ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
LNGBALBM_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 | ||
LNGBALBM_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 | |
LNGBALBM_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 | ||
LNGBALBM_00004 | 5.8e-91 | S | Protein of unknown function (DUF721) | |||
LNGBALBM_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 | |
LNGBALBM_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 | |
LNGBALBM_00007 | 6.2e-75 | S | Transmembrane domain of unknown function (DUF3566) | |||
LNGBALBM_00008 | 1.8e-217 | V | VanZ like family | |||
LNGBALBM_00009 | 1.9e-161 | yplQ | S | Haemolysin-III related | ||
LNGBALBM_00010 | 5.8e-263 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
LNGBALBM_00011 | 2e-236 | EGP | Major facilitator Superfamily | |||
LNGBALBM_00012 | 8.8e-162 | 3.2.1.78 | GH26 | G | Glycosyl hydrolase family 26 | |
LNGBALBM_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 | ||
LNGBALBM_00014 | 3.5e-51 | gcs2 | S | A circularly permuted ATPgrasp | ||
LNGBALBM_00017 | 2.4e-144 | S | Protein of unknown function DUF45 | |||
LNGBALBM_00018 | 8.1e-78 | |||||
LNGBALBM_00019 | 1.6e-154 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
LNGBALBM_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 | ||
LNGBALBM_00021 | 1.1e-149 | ybaJ | Q | ubiE/COQ5 methyltransferase family | ||
LNGBALBM_00022 | 7.7e-166 | |||||
LNGBALBM_00023 | 2e-106 | XK27_04590 | S | NADPH-dependent FMN reductase | ||
LNGBALBM_00024 | 4.9e-105 | |||||
LNGBALBM_00025 | 2.1e-22 | |||||
LNGBALBM_00028 | 4.7e-57 | mazG | S | MazG-like family | ||
LNGBALBM_00029 | 4.4e-26 | L | Uncharacterized conserved protein (DUF2075) | |||
LNGBALBM_00031 | 3.1e-194 | sinIM | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
LNGBALBM_00032 | 2e-47 | S | Type II restriction endonuclease EcoO109I | |||
LNGBALBM_00033 | 0.0 | |||||
LNGBALBM_00034 | 3.4e-111 | |||||
LNGBALBM_00035 | 1.9e-138 | |||||
LNGBALBM_00036 | 9.4e-221 | |||||
LNGBALBM_00037 | 2.8e-287 | |||||
LNGBALBM_00038 | 3.4e-38 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
LNGBALBM_00039 | 2.6e-34 | chpA | T | Toxic component of a toxin-antitoxin (TA) module | ||
LNGBALBM_00040 | 4.5e-67 | chpA | T | Toxic component of a toxin-antitoxin (TA) module | ||
LNGBALBM_00041 | 3.7e-165 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
LNGBALBM_00042 | 1.4e-24 | akr5f | 1.1.1.346 | S | reductase | |
LNGBALBM_00043 | 1.4e-121 | akr5f | 1.1.1.346 | S | Aldo/keto reductase family | |
LNGBALBM_00044 | 0.0 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
LNGBALBM_00045 | 3.6e-84 | neo | 2.7.1.87, 2.7.1.95 | F | Phosphotransferase enzyme family | |
LNGBALBM_00046 | 5.8e-21 | neo | 2.7.1.87, 2.7.1.95 | F | Phosphotransferase enzyme family | |
LNGBALBM_00047 | 1.3e-87 | S | Domain of unknown function (DUF4234) | |||
LNGBALBM_00048 | 1.8e-253 | tnpA | L | Transposase | ||
LNGBALBM_00049 | 1e-303 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
LNGBALBM_00050 | 0.0 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
LNGBALBM_00051 | 3.1e-218 | blt | G | MFS/sugar transport protein | ||
LNGBALBM_00052 | 2.8e-122 | K | Bacterial regulatory proteins, tetR family | |||
LNGBALBM_00053 | 1e-84 | dps | P | Belongs to the Dps family | ||
LNGBALBM_00054 | 9.1e-248 | ytfL | P | Transporter associated domain | ||
LNGBALBM_00055 | 2.2e-128 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
LNGBALBM_00056 | 2.4e-214 | K | helix_turn _helix lactose operon repressor | |||
LNGBALBM_00057 | 2e-35 | |||||
LNGBALBM_00058 | 2.4e-159 | xylG | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | |
LNGBALBM_00059 | 1.5e-53 | |||||
LNGBALBM_00060 | 1.5e-194 | K | helix_turn _helix lactose operon repressor | |||
LNGBALBM_00061 | 8.5e-311 | 3.2.1.55 | GH51 | G | arabinose metabolic process | |
LNGBALBM_00062 | 7.4e-305 | araB | 2.7.1.16, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
LNGBALBM_00063 | 5.1e-130 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
LNGBALBM_00064 | 1.9e-299 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
LNGBALBM_00065 | 9.1e-169 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
LNGBALBM_00066 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
LNGBALBM_00067 | 2.5e-298 | yjjP | S | Threonine/Serine exporter, ThrE | ||
LNGBALBM_00068 | 2.1e-254 | tnpA | L | Transposase | ||
LNGBALBM_00069 | 1.2e-205 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LNGBALBM_00070 | 1.2e-47 | S | Protein of unknown function (DUF3073) | |||
LNGBALBM_00071 | 1.4e-80 | I | Sterol carrier protein | |||
LNGBALBM_00072 | 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 |
LNGBALBM_00073 | 5.4e-36 | |||||
LNGBALBM_00074 | 5.7e-129 | gluP | 3.4.21.105 | S | Rhomboid family | |
LNGBALBM_00075 | 2.2e-284 | L | ribosomal rna small subunit methyltransferase | |||
LNGBALBM_00076 | 7.2e-37 | crgA | D | Involved in cell division | ||
LNGBALBM_00077 | 3.3e-141 | S | Bacterial protein of unknown function (DUF881) | |||
LNGBALBM_00078 | 9.2e-225 | srtA | 3.4.22.70 | M | Sortase family | |
LNGBALBM_00079 | 3.1e-121 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
LNGBALBM_00080 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
LNGBALBM_00081 | 1.3e-193 | T | Protein tyrosine kinase | |||
LNGBALBM_00082 | 2.2e-271 | pbpA | M | penicillin-binding protein | ||
LNGBALBM_00083 | 1.1e-290 | rodA | D | Belongs to the SEDS family | ||
LNGBALBM_00084 | 7.6e-267 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
LNGBALBM_00085 | 8e-62 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
LNGBALBM_00086 | 2.3e-130 | fhaA | T | Protein of unknown function (DUF2662) | ||
LNGBALBM_00087 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
LNGBALBM_00088 | 4.7e-127 | yicL | EG | EamA-like transporter family | ||
LNGBALBM_00089 | 3.1e-214 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
LNGBALBM_00090 | 5.7e-58 | |||||
LNGBALBM_00091 | 2.6e-180 | rrmA | 2.1.1.187 | Q | Methyltransferase domain | |
LNGBALBM_00092 | 3.1e-32 | ytgB | S | Transglycosylase associated protein | ||
LNGBALBM_00093 | 2.4e-29 | ymgJ | S | Transglycosylase associated protein | ||
LNGBALBM_00095 | 1.6e-279 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
LNGBALBM_00096 | 0.0 | cadA | P | E1-E2 ATPase | ||
LNGBALBM_00097 | 1.9e-285 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
LNGBALBM_00098 | 1.1e-115 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LNGBALBM_00099 | 8.8e-308 | S | Sel1-like repeats. | |||
LNGBALBM_00100 | 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) | |
LNGBALBM_00102 | 3.8e-179 | htpX | O | Belongs to the peptidase M48B family | ||
LNGBALBM_00103 | 4.8e-213 | lppW | 3.5.2.6 | V | Beta-lactamase | |
LNGBALBM_00104 | 2.5e-123 | E | SOS response associated peptidase (SRAP) | |||
LNGBALBM_00105 | 1.1e-228 | araJ | EGP | Major facilitator Superfamily | ||
LNGBALBM_00106 | 1.1e-11 | S | NADPH-dependent FMN reductase | |||
LNGBALBM_00107 | 7.7e-52 | relB | L | RelB antitoxin | ||
LNGBALBM_00108 | 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 | |
LNGBALBM_00109 | 1.7e-270 | 2.7.11.1 | S | cellulose binding | ||
LNGBALBM_00110 | 1.1e-141 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
LNGBALBM_00111 | 1.3e-86 | 4.1.1.44 | S | Cupin domain | ||
LNGBALBM_00112 | 8.2e-190 | S | Dienelactone hydrolase family | |||
LNGBALBM_00113 | 8.3e-162 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
LNGBALBM_00114 | 8.8e-195 | C | Aldo/keto reductase family | |||
LNGBALBM_00116 | 3.8e-251 | P | nitric oxide dioxygenase activity | |||
LNGBALBM_00117 | 9.3e-89 | C | Flavodoxin | |||
LNGBALBM_00118 | 6.3e-40 | K | helix_turn_helix, mercury resistance | |||
LNGBALBM_00119 | 5.9e-85 | fldA | C | Flavodoxin | ||
LNGBALBM_00120 | 6.9e-147 | GM | NmrA-like family | |||
LNGBALBM_00121 | 7.4e-205 | adh | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
LNGBALBM_00122 | 2e-166 | K | LysR substrate binding domain | |||
LNGBALBM_00123 | 3.7e-254 | 3.5.1.104 | G | Polysaccharide deacetylase | ||
LNGBALBM_00124 | 3e-195 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
LNGBALBM_00125 | 2.2e-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 | |
LNGBALBM_00126 | 1.2e-174 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LNGBALBM_00127 | 6.5e-63 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
LNGBALBM_00128 | 3e-233 | U | Belongs to the binding-protein-dependent transport system permease family | |||
LNGBALBM_00129 | 9.7e-159 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
LNGBALBM_00130 | 5.3e-160 | natA | E | Branched-chain amino acid ATP-binding cassette transporter | ||
LNGBALBM_00131 | 1.6e-151 | livF | E | ATPases associated with a variety of cellular activities | ||
LNGBALBM_00132 | 1.1e-215 | natB | E | Receptor family ligand binding region | ||
LNGBALBM_00133 | 4.8e-193 | K | helix_turn _helix lactose operon repressor | |||
LNGBALBM_00134 | 7.4e-299 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
LNGBALBM_00135 | 2.4e-295 | G | Transporter major facilitator family protein | |||
LNGBALBM_00136 | 6.3e-107 | natB | E | Receptor family ligand binding region | ||
LNGBALBM_00137 | 8.5e-81 | bccA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Biotin carboxylase C-terminal domain | |
LNGBALBM_00138 | 1.9e-183 | 4.2.1.48 | S | Domain of unknown function (DUF4392) | ||
LNGBALBM_00139 | 2.3e-279 | scrT | G | Transporter major facilitator family protein | ||
LNGBALBM_00140 | 4.8e-93 | S | Acetyltransferase (GNAT) family | |||
LNGBALBM_00141 | 2.7e-48 | S | Protein of unknown function (DUF1778) | |||
LNGBALBM_00142 | 3.9e-15 | |||||
LNGBALBM_00143 | 3.8e-257 | yhjE | EGP | Sugar (and other) transporter | ||
LNGBALBM_00144 | 1.1e-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 | |
LNGBALBM_00145 | 0.0 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
LNGBALBM_00146 | 6.5e-220 | E | GDSL-like Lipase/Acylhydrolase family | |||
LNGBALBM_00147 | 8e-284 | bglA | 3.2.1.21 | G | Glycosyl hydrolase family 1 | |
LNGBALBM_00148 | 1e-136 | G | beta-mannosidase | |||
LNGBALBM_00149 | 5.2e-187 | K | helix_turn _helix lactose operon repressor | |||
LNGBALBM_00150 | 2.6e-115 | S | Protein of unknown function, DUF624 | |||
LNGBALBM_00151 | 2.6e-132 | |||||
LNGBALBM_00152 | 3e-25 | |||||
LNGBALBM_00153 | 3.3e-260 | yihS | 5.1.3.11 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
LNGBALBM_00154 | 3.1e-133 | ybbL | V | ATPases associated with a variety of cellular activities | ||
LNGBALBM_00155 | 1.9e-145 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
LNGBALBM_00156 | 6e-277 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
LNGBALBM_00158 | 1.1e-127 | V | ABC transporter | |||
LNGBALBM_00159 | 0.0 | V | FtsX-like permease family | |||
LNGBALBM_00160 | 6.4e-282 | cycA | E | Amino acid permease | ||
LNGBALBM_00161 | 4.6e-33 | V | efflux transmembrane transporter activity | |||
LNGBALBM_00162 | 2.8e-19 | MV | MacB-like periplasmic core domain | |||
LNGBALBM_00163 | 4.6e-305 | M | MacB-like periplasmic core domain | |||
LNGBALBM_00164 | 9.3e-74 | V | ABC transporter, ATP-binding protein | |||
LNGBALBM_00165 | 1.2e-106 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
LNGBALBM_00166 | 0.0 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
LNGBALBM_00167 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
LNGBALBM_00168 | 4e-268 | xynD | 3.2.1.8, 3.5.1.104, 3.5.1.41 | G | Polysaccharide deacetylase | |
LNGBALBM_00169 | 6e-123 | 3.6.1.27 | I | Acid phosphatase homologues | ||
LNGBALBM_00170 | 1.6e-114 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
LNGBALBM_00171 | 2.7e-73 | |||||
LNGBALBM_00172 | 3.7e-219 | natB | E | Receptor family ligand binding region | ||
LNGBALBM_00173 | 9.5e-102 | K | Psort location Cytoplasmic, score 8.87 | |||
LNGBALBM_00174 | 0.0 | pip | S | YhgE Pip domain protein | ||
LNGBALBM_00175 | 0.0 | pip | S | YhgE Pip domain protein | ||
LNGBALBM_00176 | 2.5e-107 | XK27_08585 | S | Hypothetical bacterial integral membrane protein (Trep_Strep) | ||
LNGBALBM_00177 | 3.4e-132 | XK26_04485 | P | Cobalt transport protein | ||
LNGBALBM_00178 | 6.2e-282 | G | ATPases associated with a variety of cellular activities | |||
LNGBALBM_00179 | 7.7e-182 | adcA | P | ZinT (YodA) periplasmic lipocalin-like zinc-recruitment | ||
LNGBALBM_00180 | 3.9e-167 | S | esterase of the alpha-beta hydrolase superfamily | |||
LNGBALBM_00181 | 5e-142 | S | esterase of the alpha-beta hydrolase superfamily | |||
LNGBALBM_00182 | 1.2e-94 | |||||
LNGBALBM_00184 | 2e-310 | pepD | E | Peptidase family C69 | ||
LNGBALBM_00185 | 3.3e-121 | icaR | K | Bacterial regulatory proteins, tetR family | ||
LNGBALBM_00186 | 1.5e-224 | 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) | ||
LNGBALBM_00187 | 9e-237 | amt | U | Ammonium Transporter Family | ||
LNGBALBM_00188 | 4.5e-55 | glnB | K | Nitrogen regulatory protein P-II | ||
LNGBALBM_00189 | 0.0 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
LNGBALBM_00190 | 2.4e-38 | K | sequence-specific DNA binding | |||
LNGBALBM_00191 | 9.8e-258 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
LNGBALBM_00192 | 1.8e-284 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
LNGBALBM_00193 | 9.7e-143 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
LNGBALBM_00194 | 1.7e-52 | S | granule-associated protein | |||
LNGBALBM_00195 | 0.0 | ubiB | S | ABC1 family | ||
LNGBALBM_00196 | 1.1e-200 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
LNGBALBM_00197 | 1e-116 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
LNGBALBM_00198 | 2e-129 | |||||
LNGBALBM_00199 | 7.3e-205 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
LNGBALBM_00200 | 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) | |
LNGBALBM_00201 | 1.2e-77 | cpaE | D | bacterial-type flagellum organization | ||
LNGBALBM_00202 | 1.3e-229 | cpaF | U | Type II IV secretion system protein | ||
LNGBALBM_00203 | 2.9e-107 | U | Type ii secretion system | |||
