ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HBJBEPIO_00001 | 4.3e-16 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
HBJBEPIO_00002 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
HBJBEPIO_00003 | 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 | |
HBJBEPIO_00004 | 5.3e-147 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
HBJBEPIO_00005 | 8e-269 | S | Glycosyl transferase, family 2 | |||
HBJBEPIO_00006 | 3.3e-222 | |||||
HBJBEPIO_00007 | 1.5e-71 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
HBJBEPIO_00008 | 1.1e-152 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
HBJBEPIO_00009 | 2.5e-138 | ctsW | S | Phosphoribosyl transferase domain | ||
HBJBEPIO_00010 | 6.4e-47 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
HBJBEPIO_00011 | 0.0 | yknV | V | ABC transporter | ||
HBJBEPIO_00012 | 0.0 | mdlA2 | V | ABC transporter | ||
HBJBEPIO_00013 | 3e-50 | lipA | I | Hydrolase, alpha beta domain protein | ||
HBJBEPIO_00014 | 3.5e-282 | G | Alpha-L-arabinofuranosidase C-terminus | |||
HBJBEPIO_00015 | 8.5e-184 | tatD | L | TatD related DNase | ||
HBJBEPIO_00016 | 0.0 | kup | P | Transport of potassium into the cell | ||
HBJBEPIO_00017 | 1.2e-80 | ybfG | M | Domain of unknown function (DUF1906) | ||
HBJBEPIO_00018 | 1.8e-22 | tccB2 | V | DivIVA protein | ||
HBJBEPIO_00019 | 2.2e-129 | efeU_1 | P | Iron permease FTR1 family | ||
HBJBEPIO_00020 | 1.4e-92 | tpd | P | Fe2+ transport protein | ||
HBJBEPIO_00021 | 1.5e-231 | S | Predicted membrane protein (DUF2318) | |||
HBJBEPIO_00022 | 8e-220 | macB_2 | V | ABC transporter permease | ||
HBJBEPIO_00023 | 3.3e-126 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HBJBEPIO_00024 | 1.8e-181 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
HBJBEPIO_00025 | 1.5e-99 | |||||
HBJBEPIO_00026 | 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 | |
HBJBEPIO_00027 | 1.5e-161 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
HBJBEPIO_00028 | 1.3e-85 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
HBJBEPIO_00029 | 4e-55 | S | Predicted membrane protein (DUF2207) | |||
HBJBEPIO_00030 | 4.5e-61 | S | Predicted membrane protein (DUF2207) | |||
HBJBEPIO_00031 | 8.5e-91 | lemA | S | LemA family | ||
HBJBEPIO_00032 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
HBJBEPIO_00033 | 2.5e-25 | xylB | 1.1.1.57, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
HBJBEPIO_00034 | 2.1e-106 | lacA | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
HBJBEPIO_00035 | 0.0 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
HBJBEPIO_00036 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
HBJBEPIO_00037 | 2.4e-164 | MA20_14020 | P | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_00038 | 6.4e-82 | MA20_14025 | U | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_00039 | 3.2e-92 | yghZ | C | Aldo/keto reductase family | ||
HBJBEPIO_00040 | 3.2e-77 | soxR | K | MerR, DNA binding | ||
HBJBEPIO_00041 | 3.6e-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 | |
HBJBEPIO_00042 | 1e-139 | 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 | |
HBJBEPIO_00043 | 1.7e-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 | |
HBJBEPIO_00044 | 6.2e-88 | G | Glycosyl hydrolase family 20, domain 2 | |||
HBJBEPIO_00045 | 3.3e-280 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_00046 | 1.7e-125 | S | Short repeat of unknown function (DUF308) | |||
HBJBEPIO_00047 | 1.1e-47 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
HBJBEPIO_00048 | 3.4e-55 | DJ | Addiction module toxin, RelE StbE family | |||
HBJBEPIO_00049 | 9.1e-14 | S | Psort location Extracellular, score 8.82 | |||
HBJBEPIO_00050 | 7e-181 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HBJBEPIO_00051 | 1.1e-197 | parB | K | Belongs to the ParB family | ||
HBJBEPIO_00052 | 4.5e-172 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
HBJBEPIO_00053 | 3.3e-128 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HBJBEPIO_00054 | 3.6e-91 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
HBJBEPIO_00055 | 6.8e-165 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
HBJBEPIO_00056 | 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 | |
HBJBEPIO_00057 | 5.9e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
HBJBEPIO_00058 | 1.6e-102 | 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 | ||
HBJBEPIO_00059 | 7.3e-67 | int8 | L | Phage integrase family | ||
HBJBEPIO_00060 | 1e-41 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00061 | 3e-110 | ytrE | V | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_00062 | 1.6e-30 | 2.7.13.3 | T | Histidine kinase | ||
HBJBEPIO_00063 | 1e-55 | T | helix_turn_helix, Lux Regulon | |||
HBJBEPIO_00064 | 4.9e-82 | |||||
HBJBEPIO_00065 | 9.9e-43 | V | N-Acetylmuramoyl-L-alanine amidase | |||
HBJBEPIO_00066 | 0.0 | cbgA_1 | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
HBJBEPIO_00068 | 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) | |
HBJBEPIO_00069 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_00070 | 1.1e-240 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
HBJBEPIO_00071 | 3.5e-34 | |||||
HBJBEPIO_00072 | 1.9e-92 | flgA | NO | SAF | ||
HBJBEPIO_00073 | 6.1e-30 | fmdB | S | Putative regulatory protein | ||
HBJBEPIO_00074 | 9e-100 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
HBJBEPIO_00075 | 1.8e-113 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
HBJBEPIO_00076 | 9e-64 | |||||
HBJBEPIO_00077 | 3.9e-76 | |||||
HBJBEPIO_00078 | 2.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HBJBEPIO_00082 | 5.5e-25 | rpmG | J | Ribosomal protein L33 | ||
HBJBEPIO_00083 | 3.2e-204 | murB | 1.3.1.98 | M | Cell wall formation | |
HBJBEPIO_00084 | 1.3e-266 | E | aromatic amino acid transport protein AroP K03293 | |||
HBJBEPIO_00085 | 3.8e-102 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HBJBEPIO_00086 | 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 | ||
HBJBEPIO_00087 | 5.9e-143 | QT | PucR C-terminal helix-turn-helix domain | |||
HBJBEPIO_00088 | 0.0 | |||||
HBJBEPIO_00089 | 4e-104 | |||||
HBJBEPIO_00090 | 0.0 | typA | T | Elongation factor G C-terminus | ||
HBJBEPIO_00091 | 1.6e-230 | naiP | U | Sugar (and other) transporter | ||
HBJBEPIO_00092 | 5.2e-218 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
HBJBEPIO_00093 | 3.3e-187 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
HBJBEPIO_00094 | 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 | ||
HBJBEPIO_00095 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
HBJBEPIO_00096 | 3.5e-180 | S | Auxin Efflux Carrier | |||
HBJBEPIO_00097 | 0.0 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HBJBEPIO_00098 | 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 | ||
HBJBEPIO_00099 | 1.1e-123 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HBJBEPIO_00100 | 5.8e-164 | nusA | K | Participates in both transcription termination and antitermination | ||
HBJBEPIO_00101 | 1.3e-101 | |||||
HBJBEPIO_00103 | 1.3e-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 | |
HBJBEPIO_00104 | 1.3e-66 | rplQ | J | Ribosomal protein L17 | ||
HBJBEPIO_00105 | 4.2e-141 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HBJBEPIO_00106 | 2.2e-232 | ctpE | P | E1-E2 ATPase | ||
HBJBEPIO_00107 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
HBJBEPIO_00108 | 4.6e-214 | VP1224 | V | Psort location CytoplasmicMembrane, score 9.99 | ||
HBJBEPIO_00109 | 4.7e-92 | maa | 2.3.1.18, 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
HBJBEPIO_00110 | 3e-193 | 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 | |
HBJBEPIO_00111 | 8.1e-191 | 3.6.1.27 | I | PAP2 superfamily | ||
HBJBEPIO_00112 | 1.2e-235 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
HBJBEPIO_00113 | 8e-168 | ino1 | 5.5.1.4 | I | Myo-inositol-1-phosphate synthase | |
HBJBEPIO_00114 | 1.5e-191 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
HBJBEPIO_00115 | 2.4e-220 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
HBJBEPIO_00116 | 8.2e-129 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_00117 | 4.7e-67 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_00118 | 1.6e-100 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_00119 | 1.2e-202 | S | Endonuclease/Exonuclease/phosphatase family | |||
HBJBEPIO_00121 | 5.3e-41 | 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 | |
HBJBEPIO_00122 | 8.9e-245 | 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 | |
HBJBEPIO_00123 | 2.7e-147 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
HBJBEPIO_00124 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
HBJBEPIO_00125 | 2.8e-175 | |||||
HBJBEPIO_00126 | 8.5e-145 | tcyC | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
HBJBEPIO_00127 | 1.5e-146 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_00128 | 7.1e-151 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HBJBEPIO_00129 | 7.2e-151 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HBJBEPIO_00130 | 1.5e-46 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HBJBEPIO_00131 | 0.0 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
HBJBEPIO_00132 | 2e-120 | K | Bacterial regulatory proteins, tetR family | |||
HBJBEPIO_00133 | 3.7e-259 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
HBJBEPIO_00134 | 0.0 | crr | G | pts system, glucose-specific IIABC component | ||
HBJBEPIO_00135 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
HBJBEPIO_00136 | 9.9e-275 | cycA | E | Amino acid permease | ||
HBJBEPIO_00137 | 2.5e-89 | S | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_00138 | 7.1e-233 | M | LPXTG cell wall anchor motif | |||
HBJBEPIO_00139 | 5.1e-34 | inlJ | M | domain protein | ||
HBJBEPIO_00140 | 0.0 | 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) | |
HBJBEPIO_00141 | 1.4e-300 | S | Calcineurin-like phosphoesterase | |||
HBJBEPIO_00142 | 1e-80 | |||||
HBJBEPIO_00143 | 1.4e-138 | G | Bacterial extracellular solute-binding protein | |||
HBJBEPIO_00144 | 3.6e-163 | G | PFAM binding-protein-dependent transport systems inner membrane component | |||
HBJBEPIO_00145 | 1.7e-145 | G | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_00146 | 7e-94 | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
HBJBEPIO_00147 | 1.8e-34 | KLT | Protein tyrosine kinase | |||
HBJBEPIO_00148 | 0.0 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
HBJBEPIO_00149 | 4.6e-19 | 3.1.21.3 | V | DivIVA protein | ||
HBJBEPIO_00150 | 4.3e-87 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HBJBEPIO_00151 | 4.9e-176 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HBJBEPIO_00152 | 1.4e-236 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
HBJBEPIO_00153 | 5.6e-112 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
HBJBEPIO_00154 | 4.1e-121 | 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 | |
HBJBEPIO_00155 | 3.4e-141 | glpR | K | DeoR C terminal sensor domain | ||
HBJBEPIO_00156 | 1.1e-250 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
HBJBEPIO_00157 | 2.7e-230 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
HBJBEPIO_00158 | 1.1e-17 | gcvR | T | Belongs to the UPF0237 family | ||
HBJBEPIO_00159 | 1.9e-101 | S | UPF0210 protein | |||
HBJBEPIO_00160 | 4.1e-206 | 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 | |
HBJBEPIO_00161 | 8.2e-205 | 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 | |
HBJBEPIO_00162 | 2.8e-179 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
HBJBEPIO_00163 | 5.4e-212 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
HBJBEPIO_00164 | 2e-82 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
HBJBEPIO_00165 | 1.8e-91 | |||||
HBJBEPIO_00167 | 4.4e-183 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
HBJBEPIO_00168 | 2e-103 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
HBJBEPIO_00169 | 2e-71 | divIC | D | Septum formation initiator | ||
HBJBEPIO_00170 | 4.6e-54 | 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 | |
HBJBEPIO_00171 | 6.9e-17 | 3.1.3.15 | E | Histidinol phosphate phosphatase, HisJ family | ||
HBJBEPIO_00172 | 1.6e-140 | 3.5.2.10 | S | Creatinine amidohydrolase | ||
HBJBEPIO_00173 | 2.2e-246 | proP | EGP | Sugar (and other) transporter | ||
HBJBEPIO_00174 | 4.7e-285 | purR | QT | Purine catabolism regulatory protein-like family | ||
HBJBEPIO_00175 | 6.1e-303 | cydD | V | ABC transporter transmembrane region | ||
HBJBEPIO_00176 | 4e-156 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
HBJBEPIO_00177 | 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 | |
HBJBEPIO_00178 | 2.1e-154 | G | Major Facilitator Superfamily | |||
HBJBEPIO_00179 | 2.5e-242 | T | PhoQ Sensor | |||
HBJBEPIO_00180 | 1.2e-78 | S | Protein of unknown function (DUF2975) | |||
HBJBEPIO_00181 | 4.2e-30 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
HBJBEPIO_00182 | 0.0 | cadA | P | E1-E2 ATPase | ||
HBJBEPIO_00183 | 2.3e-187 | ansA | 3.5.1.1 | EJ | Asparaginase | |
HBJBEPIO_00184 | 2.9e-162 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
HBJBEPIO_00185 | 3.4e-28 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
HBJBEPIO_00186 | 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) | |
HBJBEPIO_00187 | 1.5e-178 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
HBJBEPIO_00188 | 1e-153 | 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 | |
HBJBEPIO_00189 | 7e-178 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
HBJBEPIO_00190 | 2.6e-97 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HBJBEPIO_00191 | 2.3e-107 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HBJBEPIO_00192 | 4.2e-74 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
HBJBEPIO_00193 | 3e-187 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HBJBEPIO_00194 | 7e-178 | 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 | |
HBJBEPIO_00195 | 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 | |
HBJBEPIO_00196 | 0.0 | ams | 2.4.1.4, 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha amylase, catalytic domain |
HBJBEPIO_00198 | 2.4e-116 | |||||
HBJBEPIO_00199 | 1.7e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HBJBEPIO_00200 | 4.5e-84 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
HBJBEPIO_00201 | 0.0 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
HBJBEPIO_00202 | 5.9e-12 | |||||
HBJBEPIO_00203 | 3.4e-17 | yccF | S | Inner membrane component domain | ||
HBJBEPIO_00204 | 2.5e-49 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HBJBEPIO_00205 | 4.2e-72 | helD | 3.6.4.12 | L | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_00206 | 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 | ||
HBJBEPIO_00207 | 1.1e-141 | 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 | |
HBJBEPIO_00208 | 5.8e-111 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
HBJBEPIO_00209 | 1.8e-198 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HBJBEPIO_00210 | 7.2e-89 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
HBJBEPIO_00211 | 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 | |
HBJBEPIO_00212 | 1.7e-45 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
HBJBEPIO_00213 | 1.2e-238 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
HBJBEPIO_00214 | 3.4e-111 | K | Bacterial regulatory proteins, tetR family | |||
HBJBEPIO_00215 | 2.1e-224 | hsvB | 6.3.2.4 | M | Belongs to the D-alanine--D-alanine ligase family | |
HBJBEPIO_00216 | 2.2e-108 | P | Major Facilitator Superfamily | |||
HBJBEPIO_00217 | 4.4e-163 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
HBJBEPIO_00218 | 0.0 | E | Transglutaminase-like superfamily | |||
