ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
MHEKMCGP_00001 | 2.9e-277 | V | ABC transporter transmembrane region | |||
MHEKMCGP_00002 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
MHEKMCGP_00003 | 3.1e-130 | T | Transcriptional regulatory protein, C terminal | |||
MHEKMCGP_00004 | 5.2e-187 | T | GHKL domain | |||
MHEKMCGP_00005 | 3.4e-76 | S | Peptidase propeptide and YPEB domain | |||
MHEKMCGP_00006 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
MHEKMCGP_00007 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
MHEKMCGP_00008 | 3.8e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
MHEKMCGP_00009 | 7e-68 | V | ABC transporter transmembrane region | |||
MHEKMCGP_00010 | 9e-161 | V | ABC transporter transmembrane region | |||
MHEKMCGP_00011 | 2.3e-309 | oppA3 | E | ABC transporter, substratebinding protein | ||
MHEKMCGP_00012 | 2.4e-60 | ypaA | S | Protein of unknown function (DUF1304) | ||
MHEKMCGP_00013 | 2.1e-28 | S | Peptidase propeptide and YPEB domain | |||
MHEKMCGP_00014 | 7.1e-237 | L | transposase, IS605 OrfB family | |||
MHEKMCGP_00015 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
MHEKMCGP_00016 | 4.2e-150 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MHEKMCGP_00017 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
MHEKMCGP_00018 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
MHEKMCGP_00019 | 1e-226 | yhaO | L | Ser Thr phosphatase family protein | ||
MHEKMCGP_00020 | 0.0 | L | AAA domain | |||
MHEKMCGP_00021 | 1.9e-186 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
MHEKMCGP_00022 | 2.9e-23 | |||||
MHEKMCGP_00023 | 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 | |
MHEKMCGP_00024 | 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 | |
MHEKMCGP_00025 | 6.2e-246 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
MHEKMCGP_00026 | 7.5e-103 | G | Phosphoglycerate mutase family | |||
MHEKMCGP_00027 | 7.8e-140 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
MHEKMCGP_00029 | 3e-24 | |||||
MHEKMCGP_00030 | 1.5e-152 | |||||
MHEKMCGP_00031 | 2.5e-186 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
MHEKMCGP_00032 | 1.7e-129 | manY | G | PTS system | ||
MHEKMCGP_00033 | 1e-173 | manN | G | system, mannose fructose sorbose family IID component | ||
MHEKMCGP_00034 | 1.1e-62 | manO | S | Domain of unknown function (DUF956) | ||
MHEKMCGP_00035 | 3.3e-158 | K | Transcriptional regulator | |||
MHEKMCGP_00036 | 3.8e-85 | maa | S | transferase hexapeptide repeat | ||
MHEKMCGP_00037 | 6.8e-243 | cycA | E | Amino acid permease | ||
MHEKMCGP_00038 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
MHEKMCGP_00039 | 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 | |
MHEKMCGP_00040 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
MHEKMCGP_00041 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
MHEKMCGP_00042 | 2.1e-79 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
MHEKMCGP_00043 | 1e-218 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
MHEKMCGP_00044 | 3.2e-28 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
MHEKMCGP_00045 | 2.3e-78 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
MHEKMCGP_00046 | 2.1e-32 | |||||
MHEKMCGP_00047 | 3.7e-59 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
MHEKMCGP_00048 | 2.3e-156 | K | Helix-turn-helix XRE-family like proteins | |||
MHEKMCGP_00049 | 3.9e-298 | V | ABC transporter transmembrane region | |||
MHEKMCGP_00050 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
MHEKMCGP_00051 | 1.7e-193 | S | TerB-C domain | |||
MHEKMCGP_00054 | 3.9e-206 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
MHEKMCGP_00055 | 3.2e-189 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
MHEKMCGP_00056 | 1.8e-230 | steT_1 | E | amino acid | ||
MHEKMCGP_00057 | 2.2e-139 | puuD | S | peptidase C26 | ||
MHEKMCGP_00059 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
MHEKMCGP_00060 | 3.5e-32 | ykzG | S | Belongs to the UPF0356 family | ||
MHEKMCGP_00061 | 8.9e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
MHEKMCGP_00062 | 0.0 | typA | T | GTP-binding protein TypA | ||
MHEKMCGP_00063 | 5.9e-211 | ftsW | D | Belongs to the SEDS family | ||
MHEKMCGP_00064 | 5.1e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
MHEKMCGP_00065 | 4.5e-97 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
MHEKMCGP_00066 | 3.6e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
MHEKMCGP_00067 | 2.4e-187 | ylbL | T | Belongs to the peptidase S16 family | ||
MHEKMCGP_00068 | 3.1e-79 | comEA | L | Competence protein ComEA | ||
MHEKMCGP_00069 | 0.0 | comEC | S | Competence protein ComEC | ||
MHEKMCGP_00070 | 2.6e-175 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
MHEKMCGP_00071 | 2.6e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
MHEKMCGP_00072 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
MHEKMCGP_00073 | 3e-310 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
MHEKMCGP_00074 | 1.3e-148 | |||||
MHEKMCGP_00075 | 1.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
MHEKMCGP_00076 | 5.8e-215 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
MHEKMCGP_00077 | 2e-233 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
MHEKMCGP_00078 | 1.4e-104 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
MHEKMCGP_00079 | 7.8e-39 | yjeM | E | Amino Acid | ||
MHEKMCGP_00080 | 3.4e-175 | yjeM | E | Amino Acid | ||
MHEKMCGP_00081 | 2.3e-192 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
MHEKMCGP_00082 | 1.3e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
MHEKMCGP_00083 | 1.3e-246 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
MHEKMCGP_00084 | 2.3e-36 | |||||
MHEKMCGP_00085 | 3.9e-165 | EG | EamA-like transporter family | |||
MHEKMCGP_00086 | 5.9e-166 | EG | EamA-like transporter family | |||
MHEKMCGP_00087 | 7.3e-83 | yicL | EG | EamA-like transporter family | ||
MHEKMCGP_00088 | 3.5e-83 | |||||
MHEKMCGP_00089 | 1.2e-109 | |||||
MHEKMCGP_00090 | 5.4e-15 | XK27_05540 | S | DUF218 domain | ||
MHEKMCGP_00091 | 9.5e-144 | XK27_05540 | S | DUF218 domain | ||
MHEKMCGP_00092 | 9.3e-264 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
MHEKMCGP_00093 | 4.7e-85 | |||||
MHEKMCGP_00094 | 3.9e-57 | |||||
MHEKMCGP_00095 | 4.7e-25 | S | Protein conserved in bacteria | |||
MHEKMCGP_00096 | 1.3e-54 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
MHEKMCGP_00097 | 2.4e-73 | S | cog cog1373 | |||
MHEKMCGP_00098 | 5.6e-179 | S | PFAM Archaeal ATPase | |||
MHEKMCGP_00099 | 4.5e-192 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
MHEKMCGP_00100 | 7.4e-128 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
MHEKMCGP_00101 | 6.4e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
MHEKMCGP_00102 | 3.5e-277 | yjeM | E | Amino Acid | ||
MHEKMCGP_00103 | 8.9e-84 | S | Fic/DOC family | |||
MHEKMCGP_00104 | 1.3e-290 | |||||
MHEKMCGP_00105 | 6e-76 | |||||
MHEKMCGP_00106 | 5.7e-94 | S | Protein of unknown function (DUF805) | |||
MHEKMCGP_00107 | 1.9e-68 | O | OsmC-like protein | |||
MHEKMCGP_00108 | 3.6e-208 | EGP | Major facilitator Superfamily | |||
MHEKMCGP_00109 | 2.5e-215 | sptS | 2.7.13.3 | T | Histidine kinase | |
MHEKMCGP_00110 | 6.8e-186 | G | Transmembrane secretion effector | |||
MHEKMCGP_00111 | 1.2e-201 | V | ABC transporter transmembrane region | |||
MHEKMCGP_00112 | 6.5e-64 | L | RelB antitoxin | |||
MHEKMCGP_00113 | 2.1e-131 | cobQ | S | glutamine amidotransferase | ||
MHEKMCGP_00114 | 1.1e-81 | M | NlpC/P60 family | |||
MHEKMCGP_00116 | 7.5e-183 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
MHEKMCGP_00117 | 6.8e-116 | dedA | S | SNARE-like domain protein | ||
MHEKMCGP_00118 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
MHEKMCGP_00119 | 3.4e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
MHEKMCGP_00120 | 2.1e-92 | yutD | S | Protein of unknown function (DUF1027) | ||
MHEKMCGP_00121 | 5.8e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
MHEKMCGP_00122 | 4.3e-55 | |||||
MHEKMCGP_00123 | 2.3e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
MHEKMCGP_00124 | 3.2e-181 | ccpA | K | catabolite control protein A | ||
MHEKMCGP_00125 | 7e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
MHEKMCGP_00126 | 1.3e-36 | |||||
MHEKMCGP_00127 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
MHEKMCGP_00128 | 3.7e-146 | ykuT | M | mechanosensitive ion channel | ||
MHEKMCGP_00129 | 6.9e-100 | V | ATPases associated with a variety of cellular activities | |||
MHEKMCGP_00130 | 1.7e-139 | |||||
MHEKMCGP_00131 | 5.4e-113 | |||||
MHEKMCGP_00132 | 8.1e-126 | S | PAS domain | |||
MHEKMCGP_00133 | 1.6e-11 | |||||
MHEKMCGP_00134 | 2.7e-57 | |||||
MHEKMCGP_00135 | 6.6e-56 | |||||
MHEKMCGP_00136 | 4e-08 | |||||
MHEKMCGP_00137 | 4.7e-109 | glnP | P | ABC transporter permease | ||
MHEKMCGP_00138 | 1.1e-164 | S | Protein of unknown function (DUF2974) | |||
MHEKMCGP_00139 | 6.2e-85 | |||||
MHEKMCGP_00140 | 6.3e-212 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
MHEKMCGP_00141 | 5e-235 | G | Bacterial extracellular solute-binding protein | |||
MHEKMCGP_00142 | 3.4e-135 | glnQ | E | ABC transporter, ATP-binding protein | ||
MHEKMCGP_00143 | 1.3e-290 | glnP | P | ABC transporter permease | ||
MHEKMCGP_00144 | 8.9e-121 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
MHEKMCGP_00145 | 5.8e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
MHEKMCGP_00146 | 1.3e-124 | terC | P | Integral membrane protein TerC family | ||
MHEKMCGP_00147 | 9.2e-92 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
MHEKMCGP_00148 | 8.5e-133 | cobB | K | SIR2 family | ||
MHEKMCGP_00149 | 2.7e-83 | S | Protein of unknown function (DUF1211) | |||
MHEKMCGP_00150 | 3.1e-113 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
MHEKMCGP_00151 | 2.8e-119 | 3.6.1.55 | F | NUDIX domain | ||
MHEKMCGP_00152 | 3e-246 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
MHEKMCGP_00153 | 1.3e-71 | K | Helix-turn-helix domain, rpiR family | |||
MHEKMCGP_00154 | 4.1e-21 | K | Helix-turn-helix domain, rpiR family | |||
MHEKMCGP_00155 | 4.9e-82 | rarA | L | MgsA AAA+ ATPase C terminal | ||
MHEKMCGP_00156 | 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 | ||
MHEKMCGP_00157 | 5.8e-85 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
MHEKMCGP_00158 | 2e-157 | S | reductase | |||
MHEKMCGP_00159 | 9.3e-35 | |||||
MHEKMCGP_00161 | 2.9e-81 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
MHEKMCGP_00162 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
MHEKMCGP_00163 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MHEKMCGP_00164 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MHEKMCGP_00165 | 3.6e-120 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
MHEKMCGP_00166 | 7.8e-70 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
MHEKMCGP_00167 | 2.7e-82 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
MHEKMCGP_00168 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
MHEKMCGP_00169 | 4.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
MHEKMCGP_00170 | 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 | ||
MHEKMCGP_00171 | 2.1e-106 | rplD | J | Forms part of the polypeptide exit tunnel | ||
MHEKMCGP_00172 | 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 | ||
MHEKMCGP_00173 | 7.3e-155 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
MHEKMCGP_00174 | 1.1e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
MHEKMCGP_00175 | 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 | ||
MHEKMCGP_00176 | 2.7e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
MHEKMCGP_00177 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
MHEKMCGP_00178 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
MHEKMCGP_00179 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
MHEKMCGP_00180 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
MHEKMCGP_00181 | 3.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
MHEKMCGP_00182 | 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 | ||
MHEKMCGP_00183 | 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 | ||
MHEKMCGP_00184 | 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 | ||
MHEKMCGP_00185 | 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 | ||
MHEKMCGP_00186 | 1.1e-54 | 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 | ||
MHEKMCGP_00187 | 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 | ||
MHEKMCGP_00188 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
MHEKMCGP_00189 | 2.6e-71 | rplO | J | Binds to the 23S rRNA | ||
MHEKMCGP_00190 | 1.1e-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 | ||
MHEKMCGP_00191 | 3.5e-120 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
MHEKMCGP_00192 | 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 | ||
MHEKMCGP_00193 | 7.8e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
MHEKMCGP_00194 | 3.6e-55 | 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 | ||
MHEKMCGP_00195 | 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 | ||
MHEKMCGP_00196 | 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 | |
MHEKMCGP_00197 | 1.4e-60 | rplQ | J | Ribosomal protein L17 | ||
MHEKMCGP_00198 | 3.7e-154 | 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 | ||
