ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
NHNMODOO_00001 | 1.9e-245 | cydA | 1.10.3.14 | C | oxidase, subunit | |
NHNMODOO_00002 | 8.1e-188 | cydB | 1.10.3.14 | C | COG1294 Cytochrome bd-type quinol oxidase, subunit 2 | |
NHNMODOO_00003 | 8.3e-108 | |||||
NHNMODOO_00004 | 0.0 | pepF2 | E | COG1164 Oligoendopeptidase F | ||
NHNMODOO_00005 | 9.1e-294 | katB | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
NHNMODOO_00008 | 2.6e-244 | iucD_1 | 1.14.13.59 | Q | L-lysine 6-monooxygenase (NADPH-requiring) | |
NHNMODOO_00009 | 4.4e-242 | alkH | 1.2.1.3 | C | Belongs to the aldehyde dehydrogenase family | |
NHNMODOO_00010 | 7.9e-111 | rnhA | 3.1.26.4 | L | Caulimovirus viroplasmin | |
NHNMODOO_00011 | 1.4e-40 | |||||
NHNMODOO_00012 | 2.2e-45 | abrB | K | SpoVT / AbrB like domain | ||
NHNMODOO_00013 | 1e-56 | |||||
NHNMODOO_00014 | 5.4e-232 | yhdH | S | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family | ||
NHNMODOO_00015 | 3.2e-181 | mreB | D | Rod-share determining protein MreBH | ||
NHNMODOO_00016 | 0.0 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
NHNMODOO_00017 | 1.6e-163 | fruB | 2.7.1.11, 2.7.1.56 | G | Belongs to the carbohydrate kinase PfkB family | |
NHNMODOO_00018 | 7.1e-133 | fruR | K | Transcriptional regulator | ||
NHNMODOO_00019 | 0.0 | yfmR | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
NHNMODOO_00020 | 4.5e-205 | nos | 1.14.14.47 | C | Belongs to the NOS family. Bacterial NOS oxygenase subfamily | |
NHNMODOO_00021 | 7.8e-85 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
NHNMODOO_00022 | 1.7e-120 | treR | K | transcriptional | ||
NHNMODOO_00023 | 0.0 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
NHNMODOO_00024 | 1.1e-267 | treP | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NHNMODOO_00025 | 0.0 | ggtA | 2.3.2.2, 3.4.19.13 | E | gamma-glutamyltransferase | |
NHNMODOO_00026 | 1.2e-304 | yngK | T | Glycosyl hydrolase-like 10 | ||
NHNMODOO_00027 | 2.5e-234 | ykvU | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
NHNMODOO_00028 | 6e-239 | agcS | E | Sodium alanine symporter | ||
NHNMODOO_00029 | 6.1e-94 | glpP | K | Regulates expression of the glpD operon. In the presence of glycerol 3-phosphate (G3P) causes antitermination of transcription of glpD at the inverted repeat of the leader region to enhance its transcription. Binds and stabilizes glpD leader mRNA | ||
NHNMODOO_00030 | 0.0 | glpD | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
NHNMODOO_00031 | 2.1e-290 | glpK | 2.7.1.30 | C | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
NHNMODOO_00032 | 5.1e-229 | pilS | 2.7.13.3 | T | Histidine kinase | |
NHNMODOO_00033 | 0.0 | yfiC | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
NHNMODOO_00034 | 4.6e-305 | yfiB3 | V | ABC transporter | ||
NHNMODOO_00035 | 0.0 | uvrD | 3.6.4.12 | L | DNA helicase | |
NHNMODOO_00036 | 4.5e-169 | phnD | P | Phosphonate ABC transporter | ||
NHNMODOO_00037 | 9.1e-139 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
NHNMODOO_00038 | 2.4e-136 | phnE | 3.6.1.63 | P | ABC transporter | |
NHNMODOO_00039 | 6.8e-142 | phnE | 3.6.1.63 | P | ABC transporter | |
NHNMODOO_00040 | 3.1e-139 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
NHNMODOO_00041 | 1.1e-242 | matE | V | MatE | ||
NHNMODOO_00042 | 1.5e-101 | tetR | K | Bacterial regulatory proteins, tetR family | ||
NHNMODOO_00043 | 6.6e-164 | 3.4.11.5 | I | Alpha/beta hydrolase family | ||
NHNMODOO_00044 | 2.2e-160 | dppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHNMODOO_00045 | 9.9e-183 | dppB | EP | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHNMODOO_00046 | 3e-301 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | |||
NHNMODOO_00047 | 4.7e-185 | appF | E | Belongs to the ABC transporter superfamily | ||
NHNMODOO_00048 | 3.7e-182 | dppD | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_00049 | 0.0 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
NHNMODOO_00050 | 7.3e-56 | XK27_04860 | S | Domain of unknown function (DUF4440) | ||
NHNMODOO_00051 | 2.3e-101 | ynaD | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_00052 | 2.1e-227 | S | Sulphur transport | |||
NHNMODOO_00053 | 3.3e-175 | S | transport system, periplasmic component | |||
NHNMODOO_00054 | 5.7e-170 | S | Belongs to the binding-protein-dependent transport system permease family | |||
NHNMODOO_00055 | 1.3e-137 | S | transport system, ATPase component | |||
NHNMODOO_00056 | 1.2e-180 | |||||
NHNMODOO_00057 | 6.4e-196 | cysA | 3.6.3.25, 3.6.3.29 | P | Part of the ABC transporter complex CysAWTP involved in sulfate thiosulfate import. Responsible for energy coupling to the transport system | |
NHNMODOO_00058 | 5.4e-136 | cysW | P | COG4208 ABC-type sulfate transport system, permease component | ||
NHNMODOO_00059 | 1.2e-130 | cysT | O | COG0555 ABC-type sulfate transport system, permease component | ||
NHNMODOO_00060 | 3e-195 | sbp | P | COG1613 ABC-type sulfate transport system, periplasmic component | ||
NHNMODOO_00061 | 1.7e-79 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
NHNMODOO_00062 | 4.3e-297 | T | COG0642 Signal transduction histidine kinase | |||
NHNMODOO_00063 | 1.9e-256 | dld | 1.1.1.303, 1.1.1.4, 1.1.2.4, 1.1.3.15 | C | Glycolate oxidase subunit | |
NHNMODOO_00064 | 3.8e-155 | yocS | S | -transporter | ||
NHNMODOO_00065 | 6.4e-238 | aroA | 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 | |
NHNMODOO_00066 | 5.9e-155 | nhaR | K | LysR substrate binding domain | ||
NHNMODOO_00067 | 2e-294 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | |||
NHNMODOO_00068 | 1.3e-204 | ytpB | 4.2.3.130 | S | Tetraprenyl-beta-curcumene synthase | |
NHNMODOO_00069 | 1.9e-63 | K | Helix-turn-helix XRE-family like proteins | |||
NHNMODOO_00070 | 2e-94 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_00071 | 6.3e-151 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00072 | 6.4e-168 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00073 | 1.9e-266 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_00074 | 0.0 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
NHNMODOO_00075 | 1.7e-170 | yisR1 | K | AraC-like ligand binding domain | ||
NHNMODOO_00076 | 2.2e-120 | mutF | V | ABC transporter, ATP-binding protein | ||
NHNMODOO_00077 | 1.2e-119 | spaE | S | ABC-2 family transporter protein | ||
NHNMODOO_00078 | 6.4e-126 | mutG | S | ABC-2 family transporter protein | ||
NHNMODOO_00079 | 9.3e-121 | K | Transcriptional regulatory protein, C terminal | |||
NHNMODOO_00080 | 8.5e-249 | T | His Kinase A (phosphoacceptor) domain | |||
NHNMODOO_00081 | 1.7e-72 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | |||
NHNMODOO_00082 | 2.7e-73 | lrpC | K | helix_turn_helix ASNC type | ||
NHNMODOO_00083 | 3.9e-105 | argO | S | Lysine exporter protein LysE YggA | ||
NHNMODOO_00084 | 5.5e-272 | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |||
NHNMODOO_00085 | 9.8e-94 | ykkA | S | Protein of unknown function (DUF664) | ||
NHNMODOO_00086 | 2.4e-74 | yuxK | S | protein conserved in bacteria | ||
NHNMODOO_00087 | 2.1e-84 | S | Protein of unknown function (DUF1569) | |||
NHNMODOO_00088 | 1.8e-56 | |||||
NHNMODOO_00089 | 1e-59 | |||||
NHNMODOO_00090 | 4.6e-73 | S | Protein of unknown function, DUF600 | |||
NHNMODOO_00091 | 1.8e-80 | S | SMI1-KNR4 cell-wall | |||
NHNMODOO_00092 | 7.6e-66 | |||||
NHNMODOO_00093 | 6.2e-194 | S | LXG domain of WXG superfamily | |||
NHNMODOO_00094 | 3.5e-147 | yjqC | P | Catalase | ||
NHNMODOO_00095 | 5e-108 | E | Lysine exporter protein LysE YggA | |||
NHNMODOO_00096 | 1.6e-244 | ycgH | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
NHNMODOO_00097 | 4.6e-117 | yhcQ | M | Spore coat protein | ||
NHNMODOO_00099 | 2.7e-174 | eutC | 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | |
NHNMODOO_00100 | 8.1e-174 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
NHNMODOO_00101 | 2.6e-209 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
NHNMODOO_00102 | 5.1e-116 | S | HTH domain | |||
NHNMODOO_00103 | 1.1e-188 | speB | 3.5.3.11 | E | Arginase family | |
NHNMODOO_00104 | 4.5e-126 | T | Transcriptional regulator | |||
NHNMODOO_00105 | 5.1e-196 | T | PhoQ Sensor | |||
NHNMODOO_00106 | 1.4e-164 | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | ||
NHNMODOO_00107 | 1.1e-119 | ydfF | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
NHNMODOO_00108 | 3e-113 | ydfE | S | Flavin reductase like domain | ||
NHNMODOO_00109 | 8.6e-142 | C | KR domain | |||
NHNMODOO_00110 | 1.1e-54 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
NHNMODOO_00111 | 2.3e-171 | srlE | 2.7.1.198 | G | PTS system glucitol sorbitol-specific transporter subunit IIB | |
NHNMODOO_00112 | 2.5e-98 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
NHNMODOO_00113 | 3.1e-75 | gutM | K | Glucitol operon activator | ||
NHNMODOO_00114 | 6.5e-171 | sorC | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
NHNMODOO_00115 | 3.6e-274 | uxaB | 1.1.1.17, 1.1.1.58 | G | tagaturonate reductase activity | |
NHNMODOO_00116 | 6.6e-284 | uxaA | 4.2.1.7 | G | Altronate | |
NHNMODOO_00117 | 3.9e-248 | yteT | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
NHNMODOO_00118 | 2.6e-121 | S | Integral membrane protein | |||
NHNMODOO_00119 | 9.5e-78 | G | carbohydrate transport | |||
NHNMODOO_00120 | 8.3e-223 | yteR | 3.2.1.172 | GH105 | G | unsaturated glucuronyl hydrolase involved in regulation of bacterial surface properties, and related proteins |
NHNMODOO_00121 | 2.2e-311 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Belongs to the glycosyl hydrolase 43 family | |
NHNMODOO_00122 | 9.2e-167 | E | Abhydrolase family | |||
NHNMODOO_00123 | 2.7e-144 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00124 | 1.3e-179 | G | COG4209 ABC-type polysaccharide transport system, permease component | |||
NHNMODOO_00125 | 1.4e-294 | G | ABC transporter substrate-binding protein | |||
NHNMODOO_00126 | 0.0 | K | Transcriptional regulator | |||
NHNMODOO_00127 | 1.6e-157 | 3.2.2.21 | K | AraC-like ligand binding domain | ||
NHNMODOO_00128 | 1.5e-194 | pelE | 3.4.11.10, 3.4.11.6, 4.2.2.2 | M | Pectic acid lyase | |
NHNMODOO_00129 | 1.9e-104 | J | Acetyltransferase (GNAT) domain | |||
NHNMODOO_00130 | 2.1e-129 | udh | 1.1.1.203, 1.1.1.388 | GM | NAD dependent epimerase/dehydratase family | |
NHNMODOO_00131 | 0.0 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
NHNMODOO_00132 | 0.0 | lplA7 | G | Bacterial extracellular solute-binding protein | ||
NHNMODOO_00133 | 3.7e-168 | lplC1 | G | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_00134 | 1.1e-173 | lplB | P | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_00135 | 1.3e-271 | araC7 | T | helix_turn_helix, arabinose operon control protein | ||
NHNMODOO_00136 | 0.0 | 2.7.13.3 | T | Histidine kinase | ||
NHNMODOO_00137 | 0.0 | yicI | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
NHNMODOO_00138 | 3.6e-203 | glcP | G | Major Facilitator Superfamily | ||
NHNMODOO_00139 | 9.5e-178 | xylR3 | 2.7.1.2 | GK | ROK family | |
NHNMODOO_00140 | 3.2e-275 | M1-1044 | S | Belongs to the UPF0061 (SELO) family | ||
NHNMODOO_00141 | 3.9e-73 | S | DinB superfamily | |||
NHNMODOO_00142 | 1.1e-164 | Q | COG0179 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) | |||
NHNMODOO_00143 | 5.4e-129 | ygaJ | E | Belongs to the peptidase S51 family | ||
NHNMODOO_00144 | 3.5e-162 | S | Alpha beta hydrolase | |||
NHNMODOO_00146 | 2.7e-73 | dcd | 3.5.4.13 | F | 2'-deoxycytidine 5'-triphosphate deaminase (DCD) | |
NHNMODOO_00147 | 5.7e-151 | P | COG0370 Fe2 transport system protein B | |||
NHNMODOO_00148 | 3.4e-164 | yjiA | S | Cobalamin biosynthesis protein CobW | ||
NHNMODOO_00149 | 4.8e-177 | adcA | S | ZinT (YodA) periplasmic lipocalin-like zinc-recruitment | ||
NHNMODOO_00150 | 4.2e-228 | adcA | P | Zinc-uptake complex component A periplasmic | ||
NHNMODOO_00151 | 2.3e-125 | adcC | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
NHNMODOO_00152 | 2e-128 | adcB | P | ABC 3 transport family | ||
NHNMODOO_00153 | 6.8e-265 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |||
NHNMODOO_00154 | 5.3e-167 | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | ||
NHNMODOO_00155 | 3.4e-163 | MA20_14845 | 4.2.1.141 | S | Fumarylacetoacetate (FAA) hydrolase family | |
NHNMODOO_00156 | 4e-139 | K | helix_turn_helix isocitrate lyase regulation | |||
NHNMODOO_00157 | 0.0 | yjhG | 4.2.1.82 | EG | Dehydratase family | |
NHNMODOO_00158 | 4.8e-239 | yjhF | EG | COG2610 H gluconate symporter and related permeases | ||
NHNMODOO_00159 | 2.3e-31 | K | MerR family transcriptional regulator | |||
NHNMODOO_00160 | 4.9e-134 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHNMODOO_00161 | 3.8e-97 | |||||
NHNMODOO_00162 | 7.3e-261 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NHNMODOO_00163 | 1.1e-77 | fld | C | Flavodoxin | ||
NHNMODOO_00164 | 1.8e-167 | yegS | 2.7.1.107 | I | COG1597 Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
NHNMODOO_00165 | 6.6e-273 | 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) | |
NHNMODOO_00166 | 2.7e-274 | 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) | |
NHNMODOO_00167 | 1.8e-44 | 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) | |
NHNMODOO_00168 | 2e-88 | yizA | S | DinB family | ||
NHNMODOO_00169 | 1.5e-172 | |||||
NHNMODOO_00171 | 9.8e-156 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
NHNMODOO_00172 | 1.3e-188 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
NHNMODOO_00173 | 2.7e-280 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
NHNMODOO_00174 | 3.2e-203 | bmpA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
NHNMODOO_00175 | 4e-220 | camS | S | COG4851 Protein involved in sex pheromone biosynthesis | ||
NHNMODOO_00176 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
NHNMODOO_00177 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
NHNMODOO_00178 | 6.8e-122 | 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 | ||
NHNMODOO_00180 | 5.7e-152 | fhuC | 3.6.3.34 | HP | ABC transporter | |
NHNMODOO_00181 | 3.7e-169 | fhuG | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_00182 | 4.3e-175 | fhuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_00184 | 2e-27 | mepA | V | MATE efflux family protein | ||
NHNMODOO_00185 | 1.2e-163 | lacX | G | Aldose 1-epimerase | ||
NHNMODOO_00186 | 0.0 | acyII | 3.5.1.11, 3.5.1.97 | S | Penicillin amidase | |
NHNMODOO_00187 | 0.0 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
NHNMODOO_00188 | 1.2e-49 | yerC | S | protein conserved in bacteria | ||
NHNMODOO_00189 | 0.0 | 3.5.4.2 | F | adenine deaminase | ||
NHNMODOO_00190 | 1.2e-155 | opuAC | E | glycine betaine | ||
NHNMODOO_00191 | 5.6e-147 | proW | P | glycine betaine | ||
NHNMODOO_00192 | 4.7e-219 | gbuA | 3.6.3.32 | E | glycine betaine | |
NHNMODOO_00193 | 2.5e-95 | K | Belongs to the GbsR family | |||
NHNMODOO_00194 | 8.5e-23 | |||||
NHNMODOO_00195 | 5.8e-40 | |||||
NHNMODOO_00196 | 2.5e-37 | |||||
NHNMODOO_00197 | 2.1e-32 | T | Protein conserved in bacteria | |||
NHNMODOO_00198 | 1.9e-81 | yokJ | S | SMI1 / KNR4 family (SUKH-1) | ||
NHNMODOO_00199 | 2.8e-61 | U | LXG domain of WXG superfamily | |||
NHNMODOO_00200 | 8.8e-59 | |||||
NHNMODOO_00201 | 5.1e-246 | S | LXG domain of WXG superfamily | |||
NHNMODOO_00202 | 6.7e-38 | S | Family of unknown function (DUF5344) | |||
NHNMODOO_00203 | 2.8e-21 | S | Domain of unknown function (DUF5082) | |||
NHNMODOO_00205 | 1.2e-186 | V | COG0842 ABC-type multidrug transport system, permease component | |||
NHNMODOO_00206 | 4.4e-217 | V | COG0842 ABC-type multidrug transport system, permease component | |||
NHNMODOO_00207 | 2e-169 | yfiL | V | COG1131 ABC-type multidrug transport system, ATPase component | ||
NHNMODOO_00208 | 1.1e-107 | KT | LuxR family transcriptional regulator | |||
NHNMODOO_00209 | 8.3e-199 | yxjM | T | Signal transduction histidine kinase | ||
NHNMODOO_00210 | 1.6e-88 | ttr | K | GCN5 family acetyltransferase | ||
NHNMODOO_00211 | 1.7e-147 | fhuD | P | Periplasmic binding protein | ||
NHNMODOO_00212 | 5.3e-201 | cpg2 | 3.4.17.11 | E | Peptidase dimerisation domain | |
NHNMODOO_00213 | 3.4e-21 | rimL | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
NHNMODOO_00214 | 5.9e-09 | rimL | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
NHNMODOO_00215 | 2.1e-191 | bdhA | 1.1.1.303, 1.1.1.4 | E | Dehydrogenase | |
NHNMODOO_00216 | 1.9e-104 | E | GDSL-like Lipase/Acylhydrolase | |||
NHNMODOO_00217 | 3.8e-290 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | |||
NHNMODOO_00220 | 1.2e-07 | |||||
NHNMODOO_00223 | 5.5e-98 | sigW | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
NHNMODOO_00224 | 2.1e-120 | 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 | ||
NHNMODOO_00225 | 5.7e-144 | 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 | |
NHNMODOO_00226 | 5.2e-218 | ybbR | S | protein conserved in bacteria | ||
NHNMODOO_00227 | 4e-248 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
NHNMODOO_00229 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
NHNMODOO_00230 | 3.9e-153 | ybfI | K | AraC-like ligand binding domain | ||
NHNMODOO_00231 | 1e-173 | E | Proline dehydrogenase | |||
NHNMODOO_00232 | 1.6e-196 | V | Beta-lactamase | |||
NHNMODOO_00233 | 2.6e-32 | 2.7.1.163 | S | Aminoglycoside phosphotransferase | ||
NHNMODOO_00234 | 1.1e-172 | 2.7.1.163 | S | Aminoglycoside phosphotransferase | ||
NHNMODOO_00235 | 1.6e-73 | K | SpoVT / AbrB like domain | |||
NHNMODOO_00236 | 4.3e-222 | CG | COG1819 Glycosyl transferases, related to UDP-glucuronosyltransferase | |||
NHNMODOO_00237 | 3.6e-140 | V | ABC transporter, ATP-binding protein | |||
NHNMODOO_00238 | 0.0 | V | FtsX-like permease family | |||
NHNMODOO_00239 | 2.5e-121 | T | Transcriptional regulatory protein, C terminal | |||
NHNMODOO_00240 | 6.8e-187 | T | Histidine kinase-like ATPases | |||
NHNMODOO_00241 | 2e-107 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_00242 | 1.6e-225 | mefE | EGP | Transmembrane secretion effector | ||
NHNMODOO_00243 | 0.0 | V | FtsX-like permease family | |||
NHNMODOO_00244 | 3.6e-132 | V | ABC transporter | |||
NHNMODOO_00245 | 8.5e-55 | ytrA | K | GntR family transcriptional regulator | ||
NHNMODOO_00246 | 1.8e-156 | V | ABC transporter, ATP-binding protein | |||
NHNMODOO_00247 | 4.1e-91 | S | ABC-2 family transporter protein | |||
NHNMODOO_00248 | 5.5e-56 | gluQ | 6.1.1.17 | 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) | |
NHNMODOO_00249 | 2.5e-153 | bla | 3.5.2.6 | V | beta-lactamase | |
NHNMODOO_00250 | 2.6e-303 | blaR | 3.5.2.6 | KTV | BlaR1 peptidase M56 | |
NHNMODOO_00251 | 6.6e-63 | blaI | K | Penicillinase repressor | ||
NHNMODOO_00252 | 8.5e-142 | aadD | H | KNTase C-terminal domain | ||
NHNMODOO_00253 | 1.4e-62 | cadC | K | transcriptional | ||
NHNMODOO_00254 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
NHNMODOO_00255 | 6.4e-193 | P | Oxidoreductase | |||
NHNMODOO_00256 | 2.3e-82 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_00257 | 1.8e-79 | |||||
NHNMODOO_00258 | 3.1e-136 | Q | ubiE/COQ5 methyltransferase family | |||
NHNMODOO_00259 | 7e-181 | trpS | 6.1.1.2 | J | Catalyzes a two-step reaction, first charging a tryptophan molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
NHNMODOO_00260 | 5.6e-113 | Q | SAM-dependent methyltransferase | |||
NHNMODOO_00261 | 2.3e-140 | ydfC | EG | EamA-like transporter family | ||
NHNMODOO_00262 | 9.7e-136 | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |||
NHNMODOO_00263 | 4.6e-106 | panZ | K | Acetyltransferase (GNAT) domain | ||
NHNMODOO_00264 | 5.9e-64 | |||||
NHNMODOO_00265 | 9.3e-69 | S | Protein of unknown function (DUF2512) | |||
NHNMODOO_00266 | 1.1e-112 | yjhB | 3.6.1.13, 3.6.1.55 | F | ADP-ribose pyrophosphatase | |
NHNMODOO_00267 | 1.2e-82 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_00268 | 1.1e-297 | siaT_1 | S | Tripartite ATP-independent periplasmic transporter, DctM component | ||
NHNMODOO_00269 | 3.3e-52 | S | Domain of unknown function (DUF1850) | |||
NHNMODOO_00270 | 2e-119 | thyA | S | NMT1-like family | ||
NHNMODOO_00271 | 4e-302 | opuD | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
NHNMODOO_00272 | 5.2e-116 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
NHNMODOO_00273 | 3.6e-165 | I | alpha/beta hydrolase fold | |||
NHNMODOO_00274 | 2.7e-211 | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | |||
NHNMODOO_00275 | 2.8e-96 | adk | 2.7.4.3 | F | topology modulation protein | |
NHNMODOO_00278 | 2.1e-85 | ftnA | 1.16.3.2 | P | Iron-storage protein | |
NHNMODOO_00279 | 2.7e-157 | yueF | S | transporter activity | ||
NHNMODOO_00280 | 2.3e-276 | 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 | |
NHNMODOO_00281 | 3.5e-90 | S | Peptidase propeptide and YPEB domain | |||
NHNMODOO_00282 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
NHNMODOO_00283 | 1.1e-205 | G | COG1593 TRAP-type C4-dicarboxylate transport system, large permease component | |||
NHNMODOO_00284 | 1.4e-81 | G | Tripartite ATP-independent periplasmic transporters, DctQ component | |||
NHNMODOO_00285 | 2.5e-181 | G | Bacterial extracellular solute-binding protein, family 7 | |||
NHNMODOO_00286 | 1.3e-168 | K | helix_turn _helix lactose operon repressor | |||
NHNMODOO_00287 | 2.2e-134 | K | helix_turn_helix, mercury resistance | |||
NHNMODOO_00288 | 0.0 | msbA2 | 3.6.3.44 | V | ABC transporter | |
NHNMODOO_00289 | 8.2e-146 | ybbH_2 | K | Transcriptional regulator | ||
NHNMODOO_00290 | 3.1e-181 | pdxA | 1.1.1.262, 1.1.1.408, 1.1.1.409 | H | Belongs to the PdxA family | |
NHNMODOO_00291 | 5.3e-237 | 2.7.1.219, 2.7.1.220 | S | Putative nucleotide-binding of sugar-metabolising enzyme | ||
NHNMODOO_00292 | 1.5e-167 | kdgT | P | The 2-keto-3-deoxygluconate permease transports the degraded pectin products into the bacterial cell, where they serve as carbon and energy sources. This is a hydrogen coupled transport system | ||
NHNMODOO_00294 | 4.4e-286 | K | Propionate catabolism activator | |||
NHNMODOO_00295 | 8e-152 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
NHNMODOO_00296 | 7e-232 | ybbF | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NHNMODOO_00297 | 1.1e-121 | yleB | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | |
NHNMODOO_00298 | 2.8e-49 | yleB | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | |
NHNMODOO_00299 | 5.1e-179 | purR15 | K | Bacterial regulatory proteins, lacI family | ||
NHNMODOO_00300 | 2e-274 | ydhP | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHNMODOO_00301 | 9.6e-151 | ypbG | 2.7.1.2 | GK | ROK family | |
NHNMODOO_00302 | 1.4e-140 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00303 | 3.6e-163 | P | COG0395 ABC-type sugar transport system, permease component | |||
NHNMODOO_00304 | 4.7e-214 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_00305 | 4.9e-139 | manA3 | 3.2.1.78 | GH26 | G | Endoglucanase |
NHNMODOO_00306 | 1e-35 | S | Protein of unknown function (DUF2642) | |||
NHNMODOO_00307 | 4.2e-12 | |||||
NHNMODOO_00308 | 1.5e-97 | yorS | 3.1.3.5 | S | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | |
NHNMODOO_00309 | 8e-137 | 1.6.5.5 | C | alcohol dehydrogenase | ||
NHNMODOO_00310 | 3.2e-77 | K | Transcriptional regulator | |||
NHNMODOO_00311 | 2.4e-53 | fdx5 | C | 2Fe-2S iron-sulfur cluster binding domain | ||
NHNMODOO_00312 | 5.9e-20 | |||||
NHNMODOO_00313 | 8.3e-299 | KT | Transcriptional regulator | |||
NHNMODOO_00314 | 6.8e-215 | adhB | 1.1.1.1, 1.1.1.202 | C | alcohol dehydrogenase | |
NHNMODOO_00315 | 2.2e-222 | EG | COG2610 H gluconate symporter and related permeases | |||
NHNMODOO_00316 | 4.3e-172 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
NHNMODOO_00317 | 1.6e-197 | eutG | C | alcohol dehydrogenase | ||
NHNMODOO_00318 | 6.1e-263 | 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 | |
NHNMODOO_00319 | 3.8e-260 | EG | Bacillus/Clostridium GerA spore germination protein | |||
NHNMODOO_00320 | 3.1e-50 | |||||
NHNMODOO_00321 | 1e-87 | ectA | 2.3.1.178 | K | L-2,4-diaminobutyric acid acetyltransferase | |
NHNMODOO_00322 | 6.8e-245 | ectB | 2.6.1.76 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
NHNMODOO_00323 | 9.5e-76 | 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 | |
NHNMODOO_00324 | 2.3e-248 | G | Glycerol-3-phosphate ABC transporter substrate-binding protein | |||
NHNMODOO_00325 | 1.2e-146 | G | Xylose isomerase-like TIM barrel | |||
NHNMODOO_00326 | 1.9e-164 | G | ABC transporter (permease) | |||
NHNMODOO_00327 | 3.2e-147 | ugpE | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
NHNMODOO_00328 | 1.2e-194 | 3.6.3.20 | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_00330 | 3.1e-236 | KLT | Protein kinase domain | |||
NHNMODOO_00333 | 3.9e-76 | H | Tellurite resistance protein TehB | |||
NHNMODOO_00334 | 3.5e-51 | S | ABC-2 family transporter protein | |||
NHNMODOO_00335 | 3.3e-310 | alkK | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
NHNMODOO_00336 | 6.3e-260 | yhfT | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | |
NHNMODOO_00337 | 2.7e-200 | vraB | 2.3.1.9 | I | Belongs to the thiolase family | |
NHNMODOO_00338 | 1.5e-136 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHNMODOO_00339 | 1.1e-189 | araC2 | K | Arabinose-binding domain of AraC transcription regulator, N-term | ||
NHNMODOO_00341 | 4.4e-74 | nsrR | K | Transcriptional regulator | ||
NHNMODOO_00342 | 4.1e-231 | 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 | |
NHNMODOO_00343 | 0.0 | glpQ1 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
NHNMODOO_00344 | 4.1e-198 | ugpC | 3.6.3.20 | P | Belongs to the ABC transporter superfamily | |
NHNMODOO_00345 | 1.8e-162 | ugpA | G | ABC transporter (permease) | ||
NHNMODOO_00346 | 3.5e-138 | ugpE | P | Glycerol-3-phosphate ABC transporter permease | ||
NHNMODOO_00347 | 2.9e-230 | ugpB | G | Glycerol-3-phosphate ABC transporter substrate-binding protein | ||
NHNMODOO_00348 | 7.3e-138 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NHNMODOO_00349 | 6.1e-208 | yceL | EGP | Major Facilitator Superfamily | ||
NHNMODOO_00350 | 5.4e-308 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_00351 | 8.2e-148 | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | ||
NHNMODOO_00352 | 1.6e-91 | K | Regulates expression of the glpD operon. In the presence of glycerol 3-phosphate (G3P) causes antitermination of transcription of glpD at the inverted repeat of the leader region to enhance its transcription. Binds and stabilizes glpD leader mRNA | |||
NHNMODOO_00353 | 1.8e-173 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00354 | 2.8e-157 | G | COG0395 ABC-type sugar transport system, permease component | |||
NHNMODOO_00355 | 5.4e-119 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NHNMODOO_00356 | 9.1e-175 | G | Xylose isomerase-like TIM barrel | |||
NHNMODOO_00357 | 3.4e-194 | S | Oxidoreductase family, C-terminal alpha/beta domain | |||
NHNMODOO_00358 | 2.3e-99 | ykoP | G | polysaccharide deacetylase | ||
NHNMODOO_00359 | 7.5e-158 | |||||
NHNMODOO_00360 | 3.1e-139 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_00361 | 1.9e-139 | K | helix_turn_helix, arabinose operon control protein | |||
NHNMODOO_00362 | 2e-64 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
NHNMODOO_00363 | 6.2e-168 | 3.5.3.11, 3.5.3.8 | E | Catalyzes the conversion of N-formimidoyl-L-glutamate to L-glutamate and formamide | ||
NHNMODOO_00364 | 9.2e-251 | yhdG | E | amino acid | ||
NHNMODOO_00365 | 3.3e-175 | K | AraC-like ligand binding domain | |||
NHNMODOO_00366 | 0.0 | rhaA | 2.7.1.12, 2.7.1.17, 2.7.1.5, 5.3.1.14 | G | Belongs to the rhamnose isomerase family | |
NHNMODOO_00367 | 0.0 | rhaD | 1.1.1.1, 4.1.2.19 | IQ | Class II Aldolase and Adducin N-terminal domain | |
NHNMODOO_00368 | 4.8e-51 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
NHNMODOO_00369 | 9.5e-223 | iolF | EGP | Major facilitator Superfamily | ||
NHNMODOO_00370 | 3.6e-146 | K | AraC-like ligand binding domain | |||
NHNMODOO_00371 | 7.4e-230 | MA20_16885 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
NHNMODOO_00372 | 1.6e-216 | MA20_16880 | EM | Protein of unknown function (DUF993) | ||
NHNMODOO_00373 | 7.6e-157 | MA20_16875 | G | Xylose isomerase-like TIM barrel | ||
NHNMODOO_00374 | 1.1e-209 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NHNMODOO_00375 | 2.9e-310 | 2.7.13.3 | T | Histidine kinase | ||
NHNMODOO_00376 | 4.1e-198 | T | helix_turn_helix, arabinose operon control protein | |||
NHNMODOO_00377 | 1.1e-247 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_00378 | 2.5e-175 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00379 | 9.6e-155 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00380 | 6.1e-194 | I | Acyltransferase family | |||
NHNMODOO_00381 | 4.7e-233 | arlS | T | His Kinase A (phosphoacceptor) domain | ||
NHNMODOO_00382 | 1.3e-117 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_00383 | 1.7e-125 | S | L-2-amino-thiazoline-4-carboxylic acid hydrolase | |||
NHNMODOO_00385 | 1.3e-55 | |||||
NHNMODOO_00386 | 0.0 | E | cell wall organization | |||
NHNMODOO_00387 | 1.5e-236 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_00388 | 9.9e-153 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00389 | 6e-157 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00390 | 5.1e-300 | abfA | 3.2.1.55 | GH51 | G | alpha-L-arabinofuranosidase activity |
NHNMODOO_00391 | 5.9e-241 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_00392 | 6.7e-159 | amyD | G | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_00393 | 1.2e-152 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00394 | 2.4e-102 | S | Protein of unknown function, DUF624 | |||
NHNMODOO_00395 | 1.5e-169 | M1-640 | K | Transcriptional regulator | ||
NHNMODOO_00396 | 5.4e-164 | rhaR1 | K | AraC-like ligand binding domain | ||
NHNMODOO_00397 | 9.6e-141 | araL | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
NHNMODOO_00398 | 4e-215 | egsA | 1.1.1.261 | C | Catalyzes the NAD(P)H-dependent reduction of dihydroxyacetonephosphate (DHAP or glycerone phosphate) to glycerol 1-phosphate (G1P). The G1P thus generated is probably used for the synthesis of phosphoglycerolipids in Gram-positive bacterial species | |
NHNMODOO_00399 | 7.1e-135 | araD | 4.1.2.17, 5.1.3.4 | G | COG0235 Ribulose-5-phosphate 4-epimerase and related epimerases and aldolases | |
NHNMODOO_00400 | 0.0 | araB | 2.7.1.16 | C | Belongs to the ribulokinase family | |
NHNMODOO_00401 | 6.7e-281 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
NHNMODOO_00402 | 3.8e-196 | chvE | G | ABC transporter | ||
NHNMODOO_00403 | 2.5e-278 | araG | 3.6.3.17 | G | Part of the ABC transporter complex RbsABC involved in ribose import. Responsible for energy coupling to the transport system | |
NHNMODOO_00404 | 1.7e-194 | gguB | G | Belongs to the binding-protein-dependent transport system permease family | ||
NHNMODOO_00405 | 5.3e-297 | melA | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase |
NHNMODOO_00406 | 6e-129 | |||||
NHNMODOO_00408 | 9.3e-78 | S | Putative small multi-drug export protein | |||
NHNMODOO_00409 | 2.8e-107 | V | Transport permease protein | |||
NHNMODOO_00410 | 7.2e-178 | KTV | LytTr DNA-binding domain | |||
NHNMODOO_00411 | 3.8e-48 | sugE | P | Small Multidrug Resistance protein | ||
NHNMODOO_00412 | 3.2e-59 | sugE | P | Small Multidrug Resistance protein | ||
NHNMODOO_00413 | 1.9e-98 | yvdT | K | Transcriptional regulator | ||
NHNMODOO_00414 | 2.8e-239 | EGP | Major Facilitator Superfamily | |||
NHNMODOO_00415 | 5.9e-135 | iolR | K | COG1349 Transcriptional regulators of sugar metabolism | ||
NHNMODOO_00416 | 1.6e-274 | 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 | |
NHNMODOO_00417 | 6e-146 | iolB | 5.3.1.30 | G | Involved in the isomerization of 5-deoxy-glucuronate (5DG) to 5-dehydro-2-deoxy-D-gluconate (DKG or 2-deoxy-5-keto-D- gluconate) | |
NHNMODOO_00418 | 9.7e-175 | iolC | 2.7.1.92 | G | Catalyzes the phosphorylation of 5-dehydro-2-deoxy-D- gluconate (2-deoxy-5-keto-D-gluconate or DKG) to 6-phospho-5- dehydro-2-deoxy-D-gluconate (DKGP) | |
NHNMODOO_00419 | 0.0 | iolD | 3.7.1.22 | E | Involved in the cleavage of the C1-C2 bond of 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (THcHDO) to yield 5-deoxy- glucuronate (5DG) | |
NHNMODOO_00420 | 1.9e-169 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
NHNMODOO_00421 | 6.2e-188 | iolG | 1.1.1.18, 1.1.1.369 | S | Involved in the oxidation of myo-inositol (MI) and D- chiro-inositol (DCI) to 2-keto-myo-inositol (2KMI or 2-inosose) and 1-keto-D-chiro-inositol (1KDCI), respectively | |
NHNMODOO_00422 | 8.2e-98 | iolI | 5.3.99.11 | G | Involved in the reversible interconverion of 2-keto-myo- inositol (2KMI, inosose or 2,4,6 3,5-pentahydroxycyclohexanone) to 1-keto-D-chiro-inositol (1KDCI or 2,3,5 4,6- pentahydroxycyclohexanone) | |
NHNMODOO_00423 | 3.8e-154 | iolJ | 4.1.2.13, 4.1.2.29 | F | Produces dihydroxyacetone phosphate (DHAP or glycerone phosphate) and malonic semialdehyde (MSA or 3-oxopropanoate) from 6-phospho-5-dehydro-2-deoxy-D-gluconate (DKGP) | |
NHNMODOO_00424 | 8e-172 | yisS | 1.1.1.370 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
