ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
CFNOAGBM_00001 | 4.5e-120 | yfbR | S | HD containing hydrolase-like enzyme | ||
CFNOAGBM_00002 | 8.1e-210 | G | Glycosyl hydrolases family 8 | |||
CFNOAGBM_00003 | 3.7e-246 | ydaM | M | Glycosyl transferase | ||
CFNOAGBM_00005 | 5.6e-118 | |||||
CFNOAGBM_00006 | 1.7e-16 | |||||
CFNOAGBM_00007 | 3.5e-70 | S | Iron-sulphur cluster biosynthesis | |||
CFNOAGBM_00008 | 6e-181 | ybiR | P | Citrate transporter | ||
CFNOAGBM_00009 | 3.2e-90 | lemA | S | LemA family | ||
CFNOAGBM_00010 | 2e-163 | htpX | O | Belongs to the peptidase M48B family | ||
CFNOAGBM_00011 | 2.8e-168 | K | helix_turn_helix, arabinose operon control protein | |||
CFNOAGBM_00012 | 6.1e-97 | S | ABC-type cobalt transport system, permease component | |||
CFNOAGBM_00013 | 6.2e-249 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00014 | 2.1e-109 | P | Cobalt transport protein | |||
CFNOAGBM_00015 | 1.8e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
CFNOAGBM_00016 | 6.4e-176 | htrA | 3.4.21.107 | O | serine protease | |
CFNOAGBM_00017 | 1.1e-147 | vicX | 3.1.26.11 | S | domain protein | |
CFNOAGBM_00018 | 6.7e-145 | yycI | S | YycH protein | ||
CFNOAGBM_00019 | 3e-251 | yycH | S | YycH protein | ||
CFNOAGBM_00020 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
CFNOAGBM_00021 | 2.2e-128 | K | response regulator | |||
CFNOAGBM_00023 | 3.2e-247 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
CFNOAGBM_00024 | 5.4e-200 | S | Sterol carrier protein domain | |||
CFNOAGBM_00025 | 5.5e-166 | arbZ | I | Acyltransferase | ||
CFNOAGBM_00026 | 8.8e-116 | ywnB | S | NAD(P)H-binding | ||
CFNOAGBM_00027 | 4.7e-143 | ropB | K | Helix-turn-helix domain | ||
CFNOAGBM_00028 | 9.4e-200 | 2.7.7.73, 2.7.7.80 | H | Involved in molybdopterin and thiamine biosynthesis, family 2 | ||
CFNOAGBM_00029 | 8.5e-173 | yxaM | EGP | Major Facilitator Superfamily | ||
CFNOAGBM_00030 | 9.3e-132 | S | Protein of unknown function (DUF975) | |||
CFNOAGBM_00031 | 1.5e-137 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
CFNOAGBM_00032 | 1.6e-154 | yitS | S | EDD domain protein, DegV family | ||
CFNOAGBM_00033 | 3.5e-17 | |||||
CFNOAGBM_00034 | 2.7e-291 | V | ABC-type multidrug transport system, ATPase and permease components | |||
CFNOAGBM_00035 | 3.7e-140 | ropB | K | Helix-turn-helix domain | ||
CFNOAGBM_00036 | 0.0 | tetP | J | elongation factor G | ||
CFNOAGBM_00037 | 3e-102 | clcA | P | chloride | ||
CFNOAGBM_00039 | 1.1e-248 | steT | E | amino acid | ||
CFNOAGBM_00040 | 1.6e-216 | L | Belongs to the 'phage' integrase family | |||
CFNOAGBM_00041 | 1.5e-31 | |||||
CFNOAGBM_00042 | 4.6e-108 | repB | EP | Plasmid replication protein | ||
CFNOAGBM_00043 | 3.7e-83 | repB | EP | Plasmid replication protein | ||
CFNOAGBM_00044 | 1.8e-109 | |||||
CFNOAGBM_00045 | 3.6e-123 | gntR1 | K | UTRA | ||
CFNOAGBM_00046 | 7.4e-70 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
CFNOAGBM_00047 | 1.6e-134 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
CFNOAGBM_00048 | 4.9e-207 | csaB | M | Glycosyl transferases group 1 | ||
CFNOAGBM_00049 | 2.5e-29 | |||||
CFNOAGBM_00050 | 4e-86 | |||||
CFNOAGBM_00051 | 2e-12 | yttA | 2.7.13.3 | S | Pfam Transposase IS66 | |
CFNOAGBM_00052 | 3.2e-39 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
CFNOAGBM_00053 | 2.4e-191 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |||
CFNOAGBM_00054 | 5.8e-26 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
CFNOAGBM_00055 | 9.5e-235 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
CFNOAGBM_00056 | 5.3e-136 | mdtG | EGP | Major facilitator Superfamily | ||
CFNOAGBM_00057 | 1.7e-125 | puuD | S | peptidase C26 | ||
CFNOAGBM_00058 | 6.2e-296 | V | ABC transporter transmembrane region | |||
CFNOAGBM_00059 | 2.5e-86 | ymdB | S | Macro domain protein | ||
CFNOAGBM_00060 | 6.5e-36 | |||||
CFNOAGBM_00061 | 0.0 | scrA | 2.7.1.199, 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
CFNOAGBM_00062 | 2.9e-300 | scrB | 3.2.1.26 | GH32 | G | invertase |
CFNOAGBM_00063 | 6.6e-139 | scrR | K | Transcriptional regulator, LacI family | ||
CFNOAGBM_00064 | 4.4e-146 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
CFNOAGBM_00065 | 4.4e-149 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
CFNOAGBM_00066 | 7.8e-131 | cobQ | S | glutamine amidotransferase | ||
CFNOAGBM_00067 | 6e-255 | yfnA | E | Amino Acid | ||
CFNOAGBM_00068 | 4.4e-36 | EG | EamA-like transporter family | |||
CFNOAGBM_00069 | 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 | ||
CFNOAGBM_00070 | 2.7e-241 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
CFNOAGBM_00071 | 3e-181 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
CFNOAGBM_00072 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
CFNOAGBM_00073 | 3.8e-246 | yagE | E | amino acid | ||
CFNOAGBM_00074 | 1.8e-116 | GM | NmrA-like family | |||
CFNOAGBM_00075 | 4.2e-65 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
CFNOAGBM_00076 | 1.3e-96 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
CFNOAGBM_00077 | 9.7e-126 | comFC | S | Competence protein | ||
CFNOAGBM_00078 | 1.5e-225 | comFA | L | Helicase C-terminal domain protein | ||
CFNOAGBM_00079 | 4.3e-118 | yvyE | 3.4.13.9 | S | YigZ family | |
CFNOAGBM_00080 | 1.6e-192 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
CFNOAGBM_00081 | 3.3e-18 | rny | S | Endoribonuclease that initiates mRNA decay | ||
CFNOAGBM_00082 | 1.6e-123 | yoaK | S | Protein of unknown function (DUF1275) | ||
CFNOAGBM_00083 | 1.3e-110 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
CFNOAGBM_00084 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
CFNOAGBM_00085 | 2.8e-171 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
CFNOAGBM_00086 | 2.4e-178 | K | Transcriptional regulator | |||
CFNOAGBM_00087 | 2.6e-32 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
CFNOAGBM_00088 | 3.6e-25 | UW | Tetratricopeptide repeat | |||
CFNOAGBM_00089 | 7.4e-166 | cpsJ | S | glycosyl transferase family 2 | ||
CFNOAGBM_00090 | 1.3e-195 | nss | M | transferase activity, transferring glycosyl groups | ||
CFNOAGBM_00091 | 1.9e-194 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
CFNOAGBM_00092 | 1.9e-95 | S | UPF0397 protein | |||
CFNOAGBM_00093 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00094 | 4.1e-142 | cbiQ | P | cobalt transport | ||
CFNOAGBM_00095 | 2.1e-118 | ybhL | S | Belongs to the BI1 family | ||
CFNOAGBM_00096 | 0.0 | GT2,GT4 | M | family 8 | ||
CFNOAGBM_00097 | 0.0 | GT2,GT4 | M | family 8 | ||
CFNOAGBM_00098 | 4.5e-227 | M | Pfam:DUF1792 | |||
CFNOAGBM_00099 | 2.9e-75 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
CFNOAGBM_00100 | 1.9e-32 | UW | Tetratricopeptide repeat | |||
CFNOAGBM_00101 | 5.5e-62 | G | Major Facilitator | |||
CFNOAGBM_00102 | 0.0 | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
CFNOAGBM_00103 | 1.9e-158 | lysR5 | K | LysR substrate binding domain | ||
CFNOAGBM_00105 | 3.2e-65 | hsdS | 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
CFNOAGBM_00106 | 3.6e-123 | L | restriction endonuclease | |||
CFNOAGBM_00107 | 2.8e-244 | cycA | E | Amino acid permease | ||
CFNOAGBM_00108 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
CFNOAGBM_00109 | 1.5e-71 | |||||
CFNOAGBM_00110 | 9.6e-81 | 4.1.1.44 | S | decarboxylase | ||
CFNOAGBM_00111 | 4.1e-37 | 4.1.1.44 | S | decarboxylase | ||
CFNOAGBM_00112 | 0.0 | S | TerB-C domain | |||
CFNOAGBM_00113 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
CFNOAGBM_00114 | 1.3e-150 | mreB | D | cell shape determining protein MreB | ||
CFNOAGBM_00115 | 6.1e-111 | radC | L | DNA repair protein | ||
CFNOAGBM_00116 | 6.4e-125 | S | Haloacid dehalogenase-like hydrolase | |||
CFNOAGBM_00117 | 7.4e-236 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
CFNOAGBM_00118 | 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 | |
CFNOAGBM_00119 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
CFNOAGBM_00120 | 6.2e-178 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | ||
CFNOAGBM_00121 | 2.5e-124 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
CFNOAGBM_00122 | 1.1e-228 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
CFNOAGBM_00123 | 5.4e-39 | |||||
CFNOAGBM_00124 | 2.8e-216 | lmrP | E | Major Facilitator Superfamily | ||
CFNOAGBM_00125 | 1.2e-146 | pbpX2 | V | Beta-lactamase | ||
CFNOAGBM_00126 | 9e-253 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
CFNOAGBM_00127 | 6.7e-37 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
CFNOAGBM_00128 | 6.1e-235 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
CFNOAGBM_00129 | 1.9e-291 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
CFNOAGBM_00131 | 3.9e-39 | |||||
CFNOAGBM_00132 | 8.9e-204 | ywhK | S | Membrane | ||
CFNOAGBM_00134 | 5.7e-59 | |||||
CFNOAGBM_00135 | 1.1e-49 | |||||
CFNOAGBM_00136 | 2.1e-45 | |||||
CFNOAGBM_00137 | 2.7e-85 | ykuL | S | (CBS) domain | ||
CFNOAGBM_00138 | 0.0 | cadA | P | P-type ATPase | ||
CFNOAGBM_00139 | 4.9e-202 | napA | P | Sodium/hydrogen exchanger family | ||
CFNOAGBM_00140 | 1e-95 | S | Putative adhesin | |||
CFNOAGBM_00141 | 9.1e-284 | V | ABC transporter transmembrane region | |||
CFNOAGBM_00142 | 1.6e-160 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
CFNOAGBM_00143 | 3.5e-35 | |||||
CFNOAGBM_00144 | 1.7e-119 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
CFNOAGBM_00145 | 3.5e-158 | S | Protein of unknown function (DUF979) | |||
CFNOAGBM_00146 | 6.6e-114 | S | Protein of unknown function (DUF969) | |||
CFNOAGBM_00147 | 4.9e-87 | S | Protein of unknown function (DUF805) | |||
CFNOAGBM_00148 | 4.4e-07 | |||||
CFNOAGBM_00149 | 4.2e-15 | |||||
CFNOAGBM_00150 | 8.5e-268 | G | PTS system Galactitol-specific IIC component | |||
CFNOAGBM_00151 | 6.1e-96 | S | Protein of unknown function (DUF1440) | |||
CFNOAGBM_00152 | 1.8e-105 | S | CAAX protease self-immunity | |||
CFNOAGBM_00153 | 1e-204 | S | DUF218 domain | |||
CFNOAGBM_00154 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00155 | 6.2e-268 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
CFNOAGBM_00156 | 2.4e-184 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
CFNOAGBM_00157 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
CFNOAGBM_00158 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
CFNOAGBM_00159 | 1.2e-177 | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | ||
CFNOAGBM_00160 | 8.3e-168 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
CFNOAGBM_00161 | 1.9e-200 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
CFNOAGBM_00162 | 1.2e-149 | K | Helix-turn-helix domain, rpiR family | |||
CFNOAGBM_00163 | 6.6e-169 | yleB | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | |
CFNOAGBM_00164 | 4.4e-150 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
CFNOAGBM_00165 | 0.0 | sacX | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CFNOAGBM_00166 | 1.9e-130 | S | membrane transporter protein | |||
CFNOAGBM_00167 | 6.2e-162 | yeaE | S | Aldo/keto reductase family | ||
CFNOAGBM_00168 | 2.3e-133 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
CFNOAGBM_00169 | 1e-119 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
CFNOAGBM_00170 | 6.3e-125 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
CFNOAGBM_00171 | 3.3e-236 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
CFNOAGBM_00172 | 3e-232 | pbuG | S | permease | ||
CFNOAGBM_00173 | 7.9e-129 | K | helix_turn_helix, mercury resistance | |||
CFNOAGBM_00176 | 4e-29 | |||||
CFNOAGBM_00177 | 2.5e-64 | xtmA | L | Terminase small subunit | ||
CFNOAGBM_00178 | 2.4e-242 | S | Phage terminase, large subunit | |||
CFNOAGBM_00179 | 5.8e-299 | FbpA | K | Fibronectin-binding protein | ||
CFNOAGBM_00180 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
CFNOAGBM_00181 | 3e-119 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
CFNOAGBM_00182 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
CFNOAGBM_00183 | 7.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
CFNOAGBM_00184 | 1.8e-28 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