MHEKMCGP_00199 | 4.6e-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 | |
MHEKMCGP_00200 | 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 | ||
MHEKMCGP_00201 | 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 | |
MHEKMCGP_00202 | 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 | ||
MHEKMCGP_00203 | 5.1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
MHEKMCGP_00204 | 8.9e-133 | L | Phage integrase family | |||
MHEKMCGP_00205 | 2.5e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
MHEKMCGP_00206 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
MHEKMCGP_00207 | 0.0 | S | SH3-like domain | |||
MHEKMCGP_00208 | 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 | |
MHEKMCGP_00209 | 2.1e-171 | whiA | K | May be required for sporulation | ||
MHEKMCGP_00210 | 4e-195 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
MHEKMCGP_00211 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
MHEKMCGP_00212 | 4.1e-90 | S | Short repeat of unknown function (DUF308) | |||
MHEKMCGP_00213 | 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 | ||
MHEKMCGP_00214 | 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 | ||
MHEKMCGP_00215 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
MHEKMCGP_00216 | 3.9e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
MHEKMCGP_00217 | 1.1e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
MHEKMCGP_00218 | 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 | |
MHEKMCGP_00219 | 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 | ||
MHEKMCGP_00220 | 5.1e-17 | |||||
MHEKMCGP_00221 | 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 | ||
MHEKMCGP_00222 | 6.4e-131 | 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 | ||
MHEKMCGP_00223 | 7.4e-286 | 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 | ||
MHEKMCGP_00224 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
MHEKMCGP_00225 | 9.4e-132 | comFC | S | Competence protein | ||
MHEKMCGP_00226 | 4.7e-246 | comFA | L | Helicase C-terminal domain protein | ||
MHEKMCGP_00227 | 1.5e-51 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |||
MHEKMCGP_00228 | 1.1e-112 | S | SLAP domain | |||
MHEKMCGP_00229 | 8.4e-89 | |||||
MHEKMCGP_00230 | 3e-09 | isdH | M | Iron Transport-associated domain | ||
MHEKMCGP_00231 | 6.3e-123 | M | Iron Transport-associated domain | |||
MHEKMCGP_00232 | 8.7e-159 | isdE | P | Periplasmic binding protein | ||
MHEKMCGP_00233 | 7.3e-148 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
MHEKMCGP_00234 | 6.7e-139 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
MHEKMCGP_00235 | 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 | ||
MHEKMCGP_00236 | 3.4e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
MHEKMCGP_00237 | 1.3e-38 | S | RelB antitoxin | |||
MHEKMCGP_00238 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
MHEKMCGP_00239 | 0.0 | S | membrane | |||
MHEKMCGP_00240 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
MHEKMCGP_00241 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
MHEKMCGP_00242 | 2.1e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
MHEKMCGP_00243 | 3.1e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
MHEKMCGP_00244 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
MHEKMCGP_00245 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
MHEKMCGP_00246 | 1e-168 | 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) | |
MHEKMCGP_00247 | 7.8e-222 | ynbB | 4.4.1.1 | P | aluminum resistance | |
MHEKMCGP_00248 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
MHEKMCGP_00249 | 1.5e-169 | |||||
MHEKMCGP_00250 | 1.7e-147 | |||||
MHEKMCGP_00251 | 1.9e-21 | |||||
MHEKMCGP_00254 | 2.7e-34 | |||||
MHEKMCGP_00255 | 1.2e-128 | S | interspecies interaction between organisms | |||
MHEKMCGP_00257 | 9.1e-10 | K | peptidyl-tyrosine sulfation | |||
MHEKMCGP_00258 | 7.1e-263 | E | ABC transporter, substratebinding protein | |||
MHEKMCGP_00259 | 3.7e-66 | K | Helix-turn-helix domain, rpiR family | |||
MHEKMCGP_00260 | 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 | |
MHEKMCGP_00261 | 8.4e-90 | nanK | GK | ROK family | ||
MHEKMCGP_00262 | 2.3e-56 | G | Xylose isomerase domain protein TIM barrel | |||
MHEKMCGP_00263 | 1.9e-121 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
MHEKMCGP_00264 | 1e-220 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
MHEKMCGP_00265 | 1.1e-59 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
MHEKMCGP_00266 | 1.7e-36 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
MHEKMCGP_00267 | 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) | |
MHEKMCGP_00268 | 7.7e-10 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
MHEKMCGP_00269 | 4.7e-88 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
MHEKMCGP_00270 | 4.4e-172 | S | Domain of unknown function (DUF389) | |||
MHEKMCGP_00271 | 6e-86 | |||||
MHEKMCGP_00272 | 5.9e-68 | S | Protein of unknown function (DUF3021) | |||
MHEKMCGP_00273 | 2.5e-140 | V | ABC transporter | |||
MHEKMCGP_00274 | 2e-106 | S | domain protein | |||
MHEKMCGP_00275 | 8.4e-56 | S | Domain of unknown function (DUF4767) | |||
MHEKMCGP_00276 | 5.8e-244 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
MHEKMCGP_00277 | 2.5e-147 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
MHEKMCGP_00278 | 3.2e-101 | 3.6.1.27 | I | Acid phosphatase homologues | ||
MHEKMCGP_00279 | 1.1e-183 | scrR | K | helix_turn _helix lactose operon repressor | ||
MHEKMCGP_00280 | 3.7e-295 | scrB | 3.2.1.26 | GH32 | G | invertase |
MHEKMCGP_00281 | 0.0 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
MHEKMCGP_00282 | 2.3e-181 | M | CHAP domain | |||
MHEKMCGP_00283 | 3.5e-75 | |||||
MHEKMCGP_00284 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
MHEKMCGP_00285 | 5.9e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
MHEKMCGP_00286 | 4.6e-171 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
MHEKMCGP_00287 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
MHEKMCGP_00288 | 6.7e-98 | M | ErfK YbiS YcfS YnhG | |||
MHEKMCGP_00289 | 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 | |
MHEKMCGP_00290 | 1.3e-240 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
MHEKMCGP_00292 | 4.7e-46 | pspC | KT | PspC domain | ||
MHEKMCGP_00293 | 3.3e-237 | L | COG2963 Transposase and inactivated derivatives | |||
MHEKMCGP_00294 | 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) | |
MHEKMCGP_00295 | 1e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
MHEKMCGP_00296 | 6.5e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
MHEKMCGP_00297 | 2.6e-189 | cggR | K | Putative sugar-binding domain | ||
MHEKMCGP_00299 | 2.8e-290 | |||||
MHEKMCGP_00300 | 4.6e-274 | ycaM | E | amino acid | ||
MHEKMCGP_00301 | 3.1e-139 | S | Cysteine-rich secretory protein family | |||
MHEKMCGP_00302 | 4.2e-77 | K | MerR HTH family regulatory protein | |||
MHEKMCGP_00303 | 1.4e-262 | lmrB | EGP | Major facilitator Superfamily | ||
MHEKMCGP_00304 | 3.1e-48 | S | Domain of unknown function (DUF4811) | |||
MHEKMCGP_00305 | 5.9e-45 | |||||
MHEKMCGP_00306 | 3.7e-58 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
MHEKMCGP_00308 | 1.6e-07 | S | PFAM Archaeal ATPase | |||
MHEKMCGP_00310 | 1.6e-73 | |||||
MHEKMCGP_00311 | 0.0 | kup | P | Transport of potassium into the cell | ||
MHEKMCGP_00312 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
MHEKMCGP_00313 | 1.2e-108 | yttB | EGP | Major facilitator Superfamily | ||
MHEKMCGP_00314 | 6.8e-60 | divIC | D | Septum formation initiator | ||
MHEKMCGP_00315 | 1.8e-62 | yabR | J | S1 RNA binding domain | ||
MHEKMCGP_00316 | 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 | |
MHEKMCGP_00317 | 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 | ||
MHEKMCGP_00318 | 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 | ||
MHEKMCGP_00319 | 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 | ||
MHEKMCGP_00320 | 1.7e-298 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
MHEKMCGP_00321 | 2.6e-225 | V | ABC transporter transmembrane region | |||
MHEKMCGP_00322 | 1.3e-287 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
MHEKMCGP_00323 | 1e-229 | S | Tetratricopeptide repeat protein | |||
MHEKMCGP_00324 | 3e-41 | 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 | ||
MHEKMCGP_00325 | 1.9e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
MHEKMCGP_00326 | 5.5e-212 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
MHEKMCGP_00327 | 2.2e-114 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
MHEKMCGP_00328 | 2.7e-18 | M | Lysin motif | |||
MHEKMCGP_00329 | 8.7e-114 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
MHEKMCGP_00330 | 7.8e-10 | 3.6.3.2, 3.6.3.6 | P | cation transport ATPase | ||
MHEKMCGP_00331 | 4.4e-35 | 3.6.3.2, 3.6.3.6 | P | cation transport ATPase | ||
MHEKMCGP_00332 | 2.5e-264 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
MHEKMCGP_00333 | 1.9e-19 | |||||
MHEKMCGP_00334 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
MHEKMCGP_00335 | 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 | |
MHEKMCGP_00336 | 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 | ||
MHEKMCGP_00337 | 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 | ||
MHEKMCGP_00338 | 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 | ||
MHEKMCGP_00339 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
MHEKMCGP_00340 | 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 | |
MHEKMCGP_00341 | 2.1e-08 | rdgB | 3.6.1.66, 5.1.1.3 | F | Ham1 family | |
MHEKMCGP_00342 | 1.7e-78 | rdgB | 3.6.1.66, 5.1.1.3 | F | Ham1 family | |
MHEKMCGP_00343 | 3.4e-79 | |||||
MHEKMCGP_00344 | 1.4e-242 | cpdA | S | Calcineurin-like phosphoesterase | ||
MHEKMCGP_00345 | 1.6e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
MHEKMCGP_00346 | 1.1e-68 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
MHEKMCGP_00347 | 1e-107 | ypsA | S | Belongs to the UPF0398 family | ||
MHEKMCGP_00348 | 4.5e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
MHEKMCGP_00349 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
MHEKMCGP_00350 | 2.7e-114 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
MHEKMCGP_00351 | 1.3e-114 | dnaD | L | DnaD domain protein | ||
MHEKMCGP_00352 | 5.8e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
MHEKMCGP_00353 | 2.4e-89 | ypmB | S | Protein conserved in bacteria | ||
MHEKMCGP_00354 | 3e-22 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
MHEKMCGP_00355 | 9.2e-14 | |||||
MHEKMCGP_00356 | 2.3e-172 | M | Glycosyl hydrolases family 25 | |||
MHEKMCGP_00357 | 5e-29 | |||||
MHEKMCGP_00358 | 7.9e-19 | |||||
MHEKMCGP_00360 | 1.1e-07 | |||||
MHEKMCGP_00361 | 2.2e-19 | S | Phage uncharacterised protein (Phage_XkdX) | |||
MHEKMCGP_00362 | 7.1e-38 | |||||
MHEKMCGP_00364 | 4.4e-151 | S | Metal-independent alpha-mannosidase (GH125) | |||
MHEKMCGP_00365 | 3.8e-184 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
MHEKMCGP_00366 | 8.3e-24 | papP | P | ABC transporter, permease protein | ||
MHEKMCGP_00368 | 4.5e-58 | yodB | K | Transcriptional regulator, HxlR family | ||
MHEKMCGP_00369 | 2.2e-134 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
MHEKMCGP_00370 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
MHEKMCGP_00371 | 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 | ||
MHEKMCGP_00372 | 5.7e-83 | S | Aminoacyl-tRNA editing domain | |||
MHEKMCGP_00373 | 6.1e-224 | S | SLAP domain | |||
MHEKMCGP_00374 | 1.5e-97 | S | CAAX protease self-immunity | |||
MHEKMCGP_00375 | 1e-12 | |||||
MHEKMCGP_00376 | 1.3e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
MHEKMCGP_00377 | 1.2e-126 | K | response regulator | |||
MHEKMCGP_00378 | 4.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
MHEKMCGP_00379 | 4.6e-216 | ylbM | S | Belongs to the UPF0348 family | ||
MHEKMCGP_00380 | 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 | ||
MHEKMCGP_00381 | 6.6e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
MHEKMCGP_00382 | 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) | |
MHEKMCGP_00383 | 4.4e-200 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
MHEKMCGP_00384 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
MHEKMCGP_00385 | 8.6e-199 | tnpB | L | Putative transposase DNA-binding domain | ||
MHEKMCGP_00386 | 1.1e-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 | |
MHEKMCGP_00387 | 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 | ||
MHEKMCGP_00388 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
MHEKMCGP_00389 | 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 | ||
MHEKMCGP_00390 | 2.7e-36 | yyaR | K | Acetyltransferase (GNAT) domain | ||
MHEKMCGP_00391 | 3.3e-131 | S | Protein of unknown function (DUF805) | |||
MHEKMCGP_00392 | 6.4e-159 | L | HNH nucleases | |||
MHEKMCGP_00393 | 1e-119 | yfbR | S | HD containing hydrolase-like enzyme | ||
MHEKMCGP_00394 | 4e-177 | G | Glycosyl hydrolases family 8 | |||
MHEKMCGP_00395 | 4.5e-189 | ydaM | M | Glycosyl transferase | ||
MHEKMCGP_00396 | 2.3e-164 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
MHEKMCGP_00397 | 1.6e-294 | L | Nuclease-related domain | |||
MHEKMCGP_00398 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
