ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
MLDOIJIL_00001 | 1.1e-82 | lacS | G | Transporter | ||
MLDOIJIL_00002 | 8.7e-57 | lacS | G | Transporter | ||
MLDOIJIL_00003 | 2.6e-103 | lacS | G | Transporter | ||
MLDOIJIL_00004 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
MLDOIJIL_00005 | 1.7e-116 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
MLDOIJIL_00006 | 3.1e-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 | |
MLDOIJIL_00007 | 1.1e-34 | phnD | P | Phosphonate ABC transporter | ||
MLDOIJIL_00008 | 8.3e-143 | licT | K | CAT RNA binding domain | ||
MLDOIJIL_00009 | 9.5e-206 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
MLDOIJIL_00010 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
MLDOIJIL_00011 | 1e-117 | |||||
MLDOIJIL_00012 | 4.4e-62 | K | Penicillinase repressor | |||
MLDOIJIL_00013 | 3.2e-147 | S | hydrolase | |||
MLDOIJIL_00014 | 1.9e-98 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
MLDOIJIL_00015 | 9e-275 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
MLDOIJIL_00016 | 2.4e-34 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
MLDOIJIL_00018 | 2e-49 | S | Putative adhesin | |||
MLDOIJIL_00019 | 3.6e-100 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
MLDOIJIL_00020 | 4.2e-19 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
MLDOIJIL_00021 | 1.4e-83 | dps | P | Belongs to the Dps family | ||
MLDOIJIL_00022 | 6.4e-82 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
MLDOIJIL_00023 | 2.8e-16 | |||||
MLDOIJIL_00024 | 1.5e-169 | |||||
MLDOIJIL_00025 | 5.7e-149 | glnA | 6.3.1.2 | E | glutamine synthetase | |
MLDOIJIL_00026 | 3.1e-135 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
MLDOIJIL_00027 | 9e-270 | 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 | |
MLDOIJIL_00028 | 6.1e-136 | V | ABC transporter transmembrane region | |||
MLDOIJIL_00029 | 3.5e-225 | 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 | ||
MLDOIJIL_00030 | 4.5e-23 | |||||
MLDOIJIL_00031 | 3.5e-161 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
MLDOIJIL_00032 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
MLDOIJIL_00033 | 2.7e-97 | T | Transcriptional regulatory protein, C terminal | |||
MLDOIJIL_00034 | 8.6e-90 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
MLDOIJIL_00035 | 1e-24 | |||||
MLDOIJIL_00036 | 9.5e-26 | |||||
MLDOIJIL_00037 | 2.5e-33 | |||||
MLDOIJIL_00038 | 1.4e-53 | S | Enterocin A Immunity | |||
MLDOIJIL_00039 | 6.9e-36 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
MLDOIJIL_00040 | 5.7e-91 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
MLDOIJIL_00041 | 1.6e-73 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00042 | 8.4e-28 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00043 | 2.3e-196 | 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 | ||
MLDOIJIL_00044 | 3e-159 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
MLDOIJIL_00045 | 2.5e-119 | K | helix_turn_helix, mercury resistance | |||
MLDOIJIL_00046 | 5.7e-10 | pbuG | S | permease | ||
MLDOIJIL_00047 | 9e-98 | |||||
MLDOIJIL_00048 | 4.9e-108 | K | LysR substrate binding domain | |||
MLDOIJIL_00049 | 1e-20 | |||||
MLDOIJIL_00050 | 2.5e-206 | S | Sterol carrier protein domain | |||
MLDOIJIL_00051 | 9.2e-95 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
MLDOIJIL_00052 | 2e-105 | argF | 2.1.3.3, 2.7.2.2 | E | Belongs to the carbamate kinase family | |
MLDOIJIL_00053 | 9.8e-63 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
MLDOIJIL_00054 | 1.3e-148 | arcA | 3.5.3.6 | E | Arginine | |
MLDOIJIL_00055 | 2.7e-123 | oatA | I | Acyltransferase | ||
MLDOIJIL_00056 | 3.6e-149 | 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 | ||
MLDOIJIL_00057 | 1.3e-30 | |||||
MLDOIJIL_00058 | 3.6e-69 | T | Toxin-antitoxin system, toxin component, MazF family | |||
MLDOIJIL_00059 | 6.3e-87 | ntd | 2.4.2.6 | F | Nucleoside | |
MLDOIJIL_00060 | 8.6e-87 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
MLDOIJIL_00061 | 8.1e-76 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
MLDOIJIL_00062 | 4e-25 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
MLDOIJIL_00063 | 1.1e-242 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
MLDOIJIL_00064 | 7.3e-66 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
MLDOIJIL_00065 | 5.5e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
MLDOIJIL_00066 | 3.9e-44 | degV | S | DegV family | ||
MLDOIJIL_00067 | 5.5e-135 | V | ABC transporter transmembrane region | |||
MLDOIJIL_00068 | 4.3e-55 | |||||
MLDOIJIL_00069 | 6.8e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
MLDOIJIL_00070 | 1.3e-179 | ccpA | K | catabolite control protein A | ||
MLDOIJIL_00071 | 2e-50 | 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 | ||
MLDOIJIL_00072 | 1.2e-266 | dnaE | 2.7.7.7 | L | DNA polymerase | |
MLDOIJIL_00073 | 3.2e-89 | ykoD | P | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00074 | 2.3e-145 | cbiQ | P | cobalt transport | ||
MLDOIJIL_00075 | 3.5e-21 | |||||
MLDOIJIL_00076 | 9.3e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
MLDOIJIL_00077 | 2.3e-111 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
MLDOIJIL_00078 | 1.4e-147 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
MLDOIJIL_00079 | 3.3e-71 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
MLDOIJIL_00080 | 7.9e-180 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
MLDOIJIL_00081 | 2.2e-151 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
MLDOIJIL_00082 | 3.8e-145 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
MLDOIJIL_00083 | 5.6e-21 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
MLDOIJIL_00084 | 3.6e-177 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
MLDOIJIL_00085 | 3.5e-283 | 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 | ||
MLDOIJIL_00086 | 5.3e-142 | noc | K | Belongs to the ParB family | ||
MLDOIJIL_00087 | 3.4e-138 | soj | D | Sporulation initiation inhibitor | ||
MLDOIJIL_00088 | 1.1e-148 | spo0J | K | Belongs to the ParB family | ||
MLDOIJIL_00089 | 6.1e-224 | S | SLAP domain | |||
MLDOIJIL_00090 | 1.5e-97 | S | CAAX protease self-immunity | |||
MLDOIJIL_00091 | 1e-12 | |||||
MLDOIJIL_00092 | 3.4e-278 | arlS | 2.7.13.3 | T | Histidine kinase | |
MLDOIJIL_00093 | 1.2e-126 | K | response regulator | |||
MLDOIJIL_00094 | 4.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
MLDOIJIL_00095 | 1.5e-141 | ylbM | S | Belongs to the UPF0348 family | ||
MLDOIJIL_00096 | 8.4e-115 | M | Belongs to the glycosyl hydrolase 28 family | |||
MLDOIJIL_00097 | 1.2e-79 | K | Acetyltransferase (GNAT) domain | |||
MLDOIJIL_00098 | 4.2e-80 | |||||
MLDOIJIL_00099 | 5.5e-50 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
MLDOIJIL_00100 | 1.6e-180 | 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) | |
MLDOIJIL_00101 | 9.5e-152 | msmR | K | AraC-like ligand binding domain | ||
MLDOIJIL_00102 | 2.9e-120 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
MLDOIJIL_00103 | 1.6e-85 | |||||
MLDOIJIL_00104 | 6.6e-73 | |||||
MLDOIJIL_00105 | 1.3e-138 | hlyX | S | Transporter associated domain | ||
MLDOIJIL_00106 | 4e-66 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
MLDOIJIL_00107 | 1.6e-175 | 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 | ||
MLDOIJIL_00108 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
MLDOIJIL_00109 | 9.2e-89 | ypmB | S | Protein conserved in bacteria | ||
MLDOIJIL_00110 | 2.6e-133 | pbpX1 | V | Beta-lactamase | ||
MLDOIJIL_00111 | 2.5e-156 | I | Protein of unknown function (DUF2974) | |||
MLDOIJIL_00112 | 2.4e-80 | mutT | 3.6.1.55 | F | NUDIX domain | |
MLDOIJIL_00113 | 3e-122 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
MLDOIJIL_00114 | 1.4e-152 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
MLDOIJIL_00115 | 1.3e-152 | L | Transposase | |||
MLDOIJIL_00116 | 1.2e-57 | L | Transposase | |||
MLDOIJIL_00117 | 1.9e-75 | M | LysM domain | |||
MLDOIJIL_00118 | 2.4e-173 | S | SLAP domain | |||
MLDOIJIL_00119 | 1.3e-151 | M | Peptidase family M1 domain | |||
MLDOIJIL_00120 | 1e-79 | S | AAA domain | |||
MLDOIJIL_00121 | 3.9e-109 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
MLDOIJIL_00122 | 1.8e-19 | |||||
MLDOIJIL_00123 | 2.2e-41 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
MLDOIJIL_00124 | 1.2e-294 | yloV | S | DAK2 domain fusion protein YloV | ||
MLDOIJIL_00125 | 2.4e-54 | asp | S | Asp23 family, cell envelope-related function | ||
MLDOIJIL_00126 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
MLDOIJIL_00127 | 4.1e-30 | |||||
MLDOIJIL_00128 | 1.3e-162 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
MLDOIJIL_00129 | 5.1e-193 | oppA3 | E | ABC transporter, substratebinding protein | ||
MLDOIJIL_00130 | 9e-161 | V | ABC transporter transmembrane region | |||
MLDOIJIL_00131 | 2.9e-50 | 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 | ||
MLDOIJIL_00132 | 1e-23 | 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 | ||
MLDOIJIL_00133 | 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 | ||
MLDOIJIL_00134 | 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 | ||
MLDOIJIL_00135 | 6.8e-60 | coiA | 3.6.4.12 | S | Competence protein | |
MLDOIJIL_00136 | 4e-13 | coiA | 3.6.4.12 | S | Competence protein | |
MLDOIJIL_00137 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
MLDOIJIL_00138 | 6.8e-110 | yjbK | S | CYTH | ||
MLDOIJIL_00139 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
MLDOIJIL_00140 | 1.3e-67 | |||||
