ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
IBEOJHIK_00001 | 6e-117 | S | Belongs to the UPF0246 family | |||
IBEOJHIK_00002 | 1.9e-228 | tnp | L | MULE transposase domain | ||
IBEOJHIK_00003 | 4.7e-10 | |||||
IBEOJHIK_00004 | 1.7e-19 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
IBEOJHIK_00005 | 7.8e-196 | I | Acyltransferase | |||
IBEOJHIK_00006 | 3.4e-19 | |||||
IBEOJHIK_00007 | 2.1e-199 | pepF2 | E | Oligopeptidase F | ||
IBEOJHIK_00008 | 4.9e-243 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
IBEOJHIK_00009 | 3.1e-81 | |||||
IBEOJHIK_00010 | 5.3e-116 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
IBEOJHIK_00011 | 1.1e-57 | M | Lysin motif | |||
IBEOJHIK_00012 | 6.8e-20 | S | the current gene model (or a revised gene model) may contain one or more premature stops and or frameshifts | |||
IBEOJHIK_00013 | 2.4e-71 | S | COG NOG38524 non supervised orthologous group | |||
IBEOJHIK_00014 | 6.1e-35 | |||||
IBEOJHIK_00015 | 0.0 | V | ABC transporter | |||
IBEOJHIK_00016 | 8.9e-221 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
IBEOJHIK_00017 | 1.5e-236 | comFA | L | Helicase C-terminal domain protein | ||
IBEOJHIK_00018 | 1.3e-90 | comFC | S | Competence protein | ||
IBEOJHIK_00019 | 0.0 | sca1 | G | Belongs to the glycosyl hydrolase 31 family | ||
IBEOJHIK_00020 | 3.8e-210 | ftsW | D | Belongs to the SEDS family | ||
IBEOJHIK_00021 | 1.3e-44 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IBEOJHIK_00022 | 3.3e-177 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IBEOJHIK_00023 | 5.2e-153 | ptlF | S | KR domain | ||
IBEOJHIK_00024 | 7.7e-146 | CcmA5 | V | ABC transporter | ||
IBEOJHIK_00025 | 6.6e-70 | S | ECF-type riboflavin transporter, S component | |||
IBEOJHIK_00026 | 5.1e-40 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
IBEOJHIK_00027 | 8.4e-148 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
IBEOJHIK_00028 | 9.5e-220 | yttB | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00030 | 4.2e-77 | S | CAAX protease self-immunity | |||
IBEOJHIK_00031 | 1.1e-84 | V | Best Blastp hit gi 7514214 pir G75157 'abc transporter, ATP-binding protein, puta tive PAB2069 - Pyrococcus abyssi (strain Orsay)' gi 5457852 emb CAB49342.1 '(AJ248284) ABC transporter, ATP-binding protein, puta tive Pyrococcus abyssi ', score 77, E-value 3.00E-13 | |||
IBEOJHIK_00032 | 2.1e-78 | ebgA | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
IBEOJHIK_00033 | 3.9e-49 | K | Transcriptional regulator, LysR family | |||
IBEOJHIK_00034 | 1e-75 | K | DNA-binding transcription factor activity | |||
IBEOJHIK_00035 | 1.6e-74 | glnP | P | ABC transporter permease | ||
IBEOJHIK_00036 | 6.3e-215 | lsgC | M | Glycosyl transferases group 1 | ||
IBEOJHIK_00037 | 0.0 | yebA | E | Transglutaminase/protease-like homologues | ||
IBEOJHIK_00038 | 1.2e-158 | yeaD | S | Protein of unknown function DUF58 | ||
IBEOJHIK_00039 | 1.5e-169 | yeaC | S | ATPase family associated with various cellular activities (AAA) | ||
IBEOJHIK_00040 | 6.7e-105 | S | Stage II sporulation protein M | |||
IBEOJHIK_00041 | 1.1e-155 | 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 | |
IBEOJHIK_00042 | 5.4e-141 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
IBEOJHIK_00043 | 2.1e-165 | yvgN | C | Aldo keto reductase | ||
IBEOJHIK_00044 | 8.7e-142 | iolR | K | DeoR C terminal sensor domain | ||
IBEOJHIK_00045 | 2.3e-268 | iolT | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00046 | 0.0 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
IBEOJHIK_00047 | 8.9e-136 | epsG | 2.4.1.293 | GT2 | M | Glycosyltransferase like family 2 |
IBEOJHIK_00050 | 1.1e-138 | lacT | K | PRD domain | ||
IBEOJHIK_00051 | 1.1e-109 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
IBEOJHIK_00052 | 5.7e-95 | copB | 3.6.3.4 | P | P-type ATPase | |
IBEOJHIK_00053 | 1.9e-92 | |||||
IBEOJHIK_00054 | 7.7e-193 | |||||
IBEOJHIK_00055 | 6.4e-249 | |||||
IBEOJHIK_00056 | 2.1e-111 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
IBEOJHIK_00057 | 1.2e-97 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
IBEOJHIK_00058 | 5.1e-106 | nodB3 | G | Polysaccharide deacetylase | ||
IBEOJHIK_00059 | 2.6e-11 | nodB3 | G | Polysaccharide deacetylase | ||
IBEOJHIK_00060 | 1.6e-114 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
IBEOJHIK_00061 | 1.7e-257 | yifK | E | Amino acid permease | ||
IBEOJHIK_00062 | 3.1e-178 | S | Protein of unknown function (DUF3800) | |||
IBEOJHIK_00063 | 4.1e-101 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | 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 |
IBEOJHIK_00064 | 1.1e-143 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | 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 |
IBEOJHIK_00065 | 7.7e-252 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
IBEOJHIK_00066 | 6.2e-154 | 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 | |
IBEOJHIK_00067 | 8e-177 | XK27_08835 | S | ABC transporter | ||
IBEOJHIK_00068 | 2.1e-81 | F | DNA/RNA non-specific endonuclease | |||
IBEOJHIK_00069 | 2.9e-47 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
IBEOJHIK_00070 | 1.4e-43 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
IBEOJHIK_00071 | 6.7e-78 | K | Transcriptional regulator | |||
IBEOJHIK_00072 | 5.7e-239 | iolT | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00073 | 7.3e-68 | radC | L | DNA repair protein | ||
IBEOJHIK_00074 | 1.7e-56 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
IBEOJHIK_00075 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
IBEOJHIK_00076 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
IBEOJHIK_00077 | 3.6e-79 | ctsR | K | Belongs to the CtsR family | ||
IBEOJHIK_00080 | 2.7e-171 | frvR | K | Mga helix-turn-helix domain | ||
IBEOJHIK_00081 | 4.8e-16 | |||||
IBEOJHIK_00082 | 7e-24 | citM | C | Citrate transporter | ||
IBEOJHIK_00083 | 1.3e-41 | |||||
IBEOJHIK_00084 | 1.8e-101 | kptA | J | Removes the 2'-phosphate from RNA via an intermediate in which the phosphate is ADP-ribosylated by NAD followed by a presumed transesterification to release the RNA and generate ADP- ribose 1''-2''-cyclic phosphate (APPR P). May function as an ADP- ribosylase | ||
IBEOJHIK_00085 | 9.3e-89 | K | Acetyltransferase (GNAT) domain | |||
IBEOJHIK_00086 | 2.4e-110 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
IBEOJHIK_00087 | 9.9e-58 | K | Transcriptional regulator PadR-like family | |||
IBEOJHIK_00088 | 4.6e-103 | ORF00048 | ||||
IBEOJHIK_00089 | 3.3e-138 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
IBEOJHIK_00090 | 4.4e-169 | yjjC | V | ABC transporter | ||
IBEOJHIK_00091 | 3.1e-287 | M | Exporter of polyketide antibiotics | |||
IBEOJHIK_00092 | 7.3e-115 | K | Transcriptional regulator | |||
IBEOJHIK_00093 | 2.4e-259 | ypiB | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00094 | 6.7e-128 | S | membrane transporter protein | |||
IBEOJHIK_00095 | 1.7e-125 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
IBEOJHIK_00096 | 5.2e-130 | K | response regulator | |||
IBEOJHIK_00097 | 2.6e-92 | phoR | 2.7.13.3 | T | Histidine kinase | |
IBEOJHIK_00098 | 7.4e-203 | phoR | 2.7.13.3 | T | Histidine kinase | |
IBEOJHIK_00099 | 5.2e-156 | pstS | P | Phosphate | ||
IBEOJHIK_00100 | 3.4e-161 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
IBEOJHIK_00101 | 1.1e-156 | pstA | P | Phosphate transport system permease protein PstA | ||
IBEOJHIK_00102 | 2e-152 | yicL | EG | EamA-like transporter family | ||
IBEOJHIK_00103 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
IBEOJHIK_00104 | 7.6e-52 | rex | K | CoA binding domain | ||
IBEOJHIK_00105 | 8e-131 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
IBEOJHIK_00106 | 4.3e-197 | N | domain, Protein | |||
IBEOJHIK_00107 | 1.8e-78 | S | WxL domain surface cell wall-binding | |||
IBEOJHIK_00108 | 5.6e-33 | copZ | P | Heavy-metal-associated domain | ||
IBEOJHIK_00109 | 0.0 | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | ||
IBEOJHIK_00111 | 1e-69 | K | helix_turn_helix, mercury resistance | |||
IBEOJHIK_00112 | 4.5e-52 | S | Protein of unknown function (DUF2568) | |||
IBEOJHIK_00113 | 1.2e-214 | opuCA | E | ABC transporter, ATP-binding protein | ||
IBEOJHIK_00114 | 4.7e-106 | opuCB | E | ABC transporter permease | ||
IBEOJHIK_00115 | 5.4e-175 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
IBEOJHIK_00116 | 1.9e-110 | opuCD | P | Binding-protein-dependent transport system inner membrane component | ||
IBEOJHIK_00118 | 2.1e-149 | S | Protein of unknown function (DUF3100) | |||
IBEOJHIK_00119 | 1.9e-69 | S | An automated process has identified a potential problem with this gene model | |||
IBEOJHIK_00120 | 1.2e-249 | 3.5.4.28, 3.5.4.31 | F | Amidohydrolase family | ||
IBEOJHIK_00121 | 9.7e-122 | S | Sulfite exporter TauE/SafE | |||
IBEOJHIK_00122 | 2e-106 | K | Tetracycline repressor, C-terminal all-alpha domain | |||
IBEOJHIK_00123 | 0.0 | ydgH | S | MMPL family | ||
IBEOJHIK_00125 | 1.1e-119 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_00126 | 9e-220 | 3.1.1.83 | I | Alpha beta hydrolase | ||
IBEOJHIK_00127 | 3.5e-247 | EGP | Major facilitator Superfamily | |||
IBEOJHIK_00128 | 2.7e-65 | S | pyridoxamine 5-phosphate | |||
IBEOJHIK_00129 | 2.3e-59 | |||||
IBEOJHIK_00130 | 6.7e-153 | M | Glycosyl hydrolase family 59 | |||
IBEOJHIK_00131 | 0.0 | M | Glycosyl hydrolase family 59 | |||
IBEOJHIK_00132 | 4.1e-192 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
IBEOJHIK_00133 | 6.2e-230 | G | Major Facilitator | |||
IBEOJHIK_00134 | 0.0 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
IBEOJHIK_00135 | 1.7e-217 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
IBEOJHIK_00136 | 2.6e-105 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
IBEOJHIK_00137 | 1.6e-168 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
IBEOJHIK_00138 | 1.3e-179 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
IBEOJHIK_00139 | 2.3e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
IBEOJHIK_00140 | 3.7e-109 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
IBEOJHIK_00141 | 1.1e-54 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
IBEOJHIK_00142 | 2.2e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
IBEOJHIK_00143 | 5.3e-127 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
IBEOJHIK_00144 | 1.7e-60 | adhR | K | helix_turn_helix, mercury resistance | ||
IBEOJHIK_00145 | 6.1e-105 | Q | Methyltransferase | |||
IBEOJHIK_00146 | 2.5e-163 | K | helix_turn_helix, arabinose operon control protein | |||
IBEOJHIK_00147 | 1.9e-113 | lysP | E | amino acid | ||
IBEOJHIK_00148 | 1.6e-57 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
IBEOJHIK_00149 | 6e-103 | pts26BCA | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IBEOJHIK_00150 | 5.2e-96 | |||||
IBEOJHIK_00152 | 7.7e-191 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
IBEOJHIK_00153 | 1e-176 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
IBEOJHIK_00154 | 7.3e-141 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
IBEOJHIK_00155 | 5.1e-268 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
IBEOJHIK_00156 | 2.4e-47 | |||||
IBEOJHIK_00157 | 9.4e-58 | |||||
IBEOJHIK_00158 | 5.6e-193 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
IBEOJHIK_00159 | 1.1e-116 | K | sequence-specific DNA binding | |||
IBEOJHIK_00160 | 2.2e-230 | inlJ | M | MucBP domain | ||
IBEOJHIK_00161 | 7.2e-300 | V | ABC transporter transmembrane region | |||
IBEOJHIK_00162 | 2.6e-62 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
IBEOJHIK_00163 | 5.3e-160 | S | Membrane | |||
IBEOJHIK_00164 | 1.1e-147 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
IBEOJHIK_00165 | 4.2e-18 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
IBEOJHIK_00166 | 2.6e-115 | L | Resolvase, N terminal domain | |||
IBEOJHIK_00167 | 3.2e-46 | ligA | 6.5.1.2 | L | BRCA1 C Terminus (BRCT) domain | |
IBEOJHIK_00168 | 1.8e-88 | |||||
IBEOJHIK_00169 | 6.1e-67 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
IBEOJHIK_00170 | 9.2e-203 | 3.4.22.70 | M | Sortase family | ||
IBEOJHIK_00171 | 3.3e-186 | M | LPXTG cell wall anchor motif | |||
IBEOJHIK_00172 | 6.4e-48 | yhbY | J | RNA-binding protein | ||
IBEOJHIK_00173 | 5.3e-80 | perR | P | Belongs to the Fur family | ||
IBEOJHIK_00174 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
IBEOJHIK_00175 | 5.1e-44 | ykuJ | S | Protein of unknown function (DUF1797) | ||
IBEOJHIK_00176 | 1e-84 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
IBEOJHIK_00177 | 1.9e-183 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
IBEOJHIK_00178 | 1e-228 | 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) | |
IBEOJHIK_00179 | 2.1e-49 | yajC | U | Preprotein translocase | ||
IBEOJHIK_00180 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
IBEOJHIK_00181 | 4.6e-91 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
IBEOJHIK_00182 | 2.8e-105 | |||||
IBEOJHIK_00184 | 5.8e-119 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
IBEOJHIK_00185 | 4.5e-86 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
IBEOJHIK_00186 | 1.9e-56 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
IBEOJHIK_00189 | 9.4e-27 | |||||
IBEOJHIK_00190 | 5.5e-132 | |||||
IBEOJHIK_00191 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
IBEOJHIK_00192 | 2.4e-207 | yxaM | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00193 | 1.2e-55 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
IBEOJHIK_00194 | 1.5e-172 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
IBEOJHIK_00195 | 4.6e-49 | |||||
IBEOJHIK_00196 | 1.1e-80 | |||||
IBEOJHIK_00197 | 3.2e-53 | |||||
IBEOJHIK_00199 | 1.3e-48 | |||||
IBEOJHIK_00200 | 6.8e-69 | comGB | NU | type II secretion system | ||
IBEOJHIK_00201 | 8.7e-144 | V | Type II restriction enzyme, methylase subunits | |||
IBEOJHIK_00202 | 2.1e-129 | L | Belongs to the 'phage' integrase family | |||
IBEOJHIK_00203 | 9.2e-53 | L | Belongs to the 'phage' integrase family | |||
IBEOJHIK_00204 | 1.5e-233 | 2.1.1.72 | V | Eco57I restriction-modification methylase | ||
IBEOJHIK_00205 | 2.4e-133 | glnQ | E | ABC transporter, ATP-binding protein | ||
IBEOJHIK_00206 | 4e-287 | glnP | P | ABC transporter permease | ||
IBEOJHIK_00208 | 1e-68 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
IBEOJHIK_00209 | 0.0 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
IBEOJHIK_00214 | 7.8e-160 | K | sequence-specific DNA binding | |||
IBEOJHIK_00215 | 1.4e-150 | K | Helix-turn-helix XRE-family like proteins | |||
IBEOJHIK_00216 | 1e-190 | K | Helix-turn-helix XRE-family like proteins | |||
IBEOJHIK_00217 | 3.9e-17 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
IBEOJHIK_00218 | 1.6e-57 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
IBEOJHIK_00219 | 1.3e-134 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
IBEOJHIK_00220 | 4e-136 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
IBEOJHIK_00221 | 1e-113 | 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 | ||
IBEOJHIK_00222 | 1.7e-105 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
IBEOJHIK_00223 | 1.3e-82 | 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 | |
IBEOJHIK_00224 | 7e-153 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
IBEOJHIK_00225 | 1.1e-197 | pac | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
IBEOJHIK_00226 | 1.4e-166 | scrB | 3.2.1.26 | GH32 | G | invertase |
IBEOJHIK_00227 | 7.5e-304 | nagZ | 3.2.1.52 | G | Glycosyl hydrolase family 3 N terminal domain | |
IBEOJHIK_00228 | 9.4e-214 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
IBEOJHIK_00230 | 8.5e-148 | cbiQ | P | cobalt transport | ||
IBEOJHIK_00231 | 3.8e-20 | 3.6.3.24 | P | ATP-binding cassette cobalt transporter | ||
IBEOJHIK_00232 | 4.6e-31 | K | 'Cold-shock' DNA-binding domain | |||
IBEOJHIK_00233 | 2.3e-72 | |||||
IBEOJHIK_00234 | 3.5e-76 | O | OsmC-like protein | |||
IBEOJHIK_00235 | 1.2e-285 | lsa | S | ABC transporter | ||
IBEOJHIK_00236 | 7.7e-249 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
IBEOJHIK_00237 | 1.2e-17 | |||||
IBEOJHIK_00238 | 4.7e-97 | yttB | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00239 | 2.2e-108 | lmrP | E | Major Facilitator Superfamily | ||
IBEOJHIK_00241 | 1.4e-130 | ydfF | K | Transcriptional | ||
IBEOJHIK_00242 | 4.4e-135 | nodI | V | ABC transporter | ||
IBEOJHIK_00243 | 8.2e-137 | nodJ | V | ABC-2 type transporter | ||
IBEOJHIK_00244 | 8.4e-179 | shetA | P | Voltage-dependent anion channel | ||
IBEOJHIK_00245 | 7.6e-72 | S | Phage portal protein | |||
IBEOJHIK_00246 | 6.1e-185 | S | head morphogenesis protein, SPP1 gp7 family | |||
IBEOJHIK_00247 | 4.4e-28 | |||||
IBEOJHIK_00248 | 8.5e-20 | |||||
IBEOJHIK_00249 | 3.6e-90 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
IBEOJHIK_00250 | 2.2e-50 | S | GtrA-like protein | |||
IBEOJHIK_00251 | 0.0 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
IBEOJHIK_00252 | 4.6e-94 | clcA | P | chloride | ||
IBEOJHIK_00253 | 5.7e-126 | tnp | L | DDE domain | ||
IBEOJHIK_00254 | 1.7e-27 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
IBEOJHIK_00255 | 3.6e-87 | els | S | Sterol carrier protein domain | ||
IBEOJHIK_00256 | 3.6e-88 | S | Protein of unknown function (DUF3800) | |||
IBEOJHIK_00257 | 0.0 | yjcE | P | Sodium proton antiporter | ||
IBEOJHIK_00258 | 2.2e-56 | S | Protein of unknown function (DUF3021) | |||
IBEOJHIK_00259 | 4.9e-73 | K | LytTr DNA-binding domain | |||
IBEOJHIK_00260 | 1.4e-148 | cylB | V | ABC-2 type transporter | ||
IBEOJHIK_00261 | 6.6e-162 | cylA | V | ABC transporter | ||
IBEOJHIK_00262 | 8.8e-107 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
IBEOJHIK_00263 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
IBEOJHIK_00264 | 2.2e-44 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
IBEOJHIK_00265 | 2.2e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
IBEOJHIK_00266 | 4.5e-180 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
IBEOJHIK_00267 | 1.4e-71 | dho | 3.5.2.3 | S | Amidohydrolase family | |
IBEOJHIK_00268 | 9.1e-206 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
IBEOJHIK_00269 | 9.6e-138 | 4.1.2.14 | S | KDGP aldolase | ||
IBEOJHIK_00271 | 1.9e-83 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
IBEOJHIK_00272 | 2.3e-131 | K | Helix-turn-helix domain, rpiR family | |||
IBEOJHIK_00274 | 1.3e-298 | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
IBEOJHIK_00275 | 2.9e-273 | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain | |
IBEOJHIK_00276 | 9.5e-49 | |||||
IBEOJHIK_00277 | 7.3e-164 | 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 | |
IBEOJHIK_00278 | 1.6e-32 | 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 | |
IBEOJHIK_00279 | 8.3e-09 | |||||
IBEOJHIK_00280 | 1.5e-20 | |||||
IBEOJHIK_00282 | 7.5e-285 | pipD | E | Dipeptidase | ||
IBEOJHIK_00283 | 8.4e-97 | V | ABC transporter (permease) | |||
IBEOJHIK_00284 | 5.4e-41 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
IBEOJHIK_00285 | 3.1e-110 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
IBEOJHIK_00286 | 3.5e-57 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
IBEOJHIK_00287 | 5.4e-86 | yvyE | 3.4.13.9 | S | YigZ family | |
IBEOJHIK_00288 | 4.3e-113 | rny | S | Endoribonuclease that initiates mRNA decay | ||
IBEOJHIK_00289 | 1e-111 | rny | S | Endoribonuclease that initiates mRNA decay | ||
IBEOJHIK_00290 | 9e-101 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
IBEOJHIK_00291 | 5.9e-79 | F | nucleoside 2-deoxyribosyltransferase | |||
IBEOJHIK_00292 | 1.2e-64 | |||||
IBEOJHIK_00293 | 5.3e-245 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
IBEOJHIK_00294 | 2e-86 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
IBEOJHIK_00295 | 2.2e-66 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
IBEOJHIK_00296 | 3.8e-145 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
IBEOJHIK_00297 | 3.1e-105 | EGP | Major facilitator Superfamily | |||
IBEOJHIK_00298 | 1.1e-139 | EGP | Major facilitator Superfamily | |||
IBEOJHIK_00299 | 2.5e-305 | oppA | E | ABC transporter, substratebinding protein | ||
IBEOJHIK_00300 | 7.7e-88 | |||||
IBEOJHIK_00301 | 1.2e-58 | |||||
IBEOJHIK_00302 | 5.7e-12 | |||||
IBEOJHIK_00303 | 7.8e-109 | gntR | K | rpiR family | ||
IBEOJHIK_00304 | 3.1e-152 | iolH | G | Xylose isomerase-like TIM barrel | ||
IBEOJHIK_00305 | 2.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
IBEOJHIK_00306 | 1.8e-104 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
IBEOJHIK_00307 | 5.5e-56 | lutB | C | 4Fe-4S dicluster domain | ||
IBEOJHIK_00308 | 1.5e-149 | lutA | C | Cysteine-rich domain | ||
IBEOJHIK_00309 | 7.8e-98 | ecsA | V | ABC transporter, ATP-binding protein | ||
IBEOJHIK_00310 | 1.3e-75 | hit | FG | histidine triad | ||
IBEOJHIK_00311 | 7.4e-48 | yhaH | S | YtxH-like protein | ||
IBEOJHIK_00312 | 3.9e-125 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
IBEOJHIK_00313 | 2.5e-23 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
IBEOJHIK_00314 | 0.0 | mdlA | V | ABC transporter | ||
IBEOJHIK_00315 | 4.8e-29 | yneF | S | UPF0154 protein | ||
IBEOJHIK_00316 | 1.1e-37 | ynzC | S | UPF0291 protein | ||
IBEOJHIK_00317 | 1.1e-25 | |||||
IBEOJHIK_00318 | 5.4e-98 | sufB | O | assembly protein SufB | ||
IBEOJHIK_00319 | 7.6e-77 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
IBEOJHIK_00320 | 3.2e-40 | L | Resolvase, N terminal domain | |||
IBEOJHIK_00322 | 7.3e-32 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
IBEOJHIK_00323 | 2.5e-88 | 3.6.1.55 | F | NUDIX domain | ||
IBEOJHIK_00324 | 1.3e-153 | yunF | F | Protein of unknown function DUF72 | ||
IBEOJHIK_00325 | 5.7e-197 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
IBEOJHIK_00326 | 5.5e-65 | rmeD | K | helix_turn_helix, mercury resistance | ||