MHEKMCGP_00399 | 8.3e-106 | S | Repeat protein | |||
MHEKMCGP_00400 | 3.9e-127 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
MHEKMCGP_00401 | 5.1e-220 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
MHEKMCGP_00402 | 5.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
MHEKMCGP_00403 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
MHEKMCGP_00404 | 1.2e-126 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
MHEKMCGP_00405 | 6.7e-37 | |||||
MHEKMCGP_00406 | 2.8e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
MHEKMCGP_00407 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
MHEKMCGP_00408 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
MHEKMCGP_00409 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
MHEKMCGP_00410 | 5.7e-149 | ylmH | S | S4 domain protein | ||
MHEKMCGP_00411 | 1.7e-45 | yggT | S | YGGT family | ||
MHEKMCGP_00412 | 7.3e-74 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
MHEKMCGP_00413 | 1.7e-206 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
MHEKMCGP_00414 | 1.3e-246 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
MHEKMCGP_00415 | 4.5e-152 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
MHEKMCGP_00416 | 3.7e-207 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
MHEKMCGP_00417 | 5e-262 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
MHEKMCGP_00418 | 1.5e-175 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
MHEKMCGP_00419 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
MHEKMCGP_00420 | 1.8e-54 | ftsL | D | Cell division protein FtsL | ||
MHEKMCGP_00421 | 7.2e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
MHEKMCGP_00422 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
MHEKMCGP_00423 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
MHEKMCGP_00425 | 2.7e-94 | mreD | ||||
MHEKMCGP_00426 | 2e-147 | mreC | M | Involved in formation and maintenance of cell shape | ||
MHEKMCGP_00427 | 2.4e-176 | mreB | D | cell shape determining protein MreB | ||
MHEKMCGP_00428 | 2.3e-108 | radC | L | DNA repair protein | ||
MHEKMCGP_00429 | 5.7e-126 | S | Haloacid dehalogenase-like hydrolase | |||
MHEKMCGP_00430 | 1.5e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
MHEKMCGP_00431 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
MHEKMCGP_00432 | 2.5e-52 | |||||
MHEKMCGP_00433 | 1.1e-132 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
MHEKMCGP_00434 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
MHEKMCGP_00436 | 6.5e-44 | |||||
MHEKMCGP_00437 | 1.5e-94 | S | Protein of unknown function (DUF3990) | |||
MHEKMCGP_00438 | 5.2e-170 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
MHEKMCGP_00439 | 2.1e-65 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
MHEKMCGP_00440 | 5.5e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
MHEKMCGP_00441 | 3.2e-119 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
MHEKMCGP_00442 | 1.7e-184 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
MHEKMCGP_00443 | 2e-225 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
MHEKMCGP_00444 | 4.8e-213 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
MHEKMCGP_00445 | 2.1e-294 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
MHEKMCGP_00446 | 1.4e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
MHEKMCGP_00447 | 1.3e-84 | yueI | S | Protein of unknown function (DUF1694) | ||
MHEKMCGP_00448 | 2.2e-238 | rarA | L | recombination factor protein RarA | ||
MHEKMCGP_00449 | 8.4e-39 | |||||
MHEKMCGP_00450 | 1.8e-78 | usp6 | T | universal stress protein | ||
MHEKMCGP_00451 | 4.7e-216 | rodA | D | Belongs to the SEDS family | ||
MHEKMCGP_00452 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
MHEKMCGP_00453 | 1e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
MHEKMCGP_00454 | 1.2e-177 | mbl | D | Cell shape determining protein MreB Mrl | ||
MHEKMCGP_00455 | 2e-30 | ywzB | S | Protein of unknown function (DUF1146) | ||
MHEKMCGP_00456 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
MHEKMCGP_00457 | 3.3e-240 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
MHEKMCGP_00458 | 2e-172 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
MHEKMCGP_00459 | 1.8e-281 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
MHEKMCGP_00460 | 2.8e-91 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
MHEKMCGP_00461 | 3.4e-46 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
MHEKMCGP_00462 | 3.5e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
MHEKMCGP_00463 | 3.8e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
MHEKMCGP_00464 | 1.6e-20 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
MHEKMCGP_00465 | 1.4e-175 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
MHEKMCGP_00466 | 1.4e-16 | L | Transposase | |||
MHEKMCGP_00467 | 1.9e-12 | L | Transposase | |||
MHEKMCGP_00468 | 5.9e-13 | K | Acetyltransferase (GNAT) domain | |||
MHEKMCGP_00469 | 1.4e-37 | S | Putative adhesin | |||
MHEKMCGP_00470 | 3.7e-261 | V | ABC transporter transmembrane region | |||
MHEKMCGP_00471 | 1.8e-40 | |||||
MHEKMCGP_00472 | 4.5e-79 | S | helix_turn_helix, Deoxyribose operon repressor | |||
MHEKMCGP_00473 | 3.3e-140 | repB | EP | Plasmid replication protein | ||
MHEKMCGP_00474 | 2.2e-22 | |||||
MHEKMCGP_00475 | 2.5e-226 | pbuG | S | permease | ||
MHEKMCGP_00476 | 9.7e-146 | S | haloacid dehalogenase-like hydrolase | |||
MHEKMCGP_00477 | 2e-225 | S | cog cog1373 | |||
MHEKMCGP_00478 | 6.1e-61 | K | Transcriptional regulator | |||
MHEKMCGP_00479 | 1.3e-94 | K | Transcriptional regulator | |||
MHEKMCGP_00480 | 1.8e-48 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | ||
MHEKMCGP_00481 | 3.1e-16 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
MHEKMCGP_00482 | 2.5e-40 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
MHEKMCGP_00483 | 2e-234 | mepA | V | MATE efflux family protein | ||
MHEKMCGP_00484 | 3.5e-71 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
MHEKMCGP_00485 | 1.8e-58 | S | Putative adhesin | |||
MHEKMCGP_00486 | 5.6e-101 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
MHEKMCGP_00487 | 3.8e-20 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
MHEKMCGP_00488 | 1.1e-83 | dps | P | Belongs to the Dps family | ||
MHEKMCGP_00490 | 3.2e-139 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
MHEKMCGP_00491 | 8.7e-86 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
MHEKMCGP_00492 | 1.9e-75 | M | LysM domain | |||
MHEKMCGP_00493 | 1.3e-42 | |||||
MHEKMCGP_00495 | 4.9e-35 | |||||
MHEKMCGP_00496 | 4.5e-76 | yniG | EGP | Major facilitator Superfamily | ||
MHEKMCGP_00497 | 5.4e-237 | L | transposase, IS605 OrfB family | |||
MHEKMCGP_00498 | 1.4e-109 | yniG | EGP | Major facilitator Superfamily | ||
MHEKMCGP_00499 | 2.4e-128 | S | cog cog1373 | |||
MHEKMCGP_00500 | 1.5e-36 | oppA | E | ABC transporter substrate-binding protein | ||
MHEKMCGP_00502 | 1.4e-31 | O | OsmC-like protein | |||
MHEKMCGP_00503 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
MHEKMCGP_00504 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
MHEKMCGP_00505 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
MHEKMCGP_00506 | 1.4e-116 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
MHEKMCGP_00507 | 3e-209 | msmX | P | Belongs to the ABC transporter superfamily | ||
MHEKMCGP_00508 | 2.3e-213 | malE | G | Bacterial extracellular solute-binding protein | ||
MHEKMCGP_00509 | 1.1e-250 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
MHEKMCGP_00510 | 3.3e-147 | malG | P | ABC transporter permease | ||
MHEKMCGP_00511 | 4.3e-67 | K | Helix-turn-helix XRE-family like proteins | |||
MHEKMCGP_00514 | 4.8e-28 | |||||
MHEKMCGP_00515 | 1e-288 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
MHEKMCGP_00516 | 1.2e-100 | treR | K | UTRA | ||
MHEKMCGP_00517 | 3.3e-283 | treB | G | phosphotransferase system | ||
MHEKMCGP_00518 | 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 | |
MHEKMCGP_00519 | 1.9e-191 | yrvN | L | AAA C-terminal domain | ||
MHEKMCGP_00520 | 2.2e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
MHEKMCGP_00521 | 9e-83 | K | Acetyltransferase (GNAT) domain | |||
MHEKMCGP_00522 | 1.3e-229 | S | Putative peptidoglycan binding domain | |||
MHEKMCGP_00523 | 7.5e-95 | S | ECF-type riboflavin transporter, S component | |||
MHEKMCGP_00524 | 2.8e-98 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
MHEKMCGP_00525 | 9.3e-204 | pbpX1 | V | Beta-lactamase | ||
MHEKMCGP_00526 | 1.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
MHEKMCGP_00527 | 1.9e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
MHEKMCGP_00528 | 7.4e-205 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MHEKMCGP_00529 | 2.1e-114 | 3.6.1.27 | I | Acid phosphatase homologues | ||
MHEKMCGP_00530 | 1.1e-189 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
MHEKMCGP_00531 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
MHEKMCGP_00532 | 9.9e-82 | C | Flavodoxin | |||
MHEKMCGP_00533 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
MHEKMCGP_00534 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
MHEKMCGP_00535 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
MHEKMCGP_00536 | 1.7e-136 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
MHEKMCGP_00537 | 7e-178 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
MHEKMCGP_00538 | 2.1e-202 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
MHEKMCGP_00539 | 6.9e-184 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
MHEKMCGP_00540 | 1.3e-116 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | G | Sucrose-6F-phosphate phosphohydrolase | ||
MHEKMCGP_00541 | 8.3e-265 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
MHEKMCGP_00542 | 9.7e-169 | |||||
MHEKMCGP_00543 | 7.5e-143 | |||||
MHEKMCGP_00544 | 3.9e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
MHEKMCGP_00545 | 5.5e-26 | |||||
MHEKMCGP_00546 | 8.7e-145 | |||||
MHEKMCGP_00547 | 5.1e-137 | |||||
MHEKMCGP_00548 | 4.5e-141 | |||||
MHEKMCGP_00549 | 4.9e-120 | skfE | V | ATPases associated with a variety of cellular activities | ||
MHEKMCGP_00550 | 1.5e-59 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
MHEKMCGP_00551 | 1.7e-240 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
MHEKMCGP_00552 | 1.4e-152 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
MHEKMCGP_00553 | 3.5e-123 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
MHEKMCGP_00554 | 4.8e-81 | mutT | 3.6.1.55 | F | NUDIX domain | |
MHEKMCGP_00555 | 1.4e-127 | S | Peptidase family M23 | |||
MHEKMCGP_00556 | 9.9e-200 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
MHEKMCGP_00557 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
MHEKMCGP_00558 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
MHEKMCGP_00559 | 4.6e-179 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
MHEKMCGP_00560 | 4.4e-135 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
MHEKMCGP_00561 | 2.1e-168 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
MHEKMCGP_00562 | 2.2e-93 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
MHEKMCGP_00563 | 1.1e-175 | phoH | T | phosphate starvation-inducible protein PhoH | ||
MHEKMCGP_00564 | 3.5e-71 | yqeY | S | YqeY-like protein | ||
MHEKMCGP_00565 | 2e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
MHEKMCGP_00566 | 1.2e-154 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
MHEKMCGP_00567 | 1.5e-18 | S | CRISPR-associated protein (Cas_Csn2) | |||
MHEKMCGP_00568 | 3.1e-71 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
MHEKMCGP_00569 | 7.7e-26 | |||||
MHEKMCGP_00570 | 5.7e-84 | S | PFAM Archaeal ATPase | |||
MHEKMCGP_00571 | 2.2e-85 | S | PFAM Archaeal ATPase | |||
MHEKMCGP_00572 | 1.4e-52 | EGP | Sugar (and other) transporter | |||
MHEKMCGP_00573 | 1e-104 | |||||
MHEKMCGP_00574 | 8.2e-114 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
MHEKMCGP_00575 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
MHEKMCGP_00576 | 3.1e-49 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
MHEKMCGP_00577 | 4.9e-58 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
MHEKMCGP_00578 | 2.4e-36 | |||||
MHEKMCGP_00581 | 3.7e-20 | |||||
MHEKMCGP_00582 | 8.9e-79 | |||||
MHEKMCGP_00583 | 3.7e-190 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
MHEKMCGP_00584 | 7.3e-155 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
MHEKMCGP_00585 | 3.1e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
MHEKMCGP_00586 | 1.3e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
MHEKMCGP_00587 | 1.7e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
MHEKMCGP_00590 | 3.9e-195 | ampC | V | Beta-lactamase | ||
MHEKMCGP_00591 | 3.8e-217 | EGP | Major facilitator Superfamily | |||
MHEKMCGP_00592 | 3.2e-253 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
MHEKMCGP_00593 | 3.8e-105 | vanZ | V | VanZ like family | ||
MHEKMCGP_00594 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
MHEKMCGP_00595 | 7.2e-267 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
MHEKMCGP_00596 | 7.5e-132 | K | Transcriptional regulatory protein, C terminal | |||
MHEKMCGP_00597 | 7.7e-67 | S | SdpI/YhfL protein family | |||
MHEKMCGP_00598 | 7.2e-191 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
MHEKMCGP_00599 | 9.9e-227 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