MLDOIJIL_00141 | 2.5e-158 | cpdA | S | Calcineurin-like phosphoesterase | ||
MLDOIJIL_00142 | 5.4e-81 | rny | S | Endoribonuclease that initiates mRNA decay | ||
MLDOIJIL_00143 | 3.8e-210 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
MLDOIJIL_00144 | 2.1e-67 | yvyE | 3.4.13.9 | S | YigZ family | |
MLDOIJIL_00145 | 2.6e-65 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
MLDOIJIL_00146 | 2.9e-126 | crtI | 1.3.99.23, 5.2.1.13 | Q | HI0933-like protein | |
MLDOIJIL_00147 | 7.5e-17 | crtI | 1.3.99.23, 5.2.1.13 | Q | HI0933-like protein | |
MLDOIJIL_00148 | 4.3e-52 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
MLDOIJIL_00149 | 8.2e-73 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
MLDOIJIL_00150 | 3.2e-10 | S | Domain of unknown function DUF87 | |||
MLDOIJIL_00151 | 1.2e-63 | S | SIR2-like domain | |||
MLDOIJIL_00152 | 1.4e-97 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
MLDOIJIL_00153 | 1.9e-259 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
MLDOIJIL_00154 | 3.4e-42 | S | RloB-like protein | |||
MLDOIJIL_00155 | 1.2e-164 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
MLDOIJIL_00156 | 2.7e-160 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
MLDOIJIL_00157 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
MLDOIJIL_00158 | 8.2e-45 | S | SLAP domain | |||
MLDOIJIL_00159 | 7.9e-120 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
MLDOIJIL_00160 | 1.6e-85 | 3.4.21.96 | S | SLAP domain | ||
MLDOIJIL_00161 | 8.4e-128 | yagE | E | Amino acid permease | ||
MLDOIJIL_00162 | 1.5e-109 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
MLDOIJIL_00163 | 2.3e-90 | 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 | ||
MLDOIJIL_00164 | 2.4e-101 | G | Phosphoglycerate mutase family | |||
MLDOIJIL_00165 | 1.2e-137 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
MLDOIJIL_00167 | 2.5e-40 | yjcE | P | Sodium proton antiporter | ||
MLDOIJIL_00168 | 1.9e-94 | yjcE | P | Sodium proton antiporter | ||
MLDOIJIL_00169 | 1.4e-140 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
MLDOIJIL_00170 | 3.5e-71 | yqeY | S | YqeY-like protein | ||
MLDOIJIL_00171 | 2e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
MLDOIJIL_00172 | 1.1e-147 | 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 | |
MLDOIJIL_00173 | 5.5e-18 | S | CRISPR-associated protein (Cas_Csn2) | |||
MLDOIJIL_00174 | 2e-09 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
MLDOIJIL_00175 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
MLDOIJIL_00176 | 5.4e-41 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
MLDOIJIL_00177 | 1.6e-147 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
MLDOIJIL_00178 | 8.8e-58 | S | Peptidase propeptide and YPEB domain | |||
MLDOIJIL_00179 | 1.3e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
MLDOIJIL_00180 | 2.8e-168 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
MLDOIJIL_00181 | 2.4e-31 | 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 | ||
MLDOIJIL_00182 | 2.3e-111 | |||||
MLDOIJIL_00184 | 1.2e-111 | E | Belongs to the SOS response-associated peptidase family | |||
MLDOIJIL_00185 | 2e-77 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MLDOIJIL_00186 | 1e-96 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MLDOIJIL_00187 | 1.8e-86 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
MLDOIJIL_00188 | 2e-103 | S | TPM domain | |||
MLDOIJIL_00189 | 2.8e-182 | K | Transcriptional regulator | |||
MLDOIJIL_00190 | 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 | |
MLDOIJIL_00191 | 1.1e-20 | ydgH | S | MMPL family | ||
MLDOIJIL_00192 | 6.9e-105 | ydgH | S | MMPL family | ||
MLDOIJIL_00194 | 7.8e-26 | K | Acetyltransferase (GNAT) domain | |||
MLDOIJIL_00195 | 9.3e-204 | pbpX1 | V | Beta-lactamase | ||
MLDOIJIL_00196 | 2.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
MLDOIJIL_00197 | 3.9e-78 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
MLDOIJIL_00198 | 6.2e-27 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MLDOIJIL_00199 | 2.3e-150 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MLDOIJIL_00200 | 8.7e-148 | L | HNH nucleases | |||
MLDOIJIL_00201 | 2.4e-80 | yfbR | S | HD containing hydrolase-like enzyme | ||
MLDOIJIL_00202 | 3.6e-17 | yfbR | S | HD containing hydrolase-like enzyme | ||
MLDOIJIL_00203 | 4.9e-190 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
MLDOIJIL_00204 | 2.5e-89 | M | Protein of unknown function (DUF3737) | |||
MLDOIJIL_00205 | 7.6e-18 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
MLDOIJIL_00206 | 1.7e-12 | |||||
MLDOIJIL_00208 | 5e-15 | S | Domain of Unknown Function with PDB structure (DUF3850) | |||
MLDOIJIL_00209 | 2.2e-97 | D | VirC1 protein | |||
MLDOIJIL_00211 | 5e-39 | relB | L | RelB antitoxin | ||
MLDOIJIL_00212 | 1.4e-34 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
MLDOIJIL_00214 | 4e-12 | |||||
MLDOIJIL_00215 | 8e-25 | K | Helix-turn-helix XRE-family like proteins | |||
MLDOIJIL_00217 | 1.3e-102 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
MLDOIJIL_00218 | 1.1e-111 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MLDOIJIL_00219 | 2.4e-43 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
MLDOIJIL_00220 | 6.7e-184 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
MLDOIJIL_00221 | 3.4e-118 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
MLDOIJIL_00222 | 7.5e-46 | htpX | O | Belongs to the peptidase M48B family | ||
MLDOIJIL_00223 | 7.9e-174 | K | helix_turn_helix, arabinose operon control protein | |||
MLDOIJIL_00224 | 4.1e-248 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00225 | 6.8e-60 | divIC | D | Septum formation initiator | ||
MLDOIJIL_00226 | 2.6e-32 | yabR | J | S1 RNA binding domain | ||
MLDOIJIL_00227 | 1.5e-197 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
MLDOIJIL_00228 | 1.3e-14 | rarA | L | MgsA AAA+ ATPase C terminal | ||
MLDOIJIL_00229 | 3.2e-56 | 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 | ||
MLDOIJIL_00230 | 2.9e-152 | 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 | ||
MLDOIJIL_00231 | 1.4e-98 | L | Helix-turn-helix domain | |||
MLDOIJIL_00232 | 5.3e-139 | L | hmm pf00665 | |||
MLDOIJIL_00233 | 1.2e-222 | S | Cysteine-rich secretory protein family | |||
MLDOIJIL_00234 | 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) | |
MLDOIJIL_00235 | 2e-195 | camS | S | sex pheromone | ||
MLDOIJIL_00236 | 2.7e-98 | 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 | |
MLDOIJIL_00237 | 4.7e-38 | |||||
MLDOIJIL_00238 | 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) | |
MLDOIJIL_00239 | 1.2e-123 | luxT | K | Bacterial regulatory proteins, tetR family | ||
MLDOIJIL_00240 | 1.5e-197 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
MLDOIJIL_00241 | 1.4e-110 | mdlB | V | ABC transporter | ||
MLDOIJIL_00242 | 6.5e-26 | |||||
MLDOIJIL_00243 | 2.4e-28 | rpiB | 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
MLDOIJIL_00244 | 8e-22 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
MLDOIJIL_00245 | 5.4e-53 | hipB | K | sequence-specific DNA binding | ||
MLDOIJIL_00246 | 4.8e-42 | S | SnoaL-like domain | |||
MLDOIJIL_00247 | 3.4e-46 | L | PLD-like domain | |||
MLDOIJIL_00248 | 9e-26 | |||||
MLDOIJIL_00249 | 2.9e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
MLDOIJIL_00250 | 4.8e-138 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
MLDOIJIL_00251 | 2.1e-50 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
MLDOIJIL_00253 | 7.5e-68 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
MLDOIJIL_00254 | 9.6e-11 | GT2,GT4 | M | family 8 | ||
MLDOIJIL_00255 | 3.1e-206 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
MLDOIJIL_00256 | 2.4e-181 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
MLDOIJIL_00257 | 9.7e-169 | |||||
MLDOIJIL_00258 | 6.9e-32 | |||||
MLDOIJIL_00259 | 1.2e-129 | 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 | |
MLDOIJIL_00261 | 4.8e-39 | cvpA | S | Colicin V production protein | ||
MLDOIJIL_00262 | 6e-28 | G | Glycosyl hydrolases family 8 | |||
MLDOIJIL_00263 | 1.3e-188 | ydaM | M | Glycosyl transferase | ||
MLDOIJIL_00264 | 2.6e-132 | thrC | 4.2.3.1 | E | Threonine synthase | |
MLDOIJIL_00265 | 4.8e-172 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
MLDOIJIL_00266 | 3.1e-185 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
MLDOIJIL_00267 | 2.6e-35 | yaaA | S | S4 domain protein YaaA | ||
MLDOIJIL_00268 | 4.6e-141 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
MLDOIJIL_00269 | 3.7e-34 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
MLDOIJIL_00270 | 2.2e-113 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
MLDOIJIL_00271 | 4.1e-83 | ydcK | S | Belongs to the SprT family | ||
MLDOIJIL_00273 | 5.2e-84 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
MLDOIJIL_00274 | 3.4e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
MLDOIJIL_00275 | 1.3e-38 | S | RelB antitoxin | |||
MLDOIJIL_00276 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
MLDOIJIL_00277 | 4.8e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
MLDOIJIL_00278 | 1.2e-146 | glnH | ET | ABC transporter substrate-binding protein | ||
MLDOIJIL_00279 | 3.2e-86 | gluC | P | ABC transporter permease | ||
MLDOIJIL_00280 | 5.2e-108 | glnP | P | ABC transporter permease | ||
MLDOIJIL_00281 | 1.2e-187 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
MLDOIJIL_00282 | 4.6e-106 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
