ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
BLNAIMJH_00001 | 4.7e-311 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
BLNAIMJH_00002 | 2.6e-39 | rpmA | J | Ribosomal L27 protein | ||
BLNAIMJH_00003 | 2.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
BLNAIMJH_00004 | 6.6e-309 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
BLNAIMJH_00005 | 1.8e-231 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
BLNAIMJH_00006 | 1.4e-44 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
BLNAIMJH_00007 | 4.1e-18 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
BLNAIMJH_00010 | 5.5e-297 | gltX | 6.1.1.17 | 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) | |
BLNAIMJH_00011 | 6.1e-100 | S | Protein of unknown function (DUF805) | |||
BLNAIMJH_00012 | 7e-184 | |||||
BLNAIMJH_00013 | 1.5e-123 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
BLNAIMJH_00014 | 6.1e-263 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_00015 | 4.9e-96 | S | GtrA-like protein | |||
BLNAIMJH_00016 | 2.3e-62 | S | Macrophage migration inhibitory factor (MIF) | |||
BLNAIMJH_00017 | 3.8e-96 | rnj | 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 | ||
BLNAIMJH_00018 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
BLNAIMJH_00019 | 1.1e-168 | |||||
BLNAIMJH_00020 | 0.0 | O | Type VII secretion system ESX-1, transport TM domain B | |||
BLNAIMJH_00021 | 3.8e-225 | snm | S | WXG100 protein secretion system (Wss), protein YukD | ||
BLNAIMJH_00022 | 8.6e-49 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
BLNAIMJH_00023 | 4.7e-57 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
BLNAIMJH_00024 | 6.5e-102 | S | UPF0210 protein | |||
BLNAIMJH_00025 | 6.1e-13 | M | Cna protein B-type domain | |||
BLNAIMJH_00026 | 2.8e-27 | M | Cna protein B-type domain | |||
BLNAIMJH_00027 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
BLNAIMJH_00028 | 4.3e-236 | S | Uncharacterized conserved protein (DUF2183) | |||
BLNAIMJH_00029 | 3.9e-69 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
BLNAIMJH_00030 | 3e-178 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
BLNAIMJH_00031 | 1.8e-134 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
BLNAIMJH_00032 | 1.7e-140 | ybbL | V | ATPases associated with a variety of cellular activities | ||
BLNAIMJH_00033 | 2.9e-241 | S | Putative esterase | |||
BLNAIMJH_00034 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
BLNAIMJH_00035 | 1.2e-277 | 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 | |
BLNAIMJH_00036 | 1.2e-58 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BLNAIMJH_00037 | 6.6e-47 | S | Glycosyl transferase, family 2 | |||
BLNAIMJH_00038 | 8.7e-223 | |||||
BLNAIMJH_00039 | 1.5e-71 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
BLNAIMJH_00040 | 1.1e-152 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
BLNAIMJH_00041 | 2.5e-138 | ctsW | S | Phosphoribosyl transferase domain | ||
BLNAIMJH_00042 | 6.8e-188 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
BLNAIMJH_00043 | 7.8e-129 | T | Response regulator receiver domain protein | |||
BLNAIMJH_00044 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
BLNAIMJH_00045 | 1.7e-59 | carD | K | CarD-like/TRCF domain | ||
BLNAIMJH_00046 | 2.2e-50 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
BLNAIMJH_00047 | 7.7e-117 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
BLNAIMJH_00048 | 1.9e-73 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
BLNAIMJH_00049 | 4.3e-233 | aspB | E | Aminotransferase class-V | ||
BLNAIMJH_00050 | 6.4e-179 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
BLNAIMJH_00051 | 6.8e-125 | tmp1 | S | Domain of unknown function (DUF4391) | ||
BLNAIMJH_00052 | 6.7e-201 | S | Endonuclease/Exonuclease/phosphatase family | |||
BLNAIMJH_00054 | 2e-40 | 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 | |
BLNAIMJH_00055 | 2e-244 | 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 | |
BLNAIMJH_00056 | 1.7e-95 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
BLNAIMJH_00057 | 4.8e-119 | recE | 2.7.7.7, 3.6.4.12 | L | Psort location Cytoplasmic, score | |
BLNAIMJH_00058 | 5.9e-32 | typA | T | Elongation factor G C-terminus | ||
BLNAIMJH_00059 | 4e-104 | |||||
BLNAIMJH_00060 | 4.9e-50 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
BLNAIMJH_00061 | 5.4e-105 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
BLNAIMJH_00062 | 3.5e-43 | V | ATPases associated with a variety of cellular activities | |||
BLNAIMJH_00063 | 1.5e-53 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
BLNAIMJH_00064 | 6.4e-73 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
BLNAIMJH_00065 | 8e-27 | V | ATPases associated with a variety of cellular activities | |||
BLNAIMJH_00066 | 3.2e-90 | V | ABC-2 family transporter protein | |||
BLNAIMJH_00067 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
BLNAIMJH_00068 | 7.5e-103 | 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 | ||
BLNAIMJH_00070 | 1.1e-86 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
BLNAIMJH_00071 | 1.5e-92 | mntP | P | Probably functions as a manganese efflux pump | ||
BLNAIMJH_00072 | 4.9e-134 | |||||
BLNAIMJH_00073 | 4.9e-134 | KT | Transcriptional regulatory protein, C terminal | |||
BLNAIMJH_00074 | 3.2e-123 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
BLNAIMJH_00075 | 5.4e-289 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
BLNAIMJH_00076 | 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 | |
BLNAIMJH_00077 | 7.7e-172 | 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 | |
BLNAIMJH_00078 | 0.0 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
BLNAIMJH_00079 | 4.9e-81 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
BLNAIMJH_00080 | 4.4e-143 | aroK | 2.7.1.71, 4.2.3.4 | H | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
BLNAIMJH_00081 | 2.1e-69 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
BLNAIMJH_00082 | 6.6e-218 | GK | ROK family | |||
BLNAIMJH_00083 | 2.4e-164 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
BLNAIMJH_00084 | 1.3e-219 | S | Metal-independent alpha-mannosidase (GH125) | |||
BLNAIMJH_00085 | 1.6e-27 | |||||
BLNAIMJH_00086 | 4.2e-247 | yihS | 5.1.3.11 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
BLNAIMJH_00087 | 6.6e-140 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
BLNAIMJH_00088 | 6.7e-66 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
BLNAIMJH_00089 | 1.5e-153 | rarA | L | Recombination factor protein RarA | ||
BLNAIMJH_00090 | 1e-28 | rutG | F | Permease family | ||
BLNAIMJH_00091 | 1.4e-62 | rutG | F | Permease family | ||
BLNAIMJH_00092 | 7.3e-160 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
BLNAIMJH_00093 | 1.4e-141 | K | helix_turn_helix, arabinose operon control protein | |||
BLNAIMJH_00094 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
BLNAIMJH_00095 | 6.8e-92 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
BLNAIMJH_00096 | 1.1e-91 | O | peptidyl-tyrosine sulfation | |||
BLNAIMJH_00097 | 9.7e-76 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00098 | 3.7e-122 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00099 | 3e-31 | S | G5 | |||
BLNAIMJH_00101 | 7.5e-151 | O | Thioredoxin | |||
BLNAIMJH_00102 | 0.0 | KLT | Protein tyrosine kinase | |||
BLNAIMJH_00103 | 0.0 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
BLNAIMJH_00104 | 1.5e-214 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00105 | 1.2e-219 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00106 | 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 | ||
BLNAIMJH_00107 | 6.2e-79 | 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 | ||
BLNAIMJH_00108 | 9.8e-237 | G | MFS/sugar transport protein | |||
BLNAIMJH_00109 | 1.1e-117 | 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 | |
BLNAIMJH_00110 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
BLNAIMJH_00111 | 2.1e-285 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
BLNAIMJH_00112 | 7.7e-255 | nadE | 6.3.1.5, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
BLNAIMJH_00113 | 1.8e-225 | S | Peptidase dimerisation domain | |||
BLNAIMJH_00114 | 4.8e-156 | S | Sucrose-6F-phosphate phosphohydrolase | |||
BLNAIMJH_00115 | 2.8e-146 | metQ | P | NLPA lipoprotein | ||
BLNAIMJH_00116 | 5.5e-147 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
BLNAIMJH_00117 | 5.4e-108 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_00118 | 1.1e-74 | |||||
BLNAIMJH_00119 | 7.5e-84 | |||||
BLNAIMJH_00121 | 1.3e-232 | XK27_00240 | K | Fic/DOC family | ||
BLNAIMJH_00122 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
BLNAIMJH_00123 | 4.6e-302 | M | domain protein | |||
BLNAIMJH_00124 | 8e-185 | 3.4.22.70 | M | Sortase family | ||
BLNAIMJH_00125 | 1.8e-22 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
BLNAIMJH_00126 | 8.2e-73 | 3.6.1.13 | L | NUDIX domain | ||
BLNAIMJH_00127 | 3.5e-171 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
BLNAIMJH_00128 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
BLNAIMJH_00129 | 9.4e-101 | pdtaR | T | Response regulator receiver domain protein | ||
BLNAIMJH_00130 | 1.4e-169 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
BLNAIMJH_00131 | 1.6e-67 | hbd2 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase, C-terminal domain | |
BLNAIMJH_00132 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
BLNAIMJH_00133 | 2.6e-214 | ybiR | P | Citrate transporter | ||
BLNAIMJH_00135 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
BLNAIMJH_00139 | 7.7e-101 | K | acetyltransferase | |||
BLNAIMJH_00140 | 8.9e-154 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
BLNAIMJH_00141 | 1.9e-104 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
BLNAIMJH_00142 | 5.1e-149 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
BLNAIMJH_00143 | 6.1e-108 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
BLNAIMJH_00144 | 1.8e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
BLNAIMJH_00145 | 3.9e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
BLNAIMJH_00146 | 1.5e-178 | S | Endonuclease/Exonuclease/phosphatase family | |||
BLNAIMJH_00147 | 1.2e-245 | 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 | |
BLNAIMJH_00148 | 1.1e-175 | S | Protein of unknown function DUF58 | |||
BLNAIMJH_00149 | 0.0 | E | Transglutaminase-like superfamily | |||
BLNAIMJH_00150 | 4.4e-163 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
BLNAIMJH_00151 | 4.8e-104 | B | Belongs to the OprB family | |||
BLNAIMJH_00152 | 1.8e-101 | T | Forkhead associated domain | |||
BLNAIMJH_00153 | 6.2e-130 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BLNAIMJH_00154 | 9.5e-156 | U | Belongs to the binding-protein-dependent transport system permease family | |||
BLNAIMJH_00155 | 7.8e-219 | livK | E | Receptor family ligand binding region | ||
BLNAIMJH_00156 | 3.2e-172 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
BLNAIMJH_00157 | 1.4e-190 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
BLNAIMJH_00158 | 1.5e-35 | rpmE | J | Binds the 23S rRNA | ||
BLNAIMJH_00160 | 6.8e-226 | xylR | GK | ROK family | ||
BLNAIMJH_00161 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
BLNAIMJH_00162 | 2.1e-279 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
BLNAIMJH_00163 | 1.3e-276 | S | PGAP1-like protein | |||
BLNAIMJH_00164 | 5.6e-53 | |||||
BLNAIMJH_00165 | 1.1e-61 | |||||
BLNAIMJH_00166 | 1.2e-167 | G | ABC transporter permease | |||
BLNAIMJH_00167 | 0.0 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00168 | 8.9e-198 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_00169 | 3.6e-241 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BLNAIMJH_00170 | 1.6e-86 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
BLNAIMJH_00171 | 1.6e-41 | |||||
BLNAIMJH_00172 | 2.2e-197 | gguB | U | Branched-chain amino acid transport system / permease component | ||
BLNAIMJH_00173 | 3e-295 | araG | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | |
BLNAIMJH_00174 | 6.2e-205 | G | Periplasmic binding protein domain | |||
BLNAIMJH_00175 | 5e-178 | GK | ROK family | |||
BLNAIMJH_00176 | 7.1e-126 | xylG | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | |
BLNAIMJH_00177 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
BLNAIMJH_00178 | 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 | |
BLNAIMJH_00179 | 6.2e-90 | S | Protein of unknown function (DUF721) | |||
BLNAIMJH_00180 | 1.3e-235 | 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 | ||
BLNAIMJH_00181 | 8.2e-108 | 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 | |
BLNAIMJH_00182 | 2.3e-38 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
BLNAIMJH_00183 | 2.7e-288 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
BLNAIMJH_00184 | 3.1e-121 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
BLNAIMJH_00185 | 4.5e-163 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
BLNAIMJH_00186 | 1e-270 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
BLNAIMJH_00187 | 8e-31 | V | N-Acetylmuramoyl-L-alanine amidase | |||
BLNAIMJH_00188 | 9.2e-82 | |||||
BLNAIMJH_00189 | 9.2e-57 | T | helix_turn_helix, Lux Regulon | |||
BLNAIMJH_00190 | 1.6e-30 | 2.7.13.3 | T | Histidine kinase | ||
BLNAIMJH_00191 | 2.4e-113 | ytrE | V | ATPases associated with a variety of cellular activities | ||
BLNAIMJH_00192 | 1.8e-218 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_00193 | 7.4e-52 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
BLNAIMJH_00194 | 5.9e-55 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
BLNAIMJH_00195 | 4.2e-228 | 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 | |
BLNAIMJH_00196 | 1.4e-46 | 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 | |
BLNAIMJH_00197 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
BLNAIMJH_00199 | 1.2e-106 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
BLNAIMJH_00200 | 3.7e-171 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
BLNAIMJH_00201 | 7.7e-70 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
BLNAIMJH_00202 | 4.6e-140 | 3.5.2.10 | S | Creatinine amidohydrolase | ||
BLNAIMJH_00203 | 1.9e-245 | proP | EGP | Sugar (and other) transporter | ||
BLNAIMJH_00204 | 1.6e-285 | purR | QT | Purine catabolism regulatory protein-like family | ||
BLNAIMJH_00205 | 1.5e-255 | codA | 3.5.4.1, 3.5.4.21 | F | Amidohydrolase family | |
BLNAIMJH_00206 | 7.1e-16 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
BLNAIMJH_00207 | 2e-29 | ilvN | 2.2.1.6 | E | ACT domain | |
BLNAIMJH_00208 | 2.6e-89 | |||||
BLNAIMJH_00209 | 0.0 | yjjK | S | ABC transporter | ||
BLNAIMJH_00210 | 1.6e-151 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
