ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
PEEMBNCF_00001 | 2.9e-33 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
PEEMBNCF_00002 | 4.7e-294 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
PEEMBNCF_00005 | 6.8e-89 | S | radical SAM domain protein | |||
PEEMBNCF_00006 | 1e-48 | V | ABC transporter | |||
PEEMBNCF_00007 | 9.4e-114 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
PEEMBNCF_00008 | 9.3e-59 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
PEEMBNCF_00009 | 3.9e-77 | azlC | E | branched-chain amino acid | ||
PEEMBNCF_00010 | 3e-32 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
PEEMBNCF_00011 | 1.5e-56 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
PEEMBNCF_00012 | 1.6e-55 | jag | S | R3H domain protein | ||
PEEMBNCF_00013 | 1.6e-120 | sip | L | Belongs to the 'phage' integrase family | ||
PEEMBNCF_00014 | 5.8e-09 | E | IrrE N-terminal-like domain | |||
PEEMBNCF_00015 | 8.6e-35 | K | Helix-turn-helix XRE-family like proteins | |||
PEEMBNCF_00016 | 1.8e-08 | K | Helix-turn-helix XRE-family like proteins | |||
PEEMBNCF_00017 | 3.9e-20 | L | Phage regulatory protein | |||
PEEMBNCF_00023 | 6.3e-44 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
PEEMBNCF_00024 | 2.5e-132 | S | D5 N terminal like | |||
PEEMBNCF_00026 | 1.2e-10 | |||||
PEEMBNCF_00027 | 3.4e-53 | K | Transcriptional regulator C-terminal region | |||
PEEMBNCF_00028 | 1e-43 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
PEEMBNCF_00029 | 4.8e-287 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
PEEMBNCF_00030 | 5e-111 | dat | 2.6.1.21 | EH | PFAM aminotransferase, class IV | |
PEEMBNCF_00031 | 5e-09 | S | SdpI/YhfL protein family | |||
PEEMBNCF_00032 | 7.2e-91 | licD2 | M | LICD family | ||
PEEMBNCF_00033 | 4.3e-79 | MA20_43635 | M | Capsular polysaccharide synthesis protein | ||
PEEMBNCF_00034 | 8.2e-33 | M | Glycosyl transferase, family 2 | |||
PEEMBNCF_00035 | 1.4e-46 | S | Polysaccharide pyruvyl transferase | |||
PEEMBNCF_00036 | 8.5e-106 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
PEEMBNCF_00037 | 4.6e-43 | S | Psort location CytoplasmicMembrane, score | |||
PEEMBNCF_00038 | 1.2e-69 | epsB | M | biosynthesis protein | ||
PEEMBNCF_00039 | 3.9e-80 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
PEEMBNCF_00040 | 6e-111 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
PEEMBNCF_00041 | 3.7e-126 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PEEMBNCF_00042 | 9.1e-92 | rfbP | M | Bacterial sugar transferase | ||
PEEMBNCF_00043 | 3.9e-143 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
PEEMBNCF_00044 | 3.6e-100 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
PEEMBNCF_00045 | 1.6e-164 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
PEEMBNCF_00046 | 9.8e-128 | 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 | |
PEEMBNCF_00047 | 9e-65 | S | Psort location Cytoplasmic, score 8.96 | |||
PEEMBNCF_00048 | 3.9e-10 | arbx | M | family 8 | ||
PEEMBNCF_00049 | 2.3e-70 | nss | M | transferase activity, transferring glycosyl groups | ||
PEEMBNCF_00050 | 7.2e-56 | nss | M | transferase activity, transferring glycosyl groups | ||
PEEMBNCF_00051 | 4.3e-109 | 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 | ||
PEEMBNCF_00052 | 5.5e-39 | cpsJ | S | Glycosyltransferase like family 2 | ||
PEEMBNCF_00053 | 2.6e-38 | cpsJ | S | Glycosyltransferase like family 2 | ||
PEEMBNCF_00055 | 2e-137 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
PEEMBNCF_00056 | 1.3e-27 | M | Glycosyltransferase like family 2 | |||
PEEMBNCF_00057 | 2.2e-154 | 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 |
PEEMBNCF_00058 | 2.2e-40 | M | family 8 | |||
PEEMBNCF_00060 | 3.5e-33 | cadA | P | P-type ATPase | ||
PEEMBNCF_00061 | 4.1e-83 | L | hmm pf00665 | |||
PEEMBNCF_00062 | 2.2e-56 | L | Helix-turn-helix domain | |||
PEEMBNCF_00064 | 6.1e-13 | S | Cysteine-rich secretory protein family | |||
PEEMBNCF_00065 | 3.4e-57 | S | MobA/MobL family | |||
PEEMBNCF_00067 | 1.7e-72 | natA | S | Domain of unknown function (DUF4162) | ||
PEEMBNCF_00068 | 3e-40 | ysdA | CP | ABC-type Na efflux pump, permease component | ||
PEEMBNCF_00070 | 1.5e-57 | repB | L | Initiator Replication protein | ||
PEEMBNCF_00071 | 2.3e-112 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PEEMBNCF_00072 | 5.6e-190 | glnPH2 | P | ABC transporter permease | ||
PEEMBNCF_00073 | 9.4e-214 | yjeM | E | Amino Acid | ||
PEEMBNCF_00074 | 1.8e-32 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
PEEMBNCF_00075 | 2.1e-136 | tetA | EGP | Major facilitator Superfamily | ||
PEEMBNCF_00076 | 6.1e-63 | S | Glycosyltransferase like family 2 | |||
PEEMBNCF_00077 | 1.7e-116 | cps1D | M | Domain of unknown function (DUF4422) | ||
PEEMBNCF_00078 | 2.3e-39 | S | CAAX protease self-immunity | |||
PEEMBNCF_00079 | 1.6e-88 | yvyE | 3.4.13.9 | S | YigZ family | |
PEEMBNCF_00080 | 1.7e-58 | S | Haloacid dehalogenase-like hydrolase | |||
PEEMBNCF_00081 | 3.9e-107 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00082 | 4.3e-113 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
PEEMBNCF_00083 | 3.5e-132 | ABC-SBP | S | ABC transporter | ||
PEEMBNCF_00084 | 1.3e-159 | potD | P | ABC transporter | ||
PEEMBNCF_00085 | 4.5e-104 | potC | U | Binding-protein-dependent transport system inner membrane component | ||
PEEMBNCF_00086 | 1.5e-120 | potB | P | ABC transporter permease | ||
PEEMBNCF_00087 | 8.2e-167 | 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 | |
PEEMBNCF_00088 | 4.9e-29 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
PEEMBNCF_00089 | 1.5e-29 | tnp2 | L | PFAM Transposase, IS204 IS1001 IS1096 IS1165 | ||
PEEMBNCF_00090 | 3.2e-67 | yxkH | G | Polysaccharide deacetylase | ||
PEEMBNCF_00091 | 2.1e-08 | |||||
PEEMBNCF_00092 | 1.7e-53 | K | LysR substrate binding domain | |||
PEEMBNCF_00093 | 1.5e-122 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
PEEMBNCF_00094 | 1.1e-199 | nupG | F | Nucleoside | ||
PEEMBNCF_00095 | 4.1e-105 | 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 | ||
PEEMBNCF_00096 | 6.1e-33 | 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 | |
PEEMBNCF_00097 | 6.2e-114 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PEEMBNCF_00098 | 1.5e-32 | ywjH | S | Protein of unknown function (DUF1634) | ||
PEEMBNCF_00099 | 1.7e-119 | yxaA | S | membrane transporter protein | ||
PEEMBNCF_00100 | 9.9e-83 | lysR5 | K | LysR substrate binding domain | ||
PEEMBNCF_00101 | 9.4e-57 | lssY | 3.6.1.27 | I | phosphatidate phosphatase activity | |
PEEMBNCF_00102 | 3.2e-14 | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
PEEMBNCF_00103 | 1.5e-16 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
PEEMBNCF_00118 | 1.3e-107 | licA | 2.7.1.89 | M | Choline/ethanolamine kinase | |
PEEMBNCF_00119 | 5.1e-85 | M | Nucleotidyl transferase | |||
PEEMBNCF_00120 | 3.3e-150 | M | BCCT, betaine/carnitine/choline family transporter | |||
PEEMBNCF_00121 | 2.2e-55 | S | peptidoglycan catabolic process | |||
PEEMBNCF_00122 | 9.5e-127 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
PEEMBNCF_00124 | 1e-105 | yxeH | S | hydrolase | ||
PEEMBNCF_00125 | 5.5e-70 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
PEEMBNCF_00127 | 2.9e-96 | yicL | EG | EamA-like transporter family | ||
PEEMBNCF_00129 | 5.2e-72 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
PEEMBNCF_00130 | 7.9e-62 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
PEEMBNCF_00131 | 6.4e-184 | L | Probable transposase | |||
PEEMBNCF_00132 | 5.4e-95 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00133 | 1.4e-32 | tetR | K | transcriptional regulator | ||
PEEMBNCF_00135 | 4.2e-16 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
PEEMBNCF_00136 | 6.6e-60 | uspA | T | Universal stress protein family | ||
PEEMBNCF_00138 | 1.9e-211 | glnP | P | ABC transporter | ||
PEEMBNCF_00139 | 1.9e-168 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
PEEMBNCF_00140 | 5.7e-261 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
PEEMBNCF_00141 | 1.2e-235 | 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 | |
PEEMBNCF_00142 | 9.9e-64 | S | Cell surface protein | |||
PEEMBNCF_00144 | 1.2e-180 | pbuG | S | permease | ||
PEEMBNCF_00145 | 7.6e-38 | 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) | |
PEEMBNCF_00146 | 1.1e-233 | 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) | |
PEEMBNCF_00147 | 1.9e-256 | 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) | |
PEEMBNCF_00148 | 1.4e-187 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
PEEMBNCF_00149 | 1.5e-33 | M | Glycosyl hydrolases family 25 | |||
PEEMBNCF_00151 | 4.5e-102 | tcyB | E | ABC transporter | ||
PEEMBNCF_00152 | 1.6e-106 | yxeH | S | hydrolase | ||
PEEMBNCF_00153 | 9.7e-231 | V | ABC transporter transmembrane region | |||
PEEMBNCF_00154 | 1.6e-12 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00155 | 4.2e-29 | |||||
PEEMBNCF_00156 | 5.3e-246 | yjbQ | P | TrkA C-terminal domain protein | ||
PEEMBNCF_00157 | 4.6e-48 | 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 | ||
PEEMBNCF_00158 | 1.9e-125 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
PEEMBNCF_00159 | 5.5e-77 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
PEEMBNCF_00160 | 1.1e-60 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
PEEMBNCF_00161 | 1.4e-53 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
PEEMBNCF_00162 | 2.4e-190 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
PEEMBNCF_00163 | 6.9e-16 | S | Putative adhesin | |||
PEEMBNCF_00164 | 1.3e-16 | pspC | KT | PspC domain | ||
PEEMBNCF_00166 | 3.9e-13 | S | Enterocin A Immunity | |||
PEEMBNCF_00167 | 7e-234 | L | Transposase | |||
PEEMBNCF_00168 | 8.7e-44 | L | Transposase | |||
PEEMBNCF_00170 | 2.7e-32 | M | domain protein | |||
PEEMBNCF_00171 | 5.2e-143 | yfjM | S | Protein of unknown function DUF262 | ||
PEEMBNCF_00172 | 6.4e-114 | degV | S | EDD domain protein, DegV family | ||
PEEMBNCF_00173 | 1e-07 | L | Helix-turn-helix domain | |||
PEEMBNCF_00174 | 4.4e-41 | wecD | K | Acetyltransferase GNAT Family | ||
PEEMBNCF_00178 | 2.5e-12 | |||||
PEEMBNCF_00182 | 1.5e-37 | |||||
PEEMBNCF_00183 | 7.1e-07 | XK27_07075 | S | CAAX amino terminal protease family protein | ||
PEEMBNCF_00188 | 8.4e-12 | sdrF | M | domain protein | ||
PEEMBNCF_00189 | 1.3e-20 | sdrF | M | domain protein | ||
PEEMBNCF_00190 | 1.1e-108 | L | Belongs to the 'phage' integrase family | |||
PEEMBNCF_00192 | 2e-26 | D | nuclear chromosome segregation | |||
PEEMBNCF_00193 | 1.5e-78 | sspC | 2.7.7.7 | DM | Glucan-binding protein C | |
PEEMBNCF_00194 | 5.4e-19 | S | Replication initiator protein A (RepA) N-terminus | |||
PEEMBNCF_00197 | 9.1e-15 | sdrF | M | domain protein | ||
PEEMBNCF_00200 | 1.3e-16 | 3.4.21.88 | K | Peptidase S24-like | ||
PEEMBNCF_00204 | 5.1e-10 | |||||
PEEMBNCF_00205 | 1.6e-43 | M | Prophage endopeptidase tail | |||
PEEMBNCF_00212 | 9.5e-18 | ftsK | D | FtsK/SpoIIIE family | ||
PEEMBNCF_00221 | 3.3e-41 | O | Belongs to the ClpA ClpB family | |||
PEEMBNCF_00227 | 6e-94 | cps1D | M | Domain of unknown function (DUF4422) | ||
PEEMBNCF_00228 | 4.3e-58 | tlpA2 | L | Transposase IS200 like | ||
PEEMBNCF_00229 | 1.8e-160 | L | transposase, IS605 OrfB family | |||
PEEMBNCF_00239 | 3.3e-154 | V | RRXRR protein | |||
PEEMBNCF_00240 | 9.6e-23 | |||||
PEEMBNCF_00243 | 2.3e-10 | E | IrrE N-terminal-like domain | |||
PEEMBNCF_00244 | 3.7e-21 | yvaO | K | Helix-turn-helix domain | ||
PEEMBNCF_00261 | 9e-65 | S | Psort location Cytoplasmic, score 8.96 | |||
PEEMBNCF_00262 | 9.8e-128 | 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 | |
PEEMBNCF_00263 | 1.6e-164 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
PEEMBNCF_00264 | 3.6e-100 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
PEEMBNCF_00265 | 3.9e-143 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
PEEMBNCF_00266 | 9.1e-92 | rfbP | M | Bacterial sugar transferase | ||
PEEMBNCF_00267 | 3.7e-126 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PEEMBNCF_00268 | 6e-111 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
PEEMBNCF_00269 | 3.9e-80 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
PEEMBNCF_00270 | 1.2e-69 | epsB | M | biosynthesis protein | ||
PEEMBNCF_00271 | 4.6e-43 | S | Psort location CytoplasmicMembrane, score | |||
PEEMBNCF_00272 | 8.5e-106 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
PEEMBNCF_00273 | 1.4e-46 | S | Polysaccharide pyruvyl transferase | |||
PEEMBNCF_00274 | 8.2e-33 | M | Glycosyl transferase, family 2 | |||
PEEMBNCF_00275 | 4.3e-79 | MA20_43635 | M | Capsular polysaccharide synthesis protein | ||
PEEMBNCF_00276 | 7.2e-91 | licD2 | M | LICD family | ||
PEEMBNCF_00279 | 3.9e-20 | L | Phage regulatory protein | |||
PEEMBNCF_00280 | 1.8e-08 | K | Helix-turn-helix XRE-family like proteins | |||
PEEMBNCF_00281 | 8.6e-35 | K | Helix-turn-helix XRE-family like proteins | |||
PEEMBNCF_00282 | 5.8e-09 | E | IrrE N-terminal-like domain | |||
PEEMBNCF_00283 | 1.6e-120 | sip | L | Belongs to the 'phage' integrase family | ||
PEEMBNCF_00284 | 1.6e-55 | jag | S | R3H domain protein | ||
PEEMBNCF_00285 | 1.5e-56 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
PEEMBNCF_00286 | 3e-32 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
PEEMBNCF_00287 | 3.9e-77 | azlC | E | branched-chain amino acid | ||
PEEMBNCF_00288 | 9.3e-59 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
PEEMBNCF_00289 | 9.4e-114 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
PEEMBNCF_00290 | 1e-48 | V | ABC transporter | |||
PEEMBNCF_00291 | 6.8e-89 | S | radical SAM domain protein | |||
PEEMBNCF_00294 | 4.7e-294 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
PEEMBNCF_00295 | 2.9e-33 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
PEEMBNCF_00296 | 3.9e-10 | arbx | M | family 8 | ||
PEEMBNCF_00297 | 2.3e-70 | nss | M | transferase activity, transferring glycosyl groups | ||
PEEMBNCF_00298 | 7.2e-56 | nss | M | transferase activity, transferring glycosyl groups | ||
PEEMBNCF_00299 | 4.3e-109 | 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 | ||
PEEMBNCF_00300 | 5.5e-39 | cpsJ | S | Glycosyltransferase like family 2 | ||
PEEMBNCF_00301 | 2.6e-38 | cpsJ | S | Glycosyltransferase like family 2 | ||
PEEMBNCF_00303 | 2e-137 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
PEEMBNCF_00304 | 1.3e-27 | M | Glycosyltransferase like family 2 | |||
PEEMBNCF_00305 | 2.2e-154 | 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 |
PEEMBNCF_00306 | 2.2e-40 | M | family 8 | |||
PEEMBNCF_00308 | 8.6e-08 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
PEEMBNCF_00309 | 2.1e-89 | L | Lactococcus lactis RepB C-terminus | |||
PEEMBNCF_00311 | 2.3e-14 | |||||
PEEMBNCF_00317 | 2e-18 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
PEEMBNCF_00319 | 2.3e-60 | NU | StbA protein | |||
PEEMBNCF_00324 | 1e-29 | E | IrrE N-terminal-like domain | |||
PEEMBNCF_00325 | 3.5e-33 | cadA | P | P-type ATPase | ||
PEEMBNCF_00326 | 4.1e-83 | L | hmm pf00665 | |||
PEEMBNCF_00327 | 2.2e-56 | L | Helix-turn-helix domain | |||
PEEMBNCF_00329 | 6.1e-13 | S | Cysteine-rich secretory protein family | |||
PEEMBNCF_00330 | 3.4e-57 | S | MobA/MobL family | |||
PEEMBNCF_00332 | 1.7e-72 | natA | S | Domain of unknown function (DUF4162) | ||
PEEMBNCF_00333 | 3e-40 | ysdA | CP | ABC-type Na efflux pump, permease component | ||
PEEMBNCF_00335 | 1.5e-57 | repB | L | Initiator Replication protein | ||
PEEMBNCF_00336 | 3.1e-112 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
PEEMBNCF_00337 | 8.8e-230 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
PEEMBNCF_00338 | 2.1e-148 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
