ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
OKHHJBLH_00001 | 1.1e-125 | 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 | |
OKHHJBLH_00002 | 1.6e-82 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
OKHHJBLH_00003 | 2.5e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
OKHHJBLH_00004 | 9e-111 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
OKHHJBLH_00005 | 4.3e-97 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
OKHHJBLH_00006 | 7.3e-71 | S | Protein of unknown function (DUF3159) | |||
OKHHJBLH_00007 | 2.6e-83 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
OKHHJBLH_00008 | 1.3e-54 | 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 | |
OKHHJBLH_00009 | 6.9e-60 | 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 | |
OKHHJBLH_00010 | 2.5e-43 | 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 | |
OKHHJBLH_00011 | 2.8e-146 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
OKHHJBLH_00013 | 5.7e-208 | K | Cell envelope-related transcriptional attenuator domain | |||
OKHHJBLH_00014 | 3.4e-54 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
OKHHJBLH_00015 | 0.0 | S | Glycosyl transferase, family 2 | |||
OKHHJBLH_00016 | 8.7e-223 | |||||
OKHHJBLH_00017 | 1.5e-71 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
OKHHJBLH_00018 | 1.1e-152 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
OKHHJBLH_00019 | 2.5e-138 | ctsW | S | Phosphoribosyl transferase domain | ||
OKHHJBLH_00020 | 3.2e-101 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
OKHHJBLH_00021 | 7.5e-56 | yccF | S | Inner membrane component domain | ||
OKHHJBLH_00022 | 0.0 | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
OKHHJBLH_00023 | 8.7e-145 | G | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00024 | 1.4e-162 | G | PFAM binding-protein-dependent transport systems inner membrane component | |||
OKHHJBLH_00025 | 6.7e-223 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_00026 | 3.3e-178 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_00027 | 8.8e-53 | K | Psort location Cytoplasmic, score | |||
OKHHJBLH_00028 | 1.1e-95 | |||||
OKHHJBLH_00029 | 4.4e-147 | M | Conserved repeat domain | |||
OKHHJBLH_00030 | 1.5e-115 | L | DNA helicase | |||
OKHHJBLH_00031 | 1.1e-119 | L | DNA helicase | |||
OKHHJBLH_00032 | 7e-92 | mraZ | K | Belongs to the MraZ family | ||
OKHHJBLH_00033 | 1.3e-190 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
OKHHJBLH_00034 | 3.9e-62 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
OKHHJBLH_00035 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
OKHHJBLH_00036 | 1.4e-153 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
OKHHJBLH_00037 | 6.4e-263 | 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 | |
OKHHJBLH_00038 | 8.8e-193 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
OKHHJBLH_00039 | 1.2e-24 | tpd | P | Fe2+ transport protein | ||
OKHHJBLH_00040 | 9.2e-293 | efeU_1 | P | Iron permease FTR1 family | ||
OKHHJBLH_00041 | 2e-237 | G | MFS/sugar transport protein | |||
OKHHJBLH_00042 | 8.9e-117 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
OKHHJBLH_00043 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
OKHHJBLH_00044 | 7.9e-285 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
OKHHJBLH_00045 | 2.4e-70 | 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 | |
OKHHJBLH_00046 | 4.4e-121 | 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 | ||
OKHHJBLH_00047 | 3.1e-83 | yraN | L | Belongs to the UPF0102 family | ||
OKHHJBLH_00048 | 3e-113 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
OKHHJBLH_00050 | 3.5e-49 | 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 | |
OKHHJBLH_00051 | 1.1e-96 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
OKHHJBLH_00052 | 1.2e-149 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
OKHHJBLH_00053 | 0.0 | G | Glycosyl hydrolase family 20, domain 2 | |||
OKHHJBLH_00054 | 3e-173 | 2.7.1.2 | GK | ROK family | ||
OKHHJBLH_00055 | 4.4e-164 | G | ABC transporter permease | |||
OKHHJBLH_00056 | 7.5e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00057 | 1.6e-241 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_00059 | 4.6e-76 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
OKHHJBLH_00060 | 6.1e-49 | S | Psort location Cytoplasmic, score | |||
OKHHJBLH_00061 | 1e-78 | |||||
OKHHJBLH_00062 | 2.2e-125 | 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 | ||
OKHHJBLH_00063 | 1.7e-70 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
OKHHJBLH_00064 | 7.4e-151 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
OKHHJBLH_00065 | 7.8e-47 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
OKHHJBLH_00066 | 6.8e-184 | 3.4.22.70 | M | Sortase family | ||
OKHHJBLH_00067 | 3.4e-85 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
OKHHJBLH_00068 | 3.6e-102 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00069 | 2.2e-145 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
OKHHJBLH_00070 | 6e-25 | 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 | |
OKHHJBLH_00071 | 1.2e-22 | lacY | P | LacY proton/sugar symporter | ||
OKHHJBLH_00072 | 1.5e-21 | lacY | P | LacY proton/sugar symporter | ||
OKHHJBLH_00073 | 1.6e-35 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
OKHHJBLH_00074 | 1.2e-36 | |||||
OKHHJBLH_00075 | 2.3e-28 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
OKHHJBLH_00076 | 2.7e-125 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
OKHHJBLH_00077 | 8e-154 | V | ATPases associated with a variety of cellular activities | |||
OKHHJBLH_00078 | 3.2e-82 | 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 |
OKHHJBLH_00079 | 6.9e-146 | G | Protein of unknown function (DUF2961) | |||
OKHHJBLH_00080 | 2.1e-90 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
OKHHJBLH_00081 | 1.5e-83 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
OKHHJBLH_00082 | 9.3e-74 | 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) | |
OKHHJBLH_00083 | 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 | |
OKHHJBLH_00084 | 9.9e-67 | V | ATPases associated with a variety of cellular activities | |||
OKHHJBLH_00085 | 3.2e-90 | V | ABC-2 family transporter protein | |||
OKHHJBLH_00086 | 1.3e-104 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
OKHHJBLH_00087 | 8.4e-62 | V | Beta-lactamase | |||
OKHHJBLH_00088 | 2e-144 | T | Histidine kinase | |||
OKHHJBLH_00089 | 2.7e-68 | K | LysR substrate binding domain protein | |||
OKHHJBLH_00090 | 1.4e-107 | S | Patatin-like phospholipase | |||
OKHHJBLH_00091 | 0.0 | S | LPXTG-motif cell wall anchor domain protein | |||
OKHHJBLH_00092 | 1.1e-23 | cydD | V | ABC transporter transmembrane region | ||
OKHHJBLH_00093 | 4.1e-103 | 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 | |
OKHHJBLH_00094 | 4.5e-53 | trkB | P | Cation transport protein | ||
OKHHJBLH_00095 | 1.7e-50 | trkB | P | Cation transport protein | ||
OKHHJBLH_00096 | 9.5e-113 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
OKHHJBLH_00097 | 3.7e-37 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
OKHHJBLH_00098 | 1.6e-168 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
OKHHJBLH_00099 | 2.8e-117 | GK | ROK family | |||
OKHHJBLH_00100 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
OKHHJBLH_00101 | 1.4e-41 | hup | L | Belongs to the bacterial histone-like protein family | ||
OKHHJBLH_00102 | 1.8e-57 | |||||
OKHHJBLH_00103 | 9.7e-141 | C | FMN binding | |||
OKHHJBLH_00104 | 1.7e-279 | 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 | |
OKHHJBLH_00105 | 5.2e-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 | ||
OKHHJBLH_00106 | 3.3e-160 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
OKHHJBLH_00107 | 1.2e-302 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
OKHHJBLH_00108 | 1.1e-170 | |||||
OKHHJBLH_00109 | 3.5e-52 | 3.6.1.27 | I | PAP2 superfamily | ||
OKHHJBLH_00110 | 6.7e-99 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_00111 | 8.7e-75 | ytrE | V | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00112 | 1e-36 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
OKHHJBLH_00113 | 3.4e-25 | |||||
OKHHJBLH_00114 | 4.7e-23 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
OKHHJBLH_00115 | 3.5e-163 | 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 | ||
OKHHJBLH_00116 | 1.4e-22 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
OKHHJBLH_00117 | 1e-83 | |||||
OKHHJBLH_00118 | 1.8e-56 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
OKHHJBLH_00119 | 1.4e-43 | malL | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain |
OKHHJBLH_00120 | 1.3e-131 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
OKHHJBLH_00121 | 4e-170 | rapZ | S | Displays ATPase and GTPase activities | ||
OKHHJBLH_00122 | 4.8e-93 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
OKHHJBLH_00124 | 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 | ||
OKHHJBLH_00125 | 4.2e-95 | S | AAA ATPase domain | |||
OKHHJBLH_00126 | 5.8e-109 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
OKHHJBLH_00127 | 4.5e-67 | cspB | K | 'Cold-shock' DNA-binding domain | ||
OKHHJBLH_00128 | 4.7e-73 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
OKHHJBLH_00129 | 3.9e-20 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
OKHHJBLH_00130 | 8.2e-34 | |||||
OKHHJBLH_00131 | 3.2e-77 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
OKHHJBLH_00132 | 4e-178 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
OKHHJBLH_00133 | 5.6e-39 | msmE | G | Bacterial extracellular solute-binding protein | ||
OKHHJBLH_00134 | 4.1e-80 | 4.2.1.53 | S | MCRA family | ||
OKHHJBLH_00135 | 1.6e-70 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
OKHHJBLH_00136 | 2.1e-88 | 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 | ||
OKHHJBLH_00137 | 2.8e-48 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
OKHHJBLH_00138 | 1e-131 | S | Protein of unknown function (DUF975) | |||
OKHHJBLH_00139 | 5.7e-89 | S | G5 | |||
OKHHJBLH_00141 | 7.5e-151 | O | Thioredoxin | |||
OKHHJBLH_00142 | 0.0 | KLT | Protein tyrosine kinase | |||
OKHHJBLH_00143 | 0.0 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
OKHHJBLH_00144 | 1.3e-107 | kcsA | U | Ion channel | ||
OKHHJBLH_00145 | 4.9e-30 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
OKHHJBLH_00146 | 3.4e-79 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00147 | 2.3e-34 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
OKHHJBLH_00148 | 1.3e-122 | S | Haloacid dehalogenase-like hydrolase | |||
OKHHJBLH_00149 | 1.1e-19 | recN | L | May be involved in recombinational repair of damaged DNA | ||
OKHHJBLH_00150 | 9.6e-32 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
OKHHJBLH_00151 | 5e-119 | lhr | L | DEAD DEAH box helicase | ||
OKHHJBLH_00152 | 1.9e-308 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
OKHHJBLH_00153 | 2.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
OKHHJBLH_00154 | 2.6e-39 | rpmA | J | Ribosomal L27 protein | ||
OKHHJBLH_00155 | 2.3e-311 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
OKHHJBLH_00156 | 1e-204 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
OKHHJBLH_00157 | 7.4e-233 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
OKHHJBLH_00159 | 5.5e-259 | 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 | ||
OKHHJBLH_00160 | 3.9e-99 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
OKHHJBLH_00161 | 1.5e-200 | 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 | |
OKHHJBLH_00162 | 4.4e-232 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
OKHHJBLH_00163 | 6.3e-232 | epsG | M | Glycosyl transferase family 21 | ||
OKHHJBLH_00164 | 1.3e-237 | S | AI-2E family transporter | |||
OKHHJBLH_00165 | 7.7e-29 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
OKHHJBLH_00166 | 5.9e-114 | sufS | 2.8.1.7, 4.4.1.16 | H | Cysteine desulfurases mobilize the sulfur from L- cysteine to yield L-alanine, an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Component of the suf operon, which is activated and required under specific conditions such as oxidative stress and iron limitation. Acts as a potent selenocysteine lyase in vitro, that mobilizes selenium from L-selenocysteine. Selenocysteine lyase activity is however unsure in vivo | |
OKHHJBLH_00167 | 3.4e-105 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
OKHHJBLH_00168 | 6.1e-130 | 3.2.1.37 | GH43 | G | Glycosyl hydrolases family 43 | |
OKHHJBLH_00169 | 1.9e-37 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
OKHHJBLH_00170 | 9.9e-72 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
OKHHJBLH_00171 | 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 | |
OKHHJBLH_00172 | 2.1e-85 | S | LPXTG-motif cell wall anchor domain protein | |||
OKHHJBLH_00173 | 0.0 | inlJ | M | domain protein | ||
OKHHJBLH_00174 | 3.1e-204 | M | LPXTG cell wall anchor motif | |||
OKHHJBLH_00175 | 2.5e-89 | S | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_00176 | 9.9e-275 | cycA | E | Amino acid permease | ||
OKHHJBLH_00177 | 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 | |
OKHHJBLH_00178 | 3.5e-99 | thiF | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
OKHHJBLH_00180 | 2e-58 | K | Acetyltransferase (GNAT) domain | |||
OKHHJBLH_00181 | 2.3e-31 | S | Uncharacterized conserved protein (DUF2183) | |||
OKHHJBLH_00182 | 8.7e-22 | 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 | ||
OKHHJBLH_00183 | 5.7e-85 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
