ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
EKFEECJI_00001 | 5.4e-13 | |||||
EKFEECJI_00002 | 4.1e-217 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
EKFEECJI_00003 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
EKFEECJI_00004 | 8.7e-145 | I | alpha/beta hydrolase fold | |||
EKFEECJI_00005 | 4.9e-129 | yibF | S | overlaps another CDS with the same product name | ||
EKFEECJI_00006 | 2.2e-202 | yibE | S | overlaps another CDS with the same product name | ||
EKFEECJI_00007 | 1.4e-112 | |||||
EKFEECJI_00008 | 1.2e-205 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
EKFEECJI_00009 | 6.4e-224 | S | Cysteine-rich secretory protein family | |||
EKFEECJI_00010 | 2.6e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
EKFEECJI_00011 | 1.3e-258 | glnPH2 | P | ABC transporter permease | ||
EKFEECJI_00012 | 2.8e-135 | |||||
EKFEECJI_00013 | 8.4e-125 | luxT | K | Bacterial regulatory proteins, tetR family | ||
EKFEECJI_00014 | 3.3e-183 | 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) | |
EKFEECJI_00015 | 5.6e-36 | |||||
EKFEECJI_00016 | 8.1e-126 | S | PAS domain | |||
EKFEECJI_00017 | 1.6e-11 | |||||
EKFEECJI_00018 | 2.7e-57 | |||||
EKFEECJI_00019 | 6.6e-56 | |||||
EKFEECJI_00020 | 4e-08 | |||||
EKFEECJI_00021 | 1.4e-81 | L | COG3385 FOG Transposase and inactivated derivatives | |||
EKFEECJI_00022 | 1.3e-148 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
EKFEECJI_00023 | 1.4e-120 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
EKFEECJI_00024 | 3e-139 | 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 | |
EKFEECJI_00025 | 1.2e-161 | phnD | P | Phosphonate ABC transporter | ||
EKFEECJI_00027 | 9.8e-83 | uspA | T | universal stress protein | ||
EKFEECJI_00028 | 7.5e-149 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
EKFEECJI_00029 | 8.6e-87 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
EKFEECJI_00030 | 3e-89 | ntd | 2.4.2.6 | F | Nucleoside | |
EKFEECJI_00031 | 5.2e-08 | |||||
EKFEECJI_00032 | 1.6e-310 | oppA | E | ABC transporter, substratebinding protein | ||
EKFEECJI_00033 | 5e-301 | oppA | E | ABC transporter, substratebinding protein | ||
EKFEECJI_00034 | 1.3e-122 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
EKFEECJI_00035 | 4.6e-257 | pepC | 3.4.22.40 | E | aminopeptidase | |
EKFEECJI_00037 | 3.4e-53 | |||||
EKFEECJI_00038 | 4.5e-241 | 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) | |
EKFEECJI_00039 | 8.4e-265 | S | Fibronectin type III domain | |||
EKFEECJI_00040 | 8.6e-21 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
EKFEECJI_00041 | 1.1e-178 | yvdE | K | helix_turn _helix lactose operon repressor | ||
EKFEECJI_00042 | 6.3e-145 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
EKFEECJI_00043 | 5.1e-292 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
EKFEECJI_00044 | 1.5e-144 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
EKFEECJI_00045 | 1.7e-184 | G | Transmembrane secretion effector | |||
EKFEECJI_00046 | 6.1e-136 | V | ABC transporter transmembrane region | |||
EKFEECJI_00047 | 3.2e-223 | L | transposase, IS605 OrfB family | |||
EKFEECJI_00048 | 1.1e-75 | V | ABC transporter transmembrane region | |||
EKFEECJI_00049 | 6.5e-64 | L | RelB antitoxin | |||
EKFEECJI_00050 | 2.1e-131 | cobQ | S | glutamine amidotransferase | ||
EKFEECJI_00051 | 1.8e-81 | M | NlpC/P60 family | |||
EKFEECJI_00054 | 2.6e-155 | |||||
EKFEECJI_00055 | 7.8e-38 | |||||
EKFEECJI_00056 | 2e-32 | |||||
EKFEECJI_00057 | 6.2e-163 | EG | EamA-like transporter family | |||
EKFEECJI_00058 | 5e-165 | EG | EamA-like transporter family | |||
EKFEECJI_00059 | 1.2e-139 | yicL | EG | EamA-like transporter family | ||
EKFEECJI_00060 | 4.3e-107 | |||||
EKFEECJI_00061 | 1.1e-110 | |||||
EKFEECJI_00062 | 5.8e-186 | XK27_05540 | S | DUF218 domain | ||
EKFEECJI_00063 | 9.9e-152 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
EKFEECJI_00064 | 1.4e-210 | yttB | EGP | Major facilitator Superfamily | ||
EKFEECJI_00065 | 1.5e-230 | XK27_04775 | S | PAS domain | ||
EKFEECJI_00066 | 6.2e-103 | S | Iron-sulfur cluster assembly protein | |||
EKFEECJI_00067 | 8.7e-141 | 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 | |
EKFEECJI_00068 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
EKFEECJI_00069 | 5.6e-255 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
EKFEECJI_00070 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
EKFEECJI_00071 | 1.6e-271 | S | Calcineurin-like phosphoesterase | |||
EKFEECJI_00072 | 3.9e-84 | |||||
EKFEECJI_00073 | 1.6e-105 | tag | 3.2.2.20 | L | glycosylase | |
EKFEECJI_00074 | 4.5e-168 | L | COG3385 FOG Transposase and inactivated derivatives | |||
EKFEECJI_00075 | 1.2e-13 | arpU | S | Phage transcriptional regulator, ArpU family | ||
EKFEECJI_00077 | 2.1e-49 | S | HNH endonuclease | |||
EKFEECJI_00078 | 1.6e-55 | L | Phage terminase, small subunit | |||
EKFEECJI_00079 | 3.4e-18 | N | HicA toxin of bacterial toxin-antitoxin, | |||
EKFEECJI_00080 | 9e-47 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
EKFEECJI_00081 | 2.8e-210 | S | Phage Terminase | |||
EKFEECJI_00083 | 9.1e-135 | S | Phage portal protein | |||
EKFEECJI_00084 | 5.5e-87 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
EKFEECJI_00085 | 2e-55 | S | Phage capsid family | |||
EKFEECJI_00086 | 5.2e-17 | S | Phage gp6-like head-tail connector protein | |||
EKFEECJI_00088 | 8.6e-14 | S | Bacteriophage HK97-gp10, putative tail-component | |||
EKFEECJI_00090 | 3.1e-13 | S | Pfam:Phage_TTP_1 | |||
EKFEECJI_00093 | 8.1e-129 | M | Phage tail tape measure protein TP901 | |||
EKFEECJI_00094 | 4.5e-34 | S | phage tail | |||
EKFEECJI_00095 | 6e-136 | S | Phage minor structural protein | |||
EKFEECJI_00103 | 7.6e-39 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
EKFEECJI_00104 | 4e-87 | M | hydrolase, family 25 | |||
EKFEECJI_00106 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
EKFEECJI_00107 | 4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
EKFEECJI_00108 | 7.6e-305 | yloV | S | DAK2 domain fusion protein YloV | ||
EKFEECJI_00109 | 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) | |
EKFEECJI_00110 | 3.7e-182 | 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 | |
EKFEECJI_00111 | 4.9e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
EKFEECJI_00112 | 1.1e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
EKFEECJI_00113 | 1.5e-170 | oppF | P | Belongs to the ABC transporter superfamily | ||
EKFEECJI_00114 | 2.6e-172 | oppB | P | ABC transporter permease | ||
EKFEECJI_00115 | 5.6e-132 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
EKFEECJI_00116 | 9.7e-46 | oppA | E | ABC transporter substrate-binding protein | ||
EKFEECJI_00117 | 1.1e-141 | yfeO | P | Voltage gated chloride channel | ||
EKFEECJI_00118 | 1.4e-184 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
EKFEECJI_00119 | 1.4e-51 | |||||
EKFEECJI_00120 | 2.1e-42 | |||||
EKFEECJI_00121 | 6.4e-232 | 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 | |
EKFEECJI_00122 | 1.1e-295 | ybeC | E | amino acid | ||
EKFEECJI_00123 | 2.6e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
EKFEECJI_00124 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
EKFEECJI_00125 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
EKFEECJI_00126 | 8e-260 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
EKFEECJI_00127 | 4e-249 | 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 | |
EKFEECJI_00128 | 1.7e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
EKFEECJI_00129 | 1e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
EKFEECJI_00130 | 1.4e-83 | K | FR47-like protein | |||
EKFEECJI_00131 | 1.1e-297 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
EKFEECJI_00132 | 2e-194 | 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 | ||
EKFEECJI_00133 | 9.7e-166 | 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 | ||
EKFEECJI_00134 | 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 | ||
EKFEECJI_00135 | 2.6e-241 | 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 | |
EKFEECJI_00136 | 1.8e-62 | yabR | J | S1 RNA binding domain | ||
EKFEECJI_00137 | 6.8e-60 | divIC | D | Septum formation initiator | ||
EKFEECJI_00138 | 1.3e-07 | S | AAA domain | |||
EKFEECJI_00140 | 1.4e-147 | res | L | Helicase C-terminal domain protein | ||
EKFEECJI_00141 | 1.7e-30 | S | Protein of unknown function (DUF669) | |||
EKFEECJI_00142 | 2.7e-268 | S | Phage plasmid primase, P4 | |||
EKFEECJI_00153 | 3.3e-37 | S | VRR_NUC | |||
EKFEECJI_00155 | 9.8e-12 | |||||
EKFEECJI_00156 | 9.5e-245 | 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 | ||
EKFEECJI_00157 | 3.1e-185 | 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 | |
EKFEECJI_00158 | 2.6e-35 | yaaA | S | S4 domain protein YaaA | ||
EKFEECJI_00159 | 4e-209 | 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 | ||
EKFEECJI_00160 | 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 | |
EKFEECJI_00161 | 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 | |
EKFEECJI_00162 | 5.5e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
EKFEECJI_00163 | 2.7e-75 | 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 | ||
EKFEECJI_00164 | 1.2e-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 | ||
EKFEECJI_00165 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
EKFEECJI_00166 | 5.7e-69 | rplI | J | Binds to the 23S rRNA | ||
EKFEECJI_00167 | 6.7e-254 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
EKFEECJI_00168 | 2.3e-165 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
EKFEECJI_00169 | 3.7e-168 | degV | S | DegV family | ||
EKFEECJI_00170 | 4.2e-135 | V | ABC transporter transmembrane region | |||
EKFEECJI_00171 | 6.7e-167 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
EKFEECJI_00173 | 1.4e-16 | |||||
EKFEECJI_00174 | 1.6e-227 | I | Protein of unknown function (DUF2974) | |||
EKFEECJI_00175 | 9.2e-119 | yhiD | S | MgtC family | ||
EKFEECJI_00177 | 3.9e-131 | K | Helix-turn-helix XRE-family like proteins | |||
EKFEECJI_00178 | 7.4e-74 | |||||
EKFEECJI_00179 | 3.3e-87 | |||||
EKFEECJI_00180 | 3.3e-141 | D | Ftsk spoiiie family protein | |||
EKFEECJI_00181 | 5.1e-145 | S | Replication initiation factor | |||
EKFEECJI_00182 | 3.9e-55 | |||||
EKFEECJI_00183 | 2.3e-26 | |||||
EKFEECJI_00184 | 9.5e-220 | L | Belongs to the 'phage' integrase family | |||
EKFEECJI_00186 | 2.5e-62 | yfiL | V | ABC transporter | ||
EKFEECJI_00187 | 2.9e-46 | V | Transport permease protein | |||
EKFEECJI_00188 | 3.4e-09 | |||||
EKFEECJI_00189 | 1.1e-68 | sagB | C | Nitroreductase family | ||
EKFEECJI_00190 | 3.3e-55 | |||||
EKFEECJI_00191 | 2.8e-32 | sagD | S | YcaO cyclodehydratase, ATP-ad Mg2+-binding | ||
EKFEECJI_00192 | 1.7e-193 | S | TerB-C domain | |||
EKFEECJI_00193 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
EKFEECJI_00194 | 3.9e-298 | V | ABC transporter transmembrane region | |||
EKFEECJI_00195 | 2.3e-156 | K | Helix-turn-helix XRE-family like proteins | |||
EKFEECJI_00196 | 3.7e-59 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
EKFEECJI_00197 | 2.1e-32 | |||||
EKFEECJI_00198 | 2.3e-78 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
EKFEECJI_00199 | 3.2e-28 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
EKFEECJI_00200 | 1e-218 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
EKFEECJI_00201 | 2.1e-79 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
