ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
MHMNNKED_00001 | 8.1e-31 | acyP | 3.6.1.7 | C | Acylphosphatase | |
MHMNNKED_00003 | 1.9e-169 | narK | P | COG2223 Nitrate nitrite transporter | ||
MHMNNKED_00004 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
MHMNNKED_00005 | 1.6e-285 | narH | 1.7.5.1 | C | Nitrate reductase, beta | |
MHMNNKED_00006 | 1.8e-45 | narJ | 1.7.5.1 | C | nitrate reductase | |
MHMNNKED_00007 | 9.7e-97 | narI | 1.7.5.1 | C | nitrate reductase, gamma subunit | |
MHMNNKED_00008 | 2.6e-139 | S | Tetratricopeptide repeats | |||
MHMNNKED_00009 | 6.2e-32 | |||||
MHMNNKED_00010 | 1.4e-65 | ytaF | P | Probably functions as a manganese efflux pump | ||
MHMNNKED_00011 | 4.3e-123 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
MHMNNKED_00012 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
MHMNNKED_00013 | 1.4e-114 | hflC | O | HflC and HflK could regulate a protease | ||
MHMNNKED_00014 | 1.8e-96 | hflK | O | HflC and HflK could encode or regulate a protease | ||
MHMNNKED_00015 | 3.7e-193 | phoR | 2.7.13.3 | T | Signal transduction histidine kinase | |
MHMNNKED_00016 | 5.3e-106 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
MHMNNKED_00017 | 6.3e-147 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
MHMNNKED_00018 | 9.1e-226 | icd | 1.1.1.42 | C | isocitrate | |
MHMNNKED_00019 | 5.3e-177 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
MHMNNKED_00020 | 6.7e-108 | ytvI | S | sporulation integral membrane protein YtvI | ||
MHMNNKED_00021 | 1.7e-34 | fxsA | S | COG3030 Protein affecting phage T7 exclusion by the F plasmid | ||
MHMNNKED_00022 | 2e-279 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
MHMNNKED_00023 | 3.7e-147 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
MHMNNKED_00024 | 1.4e-144 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
MHMNNKED_00025 | 9.5e-126 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
MHMNNKED_00026 | 2.9e-47 | lutR_1 | K | helix_turn_helix gluconate operon transcriptional repressor | ||
MHMNNKED_00027 | 7.4e-172 | ytsJ | 1.1.1.38 | C | Malate dehydrogenase | |
MHMNNKED_00028 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
MHMNNKED_00029 | 2e-47 | ytrH | S | Sporulation protein YtrH | ||
MHMNNKED_00030 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase ammonia chain | |
MHMNNKED_00031 | 6.2e-126 | argF | 2.1.3.3 | 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 | |
MHMNNKED_00032 | 4.1e-199 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
MHMNNKED_00033 | 5.8e-218 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
MHMNNKED_00034 | 5.8e-15 | yckD | S | Protein of unknown function (DUF2680) | ||
MHMNNKED_00035 | 1.3e-29 | yhdT | S | Sodium pantothenate symporter | ||
MHMNNKED_00036 | 9.1e-206 | panF | H | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
MHMNNKED_00037 | 7e-138 | murB | 1.3.1.98 | M | cell wall formation | |
MHMNNKED_00038 | 1.4e-123 | ydbI | S | AI-2E family transporter | ||
MHMNNKED_00039 | 5.1e-162 | xylR | GK | ROK family | ||
MHMNNKED_00041 | 1.9e-10 | |||||
MHMNNKED_00042 | 1.8e-111 | sodA | 1.15.1.1 | P | Superoxide dismutase | |
MHMNNKED_00043 | 4.2e-13 | S | Carbon monoxide dehydrogenase subunit G (CoxG) | |||
MHMNNKED_00044 | 1.1e-32 | yrkD | S | protein conserved in bacteria | ||
MHMNNKED_00045 | 7e-36 | P | Rhodanese Homology Domain | |||
MHMNNKED_00046 | 1.2e-260 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
MHMNNKED_00047 | 3.5e-37 | P | Rhodanese Homology Domain | |||
MHMNNKED_00048 | 7.7e-12 | O | Glutaredoxin | |||
MHMNNKED_00049 | 6.8e-126 | pgl | 3.1.1.31 | G | 6-phosphogluconolactonase | |
MHMNNKED_00051 | 2.6e-165 | S | Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase | |||
MHMNNKED_00052 | 5.2e-131 | yclQ | P | COG4607 ABC-type enterochelin transport system, periplasmic component | ||
MHMNNKED_00053 | 1.2e-124 | yclP | 3.6.3.34 | P | ABC transporter, ATP-binding protein | |
MHMNNKED_00054 | 1.4e-133 | fatC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
MHMNNKED_00055 | 4.6e-145 | yclN | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
MHMNNKED_00056 | 7.9e-127 | ycsI | S | Belongs to the D-glutamate cyclase family | ||
MHMNNKED_00057 | 8.4e-173 | ycsG | P | COG1914 Mn2 and Fe2 transporters of the NRAMP family | ||
MHMNNKED_00058 | 2.9e-118 | ycsF | S | Belongs to the UPF0271 (lamB) family | ||
MHMNNKED_00059 | 2.2e-121 | kipA | 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
MHMNNKED_00060 | 9.4e-95 | kipI | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
MHMNNKED_00061 | 4.5e-242 | sbcC | L | COG0419 ATPase involved in DNA repair | ||
MHMNNKED_00062 | 2.3e-178 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
MHMNNKED_00063 | 1.7e-29 | S | Domain of unknown function (DUF4652) | |||
MHMNNKED_00064 | 3.6e-232 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
MHMNNKED_00065 | 8.2e-98 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase | |
MHMNNKED_00066 | 5e-140 | capA | M | Bacterial capsule synthesis protein PGA_cap | ||
MHMNNKED_00067 | 4.3e-146 | 1.6.5.5 | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | ||
MHMNNKED_00068 | 6.8e-112 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
MHMNNKED_00069 | 3.5e-139 | ydaH | H | AbgT putative transporter family | ||
MHMNNKED_00070 | 5.4e-63 | L | Replication initiation and membrane attachment | |||
MHMNNKED_00071 | 3.3e-56 | D | peptidase | |||
MHMNNKED_00072 | 1e-114 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
MHMNNKED_00073 | 3.5e-107 | ftsE | D | cell division ATP-binding protein FtsE | ||
MHMNNKED_00074 | 5.3e-203 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
MHMNNKED_00075 | 1.8e-29 | sugE | P | Multidrug resistance protein | ||
MHMNNKED_00076 | 1.1e-35 | ykkC | P | Multidrug resistance protein | ||
MHMNNKED_00077 | 7e-120 | yumC | 1.18.1.2, 1.19.1.1 | C | reductase | |
MHMNNKED_00078 | 1.7e-16 | fdxA | C | 4Fe-4S binding domain | ||
MHMNNKED_00079 | 5.3e-176 | paaK | 6.2.1.30 | H | AMP-binding enzyme | |
MHMNNKED_00080 | 1e-152 | paaA | 1.14.13.149 | S | With PaaBCDE catalyzes the hydroxylation of phenylacetyl-CoA | |
MHMNNKED_00081 | 2.1e-30 | paaB | Q | Phenylacetate-CoA oxygenase subunit PaaH | ||
MHMNNKED_00082 | 6.1e-87 | paaC | 1.14.13.149 | Q | Phenylacetate-CoA oxygenase | |
MHMNNKED_00083 | 9.7e-54 | paaD | S | Phenylacetate-CoA oxygenase | ||
MHMNNKED_00084 | 2.3e-42 | ethD | S | Ethyl tert-butyl ether degradation | ||
MHMNNKED_00085 | 9.3e-96 | paaF | 4.2.1.17 | I | Enoyl-CoA hydratase/isomerase | |
MHMNNKED_00086 | 1.1e-88 | paaG | 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
MHMNNKED_00087 | 2e-99 | paaX | K | PaaX-like protein | ||
MHMNNKED_00088 | 3.9e-104 | 1.3.1.9 | S | Dihydroorotate dehydrogenase | ||
MHMNNKED_00089 | 4.6e-49 | Q | Thioesterase superfamily | |||
MHMNNKED_00090 | 4.2e-51 | K | helix_turn_helix ASNC type | |||
MHMNNKED_00091 | 5.2e-123 | ybbF | 2.7.1.211 | G | phosphotransferase system | |
MHMNNKED_00092 | 1.9e-123 | yleB | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | |
MHMNNKED_00093 | 5.2e-205 | cshA | L | COG2256 ATPase related to the helicase subunit of the Holliday junction resolvase | ||
MHMNNKED_00094 | 1.8e-76 | yczE | S | membrane | ||
MHMNNKED_00095 | 2.5e-58 | cymR | K | Transcriptional regulator | ||
MHMNNKED_00096 | 4.3e-158 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
MHMNNKED_00097 | 9.9e-192 | 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 | |
MHMNNKED_00098 | 4e-34 | opuCD | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
MHMNNKED_00099 | 2.3e-49 | opuCD | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
MHMNNKED_00100 | 1e-133 | opuCC | M | COG1732 Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
MHMNNKED_00101 | 7.3e-94 | opuCB | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
MHMNNKED_00102 | 1.5e-46 | opuCA | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
MHMNNKED_00103 | 2.1e-166 | G | Bacterial extracellular solute-binding protein | |||
MHMNNKED_00104 | 8.6e-157 | sugA | G | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_00105 | 5.4e-110 | G | Binding-protein-dependent transport system inner membrane component | |||
MHMNNKED_00106 | 2.5e-282 | treP | 2.4.1.64 | GH65 | G | Glycoside hydrolase, family 65 |
MHMNNKED_00107 | 8.4e-80 | sfsA | S | Belongs to the SfsA family | ||
MHMNNKED_00108 | 1.7e-16 | S | Family of unknown function (DUF5327) | |||
MHMNNKED_00109 | 2.1e-37 | ywdK | S | small membrane protein | ||
MHMNNKED_00110 | 3.4e-56 | gerQ | S | Essential for the localization of CwlJ in the spore coat and for spore germination triggered by calcium and dipicolinic acid (DPA). Its assembly into the spore coat is dependent on the coat morphogenetic proteins CotE and SpoIVA | ||
MHMNNKED_00111 | 1.3e-67 | cwlJ | 3.5.1.28 | M | Cell wall | |
MHMNNKED_00112 | 1.1e-100 | bshB2 | S | deacetylase | ||
MHMNNKED_00113 | 5.8e-33 | yesJ | 3.1.3.48 | K | Acetyltransferase (GNAT) family | |
MHMNNKED_00114 | 1e-245 | aidB | I | Acyl-CoA dehydrogenase, middle domain | ||
MHMNNKED_00115 | 6.7e-195 | 6.2.1.3, 6.2.1.34 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
MHMNNKED_00116 | 1.6e-10 | 6.2.1.3, 6.2.1.34 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
MHMNNKED_00117 | 1e-45 | cueR | K | transcriptional | ||
MHMNNKED_00118 | 1e-225 | L | COG3316 Transposase and inactivated derivatives | |||
MHMNNKED_00119 | 2.5e-129 | yqhO | S | esterase of the alpha-beta hydrolase superfamily | ||
MHMNNKED_00120 | 2.2e-07 | yqhP | ||||
MHMNNKED_00121 | 7.6e-54 | yqhR | S | Conserved membrane protein YqhR | ||
MHMNNKED_00122 | 1.2e-143 | yqhT | 3.4.11.9, 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
MHMNNKED_00123 | 1.2e-89 | 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 | ||
MHMNNKED_00124 | 8.4e-128 | spoIIIAA | S | stage III sporulation protein AA | ||
MHMNNKED_00125 | 2.9e-61 | spoIIIAB | S | Stage III sporulation protein | ||
MHMNNKED_00126 | 1.3e-25 | spoIIIAC | S | stage III sporulation protein AC | ||
MHMNNKED_00127 | 7.6e-28 | spoIIIAD | S | Stage III sporulation protein AD | ||
MHMNNKED_00128 | 1.9e-148 | spoIIIAE | S | stage III sporulation protein AE | ||
MHMNNKED_00129 | 5.9e-22 | fsr | P | COG0477 Permeases of the major facilitator superfamily | ||
MHMNNKED_00130 | 5.6e-69 | |||||
MHMNNKED_00131 | 3.2e-23 | ynzC | S | Bacterial protein of unknown function (DUF896) | ||
MHMNNKED_00132 | 2.4e-29 | |||||
MHMNNKED_00133 | 2.7e-72 | S | Carboxylesterase | |||
MHMNNKED_00134 | 1.7e-44 | S | CBS domain | |||
MHMNNKED_00135 | 1.5e-23 | yuzC | ||||
MHMNNKED_00136 | 1.8e-41 | K | Transcriptional regulator PadR-like family | |||
MHMNNKED_00137 | 5.4e-96 | 1.3.1.84, 4.2.1.116, 6.2.1.36 | C | alcohol dehydrogenase | ||
MHMNNKED_00138 | 4.4e-77 | cysC | 2.7.1.25 | P | Catalyzes the synthesis of activated sulfate | |
MHMNNKED_00139 | 8.4e-154 | sat | 2.7.7.4 | P | PUA-like domain | |
MHMNNKED_00140 | 2.8e-203 | yfiU | EGP | Fungal trichothecene efflux pump (TRI12) | ||
MHMNNKED_00141 | 5.9e-204 | proP | EGP | Transporter | ||
MHMNNKED_00142 | 2e-155 | S | Domain of unknown function (DUF4317) | |||
MHMNNKED_00143 | 1.5e-54 | bar | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
MHMNNKED_00144 | 1.2e-15 | |||||
MHMNNKED_00145 | 3e-72 | yhcI | S | ABC-2 family transporter protein | ||
MHMNNKED_00146 | 1.7e-104 | yhcH | V | ABC transporter, ATP-binding protein | ||
MHMNNKED_00147 | 2.4e-85 | yhcG | V | ABC transporter, ATP-binding protein | ||
MHMNNKED_00148 | 4.5e-40 | yhcF | K | Transcriptional regulator | ||
MHMNNKED_00149 | 3.2e-24 | |||||
MHMNNKED_00150 | 1.3e-151 | sufD | O | assembly protein SufD | ||
MHMNNKED_00151 | 3.2e-191 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
MHMNNKED_00152 | 1.4e-51 | nifU | C | COG0822 NifU homolog involved in Fe-S cluster formation | ||
MHMNNKED_00153 | 3.6e-239 | sufB | O | FeS cluster assembly | ||
MHMNNKED_00154 | 3.6e-154 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
MHMNNKED_00155 | 4.9e-165 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MHMNNKED_00156 | 8.2e-114 | yunF | S | Protein of unknown function DUF72 | ||
MHMNNKED_00157 | 1.4e-182 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
MHMNNKED_00158 | 1.2e-35 | yunC | S | Domain of unknown function (DUF1805) | ||
MHMNNKED_00159 | 7.9e-42 | ssuE | 1.5.1.38 | S | NADPH-dependent FMN reductase | |
MHMNNKED_00160 | 3.6e-54 | ssuE | 1.5.1.38 | S | NADPH-dependent FMN reductase | |
MHMNNKED_00161 | 5e-153 | msuD | 1.14.14.35 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | |
MHMNNKED_00162 | 4.4e-07 | |||||
MHMNNKED_00163 | 3e-245 | dppE_1 | E | ABC transporter substrate-binding protein | ||
MHMNNKED_00164 | 2e-163 | acuC | BQ | histone deacetylase | ||
MHMNNKED_00165 | 2e-59 | acuB | S | Acetoin utilization protein AcuB | ||
MHMNNKED_00166 | 5.2e-97 | acuA | K | Part of the acuABC operon, which is possibly involved in the breakdown of acetoin and butanediol. Acts as an acetyltransferase inactivating acetyl-CoA synthetase AcsA via acetylation at a Lys residue | ||
MHMNNKED_00167 | 9.9e-21 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | COG0744 Membrane carboxypeptidase (penicillin-binding protein) |
MHMNNKED_00168 | 3e-96 | |||||
MHMNNKED_00169 | 0.0 | L | SNF2 family N-terminal domain | |||
MHMNNKED_00171 | 2.4e-57 | |||||
MHMNNKED_00172 | 4e-184 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
MHMNNKED_00173 | 2.5e-81 | tcaA | S | response to antibiotic | ||
MHMNNKED_00174 | 2.7e-40 | sigS | 2.7.7.6 | K | Belongs to the sigma-70 factor family. ECF subfamily | |
MHMNNKED_00175 | 6.6e-54 | tcaA | S | response to antibiotic | ||
MHMNNKED_00176 | 3.6e-44 | |||||
MHMNNKED_00177 | 1e-92 | flhP | N | flagellar basal body | ||
MHMNNKED_00178 | 3.1e-07 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
MHMNNKED_00179 | 1.5e-63 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
MHMNNKED_00180 | 1.8e-49 | 2.7.8.20 | M | COG COG1368 Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | ||
MHMNNKED_00181 | 1.2e-151 | gntP | S | Na+-H+ antiporter family | ||
MHMNNKED_00182 | 3.1e-56 | hutP | K | Antiterminator that binds to cis-acting regulatory sequences on the mRNA in the presence of histidine, thereby suppressing transcription termination and activating the hut operon for histidine utilization | ||
MHMNNKED_00183 | 7.2e-101 | secF | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
MHMNNKED_00184 | 1.6e-177 | iolF | EGP | Sugar (and other) transporter | ||
MHMNNKED_00185 | 1.8e-42 | rhaM | 5.1.3.32 | G | L-rhamnose mutarotase | |
MHMNNKED_00186 | 1.2e-106 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
MHMNNKED_00187 | 2e-180 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
MHMNNKED_00188 | 1.2e-181 | rhaB | 2.7.1.12, 2.7.1.16, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
MHMNNKED_00189 | 7.8e-76 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
MHMNNKED_00190 | 5.2e-288 | nrdA | 1.17.4.1 | F | Catalyzes the reduction of ribonucleotides to deoxyribonucleotides. May function to provide a pool of deoxyribonucleotide precursors for DNA repair during oxygen limitation and or for immediate growth after restoration of oxygen | |
MHMNNKED_00192 | 7.4e-125 | nrdA | 1.17.4.1 | F | Catalyzes the reduction of ribonucleotides to deoxyribonucleotides. May function to provide a pool of deoxyribonucleotide precursors for DNA repair during oxygen limitation and or for immediate growth after restoration of oxygen | |
MHMNNKED_00193 | 2.1e-48 | yqhL | P | COG0607 Rhodanese-related sulfurtransferase | ||
MHMNNKED_00194 | 2.3e-252 | gcvPB | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
MHMNNKED_00195 | 1.6e-207 | gcvPA | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
MHMNNKED_00196 | 5.3e-145 | gcvT | 1.4.4.2, 2.1.2.10 | E | The glycine cleavage system catalyzes the degradation of glycine | |
MHMNNKED_00197 | 6.4e-267 | yqhH | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
MHMNNKED_00198 | 4e-102 | yqhG | S | Bacterial protein YqhG of unknown function | ||
MHMNNKED_00199 | 2.4e-07 | yqzE | S | YqzE-like protein | ||
MHMNNKED_00200 | 2.4e-14 | |||||
MHMNNKED_00201 | 1.1e-33 | comGF | U | Putative Competence protein ComGF | ||
MHMNNKED_00202 | 1e-17 | |||||
MHMNNKED_00203 | 2.4e-35 | gspH | NU | COG2165 Type II secretory pathway, pseudopilin PulG | ||
MHMNNKED_00204 | 1.6e-27 | comGC | U | Required for transformation and DNA binding | ||
MHMNNKED_00205 | 5.7e-93 | comGB | NU | COG1459 Type II secretory pathway, component PulF | ||
MHMNNKED_00206 | 1.3e-46 | comGA | NU | COG2804 Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
MHMNNKED_00207 | 8.4e-17 | S | EpsG family | |||
MHMNNKED_00208 | 3e-132 | S | Polysaccharide biosynthesis protein | |||
MHMNNKED_00209 | 2.6e-36 | alg8 | 2.4.1.33 | GT2 | M | transferase activity, transferring glycosyl groups |
MHMNNKED_00210 | 5.8e-95 | sacB | GT2,GT4 | M | Stealth protein CR4, conserved region 4 | |
MHMNNKED_00211 | 2.7e-54 | S | Endonuclease/Exonuclease/phosphatase family | |||
MHMNNKED_00212 | 4.1e-73 | |||||
MHMNNKED_00213 | 3.3e-13 | |||||
MHMNNKED_00214 | 2.7e-37 | S | Protein of unknown function (DUF2975) | |||
MHMNNKED_00215 | 5.4e-302 | 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 | |
MHMNNKED_00216 | 2.4e-124 | camS | S | COG4851 Protein involved in sex pheromone biosynthesis | ||
MHMNNKED_00217 | 3.9e-168 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
MHMNNKED_00218 | 1e-234 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
MHMNNKED_00219 | 1.2e-65 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
MHMNNKED_00220 | 2.2e-137 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
MHMNNKED_00221 | 1.8e-206 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
MHMNNKED_00222 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
MHMNNKED_00223 | 9.4e-92 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
MHMNNKED_00224 | 2e-23 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
MHMNNKED_00225 | 6.5e-151 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
MHMNNKED_00226 | 2.6e-64 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
MHMNNKED_00227 | 1.2e-185 | ytcJ | S | amidohydrolase | ||
MHMNNKED_00228 | 3.8e-25 | sasP | S | spore protein | ||
MHMNNKED_00229 | 4.7e-171 | 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 | |
MHMNNKED_00230 | 4.3e-158 | iscS2 | 2.8.1.7 | E | Cysteine desulfurase | |
MHMNNKED_00231 | 9.7e-130 | 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 | ||
MHMNNKED_00232 | 4.5e-64 | yttP | K | Transcriptional regulator | ||
MHMNNKED_00233 | 5.2e-65 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
MHMNNKED_00234 | 3.9e-161 | ytrP | 2.7.7.65 | T | PhoQ Sensor | |
MHMNNKED_00235 | 5.9e-69 | nudL | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
MHMNNKED_00236 | 6.3e-40 | iscA | S | Heme biosynthesis protein HemY | ||
MHMNNKED_00237 | 7.7e-85 | rnhA | 3.1.26.4 | L | Caulimovirus viroplasmin | |
MHMNNKED_00238 | 1.5e-77 | motB | N | Flagellar motor protein | ||
MHMNNKED_00239 | 7.1e-99 | motA | N | flagellar motor | ||
MHMNNKED_00241 | 8.3e-118 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
MHMNNKED_00242 | 1.9e-41 | |||||
MHMNNKED_00243 | 5.5e-258 | ilvD | 4.2.1.9 | E | Dehydratase family | |
MHMNNKED_00244 | 6.5e-107 | yocS | S | -transporter | ||
MHMNNKED_00245 | 2.3e-251 | ilvB | 2.2.1.6 | E | Acetolactate synthase | |
MHMNNKED_00246 | 3.6e-72 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
MHMNNKED_00247 | 5.6e-157 | ilvC | 1.1.1.86 | EH | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
MHMNNKED_00248 | 1.7e-113 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
MHMNNKED_00249 | 1.1e-216 | XK27_08635 | S | UPF0210 protein | ||
MHMNNKED_00250 | 2.3e-25 | gcvR | 1.1.1.3, 1.1.1.399, 1.1.1.95 | T | Belongs to the UPF0237 family | |
MHMNNKED_00252 | 1.2e-141 | galM | 2.7.1.6, 5.1.3.3 | G | Converts alpha-aldose to the beta-anomer | |
MHMNNKED_00253 | 2.2e-167 | msmK | P | Belongs to the ABC transporter superfamily | ||
MHMNNKED_00254 | 8.5e-85 | QT | PucR C-terminal helix-turn-helix domain | |||
MHMNNKED_00255 | 2e-66 | K | Transcriptional regulator | |||
MHMNNKED_00256 | 3.7e-71 | S | Protein of unknown function (DUF3298) | |||
MHMNNKED_00258 | 5.8e-41 | bp26 | S | Protein of unknown function (DUF541) | ||
MHMNNKED_00259 | 6.3e-19 | gerPE | S | Spore germination protein GerPE | ||
MHMNNKED_00260 | 6.2e-11 | gerPD | S | Spore germination protein | ||
MHMNNKED_00261 | 3.4e-32 | gerPC | S | Spore germination protein | ||
MHMNNKED_00262 | 5.2e-10 | gerPB | S | cell differentiation | ||
MHMNNKED_00263 | 7.9e-24 | gerPA | S | Spore germination protein | ||
MHMNNKED_00264 | 2.6e-89 | P | Protein of unknown function (DUF418) | |||
MHMNNKED_00265 | 9.4e-108 | yisK | Q | COG0179 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) | ||
MHMNNKED_00266 | 7.4e-16 | yisL | S | UPF0344 protein | ||
MHMNNKED_00267 | 1.6e-57 | yisN | S | Protein of unknown function (DUF2777) | ||
MHMNNKED_00268 | 1.8e-99 | amyA | 3.2.1.1 | GH13 | G | Alpha amylase, catalytic domain |
MHMNNKED_00269 | 1.7e-42 | yajQ | S | Belongs to the UPF0234 family | ||
MHMNNKED_00271 | 2.6e-118 | yitS | S | protein conserved in bacteria | ||
MHMNNKED_00272 | 1.2e-60 | K | Transcriptional regulator | |||
MHMNNKED_00273 | 8.5e-91 | ykoC | P | COG0619 ABC-type cobalt transport system, permease component CbiQ and related transporters | ||
MHMNNKED_00274 | 1.8e-218 | ykoD | 3.6.3.24 | P | ABC transporter | |
MHMNNKED_00275 | 5.7e-76 | ykoE | S | ABC-type cobalt transport system, permease component | ||
MHMNNKED_00276 | 5.8e-08 | S | Protein of unknown function (DUF3936) | |||
MHMNNKED_00277 | 2.8e-123 | yqkF | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | ||
MHMNNKED_00279 | 7.7e-11 | |||||
MHMNNKED_00280 | 3.7e-128 | yqkD | S | X-Pro dipeptidyl-peptidase (S15 family) | ||
MHMNNKED_00282 | 4.4e-26 | S | YolD-like protein | |||
MHMNNKED_00283 | 2.7e-201 | dinB2 | 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 | |
MHMNNKED_00284 | 4.6e-138 | hisC | 2.6.1.9 | E | Aminotransferase class I and II | |
MHMNNKED_00285 | 1.7e-85 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | belongs to the PRA-CH family | |
MHMNNKED_00286 | 1.6e-116 | hisF | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | ||
MHMNNKED_00287 | 3.2e-82 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
MHMNNKED_00288 | 4.9e-84 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
MHMNNKED_00289 | 1.2e-87 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
MHMNNKED_00290 | 1.7e-166 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
MHMNNKED_00291 | 1.5e-78 | hisG | 2.4.2.17 | E | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
MHMNNKED_00292 | 1.7e-118 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
MHMNNKED_00293 | 1.6e-56 | MA20_02285 | 2.3.1.57 | K | PFAM Acetyltransferase (GNAT) family | |
MHMNNKED_00294 | 3.2e-272 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Polyprenyl synthetase | |
MHMNNKED_00295 | 3.7e-179 | gltT | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
MHMNNKED_00296 | 1.3e-54 | yjbF | S | SNARE associated Golgi protein | ||
MHMNNKED_00297 | 1.7e-126 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase Family 4 |
MHMNNKED_00298 | 1.1e-42 | mcpB_1 | NT | chemotaxis protein | ||
MHMNNKED_00299 | 1.2e-102 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
MHMNNKED_00300 | 1.7e-08 | S | granule-associated protein | |||
MHMNNKED_00301 | 3e-46 | fld | C | Flavodoxin | ||
MHMNNKED_00302 | 1.5e-16 | S | Bacterial-like globin | |||
MHMNNKED_00303 | 7.1e-30 | |||||
MHMNNKED_00304 | 2.8e-163 | uhpT | EGP | Mycoplasma MFS transporter | ||
MHMNNKED_00305 | 2.9e-08 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
MHMNNKED_00306 | 6.8e-67 | K | Acetyltransferase (GNAT) domain | |||
MHMNNKED_00307 | 2.8e-100 | IQ | Short-chain dehydrogenase | |||
MHMNNKED_00308 | 2.3e-08 | |||||
MHMNNKED_00309 | 4.5e-69 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
MHMNNKED_00310 | 6e-46 | S | Protein of unknown function, DUF624 | |||
MHMNNKED_00311 | 7e-123 | malR | 5.1.1.1 | K | Transcriptional regulator | |
MHMNNKED_00312 | 2.4e-110 | amyC | P | ABC-type sugar transport system, permease component | ||
MHMNNKED_00313 | 3.9e-119 | G | Binding-protein-dependent transport system inner membrane component | |||
MHMNNKED_00314 | 5.9e-172 | G | Bacterial extracellular solute-binding protein | |||
MHMNNKED_00315 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
MHMNNKED_00316 | 1.8e-98 | pcrB | I | 35 carbon atoms) to the C3 hydroxyl of sn-glycerol-1-phosphate (G1P), producing heptaprenylglyceryl phosphate (HepGP). This reaction is an ether-bond-formation step in the biosynthesis of archaea-type G1P-based membrane lipids found in Bacillales | ||
MHMNNKED_00317 | 3.1e-40 | yerC | S | protein conserved in bacteria | ||
MHMNNKED_00318 | 1.1e-117 | yerB | S | Protein of unknown function (DUF3048) C-terminal domain | ||
MHMNNKED_00319 | 2.4e-76 | yerA | 3.5.4.2 | F | adenine deaminase | |
MHMNNKED_00320 | 8.6e-104 | KLT | serine threonine protein kinase | |||
MHMNNKED_00321 | 8.3e-94 | yabS | S | protein containing a von Willebrand factor type A (vWA) domain | ||
MHMNNKED_00322 | 1.8e-281 | spoIIE | 3.1.3.16 | KT | stage II sporulation protein E | |
MHMNNKED_00323 | 9.1e-50 | yabR | J | RNA binding protein (contains ribosomal protein S1 domain) | ||
MHMNNKED_00324 | 5.5e-15 | divIC | D | Septum formation initiator | ||
MHMNNKED_00325 | 2.7e-42 | yabQ | S | spore cortex biosynthesis protein | ||
MHMNNKED_00326 | 6.1e-43 | yabP | S | Sporulation protein YabP | ||
MHMNNKED_00327 | 2.2e-28 | yabO | J | COG1188 Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
MHMNNKED_00328 | 1.6e-197 | mazG | 3.6.1.66, 3.6.1.9 | S | COG3956 Protein containing tetrapyrrole methyltransferase domain and MazG-like | |
MHMNNKED_00329 | 4.8e-131 | yabM | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
MHMNNKED_00330 | 2e-81 | spoVT | K | stage V sporulation protein | ||
MHMNNKED_00331 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
MHMNNKED_00332 | 2.5e-25 | yabK | S | Peptide ABC transporter permease | ||
MHMNNKED_00333 | 3.2e-74 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
MHMNNKED_00334 | 2.4e-57 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
MHMNNKED_00335 | 1.1e-151 | 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) | |
MHMNNKED_00336 | 1.7e-188 | 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 | |
MHMNNKED_00337 | 6.9e-44 | spoVG | D | Essential for sporulation. Interferes with or is a negative regulator of the pathway leading to asymmetric septation | ||
MHMNNKED_00338 | 2e-125 | purR | 2.4.2.7 | F | pur operon repressor | |
MHMNNKED_00339 | 1.1e-129 | ispE | 2.1.1.182, 2.7.1.148 | I | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
MHMNNKED_00340 | 8.7e-49 | spoVAE | S | SpoVAC/SpoVAEB sporulation membrane protein | ||
MHMNNKED_00341 | 1e-150 | spoVAD | I | Stage V sporulation protein AD | ||
MHMNNKED_00342 | 1.7e-71 | spoVAC | S | stage V sporulation protein AC | ||
MHMNNKED_00343 | 2.5e-32 | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | |||
MHMNNKED_00344 | 1.9e-77 | ggaB | M | Glycosyltransferase like family 2 | ||
MHMNNKED_00345 | 1.8e-145 | M | Glycosyl transferases group 1 | |||
MHMNNKED_00346 | 4.1e-99 | 3.2.1.23 | G | Sulfotransferase family | ||
MHMNNKED_00347 | 1.3e-133 | M | Glycosyltransferase Family 4 | |||
MHMNNKED_00348 | 3.1e-61 | K | Belongs to the GbsR family | |||
MHMNNKED_00349 | 9.3e-172 | opuAA | 3.6.3.32 | E | Domain in cystathionine beta-synthase and other proteins. | |
MHMNNKED_00350 | 5.7e-115 | opuAB | E | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_00351 | 3.6e-120 | gbuC_2 | E | Substrate binding domain of ABC-type glycine betaine transport system | ||
MHMNNKED_00352 | 1.6e-211 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |||
MHMNNKED_00354 | 5.2e-127 | hcaT | 1.5.1.2 | EGP | Major facilitator Superfamily | |
MHMNNKED_00355 | 1.7e-199 | E | Sodium:solute symporter family | |||
MHMNNKED_00356 | 1.9e-58 | ymdB | S | Appr-1'-p processing enzyme | ||
MHMNNKED_00357 | 0.0 | clpB | 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 | ||
MHMNNKED_00358 | 2.6e-142 | EGP | Major facilitator Superfamily | |||
MHMNNKED_00359 | 1e-16 | S | Iron-sulphur cluster biosynthesis | |||
MHMNNKED_00360 | 1.7e-120 | pldB | 3.1.1.5 | I | Alpha beta hydrolase | |
MHMNNKED_00361 | 1.8e-144 | luxA | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
MHMNNKED_00363 | 3.2e-202 | ynbB | 4.4.1.1 | P | COG4100 Cystathionine beta-lyase family protein involved in aluminum resistance | |
MHMNNKED_00364 | 1.4e-170 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
MHMNNKED_00365 | 1e-136 | spoVK | O | stage V sporulation protein K | ||
MHMNNKED_00366 | 2.4e-28 | hfq | J | RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs | ||
MHMNNKED_00367 | 2.9e-128 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
MHMNNKED_00368 | 4.2e-197 | tlyC | S | Transporter associated domain | ||
MHMNNKED_00369 | 3.1e-35 | T | Universal stress protein family | |||
MHMNNKED_00370 | 2.5e-234 | ykoS | ||||
