ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
JFKAHJIP_00001 | 2.8e-134 | fasA | KT | Response regulator of the LytR AlgR family | ||
JFKAHJIP_00002 | 4.5e-244 | fasC | 2.7.13.3 | T | protein histidine kinase activity | |
JFKAHJIP_00003 | 7.1e-210 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
JFKAHJIP_00004 | 3.7e-157 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
JFKAHJIP_00005 | 6.7e-232 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
JFKAHJIP_00006 | 3.5e-274 | 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) | |
JFKAHJIP_00007 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
JFKAHJIP_00008 | 1.4e-119 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
JFKAHJIP_00009 | 3.7e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
JFKAHJIP_00010 | 1.2e-50 | S | Protein of unknown function (DUF3397) | |||
JFKAHJIP_00011 | 9.2e-89 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
JFKAHJIP_00012 | 3.1e-127 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
JFKAHJIP_00013 | 1.1e-226 | 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 | ||
JFKAHJIP_00014 | 3.3e-73 | 3.5.1.19 | Q | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | ||
JFKAHJIP_00015 | 2e-79 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
JFKAHJIP_00016 | 6.3e-108 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
JFKAHJIP_00017 | 7.9e-230 | XK27_09615 | C | reductase | ||
JFKAHJIP_00018 | 4.8e-140 | fnt | P | Formate nitrite transporter | ||
JFKAHJIP_00019 | 3.9e-96 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
JFKAHJIP_00020 | 3.7e-185 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
JFKAHJIP_00021 | 6.1e-171 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
JFKAHJIP_00022 | 1.8e-116 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
JFKAHJIP_00023 | 1.6e-94 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
JFKAHJIP_00024 | 6.7e-220 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
JFKAHJIP_00025 | 5.3e-58 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
JFKAHJIP_00026 | 1.1e-133 | S | HAD hydrolase, family IA, variant | |||
JFKAHJIP_00027 | 8.6e-156 | rrmA | 2.1.1.187 | Q | methyltransferase | |
JFKAHJIP_00031 | 6.6e-90 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
JFKAHJIP_00032 | 6.6e-66 | ssb_2 | 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 | ||
JFKAHJIP_00033 | 8.3e-37 | yeeD | O | sulfur carrier activity | ||
JFKAHJIP_00034 | 5.8e-186 | yeeE | S | Sulphur transport | ||
JFKAHJIP_00035 | 1.1e-112 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
JFKAHJIP_00036 | 1e-53 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
JFKAHJIP_00037 | 2e-08 | XK27_10305 | S | Domain of unknown function (DUF4651) | ||
JFKAHJIP_00038 | 5.9e-202 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
JFKAHJIP_00039 | 9.7e-130 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
JFKAHJIP_00040 | 1.8e-100 | S | CAAX amino terminal protease family protein | |||
JFKAHJIP_00042 | 7.3e-110 | V | CAAX protease self-immunity | |||
JFKAHJIP_00043 | 8.8e-27 | lanR | K | sequence-specific DNA binding | ||
JFKAHJIP_00044 | 4.1e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
JFKAHJIP_00045 | 3.2e-175 | ytxK | 2.1.1.72 | L | DNA methylase | |
JFKAHJIP_00046 | 2e-12 | comGF | U | Putative Competence protein ComGF | ||
JFKAHJIP_00047 | 4.5e-71 | comGF | U | Competence protein ComGF | ||
JFKAHJIP_00048 | 3.1e-15 | NU | Type II secretory pathway pseudopilin | |||
JFKAHJIP_00049 | 6.4e-70 | cglD | NU | Competence protein | ||
JFKAHJIP_00050 | 2.2e-43 | comGC | U | Required for transformation and DNA binding | ||
JFKAHJIP_00051 | 4.1e-142 | cglB | U | protein transport across the cell outer membrane | ||
JFKAHJIP_00052 | 1.1e-175 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
JFKAHJIP_00053 | 2.9e-68 | S | cog cog4699 | |||
JFKAHJIP_00054 | 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 | |
JFKAHJIP_00055 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
JFKAHJIP_00056 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
JFKAHJIP_00057 | 4.2e-239 | 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) | |
JFKAHJIP_00058 | 2e-97 | XK27_07830 | 2.3.1.128 | J | Acetyltransferase GNAT Family | |
JFKAHJIP_00059 | 1.1e-231 | ytoI | K | transcriptional regulator containing CBS domains | ||
JFKAHJIP_00060 | 1.1e-166 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
JFKAHJIP_00061 | 3.7e-163 | rbn | E | Belongs to the UPF0761 family | ||
JFKAHJIP_00062 | 1.7e-85 | ccl | S | cog cog4708 | ||
JFKAHJIP_00063 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
JFKAHJIP_00064 | 4e-184 | yegS | 2.7.1.107 | I | Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
JFKAHJIP_00065 | 4.8e-174 | yfjR | K | regulation of single-species biofilm formation | ||
JFKAHJIP_00067 | 8.3e-71 | S | QueT transporter | |||
JFKAHJIP_00068 | 8.5e-156 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
JFKAHJIP_00070 | 2.9e-17 | yjdB | S | Domain of unknown function (DUF4767) | ||
JFKAHJIP_00071 | 6.7e-167 | tehB | 2.1.1.265 | PQ | tellurite resistance protein tehb | |
JFKAHJIP_00072 | 2.4e-189 | O | protein import | |||
JFKAHJIP_00073 | 2.1e-129 | agrA | KT | phosphorelay signal transduction system | ||
JFKAHJIP_00074 | 7.8e-198 | 2.7.13.3 | T | GHKL domain | ||
JFKAHJIP_00076 | 2.4e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
JFKAHJIP_00077 | 1.5e-36 | ylqC | L | Belongs to the UPF0109 family | ||
JFKAHJIP_00078 | 3.5e-233 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
JFKAHJIP_00079 | 0.0 | ydaO | E | amino acid | ||
JFKAHJIP_00080 | 7.7e-100 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
JFKAHJIP_00081 | 5e-145 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
JFKAHJIP_00082 | 1.7e-289 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
JFKAHJIP_00083 | 4.5e-61 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
JFKAHJIP_00084 | 4.1e-81 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
JFKAHJIP_00085 | 9.5e-169 | murB | 1.3.1.98 | M | cell wall formation | |
JFKAHJIP_00086 | 2.6e-211 | 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 | |
JFKAHJIP_00087 | 4.1e-139 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
JFKAHJIP_00088 | 2.3e-131 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
JFKAHJIP_00089 | 2.6e-205 | potD | P | spermidine putrescine ABC transporter | ||
JFKAHJIP_00090 | 1.9e-145 | XK27_08050 | O | HflC and HflK could regulate a protease | ||
JFKAHJIP_00091 | 1.8e-71 | gloA | 4.4.1.5 | E | Lactoylglutathione lyase | |
JFKAHJIP_00092 | 2.6e-158 | GK | ROK family | |||
JFKAHJIP_00093 | 1.9e-208 | 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 | |
JFKAHJIP_00094 | 1e-104 | wecD | M | Acetyltransferase (GNAT) domain | ||
JFKAHJIP_00095 | 7.4e-222 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
JFKAHJIP_00096 | 7.8e-72 | ogt | 2.1.1.63, 3.2.2.20 | L | methylated-DNA-[protein]-cysteine S-methyltransferase activity | |
JFKAHJIP_00097 | 1e-57 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
JFKAHJIP_00099 | 5e-186 | femA | 2.3.2.10, 2.3.2.16 | V | FemAB family | |
JFKAHJIP_00100 | 2.4e-16 | 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 | ||
JFKAHJIP_00101 | 9e-122 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
JFKAHJIP_00102 | 1.6e-77 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
JFKAHJIP_00103 | 1e-85 | 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 | ||
JFKAHJIP_00104 | 1e-279 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
JFKAHJIP_00105 | 4.8e-157 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
JFKAHJIP_00106 | 7.9e-263 | 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 | |
JFKAHJIP_00107 | 2.6e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
JFKAHJIP_00108 | 1.5e-215 | ftsW | D | Belongs to the SEDS family | ||
JFKAHJIP_00109 | 1.6e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
JFKAHJIP_00110 | 2.1e-143 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
JFKAHJIP_00111 | 3.8e-238 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
JFKAHJIP_00112 | 5.2e-08 | MU | outer membrane autotransporter barrel domain protein | |||
JFKAHJIP_00113 | 3.9e-158 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
JFKAHJIP_00115 | 9e-75 | XK27_03180 | T | universal stress protein | ||
JFKAHJIP_00116 | 2.9e-237 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase | |
JFKAHJIP_00117 | 8.1e-140 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
JFKAHJIP_00118 | 2e-100 | pncA | Q | isochorismatase | ||
JFKAHJIP_00119 | 2.9e-292 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
JFKAHJIP_00120 | 1.4e-41 | tagE | 2.4.1.52 | GT4 | M | transferase activity, transferring glycosyl groups |
JFKAHJIP_00121 | 1.8e-47 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
JFKAHJIP_00122 | 7.7e-269 | 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) | |
JFKAHJIP_00123 | 3e-273 | 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) | |
JFKAHJIP_00124 | 9.3e-65 | |||||
JFKAHJIP_00125 | 6.3e-152 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
JFKAHJIP_00126 | 5.1e-98 | yqeG | S | hydrolase of the HAD superfamily | ||
JFKAHJIP_00127 | 1.7e-212 | yqeH | S | in Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
JFKAHJIP_00128 | 1.9e-47 | yhbY | J | RNA-binding protein | ||
JFKAHJIP_00129 | 1.2e-117 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
JFKAHJIP_00130 | 9.2e-104 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
JFKAHJIP_00131 | 2.7e-58 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
JFKAHJIP_00132 | 8.4e-139 | yqeM | Q | Methyltransferase domain protein | ||
JFKAHJIP_00133 | 6.5e-113 | S | AAA ATPase domain | |||
JFKAHJIP_00134 | 8.5e-196 | ylbM | S | Belongs to the UPF0348 family | ||
JFKAHJIP_00135 | 3.4e-39 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
JFKAHJIP_00136 | 1.6e-44 | yoeB | S | Addiction module toxin, Txe YoeB family | ||
JFKAHJIP_00138 | 0.0 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
JFKAHJIP_00140 | 2e-101 | |||||
JFKAHJIP_00143 | 3.3e-09 | |||||
JFKAHJIP_00144 | 1e-72 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
JFKAHJIP_00145 | 1.3e-131 | ecsA | V | abc transporter atp-binding protein | ||
JFKAHJIP_00146 | 4.9e-177 | ecsB | U | Bacterial ABC transporter protein EcsB | ||
JFKAHJIP_00147 | 7.1e-152 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
JFKAHJIP_00148 | 3.1e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
JFKAHJIP_00150 | 4.7e-224 | ytfP | S | Flavoprotein | ||
JFKAHJIP_00151 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
JFKAHJIP_00152 | 8.2e-63 | XK27_02560 | S | cog cog2151 | ||
JFKAHJIP_00153 | 9.1e-42 | WQ51_02910 | S | Protein of unknown function, DUF536 | ||
JFKAHJIP_00154 | 6.4e-105 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
JFKAHJIP_00155 | 1.6e-126 | K | transcriptional regulator, MerR family | |||
JFKAHJIP_00156 | 0.0 | V | ABC transporter (Permease | |||
JFKAHJIP_00157 | 7.3e-124 | V | abc transporter atp-binding protein | |||
JFKAHJIP_00159 | 1.2e-43 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
JFKAHJIP_00160 | 1e-232 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
JFKAHJIP_00161 | 0.0 | comEC | S | Competence protein ComEC | ||
JFKAHJIP_00162 | 1.1e-92 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
JFKAHJIP_00163 | 9.8e-143 | plsC | 2.3.1.51 | I | Acyltransferase | |
JFKAHJIP_00164 | 1.2e-156 | nodB3 | G | deacetylase | ||
JFKAHJIP_00165 | 5.5e-141 | yabB | 2.1.1.223 | L | Methyltransferase | |
JFKAHJIP_00166 | 7e-43 | yazA | L | endonuclease containing a URI domain | ||
JFKAHJIP_00167 | 2.2e-245 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
JFKAHJIP_00168 | 1.6e-152 | corA | P | CorA-like protein | ||
JFKAHJIP_00169 | 2.1e-61 | yjqA | S | Bacterial PH domain | ||
JFKAHJIP_00170 | 5.8e-95 | thiT | S | Thiamine transporter | ||
JFKAHJIP_00171 | 2.3e-300 | 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 | ||
JFKAHJIP_00172 | 3.1e-116 | ywaF | S | Integral membrane protein (intg_mem_TP0381) | ||
JFKAHJIP_00173 | 9.2e-256 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
JFKAHJIP_00177 | 2.8e-154 | cjaA | ET | ABC transporter substrate-binding protein | ||
JFKAHJIP_00178 | 9.9e-135 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
JFKAHJIP_00179 | 3e-106 | P | ABC transporter (Permease | |||
JFKAHJIP_00180 | 2.5e-113 | papP | P | ABC transporter (Permease | ||
JFKAHJIP_00181 | 1.2e-191 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
JFKAHJIP_00182 | 2.7e-31 | copZ | 2.7.7.77 | P | Heavy metal-associated domain protein | |
JFKAHJIP_00183 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
JFKAHJIP_00184 | 8.8e-72 | copY | K | negative regulation of transcription, DNA-templated | ||
JFKAHJIP_00185 | 7.2e-177 | EGP | Major facilitator Superfamily | |||
JFKAHJIP_00186 | 2.3e-142 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
JFKAHJIP_00187 | 6.5e-229 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
JFKAHJIP_00188 | 1.4e-96 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | belongs to the TrpF family | |
JFKAHJIP_00189 | 9.4e-133 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
JFKAHJIP_00190 | 5.6e-178 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
JFKAHJIP_00191 | 2.7e-105 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate | |
JFKAHJIP_00192 | 2.8e-257 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
JFKAHJIP_00193 | 1.2e-40 | pchB | 2.5.1.19, 4.2.1.10, 4.2.99.21, 5.4.99.5 | E | Chorismate mutase type II | |
JFKAHJIP_00194 | 3.5e-120 | yujD | V | lipoprotein transporter activity | ||
JFKAHJIP_00195 | 0.0 | S | bacteriocin-associated integral membrane protein | |||
JFKAHJIP_00196 | 2.1e-19 | S | Bacteriocin (Lactococcin_972) | |||
JFKAHJIP_00197 | 4.3e-59 | |||||
JFKAHJIP_00198 | 0.0 | ctpE | P | E1-E2 ATPase | ||
JFKAHJIP_00199 | 1.8e-47 | |||||
JFKAHJIP_00202 | 1.7e-102 | GBS0088 | J | protein conserved in bacteria | ||
JFKAHJIP_00203 | 1.7e-133 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
JFKAHJIP_00204 | 2.4e-170 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
JFKAHJIP_00205 | 4.6e-164 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
JFKAHJIP_00206 | 1.8e-184 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
JFKAHJIP_00207 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
JFKAHJIP_00208 | 2.6e-242 | 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 | |
JFKAHJIP_00209 | 7.7e-97 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
JFKAHJIP_00210 | 2e-26 | |||||
JFKAHJIP_00211 | 1.2e-118 | 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 | |
JFKAHJIP_00212 | 0.0 | U | protein secretion | |||
JFKAHJIP_00213 | 2.6e-191 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase, group 1 family protein |
JFKAHJIP_00214 | 2.6e-247 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
JFKAHJIP_00215 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
JFKAHJIP_00216 | 1.2e-158 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
JFKAHJIP_00217 | 1.1e-200 | S | Protein of unknown function (DUF3114) | |||
JFKAHJIP_00218 | 4.1e-29 | pspC | KT | PspC domain protein | ||
JFKAHJIP_00219 | 5.2e-119 | yqfA | K | protein, Hemolysin III | ||
JFKAHJIP_00220 | 3e-78 | K | hmm pf08876 | |||
JFKAHJIP_00221 | 4.7e-230 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
JFKAHJIP_00222 | 7.9e-216 | mvaS | 2.3.3.10 | I | synthase | |
JFKAHJIP_00223 | 5.9e-168 | 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 | |
JFKAHJIP_00224 | 9.6e-94 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
JFKAHJIP_00225 | 9.7e-22 | |||||
JFKAHJIP_00226 | 2.6e-225 | 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 | ||
JFKAHJIP_00227 | 1.1e-109 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
JFKAHJIP_00228 | 1.8e-251 | mmuP | E | amino acid | ||
JFKAHJIP_00229 | 1.1e-178 | mmuM | 1.5.1.20, 2.1.1.10 | H | Homocysteine | |
JFKAHJIP_00230 | 2.2e-30 | S | Domain of unknown function (DUF1912) | |||
JFKAHJIP_00231 | 4.8e-13 | L | Helix-hairpin-helix DNA-binding motif class 1 | |||
JFKAHJIP_00232 | 1.8e-108 | 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 | |
JFKAHJIP_00233 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
JFKAHJIP_00235 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
JFKAHJIP_00236 | 2.6e-199 | ilvE | 2.6.1.42 | E | Aminotransferase | |
JFKAHJIP_00237 | 4.8e-16 | S | Protein of unknown function (DUF2969) | |||
JFKAHJIP_00240 | 2.5e-204 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
JFKAHJIP_00243 | 1.9e-107 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
JFKAHJIP_00245 | 8.3e-290 | ahpF | O | alkyl hydroperoxide reductase | ||
