiR family | ||
AHGDMNCB_00512 | 1.3e-198 | S | Bacterial protein of unknown function (DUF871) | |||
AHGDMNCB_00513 | 7.8e-155 | 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 | |
AHGDMNCB_00514 | 1.8e-270 | sacX | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
AHGDMNCB_00515 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
AHGDMNCB_00516 | 1.7e-160 | 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 | ||
AHGDMNCB_00517 | 1.5e-72 | S | Aminoacyl-tRNA editing domain | |||
AHGDMNCB_00518 | 1.2e-54 | S | Abi-like protein | |||
AHGDMNCB_00519 | 7.2e-225 | S | SLAP domain | |||
AHGDMNCB_00520 | 2.9e-131 | S | CAAX protease self-immunity | |||
AHGDMNCB_00521 | 1.3e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
AHGDMNCB_00522 | 1.2e-126 | K | response regulator | |||
AHGDMNCB_00523 | 2.2e-99 | yceD | S | Uncharacterized ACR, COG1399 | ||
AHGDMNCB_00524 | 1.2e-216 | ylbM | S | Belongs to the UPF0348 family | ||
AHGDMNCB_00525 | 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 | ||
AHGDMNCB_00526 | 6.6e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
AHGDMNCB_00527 | 1.2e-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) | |
AHGDMNCB_00528 | 1.5e-200 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHGDMNCB_00529 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
AHGDMNCB_00530 | 9.2e-201 | tnpB | L | Putative transposase DNA-binding domain | ||
AHGDMNCB_00531 | 5.6e-154 | 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 | |
AHGDMNCB_00532 | 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 | ||
AHGDMNCB_00533 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
AHGDMNCB_00534 | 2.2e-73 | 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 | ||
AHGDMNCB_00535 | 6.4e-80 | yyaR | K | Acetyltransferase (GNAT) domain | ||
AHGDMNCB_00536 | 7.9e-116 | S | domain protein | |||
AHGDMNCB_00537 | 4e-146 | V | ABC transporter | |||
AHGDMNCB_00538 | 3.8e-75 | S | Protein of unknown function (DUF3021) | |||
AHGDMNCB_00539 | 5e-75 | K | LytTr DNA-binding domain | |||
AHGDMNCB_00540 | 1.2e-38 | hxlR | K | HxlR-like helix-turn-helix | ||
AHGDMNCB_00541 | 7.7e-39 | S | Aldo keto reductase | |||
AHGDMNCB_00542 | 2.7e-40 | 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) | |
AHGDMNCB_00543 | 2.9e-159 | metQ2 | P | Belongs to the nlpA lipoprotein family | ||
AHGDMNCB_00544 | 1e-190 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AHGDMNCB_00545 | 8.1e-112 | srtA | 3.4.22.70 | M | sortase family | |
AHGDMNCB_00546 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
AHGDMNCB_00547 | 9.3e-80 | apfA | 2.7.7.72, 3.6.1.61 | F | NUDIX domain | |
AHGDMNCB_00548 | 5.8e-203 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
AHGDMNCB_00549 | 4.9e-244 | dnaK | O | Heat shock 70 kDa protein | ||
AHGDMNCB_00550 | 5.4e-71 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
AHGDMNCB_00551 | 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 | ||
AHGDMNCB_00552 | 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 | ||
AHGDMNCB_00553 | 1.1e-90 | S | Short repeat of unknown function (DUF308) | |||
AHGDMNCB_00554 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
AHGDMNCB_00555 | 1.2e-194 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
AHGDMNCB_00556 | 6.9e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AHGDMNCB_00557 | 1.3e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
AHGDMNCB_00558 | 5.8e-263 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
AHGDMNCB_00561 | 1e-195 | ampC | V | Beta-lactamase | ||
AHGDMNCB_00562 | 2.2e-217 | EGP | Major facilitator Superfamily | |||
AHGDMNCB_00563 | 6.2e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
AHGDMNCB_00564 | 8.5e-105 | vanZ | V | VanZ like family | ||
AHGDMNCB_00565 | 3.1e-87 | gtcA | S | Teichoic acid glycosylation protein | ||
AHGDMNCB_00566 | 5.9e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
AHGDMNCB_00568 | 1.4e-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 | ||
AHGDMNCB_00569 | 2.8e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AHGDMNCB_00570 | 4.7e-131 | M | Glycosyl hydrolases family 25 | |||
AHGDMNCB_00571 | 1.3e-230 | potE | E | amino acid | ||
AHGDMNCB_00572 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
AHGDMNCB_00573 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
AHGDMNCB_00574 | 3.4e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AHGDMNCB_00575 | 3.5e-79 | yhdP | S | Transporter associated domain | ||
AHGDMNCB_00579 | 4.6e-34 | |||||
AHGDMNCB_00582 | 4.2e-35 | dnaC | 3.4.21.53 | L | IstB-like ATP binding protein | |
AHGDMNCB_00583 | 3.1e-34 | L | Helix-turn-helix domain | |||
AHGDMNCB_00584 | 1.4e-111 | S | Putative HNHc nuclease | |||
AHGDMNCB_00585 | 8.7e-71 | S | ERF superfamily | |||
AHGDMNCB_00590 | 1.2e-39 | |||||
AHGDMNCB_00594 | 2.3e-09 | K | Helix-turn-helix XRE-family like proteins | |||
AHGDMNCB_00595 | 2.5e-78 | 3.4.21.88 | K | Peptidase S24-like | ||
AHGDMNCB_00596 | 4e-48 | ligA | 2.7.7.7, 6.5.1.2 | L | EXOIII | |
AHGDMNCB_00601 | 9.8e-61 | yniG | EGP | Major facilitator Superfamily | ||
AHGDMNCB_00602 | 1.1e-38 | yniG | EGP | Major facilitator Superfamily | ||
AHGDMNCB_00603 | 8.4e-183 | S | PFAM Archaeal ATPase | |||
AHGDMNCB_00604 | 2.7e-189 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
AHGDMNCB_00605 | 6.1e-122 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
AHGDMNCB_00606 | 1.2e-140 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHGDMNCB_00607 | 7.9e-111 | G | Phosphoglycerate mutase family | |||
AHGDMNCB_00608 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
AHGDMNCB_00609 | 6.5e-151 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AHGDMNCB_00610 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
AHGDMNCB_00611 | 2.1e-55 | yheA | S | Belongs to the UPF0342 family | ||
AHGDMNCB_00612 | 1.9e-233 | yhaO | L | Ser Thr phosphatase family protein | ||
AHGDMNCB_00613 | 0.0 | L | AAA domain | |||
AHGDMNCB_00614 | 1.9e-186 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHGDMNCB_00615 | 5.9e-24 | |||||
AHGDMNCB_00616 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
AHGDMNCB_00617 | 8.1e-254 | sacA | 3.2.1.26 | GH32 | G | Glycosyl hydrolases family 32 |
AHGDMNCB_00618 | 5.7e-155 | msmG | G | Binding-protein-dependent transport system inner membrane component | ||
AHGDMNCB_00619 | 3.2e-161 | msmF | P | ABC-type sugar transport systems, permease components | ||
AHGDMNCB_00620 | 1.4e-242 | msmE | G | Bacterial extracellular solute-binding protein | ||
AHGDMNCB_00621 | 1.5e-180 | msmR | K | helix_turn _helix lactose operon repressor | ||
AHGDMNCB_00622 | 4.9e-117 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AHGDMNCB_00623 | 1.1e-113 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
AHGDMNCB_00624 | 2.4e-87 | G | Histidine phosphatase superfamily (branch 1) | |||
AHGDMNCB_00625 | 1.2e-105 | G | Phosphoglycerate mutase family | |||
AHGDMNCB_00626 | 9.9e-157 | D | nuclear chromosome segregation | |||
AHGDMNCB_00627 | 1.5e-78 | M | LysM domain protein | |||
AHGDMNCB_00628 | 1.9e-99 | 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 | ||
AHGDMNCB_00629 | 3.6e-254 | L | Putative transposase DNA-binding domain | |||
AHGDMNCB_00630 | 5.9e-117 | L | Resolvase, N-terminal | |||
AHGDMNCB_00631 | 6.2e-12 | |||||
AHGDMNCB_00632 | 1.1e-172 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
AHGDMNCB_00633 | 2.5e-29 | |||||
AHGDMNCB_00637 | 1.1e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
AHGDMNCB_00638 | 1.4e-225 | slpX | S | SLAP domain | ||
AHGDMNCB_00639 | 4.4e-144 | K | SIS domain | |||
AHGDMNCB_00640 | 3e-140 | S | Phage minor structural protein | |||
AHGDMNCB_00642 | 3.2e-13 | S | Domain of unknown function (DUF2479) | |||
AHGDMNCB_00643 | 1.2e-29 | |||||
AHGDMNCB_00644 | 3.7e-17 | |||||
AHGDMNCB_00645 | 1.2e-104 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
AHGDMNCB_00650 | 9.3e-16 | |||||
AHGDMNCB_00651 | 2.8e-96 | M | hydrolase, family 25 | |||
AHGDMNCB_00652 | 8.9e-183 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
AHGDMNCB_00653 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
AHGDMNCB_00654 | 2.2e-93 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
AHGDMNCB_00655 | 2.5e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
AHGDMNCB_00656 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
AHGDMNCB_00657 | 1.4e-214 | S | SLAP domain | |||
AHGDMNCB_00658 | 1.7e-122 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
AHGDMNCB_00659 | 1.3e-145 | E | GDSL-like Lipase/Acylhydrolase family | |||
AHGDMNCB_00660 | 2e-112 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
AHGDMNCB_00661 | 3e-38 | ynzC | S | UPF0291 protein | ||
AHGDMNCB_00662 | 1.4e-76 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
AHGDMNCB_00663 | 7.4e-120 | 3.6.1.55 | F | NUDIX domain | ||
AHGDMNCB_00664 | 1.7e-246 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHGDMNCB_00665 | 0.0 | L | Plasmid pRiA4b ORF-3-like protein | |||
AHGDMNCB_00666 | 5e-87 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
AHGDMNCB_00667 | 2.1e-07 | S | Protein of unknown function (DUF3021) | |||
AHGDMNCB_00668 | 4.2e-07 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
AHGDMNCB_00669 | 1e-119 | yfbR | S | HD containing hydrolase-like enzyme | ||
AHGDMNCB_00670 | 2.8e-154 | L | HNH nucleases | |||
AHGDMNCB_00671 | 2.6e-85 | S | Protein of unknown function (DUF805) | |||
AHGDMNCB_00672 | 1.2e-135 | glnQ | E | ABC transporter, ATP-binding protein | ||
AHGDMNCB_00673 | 6e-291 | glnP | P | ABC transporter permease | ||
AHGDMNCB_00674 | 1.5e-120 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
AHGDMNCB_00675 | 2e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
AHGDMNCB_00676 | 9.6e-125 | terC | P | Integral membrane protein TerC family | ||
AHGDMNCB_00677 | 3.2e-92 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
AHGDMNCB_00678 | 7.4e-269 | S | Uncharacterised protein family (UPF0236) | |||
AHGDMNCB_00679 | 2.8e-210 | msmX | P | Belongs to the ABC transporter superfamily | ||
AHGDMNCB_00680 | 5.2e-153 | msmG | P | Binding-protein-dependent transport system inner membrane component | ||
AHGDMNCB_00681 | 6.2e-157 | msmF | P | Binding-protein-dependent transport system inner membrane component | ||
AHGDMNCB_00682 | 7.1e-239 | msmE | G | Bacterial extracellular solute-binding protein | ||
AHGDMNCB_00683 | 2.2e-171 | scrR | K | Periplasmic binding protein domain | ||
AHGDMNCB_00684 | 7.2e-36 | |||||
AHGDMNCB_00685 | 2.1e-78 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHGDMNCB_00686 | 3.8e-96 | yieF | S | NADPH-dependent FMN reductase | ||
AHGDMNCB_00687 | 1.6e-35 | L | Transposase and inactivated derivatives, IS30 family | |||
AHGDMNCB_00688 | 6.5e-64 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
AHGDMNCB_00689 | 1.8e-103 | mrr | L | restriction endonuclease | ||
AHGDMNCB_00690 | 0.0 | L | Type III restriction enzyme, res subunit | |||
AHGDMNCB_00692 | 4.4e-153 | U | TraM recognition site of TraD and TraG | |||
AHGDMNCB_00695 | 9.7e-38 | |||||
AHGDMNCB_00696 | 8e-58 | L | Lactococcus lactis RepB C-terminus | |||
AHGDMNCB_00697 | 3.8e-125 | luxT | K | Bacterial regulatory proteins, tetR family | ||