NHNMODOO_00425 | 4.7e-272 | yidK | S | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
NHNMODOO_00426 | 1.3e-103 | S | Protein of unknown function (DUF421) | |||
NHNMODOO_00427 | 1.4e-200 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
NHNMODOO_00428 | 1.1e-178 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
NHNMODOO_00429 | 7e-256 | hemG | 1.14.19.9, 1.3.3.15, 1.3.3.4 | H | Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX | |
NHNMODOO_00431 | 1.3e-99 | spo0B | T | Sporulation initiation phospho-transferase B, C-terminal | ||
NHNMODOO_00432 | 7.6e-220 | 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 | ||
NHNMODOO_00433 | 1.8e-72 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
NHNMODOO_00434 | 2.1e-160 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
NHNMODOO_00435 | 1.6e-87 | niaR | S | small molecule binding protein (contains 3H domain) | ||
NHNMODOO_00436 | 6e-205 | nifS | 2.8.1.7 | E | Cysteine desulfurase | |
NHNMODOO_00437 | 3.2e-273 | nadB | 1.3.5.4, 1.4.3.16 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
NHNMODOO_00438 | 2.6e-144 | nadC | 1.4.3.16, 2.4.2.19 | H | Belongs to the NadC ModD family | |
NHNMODOO_00439 | 6.9e-206 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
NHNMODOO_00440 | 1.2e-150 | safA | M | spore coat assembly protein SafA | ||
NHNMODOO_00441 | 1.5e-22 | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | |||
NHNMODOO_00442 | 9.4e-62 | 1.9.3.1 | C | cytochrome c oxidase subunit II | ||
NHNMODOO_00443 | 3.4e-86 | bofC | S | BofC C-terminal domain | ||
NHNMODOO_00444 | 4.6e-103 | 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 | |
NHNMODOO_00445 | 5.8e-183 | 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 | |
NHNMODOO_00446 | 1.4e-27 | yrzS | S | Protein of unknown function (DUF2905) | ||
NHNMODOO_00447 | 2e-186 | 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) | |
NHNMODOO_00448 | 3.4e-227 | 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) | |
NHNMODOO_00449 | 2.5e-37 | yajC | U | Preprotein translocase subunit YajC | ||
NHNMODOO_00450 | 3.2e-57 | yrzE | S | Protein of unknown function (DUF3792) | ||
NHNMODOO_00451 | 5.2e-70 | ycaP | S | membrane | ||
NHNMODOO_00452 | 2.1e-25 | yodI | ||||
NHNMODOO_00453 | 4.7e-248 | spoVB | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
NHNMODOO_00454 | 9.6e-22 | yrzD | S | Post-transcriptional regulator | ||
NHNMODOO_00455 | 6.7e-232 | secD | 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 | ||
NHNMODOO_00456 | 2.7e-142 | 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 | ||
NHNMODOO_00457 | 2.9e-37 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
NHNMODOO_00458 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
NHNMODOO_00459 | 1.2e-91 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
NHNMODOO_00460 | 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 | |
NHNMODOO_00461 | 6.3e-73 | 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 | ||
NHNMODOO_00462 | 9e-184 | cytR | 5.1.1.1 | K | LacI family transcriptional regulator | |
NHNMODOO_00463 | 1.2e-142 | thuA | G | Trehalose utilisation | ||
NHNMODOO_00464 | 2e-191 | S | Oxidoreductase family, C-terminal alpha/beta domain | |||
NHNMODOO_00465 | 3.8e-201 | V | Belongs to the UPF0214 family | |||
NHNMODOO_00467 | 7e-242 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
NHNMODOO_00468 | 0.0 | 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) | |
NHNMODOO_00469 | 2.8e-216 | 1.1.1.3 | E | homoserine dehydrogenase | ||
NHNMODOO_00470 | 4e-50 | |||||
NHNMODOO_00471 | 3.4e-216 | yxjG | 2.1.1.14 | E | Methionine synthase | |
NHNMODOO_00472 | 1.1e-136 | yrvM | H | COG1179 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 | ||
NHNMODOO_00473 | 7.2e-107 | rsfA | S | Transcriptional regulator | ||
NHNMODOO_00474 | 7.2e-231 | rarA | L | COG2256 ATPase related to the helicase subunit of the Holliday junction resolvase | ||
NHNMODOO_00475 | 2.8e-70 | cymR | K | Transcriptional regulator | ||
NHNMODOO_00476 | 6.4e-210 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
NHNMODOO_00477 | 1.1e-216 | 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 | |
NHNMODOO_00478 | 4.5e-67 | S | COG0457 FOG TPR repeat | |||
NHNMODOO_00479 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
NHNMODOO_00480 | 3e-81 | yrrD | S | protein conserved in bacteria | ||
NHNMODOO_00481 | 2.1e-30 | yrzR | ||||
NHNMODOO_00482 | 1.6e-183 | yrrI | S | AI-2E family transporter | ||
NHNMODOO_00483 | 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 | |
NHNMODOO_00484 | 3.2e-43 | yrzL | S | Belongs to the UPF0297 family | ||
NHNMODOO_00485 | 5.7e-71 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
NHNMODOO_00486 | 4.1e-25 | yrzB | S | Belongs to the UPF0473 family | ||
NHNMODOO_00487 | 1.2e-208 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
NHNMODOO_00488 | 2.4e-113 | yrrM | 2.1.1.104 | S | O-methyltransferase | |
NHNMODOO_00489 | 5.3e-113 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
NHNMODOO_00490 | 4.1e-78 | 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 | ||
NHNMODOO_00491 | 1.1e-11 | S | Protein of unknown function (DUF1510) | |||
NHNMODOO_00492 | 0.0 | ligD | 6.5.1.1 | L | ATP-dependent DNA ligase | |
NHNMODOO_00493 | 6e-149 | 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 | ||
NHNMODOO_00494 | 8.9e-122 | 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 | |
NHNMODOO_00495 | 1.1e-10 | S | YrhC-like protein | |||
NHNMODOO_00496 | 4.3e-77 | M1-460 | ||||
NHNMODOO_00497 | 2.8e-290 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
NHNMODOO_00498 | 1.2e-146 | appF | P | ATPases associated with a variety of cellular activities | ||
NHNMODOO_00499 | 4.4e-141 | oppD | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
NHNMODOO_00500 | 2e-155 | EP | N-terminal TM domain of oligopeptide transport permease C | |||
NHNMODOO_00501 | 2.6e-145 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_00502 | 3.5e-106 | arpR | K | Bacterial regulatory proteins, tetR family | ||
NHNMODOO_00503 | 0.0 | malS | 3.2.1.1 | GH13 | G | Carbohydrate binding domain |
NHNMODOO_00504 | 1.7e-54 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
NHNMODOO_00505 | 1.3e-103 | nudL | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
NHNMODOO_00506 | 1.5e-186 | lplJ | 6.3.1.20 | H | Lipoate-protein ligase | |
NHNMODOO_00507 | 5.3e-251 | S | Membrane | |||
NHNMODOO_00508 | 1.8e-223 | hipO3 | 3.5.1.47 | S | amidohydrolase | |
NHNMODOO_00509 | 8.6e-160 | ybaS | 1.1.1.58 | S | Na -dependent transporter | |
NHNMODOO_00510 | 2.1e-123 | sigK | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
NHNMODOO_00511 | 4.9e-176 | yfjD | P | Transporter associated domain | ||
NHNMODOO_00512 | 1.6e-24 | |||||
NHNMODOO_00513 | 6.8e-23 | S | Histidine kinase | |||
NHNMODOO_00515 | 4.4e-53 | |||||
NHNMODOO_00516 | 1.3e-249 | hemD | 2.1.1.107, 4.2.1.75 | H | Belongs to the precorrin methyltransferase family | |
NHNMODOO_00517 | 0.0 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
NHNMODOO_00518 | 8.7e-56 | nirD | 1.7.1.15 | P | Nitrite reductase | |
NHNMODOO_00519 | 0.0 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
NHNMODOO_00520 | 0.0 | nasC | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
NHNMODOO_00521 | 1e-40 | nasA | P | COG2223 Nitrate nitrite transporter | ||
NHNMODOO_00522 | 2.5e-141 | nasA | P | COG2223 Nitrate nitrite transporter | ||
NHNMODOO_00523 | 4.1e-258 | M | Belongs to the BCCT transporter (TC 2.A.15) family | |||
NHNMODOO_00525 | 2e-149 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
NHNMODOO_00526 | 1.4e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
NHNMODOO_00527 | 6.1e-62 | phaG | P | Na+/H+ antiporter subunit | ||
NHNMODOO_00528 | 3.1e-38 | phaF | P | Multiple resistance and pH regulation protein F (MrpF / PhaF) | ||
NHNMODOO_00529 | 1.1e-81 | mrpE | P | Subunit E of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
NHNMODOO_00530 | 2e-264 | mrpD | CP | Subunit D of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
NHNMODOO_00531 | 8.8e-51 | phaC | 1.6.5.3 | P | Subunit C of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | |
NHNMODOO_00532 | 7.5e-71 | mrpB | P | Subunit B of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
NHNMODOO_00533 | 0.0 | phaA | 1.6.5.3 | CP | COG1009 NADH ubiquinone oxidoreductase subunit 5 (chain L) Multisubunit Na H antiporter, MnhA subunit | |
NHNMODOO_00535 | 6.2e-96 | yqeG | S | hydrolase of the HAD superfamily | ||
NHNMODOO_00536 | 1.8e-217 | yqeH | S | In Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
NHNMODOO_00537 | 3.6e-154 | 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) | |
NHNMODOO_00538 | 1.5e-46 | yhbY | J | RNA-binding protein containing KH domain, possibly ribosomal protein | ||
NHNMODOO_00539 | 9.6e-106 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
NHNMODOO_00540 | 6.7e-107 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
NHNMODOO_00541 | 9.8e-61 | 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 | ||
NHNMODOO_00542 | 1.9e-158 | cvfB | S | protein conserved in bacteria | ||
NHNMODOO_00543 | 1.8e-133 | cmoA | S | Methyltransferase domain | ||
NHNMODOO_00544 | 4.7e-146 | comER | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | ||
NHNMODOO_00545 | 2.9e-100 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
NHNMODOO_00546 | 1e-107 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
NHNMODOO_00547 | 0.0 | comEC | S | Competence protein ComEC | ||
NHNMODOO_00548 | 2.4e-07 | S | YqzM-like protein | |||
NHNMODOO_00549 | 1.4e-176 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
NHNMODOO_00550 | 4.8e-36 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
NHNMODOO_00551 | 1.3e-204 | gpr | 3.4.24.78 | C | Initiates the rapid degradation of small, acid-soluble proteins during spore germination | |
NHNMODOO_00552 | 6.1e-200 | spoIIP | M | stage II sporulation protein P | ||
NHNMODOO_00553 | 4.8e-52 | |||||
NHNMODOO_00554 | 0.0 | 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 | ||
NHNMODOO_00555 | 1.7e-218 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
NHNMODOO_00556 | 2e-186 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
NHNMODOO_00557 | 4.2e-69 | 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 | ||
NHNMODOO_00558 | 5.1e-294 | dnaK | O | Heat shock 70 kDa protein | ||
NHNMODOO_00559 | 2.8e-194 | 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 | ||
NHNMODOO_00560 | 4.1e-170 | prmA | J | Methylates ribosomal protein L11 | ||
NHNMODOO_00561 | 3.2e-130 | 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 | |
NHNMODOO_00562 | 9.9e-255 | yqeV | 2.8.4.5 | J | ribosomal protein S12 methylthiotransferase | |
NHNMODOO_00563 | 1.7e-134 | ycgJ_1 | Q | ubiE/COQ5 methyltransferase family | ||
NHNMODOO_00564 | 6.7e-221 | gltT | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NHNMODOO_00565 | 1.5e-113 | 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 | |
NHNMODOO_00566 | 2.1e-171 | iolS | C | Aldo keto reductase | ||
NHNMODOO_00567 | 9.2e-159 | yqeW | P | COG1283 Na phosphate symporter | ||
NHNMODOO_00568 | 2.1e-19 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
NHNMODOO_00569 | 5.2e-54 | yqeY | S | Yqey-like protein | ||
NHNMODOO_00570 | 1.2e-215 | yqeZ | O | COG1030 Membrane-bound serine protease (ClpP class) | ||
NHNMODOO_00571 | 2.1e-95 | yqfA | S | UPF0365 protein | ||
NHNMODOO_00572 | 1.1e-37 | |||||
NHNMODOO_00573 | 6.7e-47 | yqfC | S | sporulation protein YqfC | ||
NHNMODOO_00574 | 5e-218 | yqfD | 3.1.3.102, 3.1.3.104 | S | Stage IV sporulation | |
NHNMODOO_00575 | 5.8e-172 | phoH | T | Phosphate starvation-inducible protein PhoH | ||
NHNMODOO_00576 | 0.0 | yqfF | S | membrane-associated HD superfamily hydrolase | ||
NHNMODOO_00577 | 6.2e-82 | 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 | |
NHNMODOO_00578 | 6.3e-61 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
NHNMODOO_00579 | 5.5e-71 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
NHNMODOO_00580 | 6.9e-167 | 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 | ||
NHNMODOO_00581 | 7.1e-18 | S | YqzL-like protein | |||
NHNMODOO_00582 | 2.2e-137 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
NHNMODOO_00584 | 9.1e-172 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
NHNMODOO_00585 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
NHNMODOO_00586 | 3.8e-111 | ccpN | K | CBS domain | ||
NHNMODOO_00587 | 1.6e-143 | 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 | |
NHNMODOO_00588 | 6.2e-79 | yaiI | S | Belongs to the UPF0178 family | ||
NHNMODOO_00589 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
NHNMODOO_00590 | 1.9e-203 | 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 | ||
NHNMODOO_00591 | 1.8e-63 | C | COG2010 Cytochrome c, mono- and diheme variants | |||
NHNMODOO_00592 | 1.7e-117 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
NHNMODOO_00593 | 2.5e-190 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
NHNMODOO_00594 | 2e-177 | 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 | |
NHNMODOO_00595 | 8.8e-84 | carD | K | Transcription factor | ||
NHNMODOO_00596 | 1.2e-43 | yqfQ | S | YqfQ-like protein | ||
NHNMODOO_00597 | 4.1e-248 | 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 | |
NHNMODOO_00598 | 2e-163 | 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 | |
NHNMODOO_00599 | 1.9e-08 | yqfT | S | Protein of unknown function (DUF2624) | ||
NHNMODOO_00600 | 3.6e-213 | pilS | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
NHNMODOO_00601 | 4.1e-130 | GH23 | M | Transglycosylase SLT domain | ||
NHNMODOO_00602 | 7.7e-143 | zurA | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
NHNMODOO_00603 | 2.4e-132 | znuB | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
NHNMODOO_00604 | 7.5e-76 | zur | P | Belongs to the Fur family | ||
NHNMODOO_00605 | 1.8e-36 | S | Domain of Unknown Function (DUF1540) | |||
NHNMODOO_00607 | 3.9e-107 | yqfW | S | Belongs to the 5'(3')-deoxyribonucleotidase family | ||
NHNMODOO_00608 | 7.3e-63 | yqfX | S | membrane | ||
NHNMODOO_00609 | 2.8e-199 | 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 | |
NHNMODOO_00610 | 4e-54 | fimV | NU | translation initiation factor activity | ||
NHNMODOO_00611 | 3.3e-174 | EGP | Major facilitator Superfamily | |||
NHNMODOO_00612 | 9.7e-150 | ypuA | S | Secreted protein | ||
NHNMODOO_00613 | 1.5e-113 | O | NfeD-like C-terminal, partner-binding | |||
NHNMODOO_00614 | 2.2e-193 | XK27_00915 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
NHNMODOO_00615 | 4e-266 | nptA | P | COG1283 Na phosphate symporter | ||
NHNMODOO_00620 | 1.3e-116 | sodA | 1.15.1.1 | P | radicals which are normally produced within the cells and which are toxic to biological systems | |
NHNMODOO_00621 | 1.3e-232 | yqgE | EGP | Major facilitator superfamily | ||
NHNMODOO_00623 | 0.0 | mrdA | 3.4.16.4 | M | penicillin-binding protein | |
NHNMODOO_00624 | 7.2e-75 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
NHNMODOO_00625 | 6.9e-60 | |||||
NHNMODOO_00626 | 2.5e-124 | G | PFAM Glycoside hydrolase 15-related | |||
NHNMODOO_00627 | 3e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
NHNMODOO_00628 | 1.8e-93 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
NHNMODOO_00629 | 2.6e-141 | S | Integral membrane protein DUF92 | |||
NHNMODOO_00630 | 7.4e-186 | moeB | 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
NHNMODOO_00631 | 1.4e-232 | nhaC | C | Na H antiporter | ||
NHNMODOO_00633 | 1.4e-292 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
NHNMODOO_00634 | 2.3e-265 | spoVAF | EG | Bacillus/Clostridium GerA spore germination protein | ||
NHNMODOO_00635 | 1e-66 | yueI | S | Protein of unknown function (DUF1694) | ||
NHNMODOO_00636 | 4.2e-81 | |||||
NHNMODOO_00637 | 5.2e-09 | yqgQ | S | protein conserved in bacteria | ||
NHNMODOO_00638 | 1.1e-173 | glcK | 2.7.1.2 | G | Glucokinase | |
NHNMODOO_00639 | 2.3e-262 | aspA | 4.2.1.2, 4.3.1.1 | E | Aspartate ammonia-lyase | |
NHNMODOO_00640 | 4.5e-109 | 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) | |
NHNMODOO_00641 | 8.8e-27 | thiS | H | ThiS family | ||
NHNMODOO_00642 | 4e-139 | 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 | |
NHNMODOO_00643 | 5.2e-209 | thiO | 1.4.3.19 | E | Glycine oxidase | |
NHNMODOO_00644 | 3.4e-141 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
NHNMODOO_00645 | 6.7e-96 | |||||
NHNMODOO_00646 | 1.2e-186 | dglA | S | Thiamine-binding protein | ||
NHNMODOO_00647 | 7.1e-72 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
NHNMODOO_00648 | 2e-91 | yjcG | J | Belongs to the 2H phosphoesterase superfamily. YjcG family | ||
NHNMODOO_00649 | 8.1e-134 | yjcH | P | COG2382 Enterochelin esterase and related enzymes | ||
NHNMODOO_00650 | 1.7e-30 | |||||
NHNMODOO_00651 | 2.3e-50 | ansR | K | Helix-turn-helix XRE-family like proteins | ||
NHNMODOO_00652 | 7.4e-30 | K | Cro/C1-type HTH DNA-binding domain | |||
NHNMODOO_00658 | 4.3e-42 | nucH | 3.1.31.1 | L | COG1525 Micrococcal nuclease (thermonuclease) homologs | |
NHNMODOO_00660 | 6.1e-95 | |||||
NHNMODOO_00663 | 1.1e-09 | S | STAS-like domain of unknown function (DUF4325) | |||
NHNMODOO_00670 | 9.9e-69 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
NHNMODOO_00672 | 3.1e-18 | |||||
NHNMODOO_00674 | 8.7e-31 | S | AP2 domain protein | |||
NHNMODOO_00679 | 2.6e-09 | |||||
NHNMODOO_00681 | 5.2e-21 | gepA | S | Protein of unknown function (DUF4065) | ||
NHNMODOO_00683 | 7.8e-117 | ligB | 6.5.1.1, 6.5.1.6, 6.5.1.7 | L | ATP-dependent DNA ligase | |
NHNMODOO_00684 | 1.2e-48 | S | YolD-like protein | |||
NHNMODOO_00689 | 1.6e-31 | tmk | 2.7.4.9 | F | Thymidylate kinase | |
NHNMODOO_00693 | 1e-38 | |||||
NHNMODOO_00694 | 1e-94 | 4.6.1.1 | T | Adenylate and Guanylate cyclase catalytic domain | ||
NHNMODOO_00700 | 1.5e-52 | L | DNA integration | |||
NHNMODOO_00703 | 4.3e-129 | L | Phage integrase family | |||
NHNMODOO_00704 | 8.5e-48 | S | MTH538 TIR-like domain (DUF1863) | |||
NHNMODOO_00705 | 1.3e-107 | S | Caspase domain | |||
NHNMODOO_00708 | 6.8e-97 | |||||
NHNMODOO_00711 | 2.8e-65 | |||||
NHNMODOO_00716 | 1.6e-112 | M | Cna protein B-type domain | |||
NHNMODOO_00717 | 3.4e-106 | virB11 | 2.1.1.37 | NU | Type II/IV secretion system protein | |
NHNMODOO_00718 | 1.9e-67 | |||||
NHNMODOO_00719 | 2.1e-49 | |||||
NHNMODOO_00728 | 4.8e-08 | S | STAS-like domain of unknown function (DUF4325) | |||
NHNMODOO_00733 | 1e-16 | |||||
NHNMODOO_00735 | 0.0 | topA2 | 5.99.1.2 | L | Topoisomerase IA | |
NHNMODOO_00736 | 3.5e-108 | tnpA1 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
NHNMODOO_00738 | 2.2e-32 | |||||
NHNMODOO_00739 | 4.7e-157 | |||||
NHNMODOO_00741 | 3e-15 | S | Toxin ToxN, type III toxin-antitoxin system | |||
NHNMODOO_00744 | 3.4e-15 | |||||
NHNMODOO_00749 | 2.2e-199 | L | Transposase, IS605 OrfB family | |||
NHNMODOO_00751 | 1.1e-33 | |||||
NHNMODOO_00752 | 5e-24 | 3.1.31.1 | L | Staphylococcal nuclease homologues | ||
NHNMODOO_00753 | 2e-42 | |||||
NHNMODOO_00754 | 2.2e-07 | |||||
NHNMODOO_00755 | 9.2e-35 | |||||
NHNMODOO_00756 | 1.5e-35 | 3.1.21.3 | D | CHAP domain | ||
NHNMODOO_00762 | 3.6e-41 | L | Transposase IS200 like | |||
NHNMODOO_00763 | 4.2e-163 | L | TIGRFAM Transposase, IS605 OrfB, C-terminal | |||
NHNMODOO_00764 | 3.7e-81 | |||||
NHNMODOO_00767 | 4.3e-10 | |||||
NHNMODOO_00770 | 2.1e-162 | clpB | O | C-terminal, D2-small domain, of ClpB protein | ||
NHNMODOO_00772 | 0.0 | U | Type IV secretory system Conjugative DNA transfer | |||
NHNMODOO_00773 | 1.6e-162 | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | ||
NHNMODOO_00775 | 1.1e-09 | hupA | 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 | ||
NHNMODOO_00783 | 2e-72 | 3.6.4.12 | L | Viral (Superfamily 1) RNA helicase | ||
NHNMODOO_00784 | 4.2e-121 | O | Sigma-54 interaction domain | |||
NHNMODOO_00786 | 9.1e-62 | |||||
NHNMODOO_00790 | 7.2e-56 | 3.1.3.1 | KLT | Associated with various cellular activities | ||
NHNMODOO_00793 | 2.3e-11 | S | LexA-binding, inner membrane-associated putative hydrolase | |||
NHNMODOO_00798 | 1.2e-32 | |||||
NHNMODOO_00799 | 8e-15 | S | CAAX protease self-immunity | |||
NHNMODOO_00804 | 3.2e-14 | |||||
NHNMODOO_00805 | 1.8e-07 | |||||
NHNMODOO_00806 | 1.8e-11 | S | hydrolase activity | |||
NHNMODOO_00809 | 3.3e-32 | |||||
NHNMODOO_00813 | 5.5e-115 | S | helicase activity | |||
NHNMODOO_00815 | 1.2e-92 | yhaM | L | Shows a 3'-5' exoribonuclease activity | ||
NHNMODOO_00817 | 1.8e-17 | S | VRR_NUC | |||
NHNMODOO_00820 | 4.2e-07 | |||||
NHNMODOO_00822 | 1.2e-124 | rarA | L | AAA C-terminal domain | ||
NHNMODOO_00828 | 1.5e-42 | O | peptidyl-tyrosine sulfation | |||
NHNMODOO_00829 | 5.9e-88 | S | response regulator aspartate phosphatase | |||
NHNMODOO_00836 | 9.2e-53 | S | dUTPase | |||
NHNMODOO_00839 | 2.7e-14 | S | YopX protein | |||
NHNMODOO_00844 | 3.6e-130 | |||||
NHNMODOO_00845 | 2.2e-211 | S | Phage plasmid primase, P4 family | |||
NHNMODOO_00848 | 5.3e-55 | recJ | L | DHH family | ||
NHNMODOO_00855 | 2.8e-14 | S | Protein of unknown function (DUF1273) | |||
NHNMODOO_00856 | 2e-08 | |||||
NHNMODOO_00859 | 1.7e-26 | S | Macro domain | |||
NHNMODOO_00873 | 1.7e-68 | soj | D | COG1192 ATPases involved in chromosome partitioning | ||
NHNMODOO_00875 | 1.2e-44 | repB | L | Initiator Replication protein | ||
NHNMODOO_00876 | 3.5e-22 | |||||
NHNMODOO_00878 | 2.9e-107 | |||||
NHNMODOO_00879 | 2.9e-15 | |||||
NHNMODOO_00880 | 1.2e-07 | |||||
NHNMODOO_00882 | 1.5e-12 | CP_0160 | L | type I site-specific deoxyribonuclease activity | ||
NHNMODOO_00884 | 7e-90 | yokH | G | SMI1 / KNR4 family | ||
NHNMODOO_00885 | 1.6e-58 | V | HNH endonuclease | |||
NHNMODOO_00887 | 4.7e-133 | UW | nuclease activity | |||
NHNMODOO_00888 | 2.6e-79 | mraZ | K | Belongs to the MraZ family | ||
NHNMODOO_00889 | 4.8e-171 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
NHNMODOO_00890 | 6e-47 | ftsL | D | cell division protein FtsL | ||
NHNMODOO_00891 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
NHNMODOO_00893 | 0.0 | ftsI | 3.4.16.4 | M | stage V sporulation protein D | |
NHNMODOO_00894 | 1.8e-270 | murE | 6.3.2.10, 6.3.2.13, 6.3.2.7 | 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 | |
NHNMODOO_00895 | 8e-244 | 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 | |
NHNMODOO_00896 | 9.3e-170 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
NHNMODOO_00897 | 3.3e-242 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
NHNMODOO_00898 | 5.2e-185 | spoVE | D | Belongs to the SEDS family | ||
NHNMODOO_00899 | 1.8e-120 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
NHNMODOO_00901 | 7.6e-220 | 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 | ||
NHNMODOO_00902 | 9e-185 | 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 | ||
NHNMODOO_00903 | 1e-159 | 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 | ||
NHNMODOO_00904 | 1.1e-124 | sigE | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
NHNMODOO_00905 | 6.2e-140 | sigG | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
NHNMODOO_00906 | 1.7e-45 | ylmC | S | sporulation protein | ||
NHNMODOO_00907 | 2.4e-142 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
NHNMODOO_00908 | 2.2e-117 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
NHNMODOO_00909 | 4.9e-60 | 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 | ||
NHNMODOO_00910 | 2e-43 | yggT | S | membrane | ||
NHNMODOO_00911 | 9e-136 | ylmH | 5.4.99.23, 5.4.99.24 | S | conserved protein, contains S4-like domain | |
NHNMODOO_00912 | 1.8e-63 | divIVA | D | Cell division initiation protein | ||
NHNMODOO_00913 | 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) | |
NHNMODOO_00914 | 2e-109 | dksA | T | COG1734 DnaK suppressor protein | ||
NHNMODOO_00915 | 1.1e-72 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
NHNMODOO_00916 | 1.9e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NHNMODOO_00917 | 2.6e-89 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
NHNMODOO_00918 | 1.3e-227 | pyrP | F | Xanthine uracil | ||
NHNMODOO_00919 | 8.7e-162 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
NHNMODOO_00920 | 6.8e-237 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
NHNMODOO_00921 | 4.3e-208 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
NHNMODOO_00922 | 0.0 | carB | 6.3.5.5 | F | Belongs to the CarB family | |
NHNMODOO_00923 | 1.2e-140 | 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( ) | ||
NHNMODOO_00924 | 5.8e-166 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
NHNMODOO_00925 | 1.2e-121 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
NHNMODOO_00926 | 7.8e-109 | 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) | |
NHNMODOO_00927 | 1.9e-113 | Q | ubiE/COQ5 methyltransferase family | |||
NHNMODOO_00929 | 0.0 | yfhO | S | Bacterial membrane protein YfhO | ||
NHNMODOO_00930 | 0.0 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
NHNMODOO_00931 | 0.0 | yloB | 3.6.3.8 | P | COG0474 Cation transport ATPase | |
NHNMODOO_00932 | 3.5e-39 | ylzA | S | Belongs to the UPF0296 family | ||
NHNMODOO_00933 | 6.9e-110 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
NHNMODOO_00934 | 1e-28 | 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 | |
NHNMODOO_00935 | 3.1e-215 | 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 | |
NHNMODOO_00936 | 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 | ||
NHNMODOO_00937 | 1e-173 | 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 | |
NHNMODOO_00938 | 6.7e-251 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
NHNMODOO_00939 | 2.9e-131 | stp | 3.1.3.16 | T | phosphatase | |
NHNMODOO_00940 | 0.0 | KLT | serine threonine protein kinase | |||
NHNMODOO_00941 | 1.5e-163 | 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 | |
NHNMODOO_00942 | 3e-116 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
NHNMODOO_00944 | 1.6e-25 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
NHNMODOO_00945 | 1.5e-59 | asp | S | protein conserved in bacteria | ||
NHNMODOO_00946 | 5.7e-300 | yloV | S | kinase related to dihydroxyacetone kinase | ||
NHNMODOO_00947 | 5.2e-148 | degV3 | S | protein conserved in bacteria | ||
NHNMODOO_00948 | 4.6e-120 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
NHNMODOO_00949 | 7.7e-147 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
NHNMODOO_00950 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
NHNMODOO_00951 | 9.6e-98 | fapR | K | Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism | ||
NHNMODOO_00952 | 1.1e-178 | 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 | |
NHNMODOO_00953 | 7.2e-167 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
NHNMODOO_00954 | 2.2e-126 | IQ | reductase | |||
NHNMODOO_00955 | 5.4e-31 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
NHNMODOO_00956 | 4.4e-138 | 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 | |
NHNMODOO_00957 | 1.5e-09 | yfkK | S | Belongs to the UPF0435 family | ||
NHNMODOO_00958 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
NHNMODOO_00959 | 2.6e-175 | 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) | ||
NHNMODOO_00960 | 3e-51 | 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 | ||
NHNMODOO_00961 | 1.6e-244 | 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 | |
NHNMODOO_00962 | 6.4e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
NHNMODOO_00963 | 2.5e-33 | ylqC | S | Belongs to the UPF0109 family | ||
NHNMODOO_00964 | 1.5e-68 | ylqD | S | YlqD protein | ||
NHNMODOO_00965 | 4.2e-92 | 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 | ||
NHNMODOO_00966 | 2.2e-131 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
NHNMODOO_00967 | 0.0 | argS | 6.1.1.19 | J | Arginyl tRNA synthetase N terminal dom | |
NHNMODOO_00968 | 2.5e-56 | 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 | ||
NHNMODOO_00970 | 2.3e-101 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NHNMODOO_00971 | 3.4e-155 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
NHNMODOO_00973 | 7.8e-135 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
NHNMODOO_00974 | 2.6e-06 | lig1 | ||||
NHNMODOO_00975 | 9.6e-75 | ylqH | S | FlhB HrpN YscU SpaS Family | ||
NHNMODOO_00976 | 1.1e-212 | 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 | |
NHNMODOO_00977 | 9.7e-169 | 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 | |
NHNMODOO_00978 | 8.6e-169 | dprA | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | ||
NHNMODOO_00979 | 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 | |
NHNMODOO_00980 | 2.1e-249 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
NHNMODOO_00981 | 1.7e-165 | xerC | L | tyrosine recombinase XerC | ||
NHNMODOO_00982 | 2.3e-93 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
NHNMODOO_00983 | 2.1e-223 | 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 | ||
NHNMODOO_00984 | 4.1e-136 | 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 | ||
NHNMODOO_00985 | 3.3e-65 | flgB | N | Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body | ||
NHNMODOO_00986 | 1.8e-72 | flgC | N | Belongs to the flagella basal body rod proteins family | ||
NHNMODOO_00987 | 9.7e-38 | fliE | N | Flagellar hook-basal body | ||
NHNMODOO_00988 | 1e-234 | fliF | N | The M ring may be actively involved in energy transduction | ||
NHNMODOO_00989 | 1.5e-175 | 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 | ||
NHNMODOO_00990 | 2.9e-73 | fliH | NU | COG1317 Flagellar biosynthesis type III secretory pathway protein | ||
NHNMODOO_00991 | 1.4e-245 | fliI | 3.6.3.14 | NU | COG1157 Flagellar biosynthesis type III secretory pathway ATPase | |
NHNMODOO_00992 | 5.4e-40 | fliJ | N | bacterial-type flagellum organization | ||
NHNMODOO_00994 | 1e-205 | N | Flagellar hook-length control protein FliK | |||
NHNMODOO_00995 | 1.2e-71 | flgD | N | Flagellar basal body rod modification protein | ||
NHNMODOO_00996 | 1.4e-139 | flgG | N | Flagellar basal body rod | ||
NHNMODOO_00997 | 1.5e-27 | flbD | N | protein, possibly involved in motility | ||
NHNMODOO_00998 | 4.1e-69 | fliL | N | Controls the rotational direction of flagella during chemotaxis | ||
NHNMODOO_00999 | 2e-175 | 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 | ||
NHNMODOO_01000 | 1.3e-205 | 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 | ||
NHNMODOO_01001 | 1.2e-58 | cheY | T | cheY-homologous receiver domain | ||
NHNMODOO_01002 | 3.5e-104 | fliZ | N | Flagellar biosynthesis protein, FliO | ||
NHNMODOO_01003 | 6.2e-112 | fliP | N | Plays a role in the flagellum-specific transport system | ||
NHNMODOO_01004 | 3.6e-39 | fliQ | N | Role in flagellar biosynthesis | ||
NHNMODOO_01005 | 2.9e-129 | fliR | N | Flagellar biosynthetic protein FliR | ||
NHNMODOO_01006 | 5.5e-187 | 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 | ||
NHNMODOO_01007 | 0.0 | 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 | ||
NHNMODOO_01008 | 1.4e-173 | flhF | N | Flagellar biosynthesis regulator FlhF | ||
NHNMODOO_01009 | 4.9e-94 | |||||
NHNMODOO_01010 | 4.9e-160 | 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 | |
NHNMODOO_01011 | 1.9e-104 | cheC | NT | COG1776 Chemotaxis protein CheC, inhibitor of MCP methylation | ||
NHNMODOO_01012 | 4.3e-83 | 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 | |
NHNMODOO_01013 | 4.9e-134 | sigD | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
NHNMODOO_01015 | 1.5e-132 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
NHNMODOO_01016 | 6.3e-149 | 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 | ||
NHNMODOO_01017 | 1.6e-123 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
NHNMODOO_01018 | 2.1e-89 | 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 | ||
NHNMODOO_01019 | 2.4e-144 | uppS | 2.5.1.31 | I | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
NHNMODOO_01020 | 1.6e-130 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
NHNMODOO_01021 | 1.1e-206 | 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) | |
NHNMODOO_01022 | 7.1e-231 | rasP | M | zinc metalloprotease | ||
NHNMODOO_01023 | 0.0 | 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 | |
NHNMODOO_01024 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NHNMODOO_01025 | 2.8e-79 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
NHNMODOO_01026 | 5e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
NHNMODOO_01027 | 1e-41 | ylxR | K | nucleic-acid-binding protein implicated in transcription termination | ||
NHNMODOO_01028 | 1.6e-46 | ylxQ | J | ribosomal protein | ||
NHNMODOO_01029 | 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 | ||
NHNMODOO_01030 | 8.9e-41 | ylxP | S | protein conserved in bacteria | ||
NHNMODOO_01031 | 3.3e-56 | 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 | ||
NHNMODOO_01032 | 7.1e-172 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
NHNMODOO_01033 | 1e-173 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
NHNMODOO_01034 | 4.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
NHNMODOO_01035 | 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 | |
NHNMODOO_01036 | 3.5e-188 | ylxY | 3.5.1.104 | G | Sporulation protein, polysaccharide deacetylase | |