IBEOJHIK_00327 | 9.5e-53 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
IBEOJHIK_00328 | 3.9e-113 | S | Bacterial protein of unknown function (DUF871) | |||
IBEOJHIK_00329 | 4e-81 | S | Bacterial protein of unknown function (DUF871) | |||
IBEOJHIK_00330 | 1.4e-178 | oppF | P | Belongs to the ABC transporter superfamily | ||
IBEOJHIK_00331 | 6.1e-37 | oppB | P | ABC transporter permease | ||
IBEOJHIK_00332 | 3.2e-107 | oppB | P | ABC transporter permease | ||
IBEOJHIK_00333 | 8.2e-136 | oppC | EP | Binding-protein-dependent transport system inner membrane component | ||
IBEOJHIK_00334 | 3.7e-165 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
IBEOJHIK_00335 | 2.1e-137 | M | Glycosyltransferase like family 2 | |||
IBEOJHIK_00336 | 2.5e-239 | malE | G | Bacterial extracellular solute-binding protein | ||
IBEOJHIK_00337 | 2.6e-83 | |||||
IBEOJHIK_00338 | 3.7e-195 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
IBEOJHIK_00339 | 3.2e-101 | cad | S | FMN_bind | ||
IBEOJHIK_00340 | 3.3e-230 | tnpB | L | Putative transposase DNA-binding domain | ||
IBEOJHIK_00341 | 8.8e-198 | 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 | |
IBEOJHIK_00342 | 3.4e-137 | cobB | K | Sir2 family | ||
IBEOJHIK_00343 | 1.3e-96 | S | SseB protein N-terminal domain | |||
IBEOJHIK_00344 | 7.3e-217 | 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 | |
IBEOJHIK_00345 | 2.9e-35 | 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 | |
IBEOJHIK_00346 | 3.2e-115 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
IBEOJHIK_00347 | 2.8e-151 | whiA | K | May be required for sporulation | ||
IBEOJHIK_00348 | 3e-51 | S | Phage tail assembly chaperone protein, TAC | |||
IBEOJHIK_00349 | 3.7e-108 | S | Phage tail tube protein | |||
IBEOJHIK_00350 | 7.8e-70 | S | Protein of unknown function (DUF3168) | |||
IBEOJHIK_00351 | 2.9e-51 | S | Bacteriophage HK97-gp10, putative tail-component | |||
IBEOJHIK_00352 | 1.2e-51 | |||||
IBEOJHIK_00353 | 1.5e-62 | S | Phage gp6-like head-tail connector protein | |||
IBEOJHIK_00354 | 4.3e-186 | gpG | ||||
IBEOJHIK_00355 | 6.7e-41 | S | Domain of unknown function (DUF4355) | |||
IBEOJHIK_00356 | 1.2e-45 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
IBEOJHIK_00357 | 1.5e-109 | XK27_02070 | S | Nitroreductase family | ||
IBEOJHIK_00358 | 3.9e-78 | M | Leucine rich repeats (6 copies) | |||
IBEOJHIK_00359 | 5.5e-225 | mtnE | 2.6.1.83 | E | Aminotransferase | |
IBEOJHIK_00360 | 7.5e-146 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
IBEOJHIK_00361 | 5.4e-150 | M | NLPA lipoprotein | |||
IBEOJHIK_00363 | 3.2e-70 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
IBEOJHIK_00364 | 1.7e-65 | amiD | P | N-terminal TM domain of oligopeptide transport permease C | ||
IBEOJHIK_00365 | 1.1e-47 | oppB | P | Binding-protein-dependent transport system inner membrane component | ||
IBEOJHIK_00366 | 5.4e-68 | msi198 | K | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_00367 | 1.3e-254 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
IBEOJHIK_00368 | 2.3e-57 | asp | S | Asp23 family, cell envelope-related function | ||
IBEOJHIK_00369 | 1.3e-85 | |||||
IBEOJHIK_00370 | 8.7e-92 | S | MucBP domain | |||
IBEOJHIK_00371 | 4.8e-34 | ywnB | S | NAD(P)H-binding | ||
IBEOJHIK_00372 | 3.3e-91 | S | VanZ like family | |||
IBEOJHIK_00373 | 3.4e-132 | yebC | K | Transcriptional regulatory protein | ||
IBEOJHIK_00374 | 1.1e-134 | comGA | NU | Type II IV secretion system protein | ||
IBEOJHIK_00375 | 4.5e-100 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
IBEOJHIK_00376 | 5.1e-254 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
IBEOJHIK_00377 | 6.6e-31 | |||||
IBEOJHIK_00378 | 2.6e-152 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
IBEOJHIK_00379 | 1.1e-170 | mleP | S | Sodium Bile acid symporter family | ||
IBEOJHIK_00380 | 8.2e-34 | treB | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IBEOJHIK_00381 | 2.8e-214 | sstT | U | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
IBEOJHIK_00382 | 1e-31 | ylmH | S | S4 domain protein | ||
IBEOJHIK_00383 | 1.1e-24 | 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 | ||
IBEOJHIK_00384 | 7.2e-286 | 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 | |
IBEOJHIK_00385 | 7e-90 | 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 | ||
IBEOJHIK_00386 | 1.5e-54 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
IBEOJHIK_00387 | 1.5e-25 | 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 | ||
IBEOJHIK_00388 | 1.4e-93 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
IBEOJHIK_00389 | 2.5e-23 | S | Protein of unknown function (DUF2508) | |||
IBEOJHIK_00390 | 7.4e-115 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
IBEOJHIK_00391 | 7.8e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
IBEOJHIK_00392 | 1.6e-42 | holB | 2.7.7.7 | L | DNA polymerase III | |
IBEOJHIK_00393 | 3.2e-119 | holB | 2.7.7.7 | L | DNA polymerase III | |
IBEOJHIK_00394 | 1.7e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
IBEOJHIK_00395 | 2.4e-153 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
IBEOJHIK_00396 | 1.1e-143 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
IBEOJHIK_00397 | 2e-146 | ansA | 3.5.1.1 | EJ | Asparaginase | |
IBEOJHIK_00398 | 1.5e-33 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
IBEOJHIK_00399 | 1e-234 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
IBEOJHIK_00400 | 9.3e-259 | arpJ | P | ABC transporter permease | ||
IBEOJHIK_00401 | 5.2e-110 | S | Alpha/beta hydrolase family | |||
IBEOJHIK_00402 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
IBEOJHIK_00403 | 8.5e-44 | ypmB | S | Protein conserved in bacteria | ||
IBEOJHIK_00404 | 2.4e-107 | 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 | |
IBEOJHIK_00405 | 8.7e-57 | yoaK | S | Protein of unknown function (DUF1275) | ||
IBEOJHIK_00406 | 2.4e-127 | yjhF | G | Phosphoglycerate mutase family | ||
IBEOJHIK_00407 | 2.2e-55 | |||||
IBEOJHIK_00409 | 1.9e-150 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
IBEOJHIK_00410 | 1.1e-81 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
IBEOJHIK_00411 | 2.4e-127 | 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 | |
IBEOJHIK_00412 | 7.2e-107 | P | cobalt transport | |||
IBEOJHIK_00413 | 2.2e-246 | P | ABC transporter | |||
IBEOJHIK_00414 | 5.1e-214 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
IBEOJHIK_00415 | 1e-176 | 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) | |
IBEOJHIK_00416 | 3.2e-53 | nudA | S | ASCH | ||
IBEOJHIK_00417 | 2.5e-77 | |||||
IBEOJHIK_00418 | 1.4e-60 | 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 | ||
IBEOJHIK_00419 | 1.1e-154 | S | DUF218 domain | |||
IBEOJHIK_00420 | 4.4e-25 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
IBEOJHIK_00421 | 4.1e-127 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
IBEOJHIK_00422 | 2.1e-67 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
IBEOJHIK_00423 | 6.6e-68 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
IBEOJHIK_00424 | 5.6e-197 | 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) | |
IBEOJHIK_00425 | 4.6e-117 | 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) | |
IBEOJHIK_00426 | 8.2e-37 | cspA | K | Cold shock protein | ||
IBEOJHIK_00427 | 1.5e-145 | pstS | P | Phosphate | ||
IBEOJHIK_00428 | 4.9e-263 | ydiC1 | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00430 | 1.4e-71 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
IBEOJHIK_00431 | 8.8e-198 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
IBEOJHIK_00432 | 1.2e-109 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
IBEOJHIK_00434 | 1.1e-184 | ynjC | S | Cell surface protein | ||
IBEOJHIK_00435 | 2.2e-124 | yqcC | S | WxL domain surface cell wall-binding | ||
IBEOJHIK_00437 | 1.7e-96 | |||||
IBEOJHIK_00438 | 6.3e-82 | pbuX | F | xanthine permease | ||
IBEOJHIK_00439 | 7.3e-39 | M | Cna protein B-type domain | |||
IBEOJHIK_00440 | 2.3e-187 | lytH | 3.5.1.28, 6.1.1.12 | M | N-acetylmuramoyl-L-alanine amidase | |
IBEOJHIK_00441 | 2.7e-177 | FbpA | K | Fibronectin-binding protein | ||
IBEOJHIK_00442 | 4.8e-87 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
IBEOJHIK_00444 | 2.7e-95 | FNV0100 | F | NUDIX domain | ||
IBEOJHIK_00445 | 4.1e-142 | 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 | |
IBEOJHIK_00446 | 3.3e-35 | yhcC | S | Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082) | ||
IBEOJHIK_00447 | 3.5e-17 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
IBEOJHIK_00448 | 4.4e-169 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
IBEOJHIK_00449 | 2.8e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
IBEOJHIK_00450 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
IBEOJHIK_00451 | 1.2e-80 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
IBEOJHIK_00452 | 3.4e-17 | uvrA2 | L | ABC transporter | ||
IBEOJHIK_00453 | 1.6e-115 | N | WxL domain surface cell wall-binding | |||
IBEOJHIK_00454 | 5.9e-64 | |||||
IBEOJHIK_00455 | 2.2e-120 | S | WxL domain surface cell wall-binding | |||
IBEOJHIK_00456 | 5.2e-156 | spo0J | K | Belongs to the ParB family | ||
IBEOJHIK_00457 | 2.5e-138 | soj | D | Sporulation initiation inhibitor | ||
IBEOJHIK_00458 | 2.4e-142 | noc | K | Belongs to the ParB family | ||
IBEOJHIK_00459 | 2.8e-134 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
IBEOJHIK_00460 | 1.3e-66 | |||||
IBEOJHIK_00461 | 1e-127 | cobQ | S | glutamine amidotransferase | ||
IBEOJHIK_00463 | 5.5e-107 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
IBEOJHIK_00464 | 7.7e-120 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
IBEOJHIK_00465 | 4.4e-22 | S | Membrane | |||
IBEOJHIK_00466 | 8.1e-131 | K | response regulator | |||
IBEOJHIK_00467 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
IBEOJHIK_00468 | 1.3e-260 | yycH | S | YycH protein | ||
IBEOJHIK_00469 | 1.1e-141 | yycI | S | YycH protein | ||
IBEOJHIK_00470 | 2.7e-154 | vicX | 3.1.26.11 | S | domain protein | |
IBEOJHIK_00471 | 2e-10 | |||||
IBEOJHIK_00472 | 2.9e-206 | htrA | 3.4.21.107 | O | serine protease | |
IBEOJHIK_00473 | 1.2e-70 | S | Iron-sulphur cluster biosynthesis | |||
IBEOJHIK_00474 | 3.2e-77 | hsp3 | O | Hsp20/alpha crystallin family | ||
IBEOJHIK_00475 | 0.0 | cadA | P | P-type ATPase | ||
IBEOJHIK_00476 | 5.7e-145 | |||||
IBEOJHIK_00478 | 3.4e-302 | E | ABC transporter, substratebinding protein | |||
IBEOJHIK_00479 | 8e-257 | E | Peptidase dimerisation domain | |||
IBEOJHIK_00480 | 2.3e-103 | |||||
IBEOJHIK_00481 | 4.8e-199 | ybiR | P | Citrate transporter | ||
IBEOJHIK_00482 | 1.4e-220 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
IBEOJHIK_00483 | 0.0 | bgaC | 3.2.1.23 | G | Glycosyl hydrolases family 35 | |
IBEOJHIK_00484 | 8.1e-82 | manX_1 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
IBEOJHIK_00485 | 1.6e-129 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
IBEOJHIK_00486 | 2.1e-146 | manZ_1 | G | PTS system mannose/fructose/sorbose family IID component | ||
IBEOJHIK_00487 | 7.1e-65 | XK27_08465 | 2.7.1.191 | G | PTS system fructose IIA component | |
IBEOJHIK_00488 | 5.8e-177 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | F | pfkB family carbohydrate kinase | |
IBEOJHIK_00489 | 1.1e-147 | IQ | KR domain | |||
IBEOJHIK_00490 | 6.1e-244 | gatC | G | PTS system sugar-specific permease component | ||
IBEOJHIK_00491 | 0.0 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
IBEOJHIK_00492 | 1.6e-55 | S | Phage head-tail joining protein | |||
IBEOJHIK_00494 | 1.8e-27 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
IBEOJHIK_00495 | 2.6e-36 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
IBEOJHIK_00496 | 2.3e-53 | yrzB | S | Belongs to the UPF0473 family | ||
IBEOJHIK_00497 | 2e-36 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
IBEOJHIK_00498 | 8.6e-93 | cvpA | S | Colicin V production protein | ||
IBEOJHIK_00499 | 1.3e-117 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
IBEOJHIK_00500 | 6.8e-147 | 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 | |
IBEOJHIK_00501 | 3.5e-132 | yvfS | V | ABC-2 type transporter | ||
IBEOJHIK_00502 | 8.5e-56 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
IBEOJHIK_00503 | 4.5e-29 | |||||
IBEOJHIK_00505 | 3.1e-195 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
IBEOJHIK_00506 | 3.7e-132 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
IBEOJHIK_00507 | 4.9e-82 | ccl | S | QueT transporter | ||
IBEOJHIK_00508 | 4.9e-128 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
IBEOJHIK_00509 | 4.8e-37 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
IBEOJHIK_00510 | 2.1e-39 | K | Cro/C1-type HTH DNA-binding domain | |||
IBEOJHIK_00511 | 2.8e-87 | F | NUDIX domain | |||
IBEOJHIK_00512 | 4.4e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
IBEOJHIK_00513 | 8.6e-09 | S | Protein of unknown function (DUF4044) | |||
IBEOJHIK_00514 | 4.2e-53 | |||||
IBEOJHIK_00516 | 4.7e-128 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
IBEOJHIK_00518 | 5.1e-210 | oatA | I | Acyltransferase | ||
IBEOJHIK_00519 | 8.7e-75 | G | Phosphoglycerate mutase family | |||
IBEOJHIK_00520 | 2.5e-155 | 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 | ||
IBEOJHIK_00521 | 3.1e-150 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
IBEOJHIK_00522 | 1.9e-55 | |||||
IBEOJHIK_00523 | 3e-95 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
IBEOJHIK_00524 | 4.7e-35 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
IBEOJHIK_00525 | 3e-130 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
IBEOJHIK_00526 | 7.5e-42 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
IBEOJHIK_00527 | 8e-134 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
IBEOJHIK_00528 | 6.1e-30 | 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) | |
IBEOJHIK_00529 | 1.8e-40 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
IBEOJHIK_00530 | 5.4e-150 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
IBEOJHIK_00532 | 3.8e-96 | |||||
IBEOJHIK_00533 | 1.2e-42 | 3.4.22.70 | M | Sortase family | ||
IBEOJHIK_00534 | 1.4e-64 | ytxH | S | YtxH-like protein | ||
IBEOJHIK_00535 | 4.4e-117 | |||||
IBEOJHIK_00536 | 8.8e-156 | S | Uncharacterised protein, DegV family COG1307 | |||
IBEOJHIK_00537 | 2.1e-75 | K | Acetyltransferase (GNAT) domain | |||
IBEOJHIK_00538 | 5.4e-222 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
IBEOJHIK_00539 | 2.2e-280 | ytgP | S | Polysaccharide biosynthesis protein | ||
IBEOJHIK_00540 | 6.5e-75 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
IBEOJHIK_00541 | 1.2e-255 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
IBEOJHIK_00542 | 1.3e-113 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
IBEOJHIK_00543 | 2.1e-57 | yjdF | S | Protein of unknown function (DUF2992) | ||
IBEOJHIK_00546 | 1.5e-124 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
IBEOJHIK_00547 | 2e-65 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
IBEOJHIK_00548 | 1.5e-223 | maeN | C | 2-hydroxycarboxylate transporter family | ||
IBEOJHIK_00549 | 3.2e-273 | dcuS | 2.7.13.3 | T | Single cache domain 3 | |
IBEOJHIK_00550 | 9.6e-121 | dpiA | KT | cheY-homologous receiver domain | ||
IBEOJHIK_00551 | 1.7e-99 | |||||
IBEOJHIK_00553 | 1e-151 | 1.1.1.31 | I | NAD binding domain of 6-phosphogluconate dehydrogenase | ||
IBEOJHIK_00554 | 1.4e-68 | |||||
IBEOJHIK_00555 | 5.4e-132 | yfeJ | 6.3.5.2 | F | Glutamine amidotransferase class-I | |
IBEOJHIK_00556 | 6.8e-170 | O | protein-N(PI)-phosphohistidine-lactose phosphotransferase system transporter activity | |||
IBEOJHIK_00557 | 9.2e-225 | sip | L | Belongs to the 'phage' integrase family | ||
IBEOJHIK_00558 | 8.3e-108 | K | sequence-specific DNA binding | |||
IBEOJHIK_00559 | 7.3e-11 | K | TRANSCRIPTIONal | |||
IBEOJHIK_00560 | 3.2e-43 | |||||
IBEOJHIK_00561 | 2.3e-31 | |||||
IBEOJHIK_00562 | 8.7e-18 | |||||
IBEOJHIK_00563 | 1.8e-29 | |||||
IBEOJHIK_00564 | 5e-41 | |||||
IBEOJHIK_00565 | 2.1e-25 | |||||
IBEOJHIK_00566 | 3.9e-161 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
IBEOJHIK_00567 | 1.9e-280 | S | Virulence-associated protein E | |||
IBEOJHIK_00568 | 4.7e-78 | |||||
IBEOJHIK_00569 | 9.8e-76 | L | Phage-associated protein | |||
IBEOJHIK_00570 | 9.6e-80 | terS | L | Phage terminase, small subunit | ||
IBEOJHIK_00571 | 0.0 | terL | S | overlaps another CDS with the same product name | ||
IBEOJHIK_00572 | 2.1e-22 | |||||
IBEOJHIK_00573 | 4.7e-224 | S | Phage portal protein | |||
IBEOJHIK_00574 | 4.3e-294 | S | Phage capsid family | |||
IBEOJHIK_00575 | 1.7e-47 | S | Phage gp6-like head-tail connector protein | |||
IBEOJHIK_00576 | 5.6e-13 | S | Phage head-tail joining protein | |||
IBEOJHIK_00577 | 2.9e-16 | |||||
IBEOJHIK_00578 | 2.2e-14 | ytgB | S | Transglycosylase associated protein | ||
IBEOJHIK_00580 | 8.8e-170 | 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) | |
IBEOJHIK_00581 | 1.5e-180 | D | Alpha beta | |||
IBEOJHIK_00582 | 5.9e-185 | lipA | I | Carboxylesterase family | ||
IBEOJHIK_00583 | 1.2e-216 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
IBEOJHIK_00584 | 1e-78 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IBEOJHIK_00585 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
IBEOJHIK_00586 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
IBEOJHIK_00587 | 9.6e-132 | 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 | |
IBEOJHIK_00588 | 4.9e-66 | yueI | S | Protein of unknown function (DUF1694) | ||
IBEOJHIK_00589 | 6.7e-276 | M | Leucine rich repeats (6 copies) | |||
IBEOJHIK_00590 | 2.8e-39 | M | Leucine rich repeats (6 copies) | |||
IBEOJHIK_00591 | 3.2e-183 | |||||
IBEOJHIK_00592 | 4.7e-208 | bacI | V | MacB-like periplasmic core domain | ||
IBEOJHIK_00593 | 2e-126 | V | ABC transporter | |||
IBEOJHIK_00594 | 9.6e-152 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
IBEOJHIK_00595 | 7.1e-124 | |||||
IBEOJHIK_00596 | 2.5e-121 | K | response regulator | |||
IBEOJHIK_00597 | 1.2e-219 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
IBEOJHIK_00598 | 1.3e-238 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
IBEOJHIK_00599 | 1.2e-85 | 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 | ||
IBEOJHIK_00600 | 5.5e-25 | cpdB | 3.1.3.6, 3.1.4.16 | F | 5'-nucleotidase, C-terminal domain | |
IBEOJHIK_00601 | 3.7e-146 | |||||
IBEOJHIK_00603 | 4.8e-79 | |||||
IBEOJHIK_00604 | 1.1e-118 | V | ATPases associated with a variety of cellular activities | |||
IBEOJHIK_00605 | 2.2e-123 | |||||
IBEOJHIK_00606 | 4.6e-118 | |||||
IBEOJHIK_00607 | 6.1e-77 | |||||
IBEOJHIK_00608 | 1.8e-303 | oppA | E | ABC transporter, substratebinding protein | ||
IBEOJHIK_00609 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
IBEOJHIK_00610 | 2.8e-70 | norB | EGP | Major Facilitator | ||
IBEOJHIK_00611 | 1e-80 | V | HNH nucleases | |||
IBEOJHIK_00612 | 4.7e-67 | L | Single-strand binding protein family | |||
IBEOJHIK_00613 | 6.5e-134 | |||||
IBEOJHIK_00615 | 4e-11 | S | HNH endonuclease | |||
IBEOJHIK_00616 | 2.1e-54 | |||||
IBEOJHIK_00617 | 3.3e-86 | corA | P | CorA-like Mg2+ transporter protein | ||
IBEOJHIK_00618 | 4.9e-162 | mleR | K | LysR family | ||
IBEOJHIK_00619 | 0.0 | bglH | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IBEOJHIK_00620 | 2.7e-97 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
IBEOJHIK_00621 | 2.1e-157 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
IBEOJHIK_00622 | 1.8e-112 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
IBEOJHIK_00623 | 1.9e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
IBEOJHIK_00624 | 1.5e-22 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
IBEOJHIK_00625 | 6.2e-196 | 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 | |
IBEOJHIK_00626 | 9.6e-203 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
IBEOJHIK_00627 | 1.4e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
IBEOJHIK_00628 | 2.1e-58 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
IBEOJHIK_00629 | 2.4e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
IBEOJHIK_00630 | 1.2e-08 | |||||
IBEOJHIK_00631 | 8.6e-108 | |||||
IBEOJHIK_00632 | 4.3e-203 | |||||
IBEOJHIK_00633 | 4.6e-163 | V | ATPases associated with a variety of cellular activities | |||
IBEOJHIK_00634 | 3.2e-136 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
IBEOJHIK_00635 | 1.2e-53 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
IBEOJHIK_00636 | 3.3e-48 | K | Transcriptional regulatory protein, C terminal | |||
IBEOJHIK_00637 | 5.5e-53 | xkdO | M | Phage tail tape measure protein TP901 | ||
IBEOJHIK_00638 | 1.8e-52 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
IBEOJHIK_00639 | 2.4e-27 | wbbX | GT2,GT4 | M | Glycosyl transferases group 1 | |
IBEOJHIK_00640 | 3.1e-23 | nusA | K | Participates in both transcription termination and antitermination | ||
IBEOJHIK_00641 | 3.2e-29 | ylxR | K | Protein of unknown function (DUF448) | ||
IBEOJHIK_00642 | 5.4e-44 | ylxQ | J | ribosomal protein | ||
IBEOJHIK_00643 | 1.3e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
IBEOJHIK_00644 | 9.2e-82 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
IBEOJHIK_00645 | 3.9e-133 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
IBEOJHIK_00646 | 8.5e-128 | skfE | V | ATPases associated with a variety of cellular activities | ||
IBEOJHIK_00647 | 2.2e-36 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
IBEOJHIK_00648 | 4.6e-17 | yhcX | S | Psort location Cytoplasmic, score | ||
IBEOJHIK_00649 | 1.9e-191 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
IBEOJHIK_00650 | 4e-62 | yeaO | S | Protein of unknown function, DUF488 | ||
IBEOJHIK_00651 | 1.4e-104 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
IBEOJHIK_00652 | 8.4e-92 | |||||
IBEOJHIK_00653 | 1.4e-107 | ywrF | S | Flavin reductase like domain | ||
