ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
DNOGIALG_00001 | 5.2e-69 | 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) | |
DNOGIALG_00002 | 2.5e-34 | secG | U | Preprotein translocase SecG subunit | ||
DNOGIALG_00003 | 4.5e-177 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
DNOGIALG_00004 | 2e-160 | S | Sucrose-6F-phosphate phosphohydrolase | |||
DNOGIALG_00005 | 3.6e-301 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
DNOGIALG_00006 | 5.8e-190 | |||||
DNOGIALG_00007 | 1.4e-240 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
DNOGIALG_00008 | 3.6e-202 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
DNOGIALG_00009 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
DNOGIALG_00010 | 1.1e-190 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
DNOGIALG_00011 | 6.8e-212 | 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 | ||
DNOGIALG_00012 | 6.2e-156 | G | Fructosamine kinase | |||
DNOGIALG_00013 | 1.8e-156 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
DNOGIALG_00014 | 1.6e-62 | S | PAC2 family | |||
DNOGIALG_00015 | 9.8e-57 | S | PAC2 family | |||
DNOGIALG_00021 | 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) | |
DNOGIALG_00022 | 3.1e-112 | hit | 2.7.7.53 | FG | HIT domain | |
DNOGIALG_00023 | 2e-111 | yebC | K | transcriptional regulatory protein | ||
DNOGIALG_00024 | 2.7e-100 | 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 | |
DNOGIALG_00025 | 9.4e-107 | 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 | |
DNOGIALG_00026 | 4.7e-199 | 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 | |
DNOGIALG_00027 | 8.1e-52 | yajC | U | Preprotein translocase subunit | ||
DNOGIALG_00028 | 1e-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 | |
DNOGIALG_00029 | 3.1e-223 | 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 | |
DNOGIALG_00030 | 1.6e-163 | 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 | |
DNOGIALG_00031 | 1.7e-235 | |||||
DNOGIALG_00032 | 0.0 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
DNOGIALG_00033 | 4.8e-32 | |||||
DNOGIALG_00034 | 2.9e-120 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
DNOGIALG_00035 | 1.2e-143 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
DNOGIALG_00036 | 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 | |
DNOGIALG_00038 | 3.9e-164 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
DNOGIALG_00039 | 4.8e-290 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
DNOGIALG_00040 | 0.0 | pafB | K | WYL domain | ||
DNOGIALG_00041 | 6.8e-53 | |||||
DNOGIALG_00042 | 0.0 | helY | L | DEAD DEAH box helicase | ||
DNOGIALG_00043 | 5.1e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
DNOGIALG_00044 | 5.7e-140 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
DNOGIALG_00045 | 4.7e-37 | |||||
DNOGIALG_00046 | 4.9e-64 | |||||
DNOGIALG_00047 | 3.2e-110 | K | helix_turn_helix, mercury resistance | |||
DNOGIALG_00048 | 6.7e-75 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
DNOGIALG_00049 | 4.2e-139 | S | Bacterial protein of unknown function (DUF881) | |||
DNOGIALG_00050 | 3.9e-35 | sbp | S | Protein of unknown function (DUF1290) | ||
DNOGIALG_00051 | 1.7e-171 | S | Bacterial protein of unknown function (DUF881) | |||
DNOGIALG_00052 | 1.2e-106 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
DNOGIALG_00053 | 7.9e-157 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