AHGDMNCB_00698 | 2.6e-183 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
AHGDMNCB_00699 | 5.6e-39 | |||||
AHGDMNCB_00700 | 2.8e-125 | S | Alpha/beta hydrolase family | |||
AHGDMNCB_00701 | 1.3e-156 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
AHGDMNCB_00702 | 4.4e-140 | ypuA | S | Protein of unknown function (DUF1002) | ||
AHGDMNCB_00703 | 2.7e-148 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AHGDMNCB_00704 | 7.7e-182 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AHGDMNCB_00705 | 2.5e-283 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AHGDMNCB_00706 | 4.2e-86 | |||||
AHGDMNCB_00707 | 3.5e-131 | cobB | K | SIR2 family | ||
AHGDMNCB_00708 | 2e-58 | ydcK | S | Belongs to the SprT family | ||
AHGDMNCB_00710 | 2.5e-86 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
AHGDMNCB_00711 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
AHGDMNCB_00712 | 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 | |
AHGDMNCB_00713 | 5.8e-203 | camS | S | sex pheromone | ||
AHGDMNCB_00714 | 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) | |
AHGDMNCB_00715 | 2.9e-268 | 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) | |
AHGDMNCB_00716 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
AHGDMNCB_00717 | 3.5e-109 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
AHGDMNCB_00719 | 3.7e-11 | V | Type II restriction enzyme, methylase subunits | |||
AHGDMNCB_00720 | 1.3e-133 | hxlA | 6.2.1.3 | H | Aldolase/RraA | |
AHGDMNCB_00721 | 2.1e-257 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHGDMNCB_00722 | 3.1e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
AHGDMNCB_00723 | 1.9e-261 | frdC | 1.3.5.4 | C | FAD binding domain | |
AHGDMNCB_00724 | 9e-267 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
AHGDMNCB_00725 | 8.9e-15 | metI | P | ABC transporter permease | ||
AHGDMNCB_00726 | 4.7e-114 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
AHGDMNCB_00727 | 9.7e-97 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
AHGDMNCB_00728 | 8.1e-201 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
AHGDMNCB_00729 | 2.8e-145 | S | Bacterial protein of unknown function (DUF871) | |||
AHGDMNCB_00730 | 6.6e-25 | S | Bacterial protein of unknown function (DUF871) | |||
AHGDMNCB_00732 | 5.6e-40 | ybhL | S | Belongs to the BI1 family | ||
AHGDMNCB_00733 | 1.4e-50 | S | Metal binding domain of Ada | |||
AHGDMNCB_00734 | 4.2e-130 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
AHGDMNCB_00735 | 4.5e-117 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
AHGDMNCB_00736 | 2.4e-16 | |||||
AHGDMNCB_00737 | 8.6e-240 | G | Bacterial extracellular solute-binding protein | |||
AHGDMNCB_00738 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
AHGDMNCB_00739 | 5.9e-238 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
AHGDMNCB_00740 | 1.8e-96 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
AHGDMNCB_00741 | 6.9e-137 | lysR5 | K | LysR substrate binding domain | ||
AHGDMNCB_00742 | 1.5e-236 | arcA | 3.5.3.6 | E | Arginine | |
AHGDMNCB_00743 | 1.6e-209 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
AHGDMNCB_00744 | 1.5e-187 | L | Transposase IS66 family | |||
AHGDMNCB_00745 | 2.7e-58 | XK27_01125 | L | PFAM IS66 Orf2 family protein | ||
AHGDMNCB_00747 | 3.4e-149 | yycI | S | YycH protein | ||
AHGDMNCB_00748 | 3.3e-258 | yycH | S | YycH protein | ||
AHGDMNCB_00749 | 2.2e-305 | vicK | 2.7.13.3 | T | Histidine kinase | |
AHGDMNCB_00750 | 4.8e-131 | K | response regulator | |||
AHGDMNCB_00752 | 4.9e-34 | |||||
AHGDMNCB_00754 | 1.4e-149 | arbV | 2.3.1.51 | I | Acyl-transferase | |
AHGDMNCB_00755 | 1.2e-157 | arbx | M | Glycosyl transferase family 8 | ||
AHGDMNCB_00756 | 4.5e-185 | arbY | M | Glycosyl transferase family 8 | ||
AHGDMNCB_00757 | 6e-182 | arbY | M | Glycosyl transferase family 8 | ||
AHGDMNCB_00758 | 4.6e-168 | arbZ | I | Phosphate acyltransferases | ||
AHGDMNCB_00759 | 1.4e-36 | S | Cytochrome B5 | |||
AHGDMNCB_00760 | 9.5e-82 | XK27_04435 | 3.5.4.5 | J | FR47-like protein | |
AHGDMNCB_00763 | 4.8e-188 | rarA | L | recombination factor protein RarA | ||
AHGDMNCB_00764 | 8.4e-39 | |||||
AHGDMNCB_00765 | 1.8e-78 | usp6 | T | universal stress protein | ||
AHGDMNCB_00766 | 1.2e-216 | rodA | D | Belongs to the SEDS family | ||
AHGDMNCB_00767 | 1.5e-33 | S | Protein of unknown function (DUF2969) | |||
AHGDMNCB_00768 | 1e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
AHGDMNCB_00769 | 7.2e-178 | mbl | D | Cell shape determining protein MreB Mrl | ||
AHGDMNCB_00770 | 6.9e-31 | ywzB | S | Protein of unknown function (DUF1146) | ||
AHGDMNCB_00771 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
AHGDMNCB_00772 | 1.2e-82 | 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 | |
AHGDMNCB_00773 | 0.0 | L | PLD-like domain | |||
AHGDMNCB_00774 | 3.1e-41 | S | SnoaL-like domain | |||
AHGDMNCB_00775 | 1.4e-29 | hipB | K | sequence-specific DNA binding | ||
AHGDMNCB_00777 | 8e-22 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
AHGDMNCB_00778 | 7.1e-74 | |||||
AHGDMNCB_00779 | 7.8e-283 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AHGDMNCB_00780 | 2.1e-280 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AHGDMNCB_00781 | 8e-95 | |||||
AHGDMNCB_00782 | 4.3e-118 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
AHGDMNCB_00783 | 9e-98 | |||||
AHGDMNCB_00784 | 2e-109 | K | LysR substrate binding domain | |||
AHGDMNCB_00785 | 1e-20 | |||||
AHGDMNCB_00786 | 1.3e-215 | S | Sterol carrier protein domain | |||
AHGDMNCB_00787 | 2e-97 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
AHGDMNCB_00788 | 1.7e-109 | argF | 2.1.3.3, 2.7.2.2 | E | Belongs to the carbamate kinase family | |
AHGDMNCB_00789 | 1.6e-168 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHGDMNCB_00790 | 4.6e-166 | degV | S | DegV family | ||
AHGDMNCB_00791 | 3.5e-166 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
AHGDMNCB_00792 | 7.4e-253 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
AHGDMNCB_00793 | 5.7e-69 | rplI | J | Binds to the 23S rRNA | ||
AHGDMNCB_00794 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
AHGDMNCB_00795 | 1.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
AHGDMNCB_00796 | 4.5e-78 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
AHGDMNCB_00797 | 9.4e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
AHGDMNCB_00798 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
AHGDMNCB_00799 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
AHGDMNCB_00800 | 6.2e-210 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
AHGDMNCB_00801 | 2.6e-35 | yaaA | S | S4 domain protein YaaA | ||
AHGDMNCB_00802 | 1.1e-185 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
AHGDMNCB_00803 | 5.5e-245 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
AHGDMNCB_00804 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
AHGDMNCB_00805 | 2.7e-61 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
AHGDMNCB_00806 | 8.4e-146 | 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 | ||
AHGDMNCB_00807 | 4.7e-252 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
AHGDMNCB_00808 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
AHGDMNCB_00809 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AHGDMNCB_00811 | 6.4e-76 | 2.7.13.3 | T | GHKL domain | ||
AHGDMNCB_00812 | 1.1e-70 | K | LytTr DNA-binding domain | |||
AHGDMNCB_00813 | 4.8e-63 | M | LysM domain | |||
AHGDMNCB_00814 | 1.3e-109 | |||||
AHGDMNCB_00815 | 8.1e-276 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
AHGDMNCB_00816 | 6.7e-287 | clcA | P | chloride | ||
AHGDMNCB_00817 | 3.1e-51 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
AHGDMNCB_00818 | 1.8e-180 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
AHGDMNCB_00819 | 5.1e-74 | C | Aldo keto reductase | |||
AHGDMNCB_00820 | 5.4e-63 | M | LysM domain protein | |||
AHGDMNCB_00821 | 8.3e-151 | |||||
AHGDMNCB_00822 | 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 | ||
AHGDMNCB_00823 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
AHGDMNCB_00824 | 6.7e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
AHGDMNCB_00825 | 2.6e-175 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
AHGDMNCB_00826 | 0.0 | comEC | S | Competence protein ComEC | ||
AHGDMNCB_00827 | 1.5e-81 | comEA | L | Competence protein ComEA | ||
AHGDMNCB_00828 | 2.5e-62 | ylbL | T | Belongs to the peptidase S16 family | ||
AHGDMNCB_00829 | 1.6e-211 | yttB | EGP | Major facilitator Superfamily | ||
AHGDMNCB_00830 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AHGDMNCB_00831 | 0.0 | kup | P | Transport of potassium into the cell | ||
AHGDMNCB_00832 | 3e-75 | |||||
AHGDMNCB_00833 | 5e-13 | L | nucleotidyltransferase activity | |||
AHGDMNCB_00834 | 3.1e-83 | xamIM | L | DNA restriction-modification system | ||
AHGDMNCB_00835 | 1.4e-74 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
AHGDMNCB_00836 | 2.6e-101 | S | Peptidase propeptide and YPEB domain | |||
AHGDMNCB_00837 | 2.3e-85 | S | Peptidase propeptide and YPEB domain | |||
AHGDMNCB_00838 | 5.3e-248 | T | GHKL domain | |||
AHGDMNCB_00839 | 1.3e-128 | T | Transcriptional regulatory protein, C terminal | |||
AHGDMNCB_00840 | 6.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
AHGDMNCB_00841 | 1.7e-277 | V | ABC transporter transmembrane region | |||
AHGDMNCB_00842 | 4.6e-129 | S | PAS domain | |||
AHGDMNCB_00843 | 1.4e-13 | |||||
AHGDMNCB_00844 | 9e-141 | pnuC | H | nicotinamide mononucleotide transporter | ||
AHGDMNCB_00845 | 1.4e-72 | S | Protein of unknown function (DUF3290) | |||
AHGDMNCB_00846 | 1.1e-115 | yviA | S | Protein of unknown function (DUF421) | ||
AHGDMNCB_00847 | 3.9e-159 | 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 | |||
AHGDMNCB_00848 | 3.2e-183 | dnaQ | 2.7.7.7 | L | EXOIII | |
AHGDMNCB_00849 | 1.9e-158 | endA | F | DNA RNA non-specific endonuclease | ||
AHGDMNCB_00850 | 2e-282 | pipD | E | Dipeptidase | ||
AHGDMNCB_00851 | 1.9e-203 | malK | P | ATPases associated with a variety of cellular activities | ||
AHGDMNCB_00852 | 7.3e-158 | gtsB | P | ABC-type sugar transport systems, permease components | ||
AHGDMNCB_00853 | 6.1e-146 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
AHGDMNCB_00854 | 2.7e-257 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
AHGDMNCB_00855 | 2.5e-239 | G | Bacterial extracellular solute-binding protein | |||
AHGDMNCB_00856 | 1.8e-154 | corA | P | CorA-like Mg2+ transporter protein | ||
AHGDMNCB_00857 | 8.8e-149 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
AHGDMNCB_00858 | 2.3e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
AHGDMNCB_00859 | 0.0 | ydgH | S | MMPL family | ||
AHGDMNCB_00860 | 4.2e-165 | |||||
AHGDMNCB_00861 | 6.6e-262 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHGDMNCB_00862 | 6.2e-93 | F | Nucleoside 2-deoxyribosyltransferase | |||
AHGDMNCB_00863 | 3.2e-158 | hipB | K | Helix-turn-helix | ||
AHGDMNCB_00864 | 6.5e-153 | I | alpha/beta hydrolase fold | |||
AHGDMNCB_00865 | 1.4e-110 | yjbF | S | SNARE associated Golgi protein | ||
AHGDMNCB_00866 | 7.5e-100 | J | Acetyltransferase (GNAT) domain | |||