OKHHJBLH_00184 | 5e-42 | G | ABC transporter substrate-binding protein | |||
OKHHJBLH_00185 | 1.8e-133 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
OKHHJBLH_00186 | 2.6e-61 | 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 | ||
OKHHJBLH_00187 | 1.3e-47 | 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 | ||
OKHHJBLH_00188 | 7.5e-35 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
OKHHJBLH_00189 | 6.4e-43 | S | Sucrose-6F-phosphate phosphohydrolase | |||
OKHHJBLH_00190 | 6e-17 | secG | U | Preprotein translocase SecG subunit | ||
OKHHJBLH_00191 | 8.6e-37 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
OKHHJBLH_00192 | 2.7e-83 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
OKHHJBLH_00193 | 1.1e-77 | soxR | K | MerR, DNA binding | ||
OKHHJBLH_00194 | 1.1e-194 | yghZ | C | Aldo/keto reductase family | ||
OKHHJBLH_00195 | 3.2e-58 | S | Protein of unknown function (DUF3039) | |||
OKHHJBLH_00196 | 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 | |
OKHHJBLH_00197 | 8.5e-134 | |||||
OKHHJBLH_00198 | 1.8e-113 | yceD | S | Uncharacterized ACR, COG1399 | ||
OKHHJBLH_00199 | 1e-19 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
OKHHJBLH_00200 | 8.3e-135 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
OKHHJBLH_00201 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
OKHHJBLH_00202 | 3.5e-12 | |||||
OKHHJBLH_00203 | 3.2e-112 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
OKHHJBLH_00204 | 1.6e-78 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
OKHHJBLH_00205 | 6.7e-19 | 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) | |
OKHHJBLH_00206 | 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) | |
OKHHJBLH_00207 | 3.8e-91 | E | aromatic amino acid transport protein AroP K03293 | |||
OKHHJBLH_00208 | 5.7e-103 | I | acetylesterase activity | |||
OKHHJBLH_00209 | 1.2e-160 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
OKHHJBLH_00210 | 1.5e-92 | clcA | P | Voltage gated chloride channel | ||
OKHHJBLH_00211 | 1.5e-58 | clcA | P | Voltage gated chloride channel | ||
OKHHJBLH_00212 | 1.6e-249 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
OKHHJBLH_00213 | 1.6e-205 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
OKHHJBLH_00214 | 0.0 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_00215 | 1.8e-92 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_00216 | 1.6e-34 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_00217 | 1.8e-84 | ctpE | P | E1-E2 ATPase | ||
OKHHJBLH_00218 | 5.8e-133 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
OKHHJBLH_00220 | 2.6e-24 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00221 | 1.9e-100 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
OKHHJBLH_00222 | 1.2e-132 | comE | S | Competence protein | ||
OKHHJBLH_00223 | 6.9e-116 | 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 | ||
OKHHJBLH_00226 | 1.5e-117 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
OKHHJBLH_00227 | 1.1e-23 | lmrB | EGP | Major facilitator Superfamily | ||
OKHHJBLH_00228 | 7.1e-43 | gcvR | T | Belongs to the UPF0237 family | ||
OKHHJBLH_00229 | 6.3e-126 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
OKHHJBLH_00230 | 1.1e-138 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
OKHHJBLH_00231 | 2.9e-31 | S | Sodium:neurotransmitter symporter family | |||
OKHHJBLH_00232 | 8.3e-79 | 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 | ||
OKHHJBLH_00233 | 3.8e-37 | 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 | |
OKHHJBLH_00234 | 1.2e-65 | 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 | |
OKHHJBLH_00235 | 2.6e-191 | 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) | |
OKHHJBLH_00236 | 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 | |
OKHHJBLH_00237 | 8.4e-143 | S | Sulfite exporter TauE/SafE | |||
OKHHJBLH_00238 | 1.3e-195 | 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) | |
OKHHJBLH_00241 | 7.4e-44 | ydeP | K | HxlR-like helix-turn-helix | ||
OKHHJBLH_00242 | 3.2e-86 | XK27_10430 | S | NAD(P)H-binding | ||
OKHHJBLH_00243 | 8.8e-160 | yicL | EG | EamA-like transporter family | ||
OKHHJBLH_00244 | 3e-193 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
OKHHJBLH_00245 | 3.2e-113 | K | helix_turn_helix, Lux Regulon | |||
OKHHJBLH_00246 | 1e-224 | 2.7.13.3 | T | Histidine kinase | ||
OKHHJBLH_00247 | 2e-48 | S | Protein of unknown function DUF58 | |||
OKHHJBLH_00248 | 1.4e-62 | S | Protein of unknown function DUF58 | |||
OKHHJBLH_00249 | 2.5e-224 | S | ATPase family associated with various cellular activities (AAA) | |||
OKHHJBLH_00250 | 0.0 | S | Fibronectin type 3 domain | |||
OKHHJBLH_00251 | 4.9e-98 | metI | P | Psort location CytoplasmicMembrane, score 9.99 | ||
OKHHJBLH_00252 | 6.5e-193 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
OKHHJBLH_00253 | 2.9e-154 | metQ | M | NLPA lipoprotein | ||
OKHHJBLH_00254 | 1.4e-200 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
OKHHJBLH_00255 | 6.9e-143 | cjaA | ET | Bacterial periplasmic substrate-binding proteins | ||
OKHHJBLH_00256 | 1.1e-150 | glnQ | 3.6.3.21 | E | ATP binding protein of ABC transporter for glutamate aspartate K02028 | |
OKHHJBLH_00257 | 3.6e-120 | E | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00258 | 3.6e-52 | papP | E | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00260 | 2.1e-106 | kup | P | Transport of potassium into the cell | ||
OKHHJBLH_00261 | 2.2e-184 | tatD | L | TatD related DNase | ||
OKHHJBLH_00262 | 0.0 | G | Alpha-L-arabinofuranosidase C-terminus | |||
OKHHJBLH_00263 | 6.6e-233 | G | Alpha galactosidase A | |||
OKHHJBLH_00264 | 3.3e-197 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
OKHHJBLH_00265 | 4.5e-224 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
OKHHJBLH_00266 | 3.9e-91 | |||||
OKHHJBLH_00267 | 2.7e-117 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
OKHHJBLH_00268 | 3.6e-207 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
OKHHJBLH_00269 | 0.0 | G | Bacterial Ig-like domain (group 4) | |||
OKHHJBLH_00270 | 0.0 | sca1 | 3.2.1.187 | GH121 | DG | Bacterial Ig-like domain (group 4) |
OKHHJBLH_00271 | 0.0 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
OKHHJBLH_00272 | 9.3e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00273 | 3.1e-167 | P | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00274 | 4e-07 | P | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00275 | 1.1e-242 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_00276 | 6.3e-193 | K | Periplasmic binding protein domain | |||
OKHHJBLH_00277 | 0.0 | ubiB | S | ABC1 family | ||
OKHHJBLH_00278 | 1e-27 | S | granule-associated protein | |||
OKHHJBLH_00279 | 2.1e-137 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
OKHHJBLH_00280 | 1.1e-251 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
OKHHJBLH_00281 | 3.3e-248 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
OKHHJBLH_00282 | 0.0 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
OKHHJBLH_00283 | 7.7e-55 | glnB | K | Nitrogen regulatory protein P-II | ||
OKHHJBLH_00284 | 4.1e-19 | amt | U | Ammonium Transporter Family | ||
OKHHJBLH_00285 | 1.8e-231 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
OKHHJBLH_00286 | 2.7e-166 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
OKHHJBLH_00287 | 1e-268 | V | Efflux ABC transporter, permease protein | |||
OKHHJBLH_00288 | 5e-128 | V | ATPases associated with a variety of cellular activities | |||
OKHHJBLH_00289 | 2.1e-137 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
OKHHJBLH_00290 | 5.9e-120 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
OKHHJBLH_00291 | 2.1e-52 | 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 | ||
OKHHJBLH_00292 | 1.6e-39 | |||||
OKHHJBLH_00293 | 9.6e-157 | T | Forkhead associated domain | |||
OKHHJBLH_00294 | 0.0 | eccCa | D | FtsK/SpoIIIE family | ||
OKHHJBLH_00295 | 1.1e-89 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
OKHHJBLH_00296 | 6.2e-90 | S | Protein of unknown function (DUF721) | |||
OKHHJBLH_00297 | 3.7e-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 | ||
OKHHJBLH_00298 | 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 | |
OKHHJBLH_00299 | 2.9e-306 | 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 | ||
OKHHJBLH_00300 | 5.9e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
OKHHJBLH_00301 | 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 | |
OKHHJBLH_00302 | 1.6e-106 | oxc | 4.1.1.8 | EH | Thiamine pyrophosphate enzyme, central domain | |
OKHHJBLH_00303 | 7.1e-175 | M | LPXTG-motif cell wall anchor domain protein | |||
OKHHJBLH_00304 | 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 |
OKHHJBLH_00305 | 3.4e-91 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
OKHHJBLH_00306 | 6.4e-37 | mntP | P | Probably functions as a manganese efflux pump | ||
OKHHJBLH_00307 | 2.2e-35 | |||||
OKHHJBLH_00308 | 4.5e-123 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
OKHHJBLH_00309 | 1.4e-100 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
OKHHJBLH_00310 | 6.1e-30 | fmdB | S | Putative regulatory protein | ||
OKHHJBLH_00311 | 5e-93 | flgA | NO | SAF | ||
OKHHJBLH_00312 | 4.8e-36 | |||||
OKHHJBLH_00313 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
OKHHJBLH_00314 | 1.7e-36 | U | Belongs to the binding-protein-dependent transport system permease family | |||
OKHHJBLH_00315 | 2.6e-22 | U | Belongs to the binding-protein-dependent transport system permease family | |||
OKHHJBLH_00316 | 1e-218 | livK | E | Receptor family ligand binding region | ||
OKHHJBLH_00317 | 3.2e-172 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
OKHHJBLH_00318 | 1.4e-190 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
OKHHJBLH_00319 | 1.5e-35 | rpmE | J | Binds the 23S rRNA | ||
OKHHJBLH_00321 | 1.7e-224 | xylR | GK | ROK family | ||
OKHHJBLH_00322 | 2.3e-92 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
OKHHJBLH_00323 | 7.1e-286 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
OKHHJBLH_00324 | 1.5e-269 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
OKHHJBLH_00325 | 2.7e-102 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
OKHHJBLH_00326 | 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) | |
OKHHJBLH_00327 | 1.6e-143 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
OKHHJBLH_00328 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
OKHHJBLH_00329 | 5.5e-246 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
OKHHJBLH_00330 | 9.8e-97 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
OKHHJBLH_00331 | 1.7e-45 | |||||
OKHHJBLH_00332 | 1.6e-28 | K | Cro/C1-type HTH DNA-binding domain | |||
OKHHJBLH_00333 | 8.5e-72 | |||||
OKHHJBLH_00334 | 3.2e-33 | amyE | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
OKHHJBLH_00335 | 1e-60 | |||||
OKHHJBLH_00336 | 1.1e-197 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_00337 | 3.6e-166 | iunH2 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
OKHHJBLH_00338 | 1.1e-259 | EGP | Major Facilitator Superfamily | |||
OKHHJBLH_00339 | 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 | |
OKHHJBLH_00340 | 4e-45 | 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) | |
OKHHJBLH_00341 | 2.5e-95 | 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) | |
OKHHJBLH_00342 | 2e-205 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
OKHHJBLH_00343 | 2.1e-51 | S | Protein of unknown function (DUF2469) | |||
OKHHJBLH_00344 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
OKHHJBLH_00345 | 2.8e-139 | 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 | ||
OKHHJBLH_00346 | 4.5e-59 | MA20_14025 | U | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00347 | 2.4e-164 | MA20_14020 | P | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00348 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
OKHHJBLH_00349 | 0.0 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
OKHHJBLH_00350 | 6.7e-10 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
OKHHJBLH_00351 | 8e-106 | lacA | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
OKHHJBLH_00352 | 9.2e-130 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
OKHHJBLH_00353 | 4.2e-10 | S | zinc-ribbon domain | |||
OKHHJBLH_00356 | 2.2e-166 | T | Pfam Adenylate and Guanylate cyclase catalytic domain | |||
OKHHJBLH_00357 | 2.4e-291 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
OKHHJBLH_00358 | 1e-39 | rplI | J | Binds to the 23S rRNA | ||
OKHHJBLH_00359 | 8e-91 | 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 | ||
OKHHJBLH_00360 | 1.1e-78 | K | helix_turn_helix ASNC type | |||
OKHHJBLH_00361 | 1e-69 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
OKHHJBLH_00362 | 0.0 | S | domain protein | |||
OKHHJBLH_00363 | 1.1e-300 | 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 | |
OKHHJBLH_00364 | 2.4e-121 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
OKHHJBLH_00365 | 4.5e-163 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
OKHHJBLH_00366 | 1.1e-269 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
OKHHJBLH_00367 | 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 | |
OKHHJBLH_00368 | 6.1e-138 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
OKHHJBLH_00369 | 1.3e-254 | codA | 3.5.4.1, 3.5.4.21 | F | Amidohydrolase family | |
OKHHJBLH_00370 | 1.4e-284 | purR | QT | Purine catabolism regulatory protein-like family | ||
OKHHJBLH_00371 | 8.7e-205 | proP | EGP | Sugar (and other) transporter | ||
