ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
DJHDMHJE_00001 | 8e-39 | comGC | U | competence protein ComGC | ||
DJHDMHJE_00002 | 9e-176 | comGB | NU | type II secretion system | ||
DJHDMHJE_00003 | 8.4e-179 | comGA | NU | Type II IV secretion system protein | ||
DJHDMHJE_00004 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
DJHDMHJE_00005 | 4.6e-91 | S | VanZ like family | |||
DJHDMHJE_00006 | 8.3e-296 | ytgP | S | Polysaccharide biosynthesis protein | ||
DJHDMHJE_00007 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
DJHDMHJE_00008 | 3.5e-120 | 3.6.1.27 | I | Acid phosphatase homologues | ||
DJHDMHJE_00009 | 6.2e-43 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
DJHDMHJE_00010 | 4.3e-158 | pstS | P | Phosphate | ||
DJHDMHJE_00011 | 3.7e-174 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
DJHDMHJE_00012 | 7e-156 | pstA | P | Phosphate transport system permease protein PstA | ||
DJHDMHJE_00013 | 1.1e-144 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
DJHDMHJE_00014 | 7.8e-140 | 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 | |
DJHDMHJE_00015 | 7.5e-118 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
DJHDMHJE_00016 | 4.3e-27 | yfdV | S | Membrane transport protein | ||
DJHDMHJE_00017 | 3.3e-156 | yfdV | S | Membrane transport protein | ||
DJHDMHJE_00018 | 5.9e-83 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
DJHDMHJE_00019 | 2.4e-54 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
DJHDMHJE_00020 | 1.1e-80 | rsmC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
DJHDMHJE_00021 | 1e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
DJHDMHJE_00022 | 2e-91 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
DJHDMHJE_00023 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
DJHDMHJE_00024 | 5e-38 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
DJHDMHJE_00025 | 4.8e-108 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
DJHDMHJE_00026 | 6.4e-35 | S | Protein of unknown function (DUF2508) | |||
DJHDMHJE_00027 | 8.7e-116 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
DJHDMHJE_00028 | 2.2e-51 | yaaQ | S | Cyclic-di-AMP receptor | ||
DJHDMHJE_00029 | 1.5e-155 | holB | 2.7.7.7 | L | DNA polymerase III | |
DJHDMHJE_00030 | 2.4e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
DJHDMHJE_00031 | 7.9e-157 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
DJHDMHJE_00032 | 1.6e-142 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
DJHDMHJE_00033 | 3.4e-86 | S | ECF transporter, substrate-specific component | |||
DJHDMHJE_00034 | 6.2e-134 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
DJHDMHJE_00035 | 1.6e-105 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
DJHDMHJE_00036 | 1.4e-198 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
DJHDMHJE_00038 | 1e-40 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00039 | 2e-172 | yjeM | E | Amino Acid | ||
DJHDMHJE_00040 | 5.2e-89 | 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) | |
DJHDMHJE_00041 | 8.4e-33 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
DJHDMHJE_00042 | 2.6e-08 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
DJHDMHJE_00044 | 6.5e-90 | |||||
DJHDMHJE_00045 | 2.3e-96 | apt | 2.4.2.22, 2.4.2.7 | F | Phosphoribosyl transferase domain | |
DJHDMHJE_00046 | 4.3e-184 | P | secondary active sulfate transmembrane transporter activity | |||
DJHDMHJE_00047 | 3.6e-108 | L | Transposase and inactivated derivatives, IS30 family | |||
DJHDMHJE_00048 | 1.5e-123 | metF | 1.5.1.20 | C | Methylenetetrahydrofolate reductase | |
DJHDMHJE_00049 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
DJHDMHJE_00050 | 5.7e-88 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
DJHDMHJE_00051 | 2.9e-63 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
DJHDMHJE_00052 | 8.4e-66 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
DJHDMHJE_00053 | 3.6e-151 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
DJHDMHJE_00055 | 1.2e-202 | lsa | S | ABC transporter | ||
DJHDMHJE_00057 | 2.2e-160 | S | SLAP domain | |||
DJHDMHJE_00058 | 3e-80 | S | Bacteriocin helveticin-J | |||
DJHDMHJE_00059 | 1.4e-42 | |||||
DJHDMHJE_00060 | 1.4e-38 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
DJHDMHJE_00061 | 2.4e-48 | E | Zn peptidase | |||
DJHDMHJE_00062 | 4.7e-198 | EGP | Major facilitator Superfamily | |||
DJHDMHJE_00063 | 1e-119 | ropB | K | Transcriptional regulator | ||
DJHDMHJE_00064 | 0.0 | traA | L | MobA MobL family protein | ||
DJHDMHJE_00065 | 2.9e-271 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
DJHDMHJE_00066 | 1.7e-18 | |||||
DJHDMHJE_00067 | 1.8e-48 | L | Psort location Cytoplasmic, score | |||
DJHDMHJE_00068 | 1.9e-139 | L | Psort location Cytoplasmic, score | |||
DJHDMHJE_00070 | 7e-07 | |||||
DJHDMHJE_00072 | 3.5e-55 | pemK | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
DJHDMHJE_00073 | 3.1e-43 | T | Antidote-toxin recognition MazE, bacterial antitoxin | |||
DJHDMHJE_00074 | 2.7e-35 | S | SnoaL-like domain | |||
DJHDMHJE_00075 | 6.1e-100 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
DJHDMHJE_00076 | 2.8e-08 | cylB | V | ABC-2 type transporter | ||
DJHDMHJE_00077 | 1.7e-221 | L | Transposase | |||
DJHDMHJE_00078 | 1.6e-153 | P | ABC transporter | |||
DJHDMHJE_00080 | 1.3e-114 | K | UTRA domain | |||
DJHDMHJE_00081 | 1.8e-59 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
DJHDMHJE_00082 | 3.6e-182 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
DJHDMHJE_00083 | 9.8e-18 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
DJHDMHJE_00084 | 3.1e-77 | L | Probable transposase | |||
DJHDMHJE_00086 | 1.7e-103 | tnpR1 | L | Resolvase, N terminal domain | ||
DJHDMHJE_00087 | 9.3e-207 | EGP | Major facilitator Superfamily | |||
DJHDMHJE_00089 | 1.2e-238 | nfrB | 2.4.1.336 | GT2 | M | Glycosyltransferase like family 2 |
DJHDMHJE_00090 | 0.0 | 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 | |||
DJHDMHJE_00091 | 1.1e-264 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
DJHDMHJE_00092 | 4.8e-146 | glcU | U | sugar transport | ||
DJHDMHJE_00094 | 3.5e-25 | |||||
DJHDMHJE_00095 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
DJHDMHJE_00096 | 3.4e-41 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00097 | 2.5e-211 | L | Probable transposase | |||
DJHDMHJE_00098 | 1.8e-18 | |||||
DJHDMHJE_00099 | 2.5e-64 | XK27_01125 | L | IS66 Orf2 like protein | ||
DJHDMHJE_00100 | 5.8e-32 | S | Transposase C of IS166 homeodomain | |||
DJHDMHJE_00101 | 1e-34 | yozG | K | Transcriptional regulator | ||
DJHDMHJE_00102 | 7.1e-33 | |||||
DJHDMHJE_00103 | 8.7e-27 | |||||
DJHDMHJE_00106 | 1.8e-139 | fruR | K | DeoR C terminal sensor domain | ||
DJHDMHJE_00107 | 1.3e-168 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
DJHDMHJE_00108 | 1.6e-57 | pacL | 3.6.3.8 | P | P-type ATPase | |
DJHDMHJE_00109 | 5.6e-21 | pacL | 3.6.3.8 | P | P-type ATPase | |
DJHDMHJE_00110 | 4.5e-32 | pacL | 3.6.3.8 | P | P-type ATPase | |
DJHDMHJE_00111 | 1.6e-68 | pacL | 3.6.3.8 | P | P-type ATPase | |
DJHDMHJE_00112 | 2.2e-168 | pacL | 3.6.3.8 | P | P-type ATPase | |
DJHDMHJE_00113 | 1.9e-225 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
DJHDMHJE_00114 | 2.6e-261 | epsU | S | Polysaccharide biosynthesis protein | ||
DJHDMHJE_00115 | 5.7e-137 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
DJHDMHJE_00116 | 2.1e-87 | ydcK | S | Belongs to the SprT family | ||
DJHDMHJE_00118 | 5e-103 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
DJHDMHJE_00119 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
DJHDMHJE_00120 | 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 | |
DJHDMHJE_00121 | 4.4e-211 | camS | S | sex pheromone | ||
DJHDMHJE_00122 | 5.2e-50 | 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) | |
DJHDMHJE_00123 | 9.9e-261 | 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) | |
DJHDMHJE_00124 | 2.9e-276 | 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) | |
DJHDMHJE_00125 | 1e-170 | yegS | 2.7.1.107 | G | Lipid kinase | |
DJHDMHJE_00126 | 1.4e-114 | S | Protein of unknown function (DUF1211) | |||
DJHDMHJE_00127 | 4.9e-120 | ybhL | S | Belongs to the BI1 family | ||
DJHDMHJE_00128 | 3.5e-55 | |||||
DJHDMHJE_00129 | 9.2e-248 | nhaC | C | Na H antiporter NhaC | ||
DJHDMHJE_00130 | 3.7e-257 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
DJHDMHJE_00131 | 1.7e-168 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
DJHDMHJE_00132 | 3.8e-184 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
DJHDMHJE_00133 | 1.7e-229 | mtnE | 2.6.1.83 | E | Aminotransferase | |
DJHDMHJE_00134 | 9.3e-152 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
DJHDMHJE_00135 | 4e-34 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
DJHDMHJE_00136 | 1.7e-168 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
DJHDMHJE_00137 | 2e-29 | cspA | K | Cold shock protein | ||
DJHDMHJE_00140 | 1.7e-95 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
DJHDMHJE_00141 | 5.2e-91 | S | domain protein | |||
DJHDMHJE_00142 | 2.8e-147 | V | ABC transporter | |||
DJHDMHJE_00143 | 1.9e-74 | S | Protein of unknown function (DUF3021) | |||
DJHDMHJE_00144 | 6.6e-75 | K | LytTr DNA-binding domain | |||
DJHDMHJE_00145 | 8.6e-136 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
DJHDMHJE_00146 | 7e-206 | csaB | M | Glycosyl transferases group 1 | ||
DJHDMHJE_00147 | 5.9e-285 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
DJHDMHJE_00148 | 2.1e-154 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
DJHDMHJE_00149 | 3.6e-271 | K | Putative DNA-binding domain | |||
DJHDMHJE_00150 | 6.1e-10 | K | Putative DNA-binding domain | |||
DJHDMHJE_00151 | 3.1e-156 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_00152 | 1.6e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
DJHDMHJE_00153 | 3.4e-158 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
DJHDMHJE_00154 | 2e-126 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
DJHDMHJE_00155 | 0.0 | kup | P | Transport of potassium into the cell | ||
DJHDMHJE_00156 | 4.8e-176 | rihB | 3.2.2.1 | F | Nucleoside | |
DJHDMHJE_00157 | 7.6e-21 | gntR | K | UbiC transcription regulator-associated domain protein | ||
DJHDMHJE_00158 | 5.6e-74 | gntR | K | UbiC transcription regulator-associated domain protein | ||
DJHDMHJE_00160 | 6.2e-39 | |||||
DJHDMHJE_00161 | 2.5e-18 | C | nitroreductase | |||
DJHDMHJE_00162 | 1.4e-47 | C | nitroreductase | |||
DJHDMHJE_00163 | 1.1e-240 | yhdP | S | Transporter associated domain | ||
DJHDMHJE_00164 | 2.2e-102 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
DJHDMHJE_00165 | 5.4e-156 | potE | E | amino acid | ||
DJHDMHJE_00166 | 4.3e-37 | potE | E | amino acid | ||
DJHDMHJE_00167 | 4.4e-129 | M | Glycosyl hydrolases family 25 | |||
DJHDMHJE_00168 | 1.1e-207 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
DJHDMHJE_00169 | 6.4e-246 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
DJHDMHJE_00171 | 1.2e-25 | |||||
DJHDMHJE_00172 | 3.8e-215 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
DJHDMHJE_00173 | 3.1e-90 | gtcA | S | Teichoic acid glycosylation protein | ||
DJHDMHJE_00174 | 1.6e-79 | fld | C | Flavodoxin | ||
DJHDMHJE_00175 | 8.5e-164 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
DJHDMHJE_00176 | 1.4e-151 | yihY | S | Belongs to the UPF0761 family | ||
DJHDMHJE_00177 | 8e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
DJHDMHJE_00178 | 9.6e-27 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00179 | 2.4e-126 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00180 | 2.7e-216 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
DJHDMHJE_00181 | 6.1e-219 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
DJHDMHJE_00182 | 1.6e-216 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
DJHDMHJE_00183 | 6.5e-47 | |||||
DJHDMHJE_00185 | 7.9e-24 | L | PFAM transposase, IS4 family protein | |||
DJHDMHJE_00186 | 6.2e-47 | L | PFAM transposase, IS4 family protein | |||
DJHDMHJE_00187 | 1.7e-40 | L | Transposase | |||
DJHDMHJE_00188 | 4.9e-116 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_00189 | 3.1e-275 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
DJHDMHJE_00190 | 5.2e-192 | V | Beta-lactamase | |||
DJHDMHJE_00191 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
DJHDMHJE_00192 | 3.3e-47 | |||||
DJHDMHJE_00193 | 3.8e-99 | |||||
DJHDMHJE_00194 | 2.2e-78 | XK27_09675 | K | Acetyltransferase (GNAT) domain | ||
DJHDMHJE_00195 | 4e-53 | S | Protein of unknown function (DUF3021) | |||
DJHDMHJE_00196 | 1.6e-76 | K | LytTr DNA-binding domain | |||
DJHDMHJE_00197 | 7.2e-43 | |||||
DJHDMHJE_00198 | 8e-125 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
DJHDMHJE_00199 | 6.5e-57 | 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 | |
DJHDMHJE_00200 | 1.3e-201 | folE | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | F | GTP cyclohydrolase 1 | |
DJHDMHJE_00201 | 2.4e-248 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
DJHDMHJE_00202 | 3.9e-201 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
DJHDMHJE_00203 | 3.1e-98 | 3.6.1.55, 3.6.1.67 | F | NUDIX domain | ||
DJHDMHJE_00204 | 1.5e-48 | hutG | 3.5.3.8 | E | N-formylglutamate amidohydrolase | |
DJHDMHJE_00205 | 3.4e-25 | S | Uncharacterized protein conserved in bacteria (DUF2255) | |||
DJHDMHJE_00206 | 6e-112 | papP | P | ABC transporter, permease protein | ||
DJHDMHJE_00207 | 4e-79 | P | ABC transporter permease | |||
DJHDMHJE_00208 | 4.3e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DJHDMHJE_00209 | 9.1e-161 | cjaA | ET | ABC transporter substrate-binding protein | ||
DJHDMHJE_00210 | 3.6e-73 | L | Helix-turn-helix domain | |||
DJHDMHJE_00211 | 1.7e-42 | L | Helix-turn-helix domain | |||
DJHDMHJE_00212 | 4.2e-197 | L | hmm pf00665 | |||
DJHDMHJE_00213 | 1.7e-90 | dam | 2.1.1.72 | H | Site-specific DNA-methyltransferase (adenine-specific) | |
DJHDMHJE_00215 | 9.9e-117 | L | Integrase | |||
DJHDMHJE_00217 | 2e-255 | gor | 1.8.1.7 | C | Glutathione reductase | |
DJHDMHJE_00218 | 7.4e-15 | S | YSIRK type signal peptide | |||
DJHDMHJE_00219 | 1.4e-68 | UW | LPXTG-motif cell wall anchor domain protein | |||
DJHDMHJE_00221 | 1.7e-34 | |||||
DJHDMHJE_00222 | 6.3e-62 | S | cog cog1373 | |||
DJHDMHJE_00223 | 1.3e-76 | S | cog cog1373 | |||
DJHDMHJE_00224 | 6.4e-88 | metI | P | ABC transporter permease | ||
DJHDMHJE_00225 | 3.9e-179 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
DJHDMHJE_00226 | 2.8e-162 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
DJHDMHJE_00227 | 0.0 | aha1 | P | E1-E2 ATPase | ||
DJHDMHJE_00228 | 2.8e-48 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_00229 | 4.6e-299 | |||||
DJHDMHJE_00230 | 2.1e-08 | |||||
DJHDMHJE_00231 | 0.0 | S | PglZ domain | |||
DJHDMHJE_00232 | 1.7e-17 | LO | the current gene model (or a revised gene model) may contain a frame shift | |||
DJHDMHJE_00233 | 3.6e-27 | LO | the current gene model (or a revised gene model) may contain a frame shift | |||
DJHDMHJE_00234 | 1.3e-34 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_00235 | 2.7e-176 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
DJHDMHJE_00236 | 1.4e-92 | P | Cobalt transport protein | |||
DJHDMHJE_00237 | 1.9e-250 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
DJHDMHJE_00238 | 5.1e-173 | K | helix_turn_helix, arabinose operon control protein | |||
DJHDMHJE_00239 | 4.1e-59 | L | hmm pf00665 | |||
DJHDMHJE_00240 | 5.6e-08 | L | hmm pf00665 | |||
DJHDMHJE_00241 | 1.8e-19 | L | hmm pf00665 | |||
DJHDMHJE_00242 | 4.1e-65 | L | Helix-turn-helix domain | |||
DJHDMHJE_00243 | 8.6e-162 | htpX | O | Belongs to the peptidase M48B family | ||
DJHDMHJE_00244 | 2.3e-96 | lemA | S | LemA family | ||
DJHDMHJE_00245 | 3.6e-194 | ybiR | P | Citrate transporter | ||
DJHDMHJE_00246 | 5.9e-70 | S | Iron-sulphur cluster biosynthesis | |||
DJHDMHJE_00247 | 4.2e-19 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
DJHDMHJE_00248 | 1.2e-17 | |||||
DJHDMHJE_00249 | 1e-151 | |||||
DJHDMHJE_00250 | 1.8e-198 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00251 | 2e-23 | G | Glycosyl hydrolases family 8 | |||
DJHDMHJE_00252 | 4.4e-64 | G | Glycosyl hydrolases family 8 | |||
DJHDMHJE_00253 | 4.7e-17 | S | Peptidase propeptide and YPEB domain | |||
DJHDMHJE_00255 | 9.9e-135 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00256 | 4e-112 | pbpX2 | V | Beta-lactamase | ||
DJHDMHJE_00257 | 8.8e-104 | 3.2.2.20 | K | acetyltransferase | ||
DJHDMHJE_00258 | 5.3e-95 | |||||
DJHDMHJE_00259 | 3.7e-32 | |||||
DJHDMHJE_00260 | 1.7e-267 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
DJHDMHJE_00261 | 4.7e-132 | glvR | K | Helix-turn-helix domain, rpiR family | ||
DJHDMHJE_00262 | 8.6e-187 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
DJHDMHJE_00263 | 3.2e-15 | |||||
DJHDMHJE_00264 | 7.7e-123 | |||||
DJHDMHJE_00265 | 1.2e-238 | S | response to antibiotic | |||
DJHDMHJE_00266 | 3.7e-134 | cysA | V | ABC transporter, ATP-binding protein | ||
DJHDMHJE_00267 | 0.0 | V | FtsX-like permease family | |||
DJHDMHJE_00268 | 1.1e-167 | aspT | P | Predicted Permease Membrane Region | ||
DJHDMHJE_00269 | 7.5e-86 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
DJHDMHJE_00270 | 1.1e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
DJHDMHJE_00271 | 3.4e-126 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
DJHDMHJE_00272 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
DJHDMHJE_00273 | 4.7e-109 | glnP | P | ABC transporter permease | ||
DJHDMHJE_00274 | 4.5e-109 | glnQ | 3.6.3.21 | E | ABC transporter | |
DJHDMHJE_00275 | 6.1e-151 | aatB | ET | ABC transporter substrate-binding protein | ||
DJHDMHJE_00276 | 2.2e-78 | yjcF | S | Acetyltransferase (GNAT) domain | ||
DJHDMHJE_00277 | 1.3e-104 | E | GDSL-like Lipase/Acylhydrolase | |||
DJHDMHJE_00278 | 2.1e-171 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
DJHDMHJE_00279 | 5.8e-103 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
DJHDMHJE_00280 | 1.4e-217 | G | Bacterial extracellular solute-binding protein | |||
DJHDMHJE_00281 | 2.8e-67 | S | Peptidase propeptide and YPEB domain | |||
DJHDMHJE_00283 | 1.3e-95 | F | Nucleoside 2-deoxyribosyltransferase | |||
DJHDMHJE_00284 | 1.6e-188 | 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 | |
DJHDMHJE_00285 | 2.4e-59 | |||||
DJHDMHJE_00287 | 1.4e-63 | V | Type II restriction enzyme, methylase subunits | |||
