ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
PJBMHNLJ_00001 | 8.9e-184 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
PJBMHNLJ_00002 | 1.3e-124 | manY | G | PTS system | ||
PJBMHNLJ_00003 | 3.3e-172 | manN | G | system, mannose fructose sorbose family IID component | ||
PJBMHNLJ_00004 | 8.8e-65 | manO | S | Domain of unknown function (DUF956) | ||
PJBMHNLJ_00005 | 1.5e-253 | yifK | E | Amino acid permease | ||
PJBMHNLJ_00006 | 3.5e-231 | yifK | E | Amino acid permease | ||
PJBMHNLJ_00007 | 1e-136 | puuD | S | peptidase C26 | ||
PJBMHNLJ_00008 | 1.2e-234 | steT_1 | E | amino acid | ||
PJBMHNLJ_00009 | 9e-192 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
PJBMHNLJ_00010 | 3.9e-162 | EG | EamA-like transporter family | |||
PJBMHNLJ_00011 | 1.3e-254 | yfnA | E | Amino Acid | ||
PJBMHNLJ_00012 | 2.1e-131 | cobQ | S | glutamine amidotransferase | ||
PJBMHNLJ_00013 | 4.4e-149 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
PJBMHNLJ_00014 | 4.4e-146 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
PJBMHNLJ_00015 | 3.6e-185 | scrR | K | Transcriptional regulator, LacI family | ||
PJBMHNLJ_00016 | 1.6e-298 | scrB | 3.2.1.26 | GH32 | G | invertase |
PJBMHNLJ_00017 | 0.0 | scrA | 2.7.1.199, 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
PJBMHNLJ_00018 | 1.9e-108 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
PJBMHNLJ_00019 | 4.7e-67 | 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 | |
PJBMHNLJ_00020 | 1.5e-65 | 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 | |
PJBMHNLJ_00021 | 6.3e-148 | 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 | |
PJBMHNLJ_00022 | 2.4e-156 | pstA | P | Phosphate transport system permease protein PstA | ||
PJBMHNLJ_00023 | 1.1e-160 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
PJBMHNLJ_00024 | 1.4e-87 | pstS | P | Phosphate | ||
PJBMHNLJ_00025 | 2.8e-96 | K | Acetyltransferase (GNAT) domain | |||
PJBMHNLJ_00026 | 1.2e-129 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PJBMHNLJ_00027 | 5.5e-254 | glnPH2 | P | ABC transporter permease | ||
PJBMHNLJ_00028 | 5.5e-158 | rssA | S | Phospholipase, patatin family | ||
PJBMHNLJ_00029 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
PJBMHNLJ_00030 | 3.3e-68 | K | LytTr DNA-binding domain | |||
PJBMHNLJ_00031 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
PJBMHNLJ_00032 | 5.4e-104 | M | Transport protein ComB | |||
PJBMHNLJ_00033 | 3.2e-20 | S | Bacteriocin class II with double-glycine leader peptide | |||
PJBMHNLJ_00036 | 5.1e-279 | S | C4-dicarboxylate anaerobic carrier | |||
PJBMHNLJ_00037 | 2.6e-85 | dps | P | Belongs to the Dps family | ||
PJBMHNLJ_00038 | 3.9e-157 | 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 | |
PJBMHNLJ_00039 | 1.8e-127 | 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 | |
PJBMHNLJ_00040 | 3.1e-189 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
PJBMHNLJ_00041 | 1e-246 | clcA | P | chloride | ||
PJBMHNLJ_00042 | 1.5e-112 | |||||
PJBMHNLJ_00043 | 1.3e-88 | gluC | P | ABC transporter permease | ||
PJBMHNLJ_00044 | 5.7e-107 | glnP | P | ABC transporter permease | ||
PJBMHNLJ_00045 | 1.9e-65 | |||||
PJBMHNLJ_00046 | 0.0 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
PJBMHNLJ_00047 | 5.1e-81 | treR | K | UTRA | ||
PJBMHNLJ_00048 | 1.8e-130 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
PJBMHNLJ_00049 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
PJBMHNLJ_00050 | 3.6e-143 | fruK | 2.7.1.11, 2.7.1.56 | G | pfkB family carbohydrate kinase | |
PJBMHNLJ_00051 | 1.3e-54 | |||||
PJBMHNLJ_00052 | 1e-267 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
PJBMHNLJ_00053 | 2.4e-95 | yutD | S | Protein of unknown function (DUF1027) | ||
PJBMHNLJ_00054 | 1.2e-148 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
PJBMHNLJ_00055 | 3.8e-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 | ||
PJBMHNLJ_00056 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
PJBMHNLJ_00057 | 1.8e-172 | 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 | ||
PJBMHNLJ_00058 | 4.7e-90 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
PJBMHNLJ_00059 | 2e-216 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
PJBMHNLJ_00060 | 1.3e-238 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
PJBMHNLJ_00061 | 7e-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 | |
PJBMHNLJ_00062 | 1.1e-34 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
PJBMHNLJ_00063 | 3e-251 | 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 | |
PJBMHNLJ_00064 | 3.9e-125 | 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 | |
PJBMHNLJ_00065 | 9.4e-272 | 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 | |
PJBMHNLJ_00066 | 7.5e-22 | 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 | ||
PJBMHNLJ_00067 | 5.6e-39 | 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 | ||
PJBMHNLJ_00068 | 6.2e-246 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
PJBMHNLJ_00069 | 2.2e-279 | E | Amino acid permease | |||
PJBMHNLJ_00070 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
PJBMHNLJ_00071 | 6.3e-50 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
PJBMHNLJ_00072 | 2.4e-65 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
PJBMHNLJ_00073 | 1.4e-13 | atkY | K | Penicillinase repressor | ||
PJBMHNLJ_00074 | 7.1e-90 | |||||
PJBMHNLJ_00075 | 3.7e-75 | |||||
PJBMHNLJ_00076 | 4.7e-70 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
PJBMHNLJ_00077 | 4.6e-77 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
PJBMHNLJ_00078 | 4.7e-225 | pbuG | S | permease | ||
PJBMHNLJ_00079 | 5.6e-90 | K | Arabinose-binding domain of AraC transcription regulator, N-term | |||
PJBMHNLJ_00080 | 1.6e-58 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
PJBMHNLJ_00081 | 1.5e-231 | pbuG | S | permease | ||
PJBMHNLJ_00082 | 4.9e-114 | 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 | |
PJBMHNLJ_00083 | 7.1e-107 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
PJBMHNLJ_00084 | 2.5e-166 | akr5f | 1.1.1.346 | S | reductase | |
PJBMHNLJ_00085 | 8.2e-73 | yqhY | S | Asp23 family, cell envelope-related function | ||
PJBMHNLJ_00086 | 1.1e-101 | 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 | ||
PJBMHNLJ_00087 | 6.4e-199 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
PJBMHNLJ_00088 | 2.8e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
PJBMHNLJ_00089 | 2.2e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
PJBMHNLJ_00090 | 1.7e-60 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
PJBMHNLJ_00091 | 4.1e-49 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
PJBMHNLJ_00092 | 0.0 | KLT | serine threonine protein kinase | |||
PJBMHNLJ_00093 | 4.1e-164 | 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 | |
PJBMHNLJ_00094 | 1.7e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
PJBMHNLJ_00095 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
PJBMHNLJ_00096 | 3.9e-139 | S | haloacid dehalogenase-like hydrolase | |||
PJBMHNLJ_00098 | 5.3e-102 | cof | S | haloacid dehalogenase-like hydrolase | ||
PJBMHNLJ_00099 | 1.2e-268 | ydgH | S | MMPL family | ||
PJBMHNLJ_00100 | 6.6e-113 | 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 | ||
PJBMHNLJ_00101 | 9.7e-103 | ypsA | S | Belongs to the UPF0398 family | ||
PJBMHNLJ_00102 | 2e-157 | oppD | P | Belongs to the ABC transporter superfamily | ||
PJBMHNLJ_00103 | 9.9e-180 | oppF | P | Belongs to the ABC transporter superfamily | ||
PJBMHNLJ_00104 | 9.2e-178 | oppB | P | ABC transporter permease | ||
PJBMHNLJ_00105 | 3.3e-161 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
PJBMHNLJ_00106 | 1.5e-250 | 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 | ||
PJBMHNLJ_00107 | 1.7e-276 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
PJBMHNLJ_00108 | 1.2e-224 | S | Sterol carrier protein domain | |||
PJBMHNLJ_00109 | 7.2e-166 | arbZ | I | Acyltransferase | ||
PJBMHNLJ_00110 | 8.8e-116 | ywnB | S | NAD(P)H-binding | ||
PJBMHNLJ_00111 | 4.8e-64 | S | Protein of unknown function (DUF975) | |||
PJBMHNLJ_00113 | 4e-130 | K | response regulator | |||
PJBMHNLJ_00114 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
PJBMHNLJ_00115 | 5.3e-158 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
PJBMHNLJ_00116 | 4.2e-40 | S | Transglycosylase associated protein | |||
PJBMHNLJ_00118 | 7.6e-154 | XK27_02480 | EGP | Major facilitator Superfamily | ||
PJBMHNLJ_00119 | 7.8e-236 | clcA | P | chloride | ||
PJBMHNLJ_00120 | 5e-248 | L | Transposase | |||
PJBMHNLJ_00121 | 0.0 | tetP | J | elongation factor G | ||
PJBMHNLJ_00122 | 3.5e-17 | |||||
PJBMHNLJ_00123 | 1.2e-152 | yitS | S | EDD domain protein, DegV family | ||
PJBMHNLJ_00124 | 4.2e-103 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
PJBMHNLJ_00125 | 7.4e-62 | rplQ | J | Ribosomal protein L17 | ||
PJBMHNLJ_00126 | 9.6e-172 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
PJBMHNLJ_00127 | 2.6e-62 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
PJBMHNLJ_00128 | 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 | ||
PJBMHNLJ_00129 | 6e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
PJBMHNLJ_00130 | 1.4e-33 | 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 | ||
PJBMHNLJ_00131 | 4.5e-120 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
PJBMHNLJ_00132 | 1.1e-53 | 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 | ||
PJBMHNLJ_00133 | 1.5e-288 | U | TraM recognition site of TraD and TraG | |||
PJBMHNLJ_00134 | 6.7e-63 | K | Helix-turn-helix domain | |||
PJBMHNLJ_00135 | 5.2e-72 | S | Psort location Cytoplasmic, score 8.96 | |||
PJBMHNLJ_00136 | 2.5e-112 | D | VirC1 protein | |||
PJBMHNLJ_00137 | 4.2e-53 | U | Relaxase/Mobilisation nuclease domain | |||
PJBMHNLJ_00138 | 6.3e-134 | cysA | V | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_00139 | 1.1e-275 | E | amino acid | |||
PJBMHNLJ_00140 | 6.4e-28 | ptsH | G | phosphocarrier protein HPR | ||
PJBMHNLJ_00141 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
PJBMHNLJ_00142 | 4e-66 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
PJBMHNLJ_00143 | 2.1e-117 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
PJBMHNLJ_00144 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
PJBMHNLJ_00145 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
PJBMHNLJ_00146 | 1.2e-166 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
PJBMHNLJ_00147 | 1.4e-136 | fruR | K | DeoR C terminal sensor domain | ||
PJBMHNLJ_00148 | 2.3e-31 | 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 | |
PJBMHNLJ_00149 | 7.3e-112 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
PJBMHNLJ_00150 | 1e-47 | |||||
PJBMHNLJ_00151 | 3.7e-266 | recN | L | May be involved in recombinational repair of damaged DNA | ||
PJBMHNLJ_00152 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
PJBMHNLJ_00153 | 5.2e-136 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
PJBMHNLJ_00154 | 1.6e-168 | 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 | ||