HBJBEPIO_00219 | 5.6e-52 | S | Protein of unknown function DUF58 | |||
HBJBEPIO_00220 | 8.2e-21 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
HBJBEPIO_00221 | 0.0 | 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 | |
HBJBEPIO_00222 | 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 | |
HBJBEPIO_00223 | 4.6e-180 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HBJBEPIO_00224 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
HBJBEPIO_00225 | 2.6e-307 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
HBJBEPIO_00226 | 0.0 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
HBJBEPIO_00227 | 9.3e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_00228 | 3.1e-167 | P | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_00229 | 2e-219 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
HBJBEPIO_00230 | 4.9e-98 | metI | P | Psort location CytoplasmicMembrane, score 9.99 | ||
HBJBEPIO_00231 | 7.2e-192 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HBJBEPIO_00232 | 3.8e-154 | metQ | M | NLPA lipoprotein | ||
HBJBEPIO_00233 | 7.1e-175 | M | LPXTG-motif cell wall anchor domain protein | |||
HBJBEPIO_00234 | 0.0 | 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 |
HBJBEPIO_00235 | 8.5e-131 | amt | U | Ammonium Transporter Family | ||
HBJBEPIO_00236 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
HBJBEPIO_00237 | 8.3e-244 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
HBJBEPIO_00238 | 8.6e-53 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
HBJBEPIO_00239 | 3.3e-248 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HBJBEPIO_00240 | 2.5e-251 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
HBJBEPIO_00241 | 3.8e-44 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
HBJBEPIO_00242 | 1e-60 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
HBJBEPIO_00243 | 1e-27 | S | granule-associated protein | |||
HBJBEPIO_00244 | 2.3e-191 | ubiB | S | ABC1 family | ||
HBJBEPIO_00245 | 8.3e-67 | ubiB | S | ABC1 family | ||
HBJBEPIO_00246 | 4.1e-192 | K | Periplasmic binding protein domain | |||
HBJBEPIO_00247 | 3.3e-242 | G | Bacterial extracellular solute-binding protein | |||
HBJBEPIO_00249 | 2.5e-101 | S | Protein of unknown function DUF45 | |||
HBJBEPIO_00250 | 2.6e-188 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HBJBEPIO_00251 | 2.8e-241 | ytfL | P | Transporter associated domain | ||
HBJBEPIO_00252 | 1.6e-14 | trkH | P | Cation transport protein | ||
HBJBEPIO_00253 | 1.1e-49 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HBJBEPIO_00254 | 5.3e-64 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HBJBEPIO_00255 | 3.7e-149 | 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 | |
HBJBEPIO_00256 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
HBJBEPIO_00257 | 1.1e-61 | 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 | ||
HBJBEPIO_00258 | 2e-39 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HBJBEPIO_00259 | 5.8e-118 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HBJBEPIO_00260 | 6e-91 | mraZ | K | Belongs to the MraZ family | ||
HBJBEPIO_00261 | 5.6e-52 | L | DNA helicase | |||
HBJBEPIO_00262 | 1.7e-306 | 3.6.3.24 | P | AAA domain, putative AbiEii toxin, Type IV TA system | ||
HBJBEPIO_00263 | 6.9e-150 | P | Cobalt transport protein | |||
HBJBEPIO_00264 | 8.2e-193 | K | helix_turn_helix ASNC type | |||
HBJBEPIO_00265 | 1.7e-47 | V | ABC transporter, ATP-binding protein | |||
HBJBEPIO_00266 | 3.3e-197 | Z012_01000 | 1.1.1.14, 1.1.1.9 | C | Zinc-binding dehydrogenase | |
HBJBEPIO_00267 | 1.3e-251 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00268 | 2e-216 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
HBJBEPIO_00269 | 5.2e-56 | 3.6.1.13 | L | NUDIX domain | ||
HBJBEPIO_00270 | 1.2e-82 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
HBJBEPIO_00271 | 8e-97 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
HBJBEPIO_00272 | 0.0 | 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 | ||
HBJBEPIO_00273 | 9.5e-175 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HBJBEPIO_00274 | 2.9e-297 | yjcE | P | Sodium/hydrogen exchanger family | ||
HBJBEPIO_00275 | 9.4e-152 | ypfH | S | Phospholipase/Carboxylesterase | ||
HBJBEPIO_00276 | 4.9e-110 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
HBJBEPIO_00277 | 9.9e-19 | L | PFAM Integrase catalytic | |||
HBJBEPIO_00278 | 8.8e-72 | L | IstB-like ATP binding protein | |||
HBJBEPIO_00279 | 1.5e-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 | ||
HBJBEPIO_00280 | 2.2e-54 | 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 | ||
HBJBEPIO_00281 | 6.8e-156 | 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 | |
HBJBEPIO_00282 | 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 | |
HBJBEPIO_00283 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
HBJBEPIO_00285 | 1.3e-96 | 3.6.1.55 | F | NUDIX domain | ||
HBJBEPIO_00286 | 0.0 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
HBJBEPIO_00287 | 5e-293 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
HBJBEPIO_00288 | 1.8e-19 | 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 | ||
HBJBEPIO_00289 | 1.8e-204 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
HBJBEPIO_00290 | 1.7e-232 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
HBJBEPIO_00292 | 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 | ||
HBJBEPIO_00293 | 2.5e-49 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HBJBEPIO_00295 | 1.7e-199 | K | Cell envelope-related transcriptional attenuator domain | |||
HBJBEPIO_00296 | 3.4e-54 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
HBJBEPIO_00297 | 3.2e-152 | S | Glycosyl transferase, family 2 | |||
HBJBEPIO_00298 | 2.7e-48 | yitI | S | Acetyltransferase (GNAT) domain | ||
HBJBEPIO_00299 | 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 | |
HBJBEPIO_00300 | 1.4e-96 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
HBJBEPIO_00301 | 3.4e-135 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
HBJBEPIO_00302 | 3e-234 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
HBJBEPIO_00303 | 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 | ||
HBJBEPIO_00304 | 2.9e-33 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
HBJBEPIO_00305 | 1.4e-225 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
HBJBEPIO_00306 | 5.6e-59 | |||||
HBJBEPIO_00308 | 1.5e-51 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00309 | 2e-29 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00310 | 4.9e-58 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00311 | 1.4e-40 | ptsH | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | ||
HBJBEPIO_00313 | 7.7e-164 | T | Pfam Adenylate and Guanylate cyclase catalytic domain | |||
HBJBEPIO_00314 | 1.8e-294 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
HBJBEPIO_00315 | 2.9e-102 | 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 | |
HBJBEPIO_00316 | 2.5e-82 | J | TM2 domain | |||
HBJBEPIO_00317 | 9.1e-217 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
HBJBEPIO_00318 | 2.3e-133 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
HBJBEPIO_00319 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
HBJBEPIO_00320 | 3.2e-75 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
HBJBEPIO_00321 | 2.8e-15 | P | Belongs to the ABC transporter superfamily | |||
HBJBEPIO_00322 | 1.4e-43 | XAC3035 | O | Glutaredoxin | ||
HBJBEPIO_00323 | 3.1e-127 | XK27_08050 | O | prohibitin homologues | ||
HBJBEPIO_00324 | 2.4e-15 | S | Domain of unknown function (DUF4143) | |||
HBJBEPIO_00325 | 4.3e-75 | |||||
HBJBEPIO_00326 | 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 | |
HBJBEPIO_00327 | 1.9e-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 | |
HBJBEPIO_00328 | 1e-47 | S | Domain of unknown function (DUF4193) | |||
HBJBEPIO_00329 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
HBJBEPIO_00330 | 3.2e-112 | S | Uncharacterized conserved protein (DUF2183) | |||
HBJBEPIO_00331 | 9.3e-223 | G | Bacterial extracellular solute-binding protein | |||
HBJBEPIO_00332 | 5.9e-183 | K | Psort location Cytoplasmic, score | |||
HBJBEPIO_00333 | 4.4e-183 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_00334 | 0.0 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
HBJBEPIO_00335 | 6.5e-181 | V | Beta-lactamase | |||
HBJBEPIO_00336 | 9.3e-74 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
HBJBEPIO_00337 | 1.3e-47 | ribD | 1.1.1.193, 3.5.4.26 | H | Cytidine and deoxycytidylate deaminase zinc-binding region | |
HBJBEPIO_00338 | 9.6e-115 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
HBJBEPIO_00339 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
HBJBEPIO_00340 | 3.9e-99 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HBJBEPIO_00341 | 4.6e-64 | 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 | |
HBJBEPIO_00343 | 6.6e-124 | |||||
HBJBEPIO_00344 | 6.8e-133 | KT | Response regulator receiver domain protein | |||
HBJBEPIO_00345 | 6.5e-271 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
HBJBEPIO_00346 | 4.5e-67 | cspB | K | 'Cold-shock' DNA-binding domain | ||
HBJBEPIO_00347 | 1.2e-182 | S | Protein of unknown function (DUF3027) | |||
HBJBEPIO_00348 | 4.6e-188 | uspA | T | Belongs to the universal stress protein A family | ||
HBJBEPIO_00349 | 4.3e-26 | 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 | |
HBJBEPIO_00350 | 0.0 | I | acetylesterase activity | |||
HBJBEPIO_00351 | 7.3e-135 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HBJBEPIO_00352 | 4e-155 | 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 | |
HBJBEPIO_00353 | 6.5e-155 | iunH1 | 3.2.2.1 | F | nucleoside hydrolase | |
HBJBEPIO_00354 | 4.4e-82 | P | NMT1/THI5 like | |||
HBJBEPIO_00355 | 3.9e-125 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HBJBEPIO_00356 | 2.3e-29 | ftsK | D | FtsK SpoIIIE family protein | ||
HBJBEPIO_00357 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
HBJBEPIO_00358 | 3.8e-193 | 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) | |
HBJBEPIO_00359 | 6.5e-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 | |
HBJBEPIO_00360 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
HBJBEPIO_00361 | 1.4e-41 | hup | L | Belongs to the bacterial histone-like protein family | ||
HBJBEPIO_00362 | 1.8e-57 | |||||
HBJBEPIO_00363 | 2.5e-203 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00364 | 4.9e-96 | S | GtrA-like protein | |||
HBJBEPIO_00365 | 6.7e-62 | S | Macrophage migration inhibitory factor (MIF) | |||
HBJBEPIO_00366 | 2.2e-221 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
HBJBEPIO_00367 | 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 | ||
HBJBEPIO_00368 | 3.8e-108 | |||||
HBJBEPIO_00370 | 2.4e-127 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HBJBEPIO_00371 | 8.9e-111 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
HBJBEPIO_00372 | 6.4e-130 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
HBJBEPIO_00373 | 8.4e-181 | 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 | |
HBJBEPIO_00374 | 1e-72 | attW | O | OsmC-like protein | ||
HBJBEPIO_00375 | 9.8e-165 | T | Universal stress protein family | |||
HBJBEPIO_00376 | 1.3e-79 | M | NlpC/P60 family | |||
HBJBEPIO_00377 | 4.8e-163 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
HBJBEPIO_00378 | 6.1e-94 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00379 | 0.0 | E | ABC transporter, substrate-binding protein, family 5 | |||
HBJBEPIO_00380 | 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 | |
HBJBEPIO_00381 | 1.4e-122 | 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 | |
HBJBEPIO_00382 | 4.5e-223 | pflA | S | Protein of unknown function (DUF4012) | ||
HBJBEPIO_00383 | 1.4e-86 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
HBJBEPIO_00384 | 4.2e-181 | S | Endonuclease/Exonuclease/phosphatase family | |||
HBJBEPIO_00385 | 2.5e-47 | |||||
HBJBEPIO_00386 | 5.9e-244 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00387 | 2.8e-262 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
HBJBEPIO_00388 | 1.1e-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 | ||
HBJBEPIO_00389 | 1.6e-166 | 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 | ||
HBJBEPIO_00390 | 3.7e-193 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_00391 | 3e-60 | S | Thiamine-binding protein | |||
HBJBEPIO_00392 | 2.9e-151 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HBJBEPIO_00393 | 1.1e-133 | 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) | |
HBJBEPIO_00394 | 3.1e-20 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
HBJBEPIO_00395 | 4.5e-61 | G | Bacterial extracellular solute-binding protein | |||
HBJBEPIO_00396 | 7.5e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_00397 | 4.4e-164 | G | ABC transporter permease | |||
HBJBEPIO_00398 | 6.2e-171 | 2.7.1.2 | GK | ROK family | ||
HBJBEPIO_00399 | 3.3e-163 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HBJBEPIO_00400 | 8e-301 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
HBJBEPIO_00401 | 1.2e-08 | pnuC | H | Nicotinamide mononucleotide transporter | ||
HBJBEPIO_00402 | 2.8e-111 | pnuC | H | Nicotinamide mononucleotide transporter | ||
HBJBEPIO_00403 | 1.1e-143 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
HBJBEPIO_00404 | 5.7e-38 | csoR | S | Metal-sensitive transcriptional repressor | ||
HBJBEPIO_00405 | 1.4e-133 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HBJBEPIO_00406 | 8.3e-137 | G | Major Facilitator Superfamily | |||
HBJBEPIO_00407 | 8.4e-46 | G | Major Facilitator Superfamily | |||
HBJBEPIO_00408 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HBJBEPIO_00409 | 2.9e-61 | S | Domain of unknown function (DUF4418) | |||
HBJBEPIO_00410 | 0.0 | pcrA | 3.6.4.12 | L | DNA helicase | |
HBJBEPIO_00411 | 2.1e-32 | 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 | |
HBJBEPIO_00413 | 1.8e-187 | yocS | S | SBF-like CPA transporter family (DUF4137) | ||
HBJBEPIO_00414 | 1.2e-61 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
HBJBEPIO_00415 | 3.3e-80 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
HBJBEPIO_00416 | 3.2e-17 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
HBJBEPIO_00417 | 3.4e-160 | mhpC | I | Alpha/beta hydrolase family | ||
HBJBEPIO_00418 | 1.7e-113 | F | Domain of unknown function (DUF4916) | |||
HBJBEPIO_00419 | 6e-61 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
HBJBEPIO_00420 | 4.7e-169 | S | G5 | |||
HBJBEPIO_00421 | 5.6e-248 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00422 | 1.1e-183 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HBJBEPIO_00423 | 7.7e-194 | 1.1.1.1 | C | Iron-containing alcohol dehydrogenase | ||
HBJBEPIO_00424 | 3.6e-17 | 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 | |
HBJBEPIO_00425 | 4.9e-194 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
HBJBEPIO_00426 | 7.6e-115 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
HBJBEPIO_00427 | 2.1e-123 | livF | E | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_00428 | 3e-63 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
HBJBEPIO_00429 | 2.3e-111 | 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 | |
HBJBEPIO_00430 | 1.1e-139 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
HBJBEPIO_00431 | 1.8e-262 | S | Calcineurin-like phosphoesterase | |||
HBJBEPIO_00435 | 4.2e-110 | 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 | |
HBJBEPIO_00436 | 4.3e-138 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HBJBEPIO_00437 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