DJHDMHJE_00288 | 1.7e-57 | V | Type II restriction enzyme, methylase subunits | |||
DJHDMHJE_00289 | 9.2e-09 | S | Hypothetical protein (DUF2513) | |||
DJHDMHJE_00290 | 7.1e-34 | |||||
DJHDMHJE_00293 | 1.6e-12 | |||||
DJHDMHJE_00294 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
DJHDMHJE_00295 | 5.3e-158 | 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 | |
DJHDMHJE_00296 | 4.5e-106 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
DJHDMHJE_00297 | 4.1e-83 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
DJHDMHJE_00298 | 2.1e-249 | dnaB | L | Replication initiation and membrane attachment | ||
DJHDMHJE_00299 | 1.3e-165 | dnaI | L | Primosomal protein DnaI | ||
DJHDMHJE_00300 | 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) | |
DJHDMHJE_00301 | 1e-90 | |||||
DJHDMHJE_00302 | 3.3e-26 | L | Transposase | |||
DJHDMHJE_00303 | 3.8e-39 | 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 | ||
DJHDMHJE_00304 | 8.5e-40 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00305 | 1.9e-94 | L | Transposase | |||
DJHDMHJE_00322 | 4.9e-109 | S | Core-2/I-Branching enzyme | |||
DJHDMHJE_00323 | 4.5e-74 | L | Transposase | |||
DJHDMHJE_00328 | 1.3e-24 | E | Preprotein translocase subunit SecB | |||
DJHDMHJE_00329 | 6.6e-33 | S | Domain of unknown function (DUF4393) | |||
DJHDMHJE_00330 | 1e-18 | |||||
DJHDMHJE_00331 | 5.3e-11 | |||||
DJHDMHJE_00332 | 1.3e-44 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_00333 | 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 | ||
DJHDMHJE_00334 | 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 | ||
DJHDMHJE_00335 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
DJHDMHJE_00336 | 8.9e-55 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
DJHDMHJE_00337 | 3e-187 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
DJHDMHJE_00338 | 3.2e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
DJHDMHJE_00339 | 7.6e-180 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
DJHDMHJE_00340 | 5.1e-19 | |||||
DJHDMHJE_00341 | 2.3e-187 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
DJHDMHJE_00342 | 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 | ||
DJHDMHJE_00343 | 2.5e-95 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
DJHDMHJE_00344 | 2.6e-134 | comFC | S | Competence protein | ||
DJHDMHJE_00345 | 4.3e-247 | comFA | L | Helicase C-terminal domain protein | ||
DJHDMHJE_00346 | 1.3e-117 | yvyE | 3.4.13.9 | S | YigZ family | |
DJHDMHJE_00347 | 1.6e-208 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
DJHDMHJE_00348 | 9.5e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
DJHDMHJE_00349 | 5.5e-195 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
DJHDMHJE_00350 | 2.5e-98 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
DJHDMHJE_00351 | 1.6e-144 | ymfM | S | Helix-turn-helix domain | ||
DJHDMHJE_00352 | 1e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
DJHDMHJE_00353 | 1e-237 | S | Peptidase M16 | |||
DJHDMHJE_00354 | 1.8e-226 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
DJHDMHJE_00355 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
DJHDMHJE_00356 | 1.4e-68 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
DJHDMHJE_00357 | 5.5e-106 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
DJHDMHJE_00358 | 1.9e-212 | yubA | S | AI-2E family transporter | ||
DJHDMHJE_00359 | 3.7e-23 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
DJHDMHJE_00360 | 1.9e-26 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
DJHDMHJE_00361 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
DJHDMHJE_00362 | 8.8e-203 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
DJHDMHJE_00363 | 1.3e-109 | S | SNARE associated Golgi protein | |||
DJHDMHJE_00364 | 5e-81 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
DJHDMHJE_00365 | 3e-264 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
DJHDMHJE_00366 | 3.3e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
DJHDMHJE_00367 | 2.7e-154 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
DJHDMHJE_00368 | 2.1e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
DJHDMHJE_00369 | 6.6e-113 | yjbK | S | CYTH | ||
DJHDMHJE_00370 | 3.3e-112 | yjbH | Q | Thioredoxin | ||
DJHDMHJE_00371 | 5e-159 | coiA | 3.6.4.12 | S | Competence protein | |
DJHDMHJE_00372 | 8.7e-136 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
DJHDMHJE_00373 | 1.1e-65 | 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 | |
DJHDMHJE_00374 | 7.1e-306 | 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) | |
DJHDMHJE_00375 | 2.5e-40 | ptsH | G | phosphocarrier protein HPR | ||
DJHDMHJE_00376 | 4.1e-26 | |||||
DJHDMHJE_00377 | 4.1e-36 | L | Transposase | |||
DJHDMHJE_00378 | 4.8e-24 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00379 | 6.6e-82 | rdgB | 3.6.1.66, 5.1.1.3 | F | Ham1 family | |
DJHDMHJE_00382 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
DJHDMHJE_00383 | 6.8e-95 | yyaR | K | Acetyltransferase (GNAT) domain | ||
DJHDMHJE_00384 | 3e-38 | mta | K | helix_turn_helix, mercury resistance | ||
DJHDMHJE_00385 | 2.2e-63 | mta | K | helix_turn_helix, mercury resistance | ||
DJHDMHJE_00386 | 6.9e-07 | S | ParE toxin of type II toxin-antitoxin system, parDE | |||
DJHDMHJE_00387 | 1.3e-60 | yyaQ | S | YjbR | ||
DJHDMHJE_00388 | 8.5e-87 | proW | P | ABC transporter, permease protein | ||
DJHDMHJE_00389 | 2.5e-109 | proV | E | ABC transporter, ATP-binding protein | ||
DJHDMHJE_00390 | 7e-89 | proWZ | P | ABC transporter permease | ||
DJHDMHJE_00391 | 1.8e-143 | proX | M | ABC transporter, substrate-binding protein, QAT family | ||
DJHDMHJE_00392 | 8e-122 | C | Zinc-binding dehydrogenase | |||
DJHDMHJE_00393 | 5.2e-49 | S | Membrane | |||
DJHDMHJE_00394 | 1.4e-39 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00395 | 5.9e-207 | S | SLAP domain | |||
DJHDMHJE_00396 | 3.5e-177 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
DJHDMHJE_00397 | 4.2e-55 | 2.7.1.2 | GK | ROK family | ||
DJHDMHJE_00398 | 2.8e-68 | GK | ROK family | |||
DJHDMHJE_00399 | 5.5e-43 | |||||
DJHDMHJE_00400 | 1.2e-268 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
DJHDMHJE_00401 | 5.5e-68 | S | Domain of unknown function (DUF1934) | |||
DJHDMHJE_00402 | 3.3e-55 | 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 | ||
DJHDMHJE_00403 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
DJHDMHJE_00404 | 3.6e-246 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
DJHDMHJE_00405 | 3.2e-33 | S | Haloacid dehalogenase-like hydrolase | |||
DJHDMHJE_00406 | 2.4e-47 | S | Haloacid dehalogenase-like hydrolase | |||
DJHDMHJE_00407 | 4.1e-283 | pipD | E | Dipeptidase | ||
DJHDMHJE_00408 | 1.1e-158 | msmR | K | AraC-like ligand binding domain | ||
DJHDMHJE_00409 | 8.6e-224 | pbuX | F | xanthine permease | ||
DJHDMHJE_00410 | 7.4e-106 | 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 | |
DJHDMHJE_00411 | 1.6e-106 | K | DNA-binding helix-turn-helix protein | |||
DJHDMHJE_00412 | 5.6e-10 | |||||
DJHDMHJE_00414 | 3.6e-35 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_00415 | 4.3e-23 | |||||
DJHDMHJE_00416 | 3e-170 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
DJHDMHJE_00417 | 7e-220 | metC | 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
DJHDMHJE_00418 | 3.3e-95 | cysE | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | |
DJHDMHJE_00419 | 9.8e-18 | IQ | reductase | |||
DJHDMHJE_00420 | 7.3e-194 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
DJHDMHJE_00421 | 9.3e-74 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
DJHDMHJE_00422 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
DJHDMHJE_00423 | 2.1e-102 | S | LexA-binding, inner membrane-associated putative hydrolase | |||
DJHDMHJE_00424 | 3.4e-22 | |||||
DJHDMHJE_00425 | 1.1e-92 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
DJHDMHJE_00427 | 3.8e-40 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00428 | 1.6e-182 | S | Putative peptidoglycan binding domain | |||
DJHDMHJE_00429 | 1.8e-24 | |||||
DJHDMHJE_00430 | 7.6e-248 | dtpT | U | amino acid peptide transporter | ||
DJHDMHJE_00431 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
DJHDMHJE_00433 | 1.2e-58 | lysM | M | LysM domain | ||
DJHDMHJE_00434 | 1.5e-172 | |||||
DJHDMHJE_00435 | 5.9e-212 | mdtG | EGP | Major facilitator Superfamily | ||
DJHDMHJE_00436 | 1.5e-112 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00437 | 4.8e-82 | racA | K | Domain of unknown function (DUF1836) | ||
DJHDMHJE_00438 | 1.8e-153 | yitS | S | EDD domain protein, DegV family | ||
DJHDMHJE_00440 | 2.1e-19 | UW | LPXTG-motif cell wall anchor domain protein | |||
DJHDMHJE_00441 | 3.1e-150 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
DJHDMHJE_00442 | 9.8e-55 | |||||
DJHDMHJE_00443 | 1.1e-138 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
DJHDMHJE_00444 | 6.9e-136 | mgtC | S | MgtC family | ||
DJHDMHJE_00445 | 1.9e-09 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
DJHDMHJE_00446 | 1.4e-21 | bglH | 3.2.1.86 | GT1 | G | beta-glucosidase activity |
DJHDMHJE_00447 | 9.4e-68 | yslB | S | Protein of unknown function (DUF2507) | ||
DJHDMHJE_00448 | 1.8e-147 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
DJHDMHJE_00449 | 4.2e-115 | 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 | |
DJHDMHJE_00450 | 9.8e-112 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_00451 | 6.3e-91 | bioY | S | BioY family | ||
DJHDMHJE_00452 | 1.8e-189 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
DJHDMHJE_00453 | 4.4e-135 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
DJHDMHJE_00454 | 9.1e-144 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
DJHDMHJE_00455 | 2.7e-157 | 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 | |
DJHDMHJE_00456 | 2.5e-261 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
DJHDMHJE_00457 | 2.7e-73 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
DJHDMHJE_00458 | 6.2e-79 | 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 | |
DJHDMHJE_00459 | 1.6e-230 | 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 | |
DJHDMHJE_00460 | 1.7e-128 | IQ | reductase | |||
DJHDMHJE_00461 | 1.5e-169 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
DJHDMHJE_00462 | 1.4e-34 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
DJHDMHJE_00463 | 4.5e-180 | 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 | |
DJHDMHJE_00464 | 9.6e-80 | marR | K | Transcriptional regulator | ||
DJHDMHJE_00465 | 3.8e-78 | 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 | |
DJHDMHJE_00466 | 2.3e-188 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
DJHDMHJE_00467 | 1.8e-13 | ytgB | S | Transglycosylase associated protein | ||
DJHDMHJE_00468 | 5.8e-103 | L | Resolvase, N terminal domain | |||
DJHDMHJE_00469 | 1e-129 | L | Transposase | |||
DJHDMHJE_00470 | 5.1e-63 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
DJHDMHJE_00471 | 5.7e-158 | glcU | U | sugar transport | ||
DJHDMHJE_00472 | 0.0 | kup | P | Transport of potassium into the cell | ||
DJHDMHJE_00473 | 7.5e-86 | |||||
DJHDMHJE_00476 | 7.9e-29 | |||||
DJHDMHJE_00477 | 6.4e-36 | S | Protein of unknown function (DUF2922) | |||
DJHDMHJE_00478 | 1.4e-176 | S | SLAP domain | |||
DJHDMHJE_00480 | 3.1e-37 | |||||
DJHDMHJE_00481 | 3.4e-209 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
DJHDMHJE_00482 | 2.4e-206 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
DJHDMHJE_00483 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
DJHDMHJE_00484 | 6.8e-116 | gepA | K | Protein of unknown function (DUF4065) | ||
DJHDMHJE_00485 | 7.5e-180 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
DJHDMHJE_00486 | 3e-118 | |||||
DJHDMHJE_00487 | 4.6e-132 | |||||
DJHDMHJE_00488 | 5e-133 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
DJHDMHJE_00489 | 3e-110 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
DJHDMHJE_00490 | 5.3e-101 | G | Aldose 1-epimerase | |||
DJHDMHJE_00491 | 8.3e-199 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
DJHDMHJE_00492 | 5.6e-112 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
DJHDMHJE_00493 | 0.0 | XK27_08315 | M | Sulfatase | ||
DJHDMHJE_00494 | 9e-267 | S | Fibronectin type III domain | |||
DJHDMHJE_00495 | 6.3e-243 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
DJHDMHJE_00496 | 1.2e-53 | |||||
DJHDMHJE_00498 | 4.6e-257 | pepC | 3.4.22.40 | E | aminopeptidase | |
DJHDMHJE_00499 | 9.8e-123 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
DJHDMHJE_00500 | 1.4e-300 | oppA | E | ABC transporter, substratebinding protein | ||
DJHDMHJE_00501 | 0.0 | oppA | E | ABC transporter, substratebinding protein | ||
DJHDMHJE_00502 | 3.4e-211 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
DJHDMHJE_00503 | 2.9e-144 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
DJHDMHJE_00504 | 4.9e-185 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
DJHDMHJE_00505 | 5e-201 | oppD | P | Belongs to the ABC transporter superfamily | ||
DJHDMHJE_00506 | 3.2e-175 | oppF | P | Belongs to the ABC transporter superfamily | ||
DJHDMHJE_00507 | 1.8e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
DJHDMHJE_00508 | 4.7e-60 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
DJHDMHJE_00509 | 1.9e-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 | ||
DJHDMHJE_00510 | 6.4e-114 | |||||
DJHDMHJE_00512 | 5.3e-115 | E | Belongs to the SOS response-associated peptidase family | |||
DJHDMHJE_00513 | 2.8e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
DJHDMHJE_00514 | 1.5e-91 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
DJHDMHJE_00515 | 1.3e-106 | S | TPM domain | |||
DJHDMHJE_00516 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
DJHDMHJE_00517 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
DJHDMHJE_00518 | 4.6e-148 | tatD | L | hydrolase, TatD family | ||
DJHDMHJE_00519 | 5e-99 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
DJHDMHJE_00520 | 1e-159 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
DJHDMHJE_00521 | 1e-38 | veg | S | Biofilm formation stimulator VEG | ||
DJHDMHJE_00522 | 2.4e-150 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
DJHDMHJE_00523 | 4.2e-208 | 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 | |
DJHDMHJE_00524 | 1.6e-89 | S | SLAP domain | |||
DJHDMHJE_00525 | 3.2e-74 | S | SLAP domain | |||
DJHDMHJE_00526 | 9.8e-164 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00527 | 2.3e-41 | S | reductase | |||
DJHDMHJE_00528 | 5e-39 | S | reductase | |||
DJHDMHJE_00529 | 4e-240 | pyrP | F | Permease | ||
DJHDMHJE_00530 | 1.5e-89 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
DJHDMHJE_00532 | 1.6e-261 | emrY | EGP | Major facilitator Superfamily | ||
DJHDMHJE_00533 | 9.6e-217 | mdtG | EGP | Major facilitator Superfamily | ||
DJHDMHJE_00534 | 1.1e-208 | pepA | E | M42 glutamyl aminopeptidase | ||
DJHDMHJE_00535 | 2.1e-45 | ybiT | S | ABC transporter, ATP-binding protein | ||
DJHDMHJE_00536 | 5.4e-178 | ybiT | S | ABC transporter, ATP-binding protein | ||
DJHDMHJE_00537 | 6.2e-11 | |||||
DJHDMHJE_00538 | 2.1e-73 | |||||
DJHDMHJE_00539 | 4.7e-63 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_00540 | 3.5e-298 | S | Domain of unknown function (DUF4430) | |||
DJHDMHJE_00541 | 9.3e-184 | U | FFAT motif binding | |||
DJHDMHJE_00542 | 4.8e-81 | S | Domain of unknown function (DUF4430) | |||
DJHDMHJE_00543 | 1.5e-15 | NU | Mycoplasma protein of unknown function, DUF285 | |||
DJHDMHJE_00544 | 6.7e-234 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
DJHDMHJE_00545 | 4.7e-96 | ywnH | 2.3.1.183 | M | acetyltransferase (GNAT) family | |
DJHDMHJE_00546 | 2.2e-15 | K | Penicillinase repressor | |||
DJHDMHJE_00547 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
DJHDMHJE_00548 | 2.7e-39 | mdt(A) | EGP | Major facilitator Superfamily | ||
DJHDMHJE_00549 | 1.7e-66 | mdt(A) | EGP | Major facilitator Superfamily | ||
DJHDMHJE_00551 | 8.6e-27 | |||||
DJHDMHJE_00552 | 8.9e-186 | malE | G | Bacterial extracellular solute-binding protein | ||
DJHDMHJE_00553 | 5.1e-107 | lacI3 | K | helix_turn _helix lactose operon repressor | ||
DJHDMHJE_00554 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
DJHDMHJE_00556 | 1.2e-216 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
DJHDMHJE_00557 | 6.4e-182 | ccpA | K | catabolite control protein A | ||
DJHDMHJE_00558 | 2.6e-263 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
DJHDMHJE_00559 | 1.1e-55 | |||||
DJHDMHJE_00560 | 1.5e-277 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
DJHDMHJE_00561 | 6.8e-77 | yutD | S | Protein of unknown function (DUF1027) | ||
DJHDMHJE_00562 | 6.2e-128 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
DJHDMHJE_00563 | 2.2e-84 | S | Protein of unknown function (DUF1461) | |||
DJHDMHJE_00564 | 1.8e-116 | dedA | S | SNARE-like domain protein | ||
DJHDMHJE_00565 | 9.1e-150 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
DJHDMHJE_00566 | 7.1e-50 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_00568 | 1.3e-73 | L | Transposase | |||
DJHDMHJE_00569 | 2.8e-27 | L | Transposase | |||
DJHDMHJE_00570 | 1.4e-95 | |||||
DJHDMHJE_00571 | 1.5e-174 | S | Aldo keto reductase | |||
DJHDMHJE_00572 | 7.5e-177 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
DJHDMHJE_00573 | 1e-82 | |||||
DJHDMHJE_00574 | 2.3e-17 | C | FMN_bind | |||
DJHDMHJE_00575 | 4.5e-302 | I | Protein of unknown function (DUF2974) | |||
DJHDMHJE_00576 | 2.1e-105 | 3.6.1.55 | F | NUDIX domain | ||
DJHDMHJE_00577 | 1.8e-206 | pbpX1 | V | Beta-lactamase | ||
DJHDMHJE_00578 | 5.7e-286 | V | ABC-type multidrug transport system, ATPase and permease components | |||
DJHDMHJE_00579 | 5.1e-274 | V | ABC-type multidrug transport system, ATPase and permease components | |||
DJHDMHJE_00581 | 7.9e-188 | 2.7.7.73, 2.7.7.80 | H | Involved in molybdopterin and thiamine biosynthesis, family 2 | ||
DJHDMHJE_00585 | 3.9e-99 | |||||
DJHDMHJE_00586 | 3.8e-279 | S | O-antigen ligase like membrane protein | |||
DJHDMHJE_00587 | 2.5e-25 | |||||
DJHDMHJE_00588 | 1.2e-94 | gmk2 | 2.7.4.8 | F | Guanylate kinase homologues. | |
DJHDMHJE_00589 | 1.9e-90 | M | NlpC/P60 family | |||
DJHDMHJE_00590 | 6.3e-31 | S | Archaea bacterial proteins of unknown function | |||
DJHDMHJE_00591 | 8.6e-46 | S | Archaea bacterial proteins of unknown function | |||
DJHDMHJE_00592 | 1.5e-122 | M | NlpC P60 family protein | |||
DJHDMHJE_00593 | 7.4e-140 | M | NlpC/P60 family | |||