OKHHJBLH_00372 | 5.1e-232 | yknV | V | ABC transporter | ||
OKHHJBLH_00373 | 8e-126 | |||||
OKHHJBLH_00374 | 0.0 | rafA | 3.2.1.22 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00375 | 2.2e-174 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_00376 | 4.4e-100 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
OKHHJBLH_00377 | 7e-184 | |||||
OKHHJBLH_00378 | 9.5e-101 | S | Protein of unknown function (DUF805) | |||
OKHHJBLH_00379 | 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) | |
OKHHJBLH_00382 | 1.1e-54 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
OKHHJBLH_00383 | 5.1e-60 | U | TadE-like protein | |||
OKHHJBLH_00384 | 1.3e-42 | S | Protein of unknown function (DUF4244) | |||
OKHHJBLH_00385 | 6.1e-91 | gspF | NU | Type II secretion system (T2SS), protein F | ||
OKHHJBLH_00386 | 1.4e-133 | U | Type ii secretion system | |||
OKHHJBLH_00387 | 1.6e-185 | cpaF | U | Type II IV secretion system protein | ||
OKHHJBLH_00388 | 8e-140 | cpaE | D | bacterial-type flagellum organization | ||
OKHHJBLH_00390 | 3.8e-184 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00391 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
OKHHJBLH_00392 | 5.7e-85 | K | Cro/C1-type HTH DNA-binding domain | |||
OKHHJBLH_00393 | 1.9e-92 | E | Transglutaminase-like superfamily | |||
OKHHJBLH_00394 | 4.4e-163 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
OKHHJBLH_00395 | 4.8e-104 | B | Belongs to the OprB family | |||
OKHHJBLH_00396 | 1.1e-101 | T | Forkhead associated domain | |||
OKHHJBLH_00397 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
OKHHJBLH_00398 | 1.4e-156 | G | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00399 | 6.6e-157 | G | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00400 | 1.5e-244 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
OKHHJBLH_00401 | 1.5e-230 | nagC | GK | ROK family | ||
OKHHJBLH_00402 | 4.7e-58 | K | Bacterial regulatory proteins, tetR family | |||
OKHHJBLH_00403 | 0.0 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
OKHHJBLH_00404 | 9.4e-115 | K | Bacterial regulatory proteins, tetR family | |||
OKHHJBLH_00405 | 1.1e-234 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
OKHHJBLH_00406 | 7.8e-38 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
OKHHJBLH_00407 | 2.2e-196 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
OKHHJBLH_00408 | 1.7e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
OKHHJBLH_00409 | 1.6e-115 | |||||
OKHHJBLH_00411 | 0.0 | ams | 2.4.1.4, 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha amylase, catalytic domain |
OKHHJBLH_00412 | 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 | |
OKHHJBLH_00413 | 0.0 | yjcE | P | Sodium/hydrogen exchanger family | ||
OKHHJBLH_00414 | 1.4e-77 | tadA | 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
OKHHJBLH_00415 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
OKHHJBLH_00416 | 1.2e-34 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_00417 | 1.3e-63 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_00418 | 1.6e-225 | S | Putative ABC-transporter type IV | |||
OKHHJBLH_00419 | 6e-38 | nrdH | O | Glutaredoxin | ||
OKHHJBLH_00420 | 1.3e-17 | M | cell wall binding repeat | |||
OKHHJBLH_00421 | 8.4e-206 | abf | G | Glycosyl hydrolases family 43 | ||
OKHHJBLH_00422 | 4.4e-294 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_00423 | 2.3e-168 | G | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00424 | 1.4e-162 | G | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00425 | 8.4e-122 | 3.2.1.14 | GH18 | S | Carbohydrate binding domain | |
OKHHJBLH_00426 | 0.0 | T | Diguanylate cyclase, GGDEF domain | |||
OKHHJBLH_00427 | 3.2e-189 | lacR | K | Transcriptional regulator, LacI family | ||
OKHHJBLH_00428 | 7.8e-151 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
OKHHJBLH_00429 | 3.2e-53 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
OKHHJBLH_00430 | 0.0 | cstA | T | 5TM C-terminal transporter carbon starvation CstA | ||
OKHHJBLH_00431 | 6.2e-40 | ybdD | S | Selenoprotein, putative | ||
OKHHJBLH_00432 | 2.4e-178 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
OKHHJBLH_00433 | 6.2e-204 | parB | K | Belongs to the ParB family | ||
OKHHJBLH_00434 | 4.5e-172 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
OKHHJBLH_00435 | 3.9e-129 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
OKHHJBLH_00436 | 3.6e-91 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
OKHHJBLH_00437 | 8.5e-125 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
OKHHJBLH_00438 | 1.7e-221 | V | ABC transporter permease | |||
OKHHJBLH_00439 | 2.4e-156 | V | ABC transporter | |||
OKHHJBLH_00440 | 5.1e-150 | T | HD domain | |||
OKHHJBLH_00441 | 1e-167 | S | Glutamine amidotransferase domain | |||
OKHHJBLH_00442 | 3.1e-62 | kup | P | Transport of potassium into the cell | ||
OKHHJBLH_00443 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
OKHHJBLH_00444 | 2.4e-47 | yhbY | J | CRS1_YhbY | ||
OKHHJBLH_00445 | 9.6e-146 | 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 | |
OKHHJBLH_00446 | 2.2e-201 | S | Glycosyltransferase, group 2 family protein | |||
OKHHJBLH_00447 | 1.6e-93 | 3.6.3.3, 3.6.3.5, 3.6.3.54 | P | Heavy metal translocating P-type atpase | ||
OKHHJBLH_00448 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
OKHHJBLH_00449 | 1.9e-172 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
OKHHJBLH_00450 | 4.7e-260 | S | AAA domain | |||
OKHHJBLH_00451 | 9.9e-74 | |||||
OKHHJBLH_00452 | 3e-10 | |||||
OKHHJBLH_00453 | 1.4e-32 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
OKHHJBLH_00454 | 2.3e-92 | mhpC | I | Alpha/beta hydrolase family | ||
OKHHJBLH_00455 | 1.1e-115 | F | Domain of unknown function (DUF4916) | |||
OKHHJBLH_00456 | 6e-61 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
OKHHJBLH_00457 | 5.6e-170 | S | G5 | |||
OKHHJBLH_00458 | 7.8e-88 | |||||
OKHHJBLH_00459 | 0.0 | 3.2.1.97 | GH101 | G | Glycosyl hydrolases family 43 | |
OKHHJBLH_00460 | 7.9e-256 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
OKHHJBLH_00461 | 3.3e-107 | macB_8 | V | MacB-like periplasmic core domain | ||
OKHHJBLH_00462 | 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) | |
OKHHJBLH_00463 | 3.3e-183 | adh3 | C | Zinc-binding dehydrogenase | ||
OKHHJBLH_00464 | 4.4e-28 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
OKHHJBLH_00465 | 8.1e-39 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
OKHHJBLH_00466 | 0.0 | helD | 3.6.4.12 | L | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00467 | 2.4e-184 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
OKHHJBLH_00468 | 1.5e-106 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
OKHHJBLH_00469 | 3.2e-248 | pbuX | F | Permease family | ||
OKHHJBLH_00470 | 0.0 | yrhL | I | Psort location CytoplasmicMembrane, score 9.99 | ||
OKHHJBLH_00471 | 1.1e-30 | 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 | |
OKHHJBLH_00472 | 4.4e-102 | |||||
OKHHJBLH_00473 | 6.1e-191 | nusA | K | Participates in both transcription termination and antitermination | ||
OKHHJBLH_00474 | 2.6e-204 | 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 | ||
OKHHJBLH_00475 | 2.8e-151 | T | LytTr DNA-binding domain | |||
OKHHJBLH_00476 | 7.4e-250 | T | GHKL domain | |||
OKHHJBLH_00477 | 4.6e-214 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
OKHHJBLH_00478 | 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 | |
OKHHJBLH_00479 | 8.2e-235 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
OKHHJBLH_00480 | 1.6e-247 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_00481 | 1.1e-183 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
OKHHJBLH_00482 | 3.7e-131 | 1.1.1.1 | C | Iron-containing alcohol dehydrogenase | ||
OKHHJBLH_00483 | 6.7e-196 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
OKHHJBLH_00484 | 4.8e-151 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
OKHHJBLH_00485 | 1.9e-124 | livF | E | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00486 | 9.9e-115 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
OKHHJBLH_00487 | 4.5e-195 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
OKHHJBLH_00488 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
OKHHJBLH_00489 | 3.7e-284 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
OKHHJBLH_00490 | 2.4e-135 | 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) | |
OKHHJBLH_00491 | 6.8e-89 | zur | P | Belongs to the Fur family | ||
OKHHJBLH_00492 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
OKHHJBLH_00493 | 5.8e-24 | psuK | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
OKHHJBLH_00494 | 3.8e-29 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
OKHHJBLH_00496 | 1.1e-84 | ptpA | 3.1.3.48 | T | low molecular weight | |
OKHHJBLH_00497 | 1.4e-129 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
OKHHJBLH_00498 | 3.8e-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 | |
OKHHJBLH_00499 | 7.7e-73 | attW | O | OsmC-like protein | ||
OKHHJBLH_00500 | 1.3e-190 | T | Universal stress protein family | |||
OKHHJBLH_00501 | 1.6e-149 | amyC5 | P | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00502 | 2.2e-162 | amyD3 | P | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00503 | 4.6e-225 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_00504 | 3.7e-146 | pspC | KT | PspC domain | ||
OKHHJBLH_00505 | 9.3e-93 | |||||
OKHHJBLH_00506 | 2.3e-116 | S | Protein of unknown function (DUF4125) | |||
OKHHJBLH_00507 | 9.6e-74 | S | Domain of unknown function (DUF4037) | |||
OKHHJBLH_00508 | 1.3e-30 | 3.1.21.3 | V | DivIVA protein | ||
OKHHJBLH_00509 | 6.9e-41 | yggT | S | YGGT family | ||
OKHHJBLH_00510 | 8.9e-81 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
OKHHJBLH_00511 | 5.6e-220 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
OKHHJBLH_00512 | 5.9e-134 | 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 |
OKHHJBLH_00513 | 1.5e-35 | |||||
OKHHJBLH_00514 | 2.8e-148 | gluP | 3.4.21.105 | S | Rhomboid family | |
OKHHJBLH_00515 | 1.9e-240 | L | ribosomal rna small subunit methyltransferase | |||
OKHHJBLH_00516 | 1.5e-39 | crgA | D | Involved in cell division | ||
OKHHJBLH_00517 | 6.5e-79 | M | NlpC/P60 family | |||
OKHHJBLH_00518 | 1.3e-165 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
OKHHJBLH_00519 | 8.2e-218 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
OKHHJBLH_00520 | 6.2e-41 | |||||
OKHHJBLH_00521 | 3.4e-155 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
OKHHJBLH_00522 | 2.8e-268 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_00523 | 1.9e-161 | P | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00524 | 6.5e-148 | P | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00525 | 5.9e-41 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
OKHHJBLH_00526 | 3.4e-252 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
OKHHJBLH_00527 | 8.6e-254 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
OKHHJBLH_00528 | 7.3e-127 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
OKHHJBLH_00529 | 3.3e-146 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
OKHHJBLH_00531 | 4.5e-207 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
OKHHJBLH_00532 | 2e-146 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
OKHHJBLH_00533 | 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 | ||
OKHHJBLH_00534 | 4.4e-57 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
OKHHJBLH_00535 | 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 | ||
OKHHJBLH_00536 | 2.1e-260 | S | Protein of unknown function DUF262 | |||
OKHHJBLH_00537 | 9e-116 | K | helix_turn_helix, Lux Regulon | |||
OKHHJBLH_00538 | 1.2e-244 | T | Histidine kinase | |||
OKHHJBLH_00539 | 1e-281 | 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 | |
OKHHJBLH_00540 | 5.5e-155 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
OKHHJBLH_00541 | 6.2e-177 | ydeD | EG | EamA-like transporter family | ||
OKHHJBLH_00542 | 3.7e-112 | ybhL | S | Belongs to the BI1 family | ||
OKHHJBLH_00543 | 9.2e-82 | |||||
OKHHJBLH_00544 | 9.2e-57 | T | helix_turn_helix, Lux Regulon | |||
OKHHJBLH_00545 | 1.5e-28 | 2.7.13.3 | T | Histidine kinase | ||
OKHHJBLH_00546 | 4.6e-85 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
OKHHJBLH_00547 | 4.1e-234 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
OKHHJBLH_00548 | 2.8e-145 | cobB2 | K | Sir2 family | ||
OKHHJBLH_00549 | 2.3e-88 | I | alpha/beta hydrolase fold | |||
OKHHJBLH_00550 | 4.3e-75 | |||||
OKHHJBLH_00551 | 1.5e-14 | S | Domain of unknown function (DUF4143) | |||
OKHHJBLH_00552 | 3.1e-127 | XK27_08050 | O | prohibitin homologues | ||
OKHHJBLH_00553 | 1.4e-43 | XAC3035 | O | Glutaredoxin | ||
OKHHJBLH_00554 | 2.5e-75 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
OKHHJBLH_00555 | 3.6e-12 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
OKHHJBLH_00556 | 4.6e-171 | tesB | I | Thioesterase-like superfamily | ||
OKHHJBLH_00557 | 4.6e-97 | S | Protein of unknown function (DUF3180) | |||
OKHHJBLH_00558 | 7.7e-288 | 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 | |
OKHHJBLH_00559 | 3.8e-96 | 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 | |
OKHHJBLH_00560 | 5.7e-175 | terC | P | Integral membrane protein, TerC family | ||
OKHHJBLH_00561 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
OKHHJBLH_00562 | 7.7e-115 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
OKHHJBLH_00563 | 2.2e-07 | rpsA | J | Ribosomal protein S1 | ||