BLNAIMJH_00211 | 9.3e-295 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BLNAIMJH_00212 | 9.1e-214 | 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 | |
BLNAIMJH_00213 | 0.0 | cbgA_1 | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
BLNAIMJH_00215 | 4.1e-135 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway. Thus, catalyzes the conversion of 4-amino-5-aminomethyl-2-methylpyrimidine to 4-amino- 5-hydroxymethyl-2-methylpyrimidine (HMP) | |
BLNAIMJH_00216 | 1.4e-291 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00217 | 1.1e-192 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
BLNAIMJH_00218 | 1.2e-193 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
BLNAIMJH_00219 | 0.0 | fas | I | MaoC like domain | ||
BLNAIMJH_00220 | 7.3e-109 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
BLNAIMJH_00221 | 2e-36 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
BLNAIMJH_00222 | 6e-236 | G | Transporter major facilitator family protein | |||
BLNAIMJH_00223 | 1.2e-109 | K | Bacterial regulatory proteins, tetR family | |||
BLNAIMJH_00224 | 0.0 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
BLNAIMJH_00225 | 4e-113 | K | Bacterial regulatory proteins, tetR family | |||
BLNAIMJH_00226 | 5.7e-42 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
BLNAIMJH_00227 | 3.8e-108 | |||||
BLNAIMJH_00228 | 4.1e-251 | 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 | ||
BLNAIMJH_00229 | 5.2e-218 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
BLNAIMJH_00230 | 5.1e-188 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
BLNAIMJH_00231 | 2.2e-69 | 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 | ||
BLNAIMJH_00232 | 3.2e-113 | 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 | ||
BLNAIMJH_00233 | 4.2e-138 | 3.6.3.44 | V | ABC transporter | ||
BLNAIMJH_00234 | 1.2e-158 | msbA2 | 3.6.3.44 | V | ABC transporter transmembrane region | |
BLNAIMJH_00235 | 1.1e-158 | O | Thioredoxin | |||
BLNAIMJH_00236 | 4e-130 | E | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00237 | 1.8e-133 | yebE | S | DUF218 domain | ||
BLNAIMJH_00238 | 1.6e-63 | 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 | ||
BLNAIMJH_00239 | 6.3e-63 | I | Sterol carrier protein | |||
BLNAIMJH_00240 | 1.4e-41 | S | Protein of unknown function (DUF3073) | |||
BLNAIMJH_00241 | 5.9e-205 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BLNAIMJH_00242 | 9.4e-300 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
BLNAIMJH_00243 | 3.8e-249 | yjjP | S | Threonine/Serine exporter, ThrE | ||
BLNAIMJH_00244 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
BLNAIMJH_00245 | 1.9e-176 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
BLNAIMJH_00246 | 6.2e-40 | ybdD | S | Selenoprotein, putative | ||
BLNAIMJH_00247 | 3.2e-256 | cstA | T | 5TM C-terminal transporter carbon starvation CstA | ||
BLNAIMJH_00248 | 2.3e-229 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
BLNAIMJH_00249 | 8.3e-12 | S | Protein of unknown function, DUF624 | |||
BLNAIMJH_00250 | 2.5e-189 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_00251 | 1.4e-38 | G | beta-mannosidase | |||
BLNAIMJH_00252 | 0.0 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
BLNAIMJH_00253 | 5.6e-82 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
BLNAIMJH_00254 | 1e-130 | 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 | |
BLNAIMJH_00255 | 2.4e-39 | 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 | |
BLNAIMJH_00256 | 0.0 | S | Tetratricopeptide repeat | |||
BLNAIMJH_00257 | 6.7e-116 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
BLNAIMJH_00258 | 1.5e-132 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
BLNAIMJH_00259 | 6.1e-82 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
BLNAIMJH_00260 | 9e-95 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
BLNAIMJH_00261 | 1.9e-112 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
BLNAIMJH_00262 | 4.9e-271 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
BLNAIMJH_00263 | 6.8e-87 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
BLNAIMJH_00264 | 2.7e-27 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
BLNAIMJH_00265 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
BLNAIMJH_00266 | 6.7e-162 | |||||
BLNAIMJH_00267 | 0.0 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
BLNAIMJH_00270 | 6.7e-57 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
BLNAIMJH_00271 | 1.3e-29 | fmdB | S | Putative regulatory protein | ||
BLNAIMJH_00272 | 1.9e-92 | flgA | NO | SAF | ||
BLNAIMJH_00273 | 7e-35 | |||||
BLNAIMJH_00274 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
BLNAIMJH_00275 | 2.4e-53 | T | Forkhead associated domain | |||
BLNAIMJH_00276 | 3.2e-59 | sufC | O | FeS assembly ATPase SufC | ||
BLNAIMJH_00277 | 6.1e-235 | sufD | O | FeS assembly protein SufD | ||
BLNAIMJH_00278 | 1.6e-290 | sufB | O | FeS assembly protein SufB | ||
BLNAIMJH_00279 | 0.0 | S | L,D-transpeptidase catalytic domain | |||
BLNAIMJH_00280 | 3.4e-85 | 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 | |
BLNAIMJH_00281 | 1.7e-187 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
BLNAIMJH_00282 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
BLNAIMJH_00283 | 8.3e-244 | cydD | V | ABC transporter transmembrane region | ||
BLNAIMJH_00284 | 4.5e-127 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
BLNAIMJH_00285 | 6.7e-191 | 3.6.1.27 | I | PAP2 superfamily | ||
BLNAIMJH_00286 | 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 | |
BLNAIMJH_00287 | 4.5e-185 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
BLNAIMJH_00288 | 2.5e-244 | 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 | ||
BLNAIMJH_00289 | 5.6e-220 | 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 | ||
BLNAIMJH_00290 | 8.9e-81 | 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 | ||
BLNAIMJH_00291 | 6.9e-41 | yggT | S | YGGT family | ||
BLNAIMJH_00292 | 1.2e-14 | 3.1.21.3 | V | DivIVA protein | ||
BLNAIMJH_00293 | 8.5e-77 | S | LytR cell envelope-related transcriptional attenuator | |||
BLNAIMJH_00294 | 4.4e-137 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
BLNAIMJH_00295 | 4e-182 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
BLNAIMJH_00296 | 1.6e-174 | S | Protein of unknown function DUF58 | |||
BLNAIMJH_00297 | 3.6e-91 | |||||
BLNAIMJH_00298 | 1.6e-191 | S | von Willebrand factor (vWF) type A domain | |||
BLNAIMJH_00299 | 2.2e-97 | S | von Willebrand factor (vWF) type A domain | |||
BLNAIMJH_00300 | 2.9e-64 | L | DNA helicase | |||
BLNAIMJH_00301 | 2.7e-91 | mraZ | K | Belongs to the MraZ family | ||
BLNAIMJH_00302 | 1.3e-190 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
BLNAIMJH_00303 | 1.8e-62 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
BLNAIMJH_00304 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
BLNAIMJH_00305 | 1.1e-153 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
BLNAIMJH_00306 | 4.6e-48 | 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 | |
BLNAIMJH_00307 | 2.6e-142 | P | Zinc-uptake complex component A periplasmic | |||
BLNAIMJH_00308 | 1.3e-246 | pbuO | S | Permease family | ||
BLNAIMJH_00309 | 1.1e-87 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
BLNAIMJH_00310 | 3.3e-38 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
BLNAIMJH_00311 | 1.5e-112 | T | Forkhead associated domain | |||
BLNAIMJH_00312 | 5.4e-29 | E | Receptor family ligand binding region | |||
BLNAIMJH_00313 | 1.1e-195 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_00314 | 3.1e-297 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
BLNAIMJH_00315 | 1.5e-115 | S | Protein of unknown function, DUF624 | |||
BLNAIMJH_00316 | 8.9e-194 | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain | |
BLNAIMJH_00317 | 5.5e-36 | adhB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
BLNAIMJH_00318 | 2e-143 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
BLNAIMJH_00319 | 2.7e-221 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
BLNAIMJH_00320 | 3.6e-76 | S | Psort location CytoplasmicMembrane, score | |||
BLNAIMJH_00321 | 1e-182 | cat | P | Cation efflux family | ||
BLNAIMJH_00324 | 1.8e-114 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
BLNAIMJH_00325 | 8.5e-218 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
BLNAIMJH_00326 | 5.6e-225 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
BLNAIMJH_00327 | 0.0 | I | acetylesterase activity | |||
BLNAIMJH_00328 | 4e-230 | pccB | I | Carboxyl transferase domain | ||
BLNAIMJH_00329 | 0.0 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
BLNAIMJH_00330 | 2.1e-79 | bioY | S | BioY family | ||
BLNAIMJH_00331 | 1.3e-162 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
BLNAIMJH_00332 | 8.9e-80 | |||||
BLNAIMJH_00333 | 3.1e-227 | S | ATPase family associated with various cellular activities (AAA) | |||
BLNAIMJH_00334 | 0.0 | S | Fibronectin type 3 domain | |||
BLNAIMJH_00335 | 1.3e-142 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
BLNAIMJH_00336 | 4.3e-95 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
BLNAIMJH_00337 | 5.1e-306 | 3.6.3.24 | P | AAA domain, putative AbiEii toxin, Type IV TA system | ||
BLNAIMJH_00338 | 6.9e-150 | P | Cobalt transport protein | |||
BLNAIMJH_00339 | 5.3e-192 | K | helix_turn_helix ASNC type | |||
BLNAIMJH_00340 | 1e-102 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
BLNAIMJH_00341 | 3.9e-156 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
BLNAIMJH_00342 | 1.9e-40 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
BLNAIMJH_00343 | 4.2e-97 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
BLNAIMJH_00344 | 1e-179 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
BLNAIMJH_00345 | 1e-162 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
BLNAIMJH_00346 | 2.4e-186 | trpB | 4.1.1.48, 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
BLNAIMJH_00347 | 4.4e-147 | pspC | KT | PspC domain | ||
BLNAIMJH_00348 | 1.3e-91 | |||||
BLNAIMJH_00349 | 1.1e-115 | S | Protein of unknown function (DUF4125) | |||
BLNAIMJH_00350 | 1.6e-149 | S | Domain of unknown function (DUF4037) | |||
BLNAIMJH_00351 | 1.1e-139 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
BLNAIMJH_00352 | 7.1e-272 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
BLNAIMJH_00353 | 1.3e-131 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
BLNAIMJH_00354 | 3.6e-200 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
BLNAIMJH_00355 | 2e-118 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
BLNAIMJH_00356 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
BLNAIMJH_00357 | 1.8e-88 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
BLNAIMJH_00358 | 6.5e-226 | M | Glycosyl transferase 4-like domain | |||
BLNAIMJH_00359 | 1.1e-197 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
BLNAIMJH_00361 | 8.1e-188 | yocS | S | SBF-like CPA transporter family (DUF4137) | ||
BLNAIMJH_00363 | 3.3e-77 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_00364 | 0.0 | E | ABC transporter, substrate-binding protein, family 5 | |||
BLNAIMJH_00365 | 1e-113 | 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 | |
BLNAIMJH_00366 | 8.6e-125 | 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 | |
BLNAIMJH_00367 | 6.1e-241 | 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 | ||
BLNAIMJH_00368 | 1.2e-48 | pcrA | 3.6.4.12 | L | DNA helicase | |
BLNAIMJH_00369 | 1.5e-106 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
BLNAIMJH_00370 | 2.8e-244 | pbuX | F | Permease family | ||
BLNAIMJH_00371 | 0.0 | yrhL | I | Psort location CytoplasmicMembrane, score 9.99 | ||
BLNAIMJH_00372 | 2.1e-70 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BLNAIMJH_00373 | 8.8e-34 | degU | K | helix_turn_helix, Lux Regulon | ||
BLNAIMJH_00375 | 1.6e-102 | Q | Isochorismatase family | |||
BLNAIMJH_00376 | 1.1e-270 | U | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
BLNAIMJH_00377 | 8.3e-190 | yegV | G | pfkB family carbohydrate kinase | ||
BLNAIMJH_00378 | 2.1e-188 | yegU | O | ADP-ribosylglycohydrolase | ||
BLNAIMJH_00379 | 1.7e-93 | L | ribosomal rna small subunit methyltransferase | |||
BLNAIMJH_00380 | 8.5e-129 | gluP | 3.4.21.105 | S | Rhomboid family | |
BLNAIMJH_00381 | 7.6e-35 | |||||
BLNAIMJH_00382 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
BLNAIMJH_00384 | 1.2e-32 | 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 | ||
BLNAIMJH_00385 | 2.9e-129 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
BLNAIMJH_00386 | 2.3e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
BLNAIMJH_00387 | 3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
BLNAIMJH_00388 | 5.9e-143 | QT | PucR C-terminal helix-turn-helix domain | |||
BLNAIMJH_00389 | 3.8e-116 | |||||
BLNAIMJH_00390 | 2.2e-54 | |||||
BLNAIMJH_00391 | 8e-64 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
BLNAIMJH_00392 | 6.8e-144 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
BLNAIMJH_00393 | 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 | |
BLNAIMJH_00394 | 2.5e-144 | tcyC | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
BLNAIMJH_00395 | 3.8e-23 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_00396 | 3.6e-72 | rpsA | J | Ribosomal protein S1 | ||
BLNAIMJH_00397 | 7.7e-115 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
BLNAIMJH_00398 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
BLNAIMJH_00399 | 5.4e-14 | 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 | ||
BLNAIMJH_00400 | 2.8e-157 | terC | P | Integral membrane protein, TerC family | ||
BLNAIMJH_00401 | 2.7e-71 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
BLNAIMJH_00402 | 8.5e-165 | tesB | I | Thioesterase-like superfamily | ||
BLNAIMJH_00403 | 1.6e-94 | S | Protein of unknown function (DUF3180) | |||
BLNAIMJH_00404 | 2.2e-279 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
BLNAIMJH_00405 | 5.8e-155 | folP | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
BLNAIMJH_00406 | 9.6e-115 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
BLNAIMJH_00407 | 9.1e-236 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
BLNAIMJH_00408 | 3.6e-304 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
BLNAIMJH_00409 | 2.6e-180 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
BLNAIMJH_00410 | 2.3e-61 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
BLNAIMJH_00411 | 1.6e-134 | 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 | |
BLNAIMJH_00412 | 5.2e-156 | hgdC | I | BadF/BadG/BcrA/BcrD ATPase family | ||
BLNAIMJH_00413 | 1e-136 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
BLNAIMJH_00414 | 4.3e-88 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
BLNAIMJH_00415 | 2.5e-247 | S | zinc finger | |||
BLNAIMJH_00416 | 7.5e-71 | S | Bacterial PH domain | |||