PJBMHNLJ_00155 | 1.4e-82 | 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 | |
PJBMHNLJ_00156 | 3.6e-174 | phoH | T | phosphate starvation-inducible protein PhoH | ||
PJBMHNLJ_00157 | 6.8e-26 | yqeY | S | YqeY-like protein | ||
PJBMHNLJ_00158 | 5.1e-18 | comFA | L | Helicase C-terminal domain protein | ||
PJBMHNLJ_00159 | 5.8e-115 | yvyE | 3.4.13.9 | S | YigZ family | |
PJBMHNLJ_00160 | 3.5e-192 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
PJBMHNLJ_00161 | 2.1e-160 | rny | S | Endoribonuclease that initiates mRNA decay | ||
PJBMHNLJ_00163 | 2.2e-145 | arbV | 2.3.1.51 | I | Acyl-transferase | |
PJBMHNLJ_00164 | 1.6e-154 | arbx | M | Glycosyl transferase family 8 | ||
PJBMHNLJ_00165 | 3.8e-184 | arbY | M | Glycosyl transferase family 8 | ||
PJBMHNLJ_00166 | 1.4e-186 | arbY | M | Glycosyl transferase family 8 | ||
PJBMHNLJ_00167 | 4.7e-165 | arbZ | I | Phosphate acyltransferases | ||
PJBMHNLJ_00168 | 2.9e-246 | yhjX_2 | P | Major Facilitator Superfamily | ||
PJBMHNLJ_00169 | 2.6e-247 | yhjX_2 | P | Major Facilitator Superfamily | ||
PJBMHNLJ_00170 | 1.6e-187 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
PJBMHNLJ_00171 | 1.2e-63 | S | Peptidase propeptide and YPEB domain | |||
PJBMHNLJ_00172 | 1e-178 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
PJBMHNLJ_00173 | 5.8e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
PJBMHNLJ_00174 | 1e-182 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
PJBMHNLJ_00175 | 5.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
PJBMHNLJ_00176 | 2.6e-92 | 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 | ||
PJBMHNLJ_00177 | 1.1e-94 | 1.6.5.5 | C | nadph quinone reductase | ||
PJBMHNLJ_00178 | 2.2e-84 | K | Helix-turn-helix | |||
PJBMHNLJ_00179 | 2.2e-56 | yjdF | S | Protein of unknown function (DUF2992) | ||
PJBMHNLJ_00180 | 3.9e-93 | K | Bacterial regulatory proteins, tetR family | |||
PJBMHNLJ_00181 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
PJBMHNLJ_00182 | 5.3e-38 | |||||
PJBMHNLJ_00185 | 2.3e-195 | ampC | V | Beta-lactamase | ||
PJBMHNLJ_00186 | 4.9e-262 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain | |
PJBMHNLJ_00187 | 3.7e-60 | 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 | ||
PJBMHNLJ_00188 | 1.3e-108 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
PJBMHNLJ_00189 | 5.3e-118 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
PJBMHNLJ_00190 | 1e-209 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
PJBMHNLJ_00191 | 2.1e-88 | yqeG | S | HAD phosphatase, family IIIA | ||
PJBMHNLJ_00192 | 0.0 | aha1 | P | E1-E2 ATPase | ||
PJBMHNLJ_00193 | 7.2e-09 | 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 | |
PJBMHNLJ_00194 | 2.7e-117 | 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 | |
PJBMHNLJ_00195 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
PJBMHNLJ_00196 | 7.9e-285 | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
PJBMHNLJ_00197 | 6.6e-251 | G | Major Facilitator | |||
PJBMHNLJ_00198 | 2.3e-124 | H | Streptomycin adenylyltransferase | |||
PJBMHNLJ_00199 | 8.5e-237 | S | response to antibiotic | |||
PJBMHNLJ_00200 | 2.2e-162 | degV | S | EDD domain protein, DegV family | ||
PJBMHNLJ_00201 | 2.2e-151 | |||||
PJBMHNLJ_00202 | 3.8e-146 | K | Transcriptional regulator | |||
PJBMHNLJ_00203 | 1.1e-124 | S | Alpha/beta hydrolase family | |||
PJBMHNLJ_00204 | 8e-154 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
PJBMHNLJ_00205 | 4.8e-158 | ypuA | S | Protein of unknown function (DUF1002) | ||
PJBMHNLJ_00207 | 7.5e-140 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
PJBMHNLJ_00208 | 7.7e-174 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
PJBMHNLJ_00209 | 2.1e-123 | yugP | S | Putative neutral zinc metallopeptidase | ||
PJBMHNLJ_00210 | 5.3e-286 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
PJBMHNLJ_00211 | 9.7e-80 | |||||
PJBMHNLJ_00212 | 2.7e-134 | cobB | K | SIR2 family | ||
PJBMHNLJ_00213 | 1.6e-86 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
PJBMHNLJ_00214 | 3.6e-124 | terC | P | Integral membrane protein TerC family | ||
PJBMHNLJ_00215 | 4.4e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
PJBMHNLJ_00216 | 2e-129 | K | Transcriptional regulatory protein, C terminal | |||
PJBMHNLJ_00217 | 5.1e-66 | S | SdpI/YhfL protein family | |||
PJBMHNLJ_00218 | 3.4e-188 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
PJBMHNLJ_00219 | 4.5e-165 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
PJBMHNLJ_00220 | 1.2e-49 | dnaB | L | Replication initiation and membrane attachment | ||
PJBMHNLJ_00221 | 2.1e-160 | dnaI | L | Primosomal protein DnaI | ||
PJBMHNLJ_00222 | 2.9e-62 | 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 | ||
PJBMHNLJ_00223 | 4e-243 | 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 | ||
PJBMHNLJ_00224 | 1.2e-236 | 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 | ||
PJBMHNLJ_00225 | 3.4e-185 | D | nuclear chromosome segregation | |||
PJBMHNLJ_00226 | 2.6e-135 | rpl | K | Helix-turn-helix domain, rpiR family | ||
PJBMHNLJ_00227 | 2e-146 | K | Transcriptional regulator | |||
PJBMHNLJ_00228 | 2.8e-171 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
PJBMHNLJ_00229 | 3.2e-130 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
PJBMHNLJ_00230 | 3.5e-140 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
PJBMHNLJ_00231 | 3.2e-48 | 1.1.1.1 | C | nadph quinone reductase | ||
PJBMHNLJ_00232 | 2.4e-72 | 1.1.1.1 | C | nadph quinone reductase | ||
PJBMHNLJ_00233 | 3.2e-81 | XK27_09675 | K | Acetyltransferase (GNAT) domain | ||
PJBMHNLJ_00234 | 4e-63 | S | Protein of unknown function (DUF3021) | |||
PJBMHNLJ_00235 | 1.1e-72 | K | LytTr DNA-binding domain | |||
PJBMHNLJ_00236 | 3.5e-102 | cylB | V | ABC-2 type transporter | ||
PJBMHNLJ_00237 | 5.3e-265 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
PJBMHNLJ_00238 | 2.1e-54 | yitW | S | Iron-sulfur cluster assembly protein | ||
PJBMHNLJ_00239 | 3.4e-274 | sufB | O | assembly protein SufB | ||
PJBMHNLJ_00240 | 5e-143 | cjaA | ET | ABC transporter substrate-binding protein | ||
PJBMHNLJ_00241 | 3.4e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PJBMHNLJ_00242 | 3.9e-106 | P | ABC transporter permease | |||
PJBMHNLJ_00243 | 5.4e-113 | papP | P | ABC transporter, permease protein | ||
PJBMHNLJ_00244 | 9e-89 | |||||
PJBMHNLJ_00245 | 4.2e-121 | frnE | Q | DSBA-like thioredoxin domain | ||
PJBMHNLJ_00246 | 2.9e-216 | |||||
PJBMHNLJ_00247 | 1e-77 | S | Domain of unknown function (DUF4767) | |||
PJBMHNLJ_00248 | 8e-49 | lctP | C | L-lactate permease | ||
PJBMHNLJ_00249 | 8.7e-134 | znuB | U | ABC 3 transport family | ||
PJBMHNLJ_00250 | 7.3e-118 | fhuC | P | ABC transporter | ||
PJBMHNLJ_00251 | 7.2e-150 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
PJBMHNLJ_00252 | 1.7e-64 | S | Iron-sulphur cluster biosynthesis | |||
PJBMHNLJ_00253 | 1.7e-16 | |||||
PJBMHNLJ_00254 | 1.7e-119 | |||||
PJBMHNLJ_00256 | 3.6e-241 | ydaM | M | Glycosyl transferase | ||
PJBMHNLJ_00257 | 1.5e-153 | G | Glycosyl hydrolases family 8 | |||
PJBMHNLJ_00258 | 4.5e-120 | yfbR | S | HD containing hydrolase-like enzyme | ||
PJBMHNLJ_00259 | 1.4e-161 | L | HNH nucleases | |||
PJBMHNLJ_00260 | 2e-45 | |||||
PJBMHNLJ_00261 | 1.8e-136 | glnQ | E | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_00262 | 2.5e-297 | glnP | P | ABC transporter permease | ||
PJBMHNLJ_00263 | 1.4e-115 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
PJBMHNLJ_00264 | 6e-219 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
PJBMHNLJ_00265 | 1.1e-116 | 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 | |
PJBMHNLJ_00266 | 2.5e-60 | 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 | |||
PJBMHNLJ_00267 | 1.7e-22 | M | Lysin motif | |||
PJBMHNLJ_00268 | 7.5e-135 | 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 | |
PJBMHNLJ_00269 | 2.2e-171 | ybbR | S | YbbR-like protein | ||
PJBMHNLJ_00270 | 4.5e-255 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
PJBMHNLJ_00271 | 0.0 | XK27_08315 | M | Sulfatase | ||
PJBMHNLJ_00272 | 2.7e-73 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
PJBMHNLJ_00273 | 2.2e-292 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
PJBMHNLJ_00274 | 7.5e-83 | |||||
PJBMHNLJ_00275 | 2.1e-258 | qacA | EGP | Major facilitator Superfamily | ||
PJBMHNLJ_00276 | 6.9e-215 | 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 | |
PJBMHNLJ_00280 | 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 | ||
PJBMHNLJ_00281 | 5.1e-15 | ykzG | S | Belongs to the UPF0356 family | ||
PJBMHNLJ_00282 | 5.8e-100 | 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 | |
PJBMHNLJ_00283 | 5.7e-266 | 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 | |
PJBMHNLJ_00284 | 0.0 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
PJBMHNLJ_00285 | 1.3e-39 | spo0J | K | Belongs to the ParB family | ||
PJBMHNLJ_00286 | 2.9e-43 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
PJBMHNLJ_00287 | 2e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
PJBMHNLJ_00288 | 4e-137 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
PJBMHNLJ_00289 | 1.2e-153 | V | ABC transporter transmembrane region | |||
PJBMHNLJ_00290 | 2.9e-173 | rihB | 3.2.2.1 | F | Nucleoside | |
PJBMHNLJ_00291 | 3.4e-132 | gntR | K | UbiC transcription regulator-associated domain protein | ||
PJBMHNLJ_00292 | 1e-44 | vanZ | V | VanZ like family | ||
PJBMHNLJ_00293 | 1.9e-261 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
PJBMHNLJ_00294 | 8.2e-24 | EGP | Major facilitator Superfamily | |||
PJBMHNLJ_00295 | 1e-173 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
PJBMHNLJ_00296 | 1.3e-185 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
PJBMHNLJ_00297 | 8.6e-156 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
PJBMHNLJ_00298 | 9.8e-172 | 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 | ||
PJBMHNLJ_00299 | 7.6e-24 | |||||
PJBMHNLJ_00300 | 3.4e-183 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
PJBMHNLJ_00301 | 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 | ||
PJBMHNLJ_00302 | 1.3e-96 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
PJBMHNLJ_00303 | 9.7e-126 | comFC | S | Competence protein | ||
PJBMHNLJ_00304 | 1.1e-51 | comFA | L | Helicase C-terminal domain protein | ||
PJBMHNLJ_00305 | 1.6e-49 | |||||
PJBMHNLJ_00308 | 4e-27 | |||||
PJBMHNLJ_00309 | 4e-39 | |||||
PJBMHNLJ_00312 | 2.1e-266 | S | ABC transporter | |||
PJBMHNLJ_00313 | 1e-118 | thrE | S | Putative threonine/serine exporter | ||
PJBMHNLJ_00314 | 4.6e-66 | S | Threonine/Serine exporter, ThrE | |||
PJBMHNLJ_00315 | 2.6e-121 | tnpB | L | Putative transposase DNA-binding domain | ||
PJBMHNLJ_00316 | 2e-34 | |||||
PJBMHNLJ_00317 | 4.4e-12 | |||||
PJBMHNLJ_00318 | 9.2e-124 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
PJBMHNLJ_00319 | 0.0 | L | Helicase C-terminal domain protein | |||
PJBMHNLJ_00320 | 6.3e-154 | V | ABC transporter transmembrane region | |||