AHGDMNCB_00867 | 1.9e-247 | 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) | |
AHGDMNCB_00868 | 8.3e-18 | UW | LPXTG-motif cell wall anchor domain protein | |||
AHGDMNCB_00869 | 3.3e-45 | UW | LPXTG-motif cell wall anchor domain protein | |||
AHGDMNCB_00870 | 0.0 | UW | LPXTG-motif cell wall anchor domain protein | |||
AHGDMNCB_00871 | 1.6e-151 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
AHGDMNCB_00872 | 2e-80 | yagE | E | amino acid | ||
AHGDMNCB_00873 | 4.4e-117 | yagE | E | Amino acid permease | ||
AHGDMNCB_00874 | 1.9e-86 | 3.4.21.96 | S | SLAP domain | ||
AHGDMNCB_00875 | 4.6e-160 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AHGDMNCB_00876 | 1.1e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
AHGDMNCB_00877 | 1.2e-107 | hlyIII | S | protein, hemolysin III | ||
AHGDMNCB_00878 | 9.8e-144 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
AHGDMNCB_00879 | 7.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
AHGDMNCB_00880 | 1.9e-113 | yjcE | P | Sodium proton antiporter | ||
AHGDMNCB_00881 | 1.8e-53 | yjcE | P | Sodium proton antiporter | ||
AHGDMNCB_00882 | 2.5e-155 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
AHGDMNCB_00883 | 4.5e-65 | S | Protein of unknown function (DUF3100) | |||
AHGDMNCB_00884 | 5.7e-83 | S | An automated process has identified a potential problem with this gene model | |||
AHGDMNCB_00885 | 1.1e-49 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
AHGDMNCB_00886 | 1.6e-111 | S | SLAP domain | |||
AHGDMNCB_00887 | 1.9e-88 | |||||
AHGDMNCB_00888 | 3e-09 | isdH | M | Iron Transport-associated domain | ||
AHGDMNCB_00889 | 5.7e-124 | M | Iron Transport-associated domain | |||
AHGDMNCB_00890 | 4.3e-158 | isdE | P | Periplasmic binding protein | ||
AHGDMNCB_00891 | 1.1e-148 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AHGDMNCB_00892 | 2.3e-139 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
AHGDMNCB_00893 | 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 | ||
AHGDMNCB_00894 | 1.2e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
AHGDMNCB_00895 | 1.3e-38 | S | RelB antitoxin | |||
AHGDMNCB_00896 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
AHGDMNCB_00897 | 0.0 | S | membrane | |||
AHGDMNCB_00898 | 2.7e-124 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
AHGDMNCB_00899 | 1.4e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
AHGDMNCB_00900 | 2.4e-242 | S | response to antibiotic | |||
AHGDMNCB_00901 | 9.3e-124 | |||||
AHGDMNCB_00902 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
AHGDMNCB_00903 | 8.7e-66 | 2.7.1.191 | G | PTS system fructose IIA component | ||
AHGDMNCB_00904 | 4.3e-43 | |||||
AHGDMNCB_00905 | 7.7e-09 | |||||
AHGDMNCB_00906 | 4.2e-186 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
AHGDMNCB_00907 | 1.8e-136 | glvR | K | Helix-turn-helix domain, rpiR family | ||
AHGDMNCB_00908 | 2.7e-268 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
AHGDMNCB_00909 | 1.8e-153 | |||||
AHGDMNCB_00910 | 1.4e-23 | |||||
AHGDMNCB_00911 | 1.5e-92 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AHGDMNCB_00912 | 5.3e-158 | S | Archaea bacterial proteins of unknown function | |||
AHGDMNCB_00913 | 2.5e-106 | 3.2.2.20 | K | acetyltransferase | ||
AHGDMNCB_00915 | 9.5e-81 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
AHGDMNCB_00916 | 7.6e-39 | KQ | helix_turn_helix, mercury resistance | |||
AHGDMNCB_00918 | 1.2e-142 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
AHGDMNCB_00919 | 0.0 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
AHGDMNCB_00920 | 1.8e-07 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
AHGDMNCB_00921 | 1.6e-20 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AHGDMNCB_00922 | 1.2e-10 | 6.3.4.4 | S | Zeta toxin | ||
AHGDMNCB_00923 | 2e-17 | 6.3.4.4 | S | Zeta toxin | ||
AHGDMNCB_00924 | 6.2e-42 | |||||
AHGDMNCB_00925 | 2.9e-31 | |||||
AHGDMNCB_00926 | 5.6e-09 | M | Host cell surface-exposed lipoprotein | |||
AHGDMNCB_00927 | 1.1e-52 | |||||
AHGDMNCB_00928 | 2e-42 | S | RelB antitoxin | |||
AHGDMNCB_00929 | 8.4e-69 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
AHGDMNCB_00931 | 0.0 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
AHGDMNCB_00932 | 4.2e-61 | V | Abi-like protein | |||
AHGDMNCB_00933 | 3.2e-84 | L | the current gene model (or a revised gene model) may contain a | |||
AHGDMNCB_00934 | 1.9e-32 | S | phage tail | |||
AHGDMNCB_00935 | 7e-192 | xkdO | D | NLP P60 protein | ||
AHGDMNCB_00938 | 7.8e-28 | S | Phage tail tube protein | |||
AHGDMNCB_00939 | 2.3e-13 | S | Protein of unknown function (DUF806) | |||
AHGDMNCB_00940 | 1.3e-29 | S | Bacteriophage HK97-gp10, putative tail-component | |||
AHGDMNCB_00941 | 3.9e-10 | S | Phage head-tail joining protein | |||
AHGDMNCB_00942 | 1.4e-13 | S | Phage gp6-like head-tail connector protein | |||
AHGDMNCB_00943 | 2.1e-89 | S | Phage capsid family | |||
AHGDMNCB_00944 | 4e-53 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
AHGDMNCB_00945 | 1.6e-99 | S | Phage portal protein | |||
AHGDMNCB_00947 | 7.8e-181 | S | overlaps another CDS with the same product name | |||
AHGDMNCB_00948 | 1.3e-27 | L | Phage terminase, small subunit | |||
AHGDMNCB_00950 | 2.3e-36 | V | HNH nucleases | |||
AHGDMNCB_00954 | 2.3e-16 | |||||
AHGDMNCB_00959 | 1.3e-18 | S | HNH endonuclease | |||
AHGDMNCB_00960 | 2.2e-09 | |||||
AHGDMNCB_00962 | 7.4e-78 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
AHGDMNCB_00963 | 2.3e-67 | L | Phage integrase, N-terminal SAM-like domain | |||
AHGDMNCB_00964 | 1.9e-93 | L | Belongs to the 'phage' integrase family | |||
AHGDMNCB_00966 | 2e-280 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
AHGDMNCB_00967 | 5.4e-256 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
AHGDMNCB_00968 | 8.3e-270 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
AHGDMNCB_00969 | 1.3e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
AHGDMNCB_00970 | 5.5e-178 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHGDMNCB_00971 | 3.3e-161 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
AHGDMNCB_00972 | 2e-230 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AHGDMNCB_00973 | 5.9e-94 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
AHGDMNCB_00974 | 9.8e-169 | K | LysR substrate binding domain | |||
AHGDMNCB_00975 | 1.2e-70 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
AHGDMNCB_00976 | 7.9e-227 | N | Uncharacterized conserved protein (DUF2075) | |||
AHGDMNCB_00977 | 6.2e-205 | pbpX1 | V | Beta-lactamase | ||
AHGDMNCB_00978 | 0.0 | L | Helicase C-terminal domain protein | |||
AHGDMNCB_00979 | 1.1e-272 | E | amino acid | |||
AHGDMNCB_00980 | 2.2e-159 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
AHGDMNCB_00983 | 1.4e-192 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHGDMNCB_00984 | 8.4e-133 | EGP | Major facilitator Superfamily | |||
AHGDMNCB_00986 | 2.1e-46 | |||||
AHGDMNCB_00987 | 2.1e-146 | 3.1.3.102, 3.1.3.104 | S | haloacid dehalogenase-like hydrolase | ||
AHGDMNCB_00988 | 0.0 | tetP | J | elongation factor G | ||
AHGDMNCB_00989 | 8.1e-119 | K | Helix-turn-helix domain | |||
AHGDMNCB_00990 | 4.6e-83 | |||||
AHGDMNCB_00992 | 2.7e-74 | M | LysM domain | |||
AHGDMNCB_00993 | 5.5e-87 | |||||
AHGDMNCB_00994 | 8.3e-136 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
AHGDMNCB_00995 | 2.1e-177 | ABC-SBP | S | ABC transporter | ||
AHGDMNCB_00996 | 2.8e-92 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
AHGDMNCB_00997 | 2.3e-22 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
AHGDMNCB_00998 | 3.1e-136 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
AHGDMNCB_00999 | 4.4e-45 | |||||
AHGDMNCB_01000 | 1.3e-37 | |||||
AHGDMNCB_01001 | 1.5e-52 | S | Bacteriocin helveticin-J | |||
AHGDMNCB_01002 | 2.1e-30 | |||||
AHGDMNCB_01003 | 1.2e-247 | G | Major Facilitator | |||
AHGDMNCB_01004 | 4.1e-18 | |||||
AHGDMNCB_01005 | 5.8e-103 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
AHGDMNCB_01006 | 2.4e-176 | K | AI-2E family transporter | |||
AHGDMNCB_01007 | 3.9e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
AHGDMNCB_01008 | 2e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
AHGDMNCB_01009 | 1.1e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
AHGDMNCB_01010 | 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 | ||
AHGDMNCB_01011 | 5.1e-17 | |||||
AHGDMNCB_01012 | 4.6e-188 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
AHGDMNCB_01013 | 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 | ||
AHGDMNCB_01014 | 7.9e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
AHGDMNCB_01015 | 1.9e-132 | comFC | S | Competence protein | ||
AHGDMNCB_01016 | 1.4e-33 | comFA | L | Helicase C-terminal domain protein | ||
AHGDMNCB_01017 | 3.1e-12 | |||||
AHGDMNCB_01018 | 2.4e-50 | L | An automated process has identified a potential problem with this gene model | |||
AHGDMNCB_01019 | 1.5e-31 | L | Belongs to the 'phage' integrase family | |||
AHGDMNCB_01020 | 1.7e-42 | |||||
AHGDMNCB_01022 | 2.6e-146 | S | Putative ABC-transporter type IV | |||
AHGDMNCB_01023 | 1.4e-06 | S | LPXTG cell wall anchor motif | |||
AHGDMNCB_01024 | 4.7e-76 | ybaT | E | Amino acid permease | ||
AHGDMNCB_01025 | 8.7e-08 | ybaT | E | Amino acid permease | ||
AHGDMNCB_01027 | 4.1e-25 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
AHGDMNCB_01030 | 7.4e-95 | S | UPF0397 protein | |||
AHGDMNCB_01031 | 2.9e-66 | S | Domain of unknown function DUF1828 | |||
AHGDMNCB_01032 | 5.5e-09 | |||||
AHGDMNCB_01033 | 3.8e-51 | |||||
AHGDMNCB_01034 | 5.8e-177 | citR | K | Putative sugar-binding domain | ||
AHGDMNCB_01035 | 2e-250 | yjjP | S | Putative threonine/serine exporter | ||
AHGDMNCB_01036 | 3.4e-46 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
AHGDMNCB_01037 | 6.5e-151 | ftsZ | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | ||
AHGDMNCB_01038 | 5.8e-112 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
AHGDMNCB_01039 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
AHGDMNCB_01040 | 1.8e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
AHGDMNCB_01041 | 3e-156 | holB | 2.7.7.7 | L | DNA polymerase III | |
AHGDMNCB_01042 | 8.9e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
AHGDMNCB_01043 | 1.6e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AHGDMNCB_01044 | 1.1e-34 | S | Protein of unknown function (DUF2508) | |||
AHGDMNCB_01045 | 1.6e-108 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
AHGDMNCB_01046 | 2.8e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
AHGDMNCB_01047 | 1.2e-35 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
AHGDMNCB_01048 | 9.4e-43 | 2.4.1.58 | GT8 | M | family 8 | |
AHGDMNCB_01049 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHGDMNCB_01050 | 2.2e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
AHGDMNCB_01051 | 9e-26 | |||||
AHGDMNCB_01052 | 1.3e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
AHGDMNCB_01053 | 6e-141 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
AHGDMNCB_01054 | 1.8e-54 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
AHGDMNCB_01055 | 7e-84 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
AHGDMNCB_01056 | 4.5e-56 | |||||
AHGDMNCB_01057 | 2.3e-109 | M | family 8 | |||