DNOGIALG_00054 | 9.9e-42 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
DNOGIALG_00055 | 9.4e-113 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
DNOGIALG_00056 | 3.1e-186 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
DNOGIALG_00057 | 2.1e-160 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
DNOGIALG_00058 | 0.0 | trpB | 4.1.1.48, 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
DNOGIALG_00059 | 1.2e-131 | S | SOS response associated peptidase (SRAP) | |||
DNOGIALG_00060 | 1.4e-156 | 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 | |
DNOGIALG_00061 | 1.1e-259 | mmuP | E | amino acid | ||
DNOGIALG_00062 | 1.9e-50 | EGP | Major facilitator Superfamily | |||
DNOGIALG_00063 | 5.5e-189 | V | VanZ like family | |||
DNOGIALG_00064 | 1.8e-65 | cefD | 5.1.1.17 | E | Aminotransferase, class V | |
DNOGIALG_00065 | 3.3e-100 | S | Acetyltransferase (GNAT) domain | |||
DNOGIALG_00066 | 1.5e-50 | |||||
DNOGIALG_00067 | 5.2e-121 | |||||
DNOGIALG_00070 | 2e-35 | 2.7.13.3 | T | Histidine kinase | ||
DNOGIALG_00071 | 1.1e-193 | 2.7.13.3 | T | Histidine kinase | ||
DNOGIALG_00072 | 5.3e-127 | K | helix_turn_helix, Lux Regulon | |||
DNOGIALG_00073 | 3e-95 | |||||
DNOGIALG_00074 | 2.8e-144 | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | |||
DNOGIALG_00075 | 5.4e-92 | lolD | Q | ATPases associated with a variety of cellular activities | ||
DNOGIALG_00076 | 1.5e-177 | V | MacB-like periplasmic core domain | |||
DNOGIALG_00077 | 3.2e-40 | relB | L | RelB antitoxin | ||
DNOGIALG_00078 | 3.8e-50 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
DNOGIALG_00079 | 8.4e-26 | 2.7.13.3 | T | Histidine kinase | ||
DNOGIALG_00080 | 7.8e-97 | rpoE4 | K | Sigma-70 region 2 | ||
DNOGIALG_00081 | 7.5e-19 | S | Psort location CytoplasmicMembrane, score | |||
DNOGIALG_00082 | 8.5e-108 | |||||
DNOGIALG_00083 | 4.6e-135 | |||||
DNOGIALG_00084 | 1.3e-162 | yfiL | V | ATPases associated with a variety of cellular activities | ||
DNOGIALG_00085 | 4.5e-70 | |||||
DNOGIALG_00086 | 1.4e-62 | |||||
DNOGIALG_00087 | 1.2e-147 | S | EamA-like transporter family | |||
DNOGIALG_00088 | 1.4e-102 | |||||
DNOGIALG_00089 | 2.5e-127 | |||||
DNOGIALG_00090 | 2.2e-122 | V | ATPases associated with a variety of cellular activities | |||
DNOGIALG_00091 | 8.8e-16 | fic | D | Fic/DOC family | ||
DNOGIALG_00092 | 4.1e-23 | |||||
DNOGIALG_00093 | 3.2e-110 | |||||
DNOGIALG_00094 | 1.3e-45 | K | sequence-specific DNA binding | |||
DNOGIALG_00095 | 1.2e-50 | hipA | 2.7.11.1 | S | kinase activity | |
DNOGIALG_00097 | 1.7e-39 | 2.6.1.76 | EGP | Major Facilitator Superfamily | ||
DNOGIALG_00098 | 6.3e-20 | G | Major facilitator Superfamily | |||
DNOGIALG_00099 | 1.4e-295 | mmuP | E | amino acid | ||
DNOGIALG_00101 | 1e-62 | yeaO | K | Protein of unknown function, DUF488 | ||
DNOGIALG_00102 | 1.3e-75 | |||||
DNOGIALG_00103 | 5e-174 | 3.6.4.12 | ||||
DNOGIALG_00104 | 1.1e-64 | yijF | S | Domain of unknown function (DUF1287) | ||
DNOGIALG_00105 | 3.2e-297 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
DNOGIALG_00106 | 5.3e-71 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
DNOGIALG_00107 | 6.1e-140 | hisF | 4.1.3.27 | 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 | |
DNOGIALG_00108 | 4.7e-76 | 3.5.1.124 | S | DJ-1/PfpI family | ||
DNOGIALG_00109 | 2.7e-224 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
DNOGIALG_00110 | 1.8e-173 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)