EKFEECJI_00202 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
EKFEECJI_00203 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
EKFEECJI_00204 | 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 | |
EKFEECJI_00205 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
EKFEECJI_00206 | 7.6e-49 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
EKFEECJI_00207 | 6.8e-243 | cycA | E | Amino acid permease | ||
EKFEECJI_00208 | 3.2e-81 | maa | S | transferase hexapeptide repeat | ||
EKFEECJI_00209 | 3.3e-158 | K | Transcriptional regulator | |||
EKFEECJI_00210 | 1.1e-62 | manO | S | Domain of unknown function (DUF956) | ||
EKFEECJI_00211 | 1e-173 | manN | G | system, mannose fructose sorbose family IID component | ||
EKFEECJI_00212 | 1.7e-129 | manY | G | PTS system | ||
EKFEECJI_00213 | 2.5e-186 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
EKFEECJI_00214 | 7.5e-231 | pbuG | S | permease | ||
EKFEECJI_00215 | 2.5e-119 | K | helix_turn_helix, mercury resistance | |||
EKFEECJI_00216 | 3.3e-37 | |||||
EKFEECJI_00217 | 1.4e-52 | EGP | Sugar (and other) transporter | |||
EKFEECJI_00218 | 1e-104 | |||||
EKFEECJI_00219 | 8.2e-114 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
EKFEECJI_00220 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
EKFEECJI_00221 | 3.1e-49 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
EKFEECJI_00222 | 4.9e-58 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
EKFEECJI_00223 | 2.4e-36 | |||||
EKFEECJI_00226 | 3.7e-20 | |||||
EKFEECJI_00227 | 1.1e-139 | |||||
EKFEECJI_00228 | 3.7e-261 | V | ABC transporter transmembrane region | |||
EKFEECJI_00229 | 9.9e-82 | C | Flavodoxin | |||
EKFEECJI_00230 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
EKFEECJI_00231 | 1.1e-189 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
EKFEECJI_00232 | 2.1e-114 | 3.6.1.27 | I | Acid phosphatase homologues | ||
EKFEECJI_00233 | 7.4e-205 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
EKFEECJI_00234 | 1.9e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
EKFEECJI_00235 | 1.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
EKFEECJI_00236 | 9.3e-204 | pbpX1 | V | Beta-lactamase | ||
EKFEECJI_00237 | 2.8e-98 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
EKFEECJI_00238 | 7.5e-95 | S | ECF-type riboflavin transporter, S component | |||
EKFEECJI_00239 | 1.3e-229 | S | Putative peptidoglycan binding domain | |||
EKFEECJI_00240 | 9e-83 | K | Acetyltransferase (GNAT) domain | |||
EKFEECJI_00241 | 2.2e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
EKFEECJI_00242 | 1.9e-191 | yrvN | L | AAA C-terminal domain | ||
EKFEECJI_00243 | 8.2e-64 | spxA_2 | 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 | |
EKFEECJI_00244 | 1.5e-283 | treB | G | phosphotransferase system | ||
EKFEECJI_00245 | 8.9e-101 | treR | K | UTRA | ||
EKFEECJI_00246 | 2.5e-287 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
EKFEECJI_00247 | 6.3e-17 | |||||
EKFEECJI_00248 | 2e-183 | G | Bacterial extracellular solute-binding protein | |||
EKFEECJI_00249 | 6.3e-176 | sip | L | Belongs to the 'phage' integrase family | ||
EKFEECJI_00253 | 4.8e-12 | |||||
EKFEECJI_00254 | 1.2e-54 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
EKFEECJI_00255 | 3e-14 | S | Pfam:Peptidase_M78 | |||
EKFEECJI_00256 | 3.7e-18 | ps115 | K | sequence-specific DNA binding | ||
EKFEECJI_00257 | 3.1e-12 | |||||
EKFEECJI_00258 | 3.7e-13 | |||||
EKFEECJI_00260 | 3.1e-88 | S | AntA/AntB antirepressor | |||
EKFEECJI_00262 | 6.8e-08 | |||||
EKFEECJI_00265 | 7.7e-48 | |||||
EKFEECJI_00267 | 2.1e-42 | S | Protein of unknown function (DUF1071) | |||
EKFEECJI_00268 | 5.8e-20 | L | Psort location Cytoplasmic, score | |||
EKFEECJI_00280 | 5.5e-49 | S | VRR_NUC | |||
EKFEECJI_00282 | 3.2e-218 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
EKFEECJI_00285 | 3.3e-09 | arpU | S | Phage transcriptional regulator, ArpU family | ||
EKFEECJI_00288 | 4e-19 | ps333 | L | Terminase small subunit | ||
EKFEECJI_00289 | 4.1e-201 | S | Terminase-like family | |||
EKFEECJI_00290 | 1.4e-134 | S | Protein of unknown function (DUF1073) | |||
EKFEECJI_00291 | 1.3e-47 | S | Phage Mu protein F like protein | |||
EKFEECJI_00292 | 6.5e-12 | S | Lysin motif | |||
EKFEECJI_00293 | 1.6e-57 | S | Uncharacterized protein conserved in bacteria (DUF2213) | |||
EKFEECJI_00294 | 1.8e-34 | |||||
EKFEECJI_00295 | 3.7e-94 | Z012_11565 | S | Uncharacterized protein conserved in bacteria (DUF2184) | ||
EKFEECJI_00296 | 9.2e-20 | S | Protein of unknown function (DUF4054) | |||
EKFEECJI_00297 | 6.5e-29 | |||||
EKFEECJI_00298 | 3.9e-24 | |||||
EKFEECJI_00299 | 2.5e-31 | |||||
EKFEECJI_00300 | 9.2e-104 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
EKFEECJI_00301 | 4.2e-29 | |||||
EKFEECJI_00302 | 2.9e-09 | |||||
EKFEECJI_00304 | 2.5e-227 | 3.4.14.13 | M | Phage tail tape measure protein TP901 | ||
EKFEECJI_00305 | 1.3e-59 | M | LysM domain | |||
EKFEECJI_00306 | 2.3e-45 | |||||
EKFEECJI_00307 | 9.6e-102 | |||||
EKFEECJI_00308 | 1.2e-37 | |||||
EKFEECJI_00309 | 6.4e-31 | |||||
EKFEECJI_00310 | 3.9e-114 | Z012_12235 | S | Baseplate J-like protein | ||
EKFEECJI_00311 | 1.4e-09 | |||||
EKFEECJI_00312 | 2.2e-34 | |||||
EKFEECJI_00318 | 2e-23 | |||||
EKFEECJI_00319 | 1.1e-18 | S | Phage uncharacterised protein (Phage_XkdX) | |||
EKFEECJI_00320 | 8.1e-08 | |||||
EKFEECJI_00322 | 2e-17 | |||||
EKFEECJI_00323 | 7.7e-30 | |||||
EKFEECJI_00325 | 1e-180 | M | Glycosyl hydrolases family 25 | |||
EKFEECJI_00327 | 7.1e-19 | |||||
EKFEECJI_00328 | 1.9e-37 | G | Bacterial extracellular solute-binding protein | |||
EKFEECJI_00329 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
EKFEECJI_00330 | 1.1e-236 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
EKFEECJI_00332 | 0.0 | S | SLAP domain | |||
EKFEECJI_00333 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
EKFEECJI_00334 | 1.2e-164 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
EKFEECJI_00335 | 3.4e-42 | S | RloB-like protein | |||
EKFEECJI_00336 | 1.9e-259 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
EKFEECJI_00337 | 5.7e-99 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
EKFEECJI_00338 | 9.5e-64 | S | SIR2-like domain | |||
EKFEECJI_00339 | 3.2e-10 | S | Domain of unknown function DUF87 | |||
EKFEECJI_00340 | 5.3e-26 | |||||
EKFEECJI_00341 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
EKFEECJI_00342 | 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) | |
EKFEECJI_00343 | 3.9e-66 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
EKFEECJI_00344 | 8.5e-139 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
EKFEECJI_00345 | 1.4e-158 | coiA | 3.6.4.12 | S | Competence protein | |
EKFEECJI_00346 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
EKFEECJI_00347 | 6.8e-110 | yjbK | S | CYTH | ||
EKFEECJI_00348 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
EKFEECJI_00349 | 3.8e-153 | 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 | |
EKFEECJI_00350 | 7.1e-172 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
EKFEECJI_00351 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
EKFEECJI_00352 | 4.2e-92 | S | SNARE associated Golgi protein | |||
EKFEECJI_00353 | 1.3e-28 | 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 | ||
EKFEECJI_00354 | 3.9e-72 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
EKFEECJI_00355 | 1.4e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
EKFEECJI_00356 | 1.9e-175 | oppF | P | Belongs to the ABC transporter superfamily | ||
EKFEECJI_00357 | 2.7e-199 | oppD | P | Belongs to the ABC transporter superfamily | ||
EKFEECJI_00358 | 8.9e-187 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
EKFEECJI_00359 | 1.1e-146 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
EKFEECJI_00360 | 8.3e-210 | 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 | |
EKFEECJI_00361 | 3.3e-261 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
EKFEECJI_00362 | 7.6e-91 | F | Nucleoside 2-deoxyribosyltransferase | |||
EKFEECJI_00363 | 1e-30 | S | cog cog1373 | |||
EKFEECJI_00364 | 1.4e-15 | S | cog cog1373 | |||
EKFEECJI_00365 | 6e-85 | hipB | K | Helix-turn-helix | ||
EKFEECJI_00366 | 3.3e-237 | L | COG2963 Transposase and inactivated derivatives | |||
EKFEECJI_00367 | 4.7e-46 | pspC | KT | PspC domain | ||
EKFEECJI_00369 | 1.3e-240 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
EKFEECJI_00370 | 2.8e-154 | 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 | |
EKFEECJI_00371 | 6.7e-98 | M | ErfK YbiS YcfS YnhG | |||
EKFEECJI_00372 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
EKFEECJI_00373 | 3e-170 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
EKFEECJI_00374 | 3e-90 | S | PFAM Archaeal ATPase | |||
EKFEECJI_00375 | 5.1e-91 | S | PFAM Archaeal ATPase | |||
EKFEECJI_00376 | 7.7e-26 | |||||
EKFEECJI_00377 | 4.3e-76 | menA | 2.5.1.74 | H | UbiA prenyltransferase family | |
EKFEECJI_00378 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
EKFEECJI_00379 | 8.4e-287 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
EKFEECJI_00380 | 1.7e-34 | |||||
EKFEECJI_00381 | 1.2e-94 | sigH | K | Belongs to the sigma-70 factor family | ||
EKFEECJI_00382 | 1.7e-139 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
EKFEECJI_00383 | 5.1e-75 | 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) | ||
EKFEECJI_00384 | 7.5e-277 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
EKFEECJI_00385 | 1.6e-290 | 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) | |
EKFEECJI_00386 | 2.3e-254 | 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 | ||
EKFEECJI_00387 | 1.8e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
EKFEECJI_00388 | 4.1e-52 | |||||
EKFEECJI_00389 | 1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
EKFEECJI_00390 | 7.3e-44 | |||||
EKFEECJI_00391 | 2.4e-183 | S | AAA domain | |||
EKFEECJI_00392 | 3.4e-126 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
EKFEECJI_00393 | 1.4e-23 | |||||
EKFEECJI_00394 | 7.3e-161 | czcD | P | cation diffusion facilitator family transporter | ||
EKFEECJI_00395 | 3.7e-125 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
EKFEECJI_00396 | 6e-132 | S | membrane transporter protein | |||
EKFEECJI_00397 | 1.9e-118 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
EKFEECJI_00398 | 6.3e-105 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
EKFEECJI_00399 | 1.2e-49 | S | Protein of unknown function (DUF3021) | |||
EKFEECJI_00400 | 2.8e-65 | K | LytTr DNA-binding domain | |||
EKFEECJI_00401 | 2.6e-138 | S | TerB-C domain | |||
EKFEECJI_00402 | 1.4e-245 | P | P-loop Domain of unknown function (DUF2791) | |||
EKFEECJI_00403 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
EKFEECJI_00404 | 1.4e-60 | |||||
EKFEECJI_00405 | 4.3e-228 | amtB | P | ammonium transporter | ||
EKFEECJI_00406 | 4.4e-135 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
EKFEECJI_00408 | 6.2e-59 | psiE | S | Phosphate-starvation-inducible E | ||
EKFEECJI_00409 | 6.5e-113 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
EKFEECJI_00410 | 2.9e-69 | S | Iron-sulphur cluster biosynthesis | |||
EKFEECJI_00412 | 2.3e-30 | |||||
EKFEECJI_00413 | 2.3e-172 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
EKFEECJI_00414 | 6.2e-12 | |||||