LNGBALBM_00204 | 3.7e-111 | U | Type II secretion system (T2SS), protein F | |||
LNGBALBM_00205 | 1.7e-39 | S | Protein of unknown function (DUF4244) | |||
LNGBALBM_00206 | 6.5e-50 | U | TadE-like protein | |||
LNGBALBM_00207 | 2.5e-75 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
LNGBALBM_00208 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
LNGBALBM_00209 | 6.7e-110 | 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 | ||
LNGBALBM_00210 | 6.9e-136 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
LNGBALBM_00211 | 2.1e-97 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
LNGBALBM_00212 | 1e-198 | 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 | |
LNGBALBM_00213 | 5.4e-121 | |||||
LNGBALBM_00214 | 0.0 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
LNGBALBM_00215 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
LNGBALBM_00216 | 5.9e-216 | ino1 | 5.5.1.4 | I | Myo-inositol-1-phosphate synthase | |
LNGBALBM_00217 | 4.1e-10 | ino1 | 5.5.1.4 | I | Myo-inositol-1-phosphate synthase | |
LNGBALBM_00218 | 3.2e-220 | 3.6.1.27 | I | PAP2 superfamily | ||
LNGBALBM_00219 | 0.0 | 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 | |
LNGBALBM_00220 | 2e-109 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
LNGBALBM_00221 | 5e-211 | holB | 2.7.7.7 | L | DNA polymerase III | |
LNGBALBM_00222 | 8.6e-141 | S | Phosphatidylethanolamine-binding protein | |||
LNGBALBM_00223 | 0.0 | pepD | E | Peptidase family C69 | ||
LNGBALBM_00224 | 0.0 | pepD | E | Peptidase family C69 | ||
LNGBALBM_00225 | 1.9e-222 | S | Domain of unknown function (DUF4143) | |||
LNGBALBM_00226 | 4.1e-289 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
LNGBALBM_00227 | 6e-63 | S | Macrophage migration inhibitory factor (MIF) | |||
LNGBALBM_00228 | 2.2e-198 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LNGBALBM_00229 | 7.6e-100 | S | GtrA-like protein | |||
LNGBALBM_00230 | 7.1e-175 | |||||
LNGBALBM_00231 | 2.6e-123 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
LNGBALBM_00232 | 6.8e-262 | EGP | Major facilitator Superfamily | |||
LNGBALBM_00233 | 6.2e-254 | tnpA | L | Transposase | ||
LNGBALBM_00234 | 1.4e-294 | gltX | 6.1.1.17 | 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) | |
LNGBALBM_00237 | 3.7e-251 | S | Calcineurin-like phosphoesterase | |||
LNGBALBM_00238 | 5.6e-144 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
LNGBALBM_00239 | 4.5e-266 | |||||
LNGBALBM_00240 | 2.3e-127 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
LNGBALBM_00241 | 1.4e-41 | QU41_18010 | 2.4.2.18 | K | Lrp/AsnC ligand binding domain | |
LNGBALBM_00242 | 1.6e-257 | nox | 1.6.3.4 | C | Pyridine nucleotide-disulphide oxidoreductase | |
LNGBALBM_00243 | 1.1e-250 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LNGBALBM_00244 | 1.2e-159 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LNGBALBM_00245 | 1.4e-160 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
LNGBALBM_00246 | 2.8e-218 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
LNGBALBM_00248 | 5.5e-113 | S | Domain of unknown function (DUF4854) | |||
LNGBALBM_00249 | 7.4e-179 | S | CAAX protease self-immunity | |||
LNGBALBM_00250 | 4.4e-144 | M | Mechanosensitive ion channel | |||
LNGBALBM_00251 | 1.9e-115 | K | Bacterial regulatory proteins, tetR family | |||
LNGBALBM_00252 | 3.9e-234 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
LNGBALBM_00253 | 3.4e-163 | S | Putative ABC-transporter type IV | |||
LNGBALBM_00254 | 2.9e-229 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
LNGBALBM_00255 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LNGBALBM_00256 | 5.6e-308 | S | Psort location Cytoplasmic, score 8.87 | |||
LNGBALBM_00257 | 1.8e-198 | yegV | G | pfkB family carbohydrate kinase | ||
LNGBALBM_00258 | 2.9e-30 | rpmB | J | Ribosomal L28 family | ||
LNGBALBM_00259 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
LNGBALBM_00260 | 0.0 | M | Spy0128-like isopeptide containing domain | |||
LNGBALBM_00261 | 8.4e-102 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
LNGBALBM_00262 | 4.8e-159 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
LNGBALBM_00263 | 2.7e-120 | 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 | ||
LNGBALBM_00264 | 1.5e-46 | CP_0960 | S | Belongs to the UPF0109 family | ||
LNGBALBM_00265 | 7.9e-66 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
LNGBALBM_00266 | 0.0 | lacZ | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LNGBALBM_00267 | 9.6e-222 | S | Endonuclease/Exonuclease/phosphatase family | |||
LNGBALBM_00268 | 1.5e-161 | P | Cation efflux family | |||
LNGBALBM_00269 | 1.5e-265 | 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 | |
LNGBALBM_00270 | 0.0 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LNGBALBM_00271 | 0.0 | yjjK | S | ABC transporter | ||
LNGBALBM_00272 | 3e-136 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
LNGBALBM_00273 | 3.4e-92 | ilvN | 2.2.1.6 | E | ACT domain | |
LNGBALBM_00274 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
LNGBALBM_00275 | 9.5e-141 | 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 | |
LNGBALBM_00276 | 1.4e-24 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
LNGBALBM_00277 | 1.9e-112 | yceD | S | Uncharacterized ACR, COG1399 | ||
LNGBALBM_00278 | 5.8e-121 | |||||
LNGBALBM_00279 | 1.3e-87 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
LNGBALBM_00280 | 1.4e-49 | S | Protein of unknown function (DUF3039) | |||
LNGBALBM_00281 | 6e-196 | yghZ | C | Aldo/keto reductase family | ||
LNGBALBM_00282 | 8.5e-251 | 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 | |
LNGBALBM_00283 | 2.4e-46 | |||||
LNGBALBM_00284 | 1.5e-135 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
LNGBALBM_00285 | 8.2e-131 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
LNGBALBM_00286 | 1e-245 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
LNGBALBM_00287 | 4e-184 | S | Auxin Efflux Carrier | |||
LNGBALBM_00290 | 1.8e-218 | manC | 2.7.7.13, 5.3.1.8 | M | Mannose-6-phosphate isomerase | |
LNGBALBM_00291 | 0.0 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
LNGBALBM_00292 | 1e-60 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
LNGBALBM_00293 | 2.7e-137 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
LNGBALBM_00294 | 2.4e-144 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LNGBALBM_00295 | 9.7e-159 | V | ATPases associated with a variety of cellular activities | |||
LNGBALBM_00296 | 2.8e-255 | V | Efflux ABC transporter, permease protein | |||
LNGBALBM_00297 | 1.9e-172 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
LNGBALBM_00298 | 1.1e-236 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
LNGBALBM_00299 | 0.0 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
LNGBALBM_00300 | 5.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
LNGBALBM_00301 | 1.5e-39 | rpmA | J | Ribosomal L27 protein | ||
LNGBALBM_00302 | 4.3e-303 | |||||
LNGBALBM_00303 | 7.9e-205 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
LNGBALBM_00304 | 3.7e-232 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
LNGBALBM_00306 | 8.7e-34 | 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 | ||
LNGBALBM_00307 | 8.4e-134 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
LNGBALBM_00308 | 1.5e-71 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
LNGBALBM_00309 | 6e-123 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
LNGBALBM_00310 | 8.4e-145 | QT | PucR C-terminal helix-turn-helix domain | |||
LNGBALBM_00311 | 5.6e-169 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
LNGBALBM_00312 | 2.6e-104 | bioY | S | BioY family | ||
LNGBALBM_00313 | 0.0 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
LNGBALBM_00314 | 3.1e-303 | pccB | I | Carboxyl transferase domain | ||
LNGBALBM_00315 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
LNGBALBM_00316 | 5.9e-79 | acpS | 2.7.8.7, 3.2.1.52 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
LNGBALBM_00318 | 2.6e-121 | |||||
LNGBALBM_00319 | 3.8e-187 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
LNGBALBM_00320 | 2e-49 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
LNGBALBM_00321 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
LNGBALBM_00322 | 2.3e-99 | lemA | S | LemA family | ||
LNGBALBM_00323 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
LNGBALBM_00324 | 4.1e-186 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LNGBALBM_00325 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LNGBALBM_00326 | 9.6e-79 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
LNGBALBM_00327 | 2e-42 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
LNGBALBM_00328 | 1.6e-168 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
LNGBALBM_00329 | 1.8e-300 | yegQ | O | Peptidase family U32 C-terminal domain | ||
LNGBALBM_00330 | 1e-226 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
LNGBALBM_00331 | 2.6e-149 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
LNGBALBM_00332 | 1e-133 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
LNGBALBM_00333 | 8.1e-84 | D | nuclear chromosome segregation | |||
LNGBALBM_00334 | 2.4e-269 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
LNGBALBM_00335 | 2.1e-218 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
LNGBALBM_00336 | 0.0 | I | Psort location CytoplasmicMembrane, score 9.99 | |||
LNGBALBM_00337 | 2.2e-240 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
LNGBALBM_00338 | 7.4e-121 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
LNGBALBM_00339 | 1.6e-219 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
LNGBALBM_00340 | 3.3e-132 | KT | Transcriptional regulatory protein, C terminal | |||
LNGBALBM_00341 | 3.2e-206 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
LNGBALBM_00342 | 8.5e-171 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
LNGBALBM_00343 | 8.3e-174 | pstA | P | Phosphate transport system permease | ||
LNGBALBM_00344 | 8.9e-147 | 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 | |
LNGBALBM_00345 | 1.3e-249 | pbuO | S | Permease family | ||
LNGBALBM_00346 | 9.3e-164 | P | Zinc-uptake complex component A periplasmic | |||
LNGBALBM_00347 | 2.1e-88 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
LNGBALBM_00348 | 2.4e-44 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
LNGBALBM_00349 | 9.2e-263 | T | Forkhead associated domain | |||
LNGBALBM_00350 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
LNGBALBM_00351 | 5.6e-39 | |||||
LNGBALBM_00352 | 7.9e-103 | flgA | NO | SAF | ||
LNGBALBM_00353 | 6.8e-32 | fmdB | S | Putative regulatory protein | ||
LNGBALBM_00354 | 4e-141 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
LNGBALBM_00355 | 3.3e-121 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
LNGBALBM_00356 | 2.5e-196 | |||||
LNGBALBM_00357 | 2.3e-47 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LNGBALBM_00361 | 1.9e-25 | rpmG | J | Ribosomal protein L33 | ||
LNGBALBM_00362 | 1.4e-226 | murB | 1.3.1.98 | M | Cell wall formation | |
LNGBALBM_00363 | 6.6e-290 | E | aromatic amino acid transport protein AroP K03293 | |||
LNGBALBM_00364 | 7.6e-60 | fdxA | C | 4Fe-4S binding domain | ||
LNGBALBM_00365 | 6.8e-220 | dapC | E | Aminotransferase class I and II | ||
LNGBALBM_00366 | 2e-252 | 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 | |
LNGBALBM_00368 | 1.3e-190 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LNGBALBM_00369 | 2.8e-114 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
LNGBALBM_00370 | 3.9e-122 | |||||
LNGBALBM_00371 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
LNGBALBM_00372 | 1.2e-79 | 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 | ||
LNGBALBM_00373 | 1.5e-62 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
LNGBALBM_00374 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LNGBALBM_00375 | 6.7e-209 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
LNGBALBM_00376 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LNGBALBM_00377 | 1.6e-190 | K | Psort location Cytoplasmic, score | |||
LNGBALBM_00378 | 1.1e-152 | ywiC | S | YwiC-like protein | ||
LNGBALBM_00379 | 8e-51 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LNGBALBM_00380 | 3.2e-118 | 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 | ||
LNGBALBM_00381 | 6.8e-116 | rplD | J | Forms part of the polypeptide exit tunnel | ||
LNGBALBM_00382 | 2.6e-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 | ||
LNGBALBM_00383 | 1.2e-154 | 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 | ||
LNGBALBM_00384 | 1.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
LNGBALBM_00385 | 6.7e-57 | 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 | ||
LNGBALBM_00386 | 3.9e-124 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
LNGBALBM_00387 | 2e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
LNGBALBM_00388 | 7e-37 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
LNGBALBM_00389 | 8.3e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
LNGBALBM_00390 | 8.7e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
LNGBALBM_00391 | 3e-51 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
LNGBALBM_00392 | 1.7e-105 | rplE | J | This is 1 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. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
LNGBALBM_00393 | 3.1e-29 | 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 | ||
LNGBALBM_00394 | 1.9e-68 | 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 | ||
LNGBALBM_00395 | 2.4e-95 | 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 | ||
LNGBALBM_00396 | 1.3e-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 | ||
LNGBALBM_00397 | 8.2e-94 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
LNGBALBM_00398 | 2.5e-23 | rpmD | J | Ribosomal protein L30p/L7e | ||
LNGBALBM_00399 | 7.4e-77 | rplO | J | binds to the 23S rRNA | ||
LNGBALBM_00400 | 1.5e-250 | 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 | ||
LNGBALBM_00401 | 3.2e-101 | 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 | |