IBEOJHIK_00654 | 2.9e-168 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
IBEOJHIK_00655 | 5.3e-78 | |||||
IBEOJHIK_00656 | 1e-97 | 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 | |
IBEOJHIK_00657 | 9.6e-29 | V | ABC transporter transmembrane region | |||
IBEOJHIK_00659 | 2.1e-207 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
IBEOJHIK_00660 | 2.5e-42 | |||||
IBEOJHIK_00661 | 5.8e-213 | mccF | V | LD-carboxypeptidase | ||
IBEOJHIK_00662 | 2.1e-182 | yveB | 2.7.4.29 | I | PAP2 superfamily | |
IBEOJHIK_00663 | 2.8e-171 | L | Transposase | |||
IBEOJHIK_00664 | 5e-54 | thrB | 2.7.1.39, 4.2.3.1 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
IBEOJHIK_00665 | 1.6e-251 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
IBEOJHIK_00666 | 1.1e-67 | usp1 | T | Universal stress protein family | ||
IBEOJHIK_00667 | 1.1e-135 | sfsA | S | Belongs to the SfsA family | ||
IBEOJHIK_00668 | 1e-221 | gbuA | 3.6.3.32 | E | glycine betaine | |
IBEOJHIK_00669 | 9.4e-126 | proW | E | glycine betaine | ||
IBEOJHIK_00670 | 1.5e-169 | gbuC | E | glycine betaine | ||
IBEOJHIK_00671 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
IBEOJHIK_00672 | 1.5e-65 | gtcA | S | Teichoic acid glycosylation protein | ||
IBEOJHIK_00673 | 1.1e-127 | srtA | 3.4.22.70 | M | Sortase family | |
IBEOJHIK_00674 | 1.5e-181 | K | AI-2E family transporter | |||
IBEOJHIK_00675 | 1.4e-166 | gmuE | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
IBEOJHIK_00676 | 1.2e-132 | K | DeoR C terminal sensor domain | |||
IBEOJHIK_00677 | 3.1e-78 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_00678 | 4.1e-53 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
IBEOJHIK_00679 | 1.9e-78 | G | Phosphotransferase System | |||
IBEOJHIK_00680 | 4.9e-73 | G | Phosphotransferase System | |||
IBEOJHIK_00681 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
IBEOJHIK_00682 | 3.8e-57 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
IBEOJHIK_00683 | 1.6e-100 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
IBEOJHIK_00684 | 1e-122 | K | response regulator | |||
IBEOJHIK_00685 | 6.5e-20 | chpR | T | PFAM SpoVT AbrB | ||
IBEOJHIK_00686 | 2e-29 | cspC | K | Cold shock protein | ||
IBEOJHIK_00687 | 3e-168 | yqjA | S | Putative aromatic acid exporter C-terminal domain | ||
IBEOJHIK_00689 | 3.7e-12 | |||||
IBEOJHIK_00690 | 1.9e-53 | |||||
IBEOJHIK_00691 | 5e-173 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
IBEOJHIK_00692 | 4.2e-101 | S | Psort location CytoplasmicMembrane, score | |||
IBEOJHIK_00693 | 3.1e-195 | S | PglZ domain | |||
IBEOJHIK_00694 | 4.3e-132 | yrjD | S | LUD domain | ||
IBEOJHIK_00695 | 6.3e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
IBEOJHIK_00696 | 1.3e-116 | ypdF | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
IBEOJHIK_00699 | 3.6e-101 | |||||
IBEOJHIK_00700 | 1.7e-210 | 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 | |
IBEOJHIK_00701 | 2.5e-275 | emrY | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00702 | 1e-81 | merR | K | MerR HTH family regulatory protein | ||
IBEOJHIK_00703 | 8.1e-266 | lmrB | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00704 | 1.1e-114 | S | Domain of unknown function (DUF4811) | |||
IBEOJHIK_00705 | 1e-122 | 3.6.1.27 | I | Acid phosphatase homologues | ||
IBEOJHIK_00706 | 2.3e-81 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
IBEOJHIK_00707 | 1.7e-229 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
IBEOJHIK_00708 | 5.6e-144 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
IBEOJHIK_00710 | 1.1e-42 | bglK_1 | 2.7.1.2 | GK | ROK family | |
IBEOJHIK_00717 | 1.1e-83 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
IBEOJHIK_00718 | 1.6e-97 | |||||
IBEOJHIK_00719 | 4.2e-100 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_00720 | 5.8e-79 | S | Calcineurin-like phosphoesterase | |||
IBEOJHIK_00721 | 3.1e-80 | yosT | L | Bacterial transcription activator, effector binding domain | ||
IBEOJHIK_00722 | 7e-138 | 3.5.1.124 | S | DJ-1/PfpI family | ||
IBEOJHIK_00723 | 6.4e-32 | ywzB | S | Protein of unknown function (DUF1146) | ||
IBEOJHIK_00724 | 4.5e-180 | mbl | D | Cell shape determining protein MreB Mrl | ||
IBEOJHIK_00725 | 1.4e-25 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
IBEOJHIK_00726 | 2.6e-25 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
IBEOJHIK_00727 | 6.2e-58 | ftsL | D | cell division protein FtsL | ||
IBEOJHIK_00728 | 4.3e-30 | S | Protein of unknown function (DUF2969) | |||
IBEOJHIK_00729 | 1e-237 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
IBEOJHIK_00732 | 4.9e-108 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
IBEOJHIK_00733 | 2.4e-104 | yjbK | S | CYTH | ||
IBEOJHIK_00734 | 1.5e-115 | yjbH | Q | Thioredoxin | ||
IBEOJHIK_00735 | 7.2e-216 | coiA | 3.6.4.12 | S | Competence protein | |
IBEOJHIK_00736 | 1.3e-41 | XK27_08635 | S | UPF0210 protein | ||
IBEOJHIK_00737 | 1.8e-176 | iolA | 1.2.1.18, 1.2.1.27 | C | Belongs to the aldehyde dehydrogenase family | |
IBEOJHIK_00738 | 7.6e-157 | iolB | 5.3.1.30 | G | Involved in the isomerization of 5-deoxy-glucuronate (5DG) to 5-dehydro-2-deoxy-D-gluconate (DKG or 2-deoxy-5-keto-D- gluconate) | |
IBEOJHIK_00739 | 3.8e-179 | iolC | 2.7.1.92 | H | Catalyzes the phosphorylation of 5-dehydro-2-deoxy-D- gluconate (2-deoxy-5-keto-D-gluconate or DKG) to 6-phospho-5- dehydro-2-deoxy-D-gluconate (DKGP) | |
IBEOJHIK_00740 | 1.7e-159 | licT | K | CAT RNA binding domain | ||
IBEOJHIK_00741 | 2.7e-43 | |||||
IBEOJHIK_00742 | 5.6e-106 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
IBEOJHIK_00743 | 1e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
IBEOJHIK_00744 | 2.3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
IBEOJHIK_00745 | 4.6e-58 | 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 | ||
IBEOJHIK_00746 | 1.2e-83 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
IBEOJHIK_00747 | 1.7e-24 | rpmD | J | Ribosomal protein L30 | ||
IBEOJHIK_00748 | 4e-41 | rplO | J | Binds to the 23S rRNA | ||
IBEOJHIK_00749 | 4.4e-109 | T | LytTr DNA-binding domain | |||
IBEOJHIK_00750 | 5.6e-169 | 2.7.13.3 | T | GHKL domain | ||
IBEOJHIK_00751 | 0.0 | V | ABC transporter | |||
IBEOJHIK_00752 | 0.0 | V | ABC transporter | |||
IBEOJHIK_00753 | 1.1e-30 | K | Transcriptional | |||
IBEOJHIK_00754 | 1.2e-68 | |||||
IBEOJHIK_00755 | 5e-201 | 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 | |
IBEOJHIK_00757 | 3.1e-164 | oppF | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
IBEOJHIK_00758 | 1.7e-201 | oppD | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
IBEOJHIK_00759 | 4.4e-49 | |||||
IBEOJHIK_00760 | 3.1e-113 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
IBEOJHIK_00761 | 8.7e-50 | |||||
IBEOJHIK_00762 | 1.6e-25 | ydcG | K | Transcriptional | ||
IBEOJHIK_00763 | 1.3e-113 | YSH1 | S | Metallo-beta-lactamase superfamily | ||
IBEOJHIK_00764 | 2.2e-24 | |||||
IBEOJHIK_00765 | 2.8e-38 | |||||
IBEOJHIK_00766 | 1.7e-66 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
IBEOJHIK_00767 | 3.9e-170 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
IBEOJHIK_00768 | 3.8e-69 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
IBEOJHIK_00769 | 8.8e-104 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
IBEOJHIK_00770 | 1.2e-128 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
IBEOJHIK_00771 | 3.4e-163 | K | LysR substrate binding domain | |||
IBEOJHIK_00772 | 3.6e-257 | S | Sulphur transport | |||
IBEOJHIK_00773 | 0.0 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
IBEOJHIK_00774 | 2.9e-142 | tauC | P | Binding-protein-dependent transport system inner membrane component | ||
IBEOJHIK_00775 | 2.6e-183 | tauA | P | NMT1-like family | ||
IBEOJHIK_00776 | 5.4e-138 | tauB | 3.6.3.36 | P | ATPases associated with a variety of cellular activities | |
IBEOJHIK_00779 | 3.3e-55 | S | DsrE/DsrF-like family | |||
IBEOJHIK_00780 | 1.4e-254 | pbuO | S | permease | ||
IBEOJHIK_00781 | 3e-54 | S | Protein of unknown function (DUF1516) | |||
IBEOJHIK_00782 | 8.1e-58 | ypaA | S | Protein of unknown function (DUF1304) | ||
IBEOJHIK_00783 | 5.9e-43 | |||||
IBEOJHIK_00784 | 1.5e-132 | K | UTRA | |||
IBEOJHIK_00785 | 1.9e-194 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
IBEOJHIK_00786 | 6.4e-138 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
IBEOJHIK_00787 | 1.9e-59 | 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 | |
IBEOJHIK_00789 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
IBEOJHIK_00790 | 5e-276 | L | PFAM Integrase core domain | |||
IBEOJHIK_00791 | 3.5e-252 | 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 | ||
IBEOJHIK_00792 | 2.7e-205 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
IBEOJHIK_00793 | 2e-32 | yaaA | S | S4 domain protein YaaA | ||
IBEOJHIK_00794 | 3.3e-203 | 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 | ||
IBEOJHIK_00795 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
IBEOJHIK_00796 | 1.1e-138 | 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 | |
IBEOJHIK_00797 | 7.9e-70 | 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 | |
IBEOJHIK_00798 | 1.3e-41 | |||||
IBEOJHIK_00799 | 1.4e-19 | L | Helix-turn-helix domain | |||
IBEOJHIK_00800 | 3.6e-162 | L | PFAM Integrase catalytic region | |||
IBEOJHIK_00801 | 1.8e-38 | M1-874 | K | Domain of unknown function (DUF1836) | ||
IBEOJHIK_00802 | 1.4e-56 | ykiI | ||||
IBEOJHIK_00803 | 1.4e-104 | S | Putative inner membrane protein (DUF1819) | |||
IBEOJHIK_00804 | 4.4e-106 | S | Domain of unknown function (DUF1788) | |||
IBEOJHIK_00805 | 1.1e-46 | purK2 | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
IBEOJHIK_00806 | 1.1e-83 | yslB | S | Protein of unknown function (DUF2507) | ||
IBEOJHIK_00807 | 5.5e-247 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
IBEOJHIK_00808 | 4e-37 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
IBEOJHIK_00809 | 1.8e-239 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
IBEOJHIK_00810 | 8.5e-295 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
IBEOJHIK_00811 | 6.6e-53 | trxA | O | Belongs to the thioredoxin family | ||
IBEOJHIK_00812 | 6.4e-57 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
IBEOJHIK_00813 | 9.9e-94 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
IBEOJHIK_00814 | 6.1e-73 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
IBEOJHIK_00815 | 1.9e-141 | lacR | K | DeoR C terminal sensor domain | ||
IBEOJHIK_00816 | 9.1e-118 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
IBEOJHIK_00817 | 5.3e-245 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
IBEOJHIK_00818 | 2e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
IBEOJHIK_00819 | 2.2e-85 | ydiN | EGP | Major Facilitator Superfamily | ||
IBEOJHIK_00820 | 8.2e-168 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
IBEOJHIK_00821 | 6.1e-162 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
IBEOJHIK_00822 | 1.8e-36 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
IBEOJHIK_00823 | 2e-28 | |||||
IBEOJHIK_00824 | 2.7e-39 | ptsH | G | phosphocarrier protein HPR | ||
IBEOJHIK_00825 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
IBEOJHIK_00826 | 5.1e-70 | rplI | J | Binds to the 23S rRNA | ||
IBEOJHIK_00827 | 1.1e-17 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
IBEOJHIK_00828 | 7.2e-303 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
IBEOJHIK_00830 | 1.1e-153 | EG | EamA-like transporter family | |||
IBEOJHIK_00831 | 1.4e-74 | 3.6.1.55 | L | NUDIX domain | ||
IBEOJHIK_00832 | 1.2e-49 | K | sequence-specific DNA binding | |||
IBEOJHIK_00833 | 6.6e-63 | |||||
IBEOJHIK_00834 | 4.2e-186 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
IBEOJHIK_00835 | 4.6e-44 | zmp3 | O | Zinc-dependent metalloprotease | ||
IBEOJHIK_00836 | 1.4e-181 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
IBEOJHIK_00837 | 8.9e-37 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
IBEOJHIK_00838 | 1.6e-61 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
IBEOJHIK_00839 | 0.0 | V | FtsX-like permease family | |||
IBEOJHIK_00840 | 1.3e-93 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
IBEOJHIK_00841 | 1.4e-115 | bdhA | C | Iron-containing alcohol dehydrogenase | ||
IBEOJHIK_00842 | 5.1e-192 | I | carboxylic ester hydrolase activity | |||
IBEOJHIK_00843 | 9e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
IBEOJHIK_00844 | 2.1e-76 | marR | K | Winged helix DNA-binding domain | ||
IBEOJHIK_00845 | 1.5e-175 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
IBEOJHIK_00846 | 4.5e-33 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
IBEOJHIK_00847 | 2.4e-173 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
IBEOJHIK_00848 | 2.7e-166 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
IBEOJHIK_00849 | 7.3e-127 | IQ | reductase | |||
IBEOJHIK_00850 | 1.6e-49 | yubA | S | AI-2E family transporter | ||
IBEOJHIK_00851 | 3.4e-80 | |||||
IBEOJHIK_00852 | 3.4e-56 | |||||
IBEOJHIK_00854 | 1.8e-139 | rrmA | 2.1.1.187 | H | Methyltransferase | |
IBEOJHIK_00855 | 1.9e-124 | |||||
IBEOJHIK_00856 | 7.3e-89 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
IBEOJHIK_00857 | 4.6e-127 | |||||
IBEOJHIK_00860 | 4e-25 | XK27_02675 | K | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_00861 | 8.3e-175 | M | Peptidoglycan-binding domain 1 protein | |||
IBEOJHIK_00862 | 7.6e-76 | ynhH | S | NusG domain II | ||
IBEOJHIK_00863 | 1.3e-102 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
IBEOJHIK_00864 | 2.7e-56 | ywjH | S | Protein of unknown function (DUF1634) | ||
IBEOJHIK_00865 | 1.1e-129 | yxaA | S | Sulfite exporter TauE/SafE | ||
IBEOJHIK_00866 | 1.8e-237 | S | TPM domain | |||
IBEOJHIK_00867 | 1.7e-116 | |||||
IBEOJHIK_00868 | 3.2e-261 | nox | 1.6.3.4 | C | NADH oxidase | |
IBEOJHIK_00869 | 0.0 | fnq20 | 1.13.12.16 | S | FAD-NAD(P)-binding | |
IBEOJHIK_00870 | 9.3e-164 | gadR | K | Transcriptional activator, Rgg GadR MutR family | ||
IBEOJHIK_00871 | 4.9e-285 | V | ABC transporter transmembrane region | |||
IBEOJHIK_00872 | 1.6e-79 | S | nuclear-transcribed mRNA catabolic process, no-go decay | |||
IBEOJHIK_00873 | 2e-74 | argR | K | Regulates arginine biosynthesis genes | ||
IBEOJHIK_00874 | 1.5e-58 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
IBEOJHIK_00875 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
IBEOJHIK_00876 | 9.6e-169 | malE | G | Bacterial extracellular solute-binding protein | ||
IBEOJHIK_00877 | 1.8e-50 | malE | G | Bacterial extracellular solute-binding protein | ||
IBEOJHIK_00878 | 1.9e-147 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
IBEOJHIK_00879 | 2.6e-166 | malG | P | ABC-type sugar transport systems, permease components | ||
IBEOJHIK_00882 | 1e-187 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
IBEOJHIK_00883 | 1.1e-272 | E | Amino acid permease | |||
IBEOJHIK_00884 | 1.6e-91 | XK27_08510 | L | Type III restriction protein res subunit | ||
IBEOJHIK_00885 | 6.5e-122 | ylbM | S | Belongs to the UPF0348 family | ||
IBEOJHIK_00886 | 2.9e-232 | ydaO | E | amino acid | ||
IBEOJHIK_00887 | 2.9e-84 | 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 | |
IBEOJHIK_00888 | 9.7e-100 | yqaB | S | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_00889 | 1.3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
IBEOJHIK_00890 | 4.8e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
IBEOJHIK_00891 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
IBEOJHIK_00892 | 5.3e-239 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
IBEOJHIK_00893 | 3.2e-78 | S | QueT transporter | |||
IBEOJHIK_00894 | 1.2e-74 | bglP | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IBEOJHIK_00895 | 7.4e-266 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
IBEOJHIK_00896 | 2.1e-55 | S | Phage tail assembly chaperone proteins, TAC | |||
IBEOJHIK_00897 | 2.9e-92 | 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 | |
IBEOJHIK_00898 | 7.1e-62 | |||||
IBEOJHIK_00899 | 2.8e-210 | csdA | 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 | |
IBEOJHIK_00900 | 5.1e-176 | ylbL | T | Belongs to the peptidase S16 family | ||
IBEOJHIK_00901 | 1.5e-25 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
IBEOJHIK_00902 | 1.1e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
IBEOJHIK_00903 | 7e-80 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
IBEOJHIK_00904 | 1.9e-104 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_00905 | 2.9e-185 | yxeA | V | FtsX-like permease family | ||
IBEOJHIK_00906 | 1.7e-128 | devA | 3.6.3.25 | V | ATPases associated with a variety of cellular activities | |
IBEOJHIK_00907 | 6.4e-34 | |||||
IBEOJHIK_00908 | 9.6e-138 | tipA | K | TipAS antibiotic-recognition domain | ||
IBEOJHIK_00909 | 1.1e-138 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
IBEOJHIK_00910 | 1.6e-143 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
IBEOJHIK_00911 | 3.2e-158 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
IBEOJHIK_00912 | 4.3e-155 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
IBEOJHIK_00913 | 2.5e-121 | |||||
IBEOJHIK_00914 | 3.1e-60 | rplQ | J | Ribosomal protein L17 | ||
IBEOJHIK_00915 | 3.6e-171 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
IBEOJHIK_00916 | 4e-63 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
IBEOJHIK_00917 | 4.7e-31 | |||||
IBEOJHIK_00918 | 2e-60 | S | Pyridoxamine 5'-phosphate oxidase | |||
IBEOJHIK_00920 | 2.4e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
IBEOJHIK_00921 | 1.7e-111 | glnPH2 | P | ABC transporter permease | ||
IBEOJHIK_00922 | 6.1e-28 | 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 | ||
IBEOJHIK_00923 | 4.3e-64 | yugI | 5.3.1.9 | J | general stress protein | |
IBEOJHIK_00924 | 1e-101 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
IBEOJHIK_00925 | 9.8e-95 | XK27_08635 | S | UPF0210 protein | ||
IBEOJHIK_00926 | 1.4e-15 | gcvR | T | Belongs to the UPF0237 family | ||
IBEOJHIK_00927 | 9.2e-13 | gcvR | T | Belongs to the UPF0237 family | ||
IBEOJHIK_00928 | 5.8e-64 | S | acid phosphatase activity | |||
IBEOJHIK_00929 | 7e-186 | cpdA | S | Calcineurin-like phosphoesterase | ||
IBEOJHIK_00930 | 2.3e-150 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
IBEOJHIK_00931 | 4.7e-49 | ydiC1 | EGP | Major facilitator Superfamily | ||
IBEOJHIK_00932 | 5.8e-71 | K | helix_turn_helix multiple antibiotic resistance protein | |||
IBEOJHIK_00933 | 7.9e-105 | |||||
IBEOJHIK_00934 | 3.5e-29 | |||||
IBEOJHIK_00935 | 5.4e-40 | K | Helix-turn-helix XRE-family like proteins | |||
IBEOJHIK_00936 | 4e-56 | |||||
IBEOJHIK_00937 | 1.6e-82 | |||||
IBEOJHIK_00938 | 6.8e-273 | manR | K | PRD domain | ||
IBEOJHIK_00939 | 1.4e-69 | manR | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
IBEOJHIK_00940 | 1.6e-76 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_00941 | 8.6e-48 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
IBEOJHIK_00942 | 9e-145 | G | Phosphotransferase System | |||
IBEOJHIK_00943 | 6.1e-120 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
IBEOJHIK_00944 | 2.5e-129 | alsE | 5.1.3.1 | G | Ribulose-phosphate 3 epimerase family | |
IBEOJHIK_00945 | 5e-78 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_00946 | 1.9e-43 | ulaB | 2.7.1.194, 2.7.1.200 | G | Phosphotransferase system galactitol-specific IIB component | |
IBEOJHIK_00947 | 1.3e-17 | S | YvrJ protein family | |||
IBEOJHIK_00948 | 8.7e-147 | yqfZ | 3.2.1.17 | M | hydrolase, family 25 | |
IBEOJHIK_00949 | 2.4e-30 | S | response to antibiotic | |||
IBEOJHIK_00950 | 1e-87 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
IBEOJHIK_00951 | 1e-185 | hrtB | V | ABC transporter permease | ||
IBEOJHIK_00952 | 2.4e-206 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
IBEOJHIK_00953 | 5.1e-162 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
IBEOJHIK_00954 | 1.3e-176 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
IBEOJHIK_00955 | 1.2e-222 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
IBEOJHIK_00956 | 8.8e-167 | natA | S | ABC transporter | ||
IBEOJHIK_00957 | 2.8e-125 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
IBEOJHIK_00958 | 3.3e-34 | V | ABC transporter transmembrane region | |||
IBEOJHIK_00959 | 4.6e-82 | bglB | 3.2.1.21 | GH3 | G | hydrolase, family 3 |
IBEOJHIK_00960 | 1.3e-234 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
IBEOJHIK_00961 | 9.1e-144 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
IBEOJHIK_00962 | 4.3e-174 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
IBEOJHIK_00963 | 1.4e-124 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
IBEOJHIK_00964 | 2.8e-31 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
IBEOJHIK_00965 | 6.1e-91 | S | nuclear-transcribed mRNA catabolic process, no-go decay | |||
IBEOJHIK_00966 | 7.9e-99 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
IBEOJHIK_00967 | 8.8e-51 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
IBEOJHIK_00968 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
IBEOJHIK_00969 | 3.7e-54 | |||||
IBEOJHIK_00970 | 1.1e-89 | 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 | |
IBEOJHIK_00971 | 5.2e-83 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
IBEOJHIK_00972 | 6.5e-93 | K | Cro/C1-type HTH DNA-binding domain | |||
IBEOJHIK_00973 | 0.0 | 3.6.4.12 | L | AAA domain | ||
IBEOJHIK_00974 | 9.4e-118 | ykcC | GT2 | M | Glycosyl transferase family 2 | |
IBEOJHIK_00975 | 2.6e-160 | XK27_08510 | L | Type III restriction protein res subunit | ||
IBEOJHIK_00976 | 1e-133 | S | Domain of unknown function (DUF4918) | |||
IBEOJHIK_00977 | 8.6e-284 | mga | K | Mga helix-turn-helix domain | ||
IBEOJHIK_00979 | 7.5e-160 | yjjH | S | Calcineurin-like phosphoesterase | ||
IBEOJHIK_00980 | 3e-257 | dtpT | U | amino acid peptide transporter | ||