HBJBEPIO_00438 | 1.6e-151 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HBJBEPIO_00439 | 1.7e-260 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
HBJBEPIO_00440 | 3.6e-155 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
HBJBEPIO_00441 | 4.7e-42 | efeU_1 | P | Iron permease FTR1 family | ||
HBJBEPIO_00442 | 3e-71 | efeU_1 | P | Iron permease FTR1 family | ||
HBJBEPIO_00443 | 4.4e-237 | G | MFS/sugar transport protein | |||
HBJBEPIO_00444 | 5.3e-49 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
HBJBEPIO_00445 | 3.6e-197 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
HBJBEPIO_00446 | 2.8e-285 | cotH | M | CotH kinase protein | ||
HBJBEPIO_00447 | 1.4e-158 | P | VTC domain | |||
HBJBEPIO_00448 | 2.5e-110 | S | Domain of unknown function (DUF4956) | |||
HBJBEPIO_00449 | 0.0 | yliE | T | Putative diguanylate phosphodiesterase | ||
HBJBEPIO_00450 | 2.9e-202 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
HBJBEPIO_00451 | 7.8e-302 | pepD | E | Peptidase family C69 | ||
HBJBEPIO_00452 | 1.2e-194 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
HBJBEPIO_00453 | 1.7e-94 | icaR | K | Bacterial regulatory proteins, tetR family | ||
HBJBEPIO_00454 | 4.5e-31 | |||||
HBJBEPIO_00455 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
HBJBEPIO_00456 | 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 | |
HBJBEPIO_00457 | 7.7e-114 | S | Protein of unknown function (DUF805) | |||
HBJBEPIO_00458 | 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) | |
HBJBEPIO_00459 | 3.3e-62 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
HBJBEPIO_00460 | 4.3e-143 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
HBJBEPIO_00461 | 9.1e-98 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
HBJBEPIO_00462 | 2.4e-80 | 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 | ||
HBJBEPIO_00463 | 3.4e-67 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HBJBEPIO_00464 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HBJBEPIO_00465 | 1.2e-126 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
HBJBEPIO_00466 | 1.3e-293 | E | ABC transporter, substrate-binding protein, family 5 | |||
HBJBEPIO_00467 | 7.5e-103 | 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) | |
HBJBEPIO_00468 | 5.1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HBJBEPIO_00469 | 6.7e-35 | D | nuclear chromosome segregation | |||
HBJBEPIO_00470 | 5.1e-150 | T | HD domain | |||
HBJBEPIO_00471 | 3.3e-153 | V | ABC transporter | |||
HBJBEPIO_00472 | 1.2e-211 | V | ABC transporter permease | |||
HBJBEPIO_00473 | 1.6e-115 | S | Uncharacterised protein family (UPF0182) | |||
HBJBEPIO_00474 | 7.4e-178 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
HBJBEPIO_00475 | 6.2e-40 | ybdD | S | Selenoprotein, putative | ||
HBJBEPIO_00476 | 3.8e-162 | cstA | T | 5TM C-terminal transporter carbon starvation CstA | ||
HBJBEPIO_00477 | 4.8e-105 | rpsA | J | Ribosomal protein S1 | ||
HBJBEPIO_00478 | 9.1e-116 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
HBJBEPIO_00479 | 6.7e-74 | 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 | ||
HBJBEPIO_00480 | 1.4e-74 | 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 | ||
HBJBEPIO_00481 | 1.4e-155 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
HBJBEPIO_00482 | 6.2e-177 | ydeD | EG | EamA-like transporter family | ||
HBJBEPIO_00483 | 4.6e-43 | ybhL | S | Belongs to the BI1 family | ||
HBJBEPIO_00484 | 4.2e-200 | L | Transposase | |||
HBJBEPIO_00485 | 1.1e-23 | relB | L | RelB antitoxin | ||
HBJBEPIO_00486 | 9.1e-222 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
HBJBEPIO_00487 | 1.8e-183 | |||||
HBJBEPIO_00488 | 0.0 | pulE | NU | Type II/IV secretion system protein | ||
HBJBEPIO_00489 | 1e-61 | ppdC | NU | Prokaryotic N-terminal methylation motif | ||
HBJBEPIO_00490 | 1.3e-79 | K | helix_turn_helix ASNC type | |||
HBJBEPIO_00491 | 1e-69 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
HBJBEPIO_00492 | 4.8e-113 | S | domain protein | |||
HBJBEPIO_00493 | 5.8e-126 | dedA | S | SNARE associated Golgi protein | ||
HBJBEPIO_00495 | 3.3e-129 | S | HAD hydrolase, family IA, variant 3 | |||
HBJBEPIO_00496 | 8.6e-47 | |||||
HBJBEPIO_00497 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HBJBEPIO_00498 | 5.1e-128 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HBJBEPIO_00499 | 8.8e-47 | |||||
HBJBEPIO_00500 | 0.0 | rafA | 3.2.1.22 | G | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_00501 | 9.9e-55 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_00502 | 4.6e-188 | yegU | O | ADP-ribosylglycohydrolase | ||
HBJBEPIO_00503 | 3.2e-189 | yegV | G | pfkB family carbohydrate kinase | ||
HBJBEPIO_00504 | 5.9e-236 | U | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
HBJBEPIO_00505 | 4.8e-102 | Q | Isochorismatase family | |||
HBJBEPIO_00506 | 2.3e-214 | S | Choline/ethanolamine kinase | |||
HBJBEPIO_00507 | 2.8e-274 | eat | E | Amino acid permease | ||
HBJBEPIO_00508 | 5.3e-264 | gabT | 2.6.1.19, 2.6.1.22 | H | Aminotransferase class-III | |
HBJBEPIO_00509 | 3.9e-142 | yidP | K | UTRA | ||
HBJBEPIO_00510 | 1.9e-121 | degU | K | helix_turn_helix, Lux Regulon | ||
HBJBEPIO_00511 | 1.3e-264 | tcsS3 | KT | PspC domain | ||
HBJBEPIO_00512 | 1.1e-145 | pspC | KT | PspC domain | ||
HBJBEPIO_00513 | 9.3e-93 | |||||
HBJBEPIO_00514 | 7.9e-117 | S | Protein of unknown function (DUF4125) | |||
HBJBEPIO_00515 | 0.0 | S | Domain of unknown function (DUF4037) | |||
HBJBEPIO_00516 | 2.6e-211 | ykiI | ||||
HBJBEPIO_00518 | 4.2e-138 | L | Phage integrase family | |||
HBJBEPIO_00519 | 6.8e-14 | |||||
HBJBEPIO_00520 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
HBJBEPIO_00521 | 3.7e-171 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
HBJBEPIO_00522 | 3.5e-42 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
HBJBEPIO_00523 | 1.7e-222 | 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 | ||
HBJBEPIO_00524 | 9.6e-118 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HBJBEPIO_00525 | 4.7e-64 | recX | S | Modulates RecA activity | ||
HBJBEPIO_00526 | 1.3e-164 | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus | |
HBJBEPIO_00527 | 6.1e-222 | blt | G | MFS/sugar transport protein | ||
HBJBEPIO_00528 | 5.9e-225 | V | ABC-2 family transporter protein | |||
HBJBEPIO_00529 | 4.4e-191 | V | ATPases associated with a variety of cellular activities | |||
HBJBEPIO_00530 | 1.7e-60 | T | Histidine kinase | |||
HBJBEPIO_00531 | 3.3e-167 | iunH2 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HBJBEPIO_00532 | 1.1e-197 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_00533 | 2.6e-61 | |||||
HBJBEPIO_00534 | 2e-177 | xerD | D | recombinase XerD | ||
HBJBEPIO_00535 | 6.8e-153 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
HBJBEPIO_00536 | 2.1e-151 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
HBJBEPIO_00537 | 2.7e-85 | S | domain protein | |||
HBJBEPIO_00538 | 1.4e-142 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
HBJBEPIO_00539 | 1.6e-273 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
HBJBEPIO_00540 | 2.6e-186 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HBJBEPIO_00541 | 0.0 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
HBJBEPIO_00543 | 5e-273 | 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 | |
HBJBEPIO_00544 | 5.9e-158 | yfdV | S | Membrane transport protein | ||
HBJBEPIO_00545 | 3.6e-96 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
HBJBEPIO_00546 | 6.2e-127 | L | Protein of unknown function (DUF1524) | |||
HBJBEPIO_00547 | 6.4e-243 | T | Diguanylate cyclase (GGDEF) domain protein | |||
HBJBEPIO_00548 | 1.5e-55 | mazG | S | MazG-like family | ||
HBJBEPIO_00549 | 8.3e-272 | L | Uncharacterized conserved protein (DUF2075) | |||
HBJBEPIO_00550 | 3e-27 | |||||
HBJBEPIO_00551 | 2e-92 | pilT | NU | Type II/IV secretion system protein | ||
HBJBEPIO_00552 | 0.0 | |||||
HBJBEPIO_00553 | 2.3e-139 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
HBJBEPIO_00554 | 1.9e-62 | S | Protein of unknown function (DUF4235) | |||
HBJBEPIO_00555 | 2.4e-135 | G | Phosphoglycerate mutase family | |||
HBJBEPIO_00556 | 6.7e-176 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
HBJBEPIO_00557 | 1.4e-50 | pknL | 2.7.11.1 | KLT | PASTA | |
HBJBEPIO_00558 | 1.1e-66 | pknL | 2.7.11.1 | KLT | PASTA | |
HBJBEPIO_00559 | 2.4e-44 | pknL | 2.7.11.1 | KLT | PASTA | |
HBJBEPIO_00560 | 3e-66 | sufC | O | FeS assembly ATPase SufC | ||
HBJBEPIO_00561 | 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 | |
HBJBEPIO_00562 | 3.4e-100 | iscU | C | SUF system FeS assembly protein, NifU family | ||
HBJBEPIO_00563 | 2.7e-108 | yitW | S | Iron-sulfur cluster assembly protein | ||
HBJBEPIO_00564 | 7.5e-181 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
HBJBEPIO_00567 | 1e-182 | cat | P | Cation efflux family | ||
HBJBEPIO_00568 | 4.3e-71 | S | Psort location CytoplasmicMembrane, score | |||
HBJBEPIO_00569 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
HBJBEPIO_00570 | 1.8e-83 | K | Cro/C1-type HTH DNA-binding domain | |||
HBJBEPIO_00571 | 5.5e-138 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
HBJBEPIO_00572 | 5.3e-138 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
HBJBEPIO_00573 | 7.8e-55 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
HBJBEPIO_00574 | 2.9e-22 | K | Bacterial regulatory proteins, tetR family | |||
HBJBEPIO_00575 | 3.2e-20 | P | Major Facilitator Superfamily | |||
HBJBEPIO_00576 | 1.9e-215 | V | FtsX-like permease family | |||
HBJBEPIO_00577 | 1.2e-253 | P | Sodium/hydrogen exchanger family | |||
HBJBEPIO_00578 | 1.9e-112 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
HBJBEPIO_00579 | 2.4e-270 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HBJBEPIO_00580 | 5.7e-34 | L | Transposase | |||
HBJBEPIO_00581 | 2.3e-37 | yxeN | P | amino acid ABC transporter | ||
HBJBEPIO_00582 | 2.1e-14 | E | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_00583 | 3.9e-15 | E | ABC transporter | |||
HBJBEPIO_00584 | 6.2e-73 | 3.6.3.21 | E | ABC transporter | ||
HBJBEPIO_00585 | 5.1e-77 | odh | 1.5.1.28 | I | glycerol-3-phosphate dehydrogenase [NAD(P)+] activity | |
HBJBEPIO_00586 | 2.4e-07 | ET | Bacterial periplasmic substrate-binding proteins | |||
HBJBEPIO_00587 | 3.7e-32 | ET | Bacterial periplasmic substrate-binding proteins | |||
HBJBEPIO_00588 | 1.4e-230 | bglA | 3.2.1.21 | G | Glycosyl hydrolase family 1 | |
HBJBEPIO_00591 | 1.4e-221 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_00592 | 2e-178 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_00593 | 1.4e-164 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HBJBEPIO_00594 | 4.5e-41 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HBJBEPIO_00595 | 7.2e-66 | |||||
HBJBEPIO_00596 | 4.6e-169 | S | Fic/DOC family | |||
HBJBEPIO_00597 | 1.9e-14 | L | Eco57I restriction-modification methylase | |||
HBJBEPIO_00598 | 2.4e-11 | L | DNA restriction-modification system | |||
HBJBEPIO_00599 | 5e-48 | L | ribosomal rna small subunit methyltransferase | |||
HBJBEPIO_00600 | 3.1e-147 | gluP | 3.4.21.105 | S | Rhomboid family | |
HBJBEPIO_00601 | 3.4e-35 | |||||
HBJBEPIO_00602 | 1.5e-143 | 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 |
HBJBEPIO_00603 | 6.5e-148 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
HBJBEPIO_00604 | 1.4e-164 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
HBJBEPIO_00605 | 3.4e-133 | 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 | ||
HBJBEPIO_00606 | 2.1e-114 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
HBJBEPIO_00607 | 9.4e-186 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HBJBEPIO_00608 | 1.1e-86 | M | Bacterial capsule synthesis protein PGA_cap | |||
HBJBEPIO_00609 | 1.1e-50 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
HBJBEPIO_00610 | 3.4e-129 | KT | Transcriptional regulatory protein, C terminal | |||
HBJBEPIO_00611 | 1.6e-197 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
HBJBEPIO_00612 | 3.4e-164 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HBJBEPIO_00613 | 4e-168 | pstA | P | Phosphate transport system permease | ||
HBJBEPIO_00614 | 3.6e-148 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
HBJBEPIO_00615 | 1.8e-143 | P | Zinc-uptake complex component A periplasmic | |||
HBJBEPIO_00616 | 1.3e-246 | pbuO | S | Permease family | ||
HBJBEPIO_00617 | 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 | ||
HBJBEPIO_00618 | 2.4e-36 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
HBJBEPIO_00619 | 1.9e-176 | T | Forkhead associated domain | |||
HBJBEPIO_00620 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
HBJBEPIO_00621 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
HBJBEPIO_00622 | 7.4e-81 | |||||
HBJBEPIO_00623 | 6.1e-191 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HBJBEPIO_00624 | 0.0 | 3.2.1.97 | GH101 | G | Glycosyl hydrolases family 43 | |
HBJBEPIO_00625 | 1.1e-195 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_00626 | 2.3e-141 | abf | G | Glycosyl hydrolases family 43 | ||
HBJBEPIO_00627 | 1.6e-43 | S | Protein of unknown function (DUF3180) | |||
HBJBEPIO_00628 | 1.7e-271 | 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 | |
HBJBEPIO_00629 | 7.2e-130 | 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 | |
HBJBEPIO_00631 | 3.6e-210 | GK | ROK family | |||
HBJBEPIO_00632 | 5.2e-12 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HBJBEPIO_00633 | 9.8e-25 | helY | L | DEAD DEAH box helicase | ||
HBJBEPIO_00634 | 1.5e-130 | helY | L | DEAD DEAH box helicase | ||
HBJBEPIO_00635 | 2.1e-54 | |||||
HBJBEPIO_00636 | 3.1e-259 | pafB | K | WYL domain | ||
HBJBEPIO_00637 | 5.1e-268 | V | Efflux ABC transporter, permease protein | |||
HBJBEPIO_00638 | 1.9e-127 | V | ATPases associated with a variety of cellular activities | |||
HBJBEPIO_00639 | 8.3e-66 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HBJBEPIO_00640 | 7e-161 | 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 | |
HBJBEPIO_00641 | 0.0 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
HBJBEPIO_00643 | 2.6e-163 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
HBJBEPIO_00644 | 8.1e-243 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
HBJBEPIO_00645 | 3.6e-100 | pdtaR | T | Response regulator receiver domain protein | ||
HBJBEPIO_00646 | 2e-94 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HBJBEPIO_00647 | 8.3e-251 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
HBJBEPIO_00648 | 1.7e-215 | S | Amidohydrolase family | |||
HBJBEPIO_00649 | 2.3e-122 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
HBJBEPIO_00650 | 7e-149 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
HBJBEPIO_00651 | 3.5e-149 | |||||
HBJBEPIO_00652 | 5.3e-229 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
HBJBEPIO_00653 | 2.3e-144 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
HBJBEPIO_00654 | 1.1e-80 | 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 | |
HBJBEPIO_00655 | 2.2e-50 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
HBJBEPIO_00656 | 5.9e-241 | 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 | ||
HBJBEPIO_00657 | 5.7e-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) | |
HBJBEPIO_00658 | 4e-201 | I | Diacylglycerol kinase catalytic domain | |||
HBJBEPIO_00659 | 1.4e-120 | M | Conserved repeat domain | |||
HBJBEPIO_00660 | 9.8e-256 | macB_8 | V | MacB-like periplasmic core domain | ||
HBJBEPIO_00661 | 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) | |
HBJBEPIO_00662 | 1.2e-183 | adh3 | C | Zinc-binding dehydrogenase | ||