BLNAIMJH_00417 | 1.5e-76 | |||||
BLNAIMJH_00418 | 7.1e-200 | V | Domain of unknown function (DUF3427) | |||
BLNAIMJH_00419 | 1.5e-134 | helD | 3.6.4.12 | L | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00420 | 5.5e-59 | murJ | KLT | MviN-like protein | ||
BLNAIMJH_00421 | 4.1e-306 | murJ | KLT | MviN-like protein | ||
BLNAIMJH_00422 | 0.0 | M | Conserved repeat domain | |||
BLNAIMJH_00423 | 9e-54 | S | Fibronectin type 3 domain | |||
BLNAIMJH_00424 | 6.2e-263 | KLT | Protein tyrosine kinase | |||
BLNAIMJH_00425 | 3.3e-62 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
BLNAIMJH_00426 | 1.4e-157 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
BLNAIMJH_00427 | 1.1e-200 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_00428 | 8.7e-58 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
BLNAIMJH_00429 | 9.4e-151 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
BLNAIMJH_00430 | 7e-281 | clcA | P | Voltage gated chloride channel | ||
BLNAIMJH_00431 | 2.3e-107 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
BLNAIMJH_00432 | 3.5e-285 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
BLNAIMJH_00433 | 2.1e-210 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_00434 | 2.2e-257 | araB | 2.7.1.16, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
BLNAIMJH_00435 | 1.8e-23 | 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 | |
BLNAIMJH_00436 | 3.1e-168 | pstA | P | Phosphate transport system permease | ||
BLNAIMJH_00437 | 1.3e-163 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
BLNAIMJH_00438 | 3e-196 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
BLNAIMJH_00439 | 3.4e-129 | KT | Transcriptional regulatory protein, C terminal | |||
BLNAIMJH_00440 | 3.8e-251 | 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 | |
BLNAIMJH_00441 | 1.7e-243 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00442 | 1.8e-221 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00444 | 3.3e-227 | P | Sodium/hydrogen exchanger family | |||
BLNAIMJH_00445 | 0.0 | V | FtsX-like permease family | |||
BLNAIMJH_00446 | 0.0 | yjcE | P | Sodium/hydrogen exchanger family | ||
BLNAIMJH_00447 | 5.9e-154 | ypfH | S | Phospholipase/Carboxylesterase | ||
BLNAIMJH_00448 | 4e-112 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
BLNAIMJH_00449 | 3.5e-117 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
BLNAIMJH_00450 | 1.3e-107 | kcsA | U | Ion channel | ||
BLNAIMJH_00451 | 5.1e-39 | pepC | 3.4.22.40 | E | homocysteine catabolic process | |
BLNAIMJH_00452 | 3.4e-79 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00453 | 3.7e-105 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00454 | 5.5e-89 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00455 | 1e-47 | S | Domain of unknown function (DUF4193) | |||
BLNAIMJH_00456 | 3.2e-83 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
BLNAIMJH_00457 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | 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 | |
BLNAIMJH_00458 | 7.9e-102 | ppiA | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
BLNAIMJH_00459 | 2.9e-232 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_00460 | 1.2e-175 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BLNAIMJH_00461 | 2e-269 | KLT | Domain of unknown function (DUF4032) | |||
BLNAIMJH_00462 | 6.6e-107 | |||||
BLNAIMJH_00463 | 7.1e-73 | |||||
BLNAIMJH_00464 | 6.1e-191 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
BLNAIMJH_00465 | 1.8e-16 | 3.2.1.78 | GH26 | G | Glycosyl hydrolase family 26 | |
BLNAIMJH_00466 | 9e-127 | dedA | S | SNARE associated Golgi protein | ||
BLNAIMJH_00468 | 1.4e-107 | S | Patatin-like phospholipase | |||
BLNAIMJH_00469 | 1.9e-186 | K | LysR substrate binding domain protein | |||
BLNAIMJH_00470 | 2.1e-240 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
BLNAIMJH_00471 | 1e-119 | S | Phospholipase/Carboxylesterase | |||
BLNAIMJH_00472 | 6.3e-136 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00473 | 1.6e-259 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
BLNAIMJH_00474 | 5.8e-208 | GK | ROK family | |||
BLNAIMJH_00475 | 2e-158 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
BLNAIMJH_00476 | 1.9e-128 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
BLNAIMJH_00477 | 5.2e-264 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
BLNAIMJH_00478 | 1.2e-75 | tcsS2 | T | Histidine kinase | ||
BLNAIMJH_00479 | 1.8e-30 | tcsS2 | T | Histidine kinase | ||
BLNAIMJH_00480 | 3.9e-254 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
BLNAIMJH_00481 | 4.6e-188 | uspA | T | Belongs to the universal stress protein A family | ||
BLNAIMJH_00482 | 1.2e-182 | S | Protein of unknown function (DUF3027) | |||
BLNAIMJH_00483 | 4.5e-67 | cspB | K | 'Cold-shock' DNA-binding domain | ||
BLNAIMJH_00484 | 0.0 | S | LPXTG-motif cell wall anchor domain protein | |||
BLNAIMJH_00485 | 1.9e-232 | dinF | V | MatE | ||
BLNAIMJH_00486 | 1.5e-97 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
BLNAIMJH_00487 | 3.3e-158 | IV02_28330 | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BLNAIMJH_00488 | 2.4e-203 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
BLNAIMJH_00489 | 1.9e-80 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
BLNAIMJH_00490 | 1.2e-111 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
BLNAIMJH_00491 | 5.6e-146 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_00492 | 2.5e-153 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_00493 | 3.2e-153 | P | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_00494 | 7.2e-233 | M | Protein of unknown function (DUF2961) | |||
BLNAIMJH_00495 | 2.1e-72 | I | alpha/beta hydrolase fold | |||
BLNAIMJH_00496 | 5e-42 | G | ABC transporter substrate-binding protein | |||
BLNAIMJH_00497 | 1.2e-230 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
BLNAIMJH_00498 | 8.4e-210 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
BLNAIMJH_00499 | 6.1e-108 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
BLNAIMJH_00500 | 9e-72 | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | |||
BLNAIMJH_00501 | 9.1e-121 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
BLNAIMJH_00502 | 5e-284 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
BLNAIMJH_00503 | 2.6e-109 | S | LytR cell envelope-related transcriptional attenuator | |||
BLNAIMJH_00504 | 1.1e-167 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
BLNAIMJH_00505 | 2.2e-105 | ksgA | 2.1.1.182, 2.1.1.184 | 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 | |
BLNAIMJH_00506 | 1.4e-176 | S | Calcineurin-like phosphoesterase | |||
BLNAIMJH_00507 | 2.4e-115 | |||||
BLNAIMJH_00508 | 2.7e-48 | yitI | S | Acetyltransferase (GNAT) domain | ||
BLNAIMJH_00509 | 1.8e-209 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
BLNAIMJH_00510 | 3.6e-32 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
BLNAIMJH_00511 | 0.0 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
BLNAIMJH_00512 | 2.1e-241 | V | ABC transporter permease | |||
BLNAIMJH_00513 | 8.4e-157 | V | ABC transporter | |||
BLNAIMJH_00514 | 5.1e-150 | T | HD domain | |||
BLNAIMJH_00515 | 1e-167 | S | Glutamine amidotransferase domain | |||
BLNAIMJH_00516 | 0.0 | kup | P | Transport of potassium into the cell | ||
BLNAIMJH_00517 | 7.7e-185 | tatD | L | TatD related DNase | ||
BLNAIMJH_00518 | 0.0 | G | Alpha-L-arabinofuranosidase C-terminus | |||
BLNAIMJH_00519 | 8.1e-22 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
BLNAIMJH_00520 | 6.6e-221 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_00521 | 0.0 | rafA | 3.2.1.22 | G | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00522 | 8e-126 | |||||
BLNAIMJH_00523 | 0.0 | yknV | V | ABC transporter | ||
BLNAIMJH_00524 | 0.0 | mdlA2 | V | ABC transporter | ||
BLNAIMJH_00525 | 1.1e-214 | lipA | I | Hydrolase, alpha beta domain protein | ||
BLNAIMJH_00526 | 8.2e-104 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00527 | 3.4e-281 | 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) | |
BLNAIMJH_00528 | 1.1e-106 | S | Phosphatidylethanolamine-binding protein | |||
BLNAIMJH_00529 | 0.0 | pepD | E | Peptidase family C69 | ||
BLNAIMJH_00530 | 0.0 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
BLNAIMJH_00531 | 8.5e-218 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
BLNAIMJH_00532 | 4.2e-17 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
BLNAIMJH_00534 | 6.3e-62 | |||||
BLNAIMJH_00535 | 3.3e-96 | M | Peptidase family M23 | |||
BLNAIMJH_00536 | 0.0 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
BLNAIMJH_00537 | 6.8e-207 | G | ABC transporter substrate-binding protein | |||
BLNAIMJH_00538 | 3.2e-88 | naiP | U | Sugar (and other) transporter | ||
BLNAIMJH_00539 | 1.4e-150 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
BLNAIMJH_00540 | 6.8e-153 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
BLNAIMJH_00541 | 2e-177 | xerD | D | recombinase XerD | ||
BLNAIMJH_00542 | 1.4e-57 | S | Domain of unknown function (DUF5067) | |||
BLNAIMJH_00543 | 1.7e-127 | ybhL | S | Belongs to the BI1 family | ||
BLNAIMJH_00544 | 1e-176 | ydeD | EG | EamA-like transporter family | ||
BLNAIMJH_00545 | 4.2e-155 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
BLNAIMJH_00546 | 1.4e-16 | |||||
BLNAIMJH_00547 | 2.4e-116 | |||||
BLNAIMJH_00549 | 0.0 | ams | 2.4.1.4, 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha amylase, catalytic domain |
BLNAIMJH_00550 | 1.2e-82 | acpS | 2.7.8.7, 3.2.1.52 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
BLNAIMJH_00551 | 5.9e-91 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
BLNAIMJH_00553 | 1.2e-247 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
BLNAIMJH_00554 | 4.3e-195 | I | Diacylglycerol kinase catalytic domain | |||
BLNAIMJH_00555 | 1.4e-153 | arbG | K | CAT RNA binding domain | ||
BLNAIMJH_00556 | 2.6e-49 | crr | G | pts system, glucose-specific IIABC component | ||
BLNAIMJH_00557 | 1.6e-169 | S | G5 | |||
BLNAIMJH_00558 | 4.6e-88 | |||||
BLNAIMJH_00560 | 7.1e-263 | rfbP | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
BLNAIMJH_00561 | 4.4e-211 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
BLNAIMJH_00562 | 3e-187 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
BLNAIMJH_00563 | 4.2e-74 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
BLNAIMJH_00564 | 1.4e-92 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
BLNAIMJH_00565 | 2e-120 | |||||
BLNAIMJH_00567 | 3.2e-179 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
BLNAIMJH_00568 | 1.1e-226 | C | Na H antiporter family protein | |||
BLNAIMJH_00569 | 2e-67 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
BLNAIMJH_00570 | 6.5e-121 | |||||
BLNAIMJH_00571 | 6.3e-122 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
BLNAIMJH_00572 | 5.4e-130 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
BLNAIMJH_00573 | 6.8e-264 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
BLNAIMJH_00574 | 1.1e-115 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
BLNAIMJH_00575 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
BLNAIMJH_00576 | 5.8e-177 | T | Protein tyrosine kinase | |||
BLNAIMJH_00577 | 3.4e-103 | malE | G | Bacterial extracellular solute-binding protein | ||
BLNAIMJH_00578 | 0.0 | malL | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain |
BLNAIMJH_00579 | 7.7e-151 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
BLNAIMJH_00580 | 1.1e-53 | DJ | Addiction module toxin, RelE StbE family | |||
BLNAIMJH_00581 | 2.7e-49 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
BLNAIMJH_00582 | 7.2e-116 | S | Short repeat of unknown function (DUF308) | |||
BLNAIMJH_00583 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00584 | 6.9e-289 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
BLNAIMJH_00585 | 2.1e-218 | luxE | 6.2.1.19 | H | long-chain-fatty-acid--luciferin-component ligase, acyl-protein synthase | |
BLNAIMJH_00586 | 5.4e-156 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
BLNAIMJH_00587 | 3.6e-70 | G | ABC transporter permease | |||
BLNAIMJH_00588 | 7.4e-116 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_00589 | 7.7e-14 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_00590 | 2.2e-235 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_00591 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
BLNAIMJH_00592 | 3.9e-108 | ribU | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
BLNAIMJH_00593 | 9.9e-132 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00594 | 4.1e-50 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
BLNAIMJH_00595 | 3.2e-75 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
BLNAIMJH_00596 | 2.8e-15 | P | Belongs to the ABC transporter superfamily | |||
BLNAIMJH_00597 | 1.4e-43 | XAC3035 | O | Glutaredoxin | ||
BLNAIMJH_00598 | 3.1e-127 | XK27_08050 | O | prohibitin homologues | ||
BLNAIMJH_00599 | 1.7e-13 | S | Domain of unknown function (DUF4143) | |||
BLNAIMJH_00600 | 4.3e-75 | |||||
BLNAIMJH_00601 | 9.6e-135 | V | ATPases associated with a variety of cellular activities | |||
BLNAIMJH_00602 | 5.7e-147 | M | Conserved repeat domain | |||
BLNAIMJH_00603 | 1.3e-255 | macB_8 | V | MacB-like periplasmic core domain | ||
BLNAIMJH_00604 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
BLNAIMJH_00605 | 1.2e-183 | adh3 | C | Zinc-binding dehydrogenase | ||
BLNAIMJH_00606 | 1.1e-84 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
BLNAIMJH_00607 | 2.4e-225 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
BLNAIMJH_00608 | 8.8e-89 | zur | P | Belongs to the Fur family | ||
BLNAIMJH_00609 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
BLNAIMJH_00610 | 2.7e-202 | psuK | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
BLNAIMJH_00611 | 9.1e-189 | yeiI | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
BLNAIMJH_00612 | 1.3e-128 | trpF | 5.3.1.24 | E | N-(5'phosphoribosyl)anthranilate (PRA) isomerase | |
BLNAIMJH_00613 | 4.8e-213 | 1.1.1.1 | C | Iron-containing alcohol dehydrogenase | ||
BLNAIMJH_00614 | 1.1e-183 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
BLNAIMJH_00615 | 2.1e-247 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_00616 | 2.8e-235 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
BLNAIMJH_00617 | 1e-78 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
BLNAIMJH_00618 | 4.5e-220 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_00619 | 2.4e-161 | amyD3 | P | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_00620 | 4.1e-57 | amyC5 | P | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_00621 | 3.2e-36 | amyC5 | P | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_00622 | 2.3e-213 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