CFNOAGBM_00185 | 3.7e-148 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
CFNOAGBM_00186 | 1.1e-56 | hxlR | K | Transcriptional regulator, HxlR family | ||
CFNOAGBM_00187 | 3e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
CFNOAGBM_00188 | 8e-132 | K | Psort location CytoplasmicMembrane, score | |||
CFNOAGBM_00189 | 1.2e-103 | 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 | |
CFNOAGBM_00190 | 3.5e-236 | pbuX | F | xanthine permease | ||
CFNOAGBM_00191 | 2.9e-240 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
CFNOAGBM_00192 | 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 | |
CFNOAGBM_00193 | 2.5e-63 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
CFNOAGBM_00194 | 4e-69 | S | Domain of unknown function (DUF1934) | |||
CFNOAGBM_00195 | 5.1e-267 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
CFNOAGBM_00196 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
CFNOAGBM_00197 | 9.3e-43 | malG | P | ABC transporter permease | ||
CFNOAGBM_00198 | 5e-290 | V | ABC-type multidrug transport system, ATPase and permease components | |||
CFNOAGBM_00199 | 1.6e-280 | V | ABC-type multidrug transport system, ATPase and permease components | |||
CFNOAGBM_00200 | 8.8e-187 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
CFNOAGBM_00201 | 2.7e-202 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
CFNOAGBM_00202 | 3.5e-67 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
CFNOAGBM_00203 | 2.3e-156 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
CFNOAGBM_00204 | 2.6e-186 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
CFNOAGBM_00205 | 9.6e-68 | metI | P | ABC transporter permease | ||
CFNOAGBM_00206 | 9e-267 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
CFNOAGBM_00207 | 2.3e-262 | frdC | 1.3.5.4 | C | FAD binding domain | |
CFNOAGBM_00208 | 6.8e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
CFNOAGBM_00209 | 4.9e-241 | yjjP | S | Putative threonine/serine exporter | ||
CFNOAGBM_00210 | 4e-116 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
CFNOAGBM_00211 | 3.7e-135 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
CFNOAGBM_00212 | 3.2e-298 | V | ABC transporter, ATP-binding protein | |||
CFNOAGBM_00213 | 0.0 | V | ABC transporter | |||
CFNOAGBM_00214 | 7.4e-121 | K | response regulator | |||
CFNOAGBM_00215 | 4.8e-205 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
CFNOAGBM_00216 | 2.2e-306 | 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 | |
CFNOAGBM_00217 | 1.3e-142 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
CFNOAGBM_00218 | 4.4e-166 | natA | S | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00219 | 1.7e-221 | natB | CP | ABC-2 family transporter protein | ||
CFNOAGBM_00220 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
CFNOAGBM_00221 | 5.9e-55 | V | ABC transporter transmembrane region | |||
CFNOAGBM_00222 | 2.9e-39 | |||||
CFNOAGBM_00223 | 1.1e-62 | |||||
CFNOAGBM_00224 | 1.4e-14 | ywnB | S | NAD(P)H-binding | ||
CFNOAGBM_00225 | 1.5e-75 | L | transposase activity | |||
CFNOAGBM_00226 | 4.7e-22 | |||||
CFNOAGBM_00227 | 1.4e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
CFNOAGBM_00228 | 2.4e-130 | |||||
CFNOAGBM_00229 | 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 | ||
CFNOAGBM_00230 | 3.5e-61 | 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 | ||
CFNOAGBM_00231 | 2.3e-167 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
CFNOAGBM_00232 | 1.5e-177 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
CFNOAGBM_00233 | 8.2e-282 | lsa | S | ABC transporter | ||
CFNOAGBM_00234 | 9.8e-96 | S | GyrI-like small molecule binding domain | |||
CFNOAGBM_00235 | 1.7e-193 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
CFNOAGBM_00236 | 5e-78 | 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 | ||
CFNOAGBM_00237 | 1.9e-77 | K | MerR HTH family regulatory protein | |||
CFNOAGBM_00238 | 4.7e-266 | lmrB | EGP | Major facilitator Superfamily | ||
CFNOAGBM_00239 | 6e-97 | S | Domain of unknown function (DUF4811) | |||
CFNOAGBM_00240 | 2.5e-141 | ppm1 | GT2 | M | Glycosyl transferase family 2 | |
CFNOAGBM_00241 | 3.2e-107 | fic | D | Fic/DOC family | ||
CFNOAGBM_00242 | 1.1e-69 | |||||
CFNOAGBM_00243 | 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 | |
CFNOAGBM_00244 | 2e-294 | V | ABC transporter transmembrane region | |||
CFNOAGBM_00246 | 2.4e-144 | S | haloacid dehalogenase-like hydrolase | |||
CFNOAGBM_00247 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
CFNOAGBM_00248 | 2.5e-08 | comGC | U | Prepilin-type cleavage methylation N-terminal domain protein | ||
CFNOAGBM_00250 | 3.7e-254 | pepC | 3.4.22.40 | E | aminopeptidase | |
CFNOAGBM_00251 | 9.8e-123 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
CFNOAGBM_00252 | 1.4e-130 | oppF | P | Belongs to the ABC transporter superfamily | ||
CFNOAGBM_00253 | 1.4e-114 | oppD | P | Belongs to the ABC transporter superfamily | ||
CFNOAGBM_00254 | 6.7e-17 | oppD | P | Belongs to the ABC transporter superfamily | ||
CFNOAGBM_00255 | 6.2e-148 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
CFNOAGBM_00256 | 3.9e-125 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
CFNOAGBM_00257 | 1.1e-137 | oppA | E | ABC transporter, substratebinding protein | ||
CFNOAGBM_00258 | 3.3e-48 | oppA | E | ABC transporter, substratebinding protein | ||
CFNOAGBM_00259 | 7.2e-258 | pepC | 3.4.22.40 | E | aminopeptidase | |
CFNOAGBM_00261 | 4.8e-243 | 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) | |
CFNOAGBM_00262 | 0.0 | XK27_08315 | M | Sulfatase | ||
CFNOAGBM_00263 | 1.9e-112 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
CFNOAGBM_00264 | 1.6e-51 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
CFNOAGBM_00265 | 7e-164 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
CFNOAGBM_00266 | 8e-148 | yisY | 1.11.1.10 | S | Alpha/beta hydrolase family | |
CFNOAGBM_00267 | 1.6e-115 | |||||
CFNOAGBM_00268 | 6.7e-68 | XK27_07525 | 3.6.1.55 | F | NUDIX domain | |
CFNOAGBM_00269 | 3.2e-141 | S | Alpha/beta hydrolase family | |||
CFNOAGBM_00270 | 5.5e-113 | |||||
CFNOAGBM_00271 | 1.9e-81 | |||||
CFNOAGBM_00272 | 2e-91 | S | AAA domain | |||
CFNOAGBM_00273 | 8.7e-153 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
CFNOAGBM_00274 | 2.2e-84 | 3.6.1.55 | F | NUDIX domain | ||
CFNOAGBM_00275 | 2e-138 | 2.4.2.3 | F | Phosphorylase superfamily | ||
CFNOAGBM_00276 | 2.8e-84 | 6.3.3.2 | S | ASCH | ||
CFNOAGBM_00277 | 3.5e-157 | 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 | |
CFNOAGBM_00278 | 3.9e-66 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
CFNOAGBM_00279 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
CFNOAGBM_00280 | 9.4e-172 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
CFNOAGBM_00281 | 5.1e-45 | |||||
CFNOAGBM_00282 | 1.4e-178 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
CFNOAGBM_00283 | 2.7e-117 | dedA | S | SNARE-like domain protein | ||
CFNOAGBM_00284 | 1.5e-104 | S | Protein of unknown function (DUF1461) | |||
CFNOAGBM_00285 | 1.2e-148 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
CFNOAGBM_00286 | 9.3e-95 | yutD | S | Protein of unknown function (DUF1027) | ||
CFNOAGBM_00287 | 1e-267 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
CFNOAGBM_00288 | 1.3e-54 | |||||
CFNOAGBM_00289 | 6.8e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
CFNOAGBM_00290 | 1.2e-95 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
CFNOAGBM_00291 | 3.7e-157 | pstA | P | Phosphate transport system permease protein PstA | ||
CFNOAGBM_00292 | 6.3e-148 | 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 | |
CFNOAGBM_00293 | 3e-139 | 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 | |
CFNOAGBM_00294 | 1.9e-108 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
CFNOAGBM_00295 | 4.6e-280 | S | C4-dicarboxylate anaerobic carrier | |||
CFNOAGBM_00296 | 2.6e-85 | dps | P | Belongs to the Dps family | ||
CFNOAGBM_00297 | 2.7e-158 | 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 | |
CFNOAGBM_00298 | 2.7e-126 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
CFNOAGBM_00299 | 8.2e-176 | rihB | 3.2.2.1 | F | Nucleoside | |
CFNOAGBM_00300 | 8.9e-133 | gntR | K | UbiC transcription regulator-associated domain protein | ||
CFNOAGBM_00301 | 3.5e-52 | S | Enterocin A Immunity | |||
CFNOAGBM_00302 | 4.7e-140 | glcR | K | DeoR C terminal sensor domain | ||
CFNOAGBM_00303 | 9.1e-148 | pbuG | S | permease | ||
CFNOAGBM_00304 | 3.9e-76 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
CFNOAGBM_00305 | 1.1e-68 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
CFNOAGBM_00306 | 2.3e-72 | |||||
CFNOAGBM_00307 | 1.4e-90 | |||||
CFNOAGBM_00308 | 4.3e-74 | atkY | K | Penicillinase repressor | ||
CFNOAGBM_00309 | 2.7e-64 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
CFNOAGBM_00310 | 2.2e-50 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
CFNOAGBM_00311 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
CFNOAGBM_00312 | 1.3e-70 | S | PFAM Archaeal ATPase | |||
CFNOAGBM_00313 | 3e-34 | S | PFAM Archaeal ATPase | |||
CFNOAGBM_00314 | 6.9e-49 | S | PFAM Archaeal ATPase | |||
CFNOAGBM_00315 | 4.9e-187 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
CFNOAGBM_00317 | 3.4e-140 | H | Nodulation protein S (NodS) | |||
CFNOAGBM_00318 | 2.5e-09 | K | Helix-turn-helix XRE-family like proteins | |||
CFNOAGBM_00319 | 1.9e-58 | S | Domain of unknown function (DUF771) | |||
CFNOAGBM_00321 | 2.9e-15 | |||||
CFNOAGBM_00322 | 7.5e-39 | |||||
CFNOAGBM_00324 | 8e-44 | S | ERF superfamily | |||
CFNOAGBM_00325 | 5.1e-67 | L | Helix-turn-helix domain | |||
CFNOAGBM_00326 | 2.4e-18 | K | Transcriptional regulator | |||
CFNOAGBM_00329 | 2.4e-133 | S | DNA binding | |||
CFNOAGBM_00330 | 1.4e-25 | |||||
CFNOAGBM_00335 | 4.1e-104 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
CFNOAGBM_00336 | 7.3e-103 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
CFNOAGBM_00337 | 4.6e-255 | 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 | ||
CFNOAGBM_00338 | 2.2e-287 | gltX | 6.1.1.17, 6.1.1.24 | 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) | |
CFNOAGBM_00339 | 3.3e-269 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
CFNOAGBM_00340 | 1.3e-78 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
CFNOAGBM_00341 | 6e-140 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
CFNOAGBM_00342 | 1e-88 | yvrI | K | sigma factor activity | ||
CFNOAGBM_00343 | 1.4e-33 | |||||
CFNOAGBM_00344 | 1.2e-25 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
CFNOAGBM_00345 | 1.4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
CFNOAGBM_00346 | 3.6e-307 | yloV | S | DAK2 domain fusion protein YloV | ||
CFNOAGBM_00347 | 7.9e-25 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
CFNOAGBM_00348 | 1.8e-102 | 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 | |
CFNOAGBM_00349 | 1.6e-07 | |||||
CFNOAGBM_00350 | 3.4e-135 | E | GDSL-like Lipase/Acylhydrolase family | |||
CFNOAGBM_00351 | 3.1e-77 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
CFNOAGBM_00352 | 1.8e-223 | patA | 2.6.1.1 | E | Aminotransferase | |
CFNOAGBM_00353 | 3.6e-94 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
CFNOAGBM_00354 | 4e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
CFNOAGBM_00355 | 7.9e-35 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
CFNOAGBM_00356 | 5.1e-58 | yqhL | P | Rhodanese-like protein | ||
CFNOAGBM_00357 | 8.1e-19 | S | Protein of unknown function (DUF3042) | |||
CFNOAGBM_00358 | 1.8e-170 | 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) | |
CFNOAGBM_00359 | 7.1e-261 | glnA | 6.3.1.2 | E | glutamine synthetase | |
CFNOAGBM_00360 | 5.3e-204 | EGP | Major facilitator Superfamily | |||
CFNOAGBM_00361 | 1.1e-152 | S | haloacid dehalogenase-like hydrolase | |||
CFNOAGBM_00363 | 1.9e-180 | D | Alpha beta | |||
CFNOAGBM_00364 | 1.4e-217 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
CFNOAGBM_00365 | 5e-221 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