EKFEECJI_00415 | 1.5e-16 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EKFEECJI_00416 | 4.1e-78 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EKFEECJI_00417 | 2.8e-86 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EKFEECJI_00418 | 5.8e-78 | M | LysM domain protein | |||
EKFEECJI_00419 | 3.1e-158 | D | nuclear chromosome segregation | |||
EKFEECJI_00420 | 1.2e-105 | G | Phosphoglycerate mutase family | |||
EKFEECJI_00421 | 2.6e-89 | G | Histidine phosphatase superfamily (branch 1) | |||
EKFEECJI_00422 | 6.6e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
EKFEECJI_00423 | 1.2e-115 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
EKFEECJI_00425 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
EKFEECJI_00427 | 6.5e-210 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
EKFEECJI_00428 | 2.7e-185 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
EKFEECJI_00429 | 8.1e-120 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
EKFEECJI_00430 | 4.4e-144 | K | SIS domain | |||
EKFEECJI_00431 | 6.7e-228 | slpX | S | SLAP domain | ||
EKFEECJI_00432 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
EKFEECJI_00433 | 6.6e-11 | |||||
EKFEECJI_00434 | 3.2e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
EKFEECJI_00437 | 4.4e-239 | oppA2 | E | ABC transporter, substratebinding protein | ||
EKFEECJI_00438 | 3.4e-45 | oppA2 | E | ABC transporter, substratebinding protein | ||
EKFEECJI_00439 | 3.3e-179 | |||||
EKFEECJI_00440 | 1.3e-125 | gntR1 | K | UTRA | ||
EKFEECJI_00441 | 5.1e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
EKFEECJI_00442 | 2.1e-134 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
EKFEECJI_00443 | 1.7e-204 | csaB | M | Glycosyl transferases group 1 | ||
EKFEECJI_00444 | 2.4e-286 | 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 | |
EKFEECJI_00445 | 3.3e-152 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
EKFEECJI_00446 | 1.4e-204 | tnpB | L | Putative transposase DNA-binding domain | ||
EKFEECJI_00447 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
EKFEECJI_00448 | 7e-225 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
EKFEECJI_00449 | 6e-258 | epsU | S | Polysaccharide biosynthesis protein | ||
EKFEECJI_00450 | 7.7e-134 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
EKFEECJI_00451 | 4.1e-83 | ydcK | S | Belongs to the SprT family | ||
EKFEECJI_00453 | 5.2e-84 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
EKFEECJI_00454 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
EKFEECJI_00455 | 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 | |
EKFEECJI_00456 | 5.8e-203 | camS | S | sex pheromone | ||
EKFEECJI_00457 | 1.5e-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) | |
EKFEECJI_00458 | 2.9e-268 | 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) | |
EKFEECJI_00459 | 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) | |
EKFEECJI_00460 | 2.7e-171 | yegS | 2.7.1.107 | G | Lipid kinase | |
EKFEECJI_00461 | 4.3e-108 | ybhL | S | Belongs to the BI1 family | ||
EKFEECJI_00462 | 2.6e-57 | |||||
EKFEECJI_00463 | 3.2e-135 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
EKFEECJI_00464 | 2.8e-244 | nhaC | C | Na H antiporter NhaC | ||
EKFEECJI_00465 | 6.3e-201 | pbpX | V | Beta-lactamase | ||
EKFEECJI_00466 | 4.9e-254 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
EKFEECJI_00467 | 1.1e-94 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
EKFEECJI_00472 | 1.9e-259 | emrY | EGP | Major facilitator Superfamily | ||
EKFEECJI_00473 | 2e-91 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
EKFEECJI_00474 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
EKFEECJI_00475 | 5.5e-148 | S | cog cog1373 | |||
EKFEECJI_00476 | 5.9e-45 | |||||
EKFEECJI_00477 | 3.7e-58 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
EKFEECJI_00479 | 2.1e-45 | S | PFAM Archaeal ATPase | |||
EKFEECJI_00480 | 7.3e-74 | |||||
EKFEECJI_00481 | 0.0 | kup | P | Transport of potassium into the cell | ||
EKFEECJI_00482 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
EKFEECJI_00483 | 1e-78 | S | helix_turn_helix, Deoxyribose operon repressor | |||
EKFEECJI_00484 | 3.3e-140 | repB | EP | Plasmid replication protein | ||
EKFEECJI_00485 | 2.2e-22 | |||||
EKFEECJI_00486 | 4.4e-62 | hipB | K | Helix-turn-helix | ||
EKFEECJI_00487 | 2.7e-151 | I | alpha/beta hydrolase fold | |||
EKFEECJI_00488 | 1.4e-110 | yjbF | S | SNARE associated Golgi protein | ||
EKFEECJI_00489 | 7.5e-100 | J | Acetyltransferase (GNAT) domain | |||
EKFEECJI_00490 | 1.3e-248 | 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) | |
EKFEECJI_00491 | 9.1e-10 | UW | LPXTG-motif cell wall anchor domain protein | |||
EKFEECJI_00492 | 3.3e-45 | UW | LPXTG-motif cell wall anchor domain protein | |||
EKFEECJI_00493 | 1.3e-161 | UW | LPXTG-motif cell wall anchor domain protein | |||
EKFEECJI_00494 | 7.9e-135 | UW | LPXTG-motif cell wall anchor domain protein | |||
EKFEECJI_00495 | 8e-141 | L | An automated process has identified a potential problem with this gene model | |||
EKFEECJI_00496 | 6.8e-156 | ypbG | 2.7.1.2 | GK | ROK family | |
EKFEECJI_00497 | 5.4e-11 | |||||
EKFEECJI_00498 | 4e-45 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
EKFEECJI_00499 | 2.3e-33 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
EKFEECJI_00501 | 7.9e-24 | |||||
EKFEECJI_00502 | 5.1e-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 | ||
EKFEECJI_00503 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
EKFEECJI_00504 | 1.7e-29 | secG | U | Preprotein translocase | ||
EKFEECJI_00505 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
EKFEECJI_00506 | 1.4e-176 | 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 | ||
EKFEECJI_00507 | 7.6e-202 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
EKFEECJI_00508 | 7.9e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
EKFEECJI_00536 | 1.4e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
EKFEECJI_00537 | 5.6e-118 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
EKFEECJI_00538 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
EKFEECJI_00539 | 1.5e-107 | glnP | P | ABC transporter permease | ||
EKFEECJI_00540 | 1e-105 | glnQ | 3.6.3.21 | E | ABC transporter | |
EKFEECJI_00541 | 1.6e-143 | aatB | ET | ABC transporter substrate-binding protein | ||
EKFEECJI_00542 | 7.5e-74 | yjcF | S | Acetyltransferase (GNAT) domain | ||
EKFEECJI_00543 | 7.1e-98 | E | GDSL-like Lipase/Acylhydrolase | |||
EKFEECJI_00544 | 2.5e-169 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
EKFEECJI_00545 | 1.3e-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 | ||
EKFEECJI_00546 | 8.8e-58 | S | Peptidase propeptide and YPEB domain | |||
EKFEECJI_00547 | 3e-37 | |||||
EKFEECJI_00548 | 2.4e-110 | K | WHG domain | |||
EKFEECJI_00549 | 6.4e-96 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
EKFEECJI_00550 | 2e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
EKFEECJI_00551 | 6e-151 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
EKFEECJI_00552 | 2.5e-180 | 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 | |
EKFEECJI_00554 | 3e-53 | cvpA | S | Colicin V production protein | ||
EKFEECJI_00556 | 5.5e-30 | |||||
EKFEECJI_00557 | 4.3e-40 | S | Protein of unknown function (DUF2922) | |||
EKFEECJI_00558 | 4.6e-127 | S | SLAP domain | |||
EKFEECJI_00560 | 5.3e-41 | |||||
EKFEECJI_00561 | 1.2e-77 | K | DNA-templated transcription, initiation | |||
EKFEECJI_00562 | 1.1e-25 | |||||
EKFEECJI_00563 | 4.3e-145 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
EKFEECJI_00564 | 6.7e-19 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
EKFEECJI_00565 | 7.2e-104 | S | SLAP domain | |||
EKFEECJI_00568 | 4.4e-17 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
EKFEECJI_00571 | 1.2e-32 | M | Peptidase family M23 | |||
EKFEECJI_00572 | 1.8e-159 | trsE | S | COG0433 Predicted ATPase | ||
EKFEECJI_00573 | 4.9e-15 | |||||
EKFEECJI_00575 | 1e-32 | I | mechanosensitive ion channel activity | |||
EKFEECJI_00576 | 1.2e-140 | U | TraM recognition site of TraD and TraG | |||
EKFEECJI_00580 | 6.6e-38 | M | domain protein | |||
EKFEECJI_00581 | 1.6e-42 | M | domain protein | |||
EKFEECJI_00583 | 1.4e-24 | srtA | 3.4.22.70 | M | sortase family | |
EKFEECJI_00584 | 1.8e-21 | S | SLAP domain | |||
EKFEECJI_00589 | 2.6e-11 | ssb | L | Single-strand binding protein family | ||
EKFEECJI_00597 | 3.2e-24 | S | Domain of unknown function (DUF771) | |||
EKFEECJI_00598 | 8.9e-32 | K | Helix-turn-helix domain | |||
EKFEECJI_00599 | 1.2e-21 | XK27_07105 | K | Helix-turn-helix XRE-family like proteins | ||
EKFEECJI_00600 | 1.2e-23 | K | Helix-turn-helix domain | |||
EKFEECJI_00601 | 5e-08 | S | Pfam:DUF955 | |||
EKFEECJI_00602 | 1.4e-153 | L | Belongs to the 'phage' integrase family | |||
EKFEECJI_00604 | 1.8e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
EKFEECJI_00605 | 1.9e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
EKFEECJI_00606 | 1.6e-21 | |||||
EKFEECJI_00607 | 3.8e-77 | comGF | U | Putative Competence protein ComGF | ||
EKFEECJI_00608 | 2.3e-41 | |||||
EKFEECJI_00609 | 1.8e-69 | |||||
EKFEECJI_00610 | 3.1e-43 | comGC | U | competence protein ComGC | ||
EKFEECJI_00611 | 1.7e-171 | comGB | NU | type II secretion system | ||
EKFEECJI_00612 | 1.7e-179 | comGA | NU | Type II IV secretion system protein | ||
EKFEECJI_00613 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
EKFEECJI_00614 | 7.6e-94 | S | VanZ like family | |||
EKFEECJI_00615 | 3.5e-101 | ylbE | GM | NAD(P)H-binding | ||
EKFEECJI_00616 | 3.7e-27 | 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 | ||
EKFEECJI_00618 | 1.3e-160 | L | hmm pf00665 | |||
EKFEECJI_00619 | 5.8e-100 | L | Helix-turn-helix domain | |||
EKFEECJI_00620 | 2e-310 | E | Amino acid permease | |||
EKFEECJI_00622 | 8.8e-82 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
EKFEECJI_00623 | 2.2e-90 | 2.7.7.65 | T | GGDEF domain | ||
EKFEECJI_00624 | 8.2e-36 | |||||
EKFEECJI_00625 | 5.2e-112 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
EKFEECJI_00626 | 3.7e-26 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
EKFEECJI_00627 | 1.2e-92 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
EKFEECJI_00628 | 1e-149 | D | Alpha beta | |||
EKFEECJI_00629 | 1e-297 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
EKFEECJI_00630 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
EKFEECJI_00631 | 8.3e-143 | licT | K | CAT RNA binding domain | ||
EKFEECJI_00632 | 3.8e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
EKFEECJI_00633 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
EKFEECJI_00634 | 1.6e-118 | |||||
EKFEECJI_00635 | 1.8e-75 | K | Penicillinase repressor | |||
EKFEECJI_00636 | 1.4e-147 | S | hydrolase | |||
EKFEECJI_00637 | 4.5e-255 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
EKFEECJI_00638 | 2e-172 | ybbR | S | YbbR-like protein | ||
EKFEECJI_00639 | 6.4e-151 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
EKFEECJI_00640 | 7.3e-208 | potD | P | ABC transporter | ||
EKFEECJI_00641 | 4.8e-127 | potC | P | ABC transporter permease | ||
EKFEECJI_00642 | 1.3e-129 | potB | P | ABC transporter permease | ||
EKFEECJI_00643 | 1.8e-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 | |
EKFEECJI_00644 | 2e-163 | murB | 1.3.1.98 | M | Cell wall formation | |
EKFEECJI_00645 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
EKFEECJI_00646 | 7e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