BLNAIMJH_00623 | 2.8e-249 | T | GHKL domain | |||
BLNAIMJH_00624 | 2.8e-151 | T | LytTr DNA-binding domain | |||
BLNAIMJH_00625 | 2.1e-88 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
BLNAIMJH_00626 | 7.9e-172 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
BLNAIMJH_00627 | 4.3e-188 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
BLNAIMJH_00628 | 1.2e-36 | |||||
BLNAIMJH_00629 | 4.8e-79 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
BLNAIMJH_00630 | 1.7e-13 | tpd | P | Fe2+ transport protein | ||
BLNAIMJH_00631 | 4.2e-231 | S | Predicted membrane protein (DUF2318) | |||
BLNAIMJH_00632 | 8e-220 | macB_2 | V | ABC transporter permease | ||
BLNAIMJH_00634 | 9.1e-206 | P | NMT1/THI5 like | |||
BLNAIMJH_00635 | 3.2e-142 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
BLNAIMJH_00636 | 5.9e-257 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
BLNAIMJH_00637 | 2.8e-249 | aroA | 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
BLNAIMJH_00639 | 1.5e-211 | ykiI | ||||
BLNAIMJH_00640 | 1.7e-68 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
BLNAIMJH_00641 | 2.2e-131 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
BLNAIMJH_00642 | 1e-53 | M | Lysin motif | |||
BLNAIMJH_00643 | 8.5e-84 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
BLNAIMJH_00644 | 1.1e-217 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
BLNAIMJH_00645 | 2.2e-73 | L | DNA helicase | |||
BLNAIMJH_00646 | 5.1e-141 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
BLNAIMJH_00648 | 3.6e-85 | ptpA | 3.1.3.48 | T | low molecular weight | |
BLNAIMJH_00649 | 2.4e-129 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
BLNAIMJH_00650 | 1.9e-180 | 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 | |
BLNAIMJH_00651 | 2.4e-26 | attW | O | OsmC-like protein | ||
BLNAIMJH_00652 | 4.5e-16 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
BLNAIMJH_00653 | 3e-25 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
BLNAIMJH_00654 | 1.4e-113 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
BLNAIMJH_00655 | 1.9e-124 | livF | E | ATPases associated with a variety of cellular activities | ||
BLNAIMJH_00656 | 4.8e-151 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
BLNAIMJH_00657 | 1.3e-134 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
BLNAIMJH_00658 | 3.2e-169 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
BLNAIMJH_00659 | 3.6e-108 | yitW | S | Iron-sulfur cluster assembly protein | ||
BLNAIMJH_00660 | 2.6e-97 | iscU | C | SUF system FeS assembly protein, NifU family | ||
BLNAIMJH_00661 | 1.9e-239 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
BLNAIMJH_00662 | 1.2e-24 | sufC | O | FeS assembly ATPase SufC | ||
BLNAIMJH_00663 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
BLNAIMJH_00664 | 1.4e-27 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
BLNAIMJH_00665 | 1.9e-26 | thiS | 2.8.1.10 | H | ThiS family | |
BLNAIMJH_00666 | 5.8e-129 | thiF | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
BLNAIMJH_00667 | 1.2e-166 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
BLNAIMJH_00668 | 3.5e-280 | cycA | E | Amino acid permease | ||
BLNAIMJH_00669 | 3.9e-12 | lon | T | Belongs to the peptidase S16 family | ||
BLNAIMJH_00670 | 2.5e-281 | S | Zincin-like metallopeptidase | |||
BLNAIMJH_00671 | 1.6e-282 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
BLNAIMJH_00672 | 1.7e-70 | 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 | |
BLNAIMJH_00673 | 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 | ||
BLNAIMJH_00674 | 8.3e-102 | ybiT | S | ABC transporter | ||
BLNAIMJH_00675 | 1.4e-157 | S | IMP dehydrogenase activity | |||
BLNAIMJH_00676 | 1.6e-279 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
BLNAIMJH_00677 | 1.4e-41 | mazG | 3.6.1.66 | S | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00678 | 8.7e-46 | S | Protein of unknown function (DUF3046) | |||
BLNAIMJH_00679 | 1.6e-80 | K | Helix-turn-helix XRE-family like proteins | |||
BLNAIMJH_00680 | 5.5e-98 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
BLNAIMJH_00681 | 4.1e-124 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
BLNAIMJH_00682 | 2.8e-29 | ftsK | D | FtsK SpoIIIE family protein | ||
BLNAIMJH_00683 | 0.0 | pcrA | 3.6.4.12 | L | DNA helicase | |
BLNAIMJH_00684 | 1.7e-61 | S | Domain of unknown function (DUF4418) | |||
BLNAIMJH_00685 | 2.3e-292 | lytC | 2.1.1.197, 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
BLNAIMJH_00686 | 3.4e-161 | rfbJ | M | Glycosyl transferase family 2 | ||
BLNAIMJH_00687 | 6.7e-186 | S | Psort location CytoplasmicMembrane, score | |||
BLNAIMJH_00688 | 2.8e-82 | S | Acyltransferase family | |||
BLNAIMJH_00689 | 6.1e-109 | rgpC | U | Transport permease protein | ||
BLNAIMJH_00690 | 1.2e-174 | rgpD | 3.6.3.38 | GM | ABC transporter, ATP-binding protein | |
BLNAIMJH_00691 | 1.4e-181 | M | Glycosyl transferases group 1 | |||
BLNAIMJH_00692 | 1.7e-136 | glfT1 | 1.1.1.133 | S | Glycosyltransferase, group 2 family protein | |
BLNAIMJH_00693 | 7.6e-222 | glfT | 2.4.1.288 | GT2 | S | Glycosyltransferase like family 2 |
BLNAIMJH_00694 | 4.3e-310 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
BLNAIMJH_00695 | 2.2e-198 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
BLNAIMJH_00696 | 4.9e-232 | S | AAA domain | |||
BLNAIMJH_00697 | 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 | ||
BLNAIMJH_00698 | 3e-234 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
BLNAIMJH_00699 | 7.1e-09 | pnuC | H | Nicotinamide mononucleotide transporter | ||
BLNAIMJH_00700 | 8e-301 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
BLNAIMJH_00701 | 2.6e-177 | S | Sucrose-6F-phosphate phosphohydrolase | |||
BLNAIMJH_00702 | 2.4e-32 | secG | U | Preprotein translocase SecG subunit | ||
BLNAIMJH_00703 | 1.6e-249 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
BLNAIMJH_00704 | 1e-204 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
BLNAIMJH_00705 | 0.0 | pip | S | YhgE Pip domain protein | ||
BLNAIMJH_00706 | 0.0 | pip | S | YhgE Pip domain protein | ||
BLNAIMJH_00707 | 7e-170 | yddG | EG | EamA-like transporter family | ||
BLNAIMJH_00708 | 3.2e-65 | K | Helix-turn-helix XRE-family like proteins | |||
BLNAIMJH_00710 | 4.7e-162 | htpX | O | Belongs to the peptidase M48B family | ||
BLNAIMJH_00711 | 3.1e-270 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
BLNAIMJH_00712 | 7.9e-188 | ansA | 3.5.1.1 | EJ | Asparaginase | |
BLNAIMJH_00713 | 0.0 | cadA | P | E1-E2 ATPase | ||
BLNAIMJH_00714 | 1.1e-283 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
BLNAIMJH_00715 | 2.7e-268 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
BLNAIMJH_00716 | 3.5e-112 | pgsA1 | 2.7.8.11, 2.7.8.5 | I | CDP-alcohol phosphatidyltransferase | |
BLNAIMJH_00717 | 5.2e-128 | yebC | K | transcriptional regulatory protein | ||
BLNAIMJH_00718 | 1e-99 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
BLNAIMJH_00719 | 1e-105 | 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 | |
BLNAIMJH_00720 | 4e-195 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
BLNAIMJH_00722 | 1.1e-107 | icaR | K | Bacterial regulatory proteins, tetR family | ||
BLNAIMJH_00724 | 6.4e-57 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
BLNAIMJH_00725 | 2.2e-263 | trkB | P | Cation transport protein | ||
BLNAIMJH_00726 | 5.2e-116 | trkA | P | TrkA-N domain | ||
BLNAIMJH_00727 | 7.3e-83 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
BLNAIMJH_00728 | 1.5e-85 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
BLNAIMJH_00729 | 1.3e-101 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
BLNAIMJH_00730 | 3.9e-92 | 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) | |
BLNAIMJH_00731 | 9.7e-305 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
BLNAIMJH_00732 | 3.7e-21 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BLNAIMJH_00733 | 1.3e-92 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
BLNAIMJH_00734 | 0.0 | comE | S | Competence protein | ||
BLNAIMJH_00735 | 7.8e-70 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
BLNAIMJH_00736 | 1.6e-146 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
BLNAIMJH_00737 | 3.3e-160 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
BLNAIMJH_00738 | 1.4e-24 | pup | S | Protein modifier that is covalently attached to lysine residues of substrate proteins, thereby targeting them for proteasomal degradation. The tagging system is termed pupylation | ||
BLNAIMJH_00739 | 6.7e-281 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
BLNAIMJH_00740 | 1.8e-181 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
BLNAIMJH_00741 | 6.8e-100 | |||||
BLNAIMJH_00742 | 8.3e-159 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BLNAIMJH_00743 | 4.2e-276 | scrT | G | Transporter major facilitator family protein | ||
BLNAIMJH_00744 | 1.3e-24 | yhjE | EGP | Sugar (and other) transporter | ||
BLNAIMJH_00745 | 5.3e-89 | yhgF | K | response to ionizing radiation | ||
BLNAIMJH_00746 | 2e-169 | 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 | ||
BLNAIMJH_00747 | 1e-196 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
BLNAIMJH_00748 | 6.3e-51 | 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 | ||
BLNAIMJH_00749 | 7.1e-183 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
BLNAIMJH_00750 | 1.1e-170 | rapZ | S | Displays ATPase and GTPase activities | ||
BLNAIMJH_00751 | 2.8e-171 | whiA | K | May be required for sporulation | ||
BLNAIMJH_00752 | 5e-54 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
BLNAIMJH_00753 | 1e-128 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
BLNAIMJH_00754 | 9.1e-240 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_00755 | 4e-47 | 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) | ||
BLNAIMJH_00756 | 1.2e-236 | amt | U | Ammonium Transporter Family | ||
BLNAIMJH_00757 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
BLNAIMJH_00758 | 1.1e-65 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
BLNAIMJH_00759 | 1.3e-53 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
BLNAIMJH_00760 | 2.7e-216 | ino1 | 5.5.1.4 | I | Myo-inositol-1-phosphate synthase | |
BLNAIMJH_00761 | 4.8e-168 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
BLNAIMJH_00762 | 0.0 | S | Protein of unknown function (DUF975) | |||
BLNAIMJH_00763 | 8.6e-137 | S | Putative ABC-transporter type IV | |||
BLNAIMJH_00764 | 3.6e-81 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
BLNAIMJH_00765 | 6e-39 | ptsH | G | PTS HPr component phosphorylation site | ||
BLNAIMJH_00766 | 7.3e-181 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_00767 | 4.2e-193 | holB | 2.7.7.7 | L | DNA polymerase III | |
BLNAIMJH_00768 | 8.7e-83 | 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 | |
BLNAIMJH_00769 | 2.5e-36 | |||||
BLNAIMJH_00770 | 3.4e-59 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
BLNAIMJH_00771 | 3.6e-128 | pgm3 | G | Phosphoglycerate mutase family | ||
BLNAIMJH_00772 | 3.4e-51 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
BLNAIMJH_00773 | 1.5e-25 | 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 | ||
BLNAIMJH_00774 | 1.7e-51 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
BLNAIMJH_00775 | 7.8e-185 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
BLNAIMJH_00776 | 1.9e-84 | argR | K | Regulates arginine biosynthesis genes | ||
BLNAIMJH_00777 | 1.3e-237 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
BLNAIMJH_00778 | 9.4e-137 | G | Periplasmic binding protein domain | |||
BLNAIMJH_00779 | 3e-271 | araG | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | |
BLNAIMJH_00780 | 5.7e-94 | gguB | U | Branched-chain amino acid transport system / permease component | ||
BLNAIMJH_00781 | 1.3e-35 | gatB | 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) | |
BLNAIMJH_00782 | 2e-205 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
BLNAIMJH_00783 | 2.1e-51 | S | Protein of unknown function (DUF2469) | |||
BLNAIMJH_00784 | 1.9e-62 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
BLNAIMJH_00785 | 4.8e-102 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
BLNAIMJH_00786 | 1.2e-137 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
BLNAIMJH_00787 | 3.9e-187 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_00788 | 2.1e-260 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_00791 | 2.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
BLNAIMJH_00792 | 1.6e-147 | |||||
BLNAIMJH_00793 | 2.9e-122 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
BLNAIMJH_00794 | 4e-34 | ybiT | S | ABC transporter | ||
BLNAIMJH_00795 | 4.7e-111 | pncA | 2.7.11.1, 3.5.1.19 | Q | Isochorismatase family | |
BLNAIMJH_00796 | 2.8e-66 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
BLNAIMJH_00798 | 2e-13 | |||||
BLNAIMJH_00799 | 1.8e-116 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00800 | 1e-82 | 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) | |
BLNAIMJH_00801 | 1.8e-141 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
BLNAIMJH_00802 | 3.2e-101 | |||||
BLNAIMJH_00803 | 2.9e-243 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
BLNAIMJH_00804 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
BLNAIMJH_00805 | 3.7e-210 | mmuP | E | amino acid | ||
BLNAIMJH_00806 | 3.6e-64 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
BLNAIMJH_00807 | 1.9e-113 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
BLNAIMJH_00808 | 0.0 | scrB | 3.2.1.26, 3.2.1.97 | GH101,GH32 | N | Glycosyl hydrolases family 43 |
BLNAIMJH_00809 | 0.0 | N | Bacterial Ig-like domain 2 | |||
BLNAIMJH_00810 | 2.4e-168 | rmuC | S | RmuC family | ||
BLNAIMJH_00811 | 5.2e-135 | 3.6.3.3, 3.6.3.5, 3.6.3.54 | P | Heavy metal translocating P-type atpase | ||
BLNAIMJH_00812 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
BLNAIMJH_00813 | 4e-164 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
BLNAIMJH_00814 | 6.5e-148 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
BLNAIMJH_00815 | 2.5e-80 | |||||
BLNAIMJH_00816 | 1.3e-23 | cjaA | ET | Bacterial periplasmic substrate-binding proteins | ||
BLNAIMJH_00817 | 9.1e-200 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
BLNAIMJH_00818 | 1.2e-152 | metQ | M | NLPA lipoprotein | ||
BLNAIMJH_00819 | 4.6e-36 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
BLNAIMJH_00820 | 1.9e-204 | murB | 1.3.1.98 | M | Cell wall formation | |
BLNAIMJH_00821 | 2.8e-266 | E | aromatic amino acid transport protein AroP K03293 | |||
BLNAIMJH_00822 | 8.3e-59 | fdxA | C | 4Fe-4S binding domain | ||
BLNAIMJH_00823 | 1.1e-214 | dapC | E | Aminotransferase class I and II | ||
BLNAIMJH_00824 | 2.9e-36 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
