ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
KEAGBMNG_00001 | 0.0 | hsdR | 3.1.21.3 | V | EcoEI R protein C-terminal | |
KEAGBMNG_00002 | 1.8e-121 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KEAGBMNG_00003 | 2.4e-178 | L | Belongs to the 'phage' integrase family | |||
KEAGBMNG_00004 | 4.6e-95 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KEAGBMNG_00005 | 1.8e-292 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KEAGBMNG_00006 | 2.6e-134 | |||||
KEAGBMNG_00007 | 0.0 | KL | domain protein | |||
KEAGBMNG_00008 | 1.1e-113 | S | Tetratricopeptide repeat protein | |||
KEAGBMNG_00009 | 2.3e-34 | S | Tetratricopeptide repeat protein | |||
KEAGBMNG_00010 | 5.6e-36 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KEAGBMNG_00011 | 5.1e-66 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KEAGBMNG_00012 | 1.3e-20 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KEAGBMNG_00013 | 1e-79 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KEAGBMNG_00014 | 2.9e-27 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KEAGBMNG_00015 | 1.1e-19 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KEAGBMNG_00016 | 5.4e-90 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KEAGBMNG_00017 | 1.5e-247 | 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 | ||
KEAGBMNG_00018 | 3.2e-206 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
KEAGBMNG_00019 | 3.9e-19 | yaaA | S | S4 domain | ||
KEAGBMNG_00020 | 4.5e-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 | ||
KEAGBMNG_00021 | 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 | |
KEAGBMNG_00022 | 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 | |
KEAGBMNG_00023 | 9.4e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
KEAGBMNG_00024 | 1.7e-82 | 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 | ||
KEAGBMNG_00025 | 6.1e-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 | ||
KEAGBMNG_00026 | 5.8e-126 | corA | P | CorA-like Mg2+ transporter protein | ||
KEAGBMNG_00027 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
KEAGBMNG_00028 | 4.8e-76 | rplI | J | Binds to the 23S rRNA | ||
KEAGBMNG_00029 | 1.1e-245 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
KEAGBMNG_00030 | 2.2e-170 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
KEAGBMNG_00031 | 3.3e-219 | I | Protein of unknown function (DUF2974) | |||
KEAGBMNG_00032 | 0.0 | |||||
KEAGBMNG_00033 | 1.7e-117 | yhiD | S | MgtC family | ||
KEAGBMNG_00035 | 7.9e-114 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
KEAGBMNG_00036 | 1.2e-20 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
KEAGBMNG_00037 | 1.3e-85 | S | Protein of unknown function (DUF3278) | |||
KEAGBMNG_00038 | 4.9e-201 | S | Aldo keto reductase | |||
KEAGBMNG_00040 | 4.6e-224 | S | Sterol carrier protein domain | |||
KEAGBMNG_00041 | 3e-116 | ywnB | S | NAD(P)H-binding | ||
KEAGBMNG_00042 | 7.1e-132 | S | Protein of unknown function (DUF975) | |||
KEAGBMNG_00043 | 3.4e-137 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
KEAGBMNG_00044 | 1.2e-154 | yitS | S | EDD domain protein, DegV family | ||
KEAGBMNG_00045 | 2.2e-19 | |||||
KEAGBMNG_00046 | 0.0 | tetP | J | elongation factor G | ||
KEAGBMNG_00047 | 9.2e-167 | P | CorA-like Mg2+ transporter protein | |||
KEAGBMNG_00049 | 2.5e-40 | S | Transglycosylase associated protein | |||
KEAGBMNG_00050 | 6.7e-161 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
KEAGBMNG_00051 | 0.0 | L | Helicase C-terminal domain protein | |||
KEAGBMNG_00052 | 2.2e-165 | S | Alpha beta hydrolase | |||
KEAGBMNG_00053 | 1.8e-40 | |||||
KEAGBMNG_00054 | 5.5e-168 | K | AI-2E family transporter | |||
KEAGBMNG_00055 | 1e-251 | gor | 1.8.1.7 | C | pyridine nucleotide-disulfide oxidoreductase | |
KEAGBMNG_00056 | 6.2e-213 | 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 | |
KEAGBMNG_00057 | 1.8e-104 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
KEAGBMNG_00058 | 1.8e-192 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KEAGBMNG_00059 | 0.0 | S | domain, Protein | |||
KEAGBMNG_00060 | 0.0 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
KEAGBMNG_00061 | 0.0 | 3.1.31.1 | M | domain protein | ||
KEAGBMNG_00062 | 1.6e-266 | E | amino acid | |||
KEAGBMNG_00063 | 1.6e-171 | K | LysR substrate binding domain | |||
KEAGBMNG_00064 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
KEAGBMNG_00065 | 1.8e-243 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
KEAGBMNG_00066 | 1.8e-133 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
KEAGBMNG_00067 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
KEAGBMNG_00068 | 1.1e-88 | S | Peptidase propeptide and YPEB domain | |||
KEAGBMNG_00069 | 1.4e-186 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
KEAGBMNG_00070 | 5.7e-250 | yhjX_2 | P | Major Facilitator Superfamily | ||
KEAGBMNG_00071 | 6.7e-61 | yhjX_2 | P | Major Facilitator Superfamily | ||
KEAGBMNG_00072 | 3.5e-132 | yhjX_2 | P | Major Facilitator Superfamily | ||
KEAGBMNG_00073 | 6.1e-165 | arbZ | I | Phosphate acyltransferases | ||
KEAGBMNG_00074 | 2.9e-184 | arbY | M | Glycosyl transferase family 8 | ||
KEAGBMNG_00075 | 1.7e-184 | arbY | M | Glycosyl transferase family 8 | ||
KEAGBMNG_00076 | 3.2e-155 | arbx | M | Glycosyl transferase family 8 | ||
KEAGBMNG_00077 | 7.8e-151 | arbV | 2.3.1.51 | I | Acyl-transferase | |
KEAGBMNG_00080 | 1.2e-129 | K | response regulator | |||
KEAGBMNG_00081 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
KEAGBMNG_00082 | 1.7e-254 | yycH | S | YycH protein | ||
KEAGBMNG_00083 | 3.7e-143 | yycI | S | YycH protein | ||
KEAGBMNG_00084 | 5.1e-150 | vicX | 3.1.26.11 | S | domain protein | |
KEAGBMNG_00085 | 2.9e-184 | htrA | 3.4.21.107 | O | serine protease | |
KEAGBMNG_00086 | 9.5e-83 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
KEAGBMNG_00087 | 1.1e-110 | P | Cobalt transport protein | |||
KEAGBMNG_00088 | 9.3e-253 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
KEAGBMNG_00089 | 1.3e-94 | S | ABC-type cobalt transport system, permease component | |||
KEAGBMNG_00090 | 2.3e-170 | K | helix_turn_helix, arabinose operon control protein | |||
KEAGBMNG_00091 | 2e-147 | htpX | O | Belongs to the peptidase M48B family | ||
KEAGBMNG_00092 | 9.9e-92 | lemA | S | LemA family | ||
KEAGBMNG_00093 | 8.3e-183 | ybiR | P | Citrate transporter | ||
KEAGBMNG_00094 | 1.3e-69 | S | Iron-sulphur cluster biosynthesis | |||
KEAGBMNG_00095 | 1.7e-16 | |||||
KEAGBMNG_00096 | 1.7e-154 | |||||
KEAGBMNG_00098 | 4.3e-247 | ydaM | M | Glycosyl transferase | ||
KEAGBMNG_00099 | 2.4e-214 | G | Glycosyl hydrolases family 8 | |||
KEAGBMNG_00100 | 4.5e-120 | yfbR | S | HD containing hydrolase-like enzyme | ||
KEAGBMNG_00101 | 6.3e-162 | L | HNH nucleases | |||
KEAGBMNG_00102 | 9.6e-138 | glnQ | E | ABC transporter, ATP-binding protein | ||
KEAGBMNG_00103 | 1.5e-281 | glnP | P | ABC transporter permease | ||
KEAGBMNG_00104 | 7.2e-106 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
KEAGBMNG_00105 | 1.5e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
KEAGBMNG_00106 | 1.6e-127 | terC | P | Integral membrane protein TerC family | ||
KEAGBMNG_00107 | 5.9e-94 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
KEAGBMNG_00108 | 5.5e-135 | cobB | K | SIR2 family | ||
KEAGBMNG_00109 | 6.7e-81 | |||||
KEAGBMNG_00110 | 6.4e-273 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
KEAGBMNG_00111 | 5.6e-124 | yugP | S | Putative neutral zinc metallopeptidase | ||
KEAGBMNG_00112 | 6.3e-176 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
KEAGBMNG_00113 | 6.2e-145 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KEAGBMNG_00114 | 8.4e-163 | ypuA | S | Protein of unknown function (DUF1002) | ||
KEAGBMNG_00115 | 2.2e-143 | 2.4.1.293 | GT2 | M | Glycosyltransferase like family 2 | |
KEAGBMNG_00116 | 6.9e-124 | S | Alpha/beta hydrolase family | |||
KEAGBMNG_00117 | 1.4e-62 | |||||
KEAGBMNG_00118 | 4.1e-181 | 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) | |
KEAGBMNG_00119 | 2.4e-220 | S | CAAX protease self-immunity | |||
KEAGBMNG_00120 | 2.8e-241 | cycA | E | Amino acid permease | ||
KEAGBMNG_00121 | 7.6e-115 | luxT | K | Bacterial regulatory proteins, tetR family | ||
KEAGBMNG_00122 | 1.1e-139 | |||||
KEAGBMNG_00123 | 7.2e-286 | S | Cysteine-rich secretory protein family | |||
KEAGBMNG_00124 | 2.8e-207 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
KEAGBMNG_00125 | 3.3e-95 | |||||
KEAGBMNG_00126 | 1.5e-273 | yjcE | P | Sodium proton antiporter | ||
KEAGBMNG_00127 | 1.4e-187 | yibE | S | overlaps another CDS with the same product name | ||
KEAGBMNG_00128 | 4.9e-118 | yibF | S | overlaps another CDS with the same product name | ||
KEAGBMNG_00129 | 7.6e-157 | I | alpha/beta hydrolase fold | |||
KEAGBMNG_00130 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
KEAGBMNG_00131 | 5.3e-130 | XK27_08435 | K | UTRA | ||
KEAGBMNG_00132 | 2.4e-217 | agaS | G | SIS domain | ||
KEAGBMNG_00133 | 1.8e-228 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
KEAGBMNG_00134 | 8.7e-84 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
KEAGBMNG_00135 | 2.9e-141 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
KEAGBMNG_00136 | 5.5e-147 | manZ_1 | G | PTS system mannose/fructose/sorbose family IID component | ||
KEAGBMNG_00137 | 9.3e-68 | 2.7.1.191 | G | PTS system fructose IIA component | ||
KEAGBMNG_00138 | 1.3e-18 | S | PD-(D/E)XK nuclease family transposase | |||
KEAGBMNG_00139 | 2.3e-207 | S | zinc-ribbon domain | |||
KEAGBMNG_00140 | 1.4e-189 | |||||
KEAGBMNG_00141 | 3.3e-88 | ntd | 2.4.2.6 | F | Nucleoside | |
KEAGBMNG_00142 | 4.9e-99 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
KEAGBMNG_00143 | 1.5e-132 | XK27_08440 | K | UTRA domain | ||
KEAGBMNG_00144 | 2e-149 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
KEAGBMNG_00145 | 3.8e-87 | uspA | T | universal stress protein | ||
KEAGBMNG_00147 | 9.8e-169 | phnD | P | Phosphonate ABC transporter | ||
KEAGBMNG_00148 | 4.3e-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 | |
KEAGBMNG_00149 | 1.6e-130 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
KEAGBMNG_00150 | 5.4e-147 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
KEAGBMNG_00151 | 7.3e-83 | |||||
KEAGBMNG_00152 | 6.2e-276 | S | Calcineurin-like phosphoesterase | |||
KEAGBMNG_00153 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
KEAGBMNG_00154 | 7.3e-266 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
KEAGBMNG_00155 | 1.2e-64 | |||||
KEAGBMNG_00156 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
KEAGBMNG_00157 | 5.3e-138 | 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 | |
KEAGBMNG_00158 | 6.4e-105 | S | Iron-sulfur cluster assembly protein | |||
KEAGBMNG_00159 | 2.2e-229 | XK27_04775 | S | PAS domain | ||
KEAGBMNG_00160 | 0.0 | UW | LPXTG-motif cell wall anchor domain protein | |||
KEAGBMNG_00161 | 0.0 | UW | LPXTG-motif cell wall anchor domain protein | |||
KEAGBMNG_00162 | 4.2e-228 | yttB | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00163 | 6.6e-187 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
KEAGBMNG_00164 | 4.1e-173 | D | nuclear chromosome segregation | |||
KEAGBMNG_00165 | 2e-135 | rpl | K | Helix-turn-helix domain, rpiR family | ||
KEAGBMNG_00166 | 1.1e-164 | pfkB | 2.7.1.11, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
KEAGBMNG_00167 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
KEAGBMNG_00168 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KEAGBMNG_00169 | 0.0 | S | Bacterial membrane protein, YfhO | |||
KEAGBMNG_00170 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
KEAGBMNG_00171 | 0.0 | kup | P | Transport of potassium into the cell | ||
KEAGBMNG_00172 | 1.7e-72 | |||||
KEAGBMNG_00173 | 3.8e-113 | |||||
KEAGBMNG_00174 | 1.7e-28 | |||||
KEAGBMNG_00175 | 1.4e-34 | S | Protein of unknown function (DUF2922) | |||
KEAGBMNG_00176 | 3e-265 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
KEAGBMNG_00177 | 4.1e-254 | lysA2 | M | Glycosyl hydrolases family 25 | ||
KEAGBMNG_00178 | 1.1e-144 | fruK | 2.7.1.11, 2.7.1.56 | G | pfkB family carbohydrate kinase | |
KEAGBMNG_00179 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
KEAGBMNG_00180 | 1.7e-179 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
KEAGBMNG_00181 | 4e-131 | |||||
KEAGBMNG_00182 | 7e-150 | |||||
KEAGBMNG_00183 | 1.4e-74 | S | PAS domain | |||
KEAGBMNG_00184 | 3.8e-133 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
KEAGBMNG_00185 | 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 | ||
KEAGBMNG_00186 | 3.2e-69 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
KEAGBMNG_00187 | 8e-179 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
KEAGBMNG_00188 | 9.3e-119 | |||||
KEAGBMNG_00189 | 7.8e-152 | glcU | U | sugar transport | ||
KEAGBMNG_00190 | 9e-172 | yqhA | G | Aldose 1-epimerase | ||
KEAGBMNG_00191 | 5.6e-195 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
KEAGBMNG_00192 | 1.1e-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 | |
KEAGBMNG_00193 | 0.0 | XK27_08315 | M | Sulfatase | ||
KEAGBMNG_00194 | 2.8e-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) | |
KEAGBMNG_00196 | 3.7e-262 | pepC | 3.4.22.40 | E | aminopeptidase | |
KEAGBMNG_00197 | 8.8e-124 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
KEAGBMNG_00198 | 3.9e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
KEAGBMNG_00199 | 7.7e-43 | |||||
KEAGBMNG_00200 | 8.8e-78 | 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 | ||
KEAGBMNG_00201 | 3.3e-77 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
KEAGBMNG_00202 | 3.4e-293 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KEAGBMNG_00203 | 3.7e-82 | |||||
KEAGBMNG_00204 | 1.4e-248 | 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 | |
KEAGBMNG_00205 | 1.3e-128 | yydK | K | UTRA | ||
KEAGBMNG_00206 | 3.4e-42 | S | Domain of unknown function (DUF3284) | |||
KEAGBMNG_00207 | 6.2e-306 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
KEAGBMNG_00208 | 1e-133 | gmuR | K | UTRA | ||
KEAGBMNG_00209 | 8.5e-51 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
KEAGBMNG_00210 | 2e-52 | ptcB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
KEAGBMNG_00211 | 1.5e-269 | pts23C | 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 | |
KEAGBMNG_00212 | 3e-283 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KEAGBMNG_00213 | 3.8e-159 | ypbG | 2.7.1.2 | GK | ROK family | |
KEAGBMNG_00214 | 1.3e-114 | |||||
KEAGBMNG_00216 | 2.3e-113 | E | Belongs to the SOS response-associated peptidase family | |||
KEAGBMNG_00217 | 2.6e-194 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KEAGBMNG_00218 | 4.3e-91 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
KEAGBMNG_00219 | 4.7e-100 | S | TPM domain | |||
KEAGBMNG_00220 | 1.8e-91 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
KEAGBMNG_00221 | 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 | |
KEAGBMNG_00222 | 1.6e-148 | tatD | L | hydrolase, TatD family | ||
KEAGBMNG_00223 | 1.9e-98 | 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 | |
KEAGBMNG_00224 | 4.7e-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 | |
KEAGBMNG_00225 | 7.4e-36 | veg | S | Biofilm formation stimulator VEG | ||
KEAGBMNG_00226 | 2.6e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
KEAGBMNG_00227 | 1.1e-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 | |
KEAGBMNG_00228 | 4.8e-174 | 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) | |
KEAGBMNG_00229 | 5.8e-177 | yvdE | K | helix_turn _helix lactose operon repressor | ||
