ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
LGALHKBE_00001 | 0.0 | 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 | ||
LGALHKBE_00002 | 1.9e-206 | 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 | |
LGALHKBE_00003 | 9.2e-267 | 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 | ||
LGALHKBE_00004 | 5.8e-91 | S | Protein of unknown function (DUF721) | |||
LGALHKBE_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 | |
LGALHKBE_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 | |
LGALHKBE_00007 | 6.2e-75 | S | Transmembrane domain of unknown function (DUF3566) | |||
LGALHKBE_00008 | 1.8e-217 | V | VanZ like family | |||
LGALHKBE_00009 | 1.9e-161 | yplQ | S | Haemolysin-III related | ||
LGALHKBE_00010 | 5.8e-263 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
LGALHKBE_00011 | 2e-236 | EGP | Major facilitator Superfamily | |||
LGALHKBE_00012 | 8.8e-162 | 3.2.1.78 | GH26 | G | Glycosyl hydrolase family 26 | |
LGALHKBE_00013 | 4e-68 | 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 | ||
LGALHKBE_00014 | 3.5e-51 | gcs2 | S | A circularly permuted ATPgrasp | ||
LGALHKBE_00017 | 2.4e-144 | S | Protein of unknown function DUF45 | |||
LGALHKBE_00018 | 8.1e-78 | |||||
LGALHKBE_00019 | 1.6e-154 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
LGALHKBE_00020 | 0.0 | uvrA3 | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | ||
LGALHKBE_00021 | 1.1e-149 | ybaJ | Q | ubiE/COQ5 methyltransferase family | ||
LGALHKBE_00022 | 7.7e-166 | |||||
LGALHKBE_00023 | 2e-106 | XK27_04590 | S | NADPH-dependent FMN reductase | ||
LGALHKBE_00024 | 4.9e-105 | |||||
LGALHKBE_00025 | 2.1e-22 | |||||
LGALHKBE_00028 | 4.7e-57 | mazG | S | MazG-like family | ||
LGALHKBE_00029 | 4.4e-26 | L | Uncharacterized conserved protein (DUF2075) | |||
LGALHKBE_00031 | 3.1e-194 | sinIM | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
LGALHKBE_00032 | 2e-47 | S | Type II restriction endonuclease EcoO109I | |||
LGALHKBE_00033 | 0.0 | |||||
LGALHKBE_00034 | 3.4e-111 | |||||
LGALHKBE_00035 | 0.0 | |||||
LGALHKBE_00036 | 2.8e-287 | |||||
LGALHKBE_00037 | 3.4e-38 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
LGALHKBE_00038 | 2.6e-34 | chpA | T | Toxic component of a toxin-antitoxin (TA) module | ||
LGALHKBE_00039 | 4.5e-67 | chpA | T | Toxic component of a toxin-antitoxin (TA) module | ||
LGALHKBE_00040 | 3.7e-165 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
LGALHKBE_00041 | 1.4e-24 | akr5f | 1.1.1.346 | S | reductase | |
LGALHKBE_00042 | 1.4e-121 | akr5f | 1.1.1.346 | S | Aldo/keto reductase family | |
LGALHKBE_00043 | 0.0 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
LGALHKBE_00044 | 3.6e-84 | neo | 2.7.1.87, 2.7.1.95 | F | Phosphotransferase enzyme family | |
LGALHKBE_00045 | 5.8e-21 | neo | 2.7.1.87, 2.7.1.95 | F | Phosphotransferase enzyme family | |
LGALHKBE_00046 | 1.3e-87 | S | Domain of unknown function (DUF4234) | |||
LGALHKBE_00047 | 2.8e-254 | tnpA | L | Transposase | ||
LGALHKBE_00048 | 1e-303 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
LGALHKBE_00049 | 0.0 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
LGALHKBE_00050 | 3.1e-218 | blt | G | MFS/sugar transport protein | ||
LGALHKBE_00051 | 2.8e-122 | K | Bacterial regulatory proteins, tetR family | |||
LGALHKBE_00052 | 1e-84 | dps | P | Belongs to the Dps family | ||
LGALHKBE_00053 | 9.1e-248 | ytfL | P | Transporter associated domain | ||
LGALHKBE_00054 | 2.2e-128 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
LGALHKBE_00055 | 2.4e-214 | K | helix_turn _helix lactose operon repressor | |||
LGALHKBE_00056 | 2e-35 | |||||