MHMNNKED_00371 | 1.9e-125 | ykoT | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
MHMNNKED_00372 | 3.8e-47 | 3.2.1.21 | GH3 | N | Listeria-Bacteroides repeat domain (List_Bact_rpt) | |
MHMNNKED_00373 | 2.3e-19 | |||||
MHMNNKED_00374 | 5.5e-104 | ysxE | S | A protein kinase that phosphorylates Ser and Thr residues. Probably acts to suppress the effects of stress linked to accumulation of reactive oxygen species. Probably involved in the extracytoplasmic stress response | ||
MHMNNKED_00375 | 3.8e-57 | spoVID | M | stage VI sporulation protein D | ||
MHMNNKED_00376 | 2.8e-206 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
MHMNNKED_00377 | 5.9e-156 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
MHMNNKED_00378 | 2.1e-71 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
MHMNNKED_00379 | 2.7e-126 | hemC | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps | |
MHMNNKED_00380 | 1.6e-77 | hemX | O | cytochrome C | ||
MHMNNKED_00381 | 4.4e-178 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
MHMNNKED_00382 | 3.8e-47 | ysxD | ||||
MHMNNKED_00383 | 2.1e-101 | rfbD | 1.1.1.133 | M | RmlD substrate binding domain | |
MHMNNKED_00384 | 5.9e-89 | gca | 1.1.1.281, 4.2.1.47, 5.1.3.2 | GM | GDP-mannose 4,6 dehydratase | |
MHMNNKED_00385 | 1.3e-74 | M | Glycosyltransferase like family 2 | |||
MHMNNKED_00386 | 1.5e-37 | ypmS | S | protein conserved in bacteria | ||
MHMNNKED_00387 | 3.2e-57 | ypmR | E | COG2755 Lysophospholipase L1 and related esterases | ||
MHMNNKED_00388 | 1.1e-67 | ypmQ | S | protein SCO1 SenC PrrC, involved in biogenesis of respiratory and photosynthetic systems | ||
MHMNNKED_00389 | 3.3e-91 | degV | S | protein conserved in bacteria | ||
MHMNNKED_00390 | 3.9e-82 | yoqW | S | Belongs to the SOS response-associated peptidase family | ||
MHMNNKED_00391 | 4.1e-65 | folA | 1.1.1.262, 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
MHMNNKED_00392 | 1.1e-139 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
MHMNNKED_00393 | 1.5e-65 | 3.4.24.89 | ||||
MHMNNKED_00394 | 1.2e-53 | ypjP | S | YpjP-like protein | ||
MHMNNKED_00395 | 2.5e-58 | yphP | S | Belongs to the UPF0403 family | ||
MHMNNKED_00396 | 2.4e-113 | ypgR | C | COG0694 Thioredoxin-like proteins and domains | ||
MHMNNKED_00397 | 7.7e-253 | yfmR | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
MHMNNKED_00398 | 1.4e-60 | ypgQ | S | phosphohydrolase | ||
MHMNNKED_00399 | 1.9e-36 | |||||
MHMNNKED_00400 | 3.9e-142 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
MHMNNKED_00401 | 1e-159 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
MHMNNKED_00402 | 2.5e-309 | 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 | ||
MHMNNKED_00403 | 4.4e-09 | NT | chemotaxis protein | |||
MHMNNKED_00404 | 4.7e-36 | 3.5.4.5 | S | ASCH | ||
MHMNNKED_00405 | 2.9e-70 | sleB | 3.5.1.28 | M | Cell wall | |
MHMNNKED_00406 | 1.7e-25 | |||||
MHMNNKED_00407 | 6.7e-94 | phaB | 5.3.3.14, 5.3.3.18 | I | Enoyl-CoA hydratase/isomerase | |
MHMNNKED_00408 | 4.3e-110 | yngG | 4.1.3.4 | E | Hydroxymethylglutaryl-CoA lyase | |
MHMNNKED_00409 | 1.6e-176 | C | acyl-CoA transferases carnitine dehydratase | |||
MHMNNKED_00410 | 1.7e-173 | I | Acyl-CoA dehydrogenase, C-terminal domain | |||
MHMNNKED_00411 | 8.7e-187 | yfkN | 3.1.3.5, 3.6.1.45 | F | COG0737 5'-nucleotidase 2',3'-cyclic phosphodiesterase and related esterases | |
MHMNNKED_00412 | 7.3e-75 | rocD | 2.6.1.11, 2.6.1.13, 2.6.1.17 | E | Catalyzes the interconversion of ornithine to glutamate semialdehyde | |
MHMNNKED_00413 | 2.1e-96 | T | Transcriptional regulatory protein, C terminal | |||
MHMNNKED_00414 | 4.8e-113 | T | PhoQ Sensor | |||
MHMNNKED_00415 | 6.9e-239 | acsA | 6.2.1.1, 6.2.1.2 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
MHMNNKED_00416 | 1.3e-65 | ymaD | O | redox protein, regulator of disulfide bond formation | ||
MHMNNKED_00417 | 2.4e-100 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
MHMNNKED_00418 | 1.1e-133 | T | PhoQ Sensor | |||
MHMNNKED_00419 | 5.1e-123 | V | ABC transporter, ATP-binding protein | |||
MHMNNKED_00420 | 4.9e-220 | V | ABC transporter (permease) | |||
MHMNNKED_00421 | 2e-78 | 5.1.1.12 | E | Alanine racemase, N-terminal domain | ||
MHMNNKED_00422 | 2.6e-92 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
MHMNNKED_00423 | 9.8e-117 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
MHMNNKED_00424 | 1.9e-95 | livF | E | Amino acid ABC transporter ATPase | ||
MHMNNKED_00425 | 2.2e-50 | lytE2 | M | Putative peptidoglycan binding domain | ||
MHMNNKED_00426 | 8.8e-66 | K | acetyltransferase | |||
MHMNNKED_00427 | 2.5e-203 | aspA | 4.2.1.2, 4.3.1.1 | E | Aspartate ammonia-lyase | |
MHMNNKED_00428 | 3.3e-42 | M | Lysin motif | |||
MHMNNKED_00429 | 3.8e-70 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
MHMNNKED_00430 | 2.9e-49 | mcpA | NT | Chemotaxis | ||
MHMNNKED_00431 | 2.6e-42 | ywlE | 3.1.3.48, 3.9.1.2, 5.3.1.6 | T | Low molecular weight phosphatase family | |
MHMNNKED_00432 | 7.2e-50 | mntP | P | Probably functions as a manganese efflux pump | ||
MHMNNKED_00433 | 1.3e-145 | 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 | |
MHMNNKED_00434 | 2.1e-71 | spoIIR | S | stage II sporulation protein R | ||
MHMNNKED_00435 | 3.2e-108 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
MHMNNKED_00436 | 9.3e-171 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
MHMNNKED_00437 | 4.4e-88 | tdk | 2.7.1.21 | F | thymidine kinase | |
MHMNNKED_00438 | 2.5e-104 | btuF | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
MHMNNKED_00439 | 4.2e-52 | S | Diphthamide synthase | |||
MHMNNKED_00440 | 4e-119 | yrdQ | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
MHMNNKED_00441 | 3.3e-127 | yrdR | EG | EamA-like transporter family | ||
MHMNNKED_00442 | 3.7e-196 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
MHMNNKED_00443 | 1.4e-98 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
MHMNNKED_00444 | 3.4e-94 | S | protein conserved in bacteria | |||
MHMNNKED_00445 | 1.1e-132 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
MHMNNKED_00447 | 1.2e-39 | S | Domain of unknown function (DUF3870) | |||
MHMNNKED_00448 | 4.2e-177 | S | Protein of unknown function (DUF819) | |||
MHMNNKED_00449 | 5.1e-145 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
MHMNNKED_00450 | 1.3e-158 | ykfC | 3.4.14.13 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
MHMNNKED_00451 | 2.4e-108 | purC | 6.3.2.6 | F | Phosphoribosylaminoimidazole-succinocarboxamide synthase | |
MHMNNKED_00452 | 6.8e-152 | ddh | 1.4.1.16 | E | Catalyzes the reversible NADPH-dependent reductive amination of L-2-amino-6-oxopimelate, the acyclic form of L- tetrahydrodipicolinate, to generate the meso compound, D,L-2,6- diaminopimelate | |
MHMNNKED_00453 | 8e-154 | 1.2.1.3 | C | Aldehyde dehydrogenase family | ||
MHMNNKED_00454 | 7.4e-45 | K | Acetyltransferase (GNAT) domain | |||
MHMNNKED_00455 | 2.1e-213 | XK27_10205 | ||||
MHMNNKED_00456 | 9.2e-33 | |||||
MHMNNKED_00457 | 2.9e-85 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
MHMNNKED_00458 | 6.8e-50 | 6.3.5.6, 6.3.5.7 | J | amidotransferase, A subunit | ||
MHMNNKED_00459 | 5.7e-81 | arsB | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
MHMNNKED_00460 | 5.1e-42 | arsB | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
MHMNNKED_00462 | 6.7e-112 | pstS | P | Phosphate | ||
MHMNNKED_00463 | 5.4e-133 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
MHMNNKED_00464 | 4.1e-116 | pstA | P | Phosphate transport system permease | ||
MHMNNKED_00465 | 1e-129 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
MHMNNKED_00466 | 1.7e-61 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
MHMNNKED_00467 | 2.6e-11 | yfhD | S | YfhD-like protein | ||
MHMNNKED_00469 | 2e-42 | recX | 2.4.1.337 | GT4 | S | Modulates RecA activity |
MHMNNKED_00470 | 5.1e-35 | yfhH | S | Protein of unknown function (DUF1811) | ||
MHMNNKED_00471 | 1.1e-14 | sspK | S | reproduction | ||
MHMNNKED_00472 | 1.4e-141 | yfhP | S | membrane-bound metal-dependent | ||
MHMNNKED_00473 | 2.3e-148 | mutY | L | A G-specific | ||
MHMNNKED_00474 | 7.7e-27 | yfhS | ||||
MHMNNKED_00475 | 6.2e-113 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
MHMNNKED_00477 | 1.4e-90 | ygaC | J | Belongs to the UPF0374 family | ||
MHMNNKED_00478 | 3.3e-258 | ygaD | V | ABC transporter | ||
MHMNNKED_00479 | 1.1e-126 | ygaE | S | Membrane | ||
MHMNNKED_00480 | 4.9e-19 | P | Ion transport | |||
MHMNNKED_00481 | 2.6e-69 | bcp | 1.11.1.15 | O | Peroxiredoxin | |
MHMNNKED_00482 | 1.4e-117 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MHMNNKED_00483 | 8.6e-72 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Adenosyltransferase | |
MHMNNKED_00484 | 3.6e-68 | perR | P | Belongs to the Fur family | ||
MHMNNKED_00485 | 3.6e-39 | ygzB | S | UPF0295 protein | ||
MHMNNKED_00486 | 1.8e-103 | ygxA | S | Nucleotidyltransferase-like | ||
MHMNNKED_00488 | 1e-14 | 2.3.1.128, 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
MHMNNKED_00489 | 2.4e-155 | yfiF5 | K | AraC-like ligand binding domain | ||
MHMNNKED_00490 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase | |
MHMNNKED_00491 | 1.3e-292 | gltD | 1.4.1.13, 1.4.1.14 | E | COG0493 NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
MHMNNKED_00492 | 2e-241 | dapL | 2.6.1.83 | E | Aminotransferase class I and II | |
MHMNNKED_00493 | 1.2e-171 | 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 | |
MHMNNKED_00494 | 2.5e-258 | glnA | 6.3.1.2 | E | glutamine synthetase | |
MHMNNKED_00495 | 0.0 | asnO | 6.3.5.4 | E | Asparagine synthase | |
MHMNNKED_00496 | 1.4e-229 | amtB | P | Ammonium transporter | ||
MHMNNKED_00497 | 1.4e-203 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
MHMNNKED_00498 | 1.6e-185 | 2.7.7.7 | T | Putative nucleotidyltransferase substrate binding domain | ||
MHMNNKED_00499 | 3.2e-122 | dnaQ2 | 2.7.7.7 | L | COG0847 DNA polymerase III, epsilon subunit and related 3'-5' exonucleases | |
MHMNNKED_00500 | 4.3e-251 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
MHMNNKED_00501 | 2e-107 | M1-161 | T | HD domain | ||
MHMNNKED_00502 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
MHMNNKED_00503 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
MHMNNKED_00504 | 5.4e-161 | 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 | ||
MHMNNKED_00505 | 2.1e-21 | yaaA | S | S4 domain | ||
MHMNNKED_00506 | 1.8e-164 | 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 | |
MHMNNKED_00507 | 4e-219 | 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 | ||
MHMNNKED_00508 | 2.2e-13 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
MHMNNKED_00509 | 9.4e-40 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
MHMNNKED_00510 | 1.2e-82 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
MHMNNKED_00511 | 3.1e-70 | jag | S | single-stranded nucleic acid binding R3H | ||
MHMNNKED_00512 | 3.2e-208 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
MHMNNKED_00513 | 1.5e-309 | 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 | ||
MHMNNKED_00514 | 1.2e-86 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of guanine in position 535 of 16S rRNA | |
MHMNNKED_00515 | 9e-116 | noc | D | Effects nucleoid occlusion by binding relatively nonspecifically to DNA and preventing the assembly of the division machinery in the vicinity of the nucleoid, especially under conditions that disturb the cell cycle. It helps to coordinate cell division and chromosome segregation by preventing the formation of the Z ring through the nucleoid, which would cause chromosome breakage | ||
MHMNNKED_00516 | 3e-123 | soj | D | COG1192 ATPases involved in chromosome partitioning | ||
MHMNNKED_00517 | 1.7e-119 | spo0J | K | Belongs to the ParB family | ||
MHMNNKED_00518 | 1.3e-80 | ydfK | S | Protein of unknown function (DUF554) | ||
MHMNNKED_00519 | 1.6e-82 | yyaC | S | Sporulation protein YyaC | ||
MHMNNKED_00520 | 2e-26 | yyzM | S | protein conserved in bacteria | ||
MHMNNKED_00521 | 1.4e-177 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
MHMNNKED_00522 | 3.3e-38 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
MHMNNKED_00523 | 1.3e-60 | 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 | ||
MHMNNKED_00524 | 4e-34 | 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 | ||
MHMNNKED_00525 | 2.4e-29 | |||||
MHMNNKED_00526 | 1.6e-33 | C | 4Fe-4S binding domain | |||
MHMNNKED_00527 | 1.9e-181 | mepA | V | MATE efflux family protein | ||
MHMNNKED_00528 | 1.9e-84 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
MHMNNKED_00529 | 1.8e-43 | gerD | S | Spore gernimation protein | ||
MHMNNKED_00530 | 3.7e-53 | kbaA | 2.7.8.43 | S | Involved in the activation of the KinB signaling pathway of sporulation | |
MHMNNKED_00531 | 1.6e-16 | gerPF | S | Spore germination protein gerPA/gerPF | ||
MHMNNKED_00532 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
MHMNNKED_00533 | 0.0 | addB | 3.1.21.3, 3.6.4.12 | L | ATP-dependent helicase deoxyribonuclease subunit B | |
MHMNNKED_00534 | 1.3e-66 | EGP | Major facilitator Superfamily | |||
MHMNNKED_00535 | 9.3e-70 | yhjE | S | SNARE associated Golgi protein | ||
MHMNNKED_00536 | 2.1e-45 | |||||
MHMNNKED_00537 | 5.7e-56 | comK | K | Competence transcription factor | ||
MHMNNKED_00538 | 4.9e-08 | S | IDEAL | |||
MHMNNKED_00539 | 3.6e-150 | yhfN | 3.4.24.84 | O | Peptidase M48 | |
MHMNNKED_00540 | 9.5e-28 | azlD | S | branched-chain amino acid | ||
MHMNNKED_00541 | 2.2e-19 | azlC | E | branched-chain amino acid | ||
MHMNNKED_00542 | 1.8e-21 | fliI | 3.6.3.14 | NU | COG1157 Flagellar biosynthesis type III secretory pathway ATPase | |
MHMNNKED_00543 | 1.2e-39 | fliJ | N | Flagellar biosynthesis chaperone | ||
MHMNNKED_00544 | 1.2e-07 | ylxF | S | MgtE intracellular N domain | ||
MHMNNKED_00545 | 2.3e-27 | fliK | N | Flagellar hook-length control | ||
MHMNNKED_00546 | 5.4e-49 | flgD | N | Flagellar basal body rod modification protein | ||
MHMNNKED_00547 | 2.1e-32 | flg | N | Putative flagellar | ||
MHMNNKED_00548 | 2.8e-72 | flgE | N | flagellar | ||
MHMNNKED_00549 | 3.6e-19 | flbD | N | protein, possibly involved in motility | ||
MHMNNKED_00550 | 1.7e-35 | fliL | N | Controls the rotational direction of flagella during chemotaxis | ||
MHMNNKED_00551 | 9.7e-138 | fliM | N | One of the proteins that forms a switch complex that is proposed to be located at the base of the basal body. This complex interacts with chemotaxis proteins (such as CheY) in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
MHMNNKED_00552 | 1.4e-130 | fliN | N | FliN is one of three proteins (FliG, FliN, FliM) that form the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
MHMNNKED_00553 | 1.3e-52 | cheY | T | Chemotaxis protein CheY | ||
MHMNNKED_00554 | 3.1e-31 | fliZ | N | Flagellar biosynthesis protein, FliO | ||
MHMNNKED_00555 | 5.1e-95 | fliP | N | Plays a role in the flagellum-specific transport system | ||
MHMNNKED_00556 | 1.2e-26 | fliQ | N | Role in flagellar biosynthesis | ||
MHMNNKED_00557 | 1.5e-88 | fliR | N | Flagellar biosynthetic protein FliR | ||
MHMNNKED_00558 | 1.3e-119 | flhB | N | Required for formation of the rod structure in the basal body of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
MHMNNKED_00559 | 9.6e-302 | flhA | N | Required for formation of the rod structure of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
MHMNNKED_00560 | 2.9e-114 | flhF | N | Flagellar biosynthesis regulator FlhF | ||
MHMNNKED_00561 | 8.9e-79 | flhG | D | Belongs to the ParA family | ||
MHMNNKED_00562 | 6.3e-119 | cheB | 3.1.1.61, 3.5.1.44 | NT | catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR | |
MHMNNKED_00563 | 3.6e-264 | cheA | 2.7.13.3 | NT | COG0643 Chemotaxis protein histidine kinase and related kinases | |
MHMNNKED_00564 | 2.3e-46 | cheW | NT | COG0835 Chemotaxis signal transduction protein | ||
MHMNNKED_00565 | 1e-71 | cheC | NT | COG1776 Chemotaxis protein CheC, inhibitor of MCP methylation | ||
MHMNNKED_00566 | 1.2e-59 | cheD | 3.5.1.44 | NT | Deamidates glutamine residues to glutamate on methyl- accepting chemotaxis receptors (MCPs). CheD-mediated MCP deamidation is required for productive communication of the conformational signals of the chemoreceptors to the CheA kinase | |
MHMNNKED_00567 | 1.9e-96 | sigD | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
MHMNNKED_00568 | 3.9e-13 | |||||
MHMNNKED_00569 | 3.5e-21 | ylxL | ||||
MHMNNKED_00570 | 1.8e-117 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
MHMNNKED_00571 | 4.3e-113 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
MHMNNKED_00572 | 1.2e-118 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
MHMNNKED_00573 | 2.2e-75 | 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 | ||
MHMNNKED_00574 | 4.4e-106 | uppS | 2.5.1.31 | I | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
MHMNNKED_00575 | 3.5e-90 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
MHMNNKED_00576 | 1.5e-155 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
MHMNNKED_00577 | 3.2e-186 | rasP | M | zinc metalloprotease | ||
MHMNNKED_00578 | 1.6e-262 | 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 | |
MHMNNKED_00579 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
MHMNNKED_00580 | 7.2e-67 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
MHMNNKED_00581 | 9.7e-182 | nusA | K | Participates in both transcription termination and antitermination | ||
MHMNNKED_00582 | 2.3e-36 | ylxR | K | nucleic-acid-binding protein implicated in transcription termination | ||
MHMNNKED_00583 | 1.3e-32 | ylxQ | J | ribosomal protein | ||
MHMNNKED_00584 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
MHMNNKED_00585 | 1.6e-29 | ylxP | S | Protein of unknown function (DUF503) | ||
MHMNNKED_00586 | 2.8e-47 | 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 | ||
MHMNNKED_00587 | 9.7e-119 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
MHMNNKED_00588 | 2.8e-118 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
MHMNNKED_00589 | 1.2e-39 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
MHMNNKED_00590 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
MHMNNKED_00591 | 1.6e-126 | ylxY | 3.5.1.104 | G | Sporulation protein, polysaccharide deacetylase | |
MHMNNKED_00592 | 2.6e-20 | pgp-8 | 3.6.3.44 | Q | ATPase activity, coupled to transmembrane movement of substances | |
MHMNNKED_00593 | 7.1e-154 | ymfD | EGP | Major facilitator Superfamily | ||
MHMNNKED_00594 | 4.4e-55 | yheN | G | deacetylase | ||
MHMNNKED_00595 | 2.5e-29 | K | Cold shock | |||
MHMNNKED_00596 | 3.9e-162 | EG | Bacillus/Clostridium GerA spore germination protein | |||
MHMNNKED_00597 | 1.8e-76 | E | Spore germination protein | |||
MHMNNKED_00598 | 5.9e-86 | S | Spore germination B3/ GerAC like, C-terminal | |||
MHMNNKED_00600 | 2.7e-117 | ku | L | With LigD forms a non-homologous end joining (NHEJ) DNA repair enzyme, which repairs dsDNA breaks with reduced fidelity. Binds linear dsDNA with 5'- and 3'- overhangs but not closed circular dsDNA nor ssDNA. Recruits and stimulates the ligase activity of LigD | ||
MHMNNKED_00601 | 3.7e-228 | ligD | 6.5.1.1 | L | ATP-dependent DNA ligase | |
MHMNNKED_00602 | 2.6e-53 | CO | alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen | |||
MHMNNKED_00604 | 5.3e-211 | araP | EGP | Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family | ||
MHMNNKED_00605 | 3.7e-256 | araB | 2.7.1.16 | G | Sugar (pentulose and hexulose) kinases | |
MHMNNKED_00606 | 1.8e-161 | araR | K | helix_turn_helix gluconate operon transcriptional repressor | ||
MHMNNKED_00607 | 6e-108 | tcyC | 3.6.3.21 | E | AAA domain, putative AbiEii toxin, Type IV TA system | |
MHMNNKED_00608 | 9e-74 | tcyB | P | COG0765 ABC-type amino acid transport system, permease component | ||
MHMNNKED_00609 | 2e-96 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
MHMNNKED_00610 | 3.8e-143 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
MHMNNKED_00612 | 4.1e-22 | P | Copper resistance protein CopZ | |||
MHMNNKED_00613 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
MHMNNKED_00614 | 5.4e-39 | csoR | S | Metal-sensitive transcriptional repressor | ||
MHMNNKED_00615 | 1e-196 | 1.7.2.1 | Q | Multicopper oxidase | ||
MHMNNKED_00616 | 2.6e-99 | yycG_2 | T | Histidine kinase | ||
MHMNNKED_00617 | 3.6e-290 | G | Right handed beta helix region | |||
MHMNNKED_00618 | 0.0 | licR | 2.7.1.202 | K | transcriptional regulator, MtlR | |
MHMNNKED_00619 | 2.2e-144 | E | Peptidase dimerisation domain | |||
MHMNNKED_00620 | 1.8e-128 | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | Peptidase family M28 | ||
MHMNNKED_00621 | 3.4e-114 | KT | transcriptional regulatory protein | |||
MHMNNKED_00622 | 2.8e-199 | abgB | S | amidohydrolase | ||
MHMNNKED_00623 | 2.6e-227 | abgT | H | AbgT putative transporter family | ||
MHMNNKED_00624 | 6.5e-171 | abgA | S | Peptidase dimerisation domain | ||
MHMNNKED_00626 | 7.3e-101 | ord | 1.4.1.12, 1.4.1.16, 1.4.1.26 | S | Dihydrodipicolinate reductase, N-terminus | |
MHMNNKED_00627 | 9.7e-92 | K | Transcriptional regulator | |||
MHMNNKED_00628 | 5.6e-48 | S | Uncharacterized protein conserved in bacteria (DUF2200) | |||
MHMNNKED_00630 | 3.6e-227 | MA20_18835 | IQ | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | ||
MHMNNKED_00631 | 3.2e-24 | bofA | S | Sigma-K factor-processing regulatory protein BofA | ||
MHMNNKED_00632 | 7.8e-11 | yaaL | S | Protein of unknown function (DUF2508) | ||
MHMNNKED_00633 | 2.1e-100 | 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 | ||
MHMNNKED_00634 | 2.3e-32 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
MHMNNKED_00635 | 5.1e-232 | 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 | |
MHMNNKED_00636 | 2.7e-64 | tadA | 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
MHMNNKED_00637 | 6.3e-182 | yaaH | M | Glycoside Hydrolase Family | ||
MHMNNKED_00638 | 7.9e-69 | dgk | 2.7.1.113 | F | deoxyguanosine kinase | |
MHMNNKED_00639 | 1.3e-101 | dck | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxycytidine kinase | |
MHMNNKED_00640 | 1.5e-08 | |||||
MHMNNKED_00641 | 1.1e-191 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
MHMNNKED_00642 | 6.5e-166 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
MHMNNKED_00643 | 2.2e-247 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
MHMNNKED_00644 | 1.6e-100 | yaaC | S | YaaC-like Protein | ||
MHMNNKED_00645 | 8.1e-132 | mviM | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
MHMNNKED_00646 | 2.2e-47 | yoaS | S | Protein of unknown function (DUF2975) | ||
MHMNNKED_00647 | 6.7e-28 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
MHMNNKED_00648 | 9.2e-79 | S | Protein of unknown function (DUF1657) | |||
MHMNNKED_00649 | 8.6e-22 | S | Domain of unknown function (DUF4363) | |||
MHMNNKED_00650 | 5.8e-09 | spoIIIAF | S | Stage III sporulation protein AF (Spore_III_AF) | ||
MHMNNKED_00651 | 3.2e-73 | spoIIIAG | S | stage III sporulation protein AG | ||
MHMNNKED_00652 | 2.7e-49 | spoIIIAH | S | SpoIIIAH-like protein | ||
MHMNNKED_00653 | 9.3e-47 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
MHMNNKED_00654 | 1.8e-227 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
MHMNNKED_00655 | 9.2e-52 | yqhY | S | protein conserved in bacteria | ||
MHMNNKED_00656 | 8.5e-37 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
MHMNNKED_00657 | 4.7e-117 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
MHMNNKED_00658 | 2.4e-163 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
MHMNNKED_00659 | 5.6e-12 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
MHMNNKED_00660 | 1e-114 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
MHMNNKED_00661 | 1.6e-303 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
MHMNNKED_00662 | 7.2e-118 | rrmJ | 2.1.1.226, 2.1.1.227 | J | rRNA methylase | |
MHMNNKED_00663 | 2.5e-61 | argR | K | Regulates arginine biosynthesis genes | ||
MHMNNKED_00664 | 5.2e-200 | recN | L | May be involved in recombinational repair of damaged DNA | ||
MHMNNKED_00665 | 1.5e-175 | rseP | 3.4.21.116 | M | Stage IV sporulation protein B | |
MHMNNKED_00666 | 4.7e-111 | KT | May play the central regulatory role in sporulation. It may be an element of the effector pathway responsible for the activation of sporulation genes in response to nutritional stress. Spo0A may act in concert with spo0H (a sigma factor) to control the expression of some genes that are critical to the sporulation process | |||
MHMNNKED_00667 | 7.2e-90 | yqiK | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
MHMNNKED_00668 | 2.2e-16 | yqzF | S | Protein of unknown function (DUF2627) | ||
MHMNNKED_00669 | 3.1e-205 | bkdR | KT | Transcriptional regulator | ||
MHMNNKED_00670 | 1.1e-166 | ldh | 1.4.1.9 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
MHMNNKED_00671 | 1.3e-183 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
MHMNNKED_00672 | 7.6e-143 | bfmBAA | 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
MHMNNKED_00673 | 1.3e-171 | bfmBAB | 1.2.4.4 | C | Transketolase, pyrimidine binding domain | |
MHMNNKED_00674 | 4.9e-158 | bfmBB | 2.3.1.168, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
MHMNNKED_00675 | 6.4e-138 | mutA | 2.7.7.7, 5.4.99.2, 5.4.99.63 | I | COG1884 Methylmalonyl-CoA mutase, N-terminal domain subunit | |
MHMNNKED_00676 | 0.0 | mutB | 5.4.99.2 | I | COG1884 Methylmalonyl-CoA mutase, N-terminal domain subunit | |
MHMNNKED_00677 | 4.4e-146 | argK | E | periplasmic protein kinase ArgK and related GTPases of G3E family | ||
MHMNNKED_00678 | 3.3e-65 | yqjB | S | protein conserved in bacteria | ||
MHMNNKED_00680 | 2.8e-65 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
MHMNNKED_00681 | 0.0 | S | Dynamin family | |||
MHMNNKED_00682 | 1.9e-79 | polA | 2.7.7.7 | L | 5'3' exonuclease | |
MHMNNKED_00683 | 3.1e-97 | yxkD | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
MHMNNKED_00684 | 8.6e-10 | sspL | ||||
MHMNNKED_00685 | 2.4e-52 | rnhA | 3.1.26.4 | L | Ribonuclease | |
MHMNNKED_00686 | 8e-159 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
MHMNNKED_00687 | 5.3e-82 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
MHMNNKED_00688 | 8.3e-298 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
MHMNNKED_00689 | 7.2e-117 | coaX | 2.7.1.33 | F | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
MHMNNKED_00690 | 1.2e-131 | 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 | ||
MHMNNKED_00691 | 7.5e-145 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
MHMNNKED_00692 | 2.2e-47 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
MHMNNKED_00693 | 2.5e-49 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
MHMNNKED_00694 | 4.9e-158 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
MHMNNKED_00695 | 1.4e-254 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
MHMNNKED_00696 | 5.2e-94 | tpiA | 2.7.2.3, 5.1.3.39, 5.3.1.1, 5.3.1.33 | G | Triosephosphate isomerase | |
MHMNNKED_00697 | 1e-79 | dhaL | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | S | Dak2 | |
MHMNNKED_00698 | 5.1e-134 | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase DhaK, subunit | ||
MHMNNKED_00699 | 2.2e-244 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
MHMNNKED_00700 | 4.3e-116 | araD | 4.1.2.17, 5.1.3.4 | G | COG0235 Ribulose-5-phosphate 4-epimerase and related epimerases and aldolases | |
MHMNNKED_00702 | 1.1e-276 | hsdR | 3.1.21.3 | L | DEAD DEAH box helicase | |
MHMNNKED_00703 | 1.3e-20 | tctC | S | Tripartite tricarboxylate transporter family receptor | ||
MHMNNKED_00704 | 7.9e-131 | prpB | 4.1.3.30 | G | Catalyzes the thermodynamically favored C-C bond cleavage of (2R,3S)-2-methylisocitrate to yield pyruvate and succinate | |
MHMNNKED_00705 | 5.2e-236 | S | Tripartite tricarboxylate transporter TctA family | |||
MHMNNKED_00706 | 1.6e-52 | S | Tripartite tricarboxylate transporter TctB family | |||
MHMNNKED_00707 | 5.9e-83 | citT | T | response regulator | ||
MHMNNKED_00708 | 7.3e-156 | citS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
MHMNNKED_00709 | 2.8e-50 | abrB | S | Transition state regulatory protein AbrB | ||
MHMNNKED_00710 | 1.9e-76 | yfkM | 3.5.1.124 | S | protease | |
MHMNNKED_00711 | 3.7e-70 | ywaF | S | Integral membrane protein | ||
MHMNNKED_00712 | 3.1e-61 | plsB | 2.3.1.15 | I | Acyl-transferase | |
MHMNNKED_00713 | 5.3e-64 | 2.4.1.83 | GT2 | M | glycosyl transferase family 2 | |
MHMNNKED_00714 | 3.1e-83 | mhqD | S | Phospholipase/Carboxylesterase | ||
MHMNNKED_00715 | 7.3e-285 | pepF2 | E | COG1164 Oligoendopeptidase F | ||
MHMNNKED_00716 | 3.5e-175 | 2.6.1.113 | H | Aminotransferase class-III | ||
MHMNNKED_00717 | 5.1e-201 | E | Amino acid permease | |||
MHMNNKED_00718 | 7.7e-53 | ysmB | 2.4.2.28 | K | transcriptional | |
MHMNNKED_00719 | 2.4e-110 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
MHMNNKED_00720 | 2.1e-119 | gerM | S | COG5401 Spore germination protein | ||
MHMNNKED_00721 | 2.8e-81 | K | Acetyltransferase (GNAT) domain | |||
MHMNNKED_00722 | 8e-73 | FG | adenosine 5'-monophosphoramidase activity | |||
MHMNNKED_00724 | 1.6e-149 | cstA_2 | T | Carbon starvation protein | ||
MHMNNKED_00725 | 2.1e-89 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
MHMNNKED_00726 | 3.9e-49 | E | bleomycin resistance protein | |||
MHMNNKED_00728 | 1.8e-127 | yeaN | P | COG2807 Cyanate permease | ||
MHMNNKED_00729 | 5.9e-73 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