MLDOIJIL_00283 | 1.1e-59 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
MLDOIJIL_00284 | 3.3e-153 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
MLDOIJIL_00285 | 3.5e-174 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
MLDOIJIL_00286 | 1.4e-192 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
MLDOIJIL_00287 | 1.7e-278 | smc | D | Required for chromosome condensation and partitioning | ||
MLDOIJIL_00288 | 1.9e-124 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
MLDOIJIL_00289 | 1.1e-306 | oppA | E | ABC transporter substrate-binding protein | ||
MLDOIJIL_00290 | 3.1e-240 | oppA | E | ABC transporter substrate-binding protein | ||
MLDOIJIL_00291 | 8.2e-29 | M | domain protein | |||
MLDOIJIL_00292 | 8.2e-85 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
MLDOIJIL_00294 | 8.8e-223 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
MLDOIJIL_00296 | 3.4e-48 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
MLDOIJIL_00297 | 1.6e-146 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
MLDOIJIL_00298 | 3e-177 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
MLDOIJIL_00299 | 7.6e-208 | XK27_08315 | M | Sulfatase | ||
MLDOIJIL_00300 | 2e-151 | XK27_08315 | M | Sulfatase | ||
MLDOIJIL_00301 | 1.3e-125 | ycaM | E | amino acid | ||
MLDOIJIL_00302 | 1.2e-138 | S | Cysteine-rich secretory protein family | |||
MLDOIJIL_00303 | 4.2e-77 | K | MerR HTH family regulatory protein | |||
MLDOIJIL_00304 | 9.7e-53 | lmrB | EGP | Major facilitator Superfamily | ||
MLDOIJIL_00305 | 2.8e-58 | 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 | ||
MLDOIJIL_00306 | 5.8e-86 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
MLDOIJIL_00307 | 6.5e-37 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
MLDOIJIL_00308 | 2.8e-60 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
MLDOIJIL_00309 | 8.1e-42 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
MLDOIJIL_00310 | 1.2e-76 | G | Aldose 1-epimerase | |||
MLDOIJIL_00311 | 1.7e-114 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
MLDOIJIL_00312 | 2e-64 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
MLDOIJIL_00315 | 1.6e-12 | 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 | |
MLDOIJIL_00316 | 2.1e-157 | 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 | |
MLDOIJIL_00317 | 4e-153 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
MLDOIJIL_00318 | 1.6e-275 | V | ABC transporter transmembrane region | |||
MLDOIJIL_00319 | 2.3e-41 | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | |||
MLDOIJIL_00320 | 1.9e-47 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
MLDOIJIL_00321 | 4.8e-205 | napA | P | Sodium/hydrogen exchanger family | ||
MLDOIJIL_00322 | 1.8e-24 | cadA | P | P-type ATPase | ||
MLDOIJIL_00323 | 4.1e-147 | vicX | 3.1.26.11 | S | domain protein | |
MLDOIJIL_00324 | 1.6e-52 | yycI | S | YycH protein | ||
MLDOIJIL_00325 | 1.1e-66 | |||||
MLDOIJIL_00326 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
MLDOIJIL_00327 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
MLDOIJIL_00328 | 3.9e-198 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
MLDOIJIL_00329 | 4.3e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MLDOIJIL_00330 | 8e-79 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
MLDOIJIL_00331 | 1.5e-25 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
MLDOIJIL_00332 | 1.8e-145 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
MLDOIJIL_00333 | 4.5e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
MLDOIJIL_00334 | 3.5e-25 | |||||
MLDOIJIL_00336 | 6.6e-44 | |||||
MLDOIJIL_00337 | 1.4e-30 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
MLDOIJIL_00338 | 7.4e-99 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
MLDOIJIL_00339 | 4.3e-40 | V | ABC transporter, ATP-binding protein | |||
MLDOIJIL_00340 | 8e-80 | E | GDSL-like Lipase/Acylhydrolase family | |||
MLDOIJIL_00341 | 3.5e-120 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
MLDOIJIL_00342 | 2.5e-197 | S | SLAP domain | |||
MLDOIJIL_00343 | 4.7e-61 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
MLDOIJIL_00344 | 3.6e-134 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
MLDOIJIL_00345 | 2.2e-93 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
MLDOIJIL_00346 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
MLDOIJIL_00347 | 8.4e-228 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
MLDOIJIL_00348 | 6e-55 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
MLDOIJIL_00349 | 6.7e-85 | S | Short repeat of unknown function (DUF308) | |||
MLDOIJIL_00350 | 1e-162 | rapZ | S | Displays ATPase and GTPase activities | ||
MLDOIJIL_00351 | 4e-195 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
MLDOIJIL_00352 | 2.2e-168 | whiA | K | May be required for sporulation | ||
MLDOIJIL_00353 | 3.5e-30 | 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 | |
MLDOIJIL_00354 | 1.3e-43 | 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 | |
MLDOIJIL_00355 | 0.0 | S | SH3-like domain | |||
MLDOIJIL_00356 | 1.9e-107 | ybbL | S | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00357 | 2e-127 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
MLDOIJIL_00358 | 9.1e-10 | UW | LPXTG-motif cell wall anchor domain protein | |||
MLDOIJIL_00359 | 6.9e-43 | UW | LPXTG-motif cell wall anchor domain protein | |||
MLDOIJIL_00360 | 5.2e-75 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
MLDOIJIL_00361 | 1.5e-107 | hlyIII | S | protein, hemolysin III | ||
MLDOIJIL_00362 | 2.2e-143 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
MLDOIJIL_00363 | 7.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
MLDOIJIL_00364 | 1.1e-66 | yjcE | P | NhaP-type Na H and K H | ||
MLDOIJIL_00365 | 1.4e-92 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
MLDOIJIL_00366 | 1.1e-14 | mrr | L | restriction endonuclease | ||
MLDOIJIL_00367 | 2.7e-42 | S | Domain of unknown function DUF87 | |||
MLDOIJIL_00368 | 7.9e-13 | S | cog cog0433 | |||
MLDOIJIL_00369 | 1.5e-161 | murB | 1.3.1.98 | M | Cell wall formation | |
MLDOIJIL_00370 | 1.3e-93 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
MLDOIJIL_00371 | 7e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
MLDOIJIL_00372 | 2.7e-18 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
MLDOIJIL_00373 | 1.5e-49 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
MLDOIJIL_00374 | 5e-184 | arbY | M | Glycosyl transferase family 8 | ||
MLDOIJIL_00375 | 7.3e-161 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
MLDOIJIL_00376 | 2.3e-20 | S | Enterocin A Immunity | |||
MLDOIJIL_00378 | 5.7e-43 | 2.4.1.33 | V | HlyD family secretion protein | ||
MLDOIJIL_00379 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
MLDOIJIL_00380 | 2.9e-79 | K | LytTr DNA-binding domain | |||
MLDOIJIL_00381 | 1.9e-78 | 2.7.13.3 | T | GHKL domain | ||
MLDOIJIL_00382 | 5.5e-57 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
MLDOIJIL_00383 | 1.1e-175 | G | MFS/sugar transport protein | |||
MLDOIJIL_00384 | 7.2e-54 | G | MFS/sugar transport protein | |||
MLDOIJIL_00385 | 1e-44 | udk | 2.7.1.48 | F | Zeta toxin | |
MLDOIJIL_00386 | 1.4e-264 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
MLDOIJIL_00387 | 2.1e-25 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
MLDOIJIL_00388 | 8.8e-84 | uspA | T | universal stress protein | ||
MLDOIJIL_00390 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
MLDOIJIL_00391 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00392 | 5.2e-42 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
MLDOIJIL_00393 | 2e-47 | |||||
MLDOIJIL_00395 | 3.3e-103 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
MLDOIJIL_00396 | 2.1e-62 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
MLDOIJIL_00397 | 1.5e-94 | S | Protein of unknown function (DUF3990) | |||
MLDOIJIL_00398 | 6.5e-44 | |||||
MLDOIJIL_00400 | 1.3e-174 | |||||
MLDOIJIL_00401 | 2.6e-111 | mdtG | EGP | Major facilitator Superfamily | ||
MLDOIJIL_00402 | 1.9e-122 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
MLDOIJIL_00403 | 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 | |
MLDOIJIL_00404 | 2e-123 | pipD | E | Dipeptidase | ||
MLDOIJIL_00405 | 4.4e-77 | malK | P | ATPases associated with a variety of cellular activities | ||
MLDOIJIL_00406 | 2.1e-100 | malK | P | ATPases associated with a variety of cellular activities | ||
MLDOIJIL_00407 | 4.6e-141 | gtsB | P | ABC-type sugar transport systems, permease components | ||
MLDOIJIL_00408 | 6.1e-146 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
MLDOIJIL_00409 | 2.5e-42 | yibE | S | overlaps another CDS with the same product name | ||
MLDOIJIL_00410 | 4.2e-128 | yibF | S | overlaps another CDS with the same product name | ||
MLDOIJIL_00411 | 2.2e-75 | 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 | |
MLDOIJIL_00412 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
MLDOIJIL_00413 | 5.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
MLDOIJIL_00414 | 1.5e-219 | 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 | |
MLDOIJIL_00415 | 8.8e-69 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
MLDOIJIL_00416 | 3.2e-28 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
MLDOIJIL_00417 | 2.3e-78 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
MLDOIJIL_00418 | 2.1e-32 | |||||
MLDOIJIL_00419 | 3.9e-59 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