KEAGBMNG_00230 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
KEAGBMNG_00231 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KEAGBMNG_00232 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
KEAGBMNG_00233 | 4.8e-109 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
KEAGBMNG_00234 | 3.6e-210 | msmX | P | Belongs to the ABC transporter superfamily | ||
KEAGBMNG_00235 | 5e-229 | malE | G | Bacterial extracellular solute-binding protein | ||
KEAGBMNG_00236 | 6.5e-254 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
KEAGBMNG_00237 | 9.7e-155 | malG | P | ABC transporter permease | ||
KEAGBMNG_00238 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
KEAGBMNG_00239 | 3.3e-266 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
KEAGBMNG_00240 | 6e-73 | S | Domain of unknown function (DUF1934) | |||
KEAGBMNG_00241 | 1.3e-64 | 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 | ||
KEAGBMNG_00242 | 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 | |
KEAGBMNG_00243 | 2.2e-240 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KEAGBMNG_00244 | 6e-236 | pbuX | F | xanthine permease | ||
KEAGBMNG_00245 | 5.3e-104 | 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 | |
KEAGBMNG_00246 | 1.6e-135 | K | DNA-binding helix-turn-helix protein | |||
KEAGBMNG_00247 | 1.6e-304 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
KEAGBMNG_00249 | 3.5e-180 | K | Helix-turn-helix | |||
KEAGBMNG_00250 | 4.1e-37 | |||||
KEAGBMNG_00251 | 3.6e-67 | doc | S | Fic/DOC family | ||
KEAGBMNG_00252 | 6.5e-93 | K | Bacterial regulatory proteins, tetR family | |||
KEAGBMNG_00253 | 1.8e-112 | 1.6.5.2 | S | Flavodoxin-like fold | ||
KEAGBMNG_00254 | 5.7e-44 | yjdF | S | Protein of unknown function (DUF2992) | ||
KEAGBMNG_00256 | 7.9e-51 | |||||
KEAGBMNG_00257 | 2.1e-50 | S | Domain of unknown function (DUF4160) | |||
KEAGBMNG_00258 | 3.1e-58 | yjdF | S | Protein of unknown function (DUF2992) | ||
KEAGBMNG_00259 | 3.9e-98 | ogt | 2.1.1.63, 3.2.2.20 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
KEAGBMNG_00260 | 2.6e-94 | |||||
KEAGBMNG_00261 | 1.8e-272 | frc | 2.8.3.16, 2.8.3.19 | 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 | |
KEAGBMNG_00262 | 0.0 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
KEAGBMNG_00263 | 8.6e-186 | yfdV | S | Membrane transport protein | ||
KEAGBMNG_00264 | 7.1e-40 | |||||
KEAGBMNG_00265 | 2.4e-22 | 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 | |
KEAGBMNG_00266 | 6.7e-188 | 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 | |
KEAGBMNG_00267 | 4.9e-67 | S | Putative adhesin | |||
KEAGBMNG_00268 | 9.3e-80 | |||||
KEAGBMNG_00269 | 9.3e-08 | |||||
KEAGBMNG_00270 | 2.6e-282 | pipD | E | Dipeptidase | ||
KEAGBMNG_00271 | 1.4e-231 | 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 | |
KEAGBMNG_00272 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
KEAGBMNG_00273 | 1e-187 | ABC-SBP | S | ABC transporter | ||
KEAGBMNG_00274 | 4.9e-141 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
KEAGBMNG_00275 | 6.9e-136 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
KEAGBMNG_00276 | 3.2e-284 | ybeC | E | amino acid | ||
KEAGBMNG_00277 | 8e-41 | rpmE2 | J | Ribosomal protein L31 | ||
KEAGBMNG_00278 | 2.9e-262 | 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 | |
KEAGBMNG_00279 | 7.7e-261 | 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 | |
KEAGBMNG_00280 | 5.9e-61 | 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 | |
KEAGBMNG_00281 | 1.1e-217 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
KEAGBMNG_00282 | 2.4e-124 | S | (CBS) domain | |||
KEAGBMNG_00283 | 8.1e-182 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KEAGBMNG_00284 | 3.9e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
KEAGBMNG_00285 | 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 | ||
KEAGBMNG_00286 | 1.8e-34 | yabO | J | S4 domain protein | ||
KEAGBMNG_00287 | 2.3e-60 | divIC | D | Septum formation initiator | ||
KEAGBMNG_00288 | 9.9e-61 | yabR | J | S1 RNA binding domain | ||
KEAGBMNG_00289 | 2.4e-250 | 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 | |
KEAGBMNG_00290 | 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 | ||
KEAGBMNG_00291 | 0.0 | S | membrane | |||
KEAGBMNG_00292 | 4.9e-162 | 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 | ||
KEAGBMNG_00293 | 8.9e-192 | 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 | ||
KEAGBMNG_00294 | 1.5e-296 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
KEAGBMNG_00295 | 1.6e-08 | |||||
KEAGBMNG_00297 | 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 | ||
KEAGBMNG_00298 | 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 | |
KEAGBMNG_00299 | 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 | |
KEAGBMNG_00300 | 4e-111 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
KEAGBMNG_00301 | 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 | ||
KEAGBMNG_00302 | 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 | ||
KEAGBMNG_00303 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
KEAGBMNG_00304 | 5.8e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
KEAGBMNG_00305 | 2.2e-111 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
KEAGBMNG_00306 | 2.3e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
KEAGBMNG_00307 | 2.2e-45 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
KEAGBMNG_00308 | 5.6e-155 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
KEAGBMNG_00309 | 5e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
KEAGBMNG_00310 | 4e-54 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
KEAGBMNG_00311 | 9.4e-121 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
KEAGBMNG_00312 | 6.6e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
KEAGBMNG_00313 | 2.2e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
KEAGBMNG_00314 | 7.7e-42 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
KEAGBMNG_00315 | 5.6e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
KEAGBMNG_00316 | 1.4e-34 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
KEAGBMNG_00317 | 4.2e-95 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
KEAGBMNG_00318 | 2.3e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
KEAGBMNG_00319 | 2.7e-67 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
KEAGBMNG_00320 | 5e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
KEAGBMNG_00321 | 1.9e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
KEAGBMNG_00322 | 1.9e-76 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
KEAGBMNG_00323 | 1.4e-23 | rpmD | J | Ribosomal protein L30 | ||
KEAGBMNG_00324 | 1.3e-70 | rplO | J | Binds to the 23S rRNA | ||
KEAGBMNG_00325 | 5.8e-236 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
KEAGBMNG_00326 | 2.7e-120 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
KEAGBMNG_00327 | 1.4e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
KEAGBMNG_00328 | 6e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
KEAGBMNG_00329 | 4.2e-56 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
KEAGBMNG_00330 | 2.6e-62 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
KEAGBMNG_00331 | 1.3e-171 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
KEAGBMNG_00332 | 1.3e-61 | rplQ | J | Ribosomal protein L17 | ||
KEAGBMNG_00333 | 5.1e-156 | 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 | ||
KEAGBMNG_00334 | 2.2e-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 | |
KEAGBMNG_00335 | 2.1e-143 | 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 | ||
KEAGBMNG_00336 | 4.2e-152 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
KEAGBMNG_00337 | 4.5e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
KEAGBMNG_00338 | 1.5e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
KEAGBMNG_00339 | 1.8e-80 | |||||
KEAGBMNG_00340 | 1.2e-160 | 1.6.5.2 | GM | NmrA-like family | ||
KEAGBMNG_00341 | 3.8e-110 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
KEAGBMNG_00342 | 4.3e-129 | pgm3 | G | Belongs to the phosphoglycerate mutase family | ||
KEAGBMNG_00343 | 2.6e-52 | K | Transcriptional regulator, ArsR family | |||
KEAGBMNG_00344 | 3.4e-155 | czcD | P | cation diffusion facilitator family transporter | ||
KEAGBMNG_00345 | 2e-42 | |||||
KEAGBMNG_00346 | 5.4e-26 | |||||
KEAGBMNG_00347 | 1.4e-127 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
KEAGBMNG_00348 | 2.6e-185 | S | AAA domain | |||
KEAGBMNG_00349 | 2.1e-257 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
KEAGBMNG_00350 | 3.6e-102 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
KEAGBMNG_00351 | 1.1e-256 | 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 | ||
KEAGBMNG_00352 | 3.1e-289 | 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) | |
KEAGBMNG_00353 | 2.6e-274 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KEAGBMNG_00354 | 1.7e-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) | ||
KEAGBMNG_00355 | 1.2e-140 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KEAGBMNG_00356 | 8.3e-154 | lacT | K | PRD domain | ||
KEAGBMNG_00357 | 1.9e-56 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
KEAGBMNG_00358 | 7.5e-292 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
KEAGBMNG_00359 | 5.3e-291 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
KEAGBMNG_00360 | 1.9e-98 | yvrI | K | sigma factor activity | ||
KEAGBMNG_00361 | 1.7e-34 | |||||
KEAGBMNG_00362 | 1.1e-289 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
KEAGBMNG_00363 | 3.3e-211 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
KEAGBMNG_00364 | 4e-253 | 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) | |
KEAGBMNG_00365 | 5.6e-228 | G | Major Facilitator Superfamily | |||
KEAGBMNG_00366 | 1.3e-193 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
KEAGBMNG_00367 | 1.8e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
KEAGBMNG_00368 | 9.1e-12 | 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 | ||
KEAGBMNG_00369 | 2e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
KEAGBMNG_00370 | 5.3e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
KEAGBMNG_00371 | 1.6e-123 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
KEAGBMNG_00372 | 4.6e-109 | glnP | P | ABC transporter permease | ||
KEAGBMNG_00373 | 8.8e-116 | glnQ | 3.6.3.21 | E | ABC transporter | |
KEAGBMNG_00374 | 6.2e-148 | aatB | ET | ABC transporter substrate-binding protein | ||
KEAGBMNG_00375 | 3.1e-96 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
KEAGBMNG_00376 | 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 | ||
KEAGBMNG_00377 | 1.3e-149 | kcsA | P | Ion transport protein | ||
KEAGBMNG_00378 | 1.6e-32 | |||||
KEAGBMNG_00379 | 3.9e-113 | rsmC | 2.1.1.172 | J | Methyltransferase | |
KEAGBMNG_00380 | 1.9e-23 | |||||
KEAGBMNG_00381 | 8.4e-81 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
KEAGBMNG_00382 | 0.0 | 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 | |
KEAGBMNG_00383 | 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 | ||
KEAGBMNG_00384 | 6.2e-108 | 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 | ||
KEAGBMNG_00385 | 2.4e-26 | S | Protein of unknown function (DUF2508) | |||
KEAGBMNG_00386 | 3.7e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
KEAGBMNG_00387 | 4.5e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
KEAGBMNG_00388 | 2.8e-154 | holB | 2.7.7.7 | L | DNA polymerase III | |
KEAGBMNG_00389 | 1.3e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
KEAGBMNG_00390 | 1.8e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
KEAGBMNG_00391 | 8.7e-128 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
KEAGBMNG_00392 | 8.9e-87 | folT | S | ECF transporter, substrate-specific component | ||
KEAGBMNG_00393 | 1.5e-132 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
KEAGBMNG_00394 | 5.8e-100 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
KEAGBMNG_00395 | 5.6e-197 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
KEAGBMNG_00396 | 4.3e-09 | D | nuclear chromosome segregation | |||
KEAGBMNG_00397 | 8.4e-10 | D | nuclear chromosome segregation | |||
KEAGBMNG_00398 | 1.3e-170 | |||||
KEAGBMNG_00399 | 4.2e-115 | |||||
KEAGBMNG_00400 | 1e-240 | clcA | P | chloride | ||
KEAGBMNG_00401 | 4.5e-48 | |||||
KEAGBMNG_00402 | 2.1e-99 | S | Protein of unknown function (DUF3990) | |||
KEAGBMNG_00403 | 1.4e-189 | guaC | 1.1.1.205, 1.7.1.7 | 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 | |
KEAGBMNG_00404 | 4.1e-250 | 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 | |
KEAGBMNG_00405 | 1.3e-246 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
KEAGBMNG_00406 | 2.3e-78 | apfA | 2.7.7.72, 3.6.1.61 | F | NUDIX domain | |
KEAGBMNG_00407 | 1.2e-48 | L | bacterial-type proximal promoter sequence-specific DNA binding | |||
KEAGBMNG_00408 | 1.7e-53 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
KEAGBMNG_00409 | 5e-234 | yfdE | 2.8.3.16, 2.8.3.19 | 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 | |
KEAGBMNG_00410 | 6.7e-153 | K | helix_turn_helix, arabinose operon control protein | |||
KEAGBMNG_00411 | 0.0 | bglX | 3.2.1.21 | GH3 | G | hydrolase, family 3 |
KEAGBMNG_00412 | 0.0 | scrA | 2.7.1.211 | G | phosphotransferase system | |
KEAGBMNG_00413 | 9.7e-307 | scrB | 2.7.1.211, 3.2.1.26 | GH32 | G | Glycosyl hydrolases family 32 |
KEAGBMNG_00414 | 9.3e-155 | K | Helix-turn-helix XRE-family like proteins | |||
KEAGBMNG_00415 | 8.3e-68 | |||||
KEAGBMNG_00416 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
KEAGBMNG_00417 | 8.7e-116 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
KEAGBMNG_00418 | 3e-104 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
KEAGBMNG_00419 | 1e-78 | XK27_02470 | K | LytTr DNA-binding domain | ||
KEAGBMNG_00420 | 1.7e-123 | liaI | S | membrane | ||
KEAGBMNG_00421 | 8.8e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
KEAGBMNG_00422 | 8.2e-296 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
KEAGBMNG_00424 | 0.0 | fhaB | 4.3.1.7 | UW | LPXTG-motif cell wall anchor domain protein | |
KEAGBMNG_00425 | 0.0 | nisT | V | ABC transporter | ||
KEAGBMNG_00426 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
KEAGBMNG_00427 | 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 | ||
KEAGBMNG_00428 | 1.6e-100 | 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 | |
KEAGBMNG_00429 | 1.4e-187 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
KEAGBMNG_00430 | 4.5e-31 | yajC | U | Preprotein translocase | ||
KEAGBMNG_00431 | 4.9e-284 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
KEAGBMNG_00432 | 1.4e-209 | 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 | |
KEAGBMNG_00433 | 6.6e-184 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
KEAGBMNG_00434 | 1.5e-229 | 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 | |
KEAGBMNG_00435 | 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 | |
KEAGBMNG_00436 | 2.6e-42 | yrzL | S | Belongs to the UPF0297 family | ||
KEAGBMNG_00437 | 1.4e-72 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
KEAGBMNG_00438 | 1.8e-50 | yrzB | S | Belongs to the UPF0473 family | ||
KEAGBMNG_00439 | 1.6e-91 | cvpA | S | Colicin V production protein | ||
KEAGBMNG_00440 | 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 | ||
KEAGBMNG_00441 | 6.6e-53 | trxA | O | Belongs to the thioredoxin family | ||
KEAGBMNG_00442 | 2.4e-68 | yslB | S | Protein of unknown function (DUF2507) | ||
KEAGBMNG_00443 | 6.5e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
KEAGBMNG_00444 | 2.2e-116 | 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 | |
