ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
OJNKIJLD_00001 | 5.2e-281 | 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 | ||
OJNKIJLD_00002 | 2.3e-204 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
OJNKIJLD_00003 | 1.3e-235 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
OJNKIJLD_00004 | 6.2e-90 | S | Protein of unknown function (DUF721) | |||
OJNKIJLD_00005 | 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 | |
OJNKIJLD_00006 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
OJNKIJLD_00007 | 3.3e-68 | S | Transmembrane domain of unknown function (DUF3566) | |||
OJNKIJLD_00008 | 1.2e-260 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
OJNKIJLD_00009 | 6.1e-56 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
OJNKIJLD_00013 | 3.1e-101 | S | Protein of unknown function DUF45 | |||
OJNKIJLD_00014 | 4.5e-188 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
OJNKIJLD_00015 | 1.8e-240 | ytfL | P | Transporter associated domain | ||
OJNKIJLD_00016 | 2e-118 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
OJNKIJLD_00017 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
OJNKIJLD_00018 | 0.0 | yjjP | S | Threonine/Serine exporter, ThrE | ||
OJNKIJLD_00019 | 9.4e-300 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
OJNKIJLD_00020 | 5.9e-205 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
OJNKIJLD_00021 | 1.4e-41 | S | Protein of unknown function (DUF3073) | |||
OJNKIJLD_00022 | 1.7e-63 | I | Sterol carrier protein | |||
OJNKIJLD_00023 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
OJNKIJLD_00024 | 1.9e-33 | |||||
OJNKIJLD_00025 | 1.4e-147 | gluP | 3.4.21.105 | S | Rhomboid family | |
OJNKIJLD_00026 | 1.1e-240 | L | ribosomal rna small subunit methyltransferase | |||
OJNKIJLD_00027 | 3.1e-57 | crgA | D | Involved in cell division | ||
OJNKIJLD_00028 | 6.8e-142 | S | Bacterial protein of unknown function (DUF881) | |||
OJNKIJLD_00029 | 6.7e-209 | srtA | 3.4.22.70 | M | Sortase family | |
OJNKIJLD_00030 | 1.7e-119 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
OJNKIJLD_00031 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
OJNKIJLD_00032 | 5.8e-177 | T | Protein tyrosine kinase | |||
OJNKIJLD_00033 | 1e-265 | pbpA | M | penicillin-binding protein | ||
OJNKIJLD_00034 | 8.5e-271 | rodA | D | Belongs to the SEDS family | ||
OJNKIJLD_00035 | 6.8e-242 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
OJNKIJLD_00036 | 9.6e-73 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
OJNKIJLD_00037 | 1.2e-131 | fhaA | T | Protein of unknown function (DUF2662) | ||
OJNKIJLD_00038 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
OJNKIJLD_00039 | 3.5e-225 | 2.7.13.3 | T | Histidine kinase | ||
OJNKIJLD_00040 | 3.2e-113 | K | helix_turn_helix, Lux Regulon | |||
OJNKIJLD_00041 | 3.9e-193 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
OJNKIJLD_00042 | 1.5e-159 | yicL | EG | EamA-like transporter family | ||
OJNKIJLD_00043 | 5.1e-11 | XK27_10430 | S | NAD(P)H-binding | ||
OJNKIJLD_00045 | 8.2e-265 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
OJNKIJLD_00046 | 6.1e-277 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
OJNKIJLD_00047 | 0.0 | cadA | P | E1-E2 ATPase | ||
OJNKIJLD_00048 | 2.3e-187 | ansA | 3.5.1.1 | EJ | Asparaginase | |
OJNKIJLD_00049 | 3.1e-270 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
OJNKIJLD_00050 | 1.7e-183 | htpX | O | Belongs to the peptidase M48B family | ||
OJNKIJLD_00052 | 3.2e-65 | K | Helix-turn-helix XRE-family like proteins | |||
OJNKIJLD_00053 | 4.7e-146 | yddG | EG | EamA-like transporter family | ||
OJNKIJLD_00054 | 0.0 | pip | S | YhgE Pip domain protein | ||
OJNKIJLD_00055 | 0.0 | pip | S | YhgE Pip domain protein | ||