AHGDMNCB_01058 | 6.4e-121 | nss | M | transferase activity, transferring glycosyl groups | ||
AHGDMNCB_01060 | 1.8e-110 | 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 | |
AHGDMNCB_01061 | 1.7e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHGDMNCB_01062 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
AHGDMNCB_01063 | 2.8e-58 | 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 | ||
AHGDMNCB_01064 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
AHGDMNCB_01065 | 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 | ||
AHGDMNCB_01066 | 1.4e-50 | yrzB | S | Belongs to the UPF0473 family | ||
AHGDMNCB_01067 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
AHGDMNCB_01068 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
AHGDMNCB_01069 | 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 | |
AHGDMNCB_01070 | 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 | |
AHGDMNCB_01071 | 4.7e-182 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
AHGDMNCB_01072 | 5.9e-216 | 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 | |
AHGDMNCB_01073 | 5.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
AHGDMNCB_01074 | 9.6e-41 | yajC | U | Preprotein translocase | ||
AHGDMNCB_01075 | 6.7e-187 | 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 | |
AHGDMNCB_01076 | 5.9e-103 | 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 | |
AHGDMNCB_01077 | 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 | ||
AHGDMNCB_01078 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
AHGDMNCB_01079 | 2.6e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
AHGDMNCB_01080 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
AHGDMNCB_01081 | 3.5e-75 | |||||
AHGDMNCB_01082 | 1.2e-180 | M | CHAP domain | |||
AHGDMNCB_01083 | 0.0 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
AHGDMNCB_01084 | 3.1e-294 | scrB | 3.2.1.26 | GH32 | G | invertase |
AHGDMNCB_01085 | 1e-184 | scrR | K | helix_turn _helix lactose operon repressor | ||
AHGDMNCB_01086 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
AHGDMNCB_01087 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
AHGDMNCB_01088 | 7.4e-32 | L | COG2963 Transposase and inactivated derivatives | |||
AHGDMNCB_01089 | 3e-105 | L | COG2963 Transposase and inactivated derivatives | |||
AHGDMNCB_01090 | 2.7e-151 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
AHGDMNCB_01091 | 1.5e-91 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
AHGDMNCB_01092 | 0.0 | aha1 | P | E1-E2 ATPase | ||
AHGDMNCB_01093 | 5.8e-177 | F | DNA/RNA non-specific endonuclease | |||
AHGDMNCB_01094 | 1.1e-264 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
AHGDMNCB_01095 | 2.2e-168 | |||||
AHGDMNCB_01096 | 1.8e-144 | |||||
AHGDMNCB_01097 | 3.9e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHGDMNCB_01098 | 3.8e-27 | |||||
AHGDMNCB_01099 | 6.7e-145 | |||||
AHGDMNCB_01100 | 1.7e-137 | |||||
AHGDMNCB_01101 | 7e-142 | |||||
AHGDMNCB_01102 | 1.2e-123 | skfE | V | ATPases associated with a variety of cellular activities | ||
AHGDMNCB_01103 | 1.6e-61 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
AHGDMNCB_01104 | 7.5e-241 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AHGDMNCB_01105 | 2.9e-153 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
AHGDMNCB_01106 | 1.2e-123 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
AHGDMNCB_01107 | 4.8e-81 | mutT | 3.6.1.55 | F | NUDIX domain | |
AHGDMNCB_01108 | 1.8e-127 | S | Peptidase family M23 | |||
AHGDMNCB_01109 | 9.9e-200 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
AHGDMNCB_01110 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
AHGDMNCB_01111 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
AHGDMNCB_01112 | 4.6e-179 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
AHGDMNCB_01113 | 2.2e-134 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
AHGDMNCB_01114 | 7.7e-55 | whiA | K | May be required for sporulation | ||
AHGDMNCB_01115 | 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 | |
AHGDMNCB_01116 | 0.0 | S | SH3-like domain | |||
AHGDMNCB_01117 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
AHGDMNCB_01118 | 2.5e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
AHGDMNCB_01120 | 2.4e-16 | |||||
AHGDMNCB_01121 | 1.7e-232 | I | Protein of unknown function (DUF2974) | |||
AHGDMNCB_01122 | 5.8e-121 | yhiD | S | MgtC family | ||
AHGDMNCB_01128 | 8.5e-40 | |||||
AHGDMNCB_01129 | 1.1e-155 | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | |||
AHGDMNCB_01131 | 4.2e-22 | |||||
AHGDMNCB_01133 | 4.6e-39 | clcA | P | chloride | ||
AHGDMNCB_01134 | 6.9e-20 | clcA | P | chloride | ||
AHGDMNCB_01135 | 2.4e-118 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
AHGDMNCB_01136 | 1.6e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
AHGDMNCB_01137 | 5.4e-167 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
AHGDMNCB_01138 | 2.7e-94 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
AHGDMNCB_01139 | 1.6e-182 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHGDMNCB_01140 | 4e-245 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
AHGDMNCB_01141 | 6.4e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHGDMNCB_01142 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHGDMNCB_01143 | 1.5e-251 | lctP | C | L-lactate permease | ||
AHGDMNCB_01144 | 1e-148 | glcU | U | sugar transport | ||
AHGDMNCB_01145 | 2.4e-46 | |||||
AHGDMNCB_01146 | 2.8e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
AHGDMNCB_01147 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
AHGDMNCB_01148 | 1.2e-42 | S | Alpha beta hydrolase | |||
AHGDMNCB_01149 | 1.9e-37 | |||||
AHGDMNCB_01150 | 2.6e-52 | |||||
AHGDMNCB_01151 | 3.1e-150 | S | haloacid dehalogenase-like hydrolase | |||
AHGDMNCB_01152 | 5.4e-292 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AHGDMNCB_01153 | 1.5e-278 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AHGDMNCB_01154 | 1.5e-64 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
AHGDMNCB_01155 | 2.9e-178 | I | Carboxylesterase family | |||
AHGDMNCB_01157 | 1.5e-89 | L | Belongs to the 'phage' integrase family | |||
AHGDMNCB_01158 | 2.8e-32 | |||||
AHGDMNCB_01160 | 3.9e-47 | 3.4.21.88 | K | Peptidase S24-like | ||
AHGDMNCB_01163 | 1.4e-20 | |||||
AHGDMNCB_01165 | 3e-28 | L | Psort location Cytoplasmic, score | |||
AHGDMNCB_01169 | 7.9e-84 | L | Belongs to the 'phage' integrase family | |||
AHGDMNCB_01170 | 5.5e-81 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
AHGDMNCB_01173 | 4.7e-36 | rbtT | P | Major Facilitator Superfamily | ||
AHGDMNCB_01174 | 5.4e-203 | XK27_00915 | C | Luciferase-like monooxygenase | ||
AHGDMNCB_01175 | 2.5e-86 | K | GNAT family | |||
AHGDMNCB_01176 | 9.8e-123 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
AHGDMNCB_01178 | 5.1e-37 | |||||
AHGDMNCB_01179 | 3.9e-19 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
AHGDMNCB_01180 | 3.7e-295 | I | Acyltransferase | |||
AHGDMNCB_01181 | 3.8e-176 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
AHGDMNCB_01182 | 6.1e-143 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AHGDMNCB_01183 | 1.5e-34 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
AHGDMNCB_01184 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
AHGDMNCB_01185 | 7.3e-310 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
AHGDMNCB_01186 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
AHGDMNCB_01187 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AHGDMNCB_01188 | 3.3e-183 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
AHGDMNCB_01189 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
AHGDMNCB_01190 | 1.9e-169 | cvfB | S | S1 domain | ||
AHGDMNCB_01191 | 3.1e-167 | xerD | D | recombinase XerD | ||
AHGDMNCB_01192 | 3.8e-60 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
AHGDMNCB_01193 | 7.6e-132 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
AHGDMNCB_01194 | 4.1e-104 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
AHGDMNCB_01195 | 3.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AHGDMNCB_01196 | 7.9e-115 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
AHGDMNCB_01197 | 2.7e-18 | M | Lysin motif | |||
AHGDMNCB_01198 | 2.2e-114 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
AHGDMNCB_01199 | 5.5e-212 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
AHGDMNCB_01200 | 1.9e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
AHGDMNCB_01201 | 2.3e-41 | 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 | ||
AHGDMNCB_01202 | 1.9e-228 | S | Tetratricopeptide repeat protein | |||
AHGDMNCB_01203 | 5.8e-288 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AHGDMNCB_01205 | 1.5e-74 | K | Copper transport repressor CopY TcrY | |||
AHGDMNCB_01206 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
AHGDMNCB_01208 | 5.9e-214 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
AHGDMNCB_01209 | 3.4e-197 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
AHGDMNCB_01210 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
AHGDMNCB_01211 | 3.6e-117 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
AHGDMNCB_01212 | 6.4e-179 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
AHGDMNCB_01213 | 9.5e-144 | |||||
AHGDMNCB_01214 | 5.8e-135 | |||||
AHGDMNCB_01215 | 5e-133 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AHGDMNCB_01216 | 4.9e-99 | G | Aldose 1-epimerase | |||
AHGDMNCB_01217 | 2.1e-202 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHGDMNCB_01218 | 1.6e-111 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
AHGDMNCB_01219 | 0.0 | XK27_08315 | M | Sulfatase | ||
AHGDMNCB_01220 | 1.6e-243 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
AHGDMNCB_01221 | 1.2e-53 | |||||
AHGDMNCB_01223 | 3.6e-257 | pepC | 3.4.22.40 | E | aminopeptidase | |
AHGDMNCB_01224 | 2.6e-123 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHGDMNCB_01225 | 5e-301 | oppA | E | ABC transporter, substratebinding protein | ||
AHGDMNCB_01226 | 9.9e-310 | oppA | E | ABC transporter, substratebinding protein | ||
AHGDMNCB_01227 | 4.8e-210 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
AHGDMNCB_01228 | 1.1e-146 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHGDMNCB_01229 | 8e-188 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AHGDMNCB_01230 | 1.2e-199 | oppD | P | Belongs to the ABC transporter superfamily | ||
AHGDMNCB_01231 | 1.9e-175 | oppF | P | Belongs to the ABC transporter superfamily | ||
AHGDMNCB_01232 | 1.4e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
AHGDMNCB_01233 | 2.6e-68 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
AHGDMNCB_01234 | 2.6e-77 | 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 | ||
AHGDMNCB_01235 | 6.7e-111 | |||||
AHGDMNCB_01237 | 1.2e-111 | E | Belongs to the SOS response-associated peptidase family | |||
AHGDMNCB_01238 | 3.7e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHGDMNCB_01239 | 5.7e-88 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
AHGDMNCB_01240 | 1e-102 | S | TPM domain | |||
AHGDMNCB_01241 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
AHGDMNCB_01242 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