KEAGBMNG_00445 | 9.1e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KEAGBMNG_00446 | 1e-159 | ykuT | M | mechanosensitive ion channel | ||
KEAGBMNG_00448 | 4e-51 | |||||
KEAGBMNG_00449 | 5.9e-213 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
KEAGBMNG_00450 | 4.3e-178 | ccpA | K | catabolite control protein A | ||
KEAGBMNG_00451 | 1.9e-300 | V | ABC transporter transmembrane region | |||
KEAGBMNG_00452 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
KEAGBMNG_00453 | 2.4e-275 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
KEAGBMNG_00454 | 8e-268 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
KEAGBMNG_00455 | 2e-55 | |||||
KEAGBMNG_00456 | 3.6e-268 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
KEAGBMNG_00457 | 9.1e-98 | yutD | S | Protein of unknown function (DUF1027) | ||
KEAGBMNG_00458 | 3.6e-148 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
KEAGBMNG_00459 | 8.6e-105 | S | Protein of unknown function (DUF1461) | |||
KEAGBMNG_00460 | 2.7e-117 | dedA | S | SNARE-like domain protein | ||
KEAGBMNG_00461 | 4.8e-179 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
KEAGBMNG_00462 | 6e-61 | yugI | 5.3.1.9 | J | general stress protein | |
KEAGBMNG_00467 | 1.1e-217 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
KEAGBMNG_00468 | 3.2e-259 | qacA | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00469 | 6.8e-130 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KEAGBMNG_00470 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KEAGBMNG_00471 | 7.1e-303 | ytgP | S | Polysaccharide biosynthesis protein | ||
KEAGBMNG_00472 | 2.2e-218 | I | Protein of unknown function (DUF2974) | |||
KEAGBMNG_00473 | 8e-121 | |||||
KEAGBMNG_00474 | 3.8e-151 | 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 | |
KEAGBMNG_00475 | 8.3e-125 | M | ErfK YbiS YcfS YnhG | |||
KEAGBMNG_00476 | 1.1e-172 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KEAGBMNG_00477 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
KEAGBMNG_00478 | 6.5e-173 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
KEAGBMNG_00479 | 2.4e-50 | |||||
KEAGBMNG_00480 | 6.9e-77 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
KEAGBMNG_00481 | 1.2e-57 | 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | ||
KEAGBMNG_00483 | 3.2e-95 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
KEAGBMNG_00484 | 2.5e-129 | yfeJ | 6.3.5.2 | F | Glutamine amidotransferase class-I | |
KEAGBMNG_00485 | 2.2e-111 | ylbE | GM | NAD(P)H-binding | ||
KEAGBMNG_00486 | 1.8e-83 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
KEAGBMNG_00487 | 3.2e-194 | S | Bacteriocin helveticin-J | |||
KEAGBMNG_00488 | 9.6e-106 | tag | 3.2.2.20 | L | glycosylase | |
KEAGBMNG_00489 | 7.9e-166 | mleP3 | S | Membrane transport protein | ||
KEAGBMNG_00490 | 6.8e-139 | S | CAAX amino terminal protease | |||
KEAGBMNG_00491 | 1.4e-144 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
KEAGBMNG_00492 | 1.5e-256 | emrY | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00493 | 4e-262 | emrY | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00494 | 2e-70 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
KEAGBMNG_00495 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
KEAGBMNG_00496 | 1.4e-77 | 2.3.1.128 | K | acetyltransferase | ||
KEAGBMNG_00497 | 3.4e-146 | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | ||
KEAGBMNG_00498 | 3.2e-103 | yagU | S | Protein of unknown function (DUF1440) | ||
KEAGBMNG_00499 | 4.7e-151 | S | hydrolase | |||
KEAGBMNG_00500 | 8e-75 | K | Transcriptional regulator | |||
KEAGBMNG_00501 | 2.9e-62 | K | Transcriptional regulator | |||
KEAGBMNG_00502 | 5.6e-242 | pyrP | F | Permease | ||
KEAGBMNG_00503 | 1.3e-137 | lacR | K | DeoR C terminal sensor domain | ||
KEAGBMNG_00504 | 9.4e-74 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
KEAGBMNG_00505 | 1.9e-106 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
KEAGBMNG_00506 | 1.6e-128 | S | Domain of unknown function (DUF4867) | |||
KEAGBMNG_00507 | 7.2e-86 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
KEAGBMNG_00508 | 6.3e-51 | 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
KEAGBMNG_00509 | 2.8e-268 | gatC | G | PTS system sugar-specific permease component | ||
KEAGBMNG_00510 | 1.3e-38 | |||||
KEAGBMNG_00511 | 2e-152 | lacT | K | CAT RNA binding domain | ||
KEAGBMNG_00512 | 8.7e-57 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
KEAGBMNG_00513 | 0.0 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
KEAGBMNG_00514 | 5.7e-293 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
KEAGBMNG_00515 | 1e-201 | S | PFAM Archaeal ATPase | |||
KEAGBMNG_00516 | 8.2e-165 | K | LysR family | |||
KEAGBMNG_00517 | 0.0 | 1.3.5.4 | C | FMN_bind | ||
KEAGBMNG_00518 | 3.7e-260 | P | Sodium:sulfate symporter transmembrane region | |||
KEAGBMNG_00519 | 5.7e-169 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
KEAGBMNG_00520 | 3.3e-112 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KEAGBMNG_00521 | 8.7e-218 | mdtG | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00522 | 1.5e-32 | |||||
KEAGBMNG_00523 | 6.1e-73 | K | helix_turn_helix multiple antibiotic resistance protein | |||
KEAGBMNG_00524 | 5.8e-82 | |||||
KEAGBMNG_00525 | 2.7e-210 | pepA | E | M42 glutamyl aminopeptidase | ||
KEAGBMNG_00527 | 5.9e-88 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
KEAGBMNG_00528 | 1.2e-103 | G | PTS system sorbose-specific iic component | |||
KEAGBMNG_00529 | 3.4e-152 | G | PTS system mannose/fructose/sorbose family IID component | |||
KEAGBMNG_00530 | 6.8e-72 | 2.7.1.191 | G | PTS system fructose IIA component | ||
KEAGBMNG_00531 | 0.0 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
KEAGBMNG_00532 | 8.2e-182 | lacI3 | K | helix_turn _helix lactose operon repressor | ||
KEAGBMNG_00533 | 0.0 | 3.2.1.177 | GH31 | G | Glycosyl hydrolases family 31 | |
KEAGBMNG_00534 | 1.6e-266 | dtpT | U | amino acid peptide transporter | ||
KEAGBMNG_00535 | 1.6e-104 | naiP | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00536 | 4.7e-86 | naiP | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00537 | 2.5e-155 | S | Alpha beta hydrolase | |||
KEAGBMNG_00538 | 4.6e-76 | K | Transcriptional regulator, MarR family | |||
KEAGBMNG_00539 | 0.0 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
KEAGBMNG_00540 | 0.0 | V | ABC transporter transmembrane region | |||
KEAGBMNG_00541 | 1.3e-148 | glnH | ET | ABC transporter | ||
KEAGBMNG_00542 | 2.7e-137 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
KEAGBMNG_00543 | 9.1e-150 | glnH | ET | ABC transporter | ||
KEAGBMNG_00544 | 3.2e-110 | gluC | P | ABC transporter permease | ||
KEAGBMNG_00545 | 2e-107 | glnP | P | ABC transporter permease | ||
KEAGBMNG_00546 | 1.3e-156 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KEAGBMNG_00547 | 0.0 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
KEAGBMNG_00548 | 1.1e-130 | treR | K | UTRA | ||
KEAGBMNG_00549 | 0.0 | treB | 2.7.1.211 | G | phosphotransferase system | |
KEAGBMNG_00550 | 8.3e-84 | S | Putative adhesin | |||
KEAGBMNG_00551 | 1.8e-116 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
KEAGBMNG_00552 | 2.6e-158 | EGP | Major facilitator superfamily | |||
KEAGBMNG_00553 | 1.3e-76 | EGP | Major facilitator superfamily | |||
KEAGBMNG_00555 | 6.8e-56 | S | Enterocin A Immunity | |||
KEAGBMNG_00556 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
KEAGBMNG_00557 | 4.3e-163 | rssA | S | Phospholipase, patatin family | ||
KEAGBMNG_00558 | 1.1e-257 | glnPH2 | P | ABC transporter permease | ||
KEAGBMNG_00559 | 1.7e-131 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
KEAGBMNG_00560 | 6.2e-96 | K | Acetyltransferase (GNAT) domain | |||
KEAGBMNG_00561 | 3.5e-160 | pstS | P | Phosphate | ||
KEAGBMNG_00562 | 2.1e-161 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
KEAGBMNG_00563 | 8.3e-157 | pstA | P | Phosphate transport system permease protein PstA | ||
KEAGBMNG_00564 | 1.1e-147 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
KEAGBMNG_00565 | 2.7e-140 | 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 | |
KEAGBMNG_00566 | 2.6e-118 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
KEAGBMNG_00567 | 7.5e-283 | S | C4-dicarboxylate anaerobic carrier | |||
KEAGBMNG_00568 | 5.8e-85 | dps | P | Belongs to the Dps family | ||
KEAGBMNG_00570 | 3.2e-164 | 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 | |
KEAGBMNG_00571 | 4.8e-128 | 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 | |
KEAGBMNG_00572 | 4.1e-175 | rihB | 3.2.2.1 | F | Nucleoside | |
KEAGBMNG_00573 | 4e-133 | gntR | K | UbiC transcription regulator-associated domain protein | ||
KEAGBMNG_00574 | 2e-52 | S | Enterocin A Immunity | |||
KEAGBMNG_00575 | 8.9e-139 | glcR | K | DeoR C terminal sensor domain | ||
KEAGBMNG_00576 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
KEAGBMNG_00577 | 1.6e-120 | C | nitroreductase | |||
KEAGBMNG_00578 | 1.1e-132 | |||||
KEAGBMNG_00579 | 1.6e-252 | yhdP | S | Transporter associated domain | ||
KEAGBMNG_00580 | 5.7e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
KEAGBMNG_00581 | 2.9e-235 | potE | E | amino acid | ||
KEAGBMNG_00582 | 2.6e-137 | M | Glycosyl hydrolases family 25 | |||
KEAGBMNG_00583 | 1.9e-207 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
KEAGBMNG_00584 | 8.6e-251 | celB | 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 | |
KEAGBMNG_00586 | 5.8e-216 | L | Belongs to the 'phage' integrase family | |||
KEAGBMNG_00588 | 3.3e-96 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
KEAGBMNG_00589 | 2.1e-87 | S | Pfam:Peptidase_M78 | |||
KEAGBMNG_00590 | 3.1e-56 | xre | K | Helix-turn-helix domain | ||
KEAGBMNG_00592 | 6e-60 | S | Domain of unknown function (DUF771) | |||
KEAGBMNG_00594 | 2.5e-18 | |||||
KEAGBMNG_00595 | 9.3e-37 | |||||
KEAGBMNG_00596 | 2.8e-154 | S | Protein of unknown function (DUF1351) | |||
KEAGBMNG_00597 | 6.6e-129 | S | ERF superfamily | |||
KEAGBMNG_00598 | 2.1e-171 | yfdO | KL | Conserved phage C-terminus (Phg_2220_C) | ||
KEAGBMNG_00599 | 5.4e-15 | S | sequence-specific DNA binding | |||
KEAGBMNG_00600 | 1.3e-145 | ps308 | K | AntA/AntB antirepressor | ||
KEAGBMNG_00602 | 1.4e-25 | |||||
KEAGBMNG_00606 | 2.4e-62 | |||||
KEAGBMNG_00608 | 1.5e-80 | rusA | 3.1.22.4 | L | Endodeoxyribonuclease RusA | |
KEAGBMNG_00610 | 1.4e-49 | |||||
KEAGBMNG_00611 | 2e-32 | |||||
KEAGBMNG_00612 | 1.8e-25 | |||||
KEAGBMNG_00613 | 2.6e-97 | |||||
KEAGBMNG_00615 | 1.1e-49 | K | chromosome segregation | |||
KEAGBMNG_00617 | 2.8e-119 | C | Domain of unknown function (DUF4145) | |||
KEAGBMNG_00619 | 8.6e-119 | |||||
KEAGBMNG_00620 | 1.7e-85 | ps333 | L | Terminase small subunit | ||
KEAGBMNG_00621 | 7.3e-143 | L | NUMOD1 domain | |||
KEAGBMNG_00622 | 4e-226 | ps334 | S | Terminase-like family | ||
KEAGBMNG_00623 | 2.3e-270 | S | Phage portal protein, SPP1 Gp6-like | |||
KEAGBMNG_00624 | 4.4e-299 | S | Phage Mu protein F like protein | |||
KEAGBMNG_00626 | 6.9e-93 | S | Phage minor structural protein GP20 | |||
KEAGBMNG_00627 | 2.2e-204 | |||||
KEAGBMNG_00628 | 3.8e-66 | |||||
KEAGBMNG_00629 | 6.3e-63 | |||||
KEAGBMNG_00630 | 2e-79 | S | Bacteriophage HK97-gp10, putative tail-component | |||
KEAGBMNG_00631 | 2.3e-69 | |||||
KEAGBMNG_00632 | 1.1e-30 | |||||
KEAGBMNG_00633 | 2.8e-249 | xkdK | S | Phage tail sheath C-terminal domain | ||
KEAGBMNG_00634 | 4.5e-85 | xkdM | S | Phage tail tube protein | ||
KEAGBMNG_00635 | 1.4e-69 | xkdN | S | Phage XkdN-like tail assembly chaperone protein, TAC | ||
KEAGBMNG_00636 | 1.9e-246 | S | phage tail tape measure protein | |||
KEAGBMNG_00637 | 1.6e-112 | ygaU | GH23 | S | protein containing LysM domain | |
KEAGBMNG_00638 | 3.6e-196 | yqbQ | G | domain, Protein | ||
KEAGBMNG_00639 | 5e-60 | S | Protein of unknown function (DUF2577) | |||
KEAGBMNG_00640 | 1.4e-62 | S | Protein of unknown function (DUF2634) | |||
KEAGBMNG_00641 | 3e-215 | xkdT | S | Baseplate J-like protein | ||
KEAGBMNG_00642 | 1.3e-96 | S | Uncharacterised protein conserved in bacteria (DUF2313) | |||
KEAGBMNG_00643 | 0.0 | |||||
KEAGBMNG_00644 | 2.1e-88 | |||||
KEAGBMNG_00646 | 2.3e-64 | |||||
KEAGBMNG_00647 | 4.3e-43 | |||||
KEAGBMNG_00648 | 1.2e-68 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
KEAGBMNG_00649 | 1.9e-180 | lysA2 | M | Glycosyl hydrolases family 25 | ||
KEAGBMNG_00651 | 3.1e-217 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
KEAGBMNG_00652 | 4.2e-89 | gtcA | S | Teichoic acid glycosylation protein | ||
KEAGBMNG_00653 | 8.5e-78 | fld | C | Flavodoxin | ||
KEAGBMNG_00654 | 6.7e-161 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
KEAGBMNG_00655 | 1.6e-166 | yihY | S | Belongs to the UPF0761 family | ||
KEAGBMNG_00656 | 2.3e-170 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
KEAGBMNG_00657 | 2.5e-155 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KEAGBMNG_00658 | 1.2e-180 | E | ABC transporter, ATP-binding protein | |||
KEAGBMNG_00659 | 1.6e-288 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
KEAGBMNG_00660 | 1.9e-68 | O | OsmC-like protein | |||
KEAGBMNG_00661 | 7.1e-20 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
KEAGBMNG_00662 | 9.2e-115 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
KEAGBMNG_00663 | 2.4e-116 | K | response regulator | |||
KEAGBMNG_00664 | 1.2e-233 | sptS | 2.7.13.3 | T | Histidine kinase | |
KEAGBMNG_00665 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
KEAGBMNG_00666 | 2.4e-56 | |||||
KEAGBMNG_00667 | 2.8e-58 | |||||
KEAGBMNG_00668 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
KEAGBMNG_00669 | 9.1e-144 | S | haloacid dehalogenase-like hydrolase | |||
KEAGBMNG_00670 | 1.8e-122 | S | CAAX protease self-immunity | |||
KEAGBMNG_00672 | 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 | |
KEAGBMNG_00673 | 6.6e-72 | |||||
KEAGBMNG_00674 | 9.6e-109 | fic | D | Fic/DOC family | ||
KEAGBMNG_00675 | 6.2e-226 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
KEAGBMNG_00676 | 3.5e-128 | pnb | C | nitroreductase | ||
KEAGBMNG_00677 | 1.1e-98 | S | Domain of unknown function (DUF4811) | |||
KEAGBMNG_00678 | 3.6e-266 | lmrB | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00679 | 4.2e-77 | K | MerR HTH family regulatory protein | |||
KEAGBMNG_00680 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
KEAGBMNG_00681 | 4.6e-61 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
KEAGBMNG_00682 | 4.7e-257 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
KEAGBMNG_00683 | 7.3e-169 | 2.7.1.2 | GK | ROK family | ||
KEAGBMNG_00684 | 3.6e-165 | rhaS6 | K | helix_turn_helix, arabinose operon control protein | ||
KEAGBMNG_00685 | 9.5e-177 | I | Carboxylesterase family | |||
KEAGBMNG_00686 | 1.1e-191 | yhjX | P | Major Facilitator Superfamily | ||
KEAGBMNG_00687 | 2.5e-306 | S | Predicted membrane protein (DUF2207) | |||
KEAGBMNG_00688 | 5.2e-56 | K | Acetyltransferase (GNAT) domain | |||
KEAGBMNG_00689 | 1.4e-59 | |||||
KEAGBMNG_00690 | 1.7e-151 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
KEAGBMNG_00691 | 1.2e-92 | S | ECF-type riboflavin transporter, S component | |||
KEAGBMNG_00692 | 1.6e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
KEAGBMNG_00693 | 1.2e-12 | |||||
KEAGBMNG_00694 | 4.4e-247 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
KEAGBMNG_00695 | 1.2e-149 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
KEAGBMNG_00696 | 7.3e-64 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
KEAGBMNG_00697 | 2e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
KEAGBMNG_00698 | 2.8e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