OJNKIJLD_00056 | 3.2e-217 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
OJNKIJLD_00057 | 3.5e-249 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
OJNKIJLD_00058 | 9.8e-155 | clcA | P | Voltage gated chloride channel | ||
OJNKIJLD_00059 | 3.8e-29 | L | transposase activity | |||
OJNKIJLD_00060 | 9.3e-108 | L | Transposase and inactivated derivatives | |||
OJNKIJLD_00061 | 3.9e-131 | clcA | P | Voltage gated chloride channel | ||
OJNKIJLD_00062 | 5e-108 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
OJNKIJLD_00063 | 3.3e-57 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
OJNKIJLD_00064 | 5.8e-197 | K | helix_turn _helix lactose operon repressor | |||
OJNKIJLD_00065 | 4.5e-296 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
OJNKIJLD_00066 | 2.6e-115 | S | Protein of unknown function, DUF624 | |||
OJNKIJLD_00067 | 0.0 | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain | |
OJNKIJLD_00068 | 3.8e-219 | G | Bacterial extracellular solute-binding protein | |||
OJNKIJLD_00069 | 2.9e-162 | amyD3 | P | Binding-protein-dependent transport system inner membrane component | ||
OJNKIJLD_00070 | 3.6e-149 | amyC5 | P | Binding-protein-dependent transport system inner membrane component | ||
OJNKIJLD_00071 | 5.8e-278 | scrT | G | Transporter major facilitator family protein | ||
OJNKIJLD_00072 | 4.6e-252 | yhjE | EGP | Sugar (and other) transporter | ||
OJNKIJLD_00073 | 1.8e-203 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
OJNKIJLD_00074 | 4e-203 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
OJNKIJLD_00075 | 0.0 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
OJNKIJLD_00076 | 1.4e-36 | G | beta-mannosidase | |||
OJNKIJLD_00077 | 6.8e-187 | K | helix_turn _helix lactose operon repressor | |||
OJNKIJLD_00078 | 4.1e-270 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
OJNKIJLD_00080 | 0.0 | V | FtsX-like permease family | |||
OJNKIJLD_00081 | 3.3e-227 | P | Sodium/hydrogen exchanger family | |||
OJNKIJLD_00082 | 1.3e-76 | S | Psort location Cytoplasmic, score 8.87 | |||
OJNKIJLD_00083 | 1e-177 | 3.4.22.70 | M | Sortase family | ||
OJNKIJLD_00084 | 0.0 | inlJ | M | domain protein | ||
OJNKIJLD_00085 | 2.9e-123 | M | domain protein | |||
OJNKIJLD_00086 | 2.5e-89 | S | Psort location Cytoplasmic, score 8.87 | |||
OJNKIJLD_00087 | 9.9e-275 | cycA | E | Amino acid permease | ||
OJNKIJLD_00088 | 1.2e-166 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
OJNKIJLD_00089 | 5.8e-129 | thiF | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
OJNKIJLD_00090 | 2.5e-26 | thiS | 2.8.1.10 | H | ThiS family | |
OJNKIJLD_00091 | 5.4e-154 | 1.1.1.65 | C | Aldo/keto reductase family | ||
OJNKIJLD_00092 | 1.9e-57 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
OJNKIJLD_00093 | 4.6e-285 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
OJNKIJLD_00094 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
OJNKIJLD_00095 | 1.2e-116 | 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 | |
OJNKIJLD_00096 | 7.5e-237 | G | MFS/sugar transport protein | |||
OJNKIJLD_00097 | 9.8e-295 | efeU_1 | P | Iron permease FTR1 family | ||
OJNKIJLD_00098 | 4.1e-92 | tpd | P | Fe2+ transport protein | ||
OJNKIJLD_00099 | 3.2e-231 | S | Predicted membrane protein (DUF2318) | |||
OJNKIJLD_00100 | 2.3e-219 | macB_2 | V | ABC transporter permease | ||
OJNKIJLD_00102 | 4.5e-201 | Z012_06715 | V | FtsX-like permease family | ||
OJNKIJLD_00103 | 2e-149 | macB | V | ABC transporter, ATP-binding protein | ||
OJNKIJLD_00104 | 1.1e-61 | S | FMN_bind | |||
OJNKIJLD_00105 | 1.7e-87 | K | Psort location Cytoplasmic, score 8.87 | |||
OJNKIJLD_00106 | 3.7e-275 | pip | S | YhgE Pip domain protein | ||
OJNKIJLD_00107 | 0.0 | pip | S | YhgE Pip domain protein |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)