NHNMODOO_01037 | 6.9e-218 | pepR | S | Belongs to the peptidase M16 family | ||
NHNMODOO_01038 | 1.2e-35 | ymxH | S | YlmC YmxH family | ||
NHNMODOO_01039 | 4.4e-158 | spoVFA | E | subunit a | ||
NHNMODOO_01040 | 5.7e-106 | spoVFB | H | Together with DpaA, catalyzes the conversion of dihydrodipicolinate to dipicolinate (DPA) | ||
NHNMODOO_01041 | 7.9e-191 | 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 | |
NHNMODOO_01042 | 2.7e-219 | dapG | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
NHNMODOO_01043 | 7.7e-155 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
NHNMODOO_01044 | 1.1e-308 | 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 | ||
NHNMODOO_01045 | 3e-128 | tepA | 3.4.21.92 | OU | COG0740 Protease subunit of ATP-dependent Clp proteases | |
NHNMODOO_01046 | 8.4e-10 | S | YlzJ-like protein | |||
NHNMODOO_01047 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
NHNMODOO_01048 | 4.9e-128 | ymfC | K | Transcriptional regulator | ||
NHNMODOO_01049 | 1.9e-226 | ymfF | S | Peptidase M16 | ||
NHNMODOO_01050 | 4.4e-244 | ymfH | S | zinc protease | ||
NHNMODOO_01051 | 7.2e-119 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_01052 | 1.3e-38 | ymfJ | S | Protein of unknown function (DUF3243) | ||
NHNMODOO_01053 | 4.6e-140 | ymfK | S | Protein of unknown function (DUF3388) | ||
NHNMODOO_01054 | 2.7e-123 | ymfM | S | protein conserved in bacteria | ||
NHNMODOO_01055 | 8.7e-99 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
NHNMODOO_01056 | 1.7e-224 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
NHNMODOO_01057 | 6.7e-290 | deaD | 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 | |
NHNMODOO_01058 | 3.3e-189 | 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 | ||
NHNMODOO_01059 | 1.3e-187 | L | Calcineurin-like phosphoesterase superfamily domain | |||
NHNMODOO_01060 | 2.6e-253 | sbcC | L | AAA domain | ||
NHNMODOO_01062 | 1.7e-114 | L | DNA recombination | |||
NHNMODOO_01063 | 1.8e-218 | rny | S | Endoribonuclease that initiates mRNA decay | ||
NHNMODOO_01064 | 6.7e-150 | ymdB | S | protein conserved in bacteria | ||
NHNMODOO_01065 | 6.7e-38 | spoVS | S | Stage V sporulation protein S | ||
NHNMODOO_01066 | 7.2e-152 | tgl | 2.3.2.13 | S | protein-glutamine gamma-glutamyltransferase activity | |
NHNMODOO_01067 | 6.7e-303 | 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 | |
NHNMODOO_01068 | 7.3e-55 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
NHNMODOO_01069 | 2.6e-103 | cotE | S | Spore coat protein | ||
NHNMODOO_01070 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
NHNMODOO_01071 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
NHNMODOO_01072 | 2.2e-134 | J | Putative SAM-dependent methyltransferase | |||
NHNMODOO_01073 | 8.3e-168 | 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) | |
NHNMODOO_01074 | 2.7e-35 | 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 | ||
NHNMODOO_01075 | 7.6e-183 | xerD | L | Belongs to the 'phage' integrase family | ||
NHNMODOO_01076 | 5.8e-169 | spoVK | O | stage V sporulation protein K | ||
NHNMODOO_01077 | 5.3e-245 | ynbB | 4.4.1.1 | P | COG4100 Cystathionine beta-lyase family protein involved in aluminum resistance | |
NHNMODOO_01078 | 3.1e-264 | glnA | 6.3.1.2 | E | glutamine synthetase | |
NHNMODOO_01079 | 2.5e-228 | amtB | P | Ammonium transporter | ||
NHNMODOO_01080 | 1.4e-167 | 2.7.7.7 | T | Putative nucleotidyltransferase substrate binding domain | ||
NHNMODOO_01081 | 3.3e-132 | dnaQ2 | 2.7.7.7 | L | COG0847 DNA polymerase III, epsilon subunit and related 3'-5' exonucleases | |
NHNMODOO_01082 | 1.2e-46 | S | Family of unknown function (DUF5327) | |||
NHNMODOO_01083 | 5.1e-268 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
NHNMODOO_01084 | 1.7e-108 | ykwB | 2.3.1.1 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
NHNMODOO_01085 | 1.3e-58 | ywdK | S | small membrane protein | ||
NHNMODOO_01086 | 9.8e-77 | 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 | ||
NHNMODOO_01087 | 2.4e-77 | cwlJ | 3.5.1.28 | M | Cell wall | |
NHNMODOO_01088 | 9.6e-127 | |||||
NHNMODOO_01089 | 1.2e-62 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
NHNMODOO_01090 | 8.4e-162 | natA1 | V | ABC transporter | ||
NHNMODOO_01091 | 5.4e-164 | yhaQ | S | ABC transporter, ATP-binding protein | ||
NHNMODOO_01092 | 2.6e-180 | yhaP | CP | COG1668 ABC-type Na efflux pump, permease component | ||
NHNMODOO_01093 | 5.8e-48 | |||||
NHNMODOO_01094 | 4.8e-132 | 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 | ||
NHNMODOO_01095 | 3e-144 | ywfI | C | May function as heme-dependent peroxidase | ||
NHNMODOO_01096 | 6.2e-140 | 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | ||
NHNMODOO_01097 | 1.4e-181 | pta | 2.3.1.8, 3.6.3.21 | C | In Salmonella this enzyme is required for ethanolamine catabolism | |
NHNMODOO_01098 | 2.8e-143 | 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 | |
NHNMODOO_01099 | 2.1e-190 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NHNMODOO_01100 | 6e-249 | ywfO | S | COG1078 HD superfamily phosphohydrolases | ||
NHNMODOO_01101 | 2.5e-89 | ywgA | 2.1.1.72, 3.1.21.3 | |||
NHNMODOO_01103 | 5.6e-26 | dmpI | 5.3.2.6 | G | 4-oxalocrotonate tautomerase | |
NHNMODOO_01104 | 1.2e-123 | 3.4.22.70 | M | COG3764 Sortase (surface protein transpeptidase) | ||
NHNMODOO_01105 | 8.5e-199 | F | S-adenosylhomocysteine deaminase activity | |||
NHNMODOO_01106 | 3.8e-99 | ywhD | S | YwhD family | ||
NHNMODOO_01107 | 0.0 | pepF | E | oligoendopeptidase F | ||
NHNMODOO_01108 | 1.7e-156 | vipF | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | |
NHNMODOO_01109 | 0.0 | pbpG | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NHNMODOO_01110 | 1.4e-158 | 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 | |
NHNMODOO_01111 | 2.3e-167 | speB | 3.5.3.11 | E | Belongs to the arginase family | |
NHNMODOO_01112 | 5.5e-74 | ywiB | S | protein conserved in bacteria | ||
NHNMODOO_01113 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
NHNMODOO_01114 | 8e-74 | yqgC | S | protein conserved in bacteria | ||
NHNMODOO_01115 | 7.5e-222 | clsB | I | Belongs to the phospholipase D family. Cardiolipin synthase subfamily | ||
NHNMODOO_01116 | 0.0 | fadF | C | COG0247 Fe-S oxidoreductase | ||
NHNMODOO_01117 | 5e-210 | 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 | |
NHNMODOO_01118 | 3.9e-148 | hbdA | 1.1.1.157 | I | Dehydrogenase | |
NHNMODOO_01119 | 2.5e-206 | mmgC | I | acyl-CoA dehydrogenase | ||
NHNMODOO_01120 | 1.1e-107 | kstR2_2 | K | Transcriptional regulator | ||
NHNMODOO_01121 | 1.1e-57 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
NHNMODOO_01122 | 3.5e-307 | 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 | |
NHNMODOO_01123 | 1.2e-86 | ywjG | S | Domain of unknown function (DUF2529) | ||
NHNMODOO_01124 | 5.5e-59 | spo0F | T | response regulator | ||
NHNMODOO_01125 | 3.8e-159 | fbaA | 4.1.2.13, 4.1.2.29 | G | Aldolase | |
NHNMODOO_01126 | 2.8e-114 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
NHNMODOO_01127 | 8.1e-206 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
NHNMODOO_01128 | 9.2e-178 | glpX | 3.1.3.11, 3.1.3.37 | G | fructose-1,6-bisphosphatase | |
NHNMODOO_01129 | 1.3e-235 | 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 | ||
NHNMODOO_01130 | 3.8e-40 | rpmE2 | J | Ribosomal protein L31 | ||
NHNMODOO_01131 | 9.3e-109 | tdk | 2.7.1.21 | F | thymidine kinase | |
NHNMODOO_01132 | 9.3e-74 | |||||
NHNMODOO_01133 | 1.8e-253 | cdr | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
NHNMODOO_01134 | 9.6e-176 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
NHNMODOO_01135 | 1.7e-159 | 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 | |
NHNMODOO_01136 | 1.4e-113 | spoIIR | S | stage II sporulation protein R | ||
NHNMODOO_01137 | 4.4e-74 | ywlB | 1.20.4.1, 2.3.1.1 | E | Belongs to the acetyltransferase family. ArgA subfamily | |
NHNMODOO_01138 | 8.1e-183 | 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 | |
NHNMODOO_01139 | 1.2e-61 | S | Regulator of ribonuclease activity B | |||
NHNMODOO_01140 | 7.8e-70 | 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 | |
NHNMODOO_01141 | 5.8e-46 | K | Helix-turn-helix domain, rpiR family | |||
NHNMODOO_01142 | 1.3e-99 | 5.3.1.5 | M | Xylose isomerase-like TIM barrel | ||
NHNMODOO_01143 | 2.9e-152 | csbX | EGP | Major facilitator Superfamily | ||
NHNMODOO_01144 | 3.7e-91 | mntP | P | Probably functions as a manganese efflux pump | ||
NHNMODOO_01145 | 3.7e-70 | ywlE | 3.1.3.48, 3.9.1.2, 5.3.1.6 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
NHNMODOO_01146 | 5.9e-119 | mcpA | NT | Chemotaxis | ||
NHNMODOO_01147 | 4.9e-81 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
NHNMODOO_01148 | 5.7e-92 | ywlG | S | Belongs to the UPF0340 family | ||
NHNMODOO_01149 | 5.3e-234 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
NHNMODOO_01150 | 1.8e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
NHNMODOO_01151 | 1.5e-88 | panZ | K | -acetyltransferase | ||
NHNMODOO_01152 | 0.0 | vpr | O | Belongs to the peptidase S8 family | ||
NHNMODOO_01153 | 5.7e-22 | atpI | S | Putative F0F1-ATPase subunit Ca2+/Mg2+ transporter | ||
NHNMODOO_01154 | 7.3e-12 | S | ATP synthase I chain | |||
NHNMODOO_01155 | 2.2e-131 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
NHNMODOO_01156 | 1.4e-14 | 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 | ||
NHNMODOO_01157 | 1.3e-31 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
NHNMODOO_01158 | 1.1e-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 | ||
NHNMODOO_01159 | 1.8e-281 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
NHNMODOO_01160 | 1.7e-151 | 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 | ||
NHNMODOO_01161 | 6.1e-263 | 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 | |
NHNMODOO_01162 | 7e-55 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
NHNMODOO_01163 | 1.5e-21 | ywmB | S | TATA-box binding | ||
NHNMODOO_01164 | 2.6e-236 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
NHNMODOO_01165 | 1.1e-187 | spoIID | D | Stage II sporulation protein D | ||
NHNMODOO_01166 | 1.9e-126 | spoIIQ | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
NHNMODOO_01167 | 7.4e-53 | sugE | P | Multidrug resistance protein | ||
NHNMODOO_01168 | 4.4e-44 | ykkD | P | Multidrug resistance protein | ||
NHNMODOO_01169 | 3.6e-45 | spoIIID | K | Stage III sporulation protein D | ||
NHNMODOO_01170 | 1.6e-180 | mbl | D | Rod shape-determining protein | ||
NHNMODOO_01171 | 4.2e-136 | flhO | N | flagellar basal body | ||
NHNMODOO_01172 | 2.2e-137 | flhP | N | flagellar basal body | ||
NHNMODOO_01173 | 3.2e-59 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
NHNMODOO_01174 | 5.9e-272 | P | Spore gernimation protein GerA | |||
NHNMODOO_01175 | 1e-196 | E | Spore germination protein | |||
NHNMODOO_01176 | 1.9e-187 | S | Spore germination B3/ GerAC like, C-terminal | |||
NHNMODOO_01177 | 6.5e-108 | 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 | ||
NHNMODOO_01178 | 2.4e-136 | estA | S | Putative esterase | ||
NHNMODOO_01179 | 4.7e-73 | 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 | |
NHNMODOO_01180 | 1.3e-290 | pip | S | YhgE Pip N-terminal domain protein | ||
NHNMODOO_01181 | 6.9e-90 | speG_2 | 2.3.1.57 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
NHNMODOO_01182 | 3.2e-78 | yisT | S | DinB family | ||
NHNMODOO_01183 | 7.1e-16 | Q | N-acetyltransferase | |||
NHNMODOO_01185 | 9e-218 | lytE | M | NlpC/P60 family | ||
NHNMODOO_01186 | 1.5e-241 | polYB | 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 | |
NHNMODOO_01187 | 4.8e-224 | |||||
NHNMODOO_01188 | 6.4e-44 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
NHNMODOO_01189 | 7.4e-161 | 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) | ||
NHNMODOO_01190 | 2.6e-191 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
NHNMODOO_01191 | 9.4e-223 | rodA | D | Belongs to the SEDS family | ||
NHNMODOO_01192 | 4.1e-93 | yjbB | G | Transmembrane secretion effector | ||
NHNMODOO_01193 | 5.6e-74 | FG | Scavenger mRNA decapping enzyme C-term binding | |||
NHNMODOO_01194 | 9e-78 | guaD | 3.5.4.12, 3.5.4.3, 3.5.4.33 | FJ | COG0590 Cytosine adenosine deaminases | |
NHNMODOO_01195 | 5.9e-80 | S | Tetratrico peptide repeat | |||
NHNMODOO_01196 | 1.2e-169 | 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) | ||
NHNMODOO_01197 | 3.6e-115 | ywqC | M | biosynthesis protein | ||
NHNMODOO_01198 | 2.2e-120 | ywqD | 2.7.10.1 | D | COG0489 ATPases involved in chromosome partitioning | |
NHNMODOO_01199 | 4.2e-141 | ywqE | 3.1.3.48 | GM | COG4464 Capsular polysaccharide biosynthesis protein | |
NHNMODOO_01200 | 3.5e-71 | S | An automated process has identified a potential problem with this gene model | |||
NHNMODOO_01201 | 1.9e-128 | S | Protein of unknown function (DUF3100) | |||
NHNMODOO_01202 | 3.4e-152 | 1.1.1.31 | I | NAD-binding of NADP-dependent 3-hydroxyisobutyrate dehydrogenase | ||
NHNMODOO_01203 | 1.6e-266 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |||
NHNMODOO_01204 | 6.8e-276 | cyaD | 2.7.11.1, 3.1.4.52, 4.6.1.1 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | |
NHNMODOO_01205 | 1.4e-167 | S | Tetratricopeptide repeat | |||
NHNMODOO_01208 | 2.2e-109 | glxR | 1.1.1.31, 1.1.1.60 | I | 3-hydroxyisobutyrate dehydrogenase | |
NHNMODOO_01209 | 3.9e-239 | S | Hypothetical glycosyl hydrolase 6 | |||
NHNMODOO_01210 | 5.6e-273 | 3.2.1.23 | G | beta-galactosidase | ||
NHNMODOO_01211 | 1.1e-146 | G | ABC-type polysaccharide transport system, permease component | |||
NHNMODOO_01212 | 9.3e-129 | G | ABC transporter permease | |||
NHNMODOO_01213 | 4.1e-225 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_01214 | 2.1e-256 | S | Hypothetical glycosyl hydrolase 6 | |||
NHNMODOO_01215 | 9.7e-226 | K | helix_turn_helix, arabinose operon control protein | |||
NHNMODOO_01216 | 3.6e-42 | S | Integral membrane protein | |||
NHNMODOO_01217 | 6.1e-62 | F | PFAM AIG2 family protein | |||
NHNMODOO_01218 | 6e-260 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |||
NHNMODOO_01219 | 6.8e-234 | amaB | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
NHNMODOO_01220 | 4.4e-07 | |||||
NHNMODOO_01221 | 2.3e-270 | hyuA | 3.5.2.2 | F | Amidohydrolase family | |
NHNMODOO_01222 | 5.5e-231 | preA | 1.3.1.1 | CF | dihydroorotate dehydrogenase | |
NHNMODOO_01223 | 6e-252 | gltD | 1.3.1.1 | E | COG0493 NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
NHNMODOO_01224 | 8.9e-62 | K | DeoR C terminal sensor domain | |||
NHNMODOO_01225 | 1.8e-132 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
NHNMODOO_01226 | 2.2e-49 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NHNMODOO_01227 | 7.2e-34 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHNMODOO_01228 | 3.3e-131 | G | Phosphotransferase system, EIIC | |||
NHNMODOO_01229 | 3.5e-73 | Z012_00995 | 5.3.1.15 | S | Pfam:DUF1498 | |
NHNMODOO_01230 | 1.1e-120 | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | ||
NHNMODOO_01231 | 1e-52 | rpiB | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15, 5.3.1.34, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
NHNMODOO_01232 | 3.1e-51 | rpiB | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15, 5.3.1.34, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
NHNMODOO_01233 | 7e-75 | tpiA | 2.7.2.3, 5.1.3.39, 5.3.1.1, 5.3.1.33 | J | Triosephosphate isomerase | |
NHNMODOO_01234 | 2.9e-77 | |||||
NHNMODOO_01236 | 3.4e-23 | tnpB | L | Belongs to the 'phage' integrase family | ||
NHNMODOO_01237 | 4.6e-20 | tnpC | ||||
NHNMODOO_01238 | 1.3e-90 | J | Acetyltransferase (GNAT) domain | |||
NHNMODOO_01239 | 1.1e-123 | MA20_01270 | K | AraC family transcriptional regulator | ||
NHNMODOO_01240 | 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 | ||
NHNMODOO_01241 | 1.7e-136 | K | helix_turn_helix, mercury resistance | |||
NHNMODOO_01242 | 2e-160 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_01243 | 5.6e-172 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_01244 | 9.2e-261 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_01245 | 3.6e-134 | kipI | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
NHNMODOO_01246 | 4.3e-178 | kipA | 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
NHNMODOO_01247 | 1.1e-209 | ycsG | P | COG1914 Mn2 and Fe2 transporters of the NRAMP family | ||
NHNMODOO_01248 | 7.1e-133 | ycsF | S | Belongs to the UPF0271 (lamB) family | ||
NHNMODOO_01249 | 1.4e-08 | |||||
NHNMODOO_01250 | 4.4e-115 | P | Pyridine nucleotide-disulphide oxidoreductase | |||
NHNMODOO_01251 | 1.3e-60 | K | helix_turn_helix, mercury resistance | |||
NHNMODOO_01252 | 2e-112 | drgA | C | nitroreductase | ||
NHNMODOO_01253 | 1.1e-170 | scrR | K | helix_turn _helix lactose operon repressor | ||
NHNMODOO_01254 | 1.8e-297 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
NHNMODOO_01255 | 2.3e-254 | scrA | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NHNMODOO_01256 | 1.9e-180 | K | Transcriptional regulator | |||
NHNMODOO_01257 | 1.7e-123 | fabG | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
NHNMODOO_01258 | 1.8e-245 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
NHNMODOO_01259 | 2.9e-179 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
NHNMODOO_01260 | 1.6e-132 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
NHNMODOO_01261 | 6.6e-165 | 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 | |
NHNMODOO_01262 | 1.6e-146 | hemX | O | cytochrome C | ||
NHNMODOO_01263 | 3.6e-244 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
NHNMODOO_01264 | 2e-106 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
NHNMODOO_01265 | 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 | |
NHNMODOO_01266 | 1.4e-306 | lonB | 2.7.7.7, 3.4.21.53 | LO | Belongs to the peptidase S16 family | |
NHNMODOO_01267 | 1e-237 | 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 | ||
NHNMODOO_01268 | 3.7e-230 | 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 | ||
NHNMODOO_01269 | 5.5e-178 | trxA2 | O | COG0457 FOG TPR repeat | ||
NHNMODOO_01270 | 2.1e-111 | 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 | |
NHNMODOO_01271 | 3.1e-267 | 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 | |
NHNMODOO_01272 | 6.7e-193 | 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 | |
NHNMODOO_01273 | 5.2e-284 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
NHNMODOO_01274 | 1.2e-178 | 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 | |
NHNMODOO_01275 | 4.2e-84 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
NHNMODOO_01276 | 0.0 | ilvB | 2.2.1.6 | E | Acetolactate synthase | |
NHNMODOO_01277 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
NHNMODOO_01278 | 2.6e-68 | |||||
NHNMODOO_01279 | 1.3e-266 | M | Glycosyl transferase family group 2 | |||
NHNMODOO_01280 | 9.1e-305 | cotA | 1.10.3.4, 1.16.3.3 | Q | multicopper oxidases | |
NHNMODOO_01281 | 3.3e-128 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
NHNMODOO_01282 | 8.1e-239 | hsdM | 2.1.1.72 | V | Type I restriction-modification system | |
NHNMODOO_01283 | 0.0 | hsdR | 3.1.21.3 | L | COG4096 Type I site-specific restriction-modification system, R (restriction) subunit and related helicases | |
NHNMODOO_01285 | 4.1e-10 | |||||
NHNMODOO_01288 | 8.8e-95 | ysnB | S | Phosphoesterase | ||
NHNMODOO_01289 | 2.4e-104 | rdgB | 3.6.1.66 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
NHNMODOO_01290 | 2e-135 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
NHNMODOO_01291 | 7.7e-176 | gerM | S | COG5401 Spore germination protein | ||
NHNMODOO_01292 | 9.2e-194 | yceA | S | Belongs to the UPF0176 family | ||
NHNMODOO_01293 | 2.5e-23 | C | 4Fe-4S binding domain | |||
NHNMODOO_01294 | 1.3e-148 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
NHNMODOO_01295 | 1.2e-79 | ysmB | 2.4.2.28 | K | transcriptional | |
NHNMODOO_01296 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
NHNMODOO_01297 | 1.3e-38 | ptsH | G | phosphocarrier protein HPr | ||
NHNMODOO_01298 | 1.6e-32 | gerE | K | Transcriptional regulator | ||
NHNMODOO_01299 | 4.3e-77 | fcbC | S | thioesterase | ||
NHNMODOO_01300 | 2.8e-145 | sdhB | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
NHNMODOO_01301 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
NHNMODOO_01302 | 2.7e-111 | sdhC | C | succinate dehydrogenase | ||
NHNMODOO_01303 | 1.4e-227 | ktrB | P | COG0168 Trk-type K transport systems, membrane components | ||
NHNMODOO_01304 | 1.3e-75 | yslB | S | Protein of unknown function (DUF2507) | ||
NHNMODOO_01305 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
NHNMODOO_01306 | 1.8e-53 | trxA | O | Belongs to the thioredoxin family | ||
NHNMODOO_01307 | 1.5e-172 | etfA | C | Electron transfer flavoprotein | ||
NHNMODOO_01308 | 5.5e-133 | etfB | C | Electron transfer flavoprotein | ||
NHNMODOO_01309 | 8.8e-131 | fadB | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
NHNMODOO_01310 | 3.2e-101 | fadR | K | Transcriptional regulator | ||
NHNMODOO_01311 | 0.0 | lcfA | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
NHNMODOO_01312 | 6.9e-66 | yshE | S | membrane | ||
NHNMODOO_01313 | 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 | ||
NHNMODOO_01314 | 0.0 | polX | L | COG1796 DNA polymerase IV (family X) | ||
NHNMODOO_01315 | 5.7e-84 | cvpA | S | membrane protein, required for colicin V production | ||
NHNMODOO_01316 | 1.3e-32 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
NHNMODOO_01317 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NHNMODOO_01318 | 6.4e-193 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
NHNMODOO_01319 | 8.8e-128 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NHNMODOO_01320 | 6.3e-31 | sspI | S | Belongs to the SspI family | ||
NHNMODOO_01322 | 2.4e-17 | |||||
NHNMODOO_01323 | 2.3e-201 | ysdC | G | COG1363 Cellulase M and related proteins | ||
NHNMODOO_01324 | 1.7e-64 | ysdB | S | Sigma-w pathway protein YsdB | ||
NHNMODOO_01325 | 1.8e-260 | actP | S | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
NHNMODOO_01326 | 5.5e-53 | S | Protein of unknown function, DUF485 | |||
NHNMODOO_01327 | 2.3e-57 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
NHNMODOO_01328 | 1.7e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
NHNMODOO_01329 | 2.1e-85 | 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 | ||
NHNMODOO_01330 | 2e-206 | yknZ | V | COG0577 ABC-type antimicrobial peptide transport system, permease component | ||
NHNMODOO_01331 | 1.2e-118 | macB | V | ABC transporter, ATP-binding protein | ||
NHNMODOO_01332 | 5.3e-232 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NHNMODOO_01333 | 2.5e-122 | |||||
NHNMODOO_01334 | 4.4e-264 | dacC | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | |
NHNMODOO_01335 | 1.1e-175 | strT | C | Aldo/keto reductase family | ||
NHNMODOO_01336 | 1.7e-182 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NHNMODOO_01337 | 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) | |
NHNMODOO_01338 | 3.1e-161 | ytxC | S | YtxC-like family | ||
NHNMODOO_01339 | 3e-223 | mqnC | 1.21.98.1, 2.5.1.120, 2.5.1.77 | H | Radical SAM enzyme that catalyzes the cyclization of dehypoxanthine futalosine (DHFL) into cyclic dehypoxanthine futalosine (CDHFL), a step in the biosynthesis of menaquinone (MK, vitamin K2) | |
NHNMODOO_01340 | 3.6e-171 | dnaI | L | Primosomal protein DnaI | ||
NHNMODOO_01341 | 7.9e-242 | dnaB | L | Membrane attachment protein | ||
NHNMODOO_01342 | 5.1e-78 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
NHNMODOO_01343 | 3.3e-65 | |||||
NHNMODOO_01344 | 5.4e-68 | speH | 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 | |
NHNMODOO_01345 | 3.2e-192 | gapB | 1.2.1.12, 1.2.1.59 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
NHNMODOO_01346 | 7.6e-98 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
NHNMODOO_01347 | 1.3e-103 | ytaF | P | Probably functions as a manganese efflux pump | ||
NHNMODOO_01348 | 1e-153 | 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 | |
NHNMODOO_01349 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
NHNMODOO_01350 | 0.0 | phoR | 2.7.13.3 | T | Signal transduction histidine kinase | |
NHNMODOO_01351 | 1.5e-132 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_01352 | 2.2e-73 | lrpC | K | helix_turn_helix ASNC type | ||
NHNMODOO_01353 | 2.6e-169 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
NHNMODOO_01354 | 4.5e-241 | icd | 1.1.1.42 | C | isocitrate | |
NHNMODOO_01355 | 2.1e-205 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
NHNMODOO_01356 | 6.7e-73 | yeaL | S | UPF0756 membrane protein | ||
NHNMODOO_01357 | 9.3e-60 | fxsA | S | COG3030 Protein affecting phage T7 exclusion by the F plasmid | ||
NHNMODOO_01358 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
NHNMODOO_01359 | 2.2e-179 | 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 | |
NHNMODOO_01360 | 7.6e-180 | 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 | |
NHNMODOO_01361 | 6.8e-153 | 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 | |
NHNMODOO_01362 | 5.8e-115 | lutR_1 | K | helix_turn_helix gluconate operon transcriptional repressor | ||
NHNMODOO_01363 | 3.4e-225 | ytsJ | 1.1.1.38 | C | Malate dehydrogenase | |
NHNMODOO_01364 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
NHNMODOO_01365 | 7.2e-53 | ytrH | S | Sporulation protein YtrH | ||
NHNMODOO_01366 | 4.2e-89 | ytrI | ||||
NHNMODOO_01367 | 4.6e-166 | nrnA | 3.1.13.3, 3.1.3.7 | S | COG0618 Exopolyphosphatase-related proteins | |
NHNMODOO_01368 | 4.6e-08 | ytpI | S | YtpI-like protein | ||
NHNMODOO_01369 | 6.7e-240 | ytoI | K | transcriptional regulator containing CBS domains | ||
NHNMODOO_01371 | 1.3e-125 | ytkL | S | Belongs to the UPF0173 family | ||
NHNMODOO_01372 | 4.4e-200 | pepQ | 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
NHNMODOO_01373 | 1e-63 | |||||
NHNMODOO_01374 | 4.7e-137 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_01376 | 7.1e-256 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
NHNMODOO_01377 | 1.4e-231 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
NHNMODOO_01378 | 2.1e-10 | S | EcsC protein family | |||
NHNMODOO_01379 | 3.8e-76 | yhaM | S | 3'-5' exoribonuclease yhaM | ||
NHNMODOO_01380 | 4.6e-64 | yhaM | S | 3'-5' exoribonuclease yhaM | ||
NHNMODOO_01381 | 2.5e-217 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NHNMODOO_01382 | 1.7e-179 | ytxK | 2.1.1.72 | L | DNA methylase | |
NHNMODOO_01383 | 1.4e-84 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
NHNMODOO_01384 | 6.2e-192 | ywoG | EGP | Major facilitator Superfamily | ||
NHNMODOO_01385 | 8.4e-75 | ytfJ | S | Sporulation protein YtfJ | ||
NHNMODOO_01386 | 2.4e-119 | ytfI | S | Protein of unknown function (DUF2953) | ||
NHNMODOO_01387 | 1.3e-96 | yteJ | S | RDD family | ||
NHNMODOO_01388 | 1.9e-178 | sppA | OU | signal peptide peptidase SppA | ||
NHNMODOO_01389 | 8.1e-28 | sspB | S | spore protein | ||
NHNMODOO_01390 | 1.9e-220 | 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 | |
NHNMODOO_01391 | 3.6e-205 | iscS2 | 2.8.1.7 | E | Cysteine desulfurase | |
NHNMODOO_01392 | 1.6e-297 | 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 | ||
NHNMODOO_01393 | 8.5e-142 | hisK | 3.1.3.15 | E | COG1387 Histidinol phosphatase and related hydrolases of the PHP family | |
NHNMODOO_01394 | 2.3e-113 | yttP | K | Transcriptional regulator | ||
NHNMODOO_01395 | 6.4e-15 | L | Transposase | |||
NHNMODOO_01396 | 1.2e-85 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
NHNMODOO_01397 | 3.9e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
NHNMODOO_01398 | 8.4e-232 | 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) | |
NHNMODOO_01399 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | COG0744 Membrane carboxypeptidase (penicillin-binding protein) |
NHNMODOO_01400 | 0.0 | acsA | 6.2.1.1 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
NHNMODOO_01401 | 6.8e-121 | 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 | ||
NHNMODOO_01402 | 5e-111 | acuB | S | Acetoin utilization protein AcuB | ||
NHNMODOO_01403 | 6.8e-231 | acuC | BQ | histone deacetylase | ||
NHNMODOO_01404 | 6.6e-185 | ccpA | K | catabolite control protein A | ||
NHNMODOO_01405 | 1.2e-197 | aroA | 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 | |
NHNMODOO_01406 | 1.1e-15 | XK27_07760 | S | COG4980 Gas vesicle protein | ||
NHNMODOO_01407 | 4.3e-63 | ytxG | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
NHNMODOO_01408 | 1.1e-53 | K | Helix-turn-helix XRE-family like proteins | |||
NHNMODOO_01410 | 4.4e-246 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
NHNMODOO_01411 | 1.6e-142 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_01412 | 5.3e-127 | EP | N-terminal TM domain of oligopeptide transport permease C | |||
NHNMODOO_01413 | 8.3e-142 | oppD | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_01414 | 2.5e-152 | E | Belongs to the ABC transporter superfamily | |||
NHNMODOO_01415 | 5.4e-137 | cpg2 | 3.4.17.11 | E | Peptidase dimerisation domain | |
NHNMODOO_01417 | 8.4e-310 | msbA2 | 3.6.3.44 | V | ABC transporter | |
NHNMODOO_01418 | 3e-162 | XK27_06795 | K | sequence-specific DNA binding | ||
NHNMODOO_01420 | 0.0 | spaB | S | Lantibiotic dehydratase, C terminus | ||
NHNMODOO_01421 | 1.1e-253 | spaC1 | V | Lanthionine synthetase C-like protein | ||
NHNMODOO_01422 | 4.1e-101 | 4.1.1.36, 6.3.2.5 | H | Flavoprotein | ||
NHNMODOO_01423 | 1.1e-122 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
NHNMODOO_01424 | 7.7e-125 | S | ABC-2 family transporter protein | |||
NHNMODOO_01425 | 1.6e-124 | |||||
NHNMODOO_01426 | 7.2e-121 | T | Transcriptional regulatory protein, C terminal | |||
NHNMODOO_01427 | 8.3e-244 | 2.7.13.3 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | ||
NHNMODOO_01428 | 8.8e-36 | comEA | L | Helix-hairpin-helix motif | ||
NHNMODOO_01430 | 1.6e-174 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
NHNMODOO_01432 | 1.2e-180 | rbsR | K | transcriptional | ||
NHNMODOO_01433 | 2.2e-154 | 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 | |
NHNMODOO_01434 | 1.7e-61 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
NHNMODOO_01435 | 4.8e-274 | 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 | |
NHNMODOO_01436 | 6.3e-155 | rbsC | G | Belongs to the binding-protein-dependent transport system permease family | ||
NHNMODOO_01437 | 2.9e-160 | rbsB | G | COG1879 ABC-type sugar transport system, periplasmic component | ||
NHNMODOO_01438 | 9.7e-118 | |||||
NHNMODOO_01441 | 6.9e-75 | |||||
NHNMODOO_01442 | 1.6e-64 | K | Transcriptional regulator | |||
NHNMODOO_01443 | 5.9e-84 | |||||
NHNMODOO_01444 | 1.4e-301 | |||||
NHNMODOO_01445 | 2.5e-53 | |||||
NHNMODOO_01446 | 3.5e-169 | S | Choline/ethanolamine kinase | |||
NHNMODOO_01447 | 1e-87 | ykuD | S | protein conserved in bacteria | ||
NHNMODOO_01448 | 2.5e-209 | S | Erythromycin esterase | |||
NHNMODOO_01449 | 8.6e-166 | NT | chemotaxis protein | |||
NHNMODOO_01450 | 2.7e-132 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHNMODOO_01451 | 1.6e-253 | putP | E | Sodium:solute symporter family | ||
NHNMODOO_01452 | 2.7e-177 | 3.5.3.6 | E | Amidinotransferase | ||
NHNMODOO_01453 | 8.8e-181 | K | Transcriptional regulator | |||
NHNMODOO_01454 | 1e-148 | V | ABC transporter | |||
NHNMODOO_01455 | 3.6e-101 | S | ABC-2 family transporter protein | |||
NHNMODOO_01456 | 9.2e-147 | K | Transcriptional regulator | |||
NHNMODOO_01457 | 1.6e-149 | yxxF | EG | EamA-like transporter family | ||
NHNMODOO_01458 | 2.8e-182 | lacR | K | Transcriptional regulator | ||
NHNMODOO_01459 | 6.1e-238 | cycB | G | COG2182 Maltose-binding periplasmic proteins domains | ||
NHNMODOO_01460 | 5.8e-244 | malC | P | COG1175 ABC-type sugar transport systems, permease components | ||
NHNMODOO_01461 | 1e-148 | ganQ | P | transport | ||
NHNMODOO_01462 | 1.6e-235 | ganB | 3.2.1.89 | G | arabinogalactan | |
NHNMODOO_01463 | 0.0 | lacA | 3.2.1.23 | G | beta-galactosidase | |
NHNMODOO_01464 | 3.1e-129 | S | response regulator aspartate phosphatase | |||
NHNMODOO_01466 | 2.7e-91 | S | DinB superfamily | |||
NHNMODOO_01467 | 6.4e-204 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
NHNMODOO_01468 | 1.5e-197 | 6.3.5.5 | S | ATP-grasp domain | ||
NHNMODOO_01469 | 1e-64 | K | helix_turn_helix, mercury resistance | |||
NHNMODOO_01470 | 1.4e-54 | S | Domain of unknown function (DUF4260) | |||
NHNMODOO_01471 | 1.5e-155 | ksgA | 2.1.1.182, 2.1.1.184 | J | Ribosomal RNA adenine dimethylases | |
NHNMODOO_01473 | 1.8e-101 | 3.5.1.124 | S | DJ-1/PfpI family | ||
NHNMODOO_01475 | 2.4e-153 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
NHNMODOO_01476 | 8.9e-205 | ulaA | 2.7.1.194 | S | PTS system ascorbate-specific transporter subunit IIC | |
NHNMODOO_01477 | 3.5e-43 | ptxB | 2.7.1.194, 2.7.1.200 | G | COG3414 Phosphotransferase system, galactitol-specific IIB component | |
NHNMODOO_01478 | 3e-171 | pfkA | 2.7.1.11, 2.7.1.90 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
NHNMODOO_01479 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | ||
NHNMODOO_01480 | 8e-63 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