MLDOIJIL_00420 | 8.2e-111 | K | Helix-turn-helix XRE-family like proteins | |||
MLDOIJIL_00421 | 4.1e-26 | K | Helix-turn-helix XRE-family like proteins | |||
MLDOIJIL_00422 | 3.9e-298 | V | ABC transporter transmembrane region | |||
MLDOIJIL_00423 | 4e-161 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
MLDOIJIL_00424 | 9.3e-52 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
MLDOIJIL_00425 | 8.4e-69 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
MLDOIJIL_00426 | 1.7e-61 | qacA | EGP | Major facilitator Superfamily | ||
MLDOIJIL_00427 | 6.6e-21 | qacA | EGP | Major facilitator Superfamily | ||
MLDOIJIL_00429 | 1.3e-79 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
MLDOIJIL_00430 | 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 | |
MLDOIJIL_00431 | 1.8e-119 | S | Putative esterase | |||
MLDOIJIL_00432 | 4.7e-157 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
MLDOIJIL_00433 | 5.4e-43 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
MLDOIJIL_00434 | 1e-207 | ywhK | S | Membrane | ||
MLDOIJIL_00435 | 4.1e-44 | |||||
MLDOIJIL_00436 | 1.2e-18 | S | D-Ala-teichoic acid biosynthesis protein | |||
MLDOIJIL_00437 | 1.4e-145 | 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 | |
MLDOIJIL_00440 | 1e-246 | yjjP | S | Putative threonine/serine exporter | ||
MLDOIJIL_00441 | 2.6e-177 | citR | K | Putative sugar-binding domain | ||
MLDOIJIL_00442 | 1.5e-50 | |||||
MLDOIJIL_00443 | 5.5e-09 | |||||
MLDOIJIL_00444 | 8.8e-134 | cof | S | haloacid dehalogenase-like hydrolase | ||
MLDOIJIL_00445 | 9.4e-72 | |||||
MLDOIJIL_00446 | 7.6e-118 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
MLDOIJIL_00447 | 9.6e-119 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
MLDOIJIL_00448 | 2.8e-131 | 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 | |
MLDOIJIL_00449 | 7.8e-48 | yeaE | S | Aldo/keto reductase family | ||
MLDOIJIL_00450 | 2.4e-89 | yeaE | S | Aldo/keto reductase family | ||
MLDOIJIL_00451 | 1.5e-144 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
MLDOIJIL_00452 | 3.6e-117 | |||||
MLDOIJIL_00453 | 2.1e-157 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
MLDOIJIL_00455 | 1.3e-24 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
MLDOIJIL_00456 | 1.4e-110 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
MLDOIJIL_00457 | 3.5e-71 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
MLDOIJIL_00458 | 1.5e-60 | S | Protein of unknown function (DUF2974) | |||
MLDOIJIL_00459 | 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 | |
MLDOIJIL_00460 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
MLDOIJIL_00461 | 7.4e-37 | S | PFAM Archaeal ATPase | |||
MLDOIJIL_00462 | 2.1e-83 | S | PFAM Archaeal ATPase | |||
MLDOIJIL_00463 | 7.7e-26 | |||||
MLDOIJIL_00464 | 4.9e-69 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
MLDOIJIL_00465 | 1.5e-172 | EGP | Sugar (and other) transporter | |||
MLDOIJIL_00466 | 1e-14 | |||||
MLDOIJIL_00467 | 9.2e-206 | |||||
MLDOIJIL_00468 | 1.4e-120 | S | SLAP domain | |||
MLDOIJIL_00469 | 2.3e-48 | S | SLAP domain | |||
MLDOIJIL_00470 | 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) | |
MLDOIJIL_00471 | 6e-199 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
MLDOIJIL_00472 | 1.4e-40 | |||||
MLDOIJIL_00473 | 1e-107 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
MLDOIJIL_00474 | 4.9e-271 | glnP | P | ABC transporter permease | ||
MLDOIJIL_00475 | 1.8e-44 | K | SIS domain | |||
MLDOIJIL_00476 | 4.7e-143 | slpX | S | SLAP domain | ||
MLDOIJIL_00477 | 3e-65 | slpX | S | SLAP domain | ||
MLDOIJIL_00478 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
MLDOIJIL_00479 | 6.6e-11 | |||||
MLDOIJIL_00480 | 4.4e-92 | clcA | P | chloride | ||
MLDOIJIL_00481 | 4e-32 | E | Zn peptidase | |||
MLDOIJIL_00482 | 3.7e-58 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
MLDOIJIL_00483 | 1.2e-44 | |||||
MLDOIJIL_00484 | 9.1e-106 | S | Bacteriocin helveticin-J | |||
MLDOIJIL_00485 | 5.7e-62 | S | SLAP domain | |||
MLDOIJIL_00486 | 5.5e-53 | |||||
MLDOIJIL_00488 | 2.7e-34 | S | YSIRK type signal peptide | |||
MLDOIJIL_00489 | 3.1e-31 | F | DNA/RNA non-specific endonuclease | |||
MLDOIJIL_00491 | 7.7e-100 | 3.6.1.27 | I | Acid phosphatase homologues | ||
MLDOIJIL_00492 | 2.6e-79 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
MLDOIJIL_00493 | 2.3e-78 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
MLDOIJIL_00494 | 1.4e-107 | uvrA3 | L | excinuclease ABC, A subunit | ||
MLDOIJIL_00495 | 2.9e-15 | M | LysM domain protein | |||
MLDOIJIL_00496 | 3.8e-48 | M | LysM domain protein | |||
MLDOIJIL_00497 | 1.4e-86 | C | Aldo keto reductase | |||
MLDOIJIL_00498 | 8.3e-181 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
MLDOIJIL_00499 | 8.2e-236 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
MLDOIJIL_00500 | 7.9e-12 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
MLDOIJIL_00501 | 3.7e-250 | lctP | C | L-lactate permease | ||
MLDOIJIL_00502 | 2.1e-67 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
MLDOIJIL_00503 | 1.3e-274 | mdlA | V | ABC transporter | ||
MLDOIJIL_00504 | 5.2e-31 | mdlA | V | ABC transporter | ||
MLDOIJIL_00505 | 5.5e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
MLDOIJIL_00506 | 3e-38 | ynzC | S | UPF0291 protein | ||
MLDOIJIL_00507 | 2.8e-290 | |||||
MLDOIJIL_00509 | 2.3e-39 | L | Protein of unknown function (DUF3991) | |||
MLDOIJIL_00511 | 8e-45 | S | COG0790 FOG TPR repeat, SEL1 subfamily | |||
MLDOIJIL_00513 | 2.2e-151 | yfnA | E | amino acid | ||
MLDOIJIL_00514 | 0.0 | V | FtsX-like permease family | |||
MLDOIJIL_00515 | 3.5e-132 | cysA | V | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00516 | 3.4e-23 | |||||
MLDOIJIL_00518 | 2.4e-225 | pipD | E | Dipeptidase | ||
MLDOIJIL_00519 | 7.3e-68 | S | Iron-sulphur cluster biosynthesis | |||
MLDOIJIL_00520 | 5.2e-21 | 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 | ||
MLDOIJIL_00521 | 5.4e-203 | xerS | L | Belongs to the 'phage' integrase family | ||
MLDOIJIL_00522 | 4.1e-67 | |||||
MLDOIJIL_00523 | 8e-111 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
MLDOIJIL_00524 | 1.9e-86 | M | Glycosyl hydrolases family 25 | |||
MLDOIJIL_00525 | 1.4e-47 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
MLDOIJIL_00526 | 2e-172 | ybbR | S | YbbR-like protein | ||
MLDOIJIL_00527 | 5.3e-40 | 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 | |
MLDOIJIL_00528 | 1.5e-180 | helD | 3.6.4.12 | L | DNA helicase | |
MLDOIJIL_00529 | 7.9e-57 | 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 | |
MLDOIJIL_00530 | 1.7e-111 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
MLDOIJIL_00531 | 3.8e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
MLDOIJIL_00532 | 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 | ||
MLDOIJIL_00533 | 3.7e-45 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
MLDOIJIL_00534 | 7e-90 | 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 | ||
MLDOIJIL_00535 | 6.4e-50 | |||||
MLDOIJIL_00536 | 6e-153 | EGP | Major facilitator Superfamily | |||
MLDOIJIL_00537 | 3e-111 | ropB | K | Transcriptional regulator | ||
MLDOIJIL_00538 | 2.7e-120 | S | CAAX protease self-immunity | |||
MLDOIJIL_00539 | 5.6e-144 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
MLDOIJIL_00540 | 4.5e-15 | G | Transmembrane secretion effector | |||
MLDOIJIL_00541 | 1.1e-106 | G | Transmembrane secretion effector | |||
MLDOIJIL_00542 | 1e-142 | nhaC | C | Na H antiporter NhaC | ||
MLDOIJIL_00543 | 1.4e-147 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
MLDOIJIL_00544 | 9.8e-57 | |||||
MLDOIJIL_00545 | 1.3e-133 | ynbB | 4.4.1.1 | P | aluminum resistance | |
MLDOIJIL_00546 | 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 | |
MLDOIJIL_00547 | 3.9e-37 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
MLDOIJIL_00548 | 1.3e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
MLDOIJIL_00549 | 1.2e-06 | fhaB | 4.3.1.7 | UW | LPXTG-motif cell wall anchor domain protein | |
MLDOIJIL_00550 | 1.2e-47 | L | Transposase, IS116 IS110 IS902 family | |||
MLDOIJIL_00551 | 4e-24 | S | SLAP domain | |||
MLDOIJIL_00552 | 6.4e-24 | S | SLAP domain | |||
MLDOIJIL_00554 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
MLDOIJIL_00555 | 2.3e-210 | yubA | S | AI-2E family transporter | ||
MLDOIJIL_00556 | 8.9e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
MLDOIJIL_00557 | 4.1e-52 | |||||
MLDOIJIL_00558 | 9.9e-263 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
MLDOIJIL_00559 | 8.1e-43 | |||||
MLDOIJIL_00560 | 1.7e-181 | S | AAA domain | |||
MLDOIJIL_00561 | 4.6e-123 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
MLDOIJIL_00562 | 1.4e-23 | |||||
MLDOIJIL_00563 | 6.6e-162 | czcD | P | cation diffusion facilitator family transporter | ||
MLDOIJIL_00564 | 4.1e-124 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
MLDOIJIL_00565 | 1.5e-130 | S | membrane transporter protein | |||
MLDOIJIL_00566 | 6.6e-35 | mtlR | K | Mga helix-turn-helix domain | ||
MLDOIJIL_00567 | 2.4e-44 | 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 | |
MLDOIJIL_00568 | 3e-196 | 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 | |
MLDOIJIL_00569 | 2.4e-127 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
MLDOIJIL_00570 | 1e-84 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
MLDOIJIL_00571 | 2.2e-31 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
MLDOIJIL_00572 | 3e-127 | ybbH_2 | K | rpiR family | ||