IBEOJHIK_00981 | 1.5e-113 | macB_3 | V | ABC transporter, ATP-binding protein | ||
IBEOJHIK_00982 | 1.2e-76 | 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 | ||
IBEOJHIK_00983 | 7.3e-195 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
IBEOJHIK_00984 | 2.1e-233 | 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 | ||
IBEOJHIK_00985 | 1.7e-43 | fruR | K | DeoR C terminal sensor domain | ||
IBEOJHIK_00986 | 1.5e-135 | stp | 3.1.3.16 | T | phosphatase | |
IBEOJHIK_00987 | 2.5e-172 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
IBEOJHIK_00988 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
IBEOJHIK_00989 | 4.2e-286 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
IBEOJHIK_00990 | 2e-174 | S | Aldo keto reductase | |||
IBEOJHIK_00991 | 5.9e-157 | bioC | 2.1.1.187, 2.1.1.197 | Q | Protein-L-isoaspartate(D-aspartate) O-methyltransferase (PCMT) | |
IBEOJHIK_00992 | 2.3e-92 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
IBEOJHIK_00993 | 5.1e-60 | dinF | V | MatE | ||
IBEOJHIK_00994 | 1.3e-223 | queG | 1.17.99.6 | C | Domain of unknown function (DUF1730) | |
IBEOJHIK_00995 | 8.3e-63 | |||||
IBEOJHIK_00996 | 2.2e-88 | bioY | S | BioY family | ||
IBEOJHIK_00997 | 1.4e-136 | cggR | K | Putative sugar-binding domain | ||
IBEOJHIK_00998 | 2.2e-193 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
IBEOJHIK_00999 | 3.6e-82 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
IBEOJHIK_01000 | 2.9e-301 | S | Psort location CytoplasmicMembrane, score | |||
IBEOJHIK_01001 | 3.2e-130 | XK27_12140 | V | ATPases associated with a variety of cellular activities | ||
IBEOJHIK_01002 | 6.8e-204 | |||||
IBEOJHIK_01003 | 8e-129 | S | membrane transporter protein | |||
IBEOJHIK_01004 | 4e-59 | hxlR | K | Transcriptional regulator, HxlR family | ||
IBEOJHIK_01005 | 1.9e-197 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
IBEOJHIK_01006 | 2.6e-149 | morA2 | S | reductase | ||
IBEOJHIK_01007 | 1e-75 | K | helix_turn_helix, mercury resistance | |||
IBEOJHIK_01009 | 2.8e-57 | E | Amino acid permease | |||
IBEOJHIK_01010 | 5.4e-175 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
IBEOJHIK_01011 | 1e-257 | wcaJ | M | Bacterial sugar transferase | ||
IBEOJHIK_01012 | 7.2e-110 | 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) | |
IBEOJHIK_01013 | 9.2e-186 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
IBEOJHIK_01014 | 1.2e-128 | pgm3 | G | Phosphoglycerate mutase family | ||
IBEOJHIK_01015 | 0.0 | uvrA3 | L | excinuclease ABC | ||
IBEOJHIK_01016 | 1.3e-99 | yghZ | C | Aldo keto reductase family protein | ||
IBEOJHIK_01017 | 1.6e-82 | yghZ | C | Aldo keto reductase family protein | ||
IBEOJHIK_01018 | 2.9e-51 | S | hydrolase | |||
IBEOJHIK_01020 | 1.2e-151 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
IBEOJHIK_01021 | 1.1e-65 | 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 | ||
IBEOJHIK_01022 | 6.7e-35 | 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 | ||
IBEOJHIK_01023 | 3.4e-208 | V | ABC transporter transmembrane region | |||
IBEOJHIK_01024 | 5.7e-183 | 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) | ||
IBEOJHIK_01025 | 3.7e-90 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
IBEOJHIK_01026 | 6.9e-72 | K | Transcriptional regulator | |||
IBEOJHIK_01027 | 8.9e-78 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
IBEOJHIK_01028 | 9e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
IBEOJHIK_01029 | 1.1e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
IBEOJHIK_01030 | 5.6e-47 | nifU | C | SUF system FeS assembly protein, NifU family | ||
IBEOJHIK_01031 | 2e-219 | agaS | G | SIS domain | ||
IBEOJHIK_01032 | 9e-130 | XK27_08435 | K | UTRA | ||
IBEOJHIK_01033 | 2.6e-137 | S | Phage tail protein | |||
IBEOJHIK_01034 | 4.5e-85 | G | Phosphoglycerate mutase family | |||
IBEOJHIK_01035 | 9.2e-69 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
IBEOJHIK_01036 | 1.7e-64 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
IBEOJHIK_01037 | 5.5e-141 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
IBEOJHIK_01038 | 1.6e-210 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
IBEOJHIK_01039 | 8.7e-137 | S | E1-E2 ATPase | |||
IBEOJHIK_01040 | 2.5e-155 | 1.1.1.346 | S | reductase | ||
IBEOJHIK_01041 | 2e-174 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
IBEOJHIK_01042 | 2.4e-203 | S | endonuclease exonuclease phosphatase family protein | |||
IBEOJHIK_01044 | 3.3e-131 | G | PTS system sorbose-specific iic component | |||
IBEOJHIK_01045 | 1.3e-131 | G | PTS system mannose/fructose/sorbose family IID component | |||
IBEOJHIK_01046 | 1.5e-80 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
IBEOJHIK_01047 | 5.1e-178 | ebgA | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
IBEOJHIK_01048 | 8.6e-129 | S | zinc-ribbon domain | |||
IBEOJHIK_01049 | 5.1e-29 | |||||
IBEOJHIK_01050 | 3.9e-110 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
IBEOJHIK_01051 | 2.9e-116 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
IBEOJHIK_01052 | 1.3e-84 | nrdI | F | Belongs to the NrdI family | ||
IBEOJHIK_01053 | 7.2e-39 | D | Alpha beta | |||
IBEOJHIK_01054 | 1.6e-27 | D | Alpha beta | |||
IBEOJHIK_01055 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
IBEOJHIK_01057 | 4e-261 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
IBEOJHIK_01058 | 2.9e-81 | K | Acetyltransferase (GNAT) domain | |||
IBEOJHIK_01059 | 1.2e-165 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
IBEOJHIK_01060 | 1.3e-120 | qmcA | O | prohibitin homologues | ||
IBEOJHIK_01061 | 8.4e-30 | |||||
IBEOJHIK_01062 | 3.2e-119 | ybhL | S | Inhibitor of apoptosis-promoting Bax1 | ||
IBEOJHIK_01063 | 1.2e-38 | ykuT | M | mechanosensitive ion channel | ||
IBEOJHIK_01064 | 1.8e-96 | ykuT | M | mechanosensitive ion channel | ||
IBEOJHIK_01065 | 2e-158 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
IBEOJHIK_01066 | 3.5e-85 | ykuL | S | CBS domain | ||
IBEOJHIK_01067 | 5.2e-133 | gla | U | Major intrinsic protein | ||
IBEOJHIK_01068 | 4.4e-35 | S | Phosphoesterase | |||
IBEOJHIK_01069 | 7.6e-258 | yhdP | S | Transporter associated domain | ||
IBEOJHIK_01070 | 1.6e-140 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
IBEOJHIK_01071 | 3.2e-115 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
IBEOJHIK_01072 | 1.9e-101 | T | Sh3 type 3 domain protein | |||
IBEOJHIK_01073 | 4.8e-102 | Q | methyltransferase | |||
IBEOJHIK_01074 | 1.8e-37 | gcdC | 2.3.1.12 | I | Biotin-requiring enzyme | |
IBEOJHIK_01075 | 1.2e-100 | 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 | |
IBEOJHIK_01076 | 7.5e-197 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
IBEOJHIK_01077 | 2.5e-77 | copR | K | Copper transport repressor CopY TcrY | ||
IBEOJHIK_01078 | 2.3e-158 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
IBEOJHIK_01079 | 1.4e-127 | oppA | E | ABC transporter, substratebinding protein | ||
IBEOJHIK_01080 | 1.2e-132 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
IBEOJHIK_01081 | 4.7e-120 | |||||
IBEOJHIK_01082 | 6.2e-162 | sepS16B | ||||
IBEOJHIK_01083 | 1e-262 | nox | 1.6.3.4 | C | NADH oxidase | |
IBEOJHIK_01084 | 2e-70 | p75 | M | NlpC P60 family protein | ||
IBEOJHIK_01085 | 1.1e-83 | p75 | M | NlpC P60 family protein | ||
IBEOJHIK_01086 | 3.4e-129 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
IBEOJHIK_01087 | 3.6e-232 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
IBEOJHIK_01088 | 6e-117 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
IBEOJHIK_01089 | 1.2e-233 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IBEOJHIK_01090 | 1.4e-167 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
IBEOJHIK_01091 | 8.9e-60 | |||||
IBEOJHIK_01092 | 8.4e-64 | |||||
IBEOJHIK_01093 | 8.4e-128 | |||||
IBEOJHIK_01094 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
IBEOJHIK_01095 | 1e-167 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
IBEOJHIK_01096 | 1.1e-33 | |||||
IBEOJHIK_01097 | 3e-107 | tag | 3.2.2.20 | L | glycosylase | |
IBEOJHIK_01098 | 1.7e-160 | yceJ | EGP | Major facilitator Superfamily | ||
IBEOJHIK_01099 | 7.9e-61 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
IBEOJHIK_01100 | 1.4e-71 | xkdO | M | Phage tail tape measure protein TP901 | ||
IBEOJHIK_01101 | 7.1e-32 | |||||
IBEOJHIK_01102 | 1.3e-46 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
IBEOJHIK_01103 | 2.8e-174 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
IBEOJHIK_01104 | 1.4e-50 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
IBEOJHIK_01105 | 5.7e-88 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
IBEOJHIK_01106 | 2.2e-54 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
IBEOJHIK_01107 | 5e-70 | 6.3.3.2 | S | ASCH | ||
IBEOJHIK_01108 | 3.1e-124 | |||||
IBEOJHIK_01109 | 1.1e-86 | K | Acetyltransferase (GNAT) domain | |||
IBEOJHIK_01110 | 6.8e-136 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
IBEOJHIK_01111 | 2.8e-90 | MA20_25245 | K | FR47-like protein | ||
IBEOJHIK_01112 | 2.4e-110 | S | alpha beta | |||
IBEOJHIK_01113 | 1.2e-36 | |||||
IBEOJHIK_01114 | 3.1e-61 | |||||
IBEOJHIK_01117 | 1.7e-51 | sugE | U | Multidrug resistance protein | ||
IBEOJHIK_01118 | 1.2e-85 | aatB | ET | ABC transporter substrate-binding protein | ||
IBEOJHIK_01119 | 2.5e-82 | yuxL | 3.4.19.1 | E | Prolyl oligopeptidase family | |
IBEOJHIK_01120 | 3.5e-28 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
IBEOJHIK_01121 | 5.8e-39 | L | Transposase and inactivated derivatives | |||
IBEOJHIK_01122 | 2.1e-148 | L | Integrase core domain | |||
IBEOJHIK_01124 | 3.4e-94 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
IBEOJHIK_01125 | 2.4e-184 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
IBEOJHIK_01126 | 3.6e-45 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
IBEOJHIK_01128 | 4.2e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
IBEOJHIK_01129 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
IBEOJHIK_01130 | 1.6e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
IBEOJHIK_01131 | 1.8e-187 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
IBEOJHIK_01132 | 6.2e-99 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
IBEOJHIK_01133 | 4.9e-168 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
IBEOJHIK_01134 | 7.8e-180 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
IBEOJHIK_01135 | 3.1e-86 | hsp1 | O | Belongs to the small heat shock protein (HSP20) family | ||
IBEOJHIK_01136 | 1.1e-112 | D | Putative exonuclease SbcCD, C subunit | |||
IBEOJHIK_01137 | 0.0 | D | Putative exonuclease SbcCD, C subunit | |||
IBEOJHIK_01138 | 2.6e-61 | salL | 2.5.1.63, 2.5.1.94 | K | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
IBEOJHIK_01139 | 8.3e-42 | 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 | ||
IBEOJHIK_01140 | 3.3e-10 | |||||
IBEOJHIK_01141 | 2.3e-249 | 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 | |
IBEOJHIK_01142 | 1.6e-52 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
IBEOJHIK_01143 | 1.2e-103 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
IBEOJHIK_01144 | 2e-116 | ymfM | S | Helix-turn-helix domain | ||
IBEOJHIK_01145 | 6e-129 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
IBEOJHIK_01146 | 8.1e-246 | ymfH | S | Peptidase M16 | ||
IBEOJHIK_01147 | 1.9e-43 | ymfF | S | Peptidase M16 inactive domain protein | ||
IBEOJHIK_01148 | 1.5e-112 | tag | 3.2.2.20 | L | glycosylase | |
IBEOJHIK_01149 | 3.6e-163 | yicL | EG | EamA-like transporter family | ||
IBEOJHIK_01151 | 1.2e-82 | FG | adenosine 5'-monophosphoramidase activity | |||
IBEOJHIK_01152 | 2.5e-91 | cps1D | M | Domain of unknown function (DUF4422) | ||
IBEOJHIK_01154 | 3e-262 | L | Exonuclease | |||
IBEOJHIK_01155 | 2.9e-44 | relB | L | RelB antitoxin | ||
IBEOJHIK_01156 | 1.2e-48 | K | Helix-turn-helix domain | |||
IBEOJHIK_01157 | 1.4e-90 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
IBEOJHIK_01158 | 1.1e-120 | |||||
IBEOJHIK_01159 | 4.1e-158 | dkgB | S | reductase | ||
IBEOJHIK_01161 | 2.5e-101 | 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 | |
IBEOJHIK_01162 | 1e-37 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
IBEOJHIK_01163 | 2.6e-77 | clcA | P | chloride | ||
IBEOJHIK_01164 | 1.1e-11 | clcA | P | chloride | ||
IBEOJHIK_01165 | 2.3e-84 | |||||
IBEOJHIK_01166 | 4.7e-82 | yabR | J | RNA binding | ||
IBEOJHIK_01167 | 4.4e-65 | divIC | D | cell cycle | ||
IBEOJHIK_01168 | 1.8e-38 | yabO | J | S4 domain protein | ||
IBEOJHIK_01169 | 2.9e-282 | yabM | S | Polysaccharide biosynthesis protein | ||
IBEOJHIK_01170 | 3.5e-177 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
IBEOJHIK_01171 | 6.5e-54 | dnaE | 2.7.7.7 | L | DNA polymerase | |
IBEOJHIK_01172 | 1.5e-130 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
IBEOJHIK_01173 | 8.3e-157 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
IBEOJHIK_01174 | 1.4e-46 | yktA | S | Belongs to the UPF0223 family | ||
IBEOJHIK_01175 | 5.9e-146 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
IBEOJHIK_01176 | 1.7e-57 | typA | T | GTP-binding protein TypA | ||
IBEOJHIK_01177 | 1.3e-287 | GK | helix_turn_helix, arabinose operon control protein | |||
IBEOJHIK_01178 | 2.1e-211 | G | Major Facilitator Superfamily | |||
IBEOJHIK_01179 | 3.5e-28 | abgB | 3.5.1.47 | S | Peptidase dimerisation domain | |
IBEOJHIK_01180 | 6e-109 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
IBEOJHIK_01181 | 2.6e-49 | |||||
IBEOJHIK_01182 | 8.4e-156 | S | Protein of unknown function (DUF2785) | |||
IBEOJHIK_01187 | 3.8e-24 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
IBEOJHIK_01188 | 1.3e-102 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
IBEOJHIK_01189 | 2.5e-50 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
IBEOJHIK_01190 | 2.2e-143 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
IBEOJHIK_01191 | 1.2e-179 | ybbR | S | YbbR-like protein | ||
IBEOJHIK_01192 | 1.2e-202 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
IBEOJHIK_01193 | 2.7e-32 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
IBEOJHIK_01194 | 4.5e-137 | lys | M | Glycosyl hydrolases family 25 | ||
IBEOJHIK_01195 | 8.1e-119 | |||||
IBEOJHIK_01196 | 5e-281 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
IBEOJHIK_01197 | 6.1e-48 | |||||
IBEOJHIK_01198 | 2e-44 | hol | S | Bacteriophage holin | ||
IBEOJHIK_01199 | 1.1e-164 | ecsB | U | ABC transporter | ||
IBEOJHIK_01200 | 1.2e-148 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
IBEOJHIK_01201 | 2.9e-87 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
IBEOJHIK_01202 | 4.2e-21 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
IBEOJHIK_01203 | 2.7e-151 | cytC6 | I | alpha/beta hydrolase fold | ||
IBEOJHIK_01204 | 3.1e-122 | yrkL | S | Flavodoxin-like fold | ||
IBEOJHIK_01206 | 1.7e-88 | S | Short repeat of unknown function (DUF308) | |||
IBEOJHIK_01207 | 7.9e-154 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
IBEOJHIK_01208 | 1.2e-199 | |||||
IBEOJHIK_01209 | 7.6e-07 | |||||
IBEOJHIK_01210 | 1.7e-19 | ywnB | S | NmrA-like family | ||
IBEOJHIK_01211 | 7.1e-71 | ywnB | S | NmrA-like family | ||
IBEOJHIK_01212 | 8.8e-110 | T | Transcriptional regulatory protein, C terminal | |||
IBEOJHIK_01213 | 2.5e-175 | T | Histidine kinase-like ATPases | |||
IBEOJHIK_01214 | 6.6e-09 | XK27_05695 | V | ABC transporter, ATP-binding protein | ||
IBEOJHIK_01215 | 9.2e-124 | 1.5.1.40 | S | Rossmann-like domain | ||
IBEOJHIK_01216 | 6.5e-193 | XK27_00915 | C | Luciferase-like monooxygenase | ||
IBEOJHIK_01217 | 1.2e-97 | yacP | S | YacP-like NYN domain | ||
IBEOJHIK_01218 | 3.2e-144 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
IBEOJHIK_01219 | 0.0 | G | Phosphodiester glycosidase | |||
IBEOJHIK_01220 | 2e-96 | G | Phosphodiester glycosidase | |||
IBEOJHIK_01221 | 4.1e-188 | 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 | ||
IBEOJHIK_01222 | 2.9e-36 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
IBEOJHIK_01224 | 3.2e-50 | lciIC | K | Helix-turn-helix XRE-family like proteins | ||
IBEOJHIK_01226 | 7.8e-61 | L | Helix-turn-helix domain | |||
IBEOJHIK_01227 | 5.9e-68 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
IBEOJHIK_01228 | 3.3e-266 | ywfO | S | HD domain protein | ||
IBEOJHIK_01229 | 2.2e-131 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
IBEOJHIK_01230 | 2.6e-34 | |||||
IBEOJHIK_01231 | 3.1e-98 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
IBEOJHIK_01232 | 3.7e-14 | |||||
IBEOJHIK_01233 | 3.4e-94 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
IBEOJHIK_01234 | 6.8e-73 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
IBEOJHIK_01235 | 5.7e-115 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
IBEOJHIK_01236 | 8e-185 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
IBEOJHIK_01237 | 1.4e-45 | fer | C | 4Fe-4S single cluster domain of Ferredoxin I | ||
IBEOJHIK_01238 | 2.4e-96 | 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 | |||
IBEOJHIK_01239 | 3.1e-22 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
IBEOJHIK_01240 | 9.2e-107 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
IBEOJHIK_01241 | 9.4e-101 | malE | G | Bacterial extracellular solute-binding protein | ||
IBEOJHIK_01242 | 7.4e-115 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
IBEOJHIK_01243 | 3.7e-45 | sgaB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
IBEOJHIK_01244 | 3.1e-101 | S | Haloacid dehalogenase-like hydrolase | |||
IBEOJHIK_01245 | 6.9e-181 | oppF | P | Belongs to the ABC transporter superfamily | ||
IBEOJHIK_01246 | 1.9e-197 | oppD | P | Belongs to the ABC transporter superfamily | ||
IBEOJHIK_01247 | 1.7e-168 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
IBEOJHIK_01248 | 1.8e-134 | arlS | 2.7.13.3 | T | Histidine kinase | |
IBEOJHIK_01249 | 5.4e-198 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
IBEOJHIK_01250 | 1.4e-78 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
IBEOJHIK_01251 | 3.6e-196 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
IBEOJHIK_01252 | 9e-107 | rsmC | 2.1.1.172 | J | Methyltransferase | |
IBEOJHIK_01253 | 1.2e-49 | |||||
IBEOJHIK_01254 | 5.2e-77 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
IBEOJHIK_01255 | 3e-298 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
IBEOJHIK_01256 | 1.5e-33 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
IBEOJHIK_01257 | 5.6e-109 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
IBEOJHIK_01258 | 5.1e-57 | glk | 2.7.1.2 | G | Glucokinase | |
IBEOJHIK_01259 | 6.6e-74 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
IBEOJHIK_01260 | 2.5e-115 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
IBEOJHIK_01261 | 1.9e-59 | |||||
IBEOJHIK_01262 | 7.6e-117 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
IBEOJHIK_01263 | 2.6e-132 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
IBEOJHIK_01264 | 1.8e-116 | |||||
IBEOJHIK_01265 | 4.7e-09 | |||||
IBEOJHIK_01266 | 4.6e-55 | yheA | S | Control of competence regulator ComK, YlbF/YmcA | ||
IBEOJHIK_01267 | 1.4e-90 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
IBEOJHIK_01268 | 1.4e-270 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IBEOJHIK_01269 | 8.6e-145 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
IBEOJHIK_01270 | 4.6e-55 | tcyB | E | ABC transporter | ||
IBEOJHIK_01271 | 1.8e-23 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
IBEOJHIK_01272 | 5.7e-30 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
IBEOJHIK_01273 | 1.1e-172 | yqhA | G | Aldose 1-epimerase | ||
IBEOJHIK_01274 | 7.8e-137 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
IBEOJHIK_01275 | 7.2e-225 | spiA | K | IrrE N-terminal-like domain | ||
IBEOJHIK_01276 | 5.2e-139 | |||||
IBEOJHIK_01277 | 1.7e-16 | |||||
IBEOJHIK_01278 | 2.8e-44 | |||||
IBEOJHIK_01279 | 8.6e-150 | S | haloacid dehalogenase-like hydrolase | |||
IBEOJHIK_01280 | 0.0 | M | Glycosyl hydrolase family 59 | |||
IBEOJHIK_01281 | 0.0 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
IBEOJHIK_01282 | 1.5e-50 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
IBEOJHIK_01283 | 1.4e-122 | azlC | E | branched-chain amino acid | ||
IBEOJHIK_01284 | 0.0 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
IBEOJHIK_01285 | 6.6e-49 | |||||
IBEOJHIK_01286 | 1.2e-180 | M | Peptidoglycan-binding domain 1 protein | |||
IBEOJHIK_01288 | 2.9e-52 | |||||
IBEOJHIK_01289 | 2.2e-88 | |||||
IBEOJHIK_01290 | 1.6e-106 | S | Membrane | |||
IBEOJHIK_01291 | 5.5e-129 | pipD | E | Dipeptidase | ||
IBEOJHIK_01292 | 8.9e-107 | pipD | E | Dipeptidase | ||
IBEOJHIK_01293 | 4.5e-55 | |||||
IBEOJHIK_01294 | 1.7e-113 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
IBEOJHIK_01295 | 2.1e-103 | S | Protein of unknown function (DUF1211) | |||
IBEOJHIK_01296 | 4.1e-128 | S | membrane transporter protein | |||
IBEOJHIK_01297 | 4.3e-47 | |||||
IBEOJHIK_01298 | 1e-153 | supH | G | Sucrose-6F-phosphate phosphohydrolase | ||
IBEOJHIK_01299 | 1e-96 | K | transcriptional regulator | |||
IBEOJHIK_01300 | 6.3e-128 | macB | V | ABC transporter, ATP-binding protein | ||
IBEOJHIK_01301 | 0.0 | ylbB | V | ABC transporter permease | ||
IBEOJHIK_01302 | 1.4e-125 | usp | 3.5.1.28 | CBM50 | D | CHAP domain |
IBEOJHIK_01303 | 2.8e-215 | P | Pyridine nucleotide-disulphide oxidoreductase | |||
IBEOJHIK_01304 | 2.2e-196 | amtB | P | Ammonium Transporter Family | ||
IBEOJHIK_01305 | 1.9e-164 | V | ABC transporter | |||
IBEOJHIK_01306 | 7.9e-109 | gluC | P | ABC transporter permease | ||
IBEOJHIK_01307 | 3.4e-149 | glnH | ET | ABC transporter substrate-binding protein | ||
IBEOJHIK_01308 | 3.6e-48 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
IBEOJHIK_01309 | 0.0 | nisT | V | ABC transporter | ||
IBEOJHIK_01310 | 3.4e-149 | V | ABC transporter | |||