PEEMBNCF_00339 | 1.4e-56 | S | Protein of unknown function (DUF975) | |||
PEEMBNCF_00340 | 1.4e-76 | E | GDSL-like Lipase/Acylhydrolase family | |||
PEEMBNCF_00341 | 1e-38 | |||||
PEEMBNCF_00342 | 4.1e-27 | gcvR | T | Belongs to the UPF0237 family | ||
PEEMBNCF_00343 | 2.1e-220 | XK27_08635 | S | UPF0210 protein | ||
PEEMBNCF_00344 | 2.2e-86 | fruR | K | DeoR C terminal sensor domain | ||
PEEMBNCF_00345 | 4.1e-151 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
PEEMBNCF_00346 | 1.5e-283 | fruA | 2.7.1.202 | GT | Phosphotransferase System | |
PEEMBNCF_00347 | 9e-20 | yaaA | S | S4 domain protein YaaA | ||
PEEMBNCF_00348 | 2.1e-152 | 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 | ||
PEEMBNCF_00349 | 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 | |
PEEMBNCF_00350 | 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 | |
PEEMBNCF_00351 | 4.8e-45 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
PEEMBNCF_00352 | 2.5e-63 | 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 | ||
PEEMBNCF_00353 | 6.2e-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 | ||
PEEMBNCF_00354 | 7.3e-110 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
PEEMBNCF_00355 | 2.8e-116 | S | Glycosyl transferase family 2 | |||
PEEMBNCF_00356 | 5.7e-64 | D | peptidase | |||
PEEMBNCF_00357 | 1.4e-187 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
PEEMBNCF_00358 | 1.5e-33 | M | Glycosyl hydrolases family 25 | |||
PEEMBNCF_00360 | 4.5e-102 | tcyB | E | ABC transporter | ||
PEEMBNCF_00361 | 1.9e-101 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PEEMBNCF_00362 | 9.8e-96 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
PEEMBNCF_00363 | 3.6e-38 | K | Transcriptional regulator | |||
PEEMBNCF_00364 | 1.7e-107 | terC | P | Integral membrane protein TerC family | ||
PEEMBNCF_00365 | 3.2e-261 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
PEEMBNCF_00366 | 2.8e-65 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
PEEMBNCF_00367 | 6.4e-186 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
PEEMBNCF_00368 | 1.1e-41 | gntR1 | K | Transcriptional regulator, GntR family | ||
PEEMBNCF_00369 | 1.4e-95 | V | ABC transporter, ATP-binding protein | |||
PEEMBNCF_00370 | 4.6e-07 | |||||
PEEMBNCF_00372 | 7.9e-10 | S | Putative Competence protein ComGF | |||
PEEMBNCF_00374 | 1.2e-12 | |||||
PEEMBNCF_00375 | 1.8e-26 | comGC | U | competence protein ComGC | ||
PEEMBNCF_00376 | 5.7e-98 | comGB | NU | type II secretion system | ||
PEEMBNCF_00377 | 1.3e-118 | comGA | NU | Type II IV secretion system protein | ||
PEEMBNCF_00378 | 1.3e-101 | 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 | |
PEEMBNCF_00379 | 1.5e-119 | yebC | K | Transcriptional regulatory protein | ||
PEEMBNCF_00380 | 3.7e-42 | S | VanZ like family | |||
PEEMBNCF_00381 | 1.3e-158 | ccpA | K | catabolite control protein A | ||
PEEMBNCF_00382 | 1.3e-172 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
PEEMBNCF_00383 | 1.8e-14 | |||||
PEEMBNCF_00386 | 1.7e-74 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
PEEMBNCF_00387 | 1.5e-101 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
PEEMBNCF_00388 | 5e-67 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
PEEMBNCF_00389 | 7.7e-84 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
PEEMBNCF_00390 | 2.6e-11 | 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 | ||
PEEMBNCF_00391 | 2.1e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
PEEMBNCF_00392 | 7e-71 | yacP | S | YacP-like NYN domain | ||
PEEMBNCF_00393 | 3.2e-109 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
PEEMBNCF_00394 | 6.4e-56 | 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) | ||
PEEMBNCF_00395 | 4.7e-207 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
PEEMBNCF_00396 | 2.9e-247 | 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) | |
PEEMBNCF_00397 | 6.3e-154 | yacL | S | domain protein | ||
PEEMBNCF_00398 | 5.5e-193 | 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 | ||
PEEMBNCF_00399 | 6.9e-117 | lutA | C | Cysteine-rich domain | ||
PEEMBNCF_00400 | 2e-208 | yfnA | E | Amino Acid | ||
PEEMBNCF_00402 | 4.3e-61 | uspA | T | universal stress protein | ||
PEEMBNCF_00404 | 1.4e-12 | yajC | U | Preprotein translocase | ||
PEEMBNCF_00405 | 7.8e-208 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
PEEMBNCF_00406 | 7.9e-183 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
PEEMBNCF_00407 | 1.1e-152 | 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 | |
PEEMBNCF_00408 | 4.3e-72 | 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 | |
PEEMBNCF_00409 | 5.7e-149 | 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 | ||
PEEMBNCF_00410 | 2.3e-112 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PEEMBNCF_00411 | 5.6e-190 | glnPH2 | P | ABC transporter permease | ||
PEEMBNCF_00412 | 9.4e-214 | yjeM | E | Amino Acid | ||
PEEMBNCF_00413 | 1.8e-32 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
PEEMBNCF_00414 | 2.1e-136 | tetA | EGP | Major facilitator Superfamily | ||
PEEMBNCF_00415 | 6.1e-63 | S | Glycosyltransferase like family 2 | |||
PEEMBNCF_00416 | 5.8e-117 | cps1D | M | Domain of unknown function (DUF4422) | ||
PEEMBNCF_00417 | 2.3e-39 | S | CAAX protease self-immunity | |||
PEEMBNCF_00418 | 1.6e-88 | yvyE | 3.4.13.9 | S | YigZ family | |
PEEMBNCF_00419 | 1.7e-58 | S | Haloacid dehalogenase-like hydrolase | |||
PEEMBNCF_00420 | 2.5e-132 | S | D5 N terminal like | |||
PEEMBNCF_00422 | 1.2e-10 | |||||
PEEMBNCF_00423 | 3.4e-53 | K | Transcriptional regulator C-terminal region | |||
PEEMBNCF_00424 | 1e-43 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
PEEMBNCF_00425 | 4.8e-287 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
PEEMBNCF_00426 | 5e-111 | dat | 2.6.1.21 | EH | PFAM aminotransferase, class IV | |
PEEMBNCF_00427 | 5e-09 | S | SdpI/YhfL protein family | |||
PEEMBNCF_00428 | 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 | |
PEEMBNCF_00429 | 8.2e-34 | |||||
PEEMBNCF_00430 | 1.8e-141 | 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) | |
PEEMBNCF_00431 | 5.2e-157 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
PEEMBNCF_00432 | 8.7e-97 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
PEEMBNCF_00433 | 2.8e-57 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
PEEMBNCF_00434 | 8.9e-61 | EG | EamA-like transporter family | |||
PEEMBNCF_00435 | 3.9e-76 | L | haloacid dehalogenase-like hydrolase | |||
PEEMBNCF_00436 | 7.6e-117 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
PEEMBNCF_00437 | 1.7e-67 | 1.5.1.38 | S | NADPH-dependent FMN reductase | ||
PEEMBNCF_00438 | 1.4e-163 | C | Luciferase-like monooxygenase | |||
PEEMBNCF_00439 | 1.4e-40 | K | Transcriptional regulator, HxlR family | |||
PEEMBNCF_00440 | 1.7e-171 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
PEEMBNCF_00441 | 1.7e-191 | tnpB | L | Putative transposase DNA-binding domain | ||
PEEMBNCF_00442 | 1.1e-81 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
PEEMBNCF_00443 | 2.5e-113 | K | response regulator | |||
PEEMBNCF_00444 | 3.3e-142 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
PEEMBNCF_00445 | 1.5e-89 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
PEEMBNCF_00446 | 1e-146 | G | Transporter, major facilitator family protein | |||
PEEMBNCF_00447 | 2.4e-224 | 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) | |
PEEMBNCF_00448 | 6.5e-118 | soj | D | Sporulation initiation inhibitor | ||
PEEMBNCF_00449 | 8.3e-82 | noc | K | Belongs to the ParB family | ||
PEEMBNCF_00450 | 4.7e-102 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
PEEMBNCF_00451 | 1.2e-126 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
PEEMBNCF_00452 | 3.4e-111 | 3.1.4.46 | C | phosphodiesterase | ||
PEEMBNCF_00453 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
PEEMBNCF_00454 | 2.7e-158 | lmrB | EGP | Major facilitator Superfamily | ||
PEEMBNCF_00455 | 2.1e-54 | bioY | S | BioY family | ||
PEEMBNCF_00456 | 9.6e-96 | S | Predicted membrane protein (DUF2207) | |||
PEEMBNCF_00457 | 1.3e-242 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
PEEMBNCF_00458 | 1.1e-79 | bglK_1 | GK | ROK family | ||
PEEMBNCF_00459 | 7.6e-104 | S | Phospholipase/Carboxylesterase | |||
PEEMBNCF_00460 | 6.6e-62 | G | PFAM major facilitator superfamily MFS_1 | |||
PEEMBNCF_00461 | 7.4e-80 | mmuP | E | amino acid | ||
PEEMBNCF_00462 | 7.5e-111 | mmuP | E | amino acid | ||
PEEMBNCF_00463 | 2.7e-15 | psiE | S | Phosphate-starvation-inducible E | ||
PEEMBNCF_00464 | 3.7e-155 | oppF | P | Belongs to the ABC transporter superfamily | ||
PEEMBNCF_00465 | 7.4e-181 | oppD | P | Belongs to the ABC transporter superfamily | ||
PEEMBNCF_00466 | 2.2e-169 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
PEEMBNCF_00467 | 7.9e-142 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
PEEMBNCF_00468 | 5.8e-198 | oppA | E | ABC transporter, substratebinding protein | ||
PEEMBNCF_00469 | 1.6e-113 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
PEEMBNCF_00470 | 1.7e-61 | K | Bacterial regulatory proteins, tetR family | |||
PEEMBNCF_00471 | 8.5e-209 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
PEEMBNCF_00473 | 1.7e-111 | endA | F | DNA RNA non-specific endonuclease | ||
PEEMBNCF_00474 | 4.1e-75 | XK27_02070 | S | Nitroreductase family | ||
PEEMBNCF_00475 | 1.9e-175 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
PEEMBNCF_00476 | 7.6e-37 | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
PEEMBNCF_00477 | 3.1e-28 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
PEEMBNCF_00478 | 1.5e-139 | gldA | 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
PEEMBNCF_00479 | 1.5e-20 | S | dextransucrase activity | |||
PEEMBNCF_00480 | 3.2e-42 | G | Transmembrane secretion effector | |||
PEEMBNCF_00481 | 1.4e-163 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
PEEMBNCF_00482 | 4.2e-26 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
PEEMBNCF_00483 | 1.2e-71 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
PEEMBNCF_00484 | 3.9e-49 | 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 | ||
PEEMBNCF_00485 | 1.1e-82 | H | Nodulation protein S (NodS) | |||
PEEMBNCF_00486 | 2.6e-123 | ylbM | S | Belongs to the UPF0348 family | ||
PEEMBNCF_00487 | 2e-57 | yceD | S | Uncharacterized ACR, COG1399 | ||
PEEMBNCF_00488 | 1.9e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
PEEMBNCF_00489 | 3.7e-87 | plsC | 2.3.1.51 | I | Acyltransferase | |
PEEMBNCF_00490 | 8.5e-94 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
PEEMBNCF_00491 | 1.5e-27 | yazA | L | GIY-YIG catalytic domain protein | ||
PEEMBNCF_00492 | 1.9e-128 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
PEEMBNCF_00493 | 2.7e-128 | 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 | ||
PEEMBNCF_00494 | 1.5e-101 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
PEEMBNCF_00495 | 2.2e-66 | ybbL | S | ABC transporter | ||
PEEMBNCF_00496 | 3.7e-163 | oxlT | P | Major Facilitator Superfamily | ||
PEEMBNCF_00497 | 6.2e-53 | 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 | |
PEEMBNCF_00498 | 7.8e-46 | S | Short repeat of unknown function (DUF308) | |||
PEEMBNCF_00499 | 1.2e-29 | tetR | K | Transcriptional regulator C-terminal region | ||
PEEMBNCF_00500 | 1.3e-150 | yfeX | P | Peroxidase | ||
PEEMBNCF_00501 | 1.1e-16 | S | Protein of unknown function (DUF3021) | |||
PEEMBNCF_00502 | 2.4e-40 | K | LytTr DNA-binding domain | |||
PEEMBNCF_00503 | 9.1e-84 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
PEEMBNCF_00504 | 1.5e-29 | tnp2 | L | PFAM Transposase, IS204 IS1001 IS1096 IS1165 | ||
PEEMBNCF_00505 | 3.2e-67 | yxkH | G | Polysaccharide deacetylase | ||
PEEMBNCF_00506 | 2.1e-08 | |||||
PEEMBNCF_00507 | 1.7e-53 | K | LysR substrate binding domain | |||
PEEMBNCF_00508 | 1.5e-122 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
PEEMBNCF_00509 | 1.1e-199 | nupG | F | Nucleoside | ||
PEEMBNCF_00510 | 4.1e-105 | 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 | ||
PEEMBNCF_00511 | 6.1e-33 | 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 | |
PEEMBNCF_00512 | 3.4e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
PEEMBNCF_00514 | 3.9e-107 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00515 | 4.3e-113 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
PEEMBNCF_00516 | 3.5e-132 | ABC-SBP | S | ABC transporter | ||
PEEMBNCF_00517 | 1.3e-159 | potD | P | ABC transporter | ||
PEEMBNCF_00518 | 4.5e-104 | potC | U | Binding-protein-dependent transport system inner membrane component | ||
PEEMBNCF_00519 | 1.5e-120 | potB | P | ABC transporter permease | ||
PEEMBNCF_00520 | 8.2e-167 | 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 | |
PEEMBNCF_00521 | 1.7e-26 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
PEEMBNCF_00523 | 1.1e-192 | 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 | |
PEEMBNCF_00524 | 2.3e-168 | 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) | |
PEEMBNCF_00525 | 1.5e-20 | rimL | 1.1.1.25 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
PEEMBNCF_00527 | 1.2e-112 | dkg | S | reductase | ||
PEEMBNCF_00528 | 1.7e-24 | |||||
PEEMBNCF_00529 | 4.7e-76 | 2.4.2.3 | F | Phosphorylase superfamily | ||
PEEMBNCF_00530 | 1.4e-290 | ybiT | S | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00531 | 5.2e-25 | S | Domain of unknown function (DUF4828) | |||
PEEMBNCF_00532 | 3.5e-32 | mocA | S | Oxidoreductase | ||
PEEMBNCF_00533 | 2.3e-35 | mocA | S | Oxidoreductase | ||
PEEMBNCF_00534 | 3.9e-160 | yfmL | L | DEAD DEAH box helicase | ||
PEEMBNCF_00535 | 5.2e-21 | S | Domain of unknown function (DUF3284) | |||
PEEMBNCF_00537 | 2.3e-279 | kup | P | Transport of potassium into the cell | ||
PEEMBNCF_00538 | 3.6e-100 | malR | K | Transcriptional regulator, LacI family | ||
PEEMBNCF_00539 | 8.8e-199 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
PEEMBNCF_00540 | 3.6e-169 | 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 | ||
PEEMBNCF_00541 | 3.2e-132 | 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 | ||
PEEMBNCF_00542 | 4.6e-283 | 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 | ||
PEEMBNCF_00543 | 1.5e-76 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
PEEMBNCF_00544 | 1.9e-90 | 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 | |
PEEMBNCF_00545 | 1.9e-28 | K | response regulator | |||
PEEMBNCF_00546 | 7.3e-272 | vicK | 2.7.13.3 | T | Histidine kinase | |
PEEMBNCF_00547 | 6e-103 | yycH | S | YycH protein | ||
PEEMBNCF_00548 | 4.3e-80 | yycI | S | YycH protein | ||
PEEMBNCF_00549 | 8e-31 | yyaQ | S | YjbR | ||
PEEMBNCF_00550 | 1.3e-116 | vicX | 3.1.26.11 | S | domain protein | |
PEEMBNCF_00551 | 1.7e-145 | htrA | 3.4.21.107 | O | serine protease | |
PEEMBNCF_00552 | 7.1e-128 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
PEEMBNCF_00553 | 8.8e-171 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
PEEMBNCF_00554 | 4.4e-103 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
PEEMBNCF_00555 | 2.1e-47 | ybhF_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
PEEMBNCF_00556 | 3.5e-09 | ybhF_2 | V | abc transporter atp-binding protein | ||
PEEMBNCF_00557 | 2e-104 | ybhR | V | ABC transporter | ||
PEEMBNCF_00558 | 7.9e-32 | K | Bacterial regulatory proteins, tetR family | |||
PEEMBNCF_00559 | 7.9e-28 | VPA1512 | ET | Bacterial extracellular solute-binding proteins, family 3 | ||
PEEMBNCF_00560 | 1.7e-95 | RB5993 | 3.1.1.3 | I | Pfam Lipase (class 3) | |
PEEMBNCF_00561 | 3.5e-14 | |||||
PEEMBNCF_00562 | 3.5e-65 | secY2 | U | SecY translocase | ||
PEEMBNCF_00563 | 2.1e-61 | S | PFAM Archaeal ATPase | |||