PJBMHNLJ_00321 | 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 | |
PJBMHNLJ_00322 | 6.8e-156 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
PJBMHNLJ_00323 | 3.4e-134 | 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 | |
PJBMHNLJ_00324 | 3.2e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
PJBMHNLJ_00325 | 3.3e-138 | soj | D | Sporulation initiation inhibitor | ||
PJBMHNLJ_00326 | 3.8e-154 | noc | K | Belongs to the ParB family | ||
PJBMHNLJ_00327 | 7e-130 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
PJBMHNLJ_00328 | 3.4e-166 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
PJBMHNLJ_00329 | 1e-96 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
PJBMHNLJ_00330 | 3.5e-67 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
PJBMHNLJ_00331 | 1.5e-230 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
PJBMHNLJ_00332 | 2.9e-116 | plsC | 2.3.1.51 | I | Acyltransferase | |
PJBMHNLJ_00333 | 4.5e-183 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
PJBMHNLJ_00334 | 2.7e-274 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
PJBMHNLJ_00335 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
PJBMHNLJ_00336 | 0.0 | gph | G | Transporter | ||
PJBMHNLJ_00337 | 5e-156 | msmR | K | AraC-like ligand binding domain | ||
PJBMHNLJ_00338 | 2.6e-282 | pipD | E | Dipeptidase | ||
PJBMHNLJ_00339 | 2e-43 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
PJBMHNLJ_00340 | 1.7e-81 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
PJBMHNLJ_00341 | 6.1e-32 | L | Helicase C-terminal domain protein | |||
PJBMHNLJ_00342 | 2.1e-62 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
PJBMHNLJ_00343 | 1.9e-161 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
PJBMHNLJ_00344 | 1.3e-168 | yttB | EGP | Major facilitator Superfamily | ||
PJBMHNLJ_00345 | 1.5e-186 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
PJBMHNLJ_00346 | 2.3e-34 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
PJBMHNLJ_00347 | 2e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
PJBMHNLJ_00348 | 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 | ||
PJBMHNLJ_00349 | 0.0 | V | ABC transporter | |||
PJBMHNLJ_00350 | 7e-184 | V | ABC transporter, ATP-binding protein | |||
PJBMHNLJ_00351 | 1.3e-57 | yrvN | L | AAA C-terminal domain | ||
PJBMHNLJ_00352 | 4.5e-13 | rarA | L | atpase related to the helicase subunit of the holliday junction resolvase | ||
PJBMHNLJ_00353 | 6.7e-154 | 4.1.1.45 | S | Amidohydrolase | ||
PJBMHNLJ_00354 | 1.3e-32 | |||||
PJBMHNLJ_00355 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
PJBMHNLJ_00356 | 1.2e-140 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
PJBMHNLJ_00357 | 1.1e-175 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
PJBMHNLJ_00358 | 6.6e-119 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
PJBMHNLJ_00359 | 5.4e-256 | 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 | ||
PJBMHNLJ_00360 | 7.3e-103 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
PJBMHNLJ_00361 | 1.5e-77 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PJBMHNLJ_00362 | 1.1e-42 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PJBMHNLJ_00363 | 2.5e-308 | S | Bacterial membrane protein, YfhO | |||
PJBMHNLJ_00364 | 5.1e-220 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
PJBMHNLJ_00365 | 2.6e-35 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
PJBMHNLJ_00366 | 3e-130 | 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 | |
PJBMHNLJ_00367 | 6.6e-131 | S | membrane transporter protein | |||
PJBMHNLJ_00368 | 3.9e-156 | yeaE | S | Aldo/keto reductase family | ||
PJBMHNLJ_00369 | 2.3e-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 | |
PJBMHNLJ_00370 | 2.9e-119 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
PJBMHNLJ_00371 | 8.5e-122 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
PJBMHNLJ_00372 | 6.8e-212 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
PJBMHNLJ_00374 | 4e-232 | pbuG | S | permease | ||
PJBMHNLJ_00375 | 3.2e-111 | K | helix_turn_helix, mercury resistance | |||
PJBMHNLJ_00376 | 6.4e-96 | cvpA | S | Colicin V production protein | ||
PJBMHNLJ_00377 | 1.2e-179 | 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 | |
PJBMHNLJ_00378 | 6.3e-148 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
PJBMHNLJ_00379 | 1.5e-73 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
PJBMHNLJ_00380 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
PJBMHNLJ_00381 | 3e-215 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
PJBMHNLJ_00382 | 6e-139 | ykuT | M | mechanosensitive ion channel | ||
PJBMHNLJ_00383 | 1.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
PJBMHNLJ_00384 | 9.1e-130 | glnH | ET | ABC transporter | ||
PJBMHNLJ_00385 | 3.6e-137 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
PJBMHNLJ_00386 | 3.1e-150 | glnH | ET | ABC transporter | ||
PJBMHNLJ_00387 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
PJBMHNLJ_00388 | 4.9e-74 | uvrA3 | L | excinuclease ABC, A subunit | ||
PJBMHNLJ_00389 | 2.3e-57 | gpsB | D | DivIVA domain protein | ||
PJBMHNLJ_00390 | 1.2e-91 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
PJBMHNLJ_00391 | 4.6e-111 | G | phosphoglycerate mutase | |||
PJBMHNLJ_00392 | 5.2e-113 | G | Phosphoglycerate mutase family | |||
PJBMHNLJ_00393 | 1.3e-218 | 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 | |
PJBMHNLJ_00394 | 1.3e-243 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
PJBMHNLJ_00395 | 1.1e-264 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
PJBMHNLJ_00396 | 9e-173 | |||||
PJBMHNLJ_00397 | 5.4e-39 | |||||
PJBMHNLJ_00398 | 1.8e-215 | lmrP | E | Major Facilitator Superfamily | ||
PJBMHNLJ_00399 | 2.7e-143 | pbpX2 | V | Beta-lactamase | ||
PJBMHNLJ_00400 | 1.5e-252 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
PJBMHNLJ_00401 | 8.8e-37 | 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 | |
PJBMHNLJ_00402 | 6.1e-235 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
PJBMHNLJ_00403 | 1.9e-291 | 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 | |
PJBMHNLJ_00405 | 3.9e-39 | |||||
PJBMHNLJ_00406 | 7.5e-203 | ywhK | S | Membrane | ||
PJBMHNLJ_00407 | 4.5e-222 | ecsB | U | ABC transporter | ||
PJBMHNLJ_00408 | 5.2e-124 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
PJBMHNLJ_00409 | 1.1e-62 | |||||
PJBMHNLJ_00410 | 1.1e-191 | L | COG3547 Transposase and inactivated derivatives | |||
PJBMHNLJ_00411 | 2.8e-25 | |||||
PJBMHNLJ_00412 | 1.1e-48 | XK27_01125 | L | PFAM IS66 Orf2 family protein | ||
PJBMHNLJ_00413 | 7.4e-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 | |
PJBMHNLJ_00414 | 2.3e-196 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PJBMHNLJ_00415 | 1.5e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
PJBMHNLJ_00416 | 2.5e-155 | 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 | |
PJBMHNLJ_00417 | 4.1e-50 | S | Iron-sulfur cluster assembly protein | |||
PJBMHNLJ_00418 | 6.7e-151 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
PJBMHNLJ_00419 | 3e-125 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
PJBMHNLJ_00420 | 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 | |
PJBMHNLJ_00421 | 2.8e-244 | yjjP | S | Putative threonine/serine exporter | ||
PJBMHNLJ_00422 | 1.7e-227 | sptS | 2.7.13.3 | T | Histidine kinase | |
PJBMHNLJ_00423 | 1.8e-116 | K | response regulator | |||
PJBMHNLJ_00424 | 1.2e-111 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
PJBMHNLJ_00425 | 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 | ||
PJBMHNLJ_00426 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
PJBMHNLJ_00427 | 5.1e-58 | yqhL | P | Rhodanese-like protein | ||
PJBMHNLJ_00428 | 8.1e-19 | S | Protein of unknown function (DUF3042) | |||
PJBMHNLJ_00429 | 2e-169 | 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) | |
PJBMHNLJ_00430 | 6.3e-142 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
PJBMHNLJ_00431 | 2.4e-254 | emrY | EGP | Major facilitator Superfamily | ||
PJBMHNLJ_00432 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
PJBMHNLJ_00433 | 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 | ||
PJBMHNLJ_00434 | 9.3e-101 | 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 | |
PJBMHNLJ_00435 | 1.4e-184 | 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 | |
PJBMHNLJ_00436 | 3.5e-39 | yajC | U | Preprotein translocase | ||
PJBMHNLJ_00437 | 1e-281 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
PJBMHNLJ_00438 | 1.3e-207 | 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 | |
PJBMHNLJ_00439 | 1.9e-183 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
PJBMHNLJ_00440 | 2.6e-226 | 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 | |
PJBMHNLJ_00441 | 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 | |
PJBMHNLJ_00442 | 2.6e-42 | yrzL | S | Belongs to the UPF0297 family | ||
PJBMHNLJ_00443 | 3e-72 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
PJBMHNLJ_00444 | 4.2e-39 | yrzB | S | Belongs to the UPF0473 family | ||
PJBMHNLJ_00445 | 3.9e-93 | cvpA | S | Colicin V production protein | ||
PJBMHNLJ_00446 | 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 | ||
PJBMHNLJ_00447 | 1.1e-52 | trxA | O | Belongs to the thioredoxin family | ||
PJBMHNLJ_00448 | 3.2e-68 | yslB | S | Protein of unknown function (DUF2507) | ||
PJBMHNLJ_00449 | 5.4e-170 | 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 | ||
PJBMHNLJ_00450 | 3.3e-283 | 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 | |
PJBMHNLJ_00451 | 9.8e-92 | 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 | ||
PJBMHNLJ_00452 | 3.1e-52 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
PJBMHNLJ_00453 | 4.7e-26 | 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 | ||
PJBMHNLJ_00454 | 5e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
PJBMHNLJ_00455 | 1.5e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
PJBMHNLJ_00456 | 5.9e-188 | 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 | |
PJBMHNLJ_00457 | 7.1e-158 | 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 | |
PJBMHNLJ_00458 | 2.9e-196 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
PJBMHNLJ_00459 | 1.3e-221 | sufD | O | FeS assembly protein SufD | ||
PJBMHNLJ_00460 | 1.4e-47 | sufC | O | FeS assembly ATPase SufC | ||
PJBMHNLJ_00461 | 1.7e-38 | asp1 | S | Accessory Sec system protein Asp1 | ||
PJBMHNLJ_00462 | 2.2e-31 | asp1 | S | Accessory Sec system protein Asp1 | ||
PJBMHNLJ_00463 | 3.1e-300 | asp2 | 3.4.11.5 | S | Accessory Sec system GspB-transporter | |
PJBMHNLJ_00464 | 2.1e-18 | naiP | EGP | Major facilitator Superfamily | ||
PJBMHNLJ_00465 | 2.1e-279 | pipD | E | Peptidase family C69 | ||
PJBMHNLJ_00466 | 1.4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
PJBMHNLJ_00467 | 1.6e-307 | yloV | S | DAK2 domain fusion protein YloV | ||
PJBMHNLJ_00468 | 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 | |
PJBMHNLJ_00469 | 5.1e-19 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
PJBMHNLJ_00470 | 3.3e-191 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