LGALHKBE_00057 | 2.4e-159 | xylG | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | |
LGALHKBE_00058 | 1.5e-53 | |||||
LGALHKBE_00059 | 1.5e-194 | K | helix_turn _helix lactose operon repressor | |||
LGALHKBE_00060 | 8.5e-311 | 3.2.1.55 | GH51 | G | arabinose metabolic process | |
LGALHKBE_00061 | 7.4e-305 | araB | 2.7.1.16, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
LGALHKBE_00062 | 5.1e-130 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
LGALHKBE_00063 | 1.9e-299 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
LGALHKBE_00064 | 9.1e-169 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
LGALHKBE_00065 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
LGALHKBE_00066 | 2.5e-298 | yjjP | S | Threonine/Serine exporter, ThrE | ||
LGALHKBE_00067 | 2.1e-254 | tnpA | L | Transposase | ||
LGALHKBE_00068 | 1.2e-205 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LGALHKBE_00069 | 1.2e-47 | S | Protein of unknown function (DUF3073) | |||
LGALHKBE_00070 | 1.4e-80 | I | Sterol carrier protein | |||
LGALHKBE_00071 | 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 |
LGALHKBE_00072 | 5.4e-36 | |||||
LGALHKBE_00073 | 5.7e-129 | gluP | 3.4.21.105 | S | Rhomboid family | |
LGALHKBE_00074 | 2.2e-284 | L | ribosomal rna small subunit methyltransferase | |||
LGALHKBE_00075 | 7.2e-37 | crgA | D | Involved in cell division | ||
LGALHKBE_00076 | 3.3e-141 | S | Bacterial protein of unknown function (DUF881) | |||
LGALHKBE_00077 | 9.2e-225 | srtA | 3.4.22.70 | M | Sortase family | |
LGALHKBE_00078 | 3.1e-121 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
LGALHKBE_00079 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
LGALHKBE_00080 | 1.3e-193 | T | Protein tyrosine kinase | |||
LGALHKBE_00081 | 2.2e-271 | pbpA | M | penicillin-binding protein | ||
LGALHKBE_00082 | 1.1e-290 | rodA | D | Belongs to the SEDS family | ||
LGALHKBE_00083 | 7.6e-267 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
LGALHKBE_00084 | 8e-62 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
LGALHKBE_00085 | 2.3e-130 | fhaA | T | Protein of unknown function (DUF2662) | ||
LGALHKBE_00086 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
LGALHKBE_00087 | 4.7e-127 | yicL | EG | EamA-like transporter family | ||
LGALHKBE_00088 | 3.1e-214 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
LGALHKBE_00089 | 5.7e-58 | |||||
LGALHKBE_00090 | 2.6e-180 | rrmA | 2.1.1.187 | Q | Methyltransferase domain | |
LGALHKBE_00091 | 3.1e-32 | ytgB | S | Transglycosylase associated protein | ||
LGALHKBE_00092 | 2.4e-29 | ymgJ | S | Transglycosylase associated protein | ||
LGALHKBE_00094 | 1.6e-279 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
LGALHKBE_00095 | 0.0 | cadA | P | E1-E2 ATPase | ||
LGALHKBE_00096 | 1.9e-285 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
LGALHKBE_00097 | 1.1e-115 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LGALHKBE_00098 | 8.8e-308 | S | Sel1-like repeats. | |||
LGALHKBE_00099 | 4.6e-279 | 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) | |
LGALHKBE_00101 | 3.8e-179 | htpX | O | Belongs to the peptidase M48B family | ||
LGALHKBE_00102 | 4.8e-213 | lppW | 3.5.2.6 | V | Beta-lactamase | |
LGALHKBE_00103 | 2.5e-123 | E | SOS response associated peptidase (SRAP) | |||
LGALHKBE_00104 | 1.1e-228 | araJ | EGP | Major facilitator Superfamily | ||
LGALHKBE_00105 | 1.1e-11 | S | NADPH-dependent FMN reductase | |||
LGALHKBE_00106 | 7.7e-52 | relB | L | RelB antitoxin | ||
LGALHKBE_00107 | 4.9e-87 | ogt | 2.1.1.63, 3.2.2.21 | 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 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)