PEEMBNCF_00564 | 1.4e-225 | uxuT | G | MFS/sugar transport protein | ||
PEEMBNCF_00565 | 8.7e-193 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
PEEMBNCF_00566 | 2.6e-173 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
PEEMBNCF_00567 | 3.8e-208 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
PEEMBNCF_00568 | 2.4e-64 | whiA | K | May be required for sporulation | ||
PEEMBNCF_00569 | 3.5e-50 | sip | L | Belongs to the 'phage' integrase family | ||
PEEMBNCF_00570 | 1.1e-09 | sip | L | Belongs to the 'phage' integrase family | ||
PEEMBNCF_00573 | 9.5e-33 | C | FMN binding | |||
PEEMBNCF_00574 | 7.4e-231 | 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 | |
PEEMBNCF_00576 | 3.3e-156 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
PEEMBNCF_00577 | 2.8e-59 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
PEEMBNCF_00578 | 5.1e-11 | S | CAAX protease self-immunity | |||
PEEMBNCF_00579 | 2.5e-82 | S | Belongs to the UPF0246 family | |||
PEEMBNCF_00580 | 1.8e-68 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
PEEMBNCF_00581 | 7e-28 | adhR | K | Transcriptional regulator | ||
PEEMBNCF_00582 | 3.5e-90 | S | NADPH-dependent FMN reductase | |||
PEEMBNCF_00583 | 2.2e-100 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
PEEMBNCF_00584 | 1.5e-55 | S | ECF transporter, substrate-specific component | |||
PEEMBNCF_00585 | 1.6e-95 | znuB | U | ABC 3 transport family | ||
PEEMBNCF_00586 | 3.8e-98 | fhuC | P | ABC transporter | ||
PEEMBNCF_00587 | 2.7e-104 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
PEEMBNCF_00588 | 5.2e-116 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
PEEMBNCF_00589 | 1.5e-53 | 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 | ||
PEEMBNCF_00590 | 1e-44 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
PEEMBNCF_00591 | 1.4e-142 | 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 | ||
PEEMBNCF_00592 | 3.8e-39 | 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 | ||
PEEMBNCF_00593 | 1e-100 | rplD | J | Forms part of the polypeptide exit tunnel | ||
PEEMBNCF_00594 | 4.5e-109 | 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 | ||
PEEMBNCF_00595 | 2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
PEEMBNCF_00596 | 9.5e-167 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
PEEMBNCF_00597 | 7.4e-25 | K | SIS domain | |||
PEEMBNCF_00600 | 6.2e-09 | S | zinc-ribbon domain | |||
PEEMBNCF_00602 | 3.4e-10 | S | Mor transcription activator family | |||
PEEMBNCF_00603 | 1.7e-59 | yfjR | K | WYL domain | ||
PEEMBNCF_00604 | 6e-123 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
PEEMBNCF_00605 | 8.4e-173 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
PEEMBNCF_00606 | 1.1e-72 | K | AI-2E family transporter | |||
PEEMBNCF_00607 | 2.5e-126 | S | overlaps another CDS with the same product name | |||
PEEMBNCF_00608 | 4.9e-86 | S | overlaps another CDS with the same product name | |||
PEEMBNCF_00610 | 2.7e-57 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
PEEMBNCF_00611 | 6.2e-114 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PEEMBNCF_00612 | 1.5e-32 | ywjH | S | Protein of unknown function (DUF1634) | ||
PEEMBNCF_00613 | 1.7e-119 | yxaA | S | membrane transporter protein | ||
PEEMBNCF_00614 | 9.9e-83 | lysR5 | K | LysR substrate binding domain | ||
PEEMBNCF_00615 | 9.4e-57 | lssY | 3.6.1.27 | I | phosphatidate phosphatase activity | |
PEEMBNCF_00616 | 3.2e-14 | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
PEEMBNCF_00617 | 1.5e-16 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
PEEMBNCF_00618 | 8.1e-77 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
PEEMBNCF_00619 | 4e-45 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
PEEMBNCF_00621 | 3e-100 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
PEEMBNCF_00622 | 1.6e-98 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
PEEMBNCF_00623 | 4.2e-71 | ecsB | U | ABC transporter | ||
PEEMBNCF_00624 | 9.8e-95 | ecsA | V | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00625 | 3.6e-57 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
PEEMBNCF_00626 | 8.6e-141 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
PEEMBNCF_00627 | 1.7e-200 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
PEEMBNCF_00628 | 1e-117 | pepL | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
PEEMBNCF_00629 | 8e-43 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
PEEMBNCF_00630 | 1.8e-63 | 1.3.5.4 | C | FMN_bind | ||
PEEMBNCF_00631 | 9.1e-122 | glpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
PEEMBNCF_00633 | 1.8e-112 | lacI3 | K | helix_turn _helix lactose operon repressor | ||
PEEMBNCF_00634 | 4e-229 | malL | 3.2.1.10 | GH13 | G | Psort location Cytoplasmic, score |
PEEMBNCF_00635 | 2e-39 | 2.7.1.191 | G | PTS system fructose IIA component | ||
PEEMBNCF_00636 | 2e-70 | G | PTS system mannose/fructose/sorbose family IID component | |||
PEEMBNCF_00637 | 4.7e-88 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
PEEMBNCF_00638 | 2.3e-168 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
PEEMBNCF_00639 | 3.1e-128 | 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 | |
PEEMBNCF_00640 | 5.4e-177 | thrC | 4.2.3.1 | E | Threonine synthase | |
PEEMBNCF_00641 | 2.3e-49 | XK27_08315 | M | Sulfatase | ||
PEEMBNCF_00642 | 2.7e-182 | pepS | E | Thermophilic metalloprotease (M29) | ||
PEEMBNCF_00643 | 2.1e-168 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
PEEMBNCF_00644 | 6.2e-71 | K | Sugar-specific transcriptional regulator TrmB | |||
PEEMBNCF_00645 | 1.7e-122 | S | Sulfite exporter TauE/SafE | |||
PEEMBNCF_00646 | 2.1e-30 | minD | D | Belongs to the ParA family | ||
PEEMBNCF_00647 | 2.7e-93 | glnP | P | ABC transporter permease | ||
PEEMBNCF_00648 | 1.1e-89 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PEEMBNCF_00649 | 1.3e-109 | aatB | ET | ABC transporter substrate-binding protein | ||
PEEMBNCF_00650 | 9.8e-100 | D | Alpha beta | |||
PEEMBNCF_00651 | 4.3e-43 | isp2 | L | Transposase | ||
PEEMBNCF_00652 | 1e-47 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
PEEMBNCF_00653 | 3.1e-75 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
PEEMBNCF_00654 | 4.9e-165 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
PEEMBNCF_00655 | 1.1e-129 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
PEEMBNCF_00656 | 6.4e-36 | S | Enterocin A Immunity | |||
PEEMBNCF_00657 | 2.5e-16 | |||||
PEEMBNCF_00658 | 8.2e-16 | 3.1.3.48 | D | FIVAR domain | ||
PEEMBNCF_00659 | 9.5e-127 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
PEEMBNCF_00661 | 1e-105 | yxeH | S | hydrolase | ||
PEEMBNCF_00662 | 5.5e-70 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
PEEMBNCF_00664 | 2.9e-96 | yicL | EG | EamA-like transporter family | ||
PEEMBNCF_00665 | 8.8e-90 | pepF | E | Oligopeptidase F | ||
PEEMBNCF_00666 | 6.9e-170 | 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) | |
PEEMBNCF_00667 | 3.2e-141 | 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 | |
PEEMBNCF_00668 | 7e-26 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
PEEMBNCF_00669 | 9.5e-100 | 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 | |
PEEMBNCF_00670 | 4.8e-182 | EG | GntP family permease | |||
PEEMBNCF_00671 | 6.7e-151 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
PEEMBNCF_00672 | 1.5e-43 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
PEEMBNCF_00673 | 3.3e-21 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
PEEMBNCF_00674 | 5.5e-251 | ctpA | 3.6.3.54 | P | P-type ATPase | |
PEEMBNCF_00675 | 4.3e-82 | thrE | S | Putative threonine/serine exporter | ||
PEEMBNCF_00676 | 6.3e-49 | S | Threonine/Serine exporter, ThrE | |||
PEEMBNCF_00677 | 2.4e-124 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PEEMBNCF_00678 | 6.5e-87 | S | Sucrose-6F-phosphate phosphohydrolase | |||
PEEMBNCF_00679 | 1.9e-34 | trxA | O | Belongs to the thioredoxin family | ||
PEEMBNCF_00680 | 2.8e-21 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
PEEMBNCF_00681 | 2.8e-20 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
PEEMBNCF_00682 | 4.5e-43 | S | Peptidase_C39 like family | |||
PEEMBNCF_00683 | 8.6e-39 | S | Acyltransferase family | |||
PEEMBNCF_00684 | 8.6e-196 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
PEEMBNCF_00685 | 5.4e-59 | S | Phage head-tail joining protein | |||
PEEMBNCF_00686 | 4.8e-22 | S | Phage gp6-like head-tail connector protein | |||
PEEMBNCF_00687 | 5.8e-222 | S | Phage capsid family | |||
PEEMBNCF_00688 | 9.3e-119 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
PEEMBNCF_00689 | 1.5e-214 | S | Phage portal protein | |||
PEEMBNCF_00691 | 4.2e-258 | S | Phage Terminase | |||
PEEMBNCF_00696 | 7.5e-271 | M | Phage tail tape measure protein TP901 | |||
PEEMBNCF_00697 | 4.6e-77 | S | Phage tail protein | |||
PEEMBNCF_00698 | 1.3e-121 | rny | D | peptidase | ||
PEEMBNCF_00699 | 9.9e-64 | S | Cell surface protein | |||
PEEMBNCF_00701 | 1.2e-180 | pbuG | S | permease | ||
PEEMBNCF_00702 | 2.3e-71 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
PEEMBNCF_00703 | 6e-59 | M | Glycosyltransferase like family 2 | |||
PEEMBNCF_00704 | 6.2e-74 | M | LicD family | |||
PEEMBNCF_00705 | 1.1e-57 | cps3F | ||||
PEEMBNCF_00706 | 6.8e-94 | M | transferase activity, transferring glycosyl groups | |||
PEEMBNCF_00707 | 6.3e-76 | waaB | GT4 | M | Glycosyl transferases group 1 | |
PEEMBNCF_00708 | 8.5e-23 | M | Core-2/I-Branching enzyme | |||
PEEMBNCF_00709 | 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 | ||
PEEMBNCF_00710 | 2.2e-164 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
PEEMBNCF_00711 | 1.4e-68 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
PEEMBNCF_00712 | 1e-55 | S | CAAX protease self-immunity | |||
PEEMBNCF_00713 | 5.7e-48 | C | Flavodoxin | |||
PEEMBNCF_00714 | 3.7e-59 | yphH | S | Cupin domain | ||
PEEMBNCF_00715 | 3e-45 | yphJ | 4.1.1.44 | S | decarboxylase | |
PEEMBNCF_00716 | 1.2e-144 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
PEEMBNCF_00717 | 2.2e-30 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
PEEMBNCF_00718 | 2e-17 | |||||
PEEMBNCF_00719 | 1.3e-119 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
PEEMBNCF_00720 | 1e-113 | V | domain protein | |||
PEEMBNCF_00722 | 2.6e-34 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
PEEMBNCF_00723 | 2.6e-38 | ulaB | 2.7.1.194 | G | Phosphotransferase system galactitol-specific IIB component | |
PEEMBNCF_00724 | 8.6e-190 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
PEEMBNCF_00725 | 1.5e-91 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
PEEMBNCF_00726 | 1.4e-161 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
PEEMBNCF_00727 | 1.8e-17 | S | Bacterial membrane protein YfhO | |||
PEEMBNCF_00728 | 5.7e-52 | gtcA | S | Teichoic acid glycosylation protein | ||
PEEMBNCF_00729 | 5.1e-54 | fld | C | Flavodoxin | ||
PEEMBNCF_00730 | 2.3e-142 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
PEEMBNCF_00731 | 1.3e-151 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
PEEMBNCF_00734 | 1.7e-25 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
PEEMBNCF_00735 | 7.7e-97 | ypuA | S | Protein of unknown function (DUF1002) | ||
PEEMBNCF_00736 | 4e-09 | yhcA | V | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00737 | 5.8e-35 | K | Bacterial regulatory proteins, tetR family | |||
PEEMBNCF_00738 | 4.9e-222 | lmrA | V | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00739 | 3.3e-253 | yfiC | V | ABC transporter | ||
PEEMBNCF_00741 | 5e-62 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
PEEMBNCF_00742 | 2.8e-68 | dhaL | 2.7.1.121 | S | Dak2 | |
PEEMBNCF_00743 | 1.4e-49 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
PEEMBNCF_00744 | 8.4e-104 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
PEEMBNCF_00745 | 9.8e-177 | yjcE | P | Sodium proton antiporter | ||
PEEMBNCF_00746 | 1.3e-107 | licA | 2.7.1.89 | M | Choline/ethanolamine kinase | |
PEEMBNCF_00747 | 5.1e-85 | M | Nucleotidyl transferase | |||
PEEMBNCF_00748 | 3.3e-150 | M | BCCT, betaine/carnitine/choline family transporter | |||
PEEMBNCF_00749 | 2.2e-55 | S | peptidoglycan catabolic process | |||
PEEMBNCF_00750 | 7.6e-87 | 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 | |
PEEMBNCF_00751 | 4.1e-104 | tatD | L | hydrolase, TatD family | ||
PEEMBNCF_00752 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
PEEMBNCF_00753 | 7.6e-106 | |||||
PEEMBNCF_00755 | 3.4e-180 | 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 | ||
PEEMBNCF_00756 | 4e-190 | 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 | ||
PEEMBNCF_00757 | 1.6e-61 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
PEEMBNCF_00758 | 3.8e-94 | 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) |
PEEMBNCF_00759 | 1.6e-147 | manN | G | system, mannose fructose sorbose family IID component | ||
PEEMBNCF_00760 | 6.4e-116 | manY | G | PTS system sorbose-specific iic component | ||
PEEMBNCF_00761 | 9e-152 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
PEEMBNCF_00762 | 4.1e-80 | rbsB | G | sugar-binding domain protein | ||
PEEMBNCF_00763 | 6e-30 | yhbY | J | RNA-binding protein | ||
PEEMBNCF_00764 | 6.1e-181 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
PEEMBNCF_00765 | 2.5e-71 | yqeG | S | HAD phosphatase, family IIIA | ||
PEEMBNCF_00766 | 2.2e-52 | 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 | ||
PEEMBNCF_00767 | 1.4e-24 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
PEEMBNCF_00768 | 1.3e-79 | 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 | ||
PEEMBNCF_00769 | 6.3e-149 | 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) | |
PEEMBNCF_00770 | 4.2e-16 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
PEEMBNCF_00771 | 6.6e-60 | uspA | T | Universal stress protein family | ||
PEEMBNCF_00773 | 1.9e-211 | glnP | P | ABC transporter | ||
PEEMBNCF_00774 | 1.9e-168 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
PEEMBNCF_00775 | 2.6e-45 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
PEEMBNCF_00776 | 5.1e-63 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
PEEMBNCF_00777 | 5.6e-110 | glcU | U | sugar transport | ||
PEEMBNCF_00778 | 2.6e-15 | yobS | K | transcriptional regulator | ||
PEEMBNCF_00779 | 1.7e-152 | mdtG | EGP | Major facilitator Superfamily | ||
PEEMBNCF_00780 | 6.4e-54 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
PEEMBNCF_00781 | 2.1e-190 | 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) | |
PEEMBNCF_00782 | 7.2e-243 | lysP | E | amino acid | ||
PEEMBNCF_00783 | 3.1e-69 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
PEEMBNCF_00785 | 5.2e-72 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
PEEMBNCF_00786 | 7.9e-62 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
PEEMBNCF_00787 | 6.4e-184 | L | Probable transposase | |||
PEEMBNCF_00788 | 5.4e-95 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
PEEMBNCF_00789 | 1.4e-32 | tetR | K | transcriptional regulator | ||
PEEMBNCF_00799 | 2.4e-175 | 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 | |
PEEMBNCF_00800 | 9.2e-32 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
PEEMBNCF_00802 | 1.8e-207 | 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 | ||
PEEMBNCF_00803 | 7.6e-24 | 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 | ||
PEEMBNCF_00814 | 4.1e-24 | S | Addiction module toxin RelE StbE family | |||
PEEMBNCF_00815 | 2.9e-24 | L | Addiction module antitoxin, RelB DinJ family | |||
PEEMBNCF_00816 | 9.5e-63 | hsdS-1 | 3.1.21.3 | L | Belongs to the 'phage' integrase family | |
PEEMBNCF_00817 | 2e-40 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
PEEMBNCF_00818 | 9.9e-47 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