BLNAIMJH_00825 | 0.0 | G | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00826 | 2e-232 | 3.2.1.156 | GH8 | G | CBM9 module, glycoside hydrolase family 8 protein and carbohydrate esterase family 4 protein K01238 | |
BLNAIMJH_00827 | 0.0 | G | candidate polyfunctional acetylxylan esterase b-xylosidase A-L-arabinofuranosidase, CBM9 module, glycoside hydrolase family 43 protein and carbohydrate esterase family 6 protein K01238 | |||
BLNAIMJH_00828 | 5.4e-299 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
BLNAIMJH_00830 | 6.5e-227 | 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 | |
BLNAIMJH_00831 | 6.1e-252 | M | Bacterial capsule synthesis protein PGA_cap | |||
BLNAIMJH_00832 | 2.7e-185 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BLNAIMJH_00833 | 2.1e-114 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
BLNAIMJH_00834 | 6.9e-122 | |||||
BLNAIMJH_00835 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
BLNAIMJH_00836 | 2.6e-160 | glnA | 6.3.1.2 | E | glutamine synthetase | |
BLNAIMJH_00837 | 4e-42 | V | DNA modification | |||
BLNAIMJH_00838 | 2.2e-113 | ung2 | 3.2.2.27 | L | Uracil DNA glycosylase superfamily | |
BLNAIMJH_00839 | 1.5e-17 | L | HNH endonuclease | |||
BLNAIMJH_00840 | 4.5e-37 | |||||
BLNAIMJH_00841 | 5e-156 | NT | phage tail tape measure protein | |||
BLNAIMJH_00842 | 1.2e-107 | |||||
BLNAIMJH_00843 | 8.9e-45 | |||||
BLNAIMJH_00844 | 1.4e-28 | S | Bacteriophage holin family | |||
BLNAIMJH_00845 | 1.4e-81 | 3.2.1.20, 3.5.1.28 | GH31 | V | N-acetylmuramoyl-L-alanine amidase | |
BLNAIMJH_00846 | 4.8e-90 | L | Phage integrase family | |||
BLNAIMJH_00847 | 1.4e-272 | 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 | |
BLNAIMJH_00848 | 3.3e-192 | yfdV | S | Membrane transport protein | ||
BLNAIMJH_00849 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
BLNAIMJH_00850 | 1e-257 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
BLNAIMJH_00851 | 9e-184 | lacR | K | Transcriptional regulator, LacI family | ||
BLNAIMJH_00852 | 1.3e-28 | |||||
BLNAIMJH_00853 | 4.5e-213 | xylE | U | Sugar (and other) transporter | ||
BLNAIMJH_00854 | 2.8e-25 | G | Domain of unknown function (DUF4432) | |||
BLNAIMJH_00856 | 1.6e-156 | S | PAC2 family | |||
BLNAIMJH_00857 | 6.9e-156 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
BLNAIMJH_00858 | 5.1e-158 | G | Fructosamine kinase | |||
BLNAIMJH_00859 | 3.1e-29 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
BLNAIMJH_00860 | 1.4e-126 | L | Protein of unknown function (DUF1524) | |||
BLNAIMJH_00861 | 1.6e-233 | T | Diguanylate cyclase (GGDEF) domain protein | |||
BLNAIMJH_00862 | 8.2e-78 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BLNAIMJH_00863 | 9.5e-09 | M | Protein of unknown function (DUF3152) | |||
BLNAIMJH_00864 | 9.2e-130 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
BLNAIMJH_00865 | 1.3e-30 | S | zinc-ribbon domain | |||
BLNAIMJH_00866 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
BLNAIMJH_00867 | 4.5e-224 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
BLNAIMJH_00868 | 5e-91 | |||||
BLNAIMJH_00869 | 2.7e-117 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
BLNAIMJH_00870 | 9.4e-208 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
BLNAIMJH_00871 | 0.0 | G | Bacterial Ig-like domain (group 4) | |||
BLNAIMJH_00872 | 0.0 | sca1 | 3.2.1.187 | GH121 | DG | Bacterial Ig-like domain (group 4) |
BLNAIMJH_00873 | 0.0 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
BLNAIMJH_00874 | 9.3e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_00875 | 3.1e-167 | P | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_00876 | 1.6e-241 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
BLNAIMJH_00877 | 8.2e-221 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
BLNAIMJH_00878 | 2.9e-69 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
BLNAIMJH_00879 | 1.9e-192 | 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) | |
BLNAIMJH_00880 | 7.2e-11 | 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) | |
BLNAIMJH_00881 | 4.7e-132 | ftsK | D | FtsK SpoIIIE family protein | ||
BLNAIMJH_00882 | 2.5e-65 | ftsK | D | FtsK SpoIIIE family protein | ||
BLNAIMJH_00883 | 0.0 | G | Glycosyl hydrolase family 20, domain 2 | |||
BLNAIMJH_00884 | 1.9e-172 | 2.7.1.2 | GK | ROK family | ||
BLNAIMJH_00885 | 3.1e-157 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
BLNAIMJH_00886 | 9.6e-124 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
BLNAIMJH_00887 | 8.1e-196 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
BLNAIMJH_00888 | 7.1e-264 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_00889 | 1.2e-74 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
BLNAIMJH_00890 | 2.1e-28 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
BLNAIMJH_00891 | 4.5e-115 | hspR | K | transcriptional regulator, MerR family | ||
BLNAIMJH_00892 | 8.6e-47 | |||||
BLNAIMJH_00893 | 2.3e-130 | S | HAD hydrolase, family IA, variant 3 | |||
BLNAIMJH_00894 | 5.3e-33 | S | AIG2-like family | |||
BLNAIMJH_00895 | 1.8e-73 | 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 | ||
BLNAIMJH_00896 | 1.9e-139 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
BLNAIMJH_00897 | 1.1e-83 | def | 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 | |
BLNAIMJH_00898 | 5.2e-115 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
BLNAIMJH_00899 | 2e-09 | |||||
BLNAIMJH_00900 | 1.8e-50 | sdpR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
BLNAIMJH_00901 | 8.8e-139 | S | SdpI/YhfL protein family | |||
BLNAIMJH_00902 | 2.1e-109 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
BLNAIMJH_00903 | 5.5e-161 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
BLNAIMJH_00904 | 2e-102 | |||||
BLNAIMJH_00905 | 6.1e-191 | nusA | K | Participates in both transcription termination and antitermination | ||
BLNAIMJH_00906 | 3.4e-28 | |||||
BLNAIMJH_00907 | 2.8e-90 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
BLNAIMJH_00908 | 0.0 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
BLNAIMJH_00909 | 2.4e-69 | yhjX | EGP | Major facilitator Superfamily | ||
BLNAIMJH_00910 | 1.7e-81 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BLNAIMJH_00911 | 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 | |
BLNAIMJH_00912 | 1.8e-83 | K | Cro/C1-type HTH DNA-binding domain | |||
BLNAIMJH_00913 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
BLNAIMJH_00914 | 1.8e-75 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
BLNAIMJH_00915 | 1.1e-239 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
BLNAIMJH_00916 | 7.8e-132 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
BLNAIMJH_00917 | 6.8e-34 | E | ABC transporter, substrate-binding protein, family 5 | |||
BLNAIMJH_00919 | 1.6e-171 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
BLNAIMJH_00920 | 5.2e-08 | |||||
BLNAIMJH_00921 | 2.8e-34 | |||||
BLNAIMJH_00922 | 2.8e-165 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
BLNAIMJH_00923 | 3.5e-225 | 2.7.13.3 | T | Histidine kinase | ||
BLNAIMJH_00924 | 3.2e-113 | K | helix_turn_helix, Lux Regulon | |||
BLNAIMJH_00925 | 2.2e-114 | V | ATPases associated with a variety of cellular activities | |||
BLNAIMJH_00926 | 7.2e-245 | T | Histidine kinase | |||
BLNAIMJH_00927 | 9e-116 | K | helix_turn_helix, Lux Regulon | |||
BLNAIMJH_00928 | 1.5e-106 | S | Protein of unknown function, DUF624 | |||
BLNAIMJH_00929 | 2.9e-13 | S | Transposon-encoded protein TnpV | |||
BLNAIMJH_00930 | 2.2e-108 | pepE | 3.4.13.21 | E | Peptidase family S51 | |
BLNAIMJH_00931 | 2.5e-149 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
BLNAIMJH_00932 | 1.1e-65 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
BLNAIMJH_00933 | 2.4e-71 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
BLNAIMJH_00934 | 1.2e-131 | fhaA | T | Protein of unknown function (DUF2662) | ||
BLNAIMJH_00935 | 4.5e-65 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
BLNAIMJH_00936 | 2.6e-55 | ytfL | P | Transporter associated domain | ||
BLNAIMJH_00937 | 1e-187 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
BLNAIMJH_00938 | 3.1e-101 | S | Protein of unknown function DUF45 | |||
BLNAIMJH_00942 | 2.2e-172 | P | Zinc-uptake complex component A periplasmic | |||
BLNAIMJH_00943 | 2e-160 | znuC | P | ATPases associated with a variety of cellular activities | ||
BLNAIMJH_00944 | 1.4e-237 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
BLNAIMJH_00945 | 2.5e-98 | 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 | |
BLNAIMJH_00946 | 1.6e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
BLNAIMJH_00947 | 8.4e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
BLNAIMJH_00948 | 7.8e-44 | ydeP | K | HxlR-like helix-turn-helix | ||
BLNAIMJH_00949 | 3.2e-86 | XK27_10430 | S | NAD(P)H-binding | ||
BLNAIMJH_00950 | 8.8e-160 | yicL | EG | EamA-like transporter family | ||
BLNAIMJH_00951 | 4.8e-35 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
BLNAIMJH_00952 | 6.8e-26 | yccF | S | Inner membrane component domain | ||
BLNAIMJH_00953 | 3.9e-201 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
BLNAIMJH_00954 | 1.4e-142 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
BLNAIMJH_00955 | 1.5e-24 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
BLNAIMJH_00956 | 2.6e-157 | 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 | |
BLNAIMJH_00957 | 2.3e-284 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
BLNAIMJH_00958 | 4.6e-233 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_00959 | 8.6e-107 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
BLNAIMJH_00960 | 7.4e-174 | G | Fic/DOC family | |||
BLNAIMJH_00961 | 4.5e-142 | |||||
BLNAIMJH_00962 | 9.1e-164 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BLNAIMJH_00963 | 1.4e-167 | S | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |||
BLNAIMJH_00964 | 2.3e-57 | 3.4.13.22 | S | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | ||
BLNAIMJH_00965 | 1.1e-95 | bcp | 1.11.1.15 | O | Redoxin | |
BLNAIMJH_00966 | 1.9e-25 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_00967 | 7.4e-95 | S | Pyridoxamine 5'-phosphate oxidase | |||
BLNAIMJH_00968 | 0.0 | S | Histidine phosphatase superfamily (branch 2) | |||
BLNAIMJH_00969 | 1.6e-44 | L | transposition | |||
BLNAIMJH_00970 | 4.3e-23 | C | Acetamidase/Formamidase family | |||
BLNAIMJH_00971 | 1.7e-58 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
BLNAIMJH_00972 | 2e-174 | V | ATPases associated with a variety of cellular activities | |||
BLNAIMJH_00973 | 2.8e-123 | S | ABC-2 family transporter protein | |||
BLNAIMJH_00974 | 4.4e-123 | S | Haloacid dehalogenase-like hydrolase | |||
BLNAIMJH_00975 | 6.5e-48 | recN | L | May be involved in recombinational repair of damaged DNA | ||
BLNAIMJH_00976 | 2.8e-76 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
BLNAIMJH_00977 | 7.6e-161 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
BLNAIMJH_00978 | 8.2e-34 | |||||
BLNAIMJH_00979 | 2.8e-193 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
BLNAIMJH_00980 | 1.7e-84 | 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 | ||
BLNAIMJH_00981 | 1.5e-123 | 3.2.1.8 | S | alpha beta | ||
BLNAIMJH_00982 | 1.3e-18 | 3.4.17.13 | E | Rard protein | ||
BLNAIMJH_00983 | 2.1e-08 | relB | L | RelB antitoxin | ||
BLNAIMJH_00984 | 5.5e-29 | |||||
BLNAIMJH_00985 | 1.1e-221 | L | Uncharacterized conserved protein (DUF2075) | |||
BLNAIMJH_00986 | 1.5e-55 | mazG | S | MazG-like family | ||
BLNAIMJH_00987 | 1.3e-43 | lexA | 3.6.4.12 | K | Putative DNA-binding domain | |
BLNAIMJH_00988 | 2.4e-74 | S | Putative inner membrane protein (DUF1819) | |||
BLNAIMJH_00989 | 8.4e-23 | |||||
BLNAIMJH_00990 | 0.0 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
BLNAIMJH_00991 | 4e-121 | L | DNA helicase | |||
BLNAIMJH_00992 | 5.8e-09 | XK26_04895 | ||||
BLNAIMJH_00993 | 1.3e-67 | |||||
BLNAIMJH_00994 | 8.5e-125 | |||||
BLNAIMJH_00995 | 1.5e-117 | S | phosphoesterase or phosphohydrolase | |||
BLNAIMJH_00996 | 3.5e-25 | C | Aldo/keto reductase family | |||
BLNAIMJH_00998 | 9e-159 | 2.7.13.3 | T | Histidine kinase | ||
BLNAIMJH_00999 | 6.5e-122 | K | helix_turn_helix, Lux Regulon | |||
BLNAIMJH_01000 | 1.5e-208 | KLT | Lanthionine synthetase C-like protein | |||
BLNAIMJH_01001 | 7.7e-156 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
BLNAIMJH_01002 | 1.5e-130 | S | Enoyl-(Acyl carrier protein) reductase | |||
BLNAIMJH_01003 | 9.5e-43 | rutG | F | Permease family | ||
BLNAIMJH_01004 | 6.6e-60 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_01005 | 1.8e-139 | S | Domain of unknown function (DUF4194) | |||
BLNAIMJH_01006 | 3.6e-101 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_01007 | 8.2e-145 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
BLNAIMJH_01008 | 1.3e-198 | S | Glycosyltransferase, group 2 family protein | |||
BLNAIMJH_01009 | 1.3e-23 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
BLNAIMJH_01010 | 8.2e-213 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
BLNAIMJH_01011 | 8.4e-84 | ykoE | S | ABC-type cobalt transport system, permease component | ||
BLNAIMJH_01012 | 2.2e-288 | crr | G | pts system, glucose-specific IIABC component | ||
BLNAIMJH_01013 | 2.7e-120 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
BLNAIMJH_01014 | 6.4e-112 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
BLNAIMJH_01015 | 7.1e-167 | M | LPXTG-motif cell wall anchor domain protein | |||
BLNAIMJH_01016 | 3e-57 | S | Vitamin K epoxide reductase | |||
BLNAIMJH_01017 | 9.5e-169 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine | |
BLNAIMJH_01018 | 3.1e-144 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
BLNAIMJH_01019 | 7.3e-46 | S | Patatin-like phospholipase | |||
BLNAIMJH_01020 | 1.5e-172 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
BLNAIMJH_01021 | 3.6e-32 | S | Protein of unknown function (DUF3107) | |||
BLNAIMJH_01022 | 3.9e-157 | mphA | S | Aminoglycoside phosphotransferase | ||
BLNAIMJH_01023 | 3.1e-57 | crgA | D | Involved in cell division | ||
BLNAIMJH_01024 | 6.8e-142 | S | Bacterial protein of unknown function (DUF881) | |||
BLNAIMJH_01025 | 4.6e-63 | srtA | 3.4.22.70 | M | Sortase family | |
BLNAIMJH_01026 | 6.8e-23 | srtA | 3.4.22.70 | M | Sortase family | |
BLNAIMJH_01027 | 1.1e-130 | S | membrane transporter protein | |||
BLNAIMJH_01028 | 1.1e-113 | phoA | 3.1.3.1, 3.1.3.39 | P | Alkaline phosphatase homologues | |
BLNAIMJH_01029 | 3.7e-36 | S | Mitochondrial biogenesis AIM24 | |||
BLNAIMJH_01030 | 4.6e-73 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
BLNAIMJH_01031 | 5.9e-182 | V | Beta-lactamase | |||
BLNAIMJH_01032 | 1.3e-104 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