HBJBEPIO_00663 | 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) | |
HBJBEPIO_00664 | 1.3e-226 | 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) | |
HBJBEPIO_00665 | 2.3e-89 | zur | P | Belongs to the Fur family | ||
HBJBEPIO_00666 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
HBJBEPIO_00667 | 2.5e-203 | psuK | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
HBJBEPIO_00668 | 9.1e-189 | yeiI | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
HBJBEPIO_00669 | 3.3e-129 | trpF | 5.3.1.24 | E | N-(5'phosphoribosyl)anthranilate (PRA) isomerase | |
HBJBEPIO_00670 | 5.1e-19 | 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 | ||
HBJBEPIO_00671 | 4.4e-142 | yplQ | S | Haemolysin-III related | ||
HBJBEPIO_00672 | 3.5e-280 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
HBJBEPIO_00673 | 3.5e-255 | araB | 2.7.1.16, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
HBJBEPIO_00674 | 4e-195 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_00675 | 8.7e-218 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
HBJBEPIO_00676 | 1.1e-245 | L | DNA helicase | |||
HBJBEPIO_00677 | 2.7e-88 | sixA | 3.6.1.55 | T | Phosphoglycerate mutase family | |
HBJBEPIO_00678 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
HBJBEPIO_00679 | 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 | ||
HBJBEPIO_00680 | 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 | ||
HBJBEPIO_00681 | 1.7e-63 | I | Sterol carrier protein | |||
HBJBEPIO_00682 | 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 |
HBJBEPIO_00683 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
HBJBEPIO_00684 | 9.8e-68 | S | Fibronectin type 3 domain | |||
HBJBEPIO_00685 | 4.1e-23 | S | Fibronectin type 3 domain | |||
HBJBEPIO_00686 | 7.9e-52 | S | Fibronectin type 3 domain | |||
HBJBEPIO_00687 | 5.4e-133 | |||||
HBJBEPIO_00688 | 1.5e-92 | mntP | P | Probably functions as a manganese efflux pump | ||
HBJBEPIO_00689 | 3.4e-91 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
HBJBEPIO_00690 | 5.1e-151 | S | Fibronectin type 3 domain | |||
HBJBEPIO_00691 | 3.5e-266 | KLT | Protein tyrosine kinase | |||
HBJBEPIO_00692 | 3.5e-69 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
HBJBEPIO_00693 | 1.4e-196 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
HBJBEPIO_00694 | 7.5e-125 | U | Belongs to the binding-protein-dependent transport system permease family | |||
HBJBEPIO_00695 | 2.7e-219 | livK | E | Receptor family ligand binding region | ||
HBJBEPIO_00696 | 5e-50 | 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 | |
HBJBEPIO_00697 | 4.9e-176 | iaaA | 3.4.19.5, 3.5.1.1 | E | Asparaginase | |
HBJBEPIO_00698 | 1e-156 | S | Patatin-like phospholipase | |||
HBJBEPIO_00699 | 9.6e-26 | K | LysR substrate binding domain protein | |||
HBJBEPIO_00700 | 3e-125 | G | Transmembrane secretion effector | |||
HBJBEPIO_00702 | 5.4e-225 | S | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_00703 | 5.1e-220 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
HBJBEPIO_00704 | 6.1e-122 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
HBJBEPIO_00705 | 1.1e-92 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
HBJBEPIO_00706 | 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 | ||
HBJBEPIO_00707 | 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 | ||
HBJBEPIO_00708 | 3.4e-25 | rpmD | J | Ribosomal protein L30p/L7e | ||
HBJBEPIO_00709 | 9.8e-74 | rplO | J | binds to the 23S rRNA | ||
HBJBEPIO_00710 | 3.5e-168 | I | alpha/beta hydrolase fold | |||
HBJBEPIO_00712 | 8e-145 | cobB2 | K | Sir2 family | ||
HBJBEPIO_00713 | 4.1e-234 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
HBJBEPIO_00714 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
HBJBEPIO_00715 | 2.6e-155 | G | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_00716 | 6.6e-157 | G | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_00717 | 1.5e-244 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
HBJBEPIO_00718 | 1.5e-230 | nagC | GK | ROK family | ||
HBJBEPIO_00719 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
HBJBEPIO_00720 | 8.9e-206 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_00721 | 3.3e-67 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
HBJBEPIO_00722 | 6.8e-144 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
HBJBEPIO_00723 | 1.9e-93 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
HBJBEPIO_00724 | 9.8e-222 | S | PGAP1-like protein | |||
HBJBEPIO_00725 | 3.5e-132 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
HBJBEPIO_00726 | 6.9e-239 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
HBJBEPIO_00727 | 7.1e-33 | 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 | ||
HBJBEPIO_00728 | 1.6e-48 | 3.2.1.23 | G | Domain of unknown function (DUF4982) | ||
HBJBEPIO_00729 | 1.1e-129 | 3.2.1.23 | G | Domain of unknown function (DUF4982) | ||
HBJBEPIO_00730 | 2.1e-14 | 3.2.1.23 | G | Domain of unknown function (DUF4982) | ||
HBJBEPIO_00731 | 3.2e-63 | |||||
HBJBEPIO_00732 | 9.7e-129 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N terminal domain | |
HBJBEPIO_00733 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
HBJBEPIO_00734 | 1.1e-13 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
HBJBEPIO_00735 | 1.6e-157 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
HBJBEPIO_00736 | 7.9e-48 | 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 | |
HBJBEPIO_00737 | 6e-60 | 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 | |
HBJBEPIO_00738 | 2.5e-260 | V | Domain of unknown function (DUF3427) | |||
HBJBEPIO_00739 | 1.5e-76 | |||||
HBJBEPIO_00740 | 2.5e-166 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
HBJBEPIO_00741 | 5.5e-30 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HBJBEPIO_00742 | 1e-136 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HBJBEPIO_00743 | 2.9e-14 | D | FtsK/SpoIIIE family | |||
HBJBEPIO_00744 | 6.7e-49 | D | FtsK/SpoIIIE family | |||
HBJBEPIO_00745 | 6.9e-170 | K | Cell envelope-related transcriptional attenuator domain | |||
HBJBEPIO_00746 | 0.0 | pepD | E | Peptidase family C69 | ||
HBJBEPIO_00747 | 1.2e-57 | S | Phosphatidylethanolamine-binding protein | |||
HBJBEPIO_00748 | 1.9e-146 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
HBJBEPIO_00749 | 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 | ||
HBJBEPIO_00750 | 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 | |
HBJBEPIO_00751 | 1.8e-206 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
HBJBEPIO_00752 | 3.4e-108 | 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) | |
HBJBEPIO_00753 | 1.4e-103 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
HBJBEPIO_00754 | 2.8e-182 | S | IMP dehydrogenase activity | |||
HBJBEPIO_00755 | 3.8e-218 | ybiT | S | ABC transporter | ||
HBJBEPIO_00756 | 3.5e-269 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
HBJBEPIO_00757 | 1.4e-11 | S | Protein of unknown function, DUF624 | |||
HBJBEPIO_00758 | 9.9e-17 | 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) | |
HBJBEPIO_00759 | 2.7e-171 | 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) | |
HBJBEPIO_00760 | 1.5e-123 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
HBJBEPIO_00761 | 2.4e-172 | |||||
HBJBEPIO_00762 | 1.3e-92 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
HBJBEPIO_00763 | 1.2e-08 | comE | S | Competence protein | ||
HBJBEPIO_00764 | 6.7e-72 | K | MerR family regulatory protein | |||
HBJBEPIO_00765 | 1.2e-209 | KLT | Protein tyrosine kinase | |||
HBJBEPIO_00766 | 1.4e-149 | O | Thioredoxin | |||
HBJBEPIO_00767 | 1.1e-135 | arc | O | AAA ATPase forming ring-shaped complexes | ||
HBJBEPIO_00768 | 1.7e-301 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
HBJBEPIO_00769 | 1.4e-27 | malG | G | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_00770 | 6.2e-244 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_00771 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
HBJBEPIO_00772 | 2.9e-58 | 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 | ||
HBJBEPIO_00773 | 1.1e-258 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
HBJBEPIO_00774 | 5.5e-29 | rpmB | J | Ribosomal L28 family | ||
HBJBEPIO_00775 | 1.4e-28 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
HBJBEPIO_00776 | 1.3e-237 | S | AI-2E family transporter | |||
HBJBEPIO_00777 | 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 | |
HBJBEPIO_00778 | 8.4e-16 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
HBJBEPIO_00779 | 1.5e-73 | 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 | |
HBJBEPIO_00780 | 2.7e-134 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
HBJBEPIO_00781 | 1.1e-189 | 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 | ||
HBJBEPIO_00782 | 7e-133 | S | Protein of unknown function (DUF3159) | |||
HBJBEPIO_00783 | 4.5e-241 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HBJBEPIO_00784 | 8.4e-276 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
HBJBEPIO_00785 | 2.1e-51 | S | Protein of unknown function (DUF2469) | |||
HBJBEPIO_00786 | 2e-205 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
HBJBEPIO_00787 | 2.5e-189 | pilM | NU | Type IV pilus assembly protein PilM; | ||
HBJBEPIO_00788 | 3.4e-149 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
HBJBEPIO_00789 | 5.5e-35 | |||||
HBJBEPIO_00790 | 1.7e-22 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HBJBEPIO_00791 | 5.2e-113 | yceD | S | Uncharacterized ACR, COG1399 | ||
HBJBEPIO_00792 | 2.5e-133 | |||||
HBJBEPIO_00793 | 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 | |
HBJBEPIO_00794 | 9.1e-155 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
HBJBEPIO_00795 | 6.7e-178 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
HBJBEPIO_00796 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
HBJBEPIO_00797 | 1.6e-131 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
HBJBEPIO_00798 | 5.9e-111 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
HBJBEPIO_00799 | 3.1e-297 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
HBJBEPIO_00800 | 5.5e-29 | 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 | |
HBJBEPIO_00801 | 6.2e-41 | |||||
HBJBEPIO_00802 | 9.6e-217 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
HBJBEPIO_00803 | 4.4e-66 | rapZ | S | Displays ATPase and GTPase activities | ||
HBJBEPIO_00804 | 7.1e-183 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
HBJBEPIO_00805 | 3.8e-84 | 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 | ||
HBJBEPIO_00806 | 1.8e-121 | |||||
HBJBEPIO_00807 | 9.3e-74 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
HBJBEPIO_00808 | 5.4e-52 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
HBJBEPIO_00809 | 1.9e-50 | mltE2 | M | Bacteriophage peptidoglycan hydrolase | ||
HBJBEPIO_00810 | 1e-165 | 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 | |
HBJBEPIO_00811 | 6.7e-30 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
HBJBEPIO_00812 | 2.2e-18 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
HBJBEPIO_00813 | 1.1e-63 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HBJBEPIO_00814 | 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 | ||
HBJBEPIO_00815 | 2.3e-105 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
HBJBEPIO_00816 | 1.3e-166 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HBJBEPIO_00817 | 3.4e-94 | ftsE | D | Cell division ATP-binding protein FtsE | ||
HBJBEPIO_00818 | 8.6e-137 | S | Putative ABC-transporter type IV | |||
HBJBEPIO_00819 | 3.7e-93 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HBJBEPIO_00820 | 3e-119 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
HBJBEPIO_00821 | 7.6e-199 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HBJBEPIO_00822 | 9.1e-155 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
HBJBEPIO_00823 | 0.0 | yrhL | I | Psort location CytoplasmicMembrane, score 9.99 | ||
HBJBEPIO_00824 | 7.6e-27 | M | Bacterial capsule synthesis protein PGA_cap | |||
HBJBEPIO_00825 | 4.4e-223 | 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 | |
HBJBEPIO_00827 | 1.7e-297 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
HBJBEPIO_00828 | 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 | |||
HBJBEPIO_00829 | 4.1e-233 | 3.2.1.156 | GH8 | G | CBM9 module, glycoside hydrolase family 8 protein and carbohydrate esterase family 4 protein K01238 | |
HBJBEPIO_00830 | 0.0 | G | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_00831 | 2.4e-198 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
HBJBEPIO_00832 | 2.3e-31 | S | Uncharacterized conserved protein (DUF2183) | |||
HBJBEPIO_00833 | 1e-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 | ||
HBJBEPIO_00834 | 1.9e-208 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
HBJBEPIO_00835 | 1.7e-17 | G | Major facilitator Superfamily | |||
HBJBEPIO_00836 | 8.3e-241 | vex3 | V | ABC transporter permease | ||
HBJBEPIO_00837 | 6.1e-29 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
HBJBEPIO_00838 | 5.6e-56 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
HBJBEPIO_00839 | 4.7e-58 | yccF | S | Inner membrane component domain | ||
HBJBEPIO_00840 | 1.5e-25 | S | COG NOG10880 non supervised orthologous group | |||
HBJBEPIO_00841 | 2e-103 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
HBJBEPIO_00842 | 9.5e-233 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HBJBEPIO_00843 | 3.6e-171 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
HBJBEPIO_00844 | 2.8e-34 | |||||
HBJBEPIO_00845 | 5.7e-136 | 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 | |
HBJBEPIO_00846 | 4.2e-89 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
HBJBEPIO_00847 | 2e-112 | sucC | 6.2.1.5 | F | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
HBJBEPIO_00848 | 2.6e-161 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
HBJBEPIO_00849 | 2e-144 | L | Tetratricopeptide repeat | |||
HBJBEPIO_00850 | 2.9e-27 | helY | L | DEAD DEAH box helicase | ||
HBJBEPIO_00851 | 3.9e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
HBJBEPIO_00852 | 3e-141 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
HBJBEPIO_00853 | 4.6e-61 | |||||
HBJBEPIO_00854 | 6.7e-248 | S | zinc finger | |||
HBJBEPIO_00855 | 4.9e-70 | S | Bacterial PH domain | |||
HBJBEPIO_00856 | 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 |
HBJBEPIO_00858 | 2.9e-273 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HBJBEPIO_00859 | 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) | |
HBJBEPIO_00860 | 6.2e-42 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HBJBEPIO_00861 | 1.7e-136 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_00862 | 2.6e-214 | araJ | EGP | Major facilitator Superfamily | ||
HBJBEPIO_00864 | 1.9e-108 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HBJBEPIO_00865 | 2e-62 | argE | E | Peptidase dimerisation domain | ||
HBJBEPIO_00866 | 3.6e-93 | S | Protein of unknown function (DUF3043) | |||
HBJBEPIO_00867 | 8e-53 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HBJBEPIO_00868 | 1.1e-18 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
HBJBEPIO_00869 | 1.4e-74 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
HBJBEPIO_00870 | 3.3e-52 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HBJBEPIO_00871 | 6.2e-23 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HBJBEPIO_00872 | 2.3e-156 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HBJBEPIO_00873 | 4.7e-210 | S | Amidohydrolase family | |||
HBJBEPIO_00874 | 7.9e-174 | phoH | T | PhoH-like protein | ||