PEEMBNCF_00819 | 1.2e-160 | 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 | ||
PEEMBNCF_00820 | 1.5e-274 | dnaK | O | Heat shock 70 kDa protein | ||
PEEMBNCF_00821 | 4.2e-56 | 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 | ||
PEEMBNCF_00822 | 1.7e-44 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
PEEMBNCF_00824 | 1.9e-206 | 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 | |
PEEMBNCF_00825 | 1.8e-64 | L | Transposase IS200 like | |||
PEEMBNCF_00826 | 2e-125 | |||||
PEEMBNCF_00827 | 1.6e-30 | 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 | |
PEEMBNCF_00828 | 4.8e-29 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
PEEMBNCF_00829 | 3.5e-204 | pyrP | F | Permease | ||
PEEMBNCF_00830 | 8.2e-114 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
PEEMBNCF_00831 | 2.5e-16 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
PEEMBNCF_00832 | 1.1e-12 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
PEEMBNCF_00833 | 1e-132 | arcT | 2.6.1.1 | E | Cys/Met metabolism PLP-dependent enzyme | |
PEEMBNCF_00834 | 6.6e-46 | argR | K | Regulates arginine biosynthesis genes | ||
PEEMBNCF_00835 | 3.7e-117 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
PEEMBNCF_00836 | 3.9e-155 | amtB | P | ammonium transporter | ||
PEEMBNCF_00837 | 3.6e-197 | lmrB | EGP | Major facilitator Superfamily | ||
PEEMBNCF_00838 | 1.2e-33 | S | Domain of unknown function (DUF4811) | |||
PEEMBNCF_00839 | 1.7e-60 | yceE | S | haloacid dehalogenase-like hydrolase | ||
PEEMBNCF_00840 | 7.6e-74 | glcR | K | DeoR C terminal sensor domain | ||
PEEMBNCF_00841 | 3.2e-59 | ftsW | D | Belongs to the SEDS family | ||
PEEMBNCF_00842 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
PEEMBNCF_00843 | 7.8e-19 | nss | M | transferase activity, transferring glycosyl groups | ||
PEEMBNCF_00844 | 4e-55 | M | Glycosyltransferase like family 2 | |||
PEEMBNCF_00846 | 5.3e-39 | M | family 8 | |||
PEEMBNCF_00847 | 9.3e-39 | S | glycosyl transferase family 2 | |||
PEEMBNCF_00848 | 1.4e-156 | gmuE | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
PEEMBNCF_00849 | 1.5e-64 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
PEEMBNCF_00850 | 4.3e-97 | V | ABC transporter | |||
PEEMBNCF_00852 | 3.4e-59 | |||||
PEEMBNCF_00853 | 1.8e-26 | |||||
PEEMBNCF_00854 | 1.1e-217 | L | Probable transposase | |||
PEEMBNCF_00855 | 1.3e-28 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |||
PEEMBNCF_00856 | 4.1e-92 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
PEEMBNCF_00857 | 1.4e-40 | yabA | L | Involved in initiation control of chromosome replication | ||
PEEMBNCF_00858 | 3.9e-83 | holB | 2.7.7.7 | L | DNA polymerase III | |
PEEMBNCF_00859 | 1.4e-65 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
PEEMBNCF_00860 | 9.2e-29 | yaaL | S | Protein of unknown function (DUF2508) | ||
PEEMBNCF_00861 | 2.2e-97 | 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 | ||
PEEMBNCF_00862 | 7e-34 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
PEEMBNCF_00863 | 7e-73 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
PEEMBNCF_00864 | 2.5e-86 | S | (CBS) domain | |||
PEEMBNCF_00865 | 4e-141 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
PEEMBNCF_00866 | 1.1e-207 | 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) | |
PEEMBNCF_00867 | 5.7e-261 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
PEEMBNCF_00868 | 1.2e-235 | 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 | |
PEEMBNCF_00869 | 2.6e-170 | gatC | G | PTS system sugar-specific permease component | ||
PEEMBNCF_00870 | 7.7e-35 | IQ | KR domain | |||
PEEMBNCF_00871 | 8.1e-71 | IQ | KR domain | |||
PEEMBNCF_00872 | 2.9e-115 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
PEEMBNCF_00873 | 7.5e-92 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
PEEMBNCF_00874 | 7.5e-13 | |||||
PEEMBNCF_00875 | 2.1e-121 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
PEEMBNCF_00876 | 4.3e-186 | 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 | |
PEEMBNCF_00878 | 5.9e-22 | S | Cytochrome B5 | |||
PEEMBNCF_00879 | 6e-49 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain (presumed) | |
PEEMBNCF_00880 | 9.9e-60 | |||||
PEEMBNCF_00881 | 3.7e-43 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
PEEMBNCF_00882 | 1.1e-155 | nrnB | S | DHHA1 domain | ||
PEEMBNCF_00883 | 7.3e-44 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | ||
PEEMBNCF_00884 | 1.5e-64 | rny | D | Peptidase family M23 | ||
PEEMBNCF_00886 | 3.1e-240 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
PEEMBNCF_00887 | 2.6e-137 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
PEEMBNCF_00888 | 1.3e-55 | 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 | ||
PEEMBNCF_00889 | 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 | ||
PEEMBNCF_00890 | 6.8e-26 | ylxQ | J | ribosomal protein | ||
PEEMBNCF_00891 | 1.4e-39 | ylxR | K | Protein of unknown function (DUF448) | ||
PEEMBNCF_00892 | 1.7e-69 | nusA | K | Participates in both transcription termination and antitermination | ||
PEEMBNCF_00893 | 4.4e-297 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
PEEMBNCF_00894 | 3.3e-107 | 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 | |
PEEMBNCF_00895 | 2.1e-50 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
PEEMBNCF_00896 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
PEEMBNCF_00897 | 1.5e-15 | |||||
PEEMBNCF_00898 | 9.7e-37 | ptsH | G | phosphocarrier protein HPR | ||
PEEMBNCF_00899 | 7.6e-38 | 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) | |
PEEMBNCF_00900 | 1.1e-233 | 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) | |
PEEMBNCF_00901 | 1.9e-256 | 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) | |
PEEMBNCF_00902 | 2.3e-115 | 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 | |
PEEMBNCF_00903 | 7.9e-56 | P | Plays a role in the regulation of phosphate uptake | |||
PEEMBNCF_00904 | 1.8e-148 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
PEEMBNCF_00905 | 1.1e-79 | S | VIT family | |||
PEEMBNCF_00906 | 2.1e-83 | S | membrane | |||
PEEMBNCF_00907 | 1.6e-258 | treB | G | phosphotransferase system | ||
PEEMBNCF_00908 | 4.8e-83 | treR | K | UTRA | ||
PEEMBNCF_00909 | 9.8e-184 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
PEEMBNCF_00910 | 5.2e-13 | res | L | Helicase C-terminal domain protein | ||
PEEMBNCF_00911 | 5.6e-117 | L | AAA domain | |||
PEEMBNCF_00912 | 3.7e-85 | |||||
PEEMBNCF_00913 | 4.7e-140 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
PEEMBNCF_00914 | 3.2e-231 | S | Virulence-associated protein E | |||
PEEMBNCF_00915 | 6.7e-111 | ecfA2 | 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 | |
PEEMBNCF_00916 | 1.8e-100 | 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 | ||
PEEMBNCF_00917 | 4.8e-53 | rplQ | J | Ribosomal protein L17 | ||
PEEMBNCF_00918 | 1.3e-155 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
PEEMBNCF_00919 | 1.5e-46 | 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 | ||
PEEMBNCF_00920 | 2.3e-15 | steT | E | amino acid | ||
PEEMBNCF_00921 | 6.5e-21 | K | Acetyltransferase (GNAT) domain | |||
PEEMBNCF_00922 | 5.5e-146 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
PEEMBNCF_00923 | 2.6e-54 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
PEEMBNCF_00924 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
PEEMBNCF_00925 | 7.4e-23 | pilD | 3.4.23.43 | NOU | aspartic-type endopeptidase activity | |
PEEMBNCF_00926 | 1.4e-198 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
PEEMBNCF_00927 | 1e-279 | 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 | |
PEEMBNCF_00928 | 2.6e-151 | V | RRXRR protein | |||
PEEMBNCF_00929 | 3.8e-102 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
PEEMBNCF_00930 | 3.9e-34 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
PEEMBNCF_00931 | 4.3e-54 | queT | S | QueT transporter | ||
PEEMBNCF_00934 | 1.4e-08 | S | peptidoglycan catabolic process | |||
PEEMBNCF_00937 | 8.2e-54 | S | Phage tail assembly chaperone proteins, TAC | |||
PEEMBNCF_00938 | 2.3e-78 | S | Phage tail tube protein | |||
PEEMBNCF_00939 | 8e-206 | ynbB | 4.4.1.1 | P | aluminum resistance | |
PEEMBNCF_00940 | 1.3e-45 | glnR | K | Transcriptional regulator | ||
PEEMBNCF_00941 | 9.8e-42 | glnA | 6.3.1.2 | E | glutamine synthetase | |
PEEMBNCF_00942 | 1.7e-174 | glnA | 6.3.1.2 | E | glutamine synthetase | |
PEEMBNCF_00944 | 2.2e-32 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
PEEMBNCF_00945 | 3.6e-14 | |||||
PEEMBNCF_00946 | 5.5e-146 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
PEEMBNCF_00947 | 3.4e-39 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
PEEMBNCF_00948 | 4.1e-31 | XK27_09615 | S | reductase | ||
PEEMBNCF_00949 | 1.8e-82 | pncA | Q | isochorismatase | ||
PEEMBNCF_00950 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
PEEMBNCF_00951 | 2.8e-103 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
PEEMBNCF_00952 | 2.6e-44 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
PEEMBNCF_00953 | 1.9e-67 | XK27_09620 | S | NADPH-dependent FMN reductase | ||
PEEMBNCF_00954 | 2.1e-96 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
PEEMBNCF_00955 | 9e-61 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
PEEMBNCF_00956 | 5.5e-109 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
PEEMBNCF_00957 | 2.3e-102 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
PEEMBNCF_00958 | 2.7e-125 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
PEEMBNCF_00959 | 3.5e-165 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
PEEMBNCF_00960 | 2e-83 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
PEEMBNCF_00961 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
PEEMBNCF_00962 | 5.5e-29 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
PEEMBNCF_00963 | 4.6e-99 | 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 | |
PEEMBNCF_00964 | 1.7e-153 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
PEEMBNCF_00965 | 1.9e-90 | stp | 3.1.3.16 | T | phosphatase | |
PEEMBNCF_00966 | 1.7e-81 | L | Probable transposase | |||
PEEMBNCF_00967 | 1.2e-28 | adhR | K | helix_turn_helix, mercury resistance | ||
PEEMBNCF_00968 | 3.2e-137 | purR | 2.4.2.7 | F | pur operon repressor | |
PEEMBNCF_00969 | 5.9e-111 | galR | K | Transcriptional regulator | ||
PEEMBNCF_00970 | 8.9e-289 | lacS | G | Transporter | ||
PEEMBNCF_00972 | 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 | |
PEEMBNCF_00973 | 6.5e-158 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
PEEMBNCF_00974 | 6.9e-92 | yueF | S | AI-2E family transporter | ||
PEEMBNCF_00975 | 1e-24 | ygaC | J | Belongs to the UPF0374 family | ||
PEEMBNCF_00976 | 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 | ||
PEEMBNCF_00977 | 6.3e-53 | 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 | ||
PEEMBNCF_00978 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
PEEMBNCF_00979 | 1.6e-55 | ctsR | K | Belongs to the CtsR family | ||
PEEMBNCF_00980 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
PEEMBNCF_00981 | 1.1e-71 | ywlG | S | Belongs to the UPF0340 family | ||
PEEMBNCF_00982 | 6.7e-12 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
PEEMBNCF_00983 | 9.1e-196 | tetP | J | elongation factor G | ||
PEEMBNCF_00984 | 1.7e-121 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
PEEMBNCF_00985 | 1.2e-56 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
PEEMBNCF_00986 | 2.2e-26 | ydiI | Q | Thioesterase superfamily | ||
PEEMBNCF_00987 | 1.5e-144 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
PEEMBNCF_00988 | 5.2e-15 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
PEEMBNCF_00989 | 5e-100 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
PEEMBNCF_00990 | 2.6e-97 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
PEEMBNCF_00991 | 1.8e-15 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
PEEMBNCF_00992 | 2.4e-39 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
PEEMBNCF_00993 | 4.1e-58 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
PEEMBNCF_00994 | 3.6e-79 | dnaB | L | replication initiation and membrane attachment | ||
PEEMBNCF_00995 | 9.7e-108 | dnaI | L | Primosomal protein DnaI | ||
PEEMBNCF_00996 | 8.1e-164 | yjjP | S | Putative threonine/serine exporter | ||
PEEMBNCF_00997 | 3.1e-69 | 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
PEEMBNCF_00998 | 5e-42 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
PEEMBNCF_00999 | 2.3e-63 | srtA | 3.4.22.70 | M | sortase family | |
PEEMBNCF_01000 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
PEEMBNCF_01001 | 2.2e-294 | yeeA | V | Type II restriction enzyme, methylase subunits | ||
PEEMBNCF_01002 | 3.7e-51 | |||||
PEEMBNCF_01003 | 1.1e-112 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
PEEMBNCF_01004 | 8.7e-133 | 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 | ||
PEEMBNCF_01005 | 1.6e-26 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
PEEMBNCF_01006 | 4.1e-08 | KT | PspC domain protein | |||
PEEMBNCF_01007 | 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 | ||
PEEMBNCF_01008 | 2.1e-226 | pipD | E | Dipeptidase | ||
PEEMBNCF_01009 | 1.4e-21 | K | helix_turn_helix multiple antibiotic resistance protein | |||
PEEMBNCF_01010 | 9e-157 | EGP | Major facilitator Superfamily | |||
PEEMBNCF_01011 | 1.1e-08 | yeaZ | 2.3.1.234 | O | PFAM Peptidase M22, glycoprotease | |
PEEMBNCF_01012 | 4.3e-28 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
PEEMBNCF_01013 | 3.8e-161 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
PEEMBNCF_01014 | 6.7e-188 | uup | S | ABC transporter, ATP-binding protein | ||
PEEMBNCF_01015 | 3.8e-62 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
PEEMBNCF_01016 | 2.8e-24 | relB | L | RelB antitoxin | ||
PEEMBNCF_01017 | 8.3e-172 | S | Putative peptidoglycan binding domain | |||
PEEMBNCF_01018 | 1.2e-31 | K | Transcriptional regulator, MarR family | |||
PEEMBNCF_01019 | 1.2e-60 | ubiG | 2.1.1.265 | H | Methyltransferase domain | |
PEEMBNCF_01020 | 3.5e-24 | K | Helix-turn-helix XRE-family like proteins | |||
PEEMBNCF_01021 | 6.8e-77 | XK27_02480 | EGP | Major Facilitator Superfamily | ||
PEEMBNCF_01022 | 4.9e-246 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
PEEMBNCF_01023 | 1.1e-27 | S | Protein of unknown function (DUF3290) | |||
PEEMBNCF_01025 | 4.9e-49 | yviA | S | Protein of unknown function (DUF421) | ||
PEEMBNCF_01026 | 1.7e-248 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
PEEMBNCF_01027 | 3.3e-127 | mleP | S | Sodium Bile acid symporter family | ||
PEEMBNCF_01028 | 9.5e-234 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
PEEMBNCF_01029 | 2.3e-128 | 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) | |
PEEMBNCF_01030 | 1.5e-155 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
PEEMBNCF_01031 | 4.2e-29 | |||||
PEEMBNCF_01032 | 5.3e-246 | yjbQ | P | TrkA C-terminal domain protein | ||
PEEMBNCF_01033 | 3.6e-137 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
PEEMBNCF_01034 | 1.7e-54 | rplI | J | Binds to the 23S rRNA | ||
PEEMBNCF_01035 | 8.8e-206 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
PEEMBNCF_01036 | 3.9e-73 | S | DNA primase | |||
PEEMBNCF_01037 | 2.3e-92 | L | Transposase, IS605 OrfB family | |||
PEEMBNCF_01038 | 1e-54 | tlpA2 | L | Transposase IS200 like | ||
PEEMBNCF_01039 | 3.2e-62 | XK27_08315 | M | Sulfatase | ||
PEEMBNCF_01042 | 7.1e-167 | mdtG | EGP | Major facilitator Superfamily | ||
PEEMBNCF_01043 | 2.5e-15 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
PEEMBNCF_01044 | 0.0 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