EKFEECJI_00647 | 4.1e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
EKFEECJI_00648 | 9.7e-137 | 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 | |
EKFEECJI_00649 | 3.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
EKFEECJI_00650 | 1.2e-94 | |||||
EKFEECJI_00652 | 1.9e-117 | cps1D | M | Domain of unknown function (DUF4422) | ||
EKFEECJI_00653 | 6.7e-110 | rfbP | M | Bacterial sugar transferase | ||
EKFEECJI_00654 | 1.4e-144 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
EKFEECJI_00655 | 1.3e-121 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
EKFEECJI_00656 | 6.5e-146 | epsB | M | biosynthesis protein | ||
EKFEECJI_00657 | 1.9e-176 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
EKFEECJI_00659 | 3.8e-216 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
EKFEECJI_00660 | 3.5e-175 | S | Cysteine-rich secretory protein family | |||
EKFEECJI_00661 | 1.6e-41 | |||||
EKFEECJI_00662 | 2.6e-118 | M | NlpC/P60 family | |||
EKFEECJI_00663 | 1.4e-136 | M | NlpC P60 family protein | |||
EKFEECJI_00664 | 5e-88 | M | NlpC/P60 family | |||
EKFEECJI_00665 | 2.2e-88 | gmk2 | 2.7.4.8 | F | Guanylate kinase homologues. | |
EKFEECJI_00666 | 3.9e-42 | |||||
EKFEECJI_00667 | 2.9e-279 | S | O-antigen ligase like membrane protein | |||
EKFEECJI_00668 | 3.3e-112 | |||||
EKFEECJI_00669 | 4.7e-221 | tnpB | L | Putative transposase DNA-binding domain | ||
EKFEECJI_00670 | 5.5e-77 | nrdI | F | NrdI Flavodoxin like | ||
EKFEECJI_00671 | 9.9e-177 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
EKFEECJI_00672 | 2.5e-68 | |||||
EKFEECJI_00673 | 9.1e-112 | yvpB | S | Peptidase_C39 like family | ||
EKFEECJI_00674 | 1.1e-83 | S | Threonine/Serine exporter, ThrE | |||
EKFEECJI_00675 | 2.4e-136 | thrE | S | Putative threonine/serine exporter | ||
EKFEECJI_00676 | 8.9e-292 | S | ABC transporter | |||
EKFEECJI_00677 | 8.3e-58 | |||||
EKFEECJI_00678 | 5e-72 | rimL | J | Acetyltransferase (GNAT) domain | ||
EKFEECJI_00679 | 1.4e-34 | |||||
EKFEECJI_00680 | 1.2e-30 | |||||
EKFEECJI_00681 | 1.8e-111 | S | Protein of unknown function (DUF554) | |||
EKFEECJI_00682 | 8.7e-197 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
EKFEECJI_00683 | 9.7e-234 | cycA | E | Amino acid permease | ||
EKFEECJI_00684 | 9.2e-248 | yifK | E | Amino acid permease | ||
EKFEECJI_00685 | 6.4e-135 | S | PFAM Archaeal ATPase | |||
EKFEECJI_00686 | 2.4e-172 | V | HNH endonuclease | |||
EKFEECJI_00688 | 1.1e-138 | puuD | S | peptidase C26 | ||
EKFEECJI_00689 | 1.8e-230 | steT_1 | E | amino acid | ||
EKFEECJI_00690 | 3.2e-189 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
EKFEECJI_00691 | 3.9e-206 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
EKFEECJI_00694 | 7.7e-188 | 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 | |
EKFEECJI_00695 | 6.4e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
EKFEECJI_00696 | 2.1e-246 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
EKFEECJI_00697 | 2.5e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
EKFEECJI_00698 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
EKFEECJI_00699 | 0.0 | S | SH3-like domain | |||
EKFEECJI_00700 | 2.3e-99 | 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 | |
EKFEECJI_00701 | 2.1e-171 | whiA | K | May be required for sporulation | ||
EKFEECJI_00702 | 4e-195 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
EKFEECJI_00703 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
EKFEECJI_00704 | 9.1e-90 | S | Short repeat of unknown function (DUF308) | |||
EKFEECJI_00705 | 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 | ||
EKFEECJI_00706 | 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 | ||
EKFEECJI_00707 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
EKFEECJI_00708 | 3.9e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
EKFEECJI_00709 | 1.1e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
EKFEECJI_00710 | 9.2e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
EKFEECJI_00711 | 5.8e-180 | 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 | ||
EKFEECJI_00712 | 5.1e-17 | |||||
EKFEECJI_00713 | 4.6e-188 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
EKFEECJI_00714 | 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 | ||
EKFEECJI_00715 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
EKFEECJI_00716 | 9.4e-132 | comFC | S | Competence protein | ||
EKFEECJI_00717 | 4.7e-246 | comFA | L | Helicase C-terminal domain protein | ||
EKFEECJI_00718 | 5.1e-119 | yvyE | 3.4.13.9 | S | YigZ family | |
EKFEECJI_00719 | 1.3e-210 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
EKFEECJI_00720 | 7.4e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
EKFEECJI_00721 | 4.2e-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 | ||
EKFEECJI_00722 | 1.1e-95 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
EKFEECJI_00723 | 5.2e-97 | ymfM | S | Helix-turn-helix domain | ||
EKFEECJI_00724 | 2.3e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
EKFEECJI_00725 | 1.9e-236 | S | Peptidase M16 | |||
EKFEECJI_00726 | 9e-223 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
EKFEECJI_00727 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
EKFEECJI_00728 | 1.7e-69 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
EKFEECJI_00729 | 4.2e-106 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
EKFEECJI_00730 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
EKFEECJI_00731 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
EKFEECJI_00732 | 1.8e-200 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
EKFEECJI_00733 | 9.3e-86 | |||||
EKFEECJI_00734 | 2.5e-283 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
EKFEECJI_00735 | 7.7e-182 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EKFEECJI_00736 | 3e-147 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
EKFEECJI_00737 | 4.4e-140 | ypuA | S | Protein of unknown function (DUF1002) | ||
EKFEECJI_00738 | 3.7e-156 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
EKFEECJI_00739 | 7.3e-126 | S | Alpha/beta hydrolase family | |||
EKFEECJI_00740 | 3.4e-126 | 1.3.5.4 | C | FAD binding domain | ||
EKFEECJI_00741 | 1.7e-213 | 1.3.5.4 | C | FAD binding domain | ||
EKFEECJI_00742 | 2e-49 | L | PFAM transposase, IS4 family protein | |||
EKFEECJI_00743 | 3e-88 | L | PFAM transposase, IS4 family protein | |||
EKFEECJI_00744 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
EKFEECJI_00745 | 3.4e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
EKFEECJI_00746 | 1.7e-249 | yhdP | S | Transporter associated domain | ||
EKFEECJI_00747 | 3.9e-119 | C | nitroreductase | |||
EKFEECJI_00748 | 2.1e-39 | |||||
EKFEECJI_00749 | 2.9e-87 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
EKFEECJI_00750 | 1.6e-80 | |||||
EKFEECJI_00751 | 4.1e-147 | glvR | K | Helix-turn-helix domain, rpiR family | ||
EKFEECJI_00752 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
EKFEECJI_00753 | 5.4e-147 | S | hydrolase | |||
EKFEECJI_00754 | 2e-160 | rssA | S | Phospholipase, patatin family | ||
EKFEECJI_00755 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
EKFEECJI_00756 | 3.1e-136 | glcR | K | DeoR C terminal sensor domain | ||
EKFEECJI_00757 | 2.5e-59 | S | Enterocin A Immunity | |||
EKFEECJI_00758 | 1.2e-154 | S | hydrolase | |||
EKFEECJI_00759 | 2.8e-134 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
EKFEECJI_00760 | 9.1e-175 | rihB | 3.2.2.1 | F | Nucleoside | |
EKFEECJI_00761 | 0.0 | kup | P | Transport of potassium into the cell | ||
EKFEECJI_00762 | 1e-125 | 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 | |
EKFEECJI_00763 | 2.3e-165 | 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 | |
EKFEECJI_00764 | 7.7e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
EKFEECJI_00765 | 1.3e-235 | G | Bacterial extracellular solute-binding protein | |||
EKFEECJI_00766 | 6.3e-212 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
EKFEECJI_00767 | 5.6e-86 | |||||
EKFEECJI_00768 | 1.1e-164 | S | Protein of unknown function (DUF2974) | |||
EKFEECJI_00769 | 4.7e-109 | glnP | P | ABC transporter permease | ||
EKFEECJI_00770 | 3.7e-90 | gluC | P | ABC transporter permease | ||
EKFEECJI_00771 | 1.2e-146 | glnH | ET | ABC transporter substrate-binding protein | ||
EKFEECJI_00772 | 4.8e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
EKFEECJI_00773 | 3.8e-46 | udk | 2.7.1.48 | F | Zeta toxin | |
EKFEECJI_00774 | 1e-44 | udk | 2.7.1.48 | F | Zeta toxin | |
EKFEECJI_00775 | 1e-246 | G | MFS/sugar transport protein | |||
EKFEECJI_00776 | 1.6e-100 | S | ABC-type cobalt transport system, permease component | |||
EKFEECJI_00777 | 0.0 | V | ABC transporter transmembrane region | |||
EKFEECJI_00778 | 6.9e-309 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
EKFEECJI_00779 | 1.4e-80 | K | Transcriptional regulator, MarR family | |||
EKFEECJI_00780 | 1.9e-147 | glnH | ET | ABC transporter | ||
EKFEECJI_00781 | 1.9e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
EKFEECJI_00782 | 8.6e-243 | steT | E | amino acid | ||
EKFEECJI_00783 | 2.4e-26 | steT | E | amino acid | ||
EKFEECJI_00784 | 2.8e-202 | steT | E | amino acid | ||
EKFEECJI_00785 | 2.7e-138 | |||||
EKFEECJI_00786 | 5.9e-174 | S | Aldo keto reductase | |||
EKFEECJI_00787 | 2.2e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
EKFEECJI_00788 | 4.7e-182 | pepA | E | M42 glutamyl aminopeptidase | ||
EKFEECJI_00789 | 8.3e-198 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
EKFEECJI_00790 | 5.5e-36 | |||||
EKFEECJI_00791 | 1.6e-158 | scrR | K | Periplasmic binding protein domain | ||
EKFEECJI_00792 | 4.9e-35 | msmE | G | Bacterial extracellular solute-binding protein | ||
EKFEECJI_00793 | 3.2e-172 | msmE | G | Bacterial extracellular solute-binding protein | ||
EKFEECJI_00794 | 4.8e-157 | msmF | P | Binding-protein-dependent transport system inner membrane component | ||
EKFEECJI_00795 | 2e-152 | msmG | P | Binding-protein-dependent transport system inner membrane component | ||
EKFEECJI_00796 | 2.8e-210 | msmX | P | Belongs to the ABC transporter superfamily | ||
EKFEECJI_00797 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
EKFEECJI_00798 | 6.2e-271 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
EKFEECJI_00799 | 7.5e-109 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
EKFEECJI_00800 | 6e-27 | K | response regulator | |||
EKFEECJI_00801 | 1.3e-65 | K | response regulator | |||
EKFEECJI_00802 | 5.9e-57 | sptS | 2.7.13.3 | T | Histidine kinase | |
EKFEECJI_00803 | 2.6e-141 | sptS | 2.7.13.3 | T | Histidine kinase | |
EKFEECJI_00804 | 6.7e-207 | EGP | Major facilitator Superfamily | |||
EKFEECJI_00805 | 5.6e-68 | O | OsmC-like protein | |||
EKFEECJI_00806 | 2.3e-87 | S | Protein of unknown function (DUF805) | |||
EKFEECJI_00807 | 3.2e-77 | |||||
EKFEECJI_00808 | 3.1e-278 | |||||
EKFEECJI_00809 | 2.8e-08 | S | Fic/DOC family | |||
EKFEECJI_00810 | 4.5e-49 | S | Fic/DOC family | |||
EKFEECJI_00811 | 3.2e-278 | yjeM | E | Amino Acid | ||
EKFEECJI_00812 | 1.7e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
EKFEECJI_00813 | 5.4e-242 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
EKFEECJI_00814 | 9.7e-136 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
EKFEECJI_00815 | 7.4e-40 | yabO | J | S4 domain protein | ||
EKFEECJI_00816 | 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 | ||