HBJBEPIO_00875 | 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 | |
HBJBEPIO_00876 | 1.2e-28 | S | Putative phage holin Dp-1 | |||
HBJBEPIO_00877 | 3.6e-84 | 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 | |
HBJBEPIO_00878 | 9.8e-162 | pip | S | YhgE Pip domain protein | ||
HBJBEPIO_00879 | 1.2e-169 | yddG | EG | EamA-like transporter family | ||
HBJBEPIO_00880 | 1.4e-44 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
HBJBEPIO_00881 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HBJBEPIO_00882 | 5.8e-160 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
HBJBEPIO_00883 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
HBJBEPIO_00884 | 9.1e-102 | G | Glycosyl hydrolase family 20, domain 2 | |||
HBJBEPIO_00885 | 5.8e-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 | |
HBJBEPIO_00886 | 2.3e-235 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
HBJBEPIO_00887 | 6.1e-188 | lacR | K | Transcriptional regulator, LacI family | ||
HBJBEPIO_00888 | 0.0 | T | Diguanylate cyclase, GGDEF domain | |||
HBJBEPIO_00889 | 2.9e-251 | 3.2.1.14 | GH18 | S | Carbohydrate binding domain | |
HBJBEPIO_00890 | 0.0 | M | probably involved in cell wall | |||
HBJBEPIO_00891 | 1.1e-141 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_00892 | 5e-132 | O | Thioredoxin | |||
HBJBEPIO_00894 | 1.8e-31 | S | G5 | |||
HBJBEPIO_00895 | 1.4e-37 | S | G5 | |||
HBJBEPIO_00896 | 1.3e-46 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
HBJBEPIO_00897 | 2.1e-65 | 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) | |
HBJBEPIO_00898 | 1.8e-251 | yhjE | EGP | Sugar (and other) transporter | ||
HBJBEPIO_00899 | 1.5e-55 | 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 | |
HBJBEPIO_00900 | 1.7e-119 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
HBJBEPIO_00901 | 3.9e-156 | hgdC | I | BadF/BadG/BcrA/BcrD ATPase family | ||
HBJBEPIO_00902 | 4.6e-152 | 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 | |
HBJBEPIO_00903 | 2.7e-82 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HBJBEPIO_00904 | 7.2e-189 | K | Bacterial regulatory proteins, lacI family | |||
HBJBEPIO_00905 | 9.9e-42 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Belongs to the glycosyl hydrolase 43 family | |
HBJBEPIO_00906 | 1.4e-231 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Belongs to the glycosyl hydrolase 43 family | |
HBJBEPIO_00907 | 2.7e-64 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
HBJBEPIO_00908 | 2e-211 | 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 | ||
HBJBEPIO_00909 | 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 | |
HBJBEPIO_00910 | 3.2e-210 | tcsS2 | T | Histidine kinase | ||
HBJBEPIO_00911 | 1.9e-130 | K | helix_turn_helix, Lux Regulon | |||
HBJBEPIO_00912 | 4.9e-184 | S | alpha beta | |||
HBJBEPIO_00913 | 1.3e-25 | yhjX | EGP | Major facilitator Superfamily | ||
HBJBEPIO_00914 | 2.5e-35 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_00915 | 4.8e-258 | ecfA | GP | ABC transporter, ATP-binding protein | ||
HBJBEPIO_00916 | 1.1e-09 | hutI | Q | Amidohydrolase family | ||
HBJBEPIO_00917 | 2.4e-47 | yhbY | J | CRS1_YhbY | ||
HBJBEPIO_00918 | 1.7e-271 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
HBJBEPIO_00919 | 2.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HBJBEPIO_00920 | 2.6e-39 | rpmA | J | Ribosomal L27 protein | ||
HBJBEPIO_00921 | 2.3e-284 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
HBJBEPIO_00922 | 3.6e-67 | rafG | G | ABC transporter permease | ||
HBJBEPIO_00923 | 8.2e-154 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_00924 | 2.8e-213 | dapC | E | Aminotransferase class I and II | ||
HBJBEPIO_00925 | 7e-45 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
HBJBEPIO_00926 | 5.4e-108 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_00927 | 1.1e-74 | |||||
HBJBEPIO_00929 | 1.4e-115 | 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 | |
HBJBEPIO_00930 | 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 | |
HBJBEPIO_00931 | 7.8e-149 | S | Tetratricopeptide repeat | |||
HBJBEPIO_00932 | 4.2e-161 | 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 | ||
HBJBEPIO_00933 | 1e-204 | 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 | |
HBJBEPIO_00934 | 6.3e-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 | ||
HBJBEPIO_00935 | 6.2e-90 | S | Protein of unknown function (DUF721) | |||
HBJBEPIO_00936 | 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 | |
HBJBEPIO_00937 | 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 | |
HBJBEPIO_00938 | 3.3e-68 | S | Transmembrane domain of unknown function (DUF3566) | |||
HBJBEPIO_00939 | 1.8e-232 | S | LPXTG-motif cell wall anchor domain protein | |||
HBJBEPIO_00940 | 3.4e-126 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
HBJBEPIO_00941 | 7.7e-149 | 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) | |
HBJBEPIO_00942 | 2.8e-118 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
HBJBEPIO_00943 | 8.7e-64 | inlJ | M | domain protein | ||
HBJBEPIO_00944 | 1.3e-108 | inlJ | M | domain protein | ||
HBJBEPIO_00945 | 9.4e-248 | cydD | V | ABC transporter transmembrane region | ||
HBJBEPIO_00946 | 0.0 | sca1 | 3.2.1.187 | GH121 | DG | Bacterial Ig-like domain (group 4) |
HBJBEPIO_00947 | 0.0 | G | Bacterial Ig-like domain (group 4) | |||
HBJBEPIO_00948 | 2.7e-52 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
HBJBEPIO_00949 | 1.6e-123 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
HBJBEPIO_00950 | 2.2e-96 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HBJBEPIO_00951 | 9.1e-144 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HBJBEPIO_00952 | 2.7e-89 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HBJBEPIO_00953 | 1.6e-141 | S | Bacterial protein of unknown function (DUF881) | |||
HBJBEPIO_00954 | 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) | |
HBJBEPIO_00955 | 3.6e-247 | |||||
HBJBEPIO_00956 | 1.7e-159 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HBJBEPIO_00957 | 3.3e-62 | rarA | L | Recombination factor protein RarA | ||
HBJBEPIO_00958 | 1.9e-47 | rarA | L | Recombination factor protein RarA | ||
HBJBEPIO_00959 | 4.2e-109 | abfA1 | 3.2.1.55 | GH51 | G | arabinose metabolic process |
HBJBEPIO_00961 | 3.3e-63 | ssb1 | L | Single-strand binding protein family | ||
HBJBEPIO_00963 | 1.3e-137 | MV | MacB-like periplasmic core domain | |||
HBJBEPIO_00964 | 1.8e-295 | 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 | ||
HBJBEPIO_00965 | 5.1e-128 | gntR | K | FCD | ||
HBJBEPIO_00966 | 9.2e-69 | yxiO | S | Vacuole effluxer Atg22 like | ||
HBJBEPIO_00967 | 5.2e-116 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
HBJBEPIO_00969 | 2e-178 | 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 | |
HBJBEPIO_00971 | 4.3e-63 | |||||
HBJBEPIO_00972 | 3.3e-96 | M | Peptidase family M23 | |||
HBJBEPIO_00973 | 1.9e-35 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
HBJBEPIO_00975 | 6.4e-96 | |||||
HBJBEPIO_00976 | 7.9e-120 | yjjK | S | ABC transporter | ||
HBJBEPIO_00977 | 4.3e-19 | 3.4.13.22 | S | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | ||
HBJBEPIO_00979 | 2.8e-91 | bcp | 1.11.1.15 | O | Redoxin | |
HBJBEPIO_00980 | 1.2e-28 | S | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_00981 | 3.7e-10 | S | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_00982 | 5.6e-115 | S | Protein of unknown function DUF262 | |||
HBJBEPIO_00983 | 9e-116 | K | helix_turn_helix, Lux Regulon | |||
HBJBEPIO_00984 | 1.5e-97 | T | Histidine kinase | |||
HBJBEPIO_00985 | 6.1e-36 | lon | T | Belongs to the peptidase S16 family | ||
HBJBEPIO_00986 | 8.3e-285 | S | Zincin-like metallopeptidase | |||
HBJBEPIO_00987 | 1.6e-282 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
HBJBEPIO_00988 | 4.2e-270 | mphA | S | Aminoglycoside phosphotransferase | ||
HBJBEPIO_00989 | 3.6e-32 | S | Protein of unknown function (DUF3107) | |||
HBJBEPIO_00990 | 1.9e-172 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
HBJBEPIO_00991 | 2.1e-117 | S | Vitamin K epoxide reductase | |||
HBJBEPIO_00992 | 7.8e-171 | 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 | |
HBJBEPIO_00993 | 3.7e-145 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HBJBEPIO_00994 | 4.3e-46 | S | Protein of unknown function (DUF3046) | |||
HBJBEPIO_00995 | 1.5e-15 | K | Helix-turn-helix XRE-family like proteins | |||
HBJBEPIO_00996 | 2e-191 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
HBJBEPIO_00997 | 3.9e-34 | K | Periplasmic binding protein-like domain | |||
HBJBEPIO_00998 | 9.2e-264 | amyE | G | Bacterial extracellular solute-binding protein | ||
HBJBEPIO_00999 | 7e-90 | amt | U | Ammonium Transporter Family | ||
HBJBEPIO_01000 | 3.6e-166 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
HBJBEPIO_01001 | 2.5e-08 | |||||
HBJBEPIO_01002 | 5.4e-36 | |||||
HBJBEPIO_01003 | 4.7e-76 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
HBJBEPIO_01004 | 9.7e-112 | K | helix_turn_helix, mercury resistance | |||
HBJBEPIO_01005 | 4.4e-55 | |||||
HBJBEPIO_01006 | 1.8e-172 | 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 | ||
HBJBEPIO_01008 | 4.7e-239 | rfbP | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
HBJBEPIO_01009 | 3e-173 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
HBJBEPIO_01010 | 1.4e-172 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
HBJBEPIO_01011 | 6.1e-134 | 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) | |
HBJBEPIO_01012 | 1.4e-181 | S | Protein of unknown function (DUF975) | |||
HBJBEPIO_01013 | 1.2e-241 | msmE | G | ABC transporter periplasmic binding protein YcjN precursor K02027 | ||
HBJBEPIO_01014 | 3.6e-31 | tcsS2 | T | Histidine kinase | ||
HBJBEPIO_01015 | 3.8e-142 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
HBJBEPIO_01016 | 1e-190 | 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 | ||
HBJBEPIO_01017 | 0.0 | murJ | KLT | MviN-like protein | ||
HBJBEPIO_01018 | 2.1e-305 | murJ | KLT | MviN-like protein | ||
HBJBEPIO_01019 | 0.0 | M | Conserved repeat domain | |||
HBJBEPIO_01020 | 6.3e-122 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
HBJBEPIO_01021 | 3.8e-284 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
HBJBEPIO_01022 | 2.6e-109 | S | LytR cell envelope-related transcriptional attenuator | |||
HBJBEPIO_01023 | 1.5e-77 | 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 | |
HBJBEPIO_01027 | 2.1e-111 | yhcX | S | Acetyltransferase (GNAT) family | ||
HBJBEPIO_01028 | 2.3e-139 | S | SdpI/YhfL protein family | |||
HBJBEPIO_01029 | 2.3e-108 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
HBJBEPIO_01030 | 5.3e-100 | lytC | 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
HBJBEPIO_01031 | 3.9e-251 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
HBJBEPIO_01032 | 1.4e-158 | yegQ | O | Peptidase family U32 C-terminal domain | ||
HBJBEPIO_01033 | 2.6e-70 | yegQ | O | Peptidase family U32 C-terminal domain | ||
HBJBEPIO_01034 | 9.7e-171 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
HBJBEPIO_01035 | 9e-26 | yjeE | 2.7.1.221 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
HBJBEPIO_01036 | 1.3e-148 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
HBJBEPIO_01037 | 5.7e-21 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HBJBEPIO_01038 | 8.7e-51 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HBJBEPIO_01039 | 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 | ||
HBJBEPIO_01040 | 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 | ||
HBJBEPIO_01041 | 5.5e-68 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
HBJBEPIO_01042 | 7.1e-217 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HBJBEPIO_01043 | 2.5e-107 | |||||
HBJBEPIO_01044 | 2.3e-169 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_01045 | 1.2e-174 | 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 | |
HBJBEPIO_01046 | 2.5e-36 | |||||
HBJBEPIO_01047 | 4.2e-27 | G | Bacterial extracellular solute-binding protein | |||
HBJBEPIO_01048 | 2.2e-182 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_01049 | 6.3e-61 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
HBJBEPIO_01050 | 3.7e-143 | ybbL | V | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_01051 | 4.8e-37 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
HBJBEPIO_01052 | 1.1e-33 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
HBJBEPIO_01053 | 2.1e-256 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
HBJBEPIO_01054 | 4.8e-82 | 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) | |
HBJBEPIO_01055 | 1.3e-221 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
HBJBEPIO_01056 | 6.8e-104 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HBJBEPIO_01057 | 1.6e-142 | 4.2.1.53 | S | MCRA family | ||
HBJBEPIO_01058 | 4.6e-150 | 4.2.1.53 | S | MCRA family | ||
HBJBEPIO_01059 | 1.7e-78 | araJ | EGP | Major facilitator Superfamily | ||
HBJBEPIO_01060 | 4.3e-53 | S | Domain of unknown function (DUF4037) | |||
HBJBEPIO_01061 | 1.1e-62 | S | Domain of unknown function (DUF4037) | |||
HBJBEPIO_01062 | 7.8e-302 | E | ABC transporter, substrate-binding protein, family 5 | |||
HBJBEPIO_01063 | 1.8e-50 | yajC | U | Preprotein translocase subunit | ||
HBJBEPIO_01064 | 2.1e-157 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
HBJBEPIO_01065 | 1.9e-141 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
HBJBEPIO_01066 | 1.5e-60 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
HBJBEPIO_01067 | 5.4e-121 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
HBJBEPIO_01068 | 3.8e-91 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HBJBEPIO_01069 | 6e-143 | S | Domain of unknown function (DUF4191) | |||
HBJBEPIO_01070 | 9.4e-61 | ung2 | 3.2.2.27 | L | Uracil DNA glycosylase superfamily | |
HBJBEPIO_01071 | 4e-42 | V | DNA modification | |||
HBJBEPIO_01072 | 1.2e-88 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HBJBEPIO_01073 | 6.8e-270 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 C-terminal domain | |
HBJBEPIO_01074 | 9.3e-250 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
HBJBEPIO_01075 | 3.8e-57 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
HBJBEPIO_01076 | 3.7e-69 | 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 | |
HBJBEPIO_01077 | 1.6e-123 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
HBJBEPIO_01078 | 4.8e-62 | arc | O | AAA ATPase forming ring-shaped complexes | ||
HBJBEPIO_01079 | 7.4e-27 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HBJBEPIO_01080 | 4.2e-09 | M | Protein of unknown function (DUF3152) | |||
HBJBEPIO_01081 | 3.3e-54 | M | Protein of unknown function (DUF3152) | |||
HBJBEPIO_01082 | 8.5e-50 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HBJBEPIO_01083 | 6.1e-55 | G | ABC transporter permease | |||
HBJBEPIO_01084 | 6e-149 | G | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01085 | 3.1e-163 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
HBJBEPIO_01086 | 2.6e-73 | S | Glycosyltransferase, group 2 family protein | |||
HBJBEPIO_01087 | 3.1e-36 | 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 | |
HBJBEPIO_01088 | 3.5e-230 | L | DEAD DEAH box helicase | |||
HBJBEPIO_01089 | 1.1e-79 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
HBJBEPIO_01090 | 2.1e-136 | 3.6.3.3, 3.6.3.5, 3.6.3.54 | P | Heavy metal translocating P-type atpase | ||
HBJBEPIO_01091 | 6.9e-203 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HBJBEPIO_01092 | 6.4e-122 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HBJBEPIO_01093 | 4.2e-08 | DZ | Regulator of chromosome condensation (RCC1) repeat | |||