PEEMBNCF_01045 | 5.4e-234 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
PEEMBNCF_01047 | 1.6e-12 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
PEEMBNCF_01048 | 9.7e-231 | V | ABC transporter transmembrane region | |||
PEEMBNCF_01049 | 1.6e-106 | yxeH | S | hydrolase | ||
PEEMBNCF_01050 | 1.6e-147 | 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 | ||
PEEMBNCF_01051 | 1.1e-83 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
PEEMBNCF_01052 | 2.9e-79 | ylbE | GM | NAD dependent epimerase dehydratase family protein | ||
PEEMBNCF_01053 | 5.7e-126 | rapZ | S | Displays ATPase and GTPase activities | ||
PEEMBNCF_01055 | 1e-285 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
PEEMBNCF_01056 | 7.9e-31 | drgA | C | Nitroreductase | ||
PEEMBNCF_01057 | 6.7e-84 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
PEEMBNCF_01058 | 2.9e-106 | fadB4 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
PEEMBNCF_01059 | 5.4e-94 | npr | 1.11.1.1 | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | |
PEEMBNCF_01063 | 3e-17 | yvaO | K | Helix-turn-helix XRE-family like proteins | ||
PEEMBNCF_01064 | 3.2e-15 | S | Pfam:DUF955 | |||
PEEMBNCF_01065 | 1.6e-33 | |||||
PEEMBNCF_01066 | 1.4e-120 | scrB | 3.2.1.26 | GH32 | G | invertase |
PEEMBNCF_01067 | 8e-282 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
PEEMBNCF_01068 | 1.6e-114 | ntpJ | P | Potassium uptake protein | ||
PEEMBNCF_01069 | 2.2e-58 | ktrA | P | TrkA-N domain | ||
PEEMBNCF_01070 | 5.7e-54 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
PEEMBNCF_01072 | 4.7e-178 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
PEEMBNCF_01073 | 1.3e-166 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
PEEMBNCF_01074 | 2.2e-91 | smc | D | Required for chromosome condensation and partitioning | ||
PEEMBNCF_01075 | 6.9e-149 | 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) | ||
PEEMBNCF_01076 | 7e-40 | 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 | ||
PEEMBNCF_01077 | 2.6e-80 | 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 | |
PEEMBNCF_01078 | 6.1e-230 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
PEEMBNCF_01079 | 2.7e-148 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
PEEMBNCF_01080 | 1.9e-115 | manY | G | PTS system | ||
PEEMBNCF_01081 | 8.6e-141 | manN | G | system, mannose fructose sorbose family IID component | ||
PEEMBNCF_01082 | 2.7e-79 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
PEEMBNCF_01091 | 2.4e-130 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
PEEMBNCF_01092 | 1.6e-249 | yhgF | K | Tex-like protein N-terminal domain protein | ||
PEEMBNCF_01093 | 3.3e-99 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
PEEMBNCF_01094 | 3.4e-44 | tdk | 2.7.1.21 | F | thymidine kinase | |
PEEMBNCF_01095 | 1e-177 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
PEEMBNCF_01096 | 1.4e-89 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
PEEMBNCF_01097 | 7.2e-36 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
PEEMBNCF_01098 | 4.1e-74 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
PEEMBNCF_01099 | 1.1e-160 | adhB | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
PEEMBNCF_01100 | 9.8e-57 | 3.1.3.48 | K | Transcriptional regulator | ||
PEEMBNCF_01101 | 9.6e-126 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
PEEMBNCF_01102 | 2.6e-78 | 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 | |
PEEMBNCF_01103 | 3.3e-83 | 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 | |
PEEMBNCF_01104 | 1.1e-36 | dnaD | L | DnaD domain protein | ||
PEEMBNCF_01105 | 1.2e-127 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
PEEMBNCF_01106 | 3.1e-122 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
PEEMBNCF_01107 | 7.1e-40 | hsdM | 2.1.1.72 | V | HsdM N-terminal domain | |
PEEMBNCF_01108 | 2.9e-138 | L | Belongs to the 'phage' integrase family | |||
PEEMBNCF_01109 | 7.3e-31 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
PEEMBNCF_01110 | 7.1e-40 | hsdM | 2.1.1.72 | V | HsdM N-terminal domain | |
PEEMBNCF_01111 | 1.9e-191 | res | 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
PEEMBNCF_01112 | 2.7e-30 | |||||
PEEMBNCF_01113 | 1.1e-162 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
PEEMBNCF_01114 | 4.1e-75 | azlC | E | AzlC protein | ||
PEEMBNCF_01115 | 1.3e-38 | azlD | S | branched-chain amino acid | ||
PEEMBNCF_01116 | 5.6e-67 | I | alpha/beta hydrolase fold | |||
PEEMBNCF_01117 | 6.8e-25 | |||||
PEEMBNCF_01118 | 4e-61 | L | Helicase C-terminal domain protein | |||
PEEMBNCF_01119 | 1.9e-251 | 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 | |
PEEMBNCF_01120 | 1.7e-87 | yfnA | E | Amino Acid | ||
PEEMBNCF_01122 | 3.7e-17 | |||||
PEEMBNCF_01123 | 9.1e-55 | |||||
PEEMBNCF_01124 | 1.5e-109 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
PEEMBNCF_01127 | 4.9e-09 | S | CAAX protease self-immunity | |||
PEEMBNCF_01128 | 2.5e-32 | oatA | I | Acyltransferase | ||
PEEMBNCF_01129 | 1.4e-16 | |||||
PEEMBNCF_01131 | 1.5e-140 | 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 | |
PEEMBNCF_01132 | 5.8e-101 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
PEEMBNCF_01133 | 6.8e-90 | mtlR | K | Mga helix-turn-helix domain | ||
PEEMBNCF_01134 | 2.3e-302 | 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 | |
PEEMBNCF_01135 | 3.3e-230 | 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 | |
PEEMBNCF_01136 | 4.5e-225 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
PEEMBNCF_01137 | 2.3e-196 | EGP | Major Facilitator Superfamily | |||
PEEMBNCF_01138 | 2.3e-29 | S | Domain of unknown function (DUF4811) | |||
PEEMBNCF_01139 | 1.8e-50 | L | Replication protein | |||
PEEMBNCF_01141 | 4.3e-96 | S | PFAM Archaeal ATPase | |||
PEEMBNCF_01142 | 4.5e-151 | mepA | V | MATE efflux family protein | ||
PEEMBNCF_01144 | 2.9e-85 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
PEEMBNCF_01145 | 5.9e-129 | mleP2 | S | Sodium Bile acid symporter family | ||
PEEMBNCF_01146 | 1.7e-115 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
PEEMBNCF_01148 | 3.5e-220 | gdhA | 1.4.1.4 | E | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase | |
PEEMBNCF_01149 | 2.8e-102 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
PEEMBNCF_01150 | 9.2e-180 | clcA | P | chloride | ||
PEEMBNCF_01151 | 2.8e-19 | secG | U | Preprotein translocase | ||
PEEMBNCF_01152 | 7.4e-80 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
PEEMBNCF_01153 | 1e-160 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
PEEMBNCF_01154 | 1.2e-155 | mprF | 2.3.2.3 | 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 | |
PEEMBNCF_01155 | 6.1e-70 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
PEEMBNCF_01156 | 1.3e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
PEEMBNCF_01157 | 3e-258 | 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 | ||
PEEMBNCF_01158 | 5e-43 | 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 | |
PEEMBNCF_01159 | 1.1e-135 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
PEEMBNCF_01160 | 1.6e-23 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
PEEMBNCF_01161 | 2.9e-120 | 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 | ||
PEEMBNCF_01162 | 1.1e-10 | |||||
PEEMBNCF_01164 | 7.5e-43 | srtB | 3.4.22.70 | S | Sortase family | |
PEEMBNCF_01165 | 1.6e-29 | 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 | ||
PEEMBNCF_01166 | 2.4e-45 | yqhY | S | Asp23 family, cell envelope-related function | ||
PEEMBNCF_01167 | 1.4e-36 | 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 | ||
PEEMBNCF_01168 | 5.1e-103 | 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 | |
PEEMBNCF_01169 | 1.2e-295 | ydaO | E | amino acid | ||
PEEMBNCF_01170 | 1.9e-53 | yutD | S | Protein of unknown function (DUF1027) | ||
PEEMBNCF_01171 | 3.9e-57 | S | Calcineurin-like phosphoesterase | |||
PEEMBNCF_01172 | 2.6e-158 | cycA | E | Amino acid permease | ||
PEEMBNCF_01173 | 2.3e-93 | L | AAA ATPase domain | |||
PEEMBNCF_01174 | 1.2e-29 | 3.6.4.12 | L | UvrD/REP helicase N-terminal domain | ||
PEEMBNCF_01175 | 3.4e-68 | rodA | D | Belongs to the SEDS family | ||
PEEMBNCF_01176 | 4.6e-26 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
PEEMBNCF_01177 | 9.5e-94 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
PEEMBNCF_01178 | 1.1e-102 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
PEEMBNCF_01179 | 2.5e-21 | 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 | |
PEEMBNCF_01180 | 1.1e-22 | ykzG | S | Belongs to the UPF0356 family | ||
PEEMBNCF_01181 | 1.6e-299 | 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 | ||
PEEMBNCF_01182 | 4.3e-18 | |||||
PEEMBNCF_01183 | 7.4e-08 | yfiE | K | LysR family | ||
PEEMBNCF_01184 | 1.5e-76 | |||||
PEEMBNCF_01185 | 1.8e-76 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
PEEMBNCF_01186 | 5.6e-45 | K | Copper transport repressor CopY TcrY | |||
PEEMBNCF_01187 | 3.6e-156 | mreB | D | cell shape determining protein MreB | ||
PEEMBNCF_01188 | 2.6e-21 | K | Cold shock | |||
PEEMBNCF_01189 | 6.2e-80 | radC | L | DNA repair protein | ||
PEEMBNCF_01190 | 2.6e-23 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
PEEMBNCF_01191 | 6.7e-29 | frdC | 1.3.5.4 | C | FAD binding domain | |
PEEMBNCF_01192 | 2.5e-237 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
PEEMBNCF_01193 | 5.7e-14 | ybaN | S | Protein of unknown function (DUF454) | ||
PEEMBNCF_01194 | 1.7e-31 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
PEEMBNCF_01195 | 6.3e-51 | 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 | |
PEEMBNCF_01196 | 2.3e-87 | S | Alpha beta hydrolase | |||
PEEMBNCF_01197 | 1.2e-43 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
PEEMBNCF_01198 | 1.9e-81 | V | MatE | |||
PEEMBNCF_01199 | 5.2e-53 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
PEEMBNCF_01200 | 6.4e-19 | N | HicA toxin of bacterial toxin-antitoxin, | |||
PEEMBNCF_01201 | 1.2e-31 | arpU | S | Phage transcriptional regulator, ArpU family | ||
PEEMBNCF_01206 | 4.9e-136 | EG | EamA-like transporter family | |||
PEEMBNCF_01207 | 1.2e-72 | alkD | L | DNA alkylation repair enzyme | ||
PEEMBNCF_01208 | 3.8e-127 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
PEEMBNCF_01210 | 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 | ||
PEEMBNCF_01211 | 1.6e-47 | 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 | ||
PEEMBNCF_01212 | 2e-62 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
PEEMBNCF_01213 | 1e-109 | puuD | S | peptidase C26 | ||
PEEMBNCF_01214 | 1.4e-83 | 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 | |
PEEMBNCF_01215 | 1.4e-13 | |||||
PEEMBNCF_01216 | 1e-200 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
PEEMBNCF_01218 | 8.1e-33 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
PEEMBNCF_01219 | 2.3e-89 | 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) | |
PEEMBNCF_01220 | 9.8e-135 | K | Transcriptional regulator | |||
PEEMBNCF_01221 | 3.2e-53 | zur | P | Belongs to the Fur family | ||
PEEMBNCF_01222 | 3.1e-09 | 3.2.1.14 | GH18 | |||
PEEMBNCF_01223 | 2e-105 | |||||
PEEMBNCF_01224 | 3.1e-35 | ruvB | 3.6.4.12 | L | four-way junction helicase activity | |
PEEMBNCF_01225 | 3.5e-218 | yifK | E | Amino acid permease | ||
PEEMBNCF_01227 | 4.2e-15 | yxaM | EGP | Major Facilitator Superfamily | ||
PEEMBNCF_01229 | 1.8e-37 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
PEEMBNCF_01230 | 2e-69 | S | RRXRR protein | |||
PEEMBNCF_01231 | 6.5e-73 | S | Domain of unknown function (DUF3841) | |||
PEEMBNCF_01232 | 2.9e-08 | cdd | 2.4.2.4, 3.5.4.5 | J | Acetyltransferase (GNAT) domain | |
PEEMBNCF_01233 | 3.2e-38 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
PEEMBNCF_01234 | 2.8e-102 | S | Domain of unknown function (DUF4343) | |||
PEEMBNCF_01235 | 3.7e-57 | pstS | P | T5orf172 | ||
PEEMBNCF_01236 | 2.3e-159 | 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 | ||
PEEMBNCF_01237 | 8e-43 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
PEEMBNCF_01238 | 1.5e-32 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
PEEMBNCF_01239 | 2.7e-70 | metI | P | ABC transporter permease | ||
PEEMBNCF_01240 | 2.6e-149 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
PEEMBNCF_01241 | 2.7e-75 | ykuT | M | mechanosensitive ion channel | ||
PEEMBNCF_01242 | 2.4e-177 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
PEEMBNCF_01243 | 1.7e-23 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
PEEMBNCF_01244 | 7.2e-57 | 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 | ||
PEEMBNCF_01245 | 1.1e-26 | ylqC | S | Belongs to the UPF0109 family | ||
PEEMBNCF_01246 | 3.6e-42 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
PEEMBNCF_01247 | 5.7e-84 | 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 | |
PEEMBNCF_01248 | 7.8e-118 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
PEEMBNCF_01249 | 1.5e-127 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
PEEMBNCF_01250 | 1.3e-47 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
PEEMBNCF_01251 | 1.7e-108 | S | Acyltransferase family | |||
PEEMBNCF_01252 | 2.2e-86 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
PEEMBNCF_01253 | 3.5e-100 | S | interspecies interaction between organisms | |||
PEEMBNCF_01254 | 1.2e-207 | G | glycerol-3-phosphate transporter | |||
PEEMBNCF_01255 | 6.3e-174 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
PEEMBNCF_01256 | 7.5e-101 | 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 | ||
PEEMBNCF_01257 | 6.9e-25 | yueI | S | Protein of unknown function (DUF1694) | ||
PEEMBNCF_01258 | 1.4e-218 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
PEEMBNCF_01259 | 3.8e-70 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
PEEMBNCF_01260 | 2.8e-32 | |||||
PEEMBNCF_01261 | 1.3e-178 | helD | 3.6.4.12 | L | DNA helicase | |
PEEMBNCF_01263 | 5.9e-74 | htpX | O | Belongs to the peptidase M48B family | ||
PEEMBNCF_01264 | 2.3e-163 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
PEEMBNCF_01265 | 5.4e-126 | 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) | |
PEEMBNCF_01266 | 4.6e-25 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
PEEMBNCF_01267 | 1.5e-277 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
PEEMBNCF_01268 | 9.4e-113 | rssA | S | Phospholipase, patatin family | ||
PEEMBNCF_01269 | 8.2e-16 | |||||
PEEMBNCF_01271 | 6e-81 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
PEEMBNCF_01272 | 4.3e-38 | comFC | S | Competence protein | ||
PEEMBNCF_01274 | 1.8e-85 | sip | L | Belongs to the 'phage' integrase family | ||
PEEMBNCF_01275 | 2.6e-119 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PEEMBNCF_01276 | 1.5e-31 | |||||
PEEMBNCF_01277 | 1.8e-254 | E | Amino acid permease | |||
PEEMBNCF_01278 | 2.8e-41 | cadA | P | P-type ATPase | ||
PEEMBNCF_01279 | 1.7e-23 | yktA | S | Belongs to the UPF0223 family | ||
PEEMBNCF_01280 | 3.1e-31 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
PEEMBNCF_01281 | 2.4e-85 | 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 | |
PEEMBNCF_01283 | 4.4e-41 | wecD | K | Acetyltransferase GNAT Family | ||
PEEMBNCF_01284 | 3.9e-47 | hmpT | S | ECF-type riboflavin transporter, S component | ||
PEEMBNCF_01285 | 7e-27 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
PEEMBNCF_01286 | 2.7e-66 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
PEEMBNCF_01287 | 1.1e-292 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
PEEMBNCF_01288 | 1.3e-15 | |||||
PEEMBNCF_01289 | 1.2e-94 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
PEEMBNCF_01290 | 1.1e-60 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
PEEMBNCF_01291 | 5.5e-77 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