DJHDMHJE_00596 | 1.1e-199 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
DJHDMHJE_00597 | 9.1e-179 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
DJHDMHJE_00598 | 3.2e-145 | epsB | M | biosynthesis protein | ||
DJHDMHJE_00599 | 1.6e-119 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
DJHDMHJE_00600 | 3.1e-144 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
DJHDMHJE_00601 | 9.5e-118 | rfbP | M | Bacterial sugar transferase | ||
DJHDMHJE_00602 | 9.8e-82 | cpsF | M | Oligosaccharide biosynthesis protein Alg14 like | ||
DJHDMHJE_00603 | 1.2e-77 | pssE | S | Glycosyltransferase family 28 C-terminal domain | ||
DJHDMHJE_00604 | 4.7e-08 | GT4 | M | Glycosyl transferases group 1 | ||
DJHDMHJE_00605 | 4.8e-75 | GT4 | M | Glycosyl transferases group 1 | ||
DJHDMHJE_00606 | 3.1e-75 | M | Domain of unknown function (DUF4422) | |||
DJHDMHJE_00607 | 8.3e-33 | |||||
DJHDMHJE_00608 | 3.6e-42 | M | LicD family | |||
DJHDMHJE_00609 | 3.2e-206 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
DJHDMHJE_00610 | 1.5e-176 | epsIIL | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
DJHDMHJE_00611 | 1.5e-84 | M | LicD family | |||
DJHDMHJE_00612 | 4.5e-266 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
DJHDMHJE_00613 | 2.9e-262 | frdC | 1.3.5.4 | C | FAD binding domain | |
DJHDMHJE_00615 | 1.5e-57 | M | domain protein | |||
DJHDMHJE_00616 | 6.3e-08 | M | domain protein | |||
DJHDMHJE_00617 | 6.2e-13 | M | domain protein | |||
DJHDMHJE_00618 | 7.9e-130 | S | YSIRK type signal peptide | |||
DJHDMHJE_00619 | 3.7e-69 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_00620 | 5.3e-79 | |||||
DJHDMHJE_00621 | 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 | |
DJHDMHJE_00622 | 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 | |
DJHDMHJE_00623 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
DJHDMHJE_00624 | 2.9e-81 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
DJHDMHJE_00626 | 1.6e-08 | |||||
DJHDMHJE_00627 | 7.6e-80 | |||||
DJHDMHJE_00629 | 2.4e-300 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
DJHDMHJE_00630 | 2.1e-196 | 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 | ||
DJHDMHJE_00631 | 3.1e-164 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
DJHDMHJE_00632 | 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 | ||
DJHDMHJE_00633 | 5.8e-241 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
DJHDMHJE_00634 | 2e-61 | yabR | J | S1 RNA binding domain | ||
DJHDMHJE_00635 | 9.8e-59 | divIC | D | Septum formation initiator | ||
DJHDMHJE_00636 | 1.8e-34 | yabO | J | S4 domain protein | ||
DJHDMHJE_00637 | 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 | ||
DJHDMHJE_00638 | 1.7e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
DJHDMHJE_00639 | 3.3e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
DJHDMHJE_00640 | 7.6e-129 | S | (CBS) domain | |||
DJHDMHJE_00641 | 9.7e-92 | K | transcriptional regulator | |||
DJHDMHJE_00642 | 5.3e-217 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
DJHDMHJE_00643 | 1.7e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
DJHDMHJE_00644 | 2.5e-254 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
DJHDMHJE_00645 | 5.3e-264 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
DJHDMHJE_00646 | 1.9e-39 | rpmE2 | J | Ribosomal protein L31 | ||
DJHDMHJE_00647 | 9.1e-158 | S | Sucrose-6F-phosphate phosphohydrolase | |||
DJHDMHJE_00648 | 1.4e-147 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
DJHDMHJE_00649 | 1.8e-51 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
DJHDMHJE_00650 | 5.2e-90 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
DJHDMHJE_00651 | 6.9e-84 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
DJHDMHJE_00652 | 5.6e-152 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
DJHDMHJE_00654 | 1.9e-132 | cobQ | S | glutamine amidotransferase | ||
DJHDMHJE_00655 | 1e-41 | S | Protein of unknown function (DUF3290) | |||
DJHDMHJE_00656 | 1.3e-11 | S | Protein of unknown function (DUF3290) | |||
DJHDMHJE_00657 | 1.2e-140 | pnuC | H | nicotinamide mononucleotide transporter | ||
DJHDMHJE_00658 | 2.7e-96 | V | ABC transporter transmembrane region | |||
DJHDMHJE_00659 | 1.1e-167 | V | ABC transporter transmembrane region | |||
DJHDMHJE_00660 | 9.3e-180 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
DJHDMHJE_00661 | 3.7e-69 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_00662 | 1.6e-38 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00663 | 2.2e-174 | S | cog cog1373 | |||
DJHDMHJE_00664 | 2.4e-218 | pbuG | S | permease | ||
DJHDMHJE_00665 | 1.6e-146 | cof | S | haloacid dehalogenase-like hydrolase | ||
DJHDMHJE_00666 | 1.4e-127 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
DJHDMHJE_00667 | 5.5e-118 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
DJHDMHJE_00669 | 2.8e-20 | ybbH_2 | K | rpiR family | ||
DJHDMHJE_00670 | 5.6e-13 | |||||
DJHDMHJE_00671 | 5.6e-68 | M | LysM domain protein | |||
DJHDMHJE_00672 | 1.7e-196 | D | nuclear chromosome segregation | |||
DJHDMHJE_00673 | 9e-112 | G | Phosphoglycerate mutase family | |||
DJHDMHJE_00674 | 1.7e-229 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
DJHDMHJE_00675 | 1.7e-133 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
DJHDMHJE_00676 | 8.9e-142 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00677 | 7.1e-207 | G | Major Facilitator Superfamily | |||
DJHDMHJE_00678 | 8.9e-16 | hicA | S | HicA toxin of bacterial toxin-antitoxin, | ||
DJHDMHJE_00679 | 3.4e-31 | S | HicB family | |||
DJHDMHJE_00680 | 8.7e-28 | |||||
DJHDMHJE_00681 | 5.4e-09 | |||||
DJHDMHJE_00682 | 4e-29 | S | zinc-ribbon domain | |||
DJHDMHJE_00683 | 6.7e-24 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
DJHDMHJE_00684 | 1.6e-182 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
DJHDMHJE_00685 | 2e-129 | K | UTRA | |||
DJHDMHJE_00686 | 2.9e-84 | L | Transposase | |||
DJHDMHJE_00687 | 1.4e-15 | emrY | EGP | Major facilitator Superfamily | ||
DJHDMHJE_00688 | 1e-29 | emrY | EGP | Major facilitator Superfamily | ||
DJHDMHJE_00693 | 1.8e-24 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_00694 | 3.8e-15 | |||||
DJHDMHJE_00695 | 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 | ||
DJHDMHJE_00696 | 2.1e-120 | srtA | 3.4.22.70 | M | sortase family | |
DJHDMHJE_00697 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
DJHDMHJE_00698 | 3.7e-96 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
DJHDMHJE_00699 | 8e-171 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
DJHDMHJE_00700 | 4.2e-152 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
DJHDMHJE_00701 | 1.2e-112 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
DJHDMHJE_00702 | 2e-68 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
DJHDMHJE_00703 | 1.6e-85 | 3.4.21.96 | S | SLAP domain | ||
DJHDMHJE_00704 | 0.0 | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
DJHDMHJE_00705 | 8.8e-156 | lysR5 | K | LysR substrate binding domain | ||
DJHDMHJE_00706 | 3.2e-26 | arcA | 3.5.3.6 | E | Arginine | |
DJHDMHJE_00707 | 9e-58 | arcA | 3.5.3.6 | E | Arginine | |
DJHDMHJE_00708 | 4.9e-44 | arcA | 3.5.3.6 | E | Arginine | |
DJHDMHJE_00709 | 3.9e-13 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
DJHDMHJE_00710 | 6.8e-110 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
DJHDMHJE_00711 | 1.9e-66 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
DJHDMHJE_00712 | 2.8e-52 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
DJHDMHJE_00713 | 8.9e-98 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
DJHDMHJE_00714 | 2.7e-118 | S | Sterol carrier protein domain | |||
DJHDMHJE_00715 | 5.2e-74 | S | Sterol carrier protein domain | |||
DJHDMHJE_00716 | 1.1e-19 | |||||
DJHDMHJE_00717 | 3.5e-106 | K | LysR substrate binding domain | |||
DJHDMHJE_00718 | 2.2e-25 | |||||
DJHDMHJE_00719 | 2.1e-13 | |||||
DJHDMHJE_00720 | 0.0 | O | Belongs to the peptidase S8 family | |||
DJHDMHJE_00722 | 5.2e-198 | M | Glycosyl transferase family group 2 | |||
DJHDMHJE_00724 | 6.1e-38 | |||||
DJHDMHJE_00725 | 4.4e-73 | |||||
DJHDMHJE_00726 | 2.1e-271 | S | Archaea bacterial proteins of unknown function | |||
DJHDMHJE_00727 | 5.3e-270 | hsdR | 2.1.1.72, 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
DJHDMHJE_00728 | 0.0 | yfjM | S | Protein of unknown function DUF262 | ||
DJHDMHJE_00729 | 5.9e-305 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
DJHDMHJE_00730 | 9.7e-183 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
DJHDMHJE_00731 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
DJHDMHJE_00732 | 2.7e-61 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
DJHDMHJE_00733 | 2.5e-234 | steT | E | amino acid | ||
DJHDMHJE_00734 | 1.2e-232 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
DJHDMHJE_00735 | 5.6e-49 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
DJHDMHJE_00736 | 1.6e-25 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
DJHDMHJE_00737 | 4.2e-36 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
DJHDMHJE_00738 | 1.8e-30 | mmuP | E | amino acid | ||
DJHDMHJE_00739 | 2.1e-129 | mmuP | E | amino acid | ||
DJHDMHJE_00740 | 2.1e-34 | mmuP | E | amino acid | ||
DJHDMHJE_00741 | 1.7e-248 | N | Uncharacterized conserved protein (DUF2075) | |||
DJHDMHJE_00742 | 3.3e-10 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
DJHDMHJE_00743 | 8.6e-78 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
DJHDMHJE_00744 | 1.2e-94 | S | YcaO cyclodehydratase, ATP-ad Mg2+-binding | |||
DJHDMHJE_00745 | 4.3e-194 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
DJHDMHJE_00746 | 4.8e-204 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
DJHDMHJE_00749 | 1.3e-184 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
DJHDMHJE_00750 | 6.4e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
DJHDMHJE_00751 | 8.1e-246 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
DJHDMHJE_00752 | 1.8e-57 | |||||
DJHDMHJE_00753 | 2.8e-87 | |||||
DJHDMHJE_00754 | 2.2e-74 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
DJHDMHJE_00755 | 2.7e-71 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
DJHDMHJE_00756 | 6.6e-176 | XK27_05540 | S | DUF218 domain | ||
DJHDMHJE_00757 | 1.1e-78 | |||||
DJHDMHJE_00758 | 4.6e-109 | |||||
DJHDMHJE_00759 | 4.4e-138 | EG | EamA-like transporter family | |||
DJHDMHJE_00760 | 3.6e-82 | M | NlpC/P60 family | |||
DJHDMHJE_00761 | 2.9e-40 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00762 | 1.3e-185 | S | SLAP domain | |||
DJHDMHJE_00763 | 7e-186 | S | Bacteriocin helveticin-J | |||
DJHDMHJE_00764 | 2.7e-160 | |||||
DJHDMHJE_00765 | 4e-10 | maa | S | transferase hexapeptide repeat | ||
DJHDMHJE_00766 | 3.7e-61 | maa | S | transferase hexapeptide repeat | ||
DJHDMHJE_00767 | 5.8e-242 | cycA | E | Amino acid permease | ||
DJHDMHJE_00768 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
DJHDMHJE_00769 | 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 | |
DJHDMHJE_00770 | 8.8e-47 | |||||
DJHDMHJE_00771 | 2.2e-45 | yagE | E | amino acid | ||
DJHDMHJE_00772 | 2.8e-49 | |||||
DJHDMHJE_00773 | 9.6e-89 | UW | LPXTG-motif cell wall anchor domain protein | |||
DJHDMHJE_00774 | 4.7e-35 | S | LPXTG cell wall anchor motif | |||
DJHDMHJE_00775 | 5.2e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
DJHDMHJE_00776 | 5.2e-133 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
DJHDMHJE_00777 | 6.4e-37 | |||||
DJHDMHJE_00778 | 7.7e-73 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
DJHDMHJE_00779 | 2.2e-93 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
DJHDMHJE_00780 | 8.6e-105 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
DJHDMHJE_00781 | 2.8e-29 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
DJHDMHJE_00782 | 5.4e-69 | K | DNA-binding transcription factor activity | |||
DJHDMHJE_00783 | 0.0 | O | Belongs to the peptidase S8 family | |||
DJHDMHJE_00784 | 1.2e-123 | O | Belongs to the peptidase S8 family | |||
DJHDMHJE_00785 | 5.9e-310 | nagZ | 3.2.1.52 | G | Glycosyl hydrolase family 3 N terminal domain | |
DJHDMHJE_00786 | 4e-33 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
DJHDMHJE_00787 | 6.5e-54 | eutP | E | Ethanolamine utilisation - propanediol utilisation | ||
DJHDMHJE_00788 | 1.5e-44 | U | FFAT motif binding | |||
DJHDMHJE_00789 | 8.8e-85 | U | FFAT motif binding | |||
DJHDMHJE_00790 | 8.7e-125 | S | ECF-type riboflavin transporter, S component | |||
DJHDMHJE_00791 | 0.0 | ykoD_2 | S | AAA domain, putative AbiEii toxin, Type IV TA system | ||
DJHDMHJE_00792 | 4.1e-156 | P | ABC-type cobalt transport system permease component CbiQ and related transporters | |||
DJHDMHJE_00794 | 5.1e-43 | |||||
DJHDMHJE_00796 | 6.8e-152 | glcU | U | sugar transport | ||
DJHDMHJE_00797 | 2e-48 | |||||
DJHDMHJE_00798 | 2.5e-79 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
DJHDMHJE_00799 | 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 | |
DJHDMHJE_00800 | 1.7e-21 | |||||
DJHDMHJE_00801 | 3e-65 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
DJHDMHJE_00802 | 4.5e-179 | I | Carboxylesterase family | |||
DJHDMHJE_00804 | 6.5e-213 | M | Glycosyl hydrolases family 25 | |||
DJHDMHJE_00805 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
DJHDMHJE_00806 | 2.1e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
DJHDMHJE_00807 | 2.5e-129 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
DJHDMHJE_00808 | 1.8e-200 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
DJHDMHJE_00809 | 1.3e-257 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
DJHDMHJE_00810 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
DJHDMHJE_00811 | 2.3e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
DJHDMHJE_00812 | 2e-200 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
DJHDMHJE_00813 | 2.2e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
DJHDMHJE_00814 | 1.6e-70 | yqhY | S | Asp23 family, cell envelope-related function | ||
DJHDMHJE_00815 | 8.1e-64 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
DJHDMHJE_00816 | 7.2e-16 | ps301 | K | sequence-specific DNA binding | ||
DJHDMHJE_00817 | 8.1e-96 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
DJHDMHJE_00818 | 6.7e-189 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
DJHDMHJE_00819 | 1e-38 | yifK | E | Amino acid permease | ||
DJHDMHJE_00821 | 3.3e-116 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
DJHDMHJE_00822 | 7.8e-100 | 3.6.1.27 | I | Acid phosphatase homologues | ||
DJHDMHJE_00823 | 5.9e-81 | S | Short repeat of unknown function (DUF308) | |||
DJHDMHJE_00824 | 4.8e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
DJHDMHJE_00825 | 2.6e-194 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
DJHDMHJE_00826 | 1.4e-170 | whiA | K | May be required for sporulation | ||
DJHDMHJE_00827 | 2.3e-99 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
DJHDMHJE_00828 | 0.0 | S | SH3-like domain | |||
DJHDMHJE_00829 | 6.6e-153 | S | haloacid dehalogenase-like hydrolase | |||
DJHDMHJE_00830 | 4.4e-59 | ycaM | E | amino acid | ||
DJHDMHJE_00831 | 3e-135 | ycaM | E | amino acid | ||
DJHDMHJE_00832 | 2.6e-98 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
DJHDMHJE_00833 | 9.8e-288 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
DJHDMHJE_00834 | 0.0 | hsdR | 3.1.21.3 | L | Type I restriction enzyme R protein N terminus (HSDR_N) | |
DJHDMHJE_00835 | 4.4e-149 | hsdS2 | 2.1.1.72 | L | N-6 DNA Methylase | |
DJHDMHJE_00836 | 1.6e-114 | L | Putative transposase DNA-binding domain | |||
DJHDMHJE_00837 | 1.8e-55 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
DJHDMHJE_00838 | 9.5e-71 | L | IS1381, transposase OrfA | |||
DJHDMHJE_00839 | 4.1e-153 | ykuT | M | mechanosensitive ion channel | ||
DJHDMHJE_00840 | 3.3e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
DJHDMHJE_00841 | 2e-43 | |||||
DJHDMHJE_00842 | 9.8e-64 | S | SLAP domain | |||
DJHDMHJE_00843 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
DJHDMHJE_00844 | 4.3e-69 | rplI | J | Binds to the 23S rRNA | ||
DJHDMHJE_00845 | 1.2e-255 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
DJHDMHJE_00846 | 1.7e-168 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
DJHDMHJE_00847 | 4.5e-35 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_00848 | 1.2e-13 | L | Transposase | |||
DJHDMHJE_00849 | 1e-31 | psd | 4.1.1.65 | I | Belongs to the phosphatidylserine decarboxylase family | |
DJHDMHJE_00850 | 3.4e-49 | pspC | KT | PspC domain | ||
DJHDMHJE_00852 | 2.2e-243 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
DJHDMHJE_00853 | 4.3e-155 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
DJHDMHJE_00854 | 1.5e-110 | M | ErfK YbiS YcfS YnhG | |||
DJHDMHJE_00855 | 5.2e-78 | padR | K | Virulence activator alpha C-term | ||
DJHDMHJE_00856 | 2.2e-104 | padC | Q | Phenolic acid decarboxylase | ||
DJHDMHJE_00857 | 3.9e-113 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
DJHDMHJE_00859 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
DJHDMHJE_00860 | 1e-170 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
DJHDMHJE_00861 | 1.7e-90 | 3.6.1.55 | L | NUDIX domain | ||
DJHDMHJE_00862 | 1.1e-38 | |||||
DJHDMHJE_00863 | 1.7e-31 | |||||
DJHDMHJE_00864 | 6.6e-290 | V | ABC-type multidrug transport system, ATPase and permease components | |||
DJHDMHJE_00865 | 3.4e-286 | V | ABC-type multidrug transport system, ATPase and permease components | |||
DJHDMHJE_00867 | 4.4e-16 | L | PFAM IS66 Orf2 family protein | |||
DJHDMHJE_00868 | 1.2e-08 | |||||
DJHDMHJE_00869 | 3.3e-14 | S | Phage derived protein Gp49-like (DUF891) | |||
DJHDMHJE_00870 | 2.6e-46 | K | Helix-turn-helix XRE-family like proteins | |||
DJHDMHJE_00871 | 5.3e-43 | |||||
DJHDMHJE_00872 | 1.7e-32 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
DJHDMHJE_00873 | 2.3e-243 | L | Probable transposase | |||
DJHDMHJE_00874 | 8.7e-15 | S | Fic/DOC family | |||
DJHDMHJE_00875 | 2.2e-56 | UW | LPXTG-motif cell wall anchor domain protein | |||
DJHDMHJE_00876 | 2.6e-78 | UW | LPXTG-motif cell wall anchor domain protein | |||
DJHDMHJE_00877 | 3.4e-169 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
DJHDMHJE_00878 | 3.7e-74 | fhaB | M | Rib/alpha-like repeat | ||
DJHDMHJE_00879 | 1.5e-12 | |||||
DJHDMHJE_00880 | 4.7e-20 | |||||
DJHDMHJE_00882 | 9.3e-29 | |||||
DJHDMHJE_00883 | 1.9e-258 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
DJHDMHJE_00884 | 1.3e-156 | 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 | |