MLDOIJIL_00573 | 7e-195 | S | Bacterial protein of unknown function (DUF871) | |||
MLDOIJIL_00574 | 2.3e-148 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00575 | 2.4e-131 | V | ABC transporter transmembrane region | |||
MLDOIJIL_00576 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
MLDOIJIL_00577 | 8.1e-309 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
MLDOIJIL_00578 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
MLDOIJIL_00579 | 1.5e-34 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
MLDOIJIL_00580 | 7e-22 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
MLDOIJIL_00581 | 7.3e-74 | |||||
MLDOIJIL_00582 | 2.1e-45 | S | PFAM Archaeal ATPase | |||
MLDOIJIL_00583 | 1.3e-08 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
MLDOIJIL_00584 | 3.7e-58 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
MLDOIJIL_00585 | 5.9e-45 | |||||
MLDOIJIL_00586 | 5.5e-133 | glvR | K | Helix-turn-helix domain, rpiR family | ||
MLDOIJIL_00587 | 5.1e-113 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
MLDOIJIL_00588 | 3.9e-142 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
MLDOIJIL_00589 | 3.4e-136 | lysR5 | K | LysR substrate binding domain | ||
MLDOIJIL_00590 | 6.7e-78 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
MLDOIJIL_00591 | 2.3e-161 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
MLDOIJIL_00592 | 5.4e-234 | G | Bacterial extracellular solute-binding protein | |||
MLDOIJIL_00593 | 1e-51 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
MLDOIJIL_00594 | 4.1e-121 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
MLDOIJIL_00595 | 6.6e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
MLDOIJIL_00596 | 2e-58 | 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 | ||
MLDOIJIL_00597 | 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 | |
MLDOIJIL_00598 | 3e-215 | 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) | |
MLDOIJIL_00599 | 8.3e-58 | |||||
MLDOIJIL_00600 | 5e-72 | rimL | J | Acetyltransferase (GNAT) domain | ||
MLDOIJIL_00601 | 1.4e-34 | |||||
MLDOIJIL_00602 | 1.2e-30 | |||||
MLDOIJIL_00603 | 1.8e-46 | S | Protein of unknown function (DUF554) | |||
MLDOIJIL_00604 | 3.1e-51 | |||||
MLDOIJIL_00605 | 9.9e-295 | S | SLAP domain | |||
MLDOIJIL_00606 | 2.6e-172 | 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) | |
MLDOIJIL_00607 | 2.1e-102 | pepF | E | oligoendopeptidase F | ||
MLDOIJIL_00608 | 6.1e-22 | |||||
MLDOIJIL_00609 | 4.2e-59 | doc | S | Prophage maintenance system killer protein | ||
MLDOIJIL_00612 | 4.6e-27 | S | Enterocin A Immunity | |||
MLDOIJIL_00613 | 1.7e-22 | blpT | ||||
MLDOIJIL_00614 | 5.6e-141 | 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 | |
MLDOIJIL_00615 | 1.8e-234 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
MLDOIJIL_00616 | 2.4e-34 | 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 | |
MLDOIJIL_00617 | 3.6e-246 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
MLDOIJIL_00618 | 2.9e-176 | pbpX2 | V | Beta-lactamase | ||
MLDOIJIL_00619 | 2.6e-163 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
MLDOIJIL_00620 | 2.1e-97 | 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 | |
MLDOIJIL_00621 | 5.6e-92 | 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 | |
MLDOIJIL_00622 | 5.3e-286 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
MLDOIJIL_00623 | 1e-40 | yajC | U | Preprotein translocase | ||
MLDOIJIL_00624 | 2.5e-144 | 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 | |
MLDOIJIL_00625 | 3.7e-92 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
MLDOIJIL_00626 | 1.8e-81 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
MLDOIJIL_00627 | 4e-172 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
MLDOIJIL_00628 | 6.5e-91 | G | Peptidase_C39 like family | |||
MLDOIJIL_00629 | 2.8e-162 | M | NlpC/P60 family | |||
MLDOIJIL_00630 | 8.4e-25 | G | Peptidase_C39 like family | |||
MLDOIJIL_00631 | 1e-104 | |||||
MLDOIJIL_00632 | 4.8e-50 | EGP | Sugar (and other) transporter | |||
MLDOIJIL_00633 | 2.4e-264 | S | Fibronectin type III domain | |||
MLDOIJIL_00634 | 6.7e-08 | manY | G | PTS system | ||
MLDOIJIL_00635 | 9.4e-172 | manN | G | system, mannose fructose sorbose family IID component | ||
MLDOIJIL_00636 | 3e-60 | manO | S | Domain of unknown function (DUF956) | ||
MLDOIJIL_00637 | 4.8e-157 | K | Transcriptional regulator | |||
MLDOIJIL_00638 | 1.3e-85 | maa | S | transferase hexapeptide repeat | ||
MLDOIJIL_00639 | 1.6e-239 | cycA | E | Amino acid permease | ||
MLDOIJIL_00640 | 3.6e-105 | E | Amino acid permease | |||
MLDOIJIL_00641 | 6.3e-93 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
MLDOIJIL_00642 | 1.4e-162 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
MLDOIJIL_00643 | 9.3e-77 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
MLDOIJIL_00644 | 1.5e-46 | mmuP | E | amino acid | ||
MLDOIJIL_00645 | 4.9e-145 | XK27_00915 | C | Luciferase-like monooxygenase | ||
MLDOIJIL_00646 | 2.7e-85 | K | GNAT family | |||
MLDOIJIL_00647 | 4.1e-121 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
MLDOIJIL_00649 | 4.3e-36 | |||||
MLDOIJIL_00650 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
MLDOIJIL_00651 | 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 | ||
MLDOIJIL_00652 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
MLDOIJIL_00653 | 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 | ||
MLDOIJIL_00654 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
MLDOIJIL_00655 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
MLDOIJIL_00656 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
MLDOIJIL_00657 | 1.2e-65 | 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 | |
MLDOIJIL_00658 | 1.8e-68 | S | response to antibiotic | |||
MLDOIJIL_00659 | 8.2e-19 | S | response to antibiotic | |||
MLDOIJIL_00660 | 1.1e-124 | |||||
MLDOIJIL_00661 | 1.1e-110 | |||||
MLDOIJIL_00662 | 2.2e-100 | |||||
MLDOIJIL_00663 | 5.3e-225 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
MLDOIJIL_00664 | 4.1e-119 | 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 | |
MLDOIJIL_00665 | 5e-168 | 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 | ||
MLDOIJIL_00666 | 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 | ||
MLDOIJIL_00667 | 9.9e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
MLDOIJIL_00668 | 3.4e-65 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
MLDOIJIL_00670 | 2.1e-32 | M | Peptidase family M23 | |||
MLDOIJIL_00671 | 2.6e-53 | trsE | S | COG0433 Predicted ATPase | ||
MLDOIJIL_00672 | 1.9e-32 | I | mechanosensitive ion channel activity | |||
MLDOIJIL_00673 | 9e-83 | K | Acetyltransferase (GNAT) domain | |||
MLDOIJIL_00674 | 6.4e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
MLDOIJIL_00675 | 1.9e-191 | yrvN | L | AAA C-terminal domain | ||
MLDOIJIL_00676 | 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 | |
MLDOIJIL_00677 | 1.4e-281 | treB | G | phosphotransferase system | ||
MLDOIJIL_00678 | 4.4e-100 | treR | K | UTRA | ||
MLDOIJIL_00679 | 1e-285 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
MLDOIJIL_00680 | 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) | ||
MLDOIJIL_00681 | 3.2e-144 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MLDOIJIL_00682 | 6.4e-90 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MLDOIJIL_00683 | 9.9e-288 | 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) | |
MLDOIJIL_00684 | 1.8e-53 | 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 | ||
MLDOIJIL_00685 | 3.7e-61 | 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 | ||
MLDOIJIL_00686 | 6.6e-125 | S | (CBS) domain | |||
MLDOIJIL_00687 | 1.6e-168 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
MLDOIJIL_00688 | 1.4e-76 | |||||
MLDOIJIL_00689 | 2.8e-32 | |||||
MLDOIJIL_00690 | 1.1e-11 | |||||
MLDOIJIL_00691 | 4.7e-25 | S | Protein conserved in bacteria | |||
MLDOIJIL_00692 | 8.6e-54 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
MLDOIJIL_00693 | 1.7e-51 | yaaQ | S | Cyclic-di-AMP receptor | ||
MLDOIJIL_00694 | 3.6e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
MLDOIJIL_00695 | 1.1e-34 | S | Protein of unknown function (DUF2508) | |||
MLDOIJIL_00696 | 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 | ||
MLDOIJIL_00697 | 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 | ||
MLDOIJIL_00698 | 1.3e-34 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
MLDOIJIL_00699 | 9.4e-43 | 2.4.1.58 | GT8 | M | family 8 | |
MLDOIJIL_00700 | 7.7e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
MLDOIJIL_00701 | 3.4e-85 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MLDOIJIL_00702 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
MLDOIJIL_00703 | 3.2e-92 | S | SNARE associated Golgi protein | |||
MLDOIJIL_00704 | 7.6e-20 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
MLDOIJIL_00705 | 3.3e-35 | |||||
MLDOIJIL_00706 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
MLDOIJIL_00707 | 3.7e-146 | ykuT | M | mechanosensitive ion channel | ||
MLDOIJIL_00708 | 6.9e-100 | V | ATPases associated with a variety of cellular activities | |||
MLDOIJIL_00709 | 4e-138 | |||||
MLDOIJIL_00710 | 1.9e-157 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
MLDOIJIL_00711 | 3.1e-29 | |||||
MLDOIJIL_00712 | 3.1e-26 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
MLDOIJIL_00713 | 5e-15 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
MLDOIJIL_00714 | 9.3e-18 | |||||
MLDOIJIL_00719 | 8.4e-39 | |||||