HBJBEPIO_01094 | 6.7e-41 | P | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01095 | 9.5e-230 | M | Protein of unknown function (DUF2961) | |||
HBJBEPIO_01096 | 3.4e-37 | znuB | U | ABC 3 transport family | ||
HBJBEPIO_01097 | 2e-160 | znuC | P | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_01098 | 2.5e-253 | 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 | ||
HBJBEPIO_01099 | 8e-44 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HBJBEPIO_01100 | 1.3e-51 | 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 | |
HBJBEPIO_01101 | 1.1e-79 | 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 | |
HBJBEPIO_01102 | 3.9e-49 | natB | E | Receptor family ligand binding region | ||
HBJBEPIO_01103 | 1.8e-63 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HBJBEPIO_01104 | 1.7e-14 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
HBJBEPIO_01105 | 3.8e-96 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
HBJBEPIO_01106 | 4.7e-296 | clcA | P | Voltage gated chloride channel | ||
HBJBEPIO_01107 | 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 | |
HBJBEPIO_01108 | 1.6e-205 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
HBJBEPIO_01109 | 0.0 | pip | S | YhgE Pip domain protein | ||
HBJBEPIO_01110 | 6.3e-93 | pip | S | YhgE Pip domain protein | ||
HBJBEPIO_01111 | 6.2e-34 | pip | S | YhgE Pip domain protein | ||
HBJBEPIO_01112 | 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 | |
HBJBEPIO_01113 | 8e-83 | thiF | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
HBJBEPIO_01114 | 3.8e-26 | thiS | 2.8.1.10 | H | ThiS family | |
HBJBEPIO_01115 | 2.3e-102 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HBJBEPIO_01116 | 3.1e-139 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HBJBEPIO_01117 | 2.3e-37 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
HBJBEPIO_01118 | 1.6e-147 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HBJBEPIO_01119 | 3.6e-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 | ||
HBJBEPIO_01120 | 1.8e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
HBJBEPIO_01121 | 3.9e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HBJBEPIO_01122 | 2e-178 | S | Endonuclease/Exonuclease/phosphatase family | |||
HBJBEPIO_01123 | 2.7e-270 | 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 | |
HBJBEPIO_01124 | 9.6e-300 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HBJBEPIO_01125 | 1.6e-151 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
HBJBEPIO_01126 | 7.9e-82 | yjjK | S | ABC transporter | ||
HBJBEPIO_01128 | 7.5e-31 | S | zinc-ribbon domain | |||
HBJBEPIO_01129 | 8.3e-69 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HBJBEPIO_01130 | 1.7e-49 | S | MobA/MobL family | |||
HBJBEPIO_01132 | 4.4e-57 | L | Psort location Cytoplasmic, score 8.96 | |||
HBJBEPIO_01134 | 2.5e-55 | S | MobA/MobL family | |||
HBJBEPIO_01138 | 2.5e-60 | L | Initiator Replication protein | |||
HBJBEPIO_01140 | 2.3e-107 | K | Bacterial regulatory proteins, tetR family | |||
HBJBEPIO_01141 | 1.7e-89 | S | Beta-L-arabinofuranosidase, GH127 | |||
HBJBEPIO_01142 | 8.5e-101 | S | Protein of unknown function, DUF624 | |||
HBJBEPIO_01143 | 1.8e-72 | Z012_06715 | V | FtsX-like permease family | ||
HBJBEPIO_01144 | 2.6e-149 | macB | V | ABC transporter, ATP-binding protein | ||
HBJBEPIO_01145 | 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 | |
HBJBEPIO_01146 | 6.3e-82 | 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 | |
HBJBEPIO_01147 | 5.7e-92 | ilvN | 2.2.1.6 | E | ACT domain | |
HBJBEPIO_01148 | 1.5e-205 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
HBJBEPIO_01149 | 1.2e-40 | yggT | S | YGGT family | ||
HBJBEPIO_01150 | 1.2e-14 | 3.1.21.3 | V | DivIVA protein | ||
HBJBEPIO_01151 | 8.7e-93 | U | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01152 | 1.1e-140 | U | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01153 | 1.2e-255 | codA | 3.5.4.1, 3.5.4.21 | F | Amidohydrolase family | |
HBJBEPIO_01154 | 2e-52 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
HBJBEPIO_01155 | 1.8e-198 | trmI | 2.1.1.219, 2.1.1.220 | J | Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA | |
HBJBEPIO_01156 | 2.5e-112 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
HBJBEPIO_01157 | 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 | |
HBJBEPIO_01158 | 4.7e-183 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
HBJBEPIO_01159 | 6.9e-190 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HBJBEPIO_01160 | 2.1e-48 | 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 | |
HBJBEPIO_01161 | 1.6e-27 | |||||
HBJBEPIO_01162 | 3.3e-125 | S | Metal-independent alpha-mannosidase (GH125) | |||
HBJBEPIO_01163 | 1.7e-27 | S | Metal-independent alpha-mannosidase (GH125) | |||
HBJBEPIO_01164 | 1.1e-164 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
HBJBEPIO_01165 | 1.7e-218 | GK | ROK family | |||
HBJBEPIO_01166 | 6.1e-307 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
HBJBEPIO_01167 | 1.6e-186 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01168 | 1.8e-191 | dppC | EP | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01169 | 0.0 | P | Belongs to the ABC transporter superfamily | |||
HBJBEPIO_01170 | 7.9e-202 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_01171 | 6.8e-91 | enhA_2 | S | L,D-transpeptidase catalytic domain | ||
HBJBEPIO_01172 | 1.4e-121 | 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 | ||
HBJBEPIO_01173 | 4e-87 | |||||
HBJBEPIO_01174 | 6.6e-79 | EP | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01175 | 1.4e-136 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
HBJBEPIO_01176 | 2e-47 | sapF | E | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_01177 | 3.9e-23 | sapF | E | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_01178 | 8e-182 | 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 | |
HBJBEPIO_01179 | 1.3e-82 | argR | K | Regulates arginine biosynthesis genes | ||
HBJBEPIO_01180 | 4e-13 | S | Domain of unknown function (DUF4143) | |||
HBJBEPIO_01181 | 1.4e-121 | yorS | 3.1.3.5 | S | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | |
HBJBEPIO_01182 | 7e-286 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
HBJBEPIO_01183 | 1.9e-19 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HBJBEPIO_01184 | 4.8e-79 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HBJBEPIO_01185 | 5.1e-65 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HBJBEPIO_01186 | 1.7e-201 | 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) | |
HBJBEPIO_01187 | 1.3e-121 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
HBJBEPIO_01189 | 9.1e-74 | K | Acetyltransferase (GNAT) domain | |||
HBJBEPIO_01190 | 8.5e-78 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
HBJBEPIO_01191 | 3.4e-40 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
HBJBEPIO_01192 | 2.1e-25 | rpmI | J | Ribosomal protein L35 | ||
HBJBEPIO_01193 | 2.1e-61 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
HBJBEPIO_01194 | 3.1e-53 | yicC | S | Psort location Cytoplasmic, score | ||
HBJBEPIO_01195 | 1.5e-32 | ecfA | GP | ABC transporter, ATP-binding protein | ||
HBJBEPIO_01196 | 6.1e-109 | 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 | ||
HBJBEPIO_01197 | 5.3e-98 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
HBJBEPIO_01198 | 4.5e-18 | |||||
HBJBEPIO_01200 | 1.5e-17 | L | HNH endonuclease | |||
HBJBEPIO_01201 | 1.6e-134 | tnp3512a | L | Transposase | ||
HBJBEPIO_01202 | 5.1e-187 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HBJBEPIO_01203 | 1.8e-10 | L | Transposase, Mutator family | |||
HBJBEPIO_01204 | 2.1e-117 | 3.6.4.12 | K | Putative DNA-binding domain | ||
HBJBEPIO_01205 | 1.8e-14 | S | Uncharacterised protein family (UPF0182) | |||
HBJBEPIO_01206 | 8e-99 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
HBJBEPIO_01207 | 7.4e-39 | 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 | ||
HBJBEPIO_01208 | 1.6e-132 | corC | S | CBS domain | ||
HBJBEPIO_01209 | 1.7e-38 | ptsH | G | PTS HPr component phosphorylation site | ||
HBJBEPIO_01210 | 5.3e-119 | 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) | |
HBJBEPIO_01211 | 7.4e-208 | scrT | G | Transporter major facilitator family protein | ||
HBJBEPIO_01212 | 1e-63 | K | helix_turn_helix, Lux Regulon | |||
HBJBEPIO_01213 | 1.2e-112 | S | Protein of unknown function DUF262 | |||
HBJBEPIO_01214 | 0.0 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
HBJBEPIO_01215 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
HBJBEPIO_01216 | 0.0 | S | L,D-transpeptidase catalytic domain | |||
HBJBEPIO_01217 | 4.6e-73 | V | Protein of unknown function DUF262 | |||
HBJBEPIO_01218 | 6.6e-137 | tdh | 1.1.1.14 | C | Zinc-binding dehydrogenase | |
HBJBEPIO_01219 | 1.6e-70 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HBJBEPIO_01220 | 5.7e-255 | codA | 3.5.4.1, 3.5.4.21 | F | Amidohydrolase family | |
HBJBEPIO_01221 | 3.9e-260 | comE | S | Competence protein | ||
HBJBEPIO_01223 | 4.3e-194 | 1.13.11.79 | C | Psort location Cytoplasmic, score 8.87 | ||
HBJBEPIO_01224 | 3.2e-211 | S | Polysaccharide pyruvyl transferase | |||
HBJBEPIO_01225 | 2.4e-98 | H | Hexapeptide repeat of succinyl-transferase | |||
HBJBEPIO_01226 | 9.5e-197 | S | Glycosyltransferase like family 2 | |||
HBJBEPIO_01227 | 6.3e-252 | cps2J | S | Polysaccharide biosynthesis protein | ||
HBJBEPIO_01228 | 1.7e-243 | MA20_17390 | GT4 | M | Glycosyl transferases group 1 | |
HBJBEPIO_01229 | 1.9e-203 | GT4 | M | Psort location Cytoplasmic, score 8.87 | ||
HBJBEPIO_01230 | 1.1e-77 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
HBJBEPIO_01232 | 1.5e-33 | ribD | 1.1.1.193, 3.5.4.26 | H | Cytidine and deoxycytidylate deaminase zinc-binding region | |
HBJBEPIO_01233 | 3.2e-101 | N | Glycosyl hydrolases family 43 | |||
HBJBEPIO_01234 | 7.6e-249 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
HBJBEPIO_01235 | 3.3e-129 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
HBJBEPIO_01236 | 2.2e-117 | corA | P | CorA-like Mg2+ transporter protein | ||
HBJBEPIO_01237 | 6.8e-10 | ppdK | 2.7.9.1 | G | Pyruvate phosphate dikinase, PEP/pyruvate binding domain | |
HBJBEPIO_01238 | 2.2e-41 | hsdR | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
HBJBEPIO_01239 | 1.3e-159 | E | Aminotransferase class I and II | |||
HBJBEPIO_01240 | 8e-85 | bioM | P | ATPases associated with a variety of cellular activities | ||
HBJBEPIO_01241 | 2.1e-266 | trkB | P | Cation transport protein | ||
HBJBEPIO_01242 | 1.3e-149 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
HBJBEPIO_01243 | 1.3e-66 | 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 | |
HBJBEPIO_01244 | 3.9e-91 | |||||
HBJBEPIO_01245 | 2.3e-223 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
HBJBEPIO_01246 | 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) | |
HBJBEPIO_01248 | 5.5e-141 | cpaE | D | bacterial-type flagellum organization | ||
HBJBEPIO_01249 | 2.7e-185 | cpaF | U | Type II IV secretion system protein | ||
HBJBEPIO_01250 | 1.5e-124 | U | Type ii secretion system | |||
HBJBEPIO_01251 | 8.5e-135 | 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 | ||
HBJBEPIO_01253 | 1.7e-232 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_01254 | 1.2e-175 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HBJBEPIO_01255 | 2e-269 | KLT | Domain of unknown function (DUF4032) | |||
HBJBEPIO_01256 | 1.6e-210 | ugpC | E | Belongs to the ABC transporter superfamily | ||
HBJBEPIO_01257 | 2.8e-131 | K | LytTr DNA-binding domain | |||
HBJBEPIO_01258 | 1.7e-231 | T | GHKL domain | |||
HBJBEPIO_01259 | 6.5e-37 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_01260 | 1.2e-35 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_01261 | 3.2e-38 | G | beta-mannosidase | |||
HBJBEPIO_01262 | 3.5e-153 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
HBJBEPIO_01263 | 4.1e-98 | V | Abi-like protein | |||
HBJBEPIO_01264 | 4e-153 | scrT | G | Transporter major facilitator family protein | ||
HBJBEPIO_01265 | 2.6e-225 | 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 | |
HBJBEPIO_01266 | 2.3e-93 | G | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01267 | 7.7e-230 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
HBJBEPIO_01268 | 4.1e-141 | 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 | |||
HBJBEPIO_01269 | 6.4e-15 | yoaK | S | Protein of unknown function (DUF1275) | ||
HBJBEPIO_01270 | 2.3e-74 | 3.2.1.97 | GH101 | G | Glycosyl hydrolase 101 beta sandwich domain | |
HBJBEPIO_01271 | 3.4e-39 | |||||
HBJBEPIO_01272 | 5.4e-48 | S | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_01273 | 1.1e-101 | T | Forkhead associated domain | |||
HBJBEPIO_01274 | 4e-32 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HBJBEPIO_01275 | 1.1e-23 | 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 | |
HBJBEPIO_01276 | 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 | |
HBJBEPIO_01277 | 5e-216 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
HBJBEPIO_01278 | 1e-240 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
HBJBEPIO_01279 | 3.4e-33 | S | Uncharacterised protein family (UPF0182) | |||
HBJBEPIO_01280 | 1.7e-263 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
HBJBEPIO_01281 | 6.3e-265 | 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) | |
HBJBEPIO_01284 | 3.6e-91 | yicL | EG | EamA-like transporter family | ||
HBJBEPIO_01285 | 6.6e-18 | yicL | EG | EamA-like transporter family | ||
HBJBEPIO_01286 | 1.5e-192 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
HBJBEPIO_01287 | 2.7e-112 | K | helix_turn_helix, Lux Regulon | |||
HBJBEPIO_01288 | 3.5e-225 | 2.7.13.3 | T | Histidine kinase | ||
HBJBEPIO_01289 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
HBJBEPIO_01290 | 1.2e-131 | fhaA | T | Protein of unknown function (DUF2662) | ||
HBJBEPIO_01291 | 5.2e-71 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
HBJBEPIO_01292 | 1.1e-83 | lacR | K | Transcriptional regulator, LacI family | ||
HBJBEPIO_01293 | 5e-24 | |||||
HBJBEPIO_01294 | 1.4e-37 | V | ABC transporter transmembrane region | |||
HBJBEPIO_01295 | 2.6e-246 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
HBJBEPIO_01296 | 2.3e-82 | metQ | P | NLPA lipoprotein | ||
HBJBEPIO_01297 | 1.1e-105 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HBJBEPIO_01298 | 9.8e-230 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_01299 | 7.8e-188 | V | Acetyltransferase (GNAT) domain | |||
HBJBEPIO_01300 | 1.9e-39 | 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 | |
HBJBEPIO_01301 | 6.4e-174 | 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 | |
HBJBEPIO_01302 | 1.4e-90 | 1.1.1.65 | C | Aldo/keto reductase family | ||
HBJBEPIO_01303 | 1.9e-57 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
HBJBEPIO_01304 | 1e-292 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
HBJBEPIO_01305 | 2.7e-255 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
HBJBEPIO_01306 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
HBJBEPIO_01307 | 1.5e-177 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
HBJBEPIO_01308 | 4.8e-117 | safC | S | O-methyltransferase | ||
HBJBEPIO_01309 | 1.5e-245 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
HBJBEPIO_01311 | 4.3e-14 | 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 | ||
HBJBEPIO_01312 | 1.6e-124 | MV | MacB-like periplasmic core domain | |||
HBJBEPIO_01313 | 1e-105 | S | Pilus assembly protein, PilO | |||
HBJBEPIO_01314 | 5.3e-96 | pilN | NU | PFAM Fimbrial assembly family protein | ||