MHMNNKED_00730 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
MHMNNKED_00731 | 4.2e-83 | yegQ | O | Peptidase U32 | ||
MHMNNKED_00732 | 2e-196 | yegQ | O | COG0826 Collagenase and related proteases | ||
MHMNNKED_00733 | 2.6e-96 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
MHMNNKED_00734 | 2.7e-69 | 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 | ||
MHMNNKED_00735 | 2.2e-233 | pbpI | 3.4.16.4 | M | Penicillin-binding Protein | |
MHMNNKED_00736 | 8.4e-43 | yrrS | S | Protein of unknown function (DUF1510) | ||
MHMNNKED_00737 | 1.3e-88 | 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 | |
MHMNNKED_00739 | 3.9e-112 | sigK | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
MHMNNKED_00740 | 3e-69 | yqeG | S | hydrolase of the HAD superfamily | ||
MHMNNKED_00741 | 1.5e-187 | yqeH | S | In Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
MHMNNKED_00742 | 3.5e-72 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
MHMNNKED_00743 | 5.1e-39 | yhbY | J | RNA-binding protein containing KH domain, possibly ribosomal protein | ||
MHMNNKED_00744 | 3.1e-80 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
MHMNNKED_00745 | 2.4e-69 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
MHMNNKED_00746 | 2.9e-52 | 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 | ||
MHMNNKED_00747 | 9.8e-87 | yqeM | Q | Methyltransferase | ||
MHMNNKED_00748 | 2.6e-91 | comER | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | ||
MHMNNKED_00749 | 2.9e-147 | agcS | E | Sodium alanine symporter | ||
MHMNNKED_00750 | 2.5e-90 | 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 | |
MHMNNKED_00751 | 1.7e-49 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
MHMNNKED_00752 | 1.2e-110 | opuAC | E | Glycine betaine ABC transporter | ||
MHMNNKED_00753 | 3.8e-105 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
MHMNNKED_00754 | 5.8e-32 | tetR7 | K | Bacterial regulatory proteins, tetR family | ||
MHMNNKED_00755 | 2.1e-12 | tetR7 | K | Bacterial regulatory proteins, tetR family | ||
MHMNNKED_00756 | 7.2e-124 | EG | EamA-like transporter family | |||
MHMNNKED_00757 | 3.7e-193 | lytS | 2.7.13.3 | T | Histidine kinase | |
MHMNNKED_00758 | 2e-76 | lytT | T | COG3279 Response regulator of the LytR AlgR family | ||
MHMNNKED_00759 | 3.5e-279 | cstA_2 | T | Carbon starvation protein | ||
MHMNNKED_00760 | 1.3e-108 | XK27_05795 | ET | Ligated ion channel L-glutamate- and glycine-binding site | ||
MHMNNKED_00761 | 3.6e-89 | XK27_05795 | E | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_00762 | 1e-94 | clpP | 3.4.21.92 | OU | 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 | |
MHMNNKED_00763 | 5.4e-24 | crh | G | Phosphocarrier protein Chr | ||
MHMNNKED_00764 | 4.2e-135 | whiA | K | May be required for sporulation | ||
MHMNNKED_00765 | 3.1e-141 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
MHMNNKED_00766 | 7.5e-134 | rapZ | S | Displays ATPase and GTPase activities | ||
MHMNNKED_00767 | 2.7e-55 | yvcI | 3.6.1.55 | F | Nudix hydrolase | |
MHMNNKED_00768 | 5.4e-162 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
MHMNNKED_00769 | 1.2e-95 | S | COG0457 FOG TPR repeat | |||
MHMNNKED_00770 | 1.2e-94 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
MHMNNKED_00771 | 4.6e-229 | hpaB | 1.14.14.9 | Q | 4-hydroxyphenylacetate 3-hydroxylase C terminal | |
MHMNNKED_00772 | 1.3e-55 | S | Flavin reductase like domain | |||
MHMNNKED_00773 | 5.2e-144 | hpaD | 1.13.11.2 | E | Glyoxalase bleomycin resistance protein dioxygenase | |
MHMNNKED_00774 | 3.8e-121 | G | COG1638 TRAP-type C4-dicarboxylate transport system, periplasmic component | |||
MHMNNKED_00775 | 2.4e-36 | Q | Tripartite ATP-independent periplasmic transporters, DctQ component | |||
MHMNNKED_00776 | 2.1e-164 | G | Tripartite ATP-independent periplasmic transporter, DctM component | |||
MHMNNKED_00777 | 1.1e-73 | K | FCD domain | |||
MHMNNKED_00779 | 2.4e-225 | hpaE | 1.2.1.60 | C | Catalyzes the formation of betaine from betaine aldehyde | |
MHMNNKED_00780 | 2.8e-139 | dapA | 4.3.3.7 | E | Dihydrodipicolinate synthetase family | |
MHMNNKED_00781 | 1e-81 | hpaG1 | 4.1.1.68 | Q | Fumarylacetoacetate (FAA) hydrolase family | |
MHMNNKED_00782 | 4.6e-108 | hpaG | 4.1.1.68 | Q | 4-hydroxyphenylacetate degradation bifunctional isomerase | |
MHMNNKED_00783 | 4.8e-45 | hpcD | 4.1.1.68, 5.3.3.10 | E | 5-carboxymethyl-2-hydroxymuconate isomerase | |
MHMNNKED_00784 | 4.3e-282 | EU | Dienelactone hydrolase family | |||
MHMNNKED_00785 | 1.6e-155 | norA | EGP | Major facilitator Superfamily | ||
MHMNNKED_00786 | 3.6e-27 | S | YusW-like protein | |||
MHMNNKED_00787 | 1e-113 | spoIID | D | Stage II sporulation protein D | ||
MHMNNKED_00788 | 1.7e-38 | S | VanZ like family | |||
MHMNNKED_00789 | 1.6e-85 | spoIIQ | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
MHMNNKED_00790 | 1.9e-73 | yodN | ||||
MHMNNKED_00791 | 5.3e-20 | yozE | S | Belongs to the UPF0346 family | ||
MHMNNKED_00793 | 1.7e-70 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
MHMNNKED_00794 | 6.1e-78 | 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 | |
MHMNNKED_00795 | 9.5e-253 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
MHMNNKED_00796 | 1.5e-157 | des | 1.14.19.23, 1.14.19.45 | I | fatty acid desaturase | |
MHMNNKED_00797 | 3.8e-127 | desK | 2.7.13.3 | T | Histidine kinase | |
MHMNNKED_00798 | 5.5e-31 | bofC | S | BofC C-terminal domain | ||
MHMNNKED_00799 | 7.4e-08 | safA | M | spore coat assembly protein SafA | ||
MHMNNKED_00800 | 9.9e-186 | yisQ | V | Mate efflux family protein | ||
MHMNNKED_00801 | 6.8e-84 | S | Domain of unknown function (DUF1906) | |||
MHMNNKED_00802 | 7.7e-224 | cstA | T | Carbon starvation protein | ||
MHMNNKED_00804 | 4.4e-134 | 2.1.1.72, 3.1.21.3 | AA10,CBM73 | L | Belongs to the N(4) N(6)-methyltransferase family | |
MHMNNKED_00806 | 9.1e-07 | |||||
MHMNNKED_00807 | 3e-120 | yjbB | G | Major Facilitator Superfamily | ||
MHMNNKED_00808 | 1.7e-39 | flgN | NOU | FlgN protein | ||
MHMNNKED_00809 | 1.9e-24 | flgM | N | factor) FlgM | ||
MHMNNKED_00810 | 6.6e-48 | yvyF | S | flagellar protein | ||
MHMNNKED_00811 | 2.7e-76 | comFC | S | Phosphoribosyl transferase domain | ||
MHMNNKED_00812 | 1.6e-65 | S | Nuclease-related domain | |||
MHMNNKED_00813 | 6.8e-212 | comFA | L | COG4098 Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
MHMNNKED_00814 | 6.5e-119 | degV | S | protein conserved in bacteria | ||
MHMNNKED_00815 | 4.9e-104 | degU | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
MHMNNKED_00816 | 2.6e-139 | degS | 2.7.13.3 | T | Member of the two-component regulatory system DegS DegU, which plays an important role in the transition growth phase | |
MHMNNKED_00817 | 3.2e-94 | yvyE | 3.4.13.9 | S | Domain of unknown function (DUF1949) | |
MHMNNKED_00818 | 1e-115 | K | Transcriptional regulator | |||
MHMNNKED_00819 | 2.9e-114 | galU | 2.7.7.9 | M | Nucleotidyl transferase | |
MHMNNKED_00821 | 2.2e-123 | lytR | K | May catalyze the final step in cell wall teichoic acid biosynthesis, the transfer of the anionic cell wall polymers (APs) from their lipid-linked precursor to the cell wall peptidoglycan (PG) | ||
MHMNNKED_00822 | 1.8e-146 | CP | COG1668 ABC-type Na efflux pump, permease component | |||
MHMNNKED_00823 | 2.9e-131 | ecsA_1 | S | ABC transporter, ATP-binding protein | ||
MHMNNKED_00825 | 1.8e-100 | V | abc transporter atp-binding protein | |||
MHMNNKED_00826 | 1.9e-41 | yvoA_1 | K | GntR family transcriptional regulator | ||
MHMNNKED_00827 | 3.6e-158 | sucB | 2.3.1.61 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) | |
MHMNNKED_00828 | 0.0 | odhA | 1.2.4.2 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of three enzymatic components 2- oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3) | |
MHMNNKED_00829 | 8e-234 | iolA | 1.2.1.18, 1.2.1.27 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
MHMNNKED_00830 | 2.1e-172 | EG | COG2610 H gluconate symporter and related permeases | |||
MHMNNKED_00831 | 1.5e-97 | adhB | 1.1.1.1, 1.1.1.202 | C | alcohol dehydrogenase | |
MHMNNKED_00832 | 6.6e-24 | S | Spore germination B3/ GerAC like, C-terminal | |||
MHMNNKED_00833 | 7e-109 | M | Peptidase family S41 | |||
MHMNNKED_00834 | 6.3e-40 | lutA | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
MHMNNKED_00835 | 1.5e-216 | lutB | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. Has probably a role as an electron transporter during oxidation of L-lactate | ||
MHMNNKED_00836 | 3.5e-70 | lutC | S | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
MHMNNKED_00837 | 3.1e-82 | rodA | D | Belongs to the SEDS family | ||
MHMNNKED_00838 | 2.4e-12 | |||||
MHMNNKED_00839 | 1.6e-179 | nrnB | S | phosphohydrolase (DHH superfamily) | ||
MHMNNKED_00840 | 1.5e-88 | 3.5.3.11 | E | Belongs to the arginase family | ||
MHMNNKED_00841 | 5.6e-28 | |||||
MHMNNKED_00842 | 2e-238 | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | |||
MHMNNKED_00843 | 1.5e-64 | S | Divergent PAP2 family | |||
MHMNNKED_00844 | 1.7e-49 | S | Threonine/Serine exporter, ThrE | |||
MHMNNKED_00845 | 9.1e-88 | thrE | S | Putative threonine/serine exporter | ||
MHMNNKED_00846 | 1.1e-46 | queT | S | QueT transporter | ||
MHMNNKED_00847 | 1.3e-47 | S | Bacterial PH domain | |||
MHMNNKED_00848 | 3.1e-166 | hemY2 | 1.3.3.15, 1.3.3.4 | H | Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX | |
MHMNNKED_00849 | 5.7e-58 | M1-874 | K | Domain of unknown function (DUF1836) | ||
MHMNNKED_00850 | 5.4e-81 | yplQ | S | protein, Hemolysin III | ||
MHMNNKED_00851 | 0.0 | L | ABC transporter | |||
MHMNNKED_00852 | 3.7e-183 | hssS | 2.7.13.3 | T | PhoQ Sensor | |
MHMNNKED_00853 | 8.6e-109 | T | Transcriptional regulatory protein, C terminal | |||
MHMNNKED_00854 | 6e-188 | spaC2 | V | Lanthionine synthetase C-like protein | ||
MHMNNKED_00855 | 9.9e-236 | spaT | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
MHMNNKED_00858 | 2.6e-50 | aprE | 3.4.21.62 | M | Belongs to the peptidase S8 family | |
MHMNNKED_00859 | 4.7e-14 | M | COG3209 Rhs family protein | |||
MHMNNKED_00860 | 1.1e-23 | S | Protein of unknown function (DUF2283) | |||
MHMNNKED_00861 | 5.8e-77 | 4.4.1.3 | S | Cupin | ||
MHMNNKED_00862 | 5.7e-99 | S | Uncharacterized protein conserved in bacteria (DUF2179) | |||
MHMNNKED_00863 | 2.8e-28 | cspD | K | 'Cold-shock' DNA-binding domain | ||
MHMNNKED_00864 | 5e-150 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
MHMNNKED_00865 | 2.7e-61 | ydaC | Q | Methyltransferase domain | ||
MHMNNKED_00866 | 2e-121 | S | DNA/RNA non-specific endonuclease | |||
MHMNNKED_00867 | 8.8e-73 | proA_2 | H | Methyltransferase | ||
MHMNNKED_00868 | 1.1e-52 | S | UPF0316 protein | |||
MHMNNKED_00869 | 1.1e-18 | rplGB | J | Belongs to the eukaryotic ribosomal protein eL8 family | ||
MHMNNKED_00870 | 3.1e-66 | 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 | ||
MHMNNKED_00871 | 1.1e-80 | 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 | ||
MHMNNKED_00872 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
MHMNNKED_00873 | 3e-210 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
MHMNNKED_00874 | 4.9e-219 | 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 | ||
MHMNNKED_00875 | 1.4e-42 | spo0B | T | Sporulation initiation phospho-transferase B, C-terminal | ||
MHMNNKED_00876 | 2e-43 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
MHMNNKED_00877 | 3.4e-39 | ysxB | J | ribosomal protein | ||
MHMNNKED_00878 | 5.1e-37 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
MHMNNKED_00879 | 3.3e-147 | rng | J | ribonuclease, Rne Rng family | ||
MHMNNKED_00880 | 8.8e-79 | spoIVFB | S | Peptidase family M50 | ||
MHMNNKED_00881 | 3.2e-80 | spoIVFA | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
MHMNNKED_00883 | 1.1e-116 | ykgA | E | Amidinotransferase | ||
MHMNNKED_00884 | 4.1e-123 | minD | D | Belongs to the ParA family | ||
MHMNNKED_00885 | 6.3e-72 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
MHMNNKED_00886 | 3.8e-40 | mreD | M | shape-determining protein | ||
MHMNNKED_00887 | 9.8e-105 | mreC | M | Involved in formation and maintenance of cell shape | ||
MHMNNKED_00888 | 1.3e-161 | mreB | D | Rod shape-determining protein MreB | ||
MHMNNKED_00889 | 9.8e-102 | radC | E | Belongs to the UPF0758 family | ||
MHMNNKED_00890 | 3e-59 | maf | D | septum formation protein Maf | ||
MHMNNKED_00891 | 4.8e-17 | spoIIB | ||||
MHMNNKED_00892 | 2.2e-26 | M | RHS repeat-associated core domain protein | |||
MHMNNKED_00894 | 1.7e-119 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
MHMNNKED_00895 | 3.1e-146 | ykuI | T | Diguanylate phosphodiesterase | ||
MHMNNKED_00896 | 2e-50 | NT | chemotaxis protein | |||
MHMNNKED_00897 | 7.9e-130 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
MHMNNKED_00898 | 7.6e-09 | |||||
MHMNNKED_00899 | 7.9e-117 | S | Polysaccharide biosynthesis protein | |||
MHMNNKED_00900 | 9.1e-50 | G | WxcM-like, C-terminal | |||
MHMNNKED_00901 | 1.2e-41 | S | Aminoglycoside phosphotransferase | |||
MHMNNKED_00902 | 1.3e-64 | comB | 3.1.3.71 | H | 2-phosphosulpholactate phosphatase | |
MHMNNKED_00903 | 1.1e-110 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
MHMNNKED_00904 | 1.1e-128 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
MHMNNKED_00905 | 4.7e-108 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
MHMNNKED_00906 | 6e-94 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
MHMNNKED_00907 | 4e-151 | livK | E | Receptor family ligand binding region | ||
MHMNNKED_00908 | 1.2e-216 | yhfW | CE | COG0665 Glycine D-amino acid oxidases (deaminating) | ||
MHMNNKED_00909 | 8.2e-243 | ftsA | D | Cell division protein FtsA | ||
MHMNNKED_00910 | 1.5e-159 | ccpA | K | catabolite control protein A | ||
MHMNNKED_00911 | 9.9e-101 | motA | N | flagellar motor | ||
MHMNNKED_00912 | 5.6e-85 | motS | N | Flagellar motor protein | ||
MHMNNKED_00913 | 2.4e-151 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Also phosphorylates dephosphorylates the HPr-like catabolite repression protein crh on a specific serine residue. Therefore, by controlling the phosphorylation state of HPr and crh, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
MHMNNKED_00914 | 1.8e-71 | yvlB | S | Putative adhesin | ||
MHMNNKED_00915 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
MHMNNKED_00916 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
MHMNNKED_00917 | 4.3e-15 | csbA | S | Uncharacterized protein conserved in bacteria (DUF2198) | ||
MHMNNKED_00918 | 1.2e-84 | yjcH | P | COG2382 Enterochelin esterase and related enzymes | ||
MHMNNKED_00919 | 1.1e-67 | yjcG | J | Belongs to the 2H phosphoesterase superfamily. YjcG family | ||
MHMNNKED_00921 | 1.2e-31 | spoVIF | S | Stage VI sporulation protein F | ||
MHMNNKED_00922 | 1.7e-287 | mcpC | NT | Cache domain | ||
MHMNNKED_00923 | 2.5e-288 | 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) | |
MHMNNKED_00924 | 7.1e-229 | glnA | 6.3.1.2 | E | glutamine synthetase | |
MHMNNKED_00925 | 8.6e-71 | ribE | 2.5.1.9 | H | Riboflavin synthase | |
MHMNNKED_00926 | 1.6e-74 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
MHMNNKED_00927 | 1.8e-65 | 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 | |
MHMNNKED_00928 | 1.3e-115 | ywqB | S | Zinc finger, swim domain protein | ||
MHMNNKED_00929 | 4.8e-60 | |||||
MHMNNKED_00930 | 4.3e-36 | K | Helix-turn-helix XRE-family like proteins | |||
MHMNNKED_00931 | 1.7e-198 | des | 1.14.19.23, 1.14.19.45 | I | fatty acid desaturase | |
MHMNNKED_00932 | 4.7e-31 | cspL | K | Cold shock | ||
MHMNNKED_00933 | 1.5e-188 | qor | 1.6.5.5 | C | Zinc-binding dehydrogenase | |
MHMNNKED_00934 | 9.5e-43 | yyaS | S | Membrane | ||
MHMNNKED_00935 | 4.1e-59 | ypbD | S | metal-dependent membrane protease | ||
MHMNNKED_00936 | 4.3e-174 | recQ | 3.6.4.12 | L | DNA helicase | |
MHMNNKED_00937 | 2.6e-93 | ypbB | 5.1.3.1 | S | protein conserved in bacteria | |
MHMNNKED_00938 | 3.8e-35 | fer | C | Ferredoxin | ||
MHMNNKED_00939 | 4.5e-60 | fmnP | 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 | ||
MHMNNKED_00940 | 5.1e-72 | M | COG0739 Membrane proteins related to metalloendopeptidases | |||
MHMNNKED_00941 | 3.4e-41 | rsiX | ||||
MHMNNKED_00942 | 3.1e-63 | sigX | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
MHMNNKED_00943 | 2.1e-212 | resE | 2.7.13.3 | T | Histidine kinase | |
MHMNNKED_00944 | 1.5e-121 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
MHMNNKED_00945 | 2.8e-114 | ccsA | O | 'COG0755 ABC-type transport system involved in cytochrome c biogenesis, permease component' | ||
MHMNNKED_00946 | 3.2e-200 | dld | 1.1.1.303, 1.1.1.4, 1.1.2.4 | C | Glycolate oxidase subunit | |
MHMNNKED_00947 | 7.5e-73 | K | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | |||
MHMNNKED_00950 | 1.3e-28 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
MHMNNKED_00951 | 8e-80 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
MHMNNKED_00952 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
MHMNNKED_00953 | 9.6e-58 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
MHMNNKED_00954 | 1.5e-09 | |||||
MHMNNKED_00955 | 1e-200 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
MHMNNKED_00956 | 6.4e-286 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
MHMNNKED_00958 | 1.6e-45 | ectA | 2.3.1.178 | K | L-2,4-diaminobutyric acid acetyltransferase | |
MHMNNKED_00959 | 8.5e-179 | ectB | 2.6.1.76 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
MHMNNKED_00960 | 1.4e-55 | ectC | 4.2.1.108 | S | Catalyzes the circularization of gamma-N-acetyl- alpha,gamma-diaminobutyric acid (ADABA) to ectoine (1,4,5,6- tetrahydro-2-methyl-4-pyrimidine carboxylic acid), which is an excellent osmoprotectant | |
MHMNNKED_00961 | 2.6e-128 | ybbH_2 | K | Transcriptional regulator | ||
MHMNNKED_00963 | 1.4e-22 | yozC | ||||
MHMNNKED_00964 | 1.9e-179 | nnrD | 4.2.1.136, 5.1.99.6 | G | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
MHMNNKED_00966 | 1.9e-48 | S | Cupredoxin-like domain | |||
MHMNNKED_00967 | 1.2e-30 | 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 | ||
MHMNNKED_00968 | 8.2e-10 | 6.1.1.7 | S | Threonyl and Alanyl tRNA synthetase second additional domain | ||
MHMNNKED_00969 | 3e-14 | alaS_2 | 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 | |
MHMNNKED_00970 | 7.2e-70 | yrrT | 4.4.1.21 | Q | Could be a S-adenosyl-L-methionine-dependent methyltransferase | |
MHMNNKED_00971 | 4.7e-79 | luxS | 4.4.1.21 | T | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
MHMNNKED_00972 | 1.6e-129 | mccA | 2.5.1.134, 2.5.1.47 | E | Cysteine synthase | |
MHMNNKED_00973 | 7e-169 | mccB | 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
MHMNNKED_00975 | 9.4e-76 | S | Preprotein translocase subunit SecA (ATPase, RNA helicase) | |||
MHMNNKED_00976 | 9e-146 | lipA | 2.8.1.8 | H | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | |
MHMNNKED_00977 | 6.1e-125 | lipM | 6.3.1.20 | H | Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domain of GcvH, an intermediate carrier during protein lipoylation | |
MHMNNKED_00978 | 6.3e-84 | tesE | Q | hydratase | ||
MHMNNKED_00979 | 1.9e-79 | EG | EamA-like transporter family | |||
MHMNNKED_00980 | 3.6e-152 | nhaC | C | Na H antiporter | ||
MHMNNKED_00981 | 2.4e-225 | 2.1.1.72, 3.1.21.4 | V | restriction endonuclease | ||
MHMNNKED_00982 | 0.0 | L | T5orf172 | |||
MHMNNKED_00983 | 3e-160 | putA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
MHMNNKED_00984 | 3.4e-198 | rocD | 2.6.1.11, 2.6.1.13, 2.6.1.17 | E | Catalyzes the interconversion of ornithine to glutamate semialdehyde | |
MHMNNKED_00985 | 4.9e-118 | rbsR | K | transcriptional | ||
MHMNNKED_00986 | 1e-111 | rbsK | 2.7.1.15, 2.7.1.4 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
MHMNNKED_00987 | 9e-47 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
MHMNNKED_00988 | 8.2e-218 | rbsA | 3.6.3.17 | G | Part of the ABC transporter complex RbsABC involved in ribose import. Responsible for energy coupling to the transport system | |
MHMNNKED_00989 | 6.1e-126 | rbsC | G | Branched-chain amino acid transport system / permease component | ||
MHMNNKED_00990 | 2.9e-117 | rbsB | G | COG1879 ABC-type sugar transport system, periplasmic component | ||
MHMNNKED_00991 | 2.7e-103 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
MHMNNKED_00992 | 6.7e-10 | |||||
MHMNNKED_00993 | 3.1e-188 | pepA | 3.4.11.1, 3.4.11.5 | E | Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides | |
MHMNNKED_00994 | 4.4e-84 | yuiC | S | protein conserved in bacteria | ||
MHMNNKED_00995 | 2.1e-12 | yuiB | S | Putative membrane protein | ||
MHMNNKED_00996 | 9.9e-159 | yumC | 1.18.1.2, 1.19.1.1 | C | reductase | |
MHMNNKED_00997 | 8.3e-47 | erpA | S | Belongs to the HesB IscA family | ||
MHMNNKED_00998 | 1.6e-151 | yutJ | 1.6.99.3 | C | NADH dehydrogenase | |
MHMNNKED_00999 | 1.1e-254 | L | Integrase core domain | |||
MHMNNKED_01000 | 1.3e-94 | L | PhoH-like protein | |||
MHMNNKED_01001 | 1.1e-41 | dcm | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
MHMNNKED_01002 | 4.1e-23 | |||||
MHMNNKED_01003 | 1.5e-198 | yhbH | S | Belongs to the UPF0229 family | ||
MHMNNKED_01004 | 0.0 | prkA | T | Ser protein kinase | ||
MHMNNKED_01005 | 8.1e-97 | nfrA | 1.5.1.38, 1.5.1.39 | C | Oxidoreductase | |
MHMNNKED_01006 | 5.5e-78 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
MHMNNKED_01007 | 1.4e-111 | yhbB | S | Putative amidase domain | ||
MHMNNKED_01008 | 1.8e-177 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
MHMNNKED_01010 | 1.5e-45 | yvoA | K | transcriptional | ||
MHMNNKED_01011 | 6.7e-98 | O | peptidase U32 | |||
MHMNNKED_01012 | 1.7e-212 | nagE | 2.7.1.193, 2.7.1.199 | G | COG1263 Phosphotransferase system IIC components, glucose maltose N-acetylglucosamine-specific | |
MHMNNKED_01013 | 1.8e-41 | crr | 2.7.1.193, 2.7.1.199 | G | PTS glucose transporter subunit IIA | |
MHMNNKED_01014 | 1.6e-78 | spmB | S | Spore maturation protein | ||
MHMNNKED_01015 | 8.4e-89 | spmA | S | Spore maturation protein | ||
MHMNNKED_01016 | 1.1e-153 | dacB | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
MHMNNKED_01017 | 3.8e-68 | 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 | ||
MHMNNKED_01018 | 2.5e-90 | 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 | ||
MHMNNKED_01019 | 2e-42 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
MHMNNKED_01020 | 2.9e-198 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
MHMNNKED_01021 | 1.5e-208 | spoVAF | EG | Stage V sporulation protein AF | ||
MHMNNKED_01022 | 1.8e-24 | spoVAB | S | Stage V sporulation protein AB | ||
MHMNNKED_01023 | 1.7e-76 | spoVAA | S | Stage V sporulation protein AA | ||
MHMNNKED_01024 | 9.3e-117 | sigF | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
MHMNNKED_01025 | 2e-63 | spoIIAB | 2.7.11.1 | F | Binds to sigma F and blocks its ability to form an RNA polymerase holoenzyme (E-sigma F). Phosphorylates SpoIIAA on a serine residue. This phosphorylation may enable SpoIIAA to act as an anti-anti-sigma factor that counteracts SpoIIAB and thus releases sigma F from inhibition | |
MHMNNKED_01026 | 5.1e-41 | spoIIAA | T | Belongs to the anti-sigma-factor antagonist family | ||
MHMNNKED_01027 | 2.3e-159 | dacF | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
MHMNNKED_01028 | 2.9e-12 | EGP | Major facilitator Superfamily | |||
MHMNNKED_01030 | 8.1e-290 | pepA | 3.4.11.1, 3.4.11.5 | E | Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides | |
MHMNNKED_01031 | 2.3e-85 | yuiD | S | Divergent PAP2 family | ||
MHMNNKED_01032 | 2.1e-79 | cysC | 2.7.1.25 | P | Catalyzes the synthesis of activated sulfate | |
MHMNNKED_01033 | 9.6e-158 | sat | 2.7.7.4 | P | Belongs to the sulfate adenylyltransferase family | |
MHMNNKED_01034 | 6.6e-96 | cysH | 1.8.4.10, 1.8.4.8, 2.7.1.25 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
MHMNNKED_01035 | 6.2e-51 | 3.1.3.73 | G | alpha-ribazole phosphatase activity | ||
MHMNNKED_01036 | 1e-91 | yitD | 4.4.1.19 | S | synthase | |
MHMNNKED_01037 | 1.3e-176 | yitG | EGP | Major facilitator Superfamily | ||
MHMNNKED_01038 | 5.8e-33 | |||||
MHMNNKED_01039 | 2.5e-103 | cobB | K | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form | ||
MHMNNKED_01040 | 7e-42 | pgpB | 3.6.1.27 | I | COG0671 Membrane-associated phospholipid phosphatase | |
MHMNNKED_01041 | 5.6e-280 | htpG | O | Molecular chaperone. Has ATPase activity | ||
MHMNNKED_01042 | 5.1e-79 | magIII | L | endonuclease III | ||
MHMNNKED_01043 | 6.5e-116 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
MHMNNKED_01044 | 4.1e-94 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
MHMNNKED_01045 | 2.1e-221 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
MHMNNKED_01046 | 1.6e-78 | pncA | Q | COG1335 Amidases related to nicotinamidase | ||
MHMNNKED_01047 | 0.0 | swrC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
MHMNNKED_01048 | 6.8e-60 | ycnC | K | Bacterial regulatory proteins, tetR family | ||
MHMNNKED_01049 | 7.1e-79 | ykuK | S | Ribonuclease H-like | ||
MHMNNKED_01050 | 8.7e-145 | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | |||
MHMNNKED_01051 | 5.5e-183 | rocB | E | Peptidase family M20/M25/M40 | ||
MHMNNKED_01052 | 8.7e-255 | siaT_1 | S | Tripartite ATP-independent periplasmic transporter, DctM component | ||
MHMNNKED_01053 | 1.5e-32 | S | Domain of unknown function (DUF1850) | |||
MHMNNKED_01054 | 1.1e-127 | S | NMT1-like family | |||
MHMNNKED_01055 | 2.9e-156 | 1.1.1.1 | C | alcohol dehydrogenase | ||
MHMNNKED_01056 | 1.7e-203 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
MHMNNKED_01057 | 6.4e-125 | T | PhoQ Sensor | |||
MHMNNKED_01058 | 5e-75 | L | Integrase | |||
MHMNNKED_01059 | 3e-50 | yjcF | S | Acetyltransferase (GNAT) domain | ||
MHMNNKED_01060 | 1.9e-83 | ycgF3 | E | LysE type translocator | ||
MHMNNKED_01061 | 3.1e-82 | MTH_1382 | S | Membrane transport protein | ||
MHMNNKED_01062 | 6e-106 | cpoA | GT4 | M | Glycosyltransferase Family 4 | |
MHMNNKED_01064 | 2.8e-58 | ykhA | 3.1.2.20 | I | Acyl-CoA hydrolase | |
MHMNNKED_01065 | 2.5e-168 | nrdB | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
MHMNNKED_01066 | 2.1e-52 | fld | C | Flavodoxin | ||
MHMNNKED_01067 | 4e-73 | dhaL | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | S | Dak2 | |
MHMNNKED_01068 | 2.6e-143 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
MHMNNKED_01069 | 5e-71 | 4.2.1.44 | G | Xylose isomerase-like TIM barrel | ||
MHMNNKED_01070 | 2.3e-60 | rpiB | 5.3.1.34, 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
MHMNNKED_01071 | 3.4e-74 | K | DeoR C terminal sensor domain | |||
MHMNNKED_01072 | 1.6e-176 | FOXRED | 1.5.3.1 | E | FAD dependent oxidoreductase | |
MHMNNKED_01073 | 6.7e-112 | 4.3.1.12 | E | Ornithine cyclodeaminase | ||
MHMNNKED_01074 | 2.9e-157 | dapL | 2.6.1.83 | E | Aminotransferase | |
MHMNNKED_01075 | 6e-178 | L | Resolvase, N terminal domain | |||
MHMNNKED_01076 | 1.3e-26 | adaA | 3.2.2.21 | F | Metal binding domain of Ada | |
MHMNNKED_01078 | 5.1e-82 | 1.16.3.2 | P | Ferritin-like domain | ||
MHMNNKED_01080 | 3.7e-56 | yugU | S | Uncharacterised protein family UPF0047 | ||
MHMNNKED_01082 | 8.4e-67 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
MHMNNKED_01083 | 4.9e-199 | xylE | EGP | Sugar (and other) transporter | ||
MHMNNKED_01084 | 4e-220 | xylB | 2.7.1.17 | G | xylulose kinase | |
MHMNNKED_01085 | 8.8e-70 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
MHMNNKED_01086 | 6.6e-105 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
MHMNNKED_01087 | 1.8e-124 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
MHMNNKED_01088 | 4.8e-122 | cbiO | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
MHMNNKED_01089 | 6.9e-54 | rplQ | J | Ribosomal protein L17 | ||
MHMNNKED_01090 | 5.1e-157 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MHMNNKED_01091 | 3e-63 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
MHMNNKED_01092 | 3.4e-56 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
MHMNNKED_01093 | 5.4e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
MHMNNKED_01094 | 1.1e-97 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
MHMNNKED_01095 | 1.4e-189 | 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 | ||
MHMNNKED_01096 | 8.2e-65 | rplO | J | binds to the 23S rRNA | ||
MHMNNKED_01097 | 1.2e-22 | rpmD | J | Ribosomal protein L30 | ||
MHMNNKED_01098 | 2.1e-77 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
MHMNNKED_01099 | 5e-52 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
MHMNNKED_01100 | 1.6e-83 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
MHMNNKED_01101 | 1.1e-63 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
MHMNNKED_01102 | 4.4e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
MHMNNKED_01103 | 2.6e-89 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
MHMNNKED_01104 | 1.8e-42 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
MHMNNKED_01105 | 7.3e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
MHMNNKED_01106 | 1.8e-38 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
MHMNNKED_01107 | 7.6e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
MHMNNKED_01108 | 6.4e-70 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
MHMNNKED_01109 | 6e-112 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
MHMNNKED_01110 | 2.2e-49 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