KEAGBMNG_00699 | 2e-197 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
KEAGBMNG_00700 | 8.3e-102 | 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 | ||
KEAGBMNG_00701 | 2.2e-73 | yqhY | S | Asp23 family, cell envelope-related function | ||
KEAGBMNG_00702 | 8e-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 | ||
KEAGBMNG_00703 | 2.1e-154 | 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 | |
KEAGBMNG_00704 | 1.5e-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 | |
KEAGBMNG_00705 | 3.8e-35 | 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 | |
KEAGBMNG_00706 | 7.8e-160 | 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 | |
KEAGBMNG_00707 | 3.7e-156 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
KEAGBMNG_00708 | 9.1e-266 | recN | L | May be involved in recombinational repair of damaged DNA | ||
KEAGBMNG_00709 | 4.6e-48 | |||||
KEAGBMNG_00710 | 1.6e-111 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
KEAGBMNG_00711 | 1.7e-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 | |
KEAGBMNG_00712 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
KEAGBMNG_00713 | 7.1e-175 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
KEAGBMNG_00714 | 1.2e-244 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
KEAGBMNG_00715 | 4.5e-140 | stp | 3.1.3.16 | T | phosphatase | |
KEAGBMNG_00716 | 0.0 | KLT | serine threonine protein kinase | |||
KEAGBMNG_00717 | 2.8e-165 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
KEAGBMNG_00718 | 1.8e-121 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
KEAGBMNG_00719 | 1e-122 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
KEAGBMNG_00720 | 1.6e-25 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
KEAGBMNG_00721 | 1.4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
KEAGBMNG_00722 | 9.6e-308 | yloV | S | DAK2 domain fusion protein YloV | ||
KEAGBMNG_00723 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
KEAGBMNG_00724 | 5.8e-183 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
KEAGBMNG_00725 | 2.6e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
KEAGBMNG_00726 | 1.1e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
KEAGBMNG_00727 | 4.4e-180 | oppF | P | Belongs to the ABC transporter superfamily | ||
KEAGBMNG_00728 | 7.5e-180 | oppB | P | ABC transporter permease | ||
KEAGBMNG_00729 | 2.1e-163 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
KEAGBMNG_00730 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
KEAGBMNG_00731 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
KEAGBMNG_00732 | 1.6e-123 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
KEAGBMNG_00733 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
KEAGBMNG_00734 | 7.8e-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) | ||
KEAGBMNG_00735 | 1.6e-287 | pipD | E | Dipeptidase | ||
KEAGBMNG_00736 | 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 | ||
KEAGBMNG_00737 | 1.4e-227 | 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 | |
KEAGBMNG_00738 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
KEAGBMNG_00739 | 7.4e-97 | 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 | ||
KEAGBMNG_00740 | 2.2e-136 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
KEAGBMNG_00741 | 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 | ||
KEAGBMNG_00742 | 9.3e-118 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
KEAGBMNG_00743 | 6.5e-75 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
KEAGBMNG_00744 | 1.1e-115 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
KEAGBMNG_00745 | 7.9e-114 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
KEAGBMNG_00746 | 1.5e-34 | ynzC | S | UPF0291 protein | ||
KEAGBMNG_00747 | 1.5e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
KEAGBMNG_00748 | 0.0 | mdlA | V | ABC transporter | ||
KEAGBMNG_00749 | 6.1e-300 | mdlB | V | ABC transporter | ||
KEAGBMNG_00750 | 1.1e-219 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
KEAGBMNG_00751 | 9.8e-117 | plsC | 2.3.1.51 | I | Acyltransferase | |
KEAGBMNG_00752 | 3e-195 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
KEAGBMNG_00753 | 9.6e-141 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
KEAGBMNG_00754 | 3.5e-183 | 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 | ||
KEAGBMNG_00755 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
KEAGBMNG_00756 | 3.4e-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 | ||
KEAGBMNG_00757 | 1.4e-135 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
KEAGBMNG_00758 | 3.4e-138 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
KEAGBMNG_00759 | 1.9e-231 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
KEAGBMNG_00760 | 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 | |
KEAGBMNG_00761 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KEAGBMNG_00762 | 4.7e-82 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
KEAGBMNG_00763 | 2.3e-218 | nusA | K | Participates in both transcription termination and antitermination | ||
KEAGBMNG_00764 | 2e-46 | ylxR | K | Protein of unknown function (DUF448) | ||
KEAGBMNG_00765 | 4.2e-47 | rplGA | J | ribosomal protein | ||
KEAGBMNG_00766 | 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 | ||
KEAGBMNG_00767 | 7.9e-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 | ||
KEAGBMNG_00768 | 1.4e-167 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
KEAGBMNG_00769 | 7.6e-177 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
KEAGBMNG_00770 | 1.6e-282 | lsa | S | ABC transporter | ||
KEAGBMNG_00771 | 6.7e-121 | S | GyrI-like small molecule binding domain | |||
KEAGBMNG_00772 | 2.9e-193 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
KEAGBMNG_00773 | 8.5e-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 | ||
KEAGBMNG_00774 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
KEAGBMNG_00775 | 1.6e-171 | 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 | ||
KEAGBMNG_00776 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
KEAGBMNG_00777 | 9.3e-124 | srtA | 3.4.22.70 | M | sortase family | |
KEAGBMNG_00778 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
KEAGBMNG_00779 | 1.3e-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 | |
KEAGBMNG_00780 | 1.1e-278 | yjeM | E | Amino Acid | ||
KEAGBMNG_00781 | 9.2e-286 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
KEAGBMNG_00782 | 9.4e-191 | 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 | |
KEAGBMNG_00783 | 1.6e-96 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
KEAGBMNG_00784 | 3e-251 | G | Major Facilitator | |||
KEAGBMNG_00785 | 1.5e-54 | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
KEAGBMNG_00786 | 0.0 | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
KEAGBMNG_00787 | 1.4e-158 | lysR5 | K | LysR substrate binding domain | ||
KEAGBMNG_00789 | 2.2e-102 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KEAGBMNG_00790 | 1.6e-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 | |
KEAGBMNG_00791 | 3.7e-18 | S | Sugar efflux transporter for intercellular exchange | |||
KEAGBMNG_00792 | 1.1e-310 | ybiT | S | ABC transporter, ATP-binding protein | ||
KEAGBMNG_00793 | 9.2e-42 | K | Helix-turn-helix domain | |||
KEAGBMNG_00794 | 2.8e-146 | F | DNA/RNA non-specific endonuclease | |||
KEAGBMNG_00795 | 1.5e-60 | L | nuclease | |||
KEAGBMNG_00796 | 6.1e-157 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
KEAGBMNG_00797 | 1.6e-188 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
KEAGBMNG_00798 | 2.8e-67 | metI | P | ABC transporter permease | ||
KEAGBMNG_00799 | 1e-265 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
KEAGBMNG_00800 | 7.2e-261 | frdC | 1.3.5.4 | C | FAD binding domain | |
KEAGBMNG_00801 | 2.3e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KEAGBMNG_00802 | 2.2e-257 | yjjP | S | Putative threonine/serine exporter | ||
KEAGBMNG_00803 | 2.5e-189 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
KEAGBMNG_00804 | 0.0 | aha1 | P | E1-E2 ATPase | ||
KEAGBMNG_00805 | 0.0 | S | Bacterial membrane protein, YfhO | |||
KEAGBMNG_00806 | 3e-87 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
KEAGBMNG_00807 | 4.6e-174 | prmA | J | Ribosomal protein L11 methyltransferase | ||
KEAGBMNG_00808 | 1.4e-65 | |||||
KEAGBMNG_00809 | 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 | |
KEAGBMNG_00810 | 7.3e-74 | 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 | ||
KEAGBMNG_00811 | 1.1e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
KEAGBMNG_00812 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
KEAGBMNG_00813 | 3.1e-73 | |||||
KEAGBMNG_00814 | 1.5e-82 | mutT | 3.6.1.55 | F | NUDIX domain | |
KEAGBMNG_00815 | 5.8e-35 | |||||
KEAGBMNG_00816 | 7.2e-68 | |||||
KEAGBMNG_00817 | 1.6e-64 | S | Domain of unknown function DUF1828 | |||
KEAGBMNG_00818 | 7.4e-88 | S | Rib/alpha-like repeat | |||
KEAGBMNG_00819 | 7.7e-247 | yagE | E | amino acid | ||
KEAGBMNG_00820 | 5.1e-116 | GM | NmrA-like family | |||
KEAGBMNG_00821 | 1.9e-96 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
KEAGBMNG_00822 | 1.8e-175 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
KEAGBMNG_00823 | 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 | ||
KEAGBMNG_00824 | 3.5e-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 | ||
KEAGBMNG_00825 | 0.0 | oatA | I | Acyltransferase | ||
KEAGBMNG_00826 | 1.4e-178 | 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 | |
KEAGBMNG_00827 | 9.3e-144 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
KEAGBMNG_00828 | 7.5e-47 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
KEAGBMNG_00829 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
KEAGBMNG_00830 | 4.3e-310 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KEAGBMNG_00831 | 2.1e-28 | S | Protein of unknown function (DUF2929) | |||
KEAGBMNG_00832 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
KEAGBMNG_00834 | 2.7e-182 | 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 | |
KEAGBMNG_00835 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
KEAGBMNG_00836 | 1.5e-166 | cvfB | S | S1 domain | ||
KEAGBMNG_00837 | 2.5e-169 | xerD | D | recombinase XerD | ||
KEAGBMNG_00838 | 3.1e-62 | ribT | K | acetyltransferase | ||
KEAGBMNG_00839 | 1.1e-135 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
KEAGBMNG_00840 | 2.9e-105 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
KEAGBMNG_00841 | 1.8e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KEAGBMNG_00842 | 1.9e-58 | M | Lysin motif | |||
KEAGBMNG_00843 | 3.4e-98 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the 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. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
KEAGBMNG_00844 | 1.4e-116 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
KEAGBMNG_00845 | 2.3e-218 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KEAGBMNG_00846 | 1e-240 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KEAGBMNG_00847 | 2e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KEAGBMNG_00848 | 5.9e-233 | S | Tetratricopeptide repeat protein | |||
KEAGBMNG_00849 | 0.0 | KL | domain protein | |||
KEAGBMNG_00850 | 2.6e-134 | |||||
KEAGBMNG_00851 | 5e-187 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KEAGBMNG_00852 | 1.3e-24 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KEAGBMNG_00853 | 1.6e-224 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KEAGBMNG_00854 | 2.4e-178 | L | Belongs to the 'phage' integrase family | |||
KEAGBMNG_00855 | 4.2e-195 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KEAGBMNG_00856 | 2.4e-178 | L | Belongs to the 'phage' integrase family | |||
KEAGBMNG_00857 | 2.7e-211 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KEAGBMNG_00858 | 0.0 | hsdR | 3.1.21.3 | V | EcoEI R protein C-terminal | |
KEAGBMNG_00859 | 0.0 | S | Protein of unknown function DUF262 | |||
KEAGBMNG_00860 | 0.0 | 1.3.5.4 | C | FMN_bind | ||
KEAGBMNG_00861 | 7.2e-92 | |||||
KEAGBMNG_00862 | 9.2e-109 | |||||
KEAGBMNG_00863 | 3.8e-162 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
KEAGBMNG_00864 | 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 | |
KEAGBMNG_00865 | 2.6e-115 | hlyIII | S | protein, hemolysin III | ||
KEAGBMNG_00866 | 2.6e-152 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
KEAGBMNG_00867 | 9.2e-36 | yozE | S | Belongs to the UPF0346 family | ||
KEAGBMNG_00868 | 1.3e-265 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
KEAGBMNG_00869 | 3.2e-158 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
KEAGBMNG_00870 | 9.8e-135 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KEAGBMNG_00871 | 6.6e-156 | dprA | LU | DNA protecting protein DprA | ||
KEAGBMNG_00872 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
KEAGBMNG_00873 | 3e-248 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
KEAGBMNG_00874 | 2.5e-172 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
KEAGBMNG_00875 | 9.7e-89 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
KEAGBMNG_00876 | 8.2e-252 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
KEAGBMNG_00877 | 5.3e-180 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
KEAGBMNG_00878 | 1.1e-104 | K | LysR substrate binding domain | |||
KEAGBMNG_00879 | 3.4e-100 | S | LexA-binding, inner membrane-associated putative hydrolase | |||
KEAGBMNG_00881 | 3.5e-66 | |||||
KEAGBMNG_00882 | 1.1e-179 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
KEAGBMNG_00883 | 1.1e-71 | K | Transcriptional regulator | |||
KEAGBMNG_00884 | 5.6e-52 | |||||
KEAGBMNG_00885 | 1.1e-42 | |||||
KEAGBMNG_00886 | 1.8e-41 | K | peptidyl-tyrosine sulfation | |||
KEAGBMNG_00887 | 6.6e-124 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KEAGBMNG_00888 | 2e-112 | ybbL | S | ABC transporter, ATP-binding protein | ||
KEAGBMNG_00889 | 7.9e-132 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
KEAGBMNG_00890 | 3e-98 | K | Acetyltransferase (GNAT) domain | |||
KEAGBMNG_00891 | 2.8e-51 | S | Protein of unknown function (DUF3021) | |||
KEAGBMNG_00892 | 1.3e-75 | K | LytTr DNA-binding domain | |||
KEAGBMNG_00893 | 7.9e-107 | S | Protein of unknown function (DUF1211) | |||
KEAGBMNG_00894 | 0.0 | S | domain, Protein | |||
KEAGBMNG_00896 | 0.0 | bamA | UW | LPXTG-motif cell wall anchor domain protein | ||
KEAGBMNG_00897 | 0.0 | M | domain protein | |||
KEAGBMNG_00899 | 5.7e-302 | |||||
KEAGBMNG_00900 | 6e-111 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
KEAGBMNG_00901 | 7.4e-120 | 3.6.1.55 | F | NUDIX domain | ||
KEAGBMNG_00902 | 4.4e-71 | S | Putative adhesin | |||
KEAGBMNG_00903 | 2.2e-249 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
KEAGBMNG_00904 | 4.7e-12 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
KEAGBMNG_00905 | 5.9e-17 | L | Plasmid pRiA4b ORF-3-like protein | |||
KEAGBMNG_00906 | 5.2e-68 | K | HxlR family | |||
KEAGBMNG_00907 | 2.7e-48 | |||||
KEAGBMNG_00908 | 5.1e-231 | 4.2.1.6, 5.1.2.2 | M | Mandelate racemase muconate lactonizing enzyme | ||
KEAGBMNG_00909 | 2.5e-11 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
KEAGBMNG_00910 | 3e-76 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
KEAGBMNG_00911 | 3.2e-292 | P | ABC transporter | |||
KEAGBMNG_00912 | 1.8e-292 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KEAGBMNG_00913 | 1.2e-41 | yphH | S | Cupin domain | ||
KEAGBMNG_00914 | 1.4e-189 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
KEAGBMNG_00915 | 4.4e-35 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
KEAGBMNG_00916 | 1.7e-32 | mta | K | helix_turn_helix, mercury resistance | ||