NHNMODOO_01481 | 1.7e-257 | S | Chlorophyllase enzyme | |||
NHNMODOO_01482 | 3.5e-132 | bceA | V | ABC transporter, ATP-binding protein | ||
NHNMODOO_01483 | 0.0 | bceB | V | ABC transporter (permease) | ||
NHNMODOO_01484 | 2.5e-187 | gerKC | S | Spore germination B3/ GerAC like, C-terminal | ||
NHNMODOO_01485 | 1.6e-178 | gerKB | E | Spore germination protein | ||
NHNMODOO_01486 | 2.5e-190 | gerKA | EG | Spore germination protein | ||
NHNMODOO_01487 | 5.2e-08 | gerKA | EG | Spore germination protein | ||
NHNMODOO_01488 | 1.1e-151 | |||||
NHNMODOO_01489 | 7.5e-177 | ectD | 1.14.11.55 | Q | Phytanoyl-CoA dioxygenase (PhyH) | |
NHNMODOO_01490 | 5.1e-179 | G | COG1593 TRAP-type C4-dicarboxylate transport system, large permease component | |||
NHNMODOO_01491 | 2.7e-45 | G | Tripartite ATP-independent periplasmic transporters, DctQ component | |||
NHNMODOO_01492 | 3.6e-127 | G | Bacterial extracellular solute-binding protein, family 7 | |||
NHNMODOO_01493 | 4.2e-80 | kipR | K | Transcriptional regulator | ||
NHNMODOO_01494 | 7.5e-291 | ybbB | K | COG2207 AraC-type DNA-binding domain-containing proteins | ||
NHNMODOO_01495 | 5.3e-173 | feuA | P | Iron-uptake system-binding protein | ||
NHNMODOO_01496 | 9.8e-178 | feuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_01497 | 4.5e-183 | feuC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_01498 | 3.1e-150 | besA | S | Putative esterase | ||
NHNMODOO_01499 | 1.6e-241 | amaB | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
NHNMODOO_01500 | 9.6e-121 | tcpP | 2.7.11.1 | KT | Forkhead associated domain | |
NHNMODOO_01501 | 4.3e-155 | 3.5.2.6 | V | beta-lactamase | ||
NHNMODOO_01502 | 1.5e-131 | S | Nucleotidyltransferase domain | |||
NHNMODOO_01503 | 3e-227 | hemAT | NT | chemotaxis protein | ||
NHNMODOO_01504 | 3.8e-182 | K | helix_turn _helix lactose operon repressor | |||
NHNMODOO_01505 | 6.8e-153 | dkgB | S | Aldo/keto reductase family | ||
NHNMODOO_01506 | 3.2e-170 | fhuD | P | ABC transporter | ||
NHNMODOO_01507 | 8.6e-142 | K | Helix-turn-helix domain | |||
NHNMODOO_01508 | 6.3e-55 | S | Ketosteroid isomerase-related protein | |||
NHNMODOO_01509 | 1e-182 | MA20_22185 | K | Transcriptional regulator, LacI family | ||
NHNMODOO_01510 | 1.3e-179 | S | Oxidoreductase family, C-terminal alpha/beta domain | |||
NHNMODOO_01511 | 2e-222 | cycB_1 | G | Bacterial extracellular solute-binding protein | ||
NHNMODOO_01512 | 2.7e-166 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_01513 | 5.9e-141 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_01514 | 2.3e-17 | G | Xylose isomerase | |||
NHNMODOO_01515 | 2.7e-165 | G | Xylose isomerase | |||
NHNMODOO_01516 | 2.1e-155 | S | Membrane transport protein | |||
NHNMODOO_01518 | 1.8e-108 | K | response regulator | |||
NHNMODOO_01519 | 5.8e-61 | |||||
NHNMODOO_01520 | 1.5e-22 | |||||
NHNMODOO_01521 | 1.1e-86 | M1-1022 | 1.8.5.2 | S | DoxX | |
NHNMODOO_01522 | 2.9e-276 | murE | 6.3.2.13 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
NHNMODOO_01523 | 5.1e-148 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
NHNMODOO_01524 | 8.9e-99 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_01525 | 3.1e-111 | yqeB | ||||
NHNMODOO_01526 | 3.6e-52 | K | PadR family transcriptional regulator | |||
NHNMODOO_01527 | 3.4e-71 | V | (ABC) transporter | |||
NHNMODOO_01528 | 4.5e-163 | V | VanW like protein | |||
NHNMODOO_01530 | 1.1e-123 | yoqW | S | Belongs to the SOS response-associated peptidase family | ||
NHNMODOO_01531 | 1e-176 | isp | O | Belongs to the peptidase S8 family | ||
NHNMODOO_01532 | 4.2e-162 | yjlA | EG | Putative multidrug resistance efflux transporter | ||
NHNMODOO_01533 | 4.9e-255 | |||||
NHNMODOO_01534 | 9e-196 | sstT | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NHNMODOO_01535 | 0.0 | pepF | E | oligoendopeptidase | ||
NHNMODOO_01536 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
NHNMODOO_01537 | 2.4e-78 | cwlM | 3.5.1.28 | M | COG3103 SH3 domain protein | |
NHNMODOO_01538 | 2.6e-46 | |||||
NHNMODOO_01539 | 8.3e-282 | K | Mga helix-turn-helix domain | |||
NHNMODOO_01542 | 1e-62 | S | YolD-like protein | |||
NHNMODOO_01543 | 8e-219 | P | Protein of unknown function (DUF418) | |||
NHNMODOO_01544 | 1.9e-217 | GK | ROK family | |||
NHNMODOO_01545 | 1.3e-240 | cycB_2 | G | Bacterial extracellular solute-binding protein | ||
NHNMODOO_01546 | 3.4e-169 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_01547 | 1.3e-145 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_01548 | 3.1e-184 | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
NHNMODOO_01549 | 3.1e-184 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NHNMODOO_01550 | 5.6e-147 | 5.1.3.22, 5.3.1.5 | G | Xylose isomerase-like TIM barrel | ||
NHNMODOO_01551 | 4e-175 | S | Alpha/beta hydrolase family | |||
NHNMODOO_01552 | 7.8e-149 | K | LysR substrate binding domain | |||
NHNMODOO_01553 | 3.5e-119 | IQ | Catalyzes the formation of acetoacetate from 3-hydroxybutyrate | |||
NHNMODOO_01554 | 1.6e-214 | EGP | Major facilitator Superfamily | |||
NHNMODOO_01555 | 6.6e-206 | 2.3.1.157, 2.7.7.23 | JM | Bacterial transferase hexapeptide (six repeats) | ||
NHNMODOO_01556 | 1.3e-125 | K | transcriptional | |||
NHNMODOO_01557 | 1.7e-139 | S | carbohydrate derivative metabolic process | |||
NHNMODOO_01558 | 1.9e-84 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_01559 | 2.4e-240 | ykoH | T | Histidine kinase | ||
NHNMODOO_01560 | 4.4e-116 | ykoI | S | Peptidase propeptide and YPEB domain | ||
NHNMODOO_01561 | 9.3e-82 | ykoJ | S | Peptidase propeptide and YPEB domain | ||
NHNMODOO_01562 | 8.8e-122 | glxK | 2.7.1.165 | G | Glycerate kinase family | |
NHNMODOO_01563 | 3.9e-108 | P | Sodium:sulfate symporter transmembrane region | |||
NHNMODOO_01565 | 4.3e-239 | I | radical SAM domain protein | |||
NHNMODOO_01566 | 6.4e-284 | H | Involved in the biosynthesis of porphyrin-containing compound | |||
NHNMODOO_01567 | 1.1e-10 | |||||
NHNMODOO_01568 | 5.4e-133 | yafE | Q | methyltransferase | ||
NHNMODOO_01569 | 1.8e-14 | 1.2.7.12 | S | Uncharacterised protein family UPF0066 | ||
NHNMODOO_01570 | 4.4e-88 | 1.2.7.12 | S | Uncharacterised protein family UPF0066 | ||
NHNMODOO_01571 | 4e-221 | EGP | Major facilitator Superfamily | |||
NHNMODOO_01572 | 2.5e-95 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |||
NHNMODOO_01573 | 1.9e-167 | wbpP | 5.1.3.2, 5.1.3.7 | M | GDP-mannose 4,6 dehydratase | |
NHNMODOO_01574 | 8.3e-126 | M | Glycosyl transferases group 1 | |||
NHNMODOO_01575 | 9.2e-102 | |||||
NHNMODOO_01576 | 2.4e-103 | GT2,GT4 | M | transferase activity, transferring glycosyl groups | ||
NHNMODOO_01577 | 3.3e-121 | M | transferase activity, transferring glycosyl groups | |||
NHNMODOO_01578 | 1.3e-112 | M | Glycosyl transferase family 2 | |||
NHNMODOO_01579 | 1.6e-236 | 1.1.1.136 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | ||
NHNMODOO_01580 | 1.6e-198 | M | Glycosyltransferase like family 2 | |||
NHNMODOO_01581 | 1.1e-35 | S | Protein of unknown function (DUF2642) | |||
NHNMODOO_01582 | 9.3e-24 | |||||
NHNMODOO_01583 | 8.5e-240 | ftsH2 | 3.4.21.53 | O | AAA domain (dynein-related subfamily) | |
NHNMODOO_01584 | 2.9e-92 | ycsK | E | anatomical structure formation involved in morphogenesis | ||
NHNMODOO_01585 | 6.1e-121 | K | helix_turn_helix isocitrate lyase regulation | |||
NHNMODOO_01586 | 4.4e-164 | kdgK | 2.7.1.45 | G | COG0524 Sugar kinases, ribokinase family | |
NHNMODOO_01587 | 1.1e-102 | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | ||
NHNMODOO_01588 | 9.4e-32 | dgoD | 4.2.1.6 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
NHNMODOO_01589 | 7.4e-177 | dgoD | 4.2.1.6 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
NHNMODOO_01590 | 2.3e-195 | gntU | EG | COG2610 H gluconate symporter and related permeases | ||
NHNMODOO_01591 | 3e-153 | S | Metallo-beta-lactamase superfamily | |||
NHNMODOO_01592 | 1.8e-86 | S | Predicted membrane protein (DUF2243) | |||
NHNMODOO_01593 | 9.7e-120 | S | Cytochrome c oxidase caa3 assembly factor (Caa3_CtaG) | |||
NHNMODOO_01594 | 1.3e-230 | T | COG0642 Signal transduction histidine kinase | |||
NHNMODOO_01595 | 6.4e-125 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_01596 | 7.8e-167 | 4.2.1.103 | K | DJ-1/PfpI family | ||
NHNMODOO_01597 | 4.6e-109 | S | Predicted membrane protein (DUF2306) | |||
NHNMODOO_01598 | 1.5e-200 | dadA | 1.4.5.1 | E | COG0665 Glycine D-amino acid oxidases (deaminating) | |
NHNMODOO_01599 | 9.9e-66 | S | VanZ like family | |||
NHNMODOO_01600 | 3.7e-108 | wrbA | 1.6.5.2 | S | Belongs to the WrbA family | |
NHNMODOO_01602 | 6e-82 | 2.3.1.128 | K | Acetyltransferase (GNAT) family | ||
NHNMODOO_01603 | 9.1e-128 | 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 | |
NHNMODOO_01604 | 0.0 | V | SNF2 family N-terminal domain | |||
NHNMODOO_01605 | 7.4e-09 | S | Domain of unknown function (DUF5082) | |||
NHNMODOO_01606 | 3.3e-08 | S | Family of unknown function (DUF5344) | |||
NHNMODOO_01607 | 1.9e-244 | S | LXG domain of WXG superfamily | |||
NHNMODOO_01608 | 7.4e-88 | |||||
NHNMODOO_01609 | 1.1e-149 | |||||
NHNMODOO_01610 | 3.2e-281 | E | Sodium:solute symporter family | |||
NHNMODOO_01611 | 3.5e-23 | |||||
NHNMODOO_01612 | 3.7e-224 | 2.8.3.16, 2.8.3.20 | C | acyl-CoA transferases carnitine dehydratase | ||
NHNMODOO_01613 | 2.7e-112 | K | FCD domain | |||
NHNMODOO_01614 | 9.8e-158 | 4.1.3.4, 4.1.3.46 | E | Hydroxymethylglutaryl-CoA lyase | ||
NHNMODOO_01615 | 1.5e-102 | gntR | K | RpiR family transcriptional regulator | ||
NHNMODOO_01616 | 2.5e-181 | EG | COG2610 H gluconate symporter and related permeases | |||
NHNMODOO_01617 | 9.1e-127 | garR | 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
NHNMODOO_01618 | 8.5e-188 | S | Putative nucleotide-binding of sugar-metabolising enzyme | |||
NHNMODOO_01619 | 3.7e-224 | abgB | 3.5.1.47 | S | amidohydrolase | |
NHNMODOO_01620 | 1.2e-157 | metQ | M | Belongs to the nlpA lipoprotein family | ||
NHNMODOO_01621 | 3.3e-113 | P | COG2011 ABC-type metal ion transport system, permease component | |||
NHNMODOO_01622 | 3.3e-189 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NHNMODOO_01623 | 2.8e-168 | K | helix_turn_helix, arabinose operon control protein | |||
NHNMODOO_01625 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
NHNMODOO_01626 | 0.0 | aguA | 3.2.1.139 | G | Belongs to the glycosyl hydrolase 67 family | |
NHNMODOO_01627 | 4.3e-175 | lplB | G | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_01628 | 1.3e-154 | lplC | G | COG0395 ABC-type sugar transport system, permease component | ||
NHNMODOO_01629 | 1.4e-308 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_01630 | 2.2e-112 | S | Protein of unknown function, DUF624 | |||
NHNMODOO_01631 | 5.6e-195 | gldA | 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
NHNMODOO_01632 | 6.5e-23 | D | nuclear chromosome segregation | |||
NHNMODOO_01634 | 3.2e-217 | hutI | Q | COG1228 Imidazolonepropionase and related amidohydrolases | ||
NHNMODOO_01635 | 3.4e-197 | Q | COG1228 Imidazolonepropionase and related amidohydrolases | |||
NHNMODOO_01636 | 4.4e-302 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | |||
NHNMODOO_01637 | 6e-169 | EP | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | |||
NHNMODOO_01638 | 1e-151 | dppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHNMODOO_01639 | 5.5e-189 | oppD | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_01640 | 8.3e-190 | ddpF | E | Belongs to the ABC transporter superfamily | ||
NHNMODOO_01641 | 1.8e-173 | S | Protein of unknown function (DUF1177) | |||
NHNMODOO_01642 | 8.1e-243 | 3.5.1.18 | E | Acetylornithine deacetylase | ||
NHNMODOO_01643 | 3.1e-136 | K | Transcriptional regulator | |||
NHNMODOO_01644 | 1.3e-259 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
NHNMODOO_01645 | 1.4e-278 | xylB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 5.3.1.14 | G | xylulose kinase | |
NHNMODOO_01646 | 1.9e-197 | galM | 2.7.1.6, 5.1.3.3 | G | Converts alpha-aldose to the beta-anomer | |
NHNMODOO_01647 | 2.3e-215 | xylR | GK | ROK family | ||
NHNMODOO_01648 | 8.2e-122 | MA20_14010 | S | Trehalose utilisation | ||
NHNMODOO_01649 | 5.7e-222 | yrbE | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
NHNMODOO_01650 | 6.4e-274 | KT | PucR C-terminal helix-turn-helix domain | |||
NHNMODOO_01651 | 1.3e-106 | hyuE | 5.1.99.3 | E | Asp/Glu/Hydantoin racemase | |
NHNMODOO_01652 | 1.4e-284 | S | OPT oligopeptide transporter protein | |||
NHNMODOO_01653 | 7.6e-186 | S | Protein of unknown function (DUF917) | |||
NHNMODOO_01654 | 3.8e-160 | S | Protein of unknown function (DUF1177) | |||
NHNMODOO_01655 | 9.2e-113 | aroM | E | AroM protein | ||
NHNMODOO_01656 | 5.7e-172 | E | Thermophilic metalloprotease (M29) | |||
NHNMODOO_01657 | 3.7e-208 | EGP | Major facilitator Superfamily | |||
NHNMODOO_01658 | 3.1e-30 | dmpI | 5.3.2.6 | S | Tautomerase enzyme | |
NHNMODOO_01659 | 2.4e-164 | citS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
NHNMODOO_01660 | 7.3e-68 | T | response regulator | |||
NHNMODOO_01661 | 3.9e-145 | tctC | S | Tripartite tricarboxylate transporter family receptor | ||
NHNMODOO_01662 | 1.5e-48 | S | Tripartite tricarboxylate transporter TctB family | |||
NHNMODOO_01663 | 2.3e-212 | S | Tripartite tricarboxylate transporter TctA family | |||
NHNMODOO_01664 | 1.6e-200 | chrA | P | chromate transporter, chromate ion transporter | ||
NHNMODOO_01665 | 6.7e-44 | M1-594 | S | Thiamine-binding protein | ||
NHNMODOO_01666 | 0.0 | yngI | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
NHNMODOO_01667 | 5e-238 | |||||
NHNMODOO_01669 | 1.9e-229 | gntT | EG | gluconate transmembrane transporter activity | ||
NHNMODOO_01670 | 1.1e-140 | 2.7.1.196, 2.7.1.205 | K | sequence-specific DNA binding | ||
NHNMODOO_01671 | 3.9e-119 | S | protein conserved in bacteria | |||
NHNMODOO_01673 | 2.9e-93 | ogt | 1.17.99.6, 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
NHNMODOO_01674 | 3.2e-217 | 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) | |
NHNMODOO_01675 | 6e-97 | S | B3/4 domain | |||
NHNMODOO_01676 | 5e-81 | dps | P | Belongs to the Dps family | ||
NHNMODOO_01677 | 2.1e-196 | yhfE | 3.2.1.4 | GH5,GH9 | G | peptidase M42 |
NHNMODOO_01678 | 1.2e-105 | |||||
NHNMODOO_01679 | 5.9e-118 | V | ATPases associated with a variety of cellular activities | |||
NHNMODOO_01680 | 1.8e-60 | yhcF | K | Transcriptional regulator | ||
NHNMODOO_01681 | 2e-103 | S | ABC-2 family transporter protein | |||
NHNMODOO_01682 | 4.5e-166 | yhcH | V | ABC transporter, ATP-binding protein | ||
NHNMODOO_01683 | 3.8e-90 | mepB | S | MepB protein | ||
NHNMODOO_01684 | 7e-150 | rhaR2 | K | helix_turn_helix, arabinose operon control protein | ||
NHNMODOO_01685 | 1.7e-265 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
NHNMODOO_01686 | 0.0 | bglX | 3.2.1.21 | GH3 | G | Belongs to the glycosyl hydrolase 3 family |
NHNMODOO_01687 | 1e-254 | scrA5 | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NHNMODOO_01688 | 6.5e-257 | 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 | |
NHNMODOO_01689 | 9.3e-89 | |||||
NHNMODOO_01690 | 4.5e-286 | cstA | T | Carbon starvation protein | ||
NHNMODOO_01691 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
NHNMODOO_01692 | 8.5e-182 | yccF | K | SEC-C motif | ||
NHNMODOO_01693 | 4.9e-54 | S | Regulatory protein YrvL | |||
NHNMODOO_01694 | 0.0 | 3.1.3.5, 3.1.3.6, 3.1.4.16, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | ||
NHNMODOO_01695 | 1.2e-269 | MA20_17540 | P | secondary active sulfate transmembrane transporter activity | ||
NHNMODOO_01696 | 8.8e-102 | 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 | |
NHNMODOO_01697 | 8.4e-48 | |||||
NHNMODOO_01698 | 1.6e-94 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_01699 | 6e-126 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NHNMODOO_01700 | 5.1e-142 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NHNMODOO_01701 | 3.1e-57 | yxjI | S | LURP-one-related | ||
NHNMODOO_01702 | 2.1e-143 | gspA | M | Glycosyl transferase family 8 | ||
NHNMODOO_01703 | 1.6e-189 | V | ABC-2 type transporter | |||
NHNMODOO_01704 | 5.5e-215 | V | ABC-2 family transporter protein | |||
NHNMODOO_01705 | 2e-169 | V | COG1131 ABC-type multidrug transport system, ATPase component | |||
NHNMODOO_01706 | 9.5e-107 | KT | LuxR family transcriptional regulator | |||
NHNMODOO_01707 | 6.3e-194 | yxjM | T | Signal transduction histidine kinase | ||
NHNMODOO_01708 | 1.3e-91 | 5.4.2.11 | G | Phosphoglycerate mutase family | ||
NHNMODOO_01709 | 1.1e-114 | S | AAA domain | |||
NHNMODOO_01710 | 7.9e-126 | L | DNA alkylation repair enzyme | |||
NHNMODOO_01711 | 3.5e-217 | 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) | |
NHNMODOO_01712 | 6.4e-28 | T | Histidine kinase | |||
NHNMODOO_01713 | 2e-146 | S | Alpha beta hydrolase | |||
NHNMODOO_01714 | 1.6e-68 | K | Helix-turn-helix domain | |||
NHNMODOO_01715 | 3.3e-11 | |||||
NHNMODOO_01716 | 6.7e-35 | 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) | |
NHNMODOO_01717 | 7e-143 | K | Helix-turn-helix XRE-family like proteins | |||
NHNMODOO_01718 | 4.9e-60 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_01719 | 5.4e-54 | K | Acetyltransferase (GNAT) domain | |||
NHNMODOO_01720 | 3.4e-58 | ydzF | K | HxlR-like helix-turn-helix | ||
NHNMODOO_01721 | 3.6e-141 | rocF | 3.5.3.1, 3.5.3.11 | E | Arginase agmatinase formimionoglutamate hydrolase, arginase family | |
NHNMODOO_01722 | 3.2e-114 | K | helix_turn_helix, mercury resistance | |||
NHNMODOO_01723 | 5.1e-133 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
NHNMODOO_01724 | 5e-110 | V | ABC-2 type transporter | |||
NHNMODOO_01725 | 2.4e-119 | ubiG | S | 3-demethylubiquinone-9 3-methyltransferase | ||
NHNMODOO_01726 | 3.4e-108 | mrsE3 | S | ABC-2 family transporter protein | ||
NHNMODOO_01727 | 1.2e-99 | S | ABC-2 family transporter protein | |||
NHNMODOO_01728 | 4e-117 | bcrA | V | Bacitracin ABC transporter ATP-binding protein | ||
NHNMODOO_01729 | 5.7e-136 | T | PhoQ Sensor | |||
NHNMODOO_01730 | 6.6e-117 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_01731 | 1.1e-167 | G | domain, Protein | |||
NHNMODOO_01732 | 5.2e-93 | K | helix_turn_helix, arabinose operon control protein | |||
NHNMODOO_01733 | 2.5e-56 | ccpA | K | helix_turn _helix lactose operon repressor | ||
NHNMODOO_01734 | 2.7e-192 | scrB | 3.2.1.26 | GH32 | G | invertase |
NHNMODOO_01735 | 1.2e-178 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
NHNMODOO_01736 | 2.8e-69 | yhfA | S | Haloacid dehalogenase-like hydrolase | ||
NHNMODOO_01737 | 5.9e-129 | 4.1.2.14 | S | KDGP aldolase | ||
NHNMODOO_01738 | 2.2e-199 | selA | 2.9.1.1, 4.3.1.29 | E | L-seryl-tRNA selenium transferase | |
NHNMODOO_01739 | 1.9e-113 | S | Domain of unknown function (DUF4310) | |||
NHNMODOO_01740 | 1.4e-139 | S | Domain of unknown function (DUF4311) | |||
NHNMODOO_01741 | 1e-57 | S | Domain of unknown function (DUF4312) | |||
NHNMODOO_01742 | 3.2e-59 | S | Glycine-rich SFCGS | |||
NHNMODOO_01743 | 3.3e-40 | S | PRD domain | |||
NHNMODOO_01744 | 2.4e-209 | dho | 3.5.2.3 | S | amidohydrolase | |
NHNMODOO_01745 | 0.0 | K | Mga helix-turn-helix domain | |||
NHNMODOO_01746 | 0.0 | G | alpha-L-rhamnosidase | |||
NHNMODOO_01747 | 0.0 | pbg | 3.2.1.23 | G | beta-galactosidase | |
NHNMODOO_01748 | 1.4e-158 | K | AraC-like ligand binding domain | |||
NHNMODOO_01749 | 1.5e-148 | cypA | Q | Cytochrome P450 | ||
NHNMODOO_01750 | 5.2e-130 | EGP | PFAM major facilitator superfamily MFS_1 | |||
NHNMODOO_01751 | 1.2e-56 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_01752 | 1.8e-38 | 2.3.1.60 | K | FR47-like protein | ||
NHNMODOO_01753 | 2.4e-124 | S | Nucleotidyltransferase domain | |||
NHNMODOO_01754 | 5.8e-131 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHNMODOO_01755 | 2.3e-43 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
NHNMODOO_01756 | 8.9e-251 | pbpE | V | Beta-lactamase | ||
NHNMODOO_01757 | 3.8e-129 | K | helix_turn_helix, mercury resistance | |||
NHNMODOO_01758 | 2.4e-87 | 2.7.1.48, 3.1.3.18 | F | uridine kinase | ||
NHNMODOO_01759 | 2.1e-33 | ble | E | lactoylglutathione lyase activity | ||
NHNMODOO_01761 | 1.7e-19 | M | Host cell surface-exposed lipoprotein | |||
NHNMODOO_01762 | 2e-101 | K | Bacterial transcriptional repressor C-terminal | |||
NHNMODOO_01763 | 1.9e-242 | npr | 1.11.1.1 | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | |
NHNMODOO_01764 | 2e-133 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHNMODOO_01765 | 2.8e-154 | K | DNA-binding protein | |||
NHNMODOO_01767 | 3.9e-231 | eph | 3.3.2.9 | S | Epoxide hydrolase | |
NHNMODOO_01768 | 9.8e-169 | S | thiolester hydrolase activity | |||
NHNMODOO_01769 | 1.1e-78 | yvmB1 | K | helix_turn_helix multiple antibiotic resistance protein | ||
NHNMODOO_01770 | 2.2e-45 | J | oxidation-reduction process | |||
NHNMODOO_01771 | 4.9e-279 | yhjG | CH | FAD binding domain | ||
NHNMODOO_01772 | 1.5e-198 | ybcL | EGP | Major facilitator Superfamily | ||
NHNMODOO_01773 | 2.8e-45 | ybzH | K | ArsR family transcriptional regulator | ||
NHNMODOO_01774 | 3.4e-93 | yxcB | K | Transcriptional regulator C-terminal region | ||
NHNMODOO_01775 | 1e-134 | M1-493 | S | SnoaL-like domain | ||
NHNMODOO_01776 | 1.2e-44 | S | Protein of unknown function (DUF3533) | |||
NHNMODOO_01777 | 5.4e-49 | S | Protein of unknown function (DUF3533) | |||
NHNMODOO_01778 | 1.9e-13 | S | Protein of unknown function (DUF3533) | |||
NHNMODOO_01780 | 0.0 | yobO | M | Pectate lyase superfamily protein | ||
NHNMODOO_01788 | 1.5e-07 | |||||
NHNMODOO_01792 | 1.4e-12 | exeA | ||||
NHNMODOO_01793 | 1.3e-22 | EGP | Major facilitator Superfamily | |||
NHNMODOO_01794 | 7.3e-77 | |||||
NHNMODOO_01795 | 1.3e-55 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
NHNMODOO_01796 | 9.2e-240 | S | protein conserved in bacteria | |||
NHNMODOO_01797 | 2.7e-241 | gabT | 2.6.1.19 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
NHNMODOO_01799 | 2.4e-107 | lip | 3.1.1.3 | S | acetyltransferases and hydrolases with the alpha beta hydrolase fold | |
NHNMODOO_01802 | 2.7e-120 | S | Glycosyltransferase like family | |||
NHNMODOO_01803 | 0.0 | S | Sugar transport-related sRNA regulator N-term | |||
NHNMODOO_01804 | 5.5e-215 | EGP | Major facilitator Superfamily | |||
NHNMODOO_01805 | 0.0 | fadB | 1.1.1.35, 4.2.1.17, 5.1.2.3 | I | 3-hydroxyacyl-CoA dehydrogenase | |
NHNMODOO_01806 | 6.5e-210 | fadA | 2.3.1.16 | I | Belongs to the thiolase family | |
NHNMODOO_01807 | 0.0 | fadE | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
NHNMODOO_01808 | 1.1e-62 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
NHNMODOO_01809 | 1.2e-64 | gcvH | E | Is also involved in protein lipoylation via its role as an octanoyl lipoyl carrier protein intermediate | ||
NHNMODOO_01810 | 8.3e-185 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NHNMODOO_01811 | 1.4e-113 | metI | P | COG2011 ABC-type metal ion transport system, permease component | ||
NHNMODOO_01812 | 1.8e-153 | metQ | P | Belongs to the NlpA lipoprotein family | ||
NHNMODOO_01813 | 6.1e-94 | S | Cobalamin adenosyltransferase | |||
NHNMODOO_01814 | 7.7e-166 | btuF | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
NHNMODOO_01815 | 1.7e-60 | yurZ | 2.3.1.12, 4.1.1.44 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | |
NHNMODOO_01816 | 1.6e-143 | sufC | O | COG0396 ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
NHNMODOO_01817 | 1e-243 | O | assembly protein SufD | |||
NHNMODOO_01818 | 1.4e-234 | 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 | |
NHNMODOO_01819 | 5e-78 | nifU | C | COG0822 NifU homolog involved in Fe-S cluster formation | ||
NHNMODOO_01820 | 7.4e-269 | sufB | O | FeS cluster assembly | ||
NHNMODOO_01821 | 1e-240 | aceA | 4.1.3.1 | C | Isocitrate lyase | |
NHNMODOO_01822 | 1.1e-15 | S | YhfH-like protein | |||
NHNMODOO_01823 | 3e-51 | licT | K | transcriptional antiterminator | ||
NHNMODOO_01824 | 1e-86 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHNMODOO_01825 | 1.2e-137 | bioC_2 | Q | Methyltransferase domain | ||
NHNMODOO_01826 | 1.4e-184 | gpr | C | Aldo/keto reductase family | ||
NHNMODOO_01827 | 1.4e-137 | K | AraC family transcriptional regulator | |||
NHNMODOO_01828 | 3.2e-170 | P | Periplasmic binding protein | |||
NHNMODOO_01829 | 2.2e-167 | kka | S | Phosphotransferase enzyme family | ||
NHNMODOO_01830 | 2.7e-51 | H | RibD C-terminal domain | |||
NHNMODOO_01831 | 1.2e-37 | S | Pathogenicity locus | |||
NHNMODOO_01832 | 7.5e-40 | S | Family of unknown function (DUF5344) | |||
NHNMODOO_01833 | 4.1e-161 | S | LXG domain of WXG superfamily | |||
NHNMODOO_01834 | 6.8e-43 | |||||
NHNMODOO_01835 | 9.1e-40 | |||||
NHNMODOO_01836 | 1.1e-40 | |||||
NHNMODOO_01837 | 2.2e-07 | |||||
NHNMODOO_01838 | 4e-147 | |||||
NHNMODOO_01839 | 1.1e-48 | |||||
NHNMODOO_01840 | 1e-63 | S | Domain of unknown function (DUF5082) | |||
NHNMODOO_01841 | 1.1e-163 | yunF | S | Protein of unknown function DUF72 | ||
NHNMODOO_01842 | 6.7e-137 | yunE | S | membrane transporter protein | ||
NHNMODOO_01843 | 1.4e-256 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
NHNMODOO_01844 | 9.9e-49 | yunC | S | Domain of unknown function (DUF1805) | ||
NHNMODOO_01845 | 6.2e-156 | 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 | |
NHNMODOO_01846 | 9e-89 | 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 | |
NHNMODOO_01847 | 1.5e-138 | yunB | S | Sporulation protein YunB (Spo_YunB) | ||
NHNMODOO_01848 | 9.2e-277 | nhaC | C | Na+/H+ antiporter family | ||
NHNMODOO_01849 | 5.3e-200 | lytH | M | Peptidase, M23 | ||
NHNMODOO_01850 | 3.5e-174 | 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 | |
NHNMODOO_01851 | 1.9e-92 | yutC | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
NHNMODOO_01852 | 3.7e-50 | yutD | S | protein conserved in bacteria | ||
NHNMODOO_01853 | 1.3e-43 | |||||
NHNMODOO_01854 | 2.2e-73 | yutE | S | Protein of unknown function DUF86 | ||
NHNMODOO_01855 | 1.2e-129 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
NHNMODOO_01856 | 4.6e-85 | pgpA | 3.1.3.27 | I | COG1267 Phosphatidylglycerophosphatase A and related proteins | |
NHNMODOO_01857 | 2e-202 | yutH | S | Spore coat protein | ||
NHNMODOO_01858 | 6.7e-238 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
NHNMODOO_01859 | 1.5e-197 | thrC | 4.2.3.1 | E | Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine | |
NHNMODOO_01860 | 2.2e-157 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
NHNMODOO_01861 | 9.7e-36 | yutI | O | COG0694 Thioredoxin-like proteins and domains | ||
NHNMODOO_01862 | 2.8e-51 | yuzD | S | protein conserved in bacteria | ||
NHNMODOO_01863 | 0.0 | yutJ | 1.6.99.3 | C | NADH dehydrogenase | |
NHNMODOO_01864 | 2.2e-40 | yuzB | S | Belongs to the UPF0349 family | ||
NHNMODOO_01865 | 1.4e-42 | |||||
NHNMODOO_01866 | 2.9e-159 | 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 | |
NHNMODOO_01867 | 6.7e-209 | mqnE | 1.21.98.1, 2.5.1.120, 2.5.1.77 | H | Radical SAM enzyme that catalyzes the addition of the adenosyl radical to the double bond of 3- (1- carboxyvinyl)oxy benzoate, leading to aminodeoxyfutalosine (AFL), a key intermediate in the formation of menaquinone (MK, vitamin K2) from chorismate | |
NHNMODOO_01869 | 2.9e-60 | erpA | S | Belongs to the HesB IscA family | ||
NHNMODOO_01870 | 2.2e-109 | yecS | P | COG0765 ABC-type amino acid transport system, permease component | ||
NHNMODOO_01871 | 3.6e-154 | yckB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NHNMODOO_01872 | 4.9e-307 | mtlA | 2.7.1.197 | G | COG2213 Phosphotransferase system, mannitol-specific IIBC component | |
NHNMODOO_01873 | 0.0 | mtlR | K | transcriptional regulator, MtlR | ||
NHNMODOO_01874 | 3.7e-70 | mtlF | 2.7.1.197 | G | COG4668 Mannitol fructose-specific phosphotransferase system, IIA domain | |
NHNMODOO_01875 | 6e-205 | mtlD | 1.1.1.17 | G | COG0246 Mannitol-1-phosphate altronate dehydrogenases | |
NHNMODOO_01876 | 2.1e-185 | ycgT | 1.18.1.2, 1.19.1.1 | C | reductase | |
NHNMODOO_01877 | 2.9e-229 | yumB | 1.6.99.3 | C | NADH dehydrogenase | |
NHNMODOO_01878 | 2.2e-46 | yuiB | S | Putative membrane protein | ||
NHNMODOO_01879 | 1.7e-108 | yuiC | S | protein conserved in bacteria | ||
NHNMODOO_01880 | 1.5e-77 | yuiD | S | protein conserved in bacteria | ||
NHNMODOO_01881 | 5.6e-275 | 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 | |
NHNMODOO_01882 | 2.7e-45 | |||||
NHNMODOO_01883 | 5.6e-226 | S | antiporter | |||
NHNMODOO_01884 | 1.9e-40 | 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 | ||
NHNMODOO_01885 | 1.4e-142 | yihY | S | Belongs to the UPF0761 family | ||
NHNMODOO_01886 | 1.2e-85 | 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) | |
NHNMODOO_01887 | 1.2e-83 | alaR | K | Transcriptional regulator | ||
NHNMODOO_01888 | 3.9e-223 | yugH | 2.6.1.1 | E | Aminotransferase | |
NHNMODOO_01889 | 3.5e-135 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
NHNMODOO_01890 | 1.8e-201 | yfmL | 3.6.4.13 | L | COG0513 Superfamily II DNA and RNA helicases | |
NHNMODOO_01891 | 3.3e-52 | J | RNA binding protein (contains ribosomal protein S1 domain) | |||
NHNMODOO_01892 | 1.2e-33 | yuzA | S | Domain of unknown function (DUF378) | ||
NHNMODOO_01893 | 2.2e-226 | yugK | C | oxidoreductases, Fe-dependent alcohol dehydrogenase family | ||
NHNMODOO_01894 | 2e-205 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
NHNMODOO_01895 | 3.3e-258 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
NHNMODOO_01896 | 1.2e-70 | yugN | S | YugN-like family | ||
NHNMODOO_01897 | 2.7e-21 | |||||
NHNMODOO_01899 | 1.2e-36 | yeaO | S | Protein of unknown function, DUF488 | ||
NHNMODOO_01900 | 6.6e-165 | ppaC | 3.6.1.1 | C | Inorganic pyrophosphatase | |
NHNMODOO_01901 | 6.2e-163 | 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 | |
NHNMODOO_01902 | 5.3e-78 | yneJ | O | COG4846 Membrane protein involved in cytochrome C biogenesis | ||
NHNMODOO_01903 | 6.4e-58 | S | Protein of unknown function (DUF1516) | |||
NHNMODOO_01904 | 1.7e-73 | S | DinB superfamily | |||
NHNMODOO_01905 | 1.6e-74 | S | Putative small multi-drug export protein | |||
NHNMODOO_01906 | 1.1e-232 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NHNMODOO_01907 | 3.2e-99 | pgpB3 | 3.6.1.27 | I | COG0671 Membrane-associated phospholipid phosphatase | |
NHNMODOO_01908 | 2.4e-162 | yclN | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_01909 | 2.7e-153 | fatC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_01910 | 2.6e-149 | yclP | 3.6.3.34 | P | ABC transporter, ATP-binding protein | |
NHNMODOO_01911 | 1.6e-169 | yclQ | P | COG4607 ABC-type enterochelin transport system, periplasmic component | ||
NHNMODOO_01912 | 1.3e-105 | mrr | V | Restriction endonuclease | ||
NHNMODOO_01916 | 6.9e-82 | ssuE | 1.5.1.38 | S | FMN reductase | |
NHNMODOO_01917 | 2.7e-169 | P | ABC transporter substrate-binding protein | |||
NHNMODOO_01918 | 1.8e-209 | ssuD | 1.14.14.5 | C | Catalyzes the desulfonation of aliphatic sulfonates | |
NHNMODOO_01919 | 4.6e-132 | ssuC | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
NHNMODOO_01920 | 2.9e-123 | ssuB | P | Part of the ABC transporter complex SsuABC involved in aliphatic sulfonates import. Responsible for energy coupling to the transport system | ||
NHNMODOO_01921 | 3.7e-91 | K | Transcriptional regulator PadR-like family | |||
NHNMODOO_01922 | 5.1e-156 | axeA | S | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
NHNMODOO_01923 | 3.1e-138 | cysH | 1.8.4.10, 1.8.4.8, 2.7.1.25 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
NHNMODOO_01924 | 1.2e-216 | sat | 2.7.7.4 | P | Belongs to the sulfate adenylyltransferase family | |
NHNMODOO_01925 | 2.5e-184 | cysP | P | phosphate transporter | ||
NHNMODOO_01926 | 1.6e-111 | cysC | 2.7.1.25, 2.7.7.4 | P | Catalyzes the synthesis of activated sulfate | |
NHNMODOO_01927 | 2e-261 | hemD | 2.1.1.107, 4.2.1.75 | H | Belongs to the precorrin methyltransferase family | |
NHNMODOO_01928 | 3.4e-138 | cbiX | 4.99.1.3, 4.99.1.4, 5.4.99.60, 5.4.99.61 | C | CbiX | |
NHNMODOO_01929 | 5.6e-99 | cysG | 1.3.1.76, 4.99.1.4 | H | Siroheme synthase | |
NHNMODOO_01930 | 0.0 | cysJ | 1.8.1.2 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component | |
NHNMODOO_01931 | 0.0 | cysI | 1.7.7.1, 1.8.1.2, 1.8.7.1 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate | |
NHNMODOO_01932 | 1.4e-21 | |||||
NHNMODOO_01933 | 2.7e-152 | V | ABC transporter | |||
NHNMODOO_01934 | 9.7e-59 | gntR1 | K | GntR family transcriptional regulator | ||
NHNMODOO_01935 | 2.8e-213 | mii | 5.3.3.6 | S | PrpF protein | |
NHNMODOO_01936 | 1.4e-64 | S | Tripartite tricarboxylate transporter TctB family | |||
NHNMODOO_01937 | 1.6e-261 | S | Tripartite tricarboxylate transporter TctA family | |||
NHNMODOO_01938 | 4.9e-38 | S | Tripartite tricarboxylate transporter family receptor | |||
NHNMODOO_01939 | 8.6e-167 | yraN | K | Transcriptional regulator | ||
NHNMODOO_01940 | 1.5e-189 | leuB1 | 1.1.1.85 | CE | Isocitrate/isopropylmalate dehydrogenase | |
NHNMODOO_01941 | 1.7e-271 | C | COG1053 Succinate dehydrogenase fumarate reductase, flavoprotein subunit | |||