MHMNNKED_01111 | 1.6e-45 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
MHMNNKED_01112 | 2.3e-145 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
MHMNNKED_01113 | 5e-39 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
MHMNNKED_01114 | 6.7e-89 | rplD | J | Forms part of the polypeptide exit tunnel | ||
MHMNNKED_01115 | 9.5e-99 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
MHMNNKED_01116 | 2.2e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
MHMNNKED_01117 | 2.1e-16 | |||||
MHMNNKED_01118 | 1.7e-202 | EGP | Major facilitator Superfamily | |||
MHMNNKED_01119 | 1.1e-63 | K | Transcriptional regulator | |||
MHMNNKED_01120 | 1.8e-17 | ywcB | S | Protein of unknown function, DUF485 | ||
MHMNNKED_01121 | 1.3e-139 | yjjL | G | MFS/sugar transport protein | ||
MHMNNKED_01122 | 3.8e-75 | ydaF_1 | J | Acetyltransferase (GNAT) domain | ||
MHMNNKED_01123 | 9.2e-128 | tdcB_2 | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
MHMNNKED_01124 | 6.9e-61 | fosB | 2.5.1.18 | H | Metallothiol transferase which confers resistance to fosfomycin by catalyzing the addition of a thiol cofactor to fosfomycin. L-cysteine is probably the physiological thiol donor | |
MHMNNKED_01125 | 7.3e-156 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
MHMNNKED_01126 | 6.5e-181 | paaJ | 2.3.1.16, 2.3.1.174, 2.3.1.223, 2.3.1.9 | I | Belongs to the thiolase family | |
MHMNNKED_01127 | 9.5e-102 | ybbH_1 | K | RpiR family transcriptional regulator | ||
MHMNNKED_01128 | 4.9e-174 | EG | COG2610 H gluconate symporter and related permeases | |||
MHMNNKED_01129 | 1.3e-233 | fumC | 1.1.1.38, 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
MHMNNKED_01131 | 1e-266 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
MHMNNKED_01132 | 4.1e-133 | pbuG | S | permease | ||
MHMNNKED_01133 | 1.3e-15 | yebG | S | NETI protein | ||
MHMNNKED_01134 | 3.1e-221 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
MHMNNKED_01135 | 7.8e-212 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
MHMNNKED_01136 | 4.5e-08 | ytxG | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
MHMNNKED_01137 | 4.3e-12 | XK27_07760 | D | gas vesicle protein | ||
MHMNNKED_01138 | 3.1e-31 | ytxJ | O | Protein of unknown function (DUF2847) | ||
MHMNNKED_01139 | 2.8e-179 | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | |||
MHMNNKED_01140 | 9.3e-236 | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | ||
MHMNNKED_01143 | 1e-212 | E | Sodium:solute symporter family | |||
MHMNNKED_01144 | 1.3e-247 | mtlF | 2.7.1.197 | G | COG2213 Phosphotransferase system, mannitol-specific IIBC component | |
MHMNNKED_01145 | 2.7e-166 | mtlR | K | transcriptional regulator, MtlR | ||
MHMNNKED_01146 | 1.1e-137 | mtlD | 1.1.1.17 | G | COG0246 Mannitol-1-phosphate altronate dehydrogenases | |
MHMNNKED_01147 | 6.2e-257 | 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) | |
MHMNNKED_01149 | 1.8e-83 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
MHMNNKED_01150 | 1.5e-100 | hbd2 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase, C-terminal domain | |
MHMNNKED_01151 | 1.7e-161 | gntU | EG | GntP family permease | ||
MHMNNKED_01152 | 1e-93 | G | Xylose isomerase-like TIM barrel | |||
MHMNNKED_01153 | 2.5e-112 | hprA | 1.1.1.28, 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
MHMNNKED_01155 | 2.5e-154 | G | Major Facilitator Superfamily | |||
MHMNNKED_01156 | 2.4e-114 | yagE | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
MHMNNKED_01157 | 2.6e-93 | hag | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
MHMNNKED_01158 | 3.3e-165 | 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 | ||
MHMNNKED_01159 | 1.7e-25 | 3.4.21.107 | O | serine-type endopeptidase activity | ||
MHMNNKED_01160 | 2e-240 | yyaL | O | COG1331 Highly conserved protein containing a thioredoxin domain | ||
MHMNNKED_01161 | 8.9e-20 | yyaL | O | COG1331 Highly conserved protein containing a thioredoxin domain | ||
MHMNNKED_01162 | 2.7e-102 | polC | 2.7.7.7 | L | 3' exoribonuclease, RNase T-like | |
MHMNNKED_01163 | 2.1e-210 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
MHMNNKED_01164 | 1.3e-78 | S | COG1647 Esterase lipase | |||
MHMNNKED_01165 | 1.5e-176 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
MHMNNKED_01166 | 5e-156 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
MHMNNKED_01167 | 2.8e-92 | |||||
MHMNNKED_01168 | 2.4e-147 | mgtE | P | Acts as a magnesium transporter | ||
MHMNNKED_01169 | 1.1e-192 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
MHMNNKED_01170 | 3.9e-154 | rodA | D | Belongs to the SEDS family | ||
MHMNNKED_01171 | 5.9e-45 | yneJ | O | COG4846 Membrane protein involved in cytochrome C biogenesis | ||
MHMNNKED_01173 | 4.4e-17 | |||||
MHMNNKED_01174 | 9.3e-96 | ysaA | S | HAD-hyrolase-like | ||
MHMNNKED_01175 | 2.7e-169 | yjcD | 3.6.4.12 | L | Cold-inducible protein YdjO | |
MHMNNKED_01176 | 3e-12 | |||||
MHMNNKED_01177 | 7e-20 | |||||
MHMNNKED_01178 | 3.9e-128 | uvsE | L | Component in a DNA repair pathway. Removal of UV-light damaged nucleotides. Recognizes pyrimidine dimers and cleave a phosphodiester bond immediately 5' to the lesion | ||
MHMNNKED_01179 | 5.8e-36 | |||||
MHMNNKED_01180 | 1.7e-20 | |||||
MHMNNKED_01182 | 1.9e-64 | yvgN | S | reductase | ||
MHMNNKED_01183 | 9.4e-108 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MHMNNKED_01184 | 4.8e-40 | yhcU | S | Family of unknown function (DUF5365) | ||
MHMNNKED_01185 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
MHMNNKED_01186 | 9.1e-95 | dprA | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | ||
MHMNNKED_01187 | 4.3e-161 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
MHMNNKED_01188 | 1.2e-192 | sucC | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
MHMNNKED_01189 | 8.3e-21 | ylqH | S | FlhB HrpN YscU SpaS Family | ||
MHMNNKED_01190 | 4.1e-69 | ylqG | ||||
MHMNNKED_01191 | 5.4e-91 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
MHMNNKED_01192 | 9e-124 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
MHMNNKED_01193 | 8.9e-69 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
MHMNNKED_01194 | 5.1e-54 | 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 | ||
MHMNNKED_01195 | 1.6e-113 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
MHMNNKED_01196 | 1.3e-69 | 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 | ||
MHMNNKED_01197 | 4.4e-38 | ylqD | S | YlqD protein | ||
MHMNNKED_01198 | 3.3e-20 | ylqC | S | Belongs to the UPF0109 family | ||
MHMNNKED_01199 | 1.5e-40 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
MHMNNKED_01200 | 2.8e-209 | 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 | |
MHMNNKED_01201 | 1.4e-35 | 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 | ||
MHMNNKED_01202 | 1.2e-138 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
MHMNNKED_01203 | 2.7e-275 | smc | D | Required for chromosome condensation and partitioning | ||
MHMNNKED_01204 | 7.7e-95 | 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 | |
MHMNNKED_01205 | 1.8e-29 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
MHMNNKED_01206 | 2e-100 | IQ | reductase | |||
MHMNNKED_01207 | 3.7e-123 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
MHMNNKED_01208 | 5e-139 | 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 | |
MHMNNKED_01209 | 2.5e-77 | fapR | K | Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism | ||
MHMNNKED_01210 | 8.5e-298 | 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) | |
MHMNNKED_01211 | 7.5e-236 | yloV | S | kinase related to dihydroxyacetone kinase | ||
MHMNNKED_01212 | 1.3e-52 | asp | S | protein conserved in bacteria | ||
MHMNNKED_01213 | 2.3e-24 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
MHMNNKED_01214 | 3.2e-73 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
MHMNNKED_01215 | 6.7e-103 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
MHMNNKED_01216 | 9.4e-121 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
MHMNNKED_01217 | 1.3e-226 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
MHMNNKED_01218 | 1.8e-91 | stp | 3.1.3.16 | T | phosphatase | |
MHMNNKED_01219 | 5.5e-181 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
MHMNNKED_01220 | 4.5e-137 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
MHMNNKED_01221 | 8.4e-47 | def | 2.1.2.9, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
MHMNNKED_01222 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
MHMNNKED_01223 | 1.2e-161 | 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 | |
MHMNNKED_01224 | 3.4e-13 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
MHMNNKED_01225 | 3.9e-97 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
MHMNNKED_01226 | 5.5e-29 | ylzA | S | Belongs to the UPF0296 family | ||
MHMNNKED_01227 | 5.4e-76 | yloC | S | stress-induced protein | ||
MHMNNKED_01228 | 0.0 | yloB | 3.6.3.8 | P | COG0474 Cation transport ATPase | |
MHMNNKED_01229 | 2.4e-237 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
MHMNNKED_01230 | 4.1e-78 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
MHMNNKED_01231 | 6.5e-80 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
MHMNNKED_01232 | 2.5e-140 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
MHMNNKED_01233 | 1e-89 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
MHMNNKED_01234 | 0.0 | carB | 6.3.5.5 | F | Belongs to the CarB family | |
MHMNNKED_01235 | 3.1e-181 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
MHMNNKED_01236 | 5.3e-122 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
MHMNNKED_01237 | 2.3e-77 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
MHMNNKED_01238 | 3.7e-128 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MHMNNKED_01239 | 4.3e-54 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
MHMNNKED_01240 | 3.7e-110 | yppC | S | Protein of unknown function (DUF2515) | ||
MHMNNKED_01243 | 7.4e-22 | yppE | S | Bacterial domain of unknown function (DUF1798) | ||
MHMNNKED_01244 | 1.6e-08 | yppG | S | YppG-like protein | ||
MHMNNKED_01245 | 1.1e-35 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
MHMNNKED_01246 | 0.0 | yprA | L | COG1205 Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster | ||
MHMNNKED_01247 | 7.4e-151 | yprB | L | RNase_H superfamily | ||
MHMNNKED_01248 | 3.7e-158 | 6.3.1.20 | H | Lipoate-protein ligase | ||
MHMNNKED_01249 | 3.4e-100 | yhfI | S | COG1234 Metal-dependent hydrolases of the beta-lactamase superfamily III | ||
MHMNNKED_01250 | 3.7e-11 | yhfH | S | YhfH-like protein | ||
MHMNNKED_01251 | 4.6e-142 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
MHMNNKED_01252 | 2.6e-165 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
MHMNNKED_01253 | 7.3e-101 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
MHMNNKED_01254 | 6e-88 | P | COG2011 ABC-type metal ion transport system, permease component | |||
MHMNNKED_01255 | 4.7e-106 | metQ | M | Belongs to the nlpA lipoprotein family | ||
MHMNNKED_01256 | 7.7e-166 | abgB | S | amidohydrolase | ||
MHMNNKED_01257 | 1.7e-108 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
MHMNNKED_01259 | 1.5e-11 | K | Helix-turn-helix XRE-family like proteins | |||
MHMNNKED_01260 | 1.4e-13 | 3.2.1.8 | S | protein homooligomerization | ||
MHMNNKED_01261 | 4.7e-206 | helD_2 | 3.6.4.12 | L | DNA helicase | |
MHMNNKED_01262 | 3.8e-26 | 2.7.1.11 | G | alpha-ribazole phosphatase activity | ||
MHMNNKED_01263 | 3.1e-252 | gpmI | 5.4.2.12 | F | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
MHMNNKED_01264 | 9.4e-64 | 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) | |
MHMNNKED_01265 | 3.2e-84 | 5.1.3.2 | GT2 | GM | 3-beta hydroxysteroid dehydrogenase/isomerase family | |
MHMNNKED_01266 | 9.3e-131 | rfbG | 4.2.1.45 | M | Male sterility protein | |
MHMNNKED_01267 | 6e-111 | rfbF | 2.7.7.33 | JM | Glucose-1-phosphate cytidylyltransferase | |
MHMNNKED_01268 | 1.9e-11 | O | Tetratricopeptide repeat protein | |||
MHMNNKED_01269 | 5.5e-66 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
MHMNNKED_01270 | 7.7e-71 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
MHMNNKED_01271 | 5.6e-79 | 3.5.1.124 | S | DJ-1/PfpI family | ||
MHMNNKED_01272 | 3.3e-94 | yniA | G | Fructosamine kinase | ||
MHMNNKED_01273 | 5.5e-75 | S | reductase | |||
MHMNNKED_01274 | 3.2e-171 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
MHMNNKED_01276 | 3.4e-95 | M1-592 | P | ABC transporter, ATP-binding protein | ||
MHMNNKED_01277 | 2.9e-89 | ytlD1 | P | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_01278 | 5.3e-36 | M1-594 | S | Thiamine-binding protein | ||
MHMNNKED_01279 | 6.7e-139 | M1-596 | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
MHMNNKED_01280 | 7.3e-83 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
MHMNNKED_01281 | 5.7e-40 | |||||
MHMNNKED_01282 | 4.5e-171 | traB | S | TraB family | ||
MHMNNKED_01283 | 1.7e-136 | ynfM | EGP | Major facilitator Superfamily | ||
MHMNNKED_01287 | 4.5e-112 | G | protein with SCP PR1 domains | |||
MHMNNKED_01288 | 1.5e-112 | degV1 | S | Uncharacterised protein, DegV family COG1307 | ||
MHMNNKED_01291 | 4.1e-59 | comEC | L | domain protein | ||
MHMNNKED_01294 | 2.8e-32 | |||||
MHMNNKED_01296 | 3.4e-73 | resA | CO | Thiol-disulfide oxidoreductase which is required in disulfide reduction during c-type cytochrome synthesis. May accept reducing equivalents from CcdA, leading to breakage of disulfide bonds in apocytochrome c | ||
MHMNNKED_01297 | 1.2e-90 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
MHMNNKED_01298 | 1.3e-104 | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | |||
MHMNNKED_01299 | 1.4e-199 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | |||
MHMNNKED_01300 | 7.4e-49 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
MHMNNKED_01301 | 1.4e-108 | S | Protein of unknown function (DUF1648) | |||
MHMNNKED_01302 | 3.5e-159 | S | protein conserved in bacteria | |||
MHMNNKED_01303 | 3.2e-31 | M | Belongs to the BCCT transporter (TC 2.A.15) family | |||
MHMNNKED_01304 | 4.6e-159 | namA | C | Catalyzes the reduction of the double bond of an array of alpha,beta-unsaturated aldehydes and ketones. It also reduces the nitro group of nitroester and nitroaromatic compounds. It could have a role in detoxification processes | ||
MHMNNKED_01305 | 1.9e-99 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
MHMNNKED_01306 | 6.7e-186 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
MHMNNKED_01307 | 1.8e-62 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | N-(5'phosphoribosyl)anthranilate (PRA) isomerase | |
MHMNNKED_01308 | 1.8e-83 | trpC | 4.1.1.48, 5.3.1.24 | E | Indole-3-glycerol phosphate synthase | |
MHMNNKED_01309 | 1.8e-131 | trpD | 2.4.2.18, 4.1.3.27 | E | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
MHMNNKED_01310 | 3.6e-68 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | Anthranilate synthase | |
MHMNNKED_01311 | 2.3e-166 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
MHMNNKED_01312 | 4.1e-81 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
MHMNNKED_01313 | 3.1e-13 | S | Putative adhesin | |||
MHMNNKED_01315 | 1.6e-29 | |||||
MHMNNKED_01316 | 4.2e-72 | 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 | |
MHMNNKED_01317 | 1.4e-41 | cotX | S | Spore Coat Protein X and V domain | ||
MHMNNKED_01319 | 1.4e-61 | yccU | S | CoA-binding protein | ||
MHMNNKED_01321 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
MHMNNKED_01322 | 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 | |
MHMNNKED_01323 | 2.5e-48 | carD | K | Transcription factor | ||
MHMNNKED_01324 | 9.4e-19 | S | Staygreen protein | |||
MHMNNKED_01326 | 4.1e-09 | |||||
MHMNNKED_01328 | 6.8e-79 | rrmA | 2.1.1.187 | Q | Methyltransferase | |
MHMNNKED_01329 | 6.8e-157 | EGP | Transmembrane secretion effector | |||
MHMNNKED_01330 | 2.3e-128 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
MHMNNKED_01331 | 4.7e-231 | yfbS | P | Sodium:sulfate symporter transmembrane region | ||
MHMNNKED_01333 | 7.4e-68 | yvoF | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | ||
MHMNNKED_01334 | 4.5e-75 | ppaX | 3.1.3.18, 3.6.1.1 | S | Hydrolyzes pyrophosphate formed during P-Ser-HPr dephosphorylation by HPrK P. Might play a role in controlling the intracellular pyrophosphate pool | |
MHMNNKED_01335 | 2.7e-114 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
MHMNNKED_01336 | 2.7e-145 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
MHMNNKED_01337 | 4.2e-258 | 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) | |
MHMNNKED_01338 | 1.1e-72 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
MHMNNKED_01339 | 2e-101 | ytpQ | S | Belongs to the UPF0354 family | ||
MHMNNKED_01340 | 6.1e-41 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
MHMNNKED_01341 | 1.5e-60 | yjjX | F | Phosphatase that hydrolyzes non-canonical purine nucleotides such as XTP and ITP to their respective diphosphate derivatives. Probably excludes non-canonical purines from DNA precursor pool, thus preventing their incorporation into DNA and avoiding chromosomal lesions | ||
MHMNNKED_01342 | 4.6e-178 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
MHMNNKED_01343 | 1e-21 | ytzB | S | small secreted protein | ||
MHMNNKED_01344 | 1.8e-132 | ytnP | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
MHMNNKED_01345 | 5.7e-102 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
MHMNNKED_01346 | 1.4e-97 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
MHMNNKED_01347 | 3.5e-29 | ytzH | S | YtzH-like protein | ||
MHMNNKED_01348 | 2.6e-106 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
MHMNNKED_01349 | 1.4e-90 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase accessory domain | |
MHMNNKED_01350 | 4.3e-90 | ytlQ | ||||
MHMNNKED_01351 | 5.6e-58 | ligT | 3.1.4.58, 3.5.1.42 | J | LigT like Phosphoesterase | |
MHMNNKED_01352 | 1.3e-26 | ytzE | K | helix_turn_helix, Deoxyribose operon repressor | ||
MHMNNKED_01353 | 1.2e-100 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
MHMNNKED_01355 | 1.2e-193 | ytgP | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
MHMNNKED_01356 | 1.7e-187 | ytfP | S | HI0933-like protein | ||
MHMNNKED_01357 | 3.8e-21 | yteV | S | Sporulation protein Cse60 | ||
MHMNNKED_01358 | 3.5e-193 | dppE_1 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MHMNNKED_01359 | 4.2e-36 | ytwF | P | Sulfurtransferase | ||
MHMNNKED_01360 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MHMNNKED_01361 | 3.2e-131 | fepC | 3.6.3.34 | HP | ABC transporter | |
MHMNNKED_01362 | 1.6e-148 | P | FecCD transport family | |||
MHMNNKED_01363 | 2e-154 | fepD | P | FecCD transport family | ||
MHMNNKED_01364 | 5.6e-144 | P | Periplasmic binding protein | |||
MHMNNKED_01365 | 1.5e-154 | ycgT | 1.18.1.2, 1.19.1.1 | C | reductase | |
MHMNNKED_01366 | 3e-258 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
MHMNNKED_01367 | 3.5e-40 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
MHMNNKED_01368 | 1.8e-47 | ydiL | S | CAAX protease self-immunity | ||
MHMNNKED_01370 | 8.7e-83 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
MHMNNKED_01371 | 6.1e-91 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
MHMNNKED_01372 | 2e-256 | yheS_3 | S | ABC transporter | ||
MHMNNKED_01373 | 4.7e-299 | clpE | O | Belongs to the ClpA ClpB family | ||
MHMNNKED_01374 | 1.6e-116 | ykvI | S | membrane | ||
MHMNNKED_01375 | 1.1e-72 | S | CAAX protease self-immunity | |||
MHMNNKED_01376 | 9.5e-20 | ykvS | S | protein conserved in bacteria | ||
MHMNNKED_01377 | 1e-14 | |||||
MHMNNKED_01378 | 2.4e-67 | 3.5.1.28 | M | Cell Wall Hydrolase | ||
MHMNNKED_01379 | 1.1e-24 | ptsH | G | phosphocarrier protein HPr | ||
MHMNNKED_01380 | 2.1e-128 | glxR | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
MHMNNKED_01381 | 2.9e-57 | ykyB | S | YkyB-like protein | ||
MHMNNKED_01382 | 1.5e-107 | ykuE | S | Metallophosphoesterase | ||
MHMNNKED_01383 | 3.5e-07 | |||||
MHMNNKED_01384 | 6.4e-27 | O | COG0695 Glutaredoxin and related proteins | |||
MHMNNKED_01385 | 1.2e-28 | ykuJ | S | protein conserved in bacteria | ||
MHMNNKED_01386 | 3.6e-52 | ykuL | S | COG0517 FOG CBS domain | ||
MHMNNKED_01387 | 3.7e-141 | ccpC | K | Transcriptional regulator | ||
MHMNNKED_01388 | 1.2e-28 | ykuS | S | Belongs to the UPF0180 family | ||
MHMNNKED_01389 | 2.3e-08 | csfB | S | Inhibitor of sigma-G Gin | ||
MHMNNKED_01390 | 3.4e-80 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
MHMNNKED_01391 | 3.1e-48 | yaaQ | S | protein conserved in bacteria | ||
MHMNNKED_01392 | 1.3e-38 | yaaR | S | protein conserved in bacteria | ||
MHMNNKED_01393 | 5.8e-135 | holB | 2.7.7.7 | L | DNA polymerase III | |
MHMNNKED_01394 | 1.1e-126 | yaaT | S | stage 0 sporulation protein | ||
MHMNNKED_01395 | 1.6e-21 | yabA | L | Involved in initiation control of chromosome replication | ||
MHMNNKED_01396 | 3e-112 | yabB | 2.1.1.223 | S | Conserved hypothetical protein 95 | |
MHMNNKED_01397 | 6.2e-29 | yazA | L | endonuclease containing a URI domain | ||
MHMNNKED_01398 | 5.1e-111 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
MHMNNKED_01399 | 1.5e-30 | abrB | K | COG2002 Regulators of stationary sporulation gene expression | ||
MHMNNKED_01400 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
MHMNNKED_01401 | 7.2e-117 | tatD | L | hydrolase, TatD | ||
MHMNNKED_01402 | 5.3e-21 | fimV | NU | Tfp pilus assembly protein FimV | ||
MHMNNKED_01403 | 5.8e-184 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
MHMNNKED_01404 | 1.3e-13 | S | Inner spore coat protein D | |||
MHMNNKED_01405 | 8.5e-37 | 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 | ||
MHMNNKED_01406 | 2.2e-178 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
MHMNNKED_01408 | 1.9e-26 | S | COG1734 DnaK suppressor protein | |||
MHMNNKED_01409 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
MHMNNKED_01410 | 1.6e-38 | divIVA | D | Cell division initiation protein | ||
MHMNNKED_01411 | 4.6e-87 | ylmH | 5.4.99.23, 5.4.99.24 | S | conserved protein, contains S4-like domain | |
MHMNNKED_01412 | 3.9e-22 | yggT | S | membrane | ||
MHMNNKED_01413 | 6.3e-44 | 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 | ||
MHMNNKED_01414 | 6e-91 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
MHMNNKED_01415 | 1.8e-89 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
MHMNNKED_01416 | 1.4e-131 | sigG | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
MHMNNKED_01417 | 1.3e-120 | sigE | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
MHMNNKED_01418 | 1.7e-96 | spoIIGA | M | aspartic protease that is responsible for the proteolytic cleavage of the RNA polymerase sigma E factor (SigE spoIIGB) to yield the active peptide in the mother cell during sporulation. Responds to a signal from the forespore that is triggered by the extracellular signal protein SpoIIR | ||
MHMNNKED_01419 | 8.7e-162 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
MHMNNKED_01420 | 2e-175 | 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 | ||
MHMNNKED_01421 | 1.1e-43 | sbp | S | small basic protein | ||
MHMNNKED_01422 | 2.4e-58 | ylxX | S | protein conserved in bacteria | ||
MHMNNKED_01423 | 1.7e-51 | ylxW | S | protein conserved in bacteria | ||
MHMNNKED_01424 | 1.1e-59 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
MHMNNKED_01425 | 5.1e-153 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
MHMNNKED_01426 | 9e-152 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
MHMNNKED_01428 | 1.4e-10 | |||||
MHMNNKED_01429 | 5.7e-187 | E | Sodium:solute symporter family | |||
MHMNNKED_01430 | 1.6e-124 | yjbA | S | Belongs to the UPF0736 family | ||
MHMNNKED_01431 | 1.6e-47 | yjaZ | O | Zn-dependent protease | ||
MHMNNKED_01432 | 4.4e-97 | mutF | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
MHMNNKED_01433 | 2.8e-81 | S | lantibiotic protection ABC transporter permease subunit, MutE EpiE family | |||
MHMNNKED_01434 | 3.5e-90 | S | ABC-2 family transporter protein | |||
MHMNNKED_01435 | 6.9e-40 | |||||
MHMNNKED_01436 | 1.3e-18 | S | Lanthionine-containing peptide antibiotic (lantibiotic) active on Gram-positive bacteria. The bactericidal activity of lantibiotics is based on depolarization of energized bacterial cytoplasmic membranes, initiated by the formation of aqueous transmembrane pores | |||
MHMNNKED_01437 | 2.7e-204 | L | Transposase domain (DUF772) | |||
MHMNNKED_01440 | 5.3e-156 | mmgC | I | acyl-CoA dehydrogenase | ||
MHMNNKED_01441 | 2.6e-123 | hbdA | 1.1.1.157 | I | Dehydrogenase | |
MHMNNKED_01442 | 8.6e-186 | mmgA | 2.3.1.9 | I | Catalyzes the synthesis of acetoacetyl coenzyme A from two molecules of acetyl coenzyme A. It can also act as a thiolase, catalyzing the reverse reaction and generating two-carbon units from the four-carbon product of fatty acid oxidation | |
MHMNNKED_01443 | 0.0 | fadF | C | COG0247 Fe-S oxidoreductase | ||
MHMNNKED_01444 | 2.4e-119 | cls | I | Belongs to the phospholipase D family. Cardiolipin synthase subfamily | ||
MHMNNKED_01445 | 5.6e-263 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
MHMNNKED_01446 | 5.1e-38 | ywiB | S | Domain of unknown function (DUF1934) | ||
MHMNNKED_01447 | 1.6e-272 | pbpG | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
MHMNNKED_01448 | 8e-72 | ywhD | S | YwhD family | ||
MHMNNKED_01449 | 3.3e-78 | ywhC | S | Peptidase M50 | ||
MHMNNKED_01450 | 1.3e-19 | dmpI | 5.3.2.6 | G | 4-oxalocrotonate tautomerase | |
MHMNNKED_01451 | 1.2e-67 | ywgA | 2.1.1.72, 3.1.21.3 | |||
MHMNNKED_01452 | 1.7e-214 | ywfO | S | COG1078 HD superfamily phosphohydrolases | ||
MHMNNKED_01453 | 1.3e-26 | ywzC | S | Belongs to the UPF0741 family | ||
MHMNNKED_01454 | 1.8e-74 | rsfA | S | Transcriptional regulator | ||
MHMNNKED_01455 | 5.3e-129 | lipL | 2.3.1.200, 2.3.1.204 | H | Catalyzes the amidotransfer (transamidation) of the octanoyl moiety from octanoyl-GcvH to the lipoyl domain of the E2 subunit of lipoate-dependent enzymes | |
MHMNNKED_01456 | 2.1e-145 | pta | 2.3.1.8, 3.6.3.21 | C | In Salmonella this enzyme is required for ethanolamine catabolism | |
MHMNNKED_01457 | 1.2e-108 | ywfI | C | May function as heme-dependent peroxidase | ||
MHMNNKED_01458 | 6.1e-113 | ecsA | V | transporter (ATP-binding protein) | ||
MHMNNKED_01459 | 6.3e-131 | ecsB | U | ABC transporter | ||
MHMNNKED_01460 | 1.7e-99 | ecsC | P | EcsC protein family | ||
MHMNNKED_01461 | 3.1e-175 | yhaA | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | ||
MHMNNKED_01462 | 3.5e-57 | ymcC | S | Membrane | ||
MHMNNKED_01463 | 2.6e-61 | K | BetI-type transcriptional repressor, C-terminal | |||
MHMNNKED_01464 | 2.2e-84 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
MHMNNKED_01465 | 0.0 | lon | 3.4.21.53 | O | ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner | |
MHMNNKED_01466 | 8.4e-267 | lonB | 3.4.21.53 | LO | Belongs to the peptidase S16 family | |
MHMNNKED_01467 | 2.2e-208 | 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 | ||
MHMNNKED_01468 | 4.6e-196 | 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 | ||
MHMNNKED_01469 | 6.1e-76 | trxA2 | O | COG0457 FOG TPR repeat | ||
MHMNNKED_01471 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
MHMNNKED_01472 | 3.7e-99 | |||||
MHMNNKED_01473 | 1.6e-34 | KLT | Protein tyrosine kinase | |||
MHMNNKED_01474 | 1.5e-72 | thyX | 2.1.1.148 | H | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor, and NADPH and FADH(2) as the reductant | |
MHMNNKED_01476 | 5.4e-64 | |||||
MHMNNKED_01478 | 3e-43 | gmk_1 | 2.7.4.8 | F | Guanylate kinase homologues. | |
MHMNNKED_01479 | 1.1e-57 | E | Psort location Cytoplasmic, score | |||
MHMNNKED_01480 | 8.3e-253 | aceB | 2.3.3.9 | C | Belongs to the malate synthase family | |
MHMNNKED_01481 | 4.9e-211 | aceA | 4.1.3.1 | C | Isocitrate lyase | |
MHMNNKED_01482 | 3.6e-100 | NT | chemotaxis protein | |||
MHMNNKED_01483 | 0.0 | phaA | 1.6.5.3 | CP | Domain of unknown function (DUF4040) | |
MHMNNKED_01484 | 1.1e-58 | mnhB2 | P | Domain related to MnhB subunit of Na+/H+ antiporter | ||
MHMNNKED_01485 | 5.6e-37 | phaC | 1.6.5.3 | P | NADH-ubiquinone/plastoquinone oxidoreductase chain 4L | |
MHMNNKED_01486 | 1.9e-214 | mrpD | CP | Subunit D of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
MHMNNKED_01487 | 8.9e-57 | mrpE | P | Na+/H+ ion antiporter subunit | ||
MHMNNKED_01488 | 1.9e-27 | phaF | P | Subunit F of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
MHMNNKED_01489 | 1.9e-36 | phaG | P | Mnh complex is a Na( ) H( ) antiporter involved in Na( ) excretion | ||
MHMNNKED_01490 | 6.9e-91 | 4.2.1.17 | I | Enoyl-CoA hydratase/isomerase | ||
MHMNNKED_01492 | 3.8e-50 | ydiI | Q | protein, possibly involved in aromatic compounds catabolism | ||
MHMNNKED_01493 | 3.8e-133 | yuxJ | EGP | Major facilitator Superfamily | ||
MHMNNKED_01494 | 7e-47 | kapB | G | Kinase associated protein B | ||
MHMNNKED_01495 | 5.1e-94 | ppiB | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
MHMNNKED_01496 | 5.8e-11 | |||||
MHMNNKED_01497 | 2.3e-59 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
MHMNNKED_01498 | 8.5e-162 | patB | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
MHMNNKED_01499 | 6.8e-58 | yugF | I | Hydrolase | ||
MHMNNKED_01500 | 1e-89 | I | Enoyl-CoA hydratase/isomerase | |||
MHMNNKED_01501 | 1.1e-65 | alaR | K | Transcriptional regulator | ||
MHMNNKED_01502 | 4.5e-182 | yugH | 2.6.1.1 | E | Aminotransferase | |
MHMNNKED_01503 | 1.9e-116 | sstT | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