MHEKMCGP_00600 | 2.6e-86 | M | Protein of unknown function (DUF3737) | |||
MHEKMCGP_00601 | 2e-18 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
MHEKMCGP_00602 | 2.9e-12 | |||||
MHEKMCGP_00603 | 8.2e-85 | scrR | K | Periplasmic binding protein domain | ||
MHEKMCGP_00604 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
MHEKMCGP_00605 | 5.6e-36 | |||||
MHEKMCGP_00606 | 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) | |
MHEKMCGP_00607 | 8.4e-125 | luxT | K | Bacterial regulatory proteins, tetR family | ||
MHEKMCGP_00608 | 1.1e-134 | |||||
MHEKMCGP_00609 | 1.3e-258 | glnPH2 | P | ABC transporter permease | ||
MHEKMCGP_00610 | 2.6e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MHEKMCGP_00611 | 6.4e-224 | S | Cysteine-rich secretory protein family | |||
MHEKMCGP_00612 | 2.6e-205 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
MHEKMCGP_00613 | 1.4e-112 | |||||
MHEKMCGP_00614 | 2.2e-202 | yibE | S | overlaps another CDS with the same product name | ||
MHEKMCGP_00615 | 4.9e-129 | yibF | S | overlaps another CDS with the same product name | ||
MHEKMCGP_00616 | 8.7e-145 | I | alpha/beta hydrolase fold | |||
MHEKMCGP_00617 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
MHEKMCGP_00618 | 4.1e-217 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
MHEKMCGP_00619 | 1.9e-110 | F | DNA/RNA non-specific endonuclease | |||
MHEKMCGP_00620 | 2.7e-34 | S | YSIRK type signal peptide | |||
MHEKMCGP_00622 | 5.5e-53 | |||||
MHEKMCGP_00623 | 1.8e-285 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
MHEKMCGP_00624 | 8e-79 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
MHEKMCGP_00625 | 4.3e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MHEKMCGP_00626 | 1e-198 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
MHEKMCGP_00627 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
MHEKMCGP_00628 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
MHEKMCGP_00629 | 1.1e-66 | |||||
MHEKMCGP_00630 | 1.3e-159 | degV | S | EDD domain protein, DegV family | ||
MHEKMCGP_00631 | 9e-60 | 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 | ||
MHEKMCGP_00632 | 5.8e-221 | 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 | ||
MHEKMCGP_00633 | 5.4e-203 | xerS | L | Belongs to the 'phage' integrase family | ||
MHEKMCGP_00634 | 4.1e-67 | |||||
MHEKMCGP_00635 | 8e-111 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
MHEKMCGP_00636 | 1.5e-211 | M | Glycosyl hydrolases family 25 | |||
MHEKMCGP_00637 | 2e-39 | S | Transglycosylase associated protein | |||
MHEKMCGP_00638 | 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 | |
MHEKMCGP_00639 | 5.1e-226 | N | Uncharacterized conserved protein (DUF2075) | |||
MHEKMCGP_00640 | 4.8e-205 | pbpX1 | V | Beta-lactamase | ||
MHEKMCGP_00641 | 0.0 | L | Helicase C-terminal domain protein | |||
MHEKMCGP_00642 | 1.3e-273 | E | amino acid | |||
MHEKMCGP_00643 | 1.8e-158 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
MHEKMCGP_00646 | 1.4e-192 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MHEKMCGP_00647 | 7.6e-134 | EGP | Major facilitator Superfamily | |||
MHEKMCGP_00648 | 4e-150 | 3.1.3.102, 3.1.3.104 | S | haloacid dehalogenase-like hydrolase | ||
MHEKMCGP_00649 | 0.0 | tetP | J | elongation factor G | ||
MHEKMCGP_00650 | 3.5e-160 | yvgN | C | Aldo keto reductase | ||
MHEKMCGP_00651 | 2e-155 | P | CorA-like Mg2+ transporter protein | |||
MHEKMCGP_00652 | 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 | |
MHEKMCGP_00653 | 1.7e-174 | ABC-SBP | S | ABC transporter | ||
MHEKMCGP_00654 | 5.6e-121 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
MHEKMCGP_00655 | 2.4e-136 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
MHEKMCGP_00656 | 5.2e-248 | G | Major Facilitator | |||
MHEKMCGP_00657 | 4.1e-18 | |||||
MHEKMCGP_00658 | 2.6e-103 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
MHEKMCGP_00659 | 1.4e-176 | K | AI-2E family transporter | |||
MHEKMCGP_00660 | 8.6e-97 | oppA | E | ABC transporter substrate-binding protein | ||
MHEKMCGP_00661 | 1.2e-232 | oppA | E | ABC transporter substrate-binding protein | ||
MHEKMCGP_00662 | 2e-116 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
MHEKMCGP_00663 | 1.4e-73 | 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 | ||
MHEKMCGP_00664 | 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 | ||
MHEKMCGP_00666 | 2.6e-146 | S | Putative ABC-transporter type IV | |||
MHEKMCGP_00668 | 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) | |
MHEKMCGP_00669 | 2.1e-168 | dnaI | L | Primosomal protein DnaI | ||
MHEKMCGP_00670 | 5.1e-251 | dnaB | L | Replication initiation and membrane attachment | ||
MHEKMCGP_00671 | 3.5e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
MHEKMCGP_00672 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
MHEKMCGP_00673 | 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 | |
MHEKMCGP_00674 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
MHEKMCGP_00675 | 3.5e-25 | qmcA | O | prohibitin homologues | ||
MHEKMCGP_00676 | 7.4e-105 | qmcA | O | prohibitin homologues | ||
MHEKMCGP_00677 | 8e-51 | L | RelB antitoxin | |||
MHEKMCGP_00678 | 4.5e-188 | S | Bacteriocin helveticin-J | |||
MHEKMCGP_00679 | 4.4e-283 | M | Peptidase family M1 domain | |||
MHEKMCGP_00680 | 1.8e-176 | S | SLAP domain | |||
MHEKMCGP_00681 | 6.9e-218 | mepA | V | MATE efflux family protein | ||
MHEKMCGP_00682 | 9.7e-247 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
MHEKMCGP_00683 | 1.4e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
MHEKMCGP_00684 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
MHEKMCGP_00686 | 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 | |
MHEKMCGP_00687 | 6.5e-221 | ecsB | U | ABC transporter | ||
MHEKMCGP_00688 | 5.7e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
MHEKMCGP_00689 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
MHEKMCGP_00690 | 9.7e-24 | |||||
MHEKMCGP_00691 | 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 | |
MHEKMCGP_00692 | 1.9e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
MHEKMCGP_00693 | 1.1e-265 | |||||
MHEKMCGP_00694 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
MHEKMCGP_00695 | 1.4e-110 | yjbF | S | SNARE associated Golgi protein | ||
MHEKMCGP_00696 | 7.5e-100 | J | Acetyltransferase (GNAT) domain | |||
MHEKMCGP_00697 | 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) | |
MHEKMCGP_00698 | 9.1e-10 | UW | LPXTG-motif cell wall anchor domain protein | |||
MHEKMCGP_00699 | 3.3e-45 | UW | LPXTG-motif cell wall anchor domain protein | |||
MHEKMCGP_00700 | 1.3e-161 | UW | LPXTG-motif cell wall anchor domain protein | |||
MHEKMCGP_00701 | 2.1e-135 | UW | LPXTG-motif cell wall anchor domain protein | |||
MHEKMCGP_00702 | 2.6e-61 | M | Glycosyl hydrolases family 25 | |||
MHEKMCGP_00703 | 1.3e-61 | M | Glycosyl hydrolases family 25 | |||
MHEKMCGP_00704 | 2.8e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
MHEKMCGP_00705 | 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 | ||
MHEKMCGP_00707 | 2e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
MHEKMCGP_00708 | 1.5e-234 | L | Transposase DDE domain | |||
MHEKMCGP_00709 | 7e-87 | gtcA | S | Teichoic acid glycosylation protein | ||
MHEKMCGP_00710 | 4.1e-80 | fld | C | Flavodoxin | ||
MHEKMCGP_00711 | 1.4e-163 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
MHEKMCGP_00712 | 3.6e-163 | yihY | S | Belongs to the UPF0761 family | ||
MHEKMCGP_00713 | 2.1e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
MHEKMCGP_00714 | 2.5e-214 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
MHEKMCGP_00715 | 4.6e-211 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
MHEKMCGP_00716 | 5.5e-217 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
MHEKMCGP_00717 | 1e-44 | |||||
MHEKMCGP_00718 | 1.8e-38 | D | Alpha beta | |||
MHEKMCGP_00719 | 5.7e-120 | D | Alpha beta | |||
MHEKMCGP_00720 | 9.2e-264 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
MHEKMCGP_00721 | 1.5e-144 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
MHEKMCGP_00722 | 1.6e-85 | |||||
MHEKMCGP_00723 | 2.7e-74 | |||||
MHEKMCGP_00724 | 1.4e-140 | hlyX | S | Transporter associated domain | ||
MHEKMCGP_00725 | 9.4e-305 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
MHEKMCGP_00726 | 2.3e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
MHEKMCGP_00727 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
MHEKMCGP_00728 | 1.2e-129 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
MHEKMCGP_00729 | 5e-148 | noc | K | Belongs to the ParB family | ||
MHEKMCGP_00730 | 3.4e-138 | soj | D | Sporulation initiation inhibitor | ||
MHEKMCGP_00731 | 1.5e-153 | spo0J | K | Belongs to the ParB family | ||
MHEKMCGP_00732 | 9.6e-45 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
MHEKMCGP_00733 | 3.6e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
MHEKMCGP_00734 | 3.8e-137 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
MHEKMCGP_00735 | 1.2e-145 | V | ABC transporter, ATP-binding protein | |||
MHEKMCGP_00736 | 4.2e-144 | V | ABC transporter, ATP-binding protein | |||
MHEKMCGP_00737 | 0.0 | V | ABC transporter | |||
MHEKMCGP_00739 | 9.6e-121 | K | response regulator | |||
MHEKMCGP_00740 | 1.9e-206 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
MHEKMCGP_00741 | 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 | |
MHEKMCGP_00742 | 8e-145 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
MHEKMCGP_00743 | 1.4e-53 | S | Enterocin A Immunity | |||
MHEKMCGP_00744 | 2.5e-33 | |||||
MHEKMCGP_00745 | 9.5e-26 | |||||
MHEKMCGP_00746 | 1e-24 | |||||
MHEKMCGP_00747 | 3e-270 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
MHEKMCGP_00748 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
MHEKMCGP_00749 | 2.1e-255 | S | Archaea bacterial proteins of unknown function | |||
MHEKMCGP_00750 | 1.2e-16 | |||||
MHEKMCGP_00751 | 4.4e-138 | 2.7.13.3 | T | GHKL domain | ||
MHEKMCGP_00752 | 1.2e-127 | K | LytTr DNA-binding domain | |||
MHEKMCGP_00753 | 6.1e-269 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
MHEKMCGP_00754 | 5.2e-16 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
MHEKMCGP_00755 | 2e-219 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
MHEKMCGP_00756 | 9.8e-177 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
MHEKMCGP_00757 | 7e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
MHEKMCGP_00758 | 3.2e-217 | aspC | 2.6.1.1 | E | Aminotransferase | |
MHEKMCGP_00759 | 1.1e-197 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
MHEKMCGP_00760 | 1.2e-141 | pbpX1 | V | Beta-lactamase | ||
MHEKMCGP_00761 | 7.9e-299 | I | Protein of unknown function (DUF2974) | |||
MHEKMCGP_00762 | 6.8e-31 | C | FMN_bind | |||
MHEKMCGP_00763 | 3.9e-82 | |||||
MHEKMCGP_00764 | 1.8e-175 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
MHEKMCGP_00765 | 6.4e-90 | alkD | L | DNA alkylation repair enzyme | ||
MHEKMCGP_00766 | 1.2e-293 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
MHEKMCGP_00767 | 6.4e-128 | K | UTRA domain | |||
MHEKMCGP_00768 | 1e-54 | celA1 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
MHEKMCGP_00769 | 8.7e-60 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
MHEKMCGP_00770 | 4.7e-159 | D | nuclear chromosome segregation | |||
MHEKMCGP_00771 | 1.2e-105 | G | Phosphoglycerate mutase family | |||
MHEKMCGP_00772 | 2.6e-89 | G | Histidine phosphatase superfamily (branch 1) | |||
MHEKMCGP_00773 | 6.6e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
MHEKMCGP_00774 | 1.2e-115 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
MHEKMCGP_00776 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
MHEKMCGP_00778 | 6.5e-210 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
MHEKMCGP_00779 | 2.7e-185 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
MHEKMCGP_00780 | 8.1e-120 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
MHEKMCGP_00781 | 4.4e-144 | K | SIS domain | |||
MHEKMCGP_00782 | 6.7e-228 | slpX | S | SLAP domain | ||
MHEKMCGP_00783 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
MHEKMCGP_00784 | 6.6e-11 | |||||
MHEKMCGP_00785 | 3.2e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
MHEKMCGP_00788 | 4.4e-239 | oppA2 | E | ABC transporter, substratebinding protein | ||
MHEKMCGP_00789 | 3.4e-45 | oppA2 | E | ABC transporter, substratebinding protein | ||
MHEKMCGP_00790 | 3.3e-179 | |||||
MHEKMCGP_00791 | 4.6e-123 | gntR1 | K | UTRA | ||
MHEKMCGP_00792 | 5.1e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
MHEKMCGP_00793 | 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 |
MHEKMCGP_00794 | 1.7e-204 | csaB | M | Glycosyl transferases group 1 | ||
MHEKMCGP_00795 | 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 | |
MHEKMCGP_00796 | 1.2e-152 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
MHEKMCGP_00797 | 1.4e-204 | tnpB | L | Putative transposase DNA-binding domain | ||
MHEKMCGP_00798 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
MHEKMCGP_00799 | 7e-225 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
MHEKMCGP_00800 | 3e-257 | epsU | S | Polysaccharide biosynthesis protein | ||
MHEKMCGP_00801 | 7.7e-134 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