BLNAIMJH_01033 | 4.5e-249 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
BLNAIMJH_01034 | 4.8e-51 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
BLNAIMJH_01035 | 2.3e-280 | cydD | V | ABC transporter transmembrane region | ||
BLNAIMJH_01036 | 6.9e-101 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
BLNAIMJH_01037 | 3.5e-148 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
BLNAIMJH_01038 | 3.5e-149 | |||||
BLNAIMJH_01039 | 5.3e-251 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
BLNAIMJH_01040 | 3.4e-97 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
BLNAIMJH_01041 | 2.2e-56 | MV | MacB-like periplasmic core domain | |||
BLNAIMJH_01042 | 5.5e-130 | K | helix_turn_helix, Lux Regulon | |||
BLNAIMJH_01043 | 2.4e-154 | tcsS2 | T | Histidine kinase | ||
BLNAIMJH_01044 | 3.3e-124 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
BLNAIMJH_01045 | 8.6e-17 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
BLNAIMJH_01046 | 1.1e-156 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
BLNAIMJH_01047 | 2e-77 | 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 | ||
BLNAIMJH_01048 | 2.2e-140 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
BLNAIMJH_01049 | 3.4e-161 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
BLNAIMJH_01050 | 2.3e-168 | ftsE | D | Cell division ATP-binding protein FtsE | ||
BLNAIMJH_01051 | 1.1e-190 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
BLNAIMJH_01052 | 1.2e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
BLNAIMJH_01053 | 5.8e-143 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
BLNAIMJH_01054 | 5.4e-250 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
BLNAIMJH_01055 | 1.6e-151 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
BLNAIMJH_01056 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
BLNAIMJH_01057 | 1.4e-98 | L | Single-strand binding protein family | |||
BLNAIMJH_01058 | 1.5e-65 | 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 | |
BLNAIMJH_01059 | 1.3e-17 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
BLNAIMJH_01060 | 1.3e-262 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
BLNAIMJH_01061 | 1.2e-103 | 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 | |
BLNAIMJH_01062 | 3.3e-68 | S | Transmembrane domain of unknown function (DUF3566) | |||
BLNAIMJH_01063 | 6.5e-81 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
BLNAIMJH_01064 | 1.1e-123 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
BLNAIMJH_01065 | 3e-60 | 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 | ||
BLNAIMJH_01066 | 2.9e-66 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
BLNAIMJH_01067 | 8.4e-154 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
BLNAIMJH_01068 | 1.3e-185 | |||||
BLNAIMJH_01069 | 3.8e-31 | V | N-Acetylmuramoyl-L-alanine amidase | |||
BLNAIMJH_01070 | 1.6e-160 | 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 | |
BLNAIMJH_01071 | 2e-71 | divIC | D | Septum formation initiator | ||
BLNAIMJH_01072 | 2e-103 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
BLNAIMJH_01073 | 9e-237 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
BLNAIMJH_01074 | 9.9e-80 | S | Protein of unknown function (DUF3000) | |||
BLNAIMJH_01075 | 1.7e-48 | V | ABC transporter, ATP-binding protein | |||
BLNAIMJH_01076 | 1.3e-96 | K | MarR family | |||
BLNAIMJH_01077 | 0.0 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
BLNAIMJH_01078 | 5.1e-107 | K | Bacterial regulatory proteins, tetR family | |||
BLNAIMJH_01079 | 2.3e-199 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
BLNAIMJH_01080 | 1.4e-181 | G | Transporter major facilitator family protein | |||
BLNAIMJH_01081 | 0.0 | 3.2.1.40 | E | Bacterial alpha-L-rhamnosidase C-terminal domain | ||
BLNAIMJH_01082 | 2.2e-214 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_01083 | 1.5e-117 | K | Periplasmic binding protein domain | |||
BLNAIMJH_01084 | 4.5e-14 | K | helix_turn_helix, mercury resistance | |||
BLNAIMJH_01085 | 4e-220 | lmrB | U | Major Facilitator Superfamily | ||
BLNAIMJH_01086 | 6.8e-47 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
BLNAIMJH_01087 | 4.1e-92 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
BLNAIMJH_01088 | 3.2e-54 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
BLNAIMJH_01089 | 9.1e-74 | K | Acetyltransferase (GNAT) domain | |||
BLNAIMJH_01091 | 5.4e-181 | S | Auxin Efflux Carrier | |||
BLNAIMJH_01092 | 9.7e-52 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
BLNAIMJH_01093 | 7.2e-44 | S | ECF transporter, substrate-specific component | |||
BLNAIMJH_01094 | 3.9e-148 | S | Sulfite exporter TauE/SafE | |||
BLNAIMJH_01095 | 1.5e-177 | L | Phage integrase family | |||
BLNAIMJH_01096 | 1.2e-24 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
BLNAIMJH_01097 | 1.9e-56 | 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 | ||
BLNAIMJH_01098 | 1e-97 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
BLNAIMJH_01099 | 1.7e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
BLNAIMJH_01100 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
BLNAIMJH_01101 | 4.9e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
BLNAIMJH_01102 | 3.9e-272 | S | domain protein | |||
BLNAIMJH_01103 | 1.1e-74 | 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 | |
BLNAIMJH_01104 | 3.1e-83 | yraN | L | Belongs to the UPF0102 family | ||
BLNAIMJH_01105 | 9.6e-166 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
BLNAIMJH_01106 | 4.5e-98 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
BLNAIMJH_01107 | 2.1e-119 | yoaP | E | YoaP-like | ||
BLNAIMJH_01109 | 3.1e-195 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
BLNAIMJH_01110 | 1.2e-52 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
BLNAIMJH_01111 | 1.5e-86 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
BLNAIMJH_01112 | 1.1e-78 | K | helix_turn_helix ASNC type | |||
BLNAIMJH_01113 | 1e-69 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
BLNAIMJH_01114 | 3.3e-216 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BLNAIMJH_01116 | 1.5e-142 | ET | Bacterial periplasmic substrate-binding proteins | |||
BLNAIMJH_01117 | 2.1e-28 | corA | P | CorA-like Mg2+ transporter protein | ||
BLNAIMJH_01118 | 1.1e-156 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
BLNAIMJH_01119 | 1.6e-141 | S | Bacterial protein of unknown function (DUF881) | |||
BLNAIMJH_01120 | 4.2e-45 | sbp | S | Protein of unknown function (DUF1290) | ||
BLNAIMJH_01121 | 1.9e-189 | T | Universal stress protein family | |||
BLNAIMJH_01122 | 3.8e-79 | M | NlpC/P60 family | |||
BLNAIMJH_01123 | 1.3e-165 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
BLNAIMJH_01124 | 8.2e-218 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
BLNAIMJH_01125 | 6.2e-41 | |||||
BLNAIMJH_01126 | 2.4e-215 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
BLNAIMJH_01127 | 7.4e-89 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
BLNAIMJH_01128 | 0.0 | 4.2.1.53 | S | MCRA family | ||
BLNAIMJH_01129 | 3e-139 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
BLNAIMJH_01130 | 5.6e-203 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
BLNAIMJH_01131 | 0.0 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
BLNAIMJH_01133 | 7.5e-214 | araJ | EGP | Major facilitator Superfamily | ||
BLNAIMJH_01134 | 7.9e-22 | S | Domain of unknown function (DUF4037) | |||
BLNAIMJH_01135 | 4.3e-104 | S | Domain of unknown function (DUF4037) | |||
BLNAIMJH_01136 | 5.8e-302 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
BLNAIMJH_01137 | 8.4e-30 | rpmB | J | Ribosomal L28 family | ||
BLNAIMJH_01138 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_01139 | 2.1e-228 | yxiO | S | Vacuole effluxer Atg22 like | ||
BLNAIMJH_01140 | 1.9e-127 | gntR | K | FCD | ||
BLNAIMJH_01141 | 5.6e-79 | gntK | 2.7.1.12 | F | Shikimate kinase | |
BLNAIMJH_01142 | 1.4e-231 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_01143 | 7.5e-121 | K | Bacterial regulatory proteins, tetR family | |||
BLNAIMJH_01144 | 2.4e-228 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
BLNAIMJH_01145 | 2.2e-229 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
BLNAIMJH_01146 | 1.7e-137 | M | Mechanosensitive ion channel | |||
BLNAIMJH_01147 | 6.7e-180 | S | CAAX protease self-immunity | |||
BLNAIMJH_01148 | 1.3e-102 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
BLNAIMJH_01149 | 2.2e-232 | gatA | 6.3.5.6, 6.3.5.7 | F | 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) | |
BLNAIMJH_01150 | 7.5e-115 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
BLNAIMJH_01151 | 2.1e-54 | iaaA | 3.4.19.5, 3.5.1.1 | E | Asparaginase | |
BLNAIMJH_01152 | 2.1e-291 | E | ABC transporter, substrate-binding protein, family 5 | |||
BLNAIMJH_01153 | 2e-57 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
BLNAIMJH_01154 | 3.7e-24 | S | Beta-L-arabinofuranosidase, GH127 | |||
BLNAIMJH_01155 | 5e-101 | S | Protein of unknown function, DUF624 | |||
BLNAIMJH_01156 | 3.8e-185 | G | beta-fructofuranosidase activity | |||
BLNAIMJH_01157 | 8.3e-163 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01158 | 2.3e-168 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01159 | 4.4e-294 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_01160 | 1.7e-206 | abf | G | Glycosyl hydrolases family 43 | ||
BLNAIMJH_01161 | 2.4e-195 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_01162 | 0.0 | 3.2.1.97 | GH101 | G | Glycosyl hydrolases family 43 | |
BLNAIMJH_01163 | 7.9e-256 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
BLNAIMJH_01164 | 0.0 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
BLNAIMJH_01165 | 6.1e-70 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
BLNAIMJH_01166 | 8.9e-34 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
BLNAIMJH_01167 | 2.8e-231 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
BLNAIMJH_01168 | 6.3e-232 | epsG | M | Glycosyl transferase family 21 | ||
BLNAIMJH_01169 | 5.5e-233 | S | AI-2E family transporter | |||
BLNAIMJH_01170 | 4.2e-180 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
BLNAIMJH_01171 | 1.8e-204 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
BLNAIMJH_01172 | 0.0 | yliE | T | Putative diguanylate phosphodiesterase | ||
BLNAIMJH_01173 | 3.2e-113 | S | Domain of unknown function (DUF4956) | |||
BLNAIMJH_01174 | 4.1e-158 | P | VTC domain | |||
BLNAIMJH_01175 | 0.0 | cotH | M | CotH kinase protein | ||
BLNAIMJH_01176 | 2.1e-285 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
BLNAIMJH_01177 | 9.5e-146 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
BLNAIMJH_01178 | 2.5e-47 | V | ABC transporter, ATP-binding protein | |||
BLNAIMJH_01179 | 2e-33 | MV | MacB-like periplasmic core domain | |||
BLNAIMJH_01180 | 8.7e-117 | MV | MacB-like periplasmic core domain | |||
BLNAIMJH_01181 | 6.1e-31 | helD | 3.6.4.12 | L | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_01182 | 8.2e-31 | helD | 3.6.4.12 | L | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_01183 | 6.3e-24 | helD | 3.6.4.12 | L | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_01184 | 1e-150 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
BLNAIMJH_01185 | 4.4e-18 | S | Prophage endopeptidase tail | |||
BLNAIMJH_01188 | 5.7e-39 | |||||
BLNAIMJH_01189 | 5.2e-130 | |||||
BLNAIMJH_01191 | 3.1e-85 | L | reverse transcriptase | |||
BLNAIMJH_01193 | 3.5e-17 | |||||
BLNAIMJH_01194 | 1.3e-104 | M | Glycosyl hydrolases family 25 | |||
BLNAIMJH_01195 | 6e-37 | S | Putative phage holin Dp-1 | |||
BLNAIMJH_01196 | 2.7e-37 | |||||
BLNAIMJH_01197 | 2.1e-42 | S | Ribonuclease toxin, BrnT, of type II toxin-antitoxin system | |||
BLNAIMJH_01198 | 2.6e-90 | L | Phage integrase family | |||
BLNAIMJH_01200 | 5.4e-208 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
BLNAIMJH_01201 | 2e-146 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
BLNAIMJH_01202 | 8.9e-31 | 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 | ||
BLNAIMJH_01203 | 4.4e-57 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
BLNAIMJH_01204 | 4.5e-149 | 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 | ||
BLNAIMJH_01205 | 3.3e-106 | 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 | |
BLNAIMJH_01206 | 1.5e-63 | rplQ | J | Ribosomal protein L17 | ||
BLNAIMJH_01207 | 1.7e-168 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
BLNAIMJH_01208 | 8.1e-43 | gcs2 | S | A circularly permuted ATPgrasp | ||
BLNAIMJH_01209 | 5.7e-45 | E | Transglutaminase/protease-like homologues | |||
BLNAIMJH_01211 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
BLNAIMJH_01212 | 6.5e-148 | P | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01213 | 1.7e-162 | P | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01214 | 3e-270 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_01215 | 1.4e-184 | K | Psort location Cytoplasmic, score | |||
BLNAIMJH_01216 | 2.9e-182 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_01217 | 5.1e-223 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_01218 | 4.7e-163 | G | PFAM binding-protein-dependent transport systems inner membrane component | |||
BLNAIMJH_01219 | 6.6e-145 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01220 | 0.0 | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
BLNAIMJH_01221 | 3.2e-54 | yccF | S | Inner membrane component domain | ||
BLNAIMJH_01222 | 2.7e-21 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
BLNAIMJH_01223 | 9.8e-98 | pbpA | M | penicillin-binding protein | ||
BLNAIMJH_01224 | 4.7e-24 | pbpA | M | penicillin-binding protein | ||
BLNAIMJH_01225 | 2.3e-127 | rodA | D | Belongs to the SEDS family | ||
BLNAIMJH_01226 | 1.3e-58 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
BLNAIMJH_01228 | 8.1e-122 | cyaA | 4.6.1.1 | S | CYTH | |
BLNAIMJH_01229 | 3.4e-36 | trxA2 | O | Tetratricopeptide repeat | ||
BLNAIMJH_01230 | 0.0 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
BLNAIMJH_01231 | 9e-184 | 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 | ||
BLNAIMJH_01232 | 3.3e-118 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
BLNAIMJH_01233 | 2.7e-180 | |||||
BLNAIMJH_01234 | 1.1e-110 | trxA2 | O | Tetratricopeptide repeat | ||
BLNAIMJH_01235 | 1.9e-132 | M | Converts alpha-N-acetylneuranimic acid (Neu5Ac) to the beta-anomer, accelerating the equilibrium between the alpha- and beta-anomers. Probably facilitates sialidase-negative bacteria to compete sucessfully for limited amounts of extracellular Neu5Ac, which is likely taken up in the beta-anomer. In addition, the rapid removal of sialic acid from solution might be advantageous to the bacterium to damp down host responses | |||
BLNAIMJH_01236 | 1.2e-28 | S | Domain of unknown function (DUF5067) | |||