PJBMHNLJ_00471 | 1.3e-276 | ybiT | S | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_00472 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
PJBMHNLJ_00473 | 6.2e-91 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
PJBMHNLJ_00474 | 1.9e-17 | pncA | Q | Isochorismatase family | ||
PJBMHNLJ_00475 | 7.9e-282 | 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 | ||
PJBMHNLJ_00476 | 6.1e-214 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_00477 | 2.9e-90 | ymdB | S | Macro domain protein | ||
PJBMHNLJ_00478 | 2.4e-295 | V | ABC transporter transmembrane region | |||
PJBMHNLJ_00479 | 3.2e-124 | puuD | S | peptidase C26 | ||
PJBMHNLJ_00480 | 2.5e-217 | mdtG | EGP | Major facilitator Superfamily | ||
PJBMHNLJ_00481 | 1.2e-17 | |||||
PJBMHNLJ_00482 | 3.8e-125 | |||||
PJBMHNLJ_00483 | 4.3e-71 | aroD | 1.1.1.25, 4.2.1.10 | E | 3-dehydroquinate dehydratase activity | |
PJBMHNLJ_00484 | 8e-156 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
PJBMHNLJ_00485 | 1.7e-151 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
PJBMHNLJ_00486 | 9.2e-63 | 3.4.16.4, 3.5.2.6 | V | Beta-lactamase enzyme family | ||
PJBMHNLJ_00487 | 4.9e-60 | 3.4.16.4, 3.5.2.6 | V | Beta-lactamase enzyme family | ||
PJBMHNLJ_00488 | 7.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
PJBMHNLJ_00489 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
PJBMHNLJ_00490 | 1.1e-206 | EGP | Major facilitator Superfamily | |||
PJBMHNLJ_00491 | 1.4e-89 | glnA | 6.3.1.2 | E | glutamine synthetase | |
PJBMHNLJ_00492 | 2e-57 | |||||
PJBMHNLJ_00493 | 1.9e-86 | |||||
PJBMHNLJ_00494 | 1.3e-218 | L | Initiator Replication protein | |||
PJBMHNLJ_00495 | 3.5e-68 | |||||
PJBMHNLJ_00496 | 1.2e-152 | glcU | U | sugar transport | ||
PJBMHNLJ_00497 | 2.2e-170 | yqhA | G | Aldose 1-epimerase | ||
PJBMHNLJ_00498 | 1e-81 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
PJBMHNLJ_00499 | 1e-102 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
PJBMHNLJ_00500 | 5.6e-91 | 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 | |
PJBMHNLJ_00501 | 4.2e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
PJBMHNLJ_00502 | 3.5e-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 | |
PJBMHNLJ_00503 | 1.6e-149 | 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 | ||
PJBMHNLJ_00504 | 5.9e-43 | |||||
PJBMHNLJ_00505 | 7.7e-122 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
PJBMHNLJ_00506 | 1.2e-61 | |||||
PJBMHNLJ_00507 | 3.4e-46 | S | MazG-like family | |||
PJBMHNLJ_00508 | 1.2e-82 | FG | HIT domain | |||
PJBMHNLJ_00509 | 2.8e-86 | |||||
PJBMHNLJ_00510 | 7.2e-31 | S | Membrane | |||
PJBMHNLJ_00511 | 1e-27 | ybaJ | Q | Methyltransferase domain | ||
PJBMHNLJ_00512 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
PJBMHNLJ_00513 | 2.2e-24 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
PJBMHNLJ_00514 | 6.6e-99 | aspC | 2.6.1.1 | E | Aminotransferase | |
PJBMHNLJ_00515 | 3.5e-194 | 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 | |
PJBMHNLJ_00516 | 1e-159 | ypbG | 2.7.1.2 | GK | ROK family | |
PJBMHNLJ_00517 | 6.8e-283 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
PJBMHNLJ_00518 | 1.5e-269 | 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 | ||
PJBMHNLJ_00519 | 2.6e-52 | ptcB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
PJBMHNLJ_00520 | 7.9e-41 | |||||
PJBMHNLJ_00521 | 1.5e-50 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
PJBMHNLJ_00522 | 9.5e-135 | gmuR | K | UTRA | ||
PJBMHNLJ_00523 | 3.1e-305 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
PJBMHNLJ_00524 | 2.4e-71 | S | Domain of unknown function (DUF3284) | |||
PJBMHNLJ_00525 | 8.8e-130 | yydK | K | UTRA | ||
PJBMHNLJ_00526 | 2.9e-94 | lmrA | 3.6.3.44 | V | ABC transporter | |
PJBMHNLJ_00527 | 5.6e-62 | lmrA | 3.6.3.44 | V | ABC transporter | |
PJBMHNLJ_00528 | 6.8e-133 | C | Aldo keto reductase | |||
PJBMHNLJ_00529 | 2e-18 | K | Transcriptional regulator | |||
PJBMHNLJ_00530 | 5.2e-113 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
PJBMHNLJ_00531 | 2.5e-152 | 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 | |
PJBMHNLJ_00532 | 2.4e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
PJBMHNLJ_00533 | 4e-87 | 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 | ||
PJBMHNLJ_00534 | 5e-202 | S | CAAX protease self-immunity | |||
PJBMHNLJ_00535 | 6e-76 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
PJBMHNLJ_00536 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
PJBMHNLJ_00537 | 5.8e-59 | ftsW | D | Belongs to the SEDS family | ||
PJBMHNLJ_00538 | 0.0 | typA | T | GTP-binding protein TypA | ||
PJBMHNLJ_00539 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
PJBMHNLJ_00540 | 7.6e-91 | N | Uncharacterized conserved protein (DUF2075) | |||
PJBMHNLJ_00541 | 2.7e-307 | pepF | E | oligoendopeptidase F | ||
PJBMHNLJ_00542 | 4.6e-74 | lctP | C | L-lactate permease | ||
PJBMHNLJ_00543 | 1.1e-23 | yycI | S | YycH protein | ||
PJBMHNLJ_00544 | 3.7e-148 | vicX | 3.1.26.11 | S | domain protein | |
PJBMHNLJ_00545 | 1e-69 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
PJBMHNLJ_00546 | 7.7e-82 | nrdI | F | Belongs to the NrdI family | ||
PJBMHNLJ_00547 | 1.2e-109 | |||||
PJBMHNLJ_00548 | 1.2e-65 | S | O-antigen ligase like membrane protein | |||
PJBMHNLJ_00549 | 1.1e-132 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
PJBMHNLJ_00550 | 2.4e-46 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
PJBMHNLJ_00551 | 9.7e-42 | 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 | ||
PJBMHNLJ_00552 | 3.6e-177 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
PJBMHNLJ_00553 | 4.7e-161 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
PJBMHNLJ_00554 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
PJBMHNLJ_00555 | 1.4e-167 | 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 | ||
PJBMHNLJ_00556 | 3.1e-195 | 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 | ||
PJBMHNLJ_00557 | 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 | ||
PJBMHNLJ_00558 | 4.3e-80 | pfkB | 2.7.1.11, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
PJBMHNLJ_00559 | 5.1e-226 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
PJBMHNLJ_00560 | 1.4e-153 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
PJBMHNLJ_00561 | 2.2e-75 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
PJBMHNLJ_00562 | 7.4e-247 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
PJBMHNLJ_00563 | 6.2e-212 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
PJBMHNLJ_00564 | 2.4e-144 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
PJBMHNLJ_00565 | 6.1e-243 | cpdA | S | Calcineurin-like phosphoesterase | ||
PJBMHNLJ_00566 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
PJBMHNLJ_00567 | 7.4e-203 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
PJBMHNLJ_00568 | 5.7e-10 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
PJBMHNLJ_00569 | 7.8e-136 | qmcA | O | prohibitin homologues | ||
PJBMHNLJ_00570 | 3e-68 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
PJBMHNLJ_00571 | 1e-68 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
PJBMHNLJ_00572 | 1.7e-09 | S | Peptidase propeptide and YPEB domain | |||
PJBMHNLJ_00574 | 5.6e-39 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
PJBMHNLJ_00575 | 7.3e-83 | |||||
PJBMHNLJ_00576 | 3.1e-275 | S | Calcineurin-like phosphoesterase | |||
PJBMHNLJ_00577 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
PJBMHNLJ_00578 | 3.3e-266 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
PJBMHNLJ_00579 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
PJBMHNLJ_00580 | 3.1e-130 | 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 | |
PJBMHNLJ_00581 | 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 | ||
PJBMHNLJ_00582 | 6.6e-44 | 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 | ||
PJBMHNLJ_00583 | 5.5e-259 | emrY | EGP | Major facilitator Superfamily | ||
PJBMHNLJ_00584 | 5.5e-74 | 2.3.1.128 | K | acetyltransferase | ||
PJBMHNLJ_00585 | 4.1e-66 | S | Putative adhesin | |||
PJBMHNLJ_00586 | 2.1e-79 | |||||
PJBMHNLJ_00587 | 1.1e-31 | hxlR | K | Transcriptional regulator, HxlR family | ||
PJBMHNLJ_00588 | 6.8e-286 | pipD | E | Dipeptidase | ||
PJBMHNLJ_00589 | 4.3e-89 | 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) | ||
PJBMHNLJ_00590 | 8.4e-57 | S | PAS domain | |||
PJBMHNLJ_00591 | 9.1e-142 | |||||
PJBMHNLJ_00592 | 3.6e-140 | |||||
PJBMHNLJ_00593 | 4.7e-117 | C | nitroreductase | |||
PJBMHNLJ_00594 | 3e-239 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
PJBMHNLJ_00595 | 5.9e-62 | |||||
PJBMHNLJ_00596 | 5.5e-201 | S | Cysteine-rich secretory protein family | |||
PJBMHNLJ_00597 | 6.8e-116 | EGP | Sugar (and other) transporter | |||
PJBMHNLJ_00598 | 5.1e-69 | S | Iron-sulphur cluster biosynthesis | |||
PJBMHNLJ_00599 | 3.2e-11 | S | RelB antitoxin | |||
PJBMHNLJ_00600 | 4.8e-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 | |
PJBMHNLJ_00601 | 3.1e-34 | yjeM | E | Amino Acid | ||
PJBMHNLJ_00602 | 6.7e-84 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
PJBMHNLJ_00603 | 1.8e-228 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
PJBMHNLJ_00604 | 1.6e-216 | agaS | G | SIS domain | ||
PJBMHNLJ_00605 | 1.5e-129 | XK27_08435 | K | UTRA | ||
PJBMHNLJ_00606 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
PJBMHNLJ_00607 | 1.1e-155 | I | alpha/beta hydrolase fold | |||
PJBMHNLJ_00608 | 1.2e-119 | yibF | S | overlaps another CDS with the same product name | ||
PJBMHNLJ_00609 | 3.8e-105 | K | LysR substrate binding domain | |||
PJBMHNLJ_00610 | 2.8e-173 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
PJBMHNLJ_00611 | 2.3e-51 | S | Protein of unknown function (DUF3397) | |||
PJBMHNLJ_00612 | 4.1e-77 | mraZ | K | Belongs to the MraZ family | ||
PJBMHNLJ_00613 | 3.2e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
PJBMHNLJ_00614 | 3.9e-96 | yobS | K | Bacterial regulatory proteins, tetR family | ||
PJBMHNLJ_00615 | 5.4e-145 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
PJBMHNLJ_00616 | 7.6e-126 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
PJBMHNLJ_00617 | 1.3e-173 | degV | S | DegV family | ||
PJBMHNLJ_00618 | 9.5e-79 | |||||
PJBMHNLJ_00619 | 4.8e-207 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
PJBMHNLJ_00620 | 8.2e-63 | 2.4.2.3 | F | Phosphorylase superfamily | ||
PJBMHNLJ_00621 | 4.1e-72 | 6.3.3.2 | S | ASCH | ||
PJBMHNLJ_00622 | 2.7e-79 | 5.4.2.11 | G | Phosphoglycerate mutase family | ||
PJBMHNLJ_00623 | 1.5e-86 | 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 | |
PJBMHNLJ_00624 | 2e-91 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
PJBMHNLJ_00625 | 1e-57 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
PJBMHNLJ_00626 | 1.7e-136 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
PJBMHNLJ_00627 | 2.6e-16 | UW | Tetratricopeptide repeat | |||
PJBMHNLJ_00628 | 5.5e-283 | 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 | |