KEAGBMNG_00917 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
KEAGBMNG_00918 | 3.9e-126 | lmrA | 3.6.3.44 | V | ABC transporter | |
KEAGBMNG_00919 | 3.8e-156 | C | Aldo keto reductase | |||
KEAGBMNG_00921 | 9.2e-101 | K | Transcriptional regulator C-terminal region | |||
KEAGBMNG_00922 | 1.7e-231 | E | Alpha/beta hydrolase of unknown function (DUF1100) | |||
KEAGBMNG_00923 | 2.1e-117 | GM | NAD(P)H-binding | |||
KEAGBMNG_00924 | 1.7e-216 | mdt(A) | EGP | Major facilitator Superfamily | ||
KEAGBMNG_00925 | 2.2e-61 | S | Sulfite exporter TauE/SafE | |||
KEAGBMNG_00926 | 1.9e-32 | G | Major facilitator Superfamily | |||
KEAGBMNG_00927 | 4.8e-265 | npr | 1.11.1.1 | C | NADH oxidase | |
KEAGBMNG_00928 | 2.3e-63 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
KEAGBMNG_00929 | 4.1e-30 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
KEAGBMNG_00930 | 3e-173 | yobV1 | K | WYL domain | ||
KEAGBMNG_00931 | 2.4e-68 | S | pyridoxamine 5-phosphate | |||
KEAGBMNG_00932 | 5.5e-50 | K | LytTr DNA-binding domain | |||
KEAGBMNG_00933 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
KEAGBMNG_00934 | 4.6e-35 | copZ | C | Heavy-metal-associated domain | ||
KEAGBMNG_00935 | 1.4e-93 | dps | P | Belongs to the Dps family | ||
KEAGBMNG_00936 | 1.5e-112 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | |
KEAGBMNG_00937 | 2.1e-96 | K | Acetyltransferase (GNAT) family | |||
KEAGBMNG_00938 | 6.9e-80 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
KEAGBMNG_00939 | 5.5e-50 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
KEAGBMNG_00940 | 6.2e-76 | K | Transcriptional regulator | |||
KEAGBMNG_00941 | 7.9e-69 | ogt | 2.1.1.63 | L | methylated-DNA-[protein]-cysteine S-methyltransferase activity | |
KEAGBMNG_00942 | 2.5e-86 | XK27_09675 | K | Acetyltransferase (GNAT) domain | ||
KEAGBMNG_00943 | 1e-124 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
KEAGBMNG_00944 | 6.8e-245 | yrvN | L | AAA C-terminal domain | ||
KEAGBMNG_00945 | 3e-34 | 4.1.1.45 | S | Amidohydrolase | ||
KEAGBMNG_00946 | 2.3e-105 | 4.1.1.45 | S | Amidohydrolase | ||
KEAGBMNG_00947 | 9e-122 | ybhL | S | Belongs to the BI1 family | ||
KEAGBMNG_00948 | 2.9e-14 | C | Aldo/keto reductase family | |||
KEAGBMNG_00949 | 1.1e-74 | C | Aldo/keto reductase family | |||
KEAGBMNG_00950 | 5.1e-167 | akr5f | 1.1.1.346 | S | reductase | |
KEAGBMNG_00951 | 1.8e-124 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
KEAGBMNG_00952 | 2.6e-109 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
KEAGBMNG_00953 | 8.9e-116 | plsY | 2.3.1.15, 3.5.1.104 | 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 | |
KEAGBMNG_00954 | 0.0 | parE | 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 | |
KEAGBMNG_00955 | 0.0 | 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 | |
KEAGBMNG_00956 | 2.2e-179 | K | Transcriptional regulator | |||
KEAGBMNG_00957 | 2.8e-171 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
KEAGBMNG_00958 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
KEAGBMNG_00959 | 7.7e-111 | 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 | |
KEAGBMNG_00960 | 1.5e-124 | yoaK | S | Protein of unknown function (DUF1275) | ||
KEAGBMNG_00961 | 4.9e-204 | xerS | L | Belongs to the 'phage' integrase family | ||
KEAGBMNG_00962 | 6.7e-167 | K | Transcriptional regulator | |||
KEAGBMNG_00963 | 3.7e-151 | |||||
KEAGBMNG_00964 | 2e-163 | degV | S | EDD domain protein, DegV family | ||
KEAGBMNG_00965 | 3.8e-64 | |||||
KEAGBMNG_00966 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
KEAGBMNG_00967 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
KEAGBMNG_00968 | 3.3e-197 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
KEAGBMNG_00969 | 1.3e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KEAGBMNG_00970 | 2.3e-78 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
KEAGBMNG_00971 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
KEAGBMNG_00972 | 9.9e-58 | |||||
KEAGBMNG_00973 | 1.2e-174 | degV | S | DegV family | ||
KEAGBMNG_00974 | 3.4e-241 | cpdA | S | Calcineurin-like phosphoesterase | ||
KEAGBMNG_00975 | 2.4e-217 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
KEAGBMNG_00976 | 2e-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 | ||
KEAGBMNG_00977 | 4.2e-106 | ypsA | S | Belongs to the UPF0398 family | ||
KEAGBMNG_00978 | 1.6e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
KEAGBMNG_00979 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
KEAGBMNG_00980 | 4.2e-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 | |
KEAGBMNG_00981 | 6.7e-116 | dnaD | L | DnaD domain protein | ||
KEAGBMNG_00982 | 2.9e-259 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
KEAGBMNG_00983 | 4.8e-90 | ypmB | S | Protein conserved in bacteria | ||
KEAGBMNG_00984 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
KEAGBMNG_00985 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
KEAGBMNG_00986 | 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 | |
KEAGBMNG_00987 | 4.4e-169 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
KEAGBMNG_00988 | 3e-176 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
KEAGBMNG_00989 | 4.1e-203 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
KEAGBMNG_00990 | 5.2e-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) | |
KEAGBMNG_00991 | 1.6e-272 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KEAGBMNG_00992 | 2.2e-290 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KEAGBMNG_00993 | 1.6e-159 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
KEAGBMNG_00994 | 6.1e-160 | rbsU | U | ribose uptake protein RbsU | ||
KEAGBMNG_00995 | 3.9e-66 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
KEAGBMNG_00996 | 8e-84 | 6.3.3.2 | S | ASCH | ||
KEAGBMNG_00997 | 1.2e-134 | 2.4.2.3 | F | Phosphorylase superfamily | ||
KEAGBMNG_00998 | 1.5e-88 | 2.3.1.57 | K | Acetyltransferase (GNAT) family | ||
KEAGBMNG_00999 | 1.4e-98 | rimL | J | Acetyltransferase (GNAT) domain | ||
KEAGBMNG_01000 | 2.5e-43 | |||||
KEAGBMNG_01001 | 2.7e-51 | S | endonuclease activity | |||
KEAGBMNG_01002 | 2.1e-151 | S | Fic/DOC family | |||
KEAGBMNG_01003 | 6e-143 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
KEAGBMNG_01004 | 5.6e-40 | |||||
KEAGBMNG_01005 | 1.4e-135 | |||||
KEAGBMNG_01006 | 2.1e-63 | |||||
KEAGBMNG_01007 | 1.6e-48 | S | MazG-like family | |||
KEAGBMNG_01008 | 1.9e-152 | S | Protein of unknown function (DUF2785) | |||
KEAGBMNG_01009 | 1.2e-22 | K | Acetyltransferase (GNAT) domain | |||
KEAGBMNG_01010 | 4.5e-36 | K | Acetyltransferase (GNAT) domain | |||
KEAGBMNG_01011 | 1.1e-48 | |||||
KEAGBMNG_01012 | 5e-282 | V | ABC transporter transmembrane region | |||
KEAGBMNG_01013 | 1.7e-84 | C | nitroreductase | |||
KEAGBMNG_01014 | 2e-294 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KEAGBMNG_01015 | 2e-149 | ropB | K | Helix-turn-helix domain | ||
KEAGBMNG_01016 | 1.6e-128 | qmcA | O | prohibitin homologues | ||
KEAGBMNG_01017 | 1.2e-141 | S | Protein of unknown function (DUF975) | |||
KEAGBMNG_01018 | 1.3e-54 | K | sequence-specific DNA binding | |||
KEAGBMNG_01019 | 1e-09 | K | sequence-specific DNA binding | |||
KEAGBMNG_01020 | 2e-105 | speG | J | Acetyltransferase (GNAT) domain | ||
KEAGBMNG_01021 | 2.2e-139 | |||||
KEAGBMNG_01022 | 0.0 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
KEAGBMNG_01023 | 2e-42 | rpiB | 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
KEAGBMNG_01024 | 8.4e-50 | |||||
KEAGBMNG_01025 | 2.8e-28 | |||||
KEAGBMNG_01026 | 8.4e-119 | drgA | C | nitroreductase | ||
KEAGBMNG_01027 | 0.0 | 1.3.5.4 | C | FMN_bind | ||
KEAGBMNG_01028 | 1.1e-167 | lysR7 | K | LysR substrate binding domain | ||
KEAGBMNG_01029 | 3.3e-158 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
KEAGBMNG_01030 | 5.3e-231 | hom1 | 1.1.1.3 | E | homoserine dehydrogenase | |
KEAGBMNG_01031 | 3.3e-283 | thrC | 4.2.3.1 | E | Threonine synthase | |
KEAGBMNG_01032 | 2.1e-199 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
KEAGBMNG_01033 | 4.8e-257 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
KEAGBMNG_01034 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KEAGBMNG_01035 | 0.0 | XK27_06780 | V | ABC transporter permease | ||
KEAGBMNG_01036 | 2.9e-128 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
KEAGBMNG_01037 | 5.7e-126 | alkD | L | DNA alkylation repair enzyme | ||
KEAGBMNG_01038 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
KEAGBMNG_01039 | 4.5e-105 | pncA | Q | Isochorismatase family | ||
KEAGBMNG_01040 | 3.3e-92 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
KEAGBMNG_01041 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
KEAGBMNG_01042 | 1.1e-211 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
KEAGBMNG_01043 | 3.1e-242 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
KEAGBMNG_01044 | 2.4e-181 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
KEAGBMNG_01045 | 2.1e-94 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
KEAGBMNG_01046 | 6.8e-170 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
KEAGBMNG_01047 | 3.8e-128 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
KEAGBMNG_01048 | 5.4e-118 | 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) | |
KEAGBMNG_01049 | 2.3e-303 | I | Protein of unknown function (DUF2974) | |||
KEAGBMNG_01050 | 5.1e-153 | yxeH | S | hydrolase | ||
KEAGBMNG_01051 | 1.7e-161 | XK27_05540 | S | DUF218 domain | ||
KEAGBMNG_01052 | 3.5e-52 | ybjQ | S | Belongs to the UPF0145 family | ||
KEAGBMNG_01053 | 2.3e-157 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
KEAGBMNG_01054 | 1.1e-167 | |||||
KEAGBMNG_01055 | 4e-133 | |||||
KEAGBMNG_01056 | 1e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
KEAGBMNG_01057 | 8.1e-22 | |||||
KEAGBMNG_01058 | 2.3e-108 | |||||
KEAGBMNG_01059 | 2.1e-138 | |||||
KEAGBMNG_01060 | 3.3e-124 | skfE | V | ATPases associated with a variety of cellular activities | ||
KEAGBMNG_01061 | 9.6e-59 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
KEAGBMNG_01062 | 5.4e-247 | pepT | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KEAGBMNG_01063 | 3.2e-152 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
KEAGBMNG_01064 | 2.5e-121 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
KEAGBMNG_01065 | 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 | ||
KEAGBMNG_01066 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
KEAGBMNG_01067 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
KEAGBMNG_01068 | 3.6e-179 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
KEAGBMNG_01069 | 1.6e-137 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
KEAGBMNG_01070 | 1.1e-169 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
KEAGBMNG_01071 | 1.2e-91 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
KEAGBMNG_01072 | 4.7e-174 | phoH | T | phosphate starvation-inducible protein PhoH | ||
KEAGBMNG_01073 | 4.1e-40 | yqeY | S | YqeY-like protein | ||
KEAGBMNG_01074 | 1.5e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
KEAGBMNG_01075 | 1e-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 | |
KEAGBMNG_01076 | 1.3e-159 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
KEAGBMNG_01077 | 3.8e-107 | 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 | |
KEAGBMNG_01078 | 2.4e-144 | E | GDSL-like Lipase/Acylhydrolase family | |||
KEAGBMNG_01079 | 6.1e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
KEAGBMNG_01080 | 1.4e-223 | patA | 2.6.1.1 | E | Aminotransferase | |
KEAGBMNG_01081 | 7e-32 | |||||
KEAGBMNG_01082 | 7.2e-164 | htpX | O | Peptidase family M48 | ||
KEAGBMNG_01084 | 4.5e-76 | S | HIRAN | |||
KEAGBMNG_01086 | 6.3e-190 | 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 | |
KEAGBMNG_01087 | 8.8e-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 | |
KEAGBMNG_01088 | 7.2e-169 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
KEAGBMNG_01089 | 1.3e-209 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
KEAGBMNG_01090 | 5.5e-225 | KQ | helix_turn_helix, mercury resistance | |||
KEAGBMNG_01091 | 1.1e-183 | V | Abi-like protein | |||
KEAGBMNG_01092 | 2.4e-25 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
KEAGBMNG_01093 | 1.1e-181 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
KEAGBMNG_01094 | 6.1e-172 | S | Acyltransferase family | |||
KEAGBMNG_01095 | 8.6e-265 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
KEAGBMNG_01096 | 1.1e-219 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
KEAGBMNG_01097 | 8.1e-213 | |||||
KEAGBMNG_01098 | 6.8e-195 | M | Glycosyl transferase family 2 | |||
KEAGBMNG_01099 | 4.7e-199 | wbbI | M | transferase activity, transferring glycosyl groups | ||
KEAGBMNG_01100 | 2.3e-198 | cps1B | GT2,GT4 | M | Glycosyl transferases group 1 | |
KEAGBMNG_01101 | 4.5e-160 | GT2 | S | Glycosyl transferase family 2 | ||
KEAGBMNG_01102 | 2.2e-184 | 2.4.1.308 | GT11 | S | N-acetyllactosaminide 3-alpha-galactosyltransferase activity | |
KEAGBMNG_01103 | 1.5e-124 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
KEAGBMNG_01104 | 2.9e-90 | pssE | S | Glycosyltransferase family 28 C-terminal domain | ||
KEAGBMNG_01105 | 6.8e-83 | cpsF | M | Oligosaccharide biosynthesis protein Alg14 like | ||
KEAGBMNG_01106 | 1.7e-122 | rfbP | M | Bacterial sugar transferase | ||
KEAGBMNG_01107 | 1.7e-145 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
KEAGBMNG_01108 | 2.9e-126 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
KEAGBMNG_01109 | 1.5e-142 | epsB | M | biosynthesis protein | ||
KEAGBMNG_01110 | 6.7e-163 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
KEAGBMNG_01111 | 6.7e-81 | K | DNA-templated transcription, initiation | |||
KEAGBMNG_01112 | 9.3e-166 | |||||
KEAGBMNG_01113 | 2.5e-121 | frnE | Q | DSBA-like thioredoxin domain | ||
KEAGBMNG_01114 | 7.7e-225 | |||||
KEAGBMNG_01115 | 1.2e-70 | S | Domain of unknown function (DUF4767) | |||
KEAGBMNG_01116 | 1.5e-81 | |||||
KEAGBMNG_01117 | 6.7e-89 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
KEAGBMNG_01118 | 1.2e-103 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
KEAGBMNG_01119 | 3.5e-233 | 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 | ||
KEAGBMNG_01120 | 9.5e-205 | 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 | ||
KEAGBMNG_01121 | 1.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
KEAGBMNG_01122 | 7.7e-160 | |||||
KEAGBMNG_01123 | 0.0 | rnjB | 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 | ||
KEAGBMNG_01124 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
KEAGBMNG_01125 | 7.5e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
KEAGBMNG_01126 | 1.2e-177 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
KEAGBMNG_01127 | 0.0 | comEC | S | Competence protein ComEC | ||
KEAGBMNG_01128 | 2.4e-79 | comEA | L | Competence protein ComEA | ||
KEAGBMNG_01129 | 2.5e-186 | ylbL | T | Belongs to the peptidase S16 family | ||
KEAGBMNG_01130 | 1.5e-86 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
KEAGBMNG_01131 | 7.2e-95 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
KEAGBMNG_01132 | 6.1e-52 | ylbG | S | UPF0298 protein | ||
KEAGBMNG_01133 | 5.9e-211 | ftsW | D | Belongs to the SEDS family | ||
KEAGBMNG_01134 | 0.0 | typA | T | GTP-binding protein TypA | ||
KEAGBMNG_01135 | 5.2e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
KEAGBMNG_01136 | 3e-34 | ykzG | S | Belongs to the UPF0356 family | ||
KEAGBMNG_01137 | 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 | ||
KEAGBMNG_01138 | 9.9e-177 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
KEAGBMNG_01139 | 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 | |