LNGBALBM_00402 | 1.2e-32 | 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 | ||
LNGBALBM_00403 | 6.5e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
LNGBALBM_00404 | 2.1e-61 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
LNGBALBM_00405 | 5.7e-65 | 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 | ||
LNGBALBM_00406 | 5.2e-184 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LNGBALBM_00407 | 1e-70 | rplQ | J | Ribosomal protein L17 | ||
LNGBALBM_00408 | 2.1e-148 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
LNGBALBM_00410 | 5.1e-162 | |||||
LNGBALBM_00411 | 3.2e-195 | nusA | K | Participates in both transcription termination and antitermination | ||
LNGBALBM_00412 | 0.0 | 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 | ||
LNGBALBM_00413 | 6.4e-74 | 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 | ||
LNGBALBM_00414 | 5.9e-194 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
LNGBALBM_00415 | 7.8e-233 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
LNGBALBM_00416 | 1.5e-275 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
LNGBALBM_00417 | 1.9e-92 | |||||
LNGBALBM_00419 | 1.8e-127 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
LNGBALBM_00420 | 3.5e-180 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LNGBALBM_00422 | 1.9e-242 | 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) | |
LNGBALBM_00423 | 4.4e-219 | I | Diacylglycerol kinase catalytic domain | |||
LNGBALBM_00424 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
LNGBALBM_00425 | 2.2e-290 | S | alpha beta | |||
LNGBALBM_00426 | 9.6e-112 | S | Protein of unknown function (DUF4125) | |||
LNGBALBM_00427 | 0.0 | S | Domain of unknown function (DUF4037) | |||
LNGBALBM_00428 | 6e-126 | degU | K | helix_turn_helix, Lux Regulon | ||
LNGBALBM_00429 | 2e-269 | tcsS3 | KT | PspC domain | ||
LNGBALBM_00430 | 0.0 | pspC | KT | PspC domain | ||
LNGBALBM_00431 | 7.2e-102 | |||||
LNGBALBM_00432 | 9.5e-225 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LNGBALBM_00433 | 2.4e-130 | 2.5.1.49 | E | Cys/Met metabolism PLP-dependent enzyme | ||
LNGBALBM_00434 | 1.6e-28 | 2.5.1.49 | E | Cys/Met metabolism PLP-dependent enzyme | ||
LNGBALBM_00436 | 0.0 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
LNGBALBM_00437 | 2.2e-103 | |||||
LNGBALBM_00438 | 1.4e-291 | E | Phospholipase B | |||
LNGBALBM_00439 | 1.9e-266 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
LNGBALBM_00440 | 0.0 | gadC | E | Amino acid permease | ||
LNGBALBM_00441 | 9.2e-302 | E | Serine carboxypeptidase | |||
LNGBALBM_00442 | 1.7e-274 | puuP_1 | E | Amino acid permease | ||
LNGBALBM_00443 | 9.9e-77 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
LNGBALBM_00444 | 3.4e-140 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
LNGBALBM_00445 | 0.0 | 4.2.1.53 | S | MCRA family | ||
LNGBALBM_00446 | 5.6e-64 | 3.5.1.10 | C | Zinc-binding dehydrogenase | ||
LNGBALBM_00447 | 1.2e-123 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
LNGBALBM_00448 | 6e-282 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | Phosphomannose isomerase type I | |
LNGBALBM_00449 | 6.7e-22 | |||||
LNGBALBM_00450 | 5.5e-224 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
LNGBALBM_00451 | 3.3e-121 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
LNGBALBM_00452 | 1.6e-210 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
LNGBALBM_00453 | 5.6e-173 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
LNGBALBM_00454 | 2.1e-98 | M | NlpC/P60 family | |||
LNGBALBM_00455 | 2.4e-195 | T | Universal stress protein family | |||
LNGBALBM_00456 | 5.9e-73 | attW | O | OsmC-like protein | ||
LNGBALBM_00457 | 1.1e-174 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
LNGBALBM_00458 | 4.1e-132 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
LNGBALBM_00459 | 5.6e-100 | ptpA | 3.1.3.48 | T | low molecular weight | |
LNGBALBM_00460 | 3.6e-201 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LNGBALBM_00461 | 1.1e-161 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
LNGBALBM_00463 | 2.8e-183 | XK27_05540 | S | DUF218 domain | ||
LNGBALBM_00464 | 7.7e-188 | 3.1.3.5 | S | 5'-nucleotidase | ||
LNGBALBM_00465 | 4.6e-108 | |||||
LNGBALBM_00466 | 2.8e-293 | L | AAA ATPase domain | |||
LNGBALBM_00467 | 1.1e-54 | S | Cutinase | |||
LNGBALBM_00468 | 1.4e-228 | S | Uncharacterized protein conserved in bacteria (DUF2130) | |||
LNGBALBM_00469 | 3.3e-294 | S | Psort location Cytoplasmic, score 8.87 | |||
LNGBALBM_00470 | 3e-145 | S | Domain of unknown function (DUF4194) | |||
LNGBALBM_00471 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LNGBALBM_00472 | 1.4e-236 | S | Psort location Cytoplasmic, score 8.87 | |||
LNGBALBM_00474 | 2.6e-64 | yeaO | K | Protein of unknown function, DUF488 | ||
LNGBALBM_00475 | 2.8e-274 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
LNGBALBM_00476 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LNGBALBM_00477 | 2.8e-185 | lacR | K | Transcriptional regulator, LacI family | ||
LNGBALBM_00478 | 5.7e-117 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LNGBALBM_00479 | 5.8e-62 | |||||
LNGBALBM_00480 | 7e-96 | S | Domain of unknown function (DUF4190) | |||
LNGBALBM_00482 | 1.3e-77 | S | Domain of unknown function (DUF4190) | |||
LNGBALBM_00483 | 9.4e-205 | G | Bacterial extracellular solute-binding protein | |||
LNGBALBM_00484 | 0.0 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LNGBALBM_00485 | 6.3e-174 | G | ABC transporter permease | |||
LNGBALBM_00486 | 1.8e-173 | G | Binding-protein-dependent transport system inner membrane component | |||
LNGBALBM_00487 | 8.6e-187 | K | Periplasmic binding protein domain | |||
LNGBALBM_00491 | 1.3e-182 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
LNGBALBM_00492 | 1.2e-294 | S | AI-2E family transporter | |||
LNGBALBM_00493 | 2.9e-243 | epsG | M | Glycosyl transferase family 21 | ||
LNGBALBM_00494 | 1.3e-162 | natA | V | ATPases associated with a variety of cellular activities | ||
LNGBALBM_00495 | 0.0 | |||||
LNGBALBM_00496 | 5.3e-237 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
LNGBALBM_00497 | 5.9e-216 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
LNGBALBM_00498 | 2.5e-98 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
LNGBALBM_00499 | 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 | ||
LNGBALBM_00500 | 1.1e-142 | folK | 2.5.1.15, 2.6.1.85, 2.7.6.3, 3.5.4.16, 4.1.2.25 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
LNGBALBM_00501 | 2.3e-113 | S | Protein of unknown function (DUF3180) | |||
LNGBALBM_00502 | 2.6e-174 | tesB | I | Thioesterase-like superfamily | ||
LNGBALBM_00503 | 7.3e-300 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
LNGBALBM_00504 | 3.2e-66 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
LNGBALBM_00505 | 1e-256 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
LNGBALBM_00506 | 1.3e-111 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LNGBALBM_00507 | 2.2e-133 | |||||
LNGBALBM_00509 | 1.3e-173 | |||||
LNGBALBM_00510 | 1.4e-35 | rpmE | J | Binds the 23S rRNA | ||
LNGBALBM_00511 | 4e-272 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
LNGBALBM_00512 | 0.0 | G | Belongs to the glycosyl hydrolase 43 family | |||
LNGBALBM_00513 | 4.9e-190 | K | Bacterial regulatory proteins, lacI family | |||
LNGBALBM_00514 | 8.8e-245 | msmE | G | ABC transporter periplasmic binding protein YcjN precursor K02027 | ||
LNGBALBM_00515 | 2.9e-193 | MA20_14025 | U | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_00516 | 3.3e-158 | MA20_14020 | P | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_00517 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
LNGBALBM_00518 | 0.0 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
LNGBALBM_00519 | 2.3e-236 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
LNGBALBM_00520 | 0.0 | G | candidate polyfunctional acetylxylan esterase b-xylosidase A-L-arabinofuranosidase, CBM9 module, glycoside hydrolase family 43 protein and carbohydrate esterase family 6 protein K01238 | |||
LNGBALBM_00521 | 1.7e-290 | xylB | 1.1.1.57, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
LNGBALBM_00522 | 3.6e-219 | xylR | GK | ROK family | ||
LNGBALBM_00523 | 8.6e-36 | rpmE | J | Binds the 23S rRNA | ||
LNGBALBM_00524 | 4.9e-167 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
LNGBALBM_00525 | 3.7e-176 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
LNGBALBM_00526 | 2.6e-115 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
LNGBALBM_00527 | 1.3e-197 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
LNGBALBM_00528 | 2.2e-290 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
LNGBALBM_00529 | 3.7e-122 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
LNGBALBM_00530 | 2.7e-157 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
LNGBALBM_00531 | 1.6e-277 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
LNGBALBM_00532 | 2.5e-74 | |||||
LNGBALBM_00533 | 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 | |
LNGBALBM_00534 | 1.2e-134 | L | Single-strand binding protein family | |||
LNGBALBM_00535 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LNGBALBM_00536 | 5.7e-104 | S | Short repeat of unknown function (DUF308) | |||
LNGBALBM_00537 | 2e-130 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
LNGBALBM_00538 | 2.2e-251 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
LNGBALBM_00539 | 8.6e-84 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
LNGBALBM_00540 | 2.1e-169 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
LNGBALBM_00541 | 5.1e-204 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
LNGBALBM_00542 | 3.9e-227 | ftsE | D | Cell division ATP-binding protein FtsE | ||
LNGBALBM_00543 | 9.4e-164 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
LNGBALBM_00544 | 3.3e-184 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
LNGBALBM_00545 | 4.2e-78 | 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 | ||
LNGBALBM_00546 | 2.3e-154 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
LNGBALBM_00547 | 1.9e-167 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
LNGBALBM_00548 | 4.4e-151 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_00549 | 1.1e-153 | tcyC | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
LNGBALBM_00550 | 1e-181 | K | Psort location Cytoplasmic, score | |||
LNGBALBM_00551 | 1.4e-127 | K | helix_turn_helix, Lux Regulon | |||
LNGBALBM_00552 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
LNGBALBM_00553 | 5.2e-144 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
LNGBALBM_00554 | 3.2e-68 | |||||
LNGBALBM_00555 | 1.1e-136 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
LNGBALBM_00556 | 0.0 | E | ABC transporter, substrate-binding protein, family 5 | |||
LNGBALBM_00557 | 7.8e-169 | P | Binding-protein-dependent transport system inner membrane component | |||
LNGBALBM_00558 | 1.5e-155 | EP | Binding-protein-dependent transport system inner membrane component | |||
LNGBALBM_00559 | 1.7e-140 | P | ATPases associated with a variety of cellular activities | |||
LNGBALBM_00560 | 3.6e-140 | sapF | E | ATPases associated with a variety of cellular activities | ||
LNGBALBM_00561 | 1.4e-220 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LNGBALBM_00562 | 1e-190 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
LNGBALBM_00563 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
LNGBALBM_00564 | 2.2e-173 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LNGBALBM_00565 | 6.4e-107 | J | Acetyltransferase (GNAT) domain | |||
LNGBALBM_00568 | 1.2e-38 | M1-431 | S | Protein of unknown function (DUF1706) | ||
LNGBALBM_00569 | 8.1e-22 | M1-431 | S | Protein of unknown function (DUF1706) | ||
LNGBALBM_00571 | 1.2e-58 | |||||
LNGBALBM_00572 | 2.1e-64 | |||||
LNGBALBM_00573 | 2.6e-73 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
LNGBALBM_00574 | 0.0 | KL | Domain of unknown function (DUF3427) | |||
LNGBALBM_00575 | 3.6e-63 | mloA | S | Fic/DOC family | ||
LNGBALBM_00576 | 0.0 | S | Protein of unknown function (DUF1524) | |||
LNGBALBM_00577 | 4.4e-94 | gepA | S | Protein of unknown function (DUF4065) | ||
LNGBALBM_00578 | 3.1e-92 | doc | S | Fic/DOC family | ||
LNGBALBM_00579 | 1.2e-88 | XK27_03610 | K | Acetyltransferase (GNAT) domain | ||
LNGBALBM_00580 | 3e-142 | S | 3-oxo-5-alpha-steroid 4-dehydrogenase | |||
LNGBALBM_00581 | 7e-228 | gldA | 1.1.1.1, 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
LNGBALBM_00582 | 6.6e-95 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
LNGBALBM_00583 | 5.8e-102 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
LNGBALBM_00584 | 1.1e-261 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
LNGBALBM_00585 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LNGBALBM_00586 | 3.7e-221 | ybiR | P | Citrate transporter | ||
LNGBALBM_00588 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
LNGBALBM_00589 | 2.8e-85 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
LNGBALBM_00590 | 6.3e-226 | 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) | |
LNGBALBM_00591 | 4.8e-72 | zur | P | Belongs to the Fur family | ||
LNGBALBM_00592 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
LNGBALBM_00593 | 1.7e-265 | S | Putative esterase | |||
LNGBALBM_00594 | 2.2e-240 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
LNGBALBM_00595 | 3.3e-197 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
LNGBALBM_00596 | 3e-303 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
LNGBALBM_00597 | 5.7e-280 | umuC | 2.7.7.7 | L | DNA-damage repair protein (DNA polymerase IV) K00961 | |
LNGBALBM_00598 | 1.7e-72 | |||||
LNGBALBM_00599 | 7.3e-215 | S | 50S ribosome-binding GTPase | |||
LNGBALBM_00600 | 6.9e-101 | |||||
LNGBALBM_00601 | 2.7e-89 | S | Pyridoxamine 5'-phosphate oxidase | |||
LNGBALBM_00602 | 1.4e-107 | 2.7.1.196, 2.7.1.205 | K | sequence-specific DNA binding | ||
LNGBALBM_00604 | 1e-226 | |||||
LNGBALBM_00605 | 2.8e-126 | |||||
LNGBALBM_00606 | 2.1e-68 | |||||
LNGBALBM_00607 | 1.8e-107 | |||||
LNGBALBM_00608 | 9.9e-209 | S | Short C-terminal domain | |||