CFNOAGBM_00366 | 2.4e-217 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
CFNOAGBM_00367 | 1e-75 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
CFNOAGBM_00368 | 1.5e-117 | 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 | |
CFNOAGBM_00369 | 1.7e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
CFNOAGBM_00370 | 3.2e-68 | yslB | S | Protein of unknown function (DUF2507) | ||
CFNOAGBM_00371 | 1.1e-52 | trxA | O | Belongs to the thioredoxin family | ||
CFNOAGBM_00372 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
CFNOAGBM_00373 | 3.9e-93 | cvpA | S | Colicin V production protein | ||
CFNOAGBM_00374 | 4.2e-39 | yrzB | S | Belongs to the UPF0473 family | ||
CFNOAGBM_00375 | 8.8e-72 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
CFNOAGBM_00376 | 2.6e-42 | yrzL | S | Belongs to the UPF0297 family | ||
CFNOAGBM_00377 | 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 | |
CFNOAGBM_00378 | 6e-78 | S | Domain of unknown function (DUF4767) | |||
CFNOAGBM_00379 | 7.7e-217 | |||||
CFNOAGBM_00380 | 2.5e-121 | frnE | Q | DSBA-like thioredoxin domain | ||
CFNOAGBM_00381 | 1.9e-163 | |||||
CFNOAGBM_00382 | 1.9e-78 | K | DNA-templated transcription, initiation | |||
CFNOAGBM_00383 | 6.7e-243 | EGP | Sugar (and other) transporter | |||
CFNOAGBM_00384 | 5.1e-69 | S | Iron-sulphur cluster biosynthesis | |||
CFNOAGBM_00385 | 5.8e-287 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
CFNOAGBM_00386 | 1.2e-210 | pbuG | S | permease | ||
CFNOAGBM_00387 | 2.6e-162 | add | 3.5.4.2, 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
CFNOAGBM_00388 | 1.1e-08 | S | RelB antitoxin | |||
CFNOAGBM_00389 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
CFNOAGBM_00390 | 3.5e-288 | clcA | P | chloride | ||
CFNOAGBM_00391 | 6e-271 | 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 | |
CFNOAGBM_00392 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
CFNOAGBM_00393 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
CFNOAGBM_00394 | 3.3e-251 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
CFNOAGBM_00395 | 1.6e-149 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
CFNOAGBM_00396 | 7.8e-61 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
CFNOAGBM_00397 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
CFNOAGBM_00398 | 2.4e-256 | 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 | ||
CFNOAGBM_00399 | 1.2e-205 | 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 | |
CFNOAGBM_00400 | 1.6e-20 | yaaA | S | S4 domain | ||
CFNOAGBM_00401 | 1.2e-208 | 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 | ||
CFNOAGBM_00402 | 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 | |
CFNOAGBM_00403 | 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 | |
CFNOAGBM_00404 | 9.4e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
CFNOAGBM_00405 | 7.3e-81 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
CFNOAGBM_00406 | 2.1e-35 | 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 | ||
CFNOAGBM_00407 | 3.5e-158 | corA | P | CorA-like Mg2+ transporter protein | ||
CFNOAGBM_00408 | 2e-291 | smc | D | Required for chromosome condensation and partitioning | ||
CFNOAGBM_00409 | 2.6e-167 | 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) | ||
CFNOAGBM_00410 | 3.6e-287 | pipD | E | Dipeptidase | ||
CFNOAGBM_00411 | 4.9e-57 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
CFNOAGBM_00412 | 3.8e-228 | 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 | |
CFNOAGBM_00413 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
CFNOAGBM_00414 | 7.6e-94 | 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 | ||
CFNOAGBM_00415 | 5e-136 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
CFNOAGBM_00416 | 1e-57 | 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 | ||
CFNOAGBM_00417 | 2.1e-117 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
CFNOAGBM_00418 | 1.2e-73 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
CFNOAGBM_00419 | 1.6e-180 | 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) | |
CFNOAGBM_00420 | 9.1e-62 | |||||
CFNOAGBM_00421 | 1.1e-124 | S | Alpha/beta hydrolase family | |||
CFNOAGBM_00422 | 8e-154 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
CFNOAGBM_00423 | 4.8e-158 | ypuA | S | Protein of unknown function (DUF1002) | ||
CFNOAGBM_00425 | 7.7e-140 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
CFNOAGBM_00426 | 2.2e-176 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
CFNOAGBM_00427 | 2.1e-123 | yugP | S | Putative neutral zinc metallopeptidase | ||
CFNOAGBM_00428 | 4e-113 | S | Glycosyltransferase like family 2 | |||
CFNOAGBM_00429 | 6.5e-284 | 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 | |
CFNOAGBM_00430 | 5.5e-155 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
CFNOAGBM_00431 | 0.0 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
CFNOAGBM_00432 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
CFNOAGBM_00433 | 1.5e-286 | V | ABC transporter transmembrane region | |||
CFNOAGBM_00434 | 2.8e-135 | |||||
CFNOAGBM_00435 | 3.4e-227 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
CFNOAGBM_00436 | 5.1e-257 | epsU | S | Polysaccharide biosynthesis protein | ||
CFNOAGBM_00437 | 1.2e-131 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
CFNOAGBM_00438 | 1.8e-83 | ydcK | S | Belongs to the SprT family | ||
CFNOAGBM_00439 | 4.6e-61 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
CFNOAGBM_00440 | 7.9e-257 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
CFNOAGBM_00443 | 8e-82 | K | Transcriptional regulator | |||
CFNOAGBM_00444 | 4.3e-242 | pyrP | F | Permease | ||
CFNOAGBM_00445 | 6e-132 | lacR | K | DeoR C terminal sensor domain | ||
CFNOAGBM_00446 | 5.1e-72 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
CFNOAGBM_00447 | 1.6e-105 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
CFNOAGBM_00448 | 2.5e-14 | lacT | K | CAT RNA binding domain | ||
CFNOAGBM_00449 | 3.4e-96 | lacT | K | CAT RNA binding domain | ||
CFNOAGBM_00450 | 1.5e-53 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
CFNOAGBM_00451 | 1.1e-298 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
CFNOAGBM_00452 | 4e-278 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
CFNOAGBM_00453 | 3.1e-69 | |||||
CFNOAGBM_00454 | 3.6e-258 | emrY | EGP | Major facilitator Superfamily | ||
CFNOAGBM_00455 | 4.6e-253 | emrY | EGP | Major facilitator Superfamily | ||
CFNOAGBM_00456 | 6.3e-142 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
CFNOAGBM_00457 | 9.3e-136 | S | CAAX amino terminal protease | |||
CFNOAGBM_00458 | 1.5e-161 | mleP3 | S | Membrane transport protein | ||
CFNOAGBM_00459 | 8.5e-99 | tag | 3.2.2.20 | L | glycosylase | |
CFNOAGBM_00460 | 2.1e-193 | S | Bacteriocin helveticin-J | |||
CFNOAGBM_00461 | 1.9e-220 | yfeO | P | Voltage gated chloride channel | ||
CFNOAGBM_00462 | 8.5e-81 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
CFNOAGBM_00463 | 2.2e-87 | S | Putative adhesin | |||
CFNOAGBM_00464 | 4.5e-61 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
CFNOAGBM_00465 | 7.7e-67 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
CFNOAGBM_00466 | 2.4e-147 | S | Sucrose-6F-phosphate phosphohydrolase | |||
CFNOAGBM_00467 | 4.5e-255 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
CFNOAGBM_00468 | 2.9e-171 | ybbR | S | YbbR-like protein | ||
CFNOAGBM_00469 | 2.9e-151 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
CFNOAGBM_00470 | 5.9e-210 | potD | P | ABC transporter | ||
CFNOAGBM_00471 | 8.5e-137 | potC | P | ABC transporter permease | ||
CFNOAGBM_00472 | 1e-129 | potB | P | ABC transporter permease | ||
CFNOAGBM_00473 | 3.8e-204 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
CFNOAGBM_00474 | 7.6e-166 | murB | 1.3.1.98 | M | Cell wall formation | |
CFNOAGBM_00475 | 6.8e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
CFNOAGBM_00476 | 2.5e-83 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
CFNOAGBM_00477 | 3.2e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
CFNOAGBM_00478 | 2.8e-136 | 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 | |
CFNOAGBM_00479 | 9.8e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
CFNOAGBM_00480 | 1.3e-93 | |||||
CFNOAGBM_00481 | 3.8e-176 | tktA | 2.2.1.1 | G | Transketolase, pyrimidine binding domain | |
CFNOAGBM_00482 | 8.8e-153 | 2.2.1.1 | G | Transketolase, thiamine diphosphate binding domain | ||
CFNOAGBM_00483 | 2.2e-185 | purR13 | K | Bacterial regulatory proteins, lacI family | ||
CFNOAGBM_00484 | 3.5e-290 | G | isomerase | |||
CFNOAGBM_00485 | 1.1e-186 | 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 | |
CFNOAGBM_00486 | 2e-280 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
CFNOAGBM_00487 | 1.8e-276 | yjeM | E | Amino Acid | ||
CFNOAGBM_00488 | 4.8e-96 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
CFNOAGBM_00489 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
CFNOAGBM_00490 | 6.7e-122 | srtA | 3.4.22.70 | M | sortase family | |
CFNOAGBM_00491 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
CFNOAGBM_00492 | 4.4e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
CFNOAGBM_00493 | 1.5e-175 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
CFNOAGBM_00494 | 3.1e-203 | comEC | S | Competence protein ComEC | ||
CFNOAGBM_00495 | 6.2e-63 | yodB | K | Transcriptional regulator, HxlR family | ||
CFNOAGBM_00496 | 2.8e-137 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
CFNOAGBM_00497 | 3.8e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
CFNOAGBM_00498 | 1.1e-170 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
CFNOAGBM_00499 | 4.6e-280 | arlS | 2.7.13.3 | T | Histidine kinase | |
CFNOAGBM_00500 | 1.1e-130 | K | response regulator | |||
CFNOAGBM_00501 | 4.2e-95 | yceD | S | Uncharacterized ACR, COG1399 | ||
CFNOAGBM_00502 | 1.9e-217 | ylbM | S | Belongs to the UPF0348 family | ||
CFNOAGBM_00503 | 3.7e-60 | rsfS | 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 | ||
CFNOAGBM_00504 | 1.5e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
CFNOAGBM_00505 | 1.7e-119 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
CFNOAGBM_00506 | 3.6e-210 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
CFNOAGBM_00507 | 2.4e-87 | yqeG | S | HAD phosphatase, family IIIA | ||
CFNOAGBM_00508 | 1.9e-189 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
CFNOAGBM_00509 | 3e-57 | 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 | ||
CFNOAGBM_00510 | 2.4e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
CFNOAGBM_00511 | 4e-87 | 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 | ||
CFNOAGBM_00512 | 5e-113 | S | CAAX protease self-immunity | |||
CFNOAGBM_00514 | 2.4e-278 | ycaM | E | amino acid | ||
CFNOAGBM_00515 | 2.1e-100 | 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 | |
CFNOAGBM_00516 | 6.2e-171 | whiA | K | May be required for sporulation | ||
CFNOAGBM_00517 | 5.8e-194 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
CFNOAGBM_00518 | 1.6e-160 | rapZ | S | Displays ATPase and GTPase activities | ||
CFNOAGBM_00519 | 8.1e-91 | S | Short repeat of unknown function (DUF308) | |||
CFNOAGBM_00520 | 4.4e-233 | 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 | ||
CFNOAGBM_00521 | 4.6e-272 | S | O-antigen ligase like membrane protein | |||
CFNOAGBM_00522 | 5.3e-44 | |||||
CFNOAGBM_00523 | 1.4e-98 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
CFNOAGBM_00524 | 6.9e-119 | M | NlpC P60 family protein | |||
CFNOAGBM_00525 | 5.3e-231 | S | Putative peptidoglycan binding domain | |||
CFNOAGBM_00526 | 3.4e-228 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
CFNOAGBM_00528 | 1.3e-74 | |||||
CFNOAGBM_00529 | 7e-136 | V | ABC transporter | |||
CFNOAGBM_00530 | 4.2e-122 | V | Transport permease protein | |||
CFNOAGBM_00531 | 7.7e-121 | V | ABC-2 type transporter | |||
CFNOAGBM_00532 | 6.2e-279 | E | amino acid | |||
CFNOAGBM_00533 | 6.3e-134 | cysA | V | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00534 | 0.0 | V | FtsX-like permease family | |||