OKHHJBLH_00564 | 3.8e-45 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
OKHHJBLH_00565 | 7.9e-129 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
OKHHJBLH_00566 | 5.8e-177 | T | Protein tyrosine kinase | |||
OKHHJBLH_00567 | 2.3e-265 | pbpA | M | penicillin-binding protein | ||
OKHHJBLH_00568 | 1.4e-73 | rodA | D | Belongs to the SEDS family | ||
OKHHJBLH_00569 | 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 | ||
OKHHJBLH_00570 | 8.9e-150 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
OKHHJBLH_00571 | 3.4e-161 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
OKHHJBLH_00572 | 1.4e-76 | ftsE | D | Cell division ATP-binding protein FtsE | ||
OKHHJBLH_00573 | 1.9e-35 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
OKHHJBLH_00574 | 3.3e-96 | M | Peptidase family M23 | |||
OKHHJBLH_00575 | 6.3e-62 | |||||
OKHHJBLH_00577 | 5e-125 | XK27_06785 | V | ABC transporter | ||
OKHHJBLH_00578 | 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 | |
OKHHJBLH_00579 | 4.1e-15 | G | Transporter major facilitator family protein | |||
OKHHJBLH_00580 | 2e-32 | G | Transporter major facilitator family protein | |||
OKHHJBLH_00581 | 0.0 | 3.2.1.40 | E | Bacterial alpha-L-rhamnosidase C-terminal domain | ||
OKHHJBLH_00582 | 1.9e-37 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_00583 | 2.2e-171 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
OKHHJBLH_00584 | 5.4e-144 | S | HAD-hyrolase-like | |||
OKHHJBLH_00585 | 9.7e-141 | traX | S | TraX protein | ||
OKHHJBLH_00586 | 3.3e-42 | K | Psort location Cytoplasmic, score | |||
OKHHJBLH_00587 | 7.8e-150 | |||||
OKHHJBLH_00588 | 2.5e-161 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
OKHHJBLH_00589 | 2.1e-79 | bioY | S | BioY family | ||
OKHHJBLH_00590 | 1.8e-187 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
OKHHJBLH_00591 | 6.8e-142 | S | Bacterial protein of unknown function (DUF881) | |||
OKHHJBLH_00592 | 8.7e-209 | srtA | 3.4.22.70 | M | Sortase family | |
OKHHJBLH_00593 | 1.1e-115 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
OKHHJBLH_00594 | 1.5e-132 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
OKHHJBLH_00596 | 1.1e-186 | K | Helix-turn-helix XRE-family like proteins | |||
OKHHJBLH_00597 | 6.3e-171 | yddG | EG | EamA-like transporter family | ||
OKHHJBLH_00598 | 3.6e-120 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_00599 | 6.8e-100 | |||||
OKHHJBLH_00600 | 3.5e-182 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
OKHHJBLH_00601 | 7.4e-126 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
OKHHJBLH_00602 | 7.5e-183 | S | UPF0210 protein | |||
OKHHJBLH_00603 | 1.9e-25 | S | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_00604 | 4.1e-95 | bcp | 1.11.1.15 | O | Redoxin | |
OKHHJBLH_00605 | 2.3e-57 | 3.4.13.22 | S | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | ||
OKHHJBLH_00606 | 5.3e-167 | S | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |||
OKHHJBLH_00607 | 1.2e-67 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
OKHHJBLH_00608 | 8.2e-263 | 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 | |
OKHHJBLH_00609 | 2.7e-82 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
OKHHJBLH_00610 | 8.9e-191 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
OKHHJBLH_00611 | 9.3e-57 | 3.4.23.43 | S | Type IV leader peptidase family | ||
OKHHJBLH_00612 | 7.5e-64 | 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 | |
OKHHJBLH_00613 | 4.5e-146 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
OKHHJBLH_00614 | 2.2e-237 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
OKHHJBLH_00615 | 2.5e-264 | KLT | Protein tyrosine kinase | |||
OKHHJBLH_00616 | 3.3e-62 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
OKHHJBLH_00617 | 1.4e-157 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
OKHHJBLH_00618 | 6e-100 | K | Bacterial regulatory proteins, tetR family | |||
OKHHJBLH_00619 | 0.0 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
OKHHJBLH_00620 | 1.7e-47 | lmrB | U | Major Facilitator Superfamily | ||
OKHHJBLH_00621 | 1.3e-154 | lon | T | Belongs to the peptidase S16 family | ||
OKHHJBLH_00622 | 4.1e-284 | S | Zincin-like metallopeptidase | |||
OKHHJBLH_00623 | 3.7e-207 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
OKHHJBLH_00624 | 1.7e-56 | htpX | O | Belongs to the peptidase M48B family | ||
OKHHJBLH_00625 | 3.1e-270 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
OKHHJBLH_00626 | 6.2e-114 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
OKHHJBLH_00627 | 2.7e-185 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
OKHHJBLH_00628 | 7.2e-253 | M | Bacterial capsule synthesis protein PGA_cap | |||
OKHHJBLH_00629 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
OKHHJBLH_00630 | 2.7e-302 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
OKHHJBLH_00631 | 4.3e-116 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
OKHHJBLH_00632 | 1e-35 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
OKHHJBLH_00633 | 9.2e-151 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
OKHHJBLH_00634 | 1.5e-146 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00636 | 2e-218 | macB_2 | V | ABC transporter permease | ||
OKHHJBLH_00637 | 7.2e-231 | S | Predicted membrane protein (DUF2318) | |||
OKHHJBLH_00638 | 3e-36 | tpd | P | Fe2+ transport protein | ||
OKHHJBLH_00639 | 1.3e-131 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
OKHHJBLH_00640 | 4.6e-271 | 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 | |
OKHHJBLH_00641 | 1.1e-139 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
OKHHJBLH_00642 | 3.5e-178 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
OKHHJBLH_00643 | 8.7e-19 | 3.2.1.78 | GH26 | G | Glycosyl hydrolase family 26 | |
OKHHJBLH_00644 | 4.2e-124 | dedA | S | SNARE associated Golgi protein | ||
OKHHJBLH_00645 | 0.0 | M | probably involved in cell wall | |||
OKHHJBLH_00646 | 6.4e-47 | 3.2.1.14 | GH18 | S | Carbohydrate binding domain | |
OKHHJBLH_00647 | 1.4e-272 | frc | 2.8.3.16 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
OKHHJBLH_00648 | 5.7e-192 | yfdV | S | Membrane transport protein | ||
OKHHJBLH_00649 | 1.1e-86 | oxc | 4.1.1.8 | EH | Thiamine pyrophosphate enzyme, central domain | |
OKHHJBLH_00650 | 1.2e-118 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_00651 | 2.7e-88 | K | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_00652 | 1.1e-61 | S | FMN_bind | |||
OKHHJBLH_00653 | 2.6e-149 | macB | V | ABC transporter, ATP-binding protein | ||
OKHHJBLH_00654 | 3.7e-90 | Z012_06715 | V | FtsX-like permease family | ||
OKHHJBLH_00655 | 9.1e-121 | yjjP | S | Threonine/Serine exporter, ThrE | ||
OKHHJBLH_00656 | 9.4e-300 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
OKHHJBLH_00657 | 6.3e-196 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
OKHHJBLH_00658 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
OKHHJBLH_00659 | 5.2e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
OKHHJBLH_00660 | 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 | ||
OKHHJBLH_00661 | 1.2e-158 | msbA2 | 3.6.3.44 | V | ABC transporter transmembrane region | |
OKHHJBLH_00662 | 3e-159 | O | Thioredoxin | |||
OKHHJBLH_00663 | 4.9e-128 | E | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_00664 | 2.2e-159 | 3.5.1.106 | I | carboxylic ester hydrolase activity | ||
OKHHJBLH_00665 | 7.9e-176 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
OKHHJBLH_00666 | 1.5e-45 | P | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_00667 | 8e-149 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
OKHHJBLH_00668 | 2e-269 | KLT | Domain of unknown function (DUF4032) | |||
OKHHJBLH_00669 | 3e-69 | ugpC | E | Belongs to the ABC transporter superfamily | ||
OKHHJBLH_00670 | 1.1e-175 | dnaK | O | Heat shock 70 kDa protein | ||
OKHHJBLH_00671 | 1.2e-143 | S | Mitochondrial biogenesis AIM24 | |||
OKHHJBLH_00672 | 1.1e-99 | phoA | 3.1.3.1, 3.1.3.39 | P | Alkaline phosphatase homologues | |
OKHHJBLH_00673 | 5e-30 | GT4 | M | Psort location Cytoplasmic, score 8.87 | ||
OKHHJBLH_00674 | 2e-100 | GT4 | M | Psort location Cytoplasmic, score 8.87 | ||
OKHHJBLH_00675 | 1e-215 | M | Domain of unknown function (DUF1972) | |||
OKHHJBLH_00676 | 4.3e-61 | ppiA | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
OKHHJBLH_00677 | 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 | |
OKHHJBLH_00678 | 1.5e-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 | |
OKHHJBLH_00679 | 2.5e-247 | S | zinc finger | |||
OKHHJBLH_00680 | 7.5e-71 | S | Bacterial PH domain | |||
OKHHJBLH_00681 | 1.5e-76 | |||||
OKHHJBLH_00682 | 5.7e-194 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
OKHHJBLH_00683 | 5e-145 | bioM | P | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00684 | 3.2e-228 | E | Aminotransferase class I and II | |||
OKHHJBLH_00685 | 6.1e-24 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
OKHHJBLH_00686 | 1.1e-176 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
OKHHJBLH_00687 | 1.9e-164 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
OKHHJBLH_00688 | 2.4e-116 | 3.6.1.13 | L | NUDIX domain | ||
OKHHJBLH_00689 | 1.3e-81 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
OKHHJBLH_00690 | 2.5e-166 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
OKHHJBLH_00691 | 2.7e-108 | yitW | S | Iron-sulfur cluster assembly protein | ||
OKHHJBLH_00692 | 3.4e-100 | iscU | C | SUF system FeS assembly protein, NifU family | ||
OKHHJBLH_00693 | 9.6e-200 | 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 | |
OKHHJBLH_00694 | 4.7e-126 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
OKHHJBLH_00695 | 6.8e-133 | KT | Response regulator receiver domain protein | |||
OKHHJBLH_00696 | 1.3e-124 | |||||
OKHHJBLH_00698 | 3.6e-17 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
OKHHJBLH_00699 | 3e-130 | sufD | O | FeS assembly protein SufD | ||
OKHHJBLH_00700 | 1.6e-290 | sufB | O | FeS assembly protein SufB | ||
OKHHJBLH_00701 | 2.4e-189 | S | L,D-transpeptidase catalytic domain | |||
OKHHJBLH_00702 | 2.7e-31 | L | Tetratricopeptide repeat | |||
OKHHJBLH_00703 | 5.9e-191 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
OKHHJBLH_00704 | 5.7e-130 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
OKHHJBLH_00705 | 2e-115 | trkA | P | TrkA-N domain | ||
OKHHJBLH_00706 | 6.8e-39 | trkB | P | Cation transport protein | ||
OKHHJBLH_00707 | 1.2e-131 | fhaA | T | Protein of unknown function (DUF2662) | ||
OKHHJBLH_00708 | 3.3e-143 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
OKHHJBLH_00709 | 2.2e-50 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
OKHHJBLH_00710 | 8.9e-83 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
OKHHJBLH_00711 | 2.2e-145 | 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 | |
OKHHJBLH_00712 | 2.3e-44 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
OKHHJBLH_00713 | 2.3e-122 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
OKHHJBLH_00714 | 7e-149 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
OKHHJBLH_00715 | 1.6e-56 | |||||
OKHHJBLH_00716 | 1.7e-54 | 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 | |
OKHHJBLH_00717 | 1.8e-50 | yajC | U | Preprotein translocase subunit | ||
OKHHJBLH_00718 | 1.8e-99 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
OKHHJBLH_00719 | 2.2e-221 | 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 | |
OKHHJBLH_00720 | 2.5e-96 | 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 | |
OKHHJBLH_00721 | 1e-227 | 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 | |
OKHHJBLH_00722 | 7e-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 | |
OKHHJBLH_00724 | 5.9e-197 | S | Endonuclease/Exonuclease/phosphatase family | |||
OKHHJBLH_00725 | 4.8e-122 | T | Diguanylate cyclase (GGDEF) domain protein | |||
OKHHJBLH_00726 | 1.8e-126 | L | Protein of unknown function (DUF1524) | |||
OKHHJBLH_00727 | 2.1e-165 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
OKHHJBLH_00728 | 2.3e-102 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
OKHHJBLH_00729 | 4.5e-138 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
OKHHJBLH_00730 | 9.9e-271 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
OKHHJBLH_00731 | 1.1e-122 | |||||
OKHHJBLH_00732 | 2.2e-54 | |||||
OKHHJBLH_00733 | 3.2e-115 | |||||
OKHHJBLH_00734 | 5.9e-143 | QT | PucR C-terminal helix-turn-helix domain | |||
OKHHJBLH_00735 | 3.8e-54 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
OKHHJBLH_00736 | 4.2e-45 | sbp | S | Protein of unknown function (DUF1290) | ||
OKHHJBLH_00737 | 1.6e-141 | S | Bacterial protein of unknown function (DUF881) | |||
OKHHJBLH_00738 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
OKHHJBLH_00739 | 1.1e-56 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
OKHHJBLH_00740 | 1.9e-46 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
OKHHJBLH_00741 | 0.0 | D | FtsK/SpoIIIE family | |||
OKHHJBLH_00742 | 1.1e-110 | K | Cell envelope-related transcriptional attenuator domain | |||
OKHHJBLH_00743 | 0.0 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Belongs to the glycosyl hydrolase 43 family | |
OKHHJBLH_00744 | 1.8e-187 | K | Bacterial regulatory proteins, lacI family | |||
OKHHJBLH_00745 | 1.1e-143 | |||||
OKHHJBLH_00746 | 1.4e-172 | G | Fic/DOC family | |||
OKHHJBLH_00747 | 1.9e-106 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
OKHHJBLH_00748 | 3.9e-66 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_00749 | 2.5e-82 | 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 | |