NHNMODOO_01942 | 4.1e-188 | rspB | 1.1.1.380 | E | Alcohol dehydrogenase GroES-like domain | |
NHNMODOO_01943 | 2.2e-212 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
NHNMODOO_01944 | 2.2e-151 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHNMODOO_01945 | 6.5e-102 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
NHNMODOO_01946 | 2.7e-103 | tetR | K | Bacterial regulatory proteins, tetR family | ||
NHNMODOO_01947 | 4.9e-181 | ybcL | EGP | Major facilitator Superfamily | ||
NHNMODOO_01948 | 5.4e-28 | |||||
NHNMODOO_01949 | 7.9e-20 | XK27_00085 | K | Helix-turn-helix domain | ||
NHNMODOO_01950 | 1e-228 | cstA | T | Carbon starvation protein | ||
NHNMODOO_01951 | 6.7e-198 | ycgA | S | C4-dicarboxylate anaerobic carrier | ||
NHNMODOO_01952 | 4.4e-83 | K | Helix-turn-helix domain, rpiR family | |||
NHNMODOO_01953 | 4.6e-128 | MA20_32325 | 3.4.17.11 | E | Peptidase dimerisation domain | |
NHNMODOO_01954 | 2.6e-156 | arsB | P | Arsenic resistance protein | ||
NHNMODOO_01955 | 5e-91 | |||||
NHNMODOO_01956 | 5.9e-121 | cobB | K | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form | ||
NHNMODOO_01957 | 4.1e-44 | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | ||
NHNMODOO_01958 | 2.1e-49 | celC | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
NHNMODOO_01959 | 1.7e-238 | ywbA | 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 | ||
NHNMODOO_01960 | 2.3e-243 | celF | 3.2.1.86 | GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
NHNMODOO_01961 | 1.1e-133 | chbG | 2.7.1.196, 2.7.1.205, 3.5.1.105 | G | Probably catalyzes the deacetylation of acetylated carbohydrates an important step in the degradation of oligosaccharides | |
NHNMODOO_01962 | 1e-136 | K | UTRA | |||
NHNMODOO_01963 | 0.0 | chiA | 3.2.1.14 | GH18 | G | Glycoside Hydrolase Family 18 |
NHNMODOO_01964 | 4.5e-50 | S | Protein of unknown function (DUF1093) | |||
NHNMODOO_01965 | 4.2e-220 | ybfB | G | COG0477 Permeases of the major facilitator superfamily | ||
NHNMODOO_01966 | 1.7e-204 | rlmN | 2.1.1.192, 2.1.1.224 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
NHNMODOO_01967 | 1.2e-238 | kynU | 3.7.1.3 | E | Catalyzes the cleavage of L-kynurenine (L-Kyn) and L-3- hydroxykynurenine (L-3OHKyn) into anthranilic acid (AA) and 3- hydroxyanthranilic acid (3-OHAA), respectively | |
NHNMODOO_01968 | 7.6e-112 | kynB | 3.5.1.9 | S | Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation | |
NHNMODOO_01969 | 3.3e-155 | kynA | 1.13.11.11 | E | Heme-dependent dioxygenase that catalyzes the oxidative cleavage of the L-tryptophan (L-Trp) pyrrole ring and converts L- tryptophan to N-formyl-L-kynurenine. Catalyzes the oxidative cleavage of the indole moiety | |
NHNMODOO_01970 | 3.5e-200 | E | Spore germination protein | |||
NHNMODOO_01972 | 7.3e-209 | gerKC | S | spore germination | ||
NHNMODOO_01973 | 7.2e-270 | gerKA | EG | Spore germination protein | ||
NHNMODOO_01974 | 5.4e-133 | ygbI | K | DeoR C terminal sensor domain | ||
NHNMODOO_01975 | 1.4e-234 | 2.7.1.219, 2.7.1.220 | S | Putative nucleotide-binding of sugar-metabolising enzyme | ||
NHNMODOO_01976 | 1.2e-185 | pdxA | 1.1.1.262, 1.1.1.408, 1.1.1.409 | H | Belongs to the PdxA family | |
NHNMODOO_01977 | 4.6e-215 | gntP | EG | GntP family permease | ||
NHNMODOO_01978 | 5.7e-152 | araQ5 | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
NHNMODOO_01979 | 9.6e-156 | cebF | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
NHNMODOO_01980 | 6.6e-229 | lacE3 | G | PFAM extracellular solute-binding protein family 1 | ||
NHNMODOO_01982 | 5.6e-247 | argE | 3.5.1.16 | E | Acetylornithine deacetylase | |
NHNMODOO_01983 | 7e-124 | 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 | |
NHNMODOO_01984 | 7.9e-191 | pslL | G | Acyltransferase family | ||
NHNMODOO_01985 | 4.8e-160 | 3.13.1.3 | P | YhfZ C-terminal domain | ||
NHNMODOO_01986 | 3.6e-55 | S | PRD domain | |||
NHNMODOO_01987 | 1.7e-57 | yhfU | S | Protein of unknown function DUF2620 | ||
NHNMODOO_01988 | 3.7e-222 | yhfT | S | Protein of unknown function | ||
NHNMODOO_01989 | 1.4e-172 | php | S | Phosphotriesterase family | ||
NHNMODOO_01990 | 8.6e-204 | 2.9.1.1 | E | Cys/Met metabolism PLP-dependent enzyme | ||
NHNMODOO_01991 | 1.6e-216 | yhfX | E | Alanine racemase, N-terminal domain | ||
NHNMODOO_01992 | 3e-226 | yhfW | G | Metalloenzyme superfamily | ||
NHNMODOO_01993 | 7e-14 | yhfW | G | Metalloenzyme superfamily | ||
NHNMODOO_01994 | 0.0 | O | DnaJ molecular chaperone homology domain | |||
NHNMODOO_01995 | 0.0 | hscC | O | Hsp70 protein | ||
NHNMODOO_01996 | 4.2e-141 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHNMODOO_01997 | 7.8e-152 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
NHNMODOO_01998 | 3.5e-146 | modF | 3.6.3.21, 3.6.3.34 | P | COG1119 ABC-type molybdenum transport system, ATPase component photorepair protein PhrA | |
NHNMODOO_01999 | 1.3e-173 | agpT | K | AraC-like ligand binding domain | ||
NHNMODOO_02000 | 1.4e-245 | ugpB1 | G | Bacterial extracellular solute-binding protein | ||
NHNMODOO_02001 | 1.7e-146 | M1-465 | P | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_02002 | 3.3e-158 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_02003 | 3.6e-48 | esxA | S | Belongs to the WXG100 family | ||
NHNMODOO_02004 | 7.2e-39 | yukD | S | WXG100 protein secretion system (Wss), protein YukD | ||
NHNMODOO_02005 | 1.8e-208 | essB | S | WXG100 protein secretion system (Wss), protein YukC | ||
NHNMODOO_02006 | 0.0 | essC | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | ||
NHNMODOO_02007 | 0.0 | esaA | S | domain protein | ||
NHNMODOO_02008 | 7.9e-71 | S | Family of unknown function (DUF5383) | |||
NHNMODOO_02009 | 2.4e-44 | |||||
NHNMODOO_02010 | 1.2e-46 | |||||
NHNMODOO_02011 | 1e-42 | |||||
NHNMODOO_02012 | 1.4e-244 | S | nuclease activity | |||
NHNMODOO_02013 | 9.1e-226 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
NHNMODOO_02014 | 2.9e-282 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
NHNMODOO_02015 | 3.3e-98 | 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 | |
NHNMODOO_02016 | 1.6e-188 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
NHNMODOO_02017 | 1.6e-271 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
NHNMODOO_02018 | 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 | |
NHNMODOO_02019 | 2.4e-127 | 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 | |
NHNMODOO_02020 | 1.4e-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 | |
NHNMODOO_02021 | 3.2e-127 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
NHNMODOO_02022 | 4.3e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
NHNMODOO_02023 | 5e-207 | 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) | |
NHNMODOO_02024 | 6.5e-79 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
NHNMODOO_02025 | 1.9e-127 | S | CAAX protease self-immunity | |||
NHNMODOO_02026 | 1.4e-98 | rimL | 1.1.1.25 | J | Acetyltransferase (GNAT) domain | |
NHNMODOO_02027 | 7.5e-120 | S | PFAM AIG2 family protein | |||
NHNMODOO_02028 | 1.1e-99 | |||||
NHNMODOO_02029 | 1.9e-67 | S | Calcium/calmodulin dependent protein kinase II association domain | |||
NHNMODOO_02030 | 1.4e-30 | yebG | S | NETI protein | ||
NHNMODOO_02031 | 3.1e-07 | |||||
NHNMODOO_02032 | 2e-256 | tctA | S | Tripartite tricarboxylate transporter TctA family | ||
NHNMODOO_02033 | 1.7e-68 | S | Tripartite tricarboxylate transporter TctB family | |||
NHNMODOO_02034 | 1.9e-186 | S | Tripartite tricarboxylate transporter family receptor | |||
NHNMODOO_02036 | 6.7e-111 | citT | T | response regulator | ||
NHNMODOO_02037 | 3.2e-284 | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | ||
NHNMODOO_02038 | 0.0 | yjcE | P | COG0025 NhaP-type Na H and K H antiporters | ||
NHNMODOO_02039 | 0.0 | yheH | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
NHNMODOO_02040 | 1.3e-307 | yheI | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
NHNMODOO_02041 | 1.6e-233 | G | Major facilitator Superfamily | |||
NHNMODOO_02042 | 8.7e-20 | |||||
NHNMODOO_02044 | 1e-96 | ypbQ | S | protein conserved in bacteria | ||
NHNMODOO_02045 | 1.1e-208 | bcsA | Q | Naringenin-chalcone synthase | ||
NHNMODOO_02046 | 5.6e-130 | mta | K | transcriptional | ||
NHNMODOO_02047 | 3.3e-112 | rimJ2 | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_02048 | 3.8e-273 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
NHNMODOO_02049 | 4.1e-158 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
NHNMODOO_02050 | 1.7e-131 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_02051 | 5.1e-131 | xytR | K | DeoR C terminal sensor domain | ||
NHNMODOO_02052 | 3.5e-86 | ywrA | P | COG2059 Chromate transport protein ChrA | ||
NHNMODOO_02053 | 2.7e-103 | ywrB | P | COG2059 Chromate transport protein ChrA | ||
NHNMODOO_02054 | 3.8e-156 | mqnD | S | Catalyzes the conversion of cyclic dehypoxanthine futalosine (cyclic DHFL) into 1,4-dihydroxy-6-naphthoate, a step in the biosynthesis of menaquinone (MK, vitamin K2) | ||
NHNMODOO_02055 | 1.2e-112 | mqnB | 2.4.2.1, 3.2.2.26, 3.2.2.9 | F | Catalyzes the hydrolysis of futalosine (FL) to dehypoxanthine futalosine (DHFL) and hypoxanthine, a step in the biosynthesis of menaquinone (MK, vitamin K2) | |
NHNMODOO_02056 | 8.8e-265 | lipA1 | S | acetyltransferases and hydrolases with the alpha beta hydrolase fold | ||
NHNMODOO_02057 | 9.6e-71 | K | transcriptional antiterminator | |||
NHNMODOO_02058 | 6.1e-115 | K | transcriptional antiterminator | |||
NHNMODOO_02059 | 1.2e-51 | K | transcriptional antiterminator | |||
NHNMODOO_02060 | 3.2e-104 | yhcS | 3.4.22.70 | M | COG3764 Sortase (surface protein transpeptidase) | |
NHNMODOO_02061 | 0.0 | murF | 6.3.2.10 | M | UDP-N-acetylmuramoyl-tripeptide-D-alanyl-D-alanine ligase activity | |
NHNMODOO_02062 | 5e-161 | Q | calcium- and calmodulin-responsive adenylate cyclase activity | |||
NHNMODOO_02063 | 1.8e-156 | proX | E | Substrate binding domain of ABC-type glycine betaine transport system | ||
NHNMODOO_02064 | 7.7e-100 | K | Belongs to the GbsR family | |||
NHNMODOO_02065 | 1.5e-275 | gbsA | 1.2.1.8 | C | Belongs to the aldehyde dehydrogenase family | |
NHNMODOO_02066 | 5.6e-225 | gbsB | 1.1.1.1 | C | alcohol dehydrogenase | |
NHNMODOO_02067 | 1.8e-134 | yvfI | K | COG2186 Transcriptional regulators | ||
NHNMODOO_02068 | 1.2e-123 | lutC | S | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
NHNMODOO_02069 | 2.5e-272 | 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 | ||
NHNMODOO_02070 | 9.4e-135 | lutA | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
NHNMODOO_02071 | 0.0 | lldP | C | L-lactate permease | ||
NHNMODOO_02072 | 9.1e-14 | |||||
NHNMODOO_02073 | 2.8e-224 | cypA | C | Cytochrome P450 | ||
NHNMODOO_02074 | 1.6e-253 | ydaH | H | AbgT putative transporter family | ||
NHNMODOO_02075 | 0.0 | htpG | O | Molecular chaperone. Has ATPase activity | ||
NHNMODOO_02076 | 9.9e-100 | yaaI | Q | Isochorismatase family | ||
NHNMODOO_02077 | 4.1e-75 | ygaO | ||||
NHNMODOO_02078 | 1.2e-26 | K | Transcriptional regulator | |||
NHNMODOO_02079 | 6.3e-307 | sasH | 3.1.3.5, 3.6.1.45 | F | COG0737 5'-nucleotidase 2',3'-cyclic phosphodiesterase and related esterases | |
NHNMODOO_02081 | 3.2e-289 | rocA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
NHNMODOO_02082 | 1.8e-284 | prdR | KT | Transcriptional regulator | ||
NHNMODOO_02083 | 2.8e-168 | putA | E | Proline dehydrogenase | ||
NHNMODOO_02084 | 5.3e-153 | ykoQ | S | Calcineurin-like phosphoesterase superfamily domain | ||
NHNMODOO_02085 | 2.5e-46 | yhcN | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
NHNMODOO_02086 | 7e-284 | S | proteins of the AP superfamily | |||
NHNMODOO_02088 | 7.2e-210 | pbuG | S | permease | ||
NHNMODOO_02089 | 9.9e-67 | |||||
NHNMODOO_02090 | 1.5e-174 | aph | 2.7.11.1 | S | Phosphotransferase enzyme family | |
NHNMODOO_02091 | 1.3e-216 | G | Transmembrane secretion effector | |||
NHNMODOO_02092 | 1.3e-23 | S | YfhD-like protein | |||
NHNMODOO_02093 | 1e-63 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
NHNMODOO_02094 | 8.3e-108 | dhaL | 2.7.1.121 | S | Dak2 | |
NHNMODOO_02095 | 7.4e-175 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase DhaK, subunit | |
NHNMODOO_02096 | 1.2e-82 | M1-431 | S | Protein of unknown function (DUF1706) | ||
NHNMODOO_02097 | 7.7e-74 | adcR | K | Iron dependent repressor, N-terminal DNA binding domain | ||
NHNMODOO_02098 | 1.3e-197 | yvmA | EGP | Major Facilitator Superfamily | ||
NHNMODOO_02099 | 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 | |
NHNMODOO_02100 | 2.1e-230 | ulaA | 2.7.1.194 | S | PTS system ascorbate-specific transporter subunit IIC | |
NHNMODOO_02101 | 8.9e-41 | ulaB_1 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHNMODOO_02102 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | COG3711 Transcriptional antiterminator | ||
NHNMODOO_02103 | 5.7e-181 | yxeA | V | FtsX-like permease family | ||
NHNMODOO_02104 | 2.3e-111 | devA | 3.6.3.25 | V | ATPases associated with a variety of cellular activities | |
NHNMODOO_02105 | 5e-80 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_02106 | 3.9e-20 | yisL | S | UPF0344 protein | ||
NHNMODOO_02107 | 1.4e-120 | C | Nitroreductase family | |||
NHNMODOO_02108 | 2.2e-84 | tetB | EGP | Major facilitator Superfamily | ||
NHNMODOO_02109 | 1.4e-57 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NHNMODOO_02110 | 7e-26 | 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 | ||
NHNMODOO_02111 | 4.4e-46 | K | FCD | |||
NHNMODOO_02112 | 3.7e-118 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
NHNMODOO_02113 | 9.7e-38 | gloA_3 | E | COG0346 Lactoylglutathione lyase and related lyases | ||
NHNMODOO_02114 | 3.4e-187 | P | COG2807 Cyanate permease | |||
NHNMODOO_02115 | 3.8e-179 | S | amine dehydrogenase activity | |||
NHNMODOO_02116 | 3.6e-120 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_02117 | 8.3e-252 | T | Histidine kinase | |||
NHNMODOO_02118 | 2.5e-66 | S | YtkA-like | |||
NHNMODOO_02119 | 1.3e-56 | eaeH | M | LysM domain | ||
NHNMODOO_02120 | 4.1e-26 | phhB | 3.5.4.33, 4.2.1.96 | H | pterin-4-alpha-carbinolamine dehydratase | |
NHNMODOO_02121 | 2.7e-236 | S | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family | |||
NHNMODOO_02123 | 2.2e-137 | ubiE | Q | Methyltransferase type 11 | ||
NHNMODOO_02124 | 9.1e-70 | mmyG | S | dehydrogenases and related proteins | ||
NHNMODOO_02126 | 4.5e-32 | |||||
NHNMODOO_02127 | 1.4e-51 | S | Bacterial PH domain | |||
NHNMODOO_02128 | 5.4e-32 | |||||
NHNMODOO_02130 | 7.9e-107 | M1-1017 | S | Protein of unknown function (DUF1129) | ||
NHNMODOO_02131 | 1.5e-53 | K | Transcriptional regulator | |||
NHNMODOO_02132 | 5.1e-105 | S | DUF218 domain | |||
NHNMODOO_02133 | 5.7e-147 | degV | S | protein conserved in bacteria | ||
NHNMODOO_02134 | 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 | ||
NHNMODOO_02135 | 5.6e-40 | 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 | ||
NHNMODOO_02136 | 7.7e-227 | yciC | S | GTPases (G3E family) | ||
NHNMODOO_02137 | 8.4e-128 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
NHNMODOO_02138 | 1.1e-06 | |||||
NHNMODOO_02139 | 4.9e-187 | mhqA | E | COG0346 Lactoylglutathione lyase and related lyases | ||
NHNMODOO_02140 | 0.0 | ubiD | 4.1.1.98 | H | Belongs to the UbiD family | |
NHNMODOO_02141 | 1.8e-113 | scoB | 2.8.3.5 | I | COG2057 Acyl CoA acetate 3-ketoacid CoA transferase, beta subunit | |
NHNMODOO_02142 | 1.4e-130 | scoA | 2.8.3.5 | I | COG1788 Acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
NHNMODOO_02143 | 9.8e-239 | atoE | I | Short chain fatty acid transporter | ||
NHNMODOO_02144 | 9.5e-189 | malR | 5.1.1.1 | K | Transcriptional regulator | |
NHNMODOO_02145 | 4.6e-149 | malG | P | transport | ||
NHNMODOO_02146 | 4.3e-247 | malC | P | COG1175 ABC-type sugar transport systems, permease components | ||
NHNMODOO_02147 | 1.8e-237 | G | COG2182 Maltose-binding periplasmic proteins domains | |||
NHNMODOO_02148 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Alpha amylase, N-terminal ig-like domain |
NHNMODOO_02149 | 6.5e-240 | codA | 3.5.4.1 | F | Amidohydrolase family | |
NHNMODOO_02150 | 2.1e-222 | codB | F | cytosine purines uracil thiamine allantoin | ||
NHNMODOO_02151 | 2.5e-281 | QT | COG2508 Regulator of polyketide synthase expression | |||
NHNMODOO_02152 | 4.7e-224 | lhgO | 1.1.99.2 | S | FAD dependent oxidoreductase | |
NHNMODOO_02153 | 5.3e-220 | glcF | C | Glycolate oxidase | ||
NHNMODOO_02154 | 5.2e-262 | glcD | 1.1.3.15 | C | Glycolate oxidase subunit | |
NHNMODOO_02155 | 7.2e-116 | K | COG2186 Transcriptional regulators | |||
NHNMODOO_02156 | 7.1e-119 | K | FCD | |||
NHNMODOO_02157 | 0.0 | S | Tripartite ATP-independent periplasmic transporter, DctM component | |||
NHNMODOO_02158 | 3e-184 | S | NMT1-like family | |||
NHNMODOO_02159 | 1.1e-156 | K | Transcriptional regulator | |||
NHNMODOO_02160 | 8.1e-191 | citA | 2.3.3.1 | C | Belongs to the citrate synthase family | |
NHNMODOO_02161 | 2.1e-209 | siaM | G | COG1593 TRAP-type C4-dicarboxylate transport system, large permease component | ||
NHNMODOO_02162 | 2.5e-75 | G | Tripartite ATP-independent periplasmic transporters, DctQ component | |||
NHNMODOO_02163 | 3.4e-183 | G | Bacterial extracellular solute-binding protein, family 7 | |||
NHNMODOO_02164 | 6.8e-119 | K | FCD | |||
NHNMODOO_02165 | 7.1e-192 | yjmC | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
NHNMODOO_02166 | 8.4e-250 | NT | chemotaxis protein | |||
NHNMODOO_02167 | 2.5e-86 | paiA | K | Acetyltransferase (GNAT) domain | ||
NHNMODOO_02168 | 9.3e-95 | sigV | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
NHNMODOO_02169 | 3.5e-151 | S | Domain of unknown function (DUF4179) | |||
NHNMODOO_02170 | 1e-72 | S | Domain of unknown function (DU1801) | |||
NHNMODOO_02171 | 1.3e-108 | S | CGNR zinc finger | |||
NHNMODOO_02172 | 6.8e-78 | |||||
NHNMODOO_02173 | 1.7e-102 | K | Transcriptional regulator | |||
NHNMODOO_02174 | 0.0 | ydfJ | S | MMPL family | ||
NHNMODOO_02175 | 2.3e-182 | S | domain protein | |||
NHNMODOO_02176 | 1.7e-125 | oppF3 | E | Belongs to the ABC transporter superfamily | ||
NHNMODOO_02177 | 2.1e-32 | oppF3 | E | Belongs to the ABC transporter superfamily | ||
NHNMODOO_02178 | 1.2e-177 | oppD3 | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_02179 | 2e-166 | appC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHNMODOO_02180 | 3.7e-171 | appB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHNMODOO_02181 | 0.0 | oppA5 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
NHNMODOO_02183 | 3.2e-131 | Z012_10580 | S | Sulfite exporter TauE/SafE | ||
NHNMODOO_02184 | 4.6e-16 | |||||
NHNMODOO_02186 | 9.6e-110 | S | ABC-2 family transporter protein | |||
NHNMODOO_02187 | 8.4e-151 | V | ABC transporter | |||
NHNMODOO_02188 | 4.2e-71 | 2.7.1.191 | G | PTS system fructose IIA component | ||
NHNMODOO_02189 | 2.8e-79 | 2.7.1.191 | G | PTS system mannose fructose sorbose family | ||
NHNMODOO_02190 | 1.5e-101 | G | PTS system sorbose-specific iic component | |||
NHNMODOO_02191 | 1.7e-135 | G | PFAM Phosphotransferase system, mannose fructose sorbose family IID component | |||
NHNMODOO_02192 | 1.1e-198 | M | SIS domain | |||
NHNMODOO_02193 | 0.0 | pspF | K | PTS system fructose IIA component | ||
NHNMODOO_02194 | 3.1e-12 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
NHNMODOO_02195 | 2.4e-121 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
NHNMODOO_02196 | 1.3e-208 | G | COG1593 TRAP-type C4-dicarboxylate transport system, large permease component | |||
NHNMODOO_02197 | 3e-71 | siaT_3 | G | Tripartite ATP-independent periplasmic transporters, DctQ component | ||
NHNMODOO_02198 | 2.8e-70 | G | COG1638 TRAP-type C4-dicarboxylate transport system, periplasmic component | |||
NHNMODOO_02199 | 2e-79 | G | COG1638 TRAP-type C4-dicarboxylate transport system, periplasmic component | |||
NHNMODOO_02200 | 2.8e-188 | 1.1.1.14 | E | Dehydrogenase | ||
NHNMODOO_02201 | 3.2e-107 | K | FCD domain | |||
NHNMODOO_02202 | 7.3e-242 | S | Putative nucleotide-binding of sugar-metabolising enzyme | |||
NHNMODOO_02204 | 1.8e-06 | |||||
NHNMODOO_02206 | 1e-108 | S | LXG domain of WXG superfamily | |||
NHNMODOO_02209 | 1.6e-87 | L | COG2801 Transposase and inactivated derivatives | |||
NHNMODOO_02210 | 1.4e-65 | ytcD5 | K | Transcriptional regulator | ||
NHNMODOO_02211 | 4.2e-101 | 1.6.5.2 | S | NADPH-dependent FMN reductase | ||
NHNMODOO_02213 | 4.3e-111 | S | Enoyl-(Acyl carrier protein) reductase | |||
NHNMODOO_02214 | 9.9e-49 | S | Agrobacterium tumefaciens protein Atu4866 | |||
NHNMODOO_02215 | 6e-126 | lacR | K | AraC-type transcriptional regulator N-terminus | ||
NHNMODOO_02217 | 3.3e-20 | S | Domain of unknown function (DUF3784) | |||
NHNMODOO_02218 | 2.3e-243 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
NHNMODOO_02219 | 1.9e-208 | manC | 2.7.7.13, 5.3.1.8 | G | mannose-1-phosphate guanylyltransferase | |
NHNMODOO_02220 | 1.9e-150 | wcnD | M | Glycosyl Transferase | ||
NHNMODOO_02221 | 3.1e-81 | M | Glycosyl transferases group 1 | |||
NHNMODOO_02222 | 4.8e-20 | |||||
NHNMODOO_02223 | 6.9e-71 | M | Glycosyl transferases group 1 | |||
NHNMODOO_02224 | 8.9e-63 | M | TupA-like ATPgrasp | |||
NHNMODOO_02225 | 1.5e-82 | wzxA | S | Polysaccharide biosynthesis protein | ||
NHNMODOO_02226 | 2.6e-110 | cpsE | M | Bacterial sugar transferase | ||
NHNMODOO_02227 | 3.2e-161 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NHNMODOO_02228 | 6.7e-154 | fliC | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
NHNMODOO_02231 | 1.1e-182 | S | response regulator aspartate phosphatase | |||
NHNMODOO_02232 | 1.5e-200 | gerAC | S | Spore germination B3/ GerAC like, C-terminal | ||
NHNMODOO_02233 | 2.2e-183 | gerAB | E | Spore germination protein | ||
NHNMODOO_02234 | 3e-225 | gerAA | EG | Spore germination protein | ||
NHNMODOO_02235 | 4.1e-200 | C | NADH:flavin oxidoreductase / NADH oxidase family | |||
NHNMODOO_02236 | 2.3e-102 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_02237 | 8.9e-31 | S | Domain of unknown function (DUF5082) | |||
NHNMODOO_02238 | 7.5e-48 | |||||
NHNMODOO_02244 | 1.3e-51 | S | LXG domain of WXG superfamily | |||
NHNMODOO_02245 | 1.6e-13 | S | Family of unknown function (DUF5344) | |||
NHNMODOO_02246 | 8.9e-78 | S | Bacterial PH domain | |||
NHNMODOO_02247 | 4.2e-130 | IQ | Short-chain dehydrogenase reductase sdr | |||
NHNMODOO_02248 | 1.2e-261 | alsT | E | Sodium alanine symporter | ||
NHNMODOO_02249 | 5.6e-118 | mdmC | 2.1.1.104 | S | O-methyltransferase | |
NHNMODOO_02250 | 1.9e-153 | K | LysR substrate binding domain | |||
NHNMODOO_02251 | 2.2e-44 | sdpR | K | transcriptional | ||
NHNMODOO_02252 | 2.7e-101 | S | Immunity protein that provides protection for the cell against the toxic effects of SDP, its own SdpC-derived killing factor, and that functions as a receptor signal transduction protein as well. Once SDP accumulates in the extracellular milieu, SdpI binds to SDP, causing sequestration of SdpR at the bacterial membrane | |||
NHNMODOO_02253 | 8.2e-135 | MA20_35565 | 4.1.3.30 | G | Phosphoenolpyruvate phosphomutase | |
NHNMODOO_02254 | 4.4e-160 | E | Glyoxalase-like domain | |||
NHNMODOO_02255 | 8e-185 | P | ABC transporter substrate-binding protein | |||
NHNMODOO_02256 | 1.9e-138 | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | |||
NHNMODOO_02257 | 4.8e-126 | ssuB | P | Part of the ABC transporter complex SsuABC involved in aliphatic sulfonates import. Responsible for energy coupling to the transport system | ||
NHNMODOO_02258 | 8.5e-85 | alsE | 5.1.3.1 | G | Ribulose-phosphate 3 epimerase family | |
NHNMODOO_02259 | 3.6e-174 | ulaA | 2.7.1.194 | S | PTS system ascorbate-specific transporter subunit IIC | |
NHNMODOO_02260 | 2.1e-31 | ulaB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHNMODOO_02261 | 8.6e-181 | 2.7.1.200, 2.7.1.202 | GKT | COG3711 Transcriptional antiterminator | ||
NHNMODOO_02262 | 3.2e-147 | 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 | |
NHNMODOO_02263 | 4.1e-92 | 2.3.1.59 | K | Acetyltransferase (GNAT) domain | ||
NHNMODOO_02264 | 6.1e-140 | S | Alpha/beta hydrolase family | |||
NHNMODOO_02265 | 1.9e-80 | 4.2.1.46, 5.1.3.2 | GM | NAD dependent epimerase/dehydratase family | ||
NHNMODOO_02266 | 6.4e-81 | 4.2.1.46, 5.1.3.2 | GM | NAD dependent epimerase/dehydratase family | ||
NHNMODOO_02267 | 7.9e-179 | L | Transposase | |||
NHNMODOO_02268 | 2.5e-158 | otrA | J | Elongation factor G, domain IV | ||
NHNMODOO_02269 | 2.7e-227 | S | Putative esterase | |||
NHNMODOO_02270 | 3.2e-92 | yvdQ | S | Protein of unknown function (DUF3231) | ||
NHNMODOO_02271 | 9.5e-46 | ycbP | S | Protein of unknown function (DUF2512) | ||
NHNMODOO_02272 | 1.2e-137 | yqjF | S | Uncharacterized conserved protein (COG2071) | ||
NHNMODOO_02274 | 6.9e-212 | 3.5.1.4, 6.3.5.6, 6.3.5.7 | J | Belongs to the amidase family | ||
NHNMODOO_02275 | 5.1e-243 | allB | 3.5.2.5 | F | Catalyzes the conversion of allantoin (5- ureidohydantoin) to allantoic acid by hydrolytic cleavage of the five-member hydantoin ring | |
NHNMODOO_02276 | 1.8e-249 | S | Membrane | |||
NHNMODOO_02277 | 2.4e-56 | pucM | 3.5.2.17 | S | Belongs to the transthyretin family. 5-hydroxyisourate hydrolase subfamily | |
NHNMODOO_02278 | 1.3e-176 | uox | 1.7.3.3, 4.1.1.97 | Q | Catalyzes the oxidation of uric acid to 5- hydroxyisourate, which is further processed to form (S)-allantoin | |
NHNMODOO_02279 | 3e-87 | uraD | 1.7.3.3, 3.5.1.41, 4.1.1.97 | S | OHCU decarboxylase | |
NHNMODOO_02280 | 1.9e-308 | pucR | QT | COG2508 Regulator of polyketide synthase expression | ||
NHNMODOO_02281 | 2.3e-226 | pucF | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
NHNMODOO_02282 | 5.2e-242 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | COG0075 Serine-pyruvate aminotransferase archaeal aspartate aminotransferase | |
NHNMODOO_02283 | 4.7e-85 | 1.17.1.4, 1.2.5.3, 1.3.99.16 | C | COG2080 Aerobic-type carbon monoxide dehydrogenase, small subunit CoxS CutS homologs | ||
NHNMODOO_02284 | 0.0 | xdhA | 1.17.1.4 | C | COG1529 Aerobic-type carbon monoxide dehydrogenase, large subunit CoxL CutL homologs | |
NHNMODOO_02285 | 1.8e-164 | ygfM | 1.17.1.4, 1.2.5.3 | C | COG1319 Aerobic-type carbon monoxide dehydrogenase, middle subunit CoxM CutM homologs | |
NHNMODOO_02286 | 8.4e-100 | pucB | 1.1.1.328, 1.17.1.4, 2.7.7.76 | S | MobA-like NTP transferase domain | |
NHNMODOO_02287 | 1.2e-175 | pucA | 1.17.1.4 | O | COG1975 Xanthine and CO dehydrogenases maturation factor, XdhC CoxF family | |
NHNMODOO_02288 | 1.4e-181 | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | |||
NHNMODOO_02289 | 3.2e-145 | MA20_40340 | P | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_02290 | 3.1e-139 | P | COG1116 ABC-type nitrate sulfonate bicarbonate transport system, ATPase component | |||
NHNMODOO_02292 | 3.3e-189 | P | NMT1-like family | |||
NHNMODOO_02293 | 6.6e-143 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_02294 | 7.6e-135 | P | COG1116 ABC-type nitrate sulfonate bicarbonate transport system, ATPase component | |||
NHNMODOO_02295 | 0.0 | fhuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_02296 | 8.8e-184 | cbrA5 | P | Ferrichrome ABC transporter substrate-binding protein | ||
NHNMODOO_02297 | 1e-52 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
NHNMODOO_02298 | 5.7e-77 | nsrR | K | Transcriptional regulator | ||
NHNMODOO_02299 | 2e-77 | 6.3.3.2 | S | ASCH | ||
NHNMODOO_02300 | 0.0 | uidA | G | Belongs to the glycosyl hydrolase 2 family | ||
NHNMODOO_02301 | 7e-138 | T | Calcineurin-like phosphoesterase superfamily domain | |||
NHNMODOO_02302 | 8.5e-143 | ypgR | C | COG0694 Thioredoxin-like proteins and domains | ||
NHNMODOO_02303 | 1.4e-28 | |||||
NHNMODOO_02304 | 3.9e-84 | ydbS | S | Bacterial PH domain | ||
NHNMODOO_02305 | 8.2e-234 | ydbT | S | Membrane | ||
NHNMODOO_02306 | 7.6e-191 | S | Protein of unknown function (DUF2777) | |||
NHNMODOO_02307 | 2.9e-165 | |||||
NHNMODOO_02308 | 5e-126 | telA | P | Belongs to the TelA family | ||
NHNMODOO_02310 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase | |
NHNMODOO_02311 | 1.5e-288 | gltD | 1.4.1.13, 1.4.1.14 | E | COG0493 NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
NHNMODOO_02312 | 1.1e-112 | ypjP | S | YpjP-like protein | ||
NHNMODOO_02313 | 4.2e-37 | |||||
NHNMODOO_02315 | 1.7e-60 | kapB | G | Kinase associated protein B | ||
NHNMODOO_02316 | 1.9e-153 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
NHNMODOO_02318 | 3.9e-82 | |||||
NHNMODOO_02319 | 1.9e-145 | ycsE | S | hydrolases of the HAD superfamily | ||
NHNMODOO_02320 | 3.1e-17 | |||||
NHNMODOO_02321 | 2.2e-179 | mhqA | E | COG0346 Lactoylglutathione lyase and related lyases | ||
NHNMODOO_02322 | 3.2e-107 | mhqD | S | Carboxylesterase | ||
NHNMODOO_02323 | 4.4e-92 | |||||
NHNMODOO_02324 | 2.8e-202 | gerAC | S | Spore germination B3/ GerAC like, C-terminal | ||
NHNMODOO_02325 | 1.8e-185 | gerAB | E | Spore germination protein | ||
NHNMODOO_02326 | 1.2e-258 | gerAA | EG | Spore germination protein | ||
NHNMODOO_02327 | 0.0 | pepF | E | oligoendopeptidase F | ||
NHNMODOO_02328 | 0.0 | yprA | L | COG1205 Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster | ||
NHNMODOO_02329 | 1.9e-217 | yprB | L | RNase_H superfamily | ||
NHNMODOO_02331 | 1.3e-94 | ypsA | S | Belongs to the UPF0398 family | ||
NHNMODOO_02332 | 2.3e-48 | 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 | ||
NHNMODOO_02333 | 2.5e-68 | rnhA | 3.1.26.4 | L | An endonuclease that specifically degrades the RNA strand of RNA-DNA hybrids | |
NHNMODOO_02334 | 3e-38 | |||||
NHNMODOO_02335 | 2.6e-219 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
NHNMODOO_02336 | 7.4e-175 | S | Oxidoreductase | |||
NHNMODOO_02337 | 2.4e-303 | 2.2.1.6 | EH | Thiamine pyrophosphate enzyme, central domain | ||
NHNMODOO_02338 | 2.7e-61 | pcaC | 3.1.1.24, 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
NHNMODOO_02339 | 5.6e-62 | |||||
NHNMODOO_02340 | 1.4e-154 | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | |||
NHNMODOO_02342 | 1.6e-199 | S | Spore germination B3/ GerAC like, C-terminal | |||
NHNMODOO_02343 | 7.8e-197 | E | Spore germination protein | |||
NHNMODOO_02344 | 6.1e-269 | P | Spore gernimation protein GerA | |||
NHNMODOO_02345 | 1.1e-59 | S | Src homology 3 domains | |||
NHNMODOO_02346 | 2.2e-50 | |||||
NHNMODOO_02347 | 1.3e-287 | gntK | 2.7.1.12, 2.7.1.17, 2.7.1.5, 5.3.1.14 | G | Belongs to the FGGY kinase family | |
NHNMODOO_02348 | 3.9e-20 | S | Protein of unknown function (DUF2564) | |||
NHNMODOO_02350 | 4.5e-209 | G | Transmembrane secretion effector | |||
NHNMODOO_02351 | 1.4e-82 | Q | ubiE/COQ5 methyltransferase family | |||
NHNMODOO_02352 | 3.3e-52 | S | Belongs to the HesB IscA family | |||
NHNMODOO_02353 | 5.5e-286 | ypwA | 3.4.17.19 | E | Broad specificity carboxypetidase that releases amino acids sequentially from the C-terminus, including neutral, aromatic, polar and basic residues | |
NHNMODOO_02354 | 8.4e-89 | IV02_12955 | U | MarC family integral membrane protein | ||
NHNMODOO_02355 | 1.3e-133 | K | Helix-turn-helix XRE-family like proteins | |||
NHNMODOO_02356 | 9.6e-304 | licR | 2.7.1.197 | GKT | Mga helix-turn-helix domain | |
NHNMODOO_02357 | 1.9e-72 | S | Membrane | |||
NHNMODOO_02358 | 7.9e-46 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
NHNMODOO_02359 | 1.2e-198 | 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 | |||
NHNMODOO_02360 | 2.2e-52 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
NHNMODOO_02361 | 1.1e-254 | bglH | 3.2.1.86 | GT1 | G | Glycosyl hydrolase family 1 |
NHNMODOO_02362 | 6.9e-270 | 3.2.1.86 | GT1 | G | Glycosyl hydrolase family 1 | |
NHNMODOO_02363 | 2.8e-148 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_02364 | 7.1e-184 | proV | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
NHNMODOO_02365 | 4e-276 | proWX | EM | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
NHNMODOO_02366 | 1.2e-70 | yccU | S | CoA-binding protein | ||
NHNMODOO_02367 | 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 | |
NHNMODOO_02368 | 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 | |
NHNMODOO_02369 | 2.5e-56 | S | Uncharacterized protein conserved in bacteria (DUF2200) | |||
NHNMODOO_02370 | 2.3e-82 | dksA | T | general stress protein | ||
NHNMODOO_02371 | 5.3e-201 | ytvI | S | sporulation integral membrane protein YtvI | ||
NHNMODOO_02372 | 7.6e-135 | motB | N | Flagellar motor protein | ||
NHNMODOO_02373 | 4.1e-139 | motA | N | flagellar motor | ||
NHNMODOO_02374 | 1.2e-149 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
NHNMODOO_02375 | 1.9e-105 | S | Golgi phosphoprotein 3 (GPP34) | |||
NHNMODOO_02376 | 5.3e-36 | K | COG0202 DNA-directed RNA polymerase, alpha subunit 40 kD subunit | |||
NHNMODOO_02377 | 2.5e-101 | ydeI | S | Bacteriocin-protection, YdeI or OmpD-Associated | ||
NHNMODOO_02378 | 4.4e-86 | C | HEAT repeats | |||
NHNMODOO_02379 | 2.5e-44 | CP_0264 | 3.2.2.10 | S | Belongs to the LOG family | |
NHNMODOO_02380 | 4.1e-67 | S | Bacterial PH domain | |||
NHNMODOO_02381 | 2.2e-149 | 3.4.11.5 | I | Alpha beta hydrolase | ||
NHNMODOO_02383 | 1.2e-17 | GM | PFAM NAD-dependent epimerase dehydratase | |||