CFNOAGBM_00535 | 8.8e-124 | pgm3 | G | Phosphoglycerate mutase family | ||
CFNOAGBM_00536 | 2.8e-26 | |||||
CFNOAGBM_00537 | 1.3e-52 | |||||
CFNOAGBM_00538 | 1.9e-149 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
CFNOAGBM_00539 | 0.0 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
CFNOAGBM_00540 | 3.1e-127 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
CFNOAGBM_00541 | 9.6e-144 | rpiR1 | K | Helix-turn-helix domain, rpiR family | ||
CFNOAGBM_00542 | 0.0 | 3.6.3.8 | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
CFNOAGBM_00544 | 2.1e-117 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
CFNOAGBM_00545 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
CFNOAGBM_00546 | 1.7e-75 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
CFNOAGBM_00547 | 4.6e-105 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
CFNOAGBM_00548 | 7.2e-209 | yubA | S | AI-2E family transporter | ||
CFNOAGBM_00549 | 4.9e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
CFNOAGBM_00550 | 2.2e-201 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
CFNOAGBM_00551 | 2.3e-95 | G | Protein of unknown function (DUF4038) | |||
CFNOAGBM_00552 | 1.7e-151 | licT | K | CAT RNA binding domain | ||
CFNOAGBM_00553 | 0.0 | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
CFNOAGBM_00554 | 2.7e-169 | rbsR | K | helix_turn _helix lactose operon repressor | ||
CFNOAGBM_00555 | 1.8e-170 | uhpT | EGP | Major facilitator Superfamily | ||
CFNOAGBM_00556 | 1.5e-127 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
CFNOAGBM_00557 | 2.9e-199 | 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 | ||
CFNOAGBM_00558 | 4.7e-120 | |||||
CFNOAGBM_00559 | 5.4e-92 | |||||
CFNOAGBM_00561 | 3.4e-143 | N | Uncharacterized conserved protein (DUF2075) | |||
CFNOAGBM_00562 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
CFNOAGBM_00563 | 1.3e-170 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
CFNOAGBM_00564 | 2.5e-152 | nadK | 2.7.1.23 | F | 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 | |
CFNOAGBM_00565 | 5.2e-113 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
CFNOAGBM_00566 | 1.9e-112 | yjbK | S | CYTH | ||
CFNOAGBM_00567 | 3.7e-108 | yjbH | Q | Thioredoxin | ||
CFNOAGBM_00568 | 8.2e-165 | coiA | 3.6.4.12 | S | Competence protein | |
CFNOAGBM_00569 | 5.5e-118 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
CFNOAGBM_00570 | 5.2e-66 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
CFNOAGBM_00571 | 1e-262 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
CFNOAGBM_00572 | 2.1e-289 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
CFNOAGBM_00574 | 1e-110 | 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 | ||
CFNOAGBM_00575 | 2.4e-83 | yueI | S | Protein of unknown function (DUF1694) | ||
CFNOAGBM_00576 | 3.6e-238 | rarA | L | recombination factor protein RarA | ||
CFNOAGBM_00578 | 5.2e-81 | usp6 | T | universal stress protein | ||
CFNOAGBM_00579 | 4e-301 | S | membrane | |||
CFNOAGBM_00580 | 4e-65 | 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 | ||
CFNOAGBM_00581 | 3.2e-203 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
CFNOAGBM_00582 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
CFNOAGBM_00583 | 1.5e-45 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
CFNOAGBM_00584 | 1.6e-120 | fruR | K | DeoR C terminal sensor domain | ||
CFNOAGBM_00585 | 1.2e-166 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
CFNOAGBM_00586 | 0.0 | fruA | 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
CFNOAGBM_00587 | 5.4e-67 | S | YSIRK type signal peptide | |||
CFNOAGBM_00588 | 0.0 | 2.7.7.7 | M | domain protein | ||
CFNOAGBM_00589 | 4.7e-140 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | G | Sucrose-6F-phosphate phosphohydrolase | ||
CFNOAGBM_00590 | 2.1e-42 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
CFNOAGBM_00591 | 1.2e-158 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
CFNOAGBM_00592 | 1.6e-117 | fhuC | P | ABC transporter | ||
CFNOAGBM_00593 | 8.7e-134 | znuB | U | ABC 3 transport family | ||
CFNOAGBM_00594 | 1.2e-256 | lctP | C | L-lactate permease | ||
CFNOAGBM_00595 | 0.0 | pepF | E | oligoendopeptidase F | ||
CFNOAGBM_00596 | 9e-209 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
CFNOAGBM_00597 | 6.2e-39 | |||||
CFNOAGBM_00598 | 4.3e-62 | |||||
CFNOAGBM_00599 | 3.6e-285 | S | ABC transporter | |||
CFNOAGBM_00600 | 2.4e-136 | thrE | S | Putative threonine/serine exporter | ||
CFNOAGBM_00601 | 2.8e-79 | S | Threonine/Serine exporter, ThrE | |||
CFNOAGBM_00602 | 4e-40 | |||||
CFNOAGBM_00603 | 4.7e-60 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
CFNOAGBM_00604 | 1.3e-79 | |||||
CFNOAGBM_00605 | 6.4e-176 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
CFNOAGBM_00606 | 7.7e-82 | nrdI | F | Belongs to the NrdI family | ||
CFNOAGBM_00607 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
CFNOAGBM_00608 | 2.2e-119 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
CFNOAGBM_00609 | 8.5e-299 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00610 | 8.7e-67 | K | Transcriptional regulator, MarR family | |||
CFNOAGBM_00611 | 1.7e-154 | S | Alpha beta hydrolase | |||
CFNOAGBM_00612 | 1.3e-216 | naiP | EGP | Major facilitator Superfamily | ||
CFNOAGBM_00613 | 1.6e-279 | pipD | E | Peptidase family C69 | ||
CFNOAGBM_00614 | 8.7e-284 | dtpT | U | amino acid peptide transporter | ||
CFNOAGBM_00615 | 3.9e-82 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
CFNOAGBM_00616 | 3.8e-211 | psd | 4.1.1.65 | I | Belongs to the phosphatidylserine decarboxylase family | |
CFNOAGBM_00617 | 5e-63 | lacR | K | Transcriptional regulator | ||
CFNOAGBM_00618 | 0.0 | lacS | G | Transporter | ||
CFNOAGBM_00619 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
CFNOAGBM_00620 | 3.9e-207 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
CFNOAGBM_00621 | 1.1e-254 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
CFNOAGBM_00622 | 4.7e-161 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
CFNOAGBM_00623 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
CFNOAGBM_00624 | 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 | ||
CFNOAGBM_00625 | 9.1e-141 | aroD | S | Serine hydrolase (FSH1) | ||
CFNOAGBM_00626 | 1.1e-245 | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | |||
CFNOAGBM_00627 | 5e-42 | |||||
CFNOAGBM_00628 | 3e-118 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
CFNOAGBM_00629 | 7.7e-61 | |||||
CFNOAGBM_00630 | 3.4e-46 | S | MazG-like family | |||
CFNOAGBM_00631 | 6.3e-84 | FG | HIT domain | |||
CFNOAGBM_00632 | 1.3e-76 | K | Acetyltransferase (GNAT) domain | |||
CFNOAGBM_00633 | 2.1e-55 | |||||
CFNOAGBM_00634 | 5.5e-53 | |||||
CFNOAGBM_00635 | 1.3e-219 | V | ABC transporter transmembrane region | |||
CFNOAGBM_00636 | 2.9e-48 | V | ABC transporter transmembrane region | |||
CFNOAGBM_00637 | 6.2e-54 | yitW | S | Iron-sulfur cluster assembly protein | ||
CFNOAGBM_00638 | 3.3e-194 | sufB | O | assembly protein SufB | ||
CFNOAGBM_00639 | 6.6e-176 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
CFNOAGBM_00640 | 7.1e-175 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
CFNOAGBM_00641 | 6.1e-39 | D | nuclear chromosome segregation | |||
CFNOAGBM_00643 | 9e-18 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
CFNOAGBM_00644 | 4.8e-190 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
CFNOAGBM_00645 | 2e-185 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
CFNOAGBM_00646 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
CFNOAGBM_00647 | 1.1e-131 | cjaA | ET | ABC transporter substrate-binding protein | ||
CFNOAGBM_00648 | 7.1e-116 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
CFNOAGBM_00649 | 4.6e-151 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
CFNOAGBM_00650 | 9.2e-247 | pepT | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
CFNOAGBM_00651 | 9.6e-59 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
CFNOAGBM_00652 | 7.5e-183 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
CFNOAGBM_00653 | 1.3e-124 | manY | G | PTS system | ||
CFNOAGBM_00654 | 3.3e-172 | manN | G | system, mannose fructose sorbose family IID component | ||
CFNOAGBM_00655 | 1.8e-65 | manO | S | Domain of unknown function (DUF956) | ||
CFNOAGBM_00656 | 1.5e-253 | yifK | E | Amino acid permease | ||
CFNOAGBM_00657 | 7.9e-231 | yifK | E | Amino acid permease | ||
CFNOAGBM_00658 | 3.1e-138 | puuD | S | peptidase C26 | ||
CFNOAGBM_00659 | 5.9e-234 | steT_1 | E | amino acid | ||
CFNOAGBM_00660 | 9e-192 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
CFNOAGBM_00661 | 5.9e-25 | |||||
CFNOAGBM_00662 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
CFNOAGBM_00663 | 1.1e-43 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
CFNOAGBM_00664 | 5.1e-303 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
CFNOAGBM_00665 | 6e-123 | hlyX | S | Transporter associated domain | ||
CFNOAGBM_00666 | 2.2e-170 | yqhA | G | Aldose 1-epimerase | ||
CFNOAGBM_00667 | 1.2e-152 | glcU | U | sugar transport | ||
CFNOAGBM_00668 | 1.2e-118 | |||||
CFNOAGBM_00669 | 8e-179 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
CFNOAGBM_00670 | 3.4e-71 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
CFNOAGBM_00671 | 9.7e-42 | 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 | ||
CFNOAGBM_00672 | 2.1e-45 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
CFNOAGBM_00673 | 1.1e-132 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
CFNOAGBM_00674 | 2.4e-74 | S | PAS domain | |||
CFNOAGBM_00675 | 2.9e-148 | |||||
CFNOAGBM_00676 | 9.5e-141 | |||||
CFNOAGBM_00677 | 1.4e-178 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
CFNOAGBM_00678 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
CFNOAGBM_00679 | 3.6e-143 | fruK | 2.7.1.11, 2.7.1.56 | G | pfkB family carbohydrate kinase | |
CFNOAGBM_00680 | 2.5e-231 | lysA2 | M | Glycosyl hydrolases family 25 | ||
CFNOAGBM_00681 | 2.2e-213 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
CFNOAGBM_00682 | 8.2e-35 | S | Protein of unknown function (DUF2922) | |||
CFNOAGBM_00683 | 4.2e-27 | |||||
CFNOAGBM_00684 | 5.5e-115 | |||||
CFNOAGBM_00685 | 1e-72 | |||||
CFNOAGBM_00686 | 0.0 | kup | P | Transport of potassium into the cell | ||
CFNOAGBM_00687 | 0.0 | kup | P | Transport of potassium into the cell | ||
CFNOAGBM_00688 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
CFNOAGBM_00689 | 0.0 | S | Bacterial membrane protein, YfhO | |||
CFNOAGBM_00690 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
CFNOAGBM_00691 | 0.0 | fruA | 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
CFNOAGBM_00692 | 1.3e-168 | pfkB | 2.7.1.11, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
CFNOAGBM_00693 | 2.6e-135 | rpl | K | Helix-turn-helix domain, rpiR family | ||
CFNOAGBM_00694 | 5.3e-184 | D | nuclear chromosome segregation | |||
CFNOAGBM_00695 | 1.5e-186 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
CFNOAGBM_00696 | 3.8e-134 | yttB | EGP | Major facilitator Superfamily | ||
CFNOAGBM_00697 | 1.3e-102 | 3.6.1.27 | I | Acid phosphatase homologues | ||
CFNOAGBM_00698 | 6.2e-246 | 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 | |
CFNOAGBM_00699 | 3.7e-18 | S | Sugar efflux transporter for intercellular exchange | |||
CFNOAGBM_00700 | 1.6e-304 | ybiT | S | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00701 | 6.7e-192 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
CFNOAGBM_00702 | 2.3e-48 | K | Helix-turn-helix domain | |||
CFNOAGBM_00703 | 2.6e-139 | F | DNA/RNA non-specific endonuclease | |||
CFNOAGBM_00704 | 2.6e-80 | |||||
CFNOAGBM_00705 | 5.1e-133 | cobB | K | SIR2 family | ||
CFNOAGBM_00706 | 9.2e-87 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
CFNOAGBM_00707 | 3.6e-124 | terC | P | Integral membrane protein TerC family | ||
CFNOAGBM_00708 | 4.4e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
CFNOAGBM_00709 | 5e-116 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
CFNOAGBM_00710 | 6.4e-301 | glnP | P | ABC transporter permease | ||