OKHHJBLH_00750 | 5.4e-289 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
OKHHJBLH_00751 | 6.7e-141 | 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 | |
OKHHJBLH_00752 | 7.7e-92 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
OKHHJBLH_00753 | 5.1e-188 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
OKHHJBLH_00754 | 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 | ||
OKHHJBLH_00755 | 2.7e-94 | 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 | ||
OKHHJBLH_00756 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
OKHHJBLH_00757 | 1.9e-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 | |
OKHHJBLH_00758 | 2.3e-31 | T | PhoQ Sensor | |||
OKHHJBLH_00759 | 3.5e-78 | S | Protein of unknown function (DUF2975) | |||
OKHHJBLH_00760 | 5.8e-32 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
OKHHJBLH_00761 | 4.4e-161 | cydD | V | ABC transporter transmembrane region | ||
OKHHJBLH_00762 | 1.5e-120 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
OKHHJBLH_00763 | 3.6e-102 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
OKHHJBLH_00764 | 7.2e-56 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
OKHHJBLH_00765 | 6e-120 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
OKHHJBLH_00766 | 2.7e-29 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
OKHHJBLH_00767 | 2.1e-38 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
OKHHJBLH_00768 | 3e-50 | lipA | I | Hydrolase, alpha beta domain protein | ||
OKHHJBLH_00769 | 0.0 | mdlA2 | V | ABC transporter | ||
OKHHJBLH_00770 | 7.2e-278 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
OKHHJBLH_00771 | 1.9e-236 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
OKHHJBLH_00772 | 7e-43 | E | ABC transporter, substrate-binding protein, family 5 | |||
OKHHJBLH_00773 | 8e-60 | E | ABC transporter, substrate-binding protein, family 5 | |||
OKHHJBLH_00774 | 3e-240 | 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 | |
OKHHJBLH_00775 | 1.4e-113 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
OKHHJBLH_00776 | 2.8e-214 | iunH1 | 3.2.2.1 | F | nucleoside hydrolase | |
OKHHJBLH_00777 | 5.3e-206 | P | NMT1/THI5 like | |||
OKHHJBLH_00778 | 4.8e-18 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
OKHHJBLH_00779 | 3.3e-57 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
OKHHJBLH_00780 | 5.4e-29 | E | Receptor family ligand binding region | |||
OKHHJBLH_00781 | 1.1e-195 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_00782 | 3.4e-55 | DJ | Addiction module toxin, RelE StbE family | |||
OKHHJBLH_00783 | 5.9e-49 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
OKHHJBLH_00784 | 1.7e-125 | S | Short repeat of unknown function (DUF308) | |||
OKHHJBLH_00785 | 3.5e-168 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00787 | 5e-143 | 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 | ||
OKHHJBLH_00788 | 2.1e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
OKHHJBLH_00789 | 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 | |
OKHHJBLH_00790 | 3.1e-17 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
OKHHJBLH_00791 | 1.9e-49 | 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 | |
OKHHJBLH_00792 | 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 | |
OKHHJBLH_00793 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
OKHHJBLH_00794 | 6.1e-52 | 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 | |
OKHHJBLH_00795 | 8.9e-108 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
OKHHJBLH_00796 | 2.1e-192 | holB | 2.7.7.7 | L | DNA polymerase III | |
OKHHJBLH_00797 | 4.7e-91 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_00798 | 7.5e-239 | G | Transporter major facilitator family protein | |||
OKHHJBLH_00799 | 8e-93 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
OKHHJBLH_00800 | 1.4e-50 | pknL | 2.7.11.1 | KLT | PASTA | |
OKHHJBLH_00801 | 9.1e-198 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
OKHHJBLH_00802 | 1.1e-118 | |||||
OKHHJBLH_00803 | 5e-301 | E | ABC transporter, substrate-binding protein, family 5 | |||
OKHHJBLH_00804 | 4.9e-176 | iaaA | 3.4.19.5, 3.5.1.1 | E | Asparaginase | |
OKHHJBLH_00805 | 2.2e-96 | S | GtrA-like protein | |||
OKHHJBLH_00806 | 2.1e-263 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_00807 | 5.4e-253 | 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 | |
OKHHJBLH_00808 | 4.5e-71 | yvbK | 3.1.3.25 | K | Acetyltransferase (GNAT) domain | |
OKHHJBLH_00809 | 2.5e-140 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
OKHHJBLH_00810 | 2.1e-210 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_00811 | 2.6e-98 | araB | 2.7.1.16, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
OKHHJBLH_00812 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
OKHHJBLH_00813 | 5.3e-116 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
OKHHJBLH_00814 | 1.6e-174 | S | Protein of unknown function DUF58 | |||
OKHHJBLH_00815 | 3.6e-91 | |||||
OKHHJBLH_00816 | 6.8e-34 | E | ABC transporter, substrate-binding protein, family 5 | |||
OKHHJBLH_00818 | 1.6e-171 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
OKHHJBLH_00819 | 2.8e-34 | |||||
OKHHJBLH_00820 | 1.2e-137 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
OKHHJBLH_00821 | 6.1e-257 | 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 |
OKHHJBLH_00822 | 1.7e-63 | I | Sterol carrier protein | |||
OKHHJBLH_00823 | 1.4e-41 | S | Protein of unknown function (DUF3073) | |||
OKHHJBLH_00824 | 2.1e-29 | mphA | S | Aminoglycoside phosphotransferase | ||
OKHHJBLH_00825 | 3.6e-32 | S | Protein of unknown function (DUF3107) | |||
OKHHJBLH_00826 | 5e-173 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
OKHHJBLH_00827 | 4.8e-117 | S | Vitamin K epoxide reductase | |||
OKHHJBLH_00828 | 1.9e-59 | 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 | |
OKHHJBLH_00829 | 8.6e-47 | |||||
OKHHJBLH_00830 | 3.3e-129 | S | HAD hydrolase, family IA, variant 3 | |||
OKHHJBLH_00832 | 2.6e-144 | G | MFS/sugar transport protein | |||
OKHHJBLH_00833 | 5.2e-60 | ansA | 3.5.1.1 | EJ | Asparaginase | |
OKHHJBLH_00834 | 0.0 | cadA | P | E1-E2 ATPase | ||
OKHHJBLH_00837 | 5.4e-181 | S | Auxin Efflux Carrier | |||
OKHHJBLH_00838 | 9.7e-52 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
OKHHJBLH_00839 | 3.9e-21 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_00840 | 0.0 | abfA1 | 3.2.1.55 | GH51 | G | arabinose metabolic process |
OKHHJBLH_00841 | 3.8e-38 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
OKHHJBLH_00842 | 2.5e-80 | |||||
OKHHJBLH_00843 | 6.2e-177 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
OKHHJBLH_00844 | 3.7e-53 | M | Protein of unknown function (DUF3152) | |||
OKHHJBLH_00845 | 1.1e-96 | K | Bacterial regulatory proteins, tetR family | |||
OKHHJBLH_00846 | 3.5e-193 | S | Psort location CytoplasmicMembrane, score | |||
OKHHJBLH_00847 | 2.8e-162 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
OKHHJBLH_00848 | 4.2e-223 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
OKHHJBLH_00849 | 6.9e-202 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
OKHHJBLH_00850 | 2.8e-128 | lipA | I | Hydrolase, alpha beta domain protein | ||
OKHHJBLH_00851 | 5e-27 | S | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_00852 | 3.8e-156 | I | alpha/beta hydrolase fold | |||
OKHHJBLH_00853 | 6.1e-59 | M | Protein of unknown function (DUF2961) | |||
OKHHJBLH_00854 | 1e-284 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
OKHHJBLH_00855 | 1.1e-130 | K | LytTr DNA-binding domain | |||
OKHHJBLH_00856 | 2.6e-49 | T | GHKL domain | |||
OKHHJBLH_00857 | 6.6e-15 | T | GHKL domain | |||
OKHHJBLH_00858 | 5.2e-65 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
OKHHJBLH_00859 | 1.1e-133 | S | UPF0126 domain | |||
OKHHJBLH_00860 | 2.9e-33 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
OKHHJBLH_00861 | 1.2e-141 | 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 | ||
OKHHJBLH_00862 | 1.6e-71 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
OKHHJBLH_00863 | 1.7e-140 | ybbL | V | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00864 | 5.3e-63 | S | Putative esterase | |||
OKHHJBLH_00865 | 1.3e-41 | S | Putative esterase | |||
OKHHJBLH_00866 | 3.3e-118 | K | Cro/C1-type HTH DNA-binding domain | |||
OKHHJBLH_00868 | 1.7e-87 | 3.1.21.7 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | ||
OKHHJBLH_00869 | 1.2e-88 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
OKHHJBLH_00870 | 1.4e-101 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
OKHHJBLH_00871 | 0.0 | uvrA3 | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | ||
OKHHJBLH_00872 | 2.2e-58 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_00873 | 4.6e-92 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_00875 | 5.6e-59 | |||||
OKHHJBLH_00876 | 2.7e-56 | VP1224 | V | Psort location CytoplasmicMembrane, score 9.99 | ||
OKHHJBLH_00877 | 5.2e-108 | maa | 2.3.1.18, 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
OKHHJBLH_00878 | 9.5e-141 | 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 | |
OKHHJBLH_00879 | 2.1e-109 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
OKHHJBLH_00880 | 1.4e-139 | S | SdpI/YhfL protein family | |||
OKHHJBLH_00881 | 8.4e-30 | sdpR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
OKHHJBLH_00882 | 8.6e-15 | pccB | I | Carboxyl transferase domain | ||
OKHHJBLH_00883 | 1.2e-106 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
OKHHJBLH_00884 | 6.8e-153 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
OKHHJBLH_00885 | 7.3e-109 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
OKHHJBLH_00886 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
OKHHJBLH_00887 | 1.4e-121 | S | Phospholipase/Carboxylesterase | |||
OKHHJBLH_00888 | 1.1e-239 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
OKHHJBLH_00889 | 2.7e-92 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00890 | 4.7e-67 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00891 | 7e-34 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00892 | 3.4e-49 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00893 | 7.8e-25 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
OKHHJBLH_00894 | 0.0 | MV | MacB-like periplasmic core domain | |||
OKHHJBLH_00895 | 1.8e-128 | K | helix_turn_helix, Lux Regulon | |||
OKHHJBLH_00896 | 9.3e-181 | ybiR | P | Citrate transporter | ||
OKHHJBLH_00898 | 2.3e-176 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
OKHHJBLH_00900 | 2.3e-204 | araJ | EGP | Major facilitator Superfamily | ||
OKHHJBLH_00901 | 7.9e-22 | S | Domain of unknown function (DUF4037) | |||
OKHHJBLH_00902 | 4.3e-104 | S | Domain of unknown function (DUF4037) | |||
OKHHJBLH_00903 | 6e-41 | 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 | |
OKHHJBLH_00904 | 9e-81 | S | Protein of unknown function (DUF3000) | |||
OKHHJBLH_00905 | 1.9e-234 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
OKHHJBLH_00906 | 2.8e-121 | |||||
OKHHJBLH_00907 | 6.3e-122 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
OKHHJBLH_00908 | 1.4e-130 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
OKHHJBLH_00909 | 4.3e-33 | insK | L | Integrase core domain | ||
OKHHJBLH_00910 | 1.6e-20 | V | Abi-like protein | |||
OKHHJBLH_00911 | 5.8e-130 | V | Abi-like protein | |||
OKHHJBLH_00913 | 1.4e-74 | |||||
OKHHJBLH_00914 | 0.0 | crr | G | pts system, glucose-specific IIABC component | ||
OKHHJBLH_00915 | 2.6e-80 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
OKHHJBLH_00916 | 1.2e-73 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
OKHHJBLH_00917 | 1.7e-284 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
OKHHJBLH_00918 | 1e-59 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
OKHHJBLH_00919 | 3.3e-74 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
OKHHJBLH_00920 | 1.1e-39 | nrdH | O | Glutaredoxin | ||
OKHHJBLH_00921 | 5.4e-121 | K | Bacterial regulatory proteins, tetR family | |||
OKHHJBLH_00922 | 2.5e-41 | G | Transmembrane secretion effector | |||
OKHHJBLH_00923 | 4.2e-170 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
OKHHJBLH_00924 | 1.6e-155 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00925 | 1.4e-18 | E | ABC transporter, substrate-binding protein, family 5 | |||
OKHHJBLH_00926 | 1.8e-20 | 3.6.1.27 | I | PAP2 superfamily | ||
OKHHJBLH_00927 | 2.6e-261 | 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 | |
OKHHJBLH_00928 | 1.1e-144 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
OKHHJBLH_00929 | 1.3e-92 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
OKHHJBLH_00930 | 2.7e-299 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
OKHHJBLH_00931 | 6.6e-122 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
OKHHJBLH_00932 | 1.3e-88 | asrC | C | Nitrite and sulphite reductase 4Fe-4S domain | ||
OKHHJBLH_00933 | 1.7e-67 | 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 | |
OKHHJBLH_00934 | 7e-183 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
OKHHJBLH_00935 | 9.1e-77 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00936 | 1.7e-133 | 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) | |
OKHHJBLH_00937 | 4.3e-202 | cbgA_1 | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
OKHHJBLH_00938 | 4.7e-123 | mmuP | E | amino acid | ||
OKHHJBLH_00939 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
OKHHJBLH_00940 | 6.7e-139 | glnQ | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