AHGDMNCB_01243 | 1.8e-147 | tatD | L | hydrolase, TatD family | ||
AHGDMNCB_01244 | 1e-99 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
AHGDMNCB_01245 | 4.6e-160 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
AHGDMNCB_01246 | 1.2e-39 | veg | S | Biofilm formation stimulator VEG | ||
AHGDMNCB_01247 | 7.7e-149 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
AHGDMNCB_01248 | 8.9e-174 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
AHGDMNCB_01249 | 9e-80 | |||||
AHGDMNCB_01250 | 0.0 | S | SLAP domain | |||
AHGDMNCB_01251 | 6e-177 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
AHGDMNCB_01252 | 4e-162 | 2.7.1.2 | GK | ROK family | ||
AHGDMNCB_01253 | 7e-38 | |||||
AHGDMNCB_01254 | 3.2e-269 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHGDMNCB_01255 | 7.3e-68 | S | Domain of unknown function (DUF1934) | |||
AHGDMNCB_01256 | 1.7e-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 | ||
AHGDMNCB_01257 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
AHGDMNCB_01258 | 9.6e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHGDMNCB_01259 | 8.5e-77 | K | acetyltransferase | |||
AHGDMNCB_01260 | 9.7e-285 | pipD | E | Dipeptidase | ||
AHGDMNCB_01261 | 1.1e-152 | msmR | K | AraC-like ligand binding domain | ||
AHGDMNCB_01262 | 9.6e-223 | pbuX | F | xanthine permease | ||
AHGDMNCB_01263 | 1e-102 | 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 | |
AHGDMNCB_01265 | 3.5e-304 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
AHGDMNCB_01267 | 4.7e-91 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
AHGDMNCB_01268 | 9.2e-262 | emrY | EGP | Major facilitator Superfamily | ||
AHGDMNCB_01269 | 1.1e-217 | mdtG | EGP | Major facilitator Superfamily | ||
AHGDMNCB_01270 | 2.4e-136 | |||||
AHGDMNCB_01271 | 2.6e-103 | |||||
AHGDMNCB_01272 | 6e-210 | pepA | E | M42 glutamyl aminopeptidase | ||
AHGDMNCB_01273 | 4.5e-310 | ybiT | S | ABC transporter, ATP-binding protein | ||
AHGDMNCB_01274 | 5.9e-174 | S | Aldo keto reductase | |||
AHGDMNCB_01275 | 3.5e-137 | |||||
AHGDMNCB_01276 | 2e-239 | steT | E | amino acid | ||
AHGDMNCB_01277 | 1e-243 | steT | E | amino acid | ||
AHGDMNCB_01278 | 1.4e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
AHGDMNCB_01279 | 1.9e-147 | glnH | ET | ABC transporter | ||
AHGDMNCB_01280 | 9.3e-80 | K | Transcriptional regulator, MarR family | |||
AHGDMNCB_01281 | 6.2e-310 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
AHGDMNCB_01282 | 1.6e-219 | 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 | |
AHGDMNCB_01285 | 9.1e-139 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
AHGDMNCB_01286 | 6.6e-165 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
AHGDMNCB_01289 | 6.2e-124 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
AHGDMNCB_01290 | 6.7e-151 | epsB | M | biosynthesis protein | ||
AHGDMNCB_01291 | 2.5e-176 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHGDMNCB_01292 | 1.3e-41 | relB | L | RelB antitoxin | ||
AHGDMNCB_01293 | 1.7e-117 | L | transposase, IS605 OrfB family | |||
AHGDMNCB_01294 | 1.1e-33 | |||||
AHGDMNCB_01295 | 2.8e-52 | |||||
AHGDMNCB_01296 | 8.1e-185 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
AHGDMNCB_01297 | 8.6e-82 | yfeO | P | Voltage gated chloride channel | ||
AHGDMNCB_01298 | 1.3e-176 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
AHGDMNCB_01299 | 2.3e-82 | |||||
AHGDMNCB_01300 | 3.6e-39 | C | FMN_bind | |||
AHGDMNCB_01301 | 5.4e-300 | I | Protein of unknown function (DUF2974) | |||
AHGDMNCB_01302 | 7.3e-195 | pbpX1 | V | Beta-lactamase | ||
AHGDMNCB_01303 | 1.6e-199 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
AHGDMNCB_01304 | 3.8e-218 | aspC | 2.6.1.1 | E | Aminotransferase | |
AHGDMNCB_01305 | 7e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
AHGDMNCB_01306 | 2.8e-176 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AHGDMNCB_01307 | 1.1e-220 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
AHGDMNCB_01308 | 2.8e-75 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
AHGDMNCB_01309 | 5.1e-248 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
AHGDMNCB_01310 | 1.3e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
AHGDMNCB_01311 | 1.5e-191 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
AHGDMNCB_01312 | 1.8e-96 | yjeM | E | Amino acid permease | ||
AHGDMNCB_01313 | 1.3e-22 | yjeM | E | Amino Acid | ||
AHGDMNCB_01314 | 8.3e-105 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
AHGDMNCB_01315 | 7.7e-233 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
AHGDMNCB_01316 | 4e-216 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
AHGDMNCB_01317 | 2.8e-72 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
AHGDMNCB_01318 | 4.2e-110 | ftsW | D | Belongs to the SEDS family | ||
AHGDMNCB_01319 | 5.1e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AHGDMNCB_01320 | 1.7e-96 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
AHGDMNCB_01321 | 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 | |
AHGDMNCB_01322 | 4.7e-112 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
AHGDMNCB_01323 | 7.5e-135 | 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 | |
AHGDMNCB_01324 | 2.5e-144 | 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 | |
AHGDMNCB_01325 | 2.6e-155 | pstA | P | Phosphate transport system permease protein PstA | ||
AHGDMNCB_01326 | 1.7e-174 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
AHGDMNCB_01327 | 6.6e-151 | pstS | P | Phosphate | ||
AHGDMNCB_01328 | 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 | ||
AHGDMNCB_01329 | 1.2e-68 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
AHGDMNCB_01330 | 4e-101 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
AHGDMNCB_01331 | 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 | ||
AHGDMNCB_01332 | 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) | |
AHGDMNCB_01333 | 3.4e-288 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
AHGDMNCB_01334 | 1.7e-34 | |||||
AHGDMNCB_01335 | 5.5e-95 | sigH | K | Belongs to the sigma-70 factor family | ||
AHGDMNCB_01336 | 6.6e-139 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHGDMNCB_01337 | 2.3e-75 | 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) | ||
AHGDMNCB_01338 | 1.2e-277 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHGDMNCB_01339 | 7.8e-97 | 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) | |
AHGDMNCB_01340 | 0.0 | typA | T | GTP-binding protein TypA | ||
AHGDMNCB_01341 | 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 | |
AHGDMNCB_01342 | 3.2e-33 | ykzG | S | Belongs to the UPF0356 family | ||
AHGDMNCB_01343 | 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 | ||
AHGDMNCB_01344 | 1.2e-182 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
AHGDMNCB_01345 | 4.1e-295 | L | Nuclease-related domain | |||
AHGDMNCB_01346 | 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 | |
AHGDMNCB_01347 | 5.4e-105 | S | Repeat protein | |||
AHGDMNCB_01348 | 4.6e-108 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AHGDMNCB_01349 | 1.5e-178 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
AHGDMNCB_01351 | 5.1e-192 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AHGDMNCB_01352 | 2.2e-102 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AHGDMNCB_01353 | 2.3e-148 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
AHGDMNCB_01354 | 6.8e-131 | L | Recombinase | |||
AHGDMNCB_01355 | 1e-173 | S | Domain of unknown function (DUF389) | |||
AHGDMNCB_01356 | 1.5e-31 | |||||
AHGDMNCB_01357 | 5.8e-50 | |||||
AHGDMNCB_01358 | 7.3e-35 | |||||
AHGDMNCB_01360 | 1.5e-27 | |||||
AHGDMNCB_01361 | 1.1e-47 | |||||
AHGDMNCB_01362 | 1.9e-214 | L | Belongs to the 'phage' integrase family | |||
AHGDMNCB_01363 | 1.6e-137 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
AHGDMNCB_01364 | 9.6e-136 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
AHGDMNCB_01365 | 1.3e-195 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
AHGDMNCB_01366 | 6e-133 | S | SLAP domain | |||
AHGDMNCB_01367 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
AHGDMNCB_01368 | 1.1e-215 | naiP | EGP | Major facilitator Superfamily | ||
AHGDMNCB_01369 | 4.9e-230 | S | C4-dicarboxylate anaerobic carrier | |||
AHGDMNCB_01370 | 5.4e-112 | |||||
AHGDMNCB_01371 | 1.4e-56 | 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | ||
AHGDMNCB_01372 | 5.2e-47 | yjaB_1 | K | Acetyltransferase (GNAT) domain | ||
AHGDMNCB_01373 | 1.3e-226 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AHGDMNCB_01374 | 1.6e-182 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
AHGDMNCB_01375 | 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 | |
AHGDMNCB_01376 | 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 | ||
AHGDMNCB_01377 | 1.6e-33 | yabO | J | S4 domain protein | ||
AHGDMNCB_01378 | 6.8e-60 | divIC | D | Septum formation initiator | ||
AHGDMNCB_01379 | 4.3e-24 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHGDMNCB_01380 | 1.4e-127 | K | UTRA domain | |||
AHGDMNCB_01381 | 1.6e-55 | celA1 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AHGDMNCB_01382 | 8.7e-60 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
AHGDMNCB_01383 | 4.4e-86 | |||||
AHGDMNCB_01384 | 2.5e-250 | celD | 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 | ||
AHGDMNCB_01385 | 9.3e-71 | S | Domain of unknown function (DUF3284) | |||
AHGDMNCB_01386 | 7e-302 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
AHGDMNCB_01387 | 4e-133 | gmuR | K | UTRA | ||
AHGDMNCB_01388 | 1e-40 | |||||
AHGDMNCB_01389 | 4.5e-266 | lacE | 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 | ||
AHGDMNCB_01390 | 1.9e-277 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AHGDMNCB_01391 | 3.8e-159 | ypbG | 2.7.1.2 | GK | ROK family | |
AHGDMNCB_01392 | 1.3e-63 | C | nitroreductase | |||
AHGDMNCB_01393 | 3.1e-89 | S | Domain of unknown function (DUF4767) | |||
AHGDMNCB_01394 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
AHGDMNCB_01395 | 1.7e-143 | licT | K | CAT RNA binding domain | ||
AHGDMNCB_01396 | 2.5e-206 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
AHGDMNCB_01397 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
AHGDMNCB_01398 | 2.5e-119 | |||||
AHGDMNCB_01399 | 6.7e-75 | K | Penicillinase repressor | |||
AHGDMNCB_01400 | 3.8e-148 | S | hydrolase | |||
AHGDMNCB_01401 | 3.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
AHGDMNCB_01402 | 1.1e-127 | ybbR | S | YbbR-like protein | ||
AHGDMNCB_01403 | 8.9e-87 | psd | 4.1.1.65 | I | Belongs to the phosphatidylserine decarboxylase family | |
AHGDMNCB_01404 | 5.5e-53 | |||||
AHGDMNCB_01405 | 4.1e-282 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
AHGDMNCB_01406 | 8e-79 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
AHGDMNCB_01407 | 4.3e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AHGDMNCB_01408 | 4.6e-199 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHGDMNCB_01409 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHGDMNCB_01410 | 1.2e-57 | FbpA | K | Fibronectin-binding protein | ||
AHGDMNCB_01411 | 3.5e-174 | prmA | J | Ribosomal protein L11 methyltransferase | ||
AHGDMNCB_01412 | 2.9e-60 | |||||