BLNAIMJH_01237 | 6.4e-90 | adhB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
BLNAIMJH_01238 | 6.7e-72 | K | MerR family regulatory protein | |||
BLNAIMJH_01239 | 5.3e-119 | ykoE | S | ABC-type cobalt transport system, permease component | ||
BLNAIMJH_01240 | 4.3e-138 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
BLNAIMJH_01241 | 3e-170 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
BLNAIMJH_01242 | 4.5e-86 | S | Psort location CytoplasmicMembrane, score | |||
BLNAIMJH_01243 | 2.3e-71 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
BLNAIMJH_01244 | 1.6e-88 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
BLNAIMJH_01246 | 3.5e-92 | |||||
BLNAIMJH_01247 | 1.7e-284 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
BLNAIMJH_01248 | 1.2e-73 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
BLNAIMJH_01249 | 2.6e-80 | 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 | ||
BLNAIMJH_01250 | 2.7e-144 | yplQ | S | Haemolysin-III related | ||
BLNAIMJH_01251 | 3.4e-280 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
BLNAIMJH_01252 | 1.9e-46 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
BLNAIMJH_01253 | 0.0 | D | FtsK/SpoIIIE family | |||
BLNAIMJH_01254 | 5.3e-170 | K | Cell envelope-related transcriptional attenuator domain | |||
BLNAIMJH_01256 | 5.7e-208 | K | Cell envelope-related transcriptional attenuator domain | |||
BLNAIMJH_01257 | 3.4e-54 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
BLNAIMJH_01258 | 5.1e-104 | S | Glycosyl transferase, family 2 | |||
BLNAIMJH_01259 | 6.7e-51 | S | Glycosyl transferase, family 2 | |||
BLNAIMJH_01260 | 1.3e-09 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
BLNAIMJH_01261 | 1.9e-121 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
BLNAIMJH_01262 | 2.5e-225 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
BLNAIMJH_01263 | 5.8e-49 | S | Calcineurin-like phosphoesterase | |||
BLNAIMJH_01264 | 1.8e-256 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
BLNAIMJH_01265 | 9.3e-71 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
BLNAIMJH_01266 | 4.2e-269 | S | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_01268 | 5.1e-224 | G | Transmembrane secretion effector | |||
BLNAIMJH_01269 | 5.4e-121 | K | Bacterial regulatory proteins, tetR family | |||
BLNAIMJH_01270 | 1.1e-39 | nrdH | O | Glutaredoxin | ||
BLNAIMJH_01271 | 3.3e-74 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
BLNAIMJH_01272 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BLNAIMJH_01274 | 3.1e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BLNAIMJH_01275 | 0.0 | uvrA3 | 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 | ||
BLNAIMJH_01276 | 1.3e-29 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_01277 | 6.5e-25 | yhjX | EGP | Major facilitator Superfamily | ||
BLNAIMJH_01278 | 8.5e-195 | S | alpha beta | |||
BLNAIMJH_01279 | 3e-126 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
BLNAIMJH_01280 | 6e-143 | S | Domain of unknown function (DUF4191) | |||
BLNAIMJH_01281 | 9.2e-215 | 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 | |
BLNAIMJH_01282 | 3.6e-67 | rsfS | 2.7.7.18 | 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 | |
BLNAIMJH_01283 | 3e-60 | S | Thiamine-binding protein | |||
BLNAIMJH_01284 | 1.1e-192 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_01285 | 1.4e-57 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
BLNAIMJH_01286 | 1.6e-93 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
BLNAIMJH_01287 | 2.8e-214 | iunH1 | 3.2.2.1 | F | nucleoside hydrolase | |
BLNAIMJH_01288 | 3.2e-109 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
BLNAIMJH_01289 | 2.4e-97 | metI | P | Psort location CytoplasmicMembrane, score 9.99 | ||
BLNAIMJH_01290 | 6.6e-41 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
BLNAIMJH_01291 | 2.5e-256 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
BLNAIMJH_01292 | 2.2e-65 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BLNAIMJH_01293 | 1.4e-172 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
BLNAIMJH_01294 | 1.3e-48 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
BLNAIMJH_01295 | 7.3e-118 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
BLNAIMJH_01296 | 4.7e-35 | amy | 3.1.1.53, 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | Alpha amylase, catalytic domain |
BLNAIMJH_01297 | 1.1e-178 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
BLNAIMJH_01298 | 2.7e-114 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
BLNAIMJH_01299 | 3.3e-155 | 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 | ||
BLNAIMJH_01300 | 5.3e-34 | 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 | |
BLNAIMJH_01301 | 4.7e-185 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BLNAIMJH_01302 | 1.9e-65 | 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 | ||
BLNAIMJH_01303 | 3.3e-62 | 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 | ||
BLNAIMJH_01304 | 6e-73 | xylB | 1.1.1.57, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
BLNAIMJH_01305 | 1e-105 | lacA | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
BLNAIMJH_01306 | 3.7e-08 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
BLNAIMJH_01307 | 0.0 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
BLNAIMJH_01308 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
BLNAIMJH_01309 | 2.4e-164 | MA20_14020 | P | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_01310 | 1.5e-186 | MA20_14025 | U | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_01311 | 2.4e-242 | msmE | G | ABC transporter periplasmic binding protein YcjN precursor K02027 | ||
BLNAIMJH_01312 | 7.2e-189 | K | Bacterial regulatory proteins, lacI family | |||
BLNAIMJH_01313 | 0.0 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Belongs to the glycosyl hydrolase 43 family | |
BLNAIMJH_01314 | 6.1e-243 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
BLNAIMJH_01315 | 1.6e-163 | 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 | ||
BLNAIMJH_01316 | 9.3e-107 | 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 | |
BLNAIMJH_01317 | 1.8e-182 | 1.1.1.65 | C | Aldo/keto reductase family | ||
BLNAIMJH_01318 | 1.5e-106 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
BLNAIMJH_01319 | 5.6e-222 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_01321 | 3.3e-233 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
BLNAIMJH_01322 | 5.4e-25 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
BLNAIMJH_01323 | 3.6e-179 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
BLNAIMJH_01324 | 3.8e-69 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
BLNAIMJH_01325 | 2.8e-48 | 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 | ||
BLNAIMJH_01326 | 4.6e-133 | dnaK | O | Heat shock 70 kDa protein | ||
BLNAIMJH_01327 | 3e-212 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
BLNAIMJH_01328 | 4.3e-266 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
BLNAIMJH_01329 | 7.7e-59 | D | nuclear chromosome segregation | |||
BLNAIMJH_01330 | 3.4e-126 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
BLNAIMJH_01331 | 4.6e-143 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
BLNAIMJH_01332 | 4.1e-184 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
BLNAIMJH_01333 | 2.7e-296 | yegQ | O | Peptidase family U32 C-terminal domain | ||
BLNAIMJH_01334 | 9.7e-171 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
BLNAIMJH_01335 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
BLNAIMJH_01336 | 1.7e-91 | lemA | S | LemA family | ||
BLNAIMJH_01338 | 5e-125 | XK27_06785 | V | ABC transporter | ||
BLNAIMJH_01339 | 1.9e-33 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
BLNAIMJH_01340 | 1.6e-77 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
BLNAIMJH_01341 | 1.6e-43 | pntAA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
BLNAIMJH_01342 | 2.4e-145 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
BLNAIMJH_01343 | 7.1e-43 | gcvR | T | Belongs to the UPF0237 family | ||
BLNAIMJH_01344 | 1.1e-23 | lmrB | EGP | Major facilitator Superfamily | ||
BLNAIMJH_01345 | 3.4e-233 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
BLNAIMJH_01346 | 4e-250 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
BLNAIMJH_01347 | 3.4e-141 | glpR | K | DeoR C terminal sensor domain | ||
BLNAIMJH_01348 | 8.8e-228 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
BLNAIMJH_01349 | 8.2e-213 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
BLNAIMJH_01350 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
BLNAIMJH_01351 | 5.2e-133 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
BLNAIMJH_01352 | 1.2e-200 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
BLNAIMJH_01353 | 2.3e-75 | J | TM2 domain | |||
BLNAIMJH_01354 | 1.9e-34 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
BLNAIMJH_01355 | 1e-268 | V | Efflux ABC transporter, permease protein | |||
BLNAIMJH_01356 | 2.6e-18 | V | ATPases associated with a variety of cellular activities | |||
BLNAIMJH_01357 | 3.3e-59 | 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 | ||
BLNAIMJH_01358 | 1.2e-92 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
BLNAIMJH_01359 | 3.4e-25 | rpmD | J | Ribosomal protein L30p/L7e | ||
BLNAIMJH_01360 | 2e-132 | L | Tetratricopeptide repeat | |||
BLNAIMJH_01361 | 3.8e-170 | I | alpha/beta hydrolase fold | |||
BLNAIMJH_01363 | 2.3e-144 | cobB2 | K | Sir2 family | ||
BLNAIMJH_01364 | 4.1e-234 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
BLNAIMJH_01365 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
BLNAIMJH_01366 | 3.4e-155 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01367 | 2.1e-158 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01368 | 3.8e-243 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
BLNAIMJH_01369 | 1.5e-230 | nagC | GK | ROK family | ||
BLNAIMJH_01370 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
BLNAIMJH_01371 | 3.2e-59 | 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 | ||
BLNAIMJH_01372 | 5.4e-150 | lolD | V | ABC transporter | ||
BLNAIMJH_01373 | 3.6e-29 | V | FtsX-like permease family | |||
BLNAIMJH_01374 | 9.3e-173 | T | Pfam Adenylate and Guanylate cyclase catalytic domain | |||
BLNAIMJH_01375 | 2.1e-187 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
BLNAIMJH_01376 | 7.5e-132 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
BLNAIMJH_01377 | 1.7e-70 | rplI | J | Binds to the 23S rRNA | ||
BLNAIMJH_01378 | 3.5e-36 | 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 | ||
BLNAIMJH_01379 | 9.7e-70 | ssb1 | L | Single-stranded DNA-binding protein | ||
BLNAIMJH_01380 | 2.5e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
BLNAIMJH_01381 | 3.3e-186 | 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) | |
BLNAIMJH_01382 | 5.7e-175 | 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 | |
BLNAIMJH_01383 | 1.1e-259 | EGP | Major Facilitator Superfamily | |||
BLNAIMJH_01384 | 3.3e-167 | iunH2 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
BLNAIMJH_01385 | 1.1e-197 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_01387 | 1.2e-99 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
BLNAIMJH_01388 | 1.7e-113 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
BLNAIMJH_01389 | 4e-34 | rodA | D | Belongs to the SEDS family | ||
BLNAIMJH_01390 | 5.4e-164 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
BLNAIMJH_01391 | 1.2e-163 | G | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01392 | 2e-132 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
BLNAIMJH_01393 | 1.1e-87 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
BLNAIMJH_01394 | 2.3e-179 | V | ABC-2 family transporter protein | |||
BLNAIMJH_01395 | 9.8e-213 | rhaR1 | K | helix_turn_helix, arabinose operon control protein | ||
BLNAIMJH_01396 | 4.7e-109 | maa | 2.3.1.18, 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
BLNAIMJH_01397 | 1.3e-249 | VP1224 | V | Psort location CytoplasmicMembrane, score 9.99 | ||
BLNAIMJH_01398 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
BLNAIMJH_01399 | 0.0 | ctpE | P | E1-E2 ATPase | ||
BLNAIMJH_01400 | 1.5e-98 | |||||
BLNAIMJH_01401 | 2.8e-243 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BLNAIMJH_01402 | 3.9e-119 | S | Protein of unknown function (DUF3159) | |||
BLNAIMJH_01403 | 1.2e-79 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
BLNAIMJH_01404 | 6.5e-43 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
BLNAIMJH_01405 | 1.9e-62 | S | Protein of unknown function (DUF4235) | |||
BLNAIMJH_01406 | 2.9e-136 | G | Phosphoglycerate mutase family | |||
BLNAIMJH_01407 | 3.9e-259 | amyE | G | Bacterial extracellular solute-binding protein | ||
BLNAIMJH_01408 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
BLNAIMJH_01409 | 1.4e-264 | amyE | G | Bacterial extracellular solute-binding protein | ||
BLNAIMJH_01410 | 7e-187 | K | Periplasmic binding protein-like domain | |||
BLNAIMJH_01411 | 1.1e-181 | K | Psort location Cytoplasmic, score | |||
BLNAIMJH_01412 | 4.1e-153 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_01413 | 7.6e-152 | rafG | G | ABC transporter permease | ||
BLNAIMJH_01414 | 1.2e-149 | 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 | |
BLNAIMJH_01415 | 4.2e-234 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
BLNAIMJH_01416 | 3.2e-189 | lacR | K | Transcriptional regulator, LacI family | ||
BLNAIMJH_01417 | 0.0 | T | Diguanylate cyclase, GGDEF domain | |||
BLNAIMJH_01418 | 2.5e-250 | 3.2.1.14 | GH18 | S | Carbohydrate binding domain | |
BLNAIMJH_01419 | 0.0 | M | probably involved in cell wall | |||
BLNAIMJH_01420 | 1.1e-189 | K | helix_turn _helix lactose operon repressor | |||
BLNAIMJH_01421 | 1.4e-220 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
BLNAIMJH_01422 | 1.7e-188 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_01423 | 4.7e-192 | dppC | EP | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_01424 | 0.0 | P | Belongs to the ABC transporter superfamily | |||
BLNAIMJH_01425 | 9e-95 | 3.6.1.55 | F | NUDIX domain | ||
BLNAIMJH_01426 | 0.0 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
BLNAIMJH_01427 | 1.9e-289 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
BLNAIMJH_01428 | 3.3e-186 | V | Acetyltransferase (GNAT) domain | |||
BLNAIMJH_01429 | 5.3e-276 | 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 | |
BLNAIMJH_01430 | 4.2e-176 | efeU_1 | P | Iron permease FTR1 family | ||
BLNAIMJH_01431 | 1.1e-68 | S | Fibronectin type 3 domain | |||
BLNAIMJH_01432 | 9.8e-68 | S | Fibronectin type 3 domain | |||
BLNAIMJH_01433 | 2.7e-73 | S | Protein of unknown function (DUF3052) | |||
BLNAIMJH_01435 | 8.4e-47 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