PEEMBNCF_01292 | 1.9e-125 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
PEEMBNCF_01293 | 4.6e-48 | 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 | ||
PEEMBNCF_01294 | 3.5e-231 | 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) | |
PEEMBNCF_01295 | 6.2e-49 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
PEEMBNCF_01296 | 2.3e-107 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
PEEMBNCF_01298 | 3.4e-92 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
PEEMBNCF_01299 | 7.6e-36 | |||||
PEEMBNCF_01300 | 2.1e-56 | ygaC | J | Belongs to the UPF0374 family | ||
PEEMBNCF_01301 | 1.1e-192 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
PEEMBNCF_01302 | 5.7e-14 | S | HNH endonuclease | |||
PEEMBNCF_01303 | 8.5e-59 | L | Belongs to the 'phage' integrase family | |||
PEEMBNCF_01305 | 7.4e-81 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
PEEMBNCF_01306 | 7.6e-236 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
PEEMBNCF_01307 | 2.3e-45 | coiA | 3.6.4.12 | S | Competence protein | |
PEEMBNCF_01308 | 2.4e-166 | pepF | E | oligoendopeptidase F | ||
PEEMBNCF_01309 | 1.2e-181 | XK27_06780 | V | ABC transporter permease | ||
PEEMBNCF_01310 | 2.4e-190 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
PEEMBNCF_01311 | 1.4e-53 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
PEEMBNCF_01312 | 6.6e-49 | argR | K | Regulates arginine biosynthesis genes | ||
PEEMBNCF_01313 | 3.8e-78 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
PEEMBNCF_01314 | 2.2e-26 | |||||
PEEMBNCF_01315 | 8.1e-49 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
PEEMBNCF_01316 | 2.7e-138 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
PEEMBNCF_01317 | 3.3e-140 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
PEEMBNCF_01318 | 2.5e-11 | ftsL | D | cell division protein FtsL | ||
PEEMBNCF_01319 | 8.8e-175 | rgpAc | GT4 | M | Domain of unknown function (DUF1972) | |
PEEMBNCF_01322 | 2.6e-101 | hrtB | V | ABC transporter permease | ||
PEEMBNCF_01323 | 4.6e-35 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
PEEMBNCF_01324 | 3.9e-109 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
PEEMBNCF_01325 | 2e-138 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
PEEMBNCF_01326 | 7.6e-41 | trxA | O | Belongs to the thioredoxin family | ||
PEEMBNCF_01327 | 1.7e-183 | 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 | ||
PEEMBNCF_01329 | 6.3e-159 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
PEEMBNCF_01330 | 2.6e-18 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
PEEMBNCF_01331 | 5.3e-65 | |||||
PEEMBNCF_01332 | 3e-19 | yggT | S | YGGT family | ||
PEEMBNCF_01333 | 1e-81 | ylmH | S | S4 domain protein | ||
PEEMBNCF_01334 | 5.1e-62 | divIVA | D | DivIVA domain protein | ||
PEEMBNCF_01335 | 2e-70 | S | Protein of unknown function (DUF1361) | |||
PEEMBNCF_01336 | 4e-114 | 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 | |
PEEMBNCF_01339 | 1.9e-08 | 2.3.1.19 | K | Cro/C1-type HTH DNA-binding domain | ||
PEEMBNCF_01343 | 1.6e-14 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
PEEMBNCF_01344 | 6.9e-16 | S | Putative adhesin | |||
PEEMBNCF_01345 | 1.3e-16 | pspC | KT | PspC domain | ||
PEEMBNCF_01347 | 3.9e-13 | S | Enterocin A Immunity | |||
PEEMBNCF_01348 | 3.2e-95 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
PEEMBNCF_01349 | 3.7e-117 | ylbL | T | Belongs to the peptidase S16 family | ||
PEEMBNCF_01350 | 3e-125 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
PEEMBNCF_01351 | 2.3e-43 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
PEEMBNCF_01352 | 3.2e-60 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
PEEMBNCF_01353 | 2.5e-07 | |||||
PEEMBNCF_01354 | 4.3e-57 | S | Hypothetical protein (DUF2513) | |||
PEEMBNCF_01355 | 3.3e-176 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
PEEMBNCF_01356 | 2.2e-07 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
PEEMBNCF_01357 | 7.9e-229 | aha1 | P | TIGRFAM ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
PEEMBNCF_01358 | 5.4e-107 | G | PTS system sorbose-specific iic component | |||
PEEMBNCF_01359 | 2e-64 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
PEEMBNCF_01360 | 4e-38 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
PEEMBNCF_01361 | 2.5e-61 | phaJ | I | N-terminal half of MaoC dehydratase | ||
PEEMBNCF_01362 | 8.7e-69 | ybhL | S | Belongs to the BI1 family | ||
PEEMBNCF_01363 | 4.9e-82 | lytH | 3.5.1.28 | M | Ami_3 | |
PEEMBNCF_01364 | 3.5e-35 | 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 | |
PEEMBNCF_01365 | 7e-79 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
PEEMBNCF_01366 | 7.8e-218 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
PEEMBNCF_01367 | 5.5e-149 | T | PhoQ Sensor | |||
PEEMBNCF_01368 | 1.7e-62 | lmrP | E | Major Facilitator Superfamily | ||
PEEMBNCF_01369 | 9e-98 | S | Bacterial membrane protein, YfhO | |||
PEEMBNCF_01370 | 3.6e-24 | yozE | S | Belongs to the UPF0346 family | ||
PEEMBNCF_01371 | 3e-54 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
PEEMBNCF_01372 | 3.5e-81 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
PEEMBNCF_01373 | 2.8e-220 | yeeB | L | DEAD-like helicases superfamily | ||
PEEMBNCF_01374 | 4.1e-34 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
PEEMBNCF_01375 | 6.1e-103 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
PEEMBNCF_01376 | 3.4e-27 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
PEEMBNCF_01377 | 7.5e-72 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
PEEMBNCF_01378 | 2.3e-120 | ytbE | S | reductase | ||
PEEMBNCF_01379 | 9.9e-99 | M | Exporter of polyketide antibiotics | |||
PEEMBNCF_01380 | 1.1e-100 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
PEEMBNCF_01381 | 1.7e-236 | 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 | |
PEEMBNCF_01382 | 3e-48 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
PEEMBNCF_01383 | 3.5e-66 | 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 | ||
PEEMBNCF_01384 | 2e-202 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
PEEMBNCF_01386 | 4.4e-81 | sip | L | Belongs to the 'phage' integrase family | ||
PEEMBNCF_01387 | 3.4e-48 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
PEEMBNCF_01388 | 1.4e-13 | |||||
PEEMBNCF_01389 | 7e-145 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
PEEMBNCF_01390 | 3.4e-22 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
PEEMBNCF_01391 | 1.1e-45 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
PEEMBNCF_01393 | 4.8e-219 | res | L | Helicase C-terminal domain protein | ||
PEEMBNCF_01394 | 4.7e-74 | S | Siphovirus Gp157 | |||
PEEMBNCF_01395 | 6.5e-14 | yfjM | S | Protein of unknown function DUF262 | ||
PEEMBNCF_01396 | 8.6e-40 | yfjM | S | Protein of unknown function DUF262 | ||
PEEMBNCF_01397 | 5.2e-143 | yfjM | S | Protein of unknown function DUF262 | ||
PEEMBNCF_01398 | 4.7e-107 | asp2 | 3.4.11.5 | S | Accessory Sec system protein Asp2 | |
PEEMBNCF_01399 | 4.8e-130 | 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 | ||
PEEMBNCF_01400 | 2.5e-213 | ltrA_1 | 2.7.7.49 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |
PEEMBNCF_01401 | 3.4e-83 | qorB | 1.6.5.2 | GM | NmrA-like family | |
PEEMBNCF_01402 | 1.6e-39 | K | Transcriptional regulator | |||
PEEMBNCF_01403 | 2.1e-149 | lsa | S | ABC transporter | ||
PEEMBNCF_01404 | 1.7e-105 | 2.7.7.73, 2.7.7.80 | H | Involved in molybdopterin and thiamine biosynthesis, family 2 | ||
PEEMBNCF_01405 | 5.5e-244 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
PEEMBNCF_01406 | 6.4e-55 | L | phosphatase homologous to the C-terminal domain of histone macroH2A1 | |||
PEEMBNCF_01407 | 1.4e-168 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
PEEMBNCF_01408 | 1.3e-105 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
PEEMBNCF_01409 | 7.5e-18 | ywfO | S | HD domain protein | ||
PEEMBNCF_01410 | 3.4e-88 | S | hydrolase | |||
PEEMBNCF_01411 | 1.3e-22 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
PEEMBNCF_01412 | 3.4e-08 | S | Protein of unknown function (DUF3397) | |||
PEEMBNCF_01413 | 2.7e-155 | dapG | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
PEEMBNCF_01414 | 4.9e-186 | 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 | ||
PEEMBNCF_01415 | 2.5e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
PEEMBNCF_01416 | 4.8e-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 | ||
PEEMBNCF_01417 | 4.4e-107 | 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 | |
PEEMBNCF_01418 | 9.3e-57 | 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 | ||
PEEMBNCF_01419 | 3.9e-67 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
PEEMBNCF_01420 | 1.4e-119 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
PEEMBNCF_01421 | 9.3e-85 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
PEEMBNCF_01422 | 2.5e-39 | KLT | serine threonine protein kinase | |||
PEEMBNCF_01423 | 1.9e-111 | 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 | |
PEEMBNCF_01424 | 2.9e-60 | M | ErfK YbiS YcfS YnhG | |||
PEEMBNCF_01426 | 1.5e-35 | 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 | ||
PEEMBNCF_01427 | 3.5e-228 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
PEEMBNCF_01429 | 8.7e-165 | asnB | 6.3.5.4 | E | Asparagine synthase | |
PEEMBNCF_01430 | 3.3e-61 | yiiE | S | Protein of unknown function (DUF1211) | ||
PEEMBNCF_01431 | 1.7e-66 | pgm3 | G | phosphoglycerate mutase family | ||
PEEMBNCF_01432 | 4.7e-36 | C | Aldo/keto reductase family | |||
PEEMBNCF_01433 | 7.8e-107 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
PEEMBNCF_01434 | 6.5e-37 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
PEEMBNCF_01435 | 6.9e-247 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
PEEMBNCF_01436 | 7.7e-235 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
PEEMBNCF_01439 | 1.8e-53 | 1.14.12.17 | C | Oxidoreductase NAD-binding domain | ||
PEEMBNCF_01442 | 1.8e-23 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
PEEMBNCF_01443 | 2.5e-128 | metQ | M | Belongs to the nlpA lipoprotein family | ||
PEEMBNCF_01444 | 1.3e-35 | metI | U | ABC transporter permease | ||
PEEMBNCF_01445 | 6e-233 | L | Transposase | |||
PEEMBNCF_01446 | 3.1e-22 | K | transcriptional regulator | |||
PEEMBNCF_01447 | 8.9e-92 | KT | Putative sugar diacid recognition | |||
PEEMBNCF_01448 | 3.4e-257 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
PEEMBNCF_01449 | 7e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
PEEMBNCF_01450 | 5.1e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
PEEMBNCF_01451 | 8e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
PEEMBNCF_01452 | 5.9e-18 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
PEEMBNCF_01453 | 2.8e-99 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
PEEMBNCF_01454 | 7e-34 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
PEEMBNCF_01455 | 4.5e-70 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
PEEMBNCF_01456 | 8.4e-99 | IQ | reductase | |||
PEEMBNCF_01457 | 1.7e-147 | scrR | K | helix_turn _helix lactose operon repressor | ||
PEEMBNCF_01458 | 1e-47 | scrB | 3.2.1.26 | GH32 | G | invertase |
PEEMBNCF_01459 | 3.6e-153 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
PEEMBNCF_01460 | 1.1e-25 | |||||
PEEMBNCF_01461 | 2.9e-100 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
PEEMBNCF_01463 | 1.6e-168 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
PEEMBNCF_01464 | 1.3e-73 | 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 | |
PEEMBNCF_01465 | 1.4e-42 | S | Phosphoesterase | |||
PEEMBNCF_01467 | 2.7e-48 | pstA | P | Phosphate transport system permease protein PstA | ||
PEEMBNCF_01468 | 5.5e-110 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
PEEMBNCF_01469 | 1.4e-19 | |||||
PEEMBNCF_01470 | 5.1e-36 | K | helix_turn_helix, arabinose operon control protein | |||
PEEMBNCF_01471 | 1.9e-143 | sufD | O | FeS assembly protein SufD | ||
PEEMBNCF_01472 | 3.4e-41 | sufC | O | FeS assembly ATPase SufC | ||
PEEMBNCF_01473 | 2.6e-44 | G | Bacterial extracellular solute-binding protein | |||
PEEMBNCF_01474 | 3.9e-79 | baeR | K | Bacterial regulatory proteins, luxR family | ||
PEEMBNCF_01475 | 2e-36 | baeS | T | Histidine kinase | ||
PEEMBNCF_01476 | 1.1e-23 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
PEEMBNCF_01477 | 3.5e-151 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
PEEMBNCF_01478 | 2.9e-107 | |||||
PEEMBNCF_01479 | 1.9e-75 | |||||
PEEMBNCF_01480 | 2.8e-12 | mltD | CBM50 | M | Lysin motif | |
PEEMBNCF_01481 | 2.4e-92 | yihY | S | Belongs to the UPF0761 family | ||
PEEMBNCF_01482 | 8.1e-57 | K | transcriptional | |||
PEEMBNCF_01483 | 2.6e-41 | K | Bacterial regulatory proteins, tetR family | |||
PEEMBNCF_01484 | 4.7e-24 | T | Belongs to the universal stress protein A family | |||
PEEMBNCF_01485 | 1.4e-14 | |||||
PEEMBNCF_01486 | 1.3e-102 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PEEMBNCF_01487 | 8.7e-44 | L | Transposase | |||
PEEMBNCF_01488 | 1.8e-46 | yrjD | S | LUD domain | ||
PEEMBNCF_01489 | 3.5e-20 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
PEEMBNCF_01490 | 3.8e-41 | ytgP | S | Polysaccharide biosynthesis protein | ||
PEEMBNCF_01491 | 1.4e-61 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
PEEMBNCF_01492 | 1.1e-12 | 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 | |
PEEMBNCF_01494 | 6.7e-152 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
PEEMBNCF_01495 | 2.6e-192 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
PEEMBNCF_01496 | 7.8e-169 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
PEEMBNCF_01497 | 5.5e-248 | 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 | ||
PEEMBNCF_01498 | 3.1e-179 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
PEEMBNCF_01499 | 4e-120 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
PEEMBNCF_01500 | 4.6e-40 | pfoS | S | Phosphotransferase system, EIIC | ||
PEEMBNCF_01501 | 2.5e-92 | 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 | |
PEEMBNCF_01503 | 4.2e-54 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
PEEMBNCF_01504 | 1.1e-40 | yabR | J | RNA binding | ||
PEEMBNCF_01505 | 2.2e-21 | divIC | D | Septum formation initiator | ||
PEEMBNCF_01506 | 3.6e-31 | yabO | J | S4 domain protein | ||
PEEMBNCF_01508 | 4.9e-41 | nifU | C | SUF system FeS assembly protein, NifU family | ||
PEEMBNCF_01509 | 8.4e-67 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
PEEMBNCF_01510 | 6.8e-74 | L | HNH nucleases | |||
PEEMBNCF_01513 | 2.6e-57 | 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 | |
PEEMBNCF_01514 | 1.5e-38 | |||||
PEEMBNCF_01515 | 2.5e-154 | 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) | |
PEEMBNCF_01516 | 1.3e-36 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
PEEMBNCF_01517 | 1.5e-14 | |||||
PEEMBNCF_01518 | 1.9e-128 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
PEEMBNCF_01520 | 8e-21 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
PEEMBNCF_01521 | 7.3e-56 | macB2 | V | ABC transporter, ATP-binding protein | ||
PEEMBNCF_01522 | 3.1e-16 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
PEEMBNCF_01523 | 7.9e-19 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
PEEMBNCF_01524 | 4.6e-77 | typA | T | GTP-binding protein TypA | ||
PEEMBNCF_01526 | 1.9e-73 | clpB | O | Belongs to the ClpA ClpB family | ||
PEEMBNCF_01527 | 5.6e-42 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
PEEMBNCF_01528 | 2.7e-105 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
PEEMBNCF_01529 | 5.9e-48 | L | Uncharacterised protein family (UPF0236) | |||
PEEMBNCF_01532 | 9.3e-69 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
PEEMBNCF_01533 | 1.8e-100 | 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 | |