MLDOIJIL_00720 | 1.1e-18 | S | Phage uncharacterised protein (Phage_XkdX) | |||
MLDOIJIL_00723 | 2.8e-16 | |||||
MLDOIJIL_00724 | 2.9e-29 | |||||
MLDOIJIL_00725 | 1e-53 | tnpB | L | Putative transposase DNA-binding domain | ||
MLDOIJIL_00726 | 1.5e-55 | nrdI | F | NrdI Flavodoxin like | ||
MLDOIJIL_00727 | 9.7e-83 | S | An automated process has identified a potential problem with this gene model | |||
MLDOIJIL_00728 | 1.4e-27 | S | Protein of unknown function (DUF3100) | |||
MLDOIJIL_00729 | 9.1e-81 | S | Protein of unknown function (DUF3100) | |||
MLDOIJIL_00730 | 4.5e-94 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
MLDOIJIL_00731 | 5.5e-43 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
MLDOIJIL_00732 | 3.2e-77 | 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 | ||
MLDOIJIL_00733 | 1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
MLDOIJIL_00734 | 2.1e-82 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MLDOIJIL_00735 | 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 | |
MLDOIJIL_00736 | 3.1e-73 | S | cog cog1373 | |||
MLDOIJIL_00737 | 6.3e-201 | pbpX | V | Beta-lactamase | ||
MLDOIJIL_00738 | 2.4e-54 | 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 | ||
MLDOIJIL_00739 | 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 | ||
MLDOIJIL_00740 | 6.6e-102 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
MLDOIJIL_00741 | 2.3e-38 | yjeM | E | Amino Acid | ||
MLDOIJIL_00742 | 5.4e-20 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
MLDOIJIL_00743 | 2.5e-36 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
MLDOIJIL_00744 | 1.4e-248 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
MLDOIJIL_00745 | 3e-167 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
MLDOIJIL_00746 | 5.6e-112 | kup | P | Transport of potassium into the cell | ||
MLDOIJIL_00747 | 1.9e-69 | M | Peptidase family M1 domain | |||
MLDOIJIL_00748 | 2.2e-187 | S | Bacteriocin helveticin-J | |||
MLDOIJIL_00749 | 8e-51 | L | RelB antitoxin | |||
MLDOIJIL_00750 | 7.4e-105 | qmcA | O | prohibitin homologues | ||
MLDOIJIL_00751 | 3.5e-25 | qmcA | O | prohibitin homologues | ||
MLDOIJIL_00752 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
MLDOIJIL_00753 | 1.1e-33 | 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 | |
MLDOIJIL_00754 | 3.9e-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 | |
MLDOIJIL_00755 | 4.5e-39 | veg | S | Biofilm formation stimulator VEG | ||
MLDOIJIL_00756 | 1.9e-110 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
MLDOIJIL_00757 | 3.7e-172 | 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 | |
MLDOIJIL_00758 | 4e-167 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
MLDOIJIL_00759 | 1.4e-134 | corA | P | CorA-like Mg2+ transporter protein | ||
MLDOIJIL_00760 | 1.8e-72 | 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 | ||
MLDOIJIL_00761 | 6.5e-45 | yggT | S | YGGT family | ||
MLDOIJIL_00762 | 2.9e-145 | ylmH | S | S4 domain protein | ||
MLDOIJIL_00763 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
MLDOIJIL_00766 | 2.4e-18 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
MLDOIJIL_00768 | 7.5e-49 | 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 | ||
MLDOIJIL_00769 | 1.6e-181 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
MLDOIJIL_00770 | 9.1e-10 | K | peptidyl-tyrosine sulfation | |||
MLDOIJIL_00772 | 4.5e-131 | S | interspecies interaction between organisms | |||
MLDOIJIL_00773 | 8.9e-29 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
MLDOIJIL_00774 | 4.1e-62 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
MLDOIJIL_00775 | 4.4e-247 | dnaB | L | Replication initiation and membrane attachment | ||
MLDOIJIL_00776 | 3.4e-22 | dnaI | L | Primosomal protein DnaI | ||
MLDOIJIL_00777 | 7e-77 | rfbP | M | Bacterial sugar transferase | ||
MLDOIJIL_00778 | 1.9e-117 | cps1D | M | Domain of unknown function (DUF4422) | ||
MLDOIJIL_00780 | 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 | ||
MLDOIJIL_00781 | 1e-107 | ypsA | S | Belongs to the UPF0398 family | ||
MLDOIJIL_00782 | 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 | ||
MLDOIJIL_00783 | 3.9e-64 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
MLDOIJIL_00784 | 1.5e-129 | 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 | |
MLDOIJIL_00785 | 9.9e-213 | V | N-6 DNA Methylase | |||
MLDOIJIL_00786 | 3.8e-82 | bcgIB | 2.1.1.72, 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
MLDOIJIL_00787 | 2.2e-69 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
MLDOIJIL_00788 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
MLDOIJIL_00789 | 1.6e-76 | ecsA | V | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00790 | 1.9e-220 | ecsB | U | ABC transporter | ||
MLDOIJIL_00792 | 5.5e-30 | |||||
MLDOIJIL_00793 | 4.3e-40 | S | Protein of unknown function (DUF2922) | |||
MLDOIJIL_00794 | 1.3e-110 | S | Haloacid dehalogenase-like hydrolase | |||
MLDOIJIL_00795 | 5e-108 | radC | L | DNA repair protein | ||
MLDOIJIL_00796 | 9.3e-173 | mreB | D | cell shape determining protein MreB | ||
MLDOIJIL_00797 | 2e-147 | mreC | M | Involved in formation and maintenance of cell shape | ||
MLDOIJIL_00798 | 2.7e-94 | mreD | ||||
MLDOIJIL_00800 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
MLDOIJIL_00801 | 1.2e-19 | mraZ | K | Belongs to the MraZ family | ||
MLDOIJIL_00802 | 9.2e-36 | mraZ | K | Belongs to the MraZ family | ||
MLDOIJIL_00803 | 3e-173 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
MLDOIJIL_00804 | 2.1e-42 | |||||
MLDOIJIL_00805 | 1.2e-50 | |||||
MLDOIJIL_00806 | 1.9e-147 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
MLDOIJIL_00807 | 1.3e-78 | hipB | K | Helix-turn-helix | ||
MLDOIJIL_00808 | 1.4e-15 | S | cog cog1373 | |||
MLDOIJIL_00809 | 1e-30 | S | cog cog1373 | |||
MLDOIJIL_00810 | 3.8e-90 | F | Nucleoside 2-deoxyribosyltransferase | |||
MLDOIJIL_00811 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
MLDOIJIL_00812 | 1.3e-263 | |||||
MLDOIJIL_00813 | 1.2e-71 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
MLDOIJIL_00814 | 7.1e-130 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
MLDOIJIL_00815 | 2.2e-85 | S | ECF transporter, substrate-specific component | |||
MLDOIJIL_00816 | 6.5e-131 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
MLDOIJIL_00817 | 4.1e-34 | |||||
MLDOIJIL_00818 | 1e-66 | doc | S | Fic/DOC family | ||
MLDOIJIL_00820 | 6.1e-53 | L | An automated process has identified a potential problem with this gene model | |||
MLDOIJIL_00821 | 7.9e-16 | L | An automated process has identified a potential problem with this gene model | |||
MLDOIJIL_00823 | 3e-23 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
MLDOIJIL_00824 | 1.7e-204 | gatC | G | PTS system sugar-specific permease component | ||
MLDOIJIL_00825 | 6.5e-18 | 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
MLDOIJIL_00826 | 3.5e-57 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
MLDOIJIL_00827 | 8.3e-123 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
MLDOIJIL_00828 | 4.4e-38 | L | An automated process has identified a potential problem with this gene model | |||
MLDOIJIL_00829 | 1.8e-78 | 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 | ||
MLDOIJIL_00830 | 5.6e-68 | 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 | ||
MLDOIJIL_00831 | 4.7e-120 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
MLDOIJIL_00832 | 2.1e-236 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MLDOIJIL_00833 | 7.5e-78 | fruR | K | DeoR C terminal sensor domain | ||
MLDOIJIL_00834 | 5.4e-47 | fruR | K | DeoR C terminal sensor domain | ||
MLDOIJIL_00835 | 1.7e-91 | natB | CP | ABC-2 family transporter protein | ||
MLDOIJIL_00836 | 4e-182 | oppD | P | Belongs to the ABC transporter superfamily | ||
MLDOIJIL_00837 | 8.9e-187 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
MLDOIJIL_00838 | 7.4e-80 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
MLDOIJIL_00839 | 2.2e-90 | 2.7.7.65 | T | GGDEF domain | ||
MLDOIJIL_00840 | 3.9e-07 | |||||
MLDOIJIL_00841 | 8.9e-112 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
MLDOIJIL_00842 | 3.7e-26 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
MLDOIJIL_00843 | 1.2e-92 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
MLDOIJIL_00844 | 1e-149 | D | Alpha beta | |||
MLDOIJIL_00845 | 2.6e-188 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
MLDOIJIL_00846 | 2.3e-65 | liaI | S | membrane | ||
MLDOIJIL_00847 | 6.6e-70 | XK27_02470 | K | LytTr DNA-binding domain | ||
MLDOIJIL_00848 | 1.2e-18 | S | Sugar efflux transporter for intercellular exchange | |||
MLDOIJIL_00849 | 1.2e-55 | dtpT | U | amino acid peptide transporter | ||
MLDOIJIL_00850 | 4.9e-117 | M | NlpC/P60 family | |||
MLDOIJIL_00851 | 1.4e-136 | M | NlpC P60 family protein | |||
MLDOIJIL_00852 | 3.6e-86 | M | NlpC/P60 family | |||
MLDOIJIL_00853 | 5e-77 | comEA | L | Competence protein ComEA | ||
MLDOIJIL_00854 | 1.1e-173 | ylbL | T | Belongs to the peptidase S16 family | ||
MLDOIJIL_00855 | 5.1e-205 | M | Glycosyl hydrolases family 25 | |||
MLDOIJIL_00857 | 4.9e-140 | 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 | ||
MLDOIJIL_00858 | 2.6e-84 | rny | S | Endoribonuclease that initiates mRNA decay | ||
MLDOIJIL_00859 | 1.9e-245 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
MLDOIJIL_00860 | 1.3e-277 | macB_3 | V | ABC transporter, ATP-binding protein | ||
MLDOIJIL_00861 | 2.4e-77 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