MHEKMCGP_00802 | 4.1e-83 | ydcK | S | Belongs to the SprT family | ||
MHEKMCGP_00804 | 5.2e-84 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
MHEKMCGP_00805 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
MHEKMCGP_00806 | 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 | |
MHEKMCGP_00807 | 5.8e-203 | camS | S | sex pheromone | ||
MHEKMCGP_00808 | 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) | |
MHEKMCGP_00809 | 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) | |
MHEKMCGP_00810 | 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) | |
MHEKMCGP_00811 | 2.7e-171 | yegS | 2.7.1.107 | G | Lipid kinase | |
MHEKMCGP_00812 | 4.3e-108 | ybhL | S | Belongs to the BI1 family | ||
MHEKMCGP_00813 | 2.6e-57 | |||||
MHEKMCGP_00814 | 1.4e-147 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
MHEKMCGP_00815 | 2.8e-244 | nhaC | C | Na H antiporter NhaC | ||
MHEKMCGP_00816 | 6.3e-201 | pbpX | V | Beta-lactamase | ||
MHEKMCGP_00817 | 1.4e-253 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
MHEKMCGP_00818 | 1.1e-94 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
MHEKMCGP_00820 | 1.2e-94 | |||||
MHEKMCGP_00821 | 3.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
MHEKMCGP_00822 | 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 | |
MHEKMCGP_00823 | 4.1e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
MHEKMCGP_00824 | 7e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
MHEKMCGP_00825 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
MHEKMCGP_00826 | 2e-163 | murB | 1.3.1.98 | M | Cell wall formation | |
MHEKMCGP_00827 | 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 | |
MHEKMCGP_00828 | 1.3e-129 | potB | P | ABC transporter permease | ||
MHEKMCGP_00829 | 4.8e-127 | potC | P | ABC transporter permease | ||
MHEKMCGP_00830 | 7.3e-208 | potD | P | ABC transporter | ||
MHEKMCGP_00831 | 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 | |
MHEKMCGP_00832 | 7.5e-172 | ybbR | S | YbbR-like protein | ||
MHEKMCGP_00833 | 3.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
MHEKMCGP_00834 | 1.4e-147 | S | hydrolase | |||
MHEKMCGP_00835 | 1.8e-75 | K | Penicillinase repressor | |||
MHEKMCGP_00836 | 1.6e-118 | |||||
MHEKMCGP_00837 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
MHEKMCGP_00838 | 3.8e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
MHEKMCGP_00839 | 8.3e-143 | licT | K | CAT RNA binding domain | ||
MHEKMCGP_00840 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
MHEKMCGP_00841 | 1e-297 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
MHEKMCGP_00842 | 1e-149 | D | Alpha beta | |||
MHEKMCGP_00843 | 1.2e-92 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
MHEKMCGP_00844 | 3.7e-26 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
MHEKMCGP_00845 | 5.2e-112 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
MHEKMCGP_00846 | 8.2e-36 | |||||
MHEKMCGP_00847 | 2.2e-90 | 2.7.7.65 | T | GGDEF domain | ||
MHEKMCGP_00848 | 8.8e-82 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
MHEKMCGP_00850 | 5.9e-310 | E | Amino acid permease | |||
MHEKMCGP_00851 | 5.8e-100 | L | Helix-turn-helix domain | |||
MHEKMCGP_00852 | 1.3e-160 | L | hmm pf00665 | |||
MHEKMCGP_00854 | 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 | ||
MHEKMCGP_00855 | 6.8e-50 | ylbE | GM | NAD(P)H-binding | ||
MHEKMCGP_00856 | 5.2e-08 | |||||
MHEKMCGP_00857 | 3e-89 | ntd | 2.4.2.6 | F | Nucleoside | |
MHEKMCGP_00858 | 3.9e-87 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
MHEKMCGP_00859 | 3.4e-149 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
MHEKMCGP_00860 | 6.8e-84 | uspA | T | universal stress protein | ||
MHEKMCGP_00861 | 1.2e-150 | phnD | P | Phosphonate ABC transporter | ||
MHEKMCGP_00862 | 4.1e-136 | 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 | |
MHEKMCGP_00863 | 1.2e-111 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
MHEKMCGP_00864 | 1.3e-148 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
MHEKMCGP_00865 | 1.4e-81 | L | COG3385 FOG Transposase and inactivated derivatives | |||
MHEKMCGP_00866 | 1.2e-188 | K | Periplasmic binding protein-like domain | |||
MHEKMCGP_00867 | 2e-106 | K | Transcriptional regulator, AbiEi antitoxin | |||
MHEKMCGP_00868 | 7.6e-163 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
MHEKMCGP_00869 | 2e-188 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
MHEKMCGP_00870 | 2.1e-142 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
MHEKMCGP_00871 | 9.3e-80 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
MHEKMCGP_00872 | 7.2e-221 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
MHEKMCGP_00873 | 7.1e-165 | lacR | K | Transcriptional regulator | ||
MHEKMCGP_00874 | 8.9e-207 | lacS | G | Transporter | ||
MHEKMCGP_00875 | 2.6e-103 | lacS | G | Transporter | ||
MHEKMCGP_00876 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
MHEKMCGP_00877 | 1.1e-220 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
MHEKMCGP_00878 | 1.1e-288 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
MHEKMCGP_00879 | 2e-196 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
MHEKMCGP_00880 | 5.5e-36 | |||||
MHEKMCGP_00881 | 6.4e-71 | scrR | K | Periplasmic binding protein domain | ||
MHEKMCGP_00882 | 2.6e-65 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
MHEKMCGP_00883 | 4.1e-156 | crtI | 1.3.99.23, 5.2.1.13 | Q | HI0933-like protein | |
MHEKMCGP_00884 | 4.3e-52 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
MHEKMCGP_00885 | 7.2e-183 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
MHEKMCGP_00886 | 3.8e-115 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
MHEKMCGP_00887 | 2e-10 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
MHEKMCGP_00888 | 9.5e-82 | XK27_04435 | 3.5.4.5 | J | FR47-like protein | |
MHEKMCGP_00889 | 1.4e-36 | S | Cytochrome B5 | |||
MHEKMCGP_00890 | 6e-168 | arbZ | I | Phosphate acyltransferases | ||
MHEKMCGP_00891 | 1.6e-182 | arbY | M | Glycosyl transferase family 8 | ||
MHEKMCGP_00892 | 5e-184 | arbY | M | Glycosyl transferase family 8 | ||
MHEKMCGP_00893 | 5e-156 | arbx | M | Glycosyl transferase family 8 | ||
MHEKMCGP_00894 | 1.6e-148 | arbV | 2.3.1.51 | I | Acyl-transferase | |
MHEKMCGP_00896 | 4.9e-34 | |||||
MHEKMCGP_00898 | 4.8e-131 | K | response regulator | |||
MHEKMCGP_00899 | 2.2e-305 | vicK | 2.7.13.3 | T | Histidine kinase | |
MHEKMCGP_00900 | 1.6e-257 | yycH | S | YycH protein | ||
MHEKMCGP_00901 | 2.5e-147 | yycI | S | YycH protein | ||
MHEKMCGP_00902 | 4.1e-147 | vicX | 3.1.26.11 | S | domain protein | |
MHEKMCGP_00903 | 1.6e-161 | htrA | 3.4.21.107 | O | serine protease | |
MHEKMCGP_00904 | 1e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
MHEKMCGP_00905 | 7.7e-22 | S | SLAP domain | |||
MHEKMCGP_00906 | 1e-19 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
MHEKMCGP_00907 | 4.3e-145 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
MHEKMCGP_00908 | 1.1e-25 | |||||
MHEKMCGP_00909 | 1.2e-77 | K | DNA-templated transcription, initiation | |||
MHEKMCGP_00910 | 5.3e-41 | |||||
MHEKMCGP_00912 | 1.4e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
MHEKMCGP_00913 | 5.6e-118 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
MHEKMCGP_00914 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
MHEKMCGP_00915 | 1.5e-107 | glnP | P | ABC transporter permease | ||
MHEKMCGP_00916 | 1e-105 | glnQ | 3.6.3.21 | E | ABC transporter | |
MHEKMCGP_00917 | 1.1e-142 | aatB | ET | ABC transporter substrate-binding protein | ||
MHEKMCGP_00918 | 7.5e-74 | yjcF | S | Acetyltransferase (GNAT) domain | ||
MHEKMCGP_00919 | 4.9e-99 | E | GDSL-like Lipase/Acylhydrolase | |||
MHEKMCGP_00920 | 7.4e-169 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
MHEKMCGP_00921 | 3.8e-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 | ||
MHEKMCGP_00922 | 8.8e-58 | S | Peptidase propeptide and YPEB domain | |||
MHEKMCGP_00923 | 8.4e-265 | S | Fibronectin type III domain | |||
MHEKMCGP_00924 | 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) | |
MHEKMCGP_00925 | 3.4e-53 | |||||
MHEKMCGP_00927 | 1.8e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
MHEKMCGP_00928 | 1.3e-122 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
MHEKMCGP_00929 | 3.2e-300 | oppA | E | ABC transporter, substratebinding protein | ||
MHEKMCGP_00930 | 7.7e-310 | oppA | E | ABC transporter, substratebinding protein | ||
MHEKMCGP_00931 | 1.7e-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 | |
MHEKMCGP_00932 | 1.1e-146 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
MHEKMCGP_00933 | 6.8e-187 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
MHEKMCGP_00934 | 2.7e-199 | oppD | P | Belongs to the ABC transporter superfamily | ||
MHEKMCGP_00935 | 4.2e-175 | oppF | P | Belongs to the ABC transporter superfamily | ||
MHEKMCGP_00936 | 1.8e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
MHEKMCGP_00937 | 1.5e-71 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
MHEKMCGP_00938 | 2.6e-77 | 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 | ||
MHEKMCGP_00939 | 1.2e-112 | |||||
MHEKMCGP_00941 | 3.5e-111 | E | Belongs to the SOS response-associated peptidase family | |||
MHEKMCGP_00942 | 3.7e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MHEKMCGP_00943 | 4e-89 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
MHEKMCGP_00944 | 2e-103 | S | TPM domain | |||
MHEKMCGP_00945 | 2.4e-132 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
MHEKMCGP_00946 | 2.5e-311 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
MHEKMCGP_00947 | 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 | |
MHEKMCGP_00948 | 1e-147 | tatD | L | hydrolase, TatD family | ||
MHEKMCGP_00949 | 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 | |
MHEKMCGP_00950 | 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 | |
MHEKMCGP_00951 | 4.5e-39 | veg | S | Biofilm formation stimulator VEG | ||
MHEKMCGP_00952 | 8e-146 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
MHEKMCGP_00953 | 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 | |
MHEKMCGP_00954 | 5.3e-80 | |||||
MHEKMCGP_00955 | 7.8e-292 | S | SLAP domain | |||
MHEKMCGP_00956 | 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) | |
MHEKMCGP_00957 | 4.2e-172 | 2.7.1.2 | GK | ROK family | ||
MHEKMCGP_00958 | 5.6e-43 | |||||
MHEKMCGP_00959 | 3.2e-269 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
MHEKMCGP_00960 | 6.9e-69 | S | Domain of unknown function (DUF1934) | |||
MHEKMCGP_00961 | 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 | ||
MHEKMCGP_00962 | 6.7e-311 | 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 | |
MHEKMCGP_00963 | 9.6e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
MHEKMCGP_00964 | 1.8e-74 | K | acetyltransferase | |||
MHEKMCGP_00965 | 4.4e-285 | pipD | E | Dipeptidase | ||
MHEKMCGP_00966 | 2.5e-152 | msmR | K | AraC-like ligand binding domain | ||
MHEKMCGP_00967 | 1.4e-226 | pbuX | F | xanthine permease | ||
MHEKMCGP_00968 | 3.1e-104 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
MHEKMCGP_00969 | 2.4e-43 | K | Helix-turn-helix | |||
MHEKMCGP_00970 | 7.8e-304 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
MHEKMCGP_00972 | 4.9e-99 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
MHEKMCGP_00973 | 8.7e-117 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
MHEKMCGP_00975 | 1.1e-76 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
MHEKMCGP_00976 | 1e-95 | |||||
MHEKMCGP_00977 | 2.4e-282 | phoR | 2.7.13.3 | T | Histidine kinase | |
MHEKMCGP_00978 | 9.5e-121 | T | Transcriptional regulatory protein, C terminal | |||
MHEKMCGP_00979 | 1.4e-105 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
MHEKMCGP_00980 | 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 | |
MHEKMCGP_00981 | 1.2e-152 | pstA | P | Phosphate transport system permease protein PstA | ||
MHEKMCGP_00982 | 1.1e-159 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
MHEKMCGP_00983 | 4.2e-145 | pstS | P | Phosphate | ||
MHEKMCGP_00984 | 1.3e-30 | |||||
MHEKMCGP_00985 | 3e-162 | oppA | E | ABC transporter, substratebinding protein | ||
MHEKMCGP_00986 | 4.7e-275 | ytgP | S | Polysaccharide biosynthesis protein | ||
MHEKMCGP_00987 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MHEKMCGP_00988 | 1.1e-121 | 3.6.1.27 | I | Acid phosphatase homologues | ||
MHEKMCGP_00989 | 2.8e-168 | K | LysR substrate binding domain | |||
MHEKMCGP_00990 | 2.3e-84 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
MHEKMCGP_00991 | 6.2e-43 | 1.3.5.4 | C | FAD binding domain | ||
MHEKMCGP_00992 | 2.4e-231 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
MHEKMCGP_00993 | 1.1e-161 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
MHEKMCGP_00994 | 6.1e-177 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
MHEKMCGP_00995 | 2.2e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
MHEKMCGP_00996 | 2.5e-121 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
MHEKMCGP_00997 | 9.5e-152 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
MHEKMCGP_00998 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
MHEKMCGP_00999 | 8.2e-177 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
MHEKMCGP_01000 | 1.5e-272 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