LNGBALBM_00609 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
LNGBALBM_00610 | 8.6e-139 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
LNGBALBM_00611 | 8.9e-234 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
LNGBALBM_00612 | 1.7e-234 | M | Glycosyl transferase 4-like domain | |||
LNGBALBM_00613 | 9.4e-197 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
LNGBALBM_00615 | 2.7e-61 | 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 | ||
LNGBALBM_00616 | 2.5e-80 | 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 | ||
LNGBALBM_00617 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
LNGBALBM_00618 | 1.2e-232 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LNGBALBM_00619 | 7.7e-123 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
LNGBALBM_00620 | 2.6e-95 | |||||
LNGBALBM_00621 | 5.1e-104 | 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 | ||
LNGBALBM_00622 | 9.5e-80 | 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 | ||
LNGBALBM_00623 | 2.8e-240 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
LNGBALBM_00624 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
LNGBALBM_00625 | 8.9e-181 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
LNGBALBM_00626 | 1.2e-114 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
LNGBALBM_00627 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
LNGBALBM_00628 | 4.2e-46 | 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 | |
LNGBALBM_00629 | 3.1e-215 | 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 | |
LNGBALBM_00630 | 2.5e-255 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
LNGBALBM_00631 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
LNGBALBM_00632 | 1.7e-184 | fmt | 2.1.1.176, 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 | |
LNGBALBM_00633 | 3.5e-86 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
LNGBALBM_00634 | 6.3e-128 | apl | 3.1.3.1 | S | SNARE associated Golgi protein | |
LNGBALBM_00635 | 1.2e-291 | arc | O | AAA ATPase forming ring-shaped complexes | ||
LNGBALBM_00636 | 3.3e-310 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
LNGBALBM_00637 | 2.4e-172 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
LNGBALBM_00638 | 2.5e-30 | pup | S | Protein modifier that is covalently attached to lysine residues of substrate proteins, thereby targeting them for proteasomal degradation. The tagging system is termed pupylation | ||
LNGBALBM_00639 | 5e-292 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
LNGBALBM_00640 | 6.2e-42 | hup | L | Belongs to the bacterial histone-like protein family | ||
LNGBALBM_00642 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
LNGBALBM_00643 | 3e-281 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
LNGBALBM_00644 | 2.1e-293 | S | PGAP1-like protein | |||
LNGBALBM_00646 | 3.6e-87 | |||||
LNGBALBM_00647 | 9.3e-181 | S | von Willebrand factor (vWF) type A domain | |||
LNGBALBM_00648 | 6.3e-196 | S | von Willebrand factor (vWF) type A domain | |||
LNGBALBM_00649 | 4.5e-83 | |||||
LNGBALBM_00650 | 9.8e-180 | S | Protein of unknown function DUF58 | |||
LNGBALBM_00651 | 4.2e-192 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
LNGBALBM_00652 | 2.5e-63 | 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 | |
LNGBALBM_00653 | 3.7e-80 | S | LytR cell envelope-related transcriptional attenuator | |||
LNGBALBM_00654 | 1.8e-33 | cspA | K | 'Cold-shock' DNA-binding domain | ||
LNGBALBM_00655 | 3.5e-291 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
LNGBALBM_00656 | 6.5e-42 | S | Proteins of 100 residues with WXG | |||
LNGBALBM_00657 | 5e-134 | |||||
LNGBALBM_00658 | 2.4e-133 | KT | Response regulator receiver domain protein | |||
LNGBALBM_00659 | 0.0 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
LNGBALBM_00660 | 1.2e-79 | cspB | K | 'Cold-shock' DNA-binding domain | ||
LNGBALBM_00661 | 8.2e-210 | S | Protein of unknown function (DUF3027) | |||
LNGBALBM_00662 | 7.3e-117 | |||||
LNGBALBM_00663 | 5.6e-183 | uspA | T | Belongs to the universal stress protein A family | ||
LNGBALBM_00664 | 0.0 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
LNGBALBM_00665 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
LNGBALBM_00666 | 8.7e-259 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
LNGBALBM_00667 | 3.7e-228 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
LNGBALBM_00668 | 9.6e-149 | aroD | S | Serine aminopeptidase, S33 | ||
LNGBALBM_00669 | 3e-142 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
LNGBALBM_00670 | 8.1e-154 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
LNGBALBM_00671 | 5.2e-111 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_00672 | 2.1e-202 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_00673 | 9.8e-188 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
LNGBALBM_00674 | 0.0 | L | DEAD DEAH box helicase | |||
LNGBALBM_00675 | 7.2e-262 | rarA | L | Recombination factor protein RarA | ||
LNGBALBM_00676 | 5.7e-267 | EGP | Major facilitator Superfamily | |||
LNGBALBM_00677 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LNGBALBM_00678 | 2.5e-200 | L | Transposase, Mutator family | |||
LNGBALBM_00680 | 1.4e-308 | |||||
LNGBALBM_00681 | 1.3e-142 | E | Psort location Cytoplasmic, score 8.87 | |||
LNGBALBM_00682 | 2.4e-65 | S | Zincin-like metallopeptidase | |||
LNGBALBM_00683 | 4.9e-72 | yccF | S | Inner membrane component domain | ||
LNGBALBM_00684 | 1.1e-141 | 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 | |
LNGBALBM_00685 | 2.7e-46 | yhbY | J | CRS1_YhbY | ||
LNGBALBM_00686 | 8.6e-164 | yvgN | 1.1.1.346 | S | Aldo/keto reductase family | |
LNGBALBM_00687 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
LNGBALBM_00688 | 9.9e-98 | ecfA | GP | ABC transporter, ATP-binding protein | ||
LNGBALBM_00689 | 1.3e-134 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
LNGBALBM_00690 | 1.7e-223 | E | Aminotransferase class I and II | |||
LNGBALBM_00691 | 4e-150 | bioM | P | ATPases associated with a variety of cellular activities | ||
LNGBALBM_00692 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
LNGBALBM_00693 | 0.0 | S | Tetratricopeptide repeat | |||
LNGBALBM_00694 | 0.0 | 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 | |
LNGBALBM_00695 | 3.2e-206 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
LNGBALBM_00696 | 2.6e-109 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LNGBALBM_00697 | 7e-283 | glnA | 6.3.1.2 | E | glutamine synthetase | |
LNGBALBM_00698 | 1.6e-148 | S | Domain of unknown function (DUF4191) | |||
LNGBALBM_00699 | 3.4e-280 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LNGBALBM_00700 | 9.5e-104 | S | Protein of unknown function (DUF3043) | |||
LNGBALBM_00701 | 9.7e-266 | argE | E | Peptidase dimerisation domain | ||
LNGBALBM_00702 | 1.3e-212 | 2.7.13.3 | T | Histidine kinase | ||
LNGBALBM_00703 | 2.1e-44 | |||||
LNGBALBM_00704 | 8.2e-162 | V | N-Acetylmuramoyl-L-alanine amidase | |||
LNGBALBM_00705 | 1.3e-226 | ytrE | V | lipoprotein transporter activity | ||
LNGBALBM_00706 | 3.2e-107 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LNGBALBM_00707 | 0.0 | cbiQ | P | ATPases associated with a variety of cellular activities | ||
LNGBALBM_00708 | 4.8e-131 | V | ABC transporter, ATP-binding protein | |||
LNGBALBM_00709 | 3.4e-218 | V | FtsX-like permease family | |||
LNGBALBM_00710 | 7.1e-16 | V | FtsX-like permease family | |||
LNGBALBM_00711 | 8.7e-170 | IV02_28330 | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LNGBALBM_00712 | 2.3e-177 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LNGBALBM_00713 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
LNGBALBM_00714 | 1.8e-147 | |||||
LNGBALBM_00715 | 6.5e-204 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
LNGBALBM_00716 | 5.1e-207 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
LNGBALBM_00717 | 3.3e-180 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
LNGBALBM_00718 | 3.4e-241 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
LNGBALBM_00719 | 2.9e-184 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
LNGBALBM_00720 | 1.4e-90 | argR | K | Regulates arginine biosynthesis genes | ||
LNGBALBM_00721 | 3.2e-239 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LNGBALBM_00722 | 3e-284 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
LNGBALBM_00723 | 9.5e-155 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
LNGBALBM_00724 | 6.2e-90 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
LNGBALBM_00725 | 1.4e-256 | 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) | |
LNGBALBM_00726 | 2.2e-158 | L | Tetratricopeptide repeat | |||
LNGBALBM_00727 | 1.5e-194 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
LNGBALBM_00728 | 5.4e-144 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
LNGBALBM_00729 | 3.9e-273 | trkB | P | Cation transport protein | ||
LNGBALBM_00730 | 2.7e-117 | trkA | P | TrkA-N domain | ||
LNGBALBM_00731 | 5.6e-183 | nadK | 2.7.1.23 | H | 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 | |
LNGBALBM_00732 | 0.0 | recN | L | May be involved in recombinational repair of damaged DNA | ||
LNGBALBM_00733 | 3.3e-129 | S | Haloacid dehalogenase-like hydrolase | |||
LNGBALBM_00734 | 1.5e-288 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
LNGBALBM_00735 | 3.5e-236 | 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 | |
LNGBALBM_00736 | 1.9e-115 | |||||
LNGBALBM_00737 | 7.8e-134 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
LNGBALBM_00738 | 8.2e-193 | 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) | |
LNGBALBM_00740 | 1e-262 | 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 | |
LNGBALBM_00741 | 4.2e-71 | 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 | |
LNGBALBM_00742 | 8e-122 | gpmB | 3.1.3.73, 3.1.3.85 | G | Phosphoglycerate mutase family | |
LNGBALBM_00743 | 1.8e-82 | |||||
LNGBALBM_00745 | 8.3e-72 | pdxH | S | Pfam:Pyridox_oxidase | ||
LNGBALBM_00746 | 3e-161 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
LNGBALBM_00747 | 1.2e-169 | corA | P | CorA-like Mg2+ transporter protein | ||
LNGBALBM_00748 | 6.1e-168 | ET | Bacterial periplasmic substrate-binding proteins | |||
LNGBALBM_00749 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LNGBALBM_00750 | 8.6e-118 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
LNGBALBM_00751 | 0.0 | comE | S | Competence protein | ||
LNGBALBM_00752 | 1.8e-187 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
LNGBALBM_00753 | 8e-114 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
LNGBALBM_00754 | 9.2e-158 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
LNGBALBM_00755 | 7.5e-91 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
LNGBALBM_00756 | 3.6e-196 | 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 | |
LNGBALBM_00758 | 1.9e-89 | |||||
LNGBALBM_00760 | 3.6e-61 | |||||
LNGBALBM_00761 | 4.9e-103 | M | Peptidase family M23 | |||
LNGBALBM_00762 | 2.5e-278 | G | ABC transporter substrate-binding protein | |||
LNGBALBM_00763 | 9.7e-241 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
LNGBALBM_00764 | 6.2e-210 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
LNGBALBM_00765 | 1.4e-19 | |||||
LNGBALBM_00766 | 1.5e-297 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
LNGBALBM_00767 | 8.3e-87 | def | 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 | |
LNGBALBM_00768 | 1.9e-161 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
LNGBALBM_00769 | 7.5e-139 | 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 | ||
LNGBALBM_00770 | 1.3e-134 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
LNGBALBM_00771 | 1.2e-92 | 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 | ||
LNGBALBM_00772 | 5.5e-175 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
LNGBALBM_00773 | 1.2e-230 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
LNGBALBM_00774 | 1.4e-104 | K | WHG domain | |||
LNGBALBM_00775 | 8.4e-114 | nodI | V | ATPases associated with a variety of cellular activities | ||
LNGBALBM_00776 | 2.2e-134 | S | ABC-2 type transporter | |||
LNGBALBM_00777 | 3.9e-139 | 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 | |
LNGBALBM_00778 | 3.3e-76 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
LNGBALBM_00779 | 1.5e-299 | 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 | |
LNGBALBM_00780 | 8.8e-115 | ung2 | 3.2.2.27 | L | Uracil DNA glycosylase superfamily | |
LNGBALBM_00783 | 0.0 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
LNGBALBM_00784 | 6.4e-162 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
LNGBALBM_00785 | 7.1e-183 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
LNGBALBM_00786 | 4.5e-123 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
LNGBALBM_00787 | 2.2e-41 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
LNGBALBM_00788 | 1.2e-157 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
LNGBALBM_00789 | 1.2e-109 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LNGBALBM_00790 | 8.7e-176 | S | Bacterial protein of unknown function (DUF881) | |||
LNGBALBM_00791 | 4.8e-33 | sbp | S | Protein of unknown function (DUF1290) | ||
LNGBALBM_00792 | 3.2e-153 | S | Bacterial protein of unknown function (DUF881) | |||
LNGBALBM_00793 | 1.1e-74 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
LNGBALBM_00794 | 3.1e-133 | K | helix_turn_helix, mercury resistance | |||
LNGBALBM_00795 | 5e-69 | |||||
LNGBALBM_00796 | 1.2e-64 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LNGBALBM_00797 | 8.3e-66 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LNGBALBM_00798 | 7.4e-140 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
LNGBALBM_00799 | 3.9e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
LNGBALBM_00800 | 0.0 | helY | L | DEAD DEAH box helicase | ||
LNGBALBM_00801 | 5.8e-36 | |||||
LNGBALBM_00802 | 0.0 | pafB | K | WYL domain | ||
LNGBALBM_00803 | 9.1e-283 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
LNGBALBM_00805 | 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 | |