MHMNNKED_01504 | 1.9e-28 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
MHMNNKED_01506 | 2.2e-277 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
MHMNNKED_01507 | 3.4e-50 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
MHMNNKED_01508 | 2.9e-133 | pip | S | YhgE Pip N-terminal domain protein | ||
MHMNNKED_01509 | 1.4e-81 | fucA | 4.1.2.17 | G | Aldolase | |
MHMNNKED_01510 | 2e-149 | mtnA | 5.3.1.23 | E | Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1- P) | |
MHMNNKED_01511 | 9.9e-145 | mtnK | 2.7.1.100 | F | Catalyzes the phosphorylation of methylthioribose into methylthioribose-1-phosphate | |
MHMNNKED_01512 | 2.5e-163 | aroF | 2.5.1.54, 5.4.99.5 | E | Catalyzes the formation of 3-deoxy-D-aribino-hept-2-ulosonate 7-phosphate from phosphoenolpyruvate and D-erythrose 4-phosphate and the formation of prephenate from chorismate | |
MHMNNKED_01513 | 4.2e-95 | K | Helix-turn-helix domain | |||
MHMNNKED_01514 | 3.1e-29 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
MHMNNKED_01515 | 1.8e-83 | K | Bacterial regulatory proteins, tetR family | |||
MHMNNKED_01516 | 7.5e-147 | I | Ndr family | |||
MHMNNKED_01517 | 2e-73 | yhbS | S | family acetyltransferase | ||
MHMNNKED_01518 | 4.8e-38 | K | Transcriptional regulator PadR-like family | |||
MHMNNKED_01519 | 1e-244 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
MHMNNKED_01520 | 3.2e-86 | glpF | G | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
MHMNNKED_01521 | 9.8e-100 | artM | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
MHMNNKED_01522 | 7e-84 | artQ | E | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_01523 | 7.1e-80 | artP | ET | Belongs to the bacterial solute-binding protein 3 family | ||
MHMNNKED_01524 | 1.5e-202 | sdaC | E | Tryptophan/tyrosine permease family | ||
MHMNNKED_01525 | 1e-58 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
MHMNNKED_01528 | 7e-86 | S | Spore germination B3/ GerAC like, C-terminal | |||
MHMNNKED_01529 | 4.5e-88 | E | Spore germination protein | |||
MHMNNKED_01532 | 3.9e-76 | K | Bacterial regulatory proteins, tetR family | |||
MHMNNKED_01533 | 3.1e-203 | EGP | Major facilitator Superfamily | |||
MHMNNKED_01534 | 5.4e-109 | ribA | 3.5.4.25, 4.1.99.12 | H | GTP cyclohydrolase II | |
MHMNNKED_01535 | 6.6e-148 | 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 | |
MHMNNKED_01536 | 4.3e-61 | 3.1.3.3 | E | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | ||
MHMNNKED_01537 | 8.9e-109 | yeeN | K | transcriptional regulatory protein | ||
MHMNNKED_01538 | 1.9e-166 | ctpB | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
MHMNNKED_01539 | 6.7e-146 | minJ | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | ||
MHMNNKED_01540 | 3.3e-87 | tagA | 2.4.1.187 | GT26 | M | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
MHMNNKED_01541 | 1.4e-92 | csaB | M | Glycosyl Transferase | ||
MHMNNKED_01542 | 3.3e-101 | M | Glycosyltransferase like family 2 | |||
MHMNNKED_01543 | 9.2e-10 | yhaL | S | Sporulation protein YhaL | ||
MHMNNKED_01544 | 5.8e-193 | cbf | S | 3'-5' exoribonuclease yhaM | ||
MHMNNKED_01545 | 1.6e-196 | L | AAA domain | |||
MHMNNKED_01546 | 4.2e-127 | yhaO | L | DNA repair exonuclease | ||
MHMNNKED_01547 | 7e-128 | 3.4.24.84 | O | Peptidase family M48 | ||
MHMNNKED_01548 | 2.7e-17 | S | YhzD-like protein | |||
MHMNNKED_01549 | 6e-171 | yjlD | 1.6.99.3 | C | NADH dehydrogenase | |
MHMNNKED_01550 | 1.6e-36 | yjlC | S | Protein of unknown function (DUF1641) | ||
MHMNNKED_01551 | 6.8e-258 | alkK | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
MHMNNKED_01552 | 5.1e-103 | yhaX | S | hydrolases of the HAD superfamily | ||
MHMNNKED_01553 | 1e-30 | yheA | S | Belongs to the UPF0342 family | ||
MHMNNKED_01554 | 1e-98 | yheB | S | Belongs to the UPF0754 family | ||
MHMNNKED_01555 | 8.5e-52 | gshB | 6.3.2.2, 6.3.2.3 | HJ | YheC/D like ATP-grasp | |
MHMNNKED_01556 | 2.8e-69 | yheC | HJ | YheC/D like ATP-grasp | ||
MHMNNKED_01557 | 4.4e-141 | gshB | 6.3.2.2, 6.3.2.3 | HJ | YheC/D like ATP-grasp | |
MHMNNKED_01558 | 1.4e-66 | HJ | COG0189 Glutathione synthase Ribosomal protein S6 modification enzyme (glutaminyl transferase) | |||
MHMNNKED_01559 | 1.9e-23 | |||||
MHMNNKED_01560 | 2.1e-23 | sasP | S | Small, acid-soluble spore proteins, alpha/beta type | ||
MHMNNKED_01561 | 3.3e-17 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
MHMNNKED_01562 | 1.7e-111 | yqgE | EGP | Major facilitator superfamily | ||
MHMNNKED_01563 | 1.4e-118 | pdaA | G | deacetylase | ||
MHMNNKED_01565 | 1.5e-113 | yfkD | S | YfkD-like protein | ||
MHMNNKED_01566 | 2e-142 | yfkF | EGP | Major facilitator Superfamily | ||
MHMNNKED_01567 | 9.6e-235 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
MHMNNKED_01568 | 1.6e-101 | yihY | S | Belongs to the UPF0761 family | ||
MHMNNKED_01569 | 4.5e-10 | yfkI | S | gas vesicle protein | ||
MHMNNKED_01570 | 3.8e-60 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
MHMNNKED_01571 | 2.9e-18 | yfkK | S | Belongs to the UPF0435 family | ||
MHMNNKED_01572 | 1.6e-124 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
MHMNNKED_01573 | 2.5e-38 | yhdN | S | Domain of unknown function (DUF1992) | ||
MHMNNKED_01574 | 1.4e-34 | ybaZ | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
MHMNNKED_01575 | 4.1e-162 | ampS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
MHMNNKED_01576 | 2.7e-38 | ybjQ | S | Putative heavy-metal-binding | ||
MHMNNKED_01577 | 5e-67 | yvdA | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
MHMNNKED_01578 | 1.7e-136 | ykvU | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
MHMNNKED_01579 | 2.7e-34 | yrzB | S | Belongs to the UPF0473 family | ||
MHMNNKED_01580 | 6.2e-54 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
MHMNNKED_01581 | 4.1e-35 | yrzL | S | Belongs to the UPF0297 family | ||
MHMNNKED_01582 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
MHMNNKED_01583 | 4.6e-125 | yrrI | S | AI-2E family transporter | ||
MHMNNKED_01584 | 4.2e-29 | yrzR | ||||
MHMNNKED_01585 | 6.3e-35 | fdxA | C | 4Fe-4S binding domain | ||
MHMNNKED_01586 | 9.1e-157 | mhqA | 3.4.21.26 | E | COG0346 Lactoylglutathione lyase and related lyases | |
MHMNNKED_01587 | 1.4e-99 | aatB | ET | Bacterial periplasmic substrate-binding proteins | ||
MHMNNKED_01588 | 9.3e-89 | artQ | E | COG0765 ABC-type amino acid transport system, permease component | ||
MHMNNKED_01589 | 6e-100 | glnQ3 | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
MHMNNKED_01590 | 0.0 | 3.6.3.8 | P | COG0474 Cation transport ATPase | ||
MHMNNKED_01591 | 1.4e-51 | ywnF | S | Family of unknown function (DUF5392) | ||
MHMNNKED_01592 | 4.6e-07 | S | Protein of unknown function (DUF1450) | |||
MHMNNKED_01593 | 3.6e-99 | cheV | 2.7.13.3 | T | Chemotaxis protein CheV | |
MHMNNKED_01594 | 1.2e-107 | yueF | S | transporter activity | ||
MHMNNKED_01595 | 4.1e-43 | yusN | M | Coat F domain | ||
MHMNNKED_01596 | 1.2e-23 | |||||
MHMNNKED_01597 | 1.6e-126 | fadM | E | Proline dehydrogenase | ||
MHMNNKED_01598 | 0.0 | fadB | 1.1.1.35, 4.2.1.17, 5.1.2.3 | I | 3-hydroxyacyl-CoA dehydrogenase | |
MHMNNKED_01599 | 2e-182 | fadA | 2.3.1.16 | I | Belongs to the thiolase family | |
MHMNNKED_01600 | 1.4e-288 | fadE | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
MHMNNKED_01601 | 1.3e-52 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
MHMNNKED_01602 | 3.4e-51 | gcvH | E | Is also involved in protein lipoylation via its role as an octanoyl lipoyl carrier protein intermediate | ||
MHMNNKED_01603 | 4.1e-46 | rnmV | 3.1.26.8 | L | COG1658 Small primase-like proteins (Toprim domain) | |
MHMNNKED_01604 | 2.8e-35 | yusE | CO | Thioredoxin | ||
MHMNNKED_01605 | 1.3e-09 | S | SCP-2 sterol transfer family | |||
MHMNNKED_01607 | 3.9e-142 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
MHMNNKED_01608 | 1.9e-89 | metI | P | COG2011 ABC-type metal ion transport system, permease component | ||
MHMNNKED_01609 | 4.2e-16 | yafE | Q | ubiE/COQ5 methyltransferase family | ||
MHMNNKED_01611 | 1.1e-08 | ppsA2 | 2.7.9.2 | GT | Pyruvate phosphate dikinase, PEP/pyruvate binding domain | |
MHMNNKED_01612 | 2.8e-217 | yknU | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
MHMNNKED_01613 | 3.2e-232 | yknV | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
MHMNNKED_01614 | 5.4e-92 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
MHMNNKED_01615 | 1.4e-290 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
MHMNNKED_01616 | 8e-18 | ykzG | S | Belongs to the UPF0356 family | ||
MHMNNKED_01617 | 4.2e-33 | recN | L | Putative cell-wall binding lipoprotein | ||
MHMNNKED_01618 | 2.6e-158 | pdhA | 1.2.4.1, 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
MHMNNKED_01619 | 9e-165 | pdhB | 1.2.4.1 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
MHMNNKED_01620 | 6.3e-58 | ykhA | 3.1.2.20 | I | Acyl-CoA hydrolase | |
MHMNNKED_01621 | 3.6e-29 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
MHMNNKED_01622 | 2.2e-34 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
MHMNNKED_01623 | 7.5e-139 | speB | 3.5.3.11 | E | Belongs to the arginase family | |
MHMNNKED_01624 | 1.3e-143 | speE | 2.5.1.16 | E | Catalyzes the irreversible transfer of a propylamine group from the amino donor S-adenosylmethioninamine (decarboxy- AdoMet) to putrescine (1,4-diaminobutane) to yield spermidine | |
MHMNNKED_01625 | 1.3e-64 | speH | 2.5.1.128, 2.5.1.16, 4.1.1.50 | E | Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine | |
MHMNNKED_01626 | 7.5e-211 | speA | 4.1.1.19 | E | decarboxylase | |
MHMNNKED_01627 | 2.5e-177 | metK | 2.5.1.6 | H | S-adenosylmethionine synthetase, C-terminal domain | |
MHMNNKED_01628 | 6.3e-227 | G | Major Facilitator Superfamily | |||
MHMNNKED_01629 | 1.8e-26 | yrzD | S | Post-transcriptional regulator | ||
MHMNNKED_01630 | 5.4e-204 | spoVB | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
MHMNNKED_01631 | 3.5e-64 | yrbG | S | membrane | ||
MHMNNKED_01632 | 3.7e-45 | yrzE | S | Protein of unknown function (DUF3792) | ||
MHMNNKED_01633 | 1.8e-22 | yajC | U | Preprotein translocase subunit YajC | ||
MHMNNKED_01634 | 4.4e-203 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
MHMNNKED_01635 | 9.2e-160 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
MHMNNKED_01636 | 2.4e-19 | yrzS | S | Protein of unknown function (DUF2905) | ||
MHMNNKED_01637 | 2.8e-161 | 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 | |
MHMNNKED_01638 | 5.3e-75 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
MHMNNKED_01639 | 3.8e-87 | hprK | T | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Also phosphorylates dephosphorylates the HPr-like catabolite repression protein crh on a specific serine residue. Therefore, by controlling the phosphorylation state of HPr and crh, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
MHMNNKED_01640 | 8.8e-129 | cydA | 1.10.3.14 | C | oxidase, subunit | |
MHMNNKED_01641 | 1.4e-160 | cydB | 1.10.3.14 | C | COG1294 Cytochrome bd-type quinol oxidase, subunit 2 | |
MHMNNKED_01642 | 5.3e-62 | mta | K | MerR family transcriptional regulator | ||
MHMNNKED_01643 | 3.8e-194 | yaaH | M | Glyco_18 | ||
MHMNNKED_01644 | 0.0 | S | S-layer homology domain | |||
MHMNNKED_01645 | 9.8e-190 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
MHMNNKED_01646 | 1.5e-120 | S | Aldo/keto reductase family | |||
MHMNNKED_01647 | 9.1e-69 | CO | Thioredoxin | |||
MHMNNKED_01648 | 5.2e-71 | S | Bax inhibitor 1 like | |||
MHMNNKED_01649 | 2.3e-241 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
MHMNNKED_01650 | 1.1e-148 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
MHMNNKED_01651 | 1.5e-09 | K | Belongs to the sigma-70 factor family. ECF subfamily | |||
MHMNNKED_01652 | 7.6e-58 | |||||
MHMNNKED_01653 | 9.5e-09 | |||||
MHMNNKED_01654 | 1.6e-34 | I | SCP-2 sterol transfer family | |||
MHMNNKED_01655 | 8.1e-72 | S | Psort location CytoplasmicMembrane, score | |||
MHMNNKED_01656 | 9.4e-73 | |||||
MHMNNKED_01657 | 5.7e-182 | 2.3.1.9 | I | Thiolase, N-terminal domain | ||
MHMNNKED_01658 | 7.3e-109 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
MHMNNKED_01659 | 7e-199 | MA20_26760 | 1.3.8.7 | I | COG1960 Acyl-CoA dehydrogenases | |
MHMNNKED_01660 | 4.9e-48 | I | MaoC like domain | |||
MHMNNKED_01661 | 4.8e-60 | MA20_04520 | 4.2.1.153, 4.2.1.56 | S | N-terminal half of MaoC dehydratase | |
MHMNNKED_01662 | 3.3e-114 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
MHMNNKED_01663 | 2.5e-172 | mmgC_3 | 1.3.8.7 | I | Acyl-CoA dehydrogenase, N-terminal domain | |
MHMNNKED_01664 | 1.6e-131 | yjjC | V | COG1131 ABC-type multidrug transport system, ATPase component | ||
MHMNNKED_01665 | 5.3e-67 | K | Bacterial regulatory proteins, tetR family | |||
MHMNNKED_01666 | 3.1e-102 | |||||
MHMNNKED_01667 | 4.5e-276 | H | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
MHMNNKED_01668 | 6.5e-139 | 2.1.1.113 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
MHMNNKED_01669 | 4e-125 | G | Transmembrane secretion effector | |||
MHMNNKED_01672 | 2.7e-112 | ypjC | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
MHMNNKED_01673 | 2.1e-47 | ypjD | 2.5.1.19 | S | Nucleotide pyrophosphohydrolase | |
MHMNNKED_01674 | 1.3e-105 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
MHMNNKED_01675 | 9.5e-60 | mgsA | 2.7.1.24, 4.2.3.3 | G | methylglyoxal synthase | |
MHMNNKED_01676 | 7.9e-152 | bshA | GT4 | M | N-acetyl-alpha-D-glucosaminyl L-malate synthase | |
MHMNNKED_01677 | 4.2e-140 | 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 | |
MHMNNKED_01678 | 1.3e-131 | birA | 6.3.4.15 | K | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
MHMNNKED_01679 | 1.5e-112 | panB | 2.1.2.11 | H | Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha-ketoisovalerate to form ketopantoate | |
MHMNNKED_01680 | 1.2e-107 | panC | 2.7.4.25, 6.3.2.1 | H | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate | |
MHMNNKED_01681 | 2e-51 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
MHMNNKED_01682 | 2.6e-74 | plsC | 2.3.1.51 | I | 1-acyl-sn-glycerol-3-phosphate acyltransferase | |
MHMNNKED_01683 | 4.9e-201 | yfiC | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
MHMNNKED_01684 | 3.4e-167 | yfiB3 | V | ABC transporter transmembrane region | ||
MHMNNKED_01685 | 1.2e-92 | 1.1.1.3 | E | homoserine dehydrogenase | ||
MHMNNKED_01686 | 3.6e-201 | metY | 2.5.1.49 | E | O-acetylhomoserine | |
MHMNNKED_01687 | 1.6e-100 | dksA | T | COG1734 DnaK suppressor protein | ||
MHMNNKED_01689 | 4.6e-44 | S | Protein of unknown function (DUF2512) | |||
MHMNNKED_01690 | 2.5e-84 | 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 | |
MHMNNKED_01691 | 3e-106 | EGP | Major facilitator Superfamily | |||
MHMNNKED_01692 | 9.6e-120 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
MHMNNKED_01693 | 3.2e-115 | pstA | P | Phosphate transport system permease | ||
MHMNNKED_01694 | 5.4e-124 | pstC | U | probably responsible for the translocation of the substrate across the membrane | ||
MHMNNKED_01695 | 3.3e-107 | pstS | P | Phosphate ABC transporter substrate-binding protein | ||
MHMNNKED_01697 | 4.5e-95 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
MHMNNKED_01698 | 3.5e-184 | 1.3.8.7 | I | Acyl-CoA dehydrogenase, N-terminal domain | ||
MHMNNKED_01699 | 2.4e-180 | 2.3.1.16, 2.3.1.9 | I | Belongs to the thiolase family | ||
MHMNNKED_01700 | 1.5e-152 | amacr | C | acyl-CoA transferases carnitine dehydratase | ||
MHMNNKED_01701 | 2.1e-137 | 1.13.12.16 | S | Nitronate monooxygenase | ||
MHMNNKED_01703 | 6e-33 | |||||
MHMNNKED_01704 | 1e-23 | |||||
MHMNNKED_01705 | 7.3e-109 | M | Glycosyl transferase family 2 | |||
MHMNNKED_01706 | 4.1e-142 | S | slime layer polysaccharide biosynthetic process | |||
MHMNNKED_01707 | 1.7e-156 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |||
MHMNNKED_01708 | 2.9e-10 | |||||
MHMNNKED_01709 | 2.3e-35 | |||||
MHMNNKED_01710 | 4.5e-71 | V | efflux transmembrane transporter activity | |||
MHMNNKED_01711 | 3e-44 | 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 | ||
MHMNNKED_01712 | 8.7e-302 | dnaK | O | Heat shock 70 kDa protein | ||
MHMNNKED_01713 | 3.1e-148 | 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 | ||
MHMNNKED_01714 | 6e-142 | prmA | J | Methylates ribosomal protein L11 | ||
MHMNNKED_01715 | 6.2e-81 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
MHMNNKED_01716 | 3.1e-232 | yqeV | 2.8.4.5 | J | ribosomal protein S12 methylthiotransferase | |
MHMNNKED_01717 | 2.5e-86 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
MHMNNKED_01718 | 1.6e-91 | yqeW | P | COG1283 Na phosphate symporter | ||
MHMNNKED_01719 | 2.1e-19 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
MHMNNKED_01720 | 4.4e-34 | yqeY | S | Yqey-like protein | ||
MHMNNKED_01721 | 3e-131 | yqeZ | O | COG1030 Membrane-bound serine protease (ClpP class) | ||
MHMNNKED_01722 | 2.8e-84 | yqfA | S | UPF0365 protein | ||
MHMNNKED_01724 | 2.7e-37 | yqfC | S | sporulation protein YqfC | ||
MHMNNKED_01725 | 2.5e-148 | yqfD | 3.1.3.102, 3.1.3.104 | S | Stage IV sporulation | |
MHMNNKED_01726 | 3.9e-144 | phoH | T | Phosphate starvation-inducible protein PhoH | ||
MHMNNKED_01727 | 9.7e-268 | yqfF | S | membrane-associated HD superfamily hydrolase | ||
MHMNNKED_01728 | 2.9e-60 | 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 | |
MHMNNKED_01729 | 3.2e-25 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
MHMNNKED_01730 | 8.9e-50 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
MHMNNKED_01731 | 4.2e-148 | 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 | ||
MHMNNKED_01732 | 1.7e-08 | S | YqzL-like protein | |||
MHMNNKED_01733 | 7.5e-103 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
MHMNNKED_01734 | 1.6e-93 | ccpN | K | CBS domain | ||
MHMNNKED_01735 | 1.4e-118 | yqfL | 2.7.11.33, 2.7.4.28 | S | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
MHMNNKED_01736 | 3.5e-231 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
MHMNNKED_01737 | 3.6e-173 | 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 | ||
MHMNNKED_01738 | 6.4e-178 | yngJ | 1.3.8.1, 1.3.99.12 | I | acyl-CoA dehydrogenase | |
MHMNNKED_01739 | 8.8e-33 | cccA | C | Cytochrome C oxidase, cbb3-type, subunit III | ||
MHMNNKED_01740 | 5.1e-75 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
MHMNNKED_01741 | 5.9e-168 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
MHMNNKED_01742 | 2.9e-152 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
MHMNNKED_01743 | 5.7e-30 | yqfQ | S | YqfQ-like protein | ||
MHMNNKED_01744 | 8.6e-179 | 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 | |
MHMNNKED_01745 | 7.1e-148 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
MHMNNKED_01746 | 1.8e-24 | yqfT | S | Protein of unknown function (DUF2624) | ||
MHMNNKED_01747 | 3.6e-28 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
MHMNNKED_01748 | 3.4e-40 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
MHMNNKED_01749 | 2.7e-26 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
MHMNNKED_01750 | 2.5e-10 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
MHMNNKED_01751 | 5.2e-56 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
MHMNNKED_01752 | 1.6e-70 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
MHMNNKED_01753 | 2.8e-34 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
MHMNNKED_01754 | 1.3e-31 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
MHMNNKED_01755 | 6.7e-45 | mce | 5.1.99.1, 5.4.99.2 | E | COG0346 Lactoylglutathione lyase and related lyases | |
MHMNNKED_01756 | 2.2e-266 | mmdA | 2.1.3.15, 6.4.1.3 | I | COG4799 Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
MHMNNKED_01757 | 3.2e-166 | yqjE | 3.4.11.4 | E | COG2195 Di- and tripeptidases | |
MHMNNKED_01758 | 2.2e-184 | 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 | |
MHMNNKED_01759 | 1.5e-224 | gnd | 1.1.1.343, 1.1.1.44 | G | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
MHMNNKED_01760 | 2.3e-236 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
MHMNNKED_01761 | 2.6e-129 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
MHMNNKED_01762 | 1.8e-88 | yqjP | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
MHMNNKED_01763 | 1.4e-94 | yqjQ | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
MHMNNKED_01764 | 1.4e-09 | S | zinc-ribbon domain | |||
MHMNNKED_01765 | 1.3e-43 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
MHMNNKED_01766 | 1.3e-89 | S | Abortive infection C-terminus | |||
MHMNNKED_01767 | 1.5e-15 | S | Uncharacterized protein conserved in bacteria (DUF2188) | |||
MHMNNKED_01768 | 2.9e-44 | ygzB | S | UPF0295 protein | ||
MHMNNKED_01769 | 3.4e-163 | ygxA | S | Nucleotidyltransferase-like | ||
MHMNNKED_01770 | 2.6e-115 | glcT | K | antiterminator | ||
MHMNNKED_01771 | 2.1e-183 | S | Alpha/beta hydrolase family | |||
MHMNNKED_01772 | 3.2e-95 | S | Metallo-beta-lactamase superfamily | |||
MHMNNKED_01773 | 2.4e-98 | MA20_36880 | CH | FAD binding domain | ||
MHMNNKED_01774 | 9.9e-37 | emrR | K | Sugar-specific transcriptional regulator TrmB | ||
MHMNNKED_01776 | 8.5e-159 | garK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
MHMNNKED_01777 | 3.5e-98 | murR | K | Helix-turn-helix domain, rpiR family | ||
MHMNNKED_01778 | 1.7e-227 | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase | |
MHMNNKED_01779 | 2e-32 | M | Sulfatase | |||
MHMNNKED_01780 | 4.3e-21 | S | Pfam:DUF2029 | |||
MHMNNKED_01781 | 1.1e-38 | S | Acyltransferase family | |||
MHMNNKED_01782 | 7.4e-36 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
MHMNNKED_01783 | 2.2e-61 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
MHMNNKED_01784 | 2e-21 | yazB | K | Helix-turn-helix XRE-family like proteins | ||
MHMNNKED_01785 | 3.8e-25 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
MHMNNKED_01786 | 5.5e-158 | gpr | 3.4.24.78 | C | Initiates the rapid degradation of small, acid-soluble proteins during spore germination | |
MHMNNKED_01787 | 1.6e-25 | yqxA | S | Protein of unknown function (DUF3679) | ||
MHMNNKED_01788 | 2.6e-135 | 4.2.1.115 | M | GDP-mannose 4,6 dehydratase | ||
MHMNNKED_01789 | 5.2e-169 | wecB | 5.1.3.14 | M | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
MHMNNKED_01790 | 5.4e-127 | S | Glycosyl transferases group 1 | |||
MHMNNKED_01792 | 3.1e-38 | S | Protein of unknown function (DUF1360) | |||
MHMNNKED_01793 | 6e-54 | S | Spore coat protein Z | |||
MHMNNKED_01794 | 1.9e-09 | |||||
MHMNNKED_01795 | 7e-120 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
MHMNNKED_01796 | 2.3e-189 | yjbQ | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
MHMNNKED_01797 | 3.7e-14 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
MHMNNKED_01798 | 9e-43 | xylA | 5.3.1.5 | G | xylose isomerase activity | |
MHMNNKED_01799 | 1.1e-130 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
MHMNNKED_01800 | 1.1e-251 | treP | 2.7.1.201 | G | phosphotransferase system | |
MHMNNKED_01801 | 4.3e-276 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
MHMNNKED_01802 | 1.3e-99 | treR | K | transcriptional | ||
MHMNNKED_01803 | 3.5e-273 | 3.2.1.10 | GH13 | G | COG0366 Glycosidases | |
MHMNNKED_01805 | 5.8e-167 | G | ABC transporter substrate-binding protein | |||
MHMNNKED_01806 | 7.2e-108 | gltC | K | Transcriptional regulator | ||
MHMNNKED_01807 | 3.8e-115 | 3.4.19.11 | E | Zn_pept | ||
MHMNNKED_01808 | 5.9e-28 | yhdB | S | YhdB-like protein | ||
MHMNNKED_01809 | 1.2e-44 | bdbC | O | Required for disulfide bond formation in some proteins | ||
MHMNNKED_01810 | 1.6e-30 | bdbA | CO | Thioredoxin | ||
MHMNNKED_01811 | 1.5e-14 | S | nuclease activity | |||
MHMNNKED_01812 | 1.7e-67 | 3.5.1.124 | S | DJ-1/PfpI family | ||
MHMNNKED_01813 | 2e-160 | ysfB | KT | regulator | ||
MHMNNKED_01814 | 1.1e-42 | V | ABC transporter, ATP-binding protein | |||
MHMNNKED_01815 | 7.4e-230 | V | FtsX-like permease family | |||
MHMNNKED_01816 | 6.7e-46 | adhC | 1.1.1.1 | C | Alcohol dehydrogenase GroES-like domain | |
MHMNNKED_01817 | 2.4e-150 | pepQ | 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
MHMNNKED_01818 | 7.1e-108 | ytkL | S | Belongs to the UPF0173 family | ||
MHMNNKED_01819 | 1.4e-26 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
MHMNNKED_01820 | 1.5e-66 | ygaZ | E | AzlC protein | ||
MHMNNKED_01822 | 2.7e-118 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
MHMNNKED_01823 | 1.8e-176 | T | PhoQ Sensor | |||
MHMNNKED_01824 | 5.3e-59 | S | Protein of unknown function (DUF3221) | |||
MHMNNKED_01825 | 2.6e-103 | mpr | 3.4.21.19 | E | Belongs to the peptidase S1B family | |
MHMNNKED_01826 | 6.9e-25 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
MHMNNKED_01830 | 3.9e-70 | yocA | M | Lysozyme-like | ||
MHMNNKED_01831 | 2.2e-112 | T | Transcriptional regulatory protein, C terminal | |||
MHMNNKED_01832 | 3.9e-173 | yjcL | S | integral membrane protein | ||
MHMNNKED_01833 | 4.8e-159 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
MHMNNKED_01834 | 1.9e-103 | K | Transcriptional regulator | |||
MHMNNKED_01836 | 2.9e-91 | pstB | 3.6.3.27 | P | Belongs to the ABC transporter superfamily | |
MHMNNKED_01837 | 3.8e-102 | ybbM | S | transport system, permease component | ||
MHMNNKED_01838 | 1.3e-308 | 6.2.1.1 | I | AMP-dependent synthetase | ||
MHMNNKED_01839 | 2.2e-46 | M | Protein of unknown function (DUF1541) | |||
MHMNNKED_01840 | 2.2e-56 | 1.5.1.38 | S | FMN reductase | ||
MHMNNKED_01841 | 3.7e-22 | |||||
MHMNNKED_01842 | 4.2e-74 | yieF | S | NAD(P)H-dependent FMN reductase | ||
MHMNNKED_01843 | 8.4e-88 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
MHMNNKED_01844 | 1.5e-175 | pbuO_1 | S | permease | ||
MHMNNKED_01845 | 1.3e-86 | S | Protein of unknown function (DUF4256) | |||
MHMNNKED_01846 | 3.1e-157 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
MHMNNKED_01847 | 3.4e-62 | 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 | |
MHMNNKED_01848 | 2.7e-83 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis. Acts negatively in the development of competence by binding ComK and recruiting it to the ClpCP protease. When overexpressed, inhibits sporulation. Also involved in Spx degradation by ClpC | ||
MHMNNKED_01849 | 3.2e-95 | yjbF | S | Competence protein | ||
MHMNNKED_01850 | 3.7e-305 | pepF | E | oligoendopeptidase F | ||
MHMNNKED_01852 | 1.5e-140 | lanM | V | Domain of unknown function (DUF4135) | ||
MHMNNKED_01853 | 0.0 | 3.6.3.27 | V | ABC transporter transmembrane region | ||
MHMNNKED_01854 | 5.1e-223 | S | Erythromycin esterase | |||
MHMNNKED_01856 | 4.2e-97 | |||||
MHMNNKED_01857 | 1.6e-44 | cotB | ||||
MHMNNKED_01858 | 1.4e-43 | |||||
MHMNNKED_01859 | 3.1e-71 | |||||
MHMNNKED_01860 | 1.6e-188 | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | |||
MHMNNKED_01861 | 3.9e-91 | KT | LytTr DNA-binding domain | |||
MHMNNKED_01862 | 5.7e-218 | lytS | 2.7.13.3 | T | Histidine kinase | |
MHMNNKED_01863 | 1.2e-42 | ywcA | S | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
MHMNNKED_01864 | 1.3e-121 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
MHMNNKED_01866 | 5.4e-216 | comEC | S | Competence protein ComEC | ||
MHMNNKED_01867 | 2e-74 | comEB | 3.5.4.12 | F | COG2131 Deoxycytidylate deaminase | |
MHMNNKED_01868 | 6.9e-26 | mod_1 | 2.1.1.72 | L | DNA methylase | |
MHMNNKED_01869 | 0.0 | res_1 | 3.1.21.5 | S | DEAD-like helicases superfamily | |
MHMNNKED_01870 | 1.2e-84 | yocR | S | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family | ||
MHMNNKED_01871 | 3.4e-155 | pdh | 1.4.1.20, 1.4.1.9 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
MHMNNKED_01872 | 3.3e-152 | bkdA1 | 1.2.4.1, 1.2.4.4 | C | 1-deoxy-D-xylulose-5-phosphate synthase | |
MHMNNKED_01873 | 1.9e-149 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain | |
MHMNNKED_01874 | 5.1e-120 | bkdB | 1.8.1.4, 2.3.1.12, 2.3.1.168 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
MHMNNKED_01875 | 7.8e-157 | lpdA | 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
MHMNNKED_01880 | 1.1e-96 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
MHMNNKED_01881 | 0.0 | katE | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
MHMNNKED_01882 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
MHMNNKED_01883 | 1.1e-57 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
MHMNNKED_01884 | 1.2e-109 | MA20_23325 | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
MHMNNKED_01885 | 1e-123 | MA20_23330 | P | NMT1-like family | ||
MHMNNKED_01887 | 1.8e-72 | maa | 2.3.1.79 | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | |
MHMNNKED_01889 | 2.8e-23 | ddpX | 3.4.13.22 | |||
MHMNNKED_01890 | 5.1e-37 | ddpX | 3.4.13.22 | T | protein conserved in bacteria | |
MHMNNKED_01894 | 3.1e-08 | S | growth of symbiont in host cell | |||
MHMNNKED_01895 | 2e-227 | ahpF | O | Alkyl hydroperoxide reductase | ||
MHMNNKED_01896 | 1.8e-93 | ahpC | 1.11.1.15 | O | Alkyl hydroperoxide reductase | |
MHMNNKED_01897 | 4.1e-12 | S | YuzL-like protein | |||
MHMNNKED_01898 | 2.7e-33 | tesC | S | Thioesterase-like superfamily | ||
MHMNNKED_01900 | 3.2e-197 | rnj | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
MHMNNKED_01905 | 1e-154 | ydbT | S | Membrane | ||
MHMNNKED_01906 | 3.7e-56 | S | Bacterial PH domain | |||
MHMNNKED_01908 | 5.5e-22 | |||||
MHMNNKED_01909 | 1.3e-34 | S | Protein of unknown function (DUF2089) | |||
MHMNNKED_01910 | 1e-77 | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | |||