MHEKMCGP_01001 | 3.7e-130 | ybbH_2 | K | rpiR family | ||
MHEKMCGP_01002 | 3.4e-195 | S | Bacterial protein of unknown function (DUF871) | |||
MHEKMCGP_01003 | 4.1e-214 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
MHEKMCGP_01004 | 1.8e-119 | S | Putative esterase | |||
MHEKMCGP_01005 | 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 | |
MHEKMCGP_01006 | 1.3e-79 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
MHEKMCGP_01008 | 8.5e-260 | qacA | EGP | Major facilitator Superfamily | ||
MHEKMCGP_01009 | 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 | |
MHEKMCGP_01012 | 6.2e-165 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
MHEKMCGP_01013 | 1.5e-145 | yfeO | P | Voltage gated chloride channel | ||
MHEKMCGP_01014 | 4e-184 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
MHEKMCGP_01015 | 2.8e-52 | |||||
MHEKMCGP_01019 | 7.9e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
MHEKMCGP_01020 | 7.6e-202 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
MHEKMCGP_01021 | 5.4e-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 | ||
MHEKMCGP_01022 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
MHEKMCGP_01023 | 1.7e-29 | secG | U | Preprotein translocase | ||
MHEKMCGP_01024 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
MHEKMCGP_01025 | 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 | ||
MHEKMCGP_01026 | 6.5e-154 | pstA | P | Phosphate transport system permease protein PstA | ||
MHEKMCGP_01027 | 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 | |
MHEKMCGP_01028 | 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 | |
MHEKMCGP_01029 | 2.2e-117 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
MHEKMCGP_01030 | 2.8e-90 | L | An automated process has identified a potential problem with this gene model | |||
MHEKMCGP_01031 | 1.5e-11 | GT2,GT4 | M | family 8 | ||
MHEKMCGP_01032 | 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 | ||
MHEKMCGP_01033 | 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 | ||
MHEKMCGP_01034 | 8.7e-140 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
MHEKMCGP_01035 | 1.3e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
MHEKMCGP_01036 | 1.5e-25 | |||||
MHEKMCGP_01037 | 2.2e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
MHEKMCGP_01038 | 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 | |
MHEKMCGP_01039 | 5.7e-106 | 2.4.1.58 | GT8 | M | family 8 | |
MHEKMCGP_01040 | 1.2e-35 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
MHEKMCGP_01041 | 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 | ||
MHEKMCGP_01042 | 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 | ||
MHEKMCGP_01043 | 1.1e-34 | S | Protein of unknown function (DUF2508) | |||
MHEKMCGP_01044 | 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 | |
MHEKMCGP_01045 | 8.9e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
MHEKMCGP_01046 | 1.5e-155 | holB | 2.7.7.7 | L | DNA polymerase III | |
MHEKMCGP_01047 | 1.8e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
MHEKMCGP_01048 | 5.1e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
MHEKMCGP_01049 | 1.4e-130 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
MHEKMCGP_01050 | 2.2e-85 | S | ECF transporter, substrate-specific component | |||
MHEKMCGP_01051 | 2.4e-133 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
MHEKMCGP_01052 | 7.4e-97 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
MHEKMCGP_01053 | 4.5e-194 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
MHEKMCGP_01054 | 1.9e-245 | L | Transposase IS66 family | |||
MHEKMCGP_01055 | 8.7e-34 | S | Transposase C of IS166 homeodomain | |||
MHEKMCGP_01056 | 9.3e-64 | L | PFAM IS66 Orf2 family protein | |||
MHEKMCGP_01057 | 7.7e-22 | |||||
MHEKMCGP_01058 | 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 | |
MHEKMCGP_01059 | 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 | |
MHEKMCGP_01060 | 3.4e-284 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
MHEKMCGP_01061 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
MHEKMCGP_01062 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
MHEKMCGP_01063 | 8.1e-38 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
MHEKMCGP_01064 | 5.2e-68 | L | haloacid dehalogenase-like hydrolase | |||
MHEKMCGP_01065 | 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 | |
MHEKMCGP_01066 | 7.2e-129 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
MHEKMCGP_01067 | 2.8e-90 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
MHEKMCGP_01068 | 4.1e-31 | sgaB | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
MHEKMCGP_01069 | 1.3e-231 | ulaA | S | PTS system sugar-specific permease component | ||
MHEKMCGP_01070 | 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 | |
MHEKMCGP_01071 | 7.1e-165 | ulaG | S | Beta-lactamase superfamily domain | ||
MHEKMCGP_01072 | 1.2e-17 | |||||
MHEKMCGP_01073 | 1.9e-309 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
MHEKMCGP_01074 | 2e-70 | S | Iron-sulphur cluster biosynthesis | |||
MHEKMCGP_01075 | 7.5e-192 | ybiR | P | Citrate transporter | ||
MHEKMCGP_01076 | 5.1e-96 | lemA | S | LemA family | ||
MHEKMCGP_01077 | 8.3e-157 | htpX | O | Belongs to the peptidase M48B family | ||
MHEKMCGP_01078 | 7.9e-174 | K | helix_turn_helix, arabinose operon control protein | |||
MHEKMCGP_01079 | 4.8e-249 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
MHEKMCGP_01080 | 2.8e-77 | P | Cobalt transport protein | |||
MHEKMCGP_01081 | 1.8e-175 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
MHEKMCGP_01082 | 6.5e-91 | G | Peptidase_C39 like family | |||
MHEKMCGP_01083 | 2.8e-162 | M | NlpC/P60 family | |||
MHEKMCGP_01084 | 8.4e-25 | G | Peptidase_C39 like family | |||
MHEKMCGP_01085 | 5.7e-27 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
MHEKMCGP_01086 | 2.6e-166 | xerD | D | recombinase XerD | ||
MHEKMCGP_01087 | 1.9e-169 | cvfB | S | S1 domain | ||
MHEKMCGP_01088 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
MHEKMCGP_01089 | 3.3e-183 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
MHEKMCGP_01090 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
MHEKMCGP_01091 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
MHEKMCGP_01092 | 4.3e-310 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
MHEKMCGP_01093 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
MHEKMCGP_01094 | 1.5e-34 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
MHEKMCGP_01095 | 5.1e-142 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
MHEKMCGP_01096 | 5.4e-175 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
MHEKMCGP_01097 | 2.2e-292 | I | Acyltransferase | |||
MHEKMCGP_01098 | 1.7e-243 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
MHEKMCGP_01099 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
MHEKMCGP_01100 | 6.8e-110 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
MHEKMCGP_01101 | 4e-243 | yfnA | E | Amino Acid | ||
MHEKMCGP_01102 | 6.8e-181 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MHEKMCGP_01103 | 1.3e-148 | yxeH | S | hydrolase | ||
MHEKMCGP_01104 | 2.7e-32 | S | reductase | |||
MHEKMCGP_01105 | 4.4e-39 | S | reductase | |||
MHEKMCGP_01106 | 4.8e-34 | S | reductase | |||
MHEKMCGP_01107 | 2.8e-216 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
MHEKMCGP_01108 | 4.9e-130 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
MHEKMCGP_01109 | 1.9e-147 | glnH | ET | ABC transporter | ||
MHEKMCGP_01110 | 3.5e-79 | K | Transcriptional regulator, MarR family | |||
MHEKMCGP_01111 | 1.5e-308 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
MHEKMCGP_01112 | 0.0 | V | ABC transporter transmembrane region | |||
MHEKMCGP_01113 | 1.6e-100 | S | ABC-type cobalt transport system, permease component | |||
MHEKMCGP_01114 | 1e-246 | G | MFS/sugar transport protein | |||
MHEKMCGP_01115 | 1e-44 | udk | 2.7.1.48 | F | Zeta toxin | |
MHEKMCGP_01116 | 3.8e-46 | udk | 2.7.1.48 | F | Zeta toxin | |
MHEKMCGP_01117 | 4.8e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MHEKMCGP_01118 | 1.2e-146 | glnH | ET | ABC transporter substrate-binding protein | ||
MHEKMCGP_01119 | 3.3e-77 | gluC | P | ABC transporter permease | ||
MHEKMCGP_01120 | 1e-20 | S | Enterocin A Immunity | |||
MHEKMCGP_01122 | 5.7e-43 | 2.4.1.33 | V | HlyD family secretion protein | ||
MHEKMCGP_01123 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
MHEKMCGP_01124 | 2.9e-79 | K | LytTr DNA-binding domain | |||
MHEKMCGP_01125 | 2.1e-78 | 2.7.13.3 | T | GHKL domain | ||
MHEKMCGP_01126 | 5.7e-18 | |||||
MHEKMCGP_01127 | 1.5e-239 | G | Bacterial extracellular solute-binding protein | |||
MHEKMCGP_01128 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
MHEKMCGP_01129 | 1.1e-236 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
MHEKMCGP_01131 | 0.0 | S | SLAP domain | |||
MHEKMCGP_01132 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
MHEKMCGP_01133 | 1.2e-164 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
MHEKMCGP_01134 | 3.4e-42 | S | RloB-like protein | |||
MHEKMCGP_01135 | 1.9e-259 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
MHEKMCGP_01136 | 5.7e-99 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
MHEKMCGP_01137 | 1.2e-63 | S | SIR2-like domain | |||
MHEKMCGP_01138 | 1.2e-09 | S | Domain of unknown function DUF87 | |||
MHEKMCGP_01139 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
MHEKMCGP_01140 | 3.5e-109 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
MHEKMCGP_01141 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
MHEKMCGP_01142 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
MHEKMCGP_01143 | 5.6e-183 | K | Transcriptional regulator | |||
MHEKMCGP_01144 | 2.1e-171 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
MHEKMCGP_01145 | 2.7e-111 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
MHEKMCGP_01146 | 4e-57 | K | Helix-turn-helix domain | |||
MHEKMCGP_01147 | 7.3e-126 | S | Alpha/beta hydrolase family | |||
MHEKMCGP_01148 | 3.7e-156 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
MHEKMCGP_01149 | 4.4e-140 | ypuA | S | Protein of unknown function (DUF1002) | ||
MHEKMCGP_01150 | 8.8e-147 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
MHEKMCGP_01151 | 1.6e-182 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
MHEKMCGP_01152 | 2.5e-283 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
MHEKMCGP_01153 | 9.3e-86 | |||||
MHEKMCGP_01154 | 1.1e-56 | S | Protein of unknown function (DUF3290) | |||
MHEKMCGP_01155 | 3e-116 | yviA | S | Protein of unknown function (DUF421) | ||
MHEKMCGP_01156 | 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 | |||
MHEKMCGP_01157 | 8e-182 | dnaQ | 2.7.7.7 | L | EXOIII | |
MHEKMCGP_01158 | 1.9e-158 | endA | F | DNA RNA non-specific endonuclease | ||
MHEKMCGP_01159 | 1.3e-281 | pipD | E | Dipeptidase | ||
MHEKMCGP_01160 | 1.9e-203 | malK | P | ATPases associated with a variety of cellular activities | ||
MHEKMCGP_01161 | 1.6e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
MHEKMCGP_01162 | 6.1e-146 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
MHEKMCGP_01163 | 9.2e-258 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
MHEKMCGP_01164 | 2.3e-240 | G | Bacterial extracellular solute-binding protein | |||
MHEKMCGP_01165 | 1.8e-154 | corA | P | CorA-like Mg2+ transporter protein | ||
MHEKMCGP_01166 | 3.3e-148 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
MHEKMCGP_01167 | 6.6e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
MHEKMCGP_01168 | 0.0 | ydgH | S | MMPL family | ||
MHEKMCGP_01170 | 7.8e-26 | K | Acetyltransferase (GNAT) domain | |||
MHEKMCGP_01171 | 1.8e-163 | |||||
MHEKMCGP_01172 | 2.4e-92 | V | ABC transporter, ATP-binding protein | |||
MHEKMCGP_01173 | 4.7e-60 | S | ABC-2 family transporter protein | |||
MHEKMCGP_01174 | 2.1e-76 | S | ABC-2 family transporter protein | |||
MHEKMCGP_01175 | 8.2e-230 | pbuG | S | permease | ||
MHEKMCGP_01176 | 8.2e-140 | cof | S | haloacid dehalogenase-like hydrolase | ||
MHEKMCGP_01177 | 9.4e-72 | |||||
MHEKMCGP_01178 | 9.3e-124 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
MHEKMCGP_01179 | 8.5e-119 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
MHEKMCGP_01180 | 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 | |
MHEKMCGP_01181 | 3.7e-159 | yeaE | S | Aldo/keto reductase family | ||
MHEKMCGP_01182 | 4.4e-172 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
MHEKMCGP_01183 | 1.9e-198 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
MHEKMCGP_01184 | 1.3e-282 | xylG | 3.6.3.17 | S | ABC transporter | |
MHEKMCGP_01185 | 6.9e-181 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
MHEKMCGP_01186 | 3.9e-201 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
MHEKMCGP_01187 | 2.8e-100 | S | ECF transporter, substrate-specific component | |||
MHEKMCGP_01188 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
MHEKMCGP_01189 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
MHEKMCGP_01190 | 1.6e-194 | S | DUF218 domain | |||
MHEKMCGP_01191 | 2.7e-120 | S | CAAX protease self-immunity | |||
MHEKMCGP_01192 | 3e-111 | ropB | K | Transcriptional regulator | ||
MHEKMCGP_01193 | 4.2e-154 | EGP | Major facilitator Superfamily | |||