AHGDMNCB_01413 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
AHGDMNCB_01414 | 6e-76 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
AHGDMNCB_01415 | 6.8e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
AHGDMNCB_01416 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
AHGDMNCB_01417 | 1.7e-221 | patA | 2.6.1.1 | E | Aminotransferase | |
AHGDMNCB_01418 | 2e-214 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
AHGDMNCB_01419 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
AHGDMNCB_01420 | 1.3e-136 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
AHGDMNCB_01421 | 2e-62 | |||||
AHGDMNCB_01422 | 2.5e-33 | gepA | S | Protein of unknown function (DUF4065) | ||
AHGDMNCB_01423 | 3e-35 | |||||
AHGDMNCB_01427 | 9.5e-112 | |||||
AHGDMNCB_01428 | 1.1e-134 | K | Helix-turn-helix XRE-family like proteins | |||
AHGDMNCB_01429 | 3.5e-55 | |||||
AHGDMNCB_01430 | 4.2e-56 | |||||
AHGDMNCB_01431 | 5e-184 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
AHGDMNCB_01432 | 4.4e-121 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AHGDMNCB_01433 | 1e-42 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
AHGDMNCB_01434 | 1.2e-44 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
AHGDMNCB_01435 | 6.8e-95 | S | Phage portal protein | |||
AHGDMNCB_01437 | 0.0 | oppA3 | E | ABC transporter, substratebinding protein | ||
AHGDMNCB_01438 | 9.9e-62 | ypaA | S | Protein of unknown function (DUF1304) | ||
AHGDMNCB_01439 | 1.5e-101 | S | Peptidase propeptide and YPEB domain | |||
AHGDMNCB_01440 | 4.4e-103 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
AHGDMNCB_01441 | 2.1e-171 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
AHGDMNCB_01442 | 4.9e-99 | E | GDSL-like Lipase/Acylhydrolase | |||
AHGDMNCB_01443 | 7.5e-74 | yjcF | S | Acetyltransferase (GNAT) domain | ||
AHGDMNCB_01444 | 1.7e-145 | aatB | ET | ABC transporter substrate-binding protein | ||
AHGDMNCB_01445 | 1.7e-27 | glnQ | 3.6.3.21 | E | ABC transporter | |
AHGDMNCB_01446 | 5.8e-255 | ykoD | P | ABC transporter, ATP-binding protein | ||
AHGDMNCB_01447 | 3.6e-146 | cbiQ | P | cobalt transport | ||
AHGDMNCB_01448 | 1.8e-22 | |||||
AHGDMNCB_01449 | 9.3e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
AHGDMNCB_01450 | 1.6e-288 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
AHGDMNCB_01451 | 8.2e-168 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
AHGDMNCB_01452 | 1.2e-43 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
AHGDMNCB_01453 | 2.2e-196 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
AHGDMNCB_01454 | 3.8e-153 | ydjP | I | Alpha/beta hydrolase family | ||
AHGDMNCB_01455 | 9.4e-71 | P | Sodium:sulfate symporter transmembrane region | |||
AHGDMNCB_01456 | 1.2e-41 | psd | 4.1.1.65 | I | Belongs to the phosphatidylserine decarboxylase family | |
AHGDMNCB_01458 | 2.2e-73 | S | Sel1-like repeats. | |||
AHGDMNCB_01459 | 2e-103 | 3.1.4.37 | S | AAA domain | ||
AHGDMNCB_01460 | 1.3e-185 | |||||
AHGDMNCB_01461 | 1.9e-30 | |||||
AHGDMNCB_01462 | 1e-75 | S | HIRAN | |||
AHGDMNCB_01463 | 5e-85 | |||||
AHGDMNCB_01464 | 4.5e-09 | S | Domain of unknown function (DUF3841) | |||
AHGDMNCB_01465 | 2.7e-123 | yoaK | S | Protein of unknown function (DUF1275) | ||
AHGDMNCB_01466 | 4e-57 | K | Helix-turn-helix domain | |||
AHGDMNCB_01467 | 1.1e-112 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
AHGDMNCB_01468 | 7.3e-172 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AHGDMNCB_01469 | 4.3e-183 | K | Transcriptional regulator | |||
AHGDMNCB_01470 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AHGDMNCB_01471 | 2.7e-100 | tnpR | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | ||
AHGDMNCB_01472 | 3.6e-90 | ntd | 2.4.2.6 | F | Nucleoside | |
AHGDMNCB_01473 | 8.6e-87 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AHGDMNCB_01474 | 9.8e-149 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHGDMNCB_01475 | 1.2e-83 | uspA | T | universal stress protein | ||
AHGDMNCB_01476 | 1.2e-150 | phnD | P | Phosphonate ABC transporter | ||
AHGDMNCB_01477 | 4.1e-136 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
AHGDMNCB_01478 | 2.3e-118 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
AHGDMNCB_01479 | 2.2e-148 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
AHGDMNCB_01480 | 9.5e-106 | tag | 3.2.2.20 | L | glycosylase | |
AHGDMNCB_01481 | 3.9e-84 | |||||
AHGDMNCB_01482 | 4.2e-272 | S | Calcineurin-like phosphoesterase | |||
AHGDMNCB_01483 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHGDMNCB_01484 | 5.6e-255 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
AHGDMNCB_01485 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
AHGDMNCB_01486 | 8.7e-141 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
AHGDMNCB_01487 | 2.8e-103 | S | Iron-sulfur cluster assembly protein | |||
AHGDMNCB_01488 | 5.8e-205 | XK27_04775 | S | PAS domain | ||
AHGDMNCB_01489 | 2.2e-168 | V | FtsX-like permease family | |||
AHGDMNCB_01490 | 2.9e-260 | yfnA | E | amino acid | ||
AHGDMNCB_01491 | 6e-55 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
AHGDMNCB_01492 | 2.4e-96 | V | Type II restriction enzyme, methylase subunits | |||
AHGDMNCB_01494 | 1.3e-55 | |||||
AHGDMNCB_01498 | 2e-08 | L | DnaD domain protein | |||
AHGDMNCB_01501 | 6.6e-08 | |||||
AHGDMNCB_01505 | 9.5e-43 | K | BRO family, N-terminal domain | |||
AHGDMNCB_01506 | 6.6e-16 | S | Helix-turn-helix domain | |||
AHGDMNCB_01507 | 1.1e-66 | |||||
AHGDMNCB_01508 | 1.3e-159 | degV | S | EDD domain protein, DegV family | ||
AHGDMNCB_01509 | 7.2e-304 | 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 | ||
AHGDMNCB_01510 | 1.8e-203 | xerS | L | Belongs to the 'phage' integrase family | ||
AHGDMNCB_01511 | 4.1e-67 | |||||
AHGDMNCB_01512 | 8e-111 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
AHGDMNCB_01513 | 1.5e-211 | M | Glycosyl hydrolases family 25 | |||
AHGDMNCB_01514 | 4.2e-175 | pbpX2 | V | Beta-lactamase | ||
AHGDMNCB_01515 | 5.2e-245 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
AHGDMNCB_01516 | 5.7e-36 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHGDMNCB_01517 | 1.8e-234 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
AHGDMNCB_01518 | 7.2e-286 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
AHGDMNCB_01519 | 4e-19 | S | D-Ala-teichoic acid biosynthesis protein | |||
AHGDMNCB_01520 | 4.7e-48 | |||||
AHGDMNCB_01521 | 1e-215 | ywhK | S | Membrane | ||
AHGDMNCB_01522 | 3.9e-81 | ykuL | S | (CBS) domain | ||
AHGDMNCB_01523 | 0.0 | cadA | P | P-type ATPase | ||
AHGDMNCB_01524 | 1.6e-61 | |||||
AHGDMNCB_01525 | 1.7e-205 | napA | P | Sodium/hydrogen exchanger family | ||
AHGDMNCB_01526 | 4.2e-281 | V | ABC transporter transmembrane region | |||
AHGDMNCB_01527 | 5.3e-62 | S | Putative adhesin | |||
AHGDMNCB_01528 | 1e-156 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
AHGDMNCB_01529 | 6.4e-52 | |||||
AHGDMNCB_01530 | 1.1e-121 | S | CAAX protease self-immunity | |||
AHGDMNCB_01531 | 3.6e-194 | S | DUF218 domain | |||
AHGDMNCB_01532 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
AHGDMNCB_01533 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
AHGDMNCB_01534 | 3.3e-101 | S | ECF transporter, substrate-specific component | |||
AHGDMNCB_01535 | 4.7e-202 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
AHGDMNCB_01536 | 1.5e-200 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
AHGDMNCB_01537 | 2.6e-283 | xylG | 3.6.3.17 | S | ABC transporter | |
AHGDMNCB_01538 | 2.5e-198 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
AHGDMNCB_01539 | 4.4e-172 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
AHGDMNCB_01540 | 4.3e-160 | yeaE | S | Aldo/keto reductase family | ||
AHGDMNCB_01541 | 4.7e-134 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
AHGDMNCB_01542 | 8.5e-119 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
AHGDMNCB_01543 | 1.1e-124 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
AHGDMNCB_01544 | 5.5e-72 | |||||
AHGDMNCB_01545 | 3.7e-140 | cof | S | haloacid dehalogenase-like hydrolase | ||
AHGDMNCB_01546 | 2.2e-230 | pbuG | S | permease | ||
AHGDMNCB_01547 | 6.1e-30 | S | CAAX protease self-immunity | |||
AHGDMNCB_01548 | 7.3e-127 | K | helix_turn_helix, mercury resistance | |||
AHGDMNCB_01549 | 3e-232 | pbuG | S | permease | ||
AHGDMNCB_01550 | 2.5e-40 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
AHGDMNCB_01551 | 2.8e-159 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AHGDMNCB_01552 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
AHGDMNCB_01553 | 2.1e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
AHGDMNCB_01554 | 1.1e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
AHGDMNCB_01555 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
AHGDMNCB_01556 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
AHGDMNCB_01557 | 9.2e-170 | 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) | |
AHGDMNCB_01558 | 8.4e-224 | ynbB | 4.4.1.1 | P | aluminum resistance | |
AHGDMNCB_01559 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
AHGDMNCB_01560 | 1.8e-77 | rssA | S | Phospholipase, patatin family | ||
AHGDMNCB_01561 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHGDMNCB_01562 | 3.7e-137 | glcR | K | DeoR C terminal sensor domain | ||
AHGDMNCB_01563 | 1.9e-59 | S | Enterocin A Immunity | |||
AHGDMNCB_01564 | 1.2e-154 | S | hydrolase | |||
AHGDMNCB_01565 | 1.3e-131 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
AHGDMNCB_01566 | 3.1e-175 | rihB | 3.2.2.1 | F | Nucleoside | |
AHGDMNCB_01567 | 0.0 | kup | P | Transport of potassium into the cell | ||
AHGDMNCB_01568 | 2.6e-126 | 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 | |
AHGDMNCB_01569 | 1.6e-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 | |
AHGDMNCB_01570 | 7.7e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
AHGDMNCB_01571 | 1.1e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
AHGDMNCB_01572 | 4.4e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
AHGDMNCB_01573 | 2.7e-180 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
AHGDMNCB_01574 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
AHGDMNCB_01575 | 2.4e-133 | G | Bacterial extracellular solute-binding protein | |||
AHGDMNCB_01576 | 9.8e-213 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
AHGDMNCB_01577 | 3.3e-86 | |||||
AHGDMNCB_01578 | 2.2e-165 | S | Protein of unknown function (DUF2974) | |||
AHGDMNCB_01579 | 4.7e-109 | glnP | P | ABC transporter permease | ||
AHGDMNCB_01580 | 9.7e-91 | gluC | P | ABC transporter permease | ||
AHGDMNCB_01581 | 3.4e-149 | glnH | ET | ABC transporter substrate-binding protein | ||
AHGDMNCB_01582 | 1.9e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHGDMNCB_01583 | 3.6e-114 | udk | 2.7.1.48 | F | Zeta toxin | |
AHGDMNCB_01584 | 5.1e-254 | G | MFS/sugar transport protein | |||
AHGDMNCB_01585 | 4.9e-102 | S | ABC-type cobalt transport system, permease component | |||
AHGDMNCB_01586 | 9.2e-181 | V | ABC transporter transmembrane region | |||
AHGDMNCB_01587 | 1.5e-28 | L | Phage terminase, small subunit | |||
AHGDMNCB_01588 | 1.8e-36 | L | HNH endonuclease | |||
AHGDMNCB_01598 | 1e-83 | ps308 | K | AntA/AntB antirepressor | ||
AHGDMNCB_01603 | 1.5e-19 | S | HNH endonuclease | |||