EKFEECJI_00817 | 5.1e-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 | |
EKFEECJI_00818 | 1.5e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
EKFEECJI_00819 | 3.4e-129 | S | (CBS) domain | |||
EKFEECJI_00821 | 3.5e-71 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
EKFEECJI_00822 | 2e-234 | mepA | V | MATE efflux family protein | ||
EKFEECJI_00823 | 1.2e-51 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |||
EKFEECJI_00824 | 6.4e-113 | S | SLAP domain | |||
EKFEECJI_00825 | 8.4e-89 | |||||
EKFEECJI_00826 | 3e-09 | isdH | M | Iron Transport-associated domain | ||
EKFEECJI_00827 | 6.3e-123 | M | Iron Transport-associated domain | |||
EKFEECJI_00828 | 8.7e-159 | isdE | P | Periplasmic binding protein | ||
EKFEECJI_00829 | 9.5e-148 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
EKFEECJI_00830 | 6.7e-139 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
EKFEECJI_00831 | 6.7e-44 | 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 | ||
EKFEECJI_00832 | 3.4e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
EKFEECJI_00833 | 1.3e-38 | S | RelB antitoxin | |||
EKFEECJI_00834 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
EKFEECJI_00835 | 0.0 | S | membrane | |||
EKFEECJI_00836 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
EKFEECJI_00837 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
EKFEECJI_00838 | 2.7e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
EKFEECJI_00839 | 4e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
EKFEECJI_00840 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
EKFEECJI_00841 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
EKFEECJI_00842 | 1.5e-167 | 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) | |
EKFEECJI_00843 | 7.6e-225 | ynbB | 4.4.1.1 | P | aluminum resistance | |
EKFEECJI_00844 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
EKFEECJI_00845 | 1.5e-169 | |||||
EKFEECJI_00846 | 6e-148 | |||||
EKFEECJI_00847 | 1.9e-21 | |||||
EKFEECJI_00850 | 2.7e-34 | |||||
EKFEECJI_00851 | 1.2e-128 | S | interspecies interaction between organisms | |||
EKFEECJI_00853 | 7.1e-263 | E | ABC transporter, substratebinding protein | |||
EKFEECJI_00854 | 3.7e-66 | K | Helix-turn-helix domain, rpiR family | |||
EKFEECJI_00855 | 2.9e-122 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
EKFEECJI_00856 | 8.4e-90 | nanK | GK | ROK family | ||
EKFEECJI_00857 | 2.3e-56 | G | Xylose isomerase domain protein TIM barrel | |||
EKFEECJI_00858 | 1.9e-121 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
EKFEECJI_00859 | 1e-220 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
EKFEECJI_00860 | 1.1e-59 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
EKFEECJI_00861 | 1.7e-36 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
EKFEECJI_00862 | 2.9e-109 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
EKFEECJI_00863 | 4.4e-103 | K | Putative DNA-binding domain | |||
EKFEECJI_00864 | 9.3e-35 | |||||
EKFEECJI_00865 | 2e-157 | S | reductase | |||
EKFEECJI_00866 | 5.8e-85 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
EKFEECJI_00868 | 1e-47 | L | Psort location Cytoplasmic, score | |||
EKFEECJI_00869 | 1.7e-23 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
EKFEECJI_00870 | 9.6e-18 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
EKFEECJI_00872 | 3.7e-133 | topA2 | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
EKFEECJI_00874 | 1.1e-23 | S | CAAX protease self-immunity | |||
EKFEECJI_00876 | 4.1e-34 | |||||
EKFEECJI_00877 | 1e-66 | doc | S | Fic/DOC family | ||
EKFEECJI_00879 | 9.4e-51 | L | An automated process has identified a potential problem with this gene model | |||
EKFEECJI_00880 | 7.9e-16 | L | An automated process has identified a potential problem with this gene model | |||
EKFEECJI_00882 | 1.2e-24 | 2.7.1.200, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system EIIA 2 | ||
EKFEECJI_00883 | 9.7e-205 | gatC | G | PTS system sugar-specific permease component | ||
EKFEECJI_00884 | 6.5e-18 | 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
EKFEECJI_00885 | 3.5e-57 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
EKFEECJI_00886 | 8.3e-123 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
EKFEECJI_00887 | 2.4e-99 | L | An automated process has identified a potential problem with this gene model | |||
EKFEECJI_00888 | 2.3e-28 | V | N-6 DNA Methylase | |||
EKFEECJI_00889 | 2.2e-142 | S | Belongs to the UPF0246 family | |||
EKFEECJI_00890 | 4.1e-141 | aroD | S | Alpha/beta hydrolase family | ||
EKFEECJI_00891 | 3.5e-111 | G | phosphoglycerate mutase | |||
EKFEECJI_00892 | 3.2e-92 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
EKFEECJI_00893 | 3.3e-176 | hrtB | V | ABC transporter permease | ||
EKFEECJI_00894 | 1.5e-102 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
EKFEECJI_00895 | 1.3e-273 | pipD | E | Dipeptidase | ||
EKFEECJI_00896 | 1e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
EKFEECJI_00897 | 1.6e-161 | htrA | 3.4.21.107 | O | serine protease | |
EKFEECJI_00898 | 4.1e-147 | vicX | 3.1.26.11 | S | domain protein | |
EKFEECJI_00899 | 3.4e-149 | yycI | S | YycH protein | ||
EKFEECJI_00900 | 1.6e-257 | yycH | S | YycH protein | ||
EKFEECJI_00901 | 2.2e-305 | vicK | 2.7.13.3 | T | Histidine kinase | |
EKFEECJI_00902 | 4.8e-131 | K | response regulator | |||
EKFEECJI_00904 | 4.9e-34 | |||||
EKFEECJI_00906 | 1.6e-148 | arbV | 2.3.1.51 | I | Acyl-transferase | |
EKFEECJI_00907 | 5e-156 | arbx | M | Glycosyl transferase family 8 | ||
EKFEECJI_00908 | 5e-184 | arbY | M | Glycosyl transferase family 8 | ||
EKFEECJI_00909 | 1.6e-182 | arbY | M | Glycosyl transferase family 8 | ||
EKFEECJI_00910 | 6e-168 | arbZ | I | Phosphate acyltransferases | ||
EKFEECJI_00911 | 1.4e-36 | S | Cytochrome B5 | |||
EKFEECJI_00912 | 9.5e-82 | XK27_04435 | 3.5.4.5 | J | FR47-like protein | |
EKFEECJI_00913 | 2e-10 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
EKFEECJI_00914 | 3.1e-48 | S | Domain of unknown function (DUF4811) | |||
EKFEECJI_00915 | 1.4e-262 | lmrB | EGP | Major facilitator Superfamily | ||
EKFEECJI_00916 | 4.2e-77 | K | MerR HTH family regulatory protein | |||
EKFEECJI_00917 | 3.1e-139 | S | Cysteine-rich secretory protein family | |||
EKFEECJI_00918 | 4.6e-274 | ycaM | E | amino acid | ||
EKFEECJI_00919 | 2.8e-290 | |||||
EKFEECJI_00921 | 3.3e-189 | cggR | K | Putative sugar-binding domain | ||
EKFEECJI_00922 | 6.5e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
EKFEECJI_00923 | 1e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
EKFEECJI_00924 | 1.7e-142 | 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) | |
EKFEECJI_00925 | 1.1e-282 | phoR | 2.7.13.3 | T | Histidine kinase | |
EKFEECJI_00926 | 9.5e-121 | T | Transcriptional regulatory protein, C terminal | |||
EKFEECJI_00927 | 4e-105 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
EKFEECJI_00928 | 1.3e-139 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
EKFEECJI_00929 | 1.2e-152 | pstA | P | Phosphate transport system permease protein PstA | ||
EKFEECJI_00930 | 1.1e-159 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
EKFEECJI_00931 | 4.2e-145 | pstS | P | Phosphate | ||
EKFEECJI_00932 | 1.3e-30 | |||||
EKFEECJI_00933 | 1.4e-191 | oppA | E | ABC transporter, substratebinding protein | ||
EKFEECJI_00934 | 4.7e-275 | ytgP | S | Polysaccharide biosynthesis protein | ||
EKFEECJI_00935 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
EKFEECJI_00936 | 1.1e-121 | 3.6.1.27 | I | Acid phosphatase homologues | ||
EKFEECJI_00937 | 2.8e-168 | K | LysR substrate binding domain | |||
EKFEECJI_00938 | 2.3e-84 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
EKFEECJI_00939 | 6.2e-43 | 1.3.5.4 | C | FAD binding domain | ||
EKFEECJI_00940 | 2.4e-231 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
EKFEECJI_00941 | 1.1e-161 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
EKFEECJI_00942 | 6.1e-177 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
EKFEECJI_00943 | 2.2e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
EKFEECJI_00944 | 4.1e-269 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
EKFEECJI_00945 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
EKFEECJI_00946 | 8.2e-177 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
EKFEECJI_00947 | 1.5e-272 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
EKFEECJI_00948 | 3.7e-130 | ybbH_2 | K | rpiR family | ||
EKFEECJI_00949 | 2.6e-126 | S | Bacterial protein of unknown function (DUF871) | |||
EKFEECJI_00951 | 6.2e-165 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
EKFEECJI_00954 | 1.7e-221 | 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 | |
EKFEECJI_00955 | 8.5e-260 | qacA | EGP | Major facilitator Superfamily | ||
EKFEECJI_00957 | 1.3e-79 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
EKFEECJI_00958 | 3.6e-120 | 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 | |
EKFEECJI_00959 | 1.8e-119 | S | Putative esterase | |||
EKFEECJI_00960 | 4.1e-214 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
EKFEECJI_00961 | 7.1e-56 | S | Bacterial protein of unknown function (DUF871) | |||
EKFEECJI_00962 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
EKFEECJI_00963 | 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 | ||
EKFEECJI_00964 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
EKFEECJI_00965 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
EKFEECJI_00966 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
EKFEECJI_00967 | 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 | |
EKFEECJI_00968 | 5.2e-227 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
EKFEECJI_00969 | 1.4e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
EKFEECJI_00970 | 6.2e-210 | 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 | |
EKFEECJI_00971 | 9.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
EKFEECJI_00972 | 9.6e-41 | yajC | U | Preprotein translocase | ||
EKFEECJI_00973 | 1.5e-186 | 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 | |
EKFEECJI_00974 | 1.7e-102 | 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 | |
EKFEECJI_00975 | 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 | ||
EKFEECJI_00976 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
EKFEECJI_00977 | 5.9e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
EKFEECJI_00978 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
EKFEECJI_00979 | 3.5e-75 | |||||
EKFEECJI_00980 | 2.3e-181 | M | CHAP domain | |||
EKFEECJI_00981 | 0.0 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
EKFEECJI_00982 | 3.7e-295 | scrB | 3.2.1.26 | GH32 | G | invertase |
EKFEECJI_00983 | 1.1e-183 | scrR | K | helix_turn _helix lactose operon repressor | ||
EKFEECJI_00984 | 9.7e-59 | 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 | ||
EKFEECJI_00985 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
EKFEECJI_00986 | 6.6e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
EKFEECJI_00987 | 1.1e-110 | 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 | |
EKFEECJI_00988 | 7.7e-30 | ropB | K | Helix-turn-helix domain | ||
EKFEECJI_00989 | 4.4e-151 | S | Metal-independent alpha-mannosidase (GH125) | |||
EKFEECJI_00990 | 3.8e-184 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
EKFEECJI_00992 | 1.1e-195 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