DJHDMHJE_00885 | 1.9e-104 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_00886 | 5.1e-63 | K | LysR substrate binding domain | |||
DJHDMHJE_00887 | 1e-07 | K | LysR substrate binding domain | |||
DJHDMHJE_00888 | 1.2e-41 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00889 | 4.6e-42 | L | Psort location Cytoplasmic, score | |||
DJHDMHJE_00890 | 3.9e-135 | L | Psort location Cytoplasmic, score | |||
DJHDMHJE_00891 | 2.8e-84 | FG | adenosine 5'-monophosphoramidase activity | |||
DJHDMHJE_00892 | 7.2e-47 | |||||
DJHDMHJE_00893 | 2.8e-100 | L | Integrase | |||
DJHDMHJE_00894 | 8e-42 | S | RelB antitoxin | |||
DJHDMHJE_00895 | 2.1e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
DJHDMHJE_00896 | 8.2e-25 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_00897 | 5.6e-197 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
DJHDMHJE_00898 | 3.1e-152 | mdlA | V | ABC transporter | ||
DJHDMHJE_00899 | 1.6e-271 | mdlB | V | ABC transporter | ||
DJHDMHJE_00900 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
DJHDMHJE_00901 | 1.4e-231 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
DJHDMHJE_00902 | 4.1e-115 | plsC | 2.3.1.51 | I | Acyltransferase | |
DJHDMHJE_00903 | 4.5e-199 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
DJHDMHJE_00904 | 4.2e-141 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
DJHDMHJE_00905 | 2.2e-185 | 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 | ||
DJHDMHJE_00906 | 1.8e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
DJHDMHJE_00907 | 4e-93 | 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 | ||
DJHDMHJE_00908 | 1.4e-138 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
DJHDMHJE_00909 | 1.6e-146 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
DJHDMHJE_00910 | 2.3e-197 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
DJHDMHJE_00911 | 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 | |
DJHDMHJE_00912 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
DJHDMHJE_00913 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
DJHDMHJE_00914 | 4.2e-201 | nusA | K | Participates in both transcription termination and antitermination | ||
DJHDMHJE_00915 | 8.8e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
DJHDMHJE_00916 | 1.2e-46 | rplGA | J | ribosomal protein | ||
DJHDMHJE_00917 | 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 | ||
DJHDMHJE_00918 | 4.3e-59 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
DJHDMHJE_00919 | 2e-166 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
DJHDMHJE_00920 | 2.1e-182 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
DJHDMHJE_00921 | 2.5e-192 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
DJHDMHJE_00922 | 5.1e-78 | 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 | ||
DJHDMHJE_00923 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
DJHDMHJE_00924 | 7.6e-203 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
DJHDMHJE_00925 | 3e-64 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_00926 | 5.3e-98 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_00927 | 1e-124 | GT4 | M | Glycosyl transferases group 1 | ||
DJHDMHJE_00928 | 1.2e-56 | M | LicD family | |||
DJHDMHJE_00929 | 9.2e-40 | L | Transposase DDE domain | |||
DJHDMHJE_00930 | 7e-124 | L | Transposase DDE domain | |||
DJHDMHJE_00931 | 5.2e-39 | L | Transposase and inactivated derivatives | |||
DJHDMHJE_00932 | 2.1e-85 | L | Transposase and inactivated derivatives | |||
DJHDMHJE_00933 | 1.3e-26 | S | Transposase C of IS166 homeodomain | |||
DJHDMHJE_00934 | 9.9e-31 | L | PFAM IS66 Orf2 family protein | |||
DJHDMHJE_00935 | 3.4e-22 | |||||
DJHDMHJE_00936 | 1.8e-24 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_00937 | 2.2e-36 | |||||
DJHDMHJE_00938 | 2e-166 | S | SLAP domain | |||
DJHDMHJE_00939 | 6.7e-11 | L | Transposase | |||
DJHDMHJE_00941 | 1.1e-130 | K | response regulator | |||
DJHDMHJE_00942 | 4.1e-307 | vicK | 2.7.13.3 | T | Histidine kinase | |
DJHDMHJE_00943 | 1.2e-244 | yycH | S | YycH protein | ||
DJHDMHJE_00944 | 6.9e-150 | yycI | S | YycH protein | ||
DJHDMHJE_00945 | 3.3e-149 | vicX | 3.1.26.11 | S | domain protein | |
DJHDMHJE_00946 | 1.5e-180 | htrA | 3.4.21.107 | O | serine protease | |
DJHDMHJE_00947 | 1.5e-91 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
DJHDMHJE_00948 | 6.6e-31 | K | Helix-turn-helix XRE-family like proteins | |||
DJHDMHJE_00949 | 4.5e-35 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_00950 | 6.7e-259 | ykgC | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
DJHDMHJE_00951 | 4.1e-47 | L | Psort location Cytoplasmic, score | |||
DJHDMHJE_00952 | 1.2e-151 | cbiO2 | P | ABC transporter | ||
DJHDMHJE_00953 | 7e-158 | P | ABC transporter | |||
DJHDMHJE_00954 | 2.6e-133 | cbiQ | P | Cobalt transport protein | ||
DJHDMHJE_00955 | 1.3e-89 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
DJHDMHJE_00956 | 1.8e-32 | M | NlpC/P60 family | |||
DJHDMHJE_00957 | 1.2e-70 | L | Transposase and inactivated derivatives, IS30 family | |||
DJHDMHJE_00958 | 1.5e-68 | K | Acetyltransferase (GNAT) domain | |||
DJHDMHJE_00960 | 2.4e-223 | oxlT | P | Major Facilitator Superfamily | ||
DJHDMHJE_00961 | 1e-41 | L | Helix-turn-helix domain | |||
DJHDMHJE_00962 | 3.6e-134 | yvdE | K | helix_turn _helix lactose operon repressor | ||
DJHDMHJE_00963 | 5.4e-161 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_00964 | 1.2e-79 | |||||
DJHDMHJE_00966 | 2.4e-33 | |||||
DJHDMHJE_00969 | 5.6e-19 | |||||
DJHDMHJE_00972 | 2.8e-86 | V | COG4823 Abortive infection bacteriophage resistance protein | |||
DJHDMHJE_00973 | 5e-120 | 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 | |
DJHDMHJE_00975 | 1.5e-37 | S | SIR2-like domain | |||
DJHDMHJE_00976 | 3.1e-121 | 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 | |
DJHDMHJE_00977 | 4.2e-53 | 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 | |
DJHDMHJE_00978 | 7.1e-217 | aspC | 2.6.1.1 | E | Aminotransferase | |
DJHDMHJE_00979 | 2.4e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
DJHDMHJE_00980 | 2.2e-176 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
DJHDMHJE_00981 | 4.7e-221 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
DJHDMHJE_00982 | 3.6e-78 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
DJHDMHJE_00983 | 1.7e-251 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
DJHDMHJE_00986 | 3.4e-41 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_00987 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
DJHDMHJE_00988 | 1e-41 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
DJHDMHJE_00989 | 4e-159 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
DJHDMHJE_00990 | 2.5e-118 | fhuC | P | ABC transporter | ||
DJHDMHJE_00991 | 1.1e-131 | znuB | U | ABC 3 transport family | ||
DJHDMHJE_00992 | 1.6e-239 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
DJHDMHJE_00993 | 1.9e-200 | xerS | L | Belongs to the 'phage' integrase family | ||
DJHDMHJE_00994 | 1.8e-67 | |||||
DJHDMHJE_00995 | 3.8e-87 | adk | 2.7.4.3 | F | topology modulation protein | |
DJHDMHJE_00996 | 1.2e-109 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
DJHDMHJE_00997 | 1.4e-54 | |||||
DJHDMHJE_00998 | 8.2e-28 | M | Glycosyl hydrolases family 25 | |||
DJHDMHJE_00999 | 2.5e-44 | M | Glycosyl hydrolases family 25 | |||
DJHDMHJE_01000 | 1.1e-47 | M | Glycosyl hydrolases family 25 | |||
DJHDMHJE_01001 | 3.6e-13 | lysA2 | M | Glycosyl hydrolases family 25 | ||
DJHDMHJE_01002 | 3.2e-34 | S | Transglycosylase associated protein | |||
DJHDMHJE_01003 | 6e-106 | yoaK | S | Protein of unknown function (DUF1275) | ||
DJHDMHJE_01004 | 7.3e-177 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
DJHDMHJE_01005 | 2.9e-233 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
DJHDMHJE_01006 | 1.1e-89 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
DJHDMHJE_01007 | 1.3e-168 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
DJHDMHJE_01008 | 1.9e-250 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
DJHDMHJE_01009 | 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 | |
DJHDMHJE_01010 | 1.1e-155 | dprA | LU | DNA protecting protein DprA | ||
DJHDMHJE_01011 | 2.9e-134 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
DJHDMHJE_01012 | 7.6e-160 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
DJHDMHJE_01013 | 4e-279 | yjcE | P | Sodium proton antiporter | ||
DJHDMHJE_01014 | 9.3e-36 | yozE | S | Belongs to the UPF0346 family | ||
DJHDMHJE_01015 | 7.7e-149 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
DJHDMHJE_01016 | 6.7e-114 | hlyIII | S | protein, hemolysin III | ||
DJHDMHJE_01017 | 3e-226 | 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 | |
DJHDMHJE_01018 | 3.2e-161 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
DJHDMHJE_01019 | 7.8e-230 | S | Tetratricopeptide repeat protein | |||
DJHDMHJE_01020 | 3e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
DJHDMHJE_01021 | 2.8e-246 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
DJHDMHJE_01022 | 1.3e-208 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
DJHDMHJE_01023 | 1.7e-114 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
DJHDMHJE_01024 | 2.4e-30 | M | Lysin motif | |||
DJHDMHJE_01025 | 1.8e-114 | 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 | |||
DJHDMHJE_01026 | 1e-128 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
DJHDMHJE_01027 | 4.1e-104 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
DJHDMHJE_01028 | 2.5e-130 | 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 | ||
DJHDMHJE_01029 | 4.9e-60 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
DJHDMHJE_01030 | 4e-167 | xerD | D | recombinase XerD | ||
DJHDMHJE_01031 | 5e-170 | cvfB | S | S1 domain | ||
DJHDMHJE_01032 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
DJHDMHJE_01033 | 1.9e-183 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
DJHDMHJE_01034 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
DJHDMHJE_01035 | 2.5e-22 | S | Protein of unknown function (DUF2929) | |||
DJHDMHJE_01036 | 1.3e-309 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
DJHDMHJE_01037 | 7.6e-28 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
DJHDMHJE_01038 | 6.2e-33 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
DJHDMHJE_01039 | 1.4e-144 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
DJHDMHJE_01040 | 3.1e-178 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
DJHDMHJE_01041 | 0.0 | oatA | I | Acyltransferase | ||
DJHDMHJE_01042 | 1.4e-242 | 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 | ||
DJHDMHJE_01043 | 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 | ||
DJHDMHJE_01044 | 3.4e-41 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01045 | 1e-133 | 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 | |
DJHDMHJE_01046 | 5.2e-161 | yeaE | S | Aldo/keto reductase family | ||
DJHDMHJE_01047 | 4.3e-96 | S | ECF transporter, substrate-specific component | |||
DJHDMHJE_01048 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01049 | 4.7e-45 | macB_3 | V | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01050 | 1.2e-12 | macB_3 | V | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01051 | 2.9e-196 | S | DUF218 domain | |||
DJHDMHJE_01052 | 4.6e-120 | S | CAAX protease self-immunity | |||
DJHDMHJE_01053 | 3.7e-69 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_01054 | 1.5e-223 | |||||
DJHDMHJE_01055 | 4.7e-81 | |||||
DJHDMHJE_01056 | 2.4e-109 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
DJHDMHJE_01057 | 4.7e-66 | S | ASCH domain | |||
DJHDMHJE_01058 | 5.5e-37 | 4.4.1.5 | E | lactoylglutathione lyase activity | ||
DJHDMHJE_01059 | 1e-137 | S | Protein of unknown function DUF262 | |||
DJHDMHJE_01060 | 3.4e-19 | S | Protein of unknown function DUF262 | |||
DJHDMHJE_01061 | 2.6e-67 | S | Protein of unknown function DUF262 | |||
DJHDMHJE_01062 | 2.2e-105 | S | Putative inner membrane protein (DUF1819) | |||
DJHDMHJE_01063 | 6e-111 | S | Domain of unknown function (DUF1788) | |||
DJHDMHJE_01064 | 7.8e-217 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
DJHDMHJE_01065 | 0.0 | 2.1.1.72 | V | Eco57I restriction-modification methylase | ||
DJHDMHJE_01066 | 2.3e-41 | LO | Belongs to the peptidase S16 family | |||
DJHDMHJE_01067 | 1.6e-148 | S | Putative ABC-transporter type IV | |||
DJHDMHJE_01068 | 2.8e-236 | S | LPXTG cell wall anchor motif | |||
DJHDMHJE_01069 | 1.4e-29 | pipD | E | Dipeptidase | ||
DJHDMHJE_01070 | 1.5e-77 | pipD | E | Dipeptidase | ||
DJHDMHJE_01071 | 4.5e-30 | pipD | E | Dipeptidase | ||
DJHDMHJE_01072 | 7.4e-255 | V | Restriction endonuclease | |||
DJHDMHJE_01073 | 2.3e-107 | K | Bacterial regulatory proteins, tetR family | |||
DJHDMHJE_01074 | 3e-23 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
DJHDMHJE_01075 | 8.6e-145 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
DJHDMHJE_01076 | 8.7e-131 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
DJHDMHJE_01077 | 1.4e-113 | ybbL | S | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01078 | 3.9e-30 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
DJHDMHJE_01080 | 2e-33 | |||||
DJHDMHJE_01083 | 6.2e-235 | L | Belongs to the 'phage' integrase family | |||
DJHDMHJE_01084 | 1.6e-27 | |||||
DJHDMHJE_01085 | 2.6e-59 | |||||
DJHDMHJE_01086 | 2.7e-146 | S | Replication initiation factor | |||
DJHDMHJE_01087 | 2.6e-146 | D | Ftsk spoiiie family protein | |||
DJHDMHJE_01088 | 3.3e-36 | |||||
DJHDMHJE_01089 | 3.1e-40 | |||||
DJHDMHJE_01090 | 5e-17 | |||||
DJHDMHJE_01091 | 1.5e-39 | |||||
DJHDMHJE_01092 | 5.7e-15 | K | Helix-turn-helix XRE-family like proteins | |||
DJHDMHJE_01093 | 4.9e-184 | S | AAA domain | |||
DJHDMHJE_01094 | 2.6e-126 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
DJHDMHJE_01095 | 2.5e-23 | |||||
DJHDMHJE_01096 | 1.1e-161 | czcD | P | cation diffusion facilitator family transporter | ||
DJHDMHJE_01097 | 2e-126 | pgm3 | G | Belongs to the phosphoglycerate mutase family | ||
DJHDMHJE_01098 | 3.5e-132 | S | membrane transporter protein | |||
DJHDMHJE_01099 | 9.8e-14 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
DJHDMHJE_01100 | 1.7e-64 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
DJHDMHJE_01101 | 1.1e-109 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
DJHDMHJE_01102 | 3.2e-62 | S | Protein of unknown function (DUF805) | |||
DJHDMHJE_01103 | 5.8e-11 | S | Hypothetical protein (DUF2513) | |||
DJHDMHJE_01104 | 0.0 | V | Type II restriction enzyme, methylase subunits | |||
DJHDMHJE_01105 | 2.9e-187 | |||||
DJHDMHJE_01106 | 9.6e-52 | |||||
DJHDMHJE_01107 | 1.4e-206 | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | |||
DJHDMHJE_01108 | 1.8e-90 | |||||
DJHDMHJE_01109 | 1.6e-210 | repB | EP | Plasmid replication protein | ||
DJHDMHJE_01110 | 3.8e-27 | |||||
DJHDMHJE_01111 | 3.9e-198 | L | Phage integrase family | |||
DJHDMHJE_01112 | 1.6e-67 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
DJHDMHJE_01113 | 4.5e-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 | ||
DJHDMHJE_01114 | 4.6e-151 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
DJHDMHJE_01115 | 6.7e-142 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
DJHDMHJE_01116 | 1.5e-152 | ecfA | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
DJHDMHJE_01117 | 2.2e-154 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
DJHDMHJE_01118 | 1.1e-60 | rplQ | J | Ribosomal protein L17 | ||
DJHDMHJE_01119 | 8.1e-171 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
DJHDMHJE_01120 | 5.2e-63 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
DJHDMHJE_01121 | 4.2e-56 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
DJHDMHJE_01122 | 6.6e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
DJHDMHJE_01123 | 8.4e-34 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
DJHDMHJE_01124 | 1e-119 | 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 | |
DJHDMHJE_01125 | 2.6e-236 | 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 | ||
DJHDMHJE_01126 | 1.5e-71 | rplO | J | Binds to the 23S rRNA | ||
DJHDMHJE_01127 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
DJHDMHJE_01128 | 1.8e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
DJHDMHJE_01129 | 2.2e-55 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
DJHDMHJE_01130 | 3.3e-92 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
DJHDMHJE_01131 | 7.2e-68 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
DJHDMHJE_01132 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
DJHDMHJE_01133 | 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 | ||
DJHDMHJE_01134 | 4.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
DJHDMHJE_01135 | 8.7e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
DJHDMHJE_01136 | 1.5e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
DJHDMHJE_01137 | 2.2e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
DJHDMHJE_01138 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
DJHDMHJE_01139 | 2e-110 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
DJHDMHJE_01140 | 4e-54 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
DJHDMHJE_01141 | 4.2e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
DJHDMHJE_01142 | 1.2e-154 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
DJHDMHJE_01143 | 4.1e-47 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
DJHDMHJE_01144 | 2.3e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
DJHDMHJE_01145 | 6.9e-113 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
DJHDMHJE_01146 | 4.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
DJHDMHJE_01147 | 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 | ||
DJHDMHJE_01148 | 6e-82 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
DJHDMHJE_01149 | 7.8e-70 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
DJHDMHJE_01150 | 3.9e-122 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
DJHDMHJE_01151 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
DJHDMHJE_01152 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
DJHDMHJE_01153 | 3e-198 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
DJHDMHJE_01154 | 2.5e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
DJHDMHJE_01155 | 7.3e-80 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
DJHDMHJE_01156 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
DJHDMHJE_01157 | 7e-33 | |||||
DJHDMHJE_01158 | 1.6e-80 | cpdA | S | Calcineurin-like phosphoesterase | ||