PJBMHNLJ_00629 | 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 | |
PJBMHNLJ_00630 | 0.0 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
PJBMHNLJ_00631 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
PJBMHNLJ_00632 | 5.7e-186 | V | ABC transporter transmembrane region | |||
PJBMHNLJ_00633 | 9.8e-112 | K | transcriptional regulator | |||
PJBMHNLJ_00634 | 2.3e-95 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
PJBMHNLJ_00635 | 1.4e-87 | htpX | O | Peptidase family M48 | ||
PJBMHNLJ_00636 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
PJBMHNLJ_00637 | 2.1e-67 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
PJBMHNLJ_00638 | 7.6e-79 | yjcF | S | Acetyltransferase (GNAT) domain | ||
PJBMHNLJ_00639 | 2e-166 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
PJBMHNLJ_00640 | 1.2e-296 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
PJBMHNLJ_00641 | 1.9e-109 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
PJBMHNLJ_00642 | 8.1e-51 | 1.6.5.2 | GM | NmrA-like family | ||
PJBMHNLJ_00643 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
PJBMHNLJ_00644 | 4.2e-227 | 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 | |
PJBMHNLJ_00645 | 8.1e-123 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
PJBMHNLJ_00646 | 1.8e-47 | veg | S | Biofilm formation stimulator VEG | ||
PJBMHNLJ_00647 | 5.8e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
PJBMHNLJ_00648 | 1.5e-82 | tlpA2 | L | Transposase IS200 like | ||
PJBMHNLJ_00649 | 1.2e-227 | tnp | L | MULE transposase domain | ||
PJBMHNLJ_00650 | 1.3e-52 | |||||
PJBMHNLJ_00651 | 2.7e-148 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
PJBMHNLJ_00652 | 1.7e-17 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
PJBMHNLJ_00653 | 0.0 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
PJBMHNLJ_00654 | 3.1e-127 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
PJBMHNLJ_00655 | 9.6e-144 | rpiR1 | K | Helix-turn-helix domain, rpiR family | ||
PJBMHNLJ_00656 | 0.0 | 3.6.3.8 | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
PJBMHNLJ_00657 | 4.2e-242 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
PJBMHNLJ_00658 | 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 | |
PJBMHNLJ_00661 | 6.2e-128 | mrr | L | restriction endonuclease | ||
PJBMHNLJ_00663 | 1.2e-105 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
PJBMHNLJ_00664 | 7.4e-76 | M | domain protein | |||
PJBMHNLJ_00665 | 3.2e-90 | lemA | S | LemA family | ||
PJBMHNLJ_00666 | 1.8e-157 | ybiR | P | Citrate transporter | ||
PJBMHNLJ_00667 | 7.8e-88 | |||||
PJBMHNLJ_00668 | 7e-112 | ygaC | J | Belongs to the UPF0374 family | ||
PJBMHNLJ_00669 | 7.8e-146 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
PJBMHNLJ_00671 | 4.9e-76 | S | Putative adhesin | |||
PJBMHNLJ_00673 | 8.1e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
PJBMHNLJ_00674 | 2.6e-197 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
PJBMHNLJ_00675 | 1.1e-167 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
PJBMHNLJ_00676 | 2.8e-238 | G | Bacterial extracellular solute-binding protein | |||
PJBMHNLJ_00677 | 1.7e-176 | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | ||
PJBMHNLJ_00678 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
PJBMHNLJ_00679 | 2.6e-222 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
PJBMHNLJ_00680 | 5e-63 | |||||
PJBMHNLJ_00681 | 8.9e-109 | |||||
PJBMHNLJ_00682 | 2e-188 | S | Bacteriocin helveticin-J | |||
PJBMHNLJ_00683 | 7e-240 | yagE | E | amino acid | ||
PJBMHNLJ_00684 | 6.8e-65 | S | Psort location Cytoplasmic, score 8.96 | |||
PJBMHNLJ_00686 | 4.6e-23 | S | Lipocalin-like domain | |||
PJBMHNLJ_00687 | 4.5e-127 | ptsC | G | PTS system sorbose-specific iic component | ||
PJBMHNLJ_00688 | 2e-80 | ptsB | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
PJBMHNLJ_00689 | 3.2e-55 | 2.7.1.191 | G | PTS system fructose IIA component | ||
PJBMHNLJ_00690 | 2.3e-93 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
PJBMHNLJ_00691 | 2e-126 | yfeJ | 6.3.5.2 | F | Glutamine amidotransferase class-I | |
PJBMHNLJ_00692 | 7.6e-71 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
PJBMHNLJ_00693 | 4.6e-194 | 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 | ||
PJBMHNLJ_00694 | 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 | ||
PJBMHNLJ_00695 | 1e-116 | 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) | |
PJBMHNLJ_00696 | 1.1e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
PJBMHNLJ_00697 | 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 | |
PJBMHNLJ_00698 | 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 | |
PJBMHNLJ_00699 | 6.4e-141 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
PJBMHNLJ_00700 | 4.7e-123 | ABC-SBP | S | ABC transporter | ||
PJBMHNLJ_00701 | 1.5e-220 | natB | CP | ABC-2 family transporter protein | ||
PJBMHNLJ_00702 | 3.2e-77 | natA | S | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_00703 | 5.4e-32 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
PJBMHNLJ_00704 | 5.3e-195 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
PJBMHNLJ_00705 | 4.1e-124 | S | SNARE associated Golgi protein | |||
PJBMHNLJ_00706 | 1.1e-245 | steT | E | amino acid | ||
PJBMHNLJ_00708 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
PJBMHNLJ_00709 | 2.5e-218 | 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) | |
PJBMHNLJ_00710 | 2.5e-275 | L | Psort location Cytoplasmic, score | |||
PJBMHNLJ_00711 | 5.2e-306 | gadC | E | Contains amino acid permease domain | ||
PJBMHNLJ_00713 | 4.4e-299 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
PJBMHNLJ_00714 | 2.5e-125 | K | Psort location CytoplasmicMembrane, score | |||
PJBMHNLJ_00715 | 2.4e-101 | 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 | |
PJBMHNLJ_00716 | 1.1e-232 | pbuX | F | xanthine permease | ||
PJBMHNLJ_00717 | 2.5e-239 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
PJBMHNLJ_00718 | 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 | |
PJBMHNLJ_00719 | 2.5e-63 | 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 | ||
PJBMHNLJ_00720 | 4.4e-68 | S | Domain of unknown function (DUF1934) | |||
PJBMHNLJ_00721 | 1.4e-264 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
PJBMHNLJ_00722 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
PJBMHNLJ_00723 | 1.6e-152 | malG | P | ABC transporter permease | ||
PJBMHNLJ_00724 | 2.3e-251 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
PJBMHNLJ_00725 | 7.4e-217 | malE | G | Bacterial extracellular solute-binding protein | ||
PJBMHNLJ_00726 | 1.2e-208 | msmX | P | Belongs to the ABC transporter superfamily | ||
PJBMHNLJ_00728 | 5.7e-42 | L | Replication initiation factor | |||
PJBMHNLJ_00736 | 2e-10 | S | Helix-turn-helix domain | |||
PJBMHNLJ_00737 | 1.4e-14 | K | Transcriptional | |||
PJBMHNLJ_00738 | 1.5e-78 | 3.6.1.55 | L | NUDIX domain | ||
PJBMHNLJ_00739 | 7.4e-107 | neo | 2.7.1.87, 2.7.1.95 | F | Belongs to the aminoglycoside phosphotransferase family | |
PJBMHNLJ_00740 | 2.4e-212 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
PJBMHNLJ_00741 | 6.1e-126 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
PJBMHNLJ_00742 | 2.3e-69 | K | helix_turn_helix multiple antibiotic resistance protein | |||
PJBMHNLJ_00743 | 6.7e-34 | |||||
PJBMHNLJ_00744 | 1.3e-168 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
PJBMHNLJ_00745 | 5.4e-95 | nqr | 1.5.1.36 | S | reductase | |
PJBMHNLJ_00746 | 3.7e-99 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
PJBMHNLJ_00747 | 2.3e-259 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
PJBMHNLJ_00748 | 4.9e-34 | |||||
PJBMHNLJ_00749 | 1.7e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
PJBMHNLJ_00750 | 2.3e-33 | cspA | K | 'Cold-shock' DNA-binding domain | ||
PJBMHNLJ_00751 | 4.1e-101 | 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) | |
PJBMHNLJ_00752 | 2.2e-111 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
PJBMHNLJ_00753 | 1.7e-100 | S | ECF transporter, substrate-specific component | |||
PJBMHNLJ_00755 | 8.1e-163 | mleP3 | S | Membrane transport protein | ||
PJBMHNLJ_00756 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
PJBMHNLJ_00757 | 4.9e-201 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
PJBMHNLJ_00758 | 6.2e-63 | yodB | K | Transcriptional regulator, HxlR family | ||
PJBMHNLJ_00759 | 2.8e-137 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
PJBMHNLJ_00760 | 3.8e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
PJBMHNLJ_00761 | 3.2e-170 | 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 | ||
PJBMHNLJ_00762 | 7.6e-36 | 3.6.1.55 | F | NUDIX domain | ||
PJBMHNLJ_00763 | 3.4e-114 | 2.4.2.3 | F | Phosphorylase superfamily | ||
PJBMHNLJ_00764 | 1.3e-67 | UW | Tetratricopeptide repeat | |||
PJBMHNLJ_00766 | 2.1e-230 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
PJBMHNLJ_00767 | 1.2e-227 | 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 | |
PJBMHNLJ_00768 | 1.1e-119 | ftsW | D | Belongs to the SEDS family | ||
PJBMHNLJ_00769 | 7.4e-50 | ylbG | S | UPF0298 protein | ||
PJBMHNLJ_00770 | 1.2e-94 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
PJBMHNLJ_00771 | 6.5e-32 | |||||
PJBMHNLJ_00772 | 4.6e-90 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
PJBMHNLJ_00773 | 2.4e-175 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
PJBMHNLJ_00774 | 2.6e-113 | mgtC | S | MgtC family | ||
PJBMHNLJ_00775 | 4.5e-149 | ptsD | G | PTS system mannose/fructose/sorbose family IID component | ||
PJBMHNLJ_00776 | 7.2e-68 | 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) | |
PJBMHNLJ_00777 | 2.3e-179 | 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 | |
PJBMHNLJ_00778 | 1.4e-95 | 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 | |
PJBMHNLJ_00779 | 3.7e-154 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
PJBMHNLJ_00780 | 4.4e-58 | yabA | L | Involved in initiation control of chromosome replication | ||
PJBMHNLJ_00781 | 3.1e-153 | holB | 2.7.7.7 | L | DNA polymerase III | |
PJBMHNLJ_00782 | 5e-51 | yaaQ | S | Cyclic-di-AMP receptor | ||
PJBMHNLJ_00783 | 3.1e-113 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
PJBMHNLJ_00784 | 9e-26 | S | Protein of unknown function (DUF2508) | |||
PJBMHNLJ_00785 | 8.1e-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 | ||
PJBMHNLJ_00786 | 1.7e-51 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
PJBMHNLJ_00787 | 1.7e-294 | 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 | |
PJBMHNLJ_00788 | 1e-84 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
PJBMHNLJ_00789 | 1.1e-136 | glcR | K | DeoR C terminal sensor domain | ||
PJBMHNLJ_00790 | 1e-153 | I | alpha/beta hydrolase fold | |||
PJBMHNLJ_00791 | 3.7e-134 | hipB | K | Helix-turn-helix | ||
PJBMHNLJ_00792 | 1.2e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
PJBMHNLJ_00793 | 4.6e-120 | yihY | S | Belongs to the UPF0761 family | ||
PJBMHNLJ_00794 | 1.7e-28 | S | Psort location Cytoplasmic, score 8.87 | |||