EKFEECJI_00995 | 1.5e-195 | K | IrrE N-terminal-like domain | |||
EKFEECJI_00996 | 5.2e-92 | |||||
EKFEECJI_00997 | 1.5e-30 | S | Uncharacterized protein conserved in bacteria (DUF2188) | |||
EKFEECJI_01000 | 1.3e-71 | K | Helix-turn-helix domain, rpiR family | |||
EKFEECJI_01001 | 4.1e-21 | K | Helix-turn-helix domain, rpiR family | |||
EKFEECJI_01002 | 4.9e-82 | rarA | L | MgsA AAA+ ATPase C terminal | ||
EKFEECJI_01003 | 4.3e-226 | 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 | ||
EKFEECJI_01005 | 5.7e-103 | 3.2.2.20 | K | acetyltransferase | ||
EKFEECJI_01006 | 2.3e-93 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
EKFEECJI_01007 | 6e-112 | |||||
EKFEECJI_01009 | 1.7e-110 | E | Belongs to the SOS response-associated peptidase family | |||
EKFEECJI_01010 | 3.7e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
EKFEECJI_01011 | 4e-89 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
EKFEECJI_01012 | 2e-103 | S | TPM domain | |||
EKFEECJI_01013 | 2.4e-132 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
EKFEECJI_01014 | 2.5e-311 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
EKFEECJI_01015 | 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 | |
EKFEECJI_01016 | 1e-147 | tatD | L | hydrolase, TatD family | ||
EKFEECJI_01017 | 1e-99 | 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 | |
EKFEECJI_01018 | 6.7e-151 | 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 | |
EKFEECJI_01019 | 4.5e-39 | veg | S | Biofilm formation stimulator VEG | ||
EKFEECJI_01020 | 1.5e-147 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
EKFEECJI_01021 | 2.6e-173 | 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 | |
EKFEECJI_01022 | 5.3e-80 | |||||
EKFEECJI_01023 | 7.3e-290 | S | SLAP domain | |||
EKFEECJI_01024 | 6e-177 | 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) | |
EKFEECJI_01025 | 4.2e-172 | 2.7.1.2 | GK | ROK family | ||
EKFEECJI_01026 | 5.6e-43 | |||||
EKFEECJI_01027 | 3.6e-268 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
EKFEECJI_01028 | 6.9e-69 | S | Domain of unknown function (DUF1934) | |||
EKFEECJI_01029 | 1.5e-46 | 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 | ||
EKFEECJI_01030 | 7.6e-310 | 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 | |
EKFEECJI_01031 | 9.6e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
EKFEECJI_01032 | 1.8e-74 | K | acetyltransferase | |||
EKFEECJI_01033 | 5.7e-285 | pipD | E | Dipeptidase | ||
EKFEECJI_01034 | 2.5e-152 | msmR | K | AraC-like ligand binding domain | ||
EKFEECJI_01035 | 1.4e-226 | pbuX | F | xanthine permease | ||
EKFEECJI_01036 | 4.5e-103 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
EKFEECJI_01037 | 2.4e-30 | K | Helix-turn-helix | |||
EKFEECJI_01038 | 7.8e-304 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
EKFEECJI_01040 | 4.9e-99 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
EKFEECJI_01041 | 8.7e-117 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
EKFEECJI_01043 | 7.8e-78 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
EKFEECJI_01044 | 1e-95 | |||||
EKFEECJI_01045 | 3.6e-215 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
EKFEECJI_01046 | 2.5e-214 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
EKFEECJI_01047 | 2.1e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
EKFEECJI_01048 | 3.6e-163 | yihY | S | Belongs to the UPF0761 family | ||
EKFEECJI_01049 | 1.4e-163 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
EKFEECJI_01050 | 4.1e-80 | fld | C | Flavodoxin | ||
EKFEECJI_01051 | 7e-87 | gtcA | S | Teichoic acid glycosylation protein | ||
EKFEECJI_01052 | 2.2e-200 | L | Transposase DDE domain | |||
EKFEECJI_01053 | 2e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
EKFEECJI_01055 | 4.7e-249 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EKFEECJI_01056 | 2.8e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
EKFEECJI_01057 | 1.3e-61 | M | Glycosyl hydrolases family 25 | |||
EKFEECJI_01058 | 2.6e-61 | M | Glycosyl hydrolases family 25 | |||
EKFEECJI_01059 | 4.6e-85 | L | Transposase | |||
EKFEECJI_01060 | 4.8e-28 | |||||
EKFEECJI_01063 | 4.3e-67 | K | Helix-turn-helix XRE-family like proteins | |||
EKFEECJI_01064 | 3.3e-147 | malG | P | ABC transporter permease | ||
EKFEECJI_01065 | 1.1e-250 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
EKFEECJI_01066 | 1.3e-213 | malE | G | Bacterial extracellular solute-binding protein | ||
EKFEECJI_01067 | 6.8e-209 | msmX | P | Belongs to the ABC transporter superfamily | ||
EKFEECJI_01068 | 9e-116 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
EKFEECJI_01069 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
EKFEECJI_01070 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
EKFEECJI_01071 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
EKFEECJI_01072 | 5.9e-76 | S | PAS domain | |||
EKFEECJI_01073 | 8.9e-145 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
EKFEECJI_01074 | 1.4e-107 | M | Transport protein ComB | |||
EKFEECJI_01075 | 2.2e-129 | blpT | ||||
EKFEECJI_01079 | 3e-21 | |||||
EKFEECJI_01080 | 3.7e-83 | |||||
EKFEECJI_01081 | 3.1e-30 | yozG | K | Transcriptional regulator | ||
EKFEECJI_01082 | 2e-23 | |||||
EKFEECJI_01083 | 1.7e-67 | |||||
EKFEECJI_01084 | 1.1e-164 | natA | S | ABC transporter, ATP-binding protein | ||
EKFEECJI_01085 | 1.8e-218 | natB | CP | ABC-2 family transporter protein | ||
EKFEECJI_01086 | 1.8e-136 | fruR | K | DeoR C terminal sensor domain | ||
EKFEECJI_01087 | 2.2e-168 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
EKFEECJI_01088 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
EKFEECJI_01089 | 5.4e-41 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
EKFEECJI_01090 | 1.4e-148 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
EKFEECJI_01091 | 1.6e-117 | fhuC | P | ABC transporter | ||
EKFEECJI_01092 | 5e-129 | znuB | U | ABC 3 transport family | ||
EKFEECJI_01093 | 2e-264 | lctP | C | L-lactate permease | ||
EKFEECJI_01094 | 6.7e-89 | 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) | |
EKFEECJI_01095 | 1.5e-216 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
EKFEECJI_01096 | 1.2e-11 | |||||
EKFEECJI_01097 | 1.6e-25 | K | Helix-turn-helix XRE-family like proteins | |||
EKFEECJI_01099 | 1.1e-56 | S | Protein of unknown function (DUF3290) | |||
EKFEECJI_01100 | 3e-116 | yviA | S | Protein of unknown function (DUF421) | ||
EKFEECJI_01101 | 9e-158 | 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 | |||
EKFEECJI_01102 | 8e-182 | dnaQ | 2.7.7.7 | L | EXOIII | |
EKFEECJI_01103 | 1.9e-158 | endA | F | DNA RNA non-specific endonuclease | ||
EKFEECJI_01104 | 1.3e-281 | pipD | E | Dipeptidase | ||
EKFEECJI_01105 | 1.9e-203 | malK | P | ATPases associated with a variety of cellular activities | ||
EKFEECJI_01106 | 1.6e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
EKFEECJI_01107 | 6.1e-146 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
EKFEECJI_01108 | 9.2e-258 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
EKFEECJI_01109 | 2.3e-240 | G | Bacterial extracellular solute-binding protein | |||
EKFEECJI_01110 | 1.8e-154 | corA | P | CorA-like Mg2+ transporter protein | ||
EKFEECJI_01111 | 3.3e-148 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
EKFEECJI_01112 | 6.6e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
EKFEECJI_01113 | 0.0 | ydgH | S | MMPL family | ||
EKFEECJI_01115 | 7.8e-26 | K | Acetyltransferase (GNAT) domain | |||
EKFEECJI_01116 | 1.8e-163 | |||||
EKFEECJI_01117 | 4.8e-76 | L | COG3547 Transposase and inactivated derivatives | |||
EKFEECJI_01118 | 9.7e-83 | S | An automated process has identified a potential problem with this gene model | |||
EKFEECJI_01119 | 1e-137 | S | Protein of unknown function (DUF3100) | |||
EKFEECJI_01120 | 2.7e-246 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
EKFEECJI_01121 | 3.2e-228 | Q | Imidazolonepropionase and related amidohydrolases | |||
EKFEECJI_01122 | 0.0 | oppA | E | ABC transporter | ||
EKFEECJI_01123 | 1.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
EKFEECJI_01124 | 0.0 | mco | Q | Multicopper oxidase | ||
EKFEECJI_01125 | 1.9e-25 | |||||
EKFEECJI_01126 | 7.1e-158 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
EKFEECJI_01127 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
EKFEECJI_01128 | 2e-61 | 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 | ||
EKFEECJI_01129 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
EKFEECJI_01130 | 7.1e-200 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
EKFEECJI_01131 | 6.8e-156 | cjaA | ET | ABC transporter substrate-binding protein | ||
EKFEECJI_01132 | 1.5e-127 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
EKFEECJI_01133 | 5.3e-116 | P | ABC transporter permease | |||
EKFEECJI_01134 | 9.1e-54 | papP | P | ABC transporter, permease protein | ||
EKFEECJI_01135 | 1.9e-138 | 2.4.2.3 | F | Phosphorylase superfamily | ||
EKFEECJI_01136 | 9e-144 | 2.4.2.3 | F | Phosphorylase superfamily | ||
EKFEECJI_01137 | 3.6e-151 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
EKFEECJI_01138 | 1.3e-149 | oppA | E | ABC transporter substrate-binding protein | ||
EKFEECJI_01139 | 2.2e-54 | oppA | E | ABC transporter substrate-binding protein | ||
EKFEECJI_01140 | 0.0 | pepF | E | oligoendopeptidase F | ||
EKFEECJI_01141 | 2.9e-31 | |||||
EKFEECJI_01142 | 1.3e-69 | doc | S | Prophage maintenance system killer protein | ||
EKFEECJI_01145 | 4.6e-27 | S | Enterocin A Immunity | |||
EKFEECJI_01146 | 1.7e-22 | blpT | ||||
EKFEECJI_01147 | 7.8e-140 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EKFEECJI_01148 | 3.6e-111 | G | Phosphoglycerate mutase family | |||
EKFEECJI_01149 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
EKFEECJI_01150 | 4.2e-150 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
EKFEECJI_01151 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
EKFEECJI_01152 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
EKFEECJI_01153 | 1e-226 | yhaO | L | Ser Thr phosphatase family protein | ||
EKFEECJI_01154 | 0.0 | L | AAA domain | |||
EKFEECJI_01155 | 1.9e-186 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
EKFEECJI_01156 | 2.9e-23 | |||||
EKFEECJI_01157 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
EKFEECJI_01158 | 1.1e-265 | |||||
EKFEECJI_01159 | 1.9e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
EKFEECJI_01160 | 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 | |
EKFEECJI_01161 | 3.9e-25 | |||||
EKFEECJI_01162 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
EKFEECJI_01163 | 5.7e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
EKFEECJI_01164 | 6.5e-221 | ecsB | U | ABC transporter | ||
EKFEECJI_01165 | 3.3e-126 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
EKFEECJI_01167 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
EKFEECJI_01168 | 1.4e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
EKFEECJI_01169 | 9.7e-247 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
EKFEECJI_01170 | 6.9e-218 | mepA | V | MATE efflux family protein | ||
EKFEECJI_01171 | 1.8e-176 | S | SLAP domain | |||
EKFEECJI_01172 | 4.4e-283 | M | Peptidase family M1 domain | |||
EKFEECJI_01173 | 4.5e-188 | S | Bacteriocin helveticin-J | |||
EKFEECJI_01174 | 8e-51 | L | RelB antitoxin | |||
EKFEECJI_01175 | 7.4e-105 | qmcA | O | prohibitin homologues | ||