JFKAHJIP_00246 | 1.1e-106 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
JFKAHJIP_00247 | 7.4e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
JFKAHJIP_00248 | 1e-182 | 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 | ||
JFKAHJIP_00249 | 1.2e-82 | S | Putative small multi-drug export protein | |||
JFKAHJIP_00250 | 4.8e-76 | ctsR | K | Belongs to the CtsR family | ||
JFKAHJIP_00251 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
JFKAHJIP_00252 | 2e-233 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
JFKAHJIP_00253 | 3e-229 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
JFKAHJIP_00254 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
JFKAHJIP_00255 | 1.5e-138 | S | SseB protein N-terminal domain | |||
JFKAHJIP_00256 | 3.3e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
JFKAHJIP_00258 | 8.1e-257 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JFKAHJIP_00259 | 2.7e-67 | 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) | ||
JFKAHJIP_00261 | 2.8e-134 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
JFKAHJIP_00262 | 2.7e-91 | yacP | S | RNA-binding protein containing a PIN domain | ||
JFKAHJIP_00263 | 2e-152 | degV | S | DegV family | ||
JFKAHJIP_00265 | 2.7e-20 | K | Transcriptional | |||
JFKAHJIP_00266 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
JFKAHJIP_00267 | 7.3e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
JFKAHJIP_00268 | 1.7e-89 | S | Protein conserved in bacteria | |||
JFKAHJIP_00269 | 6.7e-89 | H | Methyltransferase | |||
JFKAHJIP_00271 | 1.2e-101 | cadD | P | cadmium resistance | ||
JFKAHJIP_00272 | 4.5e-55 | cadC | K | Bacterial regulatory protein, arsR family | ||
JFKAHJIP_00273 | 2e-18 | |||||
JFKAHJIP_00274 | 1.5e-29 | K | Helix-turn-helix domain | |||
JFKAHJIP_00275 | 6e-85 | |||||
JFKAHJIP_00276 | 8.5e-140 | srtB | 3.4.22.70 | S | sortase, SrtB family | |
JFKAHJIP_00277 | 8.2e-232 | capA | M | Bacterial capsule synthesis protein | ||
JFKAHJIP_00278 | 6.1e-39 | gcvR | T | UPF0237 protein | ||
JFKAHJIP_00279 | 2.3e-243 | XK27_08635 | S | UPF0210 protein | ||
JFKAHJIP_00280 | 7.3e-132 | ais | G | Phosphoglycerate mutase | ||
JFKAHJIP_00281 | 2.3e-142 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
JFKAHJIP_00282 | 2.7e-100 | acmA | 3.2.1.17, 3.4.17.14, 3.5.1.28 | NU | Muramidase (Flagellum-specific) | |
JFKAHJIP_00283 | 1.3e-185 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
JFKAHJIP_00284 | 5.3e-63 | 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 | ||
JFKAHJIP_00285 | 6e-303 | dnaK | O | Heat shock 70 kDa protein | ||
JFKAHJIP_00286 | 1.7e-103 | thiJ-2 | 3.5.1.124 | S | DJ-1/PfpI family | |
JFKAHJIP_00287 | 8e-189 | 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 | ||
JFKAHJIP_00288 | 1e-139 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
JFKAHJIP_00289 | 4e-136 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
JFKAHJIP_00290 | 1.5e-80 | hmpT | S | cog cog4720 | ||
JFKAHJIP_00291 | 9.5e-175 | 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) | |
JFKAHJIP_00292 | 5.5e-217 | araT | 2.6.1.1 | E | Aminotransferase | |
JFKAHJIP_00293 | 6.1e-140 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
JFKAHJIP_00294 | 9.5e-181 | 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 | |
JFKAHJIP_00295 | 1.8e-29 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
JFKAHJIP_00296 | 8.9e-130 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
JFKAHJIP_00297 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
JFKAHJIP_00298 | 8.4e-276 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
JFKAHJIP_00299 | 1.4e-189 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
JFKAHJIP_00300 | 6.8e-101 | 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 | |
JFKAHJIP_00301 | 2.8e-293 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
JFKAHJIP_00302 | 3e-237 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
JFKAHJIP_00303 | 4.5e-80 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
JFKAHJIP_00304 | 2.3e-201 | 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) | |
JFKAHJIP_00305 | 1.1e-175 | 1.1.1.169 | H | Ketopantoate reductase | ||
JFKAHJIP_00306 | 6.6e-34 | |||||
JFKAHJIP_00307 | 9.6e-135 | J | Domain of unknown function (DUF4041) | |||
JFKAHJIP_00308 | 2.5e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
JFKAHJIP_00309 | 0.0 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
JFKAHJIP_00310 | 3.1e-69 | argR | K | Regulates arginine biosynthesis genes | ||
JFKAHJIP_00311 | 1.9e-56 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
JFKAHJIP_00312 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
JFKAHJIP_00313 | 1.9e-77 | S | Protein of unknown function (DUF3021) | |||
JFKAHJIP_00314 | 2.4e-69 | K | LytTr DNA-binding domain | |||
JFKAHJIP_00316 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
JFKAHJIP_00318 | 3e-102 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
JFKAHJIP_00319 | 2.3e-104 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
JFKAHJIP_00320 | 4e-229 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
JFKAHJIP_00321 | 1e-204 | 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 | ||
JFKAHJIP_00322 | 3.9e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
JFKAHJIP_00324 | 3.3e-117 | nudL | L | hydrolase | ||
JFKAHJIP_00325 | 9.1e-53 | K | transcriptional regulator, PadR family | |||
JFKAHJIP_00326 | 1.9e-61 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
JFKAHJIP_00327 | 3.7e-106 | S | Putative adhesin | |||
JFKAHJIP_00328 | 1.7e-156 | XK27_06930 | V | domain protein | ||
JFKAHJIP_00329 | 4.6e-94 | XK27_06935 | K | transcriptional regulator | ||
JFKAHJIP_00330 | 3.8e-52 | ypaA | M | Membrane | ||
JFKAHJIP_00331 | 1.1e-10 | |||||
JFKAHJIP_00332 | 5.8e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
JFKAHJIP_00333 | 1.8e-47 | veg | S | Biofilm formation stimulator VEG | ||
JFKAHJIP_00334 | 1e-246 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
JFKAHJIP_00335 | 2.2e-73 | rplI | J | binds to the 23S rRNA | ||
JFKAHJIP_00336 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
JFKAHJIP_00337 | 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 | ||
JFKAHJIP_00338 | 4.2e-99 | yvbG | U | UPF0056 membrane protein | ||
JFKAHJIP_00339 | 2.8e-218 | 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 | |
JFKAHJIP_00340 | 0.0 | S | Bacterial membrane protein, YfhO | |||
JFKAHJIP_00341 | 3.2e-63 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
JFKAHJIP_00342 | 3.3e-58 | lytE | M | LysM domain protein | ||
JFKAHJIP_00343 | 1.7e-132 | ecfT | P | 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 | ||
JFKAHJIP_00344 | 3.6e-154 | 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 | |
JFKAHJIP_00345 | 3.1e-150 | 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 | ||
JFKAHJIP_00346 | 4.1e-90 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
JFKAHJIP_00347 | 8.3e-130 | S | sequence-specific DNA binding | |||
JFKAHJIP_00348 | 9.5e-239 | ymfH | S | Peptidase M16 | ||
JFKAHJIP_00349 | 4.2e-231 | ymfF | S | Peptidase M16 | ||
JFKAHJIP_00350 | 5.8e-59 | yaaA | S | S4 domain protein YaaA | ||
JFKAHJIP_00351 | 1.2e-202 | 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 | ||
JFKAHJIP_00352 | 8.1e-274 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
JFKAHJIP_00353 | 1.2e-191 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
JFKAHJIP_00354 | 7.1e-153 | yvjA | S | membrane | ||
JFKAHJIP_00355 | 1.1e-305 | ybiT | S | abc transporter atp-binding protein | ||
JFKAHJIP_00356 | 0.0 | XK27_10405 | S | Bacterial membrane protein YfhO | ||
JFKAHJIP_00357 | 3.2e-44 | yrzB | S | Belongs to the UPF0473 family | ||
JFKAHJIP_00358 | 2.3e-69 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
JFKAHJIP_00359 | 6.3e-44 | yrzL | S | Belongs to the UPF0297 family | ||
JFKAHJIP_00360 | 8.4e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
JFKAHJIP_00361 | 7e-234 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
JFKAHJIP_00363 | 1.3e-215 | int | L | Belongs to the 'phage' integrase family | ||
JFKAHJIP_00364 | 1.9e-18 | S | Domain of unknown function (DUF3173) | |||
JFKAHJIP_00365 | 2.6e-140 | L | Replication initiation factor | |||
JFKAHJIP_00366 | 5.5e-89 | K | sequence-specific DNA binding | |||
JFKAHJIP_00367 | 4.9e-174 | yeiH | S | membrane | ||
JFKAHJIP_00368 | 4.8e-93 | adk | 2.7.4.3 | F | topology modulation protein | |
JFKAHJIP_00369 | 2.7e-249 | 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 | |
JFKAHJIP_00370 | 3.4e-79 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
JFKAHJIP_00371 | 4.8e-35 | XK27_09805 | S | MORN repeat protein | ||
JFKAHJIP_00372 | 0.0 | XK27_09800 | I | Acyltransferase | ||
JFKAHJIP_00373 | 3e-187 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
JFKAHJIP_00374 | 2.9e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
JFKAHJIP_00375 | 2.4e-110 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
JFKAHJIP_00376 | 5.7e-104 | rplD | J | Forms part of the polypeptide exit tunnel | ||
JFKAHJIP_00377 | 2.4e-44 | 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 | ||
JFKAHJIP_00378 | 6.8e-153 | 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 | ||
JFKAHJIP_00379 | 8.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
JFKAHJIP_00380 | 7.3e-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 | ||
JFKAHJIP_00381 | 1.6e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
JFKAHJIP_00382 | 1.1e-71 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
JFKAHJIP_00383 | 3.5e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
JFKAHJIP_00384 | 1.7e-38 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
JFKAHJIP_00385 | 3.9e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
JFKAHJIP_00386 | 1.4e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
JFKAHJIP_00387 | 1.6e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
JFKAHJIP_00388 | 1.5e-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 | ||
JFKAHJIP_00389 | 1.2e-67 | 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 | ||
JFKAHJIP_00390 | 6.6e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
JFKAHJIP_00391 | 1.9e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
JFKAHJIP_00392 | 1.3e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
JFKAHJIP_00393 | 1.9e-23 | rpmD | J | ribosomal protein l30 | ||
JFKAHJIP_00394 | 5.7e-58 | rplO | J | binds to the 23S rRNA | ||
JFKAHJIP_00395 | 3e-232 | 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 | ||
JFKAHJIP_00396 | 6.2e-114 | 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 | |
JFKAHJIP_00397 | 2.7e-32 | 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 | ||
JFKAHJIP_00398 | 6e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
JFKAHJIP_00399 | 4e-57 | 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 | ||
JFKAHJIP_00400 | 1.9e-62 | 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 | ||
JFKAHJIP_00401 | 1.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
JFKAHJIP_00402 | 4.4e-62 | rplQ | J | ribosomal protein l17 | ||
JFKAHJIP_00403 | 8.6e-82 | L | Transposase | |||
JFKAHJIP_00404 | 0.0 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
JFKAHJIP_00405 | 8.1e-212 | acoC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
JFKAHJIP_00406 | 1.4e-181 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
JFKAHJIP_00407 | 6.6e-184 | acoA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
JFKAHJIP_00408 | 1.1e-215 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
JFKAHJIP_00409 | 2.4e-234 | 2.7.13.3 | T | protein histidine kinase activity | ||
JFKAHJIP_00410 | 0.0 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
JFKAHJIP_00411 | 4.8e-235 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
JFKAHJIP_00412 | 1.7e-119 | 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 | |
JFKAHJIP_00413 | 4.3e-217 | yeaB | K | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
JFKAHJIP_00414 | 2.3e-246 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
JFKAHJIP_00415 | 4.4e-181 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
JFKAHJIP_00416 | 2.7e-157 | rssA | S | Phospholipase, patatin family | ||
JFKAHJIP_00417 | 3.7e-103 | estA | E | Lysophospholipase L1 and related esterases | ||
JFKAHJIP_00418 | 4.8e-285 | S | unusual protein kinase | |||
JFKAHJIP_00419 | 4.9e-39 | S | granule-associated protein | |||
JFKAHJIP_00420 | 1.2e-287 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
JFKAHJIP_00421 | 2.9e-199 | S | hmm pf01594 | |||
JFKAHJIP_00422 | 1.5e-109 | G | Belongs to the phosphoglycerate mutase family | |||
JFKAHJIP_00423 | 7e-107 | G | Belongs to the phosphoglycerate mutase family | |||
JFKAHJIP_00424 | 2.5e-109 | pgm | G | Belongs to the phosphoglycerate mutase family | ||
JFKAHJIP_00425 | 1.3e-153 | supH | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
JFKAHJIP_00426 | 1.9e-167 | L | Transposase | |||
JFKAHJIP_00427 | 7.1e-89 | L | Transposase | |||
JFKAHJIP_00435 | 5.6e-164 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
JFKAHJIP_00436 | 7.3e-104 | S | Domain of unknown function (DUF1803) | |||
JFKAHJIP_00437 | 7.8e-102 | ygaC | J | Belongs to the UPF0374 family | ||
JFKAHJIP_00438 | 2e-138 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
JFKAHJIP_00439 | 1.5e-247 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
JFKAHJIP_00440 | 1.4e-192 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
JFKAHJIP_00441 | 1.7e-257 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
JFKAHJIP_00442 | 1.6e-117 | S | HAD hydrolase, family IA, variant 3 | |||
JFKAHJIP_00443 | 2.1e-140 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
JFKAHJIP_00444 | 5.2e-72 | marR | K | Transcriptional regulator, MarR family | ||
JFKAHJIP_00445 | 1.1e-170 | 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 | |
JFKAHJIP_00446 | 3.3e-30 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
JFKAHJIP_00447 | 2e-172 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
JFKAHJIP_00448 | 3e-162 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
JFKAHJIP_00449 | 1.8e-125 | IQ | reductase | |||
JFKAHJIP_00450 | 2.6e-233 | 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 | |
JFKAHJIP_00451 | 5.6e-54 | 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 | |
JFKAHJIP_00452 | 1.5e-71 | 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 | |
JFKAHJIP_00453 | 2e-255 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
JFKAHJIP_00454 | 5e-159 | 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 | |
JFKAHJIP_00455 | 1.5e-138 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
JFKAHJIP_00456 | 4.7e-90 | 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) | |
JFKAHJIP_00457 | 7.1e-207 | rny | D | Endoribonuclease that initiates mRNA decay | ||
JFKAHJIP_00458 | 6.8e-112 | fruR | K | transcriptional | ||
JFKAHJIP_00459 | 8.4e-165 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
JFKAHJIP_00460 | 0.0 | fruA | 2.7.1.202 | G | phosphotransferase system | |
JFKAHJIP_00461 | 1.1e-256 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
JFKAHJIP_00462 | 9.5e-236 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
JFKAHJIP_00464 | 8e-213 | iscS2 | 2.8.1.7 | E | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes | |
JFKAHJIP_00465 | 1.7e-224 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
JFKAHJIP_00466 | 1.9e-291 | 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 |
JFKAHJIP_00467 | 2.8e-254 | 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 | ||
JFKAHJIP_00468 | 1.7e-93 | 2.3.1.128 | K | acetyltransferase | ||
JFKAHJIP_00469 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
JFKAHJIP_00470 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
JFKAHJIP_00471 | 3.8e-133 | ydaF_2 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
JFKAHJIP_00472 | 5e-63 | WQ51_03320 | S | cog cog4835 | ||
JFKAHJIP_00473 | 4.2e-150 | XK27_08360 | S | EDD domain protein, DegV family | ||
JFKAHJIP_00474 | 6.3e-137 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
JFKAHJIP_00475 | 9.3e-220 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
JFKAHJIP_00476 | 0.0 | yfmR | S | abc transporter atp-binding protein | ||
JFKAHJIP_00477 | 1.7e-26 | U | response to pH | |||
JFKAHJIP_00478 | 1.8e-128 | 3.6.1.13, 3.6.1.55 | F | AdP-ribose pyrophosphatase | ||
JFKAHJIP_00479 | 6.3e-215 | nadD | 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 | H | adenylyltransferase | |
JFKAHJIP_00480 | 2.8e-257 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
JFKAHJIP_00481 | 1.1e-282 | S | Psort location CytoplasmicMembrane, score | |||
JFKAHJIP_00482 | 4.6e-70 | def_1 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