DJHDMHJE_01159 | 2.6e-87 | cpdA | S | Calcineurin-like phosphoesterase | ||
DJHDMHJE_01160 | 6.5e-11 | cpdA | S | Calcineurin-like phosphoesterase | ||
DJHDMHJE_01161 | 8.7e-220 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
DJHDMHJE_01162 | 2.7e-70 | 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 | ||
DJHDMHJE_01163 | 1.7e-107 | ypsA | S | Belongs to the UPF0398 family | ||
DJHDMHJE_01164 | 1.2e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
DJHDMHJE_01165 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
DJHDMHJE_01166 | 1.9e-112 | 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 | |
DJHDMHJE_01167 | 7.4e-115 | dnaD | L | DnaD domain protein | ||
DJHDMHJE_01168 | 1.2e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
DJHDMHJE_01169 | 2.9e-90 | ypmB | S | Protein conserved in bacteria | ||
DJHDMHJE_01170 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
DJHDMHJE_01171 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
DJHDMHJE_01172 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
DJHDMHJE_01173 | 9.6e-169 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
DJHDMHJE_01174 | 7.5e-180 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
DJHDMHJE_01175 | 4.2e-203 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
DJHDMHJE_01176 | 6.7e-187 | 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) | |
DJHDMHJE_01177 | 1.7e-262 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
DJHDMHJE_01178 | 4.1e-181 | |||||
DJHDMHJE_01179 | 7.8e-140 | |||||
DJHDMHJE_01180 | 2.8e-105 | lepB | 3.4.21.89 | U | Peptidase S24-like | |
DJHDMHJE_01181 | 1.1e-130 | L | Transposase | |||
DJHDMHJE_01182 | 3.5e-71 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
DJHDMHJE_01183 | 9.9e-250 | yfnA | E | Amino Acid | ||
DJHDMHJE_01184 | 3.3e-43 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
DJHDMHJE_01185 | 9.9e-78 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
DJHDMHJE_01186 | 1.1e-14 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
DJHDMHJE_01187 | 9.6e-46 | yxeH | S | hydrolase | ||
DJHDMHJE_01188 | 1.9e-84 | yxeH | S | hydrolase | ||
DJHDMHJE_01189 | 2.4e-158 | S | reductase | |||
DJHDMHJE_01190 | 6e-219 | 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 | |
DJHDMHJE_01202 | 4.8e-221 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
DJHDMHJE_01203 | 6.4e-201 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
DJHDMHJE_01204 | 3.7e-177 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
DJHDMHJE_01205 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
DJHDMHJE_01206 | 2.3e-29 | secG | U | Preprotein translocase | ||
DJHDMHJE_01207 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
DJHDMHJE_01208 | 5.1e-78 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
DJHDMHJE_01209 | 8.1e-60 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_01210 | 6.1e-219 | naiP | EGP | Major facilitator Superfamily | ||
DJHDMHJE_01211 | 3.1e-275 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
DJHDMHJE_01212 | 1.2e-67 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
DJHDMHJE_01213 | 1.8e-76 | oppA | E | ABC transporter | ||
DJHDMHJE_01214 | 1e-46 | oppA | E | ABC transporter | ||
DJHDMHJE_01215 | 3.5e-43 | oppA | E | ABC transporter | ||
DJHDMHJE_01216 | 4.3e-63 | oppA | E | ABC transporter | ||
DJHDMHJE_01217 | 1.7e-96 | Q | Imidazolonepropionase and related amidohydrolases | |||
DJHDMHJE_01218 | 1.5e-74 | Q | Imidazolonepropionase and related amidohydrolases | |||
DJHDMHJE_01219 | 3.7e-18 | psiE | S | Phosphate-starvation-inducible E | ||
DJHDMHJE_01221 | 1.9e-222 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
DJHDMHJE_01222 | 6.7e-289 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
DJHDMHJE_01223 | 7e-197 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
DJHDMHJE_01224 | 9.2e-78 | S | SLAP domain | |||
DJHDMHJE_01225 | 2.2e-113 | S | SLAP domain | |||
DJHDMHJE_01226 | 3.6e-25 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_01227 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
DJHDMHJE_01228 | 1.4e-211 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
DJHDMHJE_01229 | 5.5e-247 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
DJHDMHJE_01230 | 3.2e-183 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
DJHDMHJE_01231 | 4.2e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
DJHDMHJE_01232 | 3.7e-168 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
DJHDMHJE_01233 | 5.4e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
DJHDMHJE_01234 | 1e-113 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
DJHDMHJE_01235 | 2.3e-33 | S | RelB antitoxin | |||
DJHDMHJE_01236 | 4.9e-58 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
DJHDMHJE_01237 | 1.4e-26 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
DJHDMHJE_01238 | 1.2e-112 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
DJHDMHJE_01239 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
DJHDMHJE_01240 | 4.3e-16 | 1.1.1.1 | C | Zinc-binding dehydrogenase | ||
DJHDMHJE_01241 | 4.4e-233 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
DJHDMHJE_01242 | 1.5e-108 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_01243 | 3.4e-41 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01244 | 6.9e-71 | S | Enterocin A Immunity | |||
DJHDMHJE_01245 | 4.1e-115 | S | Archaea bacterial proteins of unknown function | |||
DJHDMHJE_01246 | 4.2e-146 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
DJHDMHJE_01247 | 3.2e-305 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
DJHDMHJE_01248 | 1.4e-209 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
DJHDMHJE_01249 | 5.1e-122 | K | response regulator | |||
DJHDMHJE_01250 | 0.0 | V | ABC transporter | |||
DJHDMHJE_01251 | 1.7e-307 | V | ABC transporter, ATP-binding protein | |||
DJHDMHJE_01252 | 8.9e-139 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
DJHDMHJE_01253 | 1.6e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
DJHDMHJE_01254 | 2.1e-44 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
DJHDMHJE_01255 | 2.9e-154 | spo0J | K | Belongs to the ParB family | ||
DJHDMHJE_01256 | 3.4e-138 | soj | D | Sporulation initiation inhibitor | ||
DJHDMHJE_01257 | 1.6e-149 | noc | K | Belongs to the ParB family | ||
DJHDMHJE_01258 | 1.4e-130 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
DJHDMHJE_01259 | 6.6e-85 | cvpA | S | Colicin V production protein | ||
DJHDMHJE_01260 | 1.7e-181 | 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 | |
DJHDMHJE_01261 | 6.7e-150 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
DJHDMHJE_01262 | 2e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
DJHDMHJE_01263 | 5.3e-98 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
DJHDMHJE_01264 | 9.1e-36 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_01265 | 5.4e-51 | G | Major Facilitator Superfamily | |||
DJHDMHJE_01266 | 1.6e-141 | G | Major Facilitator Superfamily | |||
DJHDMHJE_01267 | 2e-61 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_01268 | 7.5e-146 | yvpB | S | Peptidase_C39 like family | ||
DJHDMHJE_01269 | 1.5e-83 | S | Threonine/Serine exporter, ThrE | |||
DJHDMHJE_01270 | 6.1e-140 | thrE | S | Putative threonine/serine exporter | ||
DJHDMHJE_01271 | 1.1e-292 | S | ABC transporter | |||
DJHDMHJE_01272 | 1e-55 | |||||
DJHDMHJE_01273 | 1.2e-85 | rimL | J | Acetyltransferase (GNAT) domain | ||
DJHDMHJE_01274 | 4e-52 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_01275 | 2e-56 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_01276 | 3.9e-46 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_01278 | 3.7e-08 | |||||
DJHDMHJE_01280 | 1.1e-88 | V | Type II restriction enzyme, methylase subunits | |||
DJHDMHJE_01281 | 7.9e-78 | V | Type II restriction enzyme, methylase subunits | |||
DJHDMHJE_01282 | 9.9e-97 | L | Transposase | |||
DJHDMHJE_01283 | 3e-139 | |||||
DJHDMHJE_01284 | 2.4e-289 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
DJHDMHJE_01285 | 8.2e-168 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
DJHDMHJE_01286 | 2.6e-43 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
DJHDMHJE_01287 | 3.3e-197 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
DJHDMHJE_01288 | 4e-155 | ydjP | I | Alpha/beta hydrolase family | ||
DJHDMHJE_01289 | 3.6e-274 | P | Sodium:sulfate symporter transmembrane region | |||
DJHDMHJE_01290 | 4.9e-96 | L | Transposase | |||
DJHDMHJE_01291 | 3.1e-49 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
DJHDMHJE_01292 | 1.2e-120 | |||||
DJHDMHJE_01293 | 5.8e-143 | S | Belongs to the UPF0246 family | |||
DJHDMHJE_01294 | 1.5e-143 | aroD | S | Alpha/beta hydrolase family | ||
DJHDMHJE_01295 | 9.3e-112 | G | phosphoglycerate mutase | |||
DJHDMHJE_01296 | 4.1e-95 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
DJHDMHJE_01297 | 5.6e-168 | hrtB | V | ABC transporter permease | ||
DJHDMHJE_01298 | 8.8e-119 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
DJHDMHJE_01299 | 2.2e-276 | pipD | E | Dipeptidase | ||
DJHDMHJE_01300 | 9.9e-49 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_01301 | 9.6e-42 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_01302 | 5.5e-97 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
DJHDMHJE_01303 | 4e-248 | yjjP | S | Putative threonine/serine exporter | ||
DJHDMHJE_01304 | 2.4e-178 | citR | K | Putative sugar-binding domain | ||
DJHDMHJE_01305 | 1.6e-52 | |||||
DJHDMHJE_01306 | 1.6e-16 | |||||
DJHDMHJE_01307 | 6.4e-66 | S | Domain of unknown function DUF1828 | |||
DJHDMHJE_01308 | 5.6e-95 | S | UPF0397 protein | |||
DJHDMHJE_01309 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01310 | 4.3e-147 | cbiQ | P | cobalt transport | ||
DJHDMHJE_01311 | 2.7e-10 | |||||
DJHDMHJE_01312 | 2.7e-71 | yeaL | S | Protein of unknown function (DUF441) | ||
DJHDMHJE_01313 | 4.7e-41 | K | Psort location Cytoplasmic, score | |||
DJHDMHJE_01314 | 1.8e-35 | K | response regulator | |||
DJHDMHJE_01315 | 6.1e-63 | sptS | 2.7.13.3 | T | Histidine kinase | |
DJHDMHJE_01316 | 7.1e-117 | sptS | 2.7.13.3 | T | Histidine kinase | |
DJHDMHJE_01317 | 5.5e-209 | EGP | Major facilitator Superfamily | |||
DJHDMHJE_01318 | 3.7e-72 | O | OsmC-like protein | |||
DJHDMHJE_01319 | 4.9e-128 | dkgA | 1.1.1.346 | S | L-ascorbic acid biosynthetic process | |
DJHDMHJE_01320 | 1.4e-26 | L | Transposase | |||
DJHDMHJE_01322 | 3.9e-246 | yifK | E | Amino acid permease | ||
DJHDMHJE_01323 | 1.1e-221 | cycA | E | Amino acid permease | ||
DJHDMHJE_01324 | 2.4e-128 | |||||
DJHDMHJE_01325 | 4.9e-119 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
DJHDMHJE_01326 | 0.0 | clpE | O | AAA domain (Cdc48 subfamily) | ||
DJHDMHJE_01327 | 7.2e-172 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
DJHDMHJE_01328 | 3e-213 | 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 | ||
DJHDMHJE_01329 | 5.4e-124 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01330 | 1.3e-113 | XK27_06780 | V | ABC transporter permease | ||
DJHDMHJE_01331 | 1.1e-228 | XK27_06780 | V | ABC transporter permease | ||
DJHDMHJE_01332 | 1.9e-36 | |||||
DJHDMHJE_01333 | 3.3e-289 | ytgP | S | Polysaccharide biosynthesis protein | ||
DJHDMHJE_01334 | 8e-146 | lysA2 | M | Glycosyl hydrolases family 25 | ||
DJHDMHJE_01335 | 2.2e-125 | S | Protein of unknown function (DUF975) | |||
DJHDMHJE_01336 | 1.9e-50 | |||||
DJHDMHJE_01337 | 4.9e-29 | |||||
DJHDMHJE_01338 | 1.1e-127 | S | CAAX protease self-immunity | |||
DJHDMHJE_01339 | 5.9e-10 | |||||
DJHDMHJE_01341 | 3.2e-175 | pbpX2 | V | Beta-lactamase | ||
DJHDMHJE_01342 | 3.5e-249 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
DJHDMHJE_01343 | 5.7e-36 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
DJHDMHJE_01344 | 3e-242 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
DJHDMHJE_01345 | 2.5e-294 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
DJHDMHJE_01346 | 2.4e-19 | S | D-Ala-teichoic acid biosynthesis protein | |||
DJHDMHJE_01347 | 2.2e-50 | |||||
DJHDMHJE_01348 | 2.6e-216 | ywhK | S | Membrane | ||
DJHDMHJE_01349 | 5.6e-25 | ykuL | S | IMP dehydrogenase activity | ||
DJHDMHJE_01350 | 1.9e-144 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01351 | 1.1e-27 | |||||
DJHDMHJE_01352 | 3.3e-289 | V | ABC transporter transmembrane region | |||
DJHDMHJE_01353 | 9.8e-118 | KLT | serine threonine protein kinase | |||
DJHDMHJE_01354 | 1.4e-75 | K | Helix-turn-helix XRE-family like proteins | |||
DJHDMHJE_01355 | 2.2e-46 | K | Helix-turn-helix XRE-family like proteins | |||
DJHDMHJE_01356 | 1.6e-22 | |||||
DJHDMHJE_01357 | 1.9e-83 | |||||
DJHDMHJE_01359 | 2.2e-71 | S | Protein of unknown function (DUF3232) | |||
DJHDMHJE_01360 | 1.2e-271 | S | SLAP domain | |||
DJHDMHJE_01361 | 9.9e-132 | K | Helix-turn-helix XRE-family like proteins | |||
DJHDMHJE_01362 | 1.1e-89 | |||||
DJHDMHJE_01363 | 3.8e-20 | |||||
DJHDMHJE_01364 | 1.1e-65 | |||||
DJHDMHJE_01365 | 2e-14 | K | Helix-turn-helix XRE-family like proteins | |||
DJHDMHJE_01366 | 4.9e-128 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
DJHDMHJE_01367 | 3.7e-141 | K | Helix-turn-helix domain | |||
DJHDMHJE_01368 | 1.7e-229 | 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 | |
DJHDMHJE_01369 | 4.2e-217 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
DJHDMHJE_01370 | 1e-280 | 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 | ||
DJHDMHJE_01371 | 1.8e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
DJHDMHJE_01372 | 2.7e-82 | yueI | S | Protein of unknown function (DUF1694) | ||
DJHDMHJE_01373 | 7.2e-242 | rarA | L | recombination factor protein RarA | ||
DJHDMHJE_01374 | 2.5e-35 | |||||
DJHDMHJE_01375 | 3.1e-78 | usp6 | T | universal stress protein | ||
DJHDMHJE_01376 | 1.5e-217 | rodA | D | Belongs to the SEDS family | ||
DJHDMHJE_01377 | 8.6e-34 | S | Protein of unknown function (DUF2969) | |||
DJHDMHJE_01378 | 3.8e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
DJHDMHJE_01379 | 6.5e-179 | mbl | D | Cell shape determining protein MreB Mrl | ||
DJHDMHJE_01380 | 3.4e-30 | ywzB | S | Protein of unknown function (DUF1146) | ||
DJHDMHJE_01381 | 7.7e-55 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
DJHDMHJE_01382 | 2.4e-238 | 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 | |
DJHDMHJE_01383 | 8.9e-173 | 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 | ||
DJHDMHJE_01384 | 2.2e-282 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
DJHDMHJE_01385 | 5.2e-93 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
DJHDMHJE_01386 | 9.5e-49 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
DJHDMHJE_01387 | 8.6e-29 | 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 | ||
DJHDMHJE_01388 | 7.6e-129 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
DJHDMHJE_01389 | 3e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
DJHDMHJE_01390 | 1.1e-189 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
DJHDMHJE_01391 | 2.3e-156 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
DJHDMHJE_01392 | 5.3e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
DJHDMHJE_01393 | 7.6e-114 | tdk | 2.7.1.21 | F | thymidine kinase | |
DJHDMHJE_01394 | 3.1e-248 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
DJHDMHJE_01397 | 4.6e-196 | ampC | V | Beta-lactamase | ||
DJHDMHJE_01398 | 4.5e-54 | |||||
DJHDMHJE_01399 | 5.6e-103 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
DJHDMHJE_01400 | 1.2e-255 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
DJHDMHJE_01401 | 1.1e-291 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
DJHDMHJE_01402 | 2.9e-276 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
DJHDMHJE_01403 | 7.9e-76 | 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) | ||
DJHDMHJE_01404 | 7.8e-140 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
DJHDMHJE_01405 | 1.4e-93 | sigH | K | Belongs to the sigma-70 factor family | ||
DJHDMHJE_01406 | 2.2e-34 | |||||
DJHDMHJE_01407 | 3.3e-283 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
DJHDMHJE_01408 | 6.4e-88 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
DJHDMHJE_01409 | 7.5e-112 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
DJHDMHJE_01410 | 2.4e-98 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
DJHDMHJE_01411 | 5.9e-24 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
DJHDMHJE_01412 | 1.4e-101 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
DJHDMHJE_01413 | 2e-68 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
DJHDMHJE_01414 | 3.2e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
DJHDMHJE_01415 | 7.6e-49 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
DJHDMHJE_01416 | 3.2e-172 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
DJHDMHJE_01417 | 1.7e-69 | yqhL | P | Rhodanese-like protein | ||
DJHDMHJE_01418 | 5.6e-33 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
DJHDMHJE_01419 | 1.1e-116 | gluP | 3.4.21.105 | S | Rhomboid family | |
DJHDMHJE_01420 | 1.7e-99 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
DJHDMHJE_01421 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
DJHDMHJE_01422 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
DJHDMHJE_01423 | 0.0 | S | membrane | |||
DJHDMHJE_01424 | 1e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
DJHDMHJE_01425 | 3.5e-160 | degV | S | EDD domain protein, DegV family | ||
DJHDMHJE_01426 | 7.7e-65 | |||||
DJHDMHJE_01427 | 3.7e-69 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_01428 | 1.6e-27 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
DJHDMHJE_01429 | 2.4e-29 | Q | DSBA-like thioredoxin domain | |||
DJHDMHJE_01430 | 1.2e-18 | frnE | Q | DSBA-like thioredoxin domain | ||
DJHDMHJE_01431 | 1.7e-10 | frnE | Q | DSBA-like thioredoxin domain | ||
DJHDMHJE_01432 | 4.1e-175 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
DJHDMHJE_01433 | 1.6e-117 | M1-798 | K | Rhodanese Homology Domain | ||
DJHDMHJE_01434 | 1.4e-57 | CO | Thioredoxin | |||
DJHDMHJE_01435 | 2.7e-19 | atl | 3.2.1.96, 3.5.1.28 | GH73 | UW | LPXTG-motif cell wall anchor domain protein |
DJHDMHJE_01436 | 9.6e-35 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
DJHDMHJE_01437 | 6.8e-18 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
DJHDMHJE_01438 | 2.5e-35 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
DJHDMHJE_01439 | 6.5e-65 | O | Belongs to the peptidase S8 family | |||
DJHDMHJE_01440 | 1.3e-93 | O | Belongs to the peptidase S8 family | |||