CFNOAGBM_00711 | 7.3e-138 | glnQ | E | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00712 | 2e-45 | |||||
CFNOAGBM_00713 | 4.8e-51 | L | HNH nucleases | |||
CFNOAGBM_00714 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
CFNOAGBM_00715 | 6.3e-90 | ypmB | S | Protein conserved in bacteria | ||
CFNOAGBM_00716 | 6.4e-259 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
CFNOAGBM_00717 | 3.7e-114 | dnaD | L | DnaD domain protein | ||
CFNOAGBM_00718 | 1.1e-115 | 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 | |
CFNOAGBM_00719 | 6.1e-303 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
CFNOAGBM_00720 | 9.9e-180 | oppF | P | Belongs to the ABC transporter superfamily | ||
CFNOAGBM_00721 | 9e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
CFNOAGBM_00722 | 4.4e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
CFNOAGBM_00724 | 5.1e-82 | |||||
CFNOAGBM_00725 | 2.2e-87 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
CFNOAGBM_00726 | 1.7e-102 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
CFNOAGBM_00727 | 1e-229 | 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 | ||
CFNOAGBM_00728 | 1.7e-51 | 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 | ||
CFNOAGBM_00729 | 8.8e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
CFNOAGBM_00730 | 1.8e-295 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
CFNOAGBM_00731 | 2.7e-14 | ropB | K | Helix-turn-helix domain | ||
CFNOAGBM_00732 | 8.1e-114 | |||||
CFNOAGBM_00734 | 0.0 | nisT | V | ABC transporter | ||
CFNOAGBM_00735 | 9.5e-16 | |||||
CFNOAGBM_00736 | 2.2e-36 | |||||
CFNOAGBM_00737 | 4.6e-76 | EGP | Major facilitator Superfamily | |||
CFNOAGBM_00738 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
CFNOAGBM_00739 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
CFNOAGBM_00740 | 9.3e-101 | 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 | |
CFNOAGBM_00741 | 9.3e-120 | gpsB | D | DivIVA domain protein | ||
CFNOAGBM_00742 | 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) | |
CFNOAGBM_00743 | 2.3e-33 | cspA | K | 'Cold-shock' DNA-binding domain | ||
CFNOAGBM_00744 | 1.7e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
CFNOAGBM_00745 | 4.9e-34 | |||||
CFNOAGBM_00746 | 1.1e-127 | 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 | |
CFNOAGBM_00747 | 3.5e-216 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
CFNOAGBM_00748 | 9.6e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
CFNOAGBM_00749 | 8.7e-220 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
CFNOAGBM_00750 | 3.1e-124 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
CFNOAGBM_00751 | 1e-116 | S | Repeat protein | |||
CFNOAGBM_00752 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
CFNOAGBM_00753 | 2.6e-177 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
CFNOAGBM_00754 | 0.0 | rnjA | 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 | ||
CFNOAGBM_00755 | 2.3e-34 | ykzG | S | Belongs to the UPF0356 family | ||
CFNOAGBM_00756 | 1.7e-199 | aha1 | P | E1-E2 ATPase | ||
CFNOAGBM_00757 | 3.5e-310 | S | Bacterial membrane protein, YfhO | |||
CFNOAGBM_00758 | 5.3e-68 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
CFNOAGBM_00759 | 9.7e-172 | prmA | J | Ribosomal protein L11 methyltransferase | ||
CFNOAGBM_00760 | 2.4e-65 | |||||
CFNOAGBM_00761 | 0.0 | relA | 2.7.6.5 | 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 | |
CFNOAGBM_00762 | 1.3e-73 | 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 | ||
CFNOAGBM_00763 | 1.9e-253 | gor | 1.8.1.7 | C | pyridine nucleotide-disulfide oxidoreductase | |
CFNOAGBM_00764 | 3.1e-212 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
CFNOAGBM_00765 | 1.5e-103 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
CFNOAGBM_00766 | 1.2e-191 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
CFNOAGBM_00767 | 0.0 | S | domain, Protein | |||
CFNOAGBM_00768 | 8.4e-215 | M | Glycosyl transferases group 1 | |||
CFNOAGBM_00769 | 2.2e-154 | spo0J | K | Belongs to the ParB family | ||
CFNOAGBM_00770 | 9.7e-138 | soj | D | Sporulation initiation inhibitor | ||
CFNOAGBM_00771 | 1.1e-142 | noc | K | Belongs to the ParB family | ||
CFNOAGBM_00772 | 1.4e-130 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
CFNOAGBM_00773 | 6.4e-96 | cvpA | S | Colicin V production protein | ||
CFNOAGBM_00774 | 4e-178 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
CFNOAGBM_00775 | 5.7e-149 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
CFNOAGBM_00776 | 1.1e-200 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
CFNOAGBM_00777 | 3.7e-99 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
CFNOAGBM_00778 | 2.2e-96 | nqr | 1.5.1.36 | S | reductase | |
CFNOAGBM_00779 | 2e-109 | K | WHG domain | |||
CFNOAGBM_00780 | 1.8e-37 | |||||
CFNOAGBM_00781 | 1.7e-273 | pipD | E | Dipeptidase | ||
CFNOAGBM_00782 | 4.1e-294 | arbB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
CFNOAGBM_00783 | 0.0 | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
CFNOAGBM_00784 | 5.1e-156 | K | CAT RNA binding domain | |||
CFNOAGBM_00785 | 3.1e-119 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
CFNOAGBM_00786 | 1.2e-183 | hrtB | V | ABC transporter permease | ||
CFNOAGBM_00787 | 2.4e-92 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
CFNOAGBM_00788 | 4.6e-111 | G | phosphoglycerate mutase | |||
CFNOAGBM_00789 | 3.6e-114 | G | Phosphoglycerate mutase family | |||
CFNOAGBM_00790 | 1e-139 | aroD | S | Alpha/beta hydrolase family | ||
CFNOAGBM_00791 | 5.4e-141 | S | Belongs to the UPF0246 family | |||
CFNOAGBM_00792 | 2.6e-40 | |||||
CFNOAGBM_00793 | 1.3e-128 | |||||
CFNOAGBM_00794 | 3.9e-162 | O | protein-N(PI)-phosphohistidine-lactose phosphotransferase system transporter activity | |||
CFNOAGBM_00795 | 7.4e-46 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
CFNOAGBM_00796 | 4.4e-149 | S | hydrolase | |||
CFNOAGBM_00797 | 5.1e-101 | yagU | S | Protein of unknown function (DUF1440) | ||
CFNOAGBM_00798 | 7.6e-146 | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | ||
CFNOAGBM_00799 | 7.9e-202 | S | PFAM Archaeal ATPase | |||
CFNOAGBM_00800 | 3.5e-82 | 2.3.1.128 | K | acetyltransferase | ||
CFNOAGBM_00801 | 4e-16 | |||||
CFNOAGBM_00803 | 1.5e-126 | yfeJ | 6.3.5.2 | F | Glutamine amidotransferase class-I | |
CFNOAGBM_00804 | 1.5e-92 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
CFNOAGBM_00806 | 2.8e-134 | K | Sigma-54 factor, core binding domain | |||
CFNOAGBM_00807 | 2.6e-113 | mgtC | S | MgtC family | ||
CFNOAGBM_00808 | 4.5e-149 | ptsD | G | PTS system mannose/fructose/sorbose family IID component | ||
CFNOAGBM_00809 | 3.1e-137 | ptsC | G | PTS system sorbose-specific iic component | ||
CFNOAGBM_00810 | 7e-81 | ptsB | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
CFNOAGBM_00811 | 3.2e-55 | 2.7.1.191 | G | PTS system fructose IIA component | ||
CFNOAGBM_00812 | 1.4e-117 | K | Sigma-54 interaction domain | |||
CFNOAGBM_00813 | 5.2e-40 | glpK_1 | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
CFNOAGBM_00814 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
CFNOAGBM_00815 | 1.8e-122 | secA2 | 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 | ||
CFNOAGBM_00816 | 1.2e-291 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
CFNOAGBM_00817 | 1.7e-198 | V | Beta-lactamase | |||
CFNOAGBM_00819 | 1.8e-37 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
CFNOAGBM_00820 | 8.1e-114 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | |
CFNOAGBM_00821 | 1.1e-92 | dps | P | Belongs to the Dps family | ||
CFNOAGBM_00822 | 7.9e-35 | copZ | C | Heavy-metal-associated domain | ||
CFNOAGBM_00823 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
CFNOAGBM_00824 | 1.6e-108 | |||||
CFNOAGBM_00825 | 1.5e-258 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
CFNOAGBM_00826 | 2.1e-120 | spaE | S | ABC-2 family transporter protein | ||
CFNOAGBM_00827 | 2e-129 | mutF | V | ABC transporter, ATP-binding protein | ||
CFNOAGBM_00828 | 4e-243 | nhaC | C | Na H antiporter NhaC | ||
CFNOAGBM_00829 | 1.7e-131 | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | |||
CFNOAGBM_00830 | 4.6e-54 | |||||
CFNOAGBM_00831 | 1.4e-181 | |||||
CFNOAGBM_00832 | 9.2e-59 | cadX | K | Bacterial regulatory protein, arsR family | ||
CFNOAGBM_00833 | 5.6e-96 | cadD | P | Cadmium resistance transporter | ||
CFNOAGBM_00835 | 0.0 | |||||
CFNOAGBM_00836 | 2.2e-218 | I | Protein of unknown function (DUF2974) | |||
CFNOAGBM_00837 | 5e-170 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
CFNOAGBM_00838 | 1.8e-243 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
CFNOAGBM_00839 | 4.8e-76 | rplI | J | Binds to the 23S rRNA | ||
CFNOAGBM_00840 | 5.6e-286 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
CFNOAGBM_00841 | 2.2e-111 | P | ABC transporter | |||
CFNOAGBM_00842 | 1e-75 | P | ABC transporter | |||
CFNOAGBM_00844 | 1.5e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
CFNOAGBM_00845 | 5e-78 | 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 | ||
CFNOAGBM_00846 | 5.1e-150 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
CFNOAGBM_00847 | 7.4e-141 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
CFNOAGBM_00848 | 1.7e-162 | ecfA | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
CFNOAGBM_00849 | 1.5e-155 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
CFNOAGBM_00850 | 2.9e-76 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
CFNOAGBM_00851 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
CFNOAGBM_00852 | 3.2e-56 | |||||
CFNOAGBM_00853 | 2e-174 | degV | S | DegV family | ||
CFNOAGBM_00854 | 7.6e-224 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
CFNOAGBM_00855 | 1.6e-265 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
CFNOAGBM_00856 | 1.3e-309 | gadC | E | Contains amino acid permease domain | ||
CFNOAGBM_00857 | 9.5e-155 | E | Amino acid permease | |||
CFNOAGBM_00858 | 1.8e-286 | 4.1.1.25 | E | Pyridoxal-dependent decarboxylase conserved domain | ||
CFNOAGBM_00859 | 1.2e-244 | yagE | E | amino acid | ||
CFNOAGBM_00860 | 3.8e-213 | mdtG | EGP | Major facilitator Superfamily | ||
CFNOAGBM_00861 | 8.6e-28 | |||||
CFNOAGBM_00862 | 6.7e-69 | K | helix_turn_helix multiple antibiotic resistance protein | |||
CFNOAGBM_00863 | 6.5e-78 | |||||
CFNOAGBM_00864 | 3.3e-208 | pepA | E | M42 glutamyl aminopeptidase | ||
CFNOAGBM_00866 | 2.3e-116 | camS | S | sex pheromone | ||
CFNOAGBM_00867 | 3.7e-48 | 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) | |
CFNOAGBM_00868 | 5.2e-270 | gatA | 6.3.5.6, 6.3.5.7 | J | 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) | |
CFNOAGBM_00869 | 6e-274 | gatB | 6.1.1.12, 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) | |
CFNOAGBM_00870 | 6.9e-167 | yegS | 2.7.1.107 | G | Lipid kinase | |
CFNOAGBM_00871 | 5.7e-85 | tlpA2 | L | Transposase IS200 like | ||
CFNOAGBM_00872 | 6.6e-251 | L | transposase, IS605 OrfB family | |||
CFNOAGBM_00873 | 3.8e-148 | S | hydrolase | |||
CFNOAGBM_00874 | 0.0 | UW | Tetratricopeptide repeat | |||
CFNOAGBM_00875 | 9.9e-175 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
CFNOAGBM_00876 | 5.5e-172 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
CFNOAGBM_00877 | 0.0 | clpE2 | O | AAA domain (Cdc48 subfamily) | ||
CFNOAGBM_00878 | 1.1e-251 | yfnA | E | Amino Acid | ||
CFNOAGBM_00879 | 2.5e-218 | 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) | |
CFNOAGBM_00880 | 2.3e-101 | J | Acetyltransferase (GNAT) domain | |||
CFNOAGBM_00881 | 5.3e-107 | yjbF | S | SNARE associated Golgi protein | ||
CFNOAGBM_00882 | 1.8e-155 | I | alpha/beta hydrolase fold | |||
CFNOAGBM_00883 | 5.6e-155 | hipB | K | Helix-turn-helix | ||
CFNOAGBM_00884 | 4.2e-261 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
CFNOAGBM_00885 | 1.6e-177 | |||||
CFNOAGBM_00886 | 9.9e-126 | S | SNARE associated Golgi protein | |||
CFNOAGBM_00887 | 1.3e-145 | cof | S | haloacid dehalogenase-like hydrolase | ||
CFNOAGBM_00888 | 0.0 | ydgH | S | MMPL family | ||