OKHHJBLH_00941 | 1.7e-171 | glnP | E | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_00942 | 9e-22 | 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 | |
OKHHJBLH_00943 | 9.5e-186 | V | Acetyltransferase (GNAT) domain | |||
OKHHJBLH_00944 | 6.1e-219 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
OKHHJBLH_00945 | 2.1e-260 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_00946 | 3.9e-187 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_00947 | 1.3e-152 | 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 | ||
OKHHJBLH_00948 | 5.1e-158 | G | Fructosamine kinase | |||
OKHHJBLH_00949 | 4.4e-59 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
OKHHJBLH_00950 | 5.4e-53 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
OKHHJBLH_00951 | 1.3e-96 | K | MarR family | |||
OKHHJBLH_00952 | 1.4e-105 | V | ABC transporter, ATP-binding protein | |||
OKHHJBLH_00954 | 3.8e-137 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
OKHHJBLH_00955 | 1.8e-56 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
OKHHJBLH_00956 | 3.6e-139 | 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 | |||
OKHHJBLH_00957 | 9e-69 | carD | K | CarD-like/TRCF domain | ||
OKHHJBLH_00958 | 7.8e-88 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
OKHHJBLH_00959 | 3.9e-140 | znuB | U | ABC 3 transport family | ||
OKHHJBLH_00960 | 1.3e-128 | znuC | P | ATPases associated with a variety of cellular activities | ||
OKHHJBLH_00961 | 1.6e-310 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
OKHHJBLH_00962 | 6.8e-118 | K | Periplasmic binding protein domain | |||
OKHHJBLH_00963 | 4.5e-217 | S | Metal-independent alpha-mannosidase (GH125) | |||
OKHHJBLH_00964 | 7.9e-27 | |||||
OKHHJBLH_00965 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
OKHHJBLH_00966 | 1e-15 | pepD | E | Peptidase family C69 | ||
OKHHJBLH_00967 | 4e-195 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
OKHHJBLH_00968 | 4.4e-86 | icaR | K | Bacterial regulatory proteins, tetR family | ||
OKHHJBLH_00969 | 1.1e-29 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
OKHHJBLH_00970 | 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 | |
OKHHJBLH_00971 | 2e-178 | S | Endonuclease/Exonuclease/phosphatase family | |||
OKHHJBLH_00972 | 3.9e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
OKHHJBLH_00973 | 1.8e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
OKHHJBLH_00974 | 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 | ||
OKHHJBLH_00975 | 2.3e-150 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
OKHHJBLH_00976 | 1.4e-104 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
OKHHJBLH_00977 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
OKHHJBLH_00978 | 8.4e-30 | rpmB | J | Ribosomal L28 family | ||
OKHHJBLH_00979 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_00980 | 4.3e-240 | yxiO | S | Vacuole effluxer Atg22 like | ||
OKHHJBLH_00981 | 9.6e-127 | gntR | K | FCD | ||
OKHHJBLH_00982 | 2.8e-83 | gntK | 2.7.1.12 | F | Shikimate kinase | |
OKHHJBLH_00983 | 3.6e-200 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
OKHHJBLH_00984 | 4e-88 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
OKHHJBLH_00985 | 0.0 | cotH | M | CotH kinase protein | ||
OKHHJBLH_00986 | 1.7e-94 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
OKHHJBLH_00987 | 2.2e-60 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
OKHHJBLH_00988 | 1.1e-178 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
OKHHJBLH_00989 | 2.7e-134 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
OKHHJBLH_00990 | 6.2e-42 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
OKHHJBLH_00991 | 2.4e-135 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00992 | 2.1e-91 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_00993 | 0.0 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
OKHHJBLH_00994 | 0.0 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
OKHHJBLH_00995 | 3.2e-204 | murB | 1.3.1.98 | M | Cell wall formation | |
OKHHJBLH_00996 | 5.5e-25 | rpmG | J | Ribosomal protein L33 | ||
OKHHJBLH_01000 | 2.5e-56 | ctpE | P | E1-E2 ATPase | ||
OKHHJBLH_01001 | 1.4e-91 | |||||
OKHHJBLH_01002 | 1.9e-62 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
OKHHJBLH_01003 | 3.8e-195 | S | alpha beta | |||
OKHHJBLH_01004 | 1.3e-25 | yhjX | EGP | Major facilitator Superfamily | ||
OKHHJBLH_01005 | 1.3e-29 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_01006 | 4.3e-159 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
OKHHJBLH_01007 | 8.6e-27 | VP1224 | V | Psort location CytoplasmicMembrane, score 9.99 | ||
OKHHJBLH_01008 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
OKHHJBLH_01009 | 1.2e-126 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
OKHHJBLH_01010 | 2.3e-176 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
OKHHJBLH_01011 | 1.9e-124 | 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 | ||
OKHHJBLH_01012 | 3.5e-252 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
OKHHJBLH_01013 | 8.1e-244 | dinF | V | MatE | ||
OKHHJBLH_01014 | 7.9e-19 | S | LPXTG-motif cell wall anchor domain protein | |||
OKHHJBLH_01015 | 1e-06 | V | ABC transporter, ATP-binding protein | |||
OKHHJBLH_01016 | 3.8e-96 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
OKHHJBLH_01018 | 2.9e-17 | |||||
OKHHJBLH_01020 | 1.5e-17 | L | HNH endonuclease | |||
OKHHJBLH_01021 | 8e-116 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
OKHHJBLH_01022 | 5e-179 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
OKHHJBLH_01023 | 1.3e-168 | pknL | 2.7.11.1 | KLT | PASTA | |
OKHHJBLH_01024 | 1.5e-132 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
OKHHJBLH_01025 | 4.1e-95 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
OKHHJBLH_01026 | 1.1e-168 | |||||
OKHHJBLH_01027 | 5.4e-127 | adhB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
OKHHJBLH_01028 | 5.3e-144 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
OKHHJBLH_01029 | 6e-108 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
OKHHJBLH_01030 | 1.8e-19 | helY | L | DEAD DEAH box helicase | ||
OKHHJBLH_01031 | 3.9e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
OKHHJBLH_01032 | 3e-141 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
OKHHJBLH_01033 | 3e-54 | |||||
OKHHJBLH_01034 | 2.5e-258 | pepD | E | Peptidase family C69 | ||
OKHHJBLH_01035 | 1.5e-145 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
OKHHJBLH_01036 | 4.9e-24 | ilvN | 2.2.1.6 | E | ACT domain | |
OKHHJBLH_01038 | 6.4e-96 | |||||
OKHHJBLH_01039 | 2.7e-120 | yjjK | S | ABC transporter | ||
OKHHJBLH_01040 | 6.5e-226 | M | Glycosyl transferase 4-like domain | |||
OKHHJBLH_01041 | 2.9e-132 | 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 | |
OKHHJBLH_01042 | 3.9e-93 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
OKHHJBLH_01043 | 1.1e-148 | rmuC | S | RmuC family | ||
OKHHJBLH_01044 | 3.7e-10 | S | LPXTG-motif cell wall anchor domain protein | |||
OKHHJBLH_01045 | 2.3e-72 | S | GtrA-like protein | |||
OKHHJBLH_01046 | 0.0 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
OKHHJBLH_01047 | 4.9e-120 | ybjG | 3.6.1.27 | I | Psort location CytoplasmicMembrane, score | |
OKHHJBLH_01048 | 5.3e-80 | ypeA | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_01049 | 1.1e-113 | vex2 | V | ABC transporter, ATP-binding protein | ||
OKHHJBLH_01050 | 1e-213 | vex1 | V | Efflux ABC transporter, permease protein | ||
OKHHJBLH_01051 | 3.4e-242 | vex3 | V | ABC transporter permease | ||
OKHHJBLH_01052 | 1.1e-17 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
OKHHJBLH_01053 | 9.7e-43 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
OKHHJBLH_01054 | 3.2e-09 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
OKHHJBLH_01055 | 1.1e-227 | yhjX | EGP | Major facilitator Superfamily | ||
OKHHJBLH_01056 | 0.0 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
OKHHJBLH_01057 | 1.7e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
OKHHJBLH_01058 | 1e-275 | 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 | |
OKHHJBLH_01059 | 1.9e-11 | V | Beta-lactamase | |||
OKHHJBLH_01060 | 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 | |
OKHHJBLH_01061 | 2.3e-98 | ribD | 1.1.1.193, 3.5.4.26 | H | Cytidine and deoxycytidylate deaminase zinc-binding region | |
OKHHJBLH_01062 | 1e-140 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
OKHHJBLH_01063 | 6.1e-122 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
OKHHJBLH_01064 | 9.7e-93 | |||||
OKHHJBLH_01065 | 9.9e-84 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
OKHHJBLH_01066 | 1.2e-111 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
OKHHJBLH_01067 | 1.6e-158 | S | IMP dehydrogenase activity | |||
OKHHJBLH_01068 | 4.8e-15 | ybiT | S | ABC transporter | ||
OKHHJBLH_01069 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
OKHHJBLH_01070 | 5.7e-21 | E | Transglutaminase-like superfamily | |||
OKHHJBLH_01071 | 1.4e-84 | E | Transglutaminase-like superfamily | |||
OKHHJBLH_01072 | 2.1e-51 | S | Protein of unknown function DUF58 | |||
OKHHJBLH_01073 | 4.2e-200 | lhr | L | DEAD DEAH box helicase | ||
OKHHJBLH_01074 | 8.3e-102 | lhr | L | DEAD DEAH box helicase | ||
OKHHJBLH_01075 | 3.5e-274 | rfbP | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
OKHHJBLH_01076 | 1e-187 | |||||
OKHHJBLH_01077 | 8.1e-40 | V | Abi-like protein | |||
OKHHJBLH_01078 | 4e-46 | V | Abi-like protein | |||
OKHHJBLH_01079 | 4.1e-35 | S | enterobacterial common antigen metabolic process | |||
OKHHJBLH_01080 | 4.6e-114 | S | enterobacterial common antigen metabolic process | |||
OKHHJBLH_01082 | 2.2e-20 | pslL | G | Acyltransferase family | ||
OKHHJBLH_01083 | 1.8e-85 | |||||
OKHHJBLH_01084 | 8.1e-69 | M | Glycosyltransferase, group 1 family protein | |||
OKHHJBLH_01085 | 3.3e-79 | H | Hexapeptide repeat of succinyl-transferase | |||
OKHHJBLH_01086 | 3.5e-90 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
OKHHJBLH_01087 | 1.8e-251 | cps2J | S | Polysaccharide biosynthesis protein | ||
OKHHJBLH_01088 | 1.5e-239 | MA20_17390 | GT4 | M | Glycosyl transferases group 1 | |
OKHHJBLH_01089 | 5e-90 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
OKHHJBLH_01090 | 5.8e-92 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
OKHHJBLH_01091 | 4.9e-36 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
OKHHJBLH_01092 | 6.3e-50 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
OKHHJBLH_01093 | 3.9e-72 | yjjP | S | Threonine/Serine exporter, ThrE | ||
OKHHJBLH_01094 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
OKHHJBLH_01096 | 8.2e-120 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
OKHHJBLH_01097 | 1e-240 | ytfL | P | Transporter associated domain | ||
OKHHJBLH_01098 | 3.8e-187 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
OKHHJBLH_01099 | 3.1e-101 | S | Protein of unknown function DUF45 | |||
OKHHJBLH_01103 | 6.1e-56 | 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 | ||
OKHHJBLH_01104 | 1.2e-260 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
OKHHJBLH_01105 | 3.3e-68 | S | Transmembrane domain of unknown function (DUF3566) | |||
OKHHJBLH_01106 | 1.4e-277 | 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 | |
OKHHJBLH_01107 | 6.1e-120 | rafG | G | ABC transporter permease | ||
OKHHJBLH_01108 | 7.6e-106 | S | Protein of unknown function, DUF624 | |||
OKHHJBLH_01109 | 7e-21 | S | Transposon-encoded protein TnpV | |||
OKHHJBLH_01110 | 5.4e-118 | 3.2.1.37 | GH43 | G | Glycosyl hydrolases family 43 | |
OKHHJBLH_01111 | 3.1e-239 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
OKHHJBLH_01112 | 4.9e-134 | |||||
OKHHJBLH_01113 | 4.9e-134 | KT | Transcriptional regulatory protein, C terminal | |||
OKHHJBLH_01114 | 2.7e-154 | ypfH | S | Phospholipase/Carboxylesterase | ||
OKHHJBLH_01115 | 4e-112 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
OKHHJBLH_01116 | 3e-47 | S | AAA domain | |||
OKHHJBLH_01118 | 1.3e-220 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
OKHHJBLH_01119 | 1.8e-122 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
OKHHJBLH_01120 | 1.3e-221 | 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) | |
OKHHJBLH_01121 | 1.1e-211 | 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) | |
OKHHJBLH_01122 | 5.1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
OKHHJBLH_01123 | 1.3e-58 | D | nuclear chromosome segregation | |||
OKHHJBLH_01124 | 3.4e-126 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
OKHHJBLH_01125 | 2.5e-144 | 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) | |
OKHHJBLH_01126 | 4.8e-185 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
OKHHJBLH_01127 | 7e-297 | yegQ | O | Peptidase family U32 C-terminal domain | ||
OKHHJBLH_01128 | 8.3e-170 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
OKHHJBLH_01129 | 5.5e-64 | S | Predicted membrane protein (DUF2207) | |||
OKHHJBLH_01130 | 2.5e-47 | |||||
OKHHJBLH_01131 | 8.3e-221 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_01132 | 3.4e-209 | clcA_2 | P | Voltage gated chloride channel | ||
OKHHJBLH_01133 | 5.7e-16 | |||||
OKHHJBLH_01134 | 4.7e-132 | ftsK | D | FtsK SpoIIIE family protein | ||
OKHHJBLH_01135 | 6.9e-167 | 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) | |
OKHHJBLH_01136 | 8.4e-72 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_01137 | 1.2e-274 | G | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_01138 | 3.2e-253 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