JFKAHJIP_00483 | 3.3e-74 | K | DNA-binding transcription factor activity | |||
JFKAHJIP_00484 | 0.0 | lmrA1 | V | abc transporter atp-binding protein | ||
JFKAHJIP_00485 | 0.0 | lmrA2 | V | abc transporter atp-binding protein | ||
JFKAHJIP_00486 | 3.3e-112 | K | Acetyltransferase (GNAT) family | |||
JFKAHJIP_00487 | 8.7e-113 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | ||
JFKAHJIP_00488 | 1.7e-117 | T | response regulator | |||
JFKAHJIP_00489 | 8.5e-213 | sptS | 2.7.13.3 | T | Histidine kinase | |
JFKAHJIP_00490 | 1.7e-131 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
JFKAHJIP_00491 | 1.7e-91 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
JFKAHJIP_00492 | 4.5e-160 | cvfB | S | Protein conserved in bacteria | ||
JFKAHJIP_00493 | 3.7e-34 | yozE | S | Belongs to the UPF0346 family | ||
JFKAHJIP_00494 | 6e-137 | sip | M | LysM domain protein | ||
JFKAHJIP_00495 | 2.8e-191 | phoH | T | phosphate starvation-inducible protein PhoH | ||
JFKAHJIP_00500 | 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 | |
JFKAHJIP_00501 | 9.6e-163 | S | reductase | |||
JFKAHJIP_00502 | 4.7e-168 | K | transcriptional regulator (lysR family) | |||
JFKAHJIP_00503 | 2.7e-105 | S | CAAX amino terminal protease family protein | |||
JFKAHJIP_00504 | 2.8e-303 | S | Glucan-binding protein C | |||
JFKAHJIP_00505 | 7.3e-163 | S | CHAP domain | |||
JFKAHJIP_00506 | 1.3e-55 | insK | L | Integrase core domain protein | ||
JFKAHJIP_00507 | 5.2e-78 | L | transposition | |||
JFKAHJIP_00508 | 3.5e-185 | coiA | 3.6.4.12 | S | Competence protein | |
JFKAHJIP_00509 | 0.0 | pepF | E | oligoendopeptidase F | ||
JFKAHJIP_00510 | 6.7e-218 | oxlT | P | COG0477 Permeases of the major facilitator superfamily | ||
JFKAHJIP_00511 | 5.4e-127 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
JFKAHJIP_00512 | 7.8e-168 | prsA | 3.1.3.16, 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
JFKAHJIP_00513 | 1.7e-84 | yxjI | S | LURP-one-related | ||
JFKAHJIP_00514 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
JFKAHJIP_00515 | 5.2e-77 | L | COG1943 Transposase and inactivated derivatives | |||
JFKAHJIP_00516 | 3.5e-59 | K | sequence-specific DNA binding | |||
JFKAHJIP_00517 | 1.2e-09 | |||||
JFKAHJIP_00519 | 0.0 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
JFKAHJIP_00520 | 4.3e-138 | agrA | KT | response regulator | ||
JFKAHJIP_00521 | 3.1e-07 | |||||
JFKAHJIP_00522 | 5.6e-135 | agrA | KT | response regulator | ||
JFKAHJIP_00523 | 3e-232 | 2.7.13.3 | T | GHKL domain | ||
JFKAHJIP_00525 | 0.0 | vanY | 3.4.17.14, 3.5.1.28 | M | D-alanyl-D-alanine carboxypeptidase | |
JFKAHJIP_00526 | 1.3e-142 | cnhA | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
JFKAHJIP_00527 | 2.4e-228 | mtnE | 2.6.1.83 | E | mutations do not affect methionine salvage in vivo however | |
JFKAHJIP_00528 | 2.7e-188 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
JFKAHJIP_00529 | 2.8e-216 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
JFKAHJIP_00530 | 5.6e-127 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
JFKAHJIP_00531 | 1.2e-205 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
JFKAHJIP_00532 | 2.7e-128 | yxkH | G | deacetylase | ||
JFKAHJIP_00533 | 6.8e-237 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
JFKAHJIP_00534 | 6.3e-154 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
JFKAHJIP_00535 | 1.1e-148 | rarD | S | Transporter | ||
JFKAHJIP_00536 | 2.6e-16 | T | peptidase | |||
JFKAHJIP_00537 | 3e-14 | coiA | 3.6.4.12 | S | Competence protein | |
JFKAHJIP_00538 | 1e-107 | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | |||
JFKAHJIP_00539 | 5.5e-106 | rimL | 2.3.1.128, 5.2.1.8 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
JFKAHJIP_00540 | 1.6e-174 | S | Helix-hairpin-helix DNA-binding motif class 1 | |||
JFKAHJIP_00541 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
JFKAHJIP_00542 | 1e-155 | S | AIPR protein | |||
JFKAHJIP_00543 | 3.5e-56 | lrgA | S | Effector of murein hydrolase LrgA | ||
JFKAHJIP_00544 | 1.6e-115 | lrgB | M | Inhibits the expression or activity of extracellular murein hydrolases by interacting, possibly with LrgA, with the holin-like proteins CidA and or CidB. The LrgAB and CidAB proteins may affect the proton motive force of the membrane. May be involved in programmed cell death (PCD), possibly triggering PCD in response to antibiotics and environmental stresses | ||
JFKAHJIP_00545 | 4.2e-98 | 3.1.3.18 | S | IA, variant 1 | ||
JFKAHJIP_00546 | 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 | |
JFKAHJIP_00547 | 6e-305 | 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 | ||
JFKAHJIP_00548 | 2.2e-114 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
JFKAHJIP_00549 | 3.2e-07 | N | PFAM Uncharacterised protein family UPF0150 | |||
JFKAHJIP_00550 | 1.1e-153 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | |||
JFKAHJIP_00552 | 6.4e-63 | ycaO | O | OsmC-like protein | ||
JFKAHJIP_00553 | 1.9e-62 | paaI | Q | protein possibly involved in aromatic compounds catabolism | ||
JFKAHJIP_00554 | 5.7e-10 | O | ADP-ribosylglycohydrolase | |||
JFKAHJIP_00555 | 1.2e-134 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
JFKAHJIP_00557 | 6.7e-248 | 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 | ||
JFKAHJIP_00558 | 1.7e-17 | XK27_00735 | ||||
JFKAHJIP_00559 | 1e-136 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
JFKAHJIP_00560 | 0.0 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
JFKAHJIP_00561 | 4.9e-168 | S | CAAX amino terminal protease family protein | |||
JFKAHJIP_00563 | 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 | ||
JFKAHJIP_00564 | 1.3e-84 | mutT | 3.6.1.55 | F | Nudix family | |
JFKAHJIP_00565 | 6.4e-140 | ET | ABC transporter | |||
JFKAHJIP_00566 | 5.9e-138 | ET | Belongs to the bacterial solute-binding protein 3 family | |||
JFKAHJIP_00567 | 1.1e-211 | arcT | 2.6.1.1 | E | Aminotransferase | |
JFKAHJIP_00568 | 1.9e-136 | gltS | ET | Belongs to the bacterial solute-binding protein 3 family | ||
JFKAHJIP_00569 | 3.2e-20 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
JFKAHJIP_00570 | 8.9e-44 | 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 | ||
JFKAHJIP_00571 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
JFKAHJIP_00572 | 2.3e-201 | 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 | ||
JFKAHJIP_00573 | 3.4e-55 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
JFKAHJIP_00574 | 2.5e-172 | yfdH | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
JFKAHJIP_00575 | 1.1e-158 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
JFKAHJIP_00576 | 6.1e-213 | rgpA | GT4 | M | Domain of unknown function (DUF1972) | |
JFKAHJIP_00577 | 1e-173 | rgpB | GT2 | M | Glycosyltransferase, group 2 family protein | |
JFKAHJIP_00578 | 5.2e-142 | rgpC | GM | Transport permease protein | ||
JFKAHJIP_00579 | 5.3e-223 | rgpD | 3.6.3.38 | P | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
JFKAHJIP_00580 | 9.2e-184 | rgpEc | GT2 | M | Glycosyl transferase family 2 | |
JFKAHJIP_00581 | 0.0 | rgpF | M | Rhamnan synthesis protein F | ||
JFKAHJIP_00582 | 4.3e-156 | rfbJ | M | Glycosyl transferase family 2 | ||
JFKAHJIP_00583 | 4.3e-46 | M | Psort location CytoplasmicMembrane, score | |||
JFKAHJIP_00584 | 7.5e-166 | |||||
JFKAHJIP_00585 | 1.2e-118 | radC | E | Belongs to the UPF0758 family | ||
JFKAHJIP_00586 | 5.3e-127 | puuD | T | peptidase C26 | ||
JFKAHJIP_00587 | 1.9e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
JFKAHJIP_00588 | 1.8e-59 | XK27_04120 | S | Putative amino acid metabolism | ||
JFKAHJIP_00589 | 1.1e-203 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
JFKAHJIP_00590 | 5.1e-176 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
JFKAHJIP_00591 | 7.1e-101 | yjbK | S | Adenylate cyclase | ||
JFKAHJIP_00592 | 3e-119 | yjbM | 2.7.6.5 | S | Gtp pyrophosphokinase | |
JFKAHJIP_00593 | 7.5e-152 | nadK | 2.7.1.23 | H | 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 | |
JFKAHJIP_00594 | 3.1e-172 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
JFKAHJIP_00595 | 6.3e-174 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
JFKAHJIP_00596 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
JFKAHJIP_00597 | 2.7e-311 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
JFKAHJIP_00598 | 4.3e-275 | amiC | P | ABC transporter (Permease | ||
JFKAHJIP_00599 | 3.5e-166 | amiD | P | ABC transporter (Permease | ||
JFKAHJIP_00600 | 1.3e-201 | oppD | P | Belongs to the ABC transporter superfamily | ||
JFKAHJIP_00601 | 3.1e-170 | oppF | P | Belongs to the ABC transporter superfamily | ||
JFKAHJIP_00602 | 1.7e-129 | V | Psort location CytoplasmicMembrane, score | |||
JFKAHJIP_00603 | 2.3e-117 | skfE | V | abc transporter atp-binding protein | ||
JFKAHJIP_00604 | 6.1e-61 | yvoA_1 | K | Transcriptional | ||
JFKAHJIP_00605 | 6.1e-143 | supH | S | overlaps another CDS with the same product name | ||
JFKAHJIP_00606 | 1.8e-142 | XK27_02985 | S | overlaps another CDS with the same product name | ||
JFKAHJIP_00607 | 1.8e-195 | 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) | ||
JFKAHJIP_00608 | 8.8e-113 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
JFKAHJIP_00609 | 3.6e-46 | rpoZ | 2.7.7.6 | K | DNA-directed 5'-3' RNA polymerase activity | |
JFKAHJIP_00610 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
JFKAHJIP_00611 | 2.8e-171 | 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 | |
JFKAHJIP_00612 | 3.2e-245 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
JFKAHJIP_00613 | 4.8e-137 | stp | 3.1.3.16 | T | phosphatase | |
JFKAHJIP_00614 | 1.4e-302 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
JFKAHJIP_00615 | 3.8e-94 | kcsA | P | Ion transport protein | ||
JFKAHJIP_00616 | 8.6e-117 | yvqF | S | Membrane | ||
JFKAHJIP_00617 | 1.9e-170 | vraS | 2.7.13.3 | T | Histidine kinase | |
JFKAHJIP_00618 | 1.4e-113 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
JFKAHJIP_00621 | 7.6e-94 | 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 | ||
JFKAHJIP_00622 | 1.9e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
JFKAHJIP_00623 | 1.2e-188 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
JFKAHJIP_00624 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
JFKAHJIP_00625 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
JFKAHJIP_00626 | 0.0 | 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 |
JFKAHJIP_00627 | 2e-187 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
JFKAHJIP_00628 | 5.2e-180 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | glucose-1-phosphate adenylyltransferase |
JFKAHJIP_00629 | 2.2e-284 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
JFKAHJIP_00630 | 0.0 | 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 |
JFKAHJIP_00631 | 6.5e-99 | 2.3.1.128 | K | Acetyltransferase GNAT Family | ||
JFKAHJIP_00632 | 5.7e-291 | S | Protein of unknown function (DUF3114) | |||
JFKAHJIP_00634 | 0.0 | gshF | 6.3.2.2, 6.3.2.29, 6.3.2.30, 6.3.2.4 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
JFKAHJIP_00635 | 3.6e-297 | V | abc transporter atp-binding protein | |||
JFKAHJIP_00636 | 0.0 | V | abc transporter atp-binding protein | |||
JFKAHJIP_00637 | 3.7e-189 | XK27_10075 | S | abc transporter atp-binding protein | ||
JFKAHJIP_00638 | 0.0 | glgE | 2.3.1.12, 2.4.99.16, 3.2.1.1, 3.2.1.14 | GH13,GH18 | M | Pilin isopeptide linkage domain protein |
JFKAHJIP_00639 | 0.0 | M | Pilin isopeptide linkage domain protein | |||
JFKAHJIP_00640 | 0.0 | zmpB | M | signal peptide protein, YSIRK family | ||
JFKAHJIP_00641 | 0.0 | GM | domain, Protein | |||
JFKAHJIP_00642 | 9e-223 | 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 | ||
JFKAHJIP_00643 | 0.0 | sbcC | L | ATPase involved in DNA repair | ||
JFKAHJIP_00644 | 6.9e-09 | |||||
JFKAHJIP_00646 | 3.4e-155 | cat | 2.3.1.28 | S | acetyltransferase' | |
JFKAHJIP_00647 | 0.0 | M | family 8 | |||
JFKAHJIP_00648 | 1e-146 | epsH | S | acetyltransferase' | ||
JFKAHJIP_00649 | 9.9e-238 | M | Glycosyltransferase, family 8 | |||
JFKAHJIP_00650 | 7.1e-286 | tagE | 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 |
JFKAHJIP_00651 | 5.8e-193 | 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 | |||
JFKAHJIP_00652 | 3.3e-186 | nss | M | transferase activity, transferring glycosyl groups | ||
JFKAHJIP_00653 | 1.9e-236 | M | Glycosyltransferase, family 8 | |||
JFKAHJIP_00654 | 2.5e-166 | cpsJ | M | Glycosyltransferase group 2 family protein | ||
JFKAHJIP_00655 | 0.0 | M | cog cog1442 | |||
JFKAHJIP_00656 | 5.8e-241 | M | family 8 | |||
JFKAHJIP_00657 | 2.3e-165 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
JFKAHJIP_00658 | 9.5e-310 | asp1 | S | Accessory Sec system protein Asp1 | ||
JFKAHJIP_00659 | 9.4e-302 | asp2 | 3.4.11.5 | S | Accessory Sec system protein Asp2 | |
JFKAHJIP_00660 | 1.6e-68 | asp3 | S | Accessory Sec system protein Asp3 | ||
JFKAHJIP_00661 | 0.0 | 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 | ||
JFKAHJIP_00662 | 3.9e-13 | S | Accessory secretory protein Sec Asp4 | |||
JFKAHJIP_00663 | 7e-12 | S | Accessory secretory protein Sec, Asp5 | |||
JFKAHJIP_00664 | 9.5e-110 | lytC | 3.4.17.14, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
JFKAHJIP_00665 | 1.5e-233 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
JFKAHJIP_00666 | 8.6e-87 | ebsA | S | Family of unknown function (DUF5322) | ||
JFKAHJIP_00667 | 2.4e-17 | M | LysM domain | |||
JFKAHJIP_00668 | 1.6e-120 | 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 | |
JFKAHJIP_00669 | 5.6e-84 | 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 | ||
JFKAHJIP_00670 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
JFKAHJIP_00671 | 1.5e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
JFKAHJIP_00672 | 5.5e-83 | XK27_03610 | K | Gnat family | ||
JFKAHJIP_00673 | 1.9e-92 | yybC | ||||
JFKAHJIP_00674 | 4.9e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
JFKAHJIP_00675 | 1.9e-272 | pepV | 3.5.1.18 | E | Dipeptidase | |
JFKAHJIP_00676 | 9.1e-112 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
JFKAHJIP_00677 | 2e-240 | cps4A | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
JFKAHJIP_00678 | 6.8e-133 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
JFKAHJIP_00679 | 7.2e-116 | cps4C | M | biosynthesis protein | ||
JFKAHJIP_00680 | 6.1e-113 | cpsD | D | COG0489 ATPases involved in chromosome partitioning | ||
JFKAHJIP_00681 | 4.8e-257 | cpsE | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
JFKAHJIP_00682 | 1.7e-126 | tagA | 2.4.1.187 | GT26 | M | 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 |
JFKAHJIP_00683 | 7.4e-160 | licD | M | LICD family | ||
JFKAHJIP_00684 | 2e-163 | S | Glycosyl transferase family 2 | |||
JFKAHJIP_00685 | 4.4e-205 | M | glycosyl transferase group 1 | |||
JFKAHJIP_00686 | 4e-85 | |||||
JFKAHJIP_00687 | 2.7e-171 | S | glycosyl transferase family 2 | |||
JFKAHJIP_00688 | 1.3e-204 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
JFKAHJIP_00689 | 0.0 | M | Polysaccharide biosynthesis protein | |||
JFKAHJIP_00690 | 1.5e-245 | S | Polysaccharide biosynthesis protein | |||
JFKAHJIP_00691 | 1.3e-96 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
JFKAHJIP_00692 | 4.4e-225 | G | COG0457 FOG TPR repeat | |||
JFKAHJIP_00693 | 4.3e-177 | yubA | S | permease | ||
JFKAHJIP_00694 | 1.9e-91 | mutX | 3.6.1.55 | F | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
JFKAHJIP_00695 | 7.3e-164 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
JFKAHJIP_00696 | 3.2e-124 | ftsE | D | cell division ATP-binding protein FtsE | ||
JFKAHJIP_00697 | 5.7e-183 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
JFKAHJIP_00698 | 5.1e-204 | queG | 1.17.99.6 | 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) | |
JFKAHJIP_00699 | 1e-156 | yjjH | S | Calcineurin-like phosphoesterase | ||
JFKAHJIP_00700 | 3.1e-133 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
JFKAHJIP_00701 | 0.0 | pacL | 3.6.3.8 | P | cation transport ATPase | |
JFKAHJIP_00702 | 4.5e-67 | ywiB | S | Domain of unknown function (DUF1934) | ||
JFKAHJIP_00703 | 4.4e-135 | XK27_00120 | 2.4.2.3 | F | Phosphorylase superfamily | |
JFKAHJIP_00704 | 1.7e-159 | XK27_00115 | 2.3.1.128 | K | Acetyltransferase GNAT family | |
JFKAHJIP_00705 | 2e-146 | yidA | S | hydrolases of the HAD superfamily | ||
JFKAHJIP_00706 | 4.1e-207 | murM | 2.3.2.10, 2.3.2.16 | V | protein involved in methicillin resistance | |
JFKAHJIP_00707 | 8.7e-57 | S | Protein of unknown function (DUF454) | |||
JFKAHJIP_00708 | 1.3e-153 | vicX | 3.1.26.11 | S | Metal-dependent hydrolases of the beta-lactamase superfamily I | |
JFKAHJIP_00709 | 3.2e-220 | vicK | 2.7.13.3 | T | Histidine kinase | |
JFKAHJIP_00710 | 3.8e-128 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