MLDOIJIL_00862 | 7.6e-163 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
MLDOIJIL_00863 | 2e-106 | K | Transcriptional regulator, AbiEi antitoxin | |||
MLDOIJIL_00864 | 9.7e-155 | phoH | T | phosphate starvation-inducible protein PhoH | ||
MLDOIJIL_00865 | 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 | |
MLDOIJIL_00866 | 6.2e-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 | ||
MLDOIJIL_00867 | 6.9e-150 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MLDOIJIL_00868 | 5.5e-36 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
MLDOIJIL_00869 | 3.5e-53 | 3.6.3.8 | P | P-type ATPase | ||
MLDOIJIL_00870 | 9.6e-132 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
MLDOIJIL_00871 | 2.5e-52 | |||||
MLDOIJIL_00872 | 2.5e-16 | M | Lysin motif | |||
MLDOIJIL_00873 | 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 | |||
MLDOIJIL_00874 | 1.9e-127 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
MLDOIJIL_00875 | 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 | ||
MLDOIJIL_00876 | 1.7e-103 | 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 | ||
MLDOIJIL_00877 | 9.6e-175 | L | Plasmid pRiA4b ORF-3-like protein | |||
MLDOIJIL_00878 | 2.6e-132 | L | Plasmid pRiA4b ORF-3-like protein | |||
MLDOIJIL_00879 | 1.5e-102 | srtA | 3.4.22.70 | M | sortase family | |
MLDOIJIL_00880 | 4.4e-169 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
MLDOIJIL_00881 | 1.4e-112 | rihB | 3.2.2.1 | F | Nucleoside | |
MLDOIJIL_00882 | 2.8e-134 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
MLDOIJIL_00883 | 1.2e-154 | S | hydrolase | |||
MLDOIJIL_00884 | 2.5e-59 | S | Enterocin A Immunity | |||
MLDOIJIL_00885 | 1.9e-56 | glcR | K | DeoR C terminal sensor domain | ||
MLDOIJIL_00886 | 4.1e-172 | L | COG3385 FOG Transposase and inactivated derivatives | |||
MLDOIJIL_00887 | 4.7e-105 | tag | 3.2.2.20 | L | glycosylase | |
MLDOIJIL_00888 | 3.9e-84 | |||||
MLDOIJIL_00889 | 1.3e-270 | S | Calcineurin-like phosphoesterase | |||
MLDOIJIL_00890 | 1.6e-32 | |||||
MLDOIJIL_00891 | 4.7e-94 | sigH | K | Belongs to the sigma-70 factor family | ||
MLDOIJIL_00892 | 1.6e-120 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
MLDOIJIL_00893 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
MLDOIJIL_00894 | 1.2e-132 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
MLDOIJIL_00895 | 2.2e-57 | yodB | K | Transcriptional regulator, HxlR family | ||
MLDOIJIL_00897 | 1.1e-22 | papP | P | ABC transporter, permease protein | ||
MLDOIJIL_00898 | 1.8e-168 | yjeM | E | Amino Acid | ||
MLDOIJIL_00899 | 2.4e-189 | 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 | |
MLDOIJIL_00900 | 1.3e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
MLDOIJIL_00901 | 2e-158 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
MLDOIJIL_00902 | 5e-93 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
MLDOIJIL_00903 | 2.3e-07 | 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 | |
MLDOIJIL_00904 | 7e-281 | ybeC | E | amino acid | ||
MLDOIJIL_00905 | 1.2e-39 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MLDOIJIL_00907 | 8.9e-15 | oppA2 | E | ABC transporter, substratebinding protein | ||
MLDOIJIL_00908 | 3.6e-210 | oppA2 | E | ABC transporter, substratebinding protein | ||
MLDOIJIL_00909 | 1.5e-26 | oppA2 | E | ABC transporter, substratebinding protein | ||
MLDOIJIL_00910 | 2.1e-39 | |||||
MLDOIJIL_00911 | 2.4e-118 | S | Aldo keto reductase | |||
MLDOIJIL_00912 | 2.7e-138 | |||||
MLDOIJIL_00913 | 1.3e-96 | potD | P | ABC transporter | ||
MLDOIJIL_00914 | 1.3e-34 | potD | P | ABC transporter | ||
MLDOIJIL_00915 | 1.6e-20 | potD | P | ABC transporter | ||
MLDOIJIL_00916 | 3.1e-51 | potC | P | ABC transporter permease | ||
MLDOIJIL_00917 | 1.1e-52 | potC | P | ABC transporter permease | ||
MLDOIJIL_00918 | 3.3e-128 | potB | P | ABC transporter permease | ||
MLDOIJIL_00919 | 4.9e-90 | 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 | |
MLDOIJIL_00920 | 2.8e-28 | 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 | |
MLDOIJIL_00921 | 3.5e-32 | ykzG | S | Belongs to the UPF0356 family | ||
MLDOIJIL_00922 | 5.7e-21 | mbl | D | Cell shape determining protein MreB Mrl | ||
MLDOIJIL_00923 | 5e-31 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
MLDOIJIL_00924 | 9.5e-33 | S | Protein of unknown function (DUF2969) | |||
MLDOIJIL_00925 | 1.8e-81 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
MLDOIJIL_00926 | 4.5e-97 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
MLDOIJIL_00927 | 5.1e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
MLDOIJIL_00928 | 4.3e-59 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
MLDOIJIL_00929 | 1.7e-91 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
MLDOIJIL_00930 | 1.8e-93 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
MLDOIJIL_00931 | 4.1e-143 | gltC_1 | 3.1.3.48 | K | LysR substrate binding domain | |
MLDOIJIL_00932 | 1.5e-54 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
MLDOIJIL_00933 | 3.2e-75 | S | ECF transporter, substrate-specific component | |||
MLDOIJIL_00934 | 3.8e-80 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
MLDOIJIL_00935 | 1.8e-117 | 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 | ||
MLDOIJIL_00936 | 3e-117 | 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 | ||
MLDOIJIL_00937 | 4.4e-80 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
MLDOIJIL_00938 | 6.6e-55 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
MLDOIJIL_00939 | 2.2e-105 | 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) |
MLDOIJIL_00941 | 1.4e-104 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
MLDOIJIL_00942 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
MLDOIJIL_00943 | 1.9e-236 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
MLDOIJIL_00944 | 5.5e-130 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
MLDOIJIL_00945 | 2.3e-16 | 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 | |
MLDOIJIL_00946 | 8e-182 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
MLDOIJIL_00947 | 3.2e-119 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
MLDOIJIL_00948 | 5.5e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
MLDOIJIL_00949 | 2.1e-65 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
MLDOIJIL_00950 | 3.1e-69 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
MLDOIJIL_00951 | 3.2e-47 | rplGA | J | ribosomal protein | ||
MLDOIJIL_00952 | 1.5e-43 | ylxR | K | Protein of unknown function (DUF448) | ||
MLDOIJIL_00953 | 1.4e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
MLDOIJIL_00954 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
MLDOIJIL_00955 | 3.6e-91 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
MLDOIJIL_00956 | 1.7e-75 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
MLDOIJIL_00957 | 1.9e-25 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
MLDOIJIL_00958 | 7e-32 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
MLDOIJIL_00959 | 7.5e-175 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
MLDOIJIL_00960 | 3.5e-152 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
MLDOIJIL_00961 | 2.3e-181 | M | CHAP domain | |||
MLDOIJIL_00962 | 3.5e-75 | |||||
MLDOIJIL_00963 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
MLDOIJIL_00964 | 4.8e-56 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
MLDOIJIL_00965 | 1.3e-114 | dnaD | L | DnaD domain protein | ||
MLDOIJIL_00966 | 1.4e-113 | 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 | |
MLDOIJIL_00967 | 1.2e-154 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
MLDOIJIL_00968 | 2.1e-164 | lacR | K | Transcriptional regulator | ||
MLDOIJIL_00969 | 1.3e-85 | thrE | S | Putative threonine/serine exporter | ||
MLDOIJIL_00971 | 5.9e-49 | S | Threonine/Serine exporter, ThrE | |||
MLDOIJIL_00972 | 2.7e-134 | yvpB | S | Peptidase_C39 like family | ||
MLDOIJIL_00973 | 2.5e-68 | |||||
MLDOIJIL_00974 | 3.3e-115 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
MLDOIJIL_00975 | 1.3e-19 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
MLDOIJIL_00976 | 3.7e-66 | K | Helix-turn-helix domain, rpiR family | |||
MLDOIJIL_00977 | 9.5e-182 | E | ABC transporter, substratebinding protein | |||
MLDOIJIL_00978 | 1.3e-150 | S | Metal-independent alpha-mannosidase (GH125) | |||
MLDOIJIL_00979 | 1.1e-25 | |||||
MLDOIJIL_00980 | 1.2e-77 | K | DNA-templated transcription, initiation | |||
MLDOIJIL_00981 | 5.7e-27 | |||||
MLDOIJIL_00983 | 2.6e-92 | S | SLAP domain | |||
MLDOIJIL_00984 | 5.5e-206 | 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 | ||
MLDOIJIL_00985 | 3.8e-20 | |||||
MLDOIJIL_00986 | 4.6e-36 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
MLDOIJIL_00987 | 6.8e-110 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
MLDOIJIL_00988 | 4.5e-177 | 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 | ||
MLDOIJIL_00989 | 3.8e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
MLDOIJIL_00990 | 3e-82 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
MLDOIJIL_00991 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
MLDOIJIL_00992 | 2.7e-62 | V | ABC-type multidrug transport system, ATPase and permease components | |||
MLDOIJIL_00993 | 3e-11 | L | DNA topoisomerase type I activity | |||
MLDOIJIL_00995 | 1.4e-23 | S | CAAX protease self-immunity | |||
MLDOIJIL_00997 | 3.5e-64 | K | response regulator | |||
MLDOIJIL_00998 | 9.2e-24 | vicK | 2.7.13.3 | T | Histidine kinase | |