MHMNNKED_01911 | 8.8e-106 | natA | V | COG1131 ABC-type multidrug transport system, ATPase component | ||
MHMNNKED_01915 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MHMNNKED_01916 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
MHMNNKED_01917 | 4.7e-74 | rsmC | 2.1.1.172 | J | Methyltransferase | |
MHMNNKED_01918 | 7.1e-46 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
MHMNNKED_01919 | 1.3e-71 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
MHMNNKED_01920 | 3.7e-96 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
MHMNNKED_01921 | 5e-67 | rplK | J | Ribosomal protein L11/L12 | ||
MHMNNKED_01922 | 1.2e-81 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
MHMNNKED_01923 | 1.9e-15 | 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 | ||
MHMNNKED_01924 | 1.4e-95 | sigH | K | Belongs to the sigma-70 factor family | ||
MHMNNKED_01925 | 9.5e-59 | yacP | S | RNA-binding protein containing a PIN domain | ||
MHMNNKED_01926 | 1.8e-117 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
MHMNNKED_01927 | 1.5e-50 | 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) | ||
MHMNNKED_01928 | 4e-230 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
MHMNNKED_01929 | 2.8e-93 | cysE | 2.3.1.30 | E | Serine acetyltransferase | |
MHMNNKED_01930 | 1.6e-226 | 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) | |
MHMNNKED_01931 | 1.3e-63 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | I | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
MHMNNKED_01932 | 4e-69 | ispD | 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
MHMNNKED_01933 | 2.7e-141 | yacL | S | COG4956 Integral membrane protein (PIN domain superfamily) | ||
MHMNNKED_01934 | 5.7e-205 | 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 | ||
MHMNNKED_01935 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
MHMNNKED_01936 | 4.4e-165 | mcsB | 2.7.14.1, 2.7.3.2, 2.7.3.3 | E | Catalyzes the specific phosphorylation of arginine residues in a large number of proteins. Is part of the bacterial stress response system. Protein arginine phosphorylation has a physiologically important role and is involved in the regulation of many critical cellular processes, such as protein homeostasis, motility, competence, and stringent and stress responses, by regulating gene expression and protein activity | |
MHMNNKED_01937 | 3.5e-78 | mcsA | 2.7.14.1 | S | protein with conserved CXXC pairs | |
MHMNNKED_01938 | 7e-59 | ctsR | K | Belongs to the CtsR family | ||
MHMNNKED_01939 | 6.8e-163 | gapB | 1.2.1.12, 1.2.1.59 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
MHMNNKED_01940 | 5.1e-65 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
MHMNNKED_01941 | 1.7e-169 | dnaB | L | Membrane attachment protein | ||
MHMNNKED_01942 | 1.6e-126 | dnaI | L | Primosomal protein DnaI | ||
MHMNNKED_01943 | 3.7e-82 | ytxC | S | YtxC-like family | ||
MHMNNKED_01944 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
MHMNNKED_01945 | 1.1e-76 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
MHMNNKED_01946 | 9.7e-23 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
MHMNNKED_01947 | 4.5e-53 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
MHMNNKED_01948 | 8.8e-08 | ysdA | S | membrane | ||
MHMNNKED_01949 | 3.8e-39 | L | Phage integrase family | |||
MHMNNKED_01950 | 3.6e-276 | 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 | |
MHMNNKED_01951 | 9.4e-221 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
MHMNNKED_01952 | 3e-120 | ybbR | S | protein conserved in bacteria | ||
MHMNNKED_01953 | 1.7e-127 | 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 | |
MHMNNKED_01954 | 4.4e-72 | rsiW | K | Is the anti-sigma factor for SigW. The presence of RsiW leads to the inactivation of SigW, and its proteolytic destruction to sigma-W activation | ||
MHMNNKED_01955 | 2.6e-84 | sigW | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
MHMNNKED_01956 | 9e-135 | rocF | 3.5.3.1, 3.5.3.11 | E | Belongs to the arginase family | |
MHMNNKED_01957 | 1.4e-41 | phaG | P | COG1320 Multisubunit Na H antiporter, MnhG subunit | ||
MHMNNKED_01958 | 1.8e-33 | phaF | P | Subunit F of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
MHMNNKED_01959 | 3.3e-59 | mrpE | P | Subunit E of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
MHMNNKED_01960 | 7.7e-208 | mrpD | CP | Subunit D of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
MHMNNKED_01961 | 7.3e-45 | phaC | 1.6.5.3 | P | Subunit C of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | |
MHMNNKED_01962 | 1.3e-56 | mrpB | P | Subunit B of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
MHMNNKED_01963 | 0.0 | phaA | 1.6.5.3 | CP | COG1009 NADH ubiquinone oxidoreductase subunit 5 (chain L) Multisubunit Na H antiporter, MnhA subunit | |
MHMNNKED_01966 | 4.9e-178 | EGP | Major facilitator Superfamily | |||
MHMNNKED_01967 | 1.1e-106 | ctaB | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
MHMNNKED_01968 | 8.6e-18 | S | Uncharacterized protein conserved in bacteria (DUF2187) | |||
MHMNNKED_01969 | 8.2e-114 | M | Glycosyl transferase family group 2 | |||
MHMNNKED_01970 | 7.7e-74 | M | Glycosyl transferase family group 2 | |||
MHMNNKED_01971 | 1.1e-38 | V | VanZ like family | |||
MHMNNKED_01972 | 5.8e-76 | cypC | 1.11.2.4, 1.14.14.1 | Q | Cytochrome P450 | |
MHMNNKED_01973 | 2.1e-96 | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | |||
MHMNNKED_01974 | 1.7e-147 | G | Major Facilitator Superfamily | |||
MHMNNKED_01975 | 6.8e-39 | S | alpha beta | |||
MHMNNKED_01976 | 5.6e-126 | yfmL | L | COG0513 Superfamily II DNA and RNA helicases | ||
MHMNNKED_01978 | 2.1e-26 | S | Cyclopropane-fatty-acyl-phospholipid synthase | |||
MHMNNKED_01979 | 2.6e-09 | T | Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase | |||
MHMNNKED_01980 | 7.5e-79 | ydjA | C | Nitroreductase family | ||
MHMNNKED_01981 | 5.4e-63 | 1.5.1.38 | S | FMN reductase | ||
MHMNNKED_01982 | 4e-177 | gabR | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
MHMNNKED_01984 | 1e-70 | S | Restriction endonuclease | |||
MHMNNKED_01986 | 4.5e-09 | |||||
MHMNNKED_01987 | 5.7e-23 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
MHMNNKED_01988 | 2.6e-197 | C | Luciferase-like monooxygenase | |||
MHMNNKED_01989 | 6.3e-103 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
MHMNNKED_01990 | 2.4e-255 | ggtA | 2.3.2.2, 3.4.19.13 | E | Gamma-glutamyltranspeptidase | |
MHMNNKED_01991 | 1.1e-42 | chrA | P | Chromate transporter | ||
MHMNNKED_01992 | 8.9e-66 | chrA | P | COG2059 Chromate transport protein ChrA | ||
MHMNNKED_01993 | 1.8e-262 | vpr | O | Belongs to the peptidase S8 family | ||
MHMNNKED_01994 | 5e-34 | atpI | S | ATP synthase I chain | ||
MHMNNKED_01995 | 4.5e-97 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
MHMNNKED_01996 | 3.2e-22 | 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 | ||
MHMNNKED_01997 | 1.6e-19 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
MHMNNKED_01998 | 1.6e-54 | 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 | ||
MHMNNKED_01999 | 1.9e-262 | 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 | |
MHMNNKED_02000 | 6e-112 | 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 | ||
MHMNNKED_02001 | 5.2e-246 | 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 | |
MHMNNKED_02002 | 8.2e-43 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
MHMNNKED_02003 | 2.3e-21 | ywzB | S | membrane | ||
MHMNNKED_02004 | 3.7e-57 | ywmB | S | TATA-box binding | ||
MHMNNKED_02005 | 2.6e-207 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
MHMNNKED_02014 | 2e-61 | ydcK | S | Belongs to the SprT family | ||
MHMNNKED_02015 | 0.0 | yhgF | K | COG2183 Transcriptional accessory protein | ||
MHMNNKED_02016 | 2.5e-56 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
MHMNNKED_02017 | 2.7e-37 | ndoAI | K | transcriptional regulators containing the CopG Arc MetJ DNA-binding domain and a metal-binding domain | ||
MHMNNKED_02018 | 4.2e-121 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
MHMNNKED_02019 | 8.4e-145 | ydcC | M | COG2834 Outer membrane lipoprotein-sorting protein | ||
MHMNNKED_02020 | 8.1e-39 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
MHMNNKED_02021 | 6.6e-46 | ydcA | 3.4.21.105 | S | membrane protein (homolog of Drosophila rhomboid) | |
MHMNNKED_02022 | 5e-48 | uvsE | L | UV damage repair endonuclease UvdE | ||
MHMNNKED_02023 | 2.2e-42 | yorS | 3.1.3.5 | S | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | |
MHMNNKED_02025 | 1.1e-151 | ybfG | M | Domain of unknown function (DUF1906) | ||
MHMNNKED_02027 | 1.3e-80 | prsW | S | Involved in the degradation of specific anti-sigma factors | ||
MHMNNKED_02028 | 4.5e-140 | ypdA | 1.18.1.2, 1.19.1.1, 1.8.1.9 | O | COG0492 Thioredoxin reductase | |
MHMNNKED_02029 | 2.5e-215 | gudB | 1.4.1.2, 1.4.1.3 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
MHMNNKED_02030 | 7.9e-28 | mecB | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis. Acts negatively in the development of competence by binding ComK and recruiting it to the ClpCP protease. When overexpressed, inhibits sporulation. Also involved in Spx degradation by ClpC | ||
MHMNNKED_02031 | 1.2e-55 | ypbF | S | Protein of unknown function (DUF2663) | ||
MHMNNKED_02033 | 2.2e-106 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | GHMP kinases C terminal | |
MHMNNKED_02034 | 3.5e-124 | mvaD | 4.1.1.33 | I | GHMP kinases N terminal domain | |
MHMNNKED_02035 | 1.6e-59 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases C terminal | |
MHMNNKED_02036 | 6e-64 | S | AAA domain | |||
MHMNNKED_02037 | 3e-88 | yrkF | OP | Sulfurtransferase TusA | ||
MHMNNKED_02038 | 5.3e-63 | perX | P | Sulfur reduction protein DsrE | ||
MHMNNKED_02039 | 2.1e-210 | yrkH | P | Rhodanese Homology Domain | ||
MHMNNKED_02040 | 6.2e-32 | O | Belongs to the sulfur carrier protein TusA family | |||
MHMNNKED_02041 | 1.2e-106 | S | membrane transporter protein | |||
MHMNNKED_02042 | 1.8e-35 | yrkD | S | Metal-sensitive transcriptional repressor | ||
MHMNNKED_02043 | 1.9e-43 | P | Rhodanese Homology Domain | |||
MHMNNKED_02044 | 8.3e-38 | P | Rhodanese domain protein | |||
MHMNNKED_02045 | 1.8e-80 | T | HD domain | |||
MHMNNKED_02046 | 1.1e-82 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
MHMNNKED_02047 | 7.1e-21 | ydcG | K | Helix-turn-helix domain | ||
MHMNNKED_02048 | 1.2e-47 | K | Helix-turn-helix XRE-family like proteins | |||
MHMNNKED_02049 | 1e-99 | V | ATPases associated with a variety of cellular activities | |||
MHMNNKED_02050 | 1.8e-73 | S | ABC-2 family transporter protein | |||
MHMNNKED_02051 | 1.1e-91 | folE | 3.5.4.16 | H | GTP cyclohydrolase | |
MHMNNKED_02052 | 3.8e-105 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
MHMNNKED_02053 | 5.7e-09 | K | sequence-specific DNA binding | |||
MHMNNKED_02055 | 1.8e-54 | E | lipolytic protein G-D-S-L family | |||
MHMNNKED_02056 | 4.7e-25 | S | GtrA-like protein | |||
MHMNNKED_02057 | 5.5e-104 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
MHMNNKED_02058 | 7.5e-37 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
MHMNNKED_02059 | 2.2e-144 | ppaC | 3.6.1.1 | C | Inorganic pyrophosphatase | |
MHMNNKED_02060 | 1.1e-13 | cvfB | S | protein conserved in bacteria | ||
MHMNNKED_02061 | 9e-160 | mbl | D | Rod shape-determining protein | ||
MHMNNKED_02062 | 1.3e-72 | |||||
MHMNNKED_02063 | 3.2e-53 | radC | L | RadC-like JAB domain | ||
MHMNNKED_02064 | 9.3e-85 | 4.6.1.1 | T | Adenylate and Guanylate cyclase catalytic domain | ||
MHMNNKED_02065 | 5.9e-25 | |||||
MHMNNKED_02067 | 1.7e-39 | |||||
MHMNNKED_02070 | 2.8e-17 | |||||
MHMNNKED_02071 | 6.8e-54 | crtF | 2.1.1.210, 2.1.1.281, 2.1.1.79 | M | Methyltransferase | |
MHMNNKED_02072 | 6.5e-66 | 1.8.5.2 | S | DoxX | ||
MHMNNKED_02073 | 2.1e-107 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
MHMNNKED_02074 | 3.3e-77 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MHMNNKED_02075 | 2e-61 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
MHMNNKED_02076 | 8.4e-84 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
MHMNNKED_02077 | 2.4e-107 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
MHMNNKED_02078 | 3.9e-66 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
MHMNNKED_02079 | 6e-107 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
MHMNNKED_02080 | 1.1e-292 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
MHMNNKED_02081 | 7.9e-29 | ypoC | ||||
MHMNNKED_02082 | 2.8e-109 | 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 | |
MHMNNKED_02083 | 3.3e-92 | dnaD | L | DNA replication protein DnaD | ||
MHMNNKED_02084 | 1.7e-109 | S | ABC-2 family transporter protein | |||
MHMNNKED_02085 | 9.3e-122 | yxlF_1 | V | ABC transporter, ATP-binding protein | ||
MHMNNKED_02086 | 6.8e-127 | 3.2.1.22 | S | NPCBM-associated, NEW3 domain of alpha-galactosidase | ||
MHMNNKED_02087 | 8.6e-70 | sigI | K | Sigma-70, region 4 | ||
MHMNNKED_02088 | 4e-45 | rskA | S | Anti-sigma-K factor rskA | ||
MHMNNKED_02089 | 4.3e-68 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
MHMNNKED_02090 | 1.8e-72 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | alcohol dehydrogenase | |
MHMNNKED_02091 | 4.5e-66 | |||||
MHMNNKED_02095 | 0.0 | icmF | 5.4.99.13 | EI | Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly | |
MHMNNKED_02096 | 1.1e-83 | kstR2_2 | K | Transcriptional regulator | ||
MHMNNKED_02097 | 2.4e-131 | acdA | 1.3.8.1, 1.3.8.7 | I | acyl-CoA dehydrogenase | |
MHMNNKED_02098 | 3.7e-59 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
MHMNNKED_02099 | 3.8e-90 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02100 | 7.4e-83 | metQ3 | M | Belongs to the nlpA lipoprotein family | ||
MHMNNKED_02101 | 5.7e-156 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
MHMNNKED_02103 | 0.0 | nrdA | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
MHMNNKED_02104 | 3.4e-55 | fld | C | Flavodoxin | ||
MHMNNKED_02105 | 1.6e-164 | nrdB | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
MHMNNKED_02106 | 2.5e-263 | S | FAD binding domain | |||
MHMNNKED_02107 | 3.3e-153 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
MHMNNKED_02108 | 2.7e-210 | pepV | 3.5.1.18 | E | Dipeptidase | |
MHMNNKED_02109 | 1.9e-30 | ytoQ | S | Nucleoside 2-deoxyribosyltransferase YtoQ | ||
MHMNNKED_02110 | 6.1e-232 | mqo | 1.1.5.4 | C | oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor | |
MHMNNKED_02111 | 1.1e-124 | nhaR | K | Transcriptional regulator | ||
MHMNNKED_02112 | 3.3e-193 | S | F420-0:Gamma-glutamyl ligase | |||
MHMNNKED_02113 | 2.1e-99 | rluC | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
MHMNNKED_02114 | 4.5e-89 | nagZ | 3.2.1.52 | G | Belongs to the glycosyl hydrolase 3 family | |
MHMNNKED_02115 | 2.6e-202 | tagD | 2.7.7.15, 2.7.7.39 | H | Oxidoreductase NAD-binding domain protein | |
MHMNNKED_02116 | 1.4e-41 | M | Glycosyl transferase, family 2 | |||
MHMNNKED_02117 | 2.7e-46 | M | transferase activity, transferring glycosyl groups | |||
MHMNNKED_02118 | 6.3e-77 | ptmE | M | Nucleotidyl transferase | ||
MHMNNKED_02119 | 9.5e-47 | ptmE | M | Nucleotidyl transferase | ||
MHMNNKED_02120 | 4.4e-87 | spoU | 2.1.1.185 | J | RNA 2'-O ribose methyltransferase substrate binding | |
MHMNNKED_02121 | 3.8e-23 | sspI | S | Small, acid-soluble spore protein I | ||
MHMNNKED_02122 | 2e-58 | slt | M | Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
MHMNNKED_02123 | 8.4e-125 | xerC | L | tyrosine recombinase XerC | ||
MHMNNKED_02124 | 1.2e-78 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
MHMNNKED_02125 | 2.1e-215 | 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 | ||
MHMNNKED_02126 | 5.8e-122 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
MHMNNKED_02127 | 6.7e-34 | flgB | N | Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body | ||
MHMNNKED_02128 | 5.7e-58 | flgC | N | Belongs to the flagella basal body rod proteins family | ||
MHMNNKED_02129 | 1.1e-23 | fliE | N | Flagellar hook-basal body | ||
MHMNNKED_02130 | 2.3e-165 | fliF | N | The M ring may be actively involved in energy transduction | ||
MHMNNKED_02131 | 2.3e-155 | fliG | N | One of the proteins that forms a switch complex that is proposed to be located at the base of the basal body. This complex interacts with chemotaxis proteins (such as CheY) in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
MHMNNKED_02132 | 4.5e-34 | fliH | NU | Flagellar assembly protein FliH | ||
MHMNNKED_02133 | 2e-68 | XK27_09665 | 5.4.2.11 | G | Phosphoglycerate mutase | |
MHMNNKED_02134 | 3.7e-67 | yybS | S | membrane | ||
MHMNNKED_02135 | 5.9e-264 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
MHMNNKED_02136 | 5.1e-46 | rplI | J | Binds to the 23S rRNA | ||
MHMNNKED_02137 | 2e-218 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
MHMNNKED_02138 | 4e-124 | nlpD | M | G5 | ||
MHMNNKED_02139 | 4.8e-46 | EGP | Major facilitator Superfamily | |||
MHMNNKED_02140 | 1.3e-36 | K | Bacterial regulatory proteins, tetR family | |||
MHMNNKED_02142 | 1e-170 | clpB | O | Belongs to the ClpA ClpB family | ||
MHMNNKED_02143 | 4.1e-56 | rpfB | GH23 | T | protein conserved in bacteria | |
MHMNNKED_02144 | 1.4e-69 | 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 | |
MHMNNKED_02145 | 4.2e-121 | 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 | |
MHMNNKED_02146 | 2.1e-128 | yabG | S | peptidase | ||
MHMNNKED_02147 | 2.3e-35 | veg | S | protein conserved in bacteria | ||
MHMNNKED_02148 | 3.6e-19 | sspF | S | DNA topological change | ||
MHMNNKED_02149 | 6.3e-56 | opuAC | E | glycine betaine | ||
MHMNNKED_02150 | 5.4e-85 | ywaC | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
MHMNNKED_02151 | 7.9e-125 | dkgB | S | Aldo/keto reductase family | ||
MHMNNKED_02152 | 4e-09 | S | Protein of unknown function (DUF4025) | |||
MHMNNKED_02153 | 2e-108 | proV | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
MHMNNKED_02154 | 1.8e-191 | proWX | EM | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
MHMNNKED_02155 | 3.8e-146 | ydbM | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
MHMNNKED_02156 | 1.4e-107 | uppS | 2.5.1.31 | I | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
MHMNNKED_02157 | 4.3e-141 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
MHMNNKED_02158 | 8.3e-210 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
MHMNNKED_02159 | 3.6e-238 | rasP | M | zinc metalloprotease | ||
MHMNNKED_02160 | 2.3e-20 | S | Domain of unknown function (DUF3899) | |||
MHMNNKED_02161 | 1.1e-199 | dppE_1 | E | Peptide ABC transporter substrate-binding protein | ||
MHMNNKED_02162 | 1.2e-137 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
MHMNNKED_02163 | 2e-163 | oppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
MHMNNKED_02164 | 2e-162 | oppD | P | Belongs to the ABC transporter superfamily | ||
MHMNNKED_02165 | 5.8e-153 | oppF | E | Belongs to the ABC transporter superfamily | ||
MHMNNKED_02166 | 4.1e-28 | |||||
MHMNNKED_02167 | 6.2e-40 | S | Psort location CytoplasmicMembrane, score | |||
MHMNNKED_02168 | 1.4e-13 | S | Domain of unknown function (DUF4430) | |||
MHMNNKED_02169 | 1.7e-66 | Q | Thioesterase superfamily | |||
MHMNNKED_02170 | 7.3e-96 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
MHMNNKED_02171 | 4.1e-23 | uraA | F | Xanthine uracil | ||
MHMNNKED_02172 | 2e-20 | |||||
MHMNNKED_02174 | 4.5e-106 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
MHMNNKED_02175 | 1.3e-33 | yphA | ||||
MHMNNKED_02176 | 9e-127 | seaA | S | YIEGIA protein | ||
MHMNNKED_02177 | 7.5e-20 | ypzH | ||||
MHMNNKED_02178 | 6.5e-227 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
MHMNNKED_02179 | 2.6e-141 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
MHMNNKED_02180 | 2.6e-38 | tagH | 3.2.1.1, 3.5.1.28, 3.6.3.40 | GH13 | M | N-acetylmuramoyl-L-alanine amidase |
MHMNNKED_02181 | 3.3e-137 | nifS | 2.8.1.7 | E | Cysteine desulfurase | |
MHMNNKED_02182 | 3.1e-175 | nadB | 1.3.5.4, 1.4.3.16 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
MHMNNKED_02183 | 2.4e-113 | nadC | 1.4.3.16, 2.4.2.19 | H | Belongs to the NadC ModD family | |
MHMNNKED_02184 | 8.7e-164 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
MHMNNKED_02185 | 4.2e-16 | yphE | S | Protein of unknown function (DUF2768) | ||
MHMNNKED_02186 | 1e-69 | yphF | ||||
MHMNNKED_02187 | 2.7e-269 | spoIVA | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | ||
MHMNNKED_02188 | 1.9e-35 | 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 | ||
MHMNNKED_02189 | 1.9e-28 | mtrB | K | Required for transcription attenuation control in the Trp operon. This trans-acting factor seems to recognize a 10 bases nucleotide sequence in the Trp leader transcript causing transcription termination. Binds the leader RNA only in presence of L-tryptophan | ||
MHMNNKED_02190 | 3.9e-52 | hepS | 2.5.1.30 | H | heptaprenyl diphosphate synthase | |
MHMNNKED_02191 | 2.7e-110 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
MHMNNKED_02192 | 1.2e-137 | hepT | 2.5.1.30, 2.5.1.83, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
MHMNNKED_02193 | 4.1e-72 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
MHMNNKED_02194 | 7.3e-109 | cheR | 2.1.1.80 | NT | COG1352 Methylase of chemotaxis methyl-accepting proteins | |
MHMNNKED_02195 | 3.7e-165 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
MHMNNKED_02196 | 7e-97 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
MHMNNKED_02197 | 1.3e-139 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
MHMNNKED_02198 | 1.4e-87 | |||||
MHMNNKED_02199 | 5.3e-133 | S | COG0457 FOG TPR repeat | |||
MHMNNKED_02200 | 1.3e-83 | ypiB | S | Belongs to the UPF0302 family | ||
MHMNNKED_02201 | 1.9e-35 | ypiF | S | Protein of unknown function (DUF2487) | ||
MHMNNKED_02202 | 3.4e-78 | qcrA | C | Menaquinol-cytochrome c reductase | ||
MHMNNKED_02203 | 9.8e-118 | petB | C | COG1290 Cytochrome b subunit of the bc complex | ||
MHMNNKED_02204 | 3.4e-127 | qcrC | C | Menaquinol-cytochrome c reductase cytochrome b c subunit | ||
MHMNNKED_02205 | 1.2e-71 | ypjA | S | membrane | ||
MHMNNKED_02206 | 4.4e-61 | ypjB | S | sporulation protein | ||
MHMNNKED_02207 | 1.9e-124 | G | COG1593 TRAP-type C4-dicarboxylate transport system, large permease component | |||
MHMNNKED_02208 | 1.7e-81 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
MHMNNKED_02209 | 1.9e-70 | yhfK | GM | Dihydrodipicolinate reductase, N-terminus | ||
MHMNNKED_02210 | 2.7e-69 | ykuD | S | L,D-transpeptidase catalytic domain | ||
MHMNNKED_02211 | 1.3e-20 | |||||
MHMNNKED_02212 | 8.1e-82 | queF | 1.7.1.13 | S | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
MHMNNKED_02213 | 1.7e-26 | mutT | 3.6.1.55 | F | NUDIX domain | |
MHMNNKED_02214 | 7.1e-24 | |||||
MHMNNKED_02215 | 1.4e-19 | V | VanZ like family | |||
MHMNNKED_02216 | 6.1e-17 | L | Phage integrase family | |||
MHMNNKED_02217 | 5.6e-197 | 3.4.11.19 | EQ | Peptidase family S58 | ||
MHMNNKED_02218 | 1.5e-65 | S | DoxX | |||
MHMNNKED_02219 | 5.6e-156 | rbsB | G | Periplasmic binding protein domain | ||
MHMNNKED_02220 | 2.1e-158 | rbsC | G | COG1172 Ribose xylose arabinose galactoside ABC-type transport systems, permease components | ||
MHMNNKED_02221 | 2.3e-44 | rbsA | 3.6.3.17 | G | Part of the ABC transporter complex RbsABC involved in ribose import. Responsible for energy coupling to the transport system | |
MHMNNKED_02222 | 2.4e-41 | betT | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
MHMNNKED_02224 | 4.6e-18 | fliT | S | bacterial-type flagellum organization | ||
MHMNNKED_02225 | 4e-50 | fliS | N | flagellar protein FliS | ||
MHMNNKED_02226 | 2.4e-165 | fliD | N | morphogenesis and for the elongation of the flagellar filament by facilitating polymerization of the flagellin monomers at the tip of growing filament. Forms a capping structure, which prevents flagellin subunits (transported through the central channel of the flagellum) from leaking out without polymerization at the distal end | ||
MHMNNKED_02227 | 4.6e-21 | flaG | N | flagellar protein FlaG | ||
MHMNNKED_02228 | 6.3e-60 | tenI | 2.5.1.3, 5.3.99.10 | H | Thiamine monophosphate synthase | |
MHMNNKED_02229 | 4.7e-15 | thiS | H | ThiS family | ||
MHMNNKED_02230 | 7.2e-125 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
MHMNNKED_02231 | 9.4e-141 | moeB | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | ||
MHMNNKED_02232 | 2.6e-153 | hmp | 1.14.12.17 | C | Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress | |
MHMNNKED_02233 | 3.7e-57 | nsrR | K | Transcriptional regulator | ||
MHMNNKED_02234 | 1.3e-197 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
MHMNNKED_02235 | 3e-250 | pckA | 4.1.1.49 | C | Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA | |
MHMNNKED_02236 | 1.8e-187 | oppA1 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
MHMNNKED_02237 | 9.2e-103 | oppC | EP | binding-protein-dependent transport systems inner membrane component | ||
MHMNNKED_02238 | 4.2e-114 | oppB | P | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02239 | 1.6e-139 | oppF | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
MHMNNKED_02240 | 1.1e-139 | oppD | P | Belongs to the ABC transporter superfamily | ||
MHMNNKED_02241 | 1.7e-16 | ytmB | S | Protein of unknown function (DUF2584) | ||
MHMNNKED_02242 | 1.6e-137 | ytlA | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
MHMNNKED_02243 | 2.3e-110 | ytlC | P | ABC transporter | ||
MHMNNKED_02244 | 9.3e-99 | ytlD | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
MHMNNKED_02245 | 9.1e-38 | ytkD | 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
MHMNNKED_02246 | 6.3e-167 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
MHMNNKED_02247 | 8e-25 | |||||
MHMNNKED_02248 | 3e-51 | dps | P | Belongs to the Dps family | ||
MHMNNKED_02249 | 1.5e-31 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
MHMNNKED_02250 | 8.3e-102 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
MHMNNKED_02251 | 3.3e-182 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
MHMNNKED_02252 | 9e-142 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
MHMNNKED_02253 | 7.1e-78 | menH | 4.2.99.20 | S | Catalyzes a proton abstraction reaction that results in 2,5-elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6- hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) | |
MHMNNKED_02254 | 4.1e-184 | menD | 2.2.1.9 | H | Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) | |
MHMNNKED_02255 | 1.5e-115 | menF | 5.4.4.2 | HQ | Isochorismate synthase | |
MHMNNKED_02256 | 1.7e-131 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
MHMNNKED_02257 | 1.1e-99 | yphA | ||||
MHMNNKED_02258 | 6.3e-157 | seaA | S | YIEGIA protein | ||
MHMNNKED_02259 | 8.3e-27 | ypzH | ||||
MHMNNKED_02261 | 4.7e-35 | GM | Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid | |||
MHMNNKED_02262 | 3.5e-24 | |||||
MHMNNKED_02263 | 6.6e-59 | EGP | Major facilitator Superfamily | |||
MHMNNKED_02264 | 1.3e-139 | KLT | Protein kinase domain | |||
MHMNNKED_02265 | 2.6e-158 | EG | of the drug metabolite transporter (DMT) superfamily | |||
MHMNNKED_02266 | 2.5e-111 | sapB | S | MgtC family | ||
MHMNNKED_02267 | 5.6e-231 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
MHMNNKED_02268 | 8.8e-112 | tepA | 3.4.21.92 | OU | COG0740 Protease subunit of ATP-dependent Clp proteases | |
MHMNNKED_02269 | 4.9e-07 | S | YlzJ-like protein | |||
MHMNNKED_02270 | 2.6e-303 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
MHMNNKED_02271 | 1.9e-126 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
MHMNNKED_02272 | 6.4e-245 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
MHMNNKED_02273 | 3.8e-153 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
MHMNNKED_02274 | 6.7e-144 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
MHMNNKED_02275 | 1.2e-172 | ymfF | S | Peptidase M16 | ||
MHMNNKED_02276 | 3.1e-189 | ymfH | S | zinc protease | ||
MHMNNKED_02277 | 5.1e-88 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
MHMNNKED_02278 | 3.5e-31 | ymfJ | S | Protein of unknown function (DUF3243) | ||
MHMNNKED_02279 | 3.1e-107 | ymfK | S | Protein of unknown function (DUF3388) | ||
MHMNNKED_02280 | 1.1e-68 | ymfM | S | protein conserved in bacteria | ||
MHMNNKED_02281 | 1.9e-82 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
MHMNNKED_02282 | 8.3e-163 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
MHMNNKED_02283 | 3.7e-266 | suv3 | 3.6.4.13 | L | COG0513 Superfamily II DNA and RNA helicases | |
MHMNNKED_02284 | 1.5e-48 | yaiI | S | Belongs to the UPF0178 family | ||
MHMNNKED_02285 | 7.2e-65 | J | protein with SCP PR1 domains | |||
MHMNNKED_02286 | 1.1e-231 | pulA | 3.2.1.41 | CBM48,GH13 | G | Carbohydrate-binding module 48 (Isoamylase N-terminal domain) |
MHMNNKED_02287 | 2.9e-284 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Alpha amylase, C-terminal all-beta domain |
MHMNNKED_02288 | 4.5e-155 | glgC | 2.7.7.27 | G | MobA-like NTP transferase domain | |
MHMNNKED_02289 | 3.9e-148 | glgD | 2.7.7.27 | G | Nucleotidyl transferase | |
MHMNNKED_02290 | 2.5e-203 | glgA | 2.4.1.21 | GT5 | G | Starch synthase catalytic domain |
MHMNNKED_02291 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Carbohydrate phosphorylase |
MHMNNKED_02293 | 2.9e-177 | splB | 4.1.99.14 | L | Radical SAM protein | |
MHMNNKED_02294 | 8e-26 | yqhV | S | Protein of unknown function (DUF2619) | ||