JFKAHJIP_00711 | 4.6e-140 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
JFKAHJIP_00712 | 3.6e-222 | sip | L | Belongs to the 'phage' integrase family | ||
JFKAHJIP_00713 | 1.2e-28 | S | MerR HTH family regulatory protein | |||
JFKAHJIP_00714 | 4.6e-201 | |||||
JFKAHJIP_00715 | 1.5e-95 | D | ftsk spoiiie | |||
JFKAHJIP_00721 | 4.1e-48 | K | DNA-binding protein | |||
JFKAHJIP_00722 | 2.5e-80 | |||||
JFKAHJIP_00723 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
JFKAHJIP_00724 | 1.5e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
JFKAHJIP_00725 | 3.3e-219 | metE | 2.1.1.14 | E | Methionine synthase | |
JFKAHJIP_00726 | 1.1e-240 | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | ||
JFKAHJIP_00727 | 2.5e-239 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
JFKAHJIP_00729 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
JFKAHJIP_00730 | 2.7e-166 | XK27_01785 | S | cog cog1284 | ||
JFKAHJIP_00731 | 8.3e-120 | yaaA | S | Belongs to the UPF0246 family | ||
JFKAHJIP_00735 | 6.2e-120 | yoaK | S | Protein of unknown function (DUF1275) | ||
JFKAHJIP_00736 | 4.8e-85 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
JFKAHJIP_00737 | 9.2e-207 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
JFKAHJIP_00738 | 1.9e-133 | parB | K | Belongs to the ParB family | ||
JFKAHJIP_00739 | 1e-254 | 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 | ||
JFKAHJIP_00740 | 7.2e-198 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
JFKAHJIP_00741 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
JFKAHJIP_00742 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
JFKAHJIP_00743 | 2e-103 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
JFKAHJIP_00744 | 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 | ||
JFKAHJIP_00745 | 6.3e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
JFKAHJIP_00746 | 3e-60 | divIC | D | Septum formation initiator | ||
JFKAHJIP_00748 | 4.5e-236 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
JFKAHJIP_00749 | 1.1e-236 | tilS | 2.4.2.8, 6.3.4.19 | D | 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 | |
JFKAHJIP_00750 | 2e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
JFKAHJIP_00751 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
JFKAHJIP_00754 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
JFKAHJIP_00755 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
JFKAHJIP_00756 | 0.0 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
JFKAHJIP_00757 | 2.1e-288 | treB | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
JFKAHJIP_00758 | 1.7e-53 | treB | 2.7.1.201 | G | pts system | |
JFKAHJIP_00759 | 2.3e-125 | treR | K | trehalose operon | ||
JFKAHJIP_00760 | 4.3e-95 | ywlG | S | Belongs to the UPF0340 family | ||
JFKAHJIP_00763 | 8.2e-165 | fba | 4.1.2.13, 4.1.2.29 | G | aldolase | |
JFKAHJIP_00765 | 8.1e-238 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
JFKAHJIP_00766 | 6.5e-154 | endA | F | DNA RNA non-specific endonuclease | ||
JFKAHJIP_00767 | 5.5e-26 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
JFKAHJIP_00768 | 2e-233 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
JFKAHJIP_00770 | 2e-208 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
JFKAHJIP_00771 | 5.5e-250 | ydaM | M | Glycosyltransferases, probably involved in cell wall biogenesis | ||
JFKAHJIP_00773 | 8.4e-137 | |||||
JFKAHJIP_00774 | 6.6e-215 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
JFKAHJIP_00775 | 8.9e-76 | L | Transposase (IS116 IS110 IS902 family) | |||
JFKAHJIP_00776 | 1.3e-276 | thrC | 4.2.3.1 | E | Threonine synthase | |
JFKAHJIP_00777 | 7.1e-226 | norN | V | Mate efflux family protein | ||
JFKAHJIP_00778 | 1.4e-57 | asp | S | cog cog1302 | ||
JFKAHJIP_00779 | 3.8e-304 | yloV | S | kinase related to dihydroxyacetone kinase | ||
JFKAHJIP_00780 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
JFKAHJIP_00781 | 0.0 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
JFKAHJIP_00782 | 2.2e-76 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
JFKAHJIP_00783 | 3e-195 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
JFKAHJIP_00784 | 3.4e-14 | rpmH | J | Ribosomal protein L34 | ||
JFKAHJIP_00785 | 6.9e-101 | 1.6.5.2 | S | NADPH-quinone reductase (modulator of drug activity B) | ||
JFKAHJIP_00786 | 2.9e-105 | K | Transcriptional regulator | |||
JFKAHJIP_00787 | 1.2e-151 | jag | S | RNA-binding protein | ||
JFKAHJIP_00788 | 9.7e-147 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
JFKAHJIP_00789 | 3.8e-54 | 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 | |
JFKAHJIP_00790 | 1.6e-263 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
JFKAHJIP_00791 | 5.8e-230 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
JFKAHJIP_00793 | 1.9e-07 | |||||
JFKAHJIP_00798 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
JFKAHJIP_00799 | 1.6e-235 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
JFKAHJIP_00800 | 1.2e-35 | XK27_02060 | S | Transglycosylase associated protein | ||
JFKAHJIP_00801 | 2e-71 | badR | K | Transcriptional regulator, marr family | ||
JFKAHJIP_00802 | 1.1e-95 | S | reductase | |||
JFKAHJIP_00804 | 9e-139 | ykuT | M | mechanosensitive ion channel | ||
JFKAHJIP_00805 | 5.2e-229 | 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 | ||
JFKAHJIP_00806 | 1e-70 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
JFKAHJIP_00807 | 5.8e-310 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
JFKAHJIP_00808 | 3.8e-84 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
JFKAHJIP_00809 | 1.1e-77 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
JFKAHJIP_00810 | 2.5e-83 | XK27_02675 | K | Acetyltransferase GNAT Family | ||
JFKAHJIP_00811 | 2.6e-177 | prmA | J | Ribosomal protein L11 methyltransferase | ||
JFKAHJIP_00812 | 3.4e-132 | 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 | |
JFKAHJIP_00813 | 0.0 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
JFKAHJIP_00814 | 9.1e-83 | nrdI | F | Belongs to the NrdI family | ||
JFKAHJIP_00815 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
JFKAHJIP_00816 | 2.8e-73 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
JFKAHJIP_00817 | 0.0 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
JFKAHJIP_00818 | 8.7e-237 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
JFKAHJIP_00819 | 3.3e-112 | 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 | |
JFKAHJIP_00820 | 1.3e-111 | fnr5 | K | Catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
JFKAHJIP_00821 | 2.9e-194 | yhjX | P | Major Facilitator | ||
JFKAHJIP_00822 | 9.2e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
JFKAHJIP_00823 | 5.4e-72 | V | VanZ like family | |||
JFKAHJIP_00824 | 1.8e-180 | D | nuclear chromosome segregation | |||
JFKAHJIP_00826 | 2.8e-17 | KT | phosphorelay signal transduction system | |||
JFKAHJIP_00827 | 1.8e-120 | agrA | KT | response regulator | ||
JFKAHJIP_00828 | 2.1e-148 | comD | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
JFKAHJIP_00829 | 1.9e-53 | |||||
JFKAHJIP_00831 | 8.5e-11 | |||||
JFKAHJIP_00832 | 1.6e-128 | V | ABC transporter | |||
JFKAHJIP_00833 | 1e-49 | |||||
JFKAHJIP_00834 | 2.2e-123 | glnQ | E | abc transporter atp-binding protein | ||
JFKAHJIP_00835 | 5.5e-273 | glnP | P | ABC transporter | ||
JFKAHJIP_00836 | 1.5e-152 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
JFKAHJIP_00837 | 6.3e-18 | S | Protein of unknown function (DUF3021) | |||
JFKAHJIP_00838 | 2e-124 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
JFKAHJIP_00839 | 3e-183 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
JFKAHJIP_00840 | 1.7e-137 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
JFKAHJIP_00841 | 1.2e-233 | sufD | O | assembly protein SufD | ||
JFKAHJIP_00842 | 2.8e-235 | 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 | |
JFKAHJIP_00843 | 9.4e-74 | nifU | C | SUF system FeS assembly protein, NifU family | ||
JFKAHJIP_00844 | 2.9e-273 | sufB | O | assembly protein SufB | ||
JFKAHJIP_00845 | 2.7e-26 | |||||
JFKAHJIP_00846 | 4e-156 | 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 | ||
JFKAHJIP_00847 | 2.8e-182 | 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 | ||
JFKAHJIP_00848 | 2e-71 | adcR | K | transcriptional | ||
JFKAHJIP_00849 | 2.4e-135 | adcC | P | ABC transporter, ATP-binding protein | ||
JFKAHJIP_00850 | 3.9e-129 | adcB | P | ABC transporter (Permease | ||
JFKAHJIP_00851 | 2.9e-160 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
JFKAHJIP_00852 | 0.0 | ptsG | 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
JFKAHJIP_00853 | 4.6e-154 | rgfB | 3.1.3.90 | L | Endonuclease/Exonuclease/phosphatase family | |
JFKAHJIP_00854 | 4.2e-253 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
JFKAHJIP_00855 | 1.4e-142 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
JFKAHJIP_00856 | 0.0 | srlM | 2.7.1.202, 2.7.1.204 | GKT | Mga helix-turn-helix domain | |
JFKAHJIP_00857 | 6.8e-84 | gutM | K | phosphoenolpyruvate-dependent sugar phosphotransferase system | ||
JFKAHJIP_00858 | 1.1e-95 | srlA | G | PTS system glucitol sorbitol-specific | ||
JFKAHJIP_00859 | 3.8e-179 | srlE | 2.7.1.198 | G | PTS sorbitol transporter subunit IIB | |
JFKAHJIP_00860 | 4.2e-59 | srlB | 2.7.1.198 | G | sorbitol-specific, IIA component | |
JFKAHJIP_00861 | 9.2e-59 | L | MULE transposase domain | |||
JFKAHJIP_00862 | 1.1e-108 | L | Transposase IS116 IS110 IS902 | |||
JFKAHJIP_00863 | 1.3e-305 | 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 | |
JFKAHJIP_00864 | 2.2e-219 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
JFKAHJIP_00865 | 1.4e-153 | Z012_04635 | K | sequence-specific DNA binding | ||
JFKAHJIP_00866 | 6.5e-282 | V | ABC transporter | |||
JFKAHJIP_00867 | 6.1e-126 | yeeN | K | transcriptional regulatory protein | ||
JFKAHJIP_00868 | 2.2e-46 | yajC | U | protein transport | ||
JFKAHJIP_00869 | 5.3e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
JFKAHJIP_00870 | 9.3e-144 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
JFKAHJIP_00871 | 2.1e-230 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
JFKAHJIP_00872 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
JFKAHJIP_00873 | 0.0 | WQ51_06230 | S | ABC transporter | ||
JFKAHJIP_00874 | 1.4e-142 | cmpC | S | abc transporter atp-binding protein | ||
JFKAHJIP_00875 | 4.9e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
JFKAHJIP_00876 | 1.5e-286 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
JFKAHJIP_00878 | 1.9e-44 | |||||
JFKAHJIP_00879 | 5.8e-55 | S | TM2 domain | |||
JFKAHJIP_00880 | 1.3e-159 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
JFKAHJIP_00881 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
JFKAHJIP_00882 | 2.8e-24 | secE | U | Belongs to the SecE SEC61-gamma family | ||
JFKAHJIP_00883 | 8.4e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
JFKAHJIP_00884 | 3e-67 | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidate phosphatase activity | ||
JFKAHJIP_00885 | 1.5e-144 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
JFKAHJIP_00886 | 3e-131 | glcR | K | transcriptional regulator (DeoR family) | ||
JFKAHJIP_00887 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JFKAHJIP_00888 | 1.4e-72 | K | transcriptional | |||
JFKAHJIP_00889 | 8e-227 | S | COG1073 Hydrolases of the alpha beta superfamily | |||
JFKAHJIP_00890 | 1.2e-41 | yjdF | S | Protein of unknown function (DUF2992) | ||
JFKAHJIP_00891 | 6.3e-48 | 3.2.2.21 | S | YCII-related domain | ||
JFKAHJIP_00892 | 3.7e-51 | K | regulation of RNA biosynthetic process | |||
JFKAHJIP_00893 | 2.2e-154 | cylA | V | abc transporter atp-binding protein | ||
JFKAHJIP_00894 | 1.6e-133 | cylB | V | ABC-2 type transporter | ||
JFKAHJIP_00895 | 2.6e-74 | K | COG3279 Response regulator of the LytR AlgR family | |||
JFKAHJIP_00896 | 1.4e-29 | S | Protein of unknown function (DUF3021) | |||
JFKAHJIP_00897 | 4.9e-120 | mta | K | Transcriptional | ||
JFKAHJIP_00898 | 8.1e-120 | yhcA | V | abc transporter atp-binding protein | ||
JFKAHJIP_00899 | 5.9e-206 | macB_2 | V | FtsX-like permease family | ||
JFKAHJIP_00900 | 5.7e-272 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
JFKAHJIP_00901 | 1.7e-148 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
JFKAHJIP_00902 | 1.1e-77 | yhaI | S | Protein of unknown function (DUF805) | ||
JFKAHJIP_00903 | 5.8e-255 | pepC | 3.4.22.40 | E | aminopeptidase | |
JFKAHJIP_00904 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
JFKAHJIP_00905 | 4.3e-109 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
JFKAHJIP_00906 | 5.8e-94 | ypsA | S | Belongs to the UPF0398 family | ||
JFKAHJIP_00907 | 1.1e-50 | 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 | ||
JFKAHJIP_00908 | 1.3e-223 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
JFKAHJIP_00909 | 4e-284 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
JFKAHJIP_00910 | 0.0 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
JFKAHJIP_00911 | 9.6e-23 | |||||
JFKAHJIP_00912 | 4.7e-257 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
JFKAHJIP_00913 | 4.1e-89 | XK27_09675 | K | histone acetyltransferase HPA2 and related acetyltransferases | ||
JFKAHJIP_00914 | 6.9e-305 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
JFKAHJIP_00915 | 1.2e-77 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
JFKAHJIP_00916 | 3.4e-166 | 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 | ||
JFKAHJIP_00917 | 2e-45 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
JFKAHJIP_00918 | 1e-128 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
JFKAHJIP_00919 | 2.5e-94 | XK27_09705 | 6.1.1.14 | S | HD superfamily hydrolase | |
JFKAHJIP_00920 | 6.9e-103 | ybhL | S | Belongs to the BI1 family | ||
JFKAHJIP_00921 | 8.4e-13 | ycdA | S | Domain of unknown function (DUF4352) | ||
JFKAHJIP_00922 | 2.1e-243 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
JFKAHJIP_00923 | 6.9e-90 | K | transcriptional regulator | |||
JFKAHJIP_00924 | 1.6e-36 | yneF | S | UPF0154 protein | ||
JFKAHJIP_00925 | 1.5e-149 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
JFKAHJIP_00926 | 3.2e-186 | 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 | |
JFKAHJIP_00927 | 3.9e-98 | XK27_09740 | S | Phosphoesterase | ||
JFKAHJIP_00928 | 8.3e-87 | ykuL | S | CBS domain | ||
JFKAHJIP_00929 | 2.7e-132 | xerD | L | tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site | ||
JFKAHJIP_00930 | 1.8e-122 | 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 | ||
JFKAHJIP_00931 | 6.5e-94 | 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 | ||
JFKAHJIP_00932 | 3.4e-132 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
JFKAHJIP_00933 | 1.4e-13 | yidD | M | Could be involved in insertion of integral membrane proteins into the membrane | ||
JFKAHJIP_00934 | 4.9e-260 | trkH | P | Cation transport protein | ||
JFKAHJIP_00935 | 1.2e-247 | trkA | P | Potassium transporter peripheral membrane component | ||
JFKAHJIP_00936 | 6.1e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
JFKAHJIP_00937 | 3.2e-90 | ribU | 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 | ||
JFKAHJIP_00938 | 2.8e-106 | bcrC | 3.6.1.27 | I | Membrane-associated phospholipid phosphatase | |
JFKAHJIP_00939 | 1.1e-137 | K | sequence-specific DNA binding | |||
JFKAHJIP_00940 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
JFKAHJIP_00941 | 6.4e-54 | yhaI | L | Membrane | ||
JFKAHJIP_00942 | 5.7e-92 | S | Domain of unknown function (DUF4173) | |||
JFKAHJIP_00943 | 1.5e-94 | ureI | S | AmiS/UreI family transporter | ||
JFKAHJIP_00944 | 7.6e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
JFKAHJIP_00945 | 7.8e-54 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
JFKAHJIP_00946 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
JFKAHJIP_00947 | 2.5e-77 | ureE | O | enzyme active site formation | ||
JFKAHJIP_00948 | 5.3e-130 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
JFKAHJIP_00949 | 3.6e-111 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
JFKAHJIP_00950 | 1.9e-158 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
JFKAHJIP_00951 | 3.9e-176 | cbiM | P | biosynthesis protein CbiM | ||
JFKAHJIP_00952 | 1.4e-136 | P | cobalt transport protein | |||
JFKAHJIP_00953 | 2.4e-130 | cbiO | P | ABC transporter | ||
JFKAHJIP_00954 | 6.3e-138 | ET | ABC transporter substrate-binding protein | |||
JFKAHJIP_00955 | 1.4e-164 | metQ | M | Belongs to the NlpA lipoprotein family | ||
JFKAHJIP_00956 | 2e-263 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
JFKAHJIP_00957 | 2.4e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
JFKAHJIP_00958 | 8e-99 | metI | P | ABC transporter (Permease | ||
JFKAHJIP_00959 | 9.7e-209 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