CFNOAGBM_00889 | 1.1e-95 | yobS | K | Bacterial regulatory proteins, tetR family | ||
CFNOAGBM_00890 | 1.9e-159 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
CFNOAGBM_00891 | 2e-166 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
CFNOAGBM_00892 | 1.1e-82 | yjcF | S | Acetyltransferase (GNAT) domain | ||
CFNOAGBM_00893 | 1.1e-92 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
CFNOAGBM_00894 | 3.9e-78 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
CFNOAGBM_00895 | 2.9e-39 | ypaA | S | Protein of unknown function (DUF1304) | ||
CFNOAGBM_00896 | 2.5e-239 | G | Bacterial extracellular solute-binding protein | |||
CFNOAGBM_00897 | 5.1e-248 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
CFNOAGBM_00898 | 1.1e-147 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
CFNOAGBM_00899 | 2.1e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
CFNOAGBM_00900 | 3.8e-204 | malK | P | ATPases associated with a variety of cellular activities | ||
CFNOAGBM_00901 | 3.3e-280 | pipD | E | Dipeptidase | ||
CFNOAGBM_00902 | 7.6e-152 | endA | F | DNA RNA non-specific endonuclease | ||
CFNOAGBM_00903 | 2.9e-156 | dkg | S | reductase | ||
CFNOAGBM_00904 | 9.3e-198 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
CFNOAGBM_00905 | 3e-181 | dnaQ | 2.7.7.7 | L | EXOIII | |
CFNOAGBM_00906 | 3e-150 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
CFNOAGBM_00907 | 4.4e-112 | yviA | S | Protein of unknown function (DUF421) | ||
CFNOAGBM_00908 | 2e-74 | S | Protein of unknown function (DUF3290) | |||
CFNOAGBM_00909 | 1e-240 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
CFNOAGBM_00910 | 2.1e-91 | S | PAS domain | |||
CFNOAGBM_00911 | 5.3e-144 | pnuC | H | nicotinamide mononucleotide transporter | ||
CFNOAGBM_00912 | 0.0 | UW | LPXTG-motif cell wall anchor domain protein | |||
CFNOAGBM_00913 | 2.9e-218 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
CFNOAGBM_00914 | 6e-139 | ykuT | M | mechanosensitive ion channel | ||
CFNOAGBM_00915 | 1.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
CFNOAGBM_00916 | 9.6e-50 | |||||
CFNOAGBM_00917 | 3.8e-212 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
CFNOAGBM_00918 | 7.6e-216 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
CFNOAGBM_00919 | 4.5e-71 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
CFNOAGBM_00920 | 3.9e-104 | ypsA | S | Belongs to the UPF0398 family | ||
CFNOAGBM_00921 | 2.9e-93 | K | acetyltransferase | |||
CFNOAGBM_00922 | 2.5e-60 | psiE | S | Phosphate-starvation-inducible E | ||
CFNOAGBM_00923 | 3.9e-133 | S | Putative ABC-transporter type IV | |||
CFNOAGBM_00924 | 3.5e-114 | M | LysM domain protein | |||
CFNOAGBM_00926 | 5.9e-188 | rfbD | 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 | |
CFNOAGBM_00927 | 6.7e-118 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
CFNOAGBM_00928 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
CFNOAGBM_00929 | 1.2e-157 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
CFNOAGBM_00930 | 3.1e-262 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
CFNOAGBM_00931 | 1.6e-35 | yozE | S | Belongs to the UPF0346 family | ||
CFNOAGBM_00932 | 1.5e-62 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
CFNOAGBM_00933 | 2.6e-61 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
CFNOAGBM_00934 | 1.4e-08 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
CFNOAGBM_00935 | 3.1e-47 | qmcA | O | prohibitin homologues | ||
CFNOAGBM_00936 | 5.8e-77 | qmcA | O | prohibitin homologues | ||
CFNOAGBM_00937 | 3.3e-227 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
CFNOAGBM_00938 | 1.7e-227 | sptS | 2.7.13.3 | T | Histidine kinase | |
CFNOAGBM_00939 | 5.3e-116 | K | response regulator | |||
CFNOAGBM_00940 | 3.5e-114 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
CFNOAGBM_00941 | 2.8e-163 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
CFNOAGBM_00942 | 2.5e-68 | O | OsmC-like protein | |||
CFNOAGBM_00943 | 9.6e-286 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
CFNOAGBM_00944 | 1.8e-181 | E | ABC transporter, ATP-binding protein | |||
CFNOAGBM_00945 | 1.2e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
CFNOAGBM_00946 | 1.1e-161 | yihY | S | Belongs to the UPF0761 family | ||
CFNOAGBM_00947 | 6.7e-161 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
CFNOAGBM_00948 | 2.5e-77 | fld | C | Flavodoxin | ||
CFNOAGBM_00949 | 3.6e-88 | gtcA | S | Teichoic acid glycosylation protein | ||
CFNOAGBM_00950 | 5.5e-214 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
CFNOAGBM_00953 | 2.3e-251 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
CFNOAGBM_00954 | 1e-205 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
CFNOAGBM_00955 | 7.6e-137 | M | Glycosyl hydrolases family 25 | |||
CFNOAGBM_00956 | 8e-233 | potE | E | amino acid | ||
CFNOAGBM_00957 | 9.8e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
CFNOAGBM_00958 | 1.1e-237 | yhdP | S | Transporter associated domain | ||
CFNOAGBM_00959 | 4.2e-109 | |||||
CFNOAGBM_00960 | 3.5e-211 | yhjX | P | Major Facilitator Superfamily | ||
CFNOAGBM_00961 | 2e-244 | eno2 | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
CFNOAGBM_00962 | 3e-295 | V | ABC-type multidrug transport system, ATPase and permease components | |||
CFNOAGBM_00963 | 1.5e-57 | P | ABC transporter | |||
CFNOAGBM_00964 | 1.5e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
CFNOAGBM_00965 | 1.7e-156 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
CFNOAGBM_00966 | 1.1e-50 | S | Iron-sulfur cluster assembly protein | |||
CFNOAGBM_00967 | 8.8e-151 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
CFNOAGBM_00968 | 1.2e-109 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
CFNOAGBM_00969 | 2.1e-149 | L | Belongs to the 'phage' integrase family | |||
CFNOAGBM_00971 | 1e-226 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
CFNOAGBM_00972 | 4.3e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
CFNOAGBM_00973 | 1.6e-32 | comGF | U | Putative Competence protein ComGF | ||
CFNOAGBM_00974 | 3.7e-29 | cycA | E | Amino acid permease | ||
CFNOAGBM_00975 | 7.6e-115 | luxT | K | Bacterial regulatory proteins, tetR family | ||
CFNOAGBM_00976 | 4.2e-126 | |||||
CFNOAGBM_00977 | 8.3e-266 | S | Cysteine-rich secretory protein family | |||
CFNOAGBM_00978 | 4.8e-207 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
CFNOAGBM_00979 | 6.8e-77 | |||||
CFNOAGBM_00980 | 1.2e-270 | yjcE | P | Sodium proton antiporter | ||
CFNOAGBM_00981 | 8.9e-169 | yibE | S | overlaps another CDS with the same product name | ||
CFNOAGBM_00982 | 1.2e-119 | yibF | S | overlaps another CDS with the same product name | ||
CFNOAGBM_00983 | 9.6e-155 | I | alpha/beta hydrolase fold | |||
CFNOAGBM_00984 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
CFNOAGBM_00985 | 9.9e-12 | |||||
CFNOAGBM_00986 | 7e-40 | |||||
CFNOAGBM_00987 | 2.2e-154 | czcD | P | cation diffusion facilitator family transporter | ||
CFNOAGBM_00988 | 4.2e-50 | K | Transcriptional regulator, ArsR family | |||
CFNOAGBM_00989 | 1.1e-129 | pgm3 | G | Belongs to the phosphoglycerate mutase family | ||
CFNOAGBM_00990 | 1.1e-109 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
CFNOAGBM_00991 | 1.9e-150 | 1.6.5.2 | GM | NmrA-like family | ||
CFNOAGBM_00992 | 1.6e-68 | pgm3 | 5.4.2.11 | G | Histidine phosphatase superfamily (branch 1) | |
CFNOAGBM_00993 | 1.2e-157 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
CFNOAGBM_00994 | 4.7e-174 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
CFNOAGBM_00995 | 7.6e-24 | |||||
CFNOAGBM_00996 | 3.4e-183 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
CFNOAGBM_00997 | 2.7e-230 | 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 | ||
CFNOAGBM_00998 | 2.7e-149 | ecsB | U | ABC transporter | ||
CFNOAGBM_00999 | 8.9e-124 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
CFNOAGBM_01000 | 1.1e-62 | |||||
CFNOAGBM_01001 | 4.7e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
CFNOAGBM_01002 | 1.5e-120 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
CFNOAGBM_01003 | 1.6e-85 | cutC | P | Participates in the control of copper homeostasis | ||
CFNOAGBM_01004 | 4.1e-253 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
CFNOAGBM_01005 | 6.5e-120 | K | UTRA | |||
CFNOAGBM_01006 | 9.2e-62 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
CFNOAGBM_01007 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
CFNOAGBM_01008 | 5.7e-160 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
CFNOAGBM_01009 | 6e-103 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
CFNOAGBM_01010 | 7.8e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
CFNOAGBM_01011 | 3.2e-237 | dnaB | L | Replication initiation and membrane attachment | ||
CFNOAGBM_01012 | 5.4e-156 | dnaI | L | Primosomal protein DnaI | ||
CFNOAGBM_01013 | 5.8e-115 | hlyIII | S | protein, hemolysin III | ||
CFNOAGBM_01014 | 6e-227 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
CFNOAGBM_01015 | 1.9e-161 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
CFNOAGBM_01016 | 3.3e-106 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
CFNOAGBM_01017 | 1.6e-163 | htpX | O | Peptidase family M48 | ||
CFNOAGBM_01019 | 6.8e-84 | |||||
CFNOAGBM_01020 | 3.7e-81 | mutT | 3.6.1.55 | F | NUDIX domain | |
CFNOAGBM_01021 | 3.9e-39 | |||||
CFNOAGBM_01022 | 2.5e-68 | |||||
CFNOAGBM_01023 | 9.9e-67 | S | Domain of unknown function DUF1828 | |||
CFNOAGBM_01024 | 3.4e-99 | S | Rib/alpha-like repeat | |||
CFNOAGBM_01027 | 3e-147 | arbV | 2.3.1.51 | I | Acyl-transferase | |
CFNOAGBM_01028 | 1.6e-154 | arbx | M | Glycosyl transferase family 8 | ||
CFNOAGBM_01029 | 1.1e-183 | arbY | M | Glycosyl transferase family 8 | ||
CFNOAGBM_01030 | 1.4e-186 | arbY | M | Glycosyl transferase family 8 | ||
CFNOAGBM_01031 | 4.7e-165 | arbZ | I | Phosphate acyltransferases | ||
CFNOAGBM_01032 | 1e-246 | yhjX_2 | P | Major Facilitator Superfamily | ||
CFNOAGBM_01033 | 2.2e-249 | yhjX_2 | P | Major Facilitator Superfamily | ||
CFNOAGBM_01034 | 2.4e-186 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
CFNOAGBM_01035 | 1.2e-63 | S | Peptidase propeptide and YPEB domain | |||
CFNOAGBM_01036 | 1.6e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
CFNOAGBM_01037 | 2.1e-134 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
CFNOAGBM_01038 | 3.4e-242 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
CFNOAGBM_01039 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
CFNOAGBM_01040 | 3.6e-171 | K | LysR substrate binding domain | |||
CFNOAGBM_01041 | 7.8e-299 | E | amino acid | |||
CFNOAGBM_01042 | 0.0 | 3.1.31.1 | M | domain protein | ||
CFNOAGBM_01043 | 6.9e-124 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
CFNOAGBM_01044 | 5.6e-222 | L | Putative transposase DNA-binding domain | |||
CFNOAGBM_01045 | 1.2e-143 | K | LytTr DNA-binding domain | |||
CFNOAGBM_01046 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
CFNOAGBM_01047 | 4.9e-105 | M | Transport protein ComB | |||
CFNOAGBM_01048 | 3.2e-20 | S | Bacteriocin class II with double-glycine leader peptide | |||
CFNOAGBM_01051 | 9.4e-219 | 2.7.7.7 | S | Domain of unknown function (DUF5060) | ||
CFNOAGBM_01052 | 2.7e-117 | drgA | C | nitroreductase | ||
CFNOAGBM_01053 | 2.9e-170 | C | Oxidoreductase | |||
CFNOAGBM_01054 | 4.3e-73 | S | SnoaL-like domain | |||
CFNOAGBM_01055 | 2.8e-09 | rpiB | 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
CFNOAGBM_01056 | 6.4e-90 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
CFNOAGBM_01057 | 6e-79 | apfA | 2.7.7.72, 3.6.1.61 | F | NUDIX domain | |
CFNOAGBM_01058 | 8.2e-142 | L | oxidized base lesion DNA N-glycosylase activity | |||
CFNOAGBM_01059 | 4.8e-246 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
CFNOAGBM_01060 | 3e-53 | 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 | |
CFNOAGBM_01061 | 5e-63 | vanZ | V | VanZ like family | ||
CFNOAGBM_01062 | 1.9e-261 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
CFNOAGBM_01063 | 2.2e-233 | EGP | Major facilitator Superfamily | |||