IBEOJHIK_01311 | 2.8e-114 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
IBEOJHIK_01312 | 1.6e-221 | yhfX | E | Alanine racemase, N-terminal domain | ||
IBEOJHIK_01313 | 2.2e-207 | bioF | 2.3.1.47, 2.8.1.6 | E | Cys/Met metabolism PLP-dependent enzyme | |
IBEOJHIK_01314 | 5.7e-166 | php | S | Phosphotriesterase family | ||
IBEOJHIK_01315 | 1e-192 | yhfT | S | Protein of unknown function | ||
IBEOJHIK_01316 | 3e-57 | yhfU | S | Protein of unknown function DUF2620 | ||
IBEOJHIK_01317 | 7.3e-08 | |||||
IBEOJHIK_01318 | 8.7e-170 | P | YhfZ C-terminal domain | |||
IBEOJHIK_01319 | 2.8e-227 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
IBEOJHIK_01320 | 2.9e-59 | |||||
IBEOJHIK_01322 | 3.7e-61 | V | ABC transporter (permease) | |||
IBEOJHIK_01323 | 3.4e-91 | traP | 1.14.99.57, 6.2.1.3 | S | Antibiotic biosynthesis monooxygenase | |
IBEOJHIK_01324 | 9.9e-140 | yhfI | S | Metallo-beta-lactamase superfamily | ||
IBEOJHIK_01325 | 1.9e-80 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
IBEOJHIK_01326 | 7.4e-141 | K | SIS domain | |||
IBEOJHIK_01327 | 0.0 | mngB | 3.2.1.170 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
IBEOJHIK_01328 | 8.5e-81 | frvA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
IBEOJHIK_01329 | 3.6e-48 | manY | 2.7.1.191, 2.7.1.202 | G | phosphotransferase system | |
IBEOJHIK_01330 | 4.3e-203 | manY | 2.7.1.191, 2.7.1.202 | G | phosphotransferase system | |
IBEOJHIK_01331 | 9.3e-161 | S | CAAX protease self-immunity | |||
IBEOJHIK_01333 | 1.5e-89 | S | Protein of unknown function with HXXEE motif | |||
IBEOJHIK_01334 | 4.1e-98 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_01335 | 1.6e-117 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
IBEOJHIK_01336 | 4.4e-28 | hisC | 2.6.1.9 | E | Cys/Met metabolism PLP-dependent enzyme | |
IBEOJHIK_01337 | 5.2e-40 | hisC | 2.6.1.9 | E | Cys/Met metabolism PLP-dependent enzyme | |
IBEOJHIK_01338 | 7.9e-123 | K | response regulator | |||
IBEOJHIK_01339 | 8.1e-99 | 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 | |
IBEOJHIK_01340 | 1.6e-148 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
IBEOJHIK_01341 | 7.6e-94 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
IBEOJHIK_01342 | 8.4e-38 | ylqC | S | Belongs to the UPF0109 family | ||
IBEOJHIK_01343 | 1e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
IBEOJHIK_01344 | 3.1e-230 | 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 | |
IBEOJHIK_01345 | 1.3e-57 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
IBEOJHIK_01346 | 5.6e-26 | |||||
IBEOJHIK_01347 | 7.5e-17 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
IBEOJHIK_01349 | 7.2e-104 | XK27_00670 | S | ABC transporter substrate binding protein | ||
IBEOJHIK_01351 | 2e-167 | XK27_00670 | S | ABC transporter | ||
IBEOJHIK_01352 | 7.6e-156 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
IBEOJHIK_01353 | 6.1e-143 | cmpC | S | ABC transporter, ATP-binding protein | ||
IBEOJHIK_01354 | 1.2e-174 | yhfP | 1.1.1.1 | C | Zinc-binding dehydrogenase | |
IBEOJHIK_01355 | 4.2e-46 | yodB | K | Transcriptional regulator, HxlR family | ||
IBEOJHIK_01356 | 1.4e-107 | yiiE | S | Protein of unknown function (DUF1211) | ||
IBEOJHIK_01357 | 5.7e-129 | cobB | K | Sir2 family | ||
IBEOJHIK_01358 | 2.8e-17 | |||||
IBEOJHIK_01359 | 3.3e-172 | |||||
IBEOJHIK_01360 | 3.8e-98 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
IBEOJHIK_01361 | 3.6e-193 | glnA | 6.3.1.2 | E | glutamine synthetase | |
IBEOJHIK_01362 | 1.5e-33 | |||||
IBEOJHIK_01363 | 1.3e-137 | repA | K | DeoR C terminal sensor domain | ||
IBEOJHIK_01364 | 1.2e-168 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
IBEOJHIK_01365 | 4.1e-150 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
IBEOJHIK_01366 | 1.6e-137 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
IBEOJHIK_01367 | 1.8e-170 | rgpB | GT2 | M | Glycosyl transferase family 2 | |
IBEOJHIK_01368 | 3.5e-45 | M | Glycosyl transferases group 1 | |||
IBEOJHIK_01369 | 2e-46 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
IBEOJHIK_01370 | 3.4e-109 | rplD | J | Forms part of the polypeptide exit tunnel | ||
IBEOJHIK_01371 | 3e-113 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
IBEOJHIK_01372 | 1.2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
IBEOJHIK_01373 | 1.2e-68 | psiE | S | Phosphate-starvation-inducible E | ||
IBEOJHIK_01374 | 1.7e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
IBEOJHIK_01375 | 5e-150 | yfjR | K | WYL domain | ||
IBEOJHIK_01376 | 4.1e-164 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
IBEOJHIK_01377 | 1.5e-141 | terC | P | membrane | ||
IBEOJHIK_01378 | 4.6e-58 | 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 | ||
IBEOJHIK_01379 | 1.3e-132 | 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 | ||
IBEOJHIK_01380 | 7.2e-96 | spl | M | NlpC/P60 family | ||
IBEOJHIK_01381 | 3e-19 | spl | M | NlpC/P60 family | ||
IBEOJHIK_01382 | 2e-233 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
IBEOJHIK_01383 | 8.3e-90 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
IBEOJHIK_01384 | 8.1e-96 | |||||
IBEOJHIK_01385 | 2.7e-177 | K | sequence-specific DNA binding | |||
IBEOJHIK_01386 | 3e-159 | iolJ | 4.1.2.13, 4.1.2.29 | G | Fructose-bisphosphate aldolase class-II | |
IBEOJHIK_01387 | 3.6e-176 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
IBEOJHIK_01388 | 1.8e-195 | iolG2 | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
IBEOJHIK_01389 | 1.1e-192 | iolG | 1.1.1.18, 1.1.1.369 | C | Involved in the oxidation of myo-inositol (MI) and D- chiro-inositol (DCI) to 2-keto-myo-inositol (2KMI or 2-inosose) and 1-keto-D-chiro-inositol (1KDCI), respectively | |
IBEOJHIK_01390 | 0.0 | iolD | 3.7.1.22 | E | Involved in the cleavage of the C1-C2 bond of 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (THcHDO) to yield 5-deoxy- glucuronate (5DG) | |
IBEOJHIK_01391 | 7.5e-89 | pacL | 3.6.3.8 | P | P-type ATPase | |
IBEOJHIK_01392 | 6.9e-113 | pacL | 3.6.3.8 | P | P-type ATPase | |
IBEOJHIK_01393 | 2e-17 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
IBEOJHIK_01394 | 6.2e-84 | ydcK | S | Belongs to the SprT family | ||
IBEOJHIK_01395 | 9.6e-45 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
IBEOJHIK_01396 | 1.1e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
IBEOJHIK_01397 | 4.9e-150 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
IBEOJHIK_01398 | 5.4e-157 | ysdA | CP | ABC-2 family transporter protein | ||
IBEOJHIK_01399 | 3.6e-64 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
IBEOJHIK_01400 | 8.9e-164 | CcmA | V | ABC transporter | ||
IBEOJHIK_01401 | 1.5e-115 | VPA0052 | I | ABC-2 family transporter protein | ||
IBEOJHIK_01402 | 4.9e-72 | IQ | reductase | |||
IBEOJHIK_01403 | 2e-91 | 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 | |
IBEOJHIK_01404 | 8.3e-221 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
IBEOJHIK_01407 | 8.4e-154 | S | Protein of unknown function (DUF1211) | |||
IBEOJHIK_01408 | 5.9e-62 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
IBEOJHIK_01409 | 3.5e-79 | ywiB | S | Domain of unknown function (DUF1934) | ||
IBEOJHIK_01411 | 1.2e-274 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
IBEOJHIK_01412 | 5.5e-133 | K | sequence-specific DNA binding | |||
IBEOJHIK_01413 | 3.2e-89 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
IBEOJHIK_01414 | 8.4e-84 | 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 | ||
IBEOJHIK_01415 | 3.6e-70 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
IBEOJHIK_01416 | 4e-84 | 3.4.23.43 | ||||
IBEOJHIK_01420 | 3.6e-32 | 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 | |
IBEOJHIK_01422 | 1e-60 | glnR | K | Transcriptional regulator | ||
IBEOJHIK_01423 | 4.9e-08 | |||||
IBEOJHIK_01424 | 1.6e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
IBEOJHIK_01425 | 5.4e-71 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
IBEOJHIK_01426 | 2.9e-56 | 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 | ||
IBEOJHIK_01427 | 1.6e-25 | 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 | ||
IBEOJHIK_01428 | 2e-71 | helD | 3.6.4.12 | L | DNA helicase | |
IBEOJHIK_01429 | 5.7e-147 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
IBEOJHIK_01430 | 6e-241 | 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 | ||
IBEOJHIK_01431 | 3.9e-75 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
IBEOJHIK_01432 | 4.8e-73 | S | phage tail tape measure protein | |||
IBEOJHIK_01433 | 4.2e-220 | |||||
IBEOJHIK_01434 | 1e-123 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
IBEOJHIK_01435 | 9.7e-161 | epsB | M | biosynthesis protein | ||
IBEOJHIK_01436 | 2e-132 | E | lipolytic protein G-D-S-L family | |||
IBEOJHIK_01437 | 2.6e-177 | ps301 | K | Protein of unknown function (DUF4065) | ||
IBEOJHIK_01438 | 1.2e-146 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
IBEOJHIK_01439 | 1.5e-169 | fba | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
IBEOJHIK_01440 | 1.6e-82 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
IBEOJHIK_01441 | 3.9e-72 | 2.7.1.191 | G | PTS system fructose IIA component | ||
IBEOJHIK_01442 | 1.6e-310 | G | PTS system sorbose-specific iic component | |||
IBEOJHIK_01443 | 7.9e-126 | tal | 2.2.1.2 | H | Transaldolase/Fructose-6-phosphate aldolase | |
IBEOJHIK_01444 | 5.8e-170 | K | helix_turn _helix lactose operon repressor | |||
IBEOJHIK_01446 | 1.6e-112 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
IBEOJHIK_01447 | 1.6e-196 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
IBEOJHIK_01448 | 5.7e-277 | pipD | E | Dipeptidase | ||
IBEOJHIK_01449 | 1.3e-42 | |||||
IBEOJHIK_01450 | 4e-54 | |||||
IBEOJHIK_01451 | 3.5e-19 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
IBEOJHIK_01452 | 1.3e-96 | 2.3.1.128, 5.2.1.8 | J | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_01454 | 3.6e-114 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
IBEOJHIK_01455 | 7e-43 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
IBEOJHIK_01456 | 2.9e-19 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
IBEOJHIK_01457 | 1.2e-52 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
IBEOJHIK_01458 | 2.3e-116 | dedA | S | SNARE-like domain protein | ||
IBEOJHIK_01459 | 1.9e-115 | S | Protein of unknown function (DUF1461) | |||
IBEOJHIK_01460 | 1.1e-78 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_01461 | 2.6e-112 | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | ||
IBEOJHIK_01463 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_01465 | 6e-49 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
IBEOJHIK_01466 | 3.5e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
IBEOJHIK_01467 | 2.3e-297 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
IBEOJHIK_01468 | 4e-40 | ypbG | 2.7.1.2 | GK | ROK family | |
IBEOJHIK_01469 | 1.6e-103 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
IBEOJHIK_01470 | 4.6e-125 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
IBEOJHIK_01471 | 1.4e-234 | rarA | L | recombination factor protein RarA | ||
IBEOJHIK_01472 | 2.2e-48 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
IBEOJHIK_01473 | 2.6e-183 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
IBEOJHIK_01475 | 1.4e-105 | oadB | 4.1.1.3 | C | Na+-transporting oxaloacetate decarboxylase beta subunit | |
IBEOJHIK_01476 | 1.6e-34 | pip | V | domain protein | ||
IBEOJHIK_01477 | 1.7e-88 | ykiI | ||||
IBEOJHIK_01478 | 2.6e-32 | pcaC | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
IBEOJHIK_01479 | 2.7e-137 | cobB | K | Sir2 family | ||
IBEOJHIK_01480 | 1.5e-123 | plsC | 2.3.1.51 | I | Acyltransferase | |
IBEOJHIK_01481 | 6.7e-19 | ybeC | E | amino acid | ||
IBEOJHIK_01482 | 1.5e-230 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
IBEOJHIK_01483 | 2.7e-196 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
IBEOJHIK_01484 | 6.9e-168 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
IBEOJHIK_01485 | 5.1e-72 | patA | 2.6.1.1 | E | Aminotransferase | |
IBEOJHIK_01486 | 2.2e-38 | V | (ABC) transporter | |||
IBEOJHIK_01487 | 1.8e-119 | V | ABC transporter transmembrane region | |||
IBEOJHIK_01488 | 3.4e-297 | E | ABC transporter, substratebinding protein | |||
IBEOJHIK_01489 | 1.6e-238 | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | ||
IBEOJHIK_01490 | 6.5e-10 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_01491 | 1.9e-43 | glcU | U | sugar transport | ||
IBEOJHIK_01492 | 1.4e-148 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
IBEOJHIK_01493 | 5.3e-89 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
IBEOJHIK_01494 | 1.2e-115 | yfnA | E | Amino Acid | ||
IBEOJHIK_01495 | 5.1e-173 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
IBEOJHIK_01496 | 1.2e-188 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
IBEOJHIK_01497 | 6.2e-260 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
IBEOJHIK_01498 | 1.7e-259 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
IBEOJHIK_01499 | 2e-73 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
IBEOJHIK_01500 | 4.6e-224 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
IBEOJHIK_01501 | 5.5e-59 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
IBEOJHIK_01502 | 2.9e-96 | puuR | K | Cupin domain | ||
IBEOJHIK_01503 | 1.2e-191 | mocA | S | Oxidoreductase | ||
IBEOJHIK_01504 | 3.6e-12 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
IBEOJHIK_01505 | 1.3e-29 | mtsB | U | ABC 3 transport family | ||
IBEOJHIK_01506 | 1.1e-175 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
IBEOJHIK_01507 | 8.7e-51 | czrA | K | Transcriptional regulator, ArsR family | ||
IBEOJHIK_01508 | 9e-113 | 2.5.1.105 | P | Cation efflux family | ||
IBEOJHIK_01509 | 1e-24 | |||||
IBEOJHIK_01510 | 4.9e-47 | F | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
IBEOJHIK_01511 | 3.1e-206 | S | Protein of unknown function (DUF917) | |||
IBEOJHIK_01512 | 2.9e-290 | apc3 | 3.5.2.9 | EQ | Hydantoinase/oxoprolinase N-terminal region | |
IBEOJHIK_01514 | 5.1e-246 | G | PTS system sugar-specific permease component | |||
IBEOJHIK_01515 | 7e-225 | dgoD | 4.2.1.6 | M | Mandelate racemase muconate lactonizing enzyme | |
IBEOJHIK_01516 | 7.7e-90 | |||||
IBEOJHIK_01517 | 2.4e-248 | ypiB | EGP | Major facilitator Superfamily | ||
IBEOJHIK_01518 | 1.8e-72 | K | Transcriptional regulator | |||
IBEOJHIK_01519 | 1.2e-76 | |||||
IBEOJHIK_01520 | 4.7e-160 | K | LysR substrate binding domain | |||
IBEOJHIK_01521 | 7.1e-248 | P | Sodium:sulfate symporter transmembrane region | |||
IBEOJHIK_01522 | 3.2e-101 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
IBEOJHIK_01523 | 4e-289 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
IBEOJHIK_01524 | 4.5e-149 | G | PTS system mannose/fructose/sorbose family IID component | |||
IBEOJHIK_01525 | 1e-129 | G | PTS system sorbose-specific iic component | |||
IBEOJHIK_01526 | 3e-162 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
IBEOJHIK_01527 | 2.9e-256 | fucA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
IBEOJHIK_01528 | 1.2e-137 | K | UTRA domain | |||
IBEOJHIK_01529 | 6.6e-91 | 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 | ||
IBEOJHIK_01530 | 2.2e-128 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
IBEOJHIK_01531 | 9.7e-22 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
IBEOJHIK_01532 | 3e-139 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
IBEOJHIK_01533 | 5e-54 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
IBEOJHIK_01534 | 5.9e-174 | 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 | ||
IBEOJHIK_01535 | 0.0 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
IBEOJHIK_01536 | 3.8e-306 | 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 | |
IBEOJHIK_01537 | 1.3e-199 | 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 | |
IBEOJHIK_01538 | 8.8e-29 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
IBEOJHIK_01539 | 1.3e-196 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
IBEOJHIK_01540 | 4.2e-110 | ydiL | S | CAAX protease self-immunity | ||
IBEOJHIK_01541 | 6.7e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
IBEOJHIK_01542 | 4.5e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
IBEOJHIK_01543 | 1.1e-56 | S | Domain of unknown function (DUF1827) | |||
IBEOJHIK_01544 | 6.2e-54 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
IBEOJHIK_01545 | 3.2e-30 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
IBEOJHIK_01546 | 6e-91 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
IBEOJHIK_01548 | 1.2e-67 | |||||
IBEOJHIK_01549 | 2.7e-22 | |||||
IBEOJHIK_01550 | 1.8e-115 | S | Calcineurin-like phosphoesterase | |||
IBEOJHIK_01551 | 5.9e-116 | yibF | S | overlaps another CDS with the same product name | ||
IBEOJHIK_01552 | 3.2e-156 | yibE | S | overlaps another CDS with the same product name | ||
IBEOJHIK_01553 | 1.1e-141 | minD | D | Belongs to the ParA family | ||
IBEOJHIK_01554 | 3.7e-114 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
IBEOJHIK_01555 | 3.6e-46 | mreD | M | rod shape-determining protein MreD | ||
IBEOJHIK_01556 | 1.9e-123 | |||||
IBEOJHIK_01557 | 0.0 | S | Protein of unknown function (DUF1524) | |||
IBEOJHIK_01558 | 1.3e-76 | S | Protein of unknown function (DUF1524) | |||
IBEOJHIK_01559 | 0.0 | 3.4.21.53 | O | Putative ATP-dependent Lon protease | ||
IBEOJHIK_01560 | 1.2e-88 | S | PglZ domain | |||
IBEOJHIK_01561 | 3.6e-108 | L | Pfam:Integrase_AP2 | |||
IBEOJHIK_01562 | 9.6e-44 | |||||
IBEOJHIK_01563 | 1.4e-56 | yqeG | S | HAD phosphatase, family IIIA | ||
IBEOJHIK_01564 | 8.5e-139 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_01565 | 2.6e-19 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_01566 | 2.4e-110 | K | Psort location Cytoplasmic, score | |||
IBEOJHIK_01567 | 4.2e-55 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
IBEOJHIK_01568 | 1.9e-79 | yphH | S | Cupin domain | ||
IBEOJHIK_01569 | 1.5e-77 | K | Transcriptional regulator | |||
IBEOJHIK_01570 | 5.4e-121 | gph | 3.1.3.18 | S | haloacid dehalogenase-like hydrolase | |
IBEOJHIK_01571 | 1.2e-126 | ssuC | U | Binding-protein-dependent transport system inner membrane component | ||
IBEOJHIK_01572 | 4e-122 | ssuB | P | ATPases associated with a variety of cellular activities | ||
IBEOJHIK_01573 | 7.6e-89 | yfiQ | I | Acyltransferase family | ||
IBEOJHIK_01574 | 6.3e-134 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
IBEOJHIK_01575 | 1.4e-42 | 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 | ||
IBEOJHIK_01576 | 1.3e-139 | puuD | S | peptidase C26 | ||
IBEOJHIK_01578 | 9.1e-27 | 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 | |
IBEOJHIK_01579 | 8.6e-162 | 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 | |
IBEOJHIK_01580 | 4.9e-224 | pimH | EGP | Major facilitator Superfamily | ||
IBEOJHIK_01581 | 3.7e-34 | |||||
IBEOJHIK_01582 | 2.5e-32 | |||||
IBEOJHIK_01583 | 5.4e-08 | |||||
IBEOJHIK_01586 | 8.8e-09 | yhjA | S | CsbD-like | ||
IBEOJHIK_01587 | 1.1e-195 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
IBEOJHIK_01588 | 7.2e-46 | |||||
IBEOJHIK_01589 | 5.6e-203 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
IBEOJHIK_01590 | 2.9e-122 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
IBEOJHIK_01591 | 1.8e-93 | ccpN | K | Domain in cystathionine beta-synthase and other proteins. | ||
IBEOJHIK_01592 | 0.0 | ppdK | 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
IBEOJHIK_01593 | 0.0 | kup | P | Transport of potassium into the cell | ||
IBEOJHIK_01594 | 2.9e-84 | V | ATPases associated with a variety of cellular activities | |||
IBEOJHIK_01595 | 1.3e-93 | sigH | K | Sigma-70 region 2 | ||
IBEOJHIK_01596 | 3.7e-207 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
IBEOJHIK_01597 | 9.2e-95 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Cobalamin adenosyltransferase | |
IBEOJHIK_01598 | 1.3e-88 | S | ECF transporter, substrate-specific component | |||
IBEOJHIK_01599 | 3.1e-63 | S | Domain of unknown function (DUF4430) | |||
IBEOJHIK_01600 | 2e-118 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
IBEOJHIK_01601 | 5.2e-30 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
IBEOJHIK_01602 | 9.5e-49 | 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 | |
IBEOJHIK_01603 | 3.2e-132 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
IBEOJHIK_01604 | 9.3e-71 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
IBEOJHIK_01605 | 2.9e-241 | ugpB | G | Bacterial extracellular solute-binding protein | ||
IBEOJHIK_01606 | 2.2e-148 | ugpE | G | ABC transporter permease | ||
IBEOJHIK_01607 | 6.6e-165 | ugpA | P | ABC-type sugar transport systems, permease components | ||
IBEOJHIK_01608 | 2.5e-211 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
IBEOJHIK_01609 | 3.2e-226 | EGP | Major facilitator Superfamily | |||
IBEOJHIK_01610 | 9.4e-70 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
IBEOJHIK_01611 | 3.4e-80 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
IBEOJHIK_01612 | 1.7e-52 | licR | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | K | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
IBEOJHIK_01613 | 9.4e-71 | ahaA | 2.7.1.191 | G | PTS system fructose IIA component | |
IBEOJHIK_01614 | 8.5e-84 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
IBEOJHIK_01615 | 3.7e-137 | G | PTS system sorbose-specific iic component | |||
IBEOJHIK_01616 | 1.3e-151 | manZ | G | PTS system mannose/fructose/sorbose family IID component | ||
IBEOJHIK_01617 | 1.2e-204 | C | Zinc-binding dehydrogenase | |||
IBEOJHIK_01618 | 1.5e-288 | xylB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
IBEOJHIK_01619 | 2.7e-97 | S | Domain of unknown function (DUF4428) | |||
IBEOJHIK_01620 | 1.4e-208 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
IBEOJHIK_01621 | 5.3e-215 | uhpT | EGP | Major facilitator Superfamily | ||