JFKAHJIP_00960 | 1.2e-157 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
JFKAHJIP_00961 | 6.7e-93 | S | UPF0397 protein | |||
JFKAHJIP_00962 | 4.3e-308 | ykoD | P | abc transporter atp-binding protein | ||
JFKAHJIP_00963 | 3.2e-147 | cbiQ | P | cobalt transport | ||
JFKAHJIP_00964 | 4.8e-117 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
JFKAHJIP_00965 | 9.8e-234 | P | COG0168 Trk-type K transport systems, membrane components | |||
JFKAHJIP_00966 | 5.5e-127 | rsmG | 2.1.1.170 | J | Ribosomal RNA small subunit methyltransferase G | |
JFKAHJIP_00967 | 3.1e-90 | yceD | K | metal-binding, possibly nucleic acid-binding protein | ||
JFKAHJIP_00968 | 7.9e-123 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
JFKAHJIP_00969 | 3.2e-281 | T | PhoQ Sensor | |||
JFKAHJIP_00970 | 1.4e-81 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
JFKAHJIP_00971 | 3.6e-216 | dnaB | L | Replication initiation and membrane attachment | ||
JFKAHJIP_00972 | 1.5e-166 | dnaI | L | Primosomal protein DnaI | ||
JFKAHJIP_00973 | 2.6e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
JFKAHJIP_00974 | 1e-113 | |||||
JFKAHJIP_00975 | 1.4e-229 | 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) | |
JFKAHJIP_00976 | 2.5e-62 | manO | S | protein conserved in bacteria | ||
JFKAHJIP_00977 | 3.3e-169 | manN | G | PTS system mannose fructose sorbose family IID component | ||
JFKAHJIP_00978 | 1.2e-117 | manM | G | pts system | ||
JFKAHJIP_00979 | 4e-176 | manL | 2.7.1.191 | G | pts system | |
JFKAHJIP_00980 | 1e-66 | manO | S | Protein conserved in bacteria | ||
JFKAHJIP_00981 | 2.8e-160 | manN | G | PTS system mannose fructose sorbose family IID component | ||
JFKAHJIP_00982 | 4.8e-132 | manY | G | pts system | ||
JFKAHJIP_00983 | 2.4e-168 | manL | 2.7.1.191 | G | pts system | |
JFKAHJIP_00984 | 3.2e-138 | XK27_00940 | 1.2.1.70, 3.5.1.9 | S | Metal-dependent hydrolase | |
JFKAHJIP_00985 | 3.5e-154 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
JFKAHJIP_00986 | 3.6e-247 | pbuO | S | permease | ||
JFKAHJIP_00987 | 4.7e-76 | ydiB | 2.7.1.221, 5.1.1.1 | M | ATPase or kinase | |
JFKAHJIP_00988 | 6e-91 | XK27_05885 | 2.3.1.82 | M | phosphinothricin N-acetyltransferase activity | |
JFKAHJIP_00989 | 4.4e-188 | brpA | K | Transcriptional | ||
JFKAHJIP_00990 | 2.3e-81 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
JFKAHJIP_00991 | 2.4e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
JFKAHJIP_00992 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
JFKAHJIP_00993 | 8e-42 | ylxQ | J | ribosomal protein | ||
JFKAHJIP_00994 | 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 | ||
JFKAHJIP_00995 | 8.6e-57 | 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 | ||
JFKAHJIP_00996 | 2.9e-99 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
JFKAHJIP_00997 | 1.9e-272 | murE | 6.3.2.13, 6.3.2.7 | M | to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
JFKAHJIP_00998 | 1.3e-282 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
JFKAHJIP_00999 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | cation transport ATPase | |
JFKAHJIP_01000 | 5.1e-201 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
JFKAHJIP_01001 | 1.5e-222 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
JFKAHJIP_01002 | 0.0 | 3.2.1.26, 3.2.1.65 | GH32 | G | Belongs to the glycosyl hydrolase 32 family | |
JFKAHJIP_01003 | 0.0 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | G | Belongs to the glycosyl hydrolase 68 family |
JFKAHJIP_01004 | 5.7e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
JFKAHJIP_01005 | 3.7e-105 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
JFKAHJIP_01006 | 9.8e-74 | ylbF | S | Belongs to the UPF0342 family | ||
JFKAHJIP_01007 | 1.9e-46 | ylbG | S | UPF0298 protein | ||
JFKAHJIP_01008 | 1.4e-212 | livJ | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
JFKAHJIP_01009 | 4.2e-145 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
JFKAHJIP_01010 | 8.3e-139 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
JFKAHJIP_01011 | 2.4e-136 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
JFKAHJIP_01012 | 5.6e-124 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
JFKAHJIP_01013 | 7.1e-113 | acuB | S | CBS domain | ||
JFKAHJIP_01014 | 6.3e-168 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
JFKAHJIP_01015 | 3.2e-107 | yvyE | 3.4.13.9 | S | YigZ family | |
JFKAHJIP_01016 | 7.5e-247 | comFA | L | Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
JFKAHJIP_01017 | 1e-82 | comFC | K | competence protein | ||
JFKAHJIP_01018 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
JFKAHJIP_01019 | 2.4e-115 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
JFKAHJIP_01020 | 4.6e-88 | XK27_10930 | K | acetyltransferase | ||
JFKAHJIP_01021 | 7.5e-14 | |||||
JFKAHJIP_01022 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
JFKAHJIP_01023 | 5.8e-289 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
JFKAHJIP_01024 | 6.6e-32 | 3.4.24.40 | U | Large extracellular alpha-helical protein | ||
JFKAHJIP_01025 | 3.5e-48 | L | COG1943 Transposase and inactivated derivatives | |||
JFKAHJIP_01026 | 1.1e-89 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
JFKAHJIP_01027 | 4.2e-84 | mreD | M | rod shape-determining protein MreD | ||
JFKAHJIP_01028 | 9.2e-110 | mreC | M | Involved in formation and maintenance of cell shape | ||
JFKAHJIP_01036 | 6.7e-139 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
JFKAHJIP_01037 | 1.4e-142 | peb1A | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
JFKAHJIP_01038 | 1.9e-116 | gltJ | P | ABC transporter (Permease | ||
JFKAHJIP_01039 | 2.8e-226 | 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) | |
JFKAHJIP_01040 | 2.1e-109 | lytC | 3.4.17.14, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
JFKAHJIP_01041 | 0.0 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
JFKAHJIP_01042 | 4.9e-146 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
JFKAHJIP_01043 | 7.6e-230 | ycdB | P | peroxidase | ||
JFKAHJIP_01044 | 5.7e-292 | ywbL | P | COG0672 High-affinity Fe2 Pb2 permease | ||
JFKAHJIP_01045 | 1.3e-123 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
JFKAHJIP_01046 | 6.1e-25 | tatA | U | protein secretion | ||
JFKAHJIP_01047 | 1.8e-212 | msmX | P | Belongs to the ABC transporter superfamily | ||
JFKAHJIP_01048 | 9.8e-152 | malG | P | ABC transporter (Permease | ||
JFKAHJIP_01049 | 9.7e-250 | malF | P | ABC transporter (Permease | ||
JFKAHJIP_01050 | 9.6e-228 | malX | G | ABC transporter | ||
JFKAHJIP_01051 | 8.7e-171 | malR | K | Transcriptional regulator | ||
JFKAHJIP_01052 | 1.2e-301 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
JFKAHJIP_01053 | 0.0 | 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 |
JFKAHJIP_01054 | 3.2e-12 | |||||
JFKAHJIP_01055 | 1.9e-186 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
JFKAHJIP_01056 | 6e-194 | xerS | D | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division | ||
JFKAHJIP_01057 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
JFKAHJIP_01058 | 3.2e-113 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
JFKAHJIP_01059 | 3.9e-139 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
JFKAHJIP_01060 | 4e-150 | 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 | |
JFKAHJIP_01061 | 1.5e-155 | pstA | P | phosphate transport system permease | ||
JFKAHJIP_01062 | 1.9e-156 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
JFKAHJIP_01063 | 9e-156 | pstS | P | phosphate | ||
JFKAHJIP_01064 | 6.9e-253 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
JFKAHJIP_01065 | 2e-143 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
JFKAHJIP_01066 | 1e-44 | yktA | S | Belongs to the UPF0223 family | ||
JFKAHJIP_01067 | 1.6e-70 | 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 | |
JFKAHJIP_01068 | 1.3e-170 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
JFKAHJIP_01069 | 3.2e-150 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
JFKAHJIP_01070 | 6.9e-248 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
JFKAHJIP_01071 | 4.7e-35 | M1-755 | S | Domain of unknown function (DUF1858) | ||
JFKAHJIP_01072 | 1.3e-111 | hsdS2 | 2.1.1.72 | V | Type I restriction modification DNA specificity domain | |
JFKAHJIP_01073 | 8.5e-87 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
JFKAHJIP_01074 | 8.7e-60 | S | haloacid dehalogenase-like hydrolase | |||
JFKAHJIP_01075 | 2.9e-27 | S | haloacid dehalogenase-like hydrolase | |||
JFKAHJIP_01076 | 4.3e-239 | metY | 2.5.1.49 | E | o-acetylhomoserine | |
JFKAHJIP_01077 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
JFKAHJIP_01078 | 4.3e-242 | agcS | E | (Alanine) symporter | ||
JFKAHJIP_01079 | 5.6e-245 | 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 | ||
JFKAHJIP_01080 | 2.7e-177 | bglC | K | Transcriptional regulator | ||
JFKAHJIP_01081 | 0.0 | sasH | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
JFKAHJIP_01082 | 6.4e-82 | yecS | P | ABC transporter (Permease | ||
JFKAHJIP_01083 | 1.3e-148 | yckB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
JFKAHJIP_01084 | 1.1e-240 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
JFKAHJIP_01085 | 4.4e-112 | 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) | |
JFKAHJIP_01086 | 4.5e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
JFKAHJIP_01087 | 6.5e-176 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
JFKAHJIP_01088 | 5e-145 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
JFKAHJIP_01089 | 2.6e-92 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1 family | |
JFKAHJIP_01090 | 1.3e-132 | S | TraX protein | |||
JFKAHJIP_01091 | 3.3e-308 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
JFKAHJIP_01092 | 2.4e-260 | S | Psort location CytoplasmicMembrane, score | |||
JFKAHJIP_01093 | 1.4e-232 | dinF | V | Mate efflux family protein | ||
JFKAHJIP_01094 | 1.9e-170 | P | abc-type fe3 -hydroxamate transport system, periplasmic component | |||
JFKAHJIP_01095 | 1.5e-21 | V | Type III restriction enzyme, res subunit | |||
JFKAHJIP_01096 | 1.2e-106 | V | Type III restriction enzyme, res subunit | |||
JFKAHJIP_01097 | 6.6e-19 | V | Type III restriction enzyme, res subunit | |||
JFKAHJIP_01098 | 5.4e-110 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant 1 | |
JFKAHJIP_01099 | 2e-236 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
JFKAHJIP_01100 | 3.4e-186 | adhB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
JFKAHJIP_01101 | 6.1e-194 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
JFKAHJIP_01102 | 7.3e-161 | czcD | P | cation diffusion facilitator family transporter | ||
JFKAHJIP_01103 | 1.4e-104 | K | Transcriptional regulator, TetR family | |||
JFKAHJIP_01104 | 5.9e-61 | S | Protein of unknown function with HXXEE motif | |||
JFKAHJIP_01105 | 1.8e-11 | |||||
JFKAHJIP_01106 | 2e-74 | pnuC | H | nicotinamide mononucleotide transporter | ||
JFKAHJIP_01107 | 3e-113 | tnp | L | DDE domain | ||
JFKAHJIP_01108 | 9.7e-149 | cbiO2 | P | 'abc transporter, ATP-binding protein | ||
JFKAHJIP_01109 | 5.9e-157 | P | abc transporter atp-binding protein | |||
JFKAHJIP_01110 | 1.3e-132 | cbiQ | P | Cobalt transport protein | ||
JFKAHJIP_01111 | 2.2e-92 | 2.7.7.65 | T | Psort location CytoplasmicMembrane, score | ||
JFKAHJIP_01112 | 4.4e-141 | S | Phenazine biosynthesis protein | |||
JFKAHJIP_01113 | 6.5e-108 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
JFKAHJIP_01114 | 1e-263 | proWX | P | ABC transporter | ||
JFKAHJIP_01115 | 4.6e-129 | proV | E | abc transporter atp-binding protein | ||
JFKAHJIP_01116 | 4.5e-169 | C | alcohol dehydrogenase | |||
JFKAHJIP_01117 | 4.6e-133 | 1.6.5.2 | GM | NmrA-like family | ||
JFKAHJIP_01118 | 2.3e-67 | mgrA | K | Transcriptional regulator, MarR family | ||
JFKAHJIP_01119 | 4e-36 | S | Macro domain | |||
JFKAHJIP_01120 | 9.4e-12 | S | Macro domain | |||
JFKAHJIP_01121 | 2.6e-96 | K | COG COG0846 NAD-dependent protein deacetylases, SIR2 family | |||
JFKAHJIP_01122 | 2.8e-41 | C | Pyridoxamine 5'-phosphate oxidase | |||
JFKAHJIP_01123 | 3.1e-130 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
JFKAHJIP_01124 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
JFKAHJIP_01127 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
JFKAHJIP_01129 | 1e-20 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
JFKAHJIP_01130 | 4e-130 | deoD | 2.4.2.1, 2.4.2.28 | F | purine nucleoside phosphorylase | |
JFKAHJIP_01131 | 5.8e-137 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
JFKAHJIP_01132 | 4.7e-182 | clcA_2 | P | Chloride transporter, ClC family | ||
JFKAHJIP_01133 | 2.9e-148 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
JFKAHJIP_01134 | 5.5e-95 | S | Protein of unknown function (DUF1697) | |||
JFKAHJIP_01135 | 1.3e-234 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
JFKAHJIP_01136 | 1.5e-121 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
JFKAHJIP_01137 | 8e-252 | V | Glucan-binding protein C | |||
JFKAHJIP_01138 | 8.6e-57 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
JFKAHJIP_01139 | 2e-111 | XK27_05470 | E | Methionine synthase | ||
JFKAHJIP_01140 | 5.9e-85 | XK27_05470 | E | Methionine synthase | ||
JFKAHJIP_01141 | 1.1e-258 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
JFKAHJIP_01142 | 4.7e-236 | T | PhoQ Sensor | |||
JFKAHJIP_01143 | 1.5e-118 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
JFKAHJIP_01144 | 2e-149 | S | TraX protein | |||
JFKAHJIP_01146 | 1.3e-51 | V | ABC-2 family transporter protein | |||
JFKAHJIP_01147 | 4.6e-83 | mutF | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
JFKAHJIP_01148 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
JFKAHJIP_01149 | 2.5e-155 | dprA | LU | DNA protecting protein DprA | ||
JFKAHJIP_01150 | 4.4e-161 | GK | ROK family | |||
JFKAHJIP_01151 | 7.7e-135 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
JFKAHJIP_01152 | 2.1e-157 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
JFKAHJIP_01153 | 4e-127 | K | DNA-binding helix-turn-helix protein | |||
JFKAHJIP_01154 | 2.7e-91 | niaR | S | small molecule binding protein (contains 3H domain) | ||
JFKAHJIP_01155 | 2.7e-86 | |||||
JFKAHJIP_01156 | 1.9e-273 | 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 | |
JFKAHJIP_01157 | 2e-55 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
JFKAHJIP_01158 | 1e-125 | gntR1 | K | transcriptional | ||
JFKAHJIP_01159 | 2.3e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
JFKAHJIP_01160 | 2.2e-102 | rimL | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | ||
JFKAHJIP_01161 | 3e-187 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
JFKAHJIP_01162 | 1.8e-44 | |||||
JFKAHJIP_01163 | 1.4e-49 | |||||
JFKAHJIP_01164 | 1.5e-269 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
JFKAHJIP_01165 | 7.9e-157 | aatB | ET | ABC transporter substrate-binding protein | ||
JFKAHJIP_01166 | 8.8e-113 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
JFKAHJIP_01167 | 1.4e-105 | artQ | P | ABC transporter (Permease | ||
JFKAHJIP_01168 | 6.6e-59 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
JFKAHJIP_01169 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
JFKAHJIP_01170 | 2.9e-165 | cpsY | K | Transcriptional regulator | ||
JFKAHJIP_01171 | 1.3e-128 | mur1 | 3.4.17.14, 3.5.1.28 | NU | muramidase | |
JFKAHJIP_01172 | 7.4e-170 | yeiH | S | Membrane | ||
JFKAHJIP_01174 | 2.6e-09 | |||||
JFKAHJIP_01175 | 5.6e-294 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JFKAHJIP_01176 | 6.1e-146 | XK27_10720 | D | peptidase activity | ||
JFKAHJIP_01177 | 4e-275 | pepD | E | Dipeptidase | ||
JFKAHJIP_01178 | 2.2e-160 | whiA | K | May be required for sporulation | ||
JFKAHJIP_01179 | 1.4e-181 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
JFKAHJIP_01180 | 1.6e-163 | rapZ | S | Displays ATPase and GTPase activities | ||
JFKAHJIP_01181 | 1.4e-136 | yejC | S | cyclic nucleotide-binding protein | ||
JFKAHJIP_01182 | 6.6e-202 | D | nuclear chromosome segregation | |||
JFKAHJIP_01183 | 1.4e-94 | queF | 1.7.1.13 | S | Belongs to the GTP cyclohydrolase I family. QueF type 1 subfamily | |
JFKAHJIP_01184 | 4.6e-134 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
JFKAHJIP_01185 | 8.2e-81 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
JFKAHJIP_01186 | 2.6e-123 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
JFKAHJIP_01187 | 2.3e-63 | tdcF | 3.5.99.10 | J | endoribonuclease L-PSP | |
JFKAHJIP_01188 | 8.1e-200 | pmrB | EGP | Major facilitator Superfamily | ||
JFKAHJIP_01189 | 1.8e-18 | |||||
JFKAHJIP_01190 | 9.3e-261 | asnS | 6.1.1.22 | J | Catalyzes a two-step reaction, first charging an asparagine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