OKHHJBLH_01139 | 1.3e-162 | 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 | |
OKHHJBLH_01140 | 1.8e-209 | 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 | |
OKHHJBLH_01141 | 4.7e-185 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
OKHHJBLH_01142 | 1.3e-66 | rplQ | J | Ribosomal protein L17 | ||
OKHHJBLH_01143 | 3.5e-41 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
OKHHJBLH_01144 | 9.2e-71 | pdxH | S | Pfam:Pyridox_oxidase | ||
OKHHJBLH_01145 | 3.5e-166 | XK27_00240 | K | Fic/DOC family | ||
OKHHJBLH_01146 | 3.5e-12 | typA | T | Elongation factor G C-terminus | ||
OKHHJBLH_01147 | 4e-104 | |||||
OKHHJBLH_01148 | 1.3e-190 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
OKHHJBLH_01149 | 1.1e-194 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
OKHHJBLH_01150 | 9.4e-88 | pdtaR | T | Response regulator receiver domain protein | ||
OKHHJBLH_01151 | 2.2e-131 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
OKHHJBLH_01152 | 4.4e-124 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
OKHHJBLH_01153 | 6.8e-153 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
OKHHJBLH_01154 | 1.4e-86 | xerD | D | recombinase XerD | ||
OKHHJBLH_01155 | 6.6e-209 | KLT | Lanthionine synthetase C-like protein | |||
OKHHJBLH_01156 | 3.2e-220 | S | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_01157 | 6.3e-72 | S | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_01158 | 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 | ||
OKHHJBLH_01159 | 2.9e-129 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
OKHHJBLH_01160 | 2.3e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
OKHHJBLH_01161 | 1.8e-28 | V | FtsX-like permease family | |||
OKHHJBLH_01162 | 4.6e-149 | lolD | V | ABC transporter | ||
OKHHJBLH_01163 | 3.1e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
OKHHJBLH_01164 | 1.2e-28 | J | TM2 domain | |||
OKHHJBLH_01165 | 9.1e-217 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
OKHHJBLH_01166 | 1.1e-125 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_01167 | 1.9e-152 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_01168 | 3.9e-179 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
OKHHJBLH_01169 | 6.2e-105 | K | Bacterial regulatory proteins, tetR family | |||
OKHHJBLH_01170 | 1.1e-127 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
OKHHJBLH_01171 | 9.2e-94 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
OKHHJBLH_01172 | 5.4e-33 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
OKHHJBLH_01173 | 4.1e-87 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
OKHHJBLH_01174 | 3.4e-25 | rpmD | J | Ribosomal protein L30p/L7e | ||
OKHHJBLH_01175 | 9.8e-74 | rplO | J | binds to the 23S rRNA | ||
OKHHJBLH_01176 | 1.2e-185 | cbgA_1 | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
OKHHJBLH_01177 | 3.3e-127 | 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 | |
OKHHJBLH_01178 | 8.3e-122 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase, C-terminal domain | |
OKHHJBLH_01179 | 1.4e-231 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_01180 | 6.3e-125 | K | Bacterial regulatory proteins, tetR family | |||
OKHHJBLH_01181 | 1.6e-227 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
OKHHJBLH_01182 | 3.8e-229 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
OKHHJBLH_01183 | 1.7e-137 | M | Mechanosensitive ion channel | |||
OKHHJBLH_01184 | 7.4e-179 | S | CAAX protease self-immunity | |||
OKHHJBLH_01185 | 2.6e-214 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
OKHHJBLH_01186 | 2.8e-141 | U | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_01187 | 1.5e-156 | U | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_01188 | 5.8e-219 | P | Bacterial extracellular solute-binding protein | |||
OKHHJBLH_01189 | 4.2e-200 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
OKHHJBLH_01190 | 5.8e-198 | scrT | G | Transporter major facilitator family protein | ||
OKHHJBLH_01191 | 1.3e-24 | yhjE | EGP | Sugar (and other) transporter | ||
OKHHJBLH_01192 | 8.1e-29 | 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 | ||
OKHHJBLH_01193 | 1.4e-234 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_01194 | 5.6e-149 | 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 | |
OKHHJBLH_01195 | 2.5e-36 | |||||
OKHHJBLH_01196 | 3.4e-59 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
OKHHJBLH_01197 | 5.9e-285 | yliE | T | Putative diguanylate phosphodiesterase | ||
OKHHJBLH_01198 | 6.1e-102 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
OKHHJBLH_01199 | 6.8e-133 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
OKHHJBLH_01200 | 7e-14 | S | Psort location Extracellular, score 8.82 | |||
OKHHJBLH_01201 | 1.4e-121 | yorS | 3.1.3.5 | S | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | |
OKHHJBLH_01202 | 2e-12 | S | Domain of unknown function (DUF4143) | |||
OKHHJBLH_01203 | 0.0 | murJ | KLT | MviN-like protein | ||
OKHHJBLH_01204 | 4.1e-306 | murJ | KLT | MviN-like protein | ||
OKHHJBLH_01205 | 0.0 | M | Conserved repeat domain | |||
OKHHJBLH_01206 | 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 | |
OKHHJBLH_01207 | 1.7e-284 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
OKHHJBLH_01208 | 2.6e-109 | S | LytR cell envelope-related transcriptional attenuator | |||
OKHHJBLH_01209 | 1.1e-167 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
OKHHJBLH_01210 | 2e-166 | 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 | |
OKHHJBLH_01211 | 4e-39 | S | G5 | |||
OKHHJBLH_01212 | 5.1e-60 | MA20_14025 | U | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_01213 | 2.1e-235 | msmE | G | ABC transporter periplasmic binding protein YcjN precursor K02027 | ||
OKHHJBLH_01214 | 8e-301 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
OKHHJBLH_01215 | 3.2e-25 | 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 | |
OKHHJBLH_01216 | 5.9e-55 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
OKHHJBLH_01217 | 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 | ||
OKHHJBLH_01218 | 1.2e-23 | azlC | E | AzlC protein | ||
OKHHJBLH_01219 | 2.1e-88 | M | Protein of unknown function (DUF3737) | |||
OKHHJBLH_01220 | 3.2e-214 | 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 | |
OKHHJBLH_01221 | 1e-116 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
OKHHJBLH_01222 | 1.6e-39 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
OKHHJBLH_01223 | 1.1e-39 | S | Predicted membrane protein (DUF2207) | |||
OKHHJBLH_01224 | 7.6e-61 | S | Predicted membrane protein (DUF2207) | |||
OKHHJBLH_01225 | 3e-51 | lemA | S | LemA family | ||
OKHHJBLH_01227 | 4.4e-42 | V | ATPases associated with a variety of cellular activities | |||
OKHHJBLH_01228 | 3e-162 | cydD | V | ABC transporter transmembrane region | ||
OKHHJBLH_01229 | 2e-288 | umuC | 2.7.7.7 | L | DNA-damage repair protein (DNA polymerase IV) K00961 | |
OKHHJBLH_01230 | 1.5e-33 | |||||
OKHHJBLH_01231 | 3.6e-179 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
OKHHJBLH_01232 | 2.6e-121 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
OKHHJBLH_01233 | 4.5e-166 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
OKHHJBLH_01234 | 1e-182 | 1.1.1.65 | C | Aldo/keto reductase family | ||
OKHHJBLH_01235 | 1.4e-172 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
OKHHJBLH_01236 | 3.2e-138 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
OKHHJBLH_01237 | 6.3e-128 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
OKHHJBLH_01238 | 9.1e-189 | yeiI | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
OKHHJBLH_01239 | 2.5e-81 | trpF | 5.3.1.24 | E | N-(5'phosphoribosyl)anthranilate (PRA) isomerase | |
OKHHJBLH_01240 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
OKHHJBLH_01241 | 1.3e-224 | amt | U | Ammonium Transporter Family | ||
OKHHJBLH_01244 | 3.6e-168 | 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 |
OKHHJBLH_01245 | 1.8e-37 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
OKHHJBLH_01246 | 2.4e-68 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
OKHHJBLH_01247 | 2e-146 | pgl | 3.1.1.31, 3.5.99.6 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
OKHHJBLH_01248 | 2.9e-11 | |||||
OKHHJBLH_01249 | 4.3e-136 | 2.7.13.3 | T | Histidine kinase | ||
OKHHJBLH_01250 | 1e-11 | C | Aldo/keto reductase family | |||
OKHHJBLH_01251 | 7.3e-118 | S | Enoyl-(Acyl carrier protein) reductase | |||
OKHHJBLH_01252 | 1.6e-139 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
OKHHJBLH_01253 | 2e-13 | |||||
OKHHJBLH_01255 | 2.8e-66 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
OKHHJBLH_01256 | 9.5e-65 | pncA | 2.7.11.1, 3.5.1.19 | Q | Isochorismatase family | |
OKHHJBLH_01257 | 2.6e-149 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
OKHHJBLH_01258 | 3e-162 | |||||
OKHHJBLH_01259 | 3.6e-154 | 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) | |
OKHHJBLH_01260 | 1.8e-65 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
OKHHJBLH_01261 | 1.1e-44 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
OKHHJBLH_01262 | 2.4e-300 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
OKHHJBLH_01263 | 3e-46 | S | Protein of unknown function (DUF3046) | |||
OKHHJBLH_01264 | 2.3e-48 | K | Helix-turn-helix XRE-family like proteins | |||
OKHHJBLH_01265 | 1.6e-197 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
OKHHJBLH_01266 | 2.5e-39 | KT | Transcriptional regulatory protein, C terminal | |||
OKHHJBLH_01267 | 3.6e-31 | tcsS2 | T | Histidine kinase | ||
OKHHJBLH_01268 | 5.8e-81 | tcsS2 | T | Histidine kinase | ||
OKHHJBLH_01269 | 6.8e-148 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
OKHHJBLH_01270 | 2.8e-50 | 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 | |
OKHHJBLH_01272 | 2.8e-243 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
OKHHJBLH_01273 | 1.9e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
OKHHJBLH_01274 | 1.2e-55 | G | ABC transporter permease | |||
OKHHJBLH_01275 | 7.5e-164 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
OKHHJBLH_01277 | 1e-36 | |||||
OKHHJBLH_01278 | 5.7e-38 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
OKHHJBLH_01279 | 8.8e-109 | J | Acetyltransferase (GNAT) domain | |||
OKHHJBLH_01281 | 2e-62 | argE | E | Peptidase dimerisation domain | ||
OKHHJBLH_01282 | 4.4e-93 | S | Protein of unknown function (DUF3043) | |||
OKHHJBLH_01283 | 5.9e-40 | P | Zinc-uptake complex component A periplasmic | |||
OKHHJBLH_01284 | 4.8e-230 | pbuO | S | Permease family | ||
OKHHJBLH_01285 | 3.2e-45 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_01286 | 2.6e-22 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_01287 | 6.3e-29 | pip | S | YhgE Pip domain protein | ||
OKHHJBLH_01288 | 3.9e-116 | ybiT | S | ABC transporter | ||
OKHHJBLH_01289 | 4e-34 | ybiT | S | ABC transporter | ||
OKHHJBLH_01290 | 5.5e-71 | K | helix_turn_helix, arabinose operon control protein | |||
OKHHJBLH_01291 | 1.9e-155 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
OKHHJBLH_01292 | 8.5e-53 | K | helix_turn_helix ASNC type | |||
OKHHJBLH_01293 | 5.1e-142 | V | ABC transporter, ATP-binding protein | |||
OKHHJBLH_01294 | 9e-43 | clcA | P | Voltage gated chloride channel | ||
OKHHJBLH_01295 | 3.1e-149 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
OKHHJBLH_01296 | 2.7e-162 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
OKHHJBLH_01297 | 7.8e-20 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
OKHHJBLH_01298 | 3.7e-19 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
OKHHJBLH_01299 | 2e-39 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
OKHHJBLH_01300 | 1.1e-74 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
OKHHJBLH_01301 | 5.6e-08 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
OKHHJBLH_01302 | 2.4e-104 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
OKHHJBLH_01303 | 4.9e-176 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
OKHHJBLH_01304 | 1.2e-120 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
OKHHJBLH_01305 | 4.6e-64 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
OKHHJBLH_01306 | 4.9e-37 | yliE | T | Putative diguanylate phosphodiesterase | ||
OKHHJBLH_01307 | 1.1e-110 | S | Domain of unknown function (DUF4956) | |||
OKHHJBLH_01308 | 1.6e-24 | P | VTC domain | |||
OKHHJBLH_01309 | 2.5e-225 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
OKHHJBLH_01310 | 1.6e-101 | S | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_01311 | 2e-103 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
OKHHJBLH_01312 | 2.6e-71 | divIC | D | Septum formation initiator | ||
OKHHJBLH_01313 | 1e-31 | 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 | |
OKHHJBLH_01314 | 1e-87 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
OKHHJBLH_01315 | 1.3e-142 | 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 | |
OKHHJBLH_01316 | 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) | ||
OKHHJBLH_01317 | 5e-80 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
OKHHJBLH_01318 | 5.2e-162 | ykiI | ||||
OKHHJBLH_01319 | 6.3e-127 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_01320 | 6.6e-218 | GK | ROK family | |||
OKHHJBLH_01321 | 3.1e-87 | pepD | E | Peptidase family C69 | ||
OKHHJBLH_01322 | 6.5e-46 | 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 | |
OKHHJBLH_01323 | 3.9e-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 | |
OKHHJBLH_01324 | 4.9e-125 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