NHNMODOO_02384 | 3.9e-82 | yfiT | S | Belongs to the metal hydrolase YfiT family | ||
NHNMODOO_02385 | 2.6e-58 | E | LysE type translocator | |||
NHNMODOO_02386 | 1.6e-100 | K | AraC family transcriptional regulator | |||
NHNMODOO_02387 | 4e-12 | |||||
NHNMODOO_02388 | 1.8e-07 | S | Family of unknown function (DUF5345) | |||
NHNMODOO_02389 | 3.3e-92 | sigY | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
NHNMODOO_02390 | 9.8e-138 | yxlG | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | ||
NHNMODOO_02391 | 4.2e-156 | yxlF | V | ABC transporter, ATP-binding protein | ||
NHNMODOO_02392 | 5.4e-11 | yxlE | S | Phospholipase_D-nuclease N-terminal | ||
NHNMODOO_02393 | 9.3e-87 | H | PFAM pyruvate carboxyltransferase | |||
NHNMODOO_02394 | 2.1e-155 | frc | 2.8.3.16 | C | acyl-CoA transferases carnitine dehydratase | |
NHNMODOO_02395 | 6.6e-86 | G | Bacterial extracellular solute-binding protein, family 7 | |||
NHNMODOO_02396 | 2.2e-23 | G | Tripartite ATP-independent periplasmic transporters, DctQ component | |||
NHNMODOO_02397 | 2.8e-118 | G | Tripartite ATP-independent periplasmic transporter, DctM component | |||
NHNMODOO_02398 | 2.7e-55 | L | COG3316 Transposase and inactivated derivatives | |||
NHNMODOO_02399 | 7.9e-97 | GBS0088 | S | protein conserved in bacteria | ||
NHNMODOO_02400 | 7.6e-217 | EGP | Major facilitator Superfamily | |||
NHNMODOO_02402 | 3.5e-28 | sdpI | S | integral membrane protein | ||
NHNMODOO_02406 | 1.8e-224 | braB | E | Component of the transport system for branched-chain amino acids | ||
NHNMODOO_02407 | 7e-59 | S | CHY zinc finger | |||
NHNMODOO_02408 | 7.8e-166 | rihB | 3.2.2.1 | F | nucleoside hydrolase | |
NHNMODOO_02409 | 9.5e-115 | idi | I | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
NHNMODOO_02410 | 4.6e-291 | dcuS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
NHNMODOO_02411 | 1.7e-126 | T | COG4565 Response regulator of citrate malate metabolism | |||
NHNMODOO_02412 | 1.1e-298 | sdcS | P | Sodium:sulfate symporter transmembrane region | ||
NHNMODOO_02413 | 7.4e-110 | lolD | V | ABC transporter | ||
NHNMODOO_02414 | 0.0 | |||||
NHNMODOO_02416 | 0.0 | 2.7.13.3 | T | Histidine kinase | ||
NHNMODOO_02418 | 1.4e-196 | 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 | |
NHNMODOO_02419 | 6e-137 | S | GNAT acetyltransferase | |||
NHNMODOO_02420 | 3.6e-67 | |||||
NHNMODOO_02421 | 6.5e-66 | |||||
NHNMODOO_02422 | 6.3e-117 | |||||
NHNMODOO_02423 | 5.5e-113 | |||||
NHNMODOO_02424 | 5.2e-75 | yosT | L | Bacterial transcription activator, effector binding domain | ||
NHNMODOO_02425 | 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) | |
NHNMODOO_02426 | 2e-103 | K | GrpB protein | |||
NHNMODOO_02427 | 1.3e-168 | O | Predicted Zn-dependent protease (DUF2268) | |||
NHNMODOO_02428 | 4e-139 | mta | K | TipAS antibiotic-recognition domain | ||
NHNMODOO_02429 | 4.3e-22 | |||||
NHNMODOO_02431 | 1.2e-163 | yegS | 2.7.1.107 | I | COG1597 Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
NHNMODOO_02432 | 3.4e-107 | yrbG3 | S | membrane | ||
NHNMODOO_02433 | 1.1e-107 | ywrF | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | ||
NHNMODOO_02434 | 2.4e-170 | murB | 1.3.1.98 | M | cell wall formation | |
NHNMODOO_02435 | 0.0 | ywjA | V | ABC transporter | ||
NHNMODOO_02436 | 1.4e-245 | katX | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
NHNMODOO_02437 | 3.2e-95 | S | DinB superfamily | |||
NHNMODOO_02438 | 2.7e-211 | yxlH | EGP | Major facilitator Superfamily | ||
NHNMODOO_02439 | 0.0 | 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 | |
NHNMODOO_02440 | 4.3e-238 | NT | chemotaxis protein | |||
NHNMODOO_02441 | 6.4e-218 | S | Acetyltransferase | |||
NHNMODOO_02442 | 6e-247 | dapE | 3.5.1.16, 3.5.1.18 | E | Peptidase dimerisation domain | |
NHNMODOO_02443 | 3.8e-145 | ycsE | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
NHNMODOO_02445 | 1.4e-173 | troA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NHNMODOO_02446 | 4.6e-140 | troB | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
NHNMODOO_02447 | 1.9e-159 | mntC | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
NHNMODOO_02448 | 1.5e-150 | troD | P | 'COG1108 ABC-type Mn2 Zn2 transport systems, permease components' | ||
NHNMODOO_02449 | 3.7e-99 | S | UPF0302 domain | |||
NHNMODOO_02450 | 6e-55 | yflT | S | Heat induced stress protein YflT | ||
NHNMODOO_02451 | 2.2e-42 | ydzA | EGP | Major facilitator Superfamily | ||
NHNMODOO_02452 | 8.4e-221 | ywbD | 2.1.1.191 | J | Methyltransferase | |
NHNMODOO_02453 | 0.0 | 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 | |
NHNMODOO_02454 | 2.2e-246 | 3.1.3.1 | P | Belongs to the alkaline phosphatase family | ||
NHNMODOO_02455 | 1.2e-129 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
NHNMODOO_02456 | 1.5e-152 | yuaG | 3.4.21.72 | S | protein conserved in bacteria | |
NHNMODOO_02457 | 6.6e-82 | yuaF | OU | Membrane protein implicated in regulation of membrane protease activity | ||
NHNMODOO_02459 | 3.6e-285 | yhfW | CE | COG0665 Glycine D-amino acid oxidases (deaminating) | ||
NHNMODOO_02460 | 4.7e-70 | bdbC | O | Required for disulfide bond formation in some proteins | ||
NHNMODOO_02461 | 6.6e-73 | bdbA | CO | Thioredoxin | ||
NHNMODOO_02462 | 1.5e-259 | 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 | |
NHNMODOO_02463 | 5e-76 | K | Acetyltransferase (GNAT) domain | |||
NHNMODOO_02464 | 5.6e-72 | S | Protein of unknown function (DUF4064) | |||
NHNMODOO_02465 | 9e-264 | 6.3.1.2 | E | Glutamine synthetase, catalytic domain | ||
NHNMODOO_02466 | 3.4e-245 | S | dienelactone hydrolase | |||
NHNMODOO_02467 | 1.6e-32 | bceB | V | ABC transporter (permease) | ||
NHNMODOO_02468 | 2.8e-24 | gntR9 | K | Alanine-glyoxylate amino-transferase | ||
NHNMODOO_02469 | 1.9e-122 | azlC | E | AzlC protein | ||
NHNMODOO_02470 | 3.4e-47 | S | Branched-chain amino acid transport protein (AzlD) | |||
NHNMODOO_02471 | 1e-276 | hutH | 4.3.1.3 | E | Histidine ammonia-lyase | |
NHNMODOO_02472 | 4e-150 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
NHNMODOO_02473 | 4.5e-231 | BH2250 | S | protein conserved in bacteria | ||
NHNMODOO_02474 | 1.4e-135 | 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 | |
NHNMODOO_02475 | 7.1e-176 | abrB | S | Pfam:AmoA | ||
NHNMODOO_02476 | 5.9e-141 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
NHNMODOO_02477 | 1.2e-88 | CO | Thioredoxin-like | |||
NHNMODOO_02479 | 8.7e-93 | nudF | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | |
NHNMODOO_02480 | 1.2e-101 | 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 | ||
NHNMODOO_02481 | 5e-87 | fur | P | Belongs to the Fur family | ||
NHNMODOO_02482 | 9.6e-14 | S | Protein of unknown function (DUF4227) | |||
NHNMODOO_02483 | 2.2e-165 | xerD | L | recombinase XerD | ||
NHNMODOO_02484 | 3.2e-225 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
NHNMODOO_02485 | 1.7e-227 | pdp | 2.4.2.2, 2.4.2.4 | F | phosphorylase | |
NHNMODOO_02486 | 1.8e-69 | ohrB | O | Organic hydroperoxide resistance protein | ||
NHNMODOO_02487 | 9.4e-120 | yocB | J | translation release factor activity | ||
NHNMODOO_02488 | 5.5e-240 | emrB_1 | EGP | Major facilitator Superfamily | ||
NHNMODOO_02489 | 2.1e-20 | yycD | S | Uncharacterized protein conserved in bacteria (DUF2188) | ||
NHNMODOO_02490 | 4.9e-52 | |||||
NHNMODOO_02491 | 2.7e-82 | yvsG | S | LexA-binding, inner membrane-associated putative hydrolase | ||
NHNMODOO_02492 | 5.2e-131 | 3.5.1.104 | G | Polysaccharide deacetylase | ||
NHNMODOO_02493 | 5.5e-209 | dacF | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NHNMODOO_02494 | 3.9e-54 | spoIIAA | T | Belongs to the anti-sigma-factor antagonist family | ||
NHNMODOO_02495 | 1.4e-72 | 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 | |
NHNMODOO_02496 | 4.8e-137 | sigF | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
NHNMODOO_02497 | 2.2e-79 | S | Pfam:SpoVA | |||
NHNMODOO_02498 | 1.1e-181 | spoVAD | I | Stage V sporulation protein AD | ||
NHNMODOO_02499 | 2.5e-56 | spoVAEB | S | Pfam:SpoVA | ||
NHNMODOO_02500 | 9.8e-106 | spoVAEA | S | Stage V sporulation protein AE | ||
NHNMODOO_02501 | 6.4e-271 | spoVAF | EG | Stage V sporulation protein AF | ||
NHNMODOO_02502 | 1.1e-250 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
NHNMODOO_02503 | 1.4e-80 | 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 | |
NHNMODOO_02504 | 1.1e-62 | tspO | T | membrane | ||
NHNMODOO_02505 | 3.3e-158 | ccpC | K | Transcriptional regulator | ||
NHNMODOO_02507 | 6.6e-196 | S | Psort location CytoplasmicMembrane, score | |||
NHNMODOO_02508 | 2e-208 | prpC | 2.3.3.1, 2.3.3.5 | C | Belongs to the citrate synthase family | |
NHNMODOO_02509 | 1.6e-271 | prpD | 4.2.1.79 | S | 2-methylcitrate dehydratase | |
NHNMODOO_02510 | 1.1e-159 | prpB | 4.1.3.30 | G | Catalyzes the thermodynamically favored C-C bond cleavage of (2R,3S)-2-methylisocitrate to yield pyruvate and succinate | |
NHNMODOO_02511 | 3.2e-156 | hgd | 1.1.1.31, 1.1.1.60 | I | 3-hydroxyisobutyrate dehydrogenase | |
NHNMODOO_02512 | 2.3e-273 | 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 | |
NHNMODOO_02513 | 4.6e-191 | echA9 | 1.1.1.31, 3.1.2.4, 4.2.1.17 | I | 3-hydroxyisobutyryl-CoA hydrolase | |
NHNMODOO_02514 | 9.4e-110 | ribE | 2.5.1.9 | H | Riboflavin synthase | |
NHNMODOO_02515 | 2.1e-224 | 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 | |
NHNMODOO_02516 | 7.9e-82 | 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 | |
NHNMODOO_02517 | 4.6e-82 | ypuF | S | Domain of unknown function (DUF309) | ||
NHNMODOO_02518 | 1.4e-125 | 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 | ||
NHNMODOO_02519 | 2e-98 | 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 | ||
NHNMODOO_02520 | 1.2e-103 | K | Uncharacterized protein conserved in bacteria (DUF2087) | |||
NHNMODOO_02521 | 3.9e-295 | aldA | C | Belongs to the aldehyde dehydrogenase family | ||
NHNMODOO_02522 | 2.7e-168 | sodA | 1.15.1.1 | P | Superoxide dismutase | |
NHNMODOO_02523 | 9.8e-280 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
NHNMODOO_02524 | 7.6e-305 | ubiB | S | ABC1 family | ||
NHNMODOO_02525 | 1.5e-44 | S | ATP synthase, subunit b | |||
NHNMODOO_02526 | 1.9e-121 | S | membrane | |||
NHNMODOO_02527 | 7.1e-45 | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | |||
NHNMODOO_02528 | 2e-77 | spoVAC | S | stage V sporulation protein AC | ||
NHNMODOO_02529 | 5.3e-192 | spoVAD | I | Stage V sporulation protein AD | ||
NHNMODOO_02530 | 1.2e-55 | spoVAE | S | stage V sporulation protein | ||
NHNMODOO_02531 | 1.8e-209 | dacB | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NHNMODOO_02532 | 9.6e-101 | spmA | S | Spore maturation protein | ||
NHNMODOO_02533 | 1.6e-75 | spmB | S | Spore maturation protein | ||
NHNMODOO_02534 | 8.3e-131 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NHNMODOO_02535 | 7.5e-97 | 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 | ||
NHNMODOO_02536 | 1.1e-297 | ccs1 | O | COG1333 ResB protein required for cytochrome c biosynthesis | ||
NHNMODOO_02537 | 3.5e-219 | ccsA | O | 'COG0755 ABC-type transport system involved in cytochrome c biogenesis, permease component' | ||
NHNMODOO_02538 | 9e-130 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_02539 | 0.0 | resE | 2.7.13.3 | T | Histidine kinase | |
NHNMODOO_02540 | 2.1e-186 | btuC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_02541 | 1.9e-136 | yvrA | 3.6.3.34 | HP | COG1120 ABC-type cobalamin Fe3 -siderophores transport systems, ATPase components | |
NHNMODOO_02542 | 1.2e-94 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Adenosyltransferase | |
NHNMODOO_02544 | 3.4e-135 | P | COG0861 Membrane protein TerC, possibly involved in tellurium resistance | |||
NHNMODOO_02545 | 3.9e-246 | nox | 1.6.3.4 | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | |
NHNMODOO_02546 | 3.9e-298 | serA | 1.1.1.399, 1.1.1.95 | E | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NHNMODOO_02547 | 3.9e-43 | fer | C | Ferredoxin | ||
NHNMODOO_02548 | 3.9e-174 | ypbB | 5.1.3.1 | S | protein conserved in bacteria | |
NHNMODOO_02549 | 8.5e-263 | recQ | 3.6.4.12 | L | DNA helicase | |
NHNMODOO_02550 | 1e-99 | ypbD | S | metal-dependent membrane protease | ||
NHNMODOO_02552 | 2.7e-09 | ypbF | S | Protein of unknown function (DUF2663) | ||
NHNMODOO_02553 | 1.3e-51 | K | Helix-turn-helix XRE-family like proteins | |||
NHNMODOO_02554 | 7.2e-37 | sinR | K | Helix-turn-helix XRE-family like proteins | ||
NHNMODOO_02555 | 5.1e-226 | mgs | 2.4.1.337 | GT4 | M | Glycosyl Transferase |
NHNMODOO_02556 | 5.6e-197 | cpoA | GT4 | M | Glycosyl transferases group 1 | |
NHNMODOO_02557 | 2.5e-176 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
NHNMODOO_02559 | 6.3e-221 | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | ||
NHNMODOO_02560 | 4.6e-143 | ypbG | S | Calcineurin-like phosphoesterase superfamily domain | ||
NHNMODOO_02561 | 1.4e-164 | merR | K | MerR family transcriptional regulator | ||
NHNMODOO_02562 | 1.6e-108 | 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 | ||
NHNMODOO_02563 | 1.7e-125 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_02564 | 5.4e-267 | T | PhoQ Sensor | |||
NHNMODOO_02565 | 1.6e-177 | |||||
NHNMODOO_02566 | 1.6e-238 | gdhA | 1.4.1.2, 1.4.1.3 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
NHNMODOO_02567 | 9.9e-180 | ypdA | 1.18.1.2, 1.19.1.1, 1.8.1.9 | O | COG0492 Thioredoxin reductase | |
NHNMODOO_02568 | 3.3e-175 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
NHNMODOO_02569 | 1.7e-111 | prsW | S | Involved in the degradation of specific anti-sigma factors | ||
NHNMODOO_02570 | 6.9e-25 | |||||
NHNMODOO_02571 | 0.0 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | Catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
NHNMODOO_02572 | 3.7e-24 | metH | 2.1.1.13 | E | Methionine synthase | |
NHNMODOO_02573 | 0.0 | metH | 2.1.1.13 | E | Methionine synthase | |
NHNMODOO_02574 | 4.5e-163 | sleB | 3.5.1.28 | M | Spore cortex-lytic enzyme | |
NHNMODOO_02575 | 8.4e-246 | hemX | 2.1.1.107, 4.2.1.75 | H | sporulation protein | |
NHNMODOO_02576 | 5.9e-130 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
NHNMODOO_02577 | 2.9e-105 | plsC | 2.3.1.51, 2.7.4.25 | I | 1-acyl-sn-glycerol-3-phosphate acyltransferase | |
NHNMODOO_02578 | 1.4e-201 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
NHNMODOO_02579 | 3e-12 | yphA | ||||
NHNMODOO_02580 | 1.2e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
NHNMODOO_02581 | 9e-102 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
NHNMODOO_02582 | 4.1e-184 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
NHNMODOO_02583 | 4e-38 | S | Stage VI sporulation protein F | |||
NHNMODOO_02585 | 5.7e-132 | yphF | ||||
NHNMODOO_02586 | 4.4e-280 | spoIVA | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | ||
NHNMODOO_02587 | 8.6e-99 | folE | 3.5.4.16 | H | GTP cyclohydrolase | |
NHNMODOO_02588 | 1.6e-35 | 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 | ||
NHNMODOO_02589 | 7.7e-58 | hepS | 2.5.1.30 | H | heptaprenyl diphosphate synthase | |
NHNMODOO_02590 | 2.2e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
NHNMODOO_02591 | 9.7e-158 | ubiA | 2.5.1.39 | H | UbiA prenyltransferase family | |
NHNMODOO_02592 | 2.9e-159 | mqnA | 1.21.98.1, 4.2.1.151 | S | Catalyzes the dehydration of chorismate into 3- (1- carboxyvinyl)oxy benzoate, a step in the biosynthesis of menaquinone (MK, vitamin K2) | |
NHNMODOO_02593 | 6.9e-181 | hepT | 2.5.1.30, 2.5.1.83, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NHNMODOO_02594 | 1.4e-77 | 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 | |
NHNMODOO_02595 | 1.2e-138 | cheR | 2.1.1.80 | NT | COG1352 Methylase of chemotaxis methyl-accepting proteins | |
NHNMODOO_02596 | 3.1e-220 | 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 | |
NHNMODOO_02597 | 9.6e-192 | 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) | |
NHNMODOO_02598 | 2.1e-58 | aroH | 2.7.4.25, 5.4.99.5 | E | Catalyzes the Claisen rearrangement of chorismate to prephenate. Probably involved in the aromatic amino acid biosynthesis | |
NHNMODOO_02599 | 3.6e-282 | 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 | |
NHNMODOO_02600 | 3.2e-181 | 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) | |
NHNMODOO_02601 | 3.7e-129 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
NHNMODOO_02602 | 1.7e-114 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | phosphoribosylanthranilate isomerase activity | |
NHNMODOO_02603 | 1.8e-223 | 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 | |
NHNMODOO_02604 | 1.7e-145 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
NHNMODOO_02605 | 2e-205 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
NHNMODOO_02606 | 1.7e-199 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
NHNMODOO_02607 | 1.2e-236 | 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 | |
NHNMODOO_02608 | 4.8e-227 | S | COG0457 FOG TPR repeat | |||
NHNMODOO_02609 | 2.6e-97 | ypiB | S | Belongs to the UPF0302 family | ||
NHNMODOO_02610 | 3.3e-80 | ypiF | S | Protein of unknown function (DUF2487) | ||
NHNMODOO_02611 | 4.8e-90 | qcrA | C | Menaquinol-cytochrome c reductase | ||
NHNMODOO_02612 | 7.7e-123 | petB | C | COG1290 Cytochrome b subunit of the bc complex | ||
NHNMODOO_02613 | 1.7e-145 | qcrC | C | Menaquinol-cytochrome c reductase cytochrome b c subunit | ||
NHNMODOO_02614 | 8.4e-108 | ypjA | S | membrane | ||
NHNMODOO_02615 | 1.5e-138 | S | Sporulation protein YpjB (SpoYpjB) | |||
NHNMODOO_02616 | 1e-117 | yugP | S | Zn-dependent protease | ||
NHNMODOO_02617 | 7.2e-212 | tcaB | EGP | Major facilitator Superfamily | ||
NHNMODOO_02618 | 9.6e-158 | ypjC | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
NHNMODOO_02619 | 1.4e-201 | L | Transposase | |||
NHNMODOO_02620 | 1.1e-59 | ypjD | 2.5.1.19 | S | Nucleotide pyrophosphohydrolase | |
NHNMODOO_02621 | 7.2e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
NHNMODOO_02622 | 6.5e-75 | mgsA | 2.7.1.24, 4.2.3.3 | G | methylglyoxal synthase | |
NHNMODOO_02623 | 4.2e-81 | M | Acetyltransferase (GNAT) domain | |||
NHNMODOO_02624 | 2.7e-235 | rtcB | 6.5.1.3 | S | tRNA-splicing ligase RtcB | |
NHNMODOO_02625 | 1.4e-37 | |||||
NHNMODOO_02626 | 2.6e-71 | yjcF | S | Acetyltransferase (GNAT) domain | ||
NHNMODOO_02627 | 2.6e-135 | Q | Methyltransferase domain | |||
NHNMODOO_02628 | 6.1e-51 | |||||
NHNMODOO_02629 | 1.1e-286 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
NHNMODOO_02630 | 4.8e-88 | S | Protein of unknown function (DUF1706) | |||
NHNMODOO_02631 | 2.5e-264 | 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 | |
NHNMODOO_02632 | 5e-128 | yodH | Q | Methyltransferase | ||
NHNMODOO_02633 | 3.3e-139 | M | 3D domain | |||
NHNMODOO_02634 | 2.9e-159 | M | 3D domain | |||
NHNMODOO_02635 | 1.5e-155 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
NHNMODOO_02636 | 1.6e-176 | L | Transposase | |||
NHNMODOO_02637 | 4.4e-205 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
NHNMODOO_02638 | 5.4e-147 | ysaA | S | HAD-hyrolase-like | ||
NHNMODOO_02639 | 1.2e-101 | ykoE | S | ABC-type cobalt transport system, permease component | ||
NHNMODOO_02640 | 5.7e-272 | ykoD | 3.6.3.24 | P | ABC transporter | |
NHNMODOO_02641 | 6.3e-140 | ykoC | P | Cobalt transport protein | ||
NHNMODOO_02642 | 1.6e-108 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
NHNMODOO_02643 | 9.8e-106 | yvdD_1 | 3.2.2.10 | S | Belongs to the LOG family | |
NHNMODOO_02644 | 7.6e-84 | lytE2 | M | COG1388 FOG LysM repeat | ||
NHNMODOO_02645 | 4.6e-227 | els | S | Acetyltransferase | ||
NHNMODOO_02646 | 8.5e-102 | yvdT | K | Transcriptional regulator | ||
NHNMODOO_02647 | 1.5e-183 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | |||
NHNMODOO_02648 | 1.5e-135 | spoIISA | S | Toxin SpoIISA, type II toxin-antitoxin system | ||
NHNMODOO_02649 | 1.8e-184 | yceB | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
NHNMODOO_02650 | 6.3e-168 | mccA | 2.5.1.134, 2.5.1.47 | E | Cysteine synthase | |
NHNMODOO_02651 | 3.5e-208 | mccB | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
NHNMODOO_02652 | 3.5e-180 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
NHNMODOO_02654 | 2.9e-102 | stoA | CO | Redoxin | ||
NHNMODOO_02655 | 5.3e-98 | yueE | S | phosphohydrolase | ||
NHNMODOO_02656 | 5.9e-112 | yplQ | S | protein, Hemolysin III | ||
NHNMODOO_02657 | 3.4e-14 | yoeD | G | Helix-turn-helix domain | ||
NHNMODOO_02658 | 1.1e-231 | S | Putative glycosyl hydrolase domain | |||
NHNMODOO_02659 | 7.7e-97 | yjbC | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
NHNMODOO_02661 | 1.3e-66 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
NHNMODOO_02662 | 6.1e-114 | 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 | ||
NHNMODOO_02663 | 1.4e-204 | yjbF | S | Competence protein | ||
NHNMODOO_02665 | 2.3e-170 | yjbH | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
NHNMODOO_02666 | 5.6e-73 | yjbI | S | COG2346 Truncated hemoglobins | ||
NHNMODOO_02667 | 3.1e-95 | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | |||
NHNMODOO_02668 | 2.2e-94 | yjbK | S | protein conserved in bacteria | ||
NHNMODOO_02669 | 2.7e-61 | yjbL | S | Belongs to the UPF0738 family | ||
NHNMODOO_02670 | 2e-109 | yjbM | 2.7.6.5 | S | GTP pyrophosphokinase | |
NHNMODOO_02671 | 8.8e-150 | 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 | |
NHNMODOO_02672 | 3e-162 | yjbO | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NHNMODOO_02673 | 8.3e-137 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
NHNMODOO_02674 | 3.8e-57 | yngL | S | Protein of unknown function (DUF1360) | ||
NHNMODOO_02675 | 1.6e-137 | Q | ubiE/COQ5 methyltransferase family | |||
NHNMODOO_02676 | 5.4e-119 | |||||
NHNMODOO_02677 | 1.1e-135 | |||||
NHNMODOO_02680 | 3.5e-60 | cotX | S | Spore Coat Protein X and V domain | ||
NHNMODOO_02681 | 2.1e-52 | |||||
NHNMODOO_02682 | 0.0 | yjcD | 3.6.4.12 | L | DNA helicase | |
NHNMODOO_02683 | 1.1e-176 | comGA | NU | COG2804 Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
NHNMODOO_02684 | 1.5e-181 | comGB | NU | COG1459 Type II secretory pathway, component PulF | ||
NHNMODOO_02692 | 1.2e-41 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
NHNMODOO_02693 | 1.4e-47 | comGC | U | Required for transformation and DNA binding | ||
NHNMODOO_02694 | 1.7e-70 | mshD | NU | general secretion pathway protein | ||
NHNMODOO_02695 | 2e-10 | |||||
NHNMODOO_02696 | 5e-78 | |||||
NHNMODOO_02699 | 2e-36 | yqgY | S | Protein of unknown function (DUF2626) | ||
NHNMODOO_02700 | 7.5e-120 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
NHNMODOO_02701 | 6.6e-08 | S | Protein of unknown function (DUF2759) | |||
NHNMODOO_02702 | 1.9e-152 | yqhG | S | Bacterial protein YqhG of unknown function | ||
NHNMODOO_02703 | 0.0 | yqhH | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
NHNMODOO_02704 | 5.5e-203 | gcvT | 1.4.4.2, 2.1.2.10 | E | The glycine cleavage system catalyzes the degradation of glycine | |
NHNMODOO_02705 | 6.2e-249 | 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 | |
NHNMODOO_02706 | 1.9e-283 | 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 | |
NHNMODOO_02707 | 1.9e-62 | yqhL | P | COG0607 Rhodanese-related sulfurtransferase | ||
NHNMODOO_02708 | 1.8e-153 | 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 | |
NHNMODOO_02709 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
NHNMODOO_02710 | 2.7e-157 | dat | 2.6.1.21 | E | Acts on the D-isomers of alanine, leucine, aspartate, glutamate, aminobutyrate, norvaline and asparagine. The enzyme transfers an amino group from a substrate D-amino acid to the pyridoxal phosphate cofactor to form pyridoxamine and an alpha- keto acid in the first half-reaction | |
NHNMODOO_02711 | 2.5e-197 | splB | 4.1.99.14 | L | Spore photoproduct lyase | |
NHNMODOO_02712 | 6.5e-75 | mntR | K | Involved in manganese homeostasis. Might activate the transcription of the mntABCD operon | ||
NHNMODOO_02713 | 5.4e-164 | yqhO | S | esterase of the alpha-beta hydrolase superfamily | ||
NHNMODOO_02714 | 4e-55 | |||||
NHNMODOO_02715 | 1.3e-87 | yqhR | S | Conserved membrane protein YqhR | ||
NHNMODOO_02716 | 3.3e-192 | yqhT | 3.4.11.9, 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
NHNMODOO_02717 | 3.2e-98 | 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 | ||
NHNMODOO_02718 | 1e-93 | 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 | |
NHNMODOO_02719 | 2.4e-47 | S | YfzA-like protein | |||
NHNMODOO_02720 | 1.7e-35 | yqhV | S | Protein of unknown function (DUF2619) | ||
NHNMODOO_02721 | 4.6e-166 | spoIIIAA | S | stage III sporulation protein AA | ||
NHNMODOO_02722 | 1.1e-81 | spoIIIAB | S | Stage III sporulation protein | ||
NHNMODOO_02723 | 4.4e-29 | spoIIIAC | S | stage III sporulation protein AC | ||
NHNMODOO_02724 | 1.6e-40 | spoIIIAD | S | Stage III sporulation protein AD | ||
NHNMODOO_02725 | 2.5e-201 | spoIIIAE | S | stage III sporulation protein AE | ||
NHNMODOO_02726 | 2.7e-87 | spoIIIAF | S | Stage III sporulation protein AF (Spore_III_AF) | ||
NHNMODOO_02727 | 7.6e-99 | spoIIIAG | S | stage III sporulation protein AG | ||
NHNMODOO_02728 | 1.7e-88 | spoIIIAH | S | SpoIIIAH-like protein | ||
NHNMODOO_02729 | 1.1e-56 | |||||
NHNMODOO_02730 | 5.1e-68 | 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 | |
NHNMODOO_02731 | 7.7e-255 | 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 | |
NHNMODOO_02732 | 6.9e-66 | yqhY | S | protein conserved in bacteria | ||
NHNMODOO_02733 | 3.3e-65 | 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 | ||
NHNMODOO_02734 | 8.7e-206 | 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 | |
NHNMODOO_02735 | 9.7e-36 | 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 | |
NHNMODOO_02736 | 2e-155 | 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 | |
NHNMODOO_02737 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
NHNMODOO_02738 | 2.4e-147 | rrmJ | 2.1.1.226, 2.1.1.227 | J | rRNA methylase | |
NHNMODOO_02739 | 1.3e-78 | argR | K | Regulates arginine biosynthesis genes | ||
NHNMODOO_02740 | 6.4e-291 | recN | L | May be involved in recombinational repair of damaged DNA | ||
NHNMODOO_02741 | 2.3e-237 | rseP | 3.4.21.116 | M | Stage IV sporulation protein B | |
NHNMODOO_02742 | 1.8e-142 | 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 | |||
NHNMODOO_02743 | 1.3e-107 | 2.7.8.33, 2.7.8.35 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | ||
NHNMODOO_02744 | 1e-34 | yqzF | S | Protein of unknown function (DUF2627) | ||
NHNMODOO_02745 | 0.0 | bkdR | KT | Transcriptional regulator | ||
NHNMODOO_02746 | 3.1e-206 | ldh | 1.4.1.9 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
NHNMODOO_02747 | 1.6e-258 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
NHNMODOO_02748 | 1.6e-185 | bfmBAA | 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
NHNMODOO_02749 | 6.9e-181 | bfmBAB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
NHNMODOO_02750 | 1.4e-221 | bfmBB | 2.3.1.168, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
NHNMODOO_02751 | 1.4e-74 | yqiW | S | Belongs to the UPF0403 family | ||
NHNMODOO_02752 | 2.3e-204 | dhaT | 1.1.1.1, 1.1.1.202 | C | alcohol dehydrogenase | |
NHNMODOO_02753 | 2.4e-11 | |||||
NHNMODOO_02754 | 9.2e-270 | cckA | 2.7.13.3 | T | GAF domain | |
NHNMODOO_02755 | 8.7e-273 | T | Sigma-54 interaction domain | |||
NHNMODOO_02756 | 6e-199 | adhA | 1.1.1.1 | C | alcohol dehydrogenase | |
NHNMODOO_02757 | 4.6e-277 | dhaS | 1.2.1.3, 1.2.1.39 | C | Belongs to the aldehyde dehydrogenase family | |
NHNMODOO_02758 | 2.7e-185 | 2.7.7.19, 2.7.7.72 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NHNMODOO_02760 | 4.1e-275 | adiA | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | Orn Lys Arg decarboxylase | |
NHNMODOO_02761 | 1.5e-115 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
NHNMODOO_02762 | 1.1e-53 | yaaQ | S | protein conserved in bacteria | ||
NHNMODOO_02763 | 9.7e-183 | holB | 2.7.7.7 | L | DNA polymerase III | |
NHNMODOO_02764 | 2.2e-143 | yaaT | S | stage 0 sporulation protein | ||
NHNMODOO_02765 | 8e-39 | yabA | L | Involved in initiation control of chromosome replication | ||
NHNMODOO_02766 | 3.9e-136 | yabB | 2.1.1.223 | S | Conserved hypothetical protein 95 | |
NHNMODOO_02767 | 3.7e-44 | yazA | L | endonuclease containing a URI domain | ||
NHNMODOO_02768 | 5.9e-160 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
NHNMODOO_02769 | 1.1e-43 | abrB | K | COG2002 Regulators of stationary sporulation gene expression | ||
NHNMODOO_02770 | 1.7e-176 | S | NurA | |||
NHNMODOO_02771 | 0.0 | S | Domain of unknown function DUF87 | |||
NHNMODOO_02772 | 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 | |
NHNMODOO_02773 | 5e-81 | K | DNA-binding transcription factor activity | |||
NHNMODOO_02774 | 1.8e-184 | pelB | 4.2.2.2 | G | Amb_all | |
NHNMODOO_02776 | 1e-282 | S | ABC transporter | |||
NHNMODOO_02777 | 8.6e-119 | T | protein histidine kinase activity | |||
NHNMODOO_02778 | 9e-269 | S | Protein of unknown function (DUF3298) | |||
NHNMODOO_02779 | 1.6e-148 | tatD | L | hydrolase, TatD | ||
NHNMODOO_02780 | 2e-215 | rpfB | GH23 | T | protein conserved in bacteria | |
NHNMODOO_02781 | 2.6e-115 | 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 | |
NHNMODOO_02782 | 6.3e-157 | 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 | |
NHNMODOO_02783 | 8.4e-162 | yabG | S | peptidase | ||
NHNMODOO_02784 | 1.2e-39 | veg | S | protein conserved in bacteria | ||
NHNMODOO_02785 | 3.3e-25 | sspF | S | DNA topological change | ||
NHNMODOO_02786 | 5.9e-163 | 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 | |
NHNMODOO_02787 | 6.6e-148 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
NHNMODOO_02788 | 1.6e-61 | yabJ | 3.5.99.10 | J | translation initiation inhibitor, yjgF family | |
NHNMODOO_02789 | 1.6e-48 | spoVG | D | Essential for sporulation. Interferes with or is a negative regulator of the pathway leading to asymmetric septation | ||
NHNMODOO_02791 | 5.2e-251 | 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 | |
NHNMODOO_02792 | 4.5e-169 | 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) | |
NHNMODOO_02793 | 1.3e-93 | 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 | ||
NHNMODOO_02794 | 1.4e-101 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
NHNMODOO_02795 | 3.1e-39 | yabK | S | Peptide ABC transporter permease | ||
NHNMODOO_02796 | 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 | ||
NHNMODOO_02797 | 1e-93 | spoVT | K | stage V sporulation protein | ||
NHNMODOO_02798 | 2.4e-97 | S | Yip1 domain | |||
NHNMODOO_02799 | 2.3e-198 | 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) |
NHNMODOO_02800 | 4.4e-88 | S | Yip1 domain | |||
NHNMODOO_02801 | 8.5e-266 | yabM | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
NHNMODOO_02802 | 1.8e-265 | mazG | 3.6.1.66, 3.6.1.9 | S | COG3956 Protein containing tetrapyrrole methyltransferase domain and MazG-like | |
NHNMODOO_02803 | 5.1e-19 | yabO | J | COG1188 Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
NHNMODOO_02804 | 1.1e-113 | S | hydrolase | |||
NHNMODOO_02805 | 2.1e-174 | ghrB | 1.1.1.215, 1.1.1.26, 1.1.1.43, 1.1.1.79, 1.1.1.81 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NHNMODOO_02806 | 2e-83 | 2.3.1.128 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
NHNMODOO_02807 | 3.6e-196 | ycgT | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
NHNMODOO_02808 | 1.9e-101 | MA20_20865 | 3.6.1.27 | S | SNARE associated Golgi protein | |
NHNMODOO_02809 | 1.3e-51 | yabP | S | Sporulation protein YabP | ||
NHNMODOO_02810 | 2.5e-66 | yabQ | S | spore cortex biosynthesis protein | ||
NHNMODOO_02811 | 8.2e-61 | divIC | D | Septum formation initiator | ||
NHNMODOO_02812 | 2.2e-70 | yabR | J | RNA binding protein (contains ribosomal protein S1 domain) | ||
NHNMODOO_02814 | 2e-223 | citM | C | Citrate transporter | ||
NHNMODOO_02815 | 0.0 | spoIIE | 3.1.3.16, 3.1.3.3 | KT | stage II sporulation protein E | |
NHNMODOO_02816 | 1.8e-128 | yabS | S | protein containing a von Willebrand factor type A (vWA) domain | ||
NHNMODOO_02817 | 1e-173 | KLT | serine threonine protein kinase | |||
NHNMODOO_02818 | 1.8e-262 | 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 | |
NHNMODOO_02819 | 3.9e-93 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
NHNMODOO_02820 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
NHNMODOO_02821 | 6.5e-142 | coaX | 2.7.1.33 | F | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
NHNMODOO_02822 | 1.1e-156 | 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 | ||
NHNMODOO_02823 | 3.3e-172 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
NHNMODOO_02824 | 2.8e-263 | pabB | 2.6.1.85 | 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 | |
NHNMODOO_02825 | 5.2e-107 | pabA | 2.6.1.85, 4.1.3.27 | EH | Anthranilate synthase | |
NHNMODOO_02826 | 1.1e-147 | pabC | 2.6.1.42, 4.1.3.38 | EH | 4-amino-4-deoxychorismate lyase | |
NHNMODOO_02827 | 1.6e-146 | 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 | |
NHNMODOO_02828 | 1.3e-60 | 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 | |