DJHDMHJE_01441 | 5.5e-21 | ynbB | 4.4.1.1 | P | aluminum resistance | |
DJHDMHJE_01442 | 5.3e-64 | ynbB | 4.4.1.1 | P | aluminum resistance | |
DJHDMHJE_01443 | 1.4e-264 | glnA | 6.3.1.2 | E | glutamine synthetase | |
DJHDMHJE_01444 | 5.5e-135 | |||||
DJHDMHJE_01445 | 1.1e-164 | |||||
DJHDMHJE_01446 | 2.9e-150 | |||||
DJHDMHJE_01447 | 3.2e-10 | S | cog cog1373 | |||
DJHDMHJE_01448 | 4e-133 | K | helix_turn_helix, mercury resistance | |||
DJHDMHJE_01449 | 1.2e-231 | pbuG | S | permease | ||
DJHDMHJE_01450 | 1.2e-76 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_01451 | 3e-26 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
DJHDMHJE_01452 | 5.3e-141 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
DJHDMHJE_01453 | 5.1e-60 | |||||
DJHDMHJE_01454 | 6e-16 | lhr | L | DEAD DEAH box helicase | ||
DJHDMHJE_01455 | 3.9e-145 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01456 | 4.6e-54 | trxA | O | Belongs to the thioredoxin family | ||
DJHDMHJE_01457 | 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 | ||
DJHDMHJE_01458 | 6.2e-51 | yrzB | S | Belongs to the UPF0473 family | ||
DJHDMHJE_01459 | 3.6e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
DJHDMHJE_01460 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
DJHDMHJE_01461 | 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 | |
DJHDMHJE_01462 | 1.3e-230 | 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 | |
DJHDMHJE_01463 | 1.6e-182 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
DJHDMHJE_01464 | 7.1e-214 | 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 | |
DJHDMHJE_01465 | 3.9e-289 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
DJHDMHJE_01466 | 7.5e-39 | yajC | U | Preprotein translocase | ||
DJHDMHJE_01467 | 2.3e-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 | |
DJHDMHJE_01468 | 7e-104 | 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 | |
DJHDMHJE_01469 | 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 | ||
DJHDMHJE_01470 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
DJHDMHJE_01471 | 2.9e-293 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
DJHDMHJE_01472 | 3.9e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
DJHDMHJE_01473 | 8.6e-116 | sip | L | Belongs to the 'phage' integrase family | ||
DJHDMHJE_01474 | 2.8e-271 | yclK | 2.7.13.3 | T | Histidine kinase | |
DJHDMHJE_01475 | 8.3e-131 | K | Transcriptional regulatory protein, C terminal | |||
DJHDMHJE_01476 | 8.3e-61 | S | SdpI/YhfL protein family | |||
DJHDMHJE_01477 | 1.7e-168 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
DJHDMHJE_01478 | 5e-72 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
DJHDMHJE_01479 | 9.5e-129 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
DJHDMHJE_01480 | 2.1e-32 | M | Protein of unknown function (DUF3737) | |||
DJHDMHJE_01481 | 2.7e-34 | M | Protein of unknown function (DUF3737) | |||
DJHDMHJE_01483 | 3e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
DJHDMHJE_01484 | 3e-187 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
DJHDMHJE_01485 | 8.9e-84 | comGF | U | Putative Competence protein ComGF | ||
DJHDMHJE_01486 | 2.3e-41 | |||||
DJHDMHJE_01487 | 2.1e-73 | |||||
DJHDMHJE_01488 | 4.3e-244 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
DJHDMHJE_01489 | 0.0 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
DJHDMHJE_01490 | 4.9e-201 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
DJHDMHJE_01491 | 2.4e-275 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
DJHDMHJE_01492 | 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 | |
DJHDMHJE_01493 | 8.8e-127 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
DJHDMHJE_01494 | 1.3e-38 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
DJHDMHJE_01495 | 1.1e-132 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
DJHDMHJE_01496 | 3.9e-220 | 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) | |
DJHDMHJE_01497 | 1.3e-84 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
DJHDMHJE_01498 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
DJHDMHJE_01499 | 6.3e-134 | 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 | |
DJHDMHJE_01500 | 1.4e-193 | ydiM | G | Major Facilitator Superfamily | ||
DJHDMHJE_01501 | 1.5e-21 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
DJHDMHJE_01502 | 1.2e-115 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
DJHDMHJE_01504 | 5.1e-97 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
DJHDMHJE_01505 | 3.3e-101 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
DJHDMHJE_01506 | 7.5e-108 | pncA | Q | Isochorismatase family | ||
DJHDMHJE_01507 | 1.2e-271 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
DJHDMHJE_01508 | 3.3e-133 | mdlA | V | ABC transporter | ||
DJHDMHJE_01509 | 1.3e-158 | KLT | Protein kinase domain | |||
DJHDMHJE_01510 | 3.7e-42 | KLT | serine threonine protein kinase | |||
DJHDMHJE_01511 | 1.9e-175 | V | ABC transporter transmembrane region | |||
DJHDMHJE_01512 | 4.2e-135 | pts23C | 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 | ||
DJHDMHJE_01513 | 1.1e-280 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
DJHDMHJE_01514 | 7.7e-80 | ypbG | 2.7.1.2 | GK | ROK family | |
DJHDMHJE_01515 | 7.7e-11 | ypbG | 2.7.1.2 | GK | ROK family | |
DJHDMHJE_01516 | 1.2e-85 | C | nitroreductase | |||
DJHDMHJE_01517 | 7.5e-69 | S | Domain of unknown function (DUF4767) | |||
DJHDMHJE_01518 | 4.7e-246 | 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 | |
DJHDMHJE_01519 | 1.1e-92 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
DJHDMHJE_01520 | 5.9e-29 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
DJHDMHJE_01521 | 2.1e-55 | K | Helix-turn-helix domain | |||
DJHDMHJE_01522 | 1.2e-108 | 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 | |
DJHDMHJE_01523 | 1.1e-164 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
DJHDMHJE_01524 | 2.4e-170 | K | Transcriptional regulator | |||
DJHDMHJE_01525 | 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 | |
DJHDMHJE_01526 | 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 | |
DJHDMHJE_01527 | 1.3e-105 | 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 | |
DJHDMHJE_01528 | 7.9e-167 | snf | 2.7.11.1 | KL | domain protein | |
DJHDMHJE_01529 | 1.2e-85 | dps | P | Belongs to the Dps family | ||
DJHDMHJE_01530 | 2e-94 | K | acetyltransferase | |||
DJHDMHJE_01531 | 8.4e-153 | K | COG COG0846 NAD-dependent protein deacetylases, SIR2 family | |||
DJHDMHJE_01532 | 5.2e-98 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
DJHDMHJE_01533 | 4.3e-109 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
DJHDMHJE_01534 | 6.6e-84 | K | Bacterial regulatory proteins, tetR family | |||
DJHDMHJE_01535 | 3.2e-47 | 1.1.1.3 | T | phosphoserine phosphatase activity | ||
DJHDMHJE_01536 | 9.9e-143 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
DJHDMHJE_01537 | 2.1e-39 | S | Hydrolases of the alpha beta superfamily | |||
DJHDMHJE_01538 | 1.4e-57 | S | Alpha beta hydrolase | |||
DJHDMHJE_01539 | 1.2e-36 | K | Acetyltransferase (GNAT) family | |||
DJHDMHJE_01540 | 6.2e-48 | K | Acetyltransferase (GNAT) family | |||
DJHDMHJE_01541 | 2.8e-38 | |||||
DJHDMHJE_01542 | 5.7e-112 | K | WHG domain | |||
DJHDMHJE_01543 | 4.9e-116 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_01544 | 2.7e-21 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
DJHDMHJE_01545 | 1.6e-48 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
DJHDMHJE_01546 | 3.9e-29 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
DJHDMHJE_01547 | 5.4e-68 | |||||
DJHDMHJE_01548 | 7.1e-32 | |||||
DJHDMHJE_01549 | 1.4e-71 | S | Iron-sulphur cluster biosynthesis | |||
DJHDMHJE_01550 | 5.3e-175 | KLT | Protein kinase domain | |||
DJHDMHJE_01551 | 1.4e-21 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01552 | 1.9e-115 | L | Transposase | |||
DJHDMHJE_01553 | 1.1e-39 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01555 | 1.3e-128 | XK27_08435 | K | UTRA | ||
DJHDMHJE_01556 | 2.8e-229 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
DJHDMHJE_01557 | 9.4e-26 | L | Transposase | |||
DJHDMHJE_01558 | 8.4e-08 | |||||
DJHDMHJE_01560 | 1.2e-13 | O | Preprotein translocase subunit SecB | |||
DJHDMHJE_01561 | 1.5e-20 | |||||
DJHDMHJE_01562 | 1.1e-21 | hicB | S | protein encoded in hypervariable junctions of pilus gene clusters | ||
DJHDMHJE_01563 | 0.0 | sacX | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
DJHDMHJE_01564 | 1e-138 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
DJHDMHJE_01565 | 8.9e-166 | yleB | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | |
DJHDMHJE_01566 | 5.5e-126 | K | Helix-turn-helix domain, rpiR family | |||
DJHDMHJE_01567 | 4.1e-26 | L | Transposase | |||
DJHDMHJE_01571 | 3.2e-118 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |||
DJHDMHJE_01572 | 1.8e-287 | V | ABC transporter transmembrane region | |||
DJHDMHJE_01574 | 5.9e-41 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01575 | 1.1e-59 | S | SLAP domain | |||
DJHDMHJE_01576 | 2.5e-109 | S | SLAP domain | |||
DJHDMHJE_01577 | 4.7e-165 | yvgN | C | Aldo keto reductase | ||
DJHDMHJE_01578 | 2.8e-68 | tetP | J | elongation factor G | ||
DJHDMHJE_01579 | 4.4e-288 | tetP | J | elongation factor G | ||
DJHDMHJE_01580 | 2.6e-77 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | haloacid dehalogenase-like hydrolase | ||
DJHDMHJE_01581 | 6.4e-63 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | haloacid dehalogenase-like hydrolase | ||
DJHDMHJE_01582 | 6.9e-192 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
DJHDMHJE_01583 | 6.4e-107 | yniA | G | Phosphotransferase enzyme family | ||
DJHDMHJE_01584 | 1.8e-43 | yniA | G | Phosphotransferase enzyme family | ||
DJHDMHJE_01585 | 3.3e-160 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
DJHDMHJE_01586 | 1.6e-44 | E | amino acid | |||
DJHDMHJE_01587 | 2.9e-88 | E | amino acid | |||
DJHDMHJE_01588 | 0.0 | L | Helicase C-terminal domain protein | |||
DJHDMHJE_01589 | 1.6e-196 | pbpX1 | V | Beta-lactamase | ||
DJHDMHJE_01590 | 7.9e-70 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
DJHDMHJE_01591 | 4e-98 | L | Transposase | |||
DJHDMHJE_01592 | 1.7e-19 | S | Toxin ToxN, type III toxin-antitoxin system | |||
DJHDMHJE_01593 | 1.7e-234 | yfdE | 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
DJHDMHJE_01594 | 1.9e-80 | frc | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
DJHDMHJE_01595 | 1.1e-74 | frc | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
DJHDMHJE_01596 | 1.1e-26 | frc | 2.8.3.16 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
DJHDMHJE_01597 | 1.1e-37 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
DJHDMHJE_01598 | 5.7e-215 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
DJHDMHJE_01599 | 1.1e-12 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
DJHDMHJE_01600 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01601 | 5.7e-116 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
DJHDMHJE_01602 | 7.9e-79 | XK27_02470 | K | LytTr DNA-binding domain | ||
DJHDMHJE_01603 | 3.6e-121 | liaI | S | membrane | ||
DJHDMHJE_01604 | 1.1e-93 | scrR | K | Transcriptional regulator, LacI family | ||
DJHDMHJE_01605 | 1.4e-15 | scrR | K | Transcriptional regulator, LacI family | ||
DJHDMHJE_01606 | 1.2e-103 | 2.7.1.199, 2.7.1.211 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
DJHDMHJE_01607 | 1.4e-49 | |||||
DJHDMHJE_01608 | 6.4e-26 | |||||
DJHDMHJE_01609 | 1.6e-91 | |||||
DJHDMHJE_01610 | 2.7e-140 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01611 | 3e-37 | |||||
DJHDMHJE_01612 | 6.4e-58 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
DJHDMHJE_01613 | 1.4e-89 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
DJHDMHJE_01614 | 1.8e-56 | |||||
DJHDMHJE_01615 | 3.3e-245 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
DJHDMHJE_01616 | 1.5e-109 | K | Transcriptional regulator, LysR family | |||
DJHDMHJE_01617 | 1.3e-34 | S | Cytochrome b5 | |||
DJHDMHJE_01618 | 1.7e-167 | arbZ | I | Phosphate acyltransferases | ||
DJHDMHJE_01619 | 4.5e-151 | arbY | M | Glycosyl transferase family 8 | ||
DJHDMHJE_01620 | 3.7e-10 | arbY | M | Glycosyl transferase family 8 | ||
DJHDMHJE_01621 | 1.8e-186 | arbY | M | Glycosyl transferase family 8 | ||
DJHDMHJE_01622 | 4.1e-158 | arbx | M | Glycosyl transferase family 8 | ||
DJHDMHJE_01623 | 4e-13 | K | Helix-turn-helix domain | |||
DJHDMHJE_01624 | 4.7e-120 | K | Helix-turn-helix domain | |||
DJHDMHJE_01626 | 1.9e-71 | S | CAAX protease self-immunity | |||
DJHDMHJE_01627 | 2.8e-159 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
DJHDMHJE_01628 | 2e-164 | dnaQ | 2.7.7.7 | L | EXOIII | |
DJHDMHJE_01629 | 8.5e-159 | endA | F | DNA RNA non-specific endonuclease | ||
DJHDMHJE_01630 | 1.1e-280 | pipD | E | Dipeptidase | ||
DJHDMHJE_01631 | 1.9e-203 | malK | P | ATPases associated with a variety of cellular activities | ||
DJHDMHJE_01632 | 8e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
DJHDMHJE_01633 | 2.3e-145 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
DJHDMHJE_01634 | 7.3e-255 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
DJHDMHJE_01635 | 6.3e-238 | G | Bacterial extracellular solute-binding protein | |||
DJHDMHJE_01636 | 7.4e-161 | corA | P | CorA-like Mg2+ transporter protein | ||
DJHDMHJE_01637 | 4.7e-158 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
DJHDMHJE_01638 | 6.6e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
DJHDMHJE_01639 | 0.0 | ydgH | S | MMPL family | ||
DJHDMHJE_01640 | 1.4e-155 | |||||
DJHDMHJE_01641 | 1.2e-263 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
DJHDMHJE_01642 | 1.3e-126 | hipB | K | Helix-turn-helix | ||
DJHDMHJE_01643 | 2.6e-154 | I | alpha/beta hydrolase fold | |||
DJHDMHJE_01644 | 2.3e-110 | yjbF | S | SNARE associated Golgi protein | ||
DJHDMHJE_01645 | 2.9e-99 | J | Acetyltransferase (GNAT) domain | |||
DJHDMHJE_01646 | 7.6e-252 | 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) | |
DJHDMHJE_01648 | 1.5e-19 | pfoS | S | Phosphotransferase system, EIIC | ||
DJHDMHJE_01649 | 2.2e-76 | pfoS | S | Phosphotransferase system, EIIC | ||
DJHDMHJE_01650 | 9.5e-11 | pfoS | S | Phosphotransferase system, EIIC | ||
DJHDMHJE_01651 | 1.1e-133 | slpX | S | SLAP domain | ||
DJHDMHJE_01654 | 4.1e-214 | |||||
DJHDMHJE_01655 | 3e-122 | gntR1 | K | UTRA | ||
DJHDMHJE_01656 | 4.5e-35 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_01657 | 2.9e-40 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01658 | 1.9e-33 | 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 | ||
DJHDMHJE_01659 | 2.6e-78 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
DJHDMHJE_01660 | 4.2e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
DJHDMHJE_01661 | 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 | |
DJHDMHJE_01662 | 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 | |
DJHDMHJE_01663 | 4e-209 | 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 | ||
DJHDMHJE_01664 | 3.7e-22 | yaaA | S | S4 domain protein YaaA | ||
DJHDMHJE_01665 | 3.9e-196 | 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 | |
DJHDMHJE_01666 | 5.3e-259 | 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 | ||
DJHDMHJE_01667 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
DJHDMHJE_01668 | 2.7e-61 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
DJHDMHJE_01669 | 6.4e-146 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
DJHDMHJE_01670 | 5.6e-253 | 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 | ||
DJHDMHJE_01671 | 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 | ||
DJHDMHJE_01672 | 2.2e-273 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
DJHDMHJE_01673 | 8.4e-290 | clcA | P | chloride | ||
DJHDMHJE_01674 | 3.5e-15 | |||||
DJHDMHJE_01675 | 1.4e-158 | |||||
DJHDMHJE_01676 | 1.2e-18 | |||||
DJHDMHJE_01677 | 3.4e-156 | EGP | Sugar (and other) transporter | |||
DJHDMHJE_01678 | 2.2e-36 | EGP | Sugar (and other) transporter | |||
DJHDMHJE_01679 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
DJHDMHJE_01680 | 1.4e-49 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
DJHDMHJE_01681 | 1.2e-64 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
DJHDMHJE_01682 | 2.1e-76 | atkY | K | Penicillinase repressor | ||
DJHDMHJE_01683 | 2.3e-35 | |||||
DJHDMHJE_01684 | 1.5e-223 | pbuG | S | permease | ||
DJHDMHJE_01685 | 9.1e-61 | pts23C | 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 | ||
DJHDMHJE_01686 | 5.5e-135 | gmuR | K | UTRA | ||
DJHDMHJE_01687 | 1.6e-121 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
DJHDMHJE_01688 | 7.9e-50 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_01689 | 1.4e-127 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
DJHDMHJE_01690 | 1.2e-18 | |||||
DJHDMHJE_01691 | 6.1e-40 | V | ABC transporter transmembrane region | |||
DJHDMHJE_01692 | 3.8e-94 | V | ABC transporter transmembrane region | |||
DJHDMHJE_01694 | 1.4e-190 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
DJHDMHJE_01695 | 3.6e-285 | xylG | 3.6.3.17 | S | ABC transporter | |
DJHDMHJE_01696 | 1e-199 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
DJHDMHJE_01697 | 4.7e-166 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
DJHDMHJE_01698 | 8.4e-143 | K | SIS domain | |||
DJHDMHJE_01699 | 2.9e-42 | |||||
DJHDMHJE_01700 | 4.2e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
DJHDMHJE_01701 | 9.9e-149 | glnH | ET | ABC transporter | ||
DJHDMHJE_01702 | 8.8e-81 | K | Transcriptional regulator, MarR family | |||
DJHDMHJE_01703 | 9.8e-287 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01704 | 0.0 | V | ABC transporter transmembrane region | |||
DJHDMHJE_01705 | 7.6e-103 | S | ABC-type cobalt transport system, permease component | |||
DJHDMHJE_01706 | 2.1e-111 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_01707 | 2e-213 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
DJHDMHJE_01708 | 0.0 | lacS | G | Transporter | ||
DJHDMHJE_01709 | 4e-57 | lacS | G | Transporter | ||
DJHDMHJE_01710 | 5.9e-70 | lacS | G | Transporter | ||
DJHDMHJE_01711 | 6.8e-48 | lacS | G | Transporter | ||
DJHDMHJE_01712 | 6e-24 | lacS | G | Transporter | ||
DJHDMHJE_01713 | 4.9e-190 | lacR | K | Transcriptional regulator | ||
DJHDMHJE_01714 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
DJHDMHJE_01715 | 9.7e-188 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