KEAGBMNG_01140 | 5.1e-116 | S | Repeat protein | |||
KEAGBMNG_01141 | 2e-123 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
KEAGBMNG_01142 | 2.3e-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 | |
KEAGBMNG_01143 | 1.6e-57 | XK27_04120 | S | Putative amino acid metabolism | ||
KEAGBMNG_01144 | 3.9e-215 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
KEAGBMNG_01145 | 1.6e-126 | 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 | |
KEAGBMNG_01147 | 9.7e-103 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
KEAGBMNG_01148 | 2e-32 | cspA | K | 'Cold-shock' DNA-binding domain | ||
KEAGBMNG_01149 | 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) | |
KEAGBMNG_01150 | 2.1e-119 | gpsB | D | DivIVA domain protein | ||
KEAGBMNG_01151 | 4.8e-148 | ylmH | S | S4 domain protein | ||
KEAGBMNG_01152 | 2e-27 | yggT | S | YGGT family | ||
KEAGBMNG_01153 | 3.6e-73 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
KEAGBMNG_01154 | 4.7e-236 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
KEAGBMNG_01155 | 4.1e-240 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
KEAGBMNG_01156 | 4.8e-154 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
KEAGBMNG_01157 | 1.2e-210 | 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) |
KEAGBMNG_01158 | 2.5e-261 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
KEAGBMNG_01159 | 1.6e-177 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
KEAGBMNG_01160 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
KEAGBMNG_01161 | 6.3e-55 | ftsL | D | Cell division protein FtsL | ||
KEAGBMNG_01162 | 1.3e-176 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
KEAGBMNG_01163 | 4.1e-77 | mraZ | K | Belongs to the MraZ family | ||
KEAGBMNG_01164 | 6.1e-52 | S | Protein of unknown function (DUF3397) | |||
KEAGBMNG_01165 | 3.6e-13 | S | Protein of unknown function (DUF4044) | |||
KEAGBMNG_01166 | 5.4e-95 | mreD | ||||
KEAGBMNG_01167 | 1e-143 | mreC | M | Involved in formation and maintenance of cell shape | ||
KEAGBMNG_01168 | 6.4e-166 | mreB | D | cell shape determining protein MreB | ||
KEAGBMNG_01169 | 9.5e-112 | radC | L | DNA repair protein | ||
KEAGBMNG_01170 | 9.2e-124 | S | Haloacid dehalogenase-like hydrolase | |||
KEAGBMNG_01171 | 2.8e-235 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
KEAGBMNG_01172 | 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 | |
KEAGBMNG_01173 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
KEAGBMNG_01174 | 4.2e-211 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | ||
KEAGBMNG_01175 | 7.8e-126 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KEAGBMNG_01176 | 5e-229 | 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 | |
KEAGBMNG_01177 | 2.1e-216 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
KEAGBMNG_01178 | 6.5e-299 | 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 | ||
KEAGBMNG_01180 | 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 | ||
KEAGBMNG_01181 | 2.7e-82 | yueI | S | Protein of unknown function (DUF1694) | ||
KEAGBMNG_01182 | 3e-240 | rarA | L | recombination factor protein RarA | ||
KEAGBMNG_01184 | 5.2e-81 | usp6 | T | universal stress protein | ||
KEAGBMNG_01185 | 7.3e-225 | rodA | D | Belongs to the SEDS family | ||
KEAGBMNG_01186 | 1.3e-34 | S | Protein of unknown function (DUF2969) | |||
KEAGBMNG_01187 | 2e-51 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
KEAGBMNG_01188 | 2.5e-15 | S | DNA-directed RNA polymerase subunit beta | |||
KEAGBMNG_01189 | 2.2e-179 | mbl | D | Cell shape determining protein MreB Mrl | ||
KEAGBMNG_01190 | 2e-30 | ywzB | S | Protein of unknown function (DUF1146) | ||
KEAGBMNG_01191 | 1.1e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
KEAGBMNG_01192 | 3.3e-248 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
KEAGBMNG_01193 | 1.4e-170 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
KEAGBMNG_01194 | 5.1e-284 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
KEAGBMNG_01195 | 5.7e-92 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
KEAGBMNG_01196 | 5.9e-51 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
KEAGBMNG_01197 | 1.2e-26 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
KEAGBMNG_01198 | 1.6e-126 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
KEAGBMNG_01199 | 3.6e-114 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
KEAGBMNG_01200 | 1.2e-188 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
KEAGBMNG_01201 | 5.4e-158 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
KEAGBMNG_01202 | 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 | ||
KEAGBMNG_01203 | 5.5e-112 | tdk | 2.7.1.21 | F | thymidine kinase | |
KEAGBMNG_01204 | 4.9e-262 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain | |
KEAGBMNG_01205 | 7.2e-197 | ampC | V | Beta-lactamase | ||
KEAGBMNG_01208 | 1.4e-72 | |||||
KEAGBMNG_01209 | 3.2e-104 | EGP | Major facilitator Superfamily | |||
KEAGBMNG_01210 | 5.6e-88 | EGP | Major facilitator Superfamily | |||
KEAGBMNG_01211 | 5.4e-261 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
KEAGBMNG_01212 | 1.4e-107 | vanZ | V | VanZ like family | ||
KEAGBMNG_01213 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
KEAGBMNG_01214 | 2.8e-271 | T | PhoQ Sensor | |||
KEAGBMNG_01215 | 9e-130 | K | Transcriptional regulatory protein, C terminal | |||
KEAGBMNG_01216 | 9.2e-68 | S | SdpI/YhfL protein family | |||
KEAGBMNG_01217 | 2.9e-192 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
KEAGBMNG_01218 | 1.8e-80 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
KEAGBMNG_01219 | 1e-76 | M | Protein of unknown function (DUF3737) | |||
KEAGBMNG_01220 | 2.7e-24 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
KEAGBMNG_01221 | 6.4e-271 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
KEAGBMNG_01223 | 7.3e-225 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KEAGBMNG_01224 | 1.5e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
KEAGBMNG_01225 | 4.7e-88 | comGF | U | Putative Competence protein ComGF | ||
KEAGBMNG_01227 | 3.7e-67 | |||||
KEAGBMNG_01228 | 1.1e-36 | comGC | U | Required for transformation and DNA binding | ||
KEAGBMNG_01229 | 4.7e-177 | comGB | NU | type II secretion system | ||
KEAGBMNG_01230 | 5.8e-180 | comGA | NU | Type II IV secretion system protein | ||
KEAGBMNG_01231 | 1.5e-132 | yebC | K | Transcriptional regulatory protein | ||
KEAGBMNG_01232 | 7.3e-97 | S | VanZ like family | |||
KEAGBMNG_01233 | 5.1e-218 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
KEAGBMNG_01234 | 4.5e-163 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
KEAGBMNG_01235 | 8.5e-150 | yisY | 1.11.1.10 | S | Alpha/beta hydrolase family | |
KEAGBMNG_01236 | 4.8e-115 | |||||
KEAGBMNG_01237 | 8e-179 | S | Putative adhesin | |||
KEAGBMNG_01238 | 5.3e-62 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
KEAGBMNG_01239 | 2.3e-66 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
KEAGBMNG_01240 | 4.4e-149 | S | Sucrose-6F-phosphate phosphohydrolase | |||
KEAGBMNG_01241 | 5.9e-255 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
KEAGBMNG_01242 | 8.1e-174 | ybbR | S | YbbR-like protein | ||
KEAGBMNG_01243 | 3.4e-152 | 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 | |
KEAGBMNG_01244 | 1.3e-209 | potD | P | ABC transporter | ||
KEAGBMNG_01245 | 2.2e-137 | potC | P | ABC transporter permease | ||
KEAGBMNG_01246 | 7.1e-131 | potB | P | ABC transporter permease | ||
KEAGBMNG_01247 | 1.1e-206 | 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 | |
KEAGBMNG_01248 | 5.2e-167 | murB | 1.3.1.98 | M | Cell wall formation | |
KEAGBMNG_01249 | 9.5e-100 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
KEAGBMNG_01250 | 1.3e-84 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
KEAGBMNG_01251 | 2.5e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
KEAGBMNG_01252 | 3.1e-135 | 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 | |
KEAGBMNG_01253 | 8e-157 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
KEAGBMNG_01254 | 2.9e-93 | |||||
KEAGBMNG_01255 | 2.3e-91 | |||||
KEAGBMNG_01257 | 1e-107 | 3.2.2.20 | K | acetyltransferase | ||
KEAGBMNG_01258 | 2.3e-78 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
KEAGBMNG_01259 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
KEAGBMNG_01260 | 2.5e-28 | secG | U | Preprotein translocase | ||
KEAGBMNG_01261 | 3.1e-245 | 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 | |
KEAGBMNG_01262 | 1.9e-141 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
KEAGBMNG_01263 | 6e-227 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
KEAGBMNG_01264 | 3.2e-189 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KEAGBMNG_01265 | 2.3e-187 | cggR | K | Putative sugar-binding domain | ||
KEAGBMNG_01267 | 1.2e-277 | ycaM | E | amino acid | ||
KEAGBMNG_01268 | 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 | |
KEAGBMNG_01269 | 6.2e-171 | whiA | K | May be required for sporulation | ||
KEAGBMNG_01270 | 4.4e-194 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
KEAGBMNG_01271 | 6e-160 | rapZ | S | Displays ATPase and GTPase activities | ||
KEAGBMNG_01272 | 1.1e-90 | S | Short repeat of unknown function (DUF308) | |||
KEAGBMNG_01273 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
KEAGBMNG_01274 | 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 | ||
KEAGBMNG_01275 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
KEAGBMNG_01276 | 1.6e-193 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
KEAGBMNG_01277 | 5.2e-289 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
KEAGBMNG_01278 | 1.4e-225 | 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) | |
KEAGBMNG_01279 | 9.2e-181 | lacR | K | Transcriptional regulator | ||
KEAGBMNG_01280 | 7.5e-191 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
KEAGBMNG_01281 | 6e-174 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
KEAGBMNG_01282 | 8.8e-187 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
KEAGBMNG_01283 | 4.1e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
KEAGBMNG_01284 | 3.8e-176 | 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 | ||
KEAGBMNG_01285 | 3.3e-35 | |||||
KEAGBMNG_01286 | 6.2e-185 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
KEAGBMNG_01287 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
KEAGBMNG_01288 | 4.5e-97 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
KEAGBMNG_01289 | 5.7e-126 | comFC | S | Competence protein | ||
KEAGBMNG_01290 | 1.1e-242 | comFA | L | Helicase C-terminal domain protein | ||
KEAGBMNG_01291 | 2.5e-118 | yvyE | 3.4.13.9 | S | YigZ family | |
KEAGBMNG_01292 | 2.7e-192 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
KEAGBMNG_01293 | 1.2e-209 | rny | S | Endoribonuclease that initiates mRNA decay | ||
KEAGBMNG_01294 | 1.9e-195 | 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 | ||
KEAGBMNG_01295 | 1.4e-96 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KEAGBMNG_01296 | 4.3e-125 | ymfM | S | Helix-turn-helix domain | ||
KEAGBMNG_01297 | 4.1e-130 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
KEAGBMNG_01298 | 2.9e-232 | S | Peptidase M16 | |||
KEAGBMNG_01299 | 2.2e-229 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
KEAGBMNG_01300 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
KEAGBMNG_01301 | 4.6e-76 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
KEAGBMNG_01302 | 2.7e-105 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
KEAGBMNG_01303 | 5.4e-212 | yubA | S | AI-2E family transporter | ||
KEAGBMNG_01304 | 9.9e-67 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
KEAGBMNG_01305 | 4.8e-201 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
KEAGBMNG_01306 | 3.9e-234 | N | Uncharacterized conserved protein (DUF2075) | |||
KEAGBMNG_01307 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
KEAGBMNG_01308 | 3.7e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KEAGBMNG_01309 | 4e-150 | 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 | |
KEAGBMNG_01310 | 6.7e-113 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
KEAGBMNG_01311 | 3.3e-112 | yjbK | S | CYTH | ||
KEAGBMNG_01312 | 7e-107 | yjbH | Q | Thioredoxin | ||
KEAGBMNG_01313 | 1.7e-162 | coiA | 3.6.4.12 | S | Competence protein | |
KEAGBMNG_01314 | 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 | ||
KEAGBMNG_01315 | 4.7e-67 | 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 | |
KEAGBMNG_01316 | 0.0 | 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) | |
KEAGBMNG_01317 | 4.2e-40 | ptsH | G | phosphocarrier protein HPR | ||
KEAGBMNG_01318 | 6.9e-26 | |||||
KEAGBMNG_01319 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
KEAGBMNG_01320 | 1.1e-43 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
KEAGBMNG_01321 | 7.9e-304 | 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 | ||
KEAGBMNG_01322 | 1.6e-157 | hlyX | S | Transporter associated domain | ||
KEAGBMNG_01323 | 3e-78 | |||||
KEAGBMNG_01324 | 4.9e-90 | |||||
KEAGBMNG_01325 | 2.4e-112 | ygaC | J | Belongs to the UPF0374 family | ||
KEAGBMNG_01326 | 7.8e-146 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
KEAGBMNG_01327 | 9.2e-264 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KEAGBMNG_01328 | 2.9e-218 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
KEAGBMNG_01329 | 3.5e-222 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
KEAGBMNG_01330 | 9.3e-217 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
KEAGBMNG_01331 | 1.3e-179 | D | Alpha beta | |||
KEAGBMNG_01332 | 2.4e-07 | |||||
KEAGBMNG_01333 | 4.3e-152 | S | haloacid dehalogenase-like hydrolase | |||
KEAGBMNG_01334 | 2.8e-205 | EGP | Major facilitator Superfamily | |||
KEAGBMNG_01335 | 1.1e-261 | glnA | 6.3.1.2 | E | glutamine synthetase | |
KEAGBMNG_01336 | 3.3e-169 | 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) | |
KEAGBMNG_01337 | 1.1e-18 | S | Protein of unknown function (DUF3042) | |||
KEAGBMNG_01338 | 1.5e-57 | yqhL | P | Rhodanese-like protein | ||
KEAGBMNG_01339 | 6e-35 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
KEAGBMNG_01340 | 2.4e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
KEAGBMNG_01341 | 5.6e-87 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
KEAGBMNG_01342 | 7.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
KEAGBMNG_01343 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
KEAGBMNG_01344 | 0.0 | S | membrane | |||
KEAGBMNG_01345 | 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 | ||
KEAGBMNG_01346 | 2.6e-205 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
KEAGBMNG_01347 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KEAGBMNG_01348 | 8.1e-204 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
KEAGBMNG_01349 | 7.3e-64 | yodB | K | Transcriptional regulator, HxlR family | ||
KEAGBMNG_01350 | 9.6e-138 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KEAGBMNG_01351 | 3.8e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
KEAGBMNG_01352 | 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 | ||
KEAGBMNG_01353 | 1.9e-281 | arlS | 2.7.13.3 | T | Histidine kinase | |
KEAGBMNG_01354 | 1.1e-130 | K | response regulator | |||
KEAGBMNG_01355 | 2.9e-96 | yceD | S | Uncharacterized ACR, COG1399 | ||
KEAGBMNG_01356 | 5.8e-219 | ylbM | S | Belongs to the UPF0348 family | ||
KEAGBMNG_01357 | 8.2e-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 | ||
KEAGBMNG_01358 | 1.7e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
KEAGBMNG_01359 | 4.4e-120 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