MHEKMCGP_01194 | 5.4e-51 | |||||
MHEKMCGP_01195 | 2.6e-155 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
MHEKMCGP_01196 | 4.1e-276 | V | ABC transporter transmembrane region | |||
MHEKMCGP_01197 | 2.3e-41 | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | |||
MHEKMCGP_01198 | 1.9e-47 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
MHEKMCGP_01199 | 2.8e-205 | napA | P | Sodium/hydrogen exchanger family | ||
MHEKMCGP_01200 | 0.0 | cadA | P | P-type ATPase | ||
MHEKMCGP_01201 | 1.5e-80 | ykuL | S | (CBS) domain | ||
MHEKMCGP_01202 | 1e-207 | ywhK | S | Membrane | ||
MHEKMCGP_01203 | 4.1e-44 | |||||
MHEKMCGP_01204 | 1.2e-18 | S | D-Ala-teichoic acid biosynthesis protein | |||
MHEKMCGP_01205 | 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 | |
MHEKMCGP_01206 | 1.9e-236 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
MHEKMCGP_01207 | 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 | |
MHEKMCGP_01208 | 1.5e-247 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
MHEKMCGP_01209 | 7.6e-177 | pbpX2 | V | Beta-lactamase | ||
MHEKMCGP_01210 | 2.3e-133 | S | Protein of unknown function (DUF975) | |||
MHEKMCGP_01211 | 2.7e-137 | lysA2 | M | Glycosyl hydrolases family 25 | ||
MHEKMCGP_01212 | 7.9e-291 | ytgP | S | Polysaccharide biosynthesis protein | ||
MHEKMCGP_01213 | 1.9e-36 | |||||
MHEKMCGP_01214 | 0.0 | XK27_06780 | V | ABC transporter permease | ||
MHEKMCGP_01215 | 5.1e-125 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
MHEKMCGP_01216 | 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 | ||
MHEKMCGP_01217 | 2.2e-165 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
MHEKMCGP_01218 | 0.0 | clpE | O | AAA domain (Cdc48 subfamily) | ||
MHEKMCGP_01219 | 4.3e-115 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
MHEKMCGP_01220 | 2.3e-72 | cycA | E | Amino acid permease | ||
MHEKMCGP_01221 | 3.4e-142 | cycA | E | Amino acid permease | ||
MHEKMCGP_01222 | 9.2e-248 | yifK | E | Amino acid permease | ||
MHEKMCGP_01223 | 6.4e-135 | S | PFAM Archaeal ATPase | |||
MHEKMCGP_01224 | 9.8e-166 | V | HNH endonuclease | |||
MHEKMCGP_01225 | 1.2e-10 | |||||
MHEKMCGP_01226 | 2.8e-65 | K | LytTr DNA-binding domain | |||
MHEKMCGP_01227 | 1.2e-49 | S | Protein of unknown function (DUF3021) | |||
MHEKMCGP_01228 | 6.3e-105 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
MHEKMCGP_01229 | 1.9e-118 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
MHEKMCGP_01230 | 6e-132 | S | membrane transporter protein | |||
MHEKMCGP_01231 | 2.2e-125 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
MHEKMCGP_01232 | 6.6e-162 | czcD | P | cation diffusion facilitator family transporter | ||
MHEKMCGP_01233 | 1.4e-23 | |||||
MHEKMCGP_01234 | 1.7e-125 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
MHEKMCGP_01235 | 2.4e-183 | S | AAA domain | |||
MHEKMCGP_01236 | 7.3e-44 | |||||
MHEKMCGP_01237 | 1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
MHEKMCGP_01238 | 4.1e-52 | |||||
MHEKMCGP_01239 | 1.8e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
MHEKMCGP_01240 | 2.7e-255 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
MHEKMCGP_01241 | 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) | |
MHEKMCGP_01242 | 7.5e-277 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MHEKMCGP_01243 | 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) | ||
MHEKMCGP_01244 | 1.7e-139 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
MHEKMCGP_01245 | 1.2e-94 | sigH | K | Belongs to the sigma-70 factor family | ||
MHEKMCGP_01246 | 1.7e-34 | |||||
MHEKMCGP_01247 | 8.4e-287 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
MHEKMCGP_01248 | 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) | |
MHEKMCGP_01249 | 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 | ||
MHEKMCGP_01250 | 1.2e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
MHEKMCGP_01251 | 1.2e-68 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
MHEKMCGP_01252 | 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 | ||
MHEKMCGP_01253 | 2.8e-157 | pstS | P | Phosphate | ||
MHEKMCGP_01254 | 2.6e-162 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
MHEKMCGP_01255 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
MHEKMCGP_01256 | 3.4e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
MHEKMCGP_01257 | 1.7e-249 | yhdP | S | Transporter associated domain | ||
MHEKMCGP_01258 | 3.9e-119 | C | nitroreductase | |||
MHEKMCGP_01259 | 2.1e-39 | |||||
MHEKMCGP_01260 | 4.2e-86 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
MHEKMCGP_01261 | 1.6e-80 | |||||
MHEKMCGP_01262 | 4.1e-147 | glvR | K | Helix-turn-helix domain, rpiR family | ||
MHEKMCGP_01263 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
MHEKMCGP_01264 | 5.4e-147 | S | hydrolase | |||
MHEKMCGP_01265 | 2e-160 | rssA | S | Phospholipase, patatin family | ||
MHEKMCGP_01266 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
MHEKMCGP_01267 | 3.1e-136 | glcR | K | DeoR C terminal sensor domain | ||
MHEKMCGP_01268 | 2.5e-59 | S | Enterocin A Immunity | |||
MHEKMCGP_01269 | 1.2e-154 | S | hydrolase | |||
MHEKMCGP_01270 | 2.8e-134 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
MHEKMCGP_01271 | 9.1e-175 | rihB | 3.2.2.1 | F | Nucleoside | |
MHEKMCGP_01272 | 0.0 | kup | P | Transport of potassium into the cell | ||
MHEKMCGP_01273 | 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 | |
MHEKMCGP_01274 | 3.5e-166 | 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 | |
MHEKMCGP_01275 | 7.7e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
MHEKMCGP_01276 | 5.8e-78 | M | LysM domain protein | |||
MHEKMCGP_01277 | 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 | ||
MHEKMCGP_01278 | 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 | ||
MHEKMCGP_01279 | 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 | ||
MHEKMCGP_01280 | 6.2e-12 | |||||
MHEKMCGP_01281 | 2.3e-172 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
MHEKMCGP_01282 | 2.3e-30 | |||||
MHEKMCGP_01284 | 2.9e-69 | S | Iron-sulphur cluster biosynthesis | |||
MHEKMCGP_01285 | 6.5e-113 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
MHEKMCGP_01286 | 6.2e-59 | psiE | S | Phosphate-starvation-inducible E | ||
MHEKMCGP_01288 | 4.4e-135 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
MHEKMCGP_01289 | 4.3e-228 | amtB | P | ammonium transporter | ||
MHEKMCGP_01290 | 1.4e-60 | |||||
MHEKMCGP_01291 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
MHEKMCGP_01292 | 5.4e-245 | P | P-loop Domain of unknown function (DUF2791) | |||
MHEKMCGP_01293 | 2.6e-138 | S | TerB-C domain | |||
MHEKMCGP_01294 | 4.6e-58 | S | PAS domain | |||
MHEKMCGP_01295 | 9.1e-204 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
MHEKMCGP_01296 | 3.1e-178 | yvdE | K | helix_turn _helix lactose operon repressor | ||
MHEKMCGP_01297 | 7e-144 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
MHEKMCGP_01298 | 3.3e-291 | 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 | |
MHEKMCGP_01299 | 9.6e-152 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
MHEKMCGP_01300 | 2.3e-18 | |||||
MHEKMCGP_01301 | 4e-137 | K | Helix-turn-helix XRE-family like proteins | |||
MHEKMCGP_01302 | 2.3e-121 | V | Abi-like protein | |||
MHEKMCGP_01306 | 0.0 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
MHEKMCGP_01307 | 4.2e-61 | V | Abi-like protein | |||
MHEKMCGP_01308 | 0.0 | L | AAA domain | |||
MHEKMCGP_01310 | 9.1e-54 | papP | P | ABC transporter, permease protein | ||
MHEKMCGP_01311 | 5.3e-116 | P | ABC transporter permease | |||
MHEKMCGP_01312 | 1.5e-127 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MHEKMCGP_01313 | 1e-156 | cjaA | ET | ABC transporter substrate-binding protein | ||
MHEKMCGP_01314 | 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 | |
MHEKMCGP_01315 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
MHEKMCGP_01316 | 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 | ||
MHEKMCGP_01317 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
MHEKMCGP_01318 | 7.1e-158 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
MHEKMCGP_01319 | 1.9e-25 | |||||
MHEKMCGP_01320 | 0.0 | mco | Q | Multicopper oxidase | ||
MHEKMCGP_01321 | 1.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MHEKMCGP_01322 | 0.0 | oppA | E | ABC transporter | ||
MHEKMCGP_01323 | 8.4e-229 | Q | Imidazolonepropionase and related amidohydrolases | |||
MHEKMCGP_01324 | 2.7e-246 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
MHEKMCGP_01325 | 1e-137 | S | Protein of unknown function (DUF3100) | |||
MHEKMCGP_01326 | 9.7e-83 | S | An automated process has identified a potential problem with this gene model | |||
MHEKMCGP_01327 | 4.2e-92 | S | SNARE associated Golgi protein | |||
MHEKMCGP_01328 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
MHEKMCGP_01329 | 6.4e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MHEKMCGP_01330 | 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 | |
MHEKMCGP_01331 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
MHEKMCGP_01332 | 6.8e-110 | yjbK | S | CYTH | ||
MHEKMCGP_01333 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
MHEKMCGP_01334 | 1.4e-158 | coiA | 3.6.4.12 | S | Competence protein | |
MHEKMCGP_01335 | 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 | ||
MHEKMCGP_01336 | 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 | |
MHEKMCGP_01337 | 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) | |
MHEKMCGP_01338 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
MHEKMCGP_01339 | 5.3e-26 | |||||
MHEKMCGP_01340 | 1.7e-22 | blpT | ||||
MHEKMCGP_01341 | 4.6e-27 | S | Enterocin A Immunity | |||
MHEKMCGP_01344 | 1.3e-69 | doc | S | Prophage maintenance system killer protein | ||
MHEKMCGP_01345 | 2.9e-31 | |||||
MHEKMCGP_01346 | 0.0 | pepF | E | oligoendopeptidase F | ||
MHEKMCGP_01347 | 8.7e-197 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MHEKMCGP_01348 | 1.8e-111 | S | Protein of unknown function (DUF554) | |||
MHEKMCGP_01349 | 1.2e-30 | |||||
MHEKMCGP_01350 | 1.4e-34 | |||||
MHEKMCGP_01351 | 5e-72 | rimL | J | Acetyltransferase (GNAT) domain | ||
MHEKMCGP_01352 | 8.3e-58 | |||||
MHEKMCGP_01353 | 8.9e-292 | S | ABC transporter | |||
MHEKMCGP_01354 | 2.4e-136 | thrE | S | Putative threonine/serine exporter | ||
MHEKMCGP_01355 | 1.1e-83 | S | Threonine/Serine exporter, ThrE | |||
MHEKMCGP_01356 | 9.1e-112 | yvpB | S | Peptidase_C39 like family | ||
MHEKMCGP_01357 | 2.5e-68 | |||||
MHEKMCGP_01358 | 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 | |
MHEKMCGP_01359 | 5.5e-77 | nrdI | F | NrdI Flavodoxin like | ||
MHEKMCGP_01360 | 4.7e-221 | tnpB | L | Putative transposase DNA-binding domain | ||
MHEKMCGP_01361 | 3.3e-112 | |||||
MHEKMCGP_01362 | 2.9e-279 | S | O-antigen ligase like membrane protein | |||
MHEKMCGP_01363 | 3.9e-42 | |||||
MHEKMCGP_01364 | 2.2e-88 | gmk2 | 2.7.4.8 | F | Guanylate kinase homologues. | |
MHEKMCGP_01365 | 5e-88 | M | NlpC/P60 family | |||
MHEKMCGP_01366 | 1.4e-136 | M | NlpC P60 family protein | |||
MHEKMCGP_01367 | 2.6e-118 | M | NlpC/P60 family | |||
MHEKMCGP_01368 | 1.6e-41 | |||||
MHEKMCGP_01369 | 3.5e-175 | S | Cysteine-rich secretory protein family | |||
MHEKMCGP_01370 | 1.1e-103 | L | AAA ATPase domain | |||
MHEKMCGP_01371 | 1.8e-121 | L | UvrD/REP helicase N-terminal domain | |||
MHEKMCGP_01372 | 7.4e-40 | yabO | J | S4 domain protein | ||
MHEKMCGP_01373 | 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 | ||
MHEKMCGP_01374 | 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 | |
MHEKMCGP_01375 | 1.5e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
MHEKMCGP_01376 | 3.4e-129 | S | (CBS) domain | |||
MHEKMCGP_01377 | 1e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
MHEKMCGP_01378 | 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 | |
MHEKMCGP_01379 | 1.9e-251 | 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 | |
MHEKMCGP_01380 | 1.3e-262 | 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 | |
MHEKMCGP_01381 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
MHEKMCGP_01382 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
MHEKMCGP_01383 | 2.6e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MHEKMCGP_01384 | 3.3e-297 | ybeC | E | amino acid | ||
MHEKMCGP_01385 | 2.4e-231 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
MHEKMCGP_01386 | 4e-22 | |||||
MHEKMCGP_01387 | 0.0 | L | Plasmid pRiA4b ORF-3-like protein | |||
MHEKMCGP_01388 | 9e-121 | |||||
MHEKMCGP_01389 | 1.9e-157 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
MHEKMCGP_01390 | 3.9e-186 | S | Putative peptidoglycan binding domain | |||
MHEKMCGP_01391 | 4e-16 | |||||
MHEKMCGP_01392 | 7.9e-92 | liaI | S | membrane | ||
MHEKMCGP_01393 | 6.6e-70 | XK27_02470 | K | LytTr DNA-binding domain | ||
MHEKMCGP_01394 | 1.2e-18 | S | Sugar efflux transporter for intercellular exchange | |||
MHEKMCGP_01395 | 1.3e-250 | dtpT | U | amino acid peptide transporter | ||
MHEKMCGP_01396 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
MHEKMCGP_01397 | 2.8e-47 | lysM | M | LysM domain | ||
MHEKMCGP_01398 | 1.3e-174 | |||||
MHEKMCGP_01399 | 1.7e-152 | mdtG | EGP | Major facilitator Superfamily | ||