DJHDMHJE_01716 | 1.2e-191 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
DJHDMHJE_01717 | 3.7e-40 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01718 | 2.4e-83 | S | COG NOG38524 non supervised orthologous group | |||
DJHDMHJE_01719 | 1.8e-86 | L | Putative transposase DNA-binding domain | |||
DJHDMHJE_01720 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
DJHDMHJE_01721 | 3.2e-228 | yttB | EGP | Major facilitator Superfamily | ||
DJHDMHJE_01722 | 6.1e-232 | XK27_04775 | S | PAS domain | ||
DJHDMHJE_01723 | 2.7e-100 | S | Iron-sulfur cluster assembly protein | |||
DJHDMHJE_01724 | 4.3e-140 | 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 | |
DJHDMHJE_01725 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
DJHDMHJE_01728 | 9.5e-255 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
DJHDMHJE_01729 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
DJHDMHJE_01730 | 1.3e-273 | S | Calcineurin-like phosphoesterase | |||
DJHDMHJE_01731 | 8.7e-84 | |||||
DJHDMHJE_01732 | 2e-108 | tag | 3.2.2.20 | L | glycosylase | |
DJHDMHJE_01733 | 1.2e-149 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
DJHDMHJE_01734 | 9.1e-131 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
DJHDMHJE_01735 | 5.2e-139 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
DJHDMHJE_01736 | 9.9e-153 | phnD | P | Phosphonate ABC transporter | ||
DJHDMHJE_01737 | 8.5e-87 | uspA | T | universal stress protein | ||
DJHDMHJE_01738 | 1.9e-11 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
DJHDMHJE_01739 | 1.7e-128 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
DJHDMHJE_01740 | 4.9e-90 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
DJHDMHJE_01741 | 5.7e-80 | ntd | 2.4.2.6 | F | Nucleoside | |
DJHDMHJE_01742 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
DJHDMHJE_01743 | 5.7e-29 | |||||
DJHDMHJE_01744 | 1.9e-160 | I | alpha/beta hydrolase fold | |||
DJHDMHJE_01745 | 1.2e-130 | yibF | S | overlaps another CDS with the same product name | ||
DJHDMHJE_01746 | 9.7e-203 | yibE | S | overlaps another CDS with the same product name | ||
DJHDMHJE_01747 | 5.4e-93 | |||||
DJHDMHJE_01748 | 4.7e-207 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
DJHDMHJE_01749 | 1.6e-230 | S | Cysteine-rich secretory protein family | |||
DJHDMHJE_01750 | 1.8e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DJHDMHJE_01751 | 2.9e-263 | glnPH2 | P | ABC transporter permease | ||
DJHDMHJE_01752 | 1e-129 | |||||
DJHDMHJE_01753 | 6.6e-122 | luxT | K | Bacterial regulatory proteins, tetR family | ||
DJHDMHJE_01754 | 3.3e-183 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
DJHDMHJE_01755 | 2.5e-55 | |||||
DJHDMHJE_01756 | 6.6e-116 | GM | NmrA-like family | |||
DJHDMHJE_01757 | 2.5e-126 | S | Alpha/beta hydrolase family | |||
DJHDMHJE_01758 | 1.8e-158 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
DJHDMHJE_01759 | 1.1e-140 | ypuA | S | Protein of unknown function (DUF1002) | ||
DJHDMHJE_01760 | 5.6e-146 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
DJHDMHJE_01761 | 3.4e-177 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
DJHDMHJE_01762 | 1.2e-285 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
DJHDMHJE_01763 | 1e-84 | |||||
DJHDMHJE_01764 | 4.3e-132 | cobB | K | SIR2 family | ||
DJHDMHJE_01765 | 4.4e-94 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
DJHDMHJE_01766 | 3.5e-119 | terC | P | Integral membrane protein TerC family | ||
DJHDMHJE_01767 | 8.2e-63 | yeaO | S | Protein of unknown function, DUF488 | ||
DJHDMHJE_01768 | 2.8e-122 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
DJHDMHJE_01769 | 2.9e-293 | glnP | P | ABC transporter permease | ||
DJHDMHJE_01770 | 3.3e-138 | glnQ | E | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01771 | 2.4e-161 | L | HNH nucleases | |||
DJHDMHJE_01772 | 2.2e-122 | yfbR | S | HD containing hydrolase-like enzyme | ||
DJHDMHJE_01774 | 1.9e-216 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
DJHDMHJE_01776 | 3.5e-37 | yafQ | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | ||
DJHDMHJE_01777 | 8.6e-24 | relB | L | RelB antitoxin | ||
DJHDMHJE_01787 | 3.2e-73 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_01788 | 1.2e-32 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_01789 | 8.6e-41 | gcvR | T | Belongs to the UPF0237 family | ||
DJHDMHJE_01790 | 4.5e-247 | XK27_08635 | S | UPF0210 protein | ||
DJHDMHJE_01791 | 6.9e-237 | G | Bacterial extracellular solute-binding protein | |||
DJHDMHJE_01792 | 8.5e-40 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_01795 | 1.2e-304 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
DJHDMHJE_01797 | 5.7e-241 | I | Protein of unknown function (DUF2974) | |||
DJHDMHJE_01798 | 1.4e-122 | yhiD | S | MgtC family | ||
DJHDMHJE_01801 | 2.1e-241 | amtB | P | ammonium transporter | ||
DJHDMHJE_01802 | 5.3e-265 | lsa | S | ABC transporter | ||
DJHDMHJE_01803 | 1.1e-41 | S | MazG-like family | |||
DJHDMHJE_01804 | 2e-80 | S | AAA domain | |||
DJHDMHJE_01805 | 9.3e-64 | 5.4.2.11 | G | Phosphoglycerate mutase family | ||
DJHDMHJE_01806 | 7.9e-81 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
DJHDMHJE_01807 | 2.1e-119 | XK27_07525 | 3.6.1.55 | F | NUDIX domain | |
DJHDMHJE_01808 | 8.7e-131 | 2.4.2.3 | F | Phosphorylase superfamily | ||
DJHDMHJE_01809 | 1.6e-51 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
DJHDMHJE_01811 | 8e-79 | K | Acetyltransferase (GNAT) domain | |||
DJHDMHJE_01812 | 2.3e-51 | |||||
DJHDMHJE_01813 | 1.7e-14 | |||||
DJHDMHJE_01814 | 9.9e-163 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
DJHDMHJE_01815 | 4.9e-207 | L | Belongs to the 'phage' integrase family | |||
DJHDMHJE_01816 | 6.2e-29 | |||||
DJHDMHJE_01817 | 2.8e-45 | |||||
DJHDMHJE_01818 | 1.6e-67 | xkdA | E | Zn peptidase | ||
DJHDMHJE_01819 | 1e-46 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
DJHDMHJE_01820 | 2.9e-12 | |||||
DJHDMHJE_01821 | 1.3e-50 | |||||
DJHDMHJE_01824 | 1.7e-79 | S | Siphovirus Gp157 | |||
DJHDMHJE_01825 | 3e-54 | |||||
DJHDMHJE_01827 | 2.6e-220 | res | L | Helicase C-terminal domain protein | ||
DJHDMHJE_01829 | 2e-21 | K | Cro/C1-type HTH DNA-binding domain | |||
DJHDMHJE_01830 | 2e-135 | L | AAA domain | |||
DJHDMHJE_01831 | 9.4e-93 | |||||
DJHDMHJE_01832 | 2.7e-138 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
DJHDMHJE_01833 | 3.3e-210 | S | Virulence-associated protein E | |||
DJHDMHJE_01836 | 6.8e-41 | S | Domain of Unknown Function (DUF1599) | |||
DJHDMHJE_01840 | 8.4e-33 | S | VRR_NUC | |||
DJHDMHJE_01843 | 1.7e-25 | arpU | S | Phage transcriptional regulator, ArpU family | ||
DJHDMHJE_01845 | 2.2e-26 | |||||
DJHDMHJE_01846 | 6.2e-126 | L | NUMOD1 domain | |||
DJHDMHJE_01847 | 1.2e-211 | ps334 | S | Terminase-like family | ||
DJHDMHJE_01848 | 3.5e-269 | S | Phage portal protein, SPP1 Gp6-like | |||
DJHDMHJE_01849 | 1.8e-190 | S | Phage Mu protein F like protein | |||
DJHDMHJE_01851 | 1.9e-87 | S | Phage minor structural protein GP20 | |||
DJHDMHJE_01852 | 2.3e-193 | |||||
DJHDMHJE_01853 | 2.8e-58 | |||||
DJHDMHJE_01854 | 2.1e-58 | |||||
DJHDMHJE_01855 | 1.9e-68 | S | Bacteriophage HK97-gp10, putative tail-component | |||
DJHDMHJE_01856 | 8.5e-27 | |||||
DJHDMHJE_01858 | 2.6e-256 | xkdK | S | Phage tail sheath C-terminal domain | ||
DJHDMHJE_01859 | 3e-81 | xkdM | S | Phage tail tube protein | ||
DJHDMHJE_01860 | 2.2e-67 | S | Pfam:Phage_TAC_5 | |||
DJHDMHJE_01861 | 2e-132 | S | phage tail tape measure protein | |||
DJHDMHJE_01862 | 6.5e-117 | ygaU | GH23 | S | protein containing LysM domain | |
DJHDMHJE_01863 | 3.5e-194 | S | amidase activity | |||
DJHDMHJE_01864 | 7.1e-56 | S | Protein of unknown function (DUF2577) | |||
DJHDMHJE_01865 | 9e-67 | S | lytic transglycosylase activity | |||
DJHDMHJE_01866 | 1.5e-198 | xkdT | S | Baseplate J-like protein | ||
DJHDMHJE_01867 | 2.9e-86 | S | Uncharacterised protein conserved in bacteria (DUF2313) | |||
DJHDMHJE_01868 | 6.4e-185 | |||||
DJHDMHJE_01871 | 2.8e-36 | |||||
DJHDMHJE_01873 | 1.9e-15 | |||||
DJHDMHJE_01875 | 4.6e-27 | |||||
DJHDMHJE_01876 | 3.5e-56 | |||||
DJHDMHJE_01877 | 4.6e-197 | M | Glycosyl hydrolases family 25 | |||
DJHDMHJE_01880 | 6.8e-83 | S | Peptidase family M23 | |||
DJHDMHJE_01881 | 5.8e-152 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
DJHDMHJE_01882 | 2e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
DJHDMHJE_01883 | 7.2e-69 | yqeY | S | YqeY-like protein | ||
DJHDMHJE_01884 | 4.2e-175 | phoH | T | phosphate starvation-inducible protein PhoH | ||
DJHDMHJE_01885 | 1.6e-96 | 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 | |
DJHDMHJE_01886 | 1.1e-169 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
DJHDMHJE_01887 | 3e-136 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
DJHDMHJE_01888 | 4.6e-179 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
DJHDMHJE_01889 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
DJHDMHJE_01890 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
DJHDMHJE_01891 | 2.9e-199 | 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 | ||
DJHDMHJE_01892 | 1.2e-125 | S | Peptidase family M23 | |||
DJHDMHJE_01893 | 1.1e-29 | mutT | 3.6.1.55 | F | NUDIX domain | |
DJHDMHJE_01894 | 2.9e-125 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
DJHDMHJE_01895 | 7.7e-154 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
DJHDMHJE_01896 | 1.1e-242 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
DJHDMHJE_01897 | 3.9e-60 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
DJHDMHJE_01898 | 2.4e-122 | skfE | V | ATPases associated with a variety of cellular activities | ||
DJHDMHJE_01899 | 6.7e-148 | |||||
DJHDMHJE_01900 | 6.5e-148 | |||||
DJHDMHJE_01901 | 1.1e-130 | |||||
DJHDMHJE_01902 | 3.9e-33 | rarA | L | recombination factor protein RarA | ||
DJHDMHJE_01903 | 7.8e-61 | rarA | L | recombination factor protein RarA | ||
DJHDMHJE_01904 | 7.8e-28 | |||||
DJHDMHJE_01905 | 1.8e-75 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
DJHDMHJE_01906 | 2.6e-129 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_01907 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
DJHDMHJE_01908 | 1.9e-247 | ynbB | 4.4.1.1 | P | aluminum resistance | |
DJHDMHJE_01909 | 8.6e-58 | ktrA | P | domain protein | ||
DJHDMHJE_01910 | 1.5e-47 | ktrA | P | domain protein | ||
DJHDMHJE_01911 | 2e-26 | ktrB | P | Potassium uptake protein | ||
DJHDMHJE_01912 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
DJHDMHJE_01913 | 1.3e-81 | C | Flavodoxin | |||
DJHDMHJE_01914 | 1.3e-111 | 3.6.1.27 | I | Acid phosphatase homologues | ||
DJHDMHJE_01915 | 2.7e-106 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
DJHDMHJE_01916 | 2.2e-207 | pbpX1 | V | Beta-lactamase | ||
DJHDMHJE_01917 | 1.2e-149 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
DJHDMHJE_01918 | 6.9e-93 | S | ECF-type riboflavin transporter, S component | |||
DJHDMHJE_01919 | 8.1e-232 | S | Putative peptidoglycan binding domain | |||
DJHDMHJE_01920 | 1.6e-236 | mepA | V | MATE efflux family protein | ||
DJHDMHJE_01921 | 1e-256 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
DJHDMHJE_01922 | 1.9e-33 | |||||
DJHDMHJE_01923 | 1.4e-29 | fic | D | Fic/DOC family | ||
DJHDMHJE_01924 | 2.2e-60 | |||||
DJHDMHJE_01925 | 2.6e-294 | P | ABC transporter | |||
DJHDMHJE_01926 | 2e-294 | V | ABC-type multidrug transport system, ATPase and permease components | |||
DJHDMHJE_01927 | 9.2e-69 | S | Putative adhesin | |||
DJHDMHJE_01928 | 1.3e-58 | ypaA | S | Protein of unknown function (DUF1304) | ||
DJHDMHJE_01930 | 3.3e-78 | |||||
DJHDMHJE_01931 | 2.4e-56 | |||||
DJHDMHJE_01932 | 2.9e-116 | S | Fic/DOC family | |||
DJHDMHJE_01933 | 1.7e-102 | |||||
DJHDMHJE_01934 | 6.1e-208 | EGP | Major facilitator Superfamily | |||
DJHDMHJE_01935 | 1.6e-134 | |||||
DJHDMHJE_01936 | 4.8e-21 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
DJHDMHJE_01938 | 1.5e-39 | |||||
DJHDMHJE_01940 | 9.7e-236 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
DJHDMHJE_01941 | 3.2e-289 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
DJHDMHJE_01942 | 1.1e-104 | 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 | |
DJHDMHJE_01943 | 3.3e-197 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
DJHDMHJE_01944 | 1.5e-275 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
DJHDMHJE_01945 | 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 | |
DJHDMHJE_01946 | 1.8e-127 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
DJHDMHJE_01947 | 6.4e-38 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
DJHDMHJE_01948 | 2.1e-134 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
DJHDMHJE_01949 | 8.2e-221 | 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) | |
DJHDMHJE_01950 | 2.7e-77 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
DJHDMHJE_01951 | 1.9e-308 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
DJHDMHJE_01952 | 3.5e-139 | qmcA | O | prohibitin homologues | ||
DJHDMHJE_01953 | 2.2e-51 | L | RelB antitoxin | |||
DJHDMHJE_01954 | 1.1e-19 | |||||
DJHDMHJE_01955 | 2.1e-193 | S | Bacteriocin helveticin-J | |||
DJHDMHJE_01956 | 4.5e-288 | M | Peptidase family M1 domain | |||
DJHDMHJE_01957 | 8.2e-174 | S | SLAP domain | |||
DJHDMHJE_01958 | 5.5e-250 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
DJHDMHJE_01959 | 9.4e-147 | S | SLAP domain | |||
DJHDMHJE_01960 | 3.8e-158 | S | SLAP domain | |||
DJHDMHJE_01961 | 3.3e-123 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
DJHDMHJE_01962 | 4.7e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
DJHDMHJE_01963 | 1e-124 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
DJHDMHJE_01964 | 1.4e-215 | ecsB | U | ABC transporter | ||
DJHDMHJE_01965 | 3.9e-136 | ecsA | V | ABC transporter, ATP-binding protein | ||
DJHDMHJE_01966 | 3.8e-54 | higA | K | Helix-turn-helix XRE-family like proteins | ||
DJHDMHJE_01967 | 3.3e-34 | S | Plasmid maintenance system killer | |||
DJHDMHJE_01968 | 8.9e-80 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
DJHDMHJE_01969 | 8e-28 | |||||
DJHDMHJE_01970 | 1e-154 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
DJHDMHJE_01971 | 6.2e-78 | S | PAS domain | |||
DJHDMHJE_01972 | 3.4e-188 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
DJHDMHJE_01973 | 0.0 | L | AAA domain | |||
DJHDMHJE_01974 | 1.2e-230 | yhaO | L | Ser Thr phosphatase family protein | ||
DJHDMHJE_01975 | 6.1e-28 | yheA | S | Belongs to the UPF0342 family | ||
DJHDMHJE_01976 | 7.9e-17 | yheA | S | Belongs to the UPF0342 family | ||
DJHDMHJE_01977 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
DJHDMHJE_01978 | 1.3e-162 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
DJHDMHJE_01979 | 8.7e-40 | L | Transposase | |||
DJHDMHJE_01980 | 1.6e-200 | V | ABC-type multidrug transport system, ATPase and permease components | |||
DJHDMHJE_01981 | 9.4e-30 | S | ABC transporter | |||
DJHDMHJE_01982 | 1.2e-25 | L | Transposase | |||
DJHDMHJE_01983 | 1.2e-87 | S | Membrane | |||
DJHDMHJE_01984 | 4.2e-25 | I | carboxylic ester hydrolase activity | |||
DJHDMHJE_01985 | 2.9e-62 | 4.2.99.20 | S | Alpha/beta hydrolase family | ||
DJHDMHJE_01986 | 2.2e-32 | S | Biotin synthase | |||
DJHDMHJE_01987 | 1.1e-28 | S | HicB family | |||
DJHDMHJE_01989 | 1.2e-58 | yafQ | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | ||
DJHDMHJE_01990 | 4.6e-45 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
DJHDMHJE_01991 | 4.9e-86 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
DJHDMHJE_01992 | 1.9e-96 | K | Transcriptional regulator, AbiEi antitoxin | |||
DJHDMHJE_01993 | 3.8e-84 | L | Integrase | |||
DJHDMHJE_01994 | 4.9e-116 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_01995 | 2.5e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
DJHDMHJE_01996 | 5.1e-38 | ynzC | S | UPF0291 protein | ||
DJHDMHJE_01997 | 3.6e-114 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
DJHDMHJE_01998 | 8.3e-148 | E | GDSL-like Lipase/Acylhydrolase family | |||
DJHDMHJE_01999 | 6e-45 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
DJHDMHJE_02000 | 1.5e-62 | 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 | ||
DJHDMHJE_02001 | 1.7e-136 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
DJHDMHJE_02002 | 9.8e-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 | ||
DJHDMHJE_02003 | 4.5e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
DJHDMHJE_02004 | 2.2e-228 | 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 | |
DJHDMHJE_02005 | 3.2e-56 | 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 | ||
DJHDMHJE_02006 | 1.4e-133 | L | Transposase and inactivated derivatives, IS30 family | |||
DJHDMHJE_02007 | 5.4e-259 | yfnA | E | amino acid | ||
DJHDMHJE_02008 | 5.2e-44 | |||||
DJHDMHJE_02009 | 1.7e-289 | pipD | E | Dipeptidase | ||
DJHDMHJE_02010 | 1.3e-166 | 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) | ||
DJHDMHJE_02011 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
DJHDMHJE_02012 | 1.3e-125 | 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 | |
DJHDMHJE_02013 | 9.4e-302 | oppA | E | ABC transporter substrate-binding protein | ||
DJHDMHJE_02014 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
DJHDMHJE_02015 | 7.3e-148 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
DJHDMHJE_02016 | 1.7e-176 | oppB | P | ABC transporter permease | ||
DJHDMHJE_02017 | 2.8e-182 | oppF | P | Belongs to the ABC transporter superfamily | ||
DJHDMHJE_02018 | 7.3e-197 | oppD | P | Belongs to the ABC transporter superfamily | ||
DJHDMHJE_02019 | 3.4e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
DJHDMHJE_02020 | 6.4e-182 | 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 | |
DJHDMHJE_02021 | 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) | |
DJHDMHJE_02022 | 1.1e-306 | yloV | S | DAK2 domain fusion protein YloV | ||
DJHDMHJE_02023 | 6.8e-57 | asp | S | Asp23 family, cell envelope-related function | ||
DJHDMHJE_02024 | 1.1e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
DJHDMHJE_02025 | 1.6e-51 | |||||
DJHDMHJE_02026 | 1.4e-127 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
DJHDMHJE_02027 | 3.8e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
DJHDMHJE_02028 | 2.6e-166 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
DJHDMHJE_02029 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
DJHDMHJE_02030 | 2.4e-147 | stp | 3.1.3.16 | T | phosphatase | |
DJHDMHJE_02031 | 5.8e-247 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