JFKAHJIP_01191 | 2.8e-213 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
JFKAHJIP_01192 | 8.6e-76 | ypmB | S | Protein conserved in bacteria | ||
JFKAHJIP_01193 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
JFKAHJIP_01194 | 6.8e-113 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
JFKAHJIP_01195 | 5e-168 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
JFKAHJIP_01196 | 5.1e-177 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
JFKAHJIP_01197 | 6.4e-282 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
JFKAHJIP_01198 | 2.8e-191 | tcsA | S | membrane | ||
JFKAHJIP_01199 | 1.3e-64 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
JFKAHJIP_01200 | 3.5e-112 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
JFKAHJIP_01201 | 1.9e-231 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
JFKAHJIP_01202 | 1.1e-104 | rsmC | 2.1.1.172 | J | Methyltransferase small domain protein | |
JFKAHJIP_01203 | 2.8e-171 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
JFKAHJIP_01204 | 1e-29 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
JFKAHJIP_01205 | 1.3e-241 | T | PhoQ Sensor | |||
JFKAHJIP_01206 | 9.4e-121 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
JFKAHJIP_01207 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
JFKAHJIP_01208 | 1.9e-116 | coaB | 4.1.1.36, 6.3.2.5 | H | Phosphopantothenate-cysteine ligase | |
JFKAHJIP_01209 | 2.2e-91 | 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 | |
JFKAHJIP_01210 | 4.1e-93 | panT | S | ECF transporter, substrate-specific component | ||
JFKAHJIP_01211 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
JFKAHJIP_01212 | 1.6e-165 | metF | 1.5.1.20 | E | reductase | |
JFKAHJIP_01213 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
JFKAHJIP_01215 | 0.0 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | EH | component I | |
JFKAHJIP_01216 | 0.0 | 3.6.3.8 | P | cation transport ATPase | ||
JFKAHJIP_01217 | 2.2e-243 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
JFKAHJIP_01218 | 2.2e-35 | dltC | 6.1.1.13 | IQ | 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 | |
JFKAHJIP_01219 | 1.7e-237 | dltB | M | Membrane protein involved in D-alanine export | ||
JFKAHJIP_01220 | 1.3e-298 | dltA | 6.1.1.13 | Q | 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 | |
JFKAHJIP_01221 | 0.0 | XK27_10035 | V | abc transporter atp-binding protein | ||
JFKAHJIP_01222 | 2.2e-294 | yfiB1 | V | abc transporter atp-binding protein | ||
JFKAHJIP_01223 | 1.4e-99 | pvaA | M | lytic transglycosylase activity | ||
JFKAHJIP_01224 | 2.1e-177 | ndpA | S | 37-kD nucleoid-associated bacterial protein | ||
JFKAHJIP_01225 | 2.7e-230 | 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 | |
JFKAHJIP_01226 | 4.5e-106 | 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 | |
JFKAHJIP_01227 | 8.3e-143 | 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 | |
JFKAHJIP_01228 | 3.6e-191 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
JFKAHJIP_01229 | 5.1e-110 | tdk | 2.7.1.21 | F | thymidine kinase | |
JFKAHJIP_01230 | 5.8e-183 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
JFKAHJIP_01231 | 4.9e-153 | gst | O | Glutathione S-transferase | ||
JFKAHJIP_01232 | 1.7e-176 | nrnA | 3.1.13.3, 3.1.3.7 | S | domain protein | |
JFKAHJIP_01233 | 4.6e-174 | 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 | |
JFKAHJIP_01234 | 4.4e-45 | rpmE2 | J | 50S ribosomal protein L31 | ||
JFKAHJIP_01235 | 3.9e-229 | mntH | P | Mn2 and Fe2 transporters of the NRAMP family | ||
JFKAHJIP_01236 | 5.8e-164 | ypuA | S | secreted protein | ||
JFKAHJIP_01237 | 2.4e-71 | yaeR | E | COG0346 Lactoylglutathione lyase and related lyases | ||
JFKAHJIP_01238 | 9.3e-133 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
JFKAHJIP_01239 | 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 | |
JFKAHJIP_01240 | 4.1e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
JFKAHJIP_01241 | 1.4e-256 | noxE | P | NADH oxidase | ||
JFKAHJIP_01242 | 1.1e-294 | yfmM | S | abc transporter atp-binding protein | ||
JFKAHJIP_01243 | 6.1e-83 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
JFKAHJIP_01244 | 1e-143 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
JFKAHJIP_01245 | 9.4e-81 | S | ECF-type riboflavin transporter, S component | |||
JFKAHJIP_01247 | 1e-237 | XK27_08130 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
JFKAHJIP_01248 | 6.6e-44 | L | Transposase | |||
JFKAHJIP_01249 | 8.6e-40 | L | Transposase | |||
JFKAHJIP_01250 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
JFKAHJIP_01251 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
JFKAHJIP_01252 | 1.1e-87 | XK27_08075 | M | glycosyl transferase family 2 | ||
JFKAHJIP_01253 | 1.2e-72 | XK27_08075 | M | glycosyl transferase family 2 | ||
JFKAHJIP_01254 | 4.9e-102 | S | Carbohydrate-binding domain-containing protein Cthe_2159 | |||
JFKAHJIP_01255 | 2.9e-142 | P | molecular chaperone | |||
JFKAHJIP_01256 | 2.2e-93 | XK27_05505 | S | Psort location CytoplasmicMembrane, score | ||
JFKAHJIP_01259 | 4.1e-50 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
JFKAHJIP_01260 | 3.6e-60 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
JFKAHJIP_01261 | 3.6e-137 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
JFKAHJIP_01262 | 2.4e-130 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
JFKAHJIP_01263 | 2.3e-110 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
JFKAHJIP_01264 | 1.1e-106 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
JFKAHJIP_01265 | 1.4e-234 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
JFKAHJIP_01266 | 5.5e-118 | hisG | 2.4.2.17 | E | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
JFKAHJIP_01267 | 5.5e-178 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
JFKAHJIP_01268 | 4.2e-192 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
JFKAHJIP_01269 | 1.8e-60 | XK27_08085 | ||||
JFKAHJIP_01270 | 4.7e-147 | XK27_08080 | 3.1.1.53 | G | Exopolysaccharide biosynthesis protein | |
JFKAHJIP_01271 | 6.7e-136 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
JFKAHJIP_01272 | 3.9e-116 | ylfI | S | tigr01906 | ||
JFKAHJIP_01273 | 1e-139 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
JFKAHJIP_01274 | 1.4e-141 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
JFKAHJIP_01275 | 8.2e-218 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
JFKAHJIP_01276 | 3.7e-30 | KT | response to antibiotic | |||
JFKAHJIP_01278 | 1.3e-204 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
JFKAHJIP_01279 | 2.7e-111 | rmlC | 1.1.1.133, 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 | |
JFKAHJIP_01280 | 2.4e-161 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
JFKAHJIP_01281 | 7.4e-258 | S | phospholipase Carboxylesterase | |||
JFKAHJIP_01282 | 1.1e-200 | yurR | 1.4.5.1 | E | oxidoreductase | |
JFKAHJIP_01283 | 8e-146 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
JFKAHJIP_01284 | 2.2e-145 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
JFKAHJIP_01285 | 2.6e-118 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
JFKAHJIP_01286 | 5e-64 | gtrA | S | GtrA-like protein | ||
JFKAHJIP_01287 | 1.3e-249 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
JFKAHJIP_01288 | 6e-169 | ybbR | S | Protein conserved in bacteria | ||
JFKAHJIP_01289 | 1.5e-147 | 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 | |
JFKAHJIP_01290 | 2.6e-255 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain protein | |
JFKAHJIP_01291 | 2.3e-150 | cobQ | S | glutamine amidotransferase | ||
JFKAHJIP_01292 | 0.0 | mprF | 2.3.2.3 | J | 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 | |
JFKAHJIP_01293 | 2e-132 | pip | 1.11.1.10 | S | Alpha beta hydrolase | |
JFKAHJIP_01294 | 5.3e-34 | MA20_06245 | S | yiaA/B two helix domain | ||
JFKAHJIP_01295 | 0.0 | uup | S | abc transporter atp-binding protein | ||
JFKAHJIP_01296 | 6.2e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
JFKAHJIP_01297 | 3.2e-179 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
JFKAHJIP_01298 | 9.9e-227 | XK27_05680 | 6.3.2.2, 6.3.2.4 | M | carbamoylphosphate synthase large subunit | |
JFKAHJIP_01299 | 2.7e-153 | XK27_05675 | S | Esterase | ||
JFKAHJIP_01300 | 6.1e-162 | XK27_05670 | S | Putative esterase | ||
JFKAHJIP_01301 | 1.1e-264 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
JFKAHJIP_01302 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
JFKAHJIP_01303 | 3e-38 | ptsH | G | phosphocarrier protein Hpr | ||
JFKAHJIP_01304 | 9.7e-222 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
JFKAHJIP_01305 | 2.5e-211 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
JFKAHJIP_01306 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
JFKAHJIP_01307 | 2.9e-34 | nrdH | O | Glutaredoxin | ||
JFKAHJIP_01308 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
JFKAHJIP_01309 | 8.5e-184 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
JFKAHJIP_01310 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
JFKAHJIP_01311 | 8.4e-138 | divIVA | D | Cell division initiation protein | ||
JFKAHJIP_01312 | 2.7e-143 | ylmH | S | conserved protein, contains S4-like domain | ||
JFKAHJIP_01313 | 6.5e-30 | yggT | D | integral membrane protein | ||
JFKAHJIP_01314 | 3.2e-101 | sepF | D | cell septum assembly | ||
JFKAHJIP_01315 | 2.1e-123 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
JFKAHJIP_01316 | 1.7e-238 | 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 | ||
JFKAHJIP_01317 | 7.1e-224 | 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 | ||
JFKAHJIP_01318 | 2.2e-133 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
JFKAHJIP_01319 | 1.9e-200 | murG | 2.4.1.227 | 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) |
JFKAHJIP_01320 | 1e-251 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
JFKAHJIP_01322 | 0.0 | typA | T | GTP-binding protein TypA | ||
JFKAHJIP_01323 | 3.5e-177 | glk | 2.7.1.2 | G | Glucokinase | |
JFKAHJIP_01324 | 2.4e-27 | yqgQ | S | protein conserved in bacteria | ||
JFKAHJIP_01325 | 5.2e-83 | perR | P | Belongs to the Fur family | ||
JFKAHJIP_01326 | 9.3e-92 | dps | P | Belongs to the Dps family | ||
JFKAHJIP_01327 | 7.5e-115 | pilD | 3.4.23.43 | NOU | Type II secretory pathway prepilin signal peptidase PulO and related peptidases | |
JFKAHJIP_01328 | 3.6e-172 | 3.5.2.6 | V | D-alanyl-D-alanine carboxypeptidase | ||
JFKAHJIP_01329 | 9.4e-112 | sodA | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
JFKAHJIP_01330 | 1.4e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
JFKAHJIP_01331 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
JFKAHJIP_01332 | 4.8e-64 | S | Domain of unknown function (DUF4430) | |||
JFKAHJIP_01333 | 6.7e-73 | S | Psort location CytoplasmicMembrane, score | |||
JFKAHJIP_01334 | 6e-129 | sitB | 3.6.3.35 | P | ABC transporter, ATP-binding protein | |
JFKAHJIP_01335 | 2.1e-133 | mtsC | P | ABC-type Mn2 Zn2 transport systems, permease components | ||
JFKAHJIP_01336 | 3.9e-165 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JFKAHJIP_01337 | 1.1e-118 | sirR | K | iron dependent repressor | ||
JFKAHJIP_01338 | 1.5e-134 | htpX | O | Belongs to the peptidase M48B family | ||
JFKAHJIP_01339 | 1.2e-92 | lemA | S | LemA family | ||
JFKAHJIP_01340 | 2.4e-176 | spd | F | DNA RNA non-specific endonuclease | ||
JFKAHJIP_01341 | 0.0 | 2.4.1.21 | GT5 | M | Right handed beta helix region | |
JFKAHJIP_01343 | 1.9e-135 | S | double-stranded DNA endodeoxyribonuclease activity | |||
JFKAHJIP_01344 | 1.8e-303 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
JFKAHJIP_01345 | 2.3e-123 | S | Protein conserved in bacteria | |||
JFKAHJIP_01346 | 2.9e-188 | S | KAP family P-loop domain | |||
JFKAHJIP_01347 | 1.3e-88 | hsdS | 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
JFKAHJIP_01348 | 1.7e-12 | |||||
JFKAHJIP_01349 | 2.4e-133 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
JFKAHJIP_01350 | 0.0 | hsdR | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
JFKAHJIP_01352 | 2e-130 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
JFKAHJIP_01353 | 2.7e-216 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
JFKAHJIP_01354 | 5.2e-113 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
JFKAHJIP_01355 | 5.7e-55 | 5.2.1.8 | G | hydrolase | ||
JFKAHJIP_01356 | 1.6e-69 | 5.2.1.8 | G | hydrolase | ||
JFKAHJIP_01357 | 5.3e-27 | P | Hemerythrin HHE cation binding domain protein | |||
JFKAHJIP_01358 | 4.8e-144 | XK27_00880 | 3.4.17.14, 3.5.1.28 | M | Glycosyl hydrolase, family 25 | |
JFKAHJIP_01359 | 1e-81 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
JFKAHJIP_01360 | 4.3e-115 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase | |
JFKAHJIP_01361 | 1.5e-174 | S | hydrolase | |||
JFKAHJIP_01362 | 8.4e-23 | |||||
JFKAHJIP_01363 | 4.6e-137 | M | LysM domain | |||
JFKAHJIP_01364 | 8.3e-287 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
JFKAHJIP_01366 | 8.7e-235 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
JFKAHJIP_01367 | 1.8e-33 | XK27_12190 | S | protein conserved in bacteria | ||
JFKAHJIP_01369 | 1e-88 | bioY | S | biotin synthase | ||
JFKAHJIP_01370 | 4.4e-252 | yegQ | O | Peptidase U32 | ||
JFKAHJIP_01371 | 6.8e-178 | yegQ | O | Peptidase U32 | ||
JFKAHJIP_01373 | 3e-67 | ytxH | S | General stress protein | ||
JFKAHJIP_01374 | 3.7e-08 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
JFKAHJIP_01375 | 1.2e-146 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
JFKAHJIP_01376 | 2.2e-168 | 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 | ||
JFKAHJIP_01377 | 2.9e-41 | pspC | KT | PspC domain | ||
JFKAHJIP_01378 | 0.0 | yhgF | K | Transcriptional accessory protein | ||
JFKAHJIP_01380 | 1.9e-156 | XK27_03015 | S | permease | ||
JFKAHJIP_01381 | 2.4e-147 | ycgQ | S | TIGR03943 family | ||
JFKAHJIP_01382 | 5.5e-168 | S | CRISPR-associated protein Csn2 subfamily St | |||
JFKAHJIP_01383 | 3.1e-53 | 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 | ||
JFKAHJIP_01384 | 3.5e-171 | 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 | ||
JFKAHJIP_01385 | 0.0 | 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 | ||
JFKAHJIP_01386 | 1.1e-284 | sulP | P | Sulfate permease and related transporters (MFS superfamily) | ||
JFKAHJIP_01387 | 3.6e-103 | |||||
JFKAHJIP_01388 | 2.9e-119 | estA | E | GDSL-like Lipase/Acylhydrolase | ||
JFKAHJIP_01389 | 2.3e-94 | S | CAAX protease self-immunity | |||
JFKAHJIP_01390 | 3e-49 | |||||
JFKAHJIP_01392 | 2.8e-63 | yqeB | S | Pyrimidine dimer DNA glycosylase | ||
JFKAHJIP_01393 | 4.1e-60 | S | Protein of unknown function (DUF1722) | |||
JFKAHJIP_01394 | 1.3e-19 | M | Bacterial lipoprotein | |||
JFKAHJIP_01395 | 1.2e-10 | |||||
JFKAHJIP_01396 | 2.8e-126 | V | CAAX protease self-immunity | |||
JFKAHJIP_01397 | 7.1e-47 | |||||
JFKAHJIP_01398 | 3.4e-74 | K | TetR family transcriptional regulator | |||
JFKAHJIP_01399 | 4.2e-80 | Q | Methyltransferase domain | |||
JFKAHJIP_01400 | 1e-141 | acoC | 2.3.1.12, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
JFKAHJIP_01401 | 1.3e-174 | acoB | C | dehydrogenase E1 component | ||
JFKAHJIP_01402 | 3.6e-167 | acoA | C | Acetoin dehydrogenase E1 component subunit alpha | ||
JFKAHJIP_01403 | 9.5e-173 | pdhD | 1.8.1.4 | C | Dehydrogenase | |
JFKAHJIP_01404 | 3.3e-08 | K | CsbD-like | |||
JFKAHJIP_01405 | 7.7e-68 | S | Asp23 family, cell envelope-related function | |||
JFKAHJIP_01406 | 1.5e-22 | S | Small integral membrane protein | |||
JFKAHJIP_01407 | 4.7e-97 | |||||
JFKAHJIP_01408 | 2.3e-29 | S | Membrane | |||
JFKAHJIP_01410 | 4.7e-172 | S | Domain of unknown function (DUF389) | |||
JFKAHJIP_01411 | 1.3e-157 | yegS | 2.7.1.107 | I | Diacylglycerol kinase | |
JFKAHJIP_01412 | 3.4e-126 | ybbA | S | Putative esterase | ||
JFKAHJIP_01413 | 2.9e-174 | fatB | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
JFKAHJIP_01414 | 9.8e-135 | fecE | 3.6.3.34 | HP | ABC transporter | |
JFKAHJIP_01415 | 3.9e-158 | fecD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
JFKAHJIP_01416 | 4.6e-116 | V | CAAX protease self-immunity | |||
JFKAHJIP_01417 | 1.2e-152 | S | Domain of unknown function (DUF4300) | |||
JFKAHJIP_01418 | 6.3e-91 | tetR | K | transcriptional regulator | ||
JFKAHJIP_01419 | 1.5e-282 | norB | P | Major facilitator superfamily | ||
JFKAHJIP_01421 | 5.9e-55 | bta | 1.8.1.8 | CO | cell redox homeostasis | |
JFKAHJIP_01422 | 8.2e-59 | L | thioesterase | |||
JFKAHJIP_01423 | 1.3e-142 | S | Macro domain protein | |||
JFKAHJIP_01424 | 6.3e-51 | trxA | O | Belongs to the thioredoxin family | ||
JFKAHJIP_01425 | 2.5e-74 | yccU | S | CoA-binding protein | ||
JFKAHJIP_01426 | 1.1e-144 | tatD | L | Hydrolase, tatd | ||
JFKAHJIP_01427 | 1.1e-98 | 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 | |