AHGDMNCB_01604 | 5.1e-251 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
AHGDMNCB_01605 | 7.9e-174 | K | helix_turn_helix, arabinose operon control protein | |||
AHGDMNCB_01606 | 2.8e-106 | K | Helix-turn-helix domain | |||
AHGDMNCB_01608 | 1.4e-87 | |||||
AHGDMNCB_01609 | 2.6e-158 | htpX | O | Belongs to the peptidase M48B family | ||
AHGDMNCB_01610 | 2.7e-97 | lemA | S | LemA family | ||
AHGDMNCB_01611 | 8.6e-196 | ybiR | P | Citrate transporter | ||
AHGDMNCB_01612 | 2.7e-70 | S | Iron-sulphur cluster biosynthesis | |||
AHGDMNCB_01613 | 4.3e-50 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
AHGDMNCB_01614 | 2.1e-247 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
AHGDMNCB_01615 | 1.2e-17 | |||||
AHGDMNCB_01616 | 4e-116 | |||||
AHGDMNCB_01618 | 1.2e-215 | ydaM | M | Glycosyl transferase | ||
AHGDMNCB_01620 | 1.8e-132 | G | Glycosyl hydrolases family 8 | |||
AHGDMNCB_01621 | 6.8e-218 | L | transposase, IS605 OrfB family | |||
AHGDMNCB_01622 | 7.5e-233 | 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 | |
AHGDMNCB_01623 | 3e-298 | ybeC | E | amino acid | ||
AHGDMNCB_01624 | 2.6e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
AHGDMNCB_01625 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
AHGDMNCB_01626 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
AHGDMNCB_01627 | 1.3e-262 | 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 | |
AHGDMNCB_01628 | 2.4e-249 | 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 | |
AHGDMNCB_01629 | 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 | |
AHGDMNCB_01630 | 1e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AHGDMNCB_01631 | 2.1e-108 | S | (CBS) domain | |||
AHGDMNCB_01632 | 7.9e-246 | ynbB | 4.4.1.1 | P | aluminum resistance | |
AHGDMNCB_01633 | 2.9e-284 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
AHGDMNCB_01634 | 1.1e-167 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHGDMNCB_01635 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AHGDMNCB_01636 | 8.3e-90 | ypmB | S | Protein conserved in bacteria | ||
AHGDMNCB_01637 | 1.5e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AHGDMNCB_01638 | 1.3e-114 | dnaD | L | DnaD domain protein | ||
AHGDMNCB_01639 | 1e-113 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
AHGDMNCB_01640 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
AHGDMNCB_01641 | 4.5e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
AHGDMNCB_01642 | 1e-107 | ypsA | S | Belongs to the UPF0398 family | ||
AHGDMNCB_01643 | 4.6e-95 | L | An automated process has identified a potential problem with this gene model | |||
AHGDMNCB_01644 | 1e-28 | yxaM | EGP | Major facilitator Superfamily | ||
AHGDMNCB_01645 | 1.4e-55 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
AHGDMNCB_01646 | 1.5e-121 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
AHGDMNCB_01647 | 6e-80 | S | AAA domain | |||
AHGDMNCB_01648 | 9.9e-143 | 2.4.2.3 | F | Phosphorylase superfamily | ||
AHGDMNCB_01649 | 1.4e-144 | 2.4.2.3 | F | Phosphorylase superfamily | ||
AHGDMNCB_01650 | 1.3e-72 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AHGDMNCB_01651 | 1.3e-151 | dprA | LU | DNA protecting protein DprA | ||
AHGDMNCB_01652 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
AHGDMNCB_01653 | 2.7e-249 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
AHGDMNCB_01654 | 2.2e-141 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
AHGDMNCB_01655 | 1.5e-74 | 2.7.11.1, 3.2.1.8 | M | Leucine-rich repeat (LRR) protein | ||
AHGDMNCB_01656 | 2.3e-14 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
AHGDMNCB_01657 | 7.1e-68 | M | Peptidase family M1 domain | |||
AHGDMNCB_01658 | 9.4e-150 | |||||
AHGDMNCB_01660 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHGDMNCB_01661 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
AHGDMNCB_01662 | 1.7e-197 | nusA | K | Participates in both transcription termination and antitermination | ||
AHGDMNCB_01663 | 8.8e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
AHGDMNCB_01664 | 3.2e-47 | rplGA | J | ribosomal protein | ||
AHGDMNCB_01665 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
AHGDMNCB_01666 | 3e-60 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
AHGDMNCB_01667 | 3.4e-158 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
AHGDMNCB_01668 | 7.5e-177 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AHGDMNCB_01669 | 4.5e-194 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
AHGDMNCB_01670 | 8e-68 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
AHGDMNCB_01671 | 1.7e-284 | E | Amino acid permease | |||
AHGDMNCB_01672 | 1.6e-93 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
AHGDMNCB_01673 | 5.4e-46 | vicX | 3.1.26.11 | S | domain protein | |
AHGDMNCB_01674 | 3.3e-151 | htrA | 3.4.21.107 | O | serine protease | |
AHGDMNCB_01675 | 1e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
AHGDMNCB_01676 | 2.1e-102 | G | Peptidase_C39 like family | |||
AHGDMNCB_01677 | 2.3e-175 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
AHGDMNCB_01678 | 6.1e-80 | P | Cobalt transport protein | |||
AHGDMNCB_01679 | 1.2e-236 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
AHGDMNCB_01680 | 2.4e-150 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
AHGDMNCB_01681 | 5.8e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
AHGDMNCB_01682 | 7.8e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
AHGDMNCB_01683 | 1e-196 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHGDMNCB_01684 | 4.9e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
AHGDMNCB_01685 | 3.4e-71 | yqhY | S | Asp23 family, cell envelope-related function | ||
AHGDMNCB_01686 | 2.1e-64 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
AHGDMNCB_01687 | 7.4e-155 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
AHGDMNCB_01688 | 7.6e-194 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
AHGDMNCB_01689 | 1.1e-34 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
AHGDMNCB_01690 | 2.4e-153 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHGDMNCB_01691 | 5.1e-153 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
AHGDMNCB_01692 | 1.8e-306 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AHGDMNCB_01693 | 4.2e-77 | 6.3.3.2 | S | ASCH | ||
AHGDMNCB_01694 | 2.1e-111 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
AHGDMNCB_01695 | 1.1e-33 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
AHGDMNCB_01696 | 1.7e-162 | M | Peptidase family M1 domain | |||
AHGDMNCB_01697 | 7.8e-51 | S | Alpha beta hydrolase | |||
AHGDMNCB_01699 | 6.5e-187 | S | Bacteriocin helveticin-J | |||
AHGDMNCB_01700 | 8e-51 | L | RelB antitoxin | |||
AHGDMNCB_01701 | 1.8e-63 | spxA_2 | 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 | |
AHGDMNCB_01702 | 7.3e-191 | yrvN | L | AAA C-terminal domain | ||
AHGDMNCB_01703 | 1.7e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AHGDMNCB_01704 | 9e-83 | K | Acetyltransferase (GNAT) domain | |||
AHGDMNCB_01705 | 2e-230 | S | Putative peptidoglycan binding domain | |||
AHGDMNCB_01706 | 3.8e-91 | S | ECF-type riboflavin transporter, S component | |||
AHGDMNCB_01707 | 3e-100 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
AHGDMNCB_01708 | 1.2e-203 | pbpX1 | V | Beta-lactamase | ||
AHGDMNCB_01709 | 1.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
AHGDMNCB_01710 | 1.9e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
AHGDMNCB_01711 | 4.4e-112 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AHGDMNCB_01712 | 4.7e-179 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AHGDMNCB_01714 | 3.8e-94 | L | Integrase | |||
AHGDMNCB_01715 | 2.9e-42 | relB | L | RelB antitoxin | ||
AHGDMNCB_01716 | 6.8e-50 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
AHGDMNCB_01718 | 1.9e-204 | |||||
AHGDMNCB_01719 | 6.9e-73 | gpsB | D | DivIVA domain protein | ||
AHGDMNCB_01720 | 1.8e-142 | ylmH | S | S4 domain protein | ||
AHGDMNCB_01721 | 1.6e-40 | yggT | S | YGGT family | ||
AHGDMNCB_01722 | 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 | ||
AHGDMNCB_01723 | 5.5e-205 | 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 | ||
AHGDMNCB_01724 | 7.7e-247 | 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 | ||
AHGDMNCB_01725 | 4.1e-153 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
AHGDMNCB_01726 | 4.4e-208 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
AHGDMNCB_01727 | 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) | |
AHGDMNCB_01728 | 1.1e-175 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
AHGDMNCB_01729 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AHGDMNCB_01730 | 1.8e-54 | ftsL | D | Cell division protein FtsL | ||
AHGDMNCB_01731 | 3.8e-176 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
AHGDMNCB_01732 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
AHGDMNCB_01733 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
AHGDMNCB_01735 | 1.2e-94 | mreD | ||||
AHGDMNCB_01736 | 6.7e-148 | mreC | M | Involved in formation and maintenance of cell shape | ||
AHGDMNCB_01737 | 9.3e-53 | mreB | D | cell shape determining protein MreB | ||
AHGDMNCB_01738 | 1.3e-107 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
AHGDMNCB_01739 | 2.3e-281 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
AHGDMNCB_01740 | 1.9e-112 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
AHGDMNCB_01741 | 1.4e-105 | K | response regulator | |||
AHGDMNCB_01742 | 4e-221 | sptS | 2.7.13.3 | T | Histidine kinase | |
AHGDMNCB_01743 | 4.2e-209 | EGP | Major facilitator Superfamily | |||
AHGDMNCB_01744 | 2.9e-69 | O | OsmC-like protein | |||
AHGDMNCB_01745 | 3.4e-94 | S | Protein of unknown function (DUF805) | |||
AHGDMNCB_01746 | 2.2e-78 | |||||
AHGDMNCB_01747 | 1.3e-284 | |||||
AHGDMNCB_01748 | 1.2e-137 | S | Fic/DOC family | |||
AHGDMNCB_01749 | 1.1e-293 | S | SLAP domain | |||
AHGDMNCB_01750 | 7.1e-278 | yjeM | E | Amino Acid | ||
AHGDMNCB_01751 | 4.4e-222 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHGDMNCB_01752 | 4.4e-244 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
AHGDMNCB_01754 | 2.7e-31 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
AHGDMNCB_01755 | 2.4e-116 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
AHGDMNCB_01756 | 3.3e-52 | S | Iron-sulfur cluster assembly protein | |||
AHGDMNCB_01757 | 1.7e-154 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
AHGDMNCB_01758 | 9e-124 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
AHGDMNCB_01759 | 3.7e-45 | |||||
AHGDMNCB_01760 | 1.6e-285 | lsa | S | ABC transporter | ||
AHGDMNCB_01766 | 2.3e-223 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
AHGDMNCB_01767 | 2.6e-202 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
AHGDMNCB_01768 | 1.4e-176 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
AHGDMNCB_01769 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHGDMNCB_01770 | 1.7e-29 | secG | U | Preprotein translocase | ||
AHGDMNCB_01771 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AHGDMNCB_01772 | 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 | ||
AHGDMNCB_01773 | 1.4e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHGDMNCB_01774 | 3.9e-237 | S | Peptidase M16 | |||