DJHDMHJE_02032 | 2.7e-174 | 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 | |
DJHDMHJE_02033 | 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 | ||
DJHDMHJE_02034 | 6.5e-34 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
DJHDMHJE_02035 | 1.9e-112 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
DJHDMHJE_02036 | 8.1e-44 | 6.3.3.2 | S | ASCH | ||
DJHDMHJE_02037 | 3.5e-21 | 6.3.3.2 | S | ASCH | ||
DJHDMHJE_02038 | 2.5e-308 | recN | L | May be involved in recombinational repair of damaged DNA | ||
DJHDMHJE_02039 | 6e-154 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
DJHDMHJE_02040 | 2.4e-161 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
DJHDMHJE_02041 | 2.9e-35 | 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 | |
DJHDMHJE_02042 | 1.2e-194 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
DJHDMHJE_02043 | 1.1e-155 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_02044 | 9.4e-142 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
DJHDMHJE_02047 | 7.2e-20 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
DJHDMHJE_02048 | 3.6e-150 | K | Transcriptional regulator | |||
DJHDMHJE_02049 | 7.6e-64 | manO | S | Domain of unknown function (DUF956) | ||
DJHDMHJE_02050 | 1.2e-174 | manN | G | system, mannose fructose sorbose family IID component | ||
DJHDMHJE_02051 | 1.4e-134 | manY | G | PTS system | ||
DJHDMHJE_02052 | 3.6e-188 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
DJHDMHJE_02053 | 6.5e-17 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
DJHDMHJE_02054 | 3.8e-33 | scrB | 3.2.1.26 | GH32 | G | invertase |
DJHDMHJE_02055 | 6.2e-67 | msmR7 | K | helix_turn_helix, arabinose operon control protein | ||
DJHDMHJE_02057 | 2.2e-54 | S | Protein of unknown function (DUF3397) | |||
DJHDMHJE_02058 | 6.5e-13 | S | Protein of unknown function (DUF4044) | |||
DJHDMHJE_02059 | 4.5e-97 | mreD | ||||
DJHDMHJE_02060 | 7.9e-149 | mreC | M | Involved in formation and maintenance of cell shape | ||
DJHDMHJE_02061 | 4.9e-174 | mreB | D | cell shape determining protein MreB | ||
DJHDMHJE_02062 | 2.1e-114 | radC | L | DNA repair protein | ||
DJHDMHJE_02063 | 5.7e-126 | S | Haloacid dehalogenase-like hydrolase | |||
DJHDMHJE_02064 | 7.2e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
DJHDMHJE_02065 | 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 | |
DJHDMHJE_02066 | 1.8e-39 | |||||
DJHDMHJE_02067 | 3.2e-127 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_02068 | 1.1e-46 | S | ACT domain | |||
DJHDMHJE_02069 | 2e-185 | S | Domain of unknown function (DUF389) | |||
DJHDMHJE_02070 | 3.5e-29 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
DJHDMHJE_02071 | 4e-237 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
DJHDMHJE_02072 | 1.5e-56 | 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 | ||
DJHDMHJE_02073 | 6.2e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
DJHDMHJE_02074 | 5.1e-57 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
DJHDMHJE_02075 | 1.3e-93 | yqeG | S | HAD phosphatase, family IIIA | ||
DJHDMHJE_02076 | 1.3e-212 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
DJHDMHJE_02077 | 1.2e-123 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
DJHDMHJE_02078 | 2.3e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
DJHDMHJE_02079 | 6.9e-59 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
DJHDMHJE_02080 | 1.7e-215 | ylbM | S | Belongs to the UPF0348 family | ||
DJHDMHJE_02081 | 4.1e-98 | yceD | S | Uncharacterized ACR, COG1399 | ||
DJHDMHJE_02082 | 3.2e-127 | K | response regulator | |||
DJHDMHJE_02083 | 1.2e-280 | arlS | 2.7.13.3 | T | Histidine kinase | |
DJHDMHJE_02084 | 2.7e-85 | S | Aminoacyl-tRNA editing domain | |||
DJHDMHJE_02085 | 2e-156 | 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 | ||
DJHDMHJE_02086 | 1.9e-43 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
DJHDMHJE_02087 | 3e-139 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
DJHDMHJE_02088 | 4.7e-63 | yodB | K | Transcriptional regulator, HxlR family | ||
DJHDMHJE_02089 | 4e-203 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
DJHDMHJE_02090 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
DJHDMHJE_02091 | 1.4e-62 | 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 | ||
DJHDMHJE_02092 | 8.7e-170 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
DJHDMHJE_02093 | 2.9e-57 | S | Phage derived protein Gp49-like (DUF891) | |||
DJHDMHJE_02094 | 6.9e-38 | K | Helix-turn-helix domain | |||
DJHDMHJE_02095 | 4.5e-50 | |||||
DJHDMHJE_02096 | 7.4e-68 | |||||
DJHDMHJE_02097 | 7.3e-269 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_02098 | 1.6e-188 | cggR | K | Putative sugar-binding domain | ||
DJHDMHJE_02099 | 1.3e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
DJHDMHJE_02100 | 9.3e-228 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
DJHDMHJE_02101 | 2e-143 | 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) | |
DJHDMHJE_02102 | 4.8e-96 | |||||
DJHDMHJE_02103 | 8.7e-159 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
DJHDMHJE_02104 | 2.2e-136 | 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 | |
DJHDMHJE_02105 | 1.8e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
DJHDMHJE_02106 | 6.4e-90 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
DJHDMHJE_02107 | 2.3e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
DJHDMHJE_02108 | 1.1e-164 | murB | 1.3.1.98 | M | Cell wall formation | |
DJHDMHJE_02109 | 2e-205 | 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 | |
DJHDMHJE_02110 | 1.3e-129 | potB | P | ABC transporter permease | ||
DJHDMHJE_02111 | 1.7e-132 | potC | P | ABC transporter permease | ||
DJHDMHJE_02112 | 5.6e-208 | potD | P | ABC transporter | ||
DJHDMHJE_02113 | 4.2e-150 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
DJHDMHJE_02114 | 2.4e-170 | ybbR | S | YbbR-like protein | ||
DJHDMHJE_02115 | 1.3e-257 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
DJHDMHJE_02116 | 1.1e-150 | S | hydrolase | |||
DJHDMHJE_02117 | 1.5e-149 | S | Sucrose-6F-phosphate phosphohydrolase | |||
DJHDMHJE_02118 | 2.1e-118 | |||||
DJHDMHJE_02119 | 1.5e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
DJHDMHJE_02120 | 2.3e-215 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
DJHDMHJE_02121 | 4.6e-64 | licT | K | CAT RNA binding domain | ||
DJHDMHJE_02122 | 3e-63 | licT | K | CAT RNA binding domain | ||
DJHDMHJE_02123 | 0.0 | bglP | G | phosphotransferase system | ||
DJHDMHJE_02124 | 9.5e-166 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
DJHDMHJE_02125 | 2.2e-39 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
DJHDMHJE_02126 | 4.3e-61 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
DJHDMHJE_02127 | 5.9e-185 | D | Alpha beta | |||
DJHDMHJE_02128 | 1.5e-16 | E | Amino acid permease | |||
DJHDMHJE_02129 | 2.9e-163 | E | Amino acid permease | |||
DJHDMHJE_02130 | 1.7e-56 | E | Amino acid permease | |||
DJHDMHJE_02131 | 0.0 | cadA | P | P-type ATPase | ||
DJHDMHJE_02132 | 1.3e-205 | napA | P | Sodium/hydrogen exchanger family | ||
DJHDMHJE_02133 | 1.5e-49 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
DJHDMHJE_02134 | 4.7e-47 | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | |||
DJHDMHJE_02135 | 9.1e-284 | V | ABC transporter transmembrane region | |||
DJHDMHJE_02136 | 4e-81 | S | Putative adhesin | |||
DJHDMHJE_02137 | 5.9e-160 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
DJHDMHJE_02138 | 6.4e-47 | |||||
DJHDMHJE_02139 | 4.9e-116 | L | COG2963 Transposase and inactivated derivatives | |||
DJHDMHJE_02140 | 1.8e-77 | mraZ | K | Belongs to the MraZ family | ||
DJHDMHJE_02141 | 1.5e-183 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
DJHDMHJE_02142 | 1.4e-54 | ftsL | D | Cell division protein FtsL | ||
DJHDMHJE_02143 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
DJHDMHJE_02144 | 1.9e-47 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
DJHDMHJE_02145 | 7.1e-178 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
DJHDMHJE_02146 | 1.6e-260 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
DJHDMHJE_02147 | 1.8e-209 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
DJHDMHJE_02148 | 3.8e-151 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
DJHDMHJE_02149 | 2.6e-231 | 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 | ||
DJHDMHJE_02150 | 2.6e-207 | 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 | ||
DJHDMHJE_02151 | 1.3e-73 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
DJHDMHJE_02152 | 9e-47 | yggT | S | YGGT family | ||
DJHDMHJE_02153 | 3.3e-149 | ylmH | S | S4 domain protein | ||
DJHDMHJE_02154 | 2e-101 | gpsB | D | DivIVA domain protein | ||
DJHDMHJE_02155 | 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) | |
DJHDMHJE_02156 | 2.1e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
DJHDMHJE_02157 | 7.5e-103 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
DJHDMHJE_02158 | 1.9e-39 | |||||
DJHDMHJE_02159 | 1.3e-125 | 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 | |
DJHDMHJE_02160 | 2.4e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
DJHDMHJE_02161 | 1.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
DJHDMHJE_02162 | 1.2e-221 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
DJHDMHJE_02163 | 5.6e-126 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
DJHDMHJE_02164 | 2e-104 | S | Repeat protein | |||
DJHDMHJE_02165 | 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 | |
DJHDMHJE_02166 | 3.5e-106 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
DJHDMHJE_02167 | 2.3e-29 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
DJHDMHJE_02168 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
DJHDMHJE_02169 | 4.2e-33 | ykzG | S | Belongs to the UPF0356 family | ||
DJHDMHJE_02170 | 8.9e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
DJHDMHJE_02171 | 0.0 | typA | T | GTP-binding protein TypA | ||
DJHDMHJE_02172 | 4.7e-208 | ftsW | D | Belongs to the SEDS family | ||
DJHDMHJE_02173 | 8.7e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
DJHDMHJE_02174 | 2.2e-96 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
DJHDMHJE_02175 | 2.7e-85 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
DJHDMHJE_02176 | 5.4e-192 | ylbL | T | Belongs to the peptidase S16 family | ||
DJHDMHJE_02177 | 6.2e-83 | comEA | L | Competence protein ComEA | ||
DJHDMHJE_02178 | 0.0 | comEC | S | Competence protein ComEC | ||
DJHDMHJE_02179 | 4.8e-174 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
DJHDMHJE_02180 | 6.7e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
DJHDMHJE_02181 | 7e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
DJHDMHJE_02182 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
DJHDMHJE_02183 | 2.2e-151 | |||||
DJHDMHJE_02184 | 3.3e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
DJHDMHJE_02185 | 2.4e-213 | 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 | ||
DJHDMHJE_02186 | 1.3e-235 | 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 | ||
DJHDMHJE_02187 | 7.5e-106 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
DJHDMHJE_02188 | 3.9e-45 | yjeM | E | Amino Acid | ||
DJHDMHJE_02189 | 5.9e-183 | yjeM | E | Amino Acid | ||
DJHDMHJE_02190 | 1.5e-191 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
DJHDMHJE_02191 | 8.3e-265 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
DJHDMHJE_02192 | 1.4e-13 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_02193 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
DJHDMHJE_02194 | 3.9e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
DJHDMHJE_02195 | 3.2e-305 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
DJHDMHJE_02196 | 1.2e-160 | hlyX | S | Transporter associated domain | ||
DJHDMHJE_02197 | 1.3e-73 | |||||
DJHDMHJE_02198 | 1.9e-86 | |||||
DJHDMHJE_02199 | 2.7e-146 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
DJHDMHJE_02200 | 3.9e-262 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
DJHDMHJE_02201 | 1.1e-112 | L | COG3385 FOG Transposase and inactivated derivatives | |||
DJHDMHJE_02202 | 3.1e-83 | L | COG3385 FOG Transposase and inactivated derivatives | |||
DJHDMHJE_02203 | 5e-41 | L | COG3385 FOG Transposase and inactivated derivatives | |||
DJHDMHJE_02204 | 2.7e-14 | |||||
DJHDMHJE_02205 | 4.5e-67 | |||||
DJHDMHJE_02206 | 7.8e-148 | arbV | 2.3.1.51 | I | Acyl-transferase | |
DJHDMHJE_02207 | 2.7e-197 | S | SLAP domain | |||
DJHDMHJE_02208 | 3.9e-18 | |||||
DJHDMHJE_02209 | 4.7e-63 | S | Uncharacterised protein family (UPF0236) | |||
DJHDMHJE_02210 | 3.3e-86 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
DJHDMHJE_02211 | 1.2e-174 | prmA | J | Ribosomal protein L11 methyltransferase | ||
DJHDMHJE_02212 | 8.5e-60 | |||||
DJHDMHJE_02213 | 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 | |
DJHDMHJE_02214 | 2.1e-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 | ||
DJHDMHJE_02215 | 2.3e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
DJHDMHJE_02216 | 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) | |
DJHDMHJE_02217 | 2.1e-224 | patA | 2.6.1.1 | E | Aminotransferase | |
DJHDMHJE_02218 | 2.1e-114 | L | Transposase IS66 family | |||
DJHDMHJE_02219 | 8.3e-63 | L | COG3547 Transposase and inactivated derivatives | |||
DJHDMHJE_02220 | 5.5e-197 | licA | 2.7.1.89 | M | Nucleotidyl transferase | |
DJHDMHJE_02221 | 2.6e-81 | M | Nucleotidyl transferase | |||
DJHDMHJE_02222 | 1.1e-161 | caiT | U | Belongs to the BCCT transporter (TC 2.A.15) family | ||
DJHDMHJE_02224 | 1.2e-137 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
DJHDMHJE_02225 | 5.5e-178 | ABC-SBP | S | ABC transporter | ||
DJHDMHJE_02226 | 1.7e-122 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
DJHDMHJE_02227 | 9.6e-138 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
DJHDMHJE_02228 | 4.1e-41 | |||||
DJHDMHJE_02229 | 4.8e-11 | |||||
DJHDMHJE_02230 | 6.2e-105 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
DJHDMHJE_02231 | 2.2e-177 | K | AI-2E family transporter | |||
DJHDMHJE_02232 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
DJHDMHJE_02233 | 2.1e-67 | S | Domain of unknown function (DUF4430) | |||
DJHDMHJE_02234 | 1.4e-87 | S | ECF transporter, substrate-specific component | |||
DJHDMHJE_02235 | 1.3e-99 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | cob(I)alamin adenosyltransferase | |
DJHDMHJE_02236 | 2e-183 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
DJHDMHJE_02237 | 5.5e-62 | S | Protein of unknown function (DUF2974) | |||
DJHDMHJE_02238 | 2.8e-109 | glnP | P | ABC transporter permease | ||
DJHDMHJE_02239 | 6.7e-108 | gluC | P | ABC transporter permease | ||
DJHDMHJE_02240 | 1.5e-152 | glnH | ET | ABC transporter substrate-binding protein | ||
DJHDMHJE_02241 | 3.3e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DJHDMHJE_02242 | 1.1e-67 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
DJHDMHJE_02243 | 5.7e-264 | qacA | EGP | Major facilitator Superfamily | ||
DJHDMHJE_02244 | 1.1e-217 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
DJHDMHJE_02247 | 8.8e-178 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
DJHDMHJE_02250 | 2e-103 | |||||
DJHDMHJE_02251 | 2.1e-26 | |||||
DJHDMHJE_02252 | 1.9e-15 | |||||
DJHDMHJE_02253 | 1.3e-44 | |||||
DJHDMHJE_02254 | 6.8e-78 | S | Domain of unknown function (DUF5067) | |||
DJHDMHJE_02255 | 5.3e-62 | |||||
DJHDMHJE_02256 | 1.5e-48 | |||||
DJHDMHJE_02257 | 3e-133 | 2.4.2.3 | F | Phosphorylase superfamily | ||
DJHDMHJE_02258 | 3.1e-26 | L | Transposase | |||
DJHDMHJE_02259 | 9e-37 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
DJHDMHJE_02260 | 2.7e-154 | S | hydrolase | |||
DJHDMHJE_02261 | 2.7e-51 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_02262 | 1.9e-34 | L | An automated process has identified a potential problem with this gene model | |||
DJHDMHJE_02263 | 3.4e-146 | sufC | O | FeS assembly ATPase SufC | ||
DJHDMHJE_02264 | 1.8e-229 | sufD | O | FeS assembly protein SufD | ||
DJHDMHJE_02265 | 1.2e-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 | |
DJHDMHJE_02266 | 3.8e-81 | nifU | C | SUF system FeS assembly protein, NifU family | ||
DJHDMHJE_02267 | 3.2e-272 | sufB | O | assembly protein SufB | ||
DJHDMHJE_02268 | 2.5e-55 | yitW | S | Iron-sulfur cluster assembly protein | ||
DJHDMHJE_02269 | 4.1e-62 | S | Enterocin A Immunity | |||
DJHDMHJE_02270 | 1.4e-128 | glcR | K | DeoR C terminal sensor domain | ||
DJHDMHJE_02271 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
DJHDMHJE_02272 | 1.1e-161 | rssA | S | Phospholipase, patatin family | ||
DJHDMHJE_02273 | 4.4e-14 | EGP | Major facilitator Superfamily | |||
DJHDMHJE_02274 | 3.8e-118 | EGP | Major facilitator Superfamily | |||
DJHDMHJE_02275 | 6.4e-262 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
DJHDMHJE_02276 | 8.3e-108 | vanZ | V | VanZ like family | ||
DJHDMHJE_02277 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
DJHDMHJE_02278 | 7.5e-23 | lctP | C | L-lactate permease | ||
DJHDMHJE_02279 | 6.1e-90 | lctP | C | L-lactate permease | ||
DJHDMHJE_02280 | 3e-51 | lctP | C | L-lactate permease | ||
DJHDMHJE_02281 | 9.3e-43 | S | Enterocin A Immunity | |||
DJHDMHJE_02282 | 1.7e-34 | D | Filamentation induced by cAMP protein fic | |||
DJHDMHJE_02283 | 0.0 | pepF | E | oligoendopeptidase F | ||
DJHDMHJE_02284 | 2.4e-215 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
DJHDMHJE_02285 | 7.2e-25 | S | Protein of unknown function (DUF554) | |||
DJHDMHJE_02286 | 1.2e-36 | L | Transposase | |||
DJHDMHJE_02287 | 1.2e-58 | |||||
DJHDMHJE_02288 | 3.5e-266 | E | Amino acid permease | |||
DJHDMHJE_02289 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
DJHDMHJE_02290 | 8.1e-62 | L | Transposase | |||
DJHDMHJE_02291 | 5.2e-225 | S | response to antibiotic | |||
DJHDMHJE_02292 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
DJHDMHJE_02293 | 1e-276 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
DJHDMHJE_02294 | 2.1e-93 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
DJHDMHJE_02295 | 5.9e-68 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | ||
DJHDMHJE_02296 | 3.1e-66 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
DJHDMHJE_02297 | 8e-171 | yfdH | GT2 | M | Glycosyltransferase like family 2 | |
DJHDMHJE_02298 | 1.4e-245 | L | transposase, IS605 OrfB family | |||
DJHDMHJE_02299 | 9e-36 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)