PJBMHNLJ_00795 | 1.9e-82 | V | ABC-type multidrug transport system, ATPase and permease components | |||
PJBMHNLJ_00796 | 9.9e-118 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
PJBMHNLJ_00797 | 9.8e-134 | hrtB | V | ABC transporter permease | ||
PJBMHNLJ_00798 | 5.7e-98 | V | FtsX-like permease family | |||
PJBMHNLJ_00799 | 4.7e-125 | pgm3 | G | Phosphoglycerate mutase family | ||
PJBMHNLJ_00800 | 2.8e-26 | |||||
PJBMHNLJ_00801 | 7.3e-228 | S | Bacterial membrane protein, YfhO | |||
PJBMHNLJ_00802 | 2.4e-256 | 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 | ||
PJBMHNLJ_00803 | 1.2e-205 | 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 | |
PJBMHNLJ_00804 | 1.6e-20 | yaaA | S | S4 domain | ||
PJBMHNLJ_00805 | 1.2e-208 | 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 | ||
PJBMHNLJ_00806 | 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 | |
PJBMHNLJ_00807 | 2.9e-45 | 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) | |
PJBMHNLJ_00808 | 2.3e-131 | 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) | |
PJBMHNLJ_00809 | 4.1e-181 | baeS | F | Sensor histidine kinase | ||
PJBMHNLJ_00810 | 2.4e-102 | baeR | K | helix_turn_helix, Lux Regulon | ||
PJBMHNLJ_00811 | 5.5e-214 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
PJBMHNLJ_00812 | 3.7e-54 | gtcA | S | Teichoic acid glycosylation protein | ||
PJBMHNLJ_00813 | 5.8e-31 | T | Transcriptional regulatory protein, C terminal | |||
PJBMHNLJ_00814 | 4.2e-237 | T | GHKL domain | |||
PJBMHNLJ_00815 | 2.3e-140 | F | DNA/RNA non-specific endonuclease | |||
PJBMHNLJ_00816 | 8.7e-50 | L | nuclease | |||
PJBMHNLJ_00817 | 2.2e-131 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
PJBMHNLJ_00818 | 3.5e-26 | treB | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
PJBMHNLJ_00819 | 5.9e-266 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
PJBMHNLJ_00820 | 5e-274 | yjcE | P | Sodium proton antiporter | ||
PJBMHNLJ_00821 | 8.1e-302 | 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 | ||
PJBMHNLJ_00822 | 1.3e-287 | clcA | P | chloride | ||
PJBMHNLJ_00823 | 6e-271 | 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 | |
PJBMHNLJ_00824 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
PJBMHNLJ_00825 | 1.1e-251 | yfnA | E | Amino Acid | ||
PJBMHNLJ_00826 | 2e-208 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PJBMHNLJ_00827 | 2.7e-46 | |||||
PJBMHNLJ_00828 | 1.6e-171 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
PJBMHNLJ_00829 | 2.2e-254 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
PJBMHNLJ_00830 | 3.7e-18 | S | Sugar efflux transporter for intercellular exchange | |||
PJBMHNLJ_00831 | 5.8e-191 | 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 | |
PJBMHNLJ_00832 | 1.9e-227 | pts29C | 2.7.1.207 | 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 | |
PJBMHNLJ_00833 | 6.3e-15 | GT2,GT4 | M | family 8 | ||
PJBMHNLJ_00834 | 4.2e-106 | 3.2.2.20 | K | acetyltransferase | ||
PJBMHNLJ_00835 | 8.7e-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 | ||
PJBMHNLJ_00836 | 1.5e-46 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
PJBMHNLJ_00837 | 3e-75 | lacR | K | DeoR C terminal sensor domain | ||
PJBMHNLJ_00838 | 2e-71 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
PJBMHNLJ_00839 | 4.7e-105 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
PJBMHNLJ_00840 | 2.8e-130 | lacT | K | CAT RNA binding domain | ||
PJBMHNLJ_00841 | 6.9e-54 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
PJBMHNLJ_00842 | 2.6e-300 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
PJBMHNLJ_00843 | 4e-278 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
PJBMHNLJ_00844 | 3.1e-75 | K | LysR family | |||
PJBMHNLJ_00845 | 2.3e-116 | GM | NAD(P)H-binding | |||
PJBMHNLJ_00846 | 1.1e-125 | S | membrane | |||
PJBMHNLJ_00847 | 1.1e-21 | |||||
PJBMHNLJ_00848 | 1.5e-136 | |||||
PJBMHNLJ_00849 | 1e-41 | |||||
PJBMHNLJ_00850 | 3.6e-140 | 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) |
PJBMHNLJ_00851 | 2.1e-218 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
PJBMHNLJ_00852 | 9.6e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
PJBMHNLJ_00853 | 5e-254 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
PJBMHNLJ_00854 | 3.3e-58 | |||||
PJBMHNLJ_00855 | 1.6e-180 | 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) | |
PJBMHNLJ_00857 | 2e-112 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
PJBMHNLJ_00858 | 1.7e-34 | |||||
PJBMHNLJ_00859 | 3.5e-89 | yvrI | K | sigma factor activity | ||
PJBMHNLJ_00860 | 2e-140 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
PJBMHNLJ_00861 | 1.3e-78 | 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) | ||
PJBMHNLJ_00862 | 1.3e-257 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
PJBMHNLJ_00863 | 1.5e-288 | 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) | |
PJBMHNLJ_00864 | 4e-215 | frdC | 1.3.5.4 | C | FAD binding domain | |
PJBMHNLJ_00865 | 9.2e-247 | pepT | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
PJBMHNLJ_00866 | 1.9e-160 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
PJBMHNLJ_00867 | 2.4e-93 | S | Domain of unknown function (DUF4811) | |||
PJBMHNLJ_00868 | 7.4e-130 | lmrB | EGP | Major facilitator Superfamily | ||
PJBMHNLJ_00869 | 7.1e-248 | yagE | E | amino acid | ||
PJBMHNLJ_00870 | 9.8e-125 | ymfM | S | Helix-turn-helix domain | ||
PJBMHNLJ_00871 | 2.7e-35 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
PJBMHNLJ_00872 | 2.1e-205 | M | Glycosyl transferases group 1 | |||
PJBMHNLJ_00873 | 2.5e-94 | 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 | |
PJBMHNLJ_00874 | 1.5e-177 | 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 | |
PJBMHNLJ_00875 | 2.1e-42 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
PJBMHNLJ_00876 | 5.8e-138 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | G | Sucrose-6F-phosphate phosphohydrolase | ||
PJBMHNLJ_00877 | 0.0 | 2.7.7.7 | M | domain protein | ||
PJBMHNLJ_00878 | 5.6e-35 | L | Belongs to the bacterial histone-like protein family | |||
PJBMHNLJ_00879 | 3.1e-81 | rbsU | U | ribose uptake protein RbsU | ||
PJBMHNLJ_00880 | 7.7e-154 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
PJBMHNLJ_00881 | 4.4e-258 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
PJBMHNLJ_00882 | 3.1e-144 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
PJBMHNLJ_00883 | 1.7e-190 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
PJBMHNLJ_00884 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
PJBMHNLJ_00885 | 5.4e-253 | P | P-loop Domain of unknown function (DUF2791) | |||
PJBMHNLJ_00886 | 2.4e-110 | rarA | L | recombination factor protein RarA | ||
PJBMHNLJ_00888 | 5.2e-81 | usp6 | T | universal stress protein | ||
PJBMHNLJ_00889 | 2.6e-222 | rodA | D | Belongs to the SEDS family | ||
PJBMHNLJ_00890 | 6.6e-34 | S | Protein of unknown function (DUF2969) | |||
PJBMHNLJ_00891 | 5.9e-51 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
PJBMHNLJ_00892 | 6.8e-13 | S | DNA-directed RNA polymerase subunit beta | |||
PJBMHNLJ_00893 | 1.7e-179 | mbl | D | Cell shape determining protein MreB Mrl | ||
PJBMHNLJ_00894 | 2.4e-31 | ywzB | S | Protein of unknown function (DUF1146) | ||
PJBMHNLJ_00895 | 1.4e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
PJBMHNLJ_00896 | 9.7e-115 | 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 | |
PJBMHNLJ_00897 | 4.1e-240 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
PJBMHNLJ_00898 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
PJBMHNLJ_00899 | 1.3e-168 | K | LysR substrate binding domain | |||
PJBMHNLJ_00900 | 1.7e-298 | E | amino acid | |||
PJBMHNLJ_00901 | 0.0 | S | domain, Protein | |||
PJBMHNLJ_00902 | 1.5e-191 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
PJBMHNLJ_00903 | 3.4e-103 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
PJBMHNLJ_00904 | 1.4e-212 | 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 | |
PJBMHNLJ_00905 | 8.9e-256 | gor | 1.8.1.7 | C | pyridine nucleotide-disulfide oxidoreductase | |
PJBMHNLJ_00906 | 1.1e-171 | K | AI-2E family transporter | |||
PJBMHNLJ_00907 | 1.4e-159 | yhaO | L | Ser Thr phosphatase family protein | ||
PJBMHNLJ_00908 | 3.6e-55 | yheA | S | Belongs to the UPF0342 family | ||
PJBMHNLJ_00909 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
PJBMHNLJ_00910 | 7.1e-158 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
PJBMHNLJ_00912 | 2.3e-167 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
PJBMHNLJ_00913 | 3.5e-61 | 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 | ||
PJBMHNLJ_00914 | 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 | ||
PJBMHNLJ_00915 | 7.1e-47 | rplGA | J | ribosomal protein | ||
PJBMHNLJ_00916 | 1.5e-46 | ylxR | K | Protein of unknown function (DUF448) | ||
PJBMHNLJ_00917 | 3.6e-219 | nusA | K | Participates in both transcription termination and antitermination | ||
PJBMHNLJ_00918 | 3e-81 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
PJBMHNLJ_00919 | 4e-298 | ytgP | S | Polysaccharide biosynthesis protein | ||
PJBMHNLJ_00920 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
PJBMHNLJ_00921 | 3.4e-100 | 3.6.1.27 | I | Acid phosphatase homologues | ||
PJBMHNLJ_00922 | 9.9e-120 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
PJBMHNLJ_00923 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
PJBMHNLJ_00924 | 2.2e-174 | ccpA | K | catabolite control protein A | ||
PJBMHNLJ_00925 | 1.9e-211 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
PJBMHNLJ_00926 | 6.4e-139 | D | Alpha beta | |||
PJBMHNLJ_00927 | 1.6e-216 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
PJBMHNLJ_00928 | 5.6e-220 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
PJBMHNLJ_00929 | 1.2e-216 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
PJBMHNLJ_00930 | 1e-248 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
PJBMHNLJ_00931 | 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 | |
PJBMHNLJ_00932 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
PJBMHNLJ_00933 | 1.4e-32 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
PJBMHNLJ_00934 | 2.1e-227 | 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 | |
PJBMHNLJ_00935 | 1.3e-215 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
PJBMHNLJ_00936 | 1.6e-289 | 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 | ||
PJBMHNLJ_00938 | 1e-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 | ||
PJBMHNLJ_00939 | 2.4e-83 | yueI | S | Protein of unknown function (DUF1694) | ||
PJBMHNLJ_00940 | 5.5e-181 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
PJBMHNLJ_00941 | 2e-98 | S | TPM domain | |||
PJBMHNLJ_00942 | 5.6e-91 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
PJBMHNLJ_00943 | 1.2e-194 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
PJBMHNLJ_00944 | 1.2e-114 | E | Belongs to the SOS response-associated peptidase family | |||
PJBMHNLJ_00946 | 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 | |
PJBMHNLJ_00947 | 2.1e-222 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