IBEOJHIK_01622 | 2.2e-131 | ymfC | K | UTRA | ||
IBEOJHIK_01623 | 5.2e-256 | 3.5.1.18 | E | Peptidase family M20/M25/M40 | ||
IBEOJHIK_01624 | 1.4e-181 | aspG | 3.4.19.5, 3.5.1.1, 3.5.1.26 | E | Asparaginase | |
IBEOJHIK_01625 | 1e-159 | bglK_1 | GK | ROK family | ||
IBEOJHIK_01626 | 1.7e-44 | |||||
IBEOJHIK_01627 | 0.0 | O | Belongs to the peptidase S8 family | |||
IBEOJHIK_01628 | 2.5e-180 | O | Belongs to the peptidase S8 family | |||
IBEOJHIK_01629 | 4.7e-215 | ulaG | S | Beta-lactamase superfamily domain | ||
IBEOJHIK_01630 | 3.8e-81 | cmtB | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
IBEOJHIK_01631 | 5.3e-281 | ulaA | S | PTS system sugar-specific permease component | ||
IBEOJHIK_01632 | 1.8e-195 | gldA | 1.1.1.1, 1.1.1.6 | C | dehydrogenase | |
IBEOJHIK_01635 | 6e-227 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
IBEOJHIK_01636 | 2.6e-80 | S | Threonine/Serine exporter, ThrE | |||
IBEOJHIK_01637 | 1.9e-133 | thrE | S | Putative threonine/serine exporter | ||
IBEOJHIK_01639 | 1.3e-31 | |||||
IBEOJHIK_01640 | 3.8e-277 | V | ABC transporter transmembrane region | |||
IBEOJHIK_01641 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
IBEOJHIK_01642 | 1.3e-252 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
IBEOJHIK_01643 | 7.4e-310 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
IBEOJHIK_01644 | 6.6e-54 | L | AAA ATPase domain | |||
IBEOJHIK_01645 | 1.1e-21 | L | AAA ATPase domain | |||
IBEOJHIK_01646 | 1.3e-265 | M | domain protein | |||
IBEOJHIK_01647 | 0.0 | M | domain protein | |||
IBEOJHIK_01648 | 1.9e-124 | ftsE | D | ABC transporter | ||
IBEOJHIK_01649 | 1.8e-159 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
IBEOJHIK_01650 | 3.7e-226 | S | Amidohydrolase | |||
IBEOJHIK_01651 | 5.2e-101 | 6.3.1.2 | E | Glutamine synthetase N-terminal domain | ||
IBEOJHIK_01652 | 4.6e-141 | 6.3.1.2 | E | Glutamine synthetase N-terminal domain | ||
IBEOJHIK_01654 | 5.7e-143 | puuD | S | peptidase C26 | ||
IBEOJHIK_01656 | 2.4e-141 | H | Protein of unknown function (DUF1698) | |||
IBEOJHIK_01657 | 3e-160 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
IBEOJHIK_01658 | 4.1e-33 | |||||
IBEOJHIK_01659 | 4e-104 | V | Beta-lactamase | |||
IBEOJHIK_01660 | 1.1e-70 | ampH | V | Beta-lactamase | ||
IBEOJHIK_01661 | 1.2e-45 | |||||
IBEOJHIK_01662 | 5.9e-132 | DegV | S | EDD domain protein, DegV family | ||
IBEOJHIK_01663 | 2.3e-179 | ccpA | K | catabolite control protein A | ||
IBEOJHIK_01664 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
IBEOJHIK_01665 | 1.9e-16 | 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 | ||
IBEOJHIK_01666 | 2.1e-102 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
IBEOJHIK_01667 | 1.3e-42 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
IBEOJHIK_01668 | 4.4e-70 | yjhE | S | Phage tail protein | ||
IBEOJHIK_01670 | 6.5e-75 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
IBEOJHIK_01671 | 1.4e-260 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
IBEOJHIK_01672 | 2.8e-171 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
IBEOJHIK_01673 | 1.1e-130 | rpl | K | Helix-turn-helix domain, rpiR family | ||
IBEOJHIK_01674 | 1.5e-166 | natA | S | ABC transporter, ATP-binding protein | ||
IBEOJHIK_01675 | 3.2e-83 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
IBEOJHIK_01676 | 6.5e-179 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
IBEOJHIK_01677 | 4.6e-131 | 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 | |
IBEOJHIK_01678 | 3e-159 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
IBEOJHIK_01679 | 9e-92 | yxjI | ||||
IBEOJHIK_01680 | 5.6e-261 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
IBEOJHIK_01681 | 1e-176 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
IBEOJHIK_01682 | 3e-39 | S | phage tail tape measure protein | |||
IBEOJHIK_01683 | 1.4e-22 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
IBEOJHIK_01684 | 1.8e-32 | fld | C | Flavodoxin | ||
IBEOJHIK_01685 | 6.5e-37 | fld | C | Flavodoxin | ||
IBEOJHIK_01686 | 1.4e-56 | yihY | S | Belongs to the UPF0761 family | ||
IBEOJHIK_01687 | 2.8e-265 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
IBEOJHIK_01688 | 8.6e-292 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
IBEOJHIK_01689 | 6.8e-28 | |||||
IBEOJHIK_01690 | 2.1e-128 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
IBEOJHIK_01691 | 1.9e-172 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
IBEOJHIK_01692 | 3.1e-203 | 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 | |
IBEOJHIK_01693 | 1.8e-113 | cutC | P | Participates in the control of copper homeostasis | ||
IBEOJHIK_01694 | 3.5e-146 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
IBEOJHIK_01695 | 7.1e-200 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
IBEOJHIK_01696 | 4.2e-62 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
IBEOJHIK_01697 | 3.5e-42 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
IBEOJHIK_01698 | 2e-175 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
IBEOJHIK_01699 | 9.3e-11 | |||||
IBEOJHIK_01700 | 4.9e-87 | |||||
IBEOJHIK_01701 | 8.8e-207 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
IBEOJHIK_01702 | 5.5e-112 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_01704 | 9.2e-112 | 1.6.5.2 | S | Flavodoxin-like fold | ||
IBEOJHIK_01705 | 2.1e-94 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_01706 | 2.5e-86 | |||||
IBEOJHIK_01707 | 3.5e-202 | T | PhoQ Sensor | |||
IBEOJHIK_01708 | 1.6e-120 | K | Transcriptional regulatory protein, C terminal | |||
IBEOJHIK_01709 | 2e-91 | ogt | 2.1.1.63 | L | Methyltransferase | |
IBEOJHIK_01710 | 1.1e-192 | ldhD3 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
IBEOJHIK_01711 | 4.5e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
IBEOJHIK_01712 | 2.6e-52 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
IBEOJHIK_01713 | 6.1e-85 | |||||
IBEOJHIK_01714 | 7.2e-253 | celD | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IBEOJHIK_01715 | 3.1e-59 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
IBEOJHIK_01716 | 2.2e-76 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
IBEOJHIK_01717 | 1.2e-114 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
IBEOJHIK_01720 | 1.3e-07 | |||||
IBEOJHIK_01722 | 2.8e-09 | |||||
IBEOJHIK_01724 | 5.2e-142 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
IBEOJHIK_01725 | 7.6e-45 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
IBEOJHIK_01726 | 5.1e-153 | S | hydrolase | |||
IBEOJHIK_01728 | 3.3e-42 | pncA | Q | Isochorismatase family | ||
IBEOJHIK_01729 | 3.5e-43 | pncA | Q | Isochorismatase family | ||
IBEOJHIK_01730 | 1.5e-132 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
IBEOJHIK_01731 | 1.4e-222 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
IBEOJHIK_01732 | 1e-38 | corA | P | CorA-like Mg2+ transporter protein | ||
IBEOJHIK_01733 | 2e-191 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
IBEOJHIK_01734 | 1.6e-49 | M | Glycosyl hydrolases family 25 | |||
IBEOJHIK_01735 | 3.4e-39 | N | Uncharacterized conserved protein (DUF2075) | |||
IBEOJHIK_01736 | 1.9e-103 | |||||
IBEOJHIK_01737 | 1.9e-156 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
IBEOJHIK_01738 | 3.9e-116 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
IBEOJHIK_01739 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
IBEOJHIK_01740 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
IBEOJHIK_01741 | 1.8e-105 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
IBEOJHIK_01742 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
IBEOJHIK_01743 | 6e-115 | S | Protein of unknown function (DUF969) | |||
IBEOJHIK_01744 | 3.7e-130 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
IBEOJHIK_01745 | 7.9e-65 | asp2 | S | Asp23 family, cell envelope-related function | ||
IBEOJHIK_01746 | 5.1e-61 | asp23 | S | Asp23 family, cell envelope-related function | ||
IBEOJHIK_01747 | 1.9e-29 | |||||
IBEOJHIK_01748 | 1.5e-89 | S | Protein conserved in bacteria | |||
IBEOJHIK_01749 | 6.4e-38 | S | Transglycosylase associated protein | |||
IBEOJHIK_01750 | 9.1e-71 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
IBEOJHIK_01751 | 4e-173 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
IBEOJHIK_01752 | 6.7e-27 | |||||
IBEOJHIK_01753 | 3.4e-36 | |||||
IBEOJHIK_01754 | 6.4e-84 | fld | C | Flavodoxin | ||
IBEOJHIK_01755 | 5.5e-52 | |||||
IBEOJHIK_01756 | 8.2e-213 | V | (ABC) transporter | |||
IBEOJHIK_01757 | 1.9e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
IBEOJHIK_01758 | 9.7e-61 | yitW | S | Iron-sulfur cluster assembly protein | ||
IBEOJHIK_01759 | 5.3e-141 | |||||
IBEOJHIK_01760 | 4.3e-211 | ciaH | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
IBEOJHIK_01761 | 1.7e-67 | yqkB | S | Belongs to the HesB IscA family | ||
IBEOJHIK_01762 | 4.8e-20 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
IBEOJHIK_01763 | 1.1e-195 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
IBEOJHIK_01764 | 4.1e-65 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
IBEOJHIK_01765 | 4.5e-123 | tal | 2.2.1.2 | H | Pfam:Transaldolase | |
IBEOJHIK_01766 | 0.0 | K | Mga helix-turn-helix domain | |||
IBEOJHIK_01767 | 3.6e-55 | S | PRD domain | |||
IBEOJHIK_01768 | 1.2e-61 | S | Glycine-rich SFCGS | |||
IBEOJHIK_01769 | 6e-53 | S | Domain of unknown function (DUF4312) | |||
IBEOJHIK_01770 | 1.7e-137 | S | Domain of unknown function (DUF4311) | |||
IBEOJHIK_01771 | 3.6e-107 | S | Domain of unknown function (DUF4310) | |||
IBEOJHIK_01773 | 1.1e-59 | |||||
IBEOJHIK_01774 | 6.2e-81 | S | Domain of unknown function (DUF5067) | |||
IBEOJHIK_01775 | 1.6e-207 | potD | P | ABC transporter | ||
IBEOJHIK_01776 | 8.9e-145 | potC | P | ABC transporter permease | ||
IBEOJHIK_01777 | 1.7e-148 | potB | P | ABC transporter permease | ||
IBEOJHIK_01778 | 9.3e-115 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
IBEOJHIK_01779 | 9.6e-194 | L | Transposase and inactivated derivatives, IS30 family | |||
IBEOJHIK_01780 | 2.6e-160 | tktN | 2.2.1.1 | G | Transketolase, thiamine diphosphate binding domain | |
IBEOJHIK_01781 | 8.1e-177 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
IBEOJHIK_01782 | 9.3e-29 | |||||
IBEOJHIK_01783 | 2.3e-159 | cydB | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit II | |
IBEOJHIK_01784 | 3.8e-77 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
IBEOJHIK_01785 | 6.7e-121 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
IBEOJHIK_01786 | 1.7e-107 | ypsA | S | Belongs to the UPF0398 family | ||
IBEOJHIK_01787 | 1.8e-66 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
IBEOJHIK_01789 | 9.2e-86 | K | Mga helix-turn-helix domain | |||
IBEOJHIK_01790 | 9.4e-84 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
IBEOJHIK_01791 | 4.2e-141 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
IBEOJHIK_01792 | 3.3e-42 | rpmE2 | J | Ribosomal protein L31 | ||
IBEOJHIK_01793 | 4.7e-73 | |||||
IBEOJHIK_01794 | 2e-123 | |||||
IBEOJHIK_01795 | 4.6e-125 | S | Tetratricopeptide repeat | |||
IBEOJHIK_01796 | 2.3e-147 | |||||
IBEOJHIK_01797 | 3e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
IBEOJHIK_01798 | 4.5e-264 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
IBEOJHIK_01799 | 1.7e-63 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
IBEOJHIK_01800 | 6.3e-218 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
IBEOJHIK_01801 | 2.4e-37 | |||||
IBEOJHIK_01802 | 5.6e-62 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
IBEOJHIK_01803 | 1.2e-46 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
IBEOJHIK_01804 | 1e-139 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
IBEOJHIK_01805 | 6.8e-107 | 1.1.1.133, 5.1.3.13 | M | dTDP-4-dehydrorhamnose 3,5-epimerase | ||
IBEOJHIK_01807 | 6.2e-123 | |||||
IBEOJHIK_01808 | 5.5e-112 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_01809 | 1.2e-123 | norB | EGP | Major Facilitator | ||
IBEOJHIK_01810 | 2e-73 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
IBEOJHIK_01811 | 2.1e-30 | M | domain protein | |||
IBEOJHIK_01812 | 0.0 | yvcC | M | Cna protein B-type domain | ||
IBEOJHIK_01813 | 0.0 | yfiC | V | ABC transporter | ||
IBEOJHIK_01814 | 1.3e-93 | S | NADPH-dependent FMN reductase | |||
IBEOJHIK_01815 | 3.4e-294 | 2.4.1.9, 3.4.24.40 | GH68 | S | peptidase inhibitor activity | |
IBEOJHIK_01816 | 2.2e-145 | IQ | NAD dependent epimerase/dehydratase family | |||
IBEOJHIK_01817 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
IBEOJHIK_01818 | 1.2e-88 | gutM | K | Glucitol operon activator protein (GutM) | ||
IBEOJHIK_01819 | 1.3e-28 | 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 | ||
IBEOJHIK_01820 | 9.7e-158 | dnaK | O | Heat shock 70 kDa protein | ||
IBEOJHIK_01821 | 1.3e-151 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
IBEOJHIK_01822 | 2.5e-200 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
IBEOJHIK_01823 | 5.1e-47 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
IBEOJHIK_01824 | 9.3e-272 | L | Uncharacterised protein family (UPF0236) | |||
IBEOJHIK_01825 | 1.2e-32 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
IBEOJHIK_01826 | 2.6e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
IBEOJHIK_01827 | 3.1e-286 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
IBEOJHIK_01828 | 3.6e-200 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
IBEOJHIK_01829 | 4e-23 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
IBEOJHIK_01830 | 1.3e-249 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
IBEOJHIK_01831 | 8.5e-84 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
IBEOJHIK_01832 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
IBEOJHIK_01833 | 6.5e-257 | glnP | P | ABC transporter | ||
IBEOJHIK_01834 | 3.7e-266 | glnP | P | ABC transporter | ||
IBEOJHIK_01835 | 4e-101 | ydaF | J | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_01836 | 6.4e-179 | metC | 4.4.1.8 | E | cystathionine | |
IBEOJHIK_01838 | 6e-57 | |||||
IBEOJHIK_01839 | 3.1e-102 | S | WxL domain surface cell wall-binding | |||
IBEOJHIK_01840 | 1.1e-95 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_01841 | 2.5e-197 | ypdE | E | M42 glutamyl aminopeptidase | ||
IBEOJHIK_01842 | 3.8e-48 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
IBEOJHIK_01843 | 1.8e-59 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
IBEOJHIK_01844 | 3.1e-253 | 2.7.1.207 | U | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
IBEOJHIK_01845 | 4.1e-203 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
IBEOJHIK_01846 | 6.6e-234 | 4.4.1.8 | E | Aminotransferase, class I | ||
IBEOJHIK_01847 | 2.2e-219 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
IBEOJHIK_01848 | 0.0 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
IBEOJHIK_01849 | 1.4e-297 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
IBEOJHIK_01851 | 5.7e-163 | |||||
IBEOJHIK_01852 | 1.5e-46 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
IBEOJHIK_01853 | 3e-87 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_01854 | 6.2e-29 | S | Threonine/Serine exporter, ThrE | |||
IBEOJHIK_01855 | 4.4e-214 | livJ | E | Receptor family ligand binding region | ||
IBEOJHIK_01856 | 6.7e-151 | livH | U | Branched-chain amino acid transport system / permease component | ||
IBEOJHIK_01857 | 1.7e-120 | livM | E | Branched-chain amino acid transport system / permease component | ||
IBEOJHIK_01860 | 3.5e-88 | E | AAA domain | |||
IBEOJHIK_01861 | 1.9e-122 | E | lipolytic protein G-D-S-L family | |||
IBEOJHIK_01862 | 2e-37 | feoA | P | FeoA | ||
IBEOJHIK_01863 | 2.4e-46 | feoA | P | FeoA | ||
IBEOJHIK_01864 | 9.4e-118 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
IBEOJHIK_01865 | 1.6e-24 | S | Virus attachment protein p12 family | |||
IBEOJHIK_01866 | 0.0 | pckG | 4.1.1.32, 4.1.1.49 | C | Phosphoenolpyruvate carboxykinase | |
IBEOJHIK_01867 | 1e-56 | |||||
IBEOJHIK_01868 | 7.8e-54 | alfA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
IBEOJHIK_01869 | 6.7e-176 | yhaI | S | Protein of unknown function (DUF805) | ||
IBEOJHIK_01870 | 9.4e-58 | |||||
IBEOJHIK_01871 | 1.4e-253 | rarA | L | recombination factor protein RarA | ||
IBEOJHIK_01872 | 1e-210 | EGP | Transmembrane secretion effector | |||
IBEOJHIK_01873 | 2e-261 | G | MFS/sugar transport protein | |||
IBEOJHIK_01874 | 5.4e-74 | S | function, without similarity to other proteins | |||
IBEOJHIK_01875 | 1.4e-65 | |||||
IBEOJHIK_01876 | 1.5e-83 | usp6 | T | universal stress protein | ||
IBEOJHIK_01877 | 1.7e-39 | |||||
IBEOJHIK_01878 | 5e-148 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
IBEOJHIK_01879 | 4.3e-126 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
IBEOJHIK_01880 | 2.7e-269 | K | Mga helix-turn-helix domain | |||
IBEOJHIK_01881 | 4.6e-94 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
IBEOJHIK_01882 | 7e-59 | |||||
IBEOJHIK_01883 | 9.9e-234 | mesE | M | Transport protein ComB | ||
IBEOJHIK_01884 | 1.3e-268 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
IBEOJHIK_01885 | 2.2e-229 | ycaM | E | amino acid | ||
IBEOJHIK_01886 | 1.1e-77 | usp5 | T | universal stress protein | ||
IBEOJHIK_01887 | 4.7e-64 | K | Helix-turn-helix XRE-family like proteins | |||
IBEOJHIK_01888 | 9e-78 | 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 | ||
IBEOJHIK_01889 | 1.2e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
IBEOJHIK_01890 | 1e-207 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
IBEOJHIK_01891 | 3.4e-195 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
IBEOJHIK_01892 | 1.1e-40 | |||||
IBEOJHIK_01893 | 1e-111 | |||||
IBEOJHIK_01894 | 9.1e-227 | EGP | Major facilitator Superfamily | |||
IBEOJHIK_01895 | 1.9e-36 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
IBEOJHIK_01896 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
IBEOJHIK_01897 | 3.3e-56 | |||||
IBEOJHIK_01898 | 1.3e-177 | S | Cell surface protein | |||
IBEOJHIK_01899 | 1.3e-114 | S | WxL domain surface cell wall-binding | |||
IBEOJHIK_01900 | 2.4e-37 | L | Transposase | |||
IBEOJHIK_01901 | 7.8e-88 | tnp2PF3 | L | Transposase | ||
IBEOJHIK_01902 | 1.4e-181 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
IBEOJHIK_01903 | 2.3e-113 | ycaC | Q | Isochorismatase family | ||
IBEOJHIK_01904 | 1e-90 | S | AAA domain | |||
IBEOJHIK_01905 | 1.1e-83 | F | NUDIX domain | |||
IBEOJHIK_01906 | 7e-30 | ydiC1 | EGP | Major Facilitator Superfamily | ||
IBEOJHIK_01907 | 2.2e-213 | yeaN | P | Transporter, major facilitator family protein | ||
IBEOJHIK_01908 | 2.9e-173 | iolS | C | Aldo keto reductase | ||
IBEOJHIK_01909 | 5.8e-64 | manO | S | Domain of unknown function (DUF956) | ||
IBEOJHIK_01910 | 8.7e-170 | manN | G | system, mannose fructose sorbose family IID component | ||
IBEOJHIK_01911 | 1.6e-122 | manY | G | PTS system | ||
IBEOJHIK_01912 | 1.3e-182 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
IBEOJHIK_01913 | 5.5e-201 | EGP | Major facilitator Superfamily | |||
IBEOJHIK_01914 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
IBEOJHIK_01915 | 4.8e-34 | |||||
IBEOJHIK_01916 | 2.3e-165 | recN | L | May be involved in recombinational repair of damaged DNA | ||
IBEOJHIK_01917 | 0.0 | lytN | 3.5.1.104 | M | LysM domain | |
IBEOJHIK_01918 | 7.6e-62 | ydfK | S | Protein of unknown function (DUF554) | ||
IBEOJHIK_01919 | 5.1e-89 | |||||
IBEOJHIK_01920 | 8.5e-119 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
IBEOJHIK_01921 | 4.5e-136 | S | response to antibiotic | |||
IBEOJHIK_01923 | 0.0 | E | amino acid | |||
IBEOJHIK_01924 | 1.4e-46 | lysP | E | amino acid | ||
IBEOJHIK_01925 | 6.3e-298 | frvR | K | Mga helix-turn-helix domain | ||
IBEOJHIK_01926 | 3e-303 | frvR | K | Mga helix-turn-helix domain | ||
IBEOJHIK_01927 | 6.2e-214 | 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) | |
IBEOJHIK_01928 | 2.6e-140 | ksgA | 2.1.1.182, 2.1.1.197, 2.5.1.134 | J | rRNA (adenine-N6,N6-)-dimethyltransferase activity | |
IBEOJHIK_01929 | 1.5e-294 | S | ABC transporter | |||
IBEOJHIK_01930 | 1.4e-175 | draG | O | ADP-ribosylglycohydrolase | ||
IBEOJHIK_01931 | 2e-107 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
IBEOJHIK_01932 | 2.6e-53 | |||||
IBEOJHIK_01933 | 4.8e-134 | XK27_06755 | S | Protein of unknown function (DUF975) | ||
IBEOJHIK_01934 | 8.9e-147 | M | Glycosyltransferase like family 2 | |||
IBEOJHIK_01935 | 2.2e-134 | glcR | K | DeoR C terminal sensor domain | ||
IBEOJHIK_01936 | 4e-181 | ybiT | S | ABC transporter, ATP-binding protein | ||
IBEOJHIK_01937 | 2e-88 | EK | Aminotransferase, class I | |||
IBEOJHIK_01938 | 2.8e-86 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
IBEOJHIK_01939 | 4.7e-165 | metF | 1.5.1.20 | C | Methylenetetrahydrofolate reductase | |
IBEOJHIK_01940 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
IBEOJHIK_01941 | 1.7e-198 | blaA6 | V | Beta-lactamase | ||
IBEOJHIK_01942 | 3.3e-150 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
IBEOJHIK_01943 | 5.6e-127 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
IBEOJHIK_01944 | 6.9e-43 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
IBEOJHIK_01945 | 9.4e-17 | |||||
IBEOJHIK_01946 | 4.9e-72 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_01947 | 5.6e-59 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
IBEOJHIK_01948 | 2.2e-215 | S | Bacterial protein of unknown function (DUF871) | |||
IBEOJHIK_01949 | 1.2e-73 | S | Domain of unknown function (DUF3284) | |||
IBEOJHIK_01950 | 2e-239 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IBEOJHIK_01951 | 8.7e-53 | K | UbiC transcription regulator-associated domain protein | |||
IBEOJHIK_01952 | 1.3e-51 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
IBEOJHIK_01953 | 4.9e-54 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