JFKAHJIP_01428 | 2.9e-154 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
JFKAHJIP_01430 | 6.4e-162 | rsgA | 3.1.3.100 | G | 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 | |
JFKAHJIP_01431 | 2.3e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
JFKAHJIP_01432 | 1.6e-117 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
JFKAHJIP_01433 | 1.6e-169 | rmuC | S | RmuC domain protein | ||
JFKAHJIP_01434 | 3.1e-178 | cbf | S | 3'-5' exoribonuclease yhaM | ||
JFKAHJIP_01435 | 4e-142 | purR | 2.4.2.7 | F | operon repressor | |
JFKAHJIP_01436 | 2.3e-69 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
JFKAHJIP_01437 | 3.9e-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 | ||
JFKAHJIP_01438 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
JFKAHJIP_01439 | 7.9e-188 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
JFKAHJIP_01440 | 7.1e-14 | |||||
JFKAHJIP_01441 | 5.8e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
JFKAHJIP_01442 | 3e-87 | S | Fusaric acid resistance protein-like | |||
JFKAHJIP_01443 | 2.5e-62 | glnR | K | Transcriptional regulator | ||
JFKAHJIP_01444 | 5.2e-264 | glnA | 6.3.1.2 | E | glutamine synthetase | |
JFKAHJIP_01445 | 6.6e-116 | pscB | M | CHAP domain protein | ||
JFKAHJIP_01446 | 0.0 | rnjA | S | 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 | ||
JFKAHJIP_01447 | 1.5e-33 | ykzG | S | Belongs to the UPF0356 family | ||
JFKAHJIP_01448 | 3.9e-114 | yeaZ | 2.3.1.234 | O | COG1214, inactive homolog of metal-dependent proteases | |
JFKAHJIP_01449 | 9e-72 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
JFKAHJIP_01450 | 1.3e-185 | tsaD | 2.3.1.234 | O | 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 | |
JFKAHJIP_01451 | 3.9e-114 | azlC | E | AzlC protein | ||
JFKAHJIP_01452 | 3.7e-46 | azlD | S | branched-chain amino acid | ||
JFKAHJIP_01453 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
JFKAHJIP_01454 | 1.5e-115 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
JFKAHJIP_01455 | 1.3e-154 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
JFKAHJIP_01456 | 9.3e-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 | ||
JFKAHJIP_01457 | 4.1e-90 | cvpA | S | toxin biosynthetic process | ||
JFKAHJIP_01458 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
JFKAHJIP_01459 | 6e-129 | V | ABC transporter, ATP-binding protein | |||
JFKAHJIP_01460 | 2.4e-228 | V | ABC transporter (Permease | |||
JFKAHJIP_01462 | 0.0 | V | ABC transporter (Permease | |||
JFKAHJIP_01463 | 5.9e-275 | 2.7.13.3 | T | Histidine kinase | ||
JFKAHJIP_01464 | 1.9e-93 | salR | K | helix_turn_helix, Lux Regulon | ||
JFKAHJIP_01465 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
JFKAHJIP_01466 | 1.3e-37 | |||||
JFKAHJIP_01469 | 3.4e-227 | mutY | L | A G-specific adenine glycosylase | ||
JFKAHJIP_01470 | 4.2e-42 | XK27_05745 | ||||
JFKAHJIP_01471 | 2.3e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
JFKAHJIP_01472 | 2.5e-81 | 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 | ||
JFKAHJIP_01473 | 1.7e-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 | ||
JFKAHJIP_01475 | 1.3e-122 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
JFKAHJIP_01476 | 4.2e-167 | corA | P | COG0598 Mg2 and Co2 transporters | ||
JFKAHJIP_01477 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | ||
JFKAHJIP_01481 | 2.8e-32 | blpT | ||||
JFKAHJIP_01483 | 5.4e-187 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
JFKAHJIP_01484 | 3.3e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
JFKAHJIP_01485 | 1.2e-97 | 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 | ||
JFKAHJIP_01486 | 1.7e-61 | yqhY | S | protein conserved in bacteria | ||
JFKAHJIP_01487 | 8.1e-73 | 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 | ||
JFKAHJIP_01488 | 4.4e-180 | scrR | K | Transcriptional regulator | ||
JFKAHJIP_01489 | 5.1e-289 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
JFKAHJIP_01490 | 0.0 | scrA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
JFKAHJIP_01491 | 7e-172 | scrK | 2.7.1.2, 2.7.1.4 | GK | Fructokinase | |
JFKAHJIP_01492 | 3.7e-187 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
JFKAHJIP_01494 | 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 | ||
JFKAHJIP_01495 | 3.3e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
JFKAHJIP_01496 | 5.5e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
JFKAHJIP_01497 | 3.4e-61 | 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 | |
JFKAHJIP_01498 | 8.8e-201 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
JFKAHJIP_01499 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
JFKAHJIP_01503 | 2.9e-31 | yozG | K | Transcriptional regulator | ||
JFKAHJIP_01504 | 1.2e-280 | V | ABC transporter transmembrane region | |||
JFKAHJIP_01505 | 6.8e-156 | K | Helix-turn-helix XRE-family like proteins | |||
JFKAHJIP_01507 | 4.6e-177 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
JFKAHJIP_01508 | 1.8e-259 | XK27_03190 | S | hydrolases of the HAD superfamily | ||
JFKAHJIP_01509 | 2.6e-110 | yebC | M | Membrane | ||
JFKAHJIP_01510 | 2.2e-307 | KT | response to antibiotic | |||
JFKAHJIP_01511 | 5.7e-74 | XK27_02470 | K | LytTr DNA-binding domain | ||
JFKAHJIP_01512 | 8.2e-120 | liaI | S | membrane | ||
JFKAHJIP_01513 | 5.6e-77 | mccF | V | LD-carboxypeptidase | ||
JFKAHJIP_01514 | 4e-43 | S | Sugar efflux transporter for intercellular exchange | |||
JFKAHJIP_01515 | 2.6e-194 | mccF | V | LD-carboxypeptidase | ||
JFKAHJIP_01516 | 9.2e-300 | O | MreB/Mbl protein | |||
JFKAHJIP_01518 | 1.3e-145 | V | Psort location CytoplasmicMembrane, score | |||
JFKAHJIP_01521 | 8.9e-14 | |||||
JFKAHJIP_01522 | 1.1e-242 | dcuS | 2.7.13.3 | T | protein histidine kinase activity | |
JFKAHJIP_01523 | 9.5e-245 | 2.7.13.3 | T | protein histidine kinase activity | ||
JFKAHJIP_01524 | 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 | |
JFKAHJIP_01525 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
JFKAHJIP_01526 | 2.3e-125 | S | Protein of unknown function (DUF554) | |||
JFKAHJIP_01527 | 3.4e-132 | ecsA_2 | V | abc transporter atp-binding protein | ||
JFKAHJIP_01528 | 2.4e-252 | XK27_00765 | ||||
JFKAHJIP_01529 | 1.3e-140 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
JFKAHJIP_01530 | 1.1e-199 | 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 | |
JFKAHJIP_01531 | 3.1e-63 | yhaI | S | Protein of unknown function (DUF805) | ||
JFKAHJIP_01532 | 5e-69 | yhaI | J | Protein of unknown function (DUF805) | ||
JFKAHJIP_01535 | 3.9e-173 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
JFKAHJIP_01536 | 2.4e-45 | ftsL | D | cell division protein FtsL | ||
JFKAHJIP_01537 | 0.0 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
JFKAHJIP_01538 | 1.7e-182 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
JFKAHJIP_01539 | 7.2e-221 | 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 | |
JFKAHJIP_01542 | 1.3e-257 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
JFKAHJIP_01543 | 4.7e-65 | yutD | J | protein conserved in bacteria | ||
JFKAHJIP_01544 | 1.8e-223 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
JFKAHJIP_01545 | 1.3e-93 | XK27_09885 | V | Glycopeptide antibiotics resistance protein | ||
JFKAHJIP_01548 | 0.0 | mdlA | V | abc transporter atp-binding protein | ||
JFKAHJIP_01549 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
JFKAHJIP_01559 | 5.2e-07 | |||||
JFKAHJIP_01560 | 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 | |
JFKAHJIP_01561 | 2e-163 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
JFKAHJIP_01562 | 4.5e-107 | V | CAAX protease self-immunity | |||
JFKAHJIP_01563 | 1.6e-140 | cppA | E | CppA N-terminal | ||
JFKAHJIP_01564 | 2.2e-176 | ampC | V | COG1680 Beta-lactamase class C and other penicillin binding proteins | ||
JFKAHJIP_01566 | 4.8e-76 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
JFKAHJIP_01567 | 4.4e-146 | cah | 4.2.1.1 | P | carbonic anhydrase | |
JFKAHJIP_01568 | 0.0 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
JFKAHJIP_01570 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase' | |
JFKAHJIP_01571 | 3.6e-202 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
JFKAHJIP_01572 | 3.6e-35 | |||||
JFKAHJIP_01573 | 3.7e-151 | yxeM | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
JFKAHJIP_01574 | 8e-163 | yxeN | P | ABC transporter (Permease | ||
JFKAHJIP_01575 | 1.2e-129 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
JFKAHJIP_01576 | 5e-10 | S | Protein of unknown function (DUF4059) | |||
JFKAHJIP_01577 | 8e-171 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
JFKAHJIP_01578 | 1.9e-92 | rsmD | 2.1.1.171 | L | Methyltransferase | |
JFKAHJIP_01579 | 8.6e-87 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
JFKAHJIP_01580 | 4.2e-187 | ylbL | T | Belongs to the peptidase S16 family | ||
JFKAHJIP_01581 | 8.4e-184 | yhcC | S | radical SAM protein | ||
JFKAHJIP_01582 | 1e-96 | ytqB | 2.1.1.176 | J | (SAM)-dependent | |
JFKAHJIP_01584 | 0.0 | yjcE | P | NhaP-type Na H and K H antiporters | ||
JFKAHJIP_01585 | 2.2e-15 | L | PFAM Integrase, catalytic core | |||
JFKAHJIP_01586 | 7e-56 | nrdD_1 | 1.1.98.6, 1.17.4.1 | F | Ribonucleoside-triphosphate reductase | |
JFKAHJIP_01588 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
JFKAHJIP_01589 | 8.4e-93 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
JFKAHJIP_01590 | 6.6e-198 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
JFKAHJIP_01591 | 2.9e-22 | WQ51_00220 | K | Helix-turn-helix domain | ||
JFKAHJIP_01592 | 1e-93 | S | Protein of unknown function (DUF3278) | |||
JFKAHJIP_01593 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
JFKAHJIP_01594 | 2.5e-124 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
JFKAHJIP_01595 | 1.7e-173 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
JFKAHJIP_01596 | 1.6e-199 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
JFKAHJIP_01597 | 1.8e-124 | alkD | L | Dna alkylation repair | ||
JFKAHJIP_01598 | 1.5e-299 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
JFKAHJIP_01599 | 1.1e-92 | pat | 2.3.1.183 | M | acetyltransferase | |
JFKAHJIP_01600 | 9.4e-272 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
JFKAHJIP_01601 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
JFKAHJIP_01602 | 2.8e-128 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
JFKAHJIP_01603 | 8.8e-119 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
JFKAHJIP_01604 | 3.4e-147 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
JFKAHJIP_01605 | 0.0 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
JFKAHJIP_01606 | 6.7e-162 | yjlA | EG | membrane | ||
JFKAHJIP_01607 | 1.3e-80 | 3.4.21.89 | S | RDD family | ||
JFKAHJIP_01608 | 7.5e-49 | |||||
JFKAHJIP_01609 | 1.7e-88 | |||||
JFKAHJIP_01610 | 2.3e-24 | |||||
JFKAHJIP_01612 | 7.4e-30 | |||||
JFKAHJIP_01613 | 9e-116 | |||||
JFKAHJIP_01616 | 7.3e-85 | yfjR | K | regulation of single-species biofilm formation | ||
JFKAHJIP_01617 | 3.9e-125 | S | Protein of unknown function DUF262 | |||
JFKAHJIP_01618 | 4.5e-203 | S | Protein of unknown function DUF262 | |||
JFKAHJIP_01619 | 3.9e-102 | desR | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
JFKAHJIP_01620 | 3.2e-187 | desK | 2.7.13.3 | T | Histidine kinase | |
JFKAHJIP_01621 | 5.3e-133 | yvfS | V | ABC-2 type transporter | ||
JFKAHJIP_01622 | 6.7e-159 | XK27_09825 | V | 'abc transporter, ATP-binding protein | ||
JFKAHJIP_01625 | 3.3e-164 | yocS | S | Transporter | ||
JFKAHJIP_01626 | 3.1e-83 | cdd | 2.4.2.4, 3.5.4.5 | F | cytidine deaminase activity | |
JFKAHJIP_01627 | 1.7e-115 | yvfS | V | Transporter | ||
JFKAHJIP_01628 | 9.7e-158 | XK27_09825 | V | abc transporter atp-binding protein | ||
JFKAHJIP_01629 | 3.7e-16 | liaI | KT | membrane | ||
JFKAHJIP_01630 | 2.2e-29 | liaI | KT | membrane | ||
JFKAHJIP_01631 | 2.3e-92 | XK27_05000 | S | metal cluster binding | ||
JFKAHJIP_01632 | 0.0 | V | ABC transporter (permease) | |||
JFKAHJIP_01633 | 1.1e-133 | macB2 | V | ABC transporter, ATP-binding protein | ||
JFKAHJIP_01634 | 2.2e-147 | T | Histidine kinase | |||
JFKAHJIP_01635 | 5.4e-124 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
JFKAHJIP_01636 | 2.5e-98 | 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 | |
JFKAHJIP_01637 | 3.8e-224 | pbuX | F | xanthine permease | ||
JFKAHJIP_01638 | 4.5e-59 | pdxH | S | pyridoxamine 5'-phosphate oxidase | ||
JFKAHJIP_01639 | 1.2e-270 | V | (ABC) transporter | |||
JFKAHJIP_01640 | 2.6e-152 | K | sequence-specific DNA binding | |||
JFKAHJIP_01641 | 8.7e-243 | norM | V | Multidrug efflux pump | ||
JFKAHJIP_01643 | 2e-180 | 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 | |
JFKAHJIP_01644 | 8.9e-232 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
JFKAHJIP_01645 | 1e-181 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
JFKAHJIP_01646 | 1.8e-59 | S | Protein of unknown function (DUF3290) | |||
JFKAHJIP_01647 | 1.5e-107 | S | Protein of unknown function (DUF421) | |||
JFKAHJIP_01648 | 1.4e-16 | csbD | S | CsbD-like | ||
JFKAHJIP_01649 | 3e-122 | S | Carbohydrate-binding domain-containing protein Cthe_2159 | |||
JFKAHJIP_01650 | 3e-51 | XK27_01300 | S | ASCH | ||
JFKAHJIP_01651 | 7.2e-216 | yfnA | E | amino acid | ||
JFKAHJIP_01652 | 0.0 | S | dextransucrase activity | |||
JFKAHJIP_01653 | 4.3e-138 | tcyC2 | 3.6.3.21 | E | abc transporter atp-binding protein | |
JFKAHJIP_01654 | 4.3e-113 | yxeN | P | ABC transporter, permease protein | ||
JFKAHJIP_01655 | 1.3e-109 | ytmL | P | ABC transporter (Permease | ||
JFKAHJIP_01656 | 6.1e-165 | ET | ABC transporter substrate-binding protein | |||
JFKAHJIP_01657 | 2.9e-174 | 4.1.1.37 | H | Uroporphyrinogen decarboxylase (URO-D) | ||
JFKAHJIP_01658 | 1.1e-83 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
JFKAHJIP_01659 | 1.5e-42 | S | Sugar efflux transporter for intercellular exchange | |||
JFKAHJIP_01660 | 4.4e-203 | P | FtsX-like permease family | |||
JFKAHJIP_01661 | 3.9e-122 | V | abc transporter atp-binding protein | |||
JFKAHJIP_01662 | 4e-96 | K | WHG domain | |||
JFKAHJIP_01663 | 1.2e-169 | ydhF | S | Aldo keto reductase | ||
JFKAHJIP_01664 | 2.1e-211 | natB | CP | ABC-type Na efflux pump, permease component | ||
JFKAHJIP_01665 | 9.8e-166 | natA | S | abc transporter atp-binding protein | ||
JFKAHJIP_01666 | 1.1e-09 | S | Protein of unknown function (DUF3169) | |||
JFKAHJIP_01667 | 5.5e-27 | XK27_07105 | K | transcriptional | ||
JFKAHJIP_01668 | 1.3e-35 | |||||
JFKAHJIP_01669 | 2.2e-108 | XK27_02070 | S | nitroreductase | ||
JFKAHJIP_01670 | 1.5e-152 | 1.13.11.2 | S | glyoxalase | ||
JFKAHJIP_01671 | 4.7e-76 | ywnA | K | Transcriptional regulator | ||
JFKAHJIP_01672 | 4.9e-154 | E | Alpha/beta hydrolase of unknown function (DUF915) | |||
JFKAHJIP_01673 | 1.2e-225 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
JFKAHJIP_01674 | 1.7e-168 | bcrA | V | abc transporter atp-binding protein | ||
JFKAHJIP_01675 | 6.8e-128 | S | ABC-2 family transporter protein | |||
JFKAHJIP_01676 | 4.3e-45 | S | Domain of unknown function (DUF4352) | |||
JFKAHJIP_01677 | 3.4e-147 | T | PhoQ Sensor | |||
JFKAHJIP_01678 | 2.1e-123 | T | Xre family transcriptional regulator | |||
JFKAHJIP_01679 | 4.1e-110 | drgA | C | nitroreductase | ||
JFKAHJIP_01680 | 1.6e-107 | yoaK | S | Protein of unknown function (DUF1275) | ||
JFKAHJIP_01681 | 7.6e-39 | DJ | nuclease activity | |||
JFKAHJIP_01682 | 3.2e-30 | XK27_10490 | ||||
JFKAHJIP_01683 | 1.2e-157 | yvgN | C | reductase | ||
JFKAHJIP_01684 | 1.4e-209 | S | Tetratricopeptide repeat | |||
JFKAHJIP_01685 | 0.0 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
JFKAHJIP_01686 | 0.0 | lacS | G | transporter | ||
JFKAHJIP_01687 | 4.2e-200 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
JFKAHJIP_01688 | 1.1e-194 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
JFKAHJIP_01689 | 6.3e-287 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
JFKAHJIP_01690 | 5.6e-222 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
JFKAHJIP_01691 | 2e-175 | galR | K | Transcriptional regulator | ||
JFKAHJIP_01692 | 3.9e-306 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | COG0366 Glycosidases |
JFKAHJIP_01693 | 2.9e-227 | vncS | 2.7.13.3 | T | Histidine kinase | |
JFKAHJIP_01694 | 2e-115 | K | Response regulator receiver domain protein | |||
JFKAHJIP_01695 | 7.8e-239 | vex3 | V | Efflux ABC transporter, permease protein | ||
JFKAHJIP_01696 | 1.9e-107 | vex2 | V | abc transporter atp-binding protein | ||
JFKAHJIP_01697 | 5.3e-210 | vex1 | V | Efflux ABC transporter, permease protein | ||
JFKAHJIP_01698 | 1.2e-282 | XK27_07020 | S | Belongs to the UPF0371 family | ||
JFKAHJIP_01700 | 9.7e-200 | gldA | 1.1.1.6 | C | glycerol dehydrogenase | |
JFKAHJIP_01701 | 1e-176 | XK27_10475 | S | oxidoreductase | ||