HBJBEPIO_01315 | 4.7e-165 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HBJBEPIO_01316 | 2.9e-37 | T | GHKL domain | |||
HBJBEPIO_01318 | 1.6e-136 | gnuT | EG | GntP family permease | ||
HBJBEPIO_01319 | 3.7e-53 | G | Concanavalin A-like lectin/glucanases superfamily | |||
HBJBEPIO_01320 | 1.9e-81 | |||||
HBJBEPIO_01321 | 3.8e-66 | M | Domain of unknown function (DUF1906) | |||
HBJBEPIO_01322 | 1e-199 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HBJBEPIO_01323 | 2.6e-25 | 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 | ||
HBJBEPIO_01324 | 4.8e-93 | yraN | L | Belongs to the UPF0102 family | ||
HBJBEPIO_01325 | 3.7e-54 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
HBJBEPIO_01326 | 1.1e-25 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
HBJBEPIO_01327 | 2.6e-105 | S | CAAX protease self-immunity | |||
HBJBEPIO_01328 | 3.7e-254 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
HBJBEPIO_01329 | 4e-240 | G | Bacterial extracellular solute-binding protein | |||
HBJBEPIO_01330 | 1.3e-99 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
HBJBEPIO_01331 | 3.6e-44 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
HBJBEPIO_01332 | 4.1e-150 | 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 | |
HBJBEPIO_01333 | 1.9e-274 | srfJ1 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain |
HBJBEPIO_01334 | 3.8e-256 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
HBJBEPIO_01335 | 7.1e-92 | P | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01336 | 3.7e-117 | P | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01337 | 1e-116 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HBJBEPIO_01338 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
HBJBEPIO_01339 | 1.5e-109 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
HBJBEPIO_01340 | 2.3e-117 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
HBJBEPIO_01341 | 7.2e-34 | U | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01342 | 1.5e-116 | U | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01343 | 4.1e-40 | K | Bacterial regulatory proteins, tetR family | |||
HBJBEPIO_01344 | 2.4e-164 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
HBJBEPIO_01345 | 1.9e-104 | 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 | ||
HBJBEPIO_01346 | 8.5e-69 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
HBJBEPIO_01347 | 2.8e-125 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
HBJBEPIO_01348 | 8.7e-77 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
HBJBEPIO_01349 | 6.3e-135 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
HBJBEPIO_01350 | 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 | |
HBJBEPIO_01351 | 4.3e-89 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
HBJBEPIO_01352 | 1e-227 | aspB | E | Aminotransferase class-V | ||
HBJBEPIO_01353 | 7.3e-18 | rpsA | J | Ribosomal protein S1 | ||
HBJBEPIO_01354 | 1.9e-92 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
HBJBEPIO_01355 | 6.3e-23 | 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 | |
HBJBEPIO_01356 | 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 | |
HBJBEPIO_01357 | 7.1e-88 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
HBJBEPIO_01358 | 6.5e-169 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HBJBEPIO_01359 | 9.4e-53 | argR | K | Regulates arginine biosynthesis genes | ||
HBJBEPIO_01360 | 1.7e-210 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
HBJBEPIO_01361 | 1.8e-147 | 3.2.1.23 | G | Domain of unknown function (DUF4982) | ||
HBJBEPIO_01362 | 4.3e-45 | KT | LytTr DNA-binding domain | |||
HBJBEPIO_01363 | 2.5e-57 | T | GHKL domain | |||
HBJBEPIO_01364 | 1.9e-31 | T | GHKL domain | |||
HBJBEPIO_01365 | 4.7e-57 | T | GHKL domain | |||
HBJBEPIO_01366 | 5.9e-86 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_01367 | 7.3e-65 | I | alpha/beta hydrolase fold | |||
HBJBEPIO_01368 | 6.4e-58 | ybiR | P | Citrate transporter | ||
HBJBEPIO_01369 | 6.3e-51 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
HBJBEPIO_01370 | 5.1e-156 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HBJBEPIO_01371 | 4.5e-137 | S | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_01372 | 5.4e-25 | L | PFAM Integrase catalytic | |||
HBJBEPIO_01373 | 3.6e-282 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
HBJBEPIO_01374 | 1.7e-95 | S | Protein of unknown function, DUF624 | |||
HBJBEPIO_01375 | 6.6e-250 | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain | |
HBJBEPIO_01376 | 2.5e-207 | G | Bacterial extracellular solute-binding protein | |||
HBJBEPIO_01377 | 1.3e-157 | amyD3 | P | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01378 | 3.1e-52 | amyC5 | P | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01379 | 2.5e-33 | amyC5 | P | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01380 | 2.3e-145 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
HBJBEPIO_01381 | 2e-48 | S | Protein of unknown function DUF58 | |||
HBJBEPIO_01382 | 7e-168 | S | ATPase family associated with various cellular activities (AAA) | |||
HBJBEPIO_01383 | 5.6e-100 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase, C-terminal domain | |
HBJBEPIO_01384 | 2.8e-32 | gnuT | EG | GntP family permease | ||
HBJBEPIO_01385 | 9.6e-149 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
HBJBEPIO_01386 | 5e-158 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
HBJBEPIO_01387 | 1.1e-231 | EGP | Major Facilitator Superfamily | |||
HBJBEPIO_01388 | 8.7e-176 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
HBJBEPIO_01389 | 2.1e-94 | 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 | ||
HBJBEPIO_01390 | 2e-106 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
HBJBEPIO_01391 | 6.8e-115 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
HBJBEPIO_01392 | 1.8e-92 | amyE | G | Bacterial extracellular solute-binding protein | ||
HBJBEPIO_01393 | 1.1e-112 | |||||
HBJBEPIO_01394 | 2.7e-29 | |||||
HBJBEPIO_01395 | 2.2e-17 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HBJBEPIO_01396 | 5.1e-153 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
HBJBEPIO_01397 | 2.6e-172 | S | Bacterial protein of unknown function (DUF881) | |||
HBJBEPIO_01398 | 1.1e-104 | 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 | |
HBJBEPIO_01399 | 9.9e-68 | recN | L | May be involved in recombinational repair of damaged DNA | ||
HBJBEPIO_01400 | 4.4e-123 | S | Haloacid dehalogenase-like hydrolase | |||
HBJBEPIO_01401 | 3.4e-121 | S | ABC-2 family transporter protein | |||
HBJBEPIO_01402 | 6e-174 | V | ATPases associated with a variety of cellular activities | |||
HBJBEPIO_01403 | 1.7e-58 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
HBJBEPIO_01404 | 1.1e-23 | C | Acetamidase/Formamidase family | |||
HBJBEPIO_01405 | 6e-44 | L | transposition | |||
HBJBEPIO_01406 | 0.0 | S | Histidine phosphatase superfamily (branch 2) | |||
HBJBEPIO_01407 | 7.4e-95 | S | Pyridoxamine 5'-phosphate oxidase | |||
HBJBEPIO_01409 | 6e-38 | nrdH | O | Glutaredoxin | ||
HBJBEPIO_01410 | 1.6e-225 | S | Putative ABC-transporter type IV | |||
HBJBEPIO_01411 | 0.0 | pip | S | YhgE Pip domain protein | ||
HBJBEPIO_01412 | 2.6e-22 | pip | S | YhgE Pip domain protein | ||
HBJBEPIO_01413 | 1.6e-51 | pip | S | YhgE Pip domain protein | ||
HBJBEPIO_01414 | 3.6e-19 | pip | S | YhgE Pip domain protein | ||
HBJBEPIO_01415 | 5.1e-41 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
HBJBEPIO_01416 | 2.7e-162 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
HBJBEPIO_01417 | 1.1e-130 | S | membrane transporter protein | |||
HBJBEPIO_01418 | 1.6e-114 | insK | L | Integrase core domain | ||
HBJBEPIO_01419 | 5.8e-57 | htpX | O | Belongs to the peptidase M48B family | ||
HBJBEPIO_01420 | 5.3e-26 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
HBJBEPIO_01421 | 5.6e-33 | dnaK | O | Heat shock 70 kDa protein | ||
HBJBEPIO_01423 | 9.8e-70 | htpX | O | Belongs to the peptidase M48B family | ||
HBJBEPIO_01424 | 7.5e-166 | 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 | |
HBJBEPIO_01425 | 1.8e-152 | V | FtsX-like permease family | |||
HBJBEPIO_01426 | 1.1e-160 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
HBJBEPIO_01427 | 1.6e-32 | lacY | P | LacY proton/sugar symporter | ||
HBJBEPIO_01428 | 1.2e-22 | lacY | P | LacY proton/sugar symporter | ||
HBJBEPIO_01429 | 1.6e-140 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
HBJBEPIO_01430 | 2e-91 | S | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_01433 | 0.0 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
HBJBEPIO_01434 | 2.5e-161 | |||||
HBJBEPIO_01435 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
HBJBEPIO_01436 | 7.5e-285 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
HBJBEPIO_01437 | 3.6e-140 | 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 | ||
HBJBEPIO_01438 | 3.6e-20 | 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 | |
HBJBEPIO_01439 | 6.5e-131 | rmuC | S | RmuC family | ||
HBJBEPIO_01440 | 2.1e-21 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
HBJBEPIO_01441 | 6.3e-23 | XK27_00515 | D | Cell surface antigen C-terminus | ||
HBJBEPIO_01442 | 4e-50 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
HBJBEPIO_01443 | 4.4e-74 | yneG | S | Domain of unknown function (DUF4186) | ||
HBJBEPIO_01444 | 5.2e-220 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HBJBEPIO_01445 | 2e-184 | S | CAAX protease self-immunity | |||
HBJBEPIO_01446 | 1.1e-136 | M | Mechanosensitive ion channel | |||
HBJBEPIO_01447 | 7.7e-230 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
HBJBEPIO_01448 | 7.1e-228 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
HBJBEPIO_01449 | 5.7e-126 | K | Bacterial regulatory proteins, tetR family | |||
HBJBEPIO_01450 | 6.1e-93 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
HBJBEPIO_01451 | 4.9e-36 | cadA | P | E1-E2 ATPase | ||
HBJBEPIO_01452 | 1.3e-171 | whiA | K | May be required for sporulation | ||
HBJBEPIO_01453 | 6.2e-232 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HBJBEPIO_01454 | 5.2e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HBJBEPIO_01455 | 2.3e-116 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
HBJBEPIO_01456 | 1.4e-116 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HBJBEPIO_01457 | 6.8e-47 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
HBJBEPIO_01458 | 6.1e-154 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
HBJBEPIO_01459 | 1.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HBJBEPIO_01460 | 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 | ||
HBJBEPIO_01461 | 1e-97 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HBJBEPIO_01462 | 1.7e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HBJBEPIO_01463 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HBJBEPIO_01464 | 4.9e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HBJBEPIO_01465 | 2e-44 | S | Protein of unknown function (DUF3052) | |||
HBJBEPIO_01467 | 1.2e-45 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
HBJBEPIO_01468 | 2.1e-96 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HBJBEPIO_01469 | 4.6e-148 | S | phosphoesterase or phosphohydrolase | |||
HBJBEPIO_01470 | 1.9e-28 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
HBJBEPIO_01471 | 1.5e-60 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
HBJBEPIO_01472 | 9.8e-47 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
HBJBEPIO_01473 | 2e-53 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HBJBEPIO_01474 | 5.3e-50 | K | Helix-turn-helix XRE-family like proteins | |||
HBJBEPIO_01475 | 2.1e-74 | EGP | Major facilitator Superfamily | |||
HBJBEPIO_01476 | 1.6e-180 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
HBJBEPIO_01477 | 6.5e-45 | 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 | ||
HBJBEPIO_01478 | 3.7e-29 | terC | P | Integral membrane protein, TerC family | ||
HBJBEPIO_01479 | 2.8e-97 | terC | P | Integral membrane protein, TerC family | ||
HBJBEPIO_01481 | 4.2e-158 | adhB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
HBJBEPIO_01482 | 9.6e-40 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
HBJBEPIO_01483 | 4.2e-138 | 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 | |
HBJBEPIO_01484 | 2.3e-83 | L | Phage integrase family | |||
HBJBEPIO_01485 | 1.1e-39 | nrdH | O | Glutaredoxin | ||
HBJBEPIO_01486 | 3.3e-74 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
HBJBEPIO_01487 | 2.3e-59 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HBJBEPIO_01488 | 1.3e-187 | luxE | 6.2.1.19 | H | long-chain-fatty-acid--luciferin-component ligase, acyl-protein synthase | |
HBJBEPIO_01489 | 1.9e-216 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
HBJBEPIO_01490 | 4.1e-156 | L | PFAM Integrase catalytic | |||
HBJBEPIO_01491 | 1.6e-67 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
HBJBEPIO_01492 | 2e-156 | G | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01493 | 9.1e-168 | G | ABC transporter permease | |||
HBJBEPIO_01494 | 0.0 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_01495 | 8.9e-198 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_01496 | 5.1e-168 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HBJBEPIO_01497 | 3.2e-181 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HBJBEPIO_01498 | 1.4e-40 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HBJBEPIO_01499 | 7.9e-85 | K | helix_turn_helix, arabinose operon control protein | |||
HBJBEPIO_01500 | 4.8e-42 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HBJBEPIO_01501 | 4.1e-71 | L | Transposase IS200 like | |||
HBJBEPIO_01502 | 8.4e-14 | lhr | L | DEAD DEAH box helicase | ||
HBJBEPIO_01503 | 1.4e-76 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
HBJBEPIO_01504 | 2.6e-26 | XK27_03610 | K | Acetyltransferase (GNAT) domain | ||
HBJBEPIO_01505 | 2.7e-78 | XK27_03610 | K | Acetyltransferase (GNAT) domain | ||
HBJBEPIO_01506 | 2.4e-115 | 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) | |
HBJBEPIO_01507 | 4.9e-81 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
HBJBEPIO_01508 | 6.6e-145 | moeB | 2.7.7.80 | H | ThiF family | |
HBJBEPIO_01509 | 7e-88 | |||||
HBJBEPIO_01510 | 3.3e-107 | S | ABC-2 family transporter protein | |||
HBJBEPIO_01511 | 3.1e-26 | scrB | 3.2.1.26, 3.2.1.97 | GH101,GH32 | N | Glycosyl hydrolases family 43 |
HBJBEPIO_01512 | 1.7e-50 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
HBJBEPIO_01513 | 1.4e-145 | vex1 | V | Efflux ABC transporter, permease protein | ||
HBJBEPIO_01514 | 1.1e-113 | vex2 | V | ABC transporter, ATP-binding protein | ||
HBJBEPIO_01515 | 2.4e-80 | ypeA | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_01516 | 2.7e-44 | ybjG | 3.6.1.27 | I | Psort location CytoplasmicMembrane, score | |
HBJBEPIO_01517 | 0.0 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
HBJBEPIO_01518 | 2.7e-73 | S | GtrA-like protein | |||
HBJBEPIO_01519 | 3.8e-179 | S | Psort location Cytoplasmic, score | |||
HBJBEPIO_01520 | 9.2e-216 | clcA_2 | P | Voltage gated chloride channel | ||
HBJBEPIO_01521 | 3.1e-30 | |||||
HBJBEPIO_01522 | 6.5e-179 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
HBJBEPIO_01523 | 2.4e-23 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
HBJBEPIO_01524 | 9.4e-172 | V | ATPases associated with a variety of cellular activities | |||
HBJBEPIO_01525 | 5.6e-170 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
HBJBEPIO_01526 | 2.9e-119 | K | Psort location Cytoplasmic, score | |||
HBJBEPIO_01527 | 1e-119 | S | Phospholipase/Carboxylesterase | |||