LNGBALBM_00806 | 1.7e-145 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LNGBALBM_00807 | 2e-167 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LNGBALBM_00808 | 5.7e-22 | |||||
LNGBALBM_00809 | 0.0 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
LNGBALBM_00810 | 2.1e-244 | |||||
LNGBALBM_00811 | 3.4e-166 | 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 | |
LNGBALBM_00812 | 1.5e-222 | 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 | |
LNGBALBM_00813 | 1.7e-102 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
LNGBALBM_00814 | 1.4e-53 | yajC | U | Preprotein translocase subunit | ||
LNGBALBM_00815 | 5e-204 | 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 | |
LNGBALBM_00816 | 1.7e-108 | 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 | |
LNGBALBM_00817 | 2.5e-101 | 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 | |
LNGBALBM_00818 | 3.6e-129 | yebC | K | transcriptional regulatory protein | ||
LNGBALBM_00819 | 8.2e-190 | pimA | 2.4.1.345 | GT4 | M | Glycosyl transferases group 1 |
LNGBALBM_00820 | 1.9e-194 | htrB | 2.3.1.241, 2.3.1.265 | M | Bacterial lipid A biosynthesis acyltransferase | |
LNGBALBM_00821 | 1.1e-116 | pgsA1 | 2.7.8.11, 2.7.8.5 | I | CDP-alcohol phosphatidyltransferase | |
LNGBALBM_00822 | 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) | |
LNGBALBM_00823 | 1.7e-98 | S | ATPases associated with a variety of cellular activities | |||
LNGBALBM_00825 | 1.4e-95 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
LNGBALBM_00826 | 1.4e-23 | |||||
LNGBALBM_00832 | 2.3e-158 | S | PAC2 family | |||
LNGBALBM_00833 | 2.6e-150 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
LNGBALBM_00834 | 4.2e-160 | G | Fructosamine kinase | |||
LNGBALBM_00835 | 2.8e-218 | 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 | ||
LNGBALBM_00836 | 3e-201 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
LNGBALBM_00837 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
LNGBALBM_00838 | 1.4e-201 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
LNGBALBM_00839 | 1.3e-66 | S | PFAM Pentapeptide repeats (8 copies) | |||
LNGBALBM_00840 | 4e-231 | yugH | 2.6.1.1 | E | Aminotransferase class I and II | |
LNGBALBM_00841 | 4.6e-91 | alaR | K | helix_turn_helix ASNC type | ||
LNGBALBM_00842 | 8.7e-309 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
LNGBALBM_00843 | 1.1e-160 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LNGBALBM_00844 | 4.7e-25 | secG | U | Preprotein translocase SecG subunit | ||
LNGBALBM_00845 | 9.5e-152 | 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) | |
LNGBALBM_00846 | 3.1e-223 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
LNGBALBM_00847 | 4.3e-175 | whiA | K | May be required for sporulation | ||
LNGBALBM_00848 | 6e-174 | rapZ | S | Displays ATPase and GTPase activities | ||
LNGBALBM_00849 | 9.8e-177 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
LNGBALBM_00850 | 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 | ||
LNGBALBM_00851 | 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 | ||
LNGBALBM_00852 | 7e-32 | 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 | ||
LNGBALBM_00853 | 9.8e-180 | wcoO | ||||
LNGBALBM_00854 | 2.1e-99 | mug | 3.2.2.28 | L | Uracil DNA glycosylase superfamily | |
LNGBALBM_00855 | 2.7e-122 | S | Phospholipase/Carboxylesterase | |||
LNGBALBM_00856 | 4.1e-300 | ybiT | S | ABC transporter | ||
LNGBALBM_00857 | 1.9e-195 | cat | P | Cation efflux family | ||
LNGBALBM_00858 | 2.2e-145 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
LNGBALBM_00859 | 6.4e-184 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
LNGBALBM_00860 | 0.0 | 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 | |
LNGBALBM_00861 | 2e-108 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
LNGBALBM_00862 | 0.0 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
LNGBALBM_00863 | 5e-173 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
LNGBALBM_00864 | 1.1e-123 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LNGBALBM_00865 | 1.8e-189 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LNGBALBM_00866 | 1.2e-182 | draG | O | ADP-ribosylglycohydrolase | ||
LNGBALBM_00867 | 2.6e-58 | ytfH | K | HxlR-like helix-turn-helix | ||
LNGBALBM_00868 | 2.8e-51 | 3.6.1.55 | L | NUDIX domain | ||
LNGBALBM_00869 | 8.9e-80 | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | ||
LNGBALBM_00870 | 1.9e-124 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
LNGBALBM_00871 | 7.7e-188 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
LNGBALBM_00872 | 3.5e-157 | pyrK | 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 | C | Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B | |
LNGBALBM_00873 | 4.5e-177 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
LNGBALBM_00874 | 9.1e-283 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
LNGBALBM_00875 | 2e-73 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
LNGBALBM_00876 | 4.6e-188 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
LNGBALBM_00877 | 3.1e-89 | yneG | S | Domain of unknown function (DUF4186) | ||
LNGBALBM_00878 | 0.0 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
LNGBALBM_00879 | 1.5e-160 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
LNGBALBM_00880 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
LNGBALBM_00881 | 1.5e-100 | sixA | 3.6.1.55 | T | Phosphoglycerate mutase family | |
LNGBALBM_00882 | 2.7e-199 | trmI | 2.1.1.219, 2.1.1.220 | J | Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA | |
LNGBALBM_00883 | 3.4e-160 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
LNGBALBM_00884 | 7.8e-246 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
LNGBALBM_00885 | 2.6e-88 | bcp | 1.11.1.15 | O | Redoxin | |
LNGBALBM_00886 | 4.2e-80 | |||||
LNGBALBM_00887 | 1.7e-306 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
LNGBALBM_00888 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
LNGBALBM_00889 | 2.8e-262 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
LNGBALBM_00890 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
LNGBALBM_00891 | 3.4e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
LNGBALBM_00892 | 5.2e-139 | S | UPF0126 domain | |||
LNGBALBM_00893 | 5.1e-228 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
LNGBALBM_00894 | 5e-108 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
LNGBALBM_00895 | 1.3e-195 | S | alpha beta | |||
LNGBALBM_00896 | 1.8e-254 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
LNGBALBM_00897 | 1.2e-46 | pntA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
LNGBALBM_00898 | 9.7e-203 | pntAA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
LNGBALBM_00899 | 1.8e-79 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LNGBALBM_00900 | 1.3e-301 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LNGBALBM_00901 | 3.4e-183 | 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 | ||
LNGBALBM_00902 | 8.4e-249 | corC | S | CBS domain | ||
LNGBALBM_00903 | 2.5e-103 | 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 | |
LNGBALBM_00904 | 1.6e-213 | phoH | T | PhoH-like protein | ||
LNGBALBM_00905 | 2.5e-58 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
LNGBALBM_00906 | 3.2e-144 | 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 | |
LNGBALBM_00908 | 2.8e-165 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
LNGBALBM_00909 | 3.1e-132 | tnp3503b | 2.7.7.7 | L | Transposase and inactivated derivatives | |
LNGBALBM_00910 | 1.6e-214 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
LNGBALBM_00911 | 3.5e-92 | yitW | S | Iron-sulfur cluster assembly protein | ||
LNGBALBM_00912 | 8.9e-104 | iscU | C | SUF system FeS assembly protein, NifU family | ||
LNGBALBM_00913 | 3.5e-241 | sufS | 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 | |
LNGBALBM_00914 | 2.3e-142 | sufC | O | FeS assembly ATPase SufC | ||
LNGBALBM_00915 | 5.5e-228 | sufD | O | FeS assembly protein SufD | ||
LNGBALBM_00916 | 1.4e-289 | sufB | O | FeS assembly protein SufB | ||
LNGBALBM_00917 | 0.0 | S | L,D-transpeptidase catalytic domain | |||
LNGBALBM_00918 | 0.0 | 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 | |
LNGBALBM_00919 | 1.7e-48 | M | Aamy_C | |||
LNGBALBM_00920 | 1e-184 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LNGBALBM_00921 | 2.8e-84 | dexB | 2.4.1.7, 3.2.1.20, 3.2.1.51, 3.2.1.70, 3.2.1.93, 3.2.1.97 | GH101,GH13,GH29,GH31 | M | Aamy_C |
LNGBALBM_00922 | 7e-95 | amy | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | Alpha amylase, catalytic domain |
LNGBALBM_00925 | 2e-222 | |||||
LNGBALBM_00926 | 8.7e-215 | |||||
LNGBALBM_00927 | 1.3e-80 | |||||
LNGBALBM_00928 | 9.9e-82 | |||||
LNGBALBM_00929 | 7.3e-191 | |||||
LNGBALBM_00930 | 1.8e-70 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
LNGBALBM_00931 | 0.0 | aroK | 2.7.1.71, 4.2.3.4 | H | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
LNGBALBM_00932 | 5.4e-220 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
LNGBALBM_00933 | 1.3e-37 | 3.4.23.43 | S | Type IV leader peptidase family | ||
LNGBALBM_00934 | 1.8e-199 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
LNGBALBM_00935 | 1.2e-85 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
LNGBALBM_00936 | 0.0 | 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 | |
LNGBALBM_00937 | 1.4e-34 | |||||
LNGBALBM_00938 | 6.3e-64 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
LNGBALBM_00939 | 1.6e-128 | pgm3 | 3.1.3.85 | G | Phosphoglycerate mutase family | |
LNGBALBM_00940 | 8.9e-63 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
LNGBALBM_00941 | 5.8e-109 | 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 | ||
LNGBALBM_00942 | 0.0 | pcrA | 3.6.4.12 | L | DNA helicase | |
LNGBALBM_00943 | 3e-91 | 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 | |
LNGBALBM_00944 | 4e-265 | pbuX | F | Permease family | ||
LNGBALBM_00945 | 1.5e-112 | M | Protein of unknown function (DUF3737) | |||
LNGBALBM_00946 | 1.8e-27 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
LNGBALBM_00947 | 4.7e-179 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
LNGBALBM_00948 | 4.2e-186 | K | TRANSCRIPTIONal | |||
LNGBALBM_00949 | 0.0 | amyA | 3.2.1.1 | GH13 | G | Glycosyl hydrolase family 70 |
LNGBALBM_00950 | 1e-141 | S | Peptidase C26 | |||
LNGBALBM_00951 | 2.3e-84 | proX | S | Aminoacyl-tRNA editing domain | ||
LNGBALBM_00952 | 3.9e-97 | S | ABC-2 family transporter protein | |||
LNGBALBM_00953 | 8.7e-167 | V | ATPases associated with a variety of cellular activities | |||
LNGBALBM_00954 | 2.4e-66 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
LNGBALBM_00955 | 2.2e-190 | K | Helix-turn-helix XRE-family like proteins | |||
LNGBALBM_00956 | 7.7e-183 | |||||
LNGBALBM_00957 | 2.3e-141 | |||||
LNGBALBM_00958 | 1.4e-50 | 4.2.99.21 | E | Chorismate mutase type II | ||
LNGBALBM_00959 | 3.4e-160 | E | -acetyltransferase | |||
LNGBALBM_00960 | 3.9e-71 | K | Acetyltransferase (GNAT) family | |||
LNGBALBM_00961 | 1e-107 | adk | 2.7.4.3 | F | adenylate kinase activity | |
LNGBALBM_00962 | 2e-64 | S | AAA domain | |||
LNGBALBM_00963 | 0.0 | tetP | J | elongation factor G | ||
LNGBALBM_00964 | 4.6e-177 | insH6 | L | Transposase domain (DUF772) | ||
LNGBALBM_00965 | 1.3e-69 | K | sequence-specific DNA binding | |||
LNGBALBM_00966 | 3.3e-302 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
LNGBALBM_00967 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
LNGBALBM_00968 | 0.0 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
LNGBALBM_00969 | 5.7e-233 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
LNGBALBM_00970 | 4e-267 | aroA | 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
LNGBALBM_00972 | 2.4e-231 | ykiI | ||||
LNGBALBM_00973 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LNGBALBM_00974 | 5.7e-123 | 3.6.1.13 | L | NUDIX domain | ||
LNGBALBM_00975 | 8.3e-184 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
LNGBALBM_00976 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
LNGBALBM_00978 | 7.1e-117 | pdtaR | T | Response regulator receiver domain protein | ||
LNGBALBM_00979 | 2.6e-120 | aspA | 3.6.1.13 | L | NUDIX domain | |
LNGBALBM_00981 | 1.4e-275 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
LNGBALBM_00982 | 2.5e-178 | terC | P | Integral membrane protein, TerC family | ||
LNGBALBM_00983 | 0.0 | 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 | ||
LNGBALBM_00984 | 3.8e-119 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
LNGBALBM_00985 | 1.1e-267 | |||||
LNGBALBM_00986 | 3.1e-164 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
LNGBALBM_00987 | 7.3e-186 | P | Zinc-uptake complex component A periplasmic | |||
LNGBALBM_00988 | 5.1e-170 | znuC | P | ATPases associated with a variety of cellular activities | ||
LNGBALBM_00989 | 1.7e-143 | znuB | U | ABC 3 transport family | ||
LNGBALBM_00990 | 1.9e-89 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
LNGBALBM_00991 | 6.6e-102 | carD | K | CarD-like/TRCF domain | ||
LNGBALBM_00992 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | 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 |
LNGBALBM_00993 | 8.2e-131 | T | Response regulator receiver domain protein | |||
LNGBALBM_00994 | 1.2e-202 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
LNGBALBM_00995 | 1.3e-145 | ctsW | S | Phosphoribosyl transferase domain | ||
LNGBALBM_00996 | 7.9e-154 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
LNGBALBM_00997 | 4.8e-78 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
LNGBALBM_00998 | 3.1e-276 | |||||
LNGBALBM_00999 | 0.0 | S | Glycosyl transferase, family 2 | |||
LNGBALBM_01000 | 5.4e-238 | K | Cell envelope-related transcriptional attenuator domain | |||
LNGBALBM_01001 | 3.5e-185 | K | Cell envelope-related transcriptional attenuator domain | |||
LNGBALBM_01002 | 1.5e-247 | D | FtsK/SpoIIIE family | |||
LNGBALBM_01003 | 1.9e-46 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
LNGBALBM_01004 | 1.7e-284 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
LNGBALBM_01005 | 8.8e-135 | yplQ | S | Haemolysin-III related | ||