JFKAHJIP_01702 | 6.3e-58 | dhaM | 2.7.1.121 | S | dihydroxyacetone kinase, phosphotransfer subunit | |
JFKAHJIP_01703 | 4.5e-95 | dhaL | 2.7.1.121 | S | Dihydroxyacetone kinase | |
JFKAHJIP_01704 | 1.7e-179 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase | |
JFKAHJIP_01705 | 2.8e-227 | thrE | K | Psort location CytoplasmicMembrane, score | ||
JFKAHJIP_01706 | 0.0 | M | Putative cell wall binding repeat | |||
JFKAHJIP_01707 | 4.1e-34 | S | Immunity protein 41 | |||
JFKAHJIP_01708 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
JFKAHJIP_01709 | 2.4e-08 | S | Enterocin A Immunity | |||
JFKAHJIP_01710 | 1.3e-190 | mccF | V | LD-carboxypeptidase | ||
JFKAHJIP_01711 | 1e-14 | S | integral membrane protein | |||
JFKAHJIP_01712 | 4.2e-43 | czrA | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
JFKAHJIP_01713 | 1.5e-116 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
JFKAHJIP_01714 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
JFKAHJIP_01716 | 1.2e-227 | S | dextransucrase activity | |||
JFKAHJIP_01717 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
JFKAHJIP_01718 | 0.0 | S | dextransucrase activity | |||
JFKAHJIP_01719 | 0.0 | S | dextransucrase activity | |||
JFKAHJIP_01720 | 0.0 | S | dextransucrase activity | |||
JFKAHJIP_01721 | 0.0 | M | Putative cell wall binding repeat | |||
JFKAHJIP_01722 | 1.6e-237 | tcdB | S | dextransucrase activity | ||
JFKAHJIP_01723 | 0.0 | S | dextransucrase activity | |||
JFKAHJIP_01724 | 2.1e-103 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
JFKAHJIP_01725 | 1.8e-156 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
JFKAHJIP_01726 | 0.0 | M | Putative cell wall binding repeat | |||
JFKAHJIP_01727 | 1.1e-302 | S | dextransucrase activity | |||
JFKAHJIP_01728 | 0.0 | S | dextransucrase activity | |||
JFKAHJIP_01729 | 0.0 | S | dextransucrase activity | |||
JFKAHJIP_01731 | 3.6e-99 | XK27_00785 | S | CAAX protease self-immunity | ||
JFKAHJIP_01732 | 3.5e-239 | EGP | Major facilitator Superfamily | |||
JFKAHJIP_01733 | 1.8e-66 | rmaI | K | Transcriptional regulator, MarR family | ||
JFKAHJIP_01734 | 6.7e-88 | maa | 2.3.1.79 | GK | Maltose O-acetyltransferase | |
JFKAHJIP_01735 | 6.1e-137 | S | N-acetylphosphatidylethanolamine-hydrolysing phospholipas activity | |||
JFKAHJIP_01736 | 0.0 | 3.5.1.28 | M | domain protein | ||
JFKAHJIP_01737 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
JFKAHJIP_01738 | 1.5e-109 | K | Helix-turn-helix domain, rpiR family | |||
JFKAHJIP_01739 | 8.3e-17 | 3.2.1.51 | GH95 | U | LPXTG cell wall anchor motif | |
JFKAHJIP_01740 | 0.0 | M | family 8 | |||
JFKAHJIP_01741 | 4e-113 | cutC | P | Participates in the control of copper homeostasis | ||
JFKAHJIP_01742 | 1.4e-129 | S | CAAX amino terminal protease family | |||
JFKAHJIP_01743 | 6.3e-94 | ypgQ | F | HD superfamily hydrolase | ||
JFKAHJIP_01744 | 2e-95 | XK27_08140 | K | Bacterial regulatory proteins, tetR family | ||
JFKAHJIP_01745 | 7.1e-150 | yitS | S | EDD domain protein, DegV family | ||
JFKAHJIP_01746 | 1e-199 | yeaN | P | transporter | ||
JFKAHJIP_01747 | 4.7e-138 | L | Transposase and inactivated derivatives | |||
JFKAHJIP_01748 | 5.3e-74 | L | Transposase | |||
JFKAHJIP_01749 | 3e-75 | XK27_04435 | 3.5.4.5 | J | Acetyltransferase GNAT family | |
JFKAHJIP_01750 | 5.9e-40 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
JFKAHJIP_01751 | 2e-158 | K | DNA-binding helix-turn-helix protein | |||
JFKAHJIP_01752 | 1.2e-138 | S | CAAX protease self-immunity | |||
JFKAHJIP_01753 | 4.3e-138 | S | Alpha beta hydrolase | |||
JFKAHJIP_01754 | 2.7e-64 | |||||
JFKAHJIP_01755 | 5e-54 | D | Plasmid stabilization system | |||
JFKAHJIP_01756 | 2.2e-45 | |||||
JFKAHJIP_01757 | 1.8e-147 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
JFKAHJIP_01758 | 2e-58 | S | ParE toxin of type II toxin-antitoxin system, parDE | |||
JFKAHJIP_01759 | 4.8e-45 | |||||
JFKAHJIP_01760 | 0.0 | O | Molecular chaperone. Has ATPase activity | |||
JFKAHJIP_01761 | 1.8e-256 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
JFKAHJIP_01762 | 2e-97 | mip | S | hydroperoxide reductase activity | ||
JFKAHJIP_01763 | 2.2e-201 | I | acyl-CoA dehydrogenase | |||
JFKAHJIP_01764 | 1.7e-152 | ydiA | P | C4-dicarboxylate transporter malic acid transport | ||
JFKAHJIP_01765 | 1.7e-244 | msrR | K | Transcriptional regulator | ||
JFKAHJIP_01766 | 2.5e-152 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
JFKAHJIP_01767 | 6.7e-76 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
JFKAHJIP_01768 | 3.7e-235 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
JFKAHJIP_01769 | 2.4e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
JFKAHJIP_01770 | 4.2e-53 | yheA | S | Belongs to the UPF0342 family | ||
JFKAHJIP_01771 | 8.3e-207 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
JFKAHJIP_01772 | 9.9e-219 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
JFKAHJIP_01773 | 5.9e-202 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
JFKAHJIP_01774 | 3.5e-160 | aroE | 1.1.1.25 | 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) | |
JFKAHJIP_01775 | 2.1e-120 | 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 | |
JFKAHJIP_01776 | 1.4e-217 | ywbD | 2.1.1.191 | J | Methyltransferase | |
JFKAHJIP_01777 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
JFKAHJIP_01778 | 4.6e-25 | WQ51_00785 | ||||
JFKAHJIP_01779 | 7.4e-247 | 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 | |
JFKAHJIP_01780 | 3.4e-74 | yueI | S | Protein of unknown function (DUF1694) | ||
JFKAHJIP_01781 | 4e-193 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
JFKAHJIP_01782 | 6.6e-193 | yyaQ | S | YjbR | ||
JFKAHJIP_01783 | 4.1e-181 | ccpA | K | Catabolite control protein A | ||
JFKAHJIP_01784 | 1.4e-195 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
JFKAHJIP_01785 | 1.3e-63 | yugI | 5.3.1.9 | J | RNA binding protein, contains ribosomal protein S1 domain | |
JFKAHJIP_01786 | 2e-274 | 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 | |
JFKAHJIP_01787 | 6.6e-81 | smpB | O | 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 | ||
JFKAHJIP_01788 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
JFKAHJIP_01789 | 2e-33 | secG | U | Preprotein translocase subunit SecG | ||
JFKAHJIP_01790 | 2.2e-221 | mdtG | EGP | Major facilitator Superfamily | ||
JFKAHJIP_01791 | 5.1e-102 | coaE | 2.7.1.24, 3.2.2.23, 4.2.99.18 | GH23 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A |
JFKAHJIP_01792 | 6.9e-150 | 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 | |
JFKAHJIP_01793 | 2.2e-165 | era | M | 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 | ||
JFKAHJIP_01794 | 2e-65 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
JFKAHJIP_01795 | 4.6e-88 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
JFKAHJIP_01796 | 4.6e-149 | licT | K | antiterminator | ||
JFKAHJIP_01797 | 1.3e-105 | 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 | ||
JFKAHJIP_01798 | 0.0 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
JFKAHJIP_01799 | 1.1e-145 | 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 | |
JFKAHJIP_01800 | 4.3e-155 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
JFKAHJIP_01801 | 2.9e-150 | I | Alpha/beta hydrolase family | |||
JFKAHJIP_01802 | 6.6e-08 | |||||
JFKAHJIP_01803 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
JFKAHJIP_01804 | 1.4e-78 | feoA | P | FeoA domain protein | ||
JFKAHJIP_01805 | 6.4e-131 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
JFKAHJIP_01806 | 5.8e-118 | WQ51_01820 | P | Binding-protein-dependent transport system inner membrane component | ||
JFKAHJIP_01807 | 1e-34 | ykuJ | S | protein conserved in bacteria | ||
JFKAHJIP_01808 | 1.4e-181 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
JFKAHJIP_01809 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
JFKAHJIP_01810 | 1.2e-82 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
JFKAHJIP_01811 | 6.2e-48 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
JFKAHJIP_01812 | 1.3e-171 | S | oxidoreductase | |||
JFKAHJIP_01813 | 9.3e-81 | M | Pfam SNARE associated Golgi protein | |||
JFKAHJIP_01814 | 2.6e-135 | 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) | |
JFKAHJIP_01815 | 0.0 | tkt | 2.2.1.1 | G | 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 | |
JFKAHJIP_01817 | 2.8e-111 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
JFKAHJIP_01818 | 9.6e-158 | holB | 2.7.7.7 | L | dna polymerase iii | |
JFKAHJIP_01819 | 8.9e-134 | yaaT | S | stage 0 sporulation protein | ||
JFKAHJIP_01820 | 1.2e-54 | yabA | L | Involved in initiation control of chromosome replication | ||
JFKAHJIP_01821 | 4e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
JFKAHJIP_01822 | 1.9e-228 | amt | P | Ammonium Transporter | ||
JFKAHJIP_01823 | 1.9e-53 | glnB | K | Belongs to the P(II) protein family | ||
JFKAHJIP_01824 | 1.6e-104 | mur1 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | |
JFKAHJIP_01825 | 1.7e-108 | S | HD domain | |||
JFKAHJIP_01826 | 7e-147 | XK27_04800 | S | Sucrose-6F-phosphate phosphohydrolase | ||
JFKAHJIP_01827 | 5.6e-84 | S | Bacterial inner membrane protein | |||
JFKAHJIP_01828 | 3.7e-111 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
JFKAHJIP_01829 | 7.2e-292 | nptA | P | COG1283 Na phosphate symporter | ||
JFKAHJIP_01830 | 2.6e-211 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
JFKAHJIP_01831 | 5.6e-220 | S | membrane | |||
JFKAHJIP_01832 | 3.7e-176 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
JFKAHJIP_01833 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
JFKAHJIP_01834 | 2e-39 | ynzC | S | UPF0291 protein | ||
JFKAHJIP_01835 | 1.2e-255 | cycA | E | permease | ||
JFKAHJIP_01836 | 6e-08 | uvrX | 2.7.7.7 | L | impB/mucB/samB family | |
JFKAHJIP_01837 | 0.0 | pts33BCA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
JFKAHJIP_01838 | 9.2e-141 | ppiA | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
JFKAHJIP_01841 | 3.4e-69 | K | Helix-turn-helix | |||
JFKAHJIP_01843 | 4.7e-168 | fhuR | K | transcriptional regulator (lysR family) | ||
JFKAHJIP_01844 | 4.8e-76 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
JFKAHJIP_01845 | 1.1e-161 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
JFKAHJIP_01846 | 4.8e-88 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
JFKAHJIP_01847 | 3.6e-222 | pyrP | F | uracil Permease | ||
JFKAHJIP_01848 | 1.3e-173 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
JFKAHJIP_01849 | 9.3e-211 | carA | 6.3.5.5 | F | carbamoyl-phosphate synthetase glutamine chain | |
JFKAHJIP_01850 | 0.0 | carB | 6.3.5.5 | F | carbamoyl-phosphate synthetase ammonia chain | |
JFKAHJIP_01851 | 2.3e-128 | 2.1.1.223 | S | Putative SAM-dependent methyltransferase | ||
JFKAHJIP_01852 | 3.6e-182 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
JFKAHJIP_01853 | 2.9e-120 | macB | V | ABC transporter, ATP-binding protein | ||
JFKAHJIP_01854 | 1.2e-211 | V | permease protein | |||
JFKAHJIP_01855 | 1.9e-78 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
JFKAHJIP_01856 | 2.1e-45 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
JFKAHJIP_01858 | 2.5e-273 | opuD | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
JFKAHJIP_01859 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
JFKAHJIP_01860 | 0.0 | lmrA | V | abc transporter atp-binding protein | ||
JFKAHJIP_01861 | 2.1e-199 | 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) | |
JFKAHJIP_01862 | 2e-121 | 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 | |
JFKAHJIP_01863 | 5.3e-213 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
JFKAHJIP_01864 | 1.2e-129 | rr02 | KT | response regulator | ||
JFKAHJIP_01865 | 5.7e-219 | 2.7.7.73, 2.7.7.80 | H | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | ||
JFKAHJIP_01866 | 9.3e-164 | V | ABC transporter | |||
JFKAHJIP_01867 | 3.3e-119 | sagI | S | ABC-2 type transporter | ||
JFKAHJIP_01868 | 7.6e-196 | yceA | S | Belongs to the UPF0176 family | ||
JFKAHJIP_01869 | 2.3e-27 | XK27_00085 | K | Transcriptional | ||
JFKAHJIP_01870 | 2.1e-24 | |||||
JFKAHJIP_01871 | 4.2e-133 | deoD_1 | 2.4.2.3 | F | Phosphorylase superfamily | |
JFKAHJIP_01872 | 3.9e-114 | S | VIT family | |||
JFKAHJIP_01873 | 7.2e-127 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
JFKAHJIP_01874 | 7e-217 | hipO | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
JFKAHJIP_01875 | 2.2e-199 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
JFKAHJIP_01878 | 4.9e-140 | E | Alpha beta hydrolase | |||
JFKAHJIP_01879 | 5.2e-248 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
JFKAHJIP_01880 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
JFKAHJIP_01881 | 1.9e-227 | rodA | D | Belongs to the SEDS family | ||
JFKAHJIP_01882 | 7.1e-223 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
JFKAHJIP_01883 | 1.2e-112 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
JFKAHJIP_01884 | 2.7e-174 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
JFKAHJIP_01885 | 9.7e-138 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
JFKAHJIP_01886 | 5.2e-66 | GnaT | 2.5.1.16 | K | acetyltransferase | |
JFKAHJIP_01887 | 0.0 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
JFKAHJIP_01888 | 1.7e-93 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
JFKAHJIP_01889 | 4.6e-182 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
JFKAHJIP_01890 | 1.1e-124 | dnaD | ||||
JFKAHJIP_01891 | 2.9e-119 | 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 | |
JFKAHJIP_01892 | 1.8e-06 | KT | response to antibiotic | |||
JFKAHJIP_01893 | 3.3e-234 | 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 | |
JFKAHJIP_01894 | 4.6e-29 | 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 | |
JFKAHJIP_01895 | 2.2e-154 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
JFKAHJIP_01896 | 2.2e-148 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
JFKAHJIP_01897 | 2.8e-73 | argR | K | Regulates arginine biosynthesis genes | ||
JFKAHJIP_01898 | 1e-301 | recN | L | May be involved in recombinational repair of damaged DNA | ||
JFKAHJIP_01899 | 9.3e-150 | DegV | S | DegV family | ||
JFKAHJIP_01900 | 2.2e-162 | ypmR | E | COG2755 Lysophospholipase L1 and related esterases | ||
JFKAHJIP_01901 | 6.2e-97 | ypmS | S | Protein conserved in bacteria | ||
JFKAHJIP_01902 | 6.3e-39 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
JFKAHJIP_01904 | 6.2e-179 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
JFKAHJIP_01905 | 4.6e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
JFKAHJIP_01906 | 4.9e-290 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
JFKAHJIP_01907 | 6.6e-190 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
JFKAHJIP_01908 | 3.5e-37 | ysdA | L | Membrane | ||
JFKAHJIP_01909 | 2.1e-276 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
JFKAHJIP_01910 | 2.4e-112 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
JFKAHJIP_01911 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
JFKAHJIP_01912 | 3.6e-188 | 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 | |
JFKAHJIP_01913 | 6e-277 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
JFKAHJIP_01914 | 4.8e-31 | L | COG1943 Transposase and inactivated derivatives | |||
JFKAHJIP_01915 | 2.9e-18 | S | Domain of unknown function (DUF4649) | |||
JFKAHJIP_01916 | 1.4e-176 | XK27_08835 | S | ABC transporter substrate binding protein | ||
JFKAHJIP_01917 | 2.6e-147 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
JFKAHJIP_01918 | 3.1e-136 | XK27_08845 | S | abc transporter atp-binding protein | ||
JFKAHJIP_01919 | 7.8e-310 | rnjB | S | 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 | ||
JFKAHJIP_01920 | 1.8e-147 | estA | CE1 | S | Esterase | |
JFKAHJIP_01921 | 1.6e-126 | XK27_08875 | O | Zinc-dependent metalloprotease | ||
JFKAHJIP_01922 | 1.1e-17 | XK27_08880 | ||||
JFKAHJIP_01923 | 1e-75 | fld | C | Flavodoxin | ||
JFKAHJIP_01924 | 3.6e-277 | clcA | P | Chloride transporter, ClC family | ||
JFKAHJIP_01925 | 4.7e-37 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase | |
JFKAHJIP_01926 | 1e-213 | XK27_05110 | P | Chloride transporter ClC family | ||
JFKAHJIP_01927 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
JFKAHJIP_01930 | 3.2e-20 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
JFKAHJIP_01931 | 4.6e-163 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
JFKAHJIP_01932 | 3.3e-86 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
JFKAHJIP_01933 | 4.6e-302 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
JFKAHJIP_01934 | 4.8e-171 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
JFKAHJIP_01935 | 1.2e-211 | 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 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)