IBEOJHIK_01954 | 4.4e-108 | speG | J | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_01956 | 7.5e-106 | L | PFAM transposase, IS4 family protein | |||
IBEOJHIK_01957 | 3.2e-80 | L | PFAM transposase, IS4 family protein | |||
IBEOJHIK_01963 | 5.8e-85 | guaD | 3.5.4.12, 3.5.4.3, 3.5.4.33 | FJ | MafB19-like deaminase | |
IBEOJHIK_01964 | 2e-39 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
IBEOJHIK_01965 | 3.6e-202 | S | Phage portal protein | |||
IBEOJHIK_01967 | 1.1e-186 | S | Phage Terminase | |||
IBEOJHIK_01968 | 9.8e-169 | S | Phage Terminase | |||
IBEOJHIK_01969 | 4.3e-77 | L | Phage terminase, small subunit | |||
IBEOJHIK_01970 | 4.1e-14 | L | Resolvase, N terminal domain | |||
IBEOJHIK_01972 | 2e-222 | M | Glycosyl hydrolases family 25 | |||
IBEOJHIK_01973 | 5e-78 | M | Glycosyl hydrolases family 25 | |||
IBEOJHIK_01974 | 9.1e-267 | L | Transposase DDE domain | |||
IBEOJHIK_01975 | 3.8e-224 | G | Major Facilitator Superfamily | |||
IBEOJHIK_01976 | 7e-26 | L | AAA ATPase domain | |||
IBEOJHIK_01978 | 1.1e-113 | ropB | K | Helix-turn-helix domain | ||
IBEOJHIK_01979 | 4.8e-108 | M | PFAM Glycosyl transferases group 1 | |||
IBEOJHIK_01980 | 2.8e-233 | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
IBEOJHIK_01981 | 5e-136 | K | UbiC transcription regulator-associated domain protein | |||
IBEOJHIK_01982 | 1.1e-133 | fcsR | K | DeoR C terminal sensor domain | ||
IBEOJHIK_01983 | 3.4e-146 | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | ||
IBEOJHIK_01984 | 6.4e-78 | fucU | 5.1.3.29 | G | RbsD / FucU transport protein family | |
IBEOJHIK_01985 | 1.8e-232 | ywtG | EGP | Major facilitator Superfamily | ||
IBEOJHIK_01986 | 8.5e-295 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 2.7.1.51 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
IBEOJHIK_01987 | 0.0 | fucI | 5.3.1.25, 5.3.1.3 | G | Converts the aldose L-fucose into the corresponding ketose L-fuculose | |
IBEOJHIK_01988 | 8e-168 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
IBEOJHIK_01989 | 1.4e-258 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
IBEOJHIK_01990 | 1.3e-56 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
IBEOJHIK_01991 | 2e-285 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
IBEOJHIK_01992 | 1.8e-227 | iolF | EGP | Major facilitator Superfamily | ||
IBEOJHIK_01993 | 1.3e-193 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
IBEOJHIK_01994 | 6.4e-215 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
IBEOJHIK_01995 | 5.8e-67 | S | Protein of unknown function (DUF1093) | |||
IBEOJHIK_01996 | 1.5e-124 | |||||
IBEOJHIK_01997 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
IBEOJHIK_01998 | 7.5e-39 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
IBEOJHIK_01999 | 1.5e-116 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
IBEOJHIK_02000 | 3.6e-95 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
IBEOJHIK_02001 | 8e-193 | S | Bacterial membrane protein YfhO | |||
IBEOJHIK_02002 | 2.9e-53 | yneR | S | Belongs to the HesB IscA family | ||
IBEOJHIK_02003 | 2e-115 | vraR | K | helix_turn_helix, Lux Regulon | ||
IBEOJHIK_02004 | 6.1e-183 | vraS | 2.7.13.3 | T | Histidine kinase | |
IBEOJHIK_02005 | 7.4e-26 | |||||
IBEOJHIK_02006 | 9.6e-197 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
IBEOJHIK_02007 | 2.8e-122 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
IBEOJHIK_02008 | 3.8e-38 | 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 | ||
IBEOJHIK_02009 | 1.3e-73 | |||||
IBEOJHIK_02010 | 3.4e-39 | |||||
IBEOJHIK_02011 | 3.8e-119 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
IBEOJHIK_02012 | 1.2e-52 | ybjQ | S | Belongs to the UPF0145 family | ||
IBEOJHIK_02013 | 1.4e-95 | nudC | 1.3.7.1, 3.6.1.22 | L | NUDIX domain | |
IBEOJHIK_02014 | 2.8e-119 | K | response regulator | |||
IBEOJHIK_02015 | 6.5e-165 | T | PhoQ Sensor | |||
IBEOJHIK_02016 | 8.2e-168 | ycbN | V | ABC transporter, ATP-binding protein | ||
IBEOJHIK_02017 | 1.3e-114 | S | ABC-2 family transporter protein | |||
IBEOJHIK_02018 | 2.9e-165 | 3.5.1.10 | C | nadph quinone reductase | ||
IBEOJHIK_02019 | 3.3e-158 | amt | P | ammonium transporter | ||
IBEOJHIK_02020 | 1.3e-207 | yjjP | S | Putative threonine/serine exporter | ||
IBEOJHIK_02021 | 7.6e-188 | tas | C | Aldo/keto reductase family | ||
IBEOJHIK_02022 | 1.3e-46 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
IBEOJHIK_02023 | 2e-102 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
IBEOJHIK_02024 | 7.7e-120 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
IBEOJHIK_02025 | 2.9e-295 | 6.2.1.3, 6.2.1.8 | IQ | AMP-binding enzyme C-terminal domain | ||
IBEOJHIK_02026 | 2.5e-170 | ssuA | P | NMT1-like family | ||
IBEOJHIK_02027 | 3.2e-291 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase concanavalin-like domain | ||
IBEOJHIK_02028 | 2e-43 | bceA | V | ABC transporter | ||
IBEOJHIK_02029 | 6.2e-257 | S | Bacterial membrane protein YfhO | |||
IBEOJHIK_02030 | 1.7e-218 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
IBEOJHIK_02031 | 2.4e-72 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
IBEOJHIK_02032 | 1.3e-151 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
IBEOJHIK_02033 | 2.6e-100 | V | Beta-lactamase | |||
IBEOJHIK_02034 | 4.9e-31 | ykzG | S | Belongs to the UPF0356 family | ||
IBEOJHIK_02036 | 3.2e-57 | |||||
IBEOJHIK_02037 | 6.3e-28 | |||||
IBEOJHIK_02038 | 1.2e-100 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
IBEOJHIK_02039 | 1.5e-222 | EGP | Transmembrane secretion effector | |||
IBEOJHIK_02040 | 4e-104 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
IBEOJHIK_02041 | 6.1e-308 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
IBEOJHIK_02042 | 2.5e-56 | yvbK | 3.1.3.25 | K | GNAT family | |
IBEOJHIK_02043 | 4.6e-43 | pyrP | F | Permease | ||
IBEOJHIK_02044 | 1.7e-96 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
IBEOJHIK_02045 | 8.2e-174 | pyrP | F | Permease | ||
IBEOJHIK_02046 | 3.7e-96 | K | Transcriptional regulator | |||
IBEOJHIK_02047 | 5.6e-55 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IBEOJHIK_02048 | 9.5e-97 | msrA | 1.8.4.11, 1.8.4.12 | C | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
IBEOJHIK_02049 | 8.1e-114 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
IBEOJHIK_02050 | 8.4e-27 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
IBEOJHIK_02051 | 1.3e-240 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
IBEOJHIK_02052 | 2.4e-32 | ampC | V | Beta-lactamase | ||
IBEOJHIK_02053 | 7.3e-166 | 1.13.11.2 | S | glyoxalase | ||
IBEOJHIK_02054 | 9.9e-09 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
IBEOJHIK_02055 | 6.3e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
IBEOJHIK_02056 | 3e-102 | lemA | S | LemA family | ||
IBEOJHIK_02057 | 6.6e-111 | S | TPM domain | |||
IBEOJHIK_02059 | 4.9e-48 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
IBEOJHIK_02060 | 7.5e-203 | camS | S | sex pheromone | ||
IBEOJHIK_02061 | 4e-43 | yrzL | S | Belongs to the UPF0297 family | ||
IBEOJHIK_02062 | 6.1e-210 | |||||
IBEOJHIK_02063 | 1.1e-87 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
IBEOJHIK_02064 | 2.3e-18 | |||||
IBEOJHIK_02065 | 2.8e-240 | pepS | E | Thermophilic metalloprotease (M29) | ||
IBEOJHIK_02066 | 2.7e-111 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_02067 | 3.5e-103 | yjbF | S | SNARE associated Golgi protein | ||
IBEOJHIK_02068 | 4.6e-64 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
IBEOJHIK_02069 | 1.3e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
IBEOJHIK_02070 | 3.9e-85 | S | Short repeat of unknown function (DUF308) | |||
IBEOJHIK_02071 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
IBEOJHIK_02072 | 3.2e-112 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
IBEOJHIK_02073 | 3e-22 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
IBEOJHIK_02074 | 2.5e-17 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
IBEOJHIK_02075 | 2.3e-32 | |||||
IBEOJHIK_02076 | 5.3e-15 | L | Psort location Cytoplasmic, score | |||
IBEOJHIK_02077 | 1.4e-83 | Z012_06740 | S | Fic/DOC family | ||
IBEOJHIK_02078 | 3.3e-153 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
IBEOJHIK_02079 | 9.5e-63 | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | ||
IBEOJHIK_02080 | 0.0 | traA | L | MobA MobL family protein | ||
IBEOJHIK_02081 | 2.5e-27 | |||||
IBEOJHIK_02082 | 1.2e-37 | |||||
IBEOJHIK_02083 | 2e-145 | 2.7.1.176 | S | Zeta toxin | ||
IBEOJHIK_02084 | 3.3e-40 | S | Bacterial epsilon antitoxin | |||
IBEOJHIK_02085 | 1.6e-38 | |||||
IBEOJHIK_02086 | 5.7e-134 | repA | S | Replication initiator protein A | ||
IBEOJHIK_02087 | 1.1e-28 | |||||
IBEOJHIK_02089 | 1.8e-139 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
IBEOJHIK_02090 | 1.3e-81 | L | COG1961 Site-specific recombinases, DNA invertase Pin homologs | |||
IBEOJHIK_02091 | 3.7e-246 | merA | 1.16.1.1, 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
IBEOJHIK_02092 | 5.4e-69 | pnuC | H | Nicotinamide mononucleotide transporter | ||
IBEOJHIK_02093 | 9.9e-39 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
IBEOJHIK_02094 | 2e-263 | S | Putative peptidoglycan binding domain | |||
IBEOJHIK_02095 | 1.3e-96 | padR | K | Transcriptional regulator PadR-like family | ||
IBEOJHIK_02096 | 6.1e-250 | XK27_06930 | S | ABC-2 family transporter protein | ||
IBEOJHIK_02097 | 2.5e-113 | 1.6.5.2 | S | Flavodoxin-like fold | ||
IBEOJHIK_02098 | 5.1e-119 | S | (CBS) domain | |||
IBEOJHIK_02099 | 2.7e-131 | yciB | M | ErfK YbiS YcfS YnhG | ||
IBEOJHIK_02100 | 7e-283 | gltD | 1.4.1.13, 1.4.1.14 | E | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
IBEOJHIK_02101 | 2.6e-52 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1, 2.1.1.21 | E | GXGXG motif | |
IBEOJHIK_02102 | 9.6e-29 | lysP | E | amino acid | ||
IBEOJHIK_02103 | 1.9e-09 | lysP | E | amino acid | ||
IBEOJHIK_02104 | 1.5e-126 | ygjI | E | Amino Acid | ||
IBEOJHIK_02106 | 3.2e-130 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
IBEOJHIK_02107 | 1.8e-217 | yqiG | C | Oxidoreductase | ||
IBEOJHIK_02108 | 6e-17 | S | Short C-terminal domain | |||
IBEOJHIK_02109 | 2.4e-113 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
IBEOJHIK_02110 | 2.3e-246 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
IBEOJHIK_02111 | 2e-200 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
IBEOJHIK_02112 | 0.0 | pepF | E | oligoendopeptidase F | ||
IBEOJHIK_02113 | 5.8e-163 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
IBEOJHIK_02114 | 1.7e-167 | T | Calcineurin-like phosphoesterase superfamily domain | |||
IBEOJHIK_02115 | 3e-134 | znuB | U | ABC 3 transport family | ||
IBEOJHIK_02116 | 4.1e-130 | fhuC | 3.6.3.35 | P | ABC transporter | |
IBEOJHIK_02117 | 2e-58 | |||||
IBEOJHIK_02118 | 1.2e-196 | S | Protein conserved in bacteria | |||
IBEOJHIK_02119 | 1.8e-262 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
IBEOJHIK_02120 | 4.5e-191 | rgpB | GT2 | M | Glycosyl transferase family 2 | |
IBEOJHIK_02121 | 2.4e-127 | welB | S | Glycosyltransferase like family 2 | ||
IBEOJHIK_02122 | 2.8e-151 | S | Glycosyl transferase family 2 | |||
IBEOJHIK_02123 | 1.1e-253 | S | O-antigen ligase like membrane protein | |||
IBEOJHIK_02124 | 3.5e-207 | gntP | EG | Gluconate | ||
IBEOJHIK_02125 | 2.1e-304 | gntK | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
IBEOJHIK_02126 | 1.6e-169 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
IBEOJHIK_02127 | 9.8e-07 | |||||
IBEOJHIK_02128 | 6.7e-128 | |||||
IBEOJHIK_02129 | 7.5e-61 | S | Protein of unknown function (DUF806) | |||
IBEOJHIK_02130 | 1.1e-10 | K | Helix-turn-helix domain | |||
IBEOJHIK_02131 | 1.7e-47 | ybiT | S | ABC transporter, ATP-binding protein | ||
IBEOJHIK_02133 | 1.7e-140 | F | DNA RNA non-specific endonuclease | |||
IBEOJHIK_02134 | 3e-119 | yhiD | S | MgtC family | ||
IBEOJHIK_02135 | 5.5e-118 | yfeX | P | Peroxidase | ||
IBEOJHIK_02136 | 1.2e-160 | 5.1.3.3 | G | Aldose 1-epimerase | ||
IBEOJHIK_02137 | 1.1e-187 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
IBEOJHIK_02138 | 1.5e-68 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
IBEOJHIK_02139 | 3.5e-74 | S | Protein of unknown function (DUF3290) | |||
IBEOJHIK_02140 | 1.2e-117 | yviA | S | Protein of unknown function (DUF421) | ||
IBEOJHIK_02141 | 2e-48 | I | alpha/beta hydrolase fold | |||
IBEOJHIK_02142 | 3.9e-49 | |||||
IBEOJHIK_02143 | 7.2e-124 | citR | K | FCD | ||
IBEOJHIK_02144 | 4.8e-51 | S | Tetratricopeptide repeat | |||
IBEOJHIK_02145 | 2.9e-190 | 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 | ||
IBEOJHIK_02146 | 3.8e-162 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
IBEOJHIK_02147 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
IBEOJHIK_02148 | 5.9e-97 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
IBEOJHIK_02149 | 5.1e-133 | S | Protein of unknown function (DUF975) | |||
IBEOJHIK_02150 | 1.5e-58 | yqkB | S | Iron-sulphur cluster biosynthesis | ||
IBEOJHIK_02151 | 1.2e-52 | |||||
IBEOJHIK_02152 | 4e-08 | dnaK | O | Heat shock 70 kDa protein | ||
IBEOJHIK_02153 | 4.7e-171 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
IBEOJHIK_02154 | 0.0 | ysaB | V | FtsX-like permease family | ||
IBEOJHIK_02155 | 2e-88 | yhfW | G | Metalloenzyme superfamily | ||
IBEOJHIK_02156 | 4e-185 | |||||
IBEOJHIK_02157 | 6.7e-171 | S | Putative esterase | |||
IBEOJHIK_02158 | 4.1e-11 | S | response to antibiotic | |||
IBEOJHIK_02160 | 4.3e-35 | K | MarR family | |||
IBEOJHIK_02161 | 2.6e-22 | K | MarR family | |||
IBEOJHIK_02162 | 4.3e-26 | |||||
IBEOJHIK_02163 | 3.1e-84 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
IBEOJHIK_02164 | 4.9e-63 | P | Rhodanese-like domain | |||
IBEOJHIK_02165 | 8.1e-232 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
IBEOJHIK_02166 | 1.9e-253 | yclM | 2.7.2.4 | E | Belongs to the aspartokinase family | |
IBEOJHIK_02167 | 2.9e-63 | yqiK | S | SPFH domain / Band 7 family | ||
IBEOJHIK_02168 | 3.6e-64 | thrC | 4.2.3.1 | E | Threonine synthase | |
IBEOJHIK_02169 | 6.6e-134 | thrE | S | Putative threonine/serine exporter | ||
IBEOJHIK_02170 | 1.7e-43 | trxC | O | Belongs to the thioredoxin family | ||
IBEOJHIK_02171 | 3.4e-169 | pacL | P | P-type ATPase | ||
IBEOJHIK_02172 | 9.8e-64 | |||||
IBEOJHIK_02173 | 4.1e-240 | EGP | Major Facilitator Superfamily | |||
IBEOJHIK_02174 | 6.6e-33 | mco | Q | Multicopper oxidase | ||
IBEOJHIK_02175 | 3.2e-10 | |||||
IBEOJHIK_02176 | 3.9e-119 | V | ATPases associated with a variety of cellular activities | |||
IBEOJHIK_02177 | 7e-19 | |||||
IBEOJHIK_02178 | 3.4e-255 | gshR | 1.8.1.7 | C | Glutathione reductase | |
IBEOJHIK_02179 | 2e-177 | proV | E | ABC transporter, ATP-binding protein | ||
IBEOJHIK_02180 | 7.7e-169 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
IBEOJHIK_02181 | 1.4e-97 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
IBEOJHIK_02182 | 5.3e-147 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
IBEOJHIK_02183 | 2.6e-123 | drgA | C | Nitroreductase family | ||
IBEOJHIK_02184 | 5.7e-208 | lctO | C | IMP dehydrogenase / GMP reductase domain | ||
IBEOJHIK_02187 | 2.1e-185 | K | sequence-specific DNA binding | |||
IBEOJHIK_02188 | 6.3e-57 | K | Transcriptional regulator PadR-like family | |||
IBEOJHIK_02189 | 7.5e-25 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
IBEOJHIK_02190 | 6.6e-50 | |||||
IBEOJHIK_02191 | 8.2e-60 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
IBEOJHIK_02192 | 4.3e-141 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
IBEOJHIK_02193 | 1.1e-231 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
IBEOJHIK_02194 | 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 | |
IBEOJHIK_02195 | 1.3e-128 | K | cheY-homologous receiver domain | |||
IBEOJHIK_02196 | 4.5e-57 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
IBEOJHIK_02197 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
IBEOJHIK_02198 | 1e-27 | |||||
IBEOJHIK_02199 | 3.9e-131 | S | ABC-2 family transporter protein | |||
IBEOJHIK_02200 | 3.7e-168 | bcrA | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
IBEOJHIK_02201 | 3.2e-121 | T | Transcriptional regulatory protein, C terminal | |||
IBEOJHIK_02202 | 1.6e-155 | T | GHKL domain | |||
IBEOJHIK_02203 | 1.6e-68 | yqeY | S | YqeY-like protein | ||
IBEOJHIK_02204 | 1.1e-101 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
IBEOJHIK_02205 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
IBEOJHIK_02206 | 2.4e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
IBEOJHIK_02207 | 7.7e-149 | P | Belongs to the nlpA lipoprotein family | |||
IBEOJHIK_02208 | 1.9e-100 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTPase | |
IBEOJHIK_02209 | 1.1e-170 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
IBEOJHIK_02210 | 7.5e-49 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
IBEOJHIK_02211 | 5.8e-118 | S | CRISPR-associated protein (Cas_Csn2) | |||
IBEOJHIK_02212 | 2.2e-128 | treR | K | UTRA | ||
IBEOJHIK_02213 | 3.2e-220 | oxlT | P | Major Facilitator Superfamily | ||
IBEOJHIK_02214 | 0.0 | V | ABC transporter | |||
IBEOJHIK_02215 | 0.0 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
IBEOJHIK_02216 | 1.1e-178 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
IBEOJHIK_02219 | 1.9e-70 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
IBEOJHIK_02220 | 1.6e-145 | L | Replication initiation and membrane attachment | |||
IBEOJHIK_02221 | 3.5e-148 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
IBEOJHIK_02222 | 9.6e-158 | recT | L | RecT family | ||
IBEOJHIK_02225 | 1.7e-15 | |||||
IBEOJHIK_02227 | 4.8e-99 | |||||
IBEOJHIK_02231 | 2e-36 | K | Helix-turn-helix XRE-family like proteins | |||
IBEOJHIK_02232 | 3.4e-55 | 3.4.21.88 | K | Helix-turn-helix domain | ||
IBEOJHIK_02233 | 1.8e-77 | E | Zn peptidase | |||
IBEOJHIK_02234 | 5.2e-105 | lmrB | EGP | Major facilitator Superfamily | ||
IBEOJHIK_02235 | 5.2e-84 | S | Domain of unknown function (DUF4811) | |||
IBEOJHIK_02236 | 1e-96 | maf | D | nucleoside-triphosphate diphosphatase activity | ||
IBEOJHIK_02237 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
IBEOJHIK_02238 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
IBEOJHIK_02239 | 5.2e-207 | yueF | S | AI-2E family transporter | ||
IBEOJHIK_02240 | 8.6e-75 | S | Acetyltransferase (GNAT) domain | |||
IBEOJHIK_02241 | 4.3e-97 | |||||
IBEOJHIK_02242 | 1.4e-104 | ygaC | J | Belongs to the UPF0374 family | ||
IBEOJHIK_02243 | 3e-75 | plnD | K | LytTr DNA-binding domain | ||
IBEOJHIK_02246 | 1.5e-46 | spiA | S | Enterocin A Immunity | ||
IBEOJHIK_02247 | 9e-22 | |||||
IBEOJHIK_02252 | 1.6e-138 | S | CAAX protease self-immunity | |||
IBEOJHIK_02253 | 3.1e-34 | K | Transcriptional regulator | |||
IBEOJHIK_02254 | 4.7e-20 | K | Transcriptional regulator | |||
IBEOJHIK_02255 | 2e-253 | EGP | Major Facilitator Superfamily | |||
IBEOJHIK_02256 | 2.2e-54 | |||||
IBEOJHIK_02257 | 1e-54 | S | Enterocin A Immunity | |||
IBEOJHIK_02258 | 8e-128 | S | Aldo keto reductase | |||
IBEOJHIK_02259 | 2.4e-33 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
IBEOJHIK_02260 | 3.9e-110 | vanZ | V | VanZ like family | ||
IBEOJHIK_02261 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
IBEOJHIK_02262 | 3.3e-103 | |||||
IBEOJHIK_02263 | 1.3e-232 | N | Uncharacterized conserved protein (DUF2075) | |||
IBEOJHIK_02264 | 2.8e-182 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
IBEOJHIK_02265 | 9.1e-113 | K | Helix-turn-helix XRE-family like proteins | |||
IBEOJHIK_02266 | 1.4e-56 | K | Transcriptional regulator PadR-like family | |||
IBEOJHIK_02267 | 2.6e-138 | |||||
IBEOJHIK_02268 | 7.5e-138 | |||||
IBEOJHIK_02269 | 3.3e-46 | S | Enterocin A Immunity | |||
IBEOJHIK_02270 | 5.2e-192 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
IBEOJHIK_02271 | 1.6e-82 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
IBEOJHIK_02272 | 7.3e-83 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | ||
IBEOJHIK_02273 | 1.2e-23 | hisC | 2.6.1.9 | E | Cys/Met metabolism PLP-dependent enzyme | |
IBEOJHIK_02274 | 9.2e-201 | |||||
IBEOJHIK_02275 | 1.9e-121 | V | ATPases associated with a variety of cellular activities | |||
IBEOJHIK_02276 | 2.4e-77 | ohr | O | OsmC-like protein | ||
IBEOJHIK_02277 | 7.1e-152 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
IBEOJHIK_02278 | 3e-11 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
IBEOJHIK_02279 | 2.8e-35 | sip | L | Phage integrase family | ||
IBEOJHIK_02280 | 1.1e-206 | 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 | |
IBEOJHIK_02281 | 5e-56 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
IBEOJHIK_02282 | 8.6e-98 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
IBEOJHIK_02283 | 3.2e-135 | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | ||
IBEOJHIK_02284 | 1.9e-50 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
IBEOJHIK_02285 | 7.4e-222 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
IBEOJHIK_02286 | 5.5e-194 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
IBEOJHIK_02287 | 5.8e-285 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
IBEOJHIK_02288 | 2.5e-108 | K | Transcriptional regulator | |||
IBEOJHIK_02289 | 5.6e-221 | gatC | G | PTS system sugar-specific permease component | ||
IBEOJHIK_02291 | 1.5e-29 | |||||
IBEOJHIK_02292 | 1.9e-189 | V | Beta-lactamase | |||
IBEOJHIK_02293 | 8e-128 | S | Domain of unknown function (DUF4867) | |||
IBEOJHIK_02294 | 9.9e-177 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
IBEOJHIK_02295 | 1.1e-138 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
IBEOJHIK_02296 | 4.2e-175 | mocA | S | Oxidoreductase | ||
IBEOJHIK_02297 | 8.5e-142 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
IBEOJHIK_02298 | 4.3e-280 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