PEEMBNCF_01534 | 5.3e-22 | 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 | |
PEEMBNCF_01535 | 6.7e-11 | yfmR | S | ABC transporter, ATP-binding protein | ||
PEEMBNCF_01536 | 4e-216 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
PEEMBNCF_01537 | 4e-59 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
PEEMBNCF_01538 | 1.8e-97 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
PEEMBNCF_01539 | 1.8e-145 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
PEEMBNCF_01540 | 2.5e-67 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
PEEMBNCF_01541 | 5.8e-133 | 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) | |
PEEMBNCF_01542 | 1e-11 | XK27_04120 | S | Putative amino acid metabolism | ||
PEEMBNCF_01543 | 4.3e-203 | 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 | |
PEEMBNCF_01544 | 1.3e-40 | |||||
PEEMBNCF_01545 | 1.9e-35 | K | GNAT family | |||
PEEMBNCF_01546 | 4.3e-19 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
PEEMBNCF_01547 | 4.4e-19 | tag | 3.2.2.20 | L | Methyladenine glycosylase | |
PEEMBNCF_01548 | 3.4e-73 | usp6 | T | universal stress protein | ||
PEEMBNCF_01550 | 1.8e-56 | yqeY | S | YqeY-like protein | ||
PEEMBNCF_01551 | 1.8e-21 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
PEEMBNCF_01553 | 2.1e-95 | trxB2 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
PEEMBNCF_01554 | 5.7e-119 | gla | U | Major intrinsic protein | ||
PEEMBNCF_01555 | 1.6e-36 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
PEEMBNCF_01556 | 6.2e-21 | 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 | |
PEEMBNCF_01558 | 4e-166 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
PEEMBNCF_01559 | 4.5e-121 | pfoS | S | Phosphotransferase system, EIIC | ||
PEEMBNCF_01562 | 8.2e-16 | P | Sodium:sulfate symporter transmembrane region | |||
PEEMBNCF_01563 | 5.1e-08 | XK27_10540 | S | ParE toxin of type II toxin-antitoxin system, parDE | ||
PEEMBNCF_01564 | 1.3e-08 | D | Antitoxin Phd_YefM, type II toxin-antitoxin system | |||
PEEMBNCF_01565 | 3.5e-76 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
PEEMBNCF_01566 | 2.3e-23 | yeaL | S | Protein of unknown function (DUF441) | ||
PEEMBNCF_01567 | 3.6e-39 | cvfB | S | S1 domain | ||
PEEMBNCF_01568 | 2.6e-70 | cvfB | S | S1 domain | ||
PEEMBNCF_01572 | 3.5e-75 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
PEEMBNCF_01573 | 2e-71 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
PEEMBNCF_01574 | 2.3e-173 | 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 | |
PEEMBNCF_01575 | 5.2e-40 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
PEEMBNCF_01576 | 4.7e-81 | S | L,D-transpeptidase catalytic domain | |||
PEEMBNCF_01577 | 1.6e-258 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
PEEMBNCF_01578 | 4.7e-59 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
PEEMBNCF_01579 | 8.8e-23 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | GHMP kinases C terminal | |
PEEMBNCF_01580 | 1.6e-89 | 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 |
PEEMBNCF_01581 | 2e-109 | yjeM | E | Amino Acid | ||
PEEMBNCF_01583 | 1.6e-31 | 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 | ||
PEEMBNCF_01584 | 4.6e-47 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
PEEMBNCF_01585 | 7.2e-100 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
PEEMBNCF_01586 | 1.1e-32 | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
PEEMBNCF_01587 | 9.2e-36 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
PEEMBNCF_01588 | 1.3e-22 | M | domain protein | |||
PEEMBNCF_01589 | 2.7e-147 | arlS | 2.7.13.3 | T | Histidine kinase | |
PEEMBNCF_01590 | 1.7e-31 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
PEEMBNCF_01591 | 6.1e-64 | topB | 5.99.1.2 | L | DNA topoisomerase | |
PEEMBNCF_01596 | 1.1e-35 | 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 | ||
PEEMBNCF_01598 | 1.3e-139 | ansA | 3.5.1.1 | EJ | Asparaginase | |
PEEMBNCF_01599 | 1.4e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
PEEMBNCF_01600 | 6e-54 | ymfF | S | Peptidase M16 inactive domain protein | ||
PEEMBNCF_01605 | 4e-57 | S | CAAX protease self-immunity | |||
PEEMBNCF_01609 | 8.4e-29 | 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 | ||
PEEMBNCF_01610 | 5.3e-32 | M | domain protein | |||
PEEMBNCF_01611 | 2.8e-45 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
PEEMBNCF_01612 | 1.2e-77 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
PEEMBNCF_01613 | 7.1e-88 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
PEEMBNCF_01614 | 7.2e-53 | perR | P | Belongs to the Fur family | ||
PEEMBNCF_01615 | 1.7e-35 | S | LexA-binding, inner membrane-associated putative hydrolase | |||
PEEMBNCF_01616 | 3.1e-105 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
PEEMBNCF_01617 | 3.5e-157 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
PEEMBNCF_01618 | 1.3e-89 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
PEEMBNCF_01619 | 6.4e-114 | degV | S | EDD domain protein, DegV family | ||
PEEMBNCF_01620 | 3.2e-75 | rsmC | 2.1.1.172 | J | Methyltransferase | |
PEEMBNCF_01621 | 3.3e-62 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
PEEMBNCF_01622 | 1e-15 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
PEEMBNCF_01623 | 1.2e-119 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
PEEMBNCF_01624 | 1.1e-47 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
PEEMBNCF_01625 | 1.5e-90 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
PEEMBNCF_01626 | 3.4e-167 | mbl | D | Cell shape determining protein MreB Mrl | ||
PEEMBNCF_01627 | 8.1e-17 | S | AAA ATPase domain | |||
PEEMBNCF_01628 | 1.6e-89 | G | Xylose isomerase-like TIM barrel | |||
PEEMBNCF_01629 | 1.4e-25 | |||||
PEEMBNCF_01631 | 4.2e-66 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
PEEMBNCF_01632 | 1.6e-54 | L | Helix-turn-helix domain | |||
PEEMBNCF_01635 | 6.6e-43 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
PEEMBNCF_01639 | 1.6e-31 | |||||
PEEMBNCF_01640 | 5.9e-83 | S | Uncharacterised protein family (UPF0236) | |||
PEEMBNCF_01641 | 1.5e-167 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
PEEMBNCF_01642 | 1.9e-113 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
PEEMBNCF_01643 | 2.7e-19 | cps3F | ||||
PEEMBNCF_01644 | 2.7e-83 | S | Membrane | |||
PEEMBNCF_01645 | 1.3e-15 | 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 | ||
PEEMBNCF_01646 | 7.2e-82 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
PEEMBNCF_01647 | 1.3e-119 | yxjG | 2.1.1.14 | E | Cobalamin-independent synthase, Catalytic domain | |
PEEMBNCF_01648 | 7.9e-51 | 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 | |
PEEMBNCF_01649 | 2.2e-125 | S | membrane | |||
PEEMBNCF_01651 | 1.6e-161 | 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 | |
PEEMBNCF_01652 | 3.8e-131 | yloV | S | DAK2 domain fusion protein YloV | ||
PEEMBNCF_01653 | 1e-07 | L | Helix-turn-helix domain | |||
PEEMBNCF_01654 | 5.9e-75 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
PEEMBNCF_01655 | 7.1e-35 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
PEEMBNCF_01656 | 7.4e-46 | 3.6.1.27 | I | Acid phosphatase homologues | ||
PEEMBNCF_01661 | 1.6e-116 | ldhA | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
PEEMBNCF_01662 | 2.3e-109 | yedE | S | Sulphur transport | ||
PEEMBNCF_01663 | 1.5e-28 | yedF | O | Belongs to the sulfur carrier protein TusA family | ||
PEEMBNCF_01664 | 2e-53 | K | Transcriptional regulator, LysR family | |||
PEEMBNCF_01665 | 2.7e-29 | EGP | Major Facilitator Superfamily | |||
PEEMBNCF_01666 | 1.6e-145 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
PEEMBNCF_01668 | 1.3e-13 | S | Protein of unknown function (DUF2969) | |||
PEEMBNCF_01670 | 4.9e-09 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
PEEMBNCF_01671 | 4.8e-83 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
PEEMBNCF_01675 | 1.1e-63 | K | response regulator | |||
PEEMBNCF_01677 | 1.3e-41 | yjbH | Q | Thioredoxin | ||
PEEMBNCF_01678 | 1.2e-07 | |||||
PEEMBNCF_01679 | 4.2e-135 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
PEEMBNCF_01680 | 2.6e-178 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
PEEMBNCF_01682 | 2.4e-32 | bcgIB | 2.1.1.72, 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
PEEMBNCF_01683 | 6.4e-116 | 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 | |
PEEMBNCF_01684 | 3.8e-71 | mreC | M | Involved in formation and maintenance of cell shape | ||
PEEMBNCF_01685 | 2.1e-22 | rpmD | J | Ribosomal protein L30 | ||
PEEMBNCF_01686 | 1.3e-82 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
PEEMBNCF_01687 | 2.7e-26 | 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 | ||
PEEMBNCF_01688 | 4.8e-67 | spaB | S | Lantibiotic dehydratase, C terminus | ||
PEEMBNCF_01689 | 6.3e-46 | |||||
PEEMBNCF_01690 | 1.7e-31 | cggR | K | Putative sugar-binding domain | ||
PEEMBNCF_01691 | 3.5e-35 | FbpA | K | Fibronectin-binding protein | ||
PEEMBNCF_01692 | 1.2e-55 | 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 | |
PEEMBNCF_01694 | 8.1e-91 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
PEEMBNCF_01695 | 2.2e-83 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
PEEMBNCF_01696 | 8.7e-43 | blpH | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
PEEMBNCF_01698 | 1.8e-33 | pbuO_1 | S | Permease family | ||
PEEMBNCF_01699 | 2.3e-65 | hly | S | protein, hemolysin III | ||
PEEMBNCF_01700 | 4e-83 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
PEEMBNCF_01701 | 3.7e-84 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
PEEMBNCF_01702 | 4.9e-83 | 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 | |
PEEMBNCF_01703 | 1.5e-44 | O | ATPase family associated with various cellular activities (AAA) | |||
PEEMBNCF_01704 | 7.7e-64 | K | helix_turn_helix, arabinose operon control protein | |||
PEEMBNCF_01705 | 1.5e-14 | epsJ1 | M | Glycosyltransferase like family 2 | ||
PEEMBNCF_01708 | 5.9e-27 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
PEEMBNCF_01709 | 6.3e-98 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
PEEMBNCF_01710 | 4.6e-75 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
PEEMBNCF_01711 | 5.5e-160 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
PEEMBNCF_01712 | 5.9e-141 | 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 | |
PEEMBNCF_01713 | 5.9e-57 | M | Peptidase family M23 | |||
PEEMBNCF_01714 | 1.6e-36 | gutB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
PEEMBNCF_01715 | 4.9e-61 | ybaK | J | Aminoacyl-tRNA editing domain | ||
PEEMBNCF_01718 | 3e-30 | nhaC | C | Na H antiporter NhaC | ||
PEEMBNCF_01720 | 3.7e-19 | corA | P | CorA-like Mg2+ transporter protein | ||
PEEMBNCF_01721 | 1.4e-50 | comEA | L | Competence protein ComEA | ||
PEEMBNCF_01722 | 5.2e-106 | 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 | |
PEEMBNCF_01723 | 1.2e-22 | veg | S | Biofilm formation stimulator VEG | ||
PEEMBNCF_01725 | 1.2e-34 | L | Helicase C-terminal domain protein | |||
PEEMBNCF_01726 | 2.2e-165 | 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 | ||
PEEMBNCF_01729 | 9.3e-19 | helD | 3.6.4.12 | L | DNA helicase | |
PEEMBNCF_01730 | 2.9e-33 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
PEEMBNCF_01732 | 2.4e-77 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
PEEMBNCF_01733 | 5.7e-94 | L | Initiator Replication protein | |||
PEEMBNCF_01734 | 2e-41 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
PEEMBNCF_01735 | 5.4e-44 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
PEEMBNCF_01736 | 1.4e-125 | pbuX | F | xanthine permease | ||
PEEMBNCF_01737 | 1.6e-15 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
PEEMBNCF_01738 | 1.9e-105 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | MucBP domain | |
PEEMBNCF_01739 | 7.4e-53 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
PEEMBNCF_01740 | 1.6e-38 | comEC | S | Competence protein ComEC | ||
PEEMBNCF_01741 | 8.1e-36 | bCE_4747 | S | Beta-lactamase superfamily domain | ||
PEEMBNCF_01742 | 4.9e-53 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
PEEMBNCF_01743 | 3.5e-12 | L | PFAM transposase IS200-family protein | |||
PEEMBNCF_01744 | 3.5e-69 | |||||
PEEMBNCF_01745 | 4.4e-24 | radC | E | Belongs to the UPF0758 family | ||
PEEMBNCF_01746 | 4.9e-54 | yvfS | V | ABC-2 type transporter | ||
PEEMBNCF_01747 | 1e-08 | yvfR | V | ABC transporter | ||
PEEMBNCF_01748 | 2.5e-13 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
PEEMBNCF_01749 | 5.1e-62 | IQ | NAD dependent epimerase/dehydratase family | |||
PEEMBNCF_01750 | 1.3e-59 | G | Bacterial extracellular solute-binding protein | |||
PEEMBNCF_01751 | 3.2e-49 | lytE | M | LysM domain protein | ||
PEEMBNCF_01753 | 5.2e-41 | acmC | 3.2.1.96 | NU | mannosyl-glycoprotein | |
PEEMBNCF_01754 | 1.1e-61 | V | site-specific DNA-methyltransferase (adenine-specific) activity | |||
PEEMBNCF_01757 | 9.8e-66 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
PEEMBNCF_01758 | 2.3e-79 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
PEEMBNCF_01760 | 7e-34 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
PEEMBNCF_01763 | 1.4e-84 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
PEEMBNCF_01764 | 1.2e-44 | S | VIT family | |||
PEEMBNCF_01765 | 3.3e-73 | mutF | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
PEEMBNCF_01766 | 6.7e-20 | U | type IV secretory pathway VirB4 | |||
PEEMBNCF_01768 | 4.3e-21 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
PEEMBNCF_01769 | 1.8e-32 | ywiB | S | Domain of unknown function (DUF1934) | ||
PEEMBNCF_01770 | 6.8e-38 | fhaB | M | Rib/alpha-like repeat | ||
PEEMBNCF_01772 | 9.4e-09 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
PEEMBNCF_01773 | 1.2e-32 | gatD | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | |
PEEMBNCF_01774 | 1.2e-102 | |||||
PEEMBNCF_01775 | 4.2e-08 | V | N-6 DNA Methylase | |||
PEEMBNCF_01780 | 5.1e-08 | |||||
PEEMBNCF_01786 | 1.4e-40 | yphA | GM | NAD dependent epimerase/dehydratase family | ||
PEEMBNCF_01787 | 1.3e-25 | K | Helix-turn-helix domain, rpiR family | |||
PEEMBNCF_01788 | 7.6e-44 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
PEEMBNCF_01789 | 4.7e-09 | M | LysM domain | |||
PEEMBNCF_01791 | 1.1e-31 | dprA | LU | DNA protecting protein DprA | ||
PEEMBNCF_01792 | 1.4e-77 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
PEEMBNCF_01793 | 2.2e-13 | prsA | 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
PEEMBNCF_01794 | 1.3e-88 | nhaC | C | Na H antiporter NhaC | ||
PEEMBNCF_01796 | 1.1e-09 | S | Replication initiator protein A (RepA) N-terminus | |||
PEEMBNCF_01797 | 6.2e-21 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
PEEMBNCF_01802 | 1.4e-43 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
PEEMBNCF_01804 | 8.8e-29 | yjjH | S | Calcineurin-like phosphoesterase | ||
PEEMBNCF_01805 | 1.6e-38 | comEC | S | Competence protein ComEC | ||
PEEMBNCF_01806 | 9.4e-83 | 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 | |
PEEMBNCF_01807 | 4.5e-36 | kdgR | K | FCD domain | ||
PEEMBNCF_01809 | 8.6e-49 | dtpT | U | amino acid peptide transporter | ||
PEEMBNCF_01810 | 5.6e-13 | S | Thioredoxin | |||
PEEMBNCF_01813 | 2e-122 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
PEEMBNCF_01814 | 1.2e-25 | ypaA | S | Protein of unknown function (DUF1304) | ||
PEEMBNCF_01816 | 4.1e-15 | ywzB | S | Protein of unknown function (DUF1146) | ||
PEEMBNCF_01817 | 9e-48 | Z012_02125 | ||||
PEEMBNCF_01819 | 3.1e-40 | K | Transcriptional regulator | |||
PEEMBNCF_01820 | 1.2e-113 | E | Amino acid permease | |||
PEEMBNCF_01821 | 3.7e-90 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
PEEMBNCF_01822 | 3.4e-40 | repE | K | Primase C terminal 1 (PriCT-1) | ||