EKFEECJI_01176 | 3.5e-25 | qmcA | O | prohibitin homologues | ||
EKFEECJI_01177 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
EKFEECJI_01178 | 4.2e-155 | 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 | |
EKFEECJI_01179 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
EKFEECJI_01180 | 3.5e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
EKFEECJI_01181 | 5.1e-251 | dnaB | L | Replication initiation and membrane attachment | ||
EKFEECJI_01182 | 2.1e-168 | dnaI | L | Primosomal protein DnaI | ||
EKFEECJI_01183 | 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) | |
EKFEECJI_01184 | 1.2e-74 | |||||
EKFEECJI_01185 | 6e-29 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
EKFEECJI_01186 | 2.4e-133 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
EKFEECJI_01187 | 2.2e-85 | S | ECF transporter, substrate-specific component | |||
EKFEECJI_01188 | 1.4e-130 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
EKFEECJI_01189 | 5.1e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
EKFEECJI_01190 | 1.8e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
EKFEECJI_01191 | 1.5e-155 | holB | 2.7.7.7 | L | DNA polymerase III | |
EKFEECJI_01192 | 2e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
EKFEECJI_01193 | 1.6e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
EKFEECJI_01194 | 1.1e-34 | S | Protein of unknown function (DUF2508) | |||
EKFEECJI_01195 | 1.6e-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 | ||
EKFEECJI_01196 | 8.2e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
EKFEECJI_01197 | 1.2e-35 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
EKFEECJI_01198 | 5.7e-106 | 2.4.1.58 | GT8 | M | family 8 | |
EKFEECJI_01199 | 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 | |
EKFEECJI_01200 | 2.2e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
EKFEECJI_01201 | 9e-26 | |||||
EKFEECJI_01202 | 1.3e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
EKFEECJI_01203 | 1.9e-139 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
EKFEECJI_01204 | 1.8e-54 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
EKFEECJI_01205 | 7e-84 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
EKFEECJI_01206 | 1.5e-11 | GT2,GT4 | M | family 8 | ||
EKFEECJI_01207 | 2.8e-90 | L | An automated process has identified a potential problem with this gene model | |||
EKFEECJI_01208 | 2.2e-117 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
EKFEECJI_01209 | 3.9e-139 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
EKFEECJI_01210 | 5e-145 | 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 | |
EKFEECJI_01211 | 6.5e-154 | pstA | P | Phosphate transport system permease protein PstA | ||
EKFEECJI_01212 | 1.9e-162 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
EKFEECJI_01213 | 2.8e-157 | pstS | P | Phosphate | ||
EKFEECJI_01214 | 3.2e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
EKFEECJI_01215 | 1.2e-68 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
EKFEECJI_01216 | 1.2e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
EKFEECJI_01217 | 3.6e-24 | 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 | ||
EKFEECJI_01218 | 1.4e-69 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
EKFEECJI_01219 | 5.1e-226 | N | Uncharacterized conserved protein (DUF2075) | |||
EKFEECJI_01220 | 4.8e-205 | pbpX1 | V | Beta-lactamase | ||
EKFEECJI_01221 | 0.0 | L | Helicase C-terminal domain protein | |||
EKFEECJI_01222 | 1.3e-273 | E | amino acid | |||
EKFEECJI_01223 | 1.8e-158 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
EKFEECJI_01226 | 1.4e-192 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
EKFEECJI_01227 | 7.6e-134 | EGP | Major facilitator Superfamily | |||
EKFEECJI_01228 | 4e-150 | 3.1.3.102, 3.1.3.104 | S | haloacid dehalogenase-like hydrolase | ||
EKFEECJI_01229 | 0.0 | tetP | J | elongation factor G | ||
EKFEECJI_01230 | 1.2e-160 | yvgN | C | Aldo keto reductase | ||
EKFEECJI_01231 | 2e-155 | P | CorA-like Mg2+ transporter protein | |||
EKFEECJI_01232 | 5.6e-132 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
EKFEECJI_01233 | 1.7e-174 | ABC-SBP | S | ABC transporter | ||
EKFEECJI_01234 | 5.6e-121 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
EKFEECJI_01235 | 2.4e-136 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
EKFEECJI_01236 | 5.2e-248 | G | Major Facilitator | |||
EKFEECJI_01237 | 4.1e-18 | |||||
EKFEECJI_01238 | 2.6e-103 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
EKFEECJI_01239 | 6.4e-177 | K | AI-2E family transporter | |||
EKFEECJI_01240 | 2.7e-109 | oppA | E | ABC transporter substrate-binding protein | ||
EKFEECJI_01241 | 4.3e-144 | oppA | E | ABC transporter substrate-binding protein | ||
EKFEECJI_01242 | 5.2e-117 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
EKFEECJI_01243 | 8.4e-74 | ftsZ | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | ||
EKFEECJI_01244 | 9.6e-28 | ftsZ | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | ||
EKFEECJI_01245 | 2.6e-146 | S | Putative ABC-transporter type IV | |||
EKFEECJI_01246 | 6.5e-07 | S | LPXTG cell wall anchor motif | |||
EKFEECJI_01247 | 1.6e-96 | ybaT | E | Amino acid permease | ||
EKFEECJI_01249 | 7.6e-26 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
EKFEECJI_01250 | 1.4e-22 | S | CAAX protease self-immunity | |||
EKFEECJI_01251 | 1.9e-25 | S | CAAX protease self-immunity | |||
EKFEECJI_01252 | 1.9e-22 | K | Putative DNA-binding domain | |||
EKFEECJI_01253 | 7.6e-239 | pyrP | F | Permease | ||
EKFEECJI_01254 | 8.8e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
EKFEECJI_01255 | 9.2e-262 | emrY | EGP | Major facilitator Superfamily | ||
EKFEECJI_01259 | 0.0 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
EKFEECJI_01260 | 4.2e-61 | V | Abi-like protein | |||
EKFEECJI_01261 | 0.0 | L | AAA domain | |||
EKFEECJI_01263 | 1.2e-241 | S | response to antibiotic | |||
EKFEECJI_01264 | 4.9e-125 | |||||
EKFEECJI_01265 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
EKFEECJI_01266 | 8.7e-66 | 2.7.1.191 | G | PTS system fructose IIA component | ||
EKFEECJI_01267 | 4.4e-43 | |||||
EKFEECJI_01268 | 5.9e-09 | |||||
EKFEECJI_01269 | 9.4e-186 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
EKFEECJI_01270 | 5.3e-136 | glvR | K | Helix-turn-helix domain, rpiR family | ||
EKFEECJI_01271 | 2.7e-268 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
EKFEECJI_01272 | 8.3e-24 | papP | P | ABC transporter, permease protein | ||
EKFEECJI_01274 | 4.5e-58 | yodB | K | Transcriptional regulator, HxlR family | ||
EKFEECJI_01275 | 2.2e-134 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
EKFEECJI_01276 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
EKFEECJI_01277 | 2.4e-162 | 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 | ||
EKFEECJI_01278 | 5.7e-83 | S | Aminoacyl-tRNA editing domain | |||
EKFEECJI_01279 | 6.1e-224 | S | SLAP domain | |||
EKFEECJI_01280 | 1.5e-97 | S | CAAX protease self-immunity | |||
EKFEECJI_01281 | 1e-12 | |||||
EKFEECJI_01282 | 1.3e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
EKFEECJI_01283 | 1.2e-126 | K | response regulator | |||
EKFEECJI_01284 | 4.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
EKFEECJI_01285 | 4.6e-216 | ylbM | S | Belongs to the UPF0348 family | ||
EKFEECJI_01286 | 5.3e-59 | 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 | ||
EKFEECJI_01287 | 6.6e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
EKFEECJI_01288 | 4.4e-123 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
EKFEECJI_01289 | 4.4e-200 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
EKFEECJI_01290 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
EKFEECJI_01291 | 8.6e-199 | tnpB | L | Putative transposase DNA-binding domain | ||
EKFEECJI_01292 | 3.1e-152 | 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 | |
EKFEECJI_01293 | 3e-57 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
EKFEECJI_01294 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
EKFEECJI_01295 | 3.2e-72 | 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 | ||
EKFEECJI_01296 | 4e-98 | rihB | 3.2.2.1 | F | Nucleoside | |
EKFEECJI_01297 | 3.8e-103 | potB | E | Binding-protein-dependent transport system inner membrane component | ||
EKFEECJI_01298 | 2e-42 | fryA | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
EKFEECJI_01299 | 5.3e-37 | mngA | 2.7.1.195, 2.7.1.202 | G | Psort location Cytoplasmic, score 9.98 | |
EKFEECJI_01300 | 1.4e-150 | mngA | 2.7.1.195, 2.7.1.202 | U | system, fructose-specific IIC component | |
EKFEECJI_01301 | 5.5e-281 | ybgG | 3.2.1.170 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
EKFEECJI_01302 | 1.4e-137 | licR | 2.7.1.200, 2.7.1.202 | G | Mga helix-turn-helix domain | |
EKFEECJI_01303 | 0.0 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
EKFEECJI_01304 | 7e-43 | 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 | |
EKFEECJI_01305 | 6.6e-182 | 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 | |
EKFEECJI_01306 | 3.4e-284 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
EKFEECJI_01307 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
EKFEECJI_01308 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
EKFEECJI_01309 | 8.9e-133 | L | Phage integrase family | |||
EKFEECJI_01310 | 5.1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
EKFEECJI_01311 | 5.9e-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 | ||
EKFEECJI_01312 | 8.4e-145 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
EKFEECJI_01313 | 7.2e-136 | 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 | ||
EKFEECJI_01314 | 3.5e-157 | 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 | |
EKFEECJI_01315 | 1.4e-153 | 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 | ||
EKFEECJI_01316 | 1.4e-60 | rplQ | J | Ribosomal protein L17 | ||
EKFEECJI_01317 | 1.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
EKFEECJI_01318 | 3e-63 | 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 | ||
EKFEECJI_01319 | 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 | ||
EKFEECJI_01320 | 7.8e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
EKFEECJI_01321 | 8.4e-34 | 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 | ||
EKFEECJI_01322 | 1e-119 | 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 | |
EKFEECJI_01323 | 9e-237 | 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 | ||
EKFEECJI_01324 | 2.6e-71 | rplO | J | Binds to the 23S rRNA | ||
EKFEECJI_01325 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
EKFEECJI_01326 | 4.1e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
EKFEECJI_01327 | 3.6e-55 | 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 | ||
EKFEECJI_01328 | 3.3e-92 | 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 | ||
EKFEECJI_01329 | 3.2e-68 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
EKFEECJI_01330 | 8.9e-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 | ||
EKFEECJI_01331 | 5.5e-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 | ||
EKFEECJI_01332 | 3.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
EKFEECJI_01333 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
EKFEECJI_01334 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
EKFEECJI_01335 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
EKFEECJI_01336 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
