ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
GFJADELN_00002 | 6.3e-62 | |||||
GFJADELN_00003 | 1.6e-95 | M | Peptidase family M23 | |||
GFJADELN_00004 | 0.0 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
GFJADELN_00005 | 4.9e-266 | G | ABC transporter substrate-binding protein | |||
GFJADELN_00006 | 3.4e-230 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
GFJADELN_00007 | 8.4e-210 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
GFJADELN_00008 | 6.1e-108 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
GFJADELN_00009 | 8.4e-70 | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | |||
GFJADELN_00010 | 2.9e-241 | 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 | |
GFJADELN_00011 | 3.6e-67 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
GFJADELN_00012 | 2.5e-143 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
GFJADELN_00013 | 8.1e-117 | |||||
GFJADELN_00016 | 1.4e-231 | XK27_00240 | K | Fic/DOC family | ||
GFJADELN_00017 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
GFJADELN_00018 | 7.9e-302 | M | domain protein | |||
GFJADELN_00019 | 5.6e-83 | 3.4.22.70 | M | Sortase family | ||
GFJADELN_00020 | 5.2e-65 | 3.4.22.70 | M | Sortase family | ||
GFJADELN_00021 | 1.5e-163 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
GFJADELN_00022 | 5.7e-172 | corA | P | CorA-like Mg2+ transporter protein | ||
GFJADELN_00023 | 1.5e-142 | ET | Bacterial periplasmic substrate-binding proteins | |||
GFJADELN_00024 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GFJADELN_00025 | 1.3e-92 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
GFJADELN_00026 | 0.0 | comE | S | Competence protein | ||
GFJADELN_00027 | 8.4e-179 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
GFJADELN_00028 | 2.1e-93 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
GFJADELN_00029 | 1.3e-148 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
GFJADELN_00030 | 7.1e-101 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
GFJADELN_00031 | 2.6e-194 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
GFJADELN_00033 | 7.1e-120 | yoaP | E | YoaP-like | ||
GFJADELN_00034 | 1.3e-184 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
GFJADELN_00035 | 5.3e-119 | ykoE | S | ABC-type cobalt transport system, permease component | ||
GFJADELN_00036 | 6.7e-72 | K | MerR family regulatory protein | |||
GFJADELN_00037 | 3.3e-197 | adhB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
GFJADELN_00038 | 2e-143 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
GFJADELN_00039 | 6e-221 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
GFJADELN_00040 | 3.6e-76 | S | Psort location CytoplasmicMembrane, score | |||
GFJADELN_00041 | 1e-182 | cat | P | Cation efflux family | ||
GFJADELN_00044 | 1e-98 | |||||
GFJADELN_00045 | 2.9e-130 | |||||
GFJADELN_00046 | 5.7e-146 | mazG | 3.6.1.66 | S | Psort location Cytoplasmic, score 8.87 | |
GFJADELN_00047 | 6.7e-278 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
GFJADELN_00048 | 1e-173 | S | IMP dehydrogenase activity | |||
GFJADELN_00049 | 1.3e-298 | ybiT | S | ABC transporter | ||
GFJADELN_00050 | 1.1e-109 | pncA | 2.7.11.1, 3.5.1.19 | Q | Isochorismatase family | |
GFJADELN_00051 | 3.5e-64 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
GFJADELN_00053 | 2e-13 | |||||
GFJADELN_00054 | 7.6e-273 | S | Psort location Cytoplasmic, score 8.87 | |||
GFJADELN_00055 | 4.7e-140 | S | Domain of unknown function (DUF4194) | |||
GFJADELN_00056 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
GFJADELN_00057 | 3.3e-178 | S | Psort location Cytoplasmic, score 8.87 | |||
GFJADELN_00058 | 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 | ||
GFJADELN_00059 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
GFJADELN_00060 | 6e-182 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
GFJADELN_00061 | 1.1e-170 | rapZ | S | Displays ATPase and GTPase activities | ||
GFJADELN_00062 | 1.3e-171 | whiA | K | May be required for sporulation | ||
GFJADELN_00063 | 1.9e-220 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
GFJADELN_00064 | 9.6e-149 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
GFJADELN_00065 | 2.4e-32 | secG | U | Preprotein translocase SecG subunit | ||
GFJADELN_00066 | 2.6e-177 | S | Sucrose-6F-phosphate phosphohydrolase | |||
GFJADELN_00067 | 8e-301 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
GFJADELN_00068 | 7.6e-09 | pnuC | H | Nicotinamide mononucleotide transporter | ||
GFJADELN_00069 | 1.3e-113 | pnuC | H | Nicotinamide mononucleotide transporter | ||
GFJADELN_00070 | 1.9e-49 | nadD | 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 | H | ATPase kinase involved in NAD metabolism | |
GFJADELN_00071 | 6.4e-41 | nadR | H | ATPase kinase involved in NAD metabolism | ||
GFJADELN_00072 | 4.2e-203 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
GFJADELN_00073 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
GFJADELN_00074 | 4.7e-197 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
GFJADELN_00075 | 1.8e-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 | ||
GFJADELN_00076 | 5.1e-158 | G | Fructosamine kinase | |||
GFJADELN_00077 | 6.9e-156 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
GFJADELN_00078 | 1.6e-156 | S | PAC2 family | |||
GFJADELN_00085 | 2.5e-08 | |||||
GFJADELN_00086 | 5.4e-36 | |||||
GFJADELN_00087 | 4.7e-76 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
GFJADELN_00088 | 9.7e-112 | K | helix_turn_helix, mercury resistance | |||
GFJADELN_00089 | 4.6e-61 | |||||
GFJADELN_00090 | 3e-141 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
GFJADELN_00091 | 3.9e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
GFJADELN_00092 | 0.0 | helY | L | DEAD DEAH box helicase | ||
GFJADELN_00093 | 2.1e-54 | |||||
GFJADELN_00094 | 0.0 | pafB | K | WYL domain | ||
GFJADELN_00095 | 1.4e-264 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
GFJADELN_00097 | 1.1e-69 | |||||
GFJADELN_00098 | 0.0 | der | 1.1.1.399, 1.1.1.95, 2.7.4.25 | F | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
GFJADELN_00099 | 9.1e-144 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
GFJADELN_00100 | 1.3e-160 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
GFJADELN_00101 | 8.2e-34 | |||||
GFJADELN_00102 | 0.0 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
GFJADELN_00103 | 1.8e-246 | |||||
GFJADELN_00104 | 2.6e-161 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
GFJADELN_00105 | 2.2e-221 | sucC | 6.2.1.5 | F | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
GFJADELN_00106 | 1.8e-99 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
GFJADELN_00107 | 1.8e-50 | yajC | U | Preprotein translocase subunit | ||
GFJADELN_00108 | 5.6e-200 | 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 | |
GFJADELN_00109 | 1e-105 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
GFJADELN_00110 | 1e-99 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
GFJADELN_00111 | 5.2e-128 | yebC | K | transcriptional regulatory protein | ||
GFJADELN_00112 | 3.5e-112 | pgsA1 | 2.7.8.11, 2.7.8.5 | I | CDP-alcohol phosphatidyltransferase | |
GFJADELN_00113 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
GFJADELN_00114 | 1.6e-141 | S | Bacterial protein of unknown function (DUF881) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)