KEAGBMNG_01360 | 7.3e-211 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
KEAGBMNG_01361 | 3.5e-91 | yqeG | S | HAD phosphatase, family IIIA | ||
KEAGBMNG_01362 | 9.8e-191 | 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 | |
KEAGBMNG_01363 | 6.6e-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 | ||
KEAGBMNG_01364 | 2.4e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
KEAGBMNG_01365 | 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 | ||
KEAGBMNG_01366 | 1.3e-131 | S | domain protein | |||
KEAGBMNG_01367 | 4.8e-171 | V | ABC transporter | |||
KEAGBMNG_01368 | 1.9e-74 | S | Protein of unknown function (DUF3021) | |||
KEAGBMNG_01369 | 4.7e-73 | K | LytTr DNA-binding domain | |||
KEAGBMNG_01370 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
KEAGBMNG_01371 | 2.7e-163 | dnaI | L | Primosomal protein DnaI | ||
KEAGBMNG_01372 | 2.3e-251 | dnaB | L | Replication initiation and membrane attachment | ||
KEAGBMNG_01373 | 1e-81 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
KEAGBMNG_01374 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
KEAGBMNG_01375 | 1.1e-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 | |
KEAGBMNG_01376 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
KEAGBMNG_01377 | 5.7e-230 | ygeX | 4.3.1.15, 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
KEAGBMNG_01378 | 1.4e-211 | EGP | Major facilitator Superfamily | |||
KEAGBMNG_01379 | 4e-69 | rmaI | K | Transcriptional regulator | ||
KEAGBMNG_01380 | 5.9e-12 | |||||
KEAGBMNG_01381 | 1.2e-76 | K | UTRA | |||
KEAGBMNG_01382 | 2.8e-254 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
KEAGBMNG_01383 | 1.2e-117 | cutC | P | Participates in the control of copper homeostasis | ||
KEAGBMNG_01384 | 2.4e-197 | 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 | |||
KEAGBMNG_01385 | 5.9e-94 | S | Glycine/sarcosine/betaine reductase selenoprotein B (GRDB) | |||
KEAGBMNG_01386 | 3.9e-181 | aspG | 3.4.19.5, 3.5.1.1, 3.5.1.26 | E | Asparaginase | |
KEAGBMNG_01387 | 6.1e-257 | 3.5.1.18 | E | Peptidase family M20/M25/M40 | ||
KEAGBMNG_01388 | 8.3e-131 | ymfC | K | UTRA | ||
KEAGBMNG_01389 | 7.4e-123 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KEAGBMNG_01390 | 1.6e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
KEAGBMNG_01391 | 3.3e-15 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KEAGBMNG_01392 | 4.4e-42 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KEAGBMNG_01393 | 3e-124 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
KEAGBMNG_01394 | 2.1e-227 | ecsB | U | ABC transporter | ||
KEAGBMNG_01395 | 8.2e-134 | ecsA | V | ABC transporter, ATP-binding protein | ||
KEAGBMNG_01396 | 2.4e-77 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
KEAGBMNG_01397 | 2e-64 | |||||
KEAGBMNG_01398 | 4.4e-37 | S | YtxH-like protein | |||
KEAGBMNG_01399 | 4.3e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
KEAGBMNG_01400 | 1.6e-185 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
KEAGBMNG_01401 | 0.0 | L | AAA domain | |||
KEAGBMNG_01402 | 1.1e-231 | yhaO | L | Ser Thr phosphatase family protein | ||
KEAGBMNG_01403 | 3.3e-56 | yheA | S | Belongs to the UPF0342 family | ||
KEAGBMNG_01404 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KEAGBMNG_01405 | 3.6e-162 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KEAGBMNG_01407 | 1.3e-259 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
KEAGBMNG_01408 | 1.3e-66 | |||||
KEAGBMNG_01409 | 2e-94 | 3.6.1.55 | L | NUDIX domain | ||
KEAGBMNG_01410 | 2.2e-153 | neo | 2.7.1.87, 2.7.1.95 | F | Belongs to the aminoglycoside phosphotransferase family | |
KEAGBMNG_01411 | 3.9e-198 | V | Beta-lactamase | |||
KEAGBMNG_01412 | 8.4e-63 | |||||
KEAGBMNG_01413 | 0.0 | L | helicase activity | |||
KEAGBMNG_01414 | 6.4e-227 | K | DNA binding | |||
KEAGBMNG_01415 | 0.0 | res | 2.1.1.72, 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
KEAGBMNG_01416 | 2.7e-128 | mod | 2.1.1.72, 3.1.21.5 | L | DNA methylase | |
KEAGBMNG_01417 | 1.5e-115 | mod | 2.1.1.72, 3.1.21.5 | L | DNA methylase | |
KEAGBMNG_01418 | 7.4e-39 | K | Cro/C1-type HTH DNA-binding domain | |||
KEAGBMNG_01419 | 3.5e-302 | |||||
KEAGBMNG_01420 | 3.2e-36 | |||||
KEAGBMNG_01421 | 2e-233 | |||||
KEAGBMNG_01423 | 2.7e-23 | |||||
KEAGBMNG_01424 | 4.9e-51 | |||||
KEAGBMNG_01425 | 1.6e-221 | L | Protein of unknown function (DUF2800) | |||
KEAGBMNG_01426 | 1.7e-99 | S | Protein of unknown function (DUF2815) | |||
KEAGBMNG_01427 | 0.0 | polA_2 | 2.7.7.7 | L | DNA polymerase | |
KEAGBMNG_01428 | 3.3e-70 | S | Psort location Cytoplasmic, score | |||
KEAGBMNG_01429 | 0.0 | S | Phage plasmid primase, P4 | |||
KEAGBMNG_01430 | 2.4e-46 | S | VRR_NUC | |||
KEAGBMNG_01431 | 2.5e-258 | L | SNF2 family N-terminal domain | |||
KEAGBMNG_01432 | 2.8e-87 | |||||
KEAGBMNG_01433 | 3.3e-100 | |||||
KEAGBMNG_01434 | 2.2e-245 | 2.1.1.72 | KL | DNA methylase | ||
KEAGBMNG_01435 | 2.3e-113 | S | Psort location Cytoplasmic, score | |||
KEAGBMNG_01436 | 6.2e-31 | S | Domain of unknown function (DUF5049) | |||
KEAGBMNG_01437 | 1.1e-111 | S | overlaps another CDS with the same product name | |||
KEAGBMNG_01438 | 4.3e-157 | S | overlaps another CDS with the same product name | |||
KEAGBMNG_01439 | 2.5e-247 | S | Phage portal protein | |||
KEAGBMNG_01440 | 2.9e-122 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
KEAGBMNG_01441 | 6.3e-221 | S | Phage capsid family | |||
KEAGBMNG_01442 | 4.3e-43 | S | Phage gp6-like head-tail connector protein | |||
KEAGBMNG_01443 | 9e-68 | S | Phage head-tail joining protein | |||
KEAGBMNG_01444 | 3e-69 | S | Bacteriophage holin family | |||
KEAGBMNG_01445 | 2.5e-145 | M | Glycosyl hydrolases family 25 | |||
KEAGBMNG_01446 | 4.3e-36 | |||||
KEAGBMNG_01447 | 0.0 | L | Recombinase zinc beta ribbon domain | |||
KEAGBMNG_01448 | 3.5e-274 | L | Recombinase | |||
KEAGBMNG_01449 | 2.7e-227 | |||||
KEAGBMNG_01450 | 1.3e-259 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KEAGBMNG_01451 | 9.6e-121 | spaE | S | ABC-2 family transporter protein | ||
KEAGBMNG_01452 | 1.8e-130 | mutF | V | ABC transporter, ATP-binding protein | ||
KEAGBMNG_01453 | 4.4e-242 | nhaC | C | Na H antiporter NhaC | ||
KEAGBMNG_01454 | 9.6e-163 | salL | 2.5.1.63, 2.5.1.94 | K | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
KEAGBMNG_01455 | 3.3e-95 | S | UPF0397 protein | |||
KEAGBMNG_01456 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
KEAGBMNG_01457 | 3.1e-142 | cbiQ | P | cobalt transport | ||
KEAGBMNG_01458 | 3.2e-119 | ybhL | S | Belongs to the BI1 family | ||
KEAGBMNG_01459 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
KEAGBMNG_01460 | 4.2e-65 | S | Domain of unknown function (DUF4430) | |||
KEAGBMNG_01461 | 8.1e-88 | S | ECF transporter, substrate-specific component | |||
KEAGBMNG_01462 | 2.1e-94 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | cob(I)alamin adenosyltransferase | |
KEAGBMNG_01463 | 4.4e-129 | L | Helix-turn-helix domain | |||
KEAGBMNG_01464 | 2.3e-23 | L | hmm pf00665 | |||
KEAGBMNG_01465 | 1.2e-39 | L | hmm pf00665 | |||
KEAGBMNG_01466 | 9.6e-152 | S | hydrolase | |||
KEAGBMNG_01468 | 7.3e-169 | yegS | 2.7.1.107 | G | Lipid kinase | |
KEAGBMNG_01469 | 2.7e-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) | |
KEAGBMNG_01470 | 8.1e-271 | 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) | |
KEAGBMNG_01471 | 1.1e-49 | 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) | |
KEAGBMNG_01472 | 1.7e-207 | camS | S | sex pheromone | ||
KEAGBMNG_01473 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
KEAGBMNG_01474 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
KEAGBMNG_01475 | 9.4e-115 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
KEAGBMNG_01476 | 5.3e-102 | S | ECF transporter, substrate-specific component | |||
KEAGBMNG_01478 | 6.7e-86 | ydcK | S | Belongs to the SprT family | ||
KEAGBMNG_01479 | 7e-135 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
KEAGBMNG_01480 | 2.1e-258 | epsU | S | Polysaccharide biosynthesis protein | ||
KEAGBMNG_01481 | 4.7e-229 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
KEAGBMNG_01482 | 7e-147 | |||||
KEAGBMNG_01483 | 1.2e-288 | V | ABC transporter transmembrane region | |||
KEAGBMNG_01484 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
KEAGBMNG_01485 | 3.6e-154 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
KEAGBMNG_01486 | 2e-285 | 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 | |
KEAGBMNG_01487 | 0.0 | tuaG | GT2 | M | Glycosyltransferase like family 2 | |
KEAGBMNG_01488 | 2.9e-204 | csaB | M | Glycosyl transferases group 1 | ||
KEAGBMNG_01489 | 4.2e-141 | 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 |
KEAGBMNG_01490 | 1.5e-67 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
KEAGBMNG_01491 | 9.5e-124 | gntR1 | K | UTRA | ||
KEAGBMNG_01492 | 9.3e-190 | |||||
KEAGBMNG_01493 | 1.4e-52 | P | Rhodanese Homology Domain | |||
KEAGBMNG_01496 | 1.2e-166 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
KEAGBMNG_01497 | 1.8e-145 | K | SIS domain | |||
KEAGBMNG_01499 | 1.4e-189 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
KEAGBMNG_01500 | 1.7e-59 | yjgN | S | Bacterial protein of unknown function (DUF898) | ||
KEAGBMNG_01502 | 4.8e-99 | M | LysM domain protein | |||
KEAGBMNG_01503 | 1.3e-110 | M | LysM domain protein | |||
KEAGBMNG_01504 | 5.5e-135 | S | Putative ABC-transporter type IV | |||
KEAGBMNG_01505 | 2.3e-61 | psiE | S | Phosphate-starvation-inducible E | ||
KEAGBMNG_01506 | 3.4e-94 | K | acetyltransferase | |||
KEAGBMNG_01507 | 1e-149 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KEAGBMNG_01509 | 5.1e-164 | yvgN | C | Aldo keto reductase | ||
KEAGBMNG_01510 | 8.1e-249 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
KEAGBMNG_01511 | 7.5e-191 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
KEAGBMNG_01512 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
KEAGBMNG_01513 | 5.4e-253 | P | P-loop Domain of unknown function (DUF2791) | |||
KEAGBMNG_01514 | 0.0 | S | TerB-C domain | |||
KEAGBMNG_01515 | 1.3e-99 | 4.1.1.44 | S | decarboxylase | ||
KEAGBMNG_01516 | 5.1e-72 | |||||
KEAGBMNG_01517 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
KEAGBMNG_01518 | 1.9e-232 | cycA | E | Amino acid permease | ||
KEAGBMNG_01536 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
KEAGBMNG_01537 | 4.5e-183 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
KEAGBMNG_01538 | 4.2e-200 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
KEAGBMNG_01539 | 2.6e-219 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
KEAGBMNG_01551 | 3.8e-60 | |||||
KEAGBMNG_01568 | 1.4e-216 | 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) | |
KEAGBMNG_01569 | 2.1e-102 | J | Acetyltransferase (GNAT) domain | |||
KEAGBMNG_01570 | 1.5e-106 | yjbF | S | SNARE associated Golgi protein | ||
KEAGBMNG_01571 | 7.1e-152 | I | alpha/beta hydrolase fold | |||
KEAGBMNG_01572 | 2.7e-29 | hipB | K | Helix-turn-helix | ||
KEAGBMNG_01573 | 2.2e-106 | hipB | K | Helix-turn-helix | ||
KEAGBMNG_01574 | 7.2e-261 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
KEAGBMNG_01575 | 6e-180 | |||||
KEAGBMNG_01576 | 2.1e-123 | S | SNARE associated Golgi protein | |||
KEAGBMNG_01577 | 6.1e-137 | cof | S | haloacid dehalogenase-like hydrolase | ||
KEAGBMNG_01578 | 0.0 | ydgH | S | MMPL family | ||
KEAGBMNG_01579 | 3.2e-98 | yobS | K | Bacterial regulatory proteins, tetR family | ||
KEAGBMNG_01580 | 1.4e-167 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
KEAGBMNG_01581 | 5.4e-167 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
KEAGBMNG_01582 | 1.4e-80 | yjcF | S | Acetyltransferase (GNAT) domain | ||
KEAGBMNG_01583 | 6e-97 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
KEAGBMNG_01584 | 1.1e-77 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
KEAGBMNG_01585 | 8.7e-52 | ypaA | S | Protein of unknown function (DUF1304) | ||
KEAGBMNG_01586 | 3e-240 | G | Bacterial extracellular solute-binding protein | |||
KEAGBMNG_01587 | 2.7e-257 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
KEAGBMNG_01588 | 5e-148 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
KEAGBMNG_01589 | 9.5e-158 | gtsB | P | ABC-type sugar transport systems, permease components | ||
KEAGBMNG_01590 | 7.1e-203 | malK | P | ATPases associated with a variety of cellular activities | ||
KEAGBMNG_01591 | 4.9e-284 | pipD | E | Dipeptidase | ||
KEAGBMNG_01592 | 6.7e-132 | endA | F | DNA RNA non-specific endonuclease | ||
KEAGBMNG_01593 | 1e-12 | dkg | S | reductase | ||
KEAGBMNG_01594 | 9.8e-77 | dkg | S | reductase | ||
KEAGBMNG_01595 | 1.1e-201 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
KEAGBMNG_01596 | 4.5e-185 | dnaQ | 2.7.7.7 | L | EXOIII | |
KEAGBMNG_01597 | 1.3e-140 | 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 | |||
KEAGBMNG_01598 | 3.1e-113 | yviA | S | Protein of unknown function (DUF421) | ||
KEAGBMNG_01599 | 4e-75 | S | Protein of unknown function (DUF3290) | |||
KEAGBMNG_01600 | 1.5e-247 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KEAGBMNG_01601 | 1.9e-95 | S | PAS domain | |||
KEAGBMNG_01602 | 6.3e-145 | pnuC | H | nicotinamide mononucleotide transporter | ||
KEAGBMNG_01603 | 0.0 | M | domain protein | |||
KEAGBMNG_01604 | 4.6e-07 | GM | domain, Protein | |||
KEAGBMNG_01605 | 2e-43 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
KEAGBMNG_01606 | 8.1e-162 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KEAGBMNG_01607 | 2.3e-128 | S | PAS domain | |||
KEAGBMNG_01608 | 2.7e-239 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
KEAGBMNG_01609 | 2.7e-218 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
KEAGBMNG_01610 | 8e-90 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
KEAGBMNG_01611 | 0.0 | dnaX | 2.4.99.16, 2.7.7.7 | GH13 | M | domain protein |
KEAGBMNG_01612 | 5e-69 | |||||
KEAGBMNG_01613 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
KEAGBMNG_01614 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
KEAGBMNG_01615 | 1.4e-162 | EG | EamA-like transporter family | |||
KEAGBMNG_01616 | 1.6e-285 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
KEAGBMNG_01617 | 0.0 | bglP | 2.7.1.211 | G | phosphotransferase system | |
KEAGBMNG_01618 | 7.1e-150 | licT | K | CAT RNA binding domain | ||
KEAGBMNG_01619 | 0.0 | fhaB | M | Rib/alpha-like repeat | ||
KEAGBMNG_01620 | 1.1e-11 | fhaB | M | Rib/alpha-like repeat | ||
KEAGBMNG_01621 | 9.8e-103 | 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 | ||
KEAGBMNG_01622 | 6.7e-164 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
KEAGBMNG_01623 | 6.2e-105 | E | GDSL-like Lipase/Acylhydrolase | |||
KEAGBMNG_01624 | 4.1e-245 | 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 | ||
KEAGBMNG_01625 | 4.9e-82 | rarA | L | MgsA AAA+ ATPase C terminal | ||
KEAGBMNG_01626 | 2.3e-122 | K | Helix-turn-helix domain, rpiR family | |||
KEAGBMNG_01627 | 1.1e-135 | yvpB | S | Peptidase_C39 like family | ||
KEAGBMNG_01628 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
KEAGBMNG_01629 | 1.2e-117 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
KEAGBMNG_01631 | 2.9e-151 | 3.6.3.8 | P | P-type ATPase | ||
KEAGBMNG_01632 | 2.3e-250 | 3.6.3.8 | P | P-type ATPase | ||
KEAGBMNG_01633 | 1.3e-251 | 3.4.16.4 | M | ErfK YbiS YcfS YnhG | ||
KEAGBMNG_01634 | 3e-48 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KEAGBMNG_01635 | 6.7e-145 | rpiR1 | K | Helix-turn-helix domain, rpiR family | ||
KEAGBMNG_01636 | 8.2e-128 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
KEAGBMNG_01637 | 0.0 | ptsG | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