CFNOAGBM_01064 | 1.2e-208 | 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 | |
CFNOAGBM_01065 | 1.9e-183 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
CFNOAGBM_01066 | 3.1e-227 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
CFNOAGBM_01067 | 7.5e-39 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
CFNOAGBM_01068 | 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) | |
CFNOAGBM_01069 | 1.3e-227 | G | Major Facilitator Superfamily | |||
CFNOAGBM_01070 | 2.8e-188 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
CFNOAGBM_01071 | 1.8e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
CFNOAGBM_01072 | 3.4e-11 | 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 | ||
CFNOAGBM_01073 | 9.8e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
CFNOAGBM_01074 | 5.3e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
CFNOAGBM_01075 | 2.3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
CFNOAGBM_01076 | 1.1e-95 | sprD | D | Domain of Unknown Function (DUF1542) | ||
CFNOAGBM_01077 | 8.4e-109 | S | Protein of unknown function (DUF1211) | |||
CFNOAGBM_01078 | 8.6e-12 | S | reductase | |||
CFNOAGBM_01079 | 3e-55 | S | reductase | |||
CFNOAGBM_01080 | 1.4e-107 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
CFNOAGBM_01081 | 2e-117 | 3.6.1.55 | F | NUDIX domain | ||
CFNOAGBM_01082 | 8.2e-128 | T | Transcriptional regulatory protein, C terminal | |||
CFNOAGBM_01083 | 3.4e-239 | T | GHKL domain | |||
CFNOAGBM_01084 | 2.4e-89 | S | Peptidase propeptide and YPEB domain | |||
CFNOAGBM_01085 | 4.4e-123 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
CFNOAGBM_01086 | 2.7e-25 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
CFNOAGBM_01087 | 2.4e-72 | S | Putative adhesin | |||
CFNOAGBM_01088 | 2.1e-244 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
CFNOAGBM_01089 | 2.2e-151 | agaS | G | SIS domain | ||
CFNOAGBM_01090 | 1.4e-228 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
CFNOAGBM_01091 | 6.7e-84 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
CFNOAGBM_01092 | 2.8e-25 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
CFNOAGBM_01093 | 2.4e-50 | 2.7.1.191 | G | PTS system fructose IIA component | ||
CFNOAGBM_01094 | 1.2e-219 | S | zinc-ribbon domain | |||
CFNOAGBM_01095 | 4.8e-87 | ntd | 2.4.2.6 | F | Nucleoside | |
CFNOAGBM_01096 | 3.4e-100 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
CFNOAGBM_01097 | 1.1e-130 | XK27_08440 | K | UTRA domain | ||
CFNOAGBM_01098 | 3.4e-149 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
CFNOAGBM_01099 | 1e-87 | uspA | T | universal stress protein | ||
CFNOAGBM_01101 | 9.8e-169 | phnD | P | Phosphonate ABC transporter | ||
CFNOAGBM_01102 | 1.9e-141 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
CFNOAGBM_01103 | 5.4e-131 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
CFNOAGBM_01104 | 7.1e-147 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
CFNOAGBM_01105 | 1.9e-83 | |||||
CFNOAGBM_01106 | 4e-275 | S | Calcineurin-like phosphoesterase | |||
CFNOAGBM_01107 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
CFNOAGBM_01108 | 3.3e-266 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
CFNOAGBM_01109 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
CFNOAGBM_01110 | 3.1e-130 | 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 | |
CFNOAGBM_01111 | 9.9e-129 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
CFNOAGBM_01112 | 1.2e-117 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
CFNOAGBM_01113 | 2e-302 | I | Protein of unknown function (DUF2974) | |||
CFNOAGBM_01114 | 1.2e-149 | yxeH | S | hydrolase | ||
CFNOAGBM_01115 | 2.7e-67 | XK27_05540 | S | DUF218 domain | ||
CFNOAGBM_01116 | 1e-27 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
CFNOAGBM_01117 | 1.6e-182 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
CFNOAGBM_01118 | 3.1e-242 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
CFNOAGBM_01119 | 2.5e-259 | qacA | EGP | Major facilitator Superfamily | ||
CFNOAGBM_01121 | 3.7e-32 | |||||
CFNOAGBM_01122 | 4.3e-169 | 4.1.1.45 | S | Amidohydrolase | ||
CFNOAGBM_01123 | 6.3e-235 | yrvN | L | AAA C-terminal domain | ||
CFNOAGBM_01124 | 1.1e-19 | K | Transcriptional regulator | |||
CFNOAGBM_01125 | 1.6e-111 | C | Aldo keto reductase | |||
CFNOAGBM_01126 | 8.7e-148 | 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 | |
CFNOAGBM_01127 | 4e-136 | |||||
CFNOAGBM_01128 | 1e-215 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
CFNOAGBM_01129 | 1.2e-299 | ytgP | S | Polysaccharide biosynthesis protein | ||
CFNOAGBM_01130 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
CFNOAGBM_01131 | 2.3e-116 | 3.6.1.27 | I | Acid phosphatase homologues | ||
CFNOAGBM_01132 | 1e-81 | 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 | ||
CFNOAGBM_01133 | 3.5e-70 | 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 | ||
CFNOAGBM_01134 | 1.3e-106 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
CFNOAGBM_01135 | 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 | |
CFNOAGBM_01136 | 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 | |
CFNOAGBM_01137 | 0.0 | clpC | 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 | ||
CFNOAGBM_01139 | 1.6e-08 | |||||
CFNOAGBM_01140 | 2.1e-301 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
CFNOAGBM_01141 | 1.5e-191 | 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 | ||
CFNOAGBM_01142 | 1.9e-161 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
CFNOAGBM_01143 | 0.0 | S | membrane | |||
CFNOAGBM_01144 | 0.0 | S | membrane | |||
CFNOAGBM_01145 | 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 | ||
CFNOAGBM_01146 | 1.1e-242 | 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 | |
CFNOAGBM_01147 | 4.9e-60 | yabR | J | S1 RNA binding domain | ||
CFNOAGBM_01148 | 4e-60 | divIC | D | Septum formation initiator | ||
CFNOAGBM_01149 | 5.4e-34 | yabO | J | S4 domain protein | ||
CFNOAGBM_01150 | 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 | ||
CFNOAGBM_01151 | 1.9e-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 | |
CFNOAGBM_01152 | 1.4e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
CFNOAGBM_01153 | 2.3e-122 | S | (CBS) domain | |||
CFNOAGBM_01154 | 2.5e-214 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
CFNOAGBM_01155 | 5e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
CFNOAGBM_01156 | 5.5e-267 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
CFNOAGBM_01157 | 7.2e-261 | 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 | |
CFNOAGBM_01158 | 8e-41 | rpmE2 | J | Ribosomal protein L31 | ||
CFNOAGBM_01159 | 4.6e-299 | ybeC | E | amino acid | ||
CFNOAGBM_01160 | 1.7e-134 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
CFNOAGBM_01161 | 6.4e-141 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
CFNOAGBM_01162 | 1.5e-178 | ABC-SBP | S | ABC transporter | ||
CFNOAGBM_01163 | 4.7e-227 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
CFNOAGBM_01164 | 2.4e-283 | pipD | E | Dipeptidase | ||
CFNOAGBM_01165 | 2.7e-140 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
CFNOAGBM_01166 | 9.8e-77 | XK27_02070 | S | Nitroreductase family | ||
CFNOAGBM_01167 | 1.1e-31 | hxlR | K | Transcriptional regulator, HxlR family | ||
CFNOAGBM_01168 | 2.1e-79 | |||||
CFNOAGBM_01169 | 3.2e-66 | S | Putative adhesin | |||
CFNOAGBM_01170 | 4.6e-39 | |||||
CFNOAGBM_01171 | 1.2e-190 | yfdV | S | Membrane transport protein | ||
CFNOAGBM_01172 | 0.0 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
CFNOAGBM_01173 | 4.1e-264 | 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 | |
CFNOAGBM_01174 | 6.8e-95 | |||||
CFNOAGBM_01175 | 5.8e-56 | K | Transcriptional regulator | |||
CFNOAGBM_01176 | 4.3e-86 | XK27_09675 | K | Acetyltransferase (GNAT) domain | ||
CFNOAGBM_01177 | 1.4e-63 | S | Protein of unknown function (DUF3021) | |||
CFNOAGBM_01178 | 2.2e-73 | K | LytTr DNA-binding domain | |||
CFNOAGBM_01179 | 1.6e-144 | cylB | V | ABC-2 type transporter | ||
CFNOAGBM_01180 | 1.7e-151 | cylA | V | ABC transporter | ||
CFNOAGBM_01181 | 7.6e-29 | S | Peptidase M16 | |||
CFNOAGBM_01182 | 3.7e-131 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CFNOAGBM_01183 | 9.8e-125 | ymfM | S | Helix-turn-helix domain | ||
CFNOAGBM_01184 | 1.4e-96 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
CFNOAGBM_01185 | 3.5e-194 | 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 | ||
CFNOAGBM_01186 | 6e-85 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
CFNOAGBM_01187 | 1.8e-153 | dprA | LU | DNA protecting protein DprA | ||
CFNOAGBM_01188 | 4.4e-58 | yabA | L | Involved in initiation control of chromosome replication | ||
CFNOAGBM_01189 | 1e-151 | holB | 2.7.7.7 | L | DNA polymerase III | |
CFNOAGBM_01190 | 5e-51 | yaaQ | S | Cyclic-di-AMP receptor | ||
CFNOAGBM_01191 | 1.2e-112 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
CFNOAGBM_01192 | 9e-26 | S | Protein of unknown function (DUF2508) | |||
CFNOAGBM_01193 | 6.9e-107 | 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 | ||
CFNOAGBM_01194 | 5.9e-52 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
CFNOAGBM_01195 | 3e-310 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
CFNOAGBM_01196 | 1e-84 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
CFNOAGBM_01197 | 1e-40 | S | Protein conserved in bacteria | |||
CFNOAGBM_01198 | 3.3e-147 | |||||
CFNOAGBM_01199 | 3.9e-21 | |||||
CFNOAGBM_01200 | 2.3e-113 | rsmC | 2.1.1.172 | J | Methyltransferase | |
CFNOAGBM_01201 | 2.7e-32 | |||||
CFNOAGBM_01202 | 3.6e-128 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
CFNOAGBM_01203 | 9.4e-51 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
CFNOAGBM_01204 | 4.2e-81 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
CFNOAGBM_01205 | 2.9e-119 | aatB | ET | ABC transporter substrate-binding protein | ||
CFNOAGBM_01206 | 5.7e-174 | 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 | ||
CFNOAGBM_01207 | 2e-223 | dnaK | O | Heat shock 70 kDa protein | ||
CFNOAGBM_01208 | 3.6e-162 | rssA | S | Phospholipase, patatin family | ||
CFNOAGBM_01209 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
CFNOAGBM_01211 | 1.8e-53 | S | Enterocin A Immunity | |||
CFNOAGBM_01215 | 9.1e-223 | S | CAAX protease self-immunity | |||
CFNOAGBM_01216 | 7.6e-152 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
CFNOAGBM_01217 | 1.5e-208 | 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) |
CFNOAGBM_01218 | 3.6e-260 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
CFNOAGBM_01219 | 1.2e-177 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
CFNOAGBM_01220 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
CFNOAGBM_01221 | 4.8e-55 | ftsL | D | Cell division protein FtsL | ||
CFNOAGBM_01222 | 1.7e-179 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
CFNOAGBM_01223 | 4.1e-77 | mraZ | K | Belongs to the MraZ family | ||
CFNOAGBM_01224 | 2.7e-52 | S | Protein of unknown function (DUF3397) | |||
CFNOAGBM_01225 | 3.6e-13 | S | Protein of unknown function (DUF4044) | |||
CFNOAGBM_01226 | 1.6e-94 | mreD | ||||
CFNOAGBM_01227 | 9.7e-65 | mreC | M | Involved in formation and maintenance of cell shape | ||
CFNOAGBM_01228 | 8.3e-204 | xerS | L | Belongs to the 'phage' integrase family | ||
CFNOAGBM_01229 | 1.4e-153 | K | Transcriptional regulator | |||
CFNOAGBM_01230 | 1e-151 | |||||
CFNOAGBM_01231 | 1e-162 | degV | S | EDD domain protein, DegV family | ||
CFNOAGBM_01232 | 2.3e-31 | 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 | |
CFNOAGBM_01233 | 7.3e-112 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
CFNOAGBM_01234 | 1e-47 | |||||
CFNOAGBM_01235 | 2.5e-295 | recN | L | May be involved in recombinational repair of damaged DNA | ||
CFNOAGBM_01236 | 4.6e-154 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
CFNOAGBM_01237 | 1.8e-57 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
CFNOAGBM_01238 | 1.6e-103 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
CFNOAGBM_01239 | 4.5e-140 | stp | 3.1.3.16 | T | phosphatase | |