OKHHJBLH_01325 | 4.2e-74 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
OKHHJBLH_01326 | 1.6e-74 | tmp1 | S | Domain of unknown function (DUF4391) | ||
OKHHJBLH_01327 | 3.9e-142 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
OKHHJBLH_01328 | 1.6e-44 | |||||
OKHHJBLH_01329 | 4.6e-12 | |||||
OKHHJBLH_01330 | 1.1e-74 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
OKHHJBLH_01331 | 5.4e-36 | |||||
OKHHJBLH_01332 | 2.5e-08 | |||||
OKHHJBLH_01334 | 2.9e-151 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
OKHHJBLH_01335 | 3e-60 | S | Thiamine-binding protein | |||
OKHHJBLH_01336 | 5.4e-60 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
OKHHJBLH_01337 | 1.4e-189 | K | Periplasmic binding protein domain | |||
OKHHJBLH_01338 | 7.4e-169 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
OKHHJBLH_01339 | 2.7e-216 | ino1 | 5.5.1.4 | I | Myo-inositol-1-phosphate synthase | |
OKHHJBLH_01340 | 3.8e-108 | |||||
OKHHJBLH_01341 | 4.6e-188 | yegU | O | ADP-ribosylglycohydrolase | ||
OKHHJBLH_01342 | 7e-189 | yegV | G | pfkB family carbohydrate kinase | ||
OKHHJBLH_01343 | 1.5e-269 | U | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
OKHHJBLH_01344 | 1.5e-103 | Q | Isochorismatase family | |||
OKHHJBLH_01345 | 2.3e-214 | S | Choline/ethanolamine kinase | |||
OKHHJBLH_01346 | 1.6e-274 | eat | E | Amino acid permease | ||
OKHHJBLH_01347 | 7.7e-263 | gabT | 2.6.1.19, 2.6.1.22 | H | Aminotransferase class-III | |
OKHHJBLH_01348 | 8.1e-140 | yidP | K | UTRA | ||
OKHHJBLH_01349 | 1.3e-120 | degU | K | helix_turn_helix, Lux Regulon | ||
OKHHJBLH_01350 | 1e-72 | tcsS3 | KT | PspC domain | ||
OKHHJBLH_01351 | 3.1e-278 | 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 | |
OKHHJBLH_01352 | 8.6e-58 | G | Major Facilitator Superfamily | |||
OKHHJBLH_01353 | 1e-168 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
OKHHJBLH_01354 | 1.2e-52 | dppC | EP | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_01355 | 7.7e-160 | P | Belongs to the ABC transporter superfamily | |||
OKHHJBLH_01356 | 1.7e-232 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_01357 | 1.9e-34 | S | lytic transglycosylase activity | |||
OKHHJBLH_01358 | 2.7e-227 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
OKHHJBLH_01359 | 6.6e-153 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
OKHHJBLH_01360 | 1.9e-33 | pcrA | 3.6.4.12 | L | DNA helicase | |
OKHHJBLH_01361 | 1.7e-61 | S | Domain of unknown function (DUF4418) | |||
OKHHJBLH_01362 | 6e-189 | 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 | |
OKHHJBLH_01364 | 3.6e-295 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
OKHHJBLH_01365 | 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 | |||
OKHHJBLH_01366 | 4.1e-233 | 3.2.1.156 | GH8 | G | CBM9 module, glycoside hydrolase family 8 protein and carbohydrate esterase family 4 protein K01238 | |
OKHHJBLH_01367 | 0.0 | G | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_01368 | 1e-36 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
OKHHJBLH_01369 | 1.5e-214 | dapC | E | Aminotransferase class I and II | ||
OKHHJBLH_01370 | 8.3e-59 | fdxA | C | 4Fe-4S binding domain | ||
OKHHJBLH_01371 | 2.5e-22 | E | aromatic amino acid transport protein AroP K03293 | |||
OKHHJBLH_01372 | 5e-34 | I | acetylesterase activity | |||
OKHHJBLH_01373 | 7.3e-135 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
OKHHJBLH_01374 | 2.3e-153 | mphA | S | Aminoglycoside phosphotransferase | ||
OKHHJBLH_01375 | 1e-108 | 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 | |
OKHHJBLH_01376 | 2.8e-111 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
OKHHJBLH_01377 | 7.6e-71 | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | |||
OKHHJBLH_01378 | 2.3e-53 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
OKHHJBLH_01379 | 7.5e-42 | typA | T | Elongation factor G C-terminus | ||
OKHHJBLH_01380 | 5.7e-146 | mazG | 3.6.1.66 | S | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_01381 | 9.1e-53 | 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 | ||
OKHHJBLH_01382 | 2.8e-202 | 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 | ||
OKHHJBLH_01383 | 3e-161 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
OKHHJBLH_01384 | 3.4e-26 | |||||
OKHHJBLH_01385 | 5.9e-131 | 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 | |
OKHHJBLH_01386 | 1.8e-15 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
OKHHJBLH_01387 | 6.3e-124 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
OKHHJBLH_01388 | 1.3e-91 | yebE | S | DUF218 domain | ||
OKHHJBLH_01389 | 9.6e-115 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
OKHHJBLH_01390 | 7.9e-85 | 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 | ||
OKHHJBLH_01391 | 5.2e-25 | L | transposition | |||
OKHHJBLH_01392 | 4.3e-23 | C | Acetamidase/Formamidase family | |||
OKHHJBLH_01393 | 1.7e-58 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
OKHHJBLH_01394 | 1e-75 | S | Amidohydrolase | |||
OKHHJBLH_01395 | 9.8e-150 | dapA | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
OKHHJBLH_01396 | 1e-76 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
OKHHJBLH_01397 | 5.3e-119 | ykoE | S | ABC-type cobalt transport system, permease component | ||
OKHHJBLH_01398 | 9.1e-98 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
OKHHJBLH_01399 | 3.3e-123 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
OKHHJBLH_01400 | 1.8e-75 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
OKHHJBLH_01401 | 1.1e-161 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
OKHHJBLH_01402 | 1.1e-11 | 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) | |
OKHHJBLH_01403 | 8e-96 | cyaA | 4.6.1.1 | S | CYTH | |
OKHHJBLH_01404 | 9.9e-144 | trxA2 | O | Tetratricopeptide repeat | ||
OKHHJBLH_01405 | 3.4e-89 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
OKHHJBLH_01406 | 3.5e-61 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
OKHHJBLH_01407 | 8e-85 | 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 | ||
OKHHJBLH_01408 | 2.3e-152 | L | Transposase IS116 IS110 IS902 family | |||
OKHHJBLH_01409 | 2.8e-64 | G | Transporter major facilitator family protein | |||
OKHHJBLH_01410 | 2e-150 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
OKHHJBLH_01411 | 4.1e-29 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
OKHHJBLH_01412 | 9.5e-46 | mmuP | E | amino acid | ||
OKHHJBLH_01413 | 6.2e-24 | mmuP | E | amino acid | ||
OKHHJBLH_01414 | 7e-60 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
OKHHJBLH_01416 | 2.1e-86 | rarA | L | Recombination factor protein RarA | ||
OKHHJBLH_01417 | 5.8e-160 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
OKHHJBLH_01418 | 1.7e-243 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_01419 | 4e-95 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
OKHHJBLH_01420 | 1.9e-40 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
OKHHJBLH_01421 | 2.3e-96 | 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) | |
OKHHJBLH_01422 | 6.6e-63 | 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 | |
OKHHJBLH_01423 | 8.3e-140 | glpR | K | DeoR C terminal sensor domain | ||
OKHHJBLH_01424 | 3.7e-171 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
OKHHJBLH_01425 | 3.6e-219 | S | Psort location Cytoplasmic, score 8.87 | |||
OKHHJBLH_01426 | 4.1e-124 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
OKHHJBLH_01428 | 4e-34 | rodA | D | Belongs to the SEDS family | ||
OKHHJBLH_01429 | 1.1e-70 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
OKHHJBLH_01430 | 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 | |
OKHHJBLH_01431 | 2.8e-128 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
OKHHJBLH_01432 | 1.6e-45 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_01433 | 4.9e-110 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
OKHHJBLH_01434 | 6.8e-87 | P | Sodium/hydrogen exchanger family | |||
OKHHJBLH_01435 | 0.0 | V | FtsX-like permease family | |||
OKHHJBLH_01436 | 4.1e-270 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
OKHHJBLH_01437 | 8.3e-12 | S | Protein of unknown function, DUF624 | |||
OKHHJBLH_01438 | 2.5e-189 | K | helix_turn _helix lactose operon repressor | |||
OKHHJBLH_01439 | 4.4e-40 | G | beta-mannosidase | |||
OKHHJBLH_01440 | 0.0 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
OKHHJBLH_01441 | 5.6e-82 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
OKHHJBLH_01442 | 8.6e-107 | 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) | |
OKHHJBLH_01443 | 2.9e-136 | G | Phosphoglycerate mutase family | |||
OKHHJBLH_01444 | 6.6e-259 | amyE | G | Bacterial extracellular solute-binding protein | ||
OKHHJBLH_01445 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
OKHHJBLH_01446 | 1.4e-264 | amyE | G | Bacterial extracellular solute-binding protein | ||
OKHHJBLH_01447 | 7e-187 | K | Periplasmic binding protein-like domain | |||
OKHHJBLH_01448 | 1.7e-182 | K | Psort location Cytoplasmic, score | |||
OKHHJBLH_01449 | 3.7e-154 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
OKHHJBLH_01450 | 3.7e-187 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
OKHHJBLH_01451 | 9.4e-33 | S | Domain of unknown function (DUF5067) | |||
OKHHJBLH_01452 | 3.2e-216 | 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 |
OKHHJBLH_01453 | 1.9e-40 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
OKHHJBLH_01454 | 2.5e-13 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
OKHHJBLH_01455 | 2.9e-113 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
OKHHJBLH_01456 | 1.1e-101 | hgdC | I | BadF/BadG/BcrA/BcrD ATPase family | ||
OKHHJBLH_01457 | 7.4e-55 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
OKHHJBLH_01458 | 5.9e-120 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
OKHHJBLH_01459 | 8.2e-57 | pepE | 3.4.13.21 | E | Peptidase family S51 | |
OKHHJBLH_01460 | 4.6e-88 | 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) | |
OKHHJBLH_01461 | 1.3e-55 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
OKHHJBLH_01462 | 1.1e-19 | S | Domain of unknown function (DUF4191) | |||
OKHHJBLH_01463 | 1.2e-144 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
OKHHJBLH_01464 | 4.6e-74 | E | ABC transporter, substrate-binding protein, family 5 | |||
OKHHJBLH_01465 | 5.1e-96 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_01466 | 8.9e-34 | 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) | |
OKHHJBLH_01467 | 1.1e-106 | S | Phosphatidylethanolamine-binding protein | |||
OKHHJBLH_01468 | 2.1e-99 | luxE | 6.2.1.19 | H | long-chain-fatty-acid--luciferin-component ligase, acyl-protein synthase | |
OKHHJBLH_01469 | 1.1e-110 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
OKHHJBLH_01470 | 1.3e-47 | K | helix_turn_helix ASNC type | |||
OKHHJBLH_01471 | 4.5e-132 | P | Cobalt transport protein | |||
OKHHJBLH_01472 | 3.2e-16 | S | Protein of unknown function (DUF3071) | |||
OKHHJBLH_01473 | 4.5e-160 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
OKHHJBLH_01474 | 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 | ||
OKHHJBLH_01475 | 3.8e-96 | 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 | ||
OKHHJBLH_01476 | 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 | |
OKHHJBLH_01477 | 1.3e-105 | phoH | T | PhoH-like protein | ||
OKHHJBLH_01478 | 8.3e-135 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
OKHHJBLH_01479 | 1.7e-60 | safC | S | O-methyltransferase | ||
OKHHJBLH_01481 | 7.7e-101 | K | acetyltransferase | |||
OKHHJBLH_01482 | 3.4e-135 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
OKHHJBLH_01483 | 1.4e-96 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
OKHHJBLH_01484 | 3.9e-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 | |
OKHHJBLH_01485 | 2.7e-48 | yitI | S | Acetyltransferase (GNAT) domain | ||
OKHHJBLH_01486 | 2.4e-115 | |||||
OKHHJBLH_01487 | 9.3e-300 | S | Calcineurin-like phosphoesterase | |||
OKHHJBLH_01488 | 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) | |
OKHHJBLH_01489 | 4e-197 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
OKHHJBLH_01490 | 5.3e-40 | GK | ROK family | |||
OKHHJBLH_01491 | 7.5e-88 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
OKHHJBLH_01492 | 1.7e-93 | 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 | |
OKHHJBLH_01494 | 4.4e-198 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
OKHHJBLH_01495 | 1.1e-184 | 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 | |
OKHHJBLH_01496 | 1.4e-26 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
OKHHJBLH_01497 | 4.9e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
OKHHJBLH_01498 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
OKHHJBLH_01499 | 1.7e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
OKHHJBLH_01501 | 1.2e-104 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
OKHHJBLH_01502 | 2.1e-182 | rhaR_1 | K | helix_turn_helix, arabinose operon control protein | ||
OKHHJBLH_01503 | 6.2e-196 | Z012_01000 | 1.1.1.14, 1.1.1.9 | C | Zinc-binding dehydrogenase | |
OKHHJBLH_01504 | 1.5e-250 | EGP | Major facilitator Superfamily | |||
OKHHJBLH_01505 | 2e-216 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
OKHHJBLH_01506 | 1.4e-76 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
OKHHJBLH_01507 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
OKHHJBLH_01508 | 3.4e-67 | rpsI | J | Belongs to the universal ribosomal protein uS9 family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)