| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| MLNPHKMC_00001 | 1.4e-124 | ywrJ | ||||
| MLNPHKMC_00002 | 1.4e-218 | ywrK | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
| MLNPHKMC_00003 | 1.1e-169 | alsR | K | LysR substrate binding domain | ||
| MLNPHKMC_00004 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
| MLNPHKMC_00005 | 1.3e-145 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
| MLNPHKMC_00006 | 9.7e-97 | ywrO | S | NADPH-quinone reductase (modulator of drug activity B) | ||
| MLNPHKMC_00007 | 8e-48 | ywsA | S | Protein of unknown function (DUF3892) | ||
| MLNPHKMC_00008 | 8.7e-93 | batE | T | Sh3 type 3 domain protein | ||
| MLNPHKMC_00009 | 2.4e-159 | rbsB | G | COG1879 ABC-type sugar transport system, periplasmic component | ||
| MLNPHKMC_00010 | 3.5e-148 | rbsC | G | Belongs to the binding-protein-dependent transport system permease family | ||
| MLNPHKMC_00011 | 8.6e-276 | rbsA | 3.6.3.17 | G | Part of the ABC transporter complex RbsABC involved in ribose import. Responsible for energy coupling to the transport system | |
| MLNPHKMC_00012 | 5.3e-63 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
| MLNPHKMC_00013 | 2.5e-161 | rbsK | 2.7.1.15, 2.7.1.4 | 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 | |
| MLNPHKMC_00014 | 5.2e-176 | rbsR | K | transcriptional | ||
| MLNPHKMC_00015 | 6.1e-224 | murD | 6.3.2.9 | M | COG0769 UDP-N-acetylmuramyl tripeptide synthase | |
| MLNPHKMC_00016 | 8.6e-70 | pgsC | S | biosynthesis protein | ||
| MLNPHKMC_00017 | 6.3e-218 | capA | M | enzyme of poly-gamma-glutamate biosynthesis (capsule formation) | ||
| MLNPHKMC_00018 | 3.6e-21 | ywtC | ||||
| MLNPHKMC_00019 | 2e-239 | pgdS | CBM50 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
| MLNPHKMC_00020 | 4.2e-158 | ywtE | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
| MLNPHKMC_00021 | 2.3e-168 | ywtF | K | Transcriptional regulator | ||
| MLNPHKMC_00022 | 1.3e-246 | ywtG | EGP | Major facilitator Superfamily | ||
| MLNPHKMC_00023 | 9.3e-206 | gerAC | S | Spore germination protein | ||
| MLNPHKMC_00024 | 8.4e-191 | gerBB | E | Spore germination protein | ||
| MLNPHKMC_00025 | 3.7e-263 | gerBA | EG | Spore germination protein | ||
| MLNPHKMC_00026 | 1.8e-186 | pmi | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
| MLNPHKMC_00027 | 1.2e-214 | atl | 3.2.1.96, 3.5.1.28 | GH73 | G | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase |
| MLNPHKMC_00028 | 2.4e-127 | M | Glycosyl transferase group 1 protein | |||
| MLNPHKMC_00029 | 2.8e-158 | wbmJ | M | Glycosyl transferases group 1 | ||
| MLNPHKMC_00031 | 1.8e-126 | M | DUF based on E. rectale Gene description (DUF3880) | |||
| MLNPHKMC_00032 | 2e-159 | wecC | 1.1.1.336 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
| MLNPHKMC_00033 | 3.5e-129 | atl | 3.2.1.96, 3.5.1.28 | GH73 | G | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase |
| MLNPHKMC_00034 | 5.6e-54 | 3.4.11.5 | S | alpha beta | ||
| MLNPHKMC_00035 | 2.5e-192 | tarL | 2.7.8.14, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
| MLNPHKMC_00036 | 2.5e-89 | 2.7.8.46 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | ||
| MLNPHKMC_00037 | 6.2e-148 | tarJ | 1.1.1.137, 1.1.1.303, 1.1.1.4, 1.1.1.405 | E | Catalyzes the NADPH dependent reduction of D-ribulose 5- phosphate to D-ribitol 5-phosphate | |
| MLNPHKMC_00038 | 2e-105 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the transfer of the cytidylyl group of CTP to D-ribitol 5-phosphate | |
| MLNPHKMC_00039 | 9.2e-96 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
| MLNPHKMC_00040 | 5.4e-88 | tagA | 2.4.1.187 | GT26 | M | 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 |
| MLNPHKMC_00041 | 1.1e-52 | tagD | 2.7.7.15, 2.7.7.39 | IM | Cytidylyltransferase | |
| MLNPHKMC_00042 | 1.2e-133 | tagG | GM | Transport permease protein | ||
| MLNPHKMC_00043 | 1.8e-271 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
| MLNPHKMC_00044 | 2e-163 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
| MLNPHKMC_00045 | 5.3e-119 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
| MLNPHKMC_00047 | 8.5e-215 | mnaA | 5.1.3.14 | M | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
| MLNPHKMC_00048 | 1.8e-162 | lytR | K | May catalyze the final step in cell wall teichoic acid biosynthesis, the transfer of the anionic cell wall polymers (APs) from their lipid-linked precursor to the cell wall peptidoglycan (PG) | ||
| MLNPHKMC_00049 | 2.1e-35 | |||||
| MLNPHKMC_00050 | 6.8e-14 | lytB | 3.5.1.28 | D | Stage II sporulation protein | |
| MLNPHKMC_00051 | 9e-265 | lytC | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