CFNOAGBM_01240 | 0.0 | KLT | serine threonine protein kinase | |||
CFNOAGBM_01241 | 2e-129 | treR | K | UTRA | ||
CFNOAGBM_01242 | 0.0 | treB | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CFNOAGBM_01243 | 6.4e-76 | S | Putative adhesin | |||
CFNOAGBM_01245 | 2.3e-113 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
CFNOAGBM_01247 | 9.2e-205 | 2.7.13.3 | T | GHKL domain | ||
CFNOAGBM_01248 | 3.1e-102 | L | PFAM Integrase catalytic region | |||
CFNOAGBM_01249 | 2e-41 | L | Helix-turn-helix domain | |||
CFNOAGBM_01250 | 1e-196 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
CFNOAGBM_01251 | 5.5e-112 | tdk | 2.7.1.21 | F | thymidine kinase | |
CFNOAGBM_01252 | 5.5e-261 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain | |
CFNOAGBM_01253 | 1.1e-194 | ampC | V | Beta-lactamase | ||
CFNOAGBM_01256 | 8.7e-116 | manR | K | PRD domain | ||
CFNOAGBM_01257 | 3.1e-69 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
CFNOAGBM_01258 | 2.3e-78 | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
CFNOAGBM_01259 | 2.5e-245 | G | PTS system sugar-specific permease component | |||
CFNOAGBM_01260 | 8e-45 | 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
CFNOAGBM_01261 | 0.0 | GH23 | S | M26 IgA1-specific Metallo-endopeptidase C-terminal region | ||
CFNOAGBM_01263 | 9e-161 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
CFNOAGBM_01264 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
CFNOAGBM_01265 | 9.5e-56 | yheA | S | Belongs to the UPF0342 family | ||
CFNOAGBM_01266 | 5.5e-220 | yhaO | L | Ser Thr phosphatase family protein | ||
CFNOAGBM_01267 | 0.0 | L | AAA domain | |||
CFNOAGBM_01268 | 3e-184 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
CFNOAGBM_01269 | 4.9e-149 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
CFNOAGBM_01270 | 9.5e-24 | S | YtxH-like protein | |||
CFNOAGBM_01271 | 2e-51 | |||||
CFNOAGBM_01272 | 3.5e-76 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
CFNOAGBM_01273 | 1.4e-147 | glnH | ET | ABC transporter | ||
CFNOAGBM_01274 | 3.6e-137 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
CFNOAGBM_01275 | 3.1e-150 | glnH | ET | ABC transporter | ||
CFNOAGBM_01276 | 2.4e-110 | gluC | P | ABC transporter permease | ||
CFNOAGBM_01277 | 5.7e-107 | glnP | P | ABC transporter permease | ||
CFNOAGBM_01278 | 1.6e-304 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
CFNOAGBM_01279 | 1e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
CFNOAGBM_01280 | 7.5e-47 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
CFNOAGBM_01281 | 3.6e-143 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
CFNOAGBM_01282 | 7.8e-54 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
CFNOAGBM_01283 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
CFNOAGBM_01284 | 1.1e-267 | T | PhoQ Sensor | |||
CFNOAGBM_01285 | 2.2e-128 | K | Transcriptional regulatory protein, C terminal | |||
CFNOAGBM_01286 | 6e-67 | S | SdpI/YhfL protein family | |||
CFNOAGBM_01287 | 5e-192 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
CFNOAGBM_01288 | 4.6e-61 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
CFNOAGBM_01289 | 1.5e-42 | S | Phage Mu protein F like protein | |||
CFNOAGBM_01290 | 1.1e-34 | 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 | |
CFNOAGBM_01291 | 7.2e-253 | 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 | |
CFNOAGBM_01292 | 3.9e-148 | 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 | |
CFNOAGBM_01293 | 3.6e-67 | 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 | ||
CFNOAGBM_01294 | 8.2e-73 | yqhY | S | Asp23 family, cell envelope-related function | ||
CFNOAGBM_01295 | 1.1e-101 | 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 | ||
CFNOAGBM_01296 | 6.4e-199 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
CFNOAGBM_01297 | 2.8e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
CFNOAGBM_01298 | 2e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
CFNOAGBM_01299 | 7.3e-64 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
CFNOAGBM_01300 | 2.9e-151 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
CFNOAGBM_01301 | 1.5e-215 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
CFNOAGBM_01302 | 3.5e-12 | |||||
CFNOAGBM_01303 | 6.3e-64 | |||||
CFNOAGBM_01304 | 2.1e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
CFNOAGBM_01305 | 3.5e-36 | S | ECF-type riboflavin transporter, S component | |||
CFNOAGBM_01306 | 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 | |
CFNOAGBM_01307 | 2.1e-230 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
CFNOAGBM_01308 | 1.5e-138 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
CFNOAGBM_01309 | 1.2e-134 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
CFNOAGBM_01310 | 2.6e-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 | ||
CFNOAGBM_01311 | 1.8e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
CFNOAGBM_01312 | 1.5e-29 | 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 | ||
CFNOAGBM_01313 | 2.2e-56 | yjdF | S | Protein of unknown function (DUF2992) | ||
CFNOAGBM_01314 | 3.9e-93 | K | Bacterial regulatory proteins, tetR family | |||
CFNOAGBM_01315 | 1.2e-111 | 1.6.5.2 | S | NADPH-dependent FMN reductase | ||
CFNOAGBM_01316 | 4.6e-63 | rfbP | 2.7.8.6 | M | Bacterial sugar transferase | |
CFNOAGBM_01317 | 5.8e-138 | cps1D | M | Domain of unknown function (DUF4422) | ||
CFNOAGBM_01318 | 1.3e-124 | waaB | GT4 | M | Glycosyl transferases group 1 | |
CFNOAGBM_01319 | 4e-40 | S | O-antigen ligase like membrane protein | |||
CFNOAGBM_01320 | 1.4e-217 | P | P-loop Domain of unknown function (DUF2791) | |||
CFNOAGBM_01321 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
CFNOAGBM_01322 | 3.7e-174 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
CFNOAGBM_01323 | 3.8e-70 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
CFNOAGBM_01324 | 2.3e-248 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
CFNOAGBM_01325 | 2.3e-164 | yvgN | C | Aldo keto reductase | ||
CFNOAGBM_01326 | 3.3e-76 | yphH | S | Cupin domain | ||
CFNOAGBM_01327 | 1.3e-87 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
CFNOAGBM_01328 | 1.5e-55 | 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | ||
CFNOAGBM_01330 | 5.8e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
CFNOAGBM_01331 | 1.8e-195 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
CFNOAGBM_01332 | 2.6e-117 | plsC | 2.3.1.51 | I | Acyltransferase | |
CFNOAGBM_01333 | 3e-231 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
CFNOAGBM_01334 | 1.4e-283 | mdlB | V | ABC transporter | ||
CFNOAGBM_01335 | 3.7e-114 | mdlA | V | ABC transporter | ||
CFNOAGBM_01336 | 5.8e-126 | 2.7.1.2 | GK | ROK family | ||
CFNOAGBM_01337 | 2.9e-62 | K | AraC-like ligand binding domain | |||
CFNOAGBM_01338 | 3.5e-43 | rhaS6 | K | helix_turn_helix, arabinose operon control protein | ||
CFNOAGBM_01339 | 1.2e-176 | I | Carboxylesterase family | |||
CFNOAGBM_01340 | 0.0 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
CFNOAGBM_01341 | 5.3e-144 | 3.4.16.4, 3.5.2.6 | V | Beta-lactamase enzyme family | ||
CFNOAGBM_01342 | 6.3e-154 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
CFNOAGBM_01343 | 8e-156 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
CFNOAGBM_01344 | 4.3e-71 | aroD | 1.1.1.25, 4.2.1.10 | E | 3-dehydroquinate dehydratase activity | |
CFNOAGBM_01345 | 4e-156 | |||||
CFNOAGBM_01346 | 3.8e-54 | K | Acetyltransferase (GNAT) domain | |||
CFNOAGBM_01347 | 8.5e-248 | ynbB | 4.4.1.1 | P | aluminum resistance | |
CFNOAGBM_01348 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
CFNOAGBM_01349 | 7.3e-283 | E | Amino acid permease | |||
CFNOAGBM_01350 | 1.2e-158 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
CFNOAGBM_01351 | 2.5e-253 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
CFNOAGBM_01352 | 2.8e-216 | malE | G | Bacterial extracellular solute-binding protein | ||
CFNOAGBM_01353 | 2.3e-209 | msmX | P | Belongs to the ABC transporter superfamily | ||
CFNOAGBM_01354 | 8.1e-117 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
CFNOAGBM_01355 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
CFNOAGBM_01356 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
CFNOAGBM_01357 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
CFNOAGBM_01358 | 3.8e-176 | yvdE | K | helix_turn _helix lactose operon repressor | ||
CFNOAGBM_01359 | 1.1e-173 | 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) | |
CFNOAGBM_01360 | 4.1e-219 | 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 | |
CFNOAGBM_01361 | 1.5e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
CFNOAGBM_01362 | 2.2e-35 | veg | S | Biofilm formation stimulator VEG | ||
CFNOAGBM_01363 | 1.2e-160 | ksgA | 2.1.1.182 | 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 | |
CFNOAGBM_01364 | 1.2e-97 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
CFNOAGBM_01365 | 3.6e-148 | tatD | L | hydrolase, TatD family | ||
CFNOAGBM_01366 | 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 | |
CFNOAGBM_01367 | 8.5e-182 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
CFNOAGBM_01368 | 4e-99 | S | TPM domain | |||
CFNOAGBM_01369 | 5.6e-91 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
CFNOAGBM_01370 | 1.2e-194 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
CFNOAGBM_01371 | 1.2e-114 | E | Belongs to the SOS response-associated peptidase family | |||
CFNOAGBM_01373 | 1.8e-116 | |||||
CFNOAGBM_01374 | 5.5e-158 | ypbG | 2.7.1.2 | GK | ROK family | |
CFNOAGBM_01375 | 1.8e-280 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
CFNOAGBM_01376 | 4.6e-263 | pts23C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
CFNOAGBM_01377 | 2.6e-52 | ptcB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
CFNOAGBM_01378 | 2.1e-41 | |||||
CFNOAGBM_01379 | 1.5e-50 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
CFNOAGBM_01380 | 2.1e-134 | gmuR | K | UTRA | ||
CFNOAGBM_01381 | 4e-305 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
CFNOAGBM_01382 | 4.6e-70 | S | Domain of unknown function (DUF3284) | |||
CFNOAGBM_01383 | 5.2e-130 | yydK | K | UTRA | ||
CFNOAGBM_01384 | 8.2e-241 | celD | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
CFNOAGBM_01385 | 7.5e-83 | |||||
CFNOAGBM_01386 | 5.9e-51 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
CFNOAGBM_01387 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
CFNOAGBM_01388 | 4.6e-35 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
CFNOAGBM_01389 | 9.6e-86 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
CFNOAGBM_01390 | 1.5e-183 | ylbL | T | Belongs to the peptidase S16 family | ||
CFNOAGBM_01391 | 1.1e-84 | comEA | L | Competence protein ComEA | ||
CFNOAGBM_01392 | 4.1e-83 | XK26_02160 | S | Pyridoxamine 5'-phosphate oxidase | ||
CFNOAGBM_01393 | 5.3e-273 | lsa | S | ABC transporter | ||
CFNOAGBM_01395 | 5.8e-149 | |||||
CFNOAGBM_01396 | 5.4e-36 | L | PFAM Integrase catalytic region | |||
CFNOAGBM_01397 | 4.1e-142 | |||||
CFNOAGBM_01398 | 3.5e-146 | |||||
CFNOAGBM_01399 | 1.2e-49 | skfE | V | ATPases associated with a variety of cellular activities | ||
CFNOAGBM_01400 | 8.7e-116 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
CFNOAGBM_01401 | 5.2e-104 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
CFNOAGBM_01402 | 6.7e-50 | ptcB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
CFNOAGBM_01403 | 2.7e-79 | XK27_02470 | K | LytTr DNA-binding domain | ||
CFNOAGBM_01404 | 4e-120 | liaI | S | membrane | ||
CFNOAGBM_01405 | 7.2e-16 | |||||
CFNOAGBM_01406 | 1.2e-09 | |||||
CFNOAGBM_01407 | 7.7e-139 | S | Alpha beta hydrolase | |||
CFNOAGBM_01408 | 0.0 | L | Helicase C-terminal domain protein | |||
CFNOAGBM_01409 | 5.7e-160 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
CFNOAGBM_01411 | 2.3e-165 | P | CorA-like Mg2+ transporter protein | |||
CFNOAGBM_01412 | 7.5e-194 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
CFNOAGBM_01413 | 2.7e-114 | ropB | K | Helix-turn-helix XRE-family like proteins |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)