LNGBALBM_01006 | 1.2e-80 | 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 | ||
LNGBALBM_01007 | 1.1e-74 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
LNGBALBM_01008 | 2.2e-287 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
LNGBALBM_01009 | 1e-105 | |||||
LNGBALBM_01011 | 2.6e-170 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
LNGBALBM_01012 | 1.4e-110 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
LNGBALBM_01013 | 5.6e-98 | divIC | D | Septum formation initiator | ||
LNGBALBM_01014 | 2e-244 | 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 | |
LNGBALBM_01015 | 1.1e-164 | ssuC | U | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01016 | 4.6e-177 | P | NMT1-like family | |||
LNGBALBM_01017 | 9.8e-129 | ssuB | P | ATPases associated with a variety of cellular activities | ||
LNGBALBM_01019 | 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 | ||
LNGBALBM_01020 | 4.6e-103 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
LNGBALBM_01021 | 7.1e-110 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
LNGBALBM_01022 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
LNGBALBM_01023 | 6.1e-225 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
LNGBALBM_01024 | 4.5e-15 | ybdD | S | Selenoprotein, putative | ||
LNGBALBM_01025 | 0.0 | cstA | T | 5TM C-terminal transporter carbon starvation CstA | ||
LNGBALBM_01026 | 5.8e-32 | V | ABC transporter transmembrane region | |||
LNGBALBM_01027 | 9.4e-72 | V | (ABC) transporter | |||
LNGBALBM_01028 | 6.3e-99 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
LNGBALBM_01030 | 3.9e-81 | K | Winged helix DNA-binding domain | |||
LNGBALBM_01031 | 1.1e-80 | F | Nucleoside 2-deoxyribosyltransferase | |||
LNGBALBM_01032 | 1.2e-280 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
LNGBALBM_01033 | 7.2e-40 | feoA | P | FeoA | ||
LNGBALBM_01034 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
LNGBALBM_01035 | 0.0 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
LNGBALBM_01036 | 8.8e-181 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
LNGBALBM_01037 | 4.8e-148 | pgl | 3.1.1.31 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
LNGBALBM_01038 | 6.1e-282 | 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 | |
LNGBALBM_01039 | 1.5e-39 | pepE | 3.4.13.21 | E | Peptidase family S51 | |
LNGBALBM_01040 | 1.4e-251 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
LNGBALBM_01041 | 7.2e-194 | 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 | |
LNGBALBM_01042 | 0.0 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
LNGBALBM_01043 | 2.2e-148 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
LNGBALBM_01044 | 1.7e-308 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
LNGBALBM_01045 | 4.9e-199 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
LNGBALBM_01046 | 8.2e-260 | rutG | F | Permease family | ||
LNGBALBM_01047 | 2.1e-215 | lipA | I | Hydrolase, alpha beta domain protein | ||
LNGBALBM_01048 | 2.8e-42 | |||||
LNGBALBM_01049 | 2.1e-58 | S | Cupin 2, conserved barrel domain protein | |||
LNGBALBM_01050 | 1e-201 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
LNGBALBM_01051 | 6.5e-145 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
LNGBALBM_01052 | 1.3e-270 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
LNGBALBM_01053 | 0.0 | tcsS2 | T | Histidine kinase | ||
LNGBALBM_01054 | 1.4e-119 | K | helix_turn_helix, Lux Regulon | |||
LNGBALBM_01055 | 0.0 | MV | MacB-like periplasmic core domain | |||
LNGBALBM_01056 | 8.1e-171 | V | ABC transporter, ATP-binding protein | |||
LNGBALBM_01057 | 1.9e-96 | ecfT | P | transmembrane transporter activity | ||
LNGBALBM_01058 | 1.8e-292 | 3.6.3.24 | P | AAA domain, putative AbiEii toxin, Type IV TA system | ||
LNGBALBM_01059 | 1.3e-10 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
LNGBALBM_01060 | 8.8e-256 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
LNGBALBM_01061 | 8.6e-167 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
LNGBALBM_01062 | 2.2e-87 | yraN | L | Belongs to the UPF0102 family | ||
LNGBALBM_01063 | 1.1e-276 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
LNGBALBM_01064 | 1.3e-218 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
LNGBALBM_01065 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
LNGBALBM_01066 | 8.8e-173 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
LNGBALBM_01067 | 1.3e-122 | safC | S | O-methyltransferase | ||
LNGBALBM_01068 | 4.7e-151 | fmt2 | 3.2.2.10 | S | Belongs to the LOG family | |
LNGBALBM_01069 | 3.7e-252 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
LNGBALBM_01070 | 4.2e-244 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
LNGBALBM_01073 | 1.1e-250 | 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 | ||
LNGBALBM_01074 | 4.3e-124 | 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 | |
LNGBALBM_01075 | 1.3e-113 | 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 | |
LNGBALBM_01076 | 1.3e-252 | clcA_2 | P | Voltage gated chloride channel | ||
LNGBALBM_01077 | 1.5e-226 | 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 | ||
LNGBALBM_01078 | 9.3e-258 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
LNGBALBM_01079 | 9.5e-177 | 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 | |
LNGBALBM_01080 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
LNGBALBM_01081 | 5.4e-32 | |||||
LNGBALBM_01082 | 0.0 | nadE | 6.3.1.5, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
LNGBALBM_01083 | 2e-227 | S | Peptidase dimerisation domain | |||
LNGBALBM_01084 | 1.3e-120 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01085 | 1.5e-86 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LNGBALBM_01086 | 3.3e-141 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LNGBALBM_01087 | 8.6e-179 | metQ | P | NLPA lipoprotein | ||
LNGBALBM_01088 | 1.6e-102 | ppiA | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
LNGBALBM_01089 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | 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 | |
LNGBALBM_01090 | 1.2e-82 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
LNGBALBM_01091 | 1.8e-47 | S | Domain of unknown function (DUF4193) | |||
LNGBALBM_01092 | 7.8e-244 | S | Protein of unknown function (DUF3071) | |||
LNGBALBM_01093 | 2.5e-215 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
LNGBALBM_01094 | 0.0 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LNGBALBM_01095 | 3.4e-172 | glcU | G | Sugar transport protein | ||
LNGBALBM_01096 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
LNGBALBM_01097 | 2.2e-68 | G | Major facilitator superfamily | |||
LNGBALBM_01098 | 4.7e-69 | G | Major facilitator superfamily | |||
LNGBALBM_01099 | 1.2e-219 | G | Major Facilitator Superfamily | |||
LNGBALBM_01100 | 2.3e-226 | 2.4.1.345 | GT4 | M | Glycosyl transferase 4-like domain | |
LNGBALBM_01101 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LNGBALBM_01102 | 1.6e-186 | 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 | ||
LNGBALBM_01103 | 4e-130 | |||||
LNGBALBM_01104 | 2.7e-202 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
LNGBALBM_01105 | 0.0 | pknL | 2.7.11.1 | KLT | PASTA | |
LNGBALBM_01106 | 4.9e-139 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LNGBALBM_01107 | 2.2e-99 | |||||
LNGBALBM_01108 | 6.9e-195 | 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) | |
LNGBALBM_01109 | 0.0 | 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 | ||
LNGBALBM_01110 | 7.1e-124 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LNGBALBM_01112 | 2.6e-112 | recX | S | Modulates RecA activity | ||
LNGBALBM_01113 | 1e-207 | 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 | ||
LNGBALBM_01114 | 1e-43 | S | Protein of unknown function (DUF3046) | |||
LNGBALBM_01115 | 5e-67 | K | Helix-turn-helix XRE-family like proteins | |||
LNGBALBM_01116 | 4.2e-107 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
LNGBALBM_01117 | 7.7e-120 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LNGBALBM_01118 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
LNGBALBM_01119 | 6.8e-195 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
LNGBALBM_01120 | 1.1e-291 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
LNGBALBM_01121 | 1.3e-142 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
LNGBALBM_01123 | 8.5e-198 | dapB | 1.4.1.12, 1.4.1.16, 1.4.1.26 | S | Dihydrodipicolinate reductase, N-terminus | |
LNGBALBM_01124 | 6.1e-233 | V | ABC-2 family transporter protein | |||
LNGBALBM_01125 | 7.5e-236 | V | ABC-2 family transporter protein | |||
LNGBALBM_01126 | 4.2e-186 | V | ATPases associated with a variety of cellular activities | |||
LNGBALBM_01127 | 1.1e-212 | T | Histidine kinase | |||
LNGBALBM_01128 | 3.1e-116 | K | helix_turn_helix, Lux Regulon | |||
LNGBALBM_01129 | 1.6e-151 | S | Protein of unknown function DUF262 | |||
LNGBALBM_01130 | 2.1e-254 | tnpA | L | Transposase | ||
LNGBALBM_01131 | 1.3e-251 | S | Protein of unknown function DUF262 | |||
LNGBALBM_01132 | 8.7e-124 | maa | 2.3.1.18, 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
LNGBALBM_01133 | 1.7e-35 | |||||
LNGBALBM_01134 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
LNGBALBM_01135 | 0.0 | ctpE | P | E1-E2 ATPase | ||
LNGBALBM_01136 | 7e-104 | |||||
LNGBALBM_01137 | 7.2e-258 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
LNGBALBM_01138 | 1.7e-137 | S | Protein of unknown function (DUF3159) | |||
LNGBALBM_01139 | 3.3e-155 | S | Protein of unknown function (DUF3710) | |||
LNGBALBM_01140 | 4.8e-170 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
LNGBALBM_01141 | 9.8e-118 | |||||
LNGBALBM_01142 | 0.0 | dppD | P | Belongs to the ABC transporter superfamily | ||
LNGBALBM_01143 | 4.4e-172 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
LNGBALBM_01144 | 4.7e-155 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01145 | 0.0 | E | ABC transporter, substrate-binding protein, family 5 | |||
LNGBALBM_01146 | 6.2e-179 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
LNGBALBM_01147 | 3.4e-149 | V | ABC transporter, ATP-binding protein | |||
LNGBALBM_01148 | 0.0 | MV | MacB-like periplasmic core domain | |||
LNGBALBM_01149 | 4e-40 | |||||
LNGBALBM_01150 | 5.5e-211 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
LNGBALBM_01151 | 2.8e-218 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
LNGBALBM_01152 | 2.2e-90 | |||||
LNGBALBM_01153 | 0.0 | typA | T | Elongation factor G C-terminus | ||
LNGBALBM_01154 | 4.8e-260 | naiP | U | Sugar (and other) transporter | ||
LNGBALBM_01155 | 2.6e-157 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
LNGBALBM_01156 | 1.2e-152 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LNGBALBM_01157 | 4.8e-168 | xerD | D | recombinase XerD | ||
LNGBALBM_01158 | 1.5e-62 | 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 | ||
LNGBALBM_01159 | 6.1e-25 | rpmI | J | Ribosomal protein L35 | ||
LNGBALBM_01160 | 4.9e-101 | 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 | ||
LNGBALBM_01161 | 6.8e-150 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
LNGBALBM_01162 | 7.4e-208 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
LNGBALBM_01163 | 8.5e-90 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
LNGBALBM_01164 | 6.5e-179 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
LNGBALBM_01165 | 1.1e-197 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
LNGBALBM_01166 | 6e-54 | |||||
LNGBALBM_01167 | 1.5e-127 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
LNGBALBM_01168 | 4.6e-296 | 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 | |
LNGBALBM_01169 | 1.1e-200 | V | Acetyltransferase (GNAT) domain | |||
LNGBALBM_01170 | 1.1e-297 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
LNGBALBM_01171 | 5e-116 | gerE | KT | cheY-homologous receiver domain | ||
LNGBALBM_01172 | 2.9e-186 | 2.7.13.3 | T | Histidine kinase | ||
LNGBALBM_01173 | 1.5e-149 | |||||
LNGBALBM_01174 | 0.0 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
LNGBALBM_01175 | 8.8e-98 | 3.6.1.55 | F | NUDIX domain | ||
LNGBALBM_01176 | 4.8e-224 | GK | ROK family | |||
LNGBALBM_01177 | 1.5e-169 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
LNGBALBM_01178 | 1.3e-84 | 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 | ||
LNGBALBM_01179 | 4.2e-211 | int8 | L | Phage integrase family | ||
LNGBALBM_01185 | 1.6e-28 | |||||
LNGBALBM_01186 | 6.4e-229 | T | AAA domain | |||
LNGBALBM_01191 | 0.0 | xkdG | S | Caudovirus prohead serine protease | ||
LNGBALBM_01194 | 0.0 | P | Belongs to the ABC transporter superfamily | |||
LNGBALBM_01195 | 1.2e-206 | dppC | EP | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01196 | 8.8e-193 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01197 | 3.1e-59 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
LNGBALBM_01198 | 2.9e-160 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
LNGBALBM_01199 | 1e-222 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
LNGBALBM_01200 | 8.6e-287 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
LNGBALBM_01201 | 2.1e-163 | 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) |
LNGBALBM_01202 | 1.4e-256 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
LNGBALBM_01203 | 3.9e-273 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
LNGBALBM_01204 | 6.3e-207 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
LNGBALBM_01205 | 6.7e-260 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
LNGBALBM_01206 | 8.7e-159 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
LNGBALBM_01207 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
LNGBALBM_01208 | 9.5e-92 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
LNGBALBM_01209 | 3.1e-195 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
LNGBALBM_01210 | 9.3e-86 | mraZ | K | Belongs to the MraZ family | ||
LNGBALBM_01211 | 0.0 | L | DNA helicase | |||
LNGBALBM_01212 | 2.7e-227 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
LNGBALBM_01213 | 9.5e-97 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