MHMNNKED_02295 | 1.4e-91 | 3.1.2.21 | I | Acyl-ACP thioesterase | ||
MHMNNKED_02296 | 3.8e-07 | 2.7.1.24 | H | dephospho-CoA kinase activity | ||
MHMNNKED_02298 | 6.6e-144 | ybdG | M | Mechanosensitive ion channel | ||
MHMNNKED_02300 | 2.9e-79 | frnE | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
MHMNNKED_02301 | 1.8e-66 | aroK | 2.7.1.71, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
MHMNNKED_02302 | 7.7e-84 | S | Predicted nucleotidyltransferase | |||
MHMNNKED_02303 | 5.4e-94 | metQ | P | COG1464 ABC-type metal ion transport system, periplasmic component surface antigen | ||
MHMNNKED_02304 | 4.5e-127 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
MHMNNKED_02305 | 1.8e-84 | metI | P | COG2011 ABC-type metal ion transport system, permease component | ||
MHMNNKED_02306 | 8.2e-209 | actP | S | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
MHMNNKED_02307 | 2e-284 | sat | 2.7.7.4 | P | the enzyme from Thermus thermophilus is dimeric and binds a zinc ion that is coordinated by cysteine and histidine residues that are not found in all related proteins but is found in some thermophilic organisms | |
MHMNNKED_02309 | 3.5e-145 | 1.13.12.16, 1.3.1.9 | S | COG2070 Dioxygenases related to 2-nitropropane dioxygenase | ||
MHMNNKED_02310 | 2.4e-27 | yktA | S | Belongs to the UPF0223 family | ||
MHMNNKED_02311 | 1.4e-81 | yktB | S | Belongs to the UPF0637 family | ||
MHMNNKED_02312 | 4.2e-107 | suhB | 3.1.3.25 | G | Inositol monophosphatase | |
MHMNNKED_02314 | 4.4e-306 | typA | T | GTP-binding protein TypA | ||
MHMNNKED_02315 | 1.6e-30 | ylaH | S | YlaH-like protein | ||
MHMNNKED_02316 | 7.9e-23 | ylaI | S | protein conserved in bacteria | ||
MHMNNKED_02317 | 3.2e-51 | ylaJ | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
MHMNNKED_02318 | 4.2e-49 | ylaL | S | Part of the MsrPQ system that repairs oxidized periplasmic proteins containing methionine sulfoxide residues (Met-O), using respiratory chain electrons. Thus protects these proteins from oxidative-stress damage caused by reactive species of oxygen and chlorine generated by the host defense mechanisms. MsrPQ is essential for the maintenance of envelope integrity under bleach stress, rescuing a wide series of structurally unrelated periplasmic proteins from methionine oxidation. The catalytic subunit MsrP is non-stereospecific, being able to reduce both (R-) and (S-) diastereoisomers of methionine sulfoxide | ||
MHMNNKED_02319 | 1.9e-38 | ylaN | S | Belongs to the UPF0358 family | ||
MHMNNKED_02320 | 1.4e-132 | ftsW | D | Belongs to the SEDS family | ||
MHMNNKED_02321 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
MHMNNKED_02322 | 1.8e-104 | ctaA | 2.5.1.141 | O | Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group | |
MHMNNKED_02323 | 1.3e-123 | ctaB | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
MHMNNKED_02324 | 7.6e-133 | ctaC | 1.9.3.1 | C | Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) | |
MHMNNKED_02325 | 0.0 | ctaD | 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
MHMNNKED_02326 | 3.9e-92 | cyoC | 1.9.3.1 | C | COG1845 Heme copper-type cytochrome quinol oxidase, subunit 3 | |
MHMNNKED_02327 | 3.1e-29 | ctaF | 1.10.3.12, 1.9.3.1 | C | COG3125 Heme copper-type cytochrome quinol oxidase, subunit 4 | |
MHMNNKED_02328 | 8.5e-93 | ctaG | S | cytochrome c oxidase | ||
MHMNNKED_02329 | 4.6e-58 | S | Protein of unknown function (DUF420) | |||
MHMNNKED_02330 | 4.6e-48 | ylbA | S | YugN-like family | ||
MHMNNKED_02331 | 4.2e-127 | ylbC | S | protein with SCP PR1 domains | ||
MHMNNKED_02332 | 2.2e-22 | ylbD | S | Putative coat protein | ||
MHMNNKED_02333 | 2.3e-18 | ylbE | S | YlbE-like protein | ||
MHMNNKED_02334 | 4.2e-53 | ylbF | S | Belongs to the UPF0342 family | ||
MHMNNKED_02335 | 2.3e-33 | ylbG | S | UPF0298 protein | ||
MHMNNKED_02336 | 4.7e-58 | |||||
MHMNNKED_02337 | 7.4e-71 | rsmD | 2.1.1.171 | L | Methyltransferase | |
MHMNNKED_02338 | 1.8e-65 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
MHMNNKED_02339 | 2.1e-147 | ylbJ | S | Sporulation integral membrane protein YlbJ | ||
MHMNNKED_02340 | 2.3e-94 | ylbK | S | esterase of the alpha-beta hydrolase superfamily | ||
MHMNNKED_02341 | 1.7e-126 | ylbL | T | Belongs to the peptidase S16 family | ||
MHMNNKED_02342 | 5.1e-141 | ylbM | S | Belongs to the UPF0348 family | ||
MHMNNKED_02343 | 1.6e-51 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
MHMNNKED_02344 | 8e-24 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
MHMNNKED_02345 | 6.8e-228 | ato-1 | 2.8.3.18, 3.1.2.1 | C | Acetyl-CoA hydrolase/transferase N-terminal domain | |
MHMNNKED_02346 | 1.3e-90 | K | LytTr DNA-binding domain | |||
MHMNNKED_02347 | 6.7e-147 | E | Belongs to the ABC transporter superfamily | |||
MHMNNKED_02348 | 1.2e-140 | oppD | P | Belongs to the ABC transporter superfamily | ||
MHMNNKED_02349 | 3.9e-43 | EP | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | |||
MHMNNKED_02350 | 6.2e-49 | L | Nuclease-related domain | |||
MHMNNKED_02351 | 3.1e-96 | comC | 3.4.23.43 | NOU | COG1989 Type II secretory pathway, prepilin signal peptidase PulO and related peptidases | |
MHMNNKED_02352 | 2.1e-35 | S | Protein of unknown function (DUF3892) | |||
MHMNNKED_02353 | 9.5e-168 | XK27_00915 | C | Luciferase-like monooxygenase | ||
MHMNNKED_02354 | 6.9e-61 | 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 | |
MHMNNKED_02355 | 2.9e-38 | czrA | K | Transcriptional regulator | ||
MHMNNKED_02356 | 2.4e-106 | czcD | P | cation diffusion facilitator family transporter | ||
MHMNNKED_02357 | 5e-122 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
MHMNNKED_02358 | 1e-154 | livJ | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
MHMNNKED_02359 | 5e-147 | lytH | M | Peptidase, M23 | ||
MHMNNKED_02360 | 1.6e-42 | yutD | S | protein conserved in bacteria | ||
MHMNNKED_02361 | 2.7e-44 | yutE | S | Protein of unknown function DUF86 | ||
MHMNNKED_02362 | 2.8e-105 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
MHMNNKED_02363 | 4.5e-67 | pgpA | 3.1.3.27 | I | COG1267 Phosphatidylglycerophosphatase A and related proteins | |
MHMNNKED_02364 | 4.9e-97 | yutH | S | Spore coat protein | ||
MHMNNKED_02365 | 1.8e-136 | gyaR | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
MHMNNKED_02366 | 4.8e-32 | yutI | O | COG0694 Thioredoxin-like proteins and domains | ||
MHMNNKED_02367 | 5.6e-40 | yuzD | S | protein conserved in bacteria | ||
MHMNNKED_02368 | 9.2e-238 | iolA | 1.2.1.18, 1.2.1.27 | C | Aldehyde dehydrogenase family | |
MHMNNKED_02369 | 1.5e-194 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |||
MHMNNKED_02370 | 3.6e-142 | QT | Regulator of polyketide synthase expression | |||
MHMNNKED_02371 | 1.4e-190 | gabP | E | Amino acid permease | ||
MHMNNKED_02372 | 3.4e-94 | devA | 3.6.3.25 | V | Hemin ABC transporter ATP-binding protein | |
MHMNNKED_02373 | 1.5e-139 | hrtB | V | FtsX-like permease family | ||
MHMNNKED_02374 | 4e-116 | yjbH | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
MHMNNKED_02375 | 6.9e-58 | yjbI | S | COG2346 Truncated hemoglobins | ||
MHMNNKED_02376 | 1.2e-51 | slt | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
MHMNNKED_02377 | 1.8e-54 | yjbK | S | protein conserved in bacteria | ||
MHMNNKED_02378 | 6e-90 | yjbM | 2.7.6.5 | S | GTP pyrophosphokinase | |
MHMNNKED_02379 | 1.6e-119 | nadK | 2.7.1.23 | G | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
MHMNNKED_02380 | 2.4e-111 | yjbO | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
MHMNNKED_02381 | 8.2e-110 | prpE | 3.1.3.16, 3.6.1.41 | T | Asymmetrically hydrolyzes Ap4p to yield AMP and ATP | |
MHMNNKED_02382 | 7.5e-25 | spoVK | O | ATPase, AAA family | ||
MHMNNKED_02387 | 9.1e-18 | |||||
MHMNNKED_02388 | 1.8e-28 | |||||
MHMNNKED_02389 | 3.9e-111 | yitT | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
MHMNNKED_02391 | 3.2e-08 | |||||
MHMNNKED_02392 | 2.3e-113 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
MHMNNKED_02393 | 4.3e-93 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
MHMNNKED_02394 | 7.9e-46 | yitW | S | metal-sulfur cluster biosynthetic enzyme | ||
MHMNNKED_02395 | 8.3e-16 | yjzC | S | YjzC-like protein | ||
MHMNNKED_02397 | 4.7e-84 | yjaU | I | carboxylic ester hydrolase activity | ||
MHMNNKED_02398 | 3.9e-11 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
MHMNNKED_02399 | 1.4e-146 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
MHMNNKED_02400 | 5.2e-210 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
MHMNNKED_02401 | 1.4e-132 | atl | 3.2.1.96, 3.5.1.28 | GH73 | G | autolysin |
MHMNNKED_02402 | 4.2e-115 | 3.5.1.28 | M | COG3103 SH3 domain protein | ||
MHMNNKED_02403 | 1.8e-80 | M | Glycosyltransferase like family 2 | |||
MHMNNKED_02404 | 3.6e-36 | tuaB | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
MHMNNKED_02405 | 1.2e-173 | potD | E | COG0687 Spermidine putrescine-binding periplasmic protein | ||
MHMNNKED_02406 | 3.9e-113 | potC | E | COG1177 ABC-type spermidine putrescine transport system, permease component II | ||
MHMNNKED_02407 | 1.2e-117 | potB | E | COG1176 ABC-type spermidine putrescine transport system, permease component I | ||
MHMNNKED_02408 | 8.7e-180 | 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 | |
MHMNNKED_02409 | 1.9e-79 | puuR | K | Cupin domain | ||
MHMNNKED_02410 | 6.1e-178 | T | PhoQ Sensor | |||
MHMNNKED_02411 | 2.7e-107 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
MHMNNKED_02412 | 1.1e-10 | ipi | S | Intracellular proteinase inhibitor | ||
MHMNNKED_02413 | 4.3e-115 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
MHMNNKED_02414 | 1.1e-83 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
MHMNNKED_02415 | 3.5e-07 | S | YpzG-like protein | |||
MHMNNKED_02416 | 3.3e-119 | cyoA | 1.10.3.10, 1.10.3.12 | C | Catalyzes quinol oxidation with the concomitant reduction of oxygen to water. Subunit II transfers the electrons from a quinol to the binuclear center of the catalytic subunit I | |
MHMNNKED_02417 | 4.6e-269 | qoxB | 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
MHMNNKED_02418 | 1.2e-82 | qoxC | 1.10.3.12 | C | quinol oxidase, subunit | |
MHMNNKED_02419 | 8.2e-24 | qoxD | 1.10.3.12 | C | quinol oxidase, subunit | |
MHMNNKED_02420 | 3.1e-28 | cidA | S | Effector of murein hydrolase LrgA | ||
MHMNNKED_02421 | 2.3e-50 | yxaC | M | effector of murein hydrolase | ||
MHMNNKED_02422 | 1.6e-51 | yceA | S | Belongs to the UPF0176 family | ||
MHMNNKED_02423 | 8.5e-183 | manR | 2.7.1.200, 2.7.1.202 | GKT | transcriptional antiterminator | |
MHMNNKED_02424 | 2.7e-51 | manP | 2.7.1.191, 2.7.1.202 | G | phosphotransferase system | |
MHMNNKED_02425 | 3.6e-180 | S | Tripartite tricarboxylate transporter TctA family | |||
MHMNNKED_02426 | 3.7e-20 | |||||
MHMNNKED_02427 | 2e-61 | K | transcriptional | |||
MHMNNKED_02428 | 2.3e-266 | topB | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
MHMNNKED_02429 | 1.2e-102 | ytnM | S | membrane transporter protein | ||
MHMNNKED_02430 | 6.6e-135 | yurR | 1.4.5.1 | E | COG0665 Glycine D-amino acid oxidases (deaminating) | |
MHMNNKED_02431 | 1.1e-35 | |||||
MHMNNKED_02432 | 3.6e-115 | sleB | 3.5.1.28 | M | Spore cortex-lytic enzyme | |
MHMNNKED_02433 | 5.2e-77 | yfcE | S | Phosphoesterase | ||
MHMNNKED_02434 | 5e-33 | |||||
MHMNNKED_02435 | 5.6e-89 | K | LysR substrate binding domain | |||
MHMNNKED_02436 | 4e-95 | hutG | 3.5.3.8 | E | Catalyzes the conversion of N-formimidoyl-L-glutamate to L-glutamate and formamide | |
MHMNNKED_02437 | 9.4e-279 | hutU | 4.2.1.49 | E | Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate | |
MHMNNKED_02438 | 2.4e-173 | hutI | 3.5.2.7 | Q | Imidazolone-5-propionate hydrolase | |
MHMNNKED_02439 | 2.1e-172 | S | Nucleoside recognition | |||
MHMNNKED_02440 | 8.1e-62 | yrkC | G | Cupin domain | ||
MHMNNKED_02441 | 1.8e-25 | yqzD | ||||
MHMNNKED_02442 | 8.5e-41 | |||||
MHMNNKED_02443 | 4.7e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
MHMNNKED_02444 | 4.1e-53 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
MHMNNKED_02445 | 4.7e-55 | S | Integral membrane protein DUF92 | |||
MHMNNKED_02447 | 2.7e-123 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
MHMNNKED_02448 | 1.1e-68 | |||||
MHMNNKED_02449 | 4.6e-221 | spoVAF | EG | Bacillus/Clostridium GerA spore germination protein | ||
MHMNNKED_02450 | 1.4e-17 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
MHMNNKED_02451 | 2.2e-110 | glk | 2.7.1.2 | G | Glucokinase | |
MHMNNKED_02452 | 8.8e-209 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
MHMNNKED_02453 | 6e-155 | yqgT | 3.4.19.11 | E | Gamma-D-glutamyl-L-diamino acid endopeptidase | |
MHMNNKED_02454 | 1.2e-229 | L | COG3316 Transposase and inactivated derivatives | |||
MHMNNKED_02455 | 1.4e-24 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
MHMNNKED_02456 | 1.8e-236 | pbpC | 3.4.16.4 | M | Penicillin-binding Protein | |
MHMNNKED_02457 | 6.2e-256 | MA20_29420 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
MHMNNKED_02458 | 2.8e-88 | S | Uncharacterized protein conserved in bacteria (DUF2332) | |||
MHMNNKED_02459 | 1.1e-33 | yneR | S | Belongs to the HesB IscA family | ||
MHMNNKED_02460 | 1.6e-62 | ywiC | S | YwiC-like protein | ||
MHMNNKED_02461 | 1.6e-170 | ycgA | S | Membrane | ||
MHMNNKED_02462 | 9.7e-167 | 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 | |
MHMNNKED_02463 | 6.1e-15 | yvlD | S | PFAM Membrane protein of | ||
MHMNNKED_02464 | 5.3e-44 | F | Nucleoside 2-deoxyribosyltransferase | |||
MHMNNKED_02465 | 3e-168 | mdxE | G | ABC transporter, substratebinding protein | ||
MHMNNKED_02466 | 9.2e-181 | malC | P | ABC transporter (Permease | ||
MHMNNKED_02467 | 8.2e-122 | malD | P | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02468 | 1.9e-51 | malA | S | maltodextrose utilization protein MalA | ||
MHMNNKED_02469 | 1.9e-63 | niaR | S | small molecule binding protein (contains 3H domain) | ||
MHMNNKED_02470 | 1.5e-26 | K | helix_turn_helix multiple antibiotic resistance protein | |||
MHMNNKED_02471 | 2.9e-45 | 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 | |
MHMNNKED_02472 | 1.5e-59 | S | Pyridoxamine 5'-phosphate oxidase | |||
MHMNNKED_02474 | 1.6e-69 | M | LysM domain | |||
MHMNNKED_02475 | 2.5e-51 | cph2 | T | Diguanylate cyclase | ||
MHMNNKED_02476 | 5.5e-33 | yocH | M | COG1388 FOG LysM repeat | ||
MHMNNKED_02477 | 1.4e-241 | dhaS | 1.2.1.3, 1.2.1.39 | C | Belongs to the aldehyde dehydrogenase family | |
MHMNNKED_02478 | 1.6e-104 | 3.4.16.4 | M | Belongs to the peptidase S11 family | ||
MHMNNKED_02479 | 1.4e-74 | ypuA | S | Secreted protein | ||
MHMNNKED_02480 | 6.4e-79 | |||||
MHMNNKED_02481 | 7.1e-258 | phnV | P | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02482 | 2.2e-23 | potA | 3.6.3.30 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
MHMNNKED_02484 | 2.1e-76 | L | viral genome integration into host DNA | |||
MHMNNKED_02485 | 1.3e-161 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
MHMNNKED_02486 | 3.6e-63 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
MHMNNKED_02487 | 1.2e-89 | yeaZ | 2.3.1.234 | O | COG1214 Inactive homolog of metal-dependent proteases | |
MHMNNKED_02488 | 1.8e-57 | ydiB | 2.7.1.221, 5.1.1.1 | S | ATPase or kinase | |
MHMNNKED_02491 | 1.2e-54 | cvpA | S | membrane protein, required for colicin V production | ||
MHMNNKED_02492 | 9.5e-234 | polX | L | COG1796 DNA polymerase IV (family X) | ||
MHMNNKED_02493 | 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 | ||
MHMNNKED_02494 | 7.6e-57 | yshE | S | membrane | ||
MHMNNKED_02495 | 1.6e-273 | lcfA | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
MHMNNKED_02496 | 2.9e-82 | fadR | K | Transcriptional regulator | ||
MHMNNKED_02497 | 4.9e-97 | fadB | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
MHMNNKED_02498 | 3.4e-114 | etfB | C | Electron transfer flavoprotein | ||
MHMNNKED_02499 | 1.7e-150 | etfA | C | Electron transfer flavoprotein | ||
MHMNNKED_02500 | 2.2e-48 | trxA | O | Belongs to the thioredoxin family | ||
MHMNNKED_02501 | 1e-286 | 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 | ||
MHMNNKED_02502 | 4.1e-154 | lysC | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
MHMNNKED_02503 | 5.3e-51 | yslB | S | Protein of unknown function (DUF2507) | ||
MHMNNKED_02504 | 7.6e-85 | sdhC | C | succinate dehydrogenase | ||
MHMNNKED_02505 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
MHMNNKED_02506 | 1.1e-141 | sdhB | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
MHMNNKED_02507 | 5.1e-49 | ysmA | S | thioesterase | ||
MHMNNKED_02510 | 4.2e-219 | fruA | 2.7.1.202 | GT | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
MHMNNKED_02511 | 5e-117 | pfkB | 2.7.1.11, 2.7.1.56 | G | Belongs to the carbohydrate kinase PfkB family | |
MHMNNKED_02512 | 5.5e-47 | acoC | 2.3.1.12, 2.3.1.61 | C | 2-oxoacid dehydrogenases acyltransferase (catalytic domain) | |
MHMNNKED_02513 | 3.6e-217 | L | Transposase | |||
MHMNNKED_02514 | 2.1e-104 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
MHMNNKED_02515 | 4.5e-09 | |||||
MHMNNKED_02516 | 5.6e-178 | ytoI | K | transcriptional regulator containing CBS domains | ||
MHMNNKED_02517 | 5.6e-25 | ytpI | S | YtpI-like protein | ||
MHMNNKED_02518 | 2.2e-139 | nrnA | 3.1.13.3, 3.1.3.7 | S | COG0618 Exopolyphosphatase-related proteins | |
MHMNNKED_02519 | 1.1e-18 | |||||
MHMNNKED_02521 | 3.5e-306 | L | COG1112 Superfamily I DNA and RNA helicases and helicase subunits | |||
MHMNNKED_02522 | 1.4e-44 | 2.8.3.12 | I | Coenzyme A transferase | ||
MHMNNKED_02523 | 1.3e-115 | 2.8.3.12 | I | Coenzyme A transferase | ||
MHMNNKED_02524 | 9e-99 | catI | 2.8.3.12 | I | acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
MHMNNKED_02525 | 7.2e-90 | catJ | 2.8.3.12 | I | PFAM Coenzyme A transferase | |
MHMNNKED_02527 | 4.2e-30 | S | DNA repair protein MmcB-like | |||
MHMNNKED_02528 | 7.2e-46 | |||||
MHMNNKED_02530 | 9.6e-99 | bxlB | G | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02531 | 1.3e-109 | bxlC | G | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02532 | 1.4e-120 | bxlD | G | Bacterial extracellular solute-binding protein | ||
MHMNNKED_02533 | 7.5e-118 | fda | 4.1.2.13 | G | Catalyzes the formation of glycerone phosphate and D-glyceraldehyde 3-phosphate from D-fructose 1,6-bisphosphate in glycolysis | |
MHMNNKED_02534 | 3.1e-156 | metE2 | 2.1.1.14 | E | Methionine synthase | |
MHMNNKED_02535 | 5.6e-104 | HJ | RimK-like ATP-grasp domain | |||
MHMNNKED_02536 | 1.1e-51 | S | DinB family | |||
MHMNNKED_02537 | 5.5e-98 | cwlD | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
MHMNNKED_02538 | 1.7e-49 | ybaK | S | Protein of unknown function (DUF2521) | ||
MHMNNKED_02539 | 1e-24 | S | Small, acid-soluble spore proteins, alpha/beta type | |||
MHMNNKED_02540 | 1.3e-27 | yqgU | ||||
MHMNNKED_02541 | 2.2e-13 | yqgW | S | Protein of unknown function (DUF2759) | ||
MHMNNKED_02542 | 3.3e-28 | yqgY | S | Protein of unknown function (DUF2626) | ||
MHMNNKED_02543 | 1.7e-88 | K | Helix-turn-helix domain | |||
MHMNNKED_02544 | 4.9e-293 | expZ | S | ABC transporter | ||
MHMNNKED_02545 | 4.4e-127 | S | Rifampin ADP-ribosyl transferase | |||
MHMNNKED_02546 | 2e-21 | S | Phage capsid protein | |||
MHMNNKED_02547 | 2e-07 | M | domain, Protein | |||
MHMNNKED_02548 | 1.5e-37 | yxeA | S | Protein of unknown function (DUF1093) | ||
MHMNNKED_02549 | 2e-70 | E | Spore germination protein | |||
MHMNNKED_02550 | 2e-113 | gerKC | S | spore germination | ||
MHMNNKED_02551 | 2.1e-169 | gerKA | EG | Spore germination protein | ||
MHMNNKED_02553 | 8.9e-271 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
MHMNNKED_02554 | 1.2e-21 | sspD | S | small acid-soluble spore protein | ||
MHMNNKED_02555 | 1.2e-162 | ktrB | P | COG0168 Trk-type K transport systems, membrane components | ||
MHMNNKED_02556 | 1.8e-115 | ykrP | G | COG3594 Fucose 4-O-acetylase and related acetyltransferases | ||
MHMNNKED_02557 | 2.9e-64 | L | PFAM transposase IS204 IS1001 IS1096 IS1165 family protein | |||
MHMNNKED_02558 | 7.7e-67 | L | Transposase | |||
MHMNNKED_02559 | 1.2e-135 | S | Protein of unknown function C-terminus (DUF2399) | |||
MHMNNKED_02560 | 1.3e-303 | D | Putative exonuclease SbcCD, C subunit | |||
MHMNNKED_02561 | 1.1e-191 | rny | S | Endoribonuclease that initiates mRNA decay | ||
MHMNNKED_02562 | 2.2e-116 | ymdB | S | protein conserved in bacteria | ||
MHMNNKED_02563 | 1.9e-37 | spoVS | S | Stage V sporulation protein S | ||
MHMNNKED_02564 | 1.2e-49 | S | Domain of unknown function (DU1801) | |||
MHMNNKED_02565 | 2.9e-253 | miaB | 2.8.4.3 | J | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
MHMNNKED_02566 | 3.9e-43 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
MHMNNKED_02567 | 3.5e-71 | ypbG | S | Calcineurin-like phosphoesterase superfamily domain | ||
MHMNNKED_02568 | 1.4e-69 | cotE | S | Spore coat protein | ||
MHMNNKED_02569 | 1.9e-220 | sdcS | P | Sodium:sulfate symporter transmembrane region | ||
MHMNNKED_02570 | 1.4e-244 | acsA | 6.2.1.1, 6.2.1.2 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
MHMNNKED_02571 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
MHMNNKED_02572 | 1.1e-262 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
MHMNNKED_02574 | 6.9e-63 | yqjT | 3.1.26.4 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
MHMNNKED_02576 | 1.7e-137 | S | Uncharacterized protein conserved in bacteria C-term(DUF2220) | |||
MHMNNKED_02577 | 1.9e-206 | |||||
MHMNNKED_02578 | 9.4e-114 | |||||
MHMNNKED_02579 | 0.0 | D | nuclear chromosome segregation | |||
MHMNNKED_02580 | 1.2e-44 | P | Nitrate nitrite transporter | |||
MHMNNKED_02581 | 2e-102 | narI | 1.7.5.1 | C | nitrate reductase, gamma subunit | |
MHMNNKED_02582 | 1e-65 | narJ | C | nitrate reductase molybdenum cofactor assembly chaperone | ||
MHMNNKED_02583 | 1.2e-288 | narH | 1.7.5.1 | C | Nitrate reductase, beta | |
MHMNNKED_02584 | 2.1e-117 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
MHMNNKED_02585 | 4.1e-82 | S | Nuclease-related domain | |||
MHMNNKED_02586 | 7e-73 | S | EcsC protein family | |||
MHMNNKED_02587 | 2.2e-57 | uspA | T | Belongs to the universal stress protein A family | ||
MHMNNKED_02588 | 3.3e-155 | ald | 1.4.1.1 | C | Alanine dehydrogenase/PNT, N-terminal domain | |
MHMNNKED_02589 | 7.1e-147 | ycsA | 1.1.1.83, 1.1.1.93, 4.1.1.73 | CE | Tartrate dehydrogenase | |
MHMNNKED_02590 | 6.8e-145 | 3.1.1.81 | S | Metallo-beta-lactamase superfamily | ||
MHMNNKED_02591 | 5.2e-133 | corA | P | Mediates influx of magnesium ions | ||
MHMNNKED_02592 | 7.9e-69 | 1.4.3.5 | S | Pyridoxamine 5'phosphate oxidase-like, FMN-binding | ||
MHMNNKED_02594 | 8.4e-08 | VPA1573 | J | acetyltransferase | ||
MHMNNKED_02595 | 3.4e-88 | P | Copper resistance protein D | |||
MHMNNKED_02596 | 9.5e-29 | copC | S | CopC domain | ||
MHMNNKED_02597 | 5.7e-59 | J | COG0457 FOG TPR repeat | |||
MHMNNKED_02598 | 2e-18 | K | Transcriptional | |||
MHMNNKED_02599 | 3.5e-21 | |||||
MHMNNKED_02600 | 1.3e-99 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
MHMNNKED_02601 | 1.1e-114 | rarD | S | -transporter | ||
MHMNNKED_02602 | 8.3e-244 | S | PFAM Uncharacterised protein family UPF0236 | |||
MHMNNKED_02603 | 1.2e-50 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
MHMNNKED_02605 | 1.5e-99 | S | membrane | |||
MHMNNKED_02606 | 2.8e-59 | M1-344 | S | Putative vitamin uptake transporter | ||
MHMNNKED_02607 | 9.1e-100 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
MHMNNKED_02608 | 5.5e-37 | V | ABC transporter, ATP-binding protein | |||
MHMNNKED_02609 | 1e-75 | mutE | S | ABC-2 family transporter protein | ||
MHMNNKED_02610 | 2.6e-63 | S | ABC-2 family transporter protein | |||
MHMNNKED_02611 | 4.8e-67 | potA3 | V | ABC transporter | ||
MHMNNKED_02612 | 2.7e-49 | S | ABC-2 family transporter protein | |||
MHMNNKED_02613 | 9.2e-82 | T | PhoP family transcriptional regulator | |||
MHMNNKED_02614 | 2.5e-71 | T | His Kinase A (phosphoacceptor) domain | |||
MHMNNKED_02615 | 5e-14 | S | Protein of unknown function (DUF3307) | |||
MHMNNKED_02616 | 8.2e-276 | ydgH | S | drug exporters of the RND superfamily | ||
MHMNNKED_02617 | 1.6e-46 | K | helix_turn_helix multiple antibiotic resistance protein | |||
MHMNNKED_02618 | 4e-144 | kinE | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
MHMNNKED_02621 | 2.5e-33 | |||||
MHMNNKED_02622 | 3.1e-20 | K | TfoX N-terminal domain | |||
MHMNNKED_02623 | 5e-173 | allC | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
MHMNNKED_02624 | 7.6e-154 | ylbA | 3.5.3.26 | S | protein, possibly involved in glyoxylate utilization | |
MHMNNKED_02625 | 7.2e-197 | allD | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
MHMNNKED_02626 | 1.6e-199 | allD | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
MHMNNKED_02627 | 0.0 | sucD | 6.2.1.5 | C | COG0074 Succinyl-CoA synthetase, alpha subunit | |
MHMNNKED_02628 | 7.9e-246 | sucD | 6.2.1.5 | C | Protein of unknown function (DUF1116) | |
MHMNNKED_02629 | 4.7e-140 | S | Protein of unknown function (DUF2877) | |||
MHMNNKED_02630 | 1.1e-170 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
MHMNNKED_02631 | 2.8e-142 | L | Transposase | |||
MHMNNKED_02632 | 1.6e-86 | L | Transposase | |||
MHMNNKED_02634 | 3.1e-14 | |||||
MHMNNKED_02635 | 1.7e-24 | narK | P | COG2223 Nitrate nitrite transporter | ||
MHMNNKED_02636 | 1.2e-151 | moaA | 4.1.99.22, 4.6.1.17 | H | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
MHMNNKED_02637 | 1.5e-130 | H | Plays a central role in 2-thiolation of mcm(5)S(2)U at tRNA wobble positions of cytosolic tRNA(Lys), tRNA(Glu) and tRNA(Gln). Also essential during biosynthesis of the molybdenum cofactor. Acts by mediating the C-terminal thiocarboxylation of sulfur carriers urm1 and mocs2a. Its N-terminus first activates urm1 and mocs2a as acyl-adenylates (-COAMP), then the persulfide sulfur on the catalytic cysteine is transferred to urm1 and mocs2a to form thiocarboxylation (-COSH) of their C-terminus. The reaction probably involves hydrogen sulfide that is generated from the persulfide intermediate and that acts as nucleophile towards urm1 and mocs2a. Subsequently, a transient disulfide bond is formed. Does not use thiosulfate as sulfur donor | |||
MHMNNKED_02638 | 1.8e-30 | mobA | 2.7.7.77 | H | Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor | |
MHMNNKED_02639 | 1.4e-55 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
MHMNNKED_02640 | 1.6e-68 | modA | P | COG0725 ABC-type molybdate transport system, periplasmic component | ||
MHMNNKED_02641 | 7.9e-72 | modB | P | COG4149 ABC-type molybdate transport system, permease component | ||
MHMNNKED_02642 | 1.1e-118 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
MHMNNKED_02643 | 1.4e-146 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
MHMNNKED_02644 | 2.8e-79 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
MHMNNKED_02645 | 6.5e-152 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
MHMNNKED_02646 | 8.2e-140 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
MHMNNKED_02647 | 1.3e-17 | S | Protein of unknown function (DUF3992) | |||
MHMNNKED_02650 | 8.7e-203 | atoE | I | Short chain fatty acid transporter | ||
MHMNNKED_02651 | 1.5e-95 | yijE | EG | EamA-like transporter family | ||
MHMNNKED_02652 | 2.5e-114 | EG | EamA-like transporter family | |||
MHMNNKED_02654 | 2.5e-28 | S | Ketosteroid isomerase-related protein | |||
MHMNNKED_02657 | 1.5e-07 | |||||
MHMNNKED_02658 | 1.9e-161 | megL | 4.4.1.1, 4.4.1.11, 4.4.1.8 | E | methionine gamma-lyase | |
MHMNNKED_02659 | 3.3e-55 | S | Protein of unknown function (DUF1284) | |||
MHMNNKED_02660 | 3.7e-22 | |||||
MHMNNKED_02661 | 4.5e-09 | S | YpzI-like protein | |||
MHMNNKED_02662 | 5.7e-10 | S | Fur-regulated basic protein A | |||
MHMNNKED_02663 | 5.3e-21 | |||||
MHMNNKED_02664 | 6.2e-66 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
MHMNNKED_02665 | 3.3e-185 | E | Hippurate hydrolase | |||
MHMNNKED_02666 | 1.4e-128 | ydjI | S | virion core protein (lumpy skin disease virus) | ||
MHMNNKED_02667 | 2.6e-58 | ydjH | S | COG1512 Beta-propeller domains of methanol dehydrogenase type | ||
MHMNNKED_02668 | 1.6e-127 | ydjG | 3.6.4.12 | 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 | |
MHMNNKED_02669 | 3.5e-54 | pspA | KT | Phage shock protein A | ||
MHMNNKED_02670 | 8.6e-100 | M | COG2834 Outer membrane lipoprotein-sorting protein | |||
MHMNNKED_02671 | 1.3e-07 | |||||
MHMNNKED_02672 | 1.5e-113 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
MHMNNKED_02673 | 2.6e-72 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
MHMNNKED_02674 | 2.6e-182 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
MHMNNKED_02675 | 1.7e-30 | S | DNA alkylation repair protein | |||
MHMNNKED_02676 | 2e-42 | yozR | S | COG0071 Molecular chaperone (small heat shock protein) | ||
MHMNNKED_02677 | 5.6e-66 | 6.1.1.5 | J | Acetyltransferase (GNAT) domain | ||
MHMNNKED_02678 | 1.4e-165 | mcrB | V | AAA domain (dynein-related subfamily) | ||
MHMNNKED_02679 | 5.8e-29 | S | Family of unknown function (DUF5316) | |||
MHMNNKED_02680 | 7.8e-91 | |||||
MHMNNKED_02681 | 1.1e-121 | V | ATPases associated with a variety of cellular activities | |||
MHMNNKED_02682 | 2.4e-253 | ywjA | V | abc transporter atp-binding protein | ||
MHMNNKED_02683 | 7.7e-104 | M | Glycosyl transferase family 8 | |||
MHMNNKED_02684 | 2.8e-195 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