| MLNPHKMC_00052 | 4.6e-112 | tuaA | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
| MLNPHKMC_00053 | 7.4e-248 | wzxC | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
| MLNPHKMC_00054 | 1.1e-220 | tuaC | 2.4.1.21, 3.2.1.1 | GH13,GT4,GT5 | GM | Teichuronic acid |
| MLNPHKMC_00055 | 1.5e-258 | tuaD | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
| MLNPHKMC_00056 | 3.7e-263 | tuaE | M | Teichuronic acid biosynthesis protein | ||
| MLNPHKMC_00057 | 5.1e-114 | tuaF | M | protein involved in exopolysaccharide biosynthesis | ||
| MLNPHKMC_00058 | 2.1e-145 | tuaG | GT2 | M | Glycosyltransferase like family 2 | |
| MLNPHKMC_00059 | 1.3e-234 | tuaH | M | Teichuronic acid biosynthesis glycosyltransferase tuaH | ||
| MLNPHKMC_00060 | 2.6e-181 | tagO | 2.7.8.33, 2.7.8.35 | M | COG0472 UDP-N-acetylmuramyl pentapeptide phosphotransferase UDP-N-acetylglucosamine-1-phosphate transferase | |
| MLNPHKMC_00061 | 6e-163 | yvhJ | K | Transcriptional regulator | ||
| MLNPHKMC_00062 | 2e-120 | yvyE | 3.4.13.9 | S | Domain of unknown function (DUF1949) | |
| MLNPHKMC_00063 | 5.1e-183 | degS | 2.7.13.3 | T | Member of the two-component regulatory system DegS DegU, which plays an important role in the transition growth phase | |
| MLNPHKMC_00064 | 2e-126 | degU | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
| MLNPHKMC_00065 | 2.1e-154 | degV | S | protein conserved in bacteria | ||
| MLNPHKMC_00066 | 5.4e-264 | comFA | L | COG4098 Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
| MLNPHKMC_00067 | 5.7e-46 | comFB | S | Late competence development protein ComFB | ||
| MLNPHKMC_00068 | 4.7e-126 | comFC | S | Phosphoribosyl transferase domain | ||
| MLNPHKMC_00069 | 7e-74 | yvyF | S | flagellar protein | ||
| MLNPHKMC_00070 | 4.7e-39 | flgM | KNU | Negative regulator of flagellin synthesis | ||
| MLNPHKMC_00071 | 4.1e-78 | flgN | NOU | FlgN protein | ||
| MLNPHKMC_00072 | 1.2e-264 | flgK | N | flagellar hook-associated protein | ||
| MLNPHKMC_00073 | 1.3e-154 | flgL | N | Belongs to the bacterial flagellin family | ||
| MLNPHKMC_00074 | 5.7e-50 | yviE | ||||
| MLNPHKMC_00075 | 2.7e-73 | fliW | S | Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum | ||
| MLNPHKMC_00076 | 9.7e-30 | csrA | T | Could accelerate the degradation of some genes transcripts potentially through selective RNA binding | ||
| MLNPHKMC_00077 | 1.4e-108 | fliC | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
| MLNPHKMC_00078 | 1.2e-55 | flaG | N | flagellar protein FlaG | ||
| MLNPHKMC_00079 | 1.5e-256 | fliD | N | morphogenesis and for the elongation of the flagellar filament by facilitating polymerization of the flagellin monomers at the tip of growing filament. Forms a capping structure, which prevents flagellin subunits (transported through the central channel of the flagellum) from leaking out without polymerization at the distal end | ||
| MLNPHKMC_00080 | 2.9e-69 | fliS | N | flagellar protein FliS | ||
| MLNPHKMC_00081 | 1.9e-08 | fliT | S | bacterial-type flagellum organization | ||
| MLNPHKMC_00082 | 1.8e-65 | |||||
| MLNPHKMC_00083 | 2.2e-102 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
| MLNPHKMC_00084 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
| MLNPHKMC_00085 | 6.1e-185 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
| MLNPHKMC_00086 | 5.5e-142 | yvjA | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
| MLNPHKMC_00087 | 1e-54 | cccB | C | COG2010 Cytochrome c, mono- and diheme variants | ||
| MLNPHKMC_00088 | 1.6e-123 | ftsE | D | cell division ATP-binding protein FtsE | ||
| MLNPHKMC_00089 | 1.6e-155 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
| MLNPHKMC_00090 | 2e-269 | ctpB | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
| MLNPHKMC_00091 | 5.3e-56 | swrA | S | Swarming motility protein | ||
| MLNPHKMC_00092 | 1.9e-220 | minJ | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | ||
| MLNPHKMC_00093 | 2.8e-225 | yvkA | EGP | Major facilitator Superfamily | ||
| MLNPHKMC_00094 | 7e-101 | yvkB | K | Transcriptional regulator | ||
| MLNPHKMC_00095 | 0.0 | yvkC | 2.7.9.2 | GT | Phosphotransferase | |
| MLNPHKMC_00096 | 1.2e-30 | csbA | S | protein conserved in bacteria | ||
| MLNPHKMC_00097 | 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 | ||
| MLNPHKMC_00098 | 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 | ||
| MLNPHKMC_00099 | 9.2e-78 | fliC | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
| MLNPHKMC_00100 | 5.7e-33 | yvkN | ||||
| MLNPHKMC_00101 | 1.8e-48 | yvlA | ||||
| MLNPHKMC_00102 | 2.4e-166 | yvlB | S | Putative adhesin |
Showing 1 to 100 of 3,917 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)