EKFEECJI_01337 | 2.7e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
EKFEECJI_01338 | 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 | ||
EKFEECJI_01339 | 1.1e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
EKFEECJI_01340 | 3.6e-154 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
EKFEECJI_01341 | 3.1e-47 | 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 | ||
EKFEECJI_01342 | 2.1e-106 | rplD | J | Forms part of the polypeptide exit tunnel | ||
EKFEECJI_01343 | 9e-113 | 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 | ||
EKFEECJI_01344 | 4.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
EKFEECJI_01345 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
EKFEECJI_01346 | 3.5e-61 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
EKFEECJI_01347 | 8.4e-146 | 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 | ||
EKFEECJI_01348 | 2.1e-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 | ||
EKFEECJI_01349 | 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 | ||
EKFEECJI_01350 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
EKFEECJI_01351 | 6.2e-276 | 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 | |
EKFEECJI_01352 | 6.6e-235 | L | transposase, IS605 OrfB family | |||
EKFEECJI_01353 | 2.1e-28 | S | Peptidase propeptide and YPEB domain | |||
EKFEECJI_01354 | 2.4e-60 | ypaA | S | Protein of unknown function (DUF1304) | ||
EKFEECJI_01355 | 2.3e-309 | oppA3 | E | ABC transporter, substratebinding protein | ||
EKFEECJI_01356 | 9e-161 | V | ABC transporter transmembrane region | |||
EKFEECJI_01357 | 7e-68 | V | ABC transporter transmembrane region | |||
EKFEECJI_01358 | 3.8e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
EKFEECJI_01359 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
EKFEECJI_01360 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
EKFEECJI_01361 | 3.4e-76 | S | Peptidase propeptide and YPEB domain | |||
EKFEECJI_01362 | 5.2e-187 | T | GHKL domain | |||
EKFEECJI_01363 | 3.1e-130 | T | Transcriptional regulatory protein, C terminal | |||
EKFEECJI_01364 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
EKFEECJI_01365 | 2.9e-277 | V | ABC transporter transmembrane region | |||
EKFEECJI_01367 | 4.7e-60 | S | ABC-2 family transporter protein | |||
EKFEECJI_01368 | 2.1e-76 | S | ABC-2 family transporter protein | |||
EKFEECJI_01369 | 8.2e-230 | pbuG | S | permease | ||
EKFEECJI_01370 | 8.2e-140 | cof | S | haloacid dehalogenase-like hydrolase | ||
EKFEECJI_01371 | 9.4e-72 | |||||
EKFEECJI_01372 | 9.3e-124 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
EKFEECJI_01373 | 8.5e-119 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
EKFEECJI_01374 | 2.1e-134 | 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 | |
EKFEECJI_01375 | 3.7e-159 | yeaE | S | Aldo/keto reductase family | ||
EKFEECJI_01376 | 4.4e-172 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
EKFEECJI_01377 | 1.9e-198 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
EKFEECJI_01378 | 1.3e-282 | xylG | 3.6.3.17 | S | ABC transporter | |
EKFEECJI_01379 | 6.9e-181 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
EKFEECJI_01380 | 3.9e-201 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
EKFEECJI_01381 | 2.8e-100 | S | ECF transporter, substrate-specific component | |||
EKFEECJI_01382 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
EKFEECJI_01383 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
EKFEECJI_01384 | 1.6e-194 | S | DUF218 domain | |||
EKFEECJI_01385 | 2.7e-120 | S | CAAX protease self-immunity | |||
EKFEECJI_01386 | 3e-111 | ropB | K | Transcriptional regulator | ||
EKFEECJI_01387 | 4.2e-154 | EGP | Major facilitator Superfamily | |||
EKFEECJI_01388 | 5.4e-51 | |||||
EKFEECJI_01389 | 2.6e-155 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
EKFEECJI_01390 | 4.1e-276 | V | ABC transporter transmembrane region | |||
EKFEECJI_01391 | 2.3e-41 | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | |||
EKFEECJI_01392 | 1.9e-47 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
EKFEECJI_01393 | 2.8e-205 | napA | P | Sodium/hydrogen exchanger family | ||
EKFEECJI_01394 | 0.0 | cadA | P | P-type ATPase | ||
EKFEECJI_01395 | 1.5e-80 | ykuL | S | (CBS) domain | ||
EKFEECJI_01396 | 1e-207 | ywhK | S | Membrane | ||
EKFEECJI_01397 | 4.1e-44 | |||||
EKFEECJI_01398 | 1.2e-18 | S | D-Ala-teichoic acid biosynthesis protein | |||
EKFEECJI_01399 | 2.1e-285 | 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 | |
EKFEECJI_01400 | 1.9e-236 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
EKFEECJI_01401 | 1.7e-35 | 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 | |
EKFEECJI_01402 | 1.5e-247 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
EKFEECJI_01403 | 7.6e-177 | pbpX2 | V | Beta-lactamase | ||
EKFEECJI_01404 | 2.3e-133 | S | Protein of unknown function (DUF975) | |||
EKFEECJI_01405 | 2.7e-137 | lysA2 | M | Glycosyl hydrolases family 25 | ||
EKFEECJI_01406 | 7.9e-291 | ytgP | S | Polysaccharide biosynthesis protein | ||
EKFEECJI_01407 | 1.9e-36 | |||||
EKFEECJI_01408 | 0.0 | XK27_06780 | V | ABC transporter permease | ||
EKFEECJI_01409 | 5.1e-125 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
EKFEECJI_01410 | 2.2e-238 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EKFEECJI_01411 | 2.2e-165 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EKFEECJI_01412 | 0.0 | clpE | O | AAA domain (Cdc48 subfamily) | ||
EKFEECJI_01413 | 4.3e-115 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
EKFEECJI_01414 | 0.0 | L | Plasmid pRiA4b ORF-3-like protein | |||
EKFEECJI_01415 | 7.3e-245 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
EKFEECJI_01416 | 2.8e-119 | 3.6.1.55 | F | NUDIX domain | ||
EKFEECJI_01417 | 7.8e-76 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
EKFEECJI_01418 | 8.1e-175 | ulaG | S | Beta-lactamase superfamily domain | ||
EKFEECJI_01419 | 1.5e-61 | cmtB | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
EKFEECJI_01420 | 1.3e-231 | ulaA | S | PTS system sugar-specific permease component | ||
EKFEECJI_01421 | 4.1e-31 | sgaB | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
EKFEECJI_01422 | 2.8e-90 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
EKFEECJI_01423 | 7.2e-129 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
EKFEECJI_01424 | 4.9e-123 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
EKFEECJI_01425 | 5.2e-68 | L | haloacid dehalogenase-like hydrolase | |||
EKFEECJI_01426 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
EKFEECJI_01427 | 1.4e-16 | L | Transposase | |||
EKFEECJI_01428 | 1.9e-12 | L | Transposase | |||
EKFEECJI_01429 | 5.9e-13 | K | Acetyltransferase (GNAT) domain | |||
EKFEECJI_01430 | 0.0 | XK27_08315 | M | Sulfatase | ||
EKFEECJI_01431 | 1.6e-111 | 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 | |
EKFEECJI_01432 | 2.7e-202 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
EKFEECJI_01433 | 1.4e-98 | G | Aldose 1-epimerase | |||
EKFEECJI_01434 | 5e-133 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
EKFEECJI_01435 | 2.1e-116 | |||||
EKFEECJI_01436 | 2.1e-130 | |||||
EKFEECJI_01437 | 2.1e-161 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
EKFEECJI_01438 | 1.7e-106 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
EKFEECJI_01439 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
EKFEECJI_01440 | 2.5e-179 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
EKFEECJI_01441 | 5.4e-215 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
EKFEECJI_01443 | 9e-121 | |||||
EKFEECJI_01444 | 1.9e-157 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
EKFEECJI_01445 | 3.9e-186 | S | Putative peptidoglycan binding domain | |||
EKFEECJI_01446 | 4e-16 | |||||
EKFEECJI_01447 | 7.9e-92 | liaI | S | membrane | ||
EKFEECJI_01448 | 6.6e-70 | XK27_02470 | K | LytTr DNA-binding domain | ||
EKFEECJI_01449 | 1.2e-18 | S | Sugar efflux transporter for intercellular exchange | |||
EKFEECJI_01450 | 1.3e-250 | dtpT | U | amino acid peptide transporter | ||
EKFEECJI_01451 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
EKFEECJI_01452 | 2.8e-47 | lysM | M | LysM domain | ||
EKFEECJI_01453 | 1.3e-174 | |||||
EKFEECJI_01454 | 1.7e-152 | mdtG | EGP | Major facilitator Superfamily | ||
EKFEECJI_01455 | 6.9e-47 | mdtG | EGP | Major facilitator Superfamily | ||
EKFEECJI_01456 | 5.4e-113 | |||||
EKFEECJI_01457 | 1.7e-139 | |||||
EKFEECJI_01458 | 6.9e-100 | V | ATPases associated with a variety of cellular activities | |||
EKFEECJI_01459 | 3.7e-146 | ykuT | M | mechanosensitive ion channel | ||
EKFEECJI_01460 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
EKFEECJI_01461 | 1.3e-36 | |||||
EKFEECJI_01462 | 7e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
EKFEECJI_01463 | 3.2e-181 | ccpA | K | catabolite control protein A | ||
EKFEECJI_01464 | 2.3e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
EKFEECJI_01465 | 4.3e-55 | |||||
EKFEECJI_01466 | 5.8e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
EKFEECJI_01467 | 2.1e-92 | yutD | S | Protein of unknown function (DUF1027) | ||
EKFEECJI_01468 | 3.4e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
EKFEECJI_01469 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
EKFEECJI_01470 | 5.7e-115 | dedA | S | SNARE-like domain protein | ||
EKFEECJI_01471 | 7.5e-183 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
EKFEECJI_01473 | 7.4e-128 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
EKFEECJI_01474 | 2.1e-194 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
EKFEECJI_01475 | 4.7e-178 | S | PFAM Archaeal ATPase | |||
EKFEECJI_01476 | 1.4e-194 | S | cog cog1373 | |||
EKFEECJI_01477 | 1.2e-129 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
EKFEECJI_01478 | 5e-148 | noc | K | Belongs to the ParB family | ||
EKFEECJI_01479 | 3.4e-138 | soj | D | Sporulation initiation inhibitor | ||
EKFEECJI_01480 | 1.5e-153 | spo0J | K | Belongs to the ParB family | ||
EKFEECJI_01481 | 9.6e-45 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
EKFEECJI_01482 | 3.6e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
EKFEECJI_01483 | 3.8e-137 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
EKFEECJI_01484 | 1.2e-145 | V | ABC transporter, ATP-binding protein | |||
EKFEECJI_01485 | 4.2e-144 | V | ABC transporter, ATP-binding protein | |||
EKFEECJI_01486 | 0.0 | V | ABC transporter | |||
EKFEECJI_01488 | 9.6e-121 | K | response regulator | |||
EKFEECJI_01489 | 6.6e-207 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
EKFEECJI_01490 | 5.5e-305 | 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 | |
EKFEECJI_01491 | 8e-145 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
EKFEECJI_01492 | 1.4e-53 | S | Enterocin A Immunity | |||
EKFEECJI_01493 | 2.5e-33 | |||||
EKFEECJI_01494 | 9.5e-26 | |||||
EKFEECJI_01495 | 1e-24 | |||||
EKFEECJI_01496 | 3e-270 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
EKFEECJI_01497 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
EKFEECJI_01498 | 2.1e-255 | S | Archaea bacterial proteins of unknown function | |||
EKFEECJI_01499 | 1.2e-16 | |||||
EKFEECJI_01500 | 4.4e-138 | 2.7.13.3 | T | GHKL domain | ||
EKFEECJI_01501 | 1.2e-127 | K | LytTr DNA-binding domain | |||
EKFEECJI_01502 | 6.1e-269 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)