AHGDMNCB_01775 | 2.6e-222 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
AHGDMNCB_01776 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
AHGDMNCB_01777 | 1.7e-69 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
AHGDMNCB_01778 | 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 | |
AHGDMNCB_01779 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
AHGDMNCB_01780 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
AHGDMNCB_01781 | 6.3e-201 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
AHGDMNCB_01782 | 2.5e-92 | S | SNARE associated Golgi protein | |||
AHGDMNCB_01783 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
AHGDMNCB_01784 | 3.2e-172 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AHGDMNCB_01785 | 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 | |
AHGDMNCB_01786 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
AHGDMNCB_01787 | 3.6e-111 | yjbK | S | CYTH | ||
AHGDMNCB_01788 | 1.2e-114 | yjbH | Q | Thioredoxin | ||
AHGDMNCB_01789 | 5.8e-160 | coiA | 3.6.4.12 | S | Competence protein | |
AHGDMNCB_01790 | 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 | ||
AHGDMNCB_01791 | 6.1e-67 | 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 | |
AHGDMNCB_01792 | 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) | |
AHGDMNCB_01793 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
AHGDMNCB_01794 | 5.3e-26 | |||||
AHGDMNCB_01795 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
AHGDMNCB_01796 | 2.3e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
AHGDMNCB_01797 | 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 | ||
AHGDMNCB_01798 | 2.3e-140 | hlyX | S | Transporter associated domain | ||
AHGDMNCB_01799 | 1.6e-74 | |||||
AHGDMNCB_01800 | 1.6e-85 | |||||
AHGDMNCB_01801 | 8.6e-145 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
AHGDMNCB_01802 | 4.1e-264 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHGDMNCB_01803 | 6.7e-178 | D | Alpha beta | |||
AHGDMNCB_01804 | 2.7e-45 | |||||
AHGDMNCB_01805 | 1.9e-217 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
AHGDMNCB_01806 | 3.4e-214 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
AHGDMNCB_01807 | 5.1e-215 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
AHGDMNCB_01808 | 7.3e-169 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
AHGDMNCB_01809 | 3.6e-163 | yihY | S | Belongs to the UPF0761 family | ||
AHGDMNCB_01810 | 6.5e-164 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
AHGDMNCB_01811 | 1.9e-80 | 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 | |
AHGDMNCB_01812 | 1.8e-228 | 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 | |
AHGDMNCB_01813 | 6.9e-107 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
AHGDMNCB_01814 | 7.8e-202 | 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 | |
AHGDMNCB_01815 | 1.2e-121 | lsa | S | ABC transporter | ||
AHGDMNCB_01816 | 6.1e-43 | S | Protein of unknown function (DUF1211) | |||
AHGDMNCB_01817 | 0.0 | mdlA | V | ABC transporter | ||
AHGDMNCB_01818 | 0.0 | mdlB | V | ABC transporter | ||
AHGDMNCB_01819 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AHGDMNCB_01820 | 3.1e-22 | npr | 1.11.1.1 | C | NADH oxidase | |
AHGDMNCB_01821 | 4.4e-85 | dps | P | Belongs to the Dps family | ||
AHGDMNCB_01822 | 4.4e-70 | S | Iron-sulphur cluster biosynthesis | |||
AHGDMNCB_01823 | 2.8e-100 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
AHGDMNCB_01824 | 1e-61 | psiE | S | Phosphate-starvation-inducible E | ||
AHGDMNCB_01826 | 1.4e-141 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
AHGDMNCB_01827 | 1.9e-59 | |||||
AHGDMNCB_01828 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
AHGDMNCB_01829 | 5.4e-253 | P | P-loop Domain of unknown function (DUF2791) | |||
AHGDMNCB_01830 | 0.0 | S | TerB-C domain | |||
AHGDMNCB_01831 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
AHGDMNCB_01832 | 4.2e-71 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
AHGDMNCB_01833 | 2.5e-33 | |||||
AHGDMNCB_01834 | 6.4e-164 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHGDMNCB_01835 | 6.7e-09 | ackA | 2.7.2.1 | F | acetate kinase activity | |
AHGDMNCB_01836 | 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 | |
AHGDMNCB_01837 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AHGDMNCB_01838 | 6.2e-244 | cycA | E | Amino acid permease | ||
AHGDMNCB_01839 | 4.7e-91 | maa | S | transferase hexapeptide repeat | ||
AHGDMNCB_01840 | 2.2e-157 | K | Transcriptional regulator | |||
AHGDMNCB_01841 | 9.9e-64 | manO | S | Domain of unknown function (DUF956) | ||
AHGDMNCB_01842 | 1e-173 | manN | G | system, mannose fructose sorbose family IID component | ||
AHGDMNCB_01843 | 1.7e-129 | manY | G | PTS system | ||
AHGDMNCB_01844 | 5.6e-186 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
AHGDMNCB_01846 | 4.6e-245 | mod | 2.1.1.72, 3.1.21.5 | L | DNA methylase | |
AHGDMNCB_01847 | 2.4e-37 | K | Cro/C1-type HTH DNA-binding domain | |||
AHGDMNCB_01848 | 2e-81 | |||||
AHGDMNCB_01849 | 9.1e-135 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
AHGDMNCB_01850 | 6.4e-260 | epsU | S | Polysaccharide biosynthesis protein | ||
AHGDMNCB_01851 | 7e-225 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
AHGDMNCB_01852 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
AHGDMNCB_01853 | 4e-153 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
AHGDMNCB_01854 | 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 | |
AHGDMNCB_01855 | 9e-206 | csaB | M | Glycosyl transferases group 1 | ||
AHGDMNCB_01856 | 4.3e-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 |
AHGDMNCB_01857 | 1.1e-70 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
AHGDMNCB_01858 | 1.3e-125 | gntR1 | K | UTRA | ||
AHGDMNCB_01859 | 1.1e-179 | |||||
AHGDMNCB_01860 | 1e-298 | oppA2 | E | ABC transporter, substratebinding protein | ||
AHGDMNCB_01861 | 1.6e-221 | sip | L | Belongs to the 'phage' integrase family | ||
AHGDMNCB_01862 | 1.7e-30 | K | sequence-specific DNA binding | |||
AHGDMNCB_01863 | 1.4e-11 | S | Helix-turn-helix domain | |||
AHGDMNCB_01865 | 1.1e-47 | |||||
AHGDMNCB_01866 | 1.1e-121 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AHGDMNCB_01867 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHGDMNCB_01868 | 1.3e-296 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHGDMNCB_01869 | 4.3e-47 | pspC | KT | PspC domain | ||
AHGDMNCB_01871 | 4.2e-242 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AHGDMNCB_01872 | 7.4e-155 | 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 | |
AHGDMNCB_01873 | 3.6e-99 | M | ErfK YbiS YcfS YnhG | |||
AHGDMNCB_01874 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
AHGDMNCB_01875 | 1.8e-170 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
AHGDMNCB_01876 | 2.2e-96 | 3.6.1.55 | L | NUDIX domain | ||
AHGDMNCB_01877 | 1.9e-70 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
AHGDMNCB_01878 | 1.9e-93 | ypsA | S | Belongs to the UPF0398 family | ||
AHGDMNCB_01879 | 4.4e-40 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
AHGDMNCB_01881 | 6.1e-114 | C | Aldo keto reductase | |||
AHGDMNCB_01883 | 2.4e-83 | L | PFAM transposase IS200-family protein | |||
AHGDMNCB_01884 | 6.5e-93 | natA | S | ABC transporter, ATP-binding protein | ||
AHGDMNCB_01885 | 3.9e-218 | natB | CP | ABC-2 family transporter protein | ||
AHGDMNCB_01886 | 1.8e-136 | fruR | K | DeoR C terminal sensor domain | ||
AHGDMNCB_01887 | 4.1e-167 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
AHGDMNCB_01888 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
AHGDMNCB_01889 | 4.4e-43 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
AHGDMNCB_01890 | 1.7e-138 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
AHGDMNCB_01891 | 1e-108 | fhuC | P | ABC transporter | ||
AHGDMNCB_01892 | 7.9e-127 | znuB | U | ABC 3 transport family | ||
AHGDMNCB_01893 | 1.7e-247 | lctP | C | L-lactate permease | ||
AHGDMNCB_01894 | 6e-29 | mloB | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
AHGDMNCB_01896 | 4.8e-27 | L | Transposase | |||
AHGDMNCB_01897 | 6.5e-192 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
AHGDMNCB_01898 | 7.7e-67 | S | SdpI/YhfL protein family | |||
AHGDMNCB_01899 | 2e-129 | K | Transcriptional regulatory protein, C terminal | |||
AHGDMNCB_01900 | 1.4e-265 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
AHGDMNCB_01901 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHGDMNCB_01902 | 2e-118 | M | NlpC/P60 family | |||
AHGDMNCB_01903 | 1.4e-136 | M | NlpC P60 family protein | |||
AHGDMNCB_01904 | 1.1e-85 | M | NlpC/P60 family | |||
AHGDMNCB_01905 | 2.9e-88 | gmk2 | 2.7.4.8 | F | Guanylate kinase homologues. | |
AHGDMNCB_01906 | 9.3e-44 | |||||
AHGDMNCB_01907 | 4.5e-280 | S | O-antigen ligase like membrane protein | |||
AHGDMNCB_01908 | 3.3e-112 | |||||
AHGDMNCB_01909 | 1.9e-77 | nrdI | F | NrdI Flavodoxin like | ||
AHGDMNCB_01910 | 2.2e-176 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHGDMNCB_01911 | 8.6e-69 | |||||
AHGDMNCB_01912 | 1.7e-110 | yvpB | S | Peptidase_C39 like family | ||
AHGDMNCB_01913 | 4.3e-83 | S | Threonine/Serine exporter, ThrE | |||
AHGDMNCB_01914 | 4.8e-137 | thrE | S | Putative threonine/serine exporter | ||
AHGDMNCB_01915 | 1.7e-290 | S | ABC transporter | |||
AHGDMNCB_01916 | 2.5e-62 | |||||
AHGDMNCB_01917 | 8.4e-102 | rimL | J | Acetyltransferase (GNAT) domain | ||
AHGDMNCB_01918 | 2.5e-124 | S | Protein of unknown function (DUF554) | |||
AHGDMNCB_01919 | 2.1e-211 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHGDMNCB_01920 | 0.0 | pepF | E | oligoendopeptidase F | ||
AHGDMNCB_01921 | 2.4e-33 | S | Enterocin A Immunity | |||
AHGDMNCB_01922 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
AHGDMNCB_01923 | 3.1e-184 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
AHGDMNCB_01924 | 3.7e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
AHGDMNCB_01925 | 2.7e-99 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
AHGDMNCB_01926 | 5.4e-217 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
AHGDMNCB_01927 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
AHGDMNCB_01928 | 4.1e-150 | I | alpha/beta hydrolase fold | |||
AHGDMNCB_01929 | 1.7e-129 | yibF | S | overlaps another CDS with the same product name | ||
AHGDMNCB_01930 | 1.8e-201 | yibE | S | overlaps another CDS with the same product name | ||
AHGDMNCB_01931 | 1.1e-112 | |||||
AHGDMNCB_01932 | 6e-202 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
AHGDMNCB_01933 | 5.8e-225 | S | Cysteine-rich secretory protein family | |||
AHGDMNCB_01934 | 1.2e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHGDMNCB_01935 | 4.8e-258 | glnPH2 | P | ABC transporter permease | ||
AHGDMNCB_01936 | 1e-94 | |||||
AHGDMNCB_01937 | 9.8e-149 | S | hydrolase | |||
AHGDMNCB_01938 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
AHGDMNCB_01939 | 6.4e-148 | glvR | K | Helix-turn-helix domain, rpiR family | ||
AHGDMNCB_01940 | 7e-81 | |||||
AHGDMNCB_01941 | 2.9e-87 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
AHGDMNCB_01942 | 2.1e-39 | |||||
AHGDMNCB_01943 | 2.3e-119 | C | nitroreductase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)