IBEOJHIK_02299 | 7.5e-194 | yegS | 2.7.1.107 | G | Lipid kinase | |
IBEOJHIK_02300 | 1.3e-257 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
IBEOJHIK_02301 | 4.2e-222 | mod | 2.1.1.72, 3.1.21.5 | L | DNA methylase | |
IBEOJHIK_02302 | 1e-56 | 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 | |
IBEOJHIK_02303 | 3.4e-86 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
IBEOJHIK_02304 | 3.9e-85 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
IBEOJHIK_02305 | 5e-35 | pyk | 2.7.1.40, 2.7.7.4, 2.7.9.2 | G | Belongs to the pyruvate kinase family | |
IBEOJHIK_02306 | 5.2e-72 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
IBEOJHIK_02307 | 7.6e-31 | |||||
IBEOJHIK_02308 | 2.7e-94 | yhbS | S | acetyltransferase | ||
IBEOJHIK_02309 | 1.5e-275 | yclK | 2.7.13.3 | T | Histidine kinase | |
IBEOJHIK_02310 | 1.4e-133 | K | response regulator | |||
IBEOJHIK_02311 | 5.8e-70 | S | SdpI/YhfL protein family | |||
IBEOJHIK_02313 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
IBEOJHIK_02314 | 2.5e-169 | arbZ | I | Phosphate acyltransferases | ||
IBEOJHIK_02315 | 4.2e-183 | arbY | M | family 8 | ||
IBEOJHIK_02316 | 1.1e-163 | arbx | M | Glycosyl transferase family 8 | ||
IBEOJHIK_02317 | 1.3e-147 | arbV | 2.3.1.51 | I | Phosphate acyltransferases | |
IBEOJHIK_02318 | 1.1e-248 | cycA | E | Amino acid permease | ||
IBEOJHIK_02319 | 2e-74 | |||||
IBEOJHIK_02320 | 2.5e-161 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
IBEOJHIK_02321 | 3.1e-98 | 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 | |
IBEOJHIK_02322 | 6.7e-159 | czcD | P | cation diffusion facilitator family transporter | ||
IBEOJHIK_02323 | 1.8e-123 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
IBEOJHIK_02324 | 6.5e-119 | ybbL | S | ABC transporter, ATP-binding protein | ||
IBEOJHIK_02325 | 1.3e-151 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
IBEOJHIK_02326 | 1e-153 | L | PFAM Integrase catalytic region | |||
IBEOJHIK_02327 | 6.6e-93 | L | Helix-turn-helix domain | |||
IBEOJHIK_02328 | 8.6e-99 | K | Helix-turn-helix domain | |||
IBEOJHIK_02330 | 1.4e-113 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
IBEOJHIK_02331 | 3.1e-92 | yjgM | K | Acetyltransferase (GNAT) domain | ||
IBEOJHIK_02332 | 2.4e-133 | farR | K | Helix-turn-helix domain | ||
IBEOJHIK_02333 | 6.9e-161 | gatY | G | Fructose-bisphosphate aldolase class-II | ||
IBEOJHIK_02334 | 9.9e-80 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
IBEOJHIK_02335 | 1.6e-48 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
IBEOJHIK_02336 | 4.7e-252 | gatC | G | PTS system sugar-specific permease component | ||
IBEOJHIK_02337 | 5.7e-280 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
IBEOJHIK_02338 | 3.7e-162 | G | Fructose-bisphosphate aldolase class-II | |||
IBEOJHIK_02340 | 1e-31 | S | Domain of unknown function (DUF3284) | |||
IBEOJHIK_02341 | 9.9e-97 | pepF | E | Oligopeptidase F | ||
IBEOJHIK_02342 | 1.1e-289 | V | ABC transporter transmembrane region | |||
IBEOJHIK_02343 | 7.7e-172 | yfgQ | P | E1-E2 ATPase | ||
IBEOJHIK_02344 | 2.2e-60 | |||||
IBEOJHIK_02345 | 5e-78 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
IBEOJHIK_02346 | 2.1e-213 | pepF | E | Oligopeptidase F | ||
IBEOJHIK_02347 | 1.1e-37 | veg | S | Biofilm formation stimulator VEG | ||
IBEOJHIK_02348 | 1.3e-157 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
IBEOJHIK_02349 | 2.9e-99 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
IBEOJHIK_02350 | 4.7e-148 | tatD | L | hydrolase, TatD family | ||
IBEOJHIK_02351 | 5.7e-80 | manR | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | |
IBEOJHIK_02353 | 5.2e-136 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
IBEOJHIK_02354 | 8.1e-128 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
IBEOJHIK_02355 | 4e-175 | comEC | S | Competence protein ComEC | ||
IBEOJHIK_02356 | 4.8e-99 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
IBEOJHIK_02357 | 2e-79 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
IBEOJHIK_02358 | 1.1e-71 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
IBEOJHIK_02359 | 1.1e-56 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
IBEOJHIK_02360 | 7.3e-206 | V | ABC transporter transmembrane region | |||
IBEOJHIK_02361 | 4.1e-14 | |||||
IBEOJHIK_02362 | 1.3e-32 | |||||
IBEOJHIK_02363 | 2.1e-183 | EGP | Major Facilitator Superfamily | |||
IBEOJHIK_02364 | 4.2e-258 | pepC | 3.4.22.40 | E | aminopeptidase | |
IBEOJHIK_02365 | 3.8e-262 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
IBEOJHIK_02366 | 1.1e-198 | |||||
IBEOJHIK_02367 | 9.2e-212 | S | ABC-2 family transporter protein | |||
IBEOJHIK_02368 | 4.5e-224 | S | GcrA cell cycle regulator | |||
IBEOJHIK_02369 | 4.8e-107 | L | NUMOD4 motif | |||
IBEOJHIK_02370 | 2.7e-57 | |||||
IBEOJHIK_02371 | 6.7e-267 | S | Terminase RNAseH like domain | |||
IBEOJHIK_02372 | 9.8e-19 | ps333 | L | Terminase small subunit | ||
IBEOJHIK_02373 | 4.6e-120 | ytoI | K | DRTGG domain | ||
IBEOJHIK_02374 | 1.3e-34 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
IBEOJHIK_02375 | 3.6e-134 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
IBEOJHIK_02376 | 1.1e-220 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
IBEOJHIK_02377 | 1.5e-172 | |||||
IBEOJHIK_02378 | 3.4e-22 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
IBEOJHIK_02379 | 3.8e-105 | P | Belongs to the nlpA lipoprotein family | |||
IBEOJHIK_02380 | 0.0 | mngB | 3.2.1.170 | GH38 | G | hydrolase, family 38 |
IBEOJHIK_02381 | 1.5e-255 | S | Metal-independent alpha-mannosidase (GH125) | |||
IBEOJHIK_02382 | 5.3e-59 | |||||
IBEOJHIK_02383 | 7.2e-71 | K | MarR family | |||
IBEOJHIK_02384 | 2e-112 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
IBEOJHIK_02385 | 2.1e-283 | V | ABC transporter transmembrane region | |||
IBEOJHIK_02387 | 1.4e-110 | S | CAAX protease self-immunity | |||
IBEOJHIK_02388 | 2.6e-183 | rodA | D | Belongs to the SEDS family | ||
IBEOJHIK_02389 | 2.4e-178 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
IBEOJHIK_02397 | 1.5e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
IBEOJHIK_02398 | 1.5e-22 | 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 | ||
IBEOJHIK_02399 | 8.5e-22 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
IBEOJHIK_02400 | 2.3e-173 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
IBEOJHIK_02401 | 9.4e-74 | menA | 2.5.1.74 | M | UbiA prenyltransferase family | |
IBEOJHIK_02402 | 1.6e-120 | P | Binding-protein-dependent transport system inner membrane component | |||
IBEOJHIK_02403 | 3.4e-115 | P | Binding-protein-dependent transport system inner membrane component | |||
IBEOJHIK_02404 | 3.4e-163 | ET | Bacterial periplasmic substrate-binding proteins | |||
IBEOJHIK_02405 | 6.2e-117 | E | ABC transporter | |||
IBEOJHIK_02406 | 2.5e-200 | odh | 1.5.1.28 | C | NAD/NADP octopine/nopaline dehydrogenase, alpha-helical domain | |
IBEOJHIK_02407 | 1.6e-216 | abgB | 3.5.1.47 | S | Peptidase dimerisation domain | |
IBEOJHIK_02409 | 4.5e-180 | S | Cell surface protein | |||
IBEOJHIK_02410 | 5.1e-251 | ykgC | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
IBEOJHIK_02411 | 1.3e-22 | |||||
IBEOJHIK_02412 | 1.2e-192 | L | Psort location Cytoplasmic, score | |||
IBEOJHIK_02413 | 1.7e-18 | |||||
IBEOJHIK_02414 | 0.0 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
IBEOJHIK_02415 | 1.6e-67 | |||||
IBEOJHIK_02416 | 2.9e-151 | |||||
IBEOJHIK_02417 | 8.8e-63 | |||||
IBEOJHIK_02418 | 1.2e-261 | traK | U | TraM recognition site of TraD and TraG | ||
IBEOJHIK_02419 | 1.8e-81 | |||||
IBEOJHIK_02420 | 2.4e-62 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
IBEOJHIK_02421 | 2.4e-86 | |||||
IBEOJHIK_02422 | 1.8e-191 | M | CHAP domain | |||
IBEOJHIK_02423 | 6.6e-217 | polC | 2.4.1.129, 2.7.7.7, 3.4.16.4 | GT51 | S | WXG100 protein secretion system (Wss), protein YukC |
IBEOJHIK_02424 | 0.0 | traE | U | AAA-like domain | ||
IBEOJHIK_02425 | 2.8e-117 | |||||
IBEOJHIK_02426 | 1.7e-36 | |||||
IBEOJHIK_02427 | 1e-51 | S | Cag pathogenicity island, type IV secretory system | |||
IBEOJHIK_02428 | 2.1e-106 | |||||
IBEOJHIK_02429 | 1.4e-50 | |||||
IBEOJHIK_02430 | 0.0 | traA | L | MobA MobL family protein | ||
IBEOJHIK_02431 | 5.5e-27 | |||||
IBEOJHIK_02432 | 3.4e-40 | |||||
IBEOJHIK_02433 | 1.3e-85 | |||||
IBEOJHIK_02434 | 8.7e-44 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
IBEOJHIK_02435 | 7.7e-152 | repA | S | Replication initiator protein A | ||
IBEOJHIK_02436 | 6.5e-32 | |||||
IBEOJHIK_02437 | 1.5e-144 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
IBEOJHIK_02438 | 4.7e-14 | |||||
IBEOJHIK_02439 | 6.5e-108 | |||||
IBEOJHIK_02441 | 6.5e-102 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
IBEOJHIK_02442 | 4.9e-48 | uvrX | 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 | |
IBEOJHIK_02443 | 1.5e-77 | |||||
IBEOJHIK_02444 | 5.3e-21 | |||||
IBEOJHIK_02445 | 2.3e-26 | |||||
IBEOJHIK_02446 | 1.9e-189 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
IBEOJHIK_02447 | 4.8e-73 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
IBEOJHIK_02448 | 1.8e-30 | cvfB | S | S1 domain | ||
IBEOJHIK_02449 | 2.6e-263 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
IBEOJHIK_02450 | 1.7e-93 | yfbR | S | HD containing hydrolase-like enzyme | ||
IBEOJHIK_02452 | 3.1e-15 | |||||
IBEOJHIK_02455 | 4.7e-08 | ssb_2 | L | Single-strand binding protein family | ||
IBEOJHIK_02456 | 1.1e-163 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
IBEOJHIK_02457 | 4.1e-245 | Z012_01130 | S | Fic/DOC family | ||
IBEOJHIK_02458 | 2e-18 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
IBEOJHIK_02459 | 7e-267 | L | Transposase DDE domain | |||
IBEOJHIK_02460 | 6e-17 | |||||
IBEOJHIK_02461 | 8.2e-31 | 2.7.1.39 | S | Phosphotransferase enzyme family | ||
IBEOJHIK_02462 | 3.6e-78 | pacL | P | P-type ATPase | ||
IBEOJHIK_02463 | 3e-73 | pacL | P | P-type ATPase | ||
IBEOJHIK_02464 | 9.3e-115 | ylbE | GM | NAD(P)H-binding | ||
IBEOJHIK_02465 | 6.8e-23 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
IBEOJHIK_02466 | 2.4e-156 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
IBEOJHIK_02467 | 7.6e-52 | |||||
IBEOJHIK_02468 | 3.7e-147 | S | cellulase activity | |||
IBEOJHIK_02469 | 1.4e-198 | |||||
IBEOJHIK_02470 | 4.9e-224 | |||||
IBEOJHIK_02471 | 2.5e-158 | V | ATPases associated with a variety of cellular activities | |||
IBEOJHIK_02473 | 4.3e-135 | |||||
IBEOJHIK_02474 | 1.1e-108 | yfnA | E | Amino Acid | ||
IBEOJHIK_02475 | 1.6e-202 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
IBEOJHIK_02476 | 9.3e-44 | K | DNA-binding helix-turn-helix protein | |||
IBEOJHIK_02477 | 1.7e-36 | |||||
IBEOJHIK_02478 | 6.4e-139 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
IBEOJHIK_02479 | 9.3e-31 | secG | U | Preprotein translocase | ||
IBEOJHIK_02480 | 1.7e-60 | |||||
IBEOJHIK_02481 | 9.4e-220 | clcA | P | chloride | ||
IBEOJHIK_02482 | 1.9e-56 | |||||
IBEOJHIK_02483 | 5.7e-65 | nrp | 1.20.4.1 | P | ArsC family | |
IBEOJHIK_02484 | 0.0 | clpL | O | associated with various cellular activities | ||
IBEOJHIK_02485 | 4.7e-20 | |||||
IBEOJHIK_02486 | 1.4e-164 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
IBEOJHIK_02487 | 1.7e-85 | |||||
IBEOJHIK_02488 | 1.4e-118 | GM | NmrA-like family | |||
IBEOJHIK_02489 | 2e-166 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
IBEOJHIK_02490 | 2.7e-42 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
IBEOJHIK_02491 | 1.3e-131 | mntB | 3.6.3.35 | P | ABC transporter | |
IBEOJHIK_02492 | 3.1e-192 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
IBEOJHIK_02493 | 1.7e-156 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
IBEOJHIK_02494 | 4.8e-191 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
IBEOJHIK_02495 | 2.7e-64 | S | Protein of unknown function (DUF1093) | |||
IBEOJHIK_02496 | 2.3e-26 | |||||
IBEOJHIK_02497 | 1.3e-38 | |||||
IBEOJHIK_02498 | 7.7e-67 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
IBEOJHIK_02499 | 2.7e-111 | tdk | 2.7.1.21 | F | thymidine kinase | |
IBEOJHIK_02500 | 4.5e-263 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
IBEOJHIK_02501 | 6.5e-69 | S | Iron-sulphur cluster biosynthesis | |||
IBEOJHIK_02502 | 2.3e-19 | res | 2.1.1.72, 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
IBEOJHIK_02503 | 1.9e-30 | fbp | 3.1.3.11 | G | phosphatase activity | |
IBEOJHIK_02504 | 1.9e-96 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
IBEOJHIK_02505 | 4.6e-35 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
IBEOJHIK_02506 | 2.5e-116 | ylcC | 3.4.22.70 | M | Sortase family | |
IBEOJHIK_02507 | 2.4e-46 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
IBEOJHIK_02508 | 8.2e-32 | S | ECF transporter, substrate-specific component | |||
IBEOJHIK_02509 | 3.6e-76 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
IBEOJHIK_02510 | 1.7e-15 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
IBEOJHIK_02511 | 3.6e-89 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
IBEOJHIK_02512 | 2.7e-71 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
IBEOJHIK_02513 | 8.2e-09 | |||||
IBEOJHIK_02514 | 9.3e-112 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
IBEOJHIK_02515 | 6e-70 | K | Acetyltransferase (GNAT) domain | |||
IBEOJHIK_02516 | 2e-28 | |||||
IBEOJHIK_02517 | 1.6e-222 | yceI | G | Sugar (and other) transporter | ||
IBEOJHIK_02518 | 3.1e-90 | |||||
IBEOJHIK_02519 | 1.7e-156 | K | acetyltransferase | |||
IBEOJHIK_02520 | 9.8e-225 | mdtG | EGP | Major facilitator Superfamily | ||
IBEOJHIK_02521 | 7.7e-83 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
IBEOJHIK_02522 | 2.5e-51 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
IBEOJHIK_02523 | 3.2e-156 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
IBEOJHIK_02524 | 0.0 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
IBEOJHIK_02525 | 0.0 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
IBEOJHIK_02526 | 3.5e-174 | ccpB | 5.1.1.1 | K | lacI family | |
IBEOJHIK_02527 | 6.6e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
IBEOJHIK_02528 | 1.4e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
IBEOJHIK_02529 | 1.4e-121 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
IBEOJHIK_02530 | 9.3e-86 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
IBEOJHIK_02531 | 1.5e-105 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
IBEOJHIK_02532 | 6.7e-79 | pfoS | S | Phosphotransferase system, EIIC | ||
IBEOJHIK_02533 | 6.2e-51 | S | MazG-like family | |||
IBEOJHIK_02534 | 8e-97 | FbpA | K | Fibronectin-binding protein | ||
IBEOJHIK_02535 | 6.8e-167 | murB | 1.3.1.98 | M | Cell wall formation | |
IBEOJHIK_02536 | 2.8e-57 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
IBEOJHIK_02537 | 4.3e-46 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
IBEOJHIK_02538 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
IBEOJHIK_02539 | 2.7e-54 | clpE | O | Belongs to the ClpA ClpB family | ||
IBEOJHIK_02540 | 1.2e-28 | 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 | |
IBEOJHIK_02541 | 1.5e-65 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
IBEOJHIK_02542 | 5.3e-22 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
IBEOJHIK_02543 | 1.2e-120 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
IBEOJHIK_02544 | 1.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
IBEOJHIK_02545 | 1.1e-69 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
IBEOJHIK_02546 | 2.7e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
IBEOJHIK_02547 | 3.5e-79 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
IBEOJHIK_02548 | 1.2e-135 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
IBEOJHIK_02549 | 2.9e-139 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
IBEOJHIK_02550 | 8.5e-43 | argR | K | Regulates arginine biosynthesis genes | ||
IBEOJHIK_02551 | 1.5e-27 | M | Protein of unknown function (DUF3737) | |||
IBEOJHIK_02552 | 6.6e-128 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
IBEOJHIK_02553 | 2.5e-135 | S | Alpha/beta hydrolase family | |||
IBEOJHIK_02554 | 3.2e-104 | K | Bacterial regulatory proteins, tetR family | |||
IBEOJHIK_02555 | 3.2e-74 | yueI | S | Protein of unknown function (DUF1694) | ||
IBEOJHIK_02556 | 2.3e-110 | yktB | S | Belongs to the UPF0637 family | ||
IBEOJHIK_02557 | 2e-123 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
IBEOJHIK_02558 | 9e-25 | 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 | ||
IBEOJHIK_02559 | 3.6e-118 | 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 | ||
IBEOJHIK_02560 | 6.7e-78 | 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 | ||
IBEOJHIK_02561 | 1.8e-44 | yggT | D | integral membrane protein | ||
IBEOJHIK_02562 | 2.6e-146 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
IBEOJHIK_02564 | 3.6e-18 | |||||
IBEOJHIK_02565 | 1.9e-256 | bmr3 | EGP | Major facilitator Superfamily | ||
IBEOJHIK_02566 | 1.4e-138 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
IBEOJHIK_02567 | 6.7e-161 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase superfamily domain | |
IBEOJHIK_02568 | 2.5e-242 | sgaT | 2.7.1.194 | S | PTS system sugar-specific permease component | |
IBEOJHIK_02569 | 6.4e-162 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
IBEOJHIK_02570 | 4.2e-286 | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
IBEOJHIK_02571 | 1.1e-133 | K | DeoR C terminal sensor domain | |||
IBEOJHIK_02572 | 1.1e-141 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
IBEOJHIK_02573 | 3.1e-111 | S | CAAX protease self-immunity | |||
IBEOJHIK_02574 | 1.6e-79 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
IBEOJHIK_02575 | 1.9e-52 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
IBEOJHIK_02576 | 1.3e-228 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
IBEOJHIK_02577 | 3.2e-153 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
IBEOJHIK_02578 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
IBEOJHIK_02579 | 5.4e-131 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
IBEOJHIK_02580 | 2.4e-95 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
IBEOJHIK_02581 | 1.3e-47 | yazA | L | GIY-YIG catalytic domain protein | ||
IBEOJHIK_02582 | 1.1e-95 | prmA | J | Ribosomal protein L11 methyltransferase | ||
IBEOJHIK_02585 | 2.3e-54 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
IBEOJHIK_02586 | 1.1e-68 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
IBEOJHIK_02587 | 1.4e-286 | G | MFS/sugar transport protein | |||
IBEOJHIK_02588 | 3.3e-53 | yfgQ | P | E1-E2 ATPase | ||
IBEOJHIK_02589 | 1.7e-181 | 3.4.11.5 | I | Releases the N-terminal proline from various substrates | ||
IBEOJHIK_02590 | 5.3e-124 | S | B3/4 domain | |||
IBEOJHIK_02591 | 3.6e-88 | |||||
IBEOJHIK_02592 | 3.5e-64 | |||||
IBEOJHIK_02593 | 6.2e-128 | |||||
IBEOJHIK_02594 | 4.5e-136 | sacX | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IBEOJHIK_02595 | 2.7e-205 | sacX | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IBEOJHIK_02596 | 1.1e-162 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
IBEOJHIK_02597 | 3.5e-199 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
IBEOJHIK_02598 | 1.6e-157 | K | Helix-turn-helix domain, rpiR family | |||
IBEOJHIK_02599 | 4.1e-83 | K | Transcriptional regulator C-terminal region | |||
IBEOJHIK_02600 | 4.9e-128 | V | ABC transporter, ATP-binding protein | |||
IBEOJHIK_02601 | 0.0 | ylbB | V | ABC transporter permease | ||
IBEOJHIK_02602 | 1.2e-207 | 4.1.1.52 | S | Amidohydrolase | ||
IBEOJHIK_02603 | 4.9e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
IBEOJHIK_02604 | 4.2e-129 | yfmR | S | ABC transporter, ATP-binding protein | ||
IBEOJHIK_02605 | 3.4e-11 | cydB | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit II | |
IBEOJHIK_02606 | 2.3e-281 | cydA | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit I | |
IBEOJHIK_02607 | 1.5e-91 | yhbO | 3.5.1.124 | S | DJ-1/PfpI family | |
IBEOJHIK_02609 | 6e-151 | T | Calcineurin-like phosphoesterase superfamily domain | |||
IBEOJHIK_02610 | 8.2e-70 | |||||
IBEOJHIK_02612 | 1.3e-159 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
IBEOJHIK_02613 | 7.2e-155 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
IBEOJHIK_02614 | 2.3e-167 | G | Xylose isomerase-like TIM barrel | |||
IBEOJHIK_02615 | 4e-167 | K | Transcriptional regulator, LysR family | |||
IBEOJHIK_02616 | 2.8e-93 | S | Protein of unknown function (DUF1440) | |||
IBEOJHIK_02617 | 2.9e-246 | G | MFS/sugar transport protein | |||
IBEOJHIK_02618 | 3e-161 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
IBEOJHIK_02619 | 3.3e-49 | |||||
IBEOJHIK_02621 | 9.6e-115 | hly | S | protein, hemolysin III | ||
IBEOJHIK_02622 | 3e-92 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
IBEOJHIK_02623 | 2.3e-221 | mvaA | 1.1.1.34, 1.1.1.88 | C | Belongs to the HMG-CoA reductase family | |
IBEOJHIK_02624 | 2e-211 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
IBEOJHIK_02625 | 7.7e-126 | 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 | |
IBEOJHIK_02626 | 1.2e-160 | smc | D | Required for chromosome condensation and partitioning | ||
IBEOJHIK_02628 | 8.7e-81 | S | Bacterial PH domain | |||
IBEOJHIK_02629 | 1.3e-287 | ydbT | S | Bacterial PH domain | ||
IBEOJHIK_02630 | 3.7e-145 | S | AAA ATPase domain | |||
IBEOJHIK_02631 | 2.4e-169 | yniA | G | Phosphotransferase enzyme family | ||
IBEOJHIK_02632 | 9.1e-33 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
IBEOJHIK_02633 | 3.6e-174 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
IBEOJHIK_02634 | 4e-15 | pfoS | S | Phosphotransferase system, EIIC | ||
IBEOJHIK_02640 | 1.6e-45 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
IBEOJHIK_02641 | 2.3e-73 | M | Leucine rich repeats (6 copies) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)