PJBMHNLJ_00948 | 9.4e-172 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
PJBMHNLJ_00949 | 2.2e-88 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
PJBMHNLJ_00950 | 0.0 | kup | P | Transport of potassium into the cell | ||
PJBMHNLJ_00951 | 1e-72 | |||||
PJBMHNLJ_00952 | 1.9e-115 | |||||
PJBMHNLJ_00953 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
PJBMHNLJ_00954 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
PJBMHNLJ_00955 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
PJBMHNLJ_00956 | 8.4e-176 | yvdE | K | helix_turn _helix lactose operon repressor | ||
PJBMHNLJ_00957 | 1.1e-173 | 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) | |
PJBMHNLJ_00958 | 1.7e-217 | 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 | |
PJBMHNLJ_00959 | 1.5e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
PJBMHNLJ_00960 | 2.2e-35 | veg | S | Biofilm formation stimulator VEG | ||
PJBMHNLJ_00961 | 5.2e-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 | |
PJBMHNLJ_00962 | 1.2e-97 | 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 | |
PJBMHNLJ_00963 | 3.6e-148 | tatD | L | hydrolase, TatD family | ||
PJBMHNLJ_00964 | 7e-107 | 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 | |
PJBMHNLJ_00965 | 9.4e-51 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
PJBMHNLJ_00966 | 1.2e-80 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
PJBMHNLJ_00967 | 2.2e-145 | aatB | ET | ABC transporter substrate-binding protein | ||
PJBMHNLJ_00968 | 5.7e-115 | glnQ | 3.6.3.21 | E | ABC transporter | |
PJBMHNLJ_00969 | 4.6e-109 | glnP | P | ABC transporter permease | ||
PJBMHNLJ_00970 | 3.6e-123 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
PJBMHNLJ_00971 | 5.3e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
PJBMHNLJ_00972 | 1.5e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
PJBMHNLJ_00973 | 3.4e-11 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
PJBMHNLJ_00974 | 1.8e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
PJBMHNLJ_00975 | 1.9e-163 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
PJBMHNLJ_00976 | 4.9e-102 | E | GDSL-like Lipase/Acylhydrolase | |||
PJBMHNLJ_00977 | 3.3e-119 | yvpB | S | Peptidase_C39 like family | ||
PJBMHNLJ_00978 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
PJBMHNLJ_00979 | 4.3e-115 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
PJBMHNLJ_00980 | 2.3e-78 | |||||
PJBMHNLJ_00981 | 1.3e-243 | G | Bacterial extracellular solute-binding protein | |||
PJBMHNLJ_00982 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_00983 | 4.4e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
PJBMHNLJ_00984 | 2.6e-103 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
PJBMHNLJ_00985 | 9.6e-175 | L | Belongs to the 'phage' integrase family | |||
PJBMHNLJ_00986 | 2e-104 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
PJBMHNLJ_00987 | 6.9e-289 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
PJBMHNLJ_00988 | 2.7e-230 | S | Tetratricopeptide repeat protein | |||
PJBMHNLJ_00989 | 2.5e-18 | 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 | ||
PJBMHNLJ_00990 | 0.0 | S | membrane | |||
PJBMHNLJ_00991 | 2.1e-160 | 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 | ||
PJBMHNLJ_00992 | 3.4e-191 | 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 | ||
PJBMHNLJ_00993 | 1.7e-298 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
PJBMHNLJ_00994 | 6.5e-179 | comGA | NU | Type II IV secretion system protein | ||
PJBMHNLJ_00995 | 1.5e-132 | yebC | K | Transcriptional regulatory protein | ||
PJBMHNLJ_00996 | 9.5e-88 | S | VanZ like family | |||
PJBMHNLJ_00997 | 4.8e-216 | 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 | |
PJBMHNLJ_00998 | 1.8e-164 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
PJBMHNLJ_00999 | 6.2e-75 | yisY | 1.11.1.10 | S | Alpha/beta hydrolase family | |
PJBMHNLJ_01000 | 3.8e-204 | malK | P | ATPases associated with a variety of cellular activities | ||
PJBMHNLJ_01001 | 2.1e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
PJBMHNLJ_01002 | 2.5e-147 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
PJBMHNLJ_01003 | 5.1e-248 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
PJBMHNLJ_01004 | 1.6e-238 | G | Bacterial extracellular solute-binding protein | |||
PJBMHNLJ_01005 | 1.2e-85 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
PJBMHNLJ_01006 | 1.2e-83 | |||||
PJBMHNLJ_01007 | 2.3e-145 | glvR | K | Helix-turn-helix domain, rpiR family | ||
PJBMHNLJ_01008 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
PJBMHNLJ_01009 | 5.2e-272 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
PJBMHNLJ_01010 | 5.7e-76 | |||||
PJBMHNLJ_01011 | 1.2e-80 | K | DNA-templated transcription, initiation | |||
PJBMHNLJ_01012 | 4.6e-156 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
PJBMHNLJ_01013 | 4.6e-144 | epsB | M | biosynthesis protein | ||
PJBMHNLJ_01014 | 1.8e-123 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
PJBMHNLJ_01015 | 8.8e-139 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
PJBMHNLJ_01016 | 1.3e-119 | rfbP | M | Bacterial sugar transferase | ||
PJBMHNLJ_01017 | 1e-156 | hlyX | S | Transporter associated domain | ||
PJBMHNLJ_01018 | 5.1e-303 | 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 | ||
PJBMHNLJ_01019 | 1.1e-43 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
PJBMHNLJ_01020 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
PJBMHNLJ_01021 | 6.4e-61 | S | Short repeat of unknown function (DUF308) | |||
PJBMHNLJ_01022 | 1.6e-160 | rapZ | S | Displays ATPase and GTPase activities | ||
PJBMHNLJ_01023 | 6.4e-193 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
PJBMHNLJ_01024 | 6.2e-171 | whiA | K | May be required for sporulation | ||
PJBMHNLJ_01025 | 2.1e-100 | 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 | |
PJBMHNLJ_01026 | 1.8e-278 | ycaM | E | amino acid | ||
PJBMHNLJ_01028 | 1.4e-187 | cggR | K | Putative sugar-binding domain | ||
PJBMHNLJ_01029 | 3.2e-189 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
PJBMHNLJ_01030 | 4.6e-227 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
PJBMHNLJ_01031 | 1.1e-141 | 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) | |
PJBMHNLJ_01032 | 3.1e-245 | 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 | |
PJBMHNLJ_01033 | 1.9e-28 | secG | U | Preprotein translocase | ||
PJBMHNLJ_01034 | 1.1e-81 | V | ABC transporter transmembrane region | |||
PJBMHNLJ_01035 | 1e-160 | V | ABC transporter transmembrane region | |||
PJBMHNLJ_01036 | 7e-153 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
PJBMHNLJ_01037 | 3.5e-35 | |||||
PJBMHNLJ_01038 | 1.7e-119 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
PJBMHNLJ_01039 | 2.9e-157 | S | Protein of unknown function (DUF979) | |||
PJBMHNLJ_01040 | 2.5e-113 | S | Protein of unknown function (DUF969) | |||
PJBMHNLJ_01041 | 1.1e-130 | XK27_08440 | K | UTRA domain | ||
PJBMHNLJ_01042 | 1.1e-147 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
PJBMHNLJ_01043 | 5.5e-86 | uspA | T | universal stress protein | ||
PJBMHNLJ_01045 | 9.8e-169 | phnD | P | Phosphonate ABC transporter | ||
PJBMHNLJ_01046 | 1.9e-141 | 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 | |
PJBMHNLJ_01047 | 1.6e-130 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
PJBMHNLJ_01048 | 3.8e-60 | GT2,GT4 | M | family 8 | ||
PJBMHNLJ_01049 | 2.1e-118 | ybhL | S | Belongs to the BI1 family | ||
PJBMHNLJ_01050 | 6.3e-143 | cbiQ | P | cobalt transport | ||
PJBMHNLJ_01051 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_01052 | 2.8e-94 | S | UPF0397 protein | |||
PJBMHNLJ_01053 | 1.3e-71 | salL | 2.5.1.63, 2.5.1.94 | K | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
PJBMHNLJ_01054 | 1.7e-232 | 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 | ||
PJBMHNLJ_01055 | 2.3e-203 | 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 | ||
PJBMHNLJ_01056 | 1.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
PJBMHNLJ_01057 | 1.7e-72 | |||||
PJBMHNLJ_01058 | 5.1e-113 | M | LysM domain protein | |||
PJBMHNLJ_01059 | 3.1e-107 | S | Putative ABC-transporter type IV | |||
PJBMHNLJ_01060 | 6.2e-59 | psiE | S | Phosphate-starvation-inducible E | ||
PJBMHNLJ_01061 | 1.9e-89 | K | acetyltransferase | |||
PJBMHNLJ_01063 | 9.7e-163 | yvgN | C | Aldo keto reductase | ||
PJBMHNLJ_01064 | 1.9e-279 | gadC | E | Contains amino acid permease domain | ||
PJBMHNLJ_01065 | 9.1e-275 | pipD | E | Peptidase family C69 | ||
PJBMHNLJ_01066 | 4e-264 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
PJBMHNLJ_01067 | 2.8e-45 | gadC | E | Contains amino acid permease domain | ||
PJBMHNLJ_01068 | 3.7e-70 | dnaE | 2.7.7.7 | L | DNA polymerase | |
PJBMHNLJ_01069 | 4.5e-26 | S | Protein of unknown function (DUF2929) | |||
PJBMHNLJ_01070 | 1e-306 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
PJBMHNLJ_01071 | 1.2e-150 | L | AAA domain | |||
PJBMHNLJ_01072 | 3e-184 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
PJBMHNLJ_01073 | 2.1e-147 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
PJBMHNLJ_01074 | 9.5e-24 | S | YtxH-like protein | |||
PJBMHNLJ_01075 | 5.2e-52 | |||||
PJBMHNLJ_01076 | 4.1e-77 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
PJBMHNLJ_01078 | 4.2e-12 | S | Protein of unknown function (DUF2922) | |||
PJBMHNLJ_01080 | 1.3e-107 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
PJBMHNLJ_01081 | 7.7e-43 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
PJBMHNLJ_01082 | 4e-83 | dhaL | 2.7.1.121 | S | Dak2 | |
PJBMHNLJ_01083 | 1.1e-157 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
PJBMHNLJ_01085 | 4.7e-94 | S | Chloramphenicol phosphotransferase-like protein | |||
PJBMHNLJ_01086 | 3.3e-77 | ant | 2.7.7.47 | S | PFAM DNA polymerase beta domain protein region | |
PJBMHNLJ_01087 | 9.4e-94 | cca | 2.7.7.19, 2.7.7.72 | J | Aminoglycoside-2''-adenylyltransferase | |
PJBMHNLJ_01088 | 1e-198 | L | transposition, DNA-mediated | |||
PJBMHNLJ_01089 | 1.7e-98 | S | Rib/alpha-like repeat | |||
PJBMHNLJ_01090 | 3.2e-65 | S | Domain of unknown function DUF1828 | |||
PJBMHNLJ_01091 | 1.3e-70 | rplO | J | Binds to the 23S rRNA | ||
PJBMHNLJ_01092 | 1.4e-23 | rpmD | J | Ribosomal protein L30 | ||
PJBMHNLJ_01093 | 1.9e-76 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
PJBMHNLJ_01094 | 1.5e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
PJBMHNLJ_01095 | 2.9e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
PJBMHNLJ_01096 | 2.1e-67 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
PJBMHNLJ_01097 | 2.3e-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 | ||
PJBMHNLJ_01098 | 7.2e-95 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
PJBMHNLJ_01099 | 1.1e-34 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
PJBMHNLJ_01100 | 5.6e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
PJBMHNLJ_01101 | 7.7e-42 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