LNGBALBM_01214 | 2.1e-10 | M | LysM domain | |||
LNGBALBM_01215 | 3.7e-128 | 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 | |
LNGBALBM_01216 | 2.1e-166 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
LNGBALBM_01217 | 1.2e-174 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
LNGBALBM_01218 | 1e-279 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LNGBALBM_01219 | 1.2e-117 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
LNGBALBM_01220 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
LNGBALBM_01221 | 2.6e-263 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
LNGBALBM_01222 | 1.2e-186 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
LNGBALBM_01223 | 4.4e-132 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
LNGBALBM_01224 | 2.4e-121 | 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 | ||
LNGBALBM_01225 | 1.6e-124 | |||||
LNGBALBM_01226 | 2.3e-110 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
LNGBALBM_01227 | 2.4e-225 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
LNGBALBM_01228 | 1.6e-255 | 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 | |
LNGBALBM_01229 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
LNGBALBM_01231 | 2.2e-176 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
LNGBALBM_01232 | 1.7e-96 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
LNGBALBM_01233 | 4.4e-33 | tccB2 | V | DivIVA protein | ||
LNGBALBM_01234 | 9.9e-43 | yggT | S | YGGT family | ||
LNGBALBM_01235 | 1.3e-79 | 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 | ||
LNGBALBM_01236 | 1e-221 | 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 | ||
LNGBALBM_01237 | 2.6e-249 | 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 | ||
LNGBALBM_01238 | 2.6e-296 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
LNGBALBM_01239 | 1.1e-98 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
LNGBALBM_01240 | 8.1e-293 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | 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) | |
LNGBALBM_01241 | 5.1e-60 | S | Thiamine-binding protein | |||
LNGBALBM_01242 | 1e-201 | K | helix_turn _helix lactose operon repressor | |||
LNGBALBM_01243 | 3.6e-249 | lacY | P | LacY proton/sugar symporter | ||
LNGBALBM_01244 | 0.0 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
LNGBALBM_01245 | 5.4e-147 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
LNGBALBM_01246 | 1.2e-194 | P | NMT1/THI5 like | |||
LNGBALBM_01247 | 4.7e-235 | iunH1 | 3.2.2.1 | F | nucleoside hydrolase | |
LNGBALBM_01249 | 1.7e-153 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
LNGBALBM_01250 | 5.7e-132 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
LNGBALBM_01251 | 0.0 | I | acetylesterase activity | |||
LNGBALBM_01252 | 2.4e-228 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
LNGBALBM_01253 | 7e-220 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
LNGBALBM_01254 | 1.2e-283 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
LNGBALBM_01256 | 4.1e-81 | |||||
LNGBALBM_01257 | 9.1e-74 | S | Protein of unknown function (DUF3052) | |||
LNGBALBM_01258 | 1.2e-182 | lon | T | Belongs to the peptidase S16 family | ||
LNGBALBM_01259 | 1.7e-259 | S | Zincin-like metallopeptidase | |||
LNGBALBM_01260 | 3.4e-302 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
LNGBALBM_01261 | 2.7e-266 | mphA | S | Aminoglycoside phosphotransferase | ||
LNGBALBM_01262 | 2.5e-17 | S | Protein of unknown function (DUF3107) | |||
LNGBALBM_01263 | 1.7e-167 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
LNGBALBM_01264 | 2.7e-120 | S | Vitamin K epoxide reductase | |||
LNGBALBM_01265 | 2.3e-175 | 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 | |
LNGBALBM_01266 | 1.5e-146 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
LNGBALBM_01267 | 3.1e-161 | S | Patatin-like phospholipase | |||
LNGBALBM_01268 | 9.7e-137 | XK27_08050 | O | prohibitin homologues | ||
LNGBALBM_01269 | 1.6e-163 | cjaA | ET | Bacterial periplasmic substrate-binding proteins | ||
LNGBALBM_01270 | 1.8e-159 | glnQ | 3.6.3.21 | E | ATP binding protein of ABC transporter for glutamate aspartate K02028 | |
LNGBALBM_01271 | 2.7e-123 | glnP | E | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01272 | 4.1e-113 | papP | E | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01273 | 1.2e-232 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
LNGBALBM_01274 | 1.1e-110 | metI | P | Psort location CytoplasmicMembrane, score 9.99 | ||
LNGBALBM_01275 | 8.3e-221 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LNGBALBM_01276 | 1e-162 | metQ | M | NLPA lipoprotein | ||
LNGBALBM_01277 | 3.9e-192 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
LNGBALBM_01278 | 6e-128 | K | acetyltransferase | |||
LNGBALBM_01279 | 1.5e-103 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
LNGBALBM_01283 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
LNGBALBM_01284 | 1.9e-286 | aaxC | E | Amino acid permease | ||
LNGBALBM_01285 | 6e-117 | |||||
LNGBALBM_01286 | 1.2e-27 | |||||
LNGBALBM_01287 | 0.0 | E | ABC transporter, substrate-binding protein, family 5 | |||
LNGBALBM_01288 | 8.5e-260 | EGP | Major Facilitator Superfamily | |||
LNGBALBM_01289 | 1.6e-107 | pspA | KT | PspA/IM30 family | ||
LNGBALBM_01290 | 4.4e-207 | S | COG1512 Beta-propeller domains of methanol dehydrogenase type | |||
LNGBALBM_01291 | 6e-08 | L | Transposase and inactivated derivatives IS30 family | |||
LNGBALBM_01292 | 0.0 | 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) | |
LNGBALBM_01293 | 2.3e-23 | |||||
LNGBALBM_01294 | 2e-146 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
LNGBALBM_01295 | 4.3e-46 | |||||
LNGBALBM_01296 | 5.6e-11 | |||||
LNGBALBM_01297 | 0.0 | V | ABC transporter transmembrane region | |||
LNGBALBM_01298 | 0.0 | V | ABC transporter, ATP-binding protein | |||
LNGBALBM_01299 | 3.2e-98 | K | MarR family | |||
LNGBALBM_01300 | 3.7e-102 | S | NADPH-dependent FMN reductase | |||
LNGBALBM_01301 | 1.7e-98 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
LNGBALBM_01304 | 5.8e-49 | |||||
LNGBALBM_01305 | 2.1e-204 | |||||
LNGBALBM_01306 | 0.0 | cas3 | L | CRISPR-associated helicase Cas3 | ||
LNGBALBM_01307 | 0.0 | |||||
LNGBALBM_01308 | 1.2e-222 | S | CRISPR-associated protein GSU0053 (Cas_GSU0053) | |||
LNGBALBM_01309 | 9.4e-17 | cas2 | L | CRISPR associated protein Cas2 | ||
LNGBALBM_01310 | 0.0 | cas4 | 3.1.12.1 | 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 | |
LNGBALBM_01311 | 6.5e-256 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
LNGBALBM_01312 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
LNGBALBM_01313 | 9.4e-101 | yiiE | S | Protein of unknown function (DUF1211) | ||
LNGBALBM_01314 | 3.5e-62 | yiiE | S | Protein of unknown function (DUF1304) | ||
LNGBALBM_01315 | 5.4e-121 | |||||
LNGBALBM_01316 | 2e-148 | 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 | |
LNGBALBM_01317 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
LNGBALBM_01318 | 2.7e-233 | 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 | |
LNGBALBM_01319 | 6.8e-45 | 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 | |
LNGBALBM_01320 | 5.9e-191 | S | Endonuclease/Exonuclease/phosphatase family | |||
LNGBALBM_01322 | 1.9e-127 | tmp1 | S | Domain of unknown function (DUF4391) | ||
LNGBALBM_01323 | 1.5e-172 | aspB | E | Aminotransferase class-V | ||
LNGBALBM_01324 | 5.6e-100 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
LNGBALBM_01325 | 9e-300 | S | zinc finger | |||
LNGBALBM_01326 | 1.9e-269 | recE | 2.7.7.7, 3.6.4.12 | L | Psort location Cytoplasmic, score | |
LNGBALBM_01327 | 2.7e-125 | def | 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 | |
LNGBALBM_01328 | 7.2e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
LNGBALBM_01329 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
LNGBALBM_01330 | 0.0 | rnj | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
LNGBALBM_01331 | 5.7e-166 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
LNGBALBM_01332 | 1.7e-134 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
LNGBALBM_01333 | 3.5e-250 | G | Major Facilitator Superfamily | |||
LNGBALBM_01334 | 3e-133 | K | -acetyltransferase | |||
LNGBALBM_01335 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
LNGBALBM_01336 | 0.0 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
LNGBALBM_01337 | 1.9e-269 | KLT | Protein tyrosine kinase | |||
LNGBALBM_01338 | 0.0 | S | Fibronectin type 3 domain | |||
LNGBALBM_01339 | 7e-130 | S | ATPase family associated with various cellular activities (AAA) | |||
LNGBALBM_01340 | 5.4e-188 | S | Protein of unknown function DUF58 | |||
LNGBALBM_01341 | 0.0 | E | Transglutaminase-like superfamily | |||
LNGBALBM_01342 | 3.6e-93 | B | Belongs to the OprB family | |||
LNGBALBM_01343 | 9.6e-104 | T | Forkhead associated domain | |||
LNGBALBM_01344 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LNGBALBM_01345 | 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 | |
LNGBALBM_01346 | 3.5e-50 | |||||
LNGBALBM_01347 | 4.2e-186 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
LNGBALBM_01348 | 1.2e-128 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
LNGBALBM_01349 | 1.4e-251 | S | UPF0210 protein | |||
LNGBALBM_01350 | 5.5e-43 | gcvR | T | Belongs to the UPF0237 family | ||
LNGBALBM_01351 | 7.9e-149 | srtC | 3.4.22.70 | M | Sortase family | |
LNGBALBM_01353 | 1.5e-233 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
LNGBALBM_01354 | 9.1e-258 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
LNGBALBM_01355 | 1.3e-143 | glpR | K | DeoR C terminal sensor domain | ||
LNGBALBM_01356 | 5.7e-194 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
LNGBALBM_01357 | 7.5e-227 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
LNGBALBM_01358 | 3.2e-222 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
LNGBALBM_01359 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
LNGBALBM_01360 | 1e-139 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
LNGBALBM_01361 | 3.3e-222 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
LNGBALBM_01362 | 1.1e-75 | J | TM2 domain | |||
LNGBALBM_01363 | 4.2e-20 | |||||
LNGBALBM_01364 | 4.2e-176 | |||||
LNGBALBM_01365 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
LNGBALBM_01366 | 4.1e-289 | S | Uncharacterized conserved protein (DUF2183) | |||
LNGBALBM_01367 | 8.4e-72 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
LNGBALBM_01368 | 1.3e-215 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
LNGBALBM_01369 | 5e-173 | mhpC | I | Alpha/beta hydrolase family | ||
LNGBALBM_01370 | 2e-88 | F | Domain of unknown function (DUF4916) | |||
LNGBALBM_01371 | 4.6e-67 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
LNGBALBM_01372 | 2e-178 | S | G5 | |||
LNGBALBM_01373 | 1.5e-286 | rfbP | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
LNGBALBM_01374 | 3.3e-77 | |||||
LNGBALBM_01375 | 1.1e-272 | S | Predicted membrane protein (DUF2142) | |||
LNGBALBM_01376 | 2.7e-188 | rfbJ | M | Glycosyl transferase family 2 | ||
LNGBALBM_01377 | 0.0 | pflA | S | Protein of unknown function (DUF4012) | ||
LNGBALBM_01378 | 5.3e-172 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
LNGBALBM_01379 | 3e-289 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
LNGBALBM_01380 | 4.9e-206 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
LNGBALBM_01381 | 3.9e-184 | GT2 | M | Glycosyl transferase family 2 | ||
LNGBALBM_01382 | 1.1e-267 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
LNGBALBM_01383 | 1.3e-170 | S | Glycosyl transferase family 2 | |||
LNGBALBM_01384 | 5.3e-192 | S | Glycosyltransferase like family 2 | |||
LNGBALBM_01385 | 4.9e-254 | |||||
LNGBALBM_01386 | 5.3e-172 | GT2 | S | Glycosyl transferase family 2 | ||
LNGBALBM_01387 | 1.5e-146 | M | Domain of unknown function (DUF4422) | |||
LNGBALBM_01388 | 3.7e-165 | rfbN | GT2 | S | Glycosyltransferase like family 2 | |
LNGBALBM_01389 | 3.2e-183 | MA20_43635 | M | Capsular polysaccharide synthesis protein | ||
LNGBALBM_01390 | 4.2e-239 | 1.1.1.22 | M | UDP binding domain | ||
LNGBALBM_01391 | 3.1e-254 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
LNGBALBM_01392 | 4.1e-197 | M | transferase activity, transferring glycosyl groups | |||
LNGBALBM_01393 | 9.8e-163 | GT2 | S | Glycosyl transferase family 2 | ||
LNGBALBM_01394 | 1.6e-288 | rfbP | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
LNGBALBM_01395 | 1.5e-45 | |||||
LNGBALBM_01396 | 0.0 | EGP | Major facilitator Superfamily | |||
LNGBALBM_01397 | 3.7e-241 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
LNGBALBM_01398 | 1.1e-135 | L | Protein of unknown function (DUF1524) | |||
LNGBALBM_01399 | 4e-156 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
LNGBALBM_01400 | 1e-119 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
LNGBALBM_01401 | 2.5e-222 | lspL | 5.1.3.6 | M | epimerase dehydratase | |
LNGBALBM_01402 | 1.3e-84 | pssD | M | Oligosaccharide biosynthesis protein Alg14 like | ||
LNGBALBM_01403 | 8.9e-92 | pssE | M | Glycosyltransferase family 28 C-terminal domain | ||
LNGBALBM_01404 | 2.6e-185 | GT2 | S | Glycosyl transferase family 2 | ||
LNGBALBM_01405 | 2.6e-160 | GT2 | S | Glycosyl transferase family 2 | ||
LNGBALBM_01406 | 3e-204 | S | EpsG family | |||
LNGBALBM_01407 | 0.0 | cydD | V | ABC transporter transmembrane region | ||
LNGBALBM_01408 | 0.0 | fadD | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
LNGBALBM_01409 | 1.6e-271 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
LNGBALBM_01410 | 1.3e-102 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
LNGBALBM_01411 | 0.0 | pflA | S | Protein of unknown function (DUF4012) | ||
LNGBALBM_01412 | 7.2e-254 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
LNGBALBM_01413 | 3.2e-57 | |||||
LNGBALBM_01414 | 8.1e-254 | tnpA | L | Transposase | ||
LNGBALBM_01415 | 2.5e-23 | cas3 | L | DEAD-like helicases superfamily | ||
LNGBALBM_01416 | 6.1e-185 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