KEAGBMNG_01638 | 3.2e-149 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
KEAGBMNG_01639 | 1.3e-52 | |||||
KEAGBMNG_01640 | 1.8e-25 | |||||
KEAGBMNG_01641 | 8e-125 | pgm3 | G | Phosphoglycerate mutase family | ||
KEAGBMNG_01642 | 0.0 | V | FtsX-like permease family | |||
KEAGBMNG_01643 | 2.2e-134 | cysA | V | ABC transporter, ATP-binding protein | ||
KEAGBMNG_01644 | 7.3e-280 | E | amino acid | |||
KEAGBMNG_01645 | 2.4e-234 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
KEAGBMNG_01646 | 1.9e-233 | S | Putative peptidoglycan binding domain | |||
KEAGBMNG_01647 | 6.8e-95 | M | NlpC P60 family protein | |||
KEAGBMNG_01649 | 1.3e-99 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
KEAGBMNG_01650 | 9e-44 | |||||
KEAGBMNG_01651 | 3.9e-279 | S | O-antigen ligase like membrane protein | |||
KEAGBMNG_01652 | 1.8e-110 | |||||
KEAGBMNG_01653 | 2.9e-81 | nrdI | F | NrdI Flavodoxin like | ||
KEAGBMNG_01654 | 3.3e-180 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
KEAGBMNG_01655 | 4.1e-81 | |||||
KEAGBMNG_01656 | 4.7e-60 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
KEAGBMNG_01657 | 1.8e-40 | |||||
KEAGBMNG_01658 | 9.6e-80 | S | Threonine/Serine exporter, ThrE | |||
KEAGBMNG_01659 | 1.5e-138 | thrE | S | Putative threonine/serine exporter | ||
KEAGBMNG_01660 | 2.8e-285 | S | ABC transporter, ATP-binding protein | |||
KEAGBMNG_01661 | 8.5e-63 | |||||
KEAGBMNG_01662 | 3.6e-39 | |||||
KEAGBMNG_01663 | 3e-212 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
KEAGBMNG_01664 | 0.0 | pepF | E | oligoendopeptidase F | ||
KEAGBMNG_01666 | 1.4e-257 | lctP | C | L-lactate permease | ||
KEAGBMNG_01667 | 5.1e-134 | znuB | U | ABC 3 transport family | ||
KEAGBMNG_01668 | 2.8e-117 | fhuC | P | ABC transporter | ||
KEAGBMNG_01669 | 8.9e-159 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
KEAGBMNG_01670 | 1.6e-42 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
KEAGBMNG_01671 | 6.9e-139 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | G | Sucrose-6F-phosphate phosphohydrolase | ||
KEAGBMNG_01672 | 0.0 | M | domain protein | |||
KEAGBMNG_01673 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
KEAGBMNG_01674 | 6.9e-167 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
KEAGBMNG_01675 | 1.5e-135 | fruR | K | DeoR C terminal sensor domain | ||
KEAGBMNG_01676 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
KEAGBMNG_01677 | 1.6e-222 | natB | CP | ABC-2 family transporter protein | ||
KEAGBMNG_01678 | 1.2e-166 | natA | S | ABC transporter, ATP-binding protein | ||
KEAGBMNG_01679 | 2.3e-144 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
KEAGBMNG_01680 | 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 | |
KEAGBMNG_01681 | 2.9e-202 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
KEAGBMNG_01682 | 7.4e-121 | K | response regulator | |||
KEAGBMNG_01683 | 0.0 | V | ABC transporter | |||
KEAGBMNG_01684 | 1e-296 | V | ABC transporter, ATP-binding protein | |||
KEAGBMNG_01685 | 3.4e-144 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
KEAGBMNG_01686 | 3.4e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
KEAGBMNG_01687 | 1.3e-43 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
KEAGBMNG_01688 | 2.2e-154 | spo0J | K | Belongs to the ParB family | ||
KEAGBMNG_01689 | 4.4e-138 | soj | D | Sporulation initiation inhibitor | ||
KEAGBMNG_01690 | 2.1e-144 | noc | K | Belongs to the ParB family | ||
KEAGBMNG_01691 | 1.2e-129 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
KEAGBMNG_01692 | 3.2e-95 | cvpA | S | Colicin V production protein | ||
KEAGBMNG_01693 | 1.2e-179 | 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 | |
KEAGBMNG_01694 | 4.4e-149 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
KEAGBMNG_01695 | 6e-199 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
KEAGBMNG_01696 | 3.7e-99 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
KEAGBMNG_01697 | 5.3e-98 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
KEAGBMNG_01698 | 4.1e-110 | K | WHG domain | |||
KEAGBMNG_01699 | 8e-38 | |||||
KEAGBMNG_01700 | 2.6e-274 | pipD | E | Dipeptidase | ||
KEAGBMNG_01701 | 6.8e-297 | arbB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KEAGBMNG_01702 | 3.8e-297 | 2.7.1.211 | G | phosphotransferase system | ||
KEAGBMNG_01703 | 4.2e-158 | K | CAT RNA binding domain | |||
KEAGBMNG_01704 | 6.8e-119 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
KEAGBMNG_01705 | 8.8e-174 | hrtB | V | ABC transporter permease | ||
KEAGBMNG_01706 | 1.9e-92 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
KEAGBMNG_01707 | 3.5e-111 | G | phosphoglycerate mutase | |||
KEAGBMNG_01708 | 5.5e-115 | G | Phosphoglycerate mutase family | |||
KEAGBMNG_01709 | 1.8e-141 | aroD | S | Alpha/beta hydrolase family | ||
KEAGBMNG_01710 | 2e-106 | S | Protein of unknown function (DUF975) | |||
KEAGBMNG_01711 | 2.1e-140 | S | Belongs to the UPF0246 family | |||
KEAGBMNG_01712 | 2.2e-52 | |||||
KEAGBMNG_01713 | 6.7e-130 | |||||
KEAGBMNG_01714 | 2.5e-161 | O | protein-N(PI)-phosphohistidine-lactose phosphotransferase system transporter activity | |||
KEAGBMNG_01715 | 0.0 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
KEAGBMNG_01716 | 3.4e-143 | 3.4.16.4, 3.5.2.6 | V | Beta-lactamase enzyme family | ||
KEAGBMNG_01717 | 6.3e-154 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
KEAGBMNG_01718 | 2.1e-173 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
KEAGBMNG_01719 | 1.4e-53 | aroD | 1.1.1.25, 4.2.1.10 | E | 3-dehydroquinate dehydratase activity | |
KEAGBMNG_01720 | 1.1e-156 | |||||
KEAGBMNG_01721 | 3e-226 | mdtG | EGP | Major facilitator Superfamily | ||
KEAGBMNG_01722 | 2.9e-125 | puuD | S | peptidase C26 | ||
KEAGBMNG_01723 | 4.3e-297 | V | ABC transporter transmembrane region | |||
KEAGBMNG_01724 | 2.4e-92 | ymdB | S | Macro domain protein | ||
KEAGBMNG_01725 | 0.0 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
KEAGBMNG_01726 | 1e-300 | scrB | 3.2.1.26 | GH32 | G | invertase |
KEAGBMNG_01727 | 1.2e-185 | scrR | K | Transcriptional regulator, LacI family | ||
KEAGBMNG_01728 | 3e-147 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
KEAGBMNG_01729 | 6.9e-150 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
KEAGBMNG_01730 | 7.1e-132 | cobQ | S | glutamine amidotransferase | ||
KEAGBMNG_01731 | 1.3e-257 | yfnA | E | Amino Acid | ||
KEAGBMNG_01732 | 1.6e-163 | EG | EamA-like transporter family | |||
KEAGBMNG_01733 | 2.8e-193 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
KEAGBMNG_01734 | 3.9e-234 | S | CAAX protease self-immunity | |||
KEAGBMNG_01735 | 1.3e-241 | steT_1 | E | amino acid | ||
KEAGBMNG_01736 | 9.1e-138 | puuD | S | peptidase C26 | ||
KEAGBMNG_01737 | 4.9e-225 | yifK | E | Amino acid permease | ||
KEAGBMNG_01738 | 3.7e-252 | yifK | E | Amino acid permease | ||
KEAGBMNG_01739 | 1.8e-65 | manO | S | Domain of unknown function (DUF956) | ||
KEAGBMNG_01740 | 3.9e-173 | manN | G | system, mannose fructose sorbose family IID component | ||
KEAGBMNG_01741 | 1.3e-124 | manY | G | PTS system | ||
KEAGBMNG_01742 | 9.5e-186 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
KEAGBMNG_01749 | 6.9e-251 | yfnA | E | Amino Acid | ||
KEAGBMNG_01750 | 0.0 | clpE2 | O | AAA domain (Cdc48 subfamily) | ||
KEAGBMNG_01751 | 6.5e-157 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
KEAGBMNG_01752 | 2.2e-243 | pts13C | 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 | |
KEAGBMNG_01753 | 1.1e-39 | |||||
KEAGBMNG_01754 | 6.2e-216 | lmrP | E | Major Facilitator Superfamily | ||
KEAGBMNG_01755 | 1.2e-174 | pbpX2 | V | Beta-lactamase | ||
KEAGBMNG_01756 | 4.5e-252 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
KEAGBMNG_01757 | 3.9e-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 | |
KEAGBMNG_01758 | 5.5e-236 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
KEAGBMNG_01759 | 2.1e-290 | 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 | |
KEAGBMNG_01761 | 2.8e-45 | |||||
KEAGBMNG_01762 | 1.7e-199 | ywhK | S | Membrane | ||
KEAGBMNG_01763 | 1.2e-58 | |||||
KEAGBMNG_01764 | 2.4e-49 | |||||
KEAGBMNG_01765 | 3.6e-45 | |||||
KEAGBMNG_01766 | 8.3e-18 | |||||
KEAGBMNG_01767 | 2.7e-85 | ykuL | S | (CBS) domain | ||
KEAGBMNG_01768 | 0.0 | cadA | P | P-type ATPase | ||
KEAGBMNG_01769 | 9.3e-201 | napA | P | Sodium/hydrogen exchanger family | ||
KEAGBMNG_01771 | 7.7e-283 | V | ABC transporter transmembrane region | |||
KEAGBMNG_01772 | 5.9e-160 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
KEAGBMNG_01773 | 8.9e-27 | |||||
KEAGBMNG_01774 | 4.1e-34 | |||||
KEAGBMNG_01775 | 2.6e-120 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
KEAGBMNG_01776 | 1.8e-159 | S | Protein of unknown function (DUF979) | |||
KEAGBMNG_01777 | 2.3e-114 | S | Protein of unknown function (DUF969) | |||
KEAGBMNG_01778 | 4.4e-240 | G | PTS system sugar-specific permease component | |||
KEAGBMNG_01779 | 2.8e-271 | G | PTS system Galactitol-specific IIC component | |||
KEAGBMNG_01780 | 2e-94 | S | Protein of unknown function (DUF1440) | |||
KEAGBMNG_01781 | 9.1e-105 | S | CAAX protease self-immunity | |||
KEAGBMNG_01782 | 6.2e-202 | S | DUF218 domain | |||
KEAGBMNG_01783 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
KEAGBMNG_01784 | 1.7e-270 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
KEAGBMNG_01785 | 7.7e-183 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
KEAGBMNG_01786 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
KEAGBMNG_01787 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
KEAGBMNG_01788 | 1.1e-175 | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | ||
KEAGBMNG_01789 | 3.1e-245 | G | Bacterial extracellular solute-binding protein | |||
KEAGBMNG_01790 | 6.4e-168 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
KEAGBMNG_01791 | 1.6e-199 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
KEAGBMNG_01792 | 1.4e-177 | fpaP | 3.4.11.5 | I | Releases the N-terminal proline from various substrates | |
KEAGBMNG_01793 | 1.3e-195 | blaA6 | V | Beta-lactamase | ||
KEAGBMNG_01794 | 1.2e-261 | pts29C | 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 | |
KEAGBMNG_01795 | 3e-159 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
KEAGBMNG_01796 | 3.1e-214 | S | Bacterial protein of unknown function (DUF871) | |||
KEAGBMNG_01797 | 1.4e-152 | S | Putative esterase | |||
KEAGBMNG_01798 | 1.5e-194 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
KEAGBMNG_01799 | 2e-132 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
KEAGBMNG_01800 | 1.7e-157 | 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 | |
KEAGBMNG_01801 | 8.4e-134 | S | membrane transporter protein | |||
KEAGBMNG_01802 | 3e-18 | S | PD-(D/E)XK nuclease family transposase | |||
KEAGBMNG_01803 | 4e-161 | yeaE | S | Aldo/keto reductase family | ||
KEAGBMNG_01804 | 1e-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 | |
KEAGBMNG_01805 | 7.7e-120 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
KEAGBMNG_01806 | 3.7e-125 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
KEAGBMNG_01807 | 6e-238 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
KEAGBMNG_01808 | 3e-232 | pbuG | S | permease | ||
KEAGBMNG_01810 | 7.4e-111 | K | helix_turn_helix, mercury resistance | |||
KEAGBMNG_01811 | 2.3e-232 | pbuG | S | permease | ||
KEAGBMNG_01812 | 3.4e-46 | I | bis(5'-adenosyl)-triphosphatase activity | |||
KEAGBMNG_01813 | 1.1e-226 | pbuG | S | permease | ||
KEAGBMNG_01814 | 3e-69 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
KEAGBMNG_01815 | 4.1e-90 | |||||
KEAGBMNG_01816 | 5.5e-90 | |||||
KEAGBMNG_01817 | 1.4e-77 | atkY | K | Penicillinase repressor | ||
KEAGBMNG_01818 | 6.3e-66 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
KEAGBMNG_01819 | 1.1e-49 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
KEAGBMNG_01820 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
KEAGBMNG_01821 | 4.4e-155 | ropB | K | Helix-turn-helix XRE-family like proteins | ||
KEAGBMNG_01822 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KEAGBMNG_01823 | 4.1e-286 | E | Amino acid permease | |||
KEAGBMNG_01824 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
KEAGBMNG_01825 | 1e-248 | ynbB | 4.4.1.1 | P | aluminum resistance | |
KEAGBMNG_01826 | 2.3e-75 | K | Acetyltransferase (GNAT) domain | |||
KEAGBMNG_01827 | 2.3e-232 | EGP | Sugar (and other) transporter | |||
KEAGBMNG_01828 | 6.5e-69 | S | Iron-sulphur cluster biosynthesis | |||
KEAGBMNG_01829 | 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 | ||
KEAGBMNG_01830 | 1.5e-115 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
KEAGBMNG_01831 | 2.2e-107 | |||||
KEAGBMNG_01832 | 2.6e-152 | ropB | K | Transcriptional regulator | ||
KEAGBMNG_01833 | 1.2e-201 | EGP | Major facilitator Superfamily | |||
KEAGBMNG_01834 | 5.8e-291 | clcA | P | chloride | ||
KEAGBMNG_01835 | 1.3e-270 | 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 | |
KEAGBMNG_01836 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
KEAGBMNG_01837 | 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 | ||
KEAGBMNG_01838 | 2.8e-252 | 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 | ||
KEAGBMNG_01839 | 3.7e-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 | ||
KEAGBMNG_01840 | 1.7e-60 | 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 | |
KEAGBMNG_01841 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
KEAGBMNG_01842 | 2e-65 | 1.3.5.4 | C | FMN_bind | ||
KEAGBMNG_01843 | 0.0 | S | Protein of unknown function DUF262 | |||
KEAGBMNG_01844 | 0.0 | hsdR | 3.1.21.3 | V | EcoEI R protein C-terminal | |
KEAGBMNG_01845 | 1.3e-209 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KEAGBMNG_01846 | 2.4e-178 | L | Belongs to the 'phage' integrase family | |||
KEAGBMNG_01847 | 1.6e-224 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KEAGBMNG_01848 | 1.8e-292 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KEAGBMNG_01849 | 2.6e-134 | |||||
KEAGBMNG_01850 | 0.0 | KL | domain protein | |||
KEAGBMNG_01851 | 3e-162 | S | Tetratricopeptide repeat protein | |||
KEAGBMNG_01852 | 1.1e-23 | S | Tetratricopeptide repeat protein | |||
KEAGBMNG_01853 | 7.8e-26 | S | Tetratricopeptide repeat protein | |||
KEAGBMNG_01854 | 2e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KEAGBMNG_01855 | 3.5e-180 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KEAGBMNG_01856 | 2.3e-81 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KEAGBMNG_01857 | 3.1e-25 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KEAGBMNG_01858 | 2.1e-23 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KEAGBMNG_01859 | 8.6e-29 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
KEAGBMNG_01860 | 1e-45 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
KEAGBMNG_01861 | 3.8e-92 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the 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. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
KEAGBMNG_01863 | 1.2e-14 | M | Lysin motif | |||
KEAGBMNG_01864 | 2.6e-65 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KEAGBMNG_01865 | 2.9e-105 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
KEAGBMNG_01866 | 1.1e-135 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
KEAGBMNG_01867 | 3.1e-62 | ribT | K | acetyltransferase | ||
KEAGBMNG_01868 | 2.5e-169 | xerD | D | recombinase XerD | ||
KEAGBMNG_01869 | 1.5e-166 | cvfB | S | S1 domain | ||
KEAGBMNG_01870 | 1.3e-21 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
KEAGBMNG_01871 | 1.1e-75 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)