HBJBEPIO_01528 | 5.2e-75 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
HBJBEPIO_01529 | 2.1e-25 | V | ABC transporter, ATP-binding protein | |||
HBJBEPIO_01530 | 2.9e-110 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
HBJBEPIO_01531 | 3.4e-109 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
HBJBEPIO_01532 | 9.6e-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 | |
HBJBEPIO_01533 | 9.4e-55 | helY | L | DEAD DEAH box helicase | ||
HBJBEPIO_01534 | 2.5e-49 | helY | L | DEAD DEAH box helicase | ||
HBJBEPIO_01535 | 1.7e-125 | xylR | GK | ROK family | ||
HBJBEPIO_01537 | 1.5e-35 | rpmE | J | Binds the 23S rRNA | ||
HBJBEPIO_01538 | 2.8e-38 | 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 | |
HBJBEPIO_01539 | 1.3e-63 | 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) | |
HBJBEPIO_01540 | 1.1e-20 | |||||
HBJBEPIO_01541 | 1.6e-60 | |||||
HBJBEPIO_01542 | 7.1e-170 | cstA | T | 5TM C-terminal transporter carbon starvation CstA | ||
HBJBEPIO_01543 | 1.2e-52 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
HBJBEPIO_01544 | 1.7e-134 | azlC | E | AzlC protein | ||
HBJBEPIO_01545 | 1.1e-86 | M | Protein of unknown function (DUF3737) | |||
HBJBEPIO_01546 | 1.8e-81 | 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 | ||
HBJBEPIO_01547 | 1.3e-145 | pgl | 3.1.1.31, 3.5.99.6 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
HBJBEPIO_01548 | 2.6e-180 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
HBJBEPIO_01549 | 4.2e-135 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
HBJBEPIO_01550 | 6.3e-114 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HBJBEPIO_01551 | 1.4e-72 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
HBJBEPIO_01552 | 1.7e-20 | V | ABC-2 family transporter protein | |||
HBJBEPIO_01553 | 4.9e-134 | KT | Transcriptional regulatory protein, C terminal | |||
HBJBEPIO_01554 | 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 | |
HBJBEPIO_01555 | 1.9e-289 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
HBJBEPIO_01556 | 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 | |
HBJBEPIO_01557 | 2.8e-174 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
HBJBEPIO_01558 | 8.3e-185 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HBJBEPIO_01559 | 2.3e-44 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HBJBEPIO_01560 | 3.3e-135 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
HBJBEPIO_01561 | 1.3e-112 | |||||
HBJBEPIO_01563 | 2.3e-185 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HBJBEPIO_01564 | 1.7e-71 | |||||
HBJBEPIO_01565 | 4.2e-93 | S | Bacterial protein of unknown function (DUF881) | |||
HBJBEPIO_01566 | 2.8e-106 | murJ | KLT | MviN-like protein | ||
HBJBEPIO_01567 | 2.9e-81 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HBJBEPIO_01568 | 2.3e-84 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HBJBEPIO_01569 | 1.1e-47 | ybhL | S | Belongs to the BI1 family | ||
HBJBEPIO_01570 | 1e-78 | ydeD | EG | EamA-like transporter family | ||
HBJBEPIO_01571 | 2.9e-162 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
HBJBEPIO_01572 | 1.4e-27 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
HBJBEPIO_01573 | 1.1e-38 | |||||
HBJBEPIO_01574 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
HBJBEPIO_01575 | 3.3e-134 | yjjP | S | Threonine/Serine exporter, ThrE | ||
HBJBEPIO_01576 | 2.5e-132 | yjjP | S | Threonine/Serine exporter, ThrE | ||
HBJBEPIO_01577 | 1.2e-104 | S | Psort location Cytoplasmic, score 8.87 | |||
HBJBEPIO_01578 | 3.4e-146 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HBJBEPIO_01579 | 7.2e-11 | XK27_00500 | L | helicase | ||
HBJBEPIO_01580 | 6.8e-127 | 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 | |
HBJBEPIO_01581 | 1.7e-28 | epsG | M | Glycosyl transferase family 21 | ||
HBJBEPIO_01582 | 8.2e-97 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
HBJBEPIO_01583 | 4.2e-68 | trkB | P | Cation transport protein | ||
HBJBEPIO_01584 | 8.1e-160 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HBJBEPIO_01585 | 2.8e-24 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
HBJBEPIO_01586 | 6.5e-101 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
HBJBEPIO_01587 | 1.9e-97 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HBJBEPIO_01588 | 1.2e-45 | K | LysR substrate binding domain protein | |||
HBJBEPIO_01589 | 1.1e-32 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
HBJBEPIO_01590 | 2.6e-183 | 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 | H | Protein of unknown function (DUF4012) | ||
HBJBEPIO_01591 | 3.1e-181 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
HBJBEPIO_01592 | 8.4e-180 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
HBJBEPIO_01593 | 2.2e-91 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
HBJBEPIO_01594 | 3.1e-68 | 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 | |
HBJBEPIO_01595 | 1.7e-80 | S | Protein of unknown function (DUF3000) | |||
HBJBEPIO_01596 | 5.1e-20 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HBJBEPIO_01597 | 3.2e-46 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HBJBEPIO_01598 | 7.3e-109 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
HBJBEPIO_01599 | 5.2e-77 | |||||
HBJBEPIO_01600 | 4.5e-127 | recE | 2.7.7.7, 3.6.4.12 | L | Psort location Cytoplasmic, score | |
HBJBEPIO_01601 | 2.5e-07 | |||||
HBJBEPIO_01602 | 2.7e-180 | |||||
HBJBEPIO_01603 | 1.9e-170 | trxA2 | O | Tetratricopeptide repeat | ||
HBJBEPIO_01604 | 4.7e-122 | cyaA | 4.6.1.1 | S | CYTH | |
HBJBEPIO_01606 | 8e-64 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
HBJBEPIO_01607 | 4.8e-271 | mmuP | E | amino acid | ||
HBJBEPIO_01608 | 5e-173 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HBJBEPIO_01609 | 9.6e-39 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Glycosyl hydrolases family 43 | |
HBJBEPIO_01610 | 3e-195 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HBJBEPIO_01611 | 2.7e-120 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
HBJBEPIO_01612 | 5.9e-35 | S | Protein of unknown function (DUF2469) | |||
HBJBEPIO_01613 | 8.1e-83 | 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) | |
HBJBEPIO_01614 | 2e-18 | 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) | |
HBJBEPIO_01615 | 4.7e-118 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01616 | 2.5e-80 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
HBJBEPIO_01617 | 2.3e-66 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01618 | 9e-44 | rafG | G | ABC transporter permease | ||
HBJBEPIO_01619 | 1.1e-52 | hsdS2 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
HBJBEPIO_01620 | 1.3e-130 | S | PAC2 family | |||
HBJBEPIO_01621 | 1.6e-113 | kcsA | U | Ion channel | ||
HBJBEPIO_01622 | 4.3e-95 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
HBJBEPIO_01623 | 5.8e-29 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
HBJBEPIO_01624 | 5.9e-143 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
HBJBEPIO_01625 | 2.3e-69 | M | Domain of unknown function (DUF1906) | |||
HBJBEPIO_01626 | 1.8e-157 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HBJBEPIO_01627 | 8.1e-157 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
HBJBEPIO_01628 | 2.1e-30 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HBJBEPIO_01629 | 3e-50 | ptsP | 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) | |
HBJBEPIO_01630 | 6e-28 | ptsP | 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) | |
HBJBEPIO_01631 | 6.2e-51 | lolD | V | ABC transporter | ||
HBJBEPIO_01632 | 5.3e-63 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
HBJBEPIO_01633 | 1.4e-50 | sca1 | 3.2.1.187 | GH121 | DG | Bacterial Ig-like domain (group 4) |
HBJBEPIO_01634 | 1.9e-20 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
HBJBEPIO_01635 | 2.8e-60 | S | Tetratricopeptide repeat | |||
HBJBEPIO_01636 | 6.9e-110 | S | Tetratricopeptide repeat | |||
HBJBEPIO_01637 | 2.4e-98 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
HBJBEPIO_01638 | 2.4e-68 | 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 | ||
HBJBEPIO_01639 | 2.6e-28 | V | FtsX-like permease family | |||
HBJBEPIO_01640 | 3.5e-48 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HBJBEPIO_01641 | 5e-75 | trkA | P | TrkA-N domain | ||
HBJBEPIO_01642 | 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 | |
HBJBEPIO_01643 | 4e-182 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
HBJBEPIO_01644 | 4.2e-175 | S | Protein of unknown function DUF58 | |||
HBJBEPIO_01645 | 3.6e-91 | |||||
HBJBEPIO_01646 | 1.8e-190 | S | von Willebrand factor (vWF) type A domain | |||
HBJBEPIO_01647 | 5e-182 | S | von Willebrand factor (vWF) type A domain | |||
HBJBEPIO_01648 | 1.1e-45 | |||||
HBJBEPIO_01649 | 7.6e-147 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HBJBEPIO_01650 | 9.1e-104 | V | ABC transporter, ATP-binding protein | |||
HBJBEPIO_01651 | 2.6e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
HBJBEPIO_01652 | 5.1e-198 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_01653 | 8.9e-62 | lmrA2 | V | ABC transporter transmembrane region | ||
HBJBEPIO_01654 | 1.3e-184 | tetP | J | Elongation factor G, domain IV | ||
HBJBEPIO_01655 | 4.4e-89 | xynD3 | 3.2.1.55 | CBM6,GH43 | G | Belongs to the glycosyl hydrolase 43 family |
HBJBEPIO_01656 | 3e-166 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
HBJBEPIO_01657 | 1.3e-42 | S | Protein of unknown function (DUF4244) | |||
HBJBEPIO_01658 | 5.1e-60 | U | TadE-like protein | |||
HBJBEPIO_01659 | 1.1e-54 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
HBJBEPIO_01660 | 5.5e-214 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
HBJBEPIO_01661 | 1.6e-193 | S | Psort location CytoplasmicMembrane, score | |||
HBJBEPIO_01662 | 1.1e-96 | K | Bacterial regulatory proteins, tetR family | |||
HBJBEPIO_01663 | 7.4e-97 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
HBJBEPIO_01664 | 7.1e-189 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HBJBEPIO_01665 | 2.5e-133 | cycA | E | Amino acid permease | ||
HBJBEPIO_01666 | 5.4e-106 | tag | 3.2.2.20 | L | Methyladenine glycosylase | |
HBJBEPIO_01667 | 6.1e-170 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
HBJBEPIO_01668 | 2e-146 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HBJBEPIO_01669 | 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 | ||
HBJBEPIO_01670 | 4.4e-57 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HBJBEPIO_01671 | 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 | ||
HBJBEPIO_01672 | 3.8e-309 | 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 | |
HBJBEPIO_01673 | 1.7e-103 | P | Binding-protein-dependent transport system inner membrane component | |||
HBJBEPIO_01674 | 8.6e-165 | S | Putative esterase | |||
HBJBEPIO_01675 | 1.4e-181 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HBJBEPIO_01676 | 2.5e-70 | L | Helix-turn-helix domain | |||
HBJBEPIO_01677 | 5.1e-70 | gguB | U | Branched-chain amino acid transport system / permease component | ||
HBJBEPIO_01678 | 8.1e-41 | |||||
HBJBEPIO_01679 | 2.1e-140 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
HBJBEPIO_01680 | 4.4e-64 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HBJBEPIO_01681 | 1.2e-193 | lytC | 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
HBJBEPIO_01682 | 1.7e-257 | S | AAA domain | |||
HBJBEPIO_01683 | 1.6e-76 | |||||
HBJBEPIO_01684 | 3.1e-33 | S | enterobacterial common antigen metabolic process | |||
HBJBEPIO_01685 | 1.8e-40 | 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 | |
HBJBEPIO_01686 | 1.1e-56 | 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 | |
HBJBEPIO_01687 | 2.2e-96 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
HBJBEPIO_01688 | 2e-112 | K | Bacterial regulatory proteins, tetR family | |||
HBJBEPIO_01689 | 3.4e-79 | G | Fructosamine kinase | |||
HBJBEPIO_01690 | 5.2e-32 | G | Fructosamine kinase | |||
HBJBEPIO_01691 | 8.8e-124 | 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 | ||
HBJBEPIO_01692 | 1.9e-71 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
HBJBEPIO_01693 | 6.5e-80 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
HBJBEPIO_01694 | 1.6e-149 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
HBJBEPIO_01695 | 4.9e-202 | rodA | D | Belongs to the SEDS family | ||
HBJBEPIO_01696 | 8e-266 | pbpA | M | penicillin-binding protein | ||
HBJBEPIO_01697 | 5.8e-177 | T | Protein tyrosine kinase | |||
HBJBEPIO_01698 | 4.3e-123 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
HBJBEPIO_01699 | 9.6e-28 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
HBJBEPIO_01700 | 2.3e-92 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
HBJBEPIO_01701 | 1.7e-119 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
HBJBEPIO_01702 | 6.7e-209 | srtA | 3.4.22.70 | M | Sortase family | |
HBJBEPIO_01703 | 6.8e-142 | S | Bacterial protein of unknown function (DUF881) | |||
HBJBEPIO_01704 | 3.1e-57 | crgA | D | Involved in cell division | ||
HBJBEPIO_01705 | 1.7e-179 | L | ribosomal rna small subunit methyltransferase | |||
HBJBEPIO_01706 | 1.7e-24 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
HBJBEPIO_01707 | 5.2e-160 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HBJBEPIO_01708 | 1.4e-83 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HBJBEPIO_01709 | 0.0 | pccB | I | Carboxyl transferase domain | ||
HBJBEPIO_01710 | 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 | |
HBJBEPIO_01711 | 2.1e-79 | bioY | S | BioY family | ||
HBJBEPIO_01712 | 1.7e-72 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
HBJBEPIO_01713 | 5.1e-28 | S | Appr-1'-p processing enzyme | |||
HBJBEPIO_01714 | 7.7e-47 | S | Appr-1'-p processing enzyme | |||
HBJBEPIO_01715 | 1.1e-136 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
HBJBEPIO_01716 | 2.6e-266 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
HBJBEPIO_01717 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
HBJBEPIO_01718 | 1.4e-98 | L | Single-strand binding protein family | |||
HBJBEPIO_01719 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HBJBEPIO_01720 | 1.6e-151 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
HBJBEPIO_01721 | 2.7e-249 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
HBJBEPIO_01722 | 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 | |
HBJBEPIO_01723 | 1.2e-56 | glnP | E | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01724 | 6.7e-139 | glnQ | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
HBJBEPIO_01725 | 4.4e-144 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
HBJBEPIO_01726 | 6.8e-153 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HBJBEPIO_01727 | 1.8e-111 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01728 | 1e-199 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
HBJBEPIO_01729 | 5.8e-186 | K | helix_turn _helix lactose operon repressor | |||
HBJBEPIO_01730 | 6.2e-89 | K | UTRA domain | |||
HBJBEPIO_01731 | 1.1e-211 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
HBJBEPIO_01732 | 9.1e-36 | ulaB | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
HBJBEPIO_01733 | 1e-46 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
HBJBEPIO_01734 | 1.4e-154 | holB | 2.7.7.7 | L | DNA polymerase III | |
HBJBEPIO_01735 | 9.2e-189 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
HBJBEPIO_01736 | 5.5e-242 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
HBJBEPIO_01737 | 2.9e-298 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HBJBEPIO_01738 | 1.2e-191 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)