BLNAIMJH_01436 | 9e-165 | S | Calcineurin-like phosphoesterase | |||
BLNAIMJH_01437 | 1.4e-50 | 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 | ||
BLNAIMJH_01438 | 3.4e-135 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
BLNAIMJH_01439 | 1.1e-138 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
BLNAIMJH_01440 | 1.2e-67 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
BLNAIMJH_01441 | 9.7e-173 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
BLNAIMJH_01442 | 5.6e-118 | |||||
BLNAIMJH_01443 | 1.3e-197 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
BLNAIMJH_01444 | 0.0 | pknL | 2.7.11.1 | KLT | PASTA | |
BLNAIMJH_01445 | 1.9e-132 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
BLNAIMJH_01446 | 3.8e-97 | |||||
BLNAIMJH_01447 | 3.4e-194 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
BLNAIMJH_01448 | 2.4e-267 | 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 | ||
BLNAIMJH_01449 | 6.5e-151 | glnQ | 3.6.3.21 | E | ATP binding protein of ABC transporter for glutamate aspartate K02028 | |
BLNAIMJH_01450 | 9.9e-94 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
BLNAIMJH_01451 | 1.1e-155 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
BLNAIMJH_01452 | 3.1e-87 | pepD | E | Peptidase family C69 | ||
BLNAIMJH_01455 | 6e-38 | nrdH | O | Glutaredoxin | ||
BLNAIMJH_01456 | 1.8e-226 | S | Putative ABC-transporter type IV | |||
BLNAIMJH_01457 | 0.0 | pip | S | YhgE Pip domain protein | ||
BLNAIMJH_01458 | 4.2e-279 | pip | S | YhgE Pip domain protein | ||
BLNAIMJH_01459 | 2.1e-88 | K | Psort location Cytoplasmic, score 8.87 | |||
BLNAIMJH_01460 | 1.1e-61 | S | FMN_bind | |||
BLNAIMJH_01461 | 5.3e-150 | macB | V | ABC transporter, ATP-binding protein | ||
BLNAIMJH_01462 | 7.6e-40 | Z012_06715 | V | FtsX-like permease family | ||
BLNAIMJH_01463 | 3.1e-80 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
BLNAIMJH_01465 | 2.7e-226 | T | GHKL domain | |||
BLNAIMJH_01466 | 5.5e-213 | clcA_2 | P | Voltage gated chloride channel | ||
BLNAIMJH_01467 | 1.9e-178 | S | Psort location Cytoplasmic, score | |||
BLNAIMJH_01468 | 3.6e-73 | S | GtrA-like protein | |||
BLNAIMJH_01469 | 0.0 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
BLNAIMJH_01471 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
BLNAIMJH_01472 | 4.1e-30 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
BLNAIMJH_01473 | 4.9e-110 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
BLNAIMJH_01474 | 1.7e-188 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
BLNAIMJH_01475 | 8e-134 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
BLNAIMJH_01476 | 9.3e-155 | pyrK | 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 | C | Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B | |
BLNAIMJH_01477 | 6.6e-179 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
BLNAIMJH_01478 | 5.5e-124 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
BLNAIMJH_01479 | 2.9e-162 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
BLNAIMJH_01480 | 0.0 | thiC | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
BLNAIMJH_01481 | 8.8e-109 | J | Acetyltransferase (GNAT) domain | |||
BLNAIMJH_01482 | 5.6e-91 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
BLNAIMJH_01483 | 1.1e-217 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
BLNAIMJH_01484 | 6.1e-122 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
BLNAIMJH_01485 | 1.8e-101 | 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 | ||
BLNAIMJH_01486 | 5.9e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
BLNAIMJH_01487 | 3e-57 | 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 | |
BLNAIMJH_01488 | 3.9e-190 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
BLNAIMJH_01489 | 8e-91 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
BLNAIMJH_01490 | 1.7e-129 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
BLNAIMJH_01491 | 4.5e-172 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
BLNAIMJH_01492 | 2e-202 | parB | K | Belongs to the ParB family | ||
BLNAIMJH_01493 | 4.1e-181 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
BLNAIMJH_01494 | 7e-14 | S | Psort location Extracellular, score 8.82 | |||
BLNAIMJH_01495 | 1.4e-121 | yorS | 3.1.3.5 | S | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | |
BLNAIMJH_01496 | 2e-12 | S | Domain of unknown function (DUF4143) | |||
BLNAIMJH_01497 | 3.7e-79 | murJ | KLT | MviN-like protein | ||
BLNAIMJH_01498 | 1.2e-210 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
BLNAIMJH_01499 | 3.4e-43 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
BLNAIMJH_01500 | 5.4e-121 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
BLNAIMJH_01501 | 9e-26 | yjeE | 2.7.1.221 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
BLNAIMJH_01502 | 6.4e-148 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
BLNAIMJH_01503 | 3.8e-255 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
BLNAIMJH_01504 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
BLNAIMJH_01505 | 5.8e-32 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
BLNAIMJH_01506 | 2.4e-79 | S | Protein of unknown function (DUF2975) | |||
BLNAIMJH_01507 | 8.1e-241 | T | PhoQ Sensor | |||
BLNAIMJH_01508 | 1.5e-222 | G | Major Facilitator Superfamily | |||
BLNAIMJH_01509 | 5.4e-98 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
BLNAIMJH_01510 | 5.4e-22 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
BLNAIMJH_01511 | 4.5e-123 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
BLNAIMJH_01512 | 2e-39 | T | Forkhead associated domain | |||
BLNAIMJH_01513 | 4e-07 | P | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01514 | 1.1e-242 | G | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_01515 | 6.3e-193 | K | Periplasmic binding protein domain | |||
BLNAIMJH_01516 | 0.0 | ubiB | S | ABC1 family | ||
BLNAIMJH_01517 | 1e-27 | S | granule-associated protein | |||
BLNAIMJH_01518 | 2.1e-137 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
BLNAIMJH_01519 | 1.1e-251 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
BLNAIMJH_01520 | 3.3e-248 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
BLNAIMJH_01521 | 1.5e-166 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
BLNAIMJH_01522 | 1.4e-115 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
BLNAIMJH_01523 | 4.9e-99 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
BLNAIMJH_01524 | 3.3e-75 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
BLNAIMJH_01525 | 1.6e-169 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
BLNAIMJH_01526 | 1.3e-182 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_01527 | 1.5e-44 | |||||
BLNAIMJH_01528 | 5.5e-181 | S | Endonuclease/Exonuclease/phosphatase family | |||
BLNAIMJH_01529 | 4.1e-86 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
BLNAIMJH_01530 | 4.6e-223 | pflA | S | Protein of unknown function (DUF4012) | ||
BLNAIMJH_01531 | 1.9e-190 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
BLNAIMJH_01532 | 1.2e-20 | |||||
BLNAIMJH_01533 | 2e-12 | |||||
BLNAIMJH_01534 | 5.9e-185 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
BLNAIMJH_01535 | 2.1e-61 | K | LytTr DNA-binding domain | |||
BLNAIMJH_01536 | 1.8e-130 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
BLNAIMJH_01537 | 1.1e-27 | C | FMN binding | |||
BLNAIMJH_01538 | 1.8e-57 | |||||
BLNAIMJH_01539 | 0.0 | L | DEAD DEAH box helicase | |||
BLNAIMJH_01540 | 4.1e-189 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
BLNAIMJH_01541 | 1.7e-199 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_01542 | 1.8e-111 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_01543 | 1.4e-153 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
BLNAIMJH_01544 | 4.4e-144 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
BLNAIMJH_01545 | 6.7e-139 | glnQ | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
BLNAIMJH_01546 | 8.9e-215 | glnP | E | Binding-protein-dependent transport system inner membrane component | ||
BLNAIMJH_01547 | 1.9e-98 | |||||
BLNAIMJH_01548 | 1.4e-19 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
BLNAIMJH_01549 | 2.3e-148 | |||||
BLNAIMJH_01550 | 4.4e-55 | |||||
BLNAIMJH_01551 | 1.9e-190 | |||||
BLNAIMJH_01552 | 6.2e-156 | T | Forkhead associated domain | |||
BLNAIMJH_01553 | 0.0 | eccCa | D | FtsK/SpoIIIE family | ||
BLNAIMJH_01554 | 3e-254 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
BLNAIMJH_01555 | 5.2e-116 | def | 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 | |
BLNAIMJH_01556 | 1.5e-46 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
BLNAIMJH_01557 | 1.1e-96 | K | Bacterial regulatory proteins, tetR family | |||
BLNAIMJH_01558 | 1.6e-193 | S | Psort location CytoplasmicMembrane, score | |||
BLNAIMJH_01559 | 1.6e-216 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
BLNAIMJH_01560 | 1.1e-54 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
BLNAIMJH_01561 | 5.1e-60 | U | TadE-like protein | |||
BLNAIMJH_01562 | 1.3e-42 | S | Protein of unknown function (DUF4244) | |||
BLNAIMJH_01563 | 1.4e-87 | gspF | NU | Type II secretion system (T2SS), protein F | ||
BLNAIMJH_01564 | 6.2e-123 | U | Type ii secretion system | |||
BLNAIMJH_01565 | 1.6e-185 | cpaF | U | Type II IV secretion system protein | ||
BLNAIMJH_01566 | 5.5e-141 | cpaE | D | bacterial-type flagellum organization | ||
BLNAIMJH_01567 | 3.6e-97 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
BLNAIMJH_01568 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
BLNAIMJH_01569 | 1.3e-179 | 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 | ||
BLNAIMJH_01570 | 1.2e-250 | corC | S | CBS domain | ||
BLNAIMJH_01571 | 9.4e-103 | 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 | |
BLNAIMJH_01572 | 5.9e-208 | phoH | T | PhoH-like protein | ||
BLNAIMJH_01573 | 1.8e-56 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
BLNAIMJH_01574 | 2e-138 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
BLNAIMJH_01576 | 2.6e-163 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
BLNAIMJH_01577 | 2.1e-141 | U | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01578 | 2.7e-158 | U | Binding-protein-dependent transport system inner membrane component | |||
BLNAIMJH_01579 | 2.2e-218 | P | Bacterial extracellular solute-binding protein | |||
BLNAIMJH_01580 | 2.2e-218 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
BLNAIMJH_01581 | 1.7e-179 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
BLNAIMJH_01582 | 1.1e-174 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
BLNAIMJH_01583 | 1e-256 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
BLNAIMJH_01584 | 2.8e-185 | typA | T | Elongation factor G C-terminus | ||
BLNAIMJH_01585 | 2.3e-47 | 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 | ||
BLNAIMJH_01586 | 3.4e-67 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
BLNAIMJH_01587 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
BLNAIMJH_01588 | 1.4e-76 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
BLNAIMJH_01589 | 5.8e-216 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
BLNAIMJH_01590 | 3.5e-252 | EGP | Major facilitator Superfamily | |||
BLNAIMJH_01591 | 3.3e-197 | Z012_01000 | 1.1.1.14, 1.1.1.9 | C | Zinc-binding dehydrogenase | |
BLNAIMJH_01592 | 4.7e-182 | rhaR_1 | K | helix_turn_helix, arabinose operon control protein | ||
BLNAIMJH_01593 | 8.8e-150 | L | DNA helicase | |||
BLNAIMJH_01594 | 3.5e-185 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
BLNAIMJH_01595 | 8.4e-125 | lacY | P | LacY proton/sugar symporter | ||
BLNAIMJH_01596 | 1.2e-22 | lacY | P | LacY proton/sugar symporter | ||
BLNAIMJH_01597 | 4.9e-30 | corA | P | CorA-like Mg2+ transporter protein | ||
BLNAIMJH_01598 | 1.6e-44 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
BLNAIMJH_01599 | 1.1e-38 | csoR | S | Metal-sensitive transcriptional repressor | ||
BLNAIMJH_01600 | 1.4e-133 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
BLNAIMJH_01601 | 6.6e-246 | G | Major Facilitator Superfamily | |||
BLNAIMJH_01602 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
BLNAIMJH_01603 | 1.6e-224 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
BLNAIMJH_01604 | 5.1e-29 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
BLNAIMJH_01605 | 1.2e-132 | S | UPF0126 domain | |||
BLNAIMJH_01606 | 3.7e-105 | S | Mitochondrial biogenesis AIM24 | |||
BLNAIMJH_01607 | 5.3e-127 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
BLNAIMJH_01608 | 5.3e-138 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
BLNAIMJH_01609 | 5.6e-44 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
BLNAIMJH_01610 | 1.7e-99 | K | Bacterial regulatory proteins, tetR family | |||
BLNAIMJH_01611 | 1.5e-252 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
BLNAIMJH_01612 | 0.0 | 3.2.1.37 | GH43 | G | Glycosyl hydrolases family 43 | |
BLNAIMJH_01613 | 2.1e-235 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
BLNAIMJH_01614 | 7.8e-304 | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus | |
BLNAIMJH_01615 | 3.9e-99 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
BLNAIMJH_01616 | 1.3e-20 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
BLNAIMJH_01617 | 1.2e-120 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
BLNAIMJH_01618 | 1.1e-77 | soxR | K | MerR, DNA binding | ||
BLNAIMJH_01619 | 4.6e-196 | yghZ | C | Aldo/keto reductase family | ||
BLNAIMJH_01620 | 7.2e-58 | S | Protein of unknown function (DUF3039) | |||
BLNAIMJH_01621 | 7.7e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
BLNAIMJH_01622 | 8.5e-134 | |||||
BLNAIMJH_01623 | 1.8e-113 | yceD | S | Uncharacterized ACR, COG1399 | ||
BLNAIMJH_01624 | 1e-19 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
BLNAIMJH_01625 | 1.7e-135 | 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 | |
BLNAIMJH_01626 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
BLNAIMJH_01627 | 2.9e-18 | L | HTH-like domain | |||
BLNAIMJH_01628 | 1.8e-114 | L | PFAM Integrase catalytic | |||
BLNAIMJH_01629 | 1.6e-118 | ybjG | 3.6.1.27 | I | Psort location CytoplasmicMembrane, score | |
BLNAIMJH_01630 | 8.4e-78 | ypeA | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | |
BLNAIMJH_01632 | 2.3e-113 | vex2 | V | ABC transporter, ATP-binding protein | ||
BLNAIMJH_01633 | 2e-209 | vex1 | V | Efflux ABC transporter, permease protein | ||
BLNAIMJH_01634 | 7e-240 | vex3 | V | ABC transporter permease | ||
BLNAIMJH_01635 | 6.7e-27 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
BLNAIMJH_01636 | 9.7e-43 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
BLNAIMJH_01637 | 4.4e-18 | yhjX | EGP | Major facilitator Superfamily | ||
BLNAIMJH_01638 | 2.4e-180 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)