MLDOIJIL_00999 | 5.7e-273 | vicK | 2.7.13.3 | T | Histidine kinase | |
MLDOIJIL_01000 | 1.6e-257 | yycH | S | YycH protein | ||
MLDOIJIL_01001 | 1.3e-11 | skfE | V | ATPases associated with a variety of cellular activities | ||
MLDOIJIL_01002 | 4e-60 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
MLDOIJIL_01003 | 1.7e-136 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
MLDOIJIL_01004 | 6e-86 | |||||
MLDOIJIL_01005 | 5.7e-33 | K | LytTr DNA-binding domain | |||
MLDOIJIL_01006 | 5.9e-68 | S | Protein of unknown function (DUF3021) | |||
MLDOIJIL_01007 | 1.5e-242 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
MLDOIJIL_01009 | 3e-271 | S | SLAP domain | |||
MLDOIJIL_01011 | 1.1e-236 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
MLDOIJIL_01012 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
MLDOIJIL_01013 | 2.7e-67 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
MLDOIJIL_01014 | 6.4e-154 | pstS | P | Phosphate | ||
MLDOIJIL_01015 | 2.6e-162 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
MLDOIJIL_01016 | 1.1e-74 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
MLDOIJIL_01017 | 2.8e-213 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
MLDOIJIL_01018 | 6.8e-47 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
MLDOIJIL_01019 | 1.6e-182 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
MLDOIJIL_01020 | 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 | |
MLDOIJIL_01021 | 1.3e-151 | 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 | |
MLDOIJIL_01022 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
MLDOIJIL_01023 | 2e-30 | ywzB | S | Protein of unknown function (DUF1146) | ||
MLDOIJIL_01024 | 1.3e-64 | K | LysR substrate binding domain | |||
MLDOIJIL_01025 | 1.6e-71 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
MLDOIJIL_01026 | 7.3e-20 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
MLDOIJIL_01027 | 6.2e-43 | 1.3.5.4 | C | FAD binding domain | ||
MLDOIJIL_01028 | 2.1e-51 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
MLDOIJIL_01029 | 7.5e-95 | S | ECF-type riboflavin transporter, S component | |||
MLDOIJIL_01030 | 2.3e-165 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
MLDOIJIL_01031 | 5.7e-69 | rplI | J | Binds to the 23S rRNA | ||
MLDOIJIL_01032 | 1.9e-170 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
MLDOIJIL_01033 | 9.1e-69 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
MLDOIJIL_01034 | 3.3e-164 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
MLDOIJIL_01035 | 4.9e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
MLDOIJIL_01036 | 1.1e-181 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
MLDOIJIL_01037 | 1.7e-85 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
MLDOIJIL_01038 | 1.4e-80 | K | Transcriptional regulator, MarR family | |||
MLDOIJIL_01039 | 1.3e-61 | ybiR | P | Citrate transporter | ||
MLDOIJIL_01040 | 5.1e-96 | lemA | S | LemA family | ||
MLDOIJIL_01041 | 2.1e-208 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
MLDOIJIL_01042 | 1.1e-62 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
MLDOIJIL_01043 | 8.8e-254 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
MLDOIJIL_01044 | 2.5e-17 | sprD | D | Domain of Unknown Function (DUF1542) | ||
MLDOIJIL_01045 | 5.5e-19 | scrR | K | Periplasmic binding protein domain | ||
MLDOIJIL_01046 | 1.7e-107 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
MLDOIJIL_01047 | 4e-20 | S | Repeat protein | |||
MLDOIJIL_01048 | 1.6e-70 | S | Repeat protein | |||
MLDOIJIL_01049 | 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 | |
MLDOIJIL_01050 | 1.2e-38 | |||||
MLDOIJIL_01051 | 7.8e-78 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
MLDOIJIL_01053 | 8.2e-130 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
MLDOIJIL_01054 | 8.7e-117 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
MLDOIJIL_01055 | 8.7e-143 | epsB | M | biosynthesis protein | ||
MLDOIJIL_01056 | 1.9e-176 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
MLDOIJIL_01060 | 2.3e-47 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
MLDOIJIL_01061 | 1.1e-201 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
MLDOIJIL_01062 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
MLDOIJIL_01063 | 1.5e-36 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
MLDOIJIL_01064 | 6.5e-160 | copA | 3.6.3.54 | P | P-type ATPase | |
MLDOIJIL_01065 | 3.1e-49 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
MLDOIJIL_01066 | 4.9e-58 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
MLDOIJIL_01067 | 2.4e-36 | |||||
MLDOIJIL_01070 | 3.5e-121 | yjeM | E | Amino Acid | ||
MLDOIJIL_01071 | 5.8e-83 | S | Fic/DOC family | |||
MLDOIJIL_01072 | 4.3e-175 | |||||
MLDOIJIL_01073 | 3.1e-93 | |||||
MLDOIJIL_01074 | 2.2e-78 | |||||
MLDOIJIL_01075 | 1.8e-84 | S | Protein of unknown function (DUF805) | |||
MLDOIJIL_01076 | 9.5e-68 | O | OsmC-like protein | |||
MLDOIJIL_01077 | 2.5e-153 | EGP | Major facilitator Superfamily | |||
MLDOIJIL_01078 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
MLDOIJIL_01079 | 5.5e-80 | stp | 3.1.3.16 | T | phosphatase | |
MLDOIJIL_01080 | 4.5e-166 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
MLDOIJIL_01081 | 7.5e-229 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
MLDOIJIL_01082 | 2.1e-76 | ylbE | GM | NAD(P)H-binding | ||
MLDOIJIL_01083 | 1.8e-90 | S | VanZ like family | |||
MLDOIJIL_01084 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
MLDOIJIL_01086 | 3.3e-67 | K | Helix-turn-helix XRE-family like proteins | |||
MLDOIJIL_01087 | 7.7e-144 | malG | P | ABC transporter permease | ||
MLDOIJIL_01088 | 1.7e-249 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
MLDOIJIL_01089 | 1.9e-212 | malE | G | Bacterial extracellular solute-binding protein | ||
MLDOIJIL_01090 | 5.9e-15 | msmX | P | Belongs to the ABC transporter superfamily | ||
MLDOIJIL_01091 | 1.1e-175 | msmX | P | Belongs to the ABC transporter superfamily | ||
MLDOIJIL_01092 | 3.6e-73 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
MLDOIJIL_01093 | 2.8e-76 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
MLDOIJIL_01095 | 2.5e-103 | pncA | Q | Isochorismatase family | ||
MLDOIJIL_01096 | 5.2e-118 | |||||
MLDOIJIL_01100 | 1.4e-24 | srtA | 3.4.22.70 | M | sortase family | |
MLDOIJIL_01102 | 1.5e-12 | S | SLAP domain | |||
MLDOIJIL_01107 | 3.7e-10 | S | Single-strand binding protein family | |||
MLDOIJIL_01108 | 2.2e-26 | S | Type I restriction modification DNA specificity domain | |||
MLDOIJIL_01109 | 1.1e-188 | L | N-6 DNA Methylase | |||
MLDOIJIL_01111 | 1e-33 | K | Helix-turn-helix XRE-family like proteins | |||
MLDOIJIL_01112 | 7.8e-34 | S | Phage derived protein Gp49-like (DUF891) | |||
MLDOIJIL_01118 | 1.5e-26 | S | Domain of unknown function (DUF771) | |||
MLDOIJIL_01119 | 4e-21 | K | Conserved phage C-terminus (Phg_2220_C) | |||
MLDOIJIL_01121 | 4.1e-09 | S | Arc-like DNA binding domain | |||
MLDOIJIL_01123 | 7.9e-26 | K | Helix-turn-helix domain | |||
MLDOIJIL_01124 | 3.1e-19 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
MLDOIJIL_01125 | 9.8e-16 | K | Helix-turn-helix XRE-family like proteins | |||
MLDOIJIL_01126 | 1e-08 | S | Pfam:DUF955 | |||
MLDOIJIL_01127 | 8.5e-151 | L | Belongs to the 'phage' integrase family | |||
MLDOIJIL_01129 | 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 | |
MLDOIJIL_01130 | 1.8e-184 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
MLDOIJIL_01131 | 1.6e-21 | |||||
MLDOIJIL_01132 | 4.5e-71 | comGF | U | Putative Competence protein ComGF | ||
MLDOIJIL_01133 | 2.3e-41 | |||||
MLDOIJIL_01134 | 7.5e-59 | |||||
MLDOIJIL_01135 | 6.2e-20 | comGC | U | competence protein ComGC | ||
MLDOIJIL_01136 | 2.5e-22 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
MLDOIJIL_01137 | 5e-63 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
MLDOIJIL_01138 | 4.6e-311 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
MLDOIJIL_01139 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
MLDOIJIL_01140 | 6.4e-199 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
MLDOIJIL_01141 | 2.1e-63 | S | Peptidase family M23 | |||
MLDOIJIL_01142 | 7.9e-291 | ytgP | S | Polysaccharide biosynthesis protein | ||
MLDOIJIL_01143 | 1.9e-36 | |||||
MLDOIJIL_01144 | 4.3e-104 | XK27_06780 | V | ABC transporter permease | ||
MLDOIJIL_01145 | 1.3e-277 | XK27_06780 | V | ABC transporter permease | ||
MLDOIJIL_01146 | 1.3e-232 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
MLDOIJIL_01147 | 6.5e-99 | S | Tetratricopeptide repeat protein | |||
MLDOIJIL_01148 | 1.4e-75 | S | Tetratricopeptide repeat protein | |||
MLDOIJIL_01149 | 2.3e-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 | ||
MLDOIJIL_01150 | 4.2e-127 | 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 | |
MLDOIJIL_01151 | 1.4e-19 | S | reductase | |||
MLDOIJIL_01152 | 4.4e-39 | S | reductase | |||
MLDOIJIL_01153 | 4.8e-34 | S | reductase | |||
MLDOIJIL_01154 | 3.7e-213 | 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 | |
MLDOIJIL_01155 | 1.9e-80 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
MLDOIJIL_01156 | 2.7e-199 | 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 | |
MLDOIJIL_01157 | 8.4e-105 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
MLDOIJIL_01158 | 6.6e-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 | |
MLDOIJIL_01159 | 3.4e-95 | lsa | S | ABC transporter |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)