PJBMHNLJ_01102 | 2.2e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
PJBMHNLJ_01103 | 6.6e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
PJBMHNLJ_01104 | 1.6e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
PJBMHNLJ_01105 | 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 | ||
PJBMHNLJ_01106 | 5e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
PJBMHNLJ_01107 | 1.6e-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 | ||
PJBMHNLJ_01108 | 1.7e-45 | 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 | ||
PJBMHNLJ_01109 | 1e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
PJBMHNLJ_01110 | 1.7e-111 | 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 | ||
PJBMHNLJ_01111 | 2.2e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
PJBMHNLJ_01112 | 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 | ||
PJBMHNLJ_01113 | 1e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
PJBMHNLJ_01114 | 3.5e-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 | ||
PJBMHNLJ_01115 | 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 | ||
PJBMHNLJ_01116 | 0.0 | S | membrane | |||
PJBMHNLJ_01117 | 5.8e-255 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
PJBMHNLJ_01118 | 2.1e-120 | spaE | S | ABC-2 family transporter protein | ||
PJBMHNLJ_01119 | 3.7e-128 | mutF | V | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_01120 | 5.8e-242 | nhaC | C | Na H antiporter NhaC | ||
PJBMHNLJ_01121 | 5.4e-214 | pipD | E | Dipeptidase | ||
PJBMHNLJ_01122 | 8.3e-295 | arbB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
PJBMHNLJ_01123 | 0.0 | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
PJBMHNLJ_01124 | 3.2e-71 | K | CAT RNA binding domain | |||
PJBMHNLJ_01125 | 1.5e-115 | camS | S | sex pheromone | ||
PJBMHNLJ_01126 | 3.3e-49 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
PJBMHNLJ_01127 | 1.4e-270 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
PJBMHNLJ_01128 | 1e-273 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
PJBMHNLJ_01129 | 7.3e-58 | dcm | 2.1.1.37 | L | C-5 cytosine-specific DNA methylase | |
PJBMHNLJ_01130 | 2.5e-39 | nlaIVR | L | NgoBV restriction endonuclease | ||
PJBMHNLJ_01131 | 8.2e-49 | S | Lysin motif | |||
PJBMHNLJ_01132 | 8.7e-126 | L | Replication initiation factor | |||
PJBMHNLJ_01133 | 3.8e-33 | L | Single-strand binding protein family | |||
PJBMHNLJ_01134 | 3.8e-78 | L | Phage integrase, N-terminal SAM-like domain | |||
PJBMHNLJ_01135 | 1.8e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
PJBMHNLJ_01136 | 5.6e-110 | P | Cobalt transport protein | |||
PJBMHNLJ_01137 | 6.9e-240 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_01138 | 7.9e-97 | S | ABC-type cobalt transport system, permease component | |||
PJBMHNLJ_01139 | 2.8e-168 | K | helix_turn_helix, arabinose operon control protein | |||
PJBMHNLJ_01140 | 3.9e-37 | htpX | O | Belongs to the peptidase M48B family | ||
PJBMHNLJ_01141 | 1.1e-144 | G | PTS system mannose/fructose/sorbose family IID component | |||
PJBMHNLJ_01142 | 4.1e-139 | G | PTS system sorbose-specific iic component | |||
PJBMHNLJ_01143 | 6.3e-160 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
PJBMHNLJ_01144 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
PJBMHNLJ_01145 | 1.1e-269 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
PJBMHNLJ_01146 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
PJBMHNLJ_01147 | 9.1e-110 | S | DUF218 domain | |||
PJBMHNLJ_01148 | 3.6e-196 | 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 | |
PJBMHNLJ_01149 | 4.1e-95 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
PJBMHNLJ_01150 | 1.2e-129 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
PJBMHNLJ_01151 | 1.3e-85 | folT | S | ECF transporter, substrate-specific component | ||
PJBMHNLJ_01152 | 2.5e-29 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
PJBMHNLJ_01153 | 2.9e-259 | pepC | 3.4.22.40 | E | aminopeptidase | |
PJBMHNLJ_01154 | 1.6e-120 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
PJBMHNLJ_01155 | 3.3e-255 | pepC | 3.4.22.40 | E | aminopeptidase | |
PJBMHNLJ_01156 | 1.2e-32 | |||||
PJBMHNLJ_01157 | 1.5e-28 | 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 | ||
PJBMHNLJ_01158 | 5e-16 | 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 | ||
PJBMHNLJ_01159 | 1.5e-289 | 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 | |
PJBMHNLJ_01160 | 9.4e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
PJBMHNLJ_01161 | 7.3e-81 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
PJBMHNLJ_01162 | 2.1e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
PJBMHNLJ_01163 | 3.5e-158 | corA | P | CorA-like Mg2+ transporter protein | ||
PJBMHNLJ_01164 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
PJBMHNLJ_01165 | 8.2e-76 | rplI | J | Binds to the 23S rRNA | ||
PJBMHNLJ_01166 | 1.6e-244 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
PJBMHNLJ_01167 | 1e-170 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
PJBMHNLJ_01168 | 2.2e-218 | I | Protein of unknown function (DUF2974) | |||
PJBMHNLJ_01169 | 0.0 | |||||
PJBMHNLJ_01170 | 3e-251 | 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 | ||
PJBMHNLJ_01171 | 3.5e-206 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
PJBMHNLJ_01172 | 5.8e-137 | M | Glycosyl hydrolases family 25 | |||
PJBMHNLJ_01173 | 1.8e-232 | potE | E | amino acid | ||
PJBMHNLJ_01174 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
PJBMHNLJ_01175 | 6.6e-242 | psd | 4.1.1.65 | I | Belongs to the phosphatidylserine decarboxylase family | |
PJBMHNLJ_01177 | 6e-252 | L | transposase, IS605 OrfB family | |||
PJBMHNLJ_01178 | 7e-83 | tlpA2 | L | Transposase IS200 like | ||
PJBMHNLJ_01179 | 1.1e-183 | pepA | E | M42 glutamyl aminopeptidase | ||
PJBMHNLJ_01180 | 2.7e-79 | XK27_02470 | K | LytTr DNA-binding domain | ||
PJBMHNLJ_01181 | 4e-120 | liaI | S | membrane | ||
PJBMHNLJ_01183 | 2e-43 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
PJBMHNLJ_01184 | 1.8e-295 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
PJBMHNLJ_01185 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
PJBMHNLJ_01186 | 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 | |
PJBMHNLJ_01187 | 8.8e-170 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
PJBMHNLJ_01188 | 1.4e-254 | P | Sodium:sulfate symporter transmembrane region | |||
PJBMHNLJ_01189 | 0.0 | 1.3.5.4 | C | FMN_bind | ||
PJBMHNLJ_01190 | 7.1e-87 | ntd | 2.4.2.6 | F | Nucleoside | |
PJBMHNLJ_01191 | 3.1e-215 | S | zinc-ribbon domain | |||
PJBMHNLJ_01192 | 7.9e-67 | 2.7.1.191 | G | PTS system fructose IIA component | ||
PJBMHNLJ_01193 | 7.1e-147 | manZ_1 | G | PTS system mannose/fructose/sorbose family IID component | ||
PJBMHNLJ_01194 | 2.5e-107 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
PJBMHNLJ_01195 | 1.2e-99 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
PJBMHNLJ_01196 | 2.2e-165 | murB | 1.3.1.98 | M | Cell wall formation | |
PJBMHNLJ_01197 | 6e-202 | 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 | |
PJBMHNLJ_01198 | 1e-129 | potB | P | ABC transporter permease | ||
PJBMHNLJ_01199 | 2.9e-137 | potC | P | ABC transporter permease | ||
PJBMHNLJ_01200 | 2.3e-150 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
PJBMHNLJ_01201 | 8.6e-232 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
PJBMHNLJ_01202 | 2.4e-206 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
PJBMHNLJ_01203 | 1.5e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
PJBMHNLJ_01204 | 5e-78 | 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 | ||
PJBMHNLJ_01205 | 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 | |
PJBMHNLJ_01206 | 4.8e-140 | 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 | ||
PJBMHNLJ_01207 | 9.8e-163 | 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 | |
PJBMHNLJ_01208 | 4.9e-131 | 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 | ||
PJBMHNLJ_01209 | 4e-60 | divIC | D | Septum formation initiator | ||
PJBMHNLJ_01210 | 5.4e-34 | yabO | J | S4 domain protein | ||
PJBMHNLJ_01211 | 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 | ||
PJBMHNLJ_01212 | 1.9e-103 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
PJBMHNLJ_01213 | 3.6e-182 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
PJBMHNLJ_01214 | 2.3e-122 | S | (CBS) domain | |||
PJBMHNLJ_01215 | 3.5e-213 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
PJBMHNLJ_01216 | 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 | |
PJBMHNLJ_01217 | 6.5e-268 | 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 | |
PJBMHNLJ_01218 | 8e-260 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
PJBMHNLJ_01219 | 8e-41 | rpmE2 | J | Ribosomal protein L31 | ||
PJBMHNLJ_01220 | 5.2e-56 | ybeC | E | amino acid | ||
PJBMHNLJ_01221 | 1.1e-53 | S | Putative adhesin | |||
PJBMHNLJ_01222 | 2.4e-201 | napA | P | Sodium/hydrogen exchanger family | ||
PJBMHNLJ_01223 | 0.0 | cadA | P | P-type ATPase | ||
PJBMHNLJ_01224 | 8.8e-84 | ykuL | S | (CBS) domain | ||
PJBMHNLJ_01225 | 1.9e-102 | S | CAAX protease self-immunity | |||
PJBMHNLJ_01226 | 2.4e-92 | S | Protein of unknown function (DUF1440) | |||
PJBMHNLJ_01227 | 9.7e-264 | G | PTS system Galactitol-specific IIC component | |||
PJBMHNLJ_01228 | 2.7e-14 | |||||
PJBMHNLJ_01229 | 4.4e-07 | |||||
PJBMHNLJ_01230 | 7.9e-191 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
PJBMHNLJ_01231 | 4.3e-228 | G | Major Facilitator Superfamily | |||
PJBMHNLJ_01232 | 4.5e-100 | 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) | |
PJBMHNLJ_01233 | 1.3e-218 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
PJBMHNLJ_01245 | 1.2e-61 | |||||
PJBMHNLJ_01246 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
PJBMHNLJ_01247 | 2e-123 | 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 | |
PJBMHNLJ_01248 | 1.4e-148 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
PJBMHNLJ_01249 | 7.8e-35 | yozE | S | Belongs to the UPF0346 family | ||
PJBMHNLJ_01250 | 5.7e-264 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
PJBMHNLJ_01251 | 4.1e-158 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
PJBMHNLJ_01252 | 1.3e-134 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
PJBMHNLJ_01253 | 2.1e-70 | K | Acetyltransferase (GNAT) domain | |||
PJBMHNLJ_01254 | 9.4e-247 | ynbB | 4.4.1.1 | P | aluminum resistance | |
PJBMHNLJ_01255 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
PJBMHNLJ_01256 | 2.2e-306 | 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 | |
PJBMHNLJ_01257 | 7.6e-203 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
PJBMHNLJ_01258 | 7.4e-121 | K | response regulator | |||
PJBMHNLJ_01259 | 2.7e-179 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
PJBMHNLJ_01260 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
PJBMHNLJ_01261 | 1.4e-155 | dkg | S | reductase | ||
PJBMHNLJ_01262 | 1.3e-156 | endA | F | DNA RNA non-specific endonuclease | ||
PJBMHNLJ_01263 | 3.9e-281 | pipD | E | Dipeptidase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)