LNGBALBM_01417 | 6.9e-245 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
LNGBALBM_01418 | 3.7e-301 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
LNGBALBM_01419 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
LNGBALBM_01420 | 1.2e-290 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
LNGBALBM_01421 | 2.1e-67 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
LNGBALBM_01422 | 1e-108 | P | Binding-protein-dependent transport system inner membrane component | |||
LNGBALBM_01423 | 9.9e-185 | cbpA | 2.4.1.20 | GT36 | G | Glycosyl hydrolase 36 superfamily, catalytic domain |
LNGBALBM_01425 | 2.6e-172 | trxA2 | O | Tetratricopeptide repeat | ||
LNGBALBM_01426 | 9.9e-183 | |||||
LNGBALBM_01427 | 1.1e-181 | |||||
LNGBALBM_01428 | 1.4e-154 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
LNGBALBM_01429 | 9.1e-141 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
LNGBALBM_01430 | 2e-49 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
LNGBALBM_01431 | 3.5e-285 | 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 | |
LNGBALBM_01432 | 7.7e-166 | 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 | ||
LNGBALBM_01433 | 2.7e-310 | 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 | |
LNGBALBM_01434 | 8.8e-153 | 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 | ||
LNGBALBM_01435 | 1e-61 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
LNGBALBM_01436 | 1.4e-31 | 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 | ||
LNGBALBM_01437 | 1e-145 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
LNGBALBM_01438 | 1.1e-205 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
LNGBALBM_01439 | 7.1e-259 | EGP | Major facilitator Superfamily | |||
LNGBALBM_01440 | 2.4e-183 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
LNGBALBM_01442 | 3e-212 | |||||
LNGBALBM_01443 | 2.9e-27 | |||||
LNGBALBM_01444 | 5.1e-66 | |||||
LNGBALBM_01445 | 2.4e-141 | D | ftsk spoiiie | |||
LNGBALBM_01446 | 6.5e-121 | S | Plasmid replication protein | |||
LNGBALBM_01447 | 1.4e-36 | |||||
LNGBALBM_01448 | 4.4e-224 | L | HNH endonuclease | |||
LNGBALBM_01449 | 1.4e-219 | 2.1.1.72 | H | Adenine-specific methyltransferase EcoRI | ||
LNGBALBM_01450 | 2.9e-229 | L | Phage integrase family | |||
LNGBALBM_01451 | 3.6e-265 | frc | 2.8.3.16 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
LNGBALBM_01452 | 1.1e-206 | 3.2.1.4, 3.2.1.78 | GH26,GH5,GH9 | G | hydrolase family 5 | |
LNGBALBM_01453 | 5.8e-176 | yfdV | S | Membrane transport protein | ||
LNGBALBM_01454 | 0.0 | oxc | 4.1.1.8 | EH | Thiamine pyrophosphate enzyme, central domain | |
LNGBALBM_01455 | 1.2e-286 | eriC | P | Voltage gated chloride channel | ||
LNGBALBM_01456 | 0.0 | M | domain protein | |||
LNGBALBM_01457 | 0.0 | K | RNA polymerase II activating transcription factor binding | |||
LNGBALBM_01458 | 0.0 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
LNGBALBM_01459 | 2.2e-93 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
LNGBALBM_01460 | 9e-153 | |||||
LNGBALBM_01461 | 1.4e-150 | KT | Transcriptional regulatory protein, C terminal | |||
LNGBALBM_01462 | 7.7e-140 | 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 | |
LNGBALBM_01463 | 1.8e-303 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
LNGBALBM_01464 | 0.0 | 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 | |
LNGBALBM_01465 | 5.4e-104 | K | helix_turn_helix ASNC type | |||
LNGBALBM_01466 | 1e-63 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
LNGBALBM_01467 | 2.7e-311 | S | domain protein | |||
LNGBALBM_01468 | 2.8e-311 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
LNGBALBM_01469 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
LNGBALBM_01470 | 7.4e-52 | S | Protein of unknown function (DUF2469) | |||
LNGBALBM_01471 | 5.1e-198 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
LNGBALBM_01472 | 6e-285 | gatB | 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) | |
LNGBALBM_01473 | 3.2e-289 | gatA | 6.3.5.6, 6.3.5.7 | F | 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) | |
LNGBALBM_01474 | 4.5e-24 | gatC | 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) | |
LNGBALBM_01475 | 4.2e-151 | S | ABC-type transport system involved in multi-copper enzyme maturation permease component | |||
LNGBALBM_01476 | 8.4e-113 | V | ABC transporter | |||
LNGBALBM_01477 | 1e-153 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
LNGBALBM_01478 | 3.4e-115 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
LNGBALBM_01479 | 2.2e-260 | ydbA | 3.6.3.4, 3.6.3.54 | P | E1-E2 ATPase | |
LNGBALBM_01480 | 0.0 | clpB | 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 | ||
LNGBALBM_01481 | 4.5e-157 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
LNGBALBM_01482 | 7.3e-81 | |||||
LNGBALBM_01483 | 3.1e-306 | M | domain protein | |||
LNGBALBM_01484 | 0.0 | Q | von Willebrand factor (vWF) type A domain | |||
LNGBALBM_01485 | 4.6e-191 | 3.4.22.70 | M | Sortase family | ||
LNGBALBM_01486 | 1.7e-151 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
LNGBALBM_01487 | 1.1e-197 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LNGBALBM_01488 | 2.4e-181 | M | Protein of unknown function (DUF3152) | |||
LNGBALBM_01489 | 7.6e-132 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LNGBALBM_01493 | 5.8e-125 | T | Pfam Adenylate and Guanylate cyclase catalytic domain | |||
LNGBALBM_01494 | 2.2e-73 | rplI | J | Binds to the 23S rRNA | ||
LNGBALBM_01495 | 1.2e-36 | 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 | ||
LNGBALBM_01496 | 2.2e-87 | ssb1 | L | Single-stranded DNA-binding protein | ||
LNGBALBM_01497 | 5.9e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
LNGBALBM_01498 | 5.3e-192 | 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) | |
LNGBALBM_01499 | 1.4e-173 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
LNGBALBM_01500 | 4.6e-269 | EGP | Major Facilitator Superfamily | |||
LNGBALBM_01501 | 5e-168 | iunH2 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
LNGBALBM_01502 | 1.1e-197 | K | helix_turn _helix lactose operon repressor | |||
LNGBALBM_01505 | 6.3e-237 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
LNGBALBM_01506 | 1.9e-208 | 2.4.1.303 | GT2 | M | Glycosyl transferase family 2 | |
LNGBALBM_01508 | 2.9e-198 | TTHA0885 | S | Glycosyltransferase, group 2 family protein | ||
LNGBALBM_01509 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
LNGBALBM_01510 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
LNGBALBM_01511 | 0.0 | glfT | 2.4.1.288 | GT2 | S | Glycosyltransferase like family 2 |
LNGBALBM_01512 | 5.4e-177 | lytC | 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
LNGBALBM_01513 | 0.0 | lytC | 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
LNGBALBM_01514 | 7.9e-187 | tnp3503b | 2.7.7.7 | L | Transposase and inactivated derivatives | |
LNGBALBM_01515 | 1.4e-56 | S | Leucine-rich repeat (LRR) protein | |||
LNGBALBM_01516 | 1.1e-100 | M | hydrolase, family 25 | |||
LNGBALBM_01517 | 5.9e-134 | |||||
LNGBALBM_01518 | 4.7e-265 | S | Polysaccharide pyruvyl transferase | |||
LNGBALBM_01519 | 1.6e-271 | rgpD | 3.6.3.38 | GM | ABC transporter, ATP-binding protein | |
LNGBALBM_01520 | 1.2e-149 | rgpC | U | Transport permease protein | ||
LNGBALBM_01521 | 0.0 | 2.4.1.288 | GT2 | S | Glycosyltransferase like family 2 | |
LNGBALBM_01523 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
LNGBALBM_01524 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
LNGBALBM_01525 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LNGBALBM_01526 | 9.6e-250 | V | ABC transporter permease | |||
LNGBALBM_01527 | 1.6e-194 | V | ABC transporter | |||
LNGBALBM_01528 | 3.2e-152 | 3.6.1.11, 3.6.1.40 | T | HD domain | ||
LNGBALBM_01529 | 3.3e-169 | S | Glutamine amidotransferase domain | |||
LNGBALBM_01530 | 0.0 | kup | P | Transport of potassium into the cell | ||
LNGBALBM_01531 | 1.7e-184 | tatD | L | TatD related DNase | ||
LNGBALBM_01532 | 0.0 | rafA | 3.2.1.22 | G | Psort location Cytoplasmic, score 8.87 | |
LNGBALBM_01533 | 3.6e-118 | |||||
LNGBALBM_01534 | 0.0 | yknV | V | ABC transporter | ||
LNGBALBM_01535 | 0.0 | mdlA2 | V | ABC transporter | ||
LNGBALBM_01536 | 0.0 | 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 | |
LNGBALBM_01537 | 1.3e-130 | |||||
LNGBALBM_01538 | 6.6e-54 | |||||
LNGBALBM_01539 | 1.1e-172 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
LNGBALBM_01540 | 0.0 | pmt | 2.4.1.109 | GT39 | O | C-terminal four TMM region of protein-O-mannosyltransferase |
LNGBALBM_01541 | 6.2e-159 | I | alpha/beta hydrolase fold | |||
LNGBALBM_01542 | 4e-136 | dedA | S | SNARE associated Golgi protein | ||
LNGBALBM_01544 | 1.4e-138 | S | GyrI-like small molecule binding domain | |||
LNGBALBM_01545 | 0.0 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
LNGBALBM_01546 | 6.2e-114 | K | Bacterial regulatory proteins, tetR family | |||
LNGBALBM_01547 | 5.6e-129 | S | HAD hydrolase, family IA, variant 3 | |||
LNGBALBM_01548 | 5.4e-92 | hspR | K | transcriptional regulator, MerR family | ||
LNGBALBM_01549 | 2.1e-167 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
LNGBALBM_01550 | 1.2e-94 | 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 | ||
LNGBALBM_01551 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
LNGBALBM_01553 | 1.3e-193 | K | Psort location Cytoplasmic, score | |||
LNGBALBM_01554 | 1.8e-144 | traX | S | TraX protein | ||
LNGBALBM_01555 | 3.1e-147 | S | HAD-hyrolase-like | |||
LNGBALBM_01556 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LNGBALBM_01557 | 7.3e-175 | malG | G | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01558 | 2.5e-269 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01559 | 8.7e-237 | malE | G | Bacterial extracellular solute-binding protein | ||
LNGBALBM_01560 | 0.0 | malL | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain |
LNGBALBM_01561 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
LNGBALBM_01562 | 1.1e-107 | S | Protein of unknown function, DUF624 | |||
LNGBALBM_01563 | 6.1e-154 | rafG | G | ABC transporter permease | ||
LNGBALBM_01564 | 8.8e-156 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
LNGBALBM_01565 | 1.1e-181 | K | Psort location Cytoplasmic, score | |||
LNGBALBM_01566 | 2.7e-09 | amyE | G | Bacterial extracellular solute-binding protein | ||
LNGBALBM_01567 | 6.2e-241 | amyE | G | Bacterial extracellular solute-binding protein | ||
LNGBALBM_01568 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
LNGBALBM_01569 | 1.9e-115 | G | Phosphoglycerate mutase family | |||
LNGBALBM_01570 | 4e-69 | S | Protein of unknown function (DUF4235) | |||
LNGBALBM_01571 | 9.5e-141 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
LNGBALBM_01572 | 7.8e-44 | |||||
LNGBALBM_01573 | 2.6e-95 | iolT | EGP | Major facilitator Superfamily | ||
LNGBALBM_01575 | 7.3e-100 | nadE | 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
LNGBALBM_01576 | 2.5e-258 | nadE | 3.5.1.53, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
LNGBALBM_01577 | 3e-41 | relB | L | RelB antitoxin | ||
LNGBALBM_01580 | 1.4e-270 | G | Psort location CytoplasmicMembrane, score 10.00 | |||
LNGBALBM_01581 | 0.0 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
LNGBALBM_01582 | 9.9e-202 | K | Periplasmic binding protein domain | |||
LNGBALBM_01583 | 1.2e-145 | cobB2 | K | Sir2 family | ||
LNGBALBM_01584 | 2.8e-224 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
LNGBALBM_01585 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
LNGBALBM_01587 | 9.1e-186 | K | Psort location Cytoplasmic, score | |||
LNGBALBM_01588 | 0.0 | rafA | 3.2.1.22 | G | Raffinose synthase or seed imbibition protein Sip1 | |
LNGBALBM_01589 | 1.5e-161 | G | Binding-protein-dependent transport system inner membrane component | |||
LNGBALBM_01590 | 6.8e-184 | G | Binding-protein-dependent transport system inner membrane component | |||
LNGBALBM_01591 | 9e-237 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
LNGBALBM_01592 | 3.6e-232 | nagC | GK | ROK family | ||
LNGBALBM_01593 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
LNGBALBM_01594 | 5.7e-85 | tadA | 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
LNGBALBM_01595 | 0.0 | yjcE | P | Sodium/hydrogen exchanger family | ||
LNGBALBM_01596 | 3.6e-171 | ypfH | S | Phospholipase/Carboxylesterase | ||
LNGBALBM_01597 | 7.9e-163 | D | nuclear chromosome segregation | |||
LNGBALBM_01598 | 6.9e-112 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
LNGBALBM_01599 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
LNGBALBM_01600 | 2.6e-175 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LNGBALBM_01601 | 3.6e-279 | KLT | Domain of unknown function (DUF4032) | |||
LNGBALBM_01602 | 4.3e-211 | ugpC | E | Belongs to the ABC transporter superfamily | ||
LNGBALBM_01603 | 5.5e-189 | U | Ion channel | |||
LNGBALBM_01604 | 0.0 | KLT | Protein tyrosine kinase | |||
LNGBALBM_01605 | 5.8e-85 | O | Thioredoxin | |||
LNGBALBM_01607 | 1.2e-219 | S | G5 | |||
LNGBALBM_01608 | 7e-164 | ksgA | 2.1.1.182, 2.1.1.184 | 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 | |
LNGBALBM_01609 | 4.1e-178 | 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 | |
LNGBALBM_01610 | 1.5e-112 | S | LytR cell envelope-related transcriptional attenuator | |||
LNGBALBM_01611 | 1.4e-308 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
LNGBALBM_01612 | 3.5e-172 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
LNGBALBM_01613 | 0.0 | |||||
LNGBALBM_01614 | 0.0 | murJ | KLT | MviN-like protein | ||
LNGBALBM_01615 | 1.3e-179 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
LNGBALBM_01616 | 1.9e-232 | parB | K | Belongs to the ParB family | ||
LNGBALBM_01617 | 8.7e-176 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LNGBALBM_01618 | 3.3e-135 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
LNGBALBM_01619 | 3.2e-95 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
LNGBALBM_01620 | 5.6e-178 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
LNGBALBM_01621 | 5.9e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)