PEEMBNCF_01823 | 5.3e-45 | sip | L | Belongs to the 'phage' integrase family | ||
PEEMBNCF_01825 | 4.6e-92 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
PEEMBNCF_01826 | 1.6e-80 | trsE | S | COG0433 Predicted ATPase | ||
PEEMBNCF_01829 | 5.1e-92 | dedA | S | SNARE associated Golgi protein | ||
PEEMBNCF_01830 | 8.6e-24 | |||||
PEEMBNCF_01831 | 4.9e-80 | ywfO | S | HD domain protein | ||
PEEMBNCF_01832 | 1.6e-92 | fbp | 3.1.3.11 | G | phosphatase activity | |
PEEMBNCF_01833 | 8.8e-90 | KT | Transcriptional regulatory protein, C terminal | |||
PEEMBNCF_01834 | 9.3e-08 | S | Uncharacterised protein family (UPF0236) | |||
PEEMBNCF_01836 | 9e-49 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
PEEMBNCF_01837 | 4e-21 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
PEEMBNCF_01838 | 1.9e-37 | lutB | C | 4Fe-4S dicluster domain | ||
PEEMBNCF_01839 | 1.1e-72 | 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 | |
PEEMBNCF_01840 | 2.3e-49 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
PEEMBNCF_01841 | 4.9e-29 | 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 | |
PEEMBNCF_01842 | 1.9e-33 | yrzB | S | Belongs to the UPF0473 family | ||
PEEMBNCF_01843 | 1.4e-15 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
PEEMBNCF_01844 | 3.9e-74 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
PEEMBNCF_01846 | 1.8e-112 | camS | S | sex pheromone | ||
PEEMBNCF_01847 | 3.2e-56 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
PEEMBNCF_01848 | 1.3e-34 | S | Protein of unknown function (DUF1440) | |||
PEEMBNCF_01849 | 1.7e-50 | recT | L | RecT family | ||
PEEMBNCF_01851 | 7.1e-24 | xerS | L | Phage integrase family | ||
PEEMBNCF_01852 | 1.5e-41 | xerS | L | Phage integrase family | ||
PEEMBNCF_01853 | 2.5e-90 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
PEEMBNCF_01856 | 4.2e-83 | |||||
PEEMBNCF_01857 | 1.4e-39 | 2.7.13.3 | T | GHKL domain | ||
PEEMBNCF_01858 | 4.3e-57 | racA | K | Domain of unknown function (DUF1836) | ||
PEEMBNCF_01860 | 4e-07 | ybbR | S | YbbR-like protein | ||
PEEMBNCF_01861 | 2.3e-11 | ybbR | S | YbbR-like protein | ||
PEEMBNCF_01862 | 9.1e-43 | yodB | K | Transcriptional regulator, HxlR family | ||
PEEMBNCF_01863 | 7.9e-79 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
PEEMBNCF_01865 | 1.4e-21 | cutC | P | Participates in the control of copper homeostasis | ||
PEEMBNCF_01866 | 1.5e-11 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
PEEMBNCF_01867 | 1e-10 | N | phage tail tape measure protein | |||
PEEMBNCF_01868 | 2.4e-33 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
PEEMBNCF_01869 | 2.5e-35 | malT | G | Transporter, major facilitator family protein | ||
PEEMBNCF_01870 | 1.1e-98 | typA | T | GTP-binding protein TypA | ||
PEEMBNCF_01871 | 1.1e-56 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
PEEMBNCF_01872 | 4.7e-53 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
PEEMBNCF_01873 | 2.2e-30 | ynzC | S | UPF0291 protein | ||
PEEMBNCF_01874 | 5.9e-27 | yneF | S | UPF0154 protein | ||
PEEMBNCF_01875 | 4.1e-22 | 2.1.1.72 | L | DNA methylase | ||
PEEMBNCF_01876 | 2.1e-28 | menA | 2.5.1.74 | H | UbiA prenyltransferase family | |
PEEMBNCF_01877 | 1.6e-73 | 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 | ||
PEEMBNCF_01878 | 8.5e-22 | ypsA | S | Belongs to the UPF0398 family | ||
PEEMBNCF_01879 | 1.8e-103 | glcR | K | DeoR C terminal sensor domain | ||
PEEMBNCF_01881 | 4.6e-15 | |||||
PEEMBNCF_01883 | 2e-29 | 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 | ||
PEEMBNCF_01884 | 2.1e-96 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
PEEMBNCF_01886 | 6.8e-26 | ykuJ | S | Protein of unknown function (DUF1797) | ||
PEEMBNCF_01887 | 3e-27 | mprF | I | 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 | ||
PEEMBNCF_01888 | 1.5e-14 | S | Bacterial membrane protein, YfhO | |||
PEEMBNCF_01890 | 3.9e-54 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
PEEMBNCF_01891 | 3.4e-13 | S | Thioredoxin | |||
PEEMBNCF_01894 | 3e-57 | 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 | ||
PEEMBNCF_01895 | 5.7e-10 | yfnA | E | amino acid | ||
PEEMBNCF_01896 | 1.2e-16 | 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 | |
PEEMBNCF_01897 | 1.6e-09 | 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 | |
PEEMBNCF_01898 | 3.7e-17 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
PEEMBNCF_01899 | 5.2e-16 | S | Uncharacterised protein family (UPF0236) | |||
PEEMBNCF_01900 | 2.2e-57 | pfoS | S | Phosphotransferase system, EIIC | ||
PEEMBNCF_01901 | 1.5e-07 | |||||
PEEMBNCF_01902 | 4.8e-09 | bcgIB | 2.1.1.72, 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
PEEMBNCF_01903 | 1.3e-19 | arpU | S | Phage transcriptional regulator, ArpU family | ||
PEEMBNCF_01904 | 8.7e-83 | 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 | ||
PEEMBNCF_01905 | 3.5e-101 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
PEEMBNCF_01907 | 3.2e-24 | 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 | |
PEEMBNCF_01908 | 2.1e-44 | yjaB_1 | K | Acetyltransferase (GNAT) domain | ||
PEEMBNCF_01909 | 9.5e-44 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
PEEMBNCF_01911 | 4.1e-16 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
PEEMBNCF_01913 | 2.3e-26 | S | ECF transporter, substrate-specific component | |||
PEEMBNCF_01916 | 1.8e-32 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
PEEMBNCF_01917 | 5.5e-41 | phoH | T | phosphate starvation-inducible protein PhoH | ||
PEEMBNCF_01919 | 1.7e-27 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
PEEMBNCF_01920 | 1.5e-29 | L | Belongs to the 'phage' integrase family | |||
PEEMBNCF_01921 | 4.5e-53 | asp | S | Asp23 family, cell envelope-related function | ||
PEEMBNCF_01922 | 1.1e-82 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
PEEMBNCF_01923 | 1.5e-39 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
PEEMBNCF_01924 | 1.4e-31 | rhaB | 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
PEEMBNCF_01925 | 1.3e-28 | K | Cro/C1-type HTH DNA-binding domain | |||
PEEMBNCF_01927 | 2e-15 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
PEEMBNCF_01929 | 8.9e-18 | S | LysM domain | |||
PEEMBNCF_01930 | 1.3e-20 | rusA | L | Endodeoxyribonuclease RusA | ||
PEEMBNCF_01932 | 6.9e-59 | yvgN | C | Aldo keto reductase | ||
PEEMBNCF_01933 | 1.8e-59 | S | Protein of unknown function (DUF806) | |||
PEEMBNCF_01934 | 2.4e-30 | S | Bacteriophage HK97-gp10, putative tail-component | |||
PEEMBNCF_01935 | 8.3e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
PEEMBNCF_01936 | 9.5e-30 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
PEEMBNCF_01937 | 4.6e-25 | potE2 | E | amino acid | ||
PEEMBNCF_01940 | 5.7e-50 | dnaE | 2.7.7.7 | L | DNA polymerase | |
PEEMBNCF_01942 | 1.7e-20 | ykuL | S | CBS domain | ||
PEEMBNCF_01944 | 7.7e-21 | 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 | ||
PEEMBNCF_01945 | 2.9e-24 | S | N-acetylmuramoyl-L-alanine amidase activity | |||
PEEMBNCF_01947 | 6.2e-17 | salK | 2.7.13.3 | T | Histidine kinase | |
PEEMBNCF_01948 | 3.6e-36 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
PEEMBNCF_01950 | 1.9e-60 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
PEEMBNCF_01951 | 2.8e-21 | 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 | |
PEEMBNCF_01953 | 5.8e-44 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
PEEMBNCF_01954 | 2.3e-65 | 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 | |
PEEMBNCF_01955 | 2.2e-18 | ssb | L | Single-strand binding protein family | ||
PEEMBNCF_01957 | 3e-68 | K | response regulator | |||
PEEMBNCF_01960 | 7.2e-38 | 3.1.3.18 | J | HAD-hyrolase-like | ||
PEEMBNCF_01961 | 1.7e-09 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
PEEMBNCF_01962 | 3.2e-24 | 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 | |||
PEEMBNCF_01963 | 1.1e-27 | hprA | 1.1.1.29 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
PEEMBNCF_01964 | 7.2e-36 | glnH | ET | ABC transporter | ||
PEEMBNCF_01965 | 4.9e-18 | 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 | |
PEEMBNCF_01970 | 2.6e-51 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
PEEMBNCF_01972 | 3.1e-34 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
PEEMBNCF_01974 | 5.5e-20 | queH | 1.17.99.6, 3.1.26.4 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
PEEMBNCF_01975 | 1.8e-78 | 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 | ||
PEEMBNCF_01977 | 2e-58 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
PEEMBNCF_01978 | 3.5e-07 | L | Integrase core domain | |||
PEEMBNCF_01979 | 8.9e-10 | 1.3.5.4 | C | FAD binding domain | ||
PEEMBNCF_01980 | 2.1e-27 | S | CAAX protease self-immunity | |||
PEEMBNCF_01981 | 1.1e-35 | M | transferase activity, transferring glycosyl groups | |||
PEEMBNCF_01982 | 2.1e-63 | S | Terminase-like family | |||
PEEMBNCF_01984 | 7.8e-48 | S | Domain of unknown function (DUF956) | |||
PEEMBNCF_01986 | 4.7e-17 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
PEEMBNCF_01987 | 9.7e-26 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
PEEMBNCF_01988 | 2.2e-41 | S | Bacterial membrane protein YfhO | |||
PEEMBNCF_01990 | 2e-60 | 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 | |
PEEMBNCF_01991 | 2.5e-30 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
PEEMBNCF_01992 | 8.3e-36 | 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 | ||
PEEMBNCF_01994 | 2.8e-33 | lutB | C | 4Fe-4S dicluster domain | ||
PEEMBNCF_01995 | 3.4e-26 | glnP | P | ABC transporter permease | ||
PEEMBNCF_01996 | 1.2e-40 | gluC | P | ABC transporter permease | ||
PEEMBNCF_01998 | 1.5e-25 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
PEEMBNCF_01999 | 1.5e-49 | nhaC | C | Na H antiporter NhaC | ||
PEEMBNCF_02000 | 3.7e-26 | XK27_08315 | M | Sulfatase | ||
PEEMBNCF_02004 | 1.7e-26 | galT | 2.7.7.12 | G | Galactose-1-phosphate uridyl transferase, C-terminal domain | |
PEEMBNCF_02005 | 2.6e-15 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
PEEMBNCF_02006 | 3.1e-27 | cspC | K | Cold shock protein | ||
PEEMBNCF_02007 | 7.3e-28 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
PEEMBNCF_02008 | 4.6e-37 | |||||
PEEMBNCF_02011 | 5.1e-19 | 3.4.22.70 | M | Sortase family | ||
PEEMBNCF_02012 | 1.7e-10 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
PEEMBNCF_02013 | 5.8e-29 | nhaC | C | Na H antiporter NhaC | ||
PEEMBNCF_02014 | 3.2e-69 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
PEEMBNCF_02015 | 8.4e-54 | patA | 2.6.1.1 | E | Aminotransferase | |
PEEMBNCF_02016 | 3.1e-09 | K | LysR substrate binding domain | |||
PEEMBNCF_02018 | 2.9e-10 | 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 | ||
PEEMBNCF_02019 | 1e-40 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
PEEMBNCF_02021 | 1.7e-07 | O | ADP-ribosylglycohydrolase | |||
PEEMBNCF_02023 | 2e-40 | L | hmm pf00665 | |||
PEEMBNCF_02025 | 1.8e-22 | yjaB_1 | K | Acetyltransferase (GNAT) domain | ||
PEEMBNCF_02027 | 1.8e-29 | 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 | ||
PEEMBNCF_02029 | 4.8e-08 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
PEEMBNCF_02030 | 3.9e-32 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
PEEMBNCF_02031 | 5e-17 | |||||
PEEMBNCF_02032 | 1e-21 | S | Domain of unknown function (DUF4355) | |||
PEEMBNCF_02033 | 2.7e-46 | yqhL | P | Rhodanese-like protein | ||
PEEMBNCF_02034 | 1.6e-19 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
PEEMBNCF_02035 | 2.6e-14 | 2.7.13.3 | T | GHKL domain | ||
PEEMBNCF_02039 | 8e-18 | helD | 3.6.4.12 | L | DNA helicase | |
PEEMBNCF_02040 | 3.3e-28 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
PEEMBNCF_02041 | 5.4e-43 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
PEEMBNCF_02042 | 3.7e-26 | yitU | 3.1.3.104 | S | hydrolase | |
PEEMBNCF_02043 | 2.1e-14 | 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 | ||
PEEMBNCF_02044 | 6.5e-55 | 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 | |
PEEMBNCF_02045 | 2.9e-40 | 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 | ||
PEEMBNCF_02046 | 3.9e-29 | pstS | P | Phosphate | ||
PEEMBNCF_02047 | 3.5e-16 | K | Acetyltransferase (GNAT) domain | |||
PEEMBNCF_02052 | 2e-22 | mgtE | P | Acts as a magnesium transporter | ||
PEEMBNCF_02053 | 6.1e-10 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
PEEMBNCF_02054 | 6.2e-12 | nss | M | transferase activity, transferring glycosyl groups | ||
PEEMBNCF_02056 | 1.4e-16 | |||||
PEEMBNCF_02057 | 2.8e-10 | S | Bacteriophage holin family | |||
PEEMBNCF_02058 | 2.4e-26 | 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 | |
PEEMBNCF_02062 | 1.3e-33 | yvgN | C | Aldo keto reductase | ||
PEEMBNCF_02064 | 3.8e-43 | marR | K | Transcriptional regulator, MarR family | ||
PEEMBNCF_02066 | 1e-13 | ymfH | S | Peptidase M16 | ||
PEEMBNCF_02067 | 8.9e-24 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
PEEMBNCF_02068 | 5.3e-17 | G | PTS system Galactitol-specific IIC component | |||
PEEMBNCF_02070 | 7.4e-28 | yitU | 3.1.3.104 | S | hydrolase | |
PEEMBNCF_02071 | 7.4e-14 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
PEEMBNCF_02072 | 1.2e-27 | nrdH | O | Glutaredoxin | ||
PEEMBNCF_02074 | 4.4e-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 | ||
PEEMBNCF_02077 | 6.4e-10 | ybjQ | S | Belongs to the UPF0145 family | ||
PEEMBNCF_02080 | 2e-31 | S | Aldo keto reductase | |||
PEEMBNCF_02082 | 4.2e-23 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
PEEMBNCF_02083 | 4.6e-17 | S | Aldo keto reductase | |||
PEEMBNCF_02086 | 1.4e-38 | 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 | ||
PEEMBNCF_02090 | 9.3e-32 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
PEEMBNCF_02091 | 1.2e-08 | yraQ | S | Predicted permease | ||
PEEMBNCF_02092 | 8.4e-25 | 3.4.22.70 | M | Sortase family | ||
PEEMBNCF_02093 | 2.1e-36 | yrzL | S | Belongs to the UPF0297 family | ||
PEEMBNCF_02094 | 7.7e-22 | |||||
PEEMBNCF_02095 | 1e-16 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
PEEMBNCF_02096 | 7.4e-13 | |||||
PEEMBNCF_02100 | 1.2e-15 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
PEEMBNCF_02101 | 5.3e-28 | G | PTS system Galactitol-specific IIC component | |||
PEEMBNCF_02102 | 6.4e-13 | L | Helicase C-terminal domain protein | |||
PEEMBNCF_02106 | 2.7e-27 | 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 | |
PEEMBNCF_02107 | 1.3e-16 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
PEEMBNCF_02108 | 1.4e-26 | K | response regulator | |||
PEEMBNCF_02110 | 6.6e-34 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
PEEMBNCF_02111 | 4.9e-15 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
PEEMBNCF_02113 | 1.5e-18 | 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 | ||
PEEMBNCF_02114 | 1.2e-11 | comFA | L | Helicase C-terminal domain protein | ||
PEEMBNCF_02115 | 4.8e-20 | glnP | P | ABC transporter | ||
PEEMBNCF_02116 | 3.7e-17 | L | Phage terminase, small subunit | |||
PEEMBNCF_02117 | 4.5e-21 | ada | 3.2.2.21 | F | the current gene model (or a revised gene model) may contain a frame shift | |
PEEMBNCF_02122 | 3.6e-11 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
PEEMBNCF_02124 | 9.9e-21 | tetP | J | elongation factor G | ||
PEEMBNCF_02125 | 3.7e-10 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
PEEMBNCF_02127 | 1.1e-29 | glxR | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
PEEMBNCF_02128 | 1.2e-14 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
PEEMBNCF_02130 | 2.6e-19 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
PEEMBNCF_02132 | 5.4e-10 | V | DNA modification | |||
PEEMBNCF_02133 | 1.3e-12 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)