MHMNNKED_02685 | 1.1e-57 | K | LysR substrate binding domain | |||
MHMNNKED_02686 | 3.5e-180 | gabT | 2.6.1.19 | E | Aminotransferase class-III | |
MHMNNKED_02687 | 3.8e-140 | E | Sodium:solute symporter family | |||
MHMNNKED_02688 | 6.4e-18 | G | Glycerol-3-phosphate ABC transporter substrate-binding protein | |||
MHMNNKED_02689 | 2e-49 | G | Binding-protein-dependent transport system inner membrane component | |||
MHMNNKED_02690 | 1.6e-51 | G | Binding-protein-dependent transport system inner membrane component | |||
MHMNNKED_02691 | 1.9e-137 | gmuE | 2.7.1.2, 2.7.1.4 | GK | COG1940 Transcriptional regulator sugar kinase | |
MHMNNKED_02692 | 2.1e-38 | ydhM | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
MHMNNKED_02693 | 1.5e-215 | 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 | ||
MHMNNKED_02694 | 8e-35 | celC | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
MHMNNKED_02695 | 3.9e-262 | gmuD | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
MHMNNKED_02696 | 3.9e-260 | licR | 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
MHMNNKED_02697 | 3e-136 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
MHMNNKED_02698 | 6e-108 | est | 3.1.1.1 | S | Carboxylesterase | |
MHMNNKED_02699 | 1.3e-21 | secG | U | Preprotein translocase subunit SecG | ||
MHMNNKED_02700 | 4.9e-08 | cobD | 6.3.1.10 | H | Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group | |
MHMNNKED_02701 | 3e-121 | cobD | 2.6.1.9, 4.1.1.81 | E | COG0079 Histidinol-phosphate aromatic aminotransferase and cobyric acid decarboxylase | |
MHMNNKED_02702 | 2.1e-47 | cobU | 2.7.1.156, 2.7.7.62 | H | COG2087 Adenosyl cobinamide kinase adenosyl cobinamide phosphate guanylyltransferase | |
MHMNNKED_02703 | 3.6e-137 | tcyN | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
MHMNNKED_02704 | 1.1e-116 | yxeN | E | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02705 | 1.1e-125 | ytmL | E | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02706 | 3.7e-271 | katA | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
MHMNNKED_02707 | 5.6e-72 | S | RloB-like protein | |||
MHMNNKED_02708 | 3.6e-169 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
MHMNNKED_02709 | 1.3e-43 | yneH | 1.20.4.1 | P | ArsC family | |
MHMNNKED_02710 | 2.2e-55 | K | Bacterial regulatory proteins, tetR family | |||
MHMNNKED_02711 | 4.9e-61 | usp | M | protein conserved in bacteria | ||
MHMNNKED_02712 | 1.6e-81 | ybaP | G | PFAM GumN family protein | ||
MHMNNKED_02713 | 1.8e-239 | bgaA | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
MHMNNKED_02714 | 9.5e-42 | 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 | ||
MHMNNKED_02715 | 4.5e-39 | zurA | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
MHMNNKED_02716 | 1e-95 | znuB | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
MHMNNKED_02717 | 8.1e-54 | zur | P | Belongs to the Fur family | ||
MHMNNKED_02718 | 2.6e-33 | yqfW | S | Belongs to the 5'(3')-deoxyribonucleotidase family | ||
MHMNNKED_02719 | 3e-127 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
MHMNNKED_02720 | 7.3e-183 | dapG | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
MHMNNKED_02721 | 3.3e-155 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
MHMNNKED_02722 | 3.3e-85 | spoVFB | H | Together with DpaA, catalyzes the conversion of dihydrodipicolinate to dipicolinate (DPA) | ||
MHMNNKED_02723 | 1.7e-133 | dpaA | 1.1.1.29, 1.1.1.399, 1.1.1.95 | CH | Dipicolinate synthase subunit A | |
MHMNNKED_02724 | 1.7e-38 | ymxH | S | YlmC YmxH family | ||
MHMNNKED_02725 | 1.1e-75 | pepR | S | Insulinase (Peptidase family M16) | ||
MHMNNKED_02726 | 3.1e-111 | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | |||
MHMNNKED_02727 | 4e-82 | sapB | S | MgtC SapB transporter | ||
MHMNNKED_02728 | 1.4e-76 | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | ||
MHMNNKED_02729 | 4.5e-74 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
MHMNNKED_02730 | 6.1e-247 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
MHMNNKED_02731 | 2e-112 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
MHMNNKED_02732 | 1.5e-07 | ypgQ | S | phosphohydrolase | ||
MHMNNKED_02734 | 2.1e-26 | T | SpoVT / AbrB like domain | |||
MHMNNKED_02735 | 4.9e-45 | doc | S | Fic/DOC family | ||
MHMNNKED_02737 | 5.1e-145 | ctaB | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
MHMNNKED_02738 | 1e-273 | 5.99.1.2 | T | diguanylate cyclase | ||
MHMNNKED_02739 | 1e-270 | dapE | 3.5.1.16, 3.5.1.18 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
MHMNNKED_02740 | 5.5e-199 | L | COG3039 Transposase and inactivated derivatives, IS5 family | |||
MHMNNKED_02741 | 1e-235 | yfkN | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
MHMNNKED_02742 | 2.2e-88 | T | PhoQ Sensor | |||
MHMNNKED_02743 | 2.8e-60 | S | ABC-2 family transporter protein | |||
MHMNNKED_02744 | 5.1e-125 | V | abc transporter atp-binding protein | |||
MHMNNKED_02745 | 1.6e-94 | T | Xre family transcriptional regulator | |||
MHMNNKED_02746 | 1.7e-57 | |||||
MHMNNKED_02747 | 1.6e-13 | 1.9.3.1 | O | COG3278 Cbb3-type cytochrome oxidase, subunit 1 | ||
MHMNNKED_02748 | 6.7e-35 | bigR | K | Bacterial regulatory protein, arsR family | ||
MHMNNKED_02749 | 7.3e-13 | |||||
MHMNNKED_02750 | 1.1e-219 | ma_1747 | S | ABC transporter | ||
MHMNNKED_02751 | 2.4e-29 | yqkA1 | S | GrpB protein | ||
MHMNNKED_02752 | 3.9e-47 | 2.3.1.128 | K | PFAM GCN5-related N-acetyltransferase | ||
MHMNNKED_02753 | 3e-52 | 3.6.1.55 | F | NUDIX domain | ||
MHMNNKED_02754 | 8.9e-145 | murG | 2.4.1.227 | 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) |
MHMNNKED_02755 | 5e-43 | csaA | 6.1.1.10, 6.1.1.20, 6.1.1.6 | J | tRNA-binding protein | |
MHMNNKED_02756 | 1e-14 | |||||
MHMNNKED_02757 | 7.2e-32 | rpmE | J | Ribosomal protein L31 | ||
MHMNNKED_02758 | 5e-219 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
MHMNNKED_02760 | 5.5e-11 | S | Belongs to the WXG100 family | |||
MHMNNKED_02761 | 1.6e-202 | M1-161 | T | HD domain | ||
MHMNNKED_02762 | 1.6e-81 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
MHMNNKED_02763 | 3.1e-57 | S | DinB family | |||
MHMNNKED_02764 | 1.8e-78 | C | Nitroreductase family | |||
MHMNNKED_02765 | 4.8e-100 | ykoY | P | Integral membrane protein TerC family | ||
MHMNNKED_02766 | 2e-90 | modF | 3.6.3.21, 3.6.3.34 | P | COG1119 ABC-type molybdenum transport system, ATPase component photorepair protein PhrA | |
MHMNNKED_02768 | 8.1e-13 | |||||
MHMNNKED_02769 | 2.4e-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 | ||
MHMNNKED_02770 | 2e-49 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
MHMNNKED_02771 | 1.1e-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 | ||
MHMNNKED_02772 | 5.3e-130 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
MHMNNKED_02773 | 2.6e-62 | atpI | S | ATP synthase I chain | ||
MHMNNKED_02774 | 2.2e-60 | vpr | O | Belongs to the peptidase S8 family | ||
MHMNNKED_02775 | 1.4e-84 | naiP | EGP | Major facilitator Superfamily | ||
MHMNNKED_02776 | 9.6e-212 | L | Transposase zinc-binding domain | |||
MHMNNKED_02777 | 2e-23 | |||||
MHMNNKED_02779 | 2.3e-91 | K | Helix-turn-helix domain, rpiR family | |||
MHMNNKED_02780 | 3.2e-228 | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system | ||
MHMNNKED_02781 | 4e-232 | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases | |
MHMNNKED_02782 | 5.8e-59 | 2.7.1.199 | G | COG2190 Phosphotransferase system IIA components | ||
MHMNNKED_02783 | 1.3e-86 | L | Phage integrase, N-terminal SAM-like domain | |||
MHMNNKED_02785 | 3.3e-182 | argH2 | 4.3.2.1 | E | argininosuccinate lyase | |
MHMNNKED_02786 | 2.5e-250 | phnV | P | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_02787 | 9.7e-144 | potA | 3.6.3.30 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
MHMNNKED_02788 | 1.9e-150 | P | Bacterial extracellular solute-binding protein | |||
MHMNNKED_02790 | 3.5e-311 | mca | M | NPCBM-associated, NEW3 domain of alpha-galactosidase | ||
MHMNNKED_02791 | 1.1e-143 | 3.4.13.19 | E | COG2355 Zn-dependent dipeptidase, microsomal dipeptidase homolog | ||
MHMNNKED_02792 | 2.5e-166 | lysDH | 1.4.1.18 | E | Saccharopine dehydrogenase C-terminal domain | |
MHMNNKED_02793 | 9.5e-147 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
MHMNNKED_02794 | 1.9e-72 | thiT | S | Proton-coupled thiamine transporter YuaJ | ||
MHMNNKED_02795 | 1.8e-206 | dapE | 3.5.1.16, 3.5.1.18 | E | Peptidase dimerisation domain | |
MHMNNKED_02796 | 7.5e-13 | hspX | O | COG0071 Molecular chaperone (small heat shock protein) | ||
MHMNNKED_02798 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
MHMNNKED_02799 | 7.1e-134 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
MHMNNKED_02801 | 2.2e-11 | sspN | S | Small acid-soluble spore protein N family | ||
MHMNNKED_02802 | 5.2e-15 | tlp | S | Belongs to the Tlp family | ||
MHMNNKED_02803 | 2.1e-276 | spoVK | O | stage V sporulation protein K | ||
MHMNNKED_02804 | 9.2e-58 | yneP | S | thioesterase | ||
MHMNNKED_02805 | 7.7e-41 | yneQ | ||||
MHMNNKED_02806 | 5e-27 | ytkA | S | YtkA-like | ||
MHMNNKED_02807 | 1e-71 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
MHMNNKED_02809 | 2.1e-128 | spoIIP | M | stage II sporulation protein P | ||
MHMNNKED_02810 | 5e-126 | rpoN | K | COG1508 DNA-directed RNA polymerase specialized sigma subunit, sigma54 homolog | ||
MHMNNKED_02811 | 6.3e-12 | XAC3035 | O | Glutaredoxin-like domain (DUF836) | ||
MHMNNKED_02812 | 3.3e-125 | cggR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
MHMNNKED_02813 | 1.4e-160 | gapA | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
MHMNNKED_02814 | 1.6e-21 | K | MerR HTH family regulatory protein | |||
MHMNNKED_02816 | 8.6e-28 | |||||
MHMNNKED_02817 | 3.5e-23 | L | Initiator Replication protein | |||
MHMNNKED_02818 | 5.5e-29 | |||||
MHMNNKED_02819 | 5.8e-163 | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | |||
MHMNNKED_02820 | 1.7e-183 | rocR | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | ||
MHMNNKED_02821 | 1.6e-240 | L | Transposase domain (DUF772) | |||
MHMNNKED_02822 | 2e-173 | 2.1.1.72, 3.1.21.3 | L | Type I restriction modification DNA specificity domain | ||
MHMNNKED_02823 | 2.9e-16 | |||||
MHMNNKED_02824 | 6.1e-151 | S | Protein of unknown function | |||
MHMNNKED_02825 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
MHMNNKED_02826 | 1.6e-159 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
MHMNNKED_02827 | 1.4e-96 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
MHMNNKED_02828 | 2.4e-22 | sspI | S | Belongs to the SspI family | ||
MHMNNKED_02829 | 8.2e-149 | M | Glycosyl Transferase | |||
MHMNNKED_02830 | 7.7e-173 | ysdC | G | COG1363 Cellulase M and related proteins | ||
MHMNNKED_02831 | 4.8e-57 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTPase | |
MHMNNKED_02832 | 7.3e-55 | ysdB | S | Sigma-w pathway protein YsdB | ||
MHMNNKED_02833 | 6.4e-70 | S | SNARE associated Golgi protein | |||
MHMNNKED_02834 | 4.2e-17 | ysdA | S | Protein of unknown function (DUF1294) | ||
MHMNNKED_02835 | 2.3e-45 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
MHMNNKED_02837 | 2.3e-24 | S | Protease prsW family | |||
MHMNNKED_02838 | 1.6e-33 | L | Restriction endonuclease BamHI | |||
MHMNNKED_02840 | 1.6e-67 | lpg2 | 2.4.1.337 | GT4 | M | Glycosyl transferases group 1 |
MHMNNKED_02841 | 3.5e-22 | S | Hexapeptide repeat of succinyl-transferase | |||
MHMNNKED_02843 | 6.7e-202 | mrdA | 3.4.16.4 | M | COG0768 Cell division protein FtsI penicillin-binding protein 2 | |
MHMNNKED_02844 | 1.6e-245 | putA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
MHMNNKED_02845 | 3.7e-39 | yueI | S | Protein of unknown function (DUF1694) | ||
MHMNNKED_02846 | 3.8e-34 | 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) | |
MHMNNKED_02847 | 7.2e-19 | P | ABC transporter | |||
MHMNNKED_02848 | 7.4e-115 | U | Binding-protein-dependent transport system inner membrane component | |||
MHMNNKED_02849 | 1.3e-31 | yeaO | S | Protein of unknown function, DUF488 | ||
MHMNNKED_02850 | 5.3e-37 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
MHMNNKED_02851 | 1.6e-126 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
MHMNNKED_02852 | 5.6e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
MHMNNKED_02854 | 1.9e-14 | |||||
MHMNNKED_02855 | 9.3e-19 | K | Helix-turn-helix XRE-family like proteins | |||
MHMNNKED_02856 | 9.3e-76 | tnpR1 | L | Resolvase, N terminal domain | ||
MHMNNKED_02857 | 1e-10 | sca1 | D | Phage tail tape measure protein | ||
MHMNNKED_02858 | 5.6e-66 | sca1 | D | Phage tail tape measure protein | ||
MHMNNKED_02862 | 9.5e-59 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
MHMNNKED_02863 | 1.5e-156 | yaaN | P | Belongs to the TelA family | ||
MHMNNKED_02864 | 1.2e-16 | yugT | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | COG0366 Glycosidases |
MHMNNKED_02865 | 2.8e-72 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | haloacid dehalogenase-like hydrolase |
MHMNNKED_02866 | 2.8e-130 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
MHMNNKED_02867 | 2.3e-83 | K | helix_turn_helix, arabinose operon control protein | |||
MHMNNKED_02868 | 1.2e-64 | V | VanZ like family | |||
MHMNNKED_02869 | 1.8e-99 | V | VanZ like family | |||
MHMNNKED_02870 | 9.8e-56 | K | Transcriptional regulator PadR-like family | |||
MHMNNKED_02871 | 6.2e-73 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
MHMNNKED_02872 | 2.5e-150 | yvjA | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
MHMNNKED_02873 | 6e-31 | cccB | C | Cytochrome c | ||
MHMNNKED_02874 | 1.3e-72 | ytoA | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
MHMNNKED_02875 | 6e-138 | ytpB | 4.2.3.130 | S | Tetraprenyl-beta-curcumene synthase | |
MHMNNKED_02876 | 5.3e-75 | bioY | S | Biotin biosynthesis protein | ||
MHMNNKED_02877 | 1.9e-149 | bioB | 2.8.1.6 | H | Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism | |
MHMNNKED_02878 | 3.3e-74 | noeI | M | Putative rRNA methylase | ||
MHMNNKED_02879 | 6.6e-160 | yhcC | S | Fe-S oxidoreductase | ||
MHMNNKED_02880 | 2.1e-23 | ytzC | S | Protein of unknown function (DUF2524) | ||
MHMNNKED_02881 | 4.5e-155 | MA20_40060 | 1.3.8.6, 1.3.8.7 | I | Acyl-CoA dehydrogenase, middle domain | |
MHMNNKED_02882 | 2.2e-82 | MA20_40065 | 1.3.8.7, 2.3.1.9 | I | Acyl-CoA dehydrogenase, C-terminal domain | |
MHMNNKED_02883 | 2.1e-111 | 5.3.3.18 | I | Enoyl-CoA hydratase/isomerase | ||
MHMNNKED_02884 | 6.5e-30 | tehB | 2.1.1.265 | Q | methyltransferase | |
MHMNNKED_02885 | 1.7e-88 | argD | 2.6.1.11, 2.6.1.17, 2.6.1.18, 2.6.1.36, 2.6.1.55, 2.6.1.62, 2.6.1.82 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
MHMNNKED_02886 | 3.6e-09 | yydH | S | Psort location CytoplasmicMembrane, score 10.00 | ||
MHMNNKED_02887 | 1.5e-52 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
MHMNNKED_02888 | 5.3e-95 | natA | S | ABC transporter, ATP-binding protein | ||
MHMNNKED_02889 | 4.3e-63 | sipS | 3.4.21.89 | U | Signal peptidase, peptidase S26 | |
MHMNNKED_02890 | 1e-63 | ykhA | 3.1.2.20 | I | Acyl-CoA hydrolase | |
MHMNNKED_02891 | 3.1e-72 | tag | 3.2.2.20 | L | Methyladenine glycosylase | |
MHMNNKED_02892 | 5.2e-136 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
MHMNNKED_02893 | 2e-304 | 6.2.1.1, 6.2.1.16 | I | AMP-dependent synthetase | ||
MHMNNKED_02894 | 4.4e-241 | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
MHMNNKED_02895 | 2.4e-34 | S | Thioesterase-like superfamily | |||
MHMNNKED_02896 | 5.5e-149 | yfmJ | S | N-terminal domain of oxidoreductase | ||
MHMNNKED_02897 | 7.4e-45 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
MHMNNKED_02898 | 6.9e-125 | haeIIIM | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
MHMNNKED_02899 | 1.6e-78 | L | HaeIII restriction endonuclease | |||
MHMNNKED_02900 | 2.4e-54 | S | Protein of unknown function DUF262 | |||
MHMNNKED_02903 | 9e-147 | vicX | 3.1.26.11 | S | COG1235 Metal-dependent hydrolases of the beta-lactamase superfamily I | |
MHMNNKED_02904 | 2e-144 | yycI | S | YycH protein | ||
MHMNNKED_02905 | 2e-61 | yycH | S | Two-component system yycF yycG regulatory protein | ||
MHMNNKED_02906 | 3.1e-242 | glpD | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
MHMNNKED_02907 | 1.4e-57 | S | Staygreen protein | |||
MHMNNKED_02910 | 2.4e-65 | S | ABC-2 family transporter protein | |||
MHMNNKED_02911 | 1.5e-31 | V | abc transporter atp-binding protein | |||
MHMNNKED_02912 | 1.3e-28 | K | Sigma-70, region 4 | |||
MHMNNKED_02914 | 7.4e-21 | XK27_00085 | K | transcriptional | ||
MHMNNKED_02915 | 1.4e-25 | |||||
MHMNNKED_02916 | 3.9e-25 | |||||
MHMNNKED_02917 | 1.3e-10 | G | Extracellular solute-binding protein | |||
MHMNNKED_02918 | 1.9e-11 | cps3F | ||||
MHMNNKED_02919 | 2.4e-272 | M | Sulfatase | |||
MHMNNKED_02920 | 2.6e-43 | |||||
MHMNNKED_02921 | 4.6e-105 | L | COG1484 DNA replication protein | |||
MHMNNKED_02922 | 6.1e-210 | L | COG4584 Transposase and inactivated derivatives | |||
MHMNNKED_02923 | 5.6e-239 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
MHMNNKED_02924 | 2.1e-08 | |||||
MHMNNKED_02925 | 5.1e-64 | mntR | K | Involved in manganese homeostasis. Might activate the transcription of the mntABCD operon | ||
MHMNNKED_02926 | 5.1e-30 | cspD | K | Cold-shock protein | ||
MHMNNKED_02927 | 6.3e-15 | ypeQ | S | Zinc-finger | ||
MHMNNKED_02928 | 2e-24 | ypeP | 3.1.26.4 | L | COG0328 Ribonuclease HI | |
MHMNNKED_02929 | 1.2e-45 | rsfA | S | SANT SWI3, ADA2, N-CoR and TFIIIB'' DNA-binding domains | ||
MHMNNKED_02930 | 1.7e-166 | accC2 | 6.3.4.14, 6.4.1.2, 6.4.1.3, 6.4.1.4 | I | Biotin carboxylase | |
MHMNNKED_02931 | 9e-09 | yngHB | 2.1.3.1, 6.4.1.1 | C | Biotin carboxyl carrier protein | |
MHMNNKED_02932 | 1.1e-241 | yngE | I | COG4799 Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | ||
MHMNNKED_02933 | 9.3e-68 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
MHMNNKED_02934 | 6.5e-168 | bshC | S | Involved in bacillithiol (BSH) biosynthesis. May catalyze the last step of the pathway, the addition of cysteine to glucosamine malate (GlcN-Mal) to generate BSH | ||
MHMNNKED_02935 | 2.8e-70 | mraZ | K | Belongs to the MraZ family | ||
MHMNNKED_02936 | 3.2e-135 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
MHMNNKED_02938 | 2.4e-282 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
MHMNNKED_02939 | 5.3e-311 | ftsI | 3.4.16.4 | M | stage V sporulation protein D | |
MHMNNKED_02940 | 2.3e-191 | murE | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
MHMNNKED_02941 | 5.1e-144 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
MHMNNKED_02942 | 9.5e-197 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
MHMNNKED_02943 | 9.1e-182 | spoVE | D | Belongs to the SEDS family | ||
MHMNNKED_02944 | 4.9e-231 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
MHMNNKED_02945 | 2.6e-29 | ptsH | G | phosphocarrier protein HPr | ||
MHMNNKED_02946 | 2.8e-268 | ptsG | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system | |
MHMNNKED_02947 | 8.3e-190 | pdp | 2.4.2.2, 2.4.2.4 | F | phosphorylase | |
MHMNNKED_02948 | 2e-203 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
MHMNNKED_02949 | 4.2e-132 | xerD | L | recombinase XerD | ||
MHMNNKED_02950 | 6.6e-26 | S | Protein of unknown function (DUF4227) | |||
MHMNNKED_02951 | 5.2e-73 | fur | P | Belongs to the Fur family | ||
MHMNNKED_02952 | 2.4e-86 | spoIIM | S | Required for complete septum migration and engulfment of the forespore compartment during sporulation. Required for stabilizing and recruiting of SpoIIP to the septal membrane | ||
MHMNNKED_02953 | 5.7e-166 | yqxK | 3.6.4.12 | L | DNA helicase | |
MHMNNKED_02954 | 1.6e-66 | nudF | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | |
MHMNNKED_02956 | 4e-59 | T | Response regulator containing a CheY-like receiver domain and an HD-GYP domain | |||
MHMNNKED_02958 | 6.8e-138 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
MHMNNKED_02959 | 1.4e-128 | vicX | 3.1.26.11 | S | COG1235 Metal-dependent hydrolases of the beta-lactamase superfamily I | |
MHMNNKED_02960 | 8.1e-63 | yycI | S | protein conserved in bacteria | ||
MHMNNKED_02961 | 2.6e-87 | yycH | S | protein conserved in bacteria | ||
MHMNNKED_02962 | 2.9e-233 | vicK | 2.7.13.3 | T | Histidine kinase | |
MHMNNKED_02963 | 1.1e-122 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
MHMNNKED_02964 | 8.7e-158 | C | 4Fe-4S single cluster domain | |||
MHMNNKED_02965 | 4.7e-41 | 4.1.1.36, 6.3.2.5 | H | Flavoprotein | ||
MHMNNKED_02966 | 1e-146 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
MHMNNKED_02967 | 3.6e-45 | ypmB | S | protein conserved in bacteria | ||
MHMNNKED_02968 | 9.6e-161 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
MHMNNKED_02969 | 4.6e-225 | asnS | 6.1.1.22 | J | asparaginyl-tRNA | |
MHMNNKED_02970 | 2.9e-34 | ypqE | 2.7.1.199 | G | COG2190 Phosphotransferase system IIA components | |
MHMNNKED_02971 | 2.6e-236 | L | Transposase | |||
MHMNNKED_02972 | 9.2e-161 | ald | 1.4.1.1 | E | Alanine dehydrogenase/PNT, N-terminal domain | |
MHMNNKED_02973 | 6.3e-110 | yukF | QT | PucR C-terminal helix-turn-helix domain | ||
MHMNNKED_02974 | 2.4e-121 | S | membrane | |||
MHMNNKED_02975 | 6.9e-150 | S | Putative nucleotide-binding of sugar-metabolising enzyme | |||
MHMNNKED_02976 | 2.5e-143 | ywaD | 3.4.11.10, 3.4.11.6 | S | Peptidase family M28 | |
MHMNNKED_02977 | 2.1e-96 | isp | O | Belongs to the peptidase S8 family | ||
MHMNNKED_02978 | 1.1e-18 | G | Belongs to the glycosyl hydrolase 43 family | |||
MHMNNKED_02979 | 6.5e-47 | V | Mate efflux family protein | |||
MHMNNKED_02980 | 2.7e-20 | uidA | G | Belongs to the glycosyl hydrolase 2 family | ||
MHMNNKED_02981 | 1.1e-60 | dam | 2.1.1.72 | L | Site-specific DNA-methyltransferase (Adenine-specific) | |
MHMNNKED_02982 | 1.1e-108 | dpnB | 3.1.21.4 | L | Recognizes the double-stranded unmethylated sequence GATC and cleaves before G-1 | |
MHMNNKED_02983 | 2.2e-98 | L | Belongs to the N(4) N(6)-methyltransferase family | |||
MHMNNKED_02984 | 1.6e-94 | L | PFAM transposase, IS4 family protein | |||
MHMNNKED_02985 | 2.5e-104 | 3.4.22.70 | M | sortase family | ||
MHMNNKED_02986 | 3.8e-94 | 3.1.1.3 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
MHMNNKED_02987 | 4.1e-227 | |||||
MHMNNKED_02988 | 7.1e-16 | rsbT | 2.7.11.1 | T | Histidine kinase-like ATPase domain | |
MHMNNKED_02989 | 1e-138 | kinE | 2.7.13.3 | T | STAS domain | |
MHMNNKED_02990 | 1.6e-93 | kinC | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
MHMNNKED_02991 | 2.1e-218 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
MHMNNKED_02992 | 9.7e-137 | G | PUCC protein | |||
MHMNNKED_02993 | 9.4e-99 | traC | L | Domain of unknown function (DUF1738) | ||
MHMNNKED_02998 | 3.9e-248 | 5.99.1.2 | G | DNA topoisomerase III | ||
MHMNNKED_03001 | 3.8e-08 | |||||
MHMNNKED_03003 | 1.4e-43 | radC | L | RadC-like JAB domain | ||
MHMNNKED_03008 | 6.6e-31 | |||||
MHMNNKED_03011 | 2.4e-60 | V | Restriction endonuclease | |||
MHMNNKED_03012 | 4.4e-80 | 5.99.1.2 | G | DNA topoisomerase III | ||
MHMNNKED_03015 | 6.3e-129 | S | CAAX protease self-immunity | |||
MHMNNKED_03016 | 1.9e-86 | S | Bacterial PH domain | |||
MHMNNKED_03017 | 8.7e-25 | wgaB | M | Psort location Cytoplasmic, score 8.87 | ||
MHMNNKED_03018 | 3.7e-51 | S | Polysaccharide biosynthesis protein | |||
MHMNNKED_03019 | 2.1e-18 | S | Glycosyltransferase like family 2 | |||
MHMNNKED_03020 | 4.4e-41 | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | ||
MHMNNKED_03021 | 6.2e-20 | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | ||
MHMNNKED_03022 | 6.8e-67 | glcR | K | DeoR C terminal sensor domain | ||
MHMNNKED_03023 | 1.4e-46 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
MHMNNKED_03025 | 3.5e-71 | |||||
MHMNNKED_03026 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase | |
MHMNNKED_03027 | 5.1e-120 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
MHMNNKED_03028 | 8e-74 | S | Protein of unknown function (DUF3298) | |||
MHMNNKED_03030 | 8.7e-16 | yisR | K | helix_turn_helix, arabinose operon control protein | ||
MHMNNKED_03031 | 1.3e-26 | yisR | K | helix_turn_helix, arabinose operon control protein | ||
MHMNNKED_03032 | 7.8e-79 | yisR | K | helix_turn_helix, arabinose operon control protein | ||
MHMNNKED_03033 | 1.9e-263 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Alpha amylase, N-terminal ig-like domain |
MHMNNKED_03034 | 1.7e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
MHMNNKED_03035 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
MHMNNKED_03036 | 1.8e-56 | msbA2 | 3.6.3.44 | V | ABC transporter | |
MHMNNKED_03038 | 2.4e-24 | O | Subtilase family | |||
MHMNNKED_03039 | 3.7e-234 | asnB | 6.3.5.4 | E | Asparagine synthase | |
MHMNNKED_03041 | 3.9e-125 | xylR | GK | ROK family | ||
MHMNNKED_03042 | 8.6e-51 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |||
MHMNNKED_03043 | 5.8e-56 | S | DinB family | |||
MHMNNKED_03044 | 7.6e-74 | L | Tn3 transposase DDE domain | |||
MHMNNKED_03045 | 7.8e-212 | L | PFAM Transposase, IS4-like | |||
MHMNNKED_03046 | 1.1e-46 | F | ATP-grasp domain | |||
MHMNNKED_03047 | 7.7e-07 | 2.3.1.128 | K | acetyltransferase | ||
MHMNNKED_03048 | 2.3e-164 | vioA | 2.6.1.33 | E | Belongs to the DegT DnrJ EryC1 family | |
MHMNNKED_03049 | 8.9e-145 | U | protein localization to endoplasmic reticulum | |||
MHMNNKED_03050 | 1.3e-63 | coaW | 2.7.1.33 | H | Pantothenate kinase | |
MHMNNKED_03051 | 1.2e-55 | yneK | S | Protein of unknown function (DUF2621) | ||
MHMNNKED_03052 | 5.4e-38 | cheB | 3.1.1.61, 3.5.1.44 | T | cheY-homologous receiver domain | |
MHMNNKED_03053 | 2.6e-97 | ccdA | O | cytochrome c biogenesis protein | ||
MHMNNKED_03054 | 2e-234 | mdlB | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
MHMNNKED_03055 | 1.8e-248 | mdlA | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
MHMNNKED_03056 | 1.3e-26 | yneF | S | UPF0154 protein | ||
MHMNNKED_03057 | 2e-45 | yneE | S | Sporulation inhibitor of replication protein sirA | ||
MHMNNKED_03059 | 6.3e-24 | ynzC | S | UPF0291 protein | ||
MHMNNKED_03060 | 1e-82 | yneB | L | resolvase | ||
MHMNNKED_03062 | 5.7e-96 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
MHMNNKED_03064 | 7e-29 | M | NLP P60 protein | |||
MHMNNKED_03065 | 3.1e-31 | L | RePlication protein | |||
MHMNNKED_03066 | 2.8e-29 | L | RePlication protein | |||
MHMNNKED_03067 | 1.3e-07 | L | Eco57I restriction-modification methylase | |||
MHMNNKED_03068 | 3e-115 | yugO | P | COG1226 Kef-type K transport systems | ||
MHMNNKED_03069 | 1.1e-229 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
MHMNNKED_03070 | 3.8e-194 | yugJ | C | oxidoreductases, Fe-dependent alcohol dehydrogenase family | ||
MHMNNKED_03071 | 3.9e-26 | yuzA | S | Domain of unknown function (DUF378) | ||
MHMNNKED_03072 | 9.7e-56 | ygzB | S | UPF0295 protein | ||
MHMNNKED_03073 | 2.4e-80 | perR | P | Belongs to the Fur family | ||
MHMNNKED_03074 | 7.6e-100 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Adenosyltransferase | |
MHMNNKED_03075 | 7.3e-78 | yrrM | 2.1.1.104 | S | O-methyltransferase | |
MHMNNKED_03076 | 5.8e-123 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
MHMNNKED_03077 | 1.6e-18 | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | ||
MHMNNKED_03079 | 2.4e-42 | S | DNA alkylation repair protein | |||
MHMNNKED_03080 | 1.8e-86 | yozR | S | COG0071 Molecular chaperone (small heat shock protein) | ||
MHMNNKED_03081 | 9.5e-106 | 6.1.1.5 | J | Acetyltransferase (GNAT) domain | ||
MHMNNKED_03082 | 7.7e-58 | ytxK | 2.1.1.72 | L | DNA methylase | |
MHMNNKED_03083 | 2.6e-190 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
MHMNNKED_03084 | 5.3e-60 | S | Domain of unknown function (DUF1837) | |||
MHMNNKED_03085 | 3.4e-21 | |||||
MHMNNKED_03086 | 8.5e-15 | 2.7.1.11 | G | alpha-ribazole phosphatase activity | ||
MHMNNKED_03087 | 4.1e-40 | |||||
MHMNNKED_03090 | 4.5e-21 | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | ||
MHMNNKED_03091 | 3e-105 | S | Sucrose-6F-phosphate phosphohydrolase | |||
MHMNNKED_03092 | 1.6e-97 | yvaK | 3.1.1.1 | S | Alpha/beta hydrolase family | |
MHMNNKED_03093 | 3.6e-08 | draG | 3.2.2.24 | O | PFAM ADP-ribosylation Crystallin J1 | |
MHMNNKED_03094 | 1.1e-49 | yabJ | 3.5.99.10 | J | Endoribonuclease L-PSP | |
MHMNNKED_03095 | 1.6e-181 | E | Sodium:solute symporter family | |||
MHMNNKED_03096 | 4.6e-207 | 1.14.14.28 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
MHMNNKED_03097 | 1.1e-56 | osmC | O | OsmC-like protein | ||
MHMNNKED_03098 | 9.4e-93 | M1-591 | L | TatD related DNase | ||
MHMNNKED_03099 | 8.4e-159 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
MHMNNKED_03100 | 5.2e-165 | proA | 1.2.1.41, 1.2.1.81 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
MHMNNKED_03102 | 2.7e-54 | M | Domain of unknown function (DUF4349) | |||
MHMNNKED_03103 | 2e-76 | S | membrane transporter protein | |||
MHMNNKED_03104 | 1.8e-71 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
MHMNNKED_03105 | 2.9e-13 | |||||
MHMNNKED_03106 | 7.1e-30 | |||||
MHMNNKED_03108 | 1.1e-110 | ehuB | ET | Bacterial periplasmic substrate-binding proteins | ||
MHMNNKED_03109 | 1.3e-77 | ehuC | E | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_03110 | 1.1e-89 | ehuD | E | Binding-protein-dependent transport system inner membrane component | ||
MHMNNKED_03111 | 1.9e-110 | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)