MHEKMCGP_01400 | 6.9e-47 | mdtG | EGP | Major facilitator Superfamily | ||
MHEKMCGP_01402 | 1.9e-259 | emrY | EGP | Major facilitator Superfamily | ||
MHEKMCGP_01403 | 3.2e-36 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
MHEKMCGP_01404 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
MHEKMCGP_01405 | 5.5e-148 | S | cog cog1373 | |||
MHEKMCGP_01406 | 7.6e-132 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
MHEKMCGP_01407 | 4.1e-104 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
MHEKMCGP_01408 | 3.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
MHEKMCGP_01410 | 5.4e-215 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
MHEKMCGP_01411 | 2.6e-181 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
MHEKMCGP_01412 | 8.8e-177 | yjbQ | P | TrkA C-terminal domain protein | ||
MHEKMCGP_01413 | 1.9e-113 | yjbQ | P | TrkA C-terminal domain protein | ||
MHEKMCGP_01414 | 1.7e-106 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
MHEKMCGP_01415 | 6e-161 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
MHEKMCGP_01416 | 4.6e-130 | |||||
MHEKMCGP_01417 | 2.1e-116 | |||||
MHEKMCGP_01418 | 5e-133 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
MHEKMCGP_01419 | 1.4e-98 | G | Aldose 1-epimerase | |||
MHEKMCGP_01420 | 2.8e-199 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MHEKMCGP_01421 | 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 | |
MHEKMCGP_01422 | 0.0 | XK27_08315 | M | Sulfatase | ||
MHEKMCGP_01423 | 9.3e-116 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
MHEKMCGP_01424 | 1.4e-107 | M | Transport protein ComB | |||
MHEKMCGP_01425 | 2.2e-129 | blpT | ||||
MHEKMCGP_01429 | 3e-21 | |||||
MHEKMCGP_01430 | 3.7e-83 | |||||
MHEKMCGP_01431 | 8.2e-31 | yozG | K | Transcriptional regulator | ||
MHEKMCGP_01432 | 2e-23 | |||||
MHEKMCGP_01433 | 1.7e-67 | |||||
MHEKMCGP_01434 | 1.1e-164 | natA | S | ABC transporter, ATP-binding protein | ||
MHEKMCGP_01435 | 1.8e-218 | natB | CP | ABC-2 family transporter protein | ||
MHEKMCGP_01436 | 1.8e-136 | fruR | K | DeoR C terminal sensor domain | ||
MHEKMCGP_01437 | 2.2e-168 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
MHEKMCGP_01438 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
MHEKMCGP_01439 | 5.4e-41 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
MHEKMCGP_01440 | 1.6e-147 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
MHEKMCGP_01441 | 1.6e-117 | fhuC | P | ABC transporter | ||
MHEKMCGP_01442 | 5e-129 | znuB | U | ABC 3 transport family | ||
MHEKMCGP_01443 | 2e-264 | lctP | C | L-lactate permease | ||
MHEKMCGP_01444 | 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) | |
MHEKMCGP_01445 | 1.5e-216 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
MHEKMCGP_01446 | 1.2e-11 | |||||
MHEKMCGP_01447 | 1.6e-25 | K | Helix-turn-helix XRE-family like proteins | |||
MHEKMCGP_01449 | 4.1e-33 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
MHEKMCGP_01450 | 2.8e-48 | S | Peptidase propeptide and YPEB domain | |||
MHEKMCGP_01451 | 6e-46 | L | An automated process has identified a potential problem with this gene model | |||
MHEKMCGP_01452 | 4.2e-63 | lmrB | EGP | Major facilitator Superfamily | ||
MHEKMCGP_01453 | 9.8e-123 | rbtT | P | Major Facilitator Superfamily | ||
MHEKMCGP_01454 | 2.7e-202 | XK27_00915 | C | Luciferase-like monooxygenase | ||
MHEKMCGP_01455 | 2.5e-86 | K | GNAT family | |||
MHEKMCGP_01456 | 1.4e-124 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
MHEKMCGP_01458 | 4.3e-36 | |||||
MHEKMCGP_01459 | 6.2e-288 | P | ABC transporter | |||
MHEKMCGP_01460 | 2.3e-07 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MHEKMCGP_01461 | 9.8e-94 | yttB | EGP | Major facilitator Superfamily | ||
MHEKMCGP_01462 | 1.5e-230 | XK27_04775 | S | PAS domain | ||
MHEKMCGP_01463 | 2.1e-103 | S | Iron-sulfur cluster assembly protein | |||
MHEKMCGP_01464 | 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 | |
MHEKMCGP_01465 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
MHEKMCGP_01466 | 5.6e-255 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
MHEKMCGP_01467 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
MHEKMCGP_01468 | 3.5e-271 | S | Calcineurin-like phosphoesterase | |||
MHEKMCGP_01469 | 3.9e-84 | |||||
MHEKMCGP_01470 | 1.6e-105 | tag | 3.2.2.20 | L | glycosylase | |
MHEKMCGP_01471 | 4.5e-168 | L | COG3385 FOG Transposase and inactivated derivatives | |||
MHEKMCGP_01472 | 4.3e-24 | S | SLAP domain | |||
MHEKMCGP_01473 | 3.8e-24 | S | SLAP domain | |||
MHEKMCGP_01474 | 3.3e-37 | |||||
MHEKMCGP_01475 | 2.5e-119 | K | helix_turn_helix, mercury resistance | |||
MHEKMCGP_01476 | 7.5e-231 | pbuG | S | permease | ||
MHEKMCGP_01477 | 7.1e-63 | M | LysM domain protein | |||
MHEKMCGP_01478 | 6.2e-151 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
MHEKMCGP_01479 | 7.9e-67 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
MHEKMCGP_01480 | 2.7e-64 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
MHEKMCGP_01481 | 3.2e-12 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
MHEKMCGP_01482 | 1.2e-116 | mmuP | E | amino acid | ||
MHEKMCGP_01483 | 6.5e-273 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
MHEKMCGP_01484 | 1.6e-93 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
MHEKMCGP_01485 | 5.5e-283 | E | Amino acid permease | |||
MHEKMCGP_01486 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
MHEKMCGP_01487 | 6.7e-245 | ynbB | 4.4.1.1 | P | aluminum resistance | |
MHEKMCGP_01488 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
MHEKMCGP_01489 | 1.8e-200 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
MHEKMCGP_01490 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
MHEKMCGP_01491 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
MHEKMCGP_01492 | 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 | |
MHEKMCGP_01493 | 1.7e-69 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
MHEKMCGP_01494 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
MHEKMCGP_01495 | 9e-223 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
MHEKMCGP_01496 | 1.9e-236 | S | Peptidase M16 | |||
MHEKMCGP_01497 | 2.3e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
MHEKMCGP_01498 | 5.2e-97 | ymfM | S | Helix-turn-helix domain | ||
MHEKMCGP_01499 | 1.1e-95 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
MHEKMCGP_01500 | 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 | ||
MHEKMCGP_01501 | 7.4e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
MHEKMCGP_01502 | 1.3e-210 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
MHEKMCGP_01503 | 5.1e-119 | yvyE | 3.4.13.9 | S | YigZ family | |
MHEKMCGP_01504 | 2.2e-142 | S | Belongs to the UPF0246 family | |||
MHEKMCGP_01505 | 4.1e-141 | aroD | S | Alpha/beta hydrolase family | ||
MHEKMCGP_01506 | 3.5e-111 | G | phosphoglycerate mutase | |||
MHEKMCGP_01507 | 3.2e-92 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
MHEKMCGP_01508 | 3.3e-176 | hrtB | V | ABC transporter permease | ||
MHEKMCGP_01509 | 1.5e-102 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
MHEKMCGP_01510 | 1.1e-272 | pipD | E | Dipeptidase | ||
MHEKMCGP_01511 | 5.9e-174 | S | Aldo keto reductase | |||
MHEKMCGP_01512 | 2.2e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
MHEKMCGP_01513 | 4.7e-182 | pepA | E | M42 glutamyl aminopeptidase | ||
MHEKMCGP_01514 | 9.1e-66 | L | An automated process has identified a potential problem with this gene model | |||
MHEKMCGP_01515 | 3e-53 | cvpA | S | Colicin V production protein | ||
MHEKMCGP_01517 | 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 | |
MHEKMCGP_01518 | 6e-151 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
MHEKMCGP_01519 | 2e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
MHEKMCGP_01520 | 6.4e-96 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
MHEKMCGP_01521 | 2.4e-110 | K | WHG domain | |||
MHEKMCGP_01522 | 3e-37 | |||||
MHEKMCGP_01523 | 2.2e-120 | lsa | S | ABC transporter | ||
MHEKMCGP_01524 | 1.7e-201 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
MHEKMCGP_01525 | 3.1e-107 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
MHEKMCGP_01526 | 1.8e-228 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
MHEKMCGP_01527 | 0.0 | L | PLD-like domain | |||
MHEKMCGP_01528 | 4.8e-42 | S | SnoaL-like domain | |||
MHEKMCGP_01529 | 5.4e-53 | hipB | K | sequence-specific DNA binding | ||
MHEKMCGP_01530 | 8e-22 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
MHEKMCGP_01531 | 3.4e-27 | |||||
MHEKMCGP_01532 | 8.8e-29 | |||||
MHEKMCGP_01535 | 4.9e-111 | K | Helix-turn-helix XRE-family like proteins | |||
MHEKMCGP_01536 | 2.5e-75 | K | Helix-turn-helix domain | |||
MHEKMCGP_01537 | 1.9e-25 | S | CAAX protease self-immunity | |||
MHEKMCGP_01538 | 1.4e-22 | S | CAAX protease self-immunity | |||
MHEKMCGP_01539 | 7.6e-26 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
MHEKMCGP_01541 | 1.6e-96 | ybaT | E | Amino acid permease | ||
MHEKMCGP_01543 | 1.2e-241 | S | response to antibiotic | |||
MHEKMCGP_01544 | 4.9e-125 | |||||
MHEKMCGP_01545 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
MHEKMCGP_01546 | 8.7e-66 | 2.7.1.191 | G | PTS system fructose IIA component | ||
MHEKMCGP_01547 | 4.4e-43 | |||||
MHEKMCGP_01548 | 5.9e-09 | |||||
MHEKMCGP_01549 | 9.4e-186 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
MHEKMCGP_01550 | 5.3e-136 | glvR | K | Helix-turn-helix domain, rpiR family | ||
MHEKMCGP_01551 | 2.7e-268 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
MHEKMCGP_01552 | 7.7e-30 | ropB | K | Helix-turn-helix domain | ||
MHEKMCGP_01553 | 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 | |
MHEKMCGP_01554 | 6.6e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
MHEKMCGP_01555 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
MHEKMCGP_01556 | 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 | ||
MHEKMCGP_01557 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
MHEKMCGP_01558 | 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 | ||
MHEKMCGP_01559 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
MHEKMCGP_01560 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
MHEKMCGP_01561 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
MHEKMCGP_01562 | 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 | |
MHEKMCGP_01563 | 2e-226 | 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 | |
MHEKMCGP_01564 | 1.4e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
MHEKMCGP_01565 | 1.7e-215 | 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 | |
MHEKMCGP_01566 | 9.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
MHEKMCGP_01567 | 9.6e-41 | yajC | U | Preprotein translocase | ||
MHEKMCGP_01568 | 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 | |
MHEKMCGP_01569 | 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 | |
MHEKMCGP_01570 | 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 | ||
MHEKMCGP_01571 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
MHEKMCGP_01572 | 2e-75 | S | cog cog0433 | |||
MHEKMCGP_01575 | 4.4e-17 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
MHEKMCGP_01578 | 1.2e-32 | M | Peptidase family M23 | |||
MHEKMCGP_01579 | 1.8e-159 | trsE | S | COG0433 Predicted ATPase | ||
MHEKMCGP_01580 | 4.9e-15 | |||||
MHEKMCGP_01582 | 1e-32 | I | mechanosensitive ion channel activity | |||
MHEKMCGP_01583 | 2e-140 | U | TraM recognition site of TraD and TraG | |||
MHEKMCGP_01587 | 5e-38 | M | domain protein | |||
MHEKMCGP_01588 | 4.6e-42 | M | domain protein | |||
MHEKMCGP_01590 | 1.4e-24 | srtA | 3.4.22.70 | M | sortase family | |
MHEKMCGP_01591 | 1.6e-21 | S | SLAP domain | |||
MHEKMCGP_01596 | 2.6e-11 | ssb | L | Single-strand binding protein family | ||
MHEKMCGP_01604 | 3.2e-24 | S | Domain of unknown function (DUF771) | |||
MHEKMCGP_01605 | 8.9e-32 | K | Helix-turn-helix domain | |||
MHEKMCGP_01606 | 1.2e-21 | XK27_07105 | K | Helix-turn-helix XRE-family like proteins | ||
MHEKMCGP_01607 | 1.2e-23 | K | Helix-turn-helix domain | |||
MHEKMCGP_01608 | 5e-08 | S | Pfam:DUF955 | |||
MHEKMCGP_01609 | 1.4e-153 | L | Belongs to the 'phage' integrase family | |||
MHEKMCGP_01611 | 6.3e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
MHEKMCGP_01612 | 1.9e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
MHEKMCGP_01613 | 1.6e-21 | |||||
MHEKMCGP_01614 | 3.8e-77 | comGF | U | Putative Competence protein ComGF | ||
MHEKMCGP_01615 | 2.3e-41 | |||||
MHEKMCGP_01616 | 1.8e-69 | |||||
MHEKMCGP_01617 | 3.1e-43 | comGC | U | competence protein ComGC | ||
MHEKMCGP_01618 | 1.7e-171 | comGB | NU | type II secretion system | ||
MHEKMCGP_01619 | 1.7e-179 | comGA | NU | Type II IV secretion system protein | ||
MHEKMCGP_01620 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
MHEKMCGP_01621 | 7.6e-94 | S | VanZ like family | |||
MHEKMCGP_01622 | 4.3e-25 | ylbE | GM | NAD(P)H-binding | ||
MHEKMCGP_01623 | 2.7e-151 | I | alpha/beta hydrolase fold | |||
MHEKMCGP_01624 | 5.2e-156 | hipB | K | Helix-turn-helix | ||
MHEKMCGP_01625 | 1.4e-15 | S | cog cog1373 | |||
MHEKMCGP_01626 | 1e-30 | S | cog cog1373 | |||
MHEKMCGP_01627 | 7.6e-91 | F | Nucleoside 2-deoxyribosyltransferase | |||
MHEKMCGP_01628 | 3.3e-261 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)