NHNMODOO_02829 | 1.3e-93 | 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 | |
NHNMODOO_02830 | 6.4e-190 | 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 | ||
NHNMODOO_02831 | 2.2e-287 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NHNMODOO_02833 | 1.5e-191 | 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 | ||
NHNMODOO_02834 | 1.1e-215 | E | Peptidase family M28 | |||
NHNMODOO_02835 | 5.3e-105 | GM | NmrA-like family | |||
NHNMODOO_02836 | 3.9e-177 | ytvI | S | AI-2E family transporter | ||
NHNMODOO_02837 | 5.3e-80 | copC | S | CopC domain | ||
NHNMODOO_02839 | 4.7e-194 | yhdY | M | Mechanosensitive ion channel | ||
NHNMODOO_02840 | 2e-183 | T | Metal dependent phosphohydrolases with conserved 'HD' motif. | |||
NHNMODOO_02841 | 1.5e-145 | S | Membrane transport protein | |||
NHNMODOO_02842 | 1.3e-75 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
NHNMODOO_02843 | 2.2e-221 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
NHNMODOO_02844 | 1.1e-211 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
NHNMODOO_02845 | 2.4e-37 | ykuS | S | Belongs to the UPF0180 family | ||
NHNMODOO_02846 | 7.9e-127 | ykuT | M | Mechanosensitive ion channel | ||
NHNMODOO_02847 | 4.7e-102 | ykuU | O | Alkyl hydroperoxide reductase | ||
NHNMODOO_02848 | 4.1e-83 | ykuV | CO | thiol-disulfide | ||
NHNMODOO_02849 | 1.1e-113 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
NHNMODOO_02850 | 0.0 | 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 | ||
NHNMODOO_02851 | 9.1e-30 | ykzG | S | Belongs to the UPF0356 family | ||
NHNMODOO_02852 | 3.7e-99 | 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 | |
NHNMODOO_02854 | 8.1e-69 | recN | L | Putative cell-wall binding lipoprotein | ||
NHNMODOO_02855 | 1.1e-201 | bkdA1 | 1.2.4.1, 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
NHNMODOO_02856 | 1.4e-178 | pdhB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
NHNMODOO_02857 | 2.6e-180 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
NHNMODOO_02858 | 2.2e-260 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
NHNMODOO_02859 | 2.8e-185 | oppD | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_02860 | 8e-185 | E | Belongs to the ABC transporter superfamily | |||
NHNMODOO_02861 | 0.0 | appA_2 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | ||
NHNMODOO_02862 | 6.8e-173 | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | |||
NHNMODOO_02863 | 2.3e-162 | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | |||
NHNMODOO_02864 | 8.5e-66 | CO | cell redox homeostasis | |||
NHNMODOO_02865 | 6.6e-277 | opuD | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
NHNMODOO_02866 | 1.4e-121 | pdaA_2 | 3.5.1.104 | G | Polysaccharide deacetylase | |
NHNMODOO_02867 | 1e-203 | legA | 3.5.1.2 | O | Peptidase family M48 | |
NHNMODOO_02868 | 4.6e-277 | speA | 4.1.1.19 | E | Arginine | |
NHNMODOO_02869 | 1.3e-38 | yktA | S | Belongs to the UPF0223 family | ||
NHNMODOO_02870 | 2.3e-113 | yktB | S | Belongs to the UPF0637 family | ||
NHNMODOO_02871 | 9.5e-152 | suhB | 3.1.3.25 | G | Inositol monophosphatase | |
NHNMODOO_02872 | 2.3e-162 | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | ||
NHNMODOO_02873 | 3.8e-11 | S | Family of unknown function (DUF5325) | |||
NHNMODOO_02874 | 0.0 | typA | T | GTP-binding protein TypA | ||
NHNMODOO_02875 | 3.3e-50 | ylaH | S | YlaH-like protein | ||
NHNMODOO_02876 | 3.2e-32 | ylaI | S | protein conserved in bacteria | ||
NHNMODOO_02877 | 3.9e-251 | phoH | T | ATPase related to phosphate starvation-inducible protein PhoH | ||
NHNMODOO_02878 | 1.6e-91 | 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 | ||
NHNMODOO_02879 | 9e-41 | ylaN | S | Belongs to the UPF0358 family | ||
NHNMODOO_02880 | 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 | |
NHNMODOO_02881 | 5.9e-158 | ctaA | 2.5.1.141 | O | Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group | |
NHNMODOO_02882 | 2.7e-199 | 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) | |
NHNMODOO_02883 | 0.0 | ctaD | 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 | |
NHNMODOO_02884 | 5.7e-104 | cyoC | 1.10.3.12, 1.9.3.1 | C | COG1845 Heme copper-type cytochrome quinol oxidase, subunit 3 | |
NHNMODOO_02885 | 1.8e-51 | ctaF | 1.10.3.12, 1.9.3.1 | C | COG3125 Heme copper-type cytochrome quinol oxidase, subunit 4 | |
NHNMODOO_02886 | 5.7e-92 | yozB | S | membrane | ||
NHNMODOO_02887 | 6.7e-84 | |||||
NHNMODOO_02888 | 6.1e-63 | ylbA | S | YugN-like family | ||
NHNMODOO_02889 | 7.3e-190 | ylbC | S | protein with SCP PR1 domains | ||
NHNMODOO_02890 | 6.6e-84 | yiiD | Q | protein, possibly involved in aromatic compounds catabolism | ||
NHNMODOO_02891 | 1.3e-70 | ylbD | S | Putative coat protein | ||
NHNMODOO_02892 | 1.2e-31 | ylbE | S | YlbE-like protein | ||
NHNMODOO_02893 | 1.5e-138 | rimK1 | HJ | Prokaryotic glutathione synthetase, ATP-grasp domain | ||
NHNMODOO_02894 | 2.2e-57 | ylbF | S | Belongs to the UPF0342 family | ||
NHNMODOO_02895 | 1.1e-46 | ylbG | S | UPF0298 protein | ||
NHNMODOO_02896 | 5.9e-64 | S | Methylthioribose kinase | |||
NHNMODOO_02897 | 6e-97 | rsmD | 2.1.1.171 | L | Methyltransferase | |
NHNMODOO_02898 | 2.8e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
NHNMODOO_02899 | 2.6e-214 | ylbJ | S | Sporulation integral membrane protein YlbJ | ||
NHNMODOO_02900 | 5.8e-138 | ylbK | S | esterase of the alpha-beta hydrolase superfamily | ||
NHNMODOO_02901 | 3.9e-190 | ylbL | T | Belongs to the peptidase S16 family | ||
NHNMODOO_02902 | 1.3e-221 | ylbM | S | Belongs to the UPF0348 family | ||
NHNMODOO_02903 | 6.4e-93 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
NHNMODOO_02904 | 1.3e-26 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
NHNMODOO_02905 | 3.6e-62 | S | SANT SWI3, ADA2, N-CoR and TFIIIB'' DNA-binding domains | |||
NHNMODOO_02906 | 5.2e-92 | ylbP | K | n-acetyltransferase | ||
NHNMODOO_02907 | 2.9e-146 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
NHNMODOO_02908 | 1e-10 | S | Protein of unknown function (DUF3397) | |||
NHNMODOO_02909 | 9.7e-305 | 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 | ||
NHNMODOO_02910 | 1.9e-153 | S | CAAX amino terminal protease family protein | |||
NHNMODOO_02911 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
NHNMODOO_02913 | 0.0 | V | ABC transporter (permease) | |||
NHNMODOO_02914 | 9.5e-141 | yvcR | V | ABC transporter, ATP-binding protein | ||
NHNMODOO_02915 | 8.2e-188 | yvcQ | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
NHNMODOO_02916 | 3.4e-129 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_02917 | 9.1e-29 | 3.1.3.48 | GM | protein tyrosine phosphatase activity | ||
NHNMODOO_02918 | 2.5e-49 | |||||
NHNMODOO_02919 | 8.8e-167 | gmuE | 2.7.1.2, 2.7.1.4 | GK | COG1940 Transcriptional regulator sugar kinase | |
NHNMODOO_02920 | 1.1e-308 | rocB | E | arginine degradation protein | ||
NHNMODOO_02921 | 1.5e-270 | mdr | EGP | Major facilitator Superfamily | ||
NHNMODOO_02923 | 3.7e-168 | Q | Exhibits S-adenosyl-L-methionine-dependent methyltransferase activity | |||
NHNMODOO_02924 | 2.9e-279 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
NHNMODOO_02925 | 2.9e-210 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
NHNMODOO_02926 | 2e-127 | lacR | K | DeoR C terminal sensor domain | ||
NHNMODOO_02927 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
NHNMODOO_02928 | 1.4e-184 | 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 | |
NHNMODOO_02929 | 6e-230 | G | ABC transporter substrate-binding protein | |||
NHNMODOO_02930 | 9.8e-158 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_02931 | 2.9e-154 | P | PFAM binding-protein-dependent transport systems inner membrane component | |||
NHNMODOO_02932 | 1.8e-59 | Z012_01525 | FJ | tRNA wobble adenosine to inosine editing | ||
NHNMODOO_02933 | 7.1e-13 | S | Inner spore coat protein D | |||
NHNMODOO_02934 | 1.8e-306 | M1-554 | G | Endonuclease Exonuclease Phosphatase | ||
NHNMODOO_02935 | 0.0 | ade | 3.5.4.2 | F | Adenine deaminase C-terminal domain | |
NHNMODOO_02936 | 3.7e-196 | potA11 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
NHNMODOO_02937 | 6.7e-134 | potC3 | P | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_02938 | 2.1e-138 | potB | E | COG1176 ABC-type spermidine putrescine transport system, permease component I | ||
NHNMODOO_02939 | 6e-166 | iunH3 | 3.2.2.1 | F | nucleoside hydrolase | |
NHNMODOO_02940 | 6.9e-195 | potD2 | E | COG0687 Spermidine putrescine-binding periplasmic protein | ||
NHNMODOO_02941 | 2.4e-56 | |||||
NHNMODOO_02942 | 2.4e-47 | |||||
NHNMODOO_02944 | 3.8e-162 | T | Belongs to the universal stress protein A family | |||
NHNMODOO_02945 | 2.8e-140 | rpl | K | Helix-turn-helix domain, rpiR family | ||
NHNMODOO_02946 | 1.2e-170 | pfkB | 2.7.1.11, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
NHNMODOO_02947 | 6.8e-230 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHNMODOO_02948 | 1.8e-75 | fruD | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
NHNMODOO_02949 | 4e-156 | kbaY | 4.1.2.13, 4.1.2.40 | G | in enteric bacteria there are two D-tagatose 1,6-bisphosphate-specific aldolases KbaY (also called AgaY), involved in catabolism of N-acetyl-galactosamine and D-galactosamine, and GatY which is part of the galactitol catabolism pathway | |
NHNMODOO_02950 | 4.7e-74 | |||||
NHNMODOO_02951 | 4.7e-85 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
NHNMODOO_02954 | 7.2e-69 | fabH | 2.3.1.180 | I | Chalcone and stilbene synthases, N-terminal domain | |
NHNMODOO_02955 | 1e-114 | K | Transcriptional regulator | |||
NHNMODOO_02956 | 2.4e-193 | V | COG0842 ABC-type multidrug transport system, permease component | |||
NHNMODOO_02957 | 2.3e-139 | V | COG1131 ABC-type multidrug transport system, ATPase component | |||
NHNMODOO_02958 | 3.9e-83 | M | PFAM secretion protein HlyD family protein | |||
NHNMODOO_02959 | 7.9e-205 | MA20_04465 | 4.2.3.1 | E | Pyridoxal-phosphate dependent enzyme | |
NHNMODOO_02960 | 2.4e-139 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
NHNMODOO_02961 | 9.5e-239 | KT | transcriptional regulatory protein | |||
NHNMODOO_02962 | 1.1e-259 | abgB | 3.5.1.47 | S | amidohydrolase | |
NHNMODOO_02963 | 2.1e-277 | abgT | H | AbgT putative transporter family | ||
NHNMODOO_02964 | 2.6e-236 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
NHNMODOO_02965 | 4.5e-68 | S | Putative glycolipid-binding | |||
NHNMODOO_02966 | 5.5e-23 | C | 4Fe-4S binding domain | |||
NHNMODOO_02967 | 6.3e-38 | S | Protein of unknown function (DUF1450) | |||
NHNMODOO_02968 | 4.3e-112 | sodA | 1.15.1.1 | P | Iron/manganese superoxide dismutases, C-terminal domain | |
NHNMODOO_02969 | 4.8e-114 | sufR | K | Transcriptional regulator | ||
NHNMODOO_02970 | 3e-249 | S | Polysaccharide biosynthesis protein | |||
NHNMODOO_02971 | 3.5e-146 | exoM | S | Glycosyl transferase family 2 | ||
NHNMODOO_02972 | 6.7e-193 | M | Glycosyl transferases group 1 | |||
NHNMODOO_02973 | 3.9e-54 | |||||
NHNMODOO_02974 | 1.4e-227 | M | -O-antigen | |||
NHNMODOO_02975 | 1.4e-251 | tuaD | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
NHNMODOO_02976 | 7.3e-68 | |||||
NHNMODOO_02977 | 1.6e-137 | tuaG | GT2 | M | Glycosyltransferase like family 2 | |
NHNMODOO_02978 | 1.6e-173 | tagO | 2.7.8.33, 2.7.8.35 | M | COG0472 UDP-N-acetylmuramyl pentapeptide phosphotransferase UDP-N-acetylglucosamine-1-phosphate transferase | |
NHNMODOO_02979 | 6.6e-176 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NHNMODOO_02981 | 2e-22 | |||||
NHNMODOO_02982 | 1.3e-33 | |||||
NHNMODOO_02983 | 2.9e-142 | pdaB | 3.5.1.104 | G | Polysaccharide deacetylase | |
NHNMODOO_02984 | 1.7e-100 | kbaA | 2.7.8.43 | S | Involved in the activation of the KinB signaling pathway of sporulation | |
NHNMODOO_02985 | 1.5e-58 | gerD | S | Spore gernimation protein | ||
NHNMODOO_02986 | 4.5e-93 | rpiR | K | transcriptional regulator, RpiR family | ||
NHNMODOO_02987 | 2.7e-171 | M1-530 | S | Protein of unknown function (DUF4127) | ||
NHNMODOO_02988 | 8.6e-73 | ywpJ_2 | S | Sucrose-6F-phosphate phosphohydrolase | ||
NHNMODOO_02989 | 9.3e-173 | 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 | |||
NHNMODOO_02990 | 2.8e-30 | licB | 2.7.1.196, 2.7.1.205 | G | PFAM Phosphotransferase system, lactose cellobiose-specific IIB subunit | |
NHNMODOO_02991 | 7.8e-75 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
NHNMODOO_02992 | 3.9e-21 | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | ||
NHNMODOO_02993 | 7.2e-192 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
NHNMODOO_02994 | 0.0 | ptsG | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NHNMODOO_02995 | 1.1e-150 | glcT | K | antiterminator | ||
NHNMODOO_02996 | 4.4e-132 | cwlD | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
NHNMODOO_02997 | 8.9e-80 | ybaK | S | Protein of unknown function (DUF2521) | ||
NHNMODOO_02998 | 5.7e-70 | guaA | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_03000 | 1.6e-29 | yozG | K | Transcriptional regulator | ||
NHNMODOO_03001 | 8.9e-82 | S | Protein of unknown function (DUF2975) | |||
NHNMODOO_03002 | 1.7e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
NHNMODOO_03003 | 4.4e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
NHNMODOO_03004 | 3.8e-145 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
NHNMODOO_03005 | 1.1e-133 | 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 | ||
NHNMODOO_03006 | 2e-144 | ecfA | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
NHNMODOO_03007 | 4.7e-157 | ecfA | 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 | ||
NHNMODOO_03008 | 4.7e-58 | rplQ | J | Ribosomal protein L17 | ||
NHNMODOO_03009 | 2.4e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NHNMODOO_03010 | 1.9e-65 | 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 | ||
NHNMODOO_03011 | 1.1e-57 | 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 | ||
NHNMODOO_03012 | 1.4e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
NHNMODOO_03013 | 1.1e-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 | ||
NHNMODOO_03014 | 4.1e-141 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
NHNMODOO_03015 | 8.6e-119 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
NHNMODOO_03016 | 1.8e-229 | 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 | ||
NHNMODOO_03017 | 3.3e-74 | rplO | J | binds to the 23S rRNA | ||
NHNMODOO_03018 | 2.7e-25 | rpmD | J | Ribosomal protein L30 | ||
NHNMODOO_03019 | 4e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
NHNMODOO_03020 | 1.3e-60 | 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 | ||
NHNMODOO_03021 | 4.9e-96 | 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 | ||
NHNMODOO_03022 | 1.3e-66 | 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 | ||
NHNMODOO_03023 | 2.3e-93 | 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 | ||
NHNMODOO_03024 | 6.8e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
NHNMODOO_03025 | 5.1e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
NHNMODOO_03026 | 3.5e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
NHNMODOO_03027 | 1.1e-27 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
NHNMODOO_03028 | 4.2e-77 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
NHNMODOO_03029 | 8.7e-119 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
NHNMODOO_03030 | 6.6e-54 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
NHNMODOO_03031 | 1.4e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
NHNMODOO_03032 | 2.2e-156 | 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 | ||
NHNMODOO_03033 | 2.3e-44 | 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 | ||
NHNMODOO_03034 | 1e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
NHNMODOO_03035 | 1.5e-109 | 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 | ||
NHNMODOO_03036 | 7.5e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
NHNMODOO_03037 | 4.7e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
NHNMODOO_03038 | 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 | ||
NHNMODOO_03039 | 9.3e-83 | 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 | ||
NHNMODOO_03040 | 3.9e-72 | 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 | ||
NHNMODOO_03041 | 5e-35 | rplGB | J | Belongs to the eukaryotic ribosomal protein eL8 family | ||
NHNMODOO_03042 | 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 | |
NHNMODOO_03043 | 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 | |
NHNMODOO_03044 | 2.6e-115 | rsmC | 2.1.1.172 | J | Methyltransferase | |
NHNMODOO_03045 | 3.2e-51 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
NHNMODOO_03046 | 3.5e-80 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
NHNMODOO_03047 | 9.4e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
NHNMODOO_03048 | 6.3e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
NHNMODOO_03049 | 8.4e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
NHNMODOO_03050 | 6.1e-25 | 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 | ||
NHNMODOO_03051 | 3.6e-117 | sigH | K | Belongs to the sigma-70 factor family | ||
NHNMODOO_03052 | 4.9e-85 | yacP | S | RNA-binding protein containing a PIN domain | ||
NHNMODOO_03053 | 1.2e-143 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NHNMODOO_03054 | 5.7e-68 | 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) | ||
NHNMODOO_03055 | 8.2e-268 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NHNMODOO_03056 | 9.3e-121 | cysE | 2.3.1.30 | E | Serine acetyltransferase | |
NHNMODOO_03057 | 6.9e-278 | 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) | |
NHNMODOO_03058 | 6.1e-82 | 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) | |
NHNMODOO_03059 | 1.9e-116 | 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) | |
NHNMODOO_03060 | 2e-197 | yacL | S | COG4956 Integral membrane protein (PIN domain superfamily) | ||
NHNMODOO_03061 | 2.7e-194 | disA | 2.7.7.85 | L | Has also diadenylate cyclase activity, catalyzing the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP). c- di-AMP acts as a signaling molecule that couples DNA integrity with progression of sporulation. The rise in c-di-AMP level generated by DisA while scanning the chromosome, operates as a positive signal that advances sporulation | |
NHNMODOO_03062 | 5.8e-250 | 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 | ||
NHNMODOO_03063 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
NHNMODOO_03064 | 2.4e-195 | 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 | |
NHNMODOO_03065 | 1.3e-93 | mcsA | 2.7.14.1 | S | protein with conserved CXXC pairs | |
NHNMODOO_03066 | 1.5e-72 | ctsR | K | Belongs to the CtsR family | ||
NHNMODOO_03067 | 7.8e-169 | yoaV3 | EG | EamA-like transporter family | ||
NHNMODOO_03068 | 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 | ||
NHNMODOO_03069 | 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 | ||
NHNMODOO_03070 | 9e-150 | yvlB | S | Putative adhesin | ||
NHNMODOO_03071 | 8.8e-11 | pspC | KT | positive regulation of macromolecule biosynthetic process | ||
NHNMODOO_03072 | 9.3e-48 | yvlD | S | Membrane | ||
NHNMODOO_03073 | 6.2e-171 | 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 | ||
NHNMODOO_03074 | 7.2e-147 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
NHNMODOO_03075 | 8.5e-160 | yvoD | P | COG0370 Fe2 transport system protein B | ||
NHNMODOO_03076 | 1.3e-116 | 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 | |
NHNMODOO_03077 | 1.3e-71 | yvoF | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | ||
NHNMODOO_03078 | 3.2e-217 | 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 | |
NHNMODOO_03079 | 9e-113 | 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 | |
NHNMODOO_03080 | 3.5e-225 | 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 | |
NHNMODOO_03081 | 1e-107 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
NHNMODOO_03082 | 3.6e-114 | 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 | ||
NHNMODOO_03083 | 7.7e-129 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
NHNMODOO_03084 | 2.6e-135 | 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 | ||
NHNMODOO_03085 | 8.1e-111 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | belongs to the PRA-CH family | |
NHNMODOO_03086 | 4.9e-126 | yobR | 2.3.1.1 | K | FR47-like protein | |
NHNMODOO_03087 | 3.4e-41 | rhaS5 | K | AraC-like ligand binding domain | ||
NHNMODOO_03088 | 2.2e-90 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
NHNMODOO_03089 | 1.1e-234 | cypC | 1.11.2.4, 1.14.14.1 | Q | Cytochrome P450 | |
NHNMODOO_03090 | 3.8e-193 | S | COG0457 FOG TPR repeat | |||
NHNMODOO_03091 | 3.8e-176 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
NHNMODOO_03092 | 1.1e-89 | yvcI | 3.6.1.55 | F | Nudix hydrolase | |
NHNMODOO_03093 | 5.2e-167 | rapZ | S | Displays ATPase and GTPase activities | ||
NHNMODOO_03094 | 4e-176 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
NHNMODOO_03095 | 1.2e-177 | whiA | K | May be required for sporulation | ||
NHNMODOO_03096 | 2.4e-37 | crh | G | Phosphocarrier protein Chr | ||
NHNMODOO_03097 | 8.7e-111 | opuCD | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
NHNMODOO_03098 | 4.1e-167 | opuCC | M | COG1732 Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
NHNMODOO_03099 | 2.5e-107 | opuCB | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
NHNMODOO_03100 | 1.8e-213 | opuCA | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
NHNMODOO_03101 | 1.5e-56 | S | Domain of unknown function (DUF4870) | |||
NHNMODOO_03102 | 2.2e-229 | E | Peptidase dimerisation domain | |||
NHNMODOO_03103 | 8.8e-74 | EGP | Major facilitator Superfamily | |||
NHNMODOO_03104 | 2.6e-46 | EGP | Major facilitator Superfamily | |||
NHNMODOO_03105 | 1.5e-15 | K | Transcriptional regulator | |||
NHNMODOO_03106 | 4.5e-103 | 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 | |
NHNMODOO_03108 | 6.7e-235 | rpoN | K | COG1508 DNA-directed RNA polymerase specialized sigma subunit, sigma54 homolog | ||
NHNMODOO_03109 | 5.8e-39 | XAC3035 | O | Has a glutathione-disulfide oxidoreductase activity in the presence of NADPH and glutathione reductase. Reduces low molecular weight disulfides and proteins | ||
NHNMODOO_03111 | 2.1e-202 | S | response regulator aspartate phosphatase | |||
NHNMODOO_03112 | 7.9e-180 | cggR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
NHNMODOO_03113 | 1.5e-186 | gapA | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
NHNMODOO_03114 | 4e-215 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
NHNMODOO_03115 | 4.1e-133 | 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) | |
NHNMODOO_03116 | 2.1e-296 | gpmI | 5.4.2.12 | G | Catalyzes the interconversion of 2-phosphoglycerate and | |
NHNMODOO_03117 | 4.3e-239 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
NHNMODOO_03118 | 6.6e-117 | MA20_15070 | K | FCD | ||
NHNMODOO_03119 | 1.4e-170 | dapAf2 | 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
NHNMODOO_03120 | 4.7e-266 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |||
NHNMODOO_03121 | 3e-223 | 4.2.1.158 | M | Mandelate racemase / muconate lactonizing enzyme, N-terminal domain | ||
NHNMODOO_03122 | 1e-163 | S | Tripartite tricarboxylate transporter family receptor | |||
NHNMODOO_03123 | 8.8e-73 | S | Tripartite tricarboxylate transporter TctB family | |||
NHNMODOO_03124 | 2.6e-264 | S | Tripartite tricarboxylate transporter TctA family | |||
NHNMODOO_03125 | 3.3e-77 | yclD | ||||
NHNMODOO_03126 | 1.2e-27 | secG | U | Preprotein translocase subunit SecG | ||
NHNMODOO_03127 | 8e-177 | yceB | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
NHNMODOO_03128 | 1.7e-136 | S | COG1647 Esterase lipase | |||
NHNMODOO_03129 | 2.5e-138 | est | 3.1.1.1 | S | Carboxylesterase | |
NHNMODOO_03130 | 0.0 | rnr | K | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
NHNMODOO_03131 | 1.8e-58 | mhqP | S | DoxX | ||
NHNMODOO_03132 | 3.1e-64 | L | Transposase | |||
NHNMODOO_03133 | 5.1e-81 | smpB | O | Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene | ||
NHNMODOO_03136 | 5e-51 | S | amino acid activation for nonribosomal peptide biosynthetic process | |||
NHNMODOO_03137 | 7.7e-264 | ydbT | S | Bacterial PH domain | ||
NHNMODOO_03138 | 1.9e-86 | S | Bacterial PH domain | |||
NHNMODOO_03139 | 1.6e-135 | S | CAAX protease self-immunity | |||
NHNMODOO_03141 | 2.1e-249 | celF | 3.2.1.86 | GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
NHNMODOO_03142 | 1.7e-45 | |||||
NHNMODOO_03143 | 1.9e-223 | 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 | |||
NHNMODOO_03144 | 2.3e-50 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
NHNMODOO_03145 | 2.8e-49 | celC | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
NHNMODOO_03146 | 1.5e-208 | ybhE | S | Bacterial protein of unknown function (DUF871) | ||
NHNMODOO_03147 | 6.4e-152 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
NHNMODOO_03148 | 4e-164 | K | Transcriptional regulator | |||
NHNMODOO_03150 | 3.5e-291 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
NHNMODOO_03151 | 1.5e-156 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03152 | 2.2e-165 | EP | N-terminal TM domain of oligopeptide transport permease C | |||
NHNMODOO_03153 | 8.8e-184 | oppD | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_03154 | 3.4e-194 | E | Belongs to the ABC transporter superfamily | |||
NHNMODOO_03155 | 4.3e-225 | E | Peptidase family M28 | |||
NHNMODOO_03156 | 4.7e-236 | P | Sodium:sulfate symporter transmembrane region | |||
NHNMODOO_03157 | 1.5e-219 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
NHNMODOO_03158 | 6.6e-226 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
NHNMODOO_03159 | 2.3e-87 | |||||
NHNMODOO_03161 | 5.5e-189 | P | Bacterial extracellular solute-binding protein | |||
NHNMODOO_03162 | 6.3e-199 | fbpC2 | 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 | |
NHNMODOO_03163 | 6.2e-291 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03164 | 5.4e-303 | 2.7.13.3 | T | Histidine kinase | ||
NHNMODOO_03165 | 8.6e-139 | T | helix_turn_helix, arabinose operon control protein | |||
NHNMODOO_03166 | 8e-202 | S | response regulator aspartate phosphatase | |||
NHNMODOO_03167 | 5.5e-127 | puuD | 4.1.3.27 | S | Peptidase C26 | |
NHNMODOO_03168 | 6.3e-149 | 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 | |
NHNMODOO_03169 | 1.4e-33 | |||||
NHNMODOO_03170 | 3.3e-37 | |||||
NHNMODOO_03171 | 1.5e-152 | S | response regulator aspartate phosphatase | |||
NHNMODOO_03172 | 1.3e-207 | S | Protein of unknown function (DUF418) | |||
NHNMODOO_03173 | 2e-14 | |||||
NHNMODOO_03174 | 2.6e-28 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_03175 | 6.3e-162 | S | Belongs to the pirin family | |||
NHNMODOO_03176 | 1.2e-58 | hxlR | K | HxlR-like helix-turn-helix | ||
NHNMODOO_03177 | 7.1e-245 | F | Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine | |||
NHNMODOO_03178 | 8.3e-170 | aadK | G | Streptomycin adenylyltransferase | ||
NHNMODOO_03179 | 2.8e-173 | cat | P | Catalase | ||
NHNMODOO_03180 | 1.4e-40 | S | Protein of unknown function (DUF2642) | |||
NHNMODOO_03183 | 2.2e-204 | S | response regulator aspartate phosphatase | |||
NHNMODOO_03184 | 6e-132 | K | Transcriptional regulator | |||
NHNMODOO_03185 | 2.1e-188 | G | COG1638 TRAP-type C4-dicarboxylate transport system, periplasmic component | |||
NHNMODOO_03186 | 4.6e-83 | dctQ1 | G | Tripartite ATP-independent periplasmic transporters, DctQ component | ||
NHNMODOO_03187 | 3.4e-215 | siaT_2 | G | Tripartite ATP-independent periplasmic transporter, DctM component | ||
NHNMODOO_03188 | 1.9e-138 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHNMODOO_03189 | 1.3e-92 | S | DNA-binding protein with PD1-like DNA-binding motif | |||
NHNMODOO_03190 | 9.8e-280 | MA20_41335 | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
NHNMODOO_03191 | 3.3e-203 | 2.3.1.16, 2.3.1.9 | I | Thiolase, C-terminal domain | ||
NHNMODOO_03192 | 7.1e-47 | S | DUF35 OB-fold domain, acyl-CoA-associated | |||
NHNMODOO_03193 | 4.6e-238 | yoaB | EGP | Major facilitator Superfamily | ||
NHNMODOO_03194 | 6.4e-212 | 1.1.1.14 | E | Dehydrogenase | ||
NHNMODOO_03195 | 4.2e-133 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_03196 | 4e-134 | K | DeoR C terminal sensor domain | |||
NHNMODOO_03197 | 9.4e-80 | rpiB | 5.3.1.34, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
NHNMODOO_03198 | 1.9e-186 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
NHNMODOO_03199 | 5.4e-110 | dhaL | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | S | Dak2 | |
NHNMODOO_03200 | 4e-173 | glpX | 2.2.1.1, 3.1.3.11, 3.1.3.37 | G | Bacterial fructose-1,6-bisphosphatase, glpX-encoded | |
NHNMODOO_03201 | 1.3e-80 | |||||
NHNMODOO_03202 | 2.7e-114 | UW | nuclease activity | |||
NHNMODOO_03208 | 2.7e-94 | ogt | 2.1.1.63, 3.2.2.21 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
NHNMODOO_03209 | 2.7e-106 | adaA | 3.2.2.21 | K | Transcriptional regulator | |
NHNMODOO_03210 | 8.2e-168 | alkA | 3.2.2.21 | L | COG0122 3-methyladenine DNA glycosylase 8-oxoguanine DNA glycosylase | |
NHNMODOO_03211 | 2.7e-210 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NHNMODOO_03212 | 7e-170 | 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) | |
NHNMODOO_03213 | 2.4e-147 | yidA | S | hydrolases of the HAD superfamily | ||
NHNMODOO_03214 | 8.6e-87 | S | DinB family | |||
NHNMODOO_03215 | 3.3e-161 | K | WYL domain | |||
NHNMODOO_03216 | 2e-100 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
NHNMODOO_03217 | 1.4e-125 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHNMODOO_03218 | 3.6e-185 | 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) | |
NHNMODOO_03220 | 1.7e-111 | yhcZ | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
NHNMODOO_03221 | 4.6e-205 | yhcY | 2.7.13.3 | T | Histidine kinase | |
NHNMODOO_03222 | 2.1e-38 | |||||
NHNMODOO_03224 | 7.5e-112 | KLT | serine threonine protein kinase | |||
NHNMODOO_03225 | 5.7e-86 | K | Transcriptional regulator | |||
NHNMODOO_03226 | 1.5e-140 | 3.1.26.11 | S | Metallo-beta-lactamase superfamily | ||
NHNMODOO_03227 | 1.7e-108 | 4.1.2.14, 4.1.3.42 | G | 2-dehydro-3-deoxy-phosphogluconate aldolase | ||
NHNMODOO_03228 | 3.8e-20 | K | sequence-specific DNA binding | |||
NHNMODOO_03230 | 2.8e-11 | |||||
NHNMODOO_03231 | 4.5e-133 | |||||
NHNMODOO_03232 | 1.5e-121 | yhcG | V | ABC transporter, ATP-binding protein | ||
NHNMODOO_03233 | 7.3e-62 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
NHNMODOO_03235 | 7.2e-123 | |||||
NHNMODOO_03236 | 2.9e-159 | S | NYN domain | |||
NHNMODOO_03237 | 4.8e-52 | K | sequence-specific DNA binding | |||
NHNMODOO_03238 | 6.7e-21 | K | sequence-specific DNA binding | |||
NHNMODOO_03239 | 1.3e-274 | 3.2.1.52 | G | Belongs to the glycosyl hydrolase 3 family | ||
NHNMODOO_03240 | 7.9e-244 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_03241 | 4.3e-161 | araP | G | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_03242 | 3.4e-155 | araQ | P | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_03243 | 1.8e-201 | msmX | E | ABC transporter | ||
NHNMODOO_03244 | 6.5e-101 | |||||
NHNMODOO_03246 | 7e-181 | scrR | K | transcriptional | ||
NHNMODOO_03247 | 4.3e-175 | lplB7 | G | COG4209 ABC-type polysaccharide transport system, permease component | ||
NHNMODOO_03248 | 1.5e-161 | lplC7 | G | COG0395 ABC-type sugar transport system, permease component | ||
NHNMODOO_03249 | 0.0 | lplA5 | G | Bacterial extracellular solute-binding protein | ||
NHNMODOO_03250 | 0.0 | sacC | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
NHNMODOO_03251 | 3.1e-289 | cscA | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
NHNMODOO_03252 | 2.3e-128 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHNMODOO_03253 | 2.5e-215 | yaaH | M | Glycoside Hydrolase Family | ||
NHNMODOO_03254 | 1.2e-26 | |||||
NHNMODOO_03255 | 7.7e-97 | pncA | Q | COG1335 Amidases related to nicotinamidase | ||
NHNMODOO_03256 | 1.5e-112 | ymaB | S | MutT family | ||
NHNMODOO_03257 | 3.4e-191 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NHNMODOO_03258 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NHNMODOO_03259 | 3.9e-63 | nrdI | 1.17.4.1 | F | Probably involved in ribonucleotide reductase function | |
NHNMODOO_03260 | 1.3e-129 | E | lipolytic protein G-D-S-L family | |||
NHNMODOO_03261 | 2e-194 | exoA | M | Glycosyltransferase like family 2 | ||
NHNMODOO_03262 | 1.5e-250 | wcaJ | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
NHNMODOO_03263 | 1.5e-230 | tagF | 2.7.8.12 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
NHNMODOO_03264 | 4.9e-134 | 2.7.8.34 | I | CDP-alcohol phosphatidyltransferase | ||
NHNMODOO_03265 | 9e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Cytidylyltransferase | |
NHNMODOO_03266 | 0.0 | tagF | 2.7.8.12 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
NHNMODOO_03267 | 4e-276 | M | Glycosyltransferase like family 2 | |||
NHNMODOO_03268 | 2.6e-163 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NHNMODOO_03269 | 6.6e-50 | atl | 3.2.1.96, 3.4.17.14, 3.5.1.28, 6.1.1.12 | GH73 | G | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase |
NHNMODOO_03270 | 5.3e-176 | S | Phosphotransferase system, EIIC | |||
NHNMODOO_03271 | 4.5e-131 | 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 | |
NHNMODOO_03272 | 1.1e-92 | tag | 3.2.2.20 | L | Methyladenine glycosylase | |
NHNMODOO_03273 | 6.3e-128 | |||||
NHNMODOO_03274 | 9.1e-95 | 3.4.21.89 | U | Signal peptidase | ||
NHNMODOO_03275 | 0.0 | vpr | O | Belongs to the peptidase S8 family | ||
NHNMODOO_03276 | 8.6e-153 | hisJ3 | 3.1.3.15 | E | PHP domain | |
NHNMODOO_03277 | 4.5e-183 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
NHNMODOO_03278 | 6.8e-113 | 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 | |
NHNMODOO_03279 | 2.7e-119 | |||||
NHNMODOO_03280 | 1.1e-195 | yetN | S | Protein of unknown function (DUF3900) | ||
NHNMODOO_03281 | 3.9e-185 | cdaR | KT | Sugar diacid utilization regulator | ||
NHNMODOO_03282 | 1.6e-200 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
NHNMODOO_03283 | 7.1e-80 | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | |||
NHNMODOO_03284 | 9.6e-146 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
NHNMODOO_03285 | 1.6e-79 | yvbK | 3.1.3.25 | K | acetyltransferase | |
NHNMODOO_03286 | 2.4e-242 | aspT | EK | Alanine-glyoxylate amino-transferase | ||
NHNMODOO_03287 | 2.7e-88 | 3.1.1.29 | K | -acetyltransferase | ||
NHNMODOO_03288 | 3e-54 | |||||
NHNMODOO_03289 | 1.8e-75 | K | transcriptional | |||
NHNMODOO_03290 | 8.1e-188 | mgtE | P | Acts as a magnesium transporter | ||
NHNMODOO_03291 | 3.4e-106 | desR | T | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
NHNMODOO_03292 | 1.2e-189 | desK | 2.7.13.3 | T | Histidine kinase | |
NHNMODOO_03293 | 1.1e-192 | des | 1.14.19.23, 1.14.19.45 | I | fatty acid desaturase | |
NHNMODOO_03294 | 1.6e-168 | agpT | K | AraC-like ligand binding domain | ||
NHNMODOO_03295 | 4.6e-249 | melA | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase |
NHNMODOO_03296 | 5.8e-108 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
NHNMODOO_03297 | 2.7e-100 | yvrI | K | RNA polymerase | ||
NHNMODOO_03298 | 1.7e-38 | |||||
NHNMODOO_03299 | 3.9e-159 | U | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03300 | 8.2e-171 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03301 | 1.5e-220 | T | cheY-homologous receiver domain | |||
NHNMODOO_03302 | 6.3e-299 | 2.7.13.3 | T | Histidine kinase | ||
NHNMODOO_03303 | 0.0 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_03304 | 4.9e-123 | ywiC | S | YwiC-like protein | ||
NHNMODOO_03306 | 3.2e-270 | narK | P | COG2223 Nitrate nitrite transporter | ||
NHNMODOO_03307 | 5e-111 | nreC | T | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
NHNMODOO_03308 | 1.4e-195 | nreB | 2.7.13.3 | T | Member of the two-component regulatory system DegS DegU, which plays an important role in the transition growth phase | |
NHNMODOO_03309 | 2.7e-82 | ptsP | 2.7.13.3, 2.7.3.9 | T | phosphoenolpyruvate-protein phosphotransferase activity | |
NHNMODOO_03310 | 1.7e-125 | narI | 1.7.5.1 | C | nitrate reductase, gamma subunit | |
NHNMODOO_03311 | 4.2e-115 | narJ | C | Nitrate reductase delta subunit | ||
NHNMODOO_03312 | 0.0 | narH | 1.7.5.1 | C | Nitrate reductase, beta | |
NHNMODOO_03313 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NHNMODOO_03314 | 4.2e-79 | scdA | D | Di-iron-containing protein involved in the repair of iron-sulfur clusters | ||
NHNMODOO_03315 | 3.3e-233 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
NHNMODOO_03316 | 9.9e-283 | ptsG | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NHNMODOO_03317 | 1e-114 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
NHNMODOO_03318 | 3.7e-140 | K | Helix-turn-helix domain, rpiR family | |||
NHNMODOO_03319 | 1.8e-87 | K | Transcriptional regulator PadR-like family | |||
NHNMODOO_03320 | 0.0 | Q | FtsX-like permease family | |||
NHNMODOO_03321 | 3.5e-129 | lolD-2 | V | COG1136 ABC-type antimicrobial peptide transport system, ATPase component | ||
NHNMODOO_03323 | 5.7e-19 | |||||
NHNMODOO_03325 | 1e-15 | |||||
NHNMODOO_03326 | 4.7e-170 | glcA | G | Glycoside hydrolase family 16 | ||
NHNMODOO_03327 | 8.2e-119 | dck | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxycytidine kinase | |
NHNMODOO_03328 | 3.6e-106 | dgk | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxyguanosine kinase | |
NHNMODOO_03329 | 3e-220 | patB | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
NHNMODOO_03331 | 7.9e-85 | ywpF | S | YwpF-like protein | ||
NHNMODOO_03332 | 1.2e-222 | ymfD | EGP | Major facilitator Superfamily | ||
NHNMODOO_03333 | 3.3e-83 | ytkD | 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
NHNMODOO_03334 | 5.5e-136 | ytlD | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
NHNMODOO_03335 | 6.2e-137 | ytlC | P | ABC transporter | ||
NHNMODOO_03336 | 1.1e-178 | ytlA | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
NHNMODOO_03337 | 7.3e-149 | ytmA | E | COG1506 Dipeptidyl aminopeptidases acylaminoacyl-peptidases | ||
NHNMODOO_03338 | 1.2e-304 | 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 | |
NHNMODOO_03339 | 5.1e-226 | 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 | |
NHNMODOO_03340 | 8.5e-64 | ytoA | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
NHNMODOO_03341 | 3.9e-150 | ytpA | 3.1.1.5 | I | Alpha beta hydrolase | |
NHNMODOO_03342 | 1.7e-105 | 4.2.1.1 | P | Reversible hydration of carbon dioxide | ||
NHNMODOO_03343 | 6.1e-100 | ytqB | J | Putative rRNA methylase | ||
NHNMODOO_03345 | 1.2e-190 | yttB | EGP | Major facilitator Superfamily | ||
NHNMODOO_03346 | 1e-173 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
NHNMODOO_03347 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NHNMODOO_03348 | 1.5e-236 | 3.5.1.47 | S | amidohydrolase | ||
NHNMODOO_03349 | 8.2e-132 | S | Protein of unknown function (DUF3100) | |||
NHNMODOO_03350 | 2.1e-77 | S | An automated process has identified a potential problem with this gene model | |||
NHNMODOO_03351 | 1.7e-36 | |||||
NHNMODOO_03352 | 5.2e-205 | ytfP | S | HI0933-like protein | ||
NHNMODOO_03353 | 1.1e-225 | yhaA1 | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
NHNMODOO_03354 | 1.2e-67 | yugU | S | Uncharacterised protein family UPF0047 | ||
NHNMODOO_03355 | 1.7e-162 | yvrE | G | SMP-30/Gluconolaconase/LRE-like region | ||
NHNMODOO_03356 | 1e-282 | ytgP | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
NHNMODOO_03357 | 1.5e-195 | ftsW | D | Belongs to the SEDS family | ||
NHNMODOO_03358 | 1.9e-209 | rodA | D | Belongs to the SEDS family | ||
NHNMODOO_03359 | 1.5e-132 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NHNMODOO_03360 | 1.5e-30 | ytzE | K | COG1349 Transcriptional regulators of sugar metabolism | ||
NHNMODOO_03361 | 4.3e-71 | 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 | |
NHNMODOO_03362 | 1.4e-162 | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | |||
NHNMODOO_03363 | 7.9e-160 | ydeE | K | AraC family transcriptional regulator | ||
NHNMODOO_03364 | 7.1e-167 | ytkP | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
NHNMODOO_03365 | 3.7e-102 | ligT | 3.1.4.58, 3.5.1.42 | J | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | |
NHNMODOO_03366 | 8.6e-61 | cidA | S | Increases the activity of extracellular murein hydrolases possibly by mediating their export via hole formation. Inhibited by the antiholin-like proteins LrgAB. In an unstressed cell, the LrgAB products probably inhibit the function of the CidA protein. When a cell is stressed by the addition of antibiotics or by other factors in the environment, CidA possibly oligomerizes within the bacterial cell membrane, creating lesions that disrupt the proton motive force, which in turn results in loss of cell viability. These lesions are also hypothesized to regulate the subsequent cell lysis by either allowing the murein hydrolases access to the cell wall substrate and or regulating their activity by a | ||
NHNMODOO_03367 | 3.4e-97 | lrgB | M | effector of murein hydrolase | ||
NHNMODOO_03368 | 0.0 | acoR | KQ | COG3284 Transcriptional activator of acetoin glycerol metabolism | ||
NHNMODOO_03369 | 1e-206 | 1.8.1.4 | C | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
NHNMODOO_03370 | 1.4e-175 | acoA | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | ||
NHNMODOO_03371 | 4.2e-192 | acoB | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | ||
NHNMODOO_03372 | 4.9e-192 | acoC | 2.3.1.12, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
NHNMODOO_03373 | 6.3e-51 | S | PFAM Uncharacterised protein family UPF0150 | |||
NHNMODOO_03374 | 1.8e-125 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_03375 | 7.5e-163 | purU | 2.7.7.72, 3.5.1.10 | F | Catalyzes the hydrolysis of 10-formyltetrahydrofolate (formyl-FH4) to formate and tetrahydrofolate (FH4) | |
NHNMODOO_03376 | 1.1e-152 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
NHNMODOO_03377 | 6.3e-14 | S | YtzH-like protein | |||
NHNMODOO_03378 | 6.4e-119 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
NHNMODOO_03379 | 8.2e-48 | ytzB | ||||
NHNMODOO_03380 | 3.1e-206 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
NHNMODOO_03381 | 2e-86 | 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 | ||
NHNMODOO_03382 | 6.1e-76 | ytoQ | S | Nucleoside 2-deoxyribosyltransferase YtoQ | ||
NHNMODOO_03383 | 2.2e-113 | S | Phosphotransferase system, EIIC | |||
NHNMODOO_03384 | 6.7e-56 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
NHNMODOO_03385 | 1.3e-145 | ytpQ | S | Belongs to the UPF0354 family | ||
NHNMODOO_03386 | 1.6e-103 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NHNMODOO_03387 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
NHNMODOO_03388 | 6.5e-251 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
NHNMODOO_03389 | 4e-44 | abrB | K | SpoVT / AbrB like domain | ||
NHNMODOO_03390 | 1.2e-213 | Q | COG1228 Imidazolonepropionase and related amidohydrolases | |||
NHNMODOO_03392 | 3.5e-117 | ung2 | 3.2.2.27 | L | Uracil DNA glycosylase superfamily | |
NHNMODOO_03393 | 3.8e-207 | dadA | 1.4.5.1 | E | COG0665 Glycine D-amino acid oxidases (deaminating) | |
NHNMODOO_03394 | 2.2e-128 | S | Peptidase C26 | |||
NHNMODOO_03395 | 5e-268 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
NHNMODOO_03396 | 3.8e-76 | S | DinB family | |||
NHNMODOO_03397 | 1e-165 | pstS | P | Phosphate | ||
NHNMODOO_03398 | 6.4e-160 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
NHNMODOO_03399 | 9.4e-161 | pstA | P | Phosphate transport system permease | ||
NHNMODOO_03400 | 7.1e-147 | 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 | |
NHNMODOO_03401 | 1.4e-144 | 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 | |
NHNMODOO_03402 | 6.1e-109 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
NHNMODOO_03403 | 7.8e-61 | |||||
NHNMODOO_03404 | 0.0 | addB | 3.6.4.12 | L | exonuclease activity | |
NHNMODOO_03405 | 0.0 | recB | 3.1.11.5, 3.1.12.1, 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
NHNMODOO_03406 | 0.0 | cheA | 2.7.13.3 | NT | COG0643 Chemotaxis protein histidine kinase and related kinases | |
NHNMODOO_03407 | 2.9e-67 | cheW | NT | chemotaxis | ||
NHNMODOO_03408 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
NHNMODOO_03409 | 4.7e-48 | S | IDEAL | |||
NHNMODOO_03410 | 5.2e-153 | ykgA | E | Amidinotransferase | ||
NHNMODOO_03411 | 7.4e-283 | mmdA | 2.1.3.15, 6.4.1.3 | I | COG4799 Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
NHNMODOO_03412 | 5.4e-90 | |||||
NHNMODOO_03413 | 1.1e-62 | ytwF | P | Sulfurtransferase | ||
NHNMODOO_03414 | 3.3e-40 | |||||
NHNMODOO_03415 | 2.6e-146 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
NHNMODOO_03416 | 1.8e-145 | yitT | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
NHNMODOO_03417 | 2.3e-31 | ipi | S | Intracellular proteinase inhibitor | ||
NHNMODOO_03419 | 0.0 | ywqA | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
NHNMODOO_03420 | 4.6e-214 | ywqB | S | zinc ion binding | ||
NHNMODOO_03421 | 1.4e-107 | |||||
NHNMODOO_03422 | 1.8e-78 | MA20_02285 | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
NHNMODOO_03423 | 3.4e-149 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
NHNMODOO_03424 | 9.7e-166 | ctaG | S | cytochrome c oxidase | ||
NHNMODOO_03425 | 4.4e-194 | 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 | |
NHNMODOO_03426 | 8.3e-224 | 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 | |
NHNMODOO_03427 | 3.7e-129 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
NHNMODOO_03428 | 4.3e-214 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
NHNMODOO_03429 | 1.7e-209 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
NHNMODOO_03430 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase ammonia chain | |
NHNMODOO_03431 | 1e-168 | 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 | |
NHNMODOO_03432 | 4.2e-116 | yjaU | I | carboxylic ester hydrolase activity | ||
NHNMODOO_03433 | 3.9e-148 | 5.1.3.2 | GM | RmlD substrate binding domain | ||
NHNMODOO_03434 | 6.6e-306 | 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 | ||
NHNMODOO_03435 | 1.4e-13 | comZ | S | ComZ | ||
NHNMODOO_03437 | 1.1e-167 | 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 | |
NHNMODOO_03438 | 7.8e-230 | 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 | |
NHNMODOO_03439 | 0.0 | cca | 2.7.7.19, 2.7.7.72, 3.1.13.3, 3.1.3.7 | J | Poly A polymerase head domain | |
NHNMODOO_03441 | 2.3e-102 | 3.5.1.28 | M | Cell Wall Hydrolase | ||
NHNMODOO_03442 | 3.9e-107 | J | protein with SCP PR1 domains | |||
NHNMODOO_03443 | 2.4e-178 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
NHNMODOO_03444 | 6.9e-136 | ywaC | 2.7.6.5 | S | protein conserved in bacteria | |
NHNMODOO_03445 | 1.7e-153 | yjaZ | O | Zn-dependent protease | ||
NHNMODOO_03446 | 2.9e-139 | yjbA | S | Belongs to the UPF0736 family | ||
NHNMODOO_03447 | 2.7e-10 | |||||
NHNMODOO_03448 | 2.2e-76 | K | Acetyltransferase (GNAT) domain | |||
NHNMODOO_03449 | 1.1e-166 | yhbB | S | Putative amidase domain | ||
NHNMODOO_03450 | 6.3e-87 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
NHNMODOO_03451 | 4.3e-87 | yufK | S | Family of unknown function (DUF5366) | ||
NHNMODOO_03452 | 2.8e-51 | hmoB | 1.14.99.48, 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | |
NHNMODOO_03453 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin-binding Protein |
NHNMODOO_03454 | 0.0 | prkA | T | Ser protein kinase | ||
NHNMODOO_03455 | 6.3e-86 | sipV | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NHNMODOO_03456 | 2.4e-101 | sipV | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NHNMODOO_03457 | 1.1e-138 | cysA1 | S | AAA domain | ||
NHNMODOO_03458 | 6.7e-215 | yhbH | S | Belongs to the UPF0229 family | ||
NHNMODOO_03461 | 2.3e-141 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_03462 | 4.7e-266 | EGP | Major facilitator Superfamily | |||
NHNMODOO_03463 | 1.1e-173 | drrA | V | COG1131 ABC-type multidrug transport system, ATPase component | ||
NHNMODOO_03464 | 1.6e-146 | drrB | V | Transport permease protein | ||
NHNMODOO_03466 | 2e-80 | S | Protein of unknown function (DUF664) | |||
NHNMODOO_03467 | 1.9e-237 | 3.2.1.51, 4.2.2.23 | GH95,PL11 | G | Right handed beta helix region | |
NHNMODOO_03468 | 3.5e-160 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_03469 | 1.1e-248 | E | Sodium:solute symporter family | |||
NHNMODOO_03470 | 7.8e-126 | K | UTRA | |||
NHNMODOO_03471 | 1.5e-264 | 4.3.2.1 | E | argininosuccinate lyase | ||
NHNMODOO_03473 | 1.8e-130 | yvoA | K | transcriptional | ||
NHNMODOO_03474 | 7.7e-219 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
NHNMODOO_03475 | 1.5e-132 | 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 | |
NHNMODOO_03476 | 9.7e-127 | frp | 1.5.1.39 | C | Oxidoreductase | |
NHNMODOO_03477 | 9e-220 | mtnE | 2.6.1.83 | E | Aminotransferase | |
NHNMODOO_03478 | 4e-113 | ycgM | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
NHNMODOO_03479 | 3.4e-132 | yqiK | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NHNMODOO_03480 | 4.6e-288 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
NHNMODOO_03481 | 7.1e-305 | yhcX | K | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | ||
NHNMODOO_03482 | 3.1e-119 | sfsA | S | Sugar fermentation stimulation protein | ||
NHNMODOO_03483 | 1.2e-299 | glpD | 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
NHNMODOO_03484 | 0.0 | pmmB | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
NHNMODOO_03485 | 2.7e-271 | ycgB | S | Stage V sporulation protein R | ||
NHNMODOO_03486 | 0.0 | yknU | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
NHNMODOO_03487 | 0.0 | yknV | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
NHNMODOO_03488 | 1.5e-230 | lysN | EK | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NHNMODOO_03489 | 8.1e-149 | htpX | O | Peptidase family M48 | ||
NHNMODOO_03490 | 7.2e-95 | lemA | S | LemA family | ||
NHNMODOO_03491 | 8.5e-218 | yngJ | 1.3.8.1, 1.3.99.12 | I | acyl-CoA dehydrogenase | |
NHNMODOO_03492 | 3.5e-255 | yngH | 6.3.4.14, 6.4.1.2, 6.4.1.3, 6.4.1.4 | I | Biotin carboxylase | |
NHNMODOO_03493 | 4.1e-30 | pycB | 2.3.1.12, 6.4.1.1 | I | Biotin carboxyl carrier protein | |
NHNMODOO_03494 | 1.6e-132 | yngF | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
NHNMODOO_03495 | 2e-283 | yngE | 2.1.3.15, 6.4.1.3 | I | COG4799 Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
NHNMODOO_03497 | 9.9e-214 | |||||
NHNMODOO_03498 | 1.4e-78 | K | Sigma-70, region 4 | |||
NHNMODOO_03499 | 2.6e-205 | msmK | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_03500 | 2.3e-159 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
NHNMODOO_03501 | 1.4e-78 | ligB | 6.5.1.1, 6.5.1.6, 6.5.1.7 | L | ATP-dependent DNA ligase | |
NHNMODOO_03502 | 8e-58 | S | YolD-like protein | |||
NHNMODOO_03503 | 1.1e-20 | |||||
NHNMODOO_03505 | 1.1e-53 | |||||
NHNMODOO_03506 | 5.7e-291 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
NHNMODOO_03507 | 2.1e-33 | |||||
NHNMODOO_03508 | 4.4e-92 | S | DinB superfamily | |||
NHNMODOO_03509 | 4.9e-56 | |||||
NHNMODOO_03510 | 1.3e-134 | 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | ||
NHNMODOO_03511 | 3.6e-285 | malX | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NHNMODOO_03512 | 8.9e-251 | 4.3.2.2, 5.5.1.2 | F | Adenylosuccinate lyase C-terminus | ||
NHNMODOO_03513 | 4.6e-113 | glvR | K | Helix-turn-helix domain, rpiR family | ||
NHNMODOO_03514 | 5.1e-74 | |||||
NHNMODOO_03518 | 5.9e-16 | |||||
NHNMODOO_03520 | 7.4e-253 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | COG1263 Phosphotransferase system IIC components, glucose maltose N-acetylglucosamine-specific | |
NHNMODOO_03521 | 2.2e-134 | celG | 3.5.1.105 | G | Probably catalyzes the deacetylation of acetylated carbohydrates an important step in the degradation of oligosaccharides | |
NHNMODOO_03522 | 4.9e-246 | pagL | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
NHNMODOO_03523 | 1.1e-124 | mngR | K | UTRA | ||
NHNMODOO_03524 | 1.2e-104 | S | CAAX protease self-immunity | |||
NHNMODOO_03525 | 1.2e-173 | 3.5.1.28 | M | COG3103 SH3 domain protein | ||
NHNMODOO_03526 | 1.3e-162 | ydhU | P | Catalase | ||
NHNMODOO_03528 | 5.9e-146 | S | Nucleotidyltransferase domain | |||
NHNMODOO_03529 | 1.1e-124 | bshB1 | S | proteins, LmbE homologs | ||
NHNMODOO_03530 | 8e-205 | bshA | GT4 | M | N-acetyl-alpha-D-glucosaminyl L-malate synthase | |
NHNMODOO_03531 | 3.2e-190 | 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 | |
NHNMODOO_03532 | 1.3e-176 | birA | 6.3.4.15 | K | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
NHNMODOO_03533 | 3.9e-148 | 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 | |
NHNMODOO_03534 | 1.4e-164 | 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 | |
NHNMODOO_03535 | 2.7e-64 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
NHNMODOO_03536 | 1.2e-174 | S | Tetratricopeptide repeat | |||
NHNMODOO_03537 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
NHNMODOO_03538 | 2.2e-243 | mtaD | 3.5.4.28, 3.5.4.31 | F | Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine | |
NHNMODOO_03539 | 1.6e-14 | |||||
NHNMODOO_03540 | 4.2e-22 | ypmA | S | Protein of unknown function (DUF4264) | ||
NHNMODOO_03541 | 5.3e-81 | ypmB | S | protein conserved in bacteria | ||
NHNMODOO_03542 | 7.6e-252 | asnS | 6.1.1.22 | J | asparaginyl-tRNA | |
NHNMODOO_03543 | 5.9e-126 | dnaD | L | DNA replication protein DnaD | ||
NHNMODOO_03544 | 2.4e-121 | 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 | |
NHNMODOO_03545 | 0.0 | ypbR | S | Dynamin family | ||
NHNMODOO_03546 | 0.0 | pbp1A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NHNMODOO_03547 | 8.5e-116 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
NHNMODOO_03548 | 2e-158 | yppC | S | Protein of unknown function (DUF2515) | ||
NHNMODOO_03550 | 2.6e-86 | racA | K | Required for the formation of axial filaments and for anchoring the origin regions at the cell poles in sporulating cells, thus ensuring proper chromosome segregation in the prespore. Binds in a dispersed manner throughout the chromosome but preferentially to sites clustered in the origin portion of the chromosome, causing condensation of the chromosome and its remodeling into an elongated, anchored structure | ||
NHNMODOO_03551 | 1.6e-45 | yppE | S | Bacterial domain of unknown function (DUF1798) | ||
NHNMODOO_03552 | 6e-15 | |||||
NHNMODOO_03553 | 6.8e-234 | 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 | |
NHNMODOO_03554 | 2.8e-96 | pfpI | 3.5.1.124 | S | DJ-1/PfpI family | |
NHNMODOO_03555 | 1.7e-168 | 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 | |
NHNMODOO_03556 | 3.5e-52 | yusE | CO | cell redox homeostasis | ||
NHNMODOO_03557 | 9.3e-77 | yphP | S | Belongs to the UPF0403 family | ||
NHNMODOO_03558 | 1.5e-73 | CO | Thioredoxin-like | |||
NHNMODOO_03560 | 8.7e-70 | puuR | K | sequence-specific DNA binding | ||
NHNMODOO_03561 | 6.3e-67 | puuR | K | sequence-specific DNA binding | ||
NHNMODOO_03562 | 7.8e-189 | V | Domain of unknown function (DUF3471) | |||
NHNMODOO_03563 | 1.3e-120 | sapB | S | MgtC SapB transporter | ||
NHNMODOO_03564 | 7.1e-59 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NHNMODOO_03565 | 1.7e-54 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NHNMODOO_03566 | 4.4e-211 | megL | 2.5.1.48, 2.5.1.49, 4.4.1.1, 4.4.1.11, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
NHNMODOO_03568 | 6.6e-179 | thiL | 2.7.4.16 | H | Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 | |
NHNMODOO_03569 | 3.9e-81 | ydiB | 2.7.1.221, 5.1.1.1 | S | ATPase or kinase | |
NHNMODOO_03570 | 3.2e-127 | yeaZ | 2.3.1.234 | O | COG1214 Inactive homolog of metal-dependent proteases | |
NHNMODOO_03571 | 2.3e-84 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
NHNMODOO_03572 | 3.3e-178 | 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 | |
NHNMODOO_03573 | 1.1e-304 | ydiF | S | ABC transporter | ||
NHNMODOO_03574 | 6.8e-113 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
NHNMODOO_03575 | 1.4e-24 | 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 | ||
NHNMODOO_03576 | 7.9e-130 | 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 | ||
NHNMODOO_03577 | 1.9e-181 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NHNMODOO_03578 | 3.9e-111 | metI | P | COG2011 ABC-type metal ion transport system, permease component | ||
NHNMODOO_03579 | 5.5e-139 | P | COG1464 ABC-type metal ion transport system, periplasmic component surface antigen | |||
NHNMODOO_03580 | 2.3e-201 | gldA | 1.1.1.1, 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
NHNMODOO_03581 | 8.9e-117 | ydiL | S | CAAX protease self-immunity | ||
NHNMODOO_03582 | 5.7e-43 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
NHNMODOO_03583 | 2.6e-281 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
NHNMODOO_03584 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Mga helix-turn-helix domain | ||
NHNMODOO_03585 | 1.8e-72 | ulaC | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
NHNMODOO_03586 | 1.4e-41 | 2.7.1.194, 2.7.1.200 | G | COG3414 Phosphotransferase system, galactitol-specific IIB component | ||
NHNMODOO_03587 | 1.9e-223 | ulaA | S | PTS system ascorbate-specific transporter subunit IIC | ||
NHNMODOO_03588 | 5.7e-127 | S | carbohydrate derivative metabolic process | |||
NHNMODOO_03589 | 1.3e-120 | ypdP | S | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | ||
NHNMODOO_03590 | 4.2e-144 | 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 | |
NHNMODOO_03591 | 2.4e-267 | hpaB | 1.14.14.9 | Q | COG2368 Aromatic ring hydroxylase | |
NHNMODOO_03592 | 8.7e-87 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
NHNMODOO_03593 | 1.8e-96 | 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 | |
NHNMODOO_03594 | 1.3e-82 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
NHNMODOO_03595 | 2.2e-182 | 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 | |
NHNMODOO_03596 | 7.6e-236 | moeA | 2.10.1.1 | H | molybdopterin | |
NHNMODOO_03597 | 5.3e-87 | mobB | 2.10.1.1, 2.7.7.77 | H | molybdopterin-guanine dinucleotide biosynthesis protein | |
NHNMODOO_03598 | 1.1e-74 | moaE | 2.8.1.12 | H | COG0314 Molybdopterin converting factor, large subunit | |
NHNMODOO_03599 | 6.9e-34 | moaD | 2.8.1.12 | H | Involved in sulfur transfer in the conversion of molybdopterin precursor Z to molybdopterin | |
NHNMODOO_03600 | 3e-137 | focA | P | Formate/nitrite transporter | ||
NHNMODOO_03601 | 0.0 | yjgC | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase (NAD+) activity | |
NHNMODOO_03602 | 1.8e-105 | yjgD | S | Protein of unknown function (DUF1641) | ||
NHNMODOO_03603 | 1.1e-133 | fdhD | C | Required for formate dehydrogenase (FDH) activity. Acts as a sulfur carrier protein that transfers sulfur from IscS to the molybdenum cofactor prior to its insertion into FDH | ||
NHNMODOO_03604 | 1.1e-76 | MA20_19235 | S | Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME) | ||
NHNMODOO_03607 | 0.0 | yfhO | S | Bacterial membrane protein YfhO | ||
NHNMODOO_03608 | 1.2e-68 | wxcN | GT2 | S | GtrA-like protein | |
NHNMODOO_03609 | 2.3e-181 | csbB | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
NHNMODOO_03610 | 1.6e-151 | S | Haloacid dehalogenase-like hydrolase | |||
NHNMODOO_03611 | 1.3e-132 | |||||
NHNMODOO_03612 | 1e-148 | ehuB | ET | Bacterial periplasmic substrate-binding proteins | ||
NHNMODOO_03613 | 6.1e-112 | ehuC | E | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_03614 | 1.7e-117 | ehuD | E | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_03615 | 5.8e-149 | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | ||
NHNMODOO_03616 | 2.5e-71 | wecC | 1.1.1.336 | M | ArpU family transcriptional regulator | |
NHNMODOO_03617 | 1.5e-244 | malK | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
NHNMODOO_03618 | 1.2e-110 | dcuR | T | COG4565 Response regulator of citrate malate metabolism | ||
NHNMODOO_03619 | 0.0 | ltaS | 2.7.8.20 | M | Sulfatase | |
NHNMODOO_03620 | 1.9e-305 | 2.6.1.52 | E | Aminotransferase class-V | ||
NHNMODOO_03621 | 1.1e-87 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
NHNMODOO_03622 | 1.3e-105 | V | Beta-lactamase | |||
NHNMODOO_03623 | 4.9e-133 | yfhB | 5.3.3.17 | S | PhzF family | |
NHNMODOO_03624 | 1e-60 | S | Protein of unknown function, DUF393 | |||
NHNMODOO_03625 | 4.6e-188 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NHNMODOO_03626 | 5.7e-169 | 3.2.2.21 | K | Cupin domain | ||
NHNMODOO_03627 | 2.6e-140 | G | Xylose isomerase-like TIM barrel | |||
NHNMODOO_03628 | 3.6e-210 | S | Oxidoreductase family, C-terminal alpha/beta domain | |||
NHNMODOO_03629 | 1e-251 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_03630 | 1e-170 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03631 | 7.3e-155 | P | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03632 | 6.4e-142 | G | Xylose isomerase-like TIM barrel | |||
NHNMODOO_03633 | 1.7e-98 | 3.2.2.21 | K | AraC-like ligand binding domain | ||
NHNMODOO_03634 | 3e-209 | S | Oxidoreductase family, C-terminal alpha/beta domain | |||
NHNMODOO_03635 | 1.7e-223 | S | Oxidoreductase family, C-terminal alpha/beta domain | |||
NHNMODOO_03636 | 4e-164 | 3.2.2.21 | K | AraC-like ligand binding domain | ||
NHNMODOO_03637 | 7.3e-211 | 3.2.1.180 | GH88 | O | Glycosyl Hydrolase Family 88 | |
NHNMODOO_03638 | 3.2e-164 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03639 | 1.6e-146 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03640 | 2.1e-257 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_03641 | 7.8e-63 | S | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
NHNMODOO_03642 | 6.9e-95 | mutT | 3.6.1.13, 3.6.1.55 | L | nUDIX hydrolase | |
NHNMODOO_03643 | 1.2e-244 | ywoF | P | Right handed beta helix region | ||
NHNMODOO_03644 | 2e-158 | EG | EamA-like transporter family | |||
NHNMODOO_03646 | 1e-102 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_03647 | 5e-55 | S | Family of unknown function (DUF5367) | |||
NHNMODOO_03648 | 2.6e-158 | rbcR1 | K | Transcriptional regulator | ||
NHNMODOO_03649 | 1.4e-178 | phnT | 3.6.3.30 | P | ABC transporter | |
NHNMODOO_03650 | 6.8e-187 | ftpB | P | Bacterial extracellular solute-binding protein | ||
NHNMODOO_03651 | 1.7e-288 | ftpA | P | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_03652 | 3.1e-206 | ysh1 | J | Metallo-beta-lactamase superfamily | ||
NHNMODOO_03653 | 7.6e-146 | |||||
NHNMODOO_03654 | 3.2e-81 | |||||
NHNMODOO_03655 | 2.2e-298 | acsA | 6.2.1.1, 6.2.1.2 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
NHNMODOO_03656 | 1.1e-26 | topA2 | 5.99.1.2 | L | Topoisomerase IA | |
NHNMODOO_03657 | 3.5e-10 | Q | Thioesterase superfamily | |||
NHNMODOO_03658 | 5.4e-178 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
NHNMODOO_03659 | 1.2e-141 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
NHNMODOO_03660 | 1.6e-233 | yxiO | S | COG2270 Permeases of the major facilitator superfamily | ||
NHNMODOO_03661 | 7.3e-203 | ysfB | KT | regulator | ||
NHNMODOO_03662 | 3.8e-257 | glcD | 1.1.3.15 | C | Glycolate oxidase subunit | |
NHNMODOO_03663 | 1e-251 | glcF | C | Glycolate oxidase | ||
NHNMODOO_03664 | 9.6e-155 | ssuB | P | COG1116 ABC-type nitrate sulfonate bicarbonate transport system, ATPase component | ||
NHNMODOO_03665 | 5.6e-104 | ssuC | P | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_03666 | 1.5e-172 | ssuA | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
NHNMODOO_03667 | 3.9e-90 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
NHNMODOO_03668 | 1.3e-76 | yybA | 2.3.1.57 | K | transcriptional | |
NHNMODOO_03669 | 2.5e-90 | S | VanZ like family | |||
NHNMODOO_03670 | 4.4e-186 | ydcC | M | COG2834 Outer membrane lipoprotein-sorting protein | ||
NHNMODOO_03671 | 1.3e-57 | 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 | |
NHNMODOO_03672 | 1.4e-128 | ydcA | 3.4.21.105 | S | membrane protein (homolog of Drosophila rhomboid) | |
NHNMODOO_03673 | 5.7e-101 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
NHNMODOO_03674 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
NHNMODOO_03675 | 1.5e-138 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
NHNMODOO_03676 | 3.2e-47 | |||||
NHNMODOO_03677 | 2.8e-106 | S | Integral membrane protein | |||
NHNMODOO_03678 | 1.8e-212 | S | Winged helix DNA-binding domain | |||
NHNMODOO_03679 | 2.1e-137 | G | Xylose isomerase-like TIM barrel | |||
NHNMODOO_03680 | 2.5e-189 | S | Oxidoreductase family, C-terminal alpha/beta domain | |||
NHNMODOO_03681 | 5e-192 | G | Xylose isomerase | |||
NHNMODOO_03682 | 3.5e-157 | S | electron transporter, transferring electrons within the cyclic electron transport pathway of photosynthesis activity | |||
NHNMODOO_03683 | 5.1e-58 | phaG | P | COG1320 Multisubunit Na H antiporter, MnhG subunit | ||
NHNMODOO_03684 | 7.2e-38 | phaF | P | Subunit F of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
NHNMODOO_03685 | 6.4e-85 | mrpE | P | Na+/H+ ion antiporter subunit | ||
NHNMODOO_03686 | 1.1e-262 | mrpD | CP | Subunit D of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
NHNMODOO_03687 | 3.8e-49 | phaC | 1.6.5.3 | P | Subunit C of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | |
NHNMODOO_03688 | 5.1e-64 | mnhB2 | P | antiporter activity | ||
NHNMODOO_03689 | 0.0 | phaA | 1.6.5.3 | CP | COG1009 NADH ubiquinone oxidoreductase subunit 5 (chain L) Multisubunit Na H antiporter, MnhA subunit | |
NHNMODOO_03690 | 5.1e-130 | T | PhoQ Sensor | |||
NHNMODOO_03691 | 8.7e-110 | S | Nitroreductase family | |||
NHNMODOO_03692 | 2e-58 | hxlR | K | transcriptional | ||
NHNMODOO_03693 | 1.2e-180 | ykfD | E | Belongs to the ABC transporter superfamily | ||
NHNMODOO_03694 | 3.8e-165 | ykfC | 3.4.14.13 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
NHNMODOO_03695 | 5.6e-172 | ykfA | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | |
NHNMODOO_03696 | 4.6e-311 | dppE | E | ABC transporter substrate-binding protein | ||
NHNMODOO_03697 | 2.4e-181 | dppD | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_03698 | 4.8e-171 | dppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHNMODOO_03699 | 4e-162 | dppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHNMODOO_03700 | 1.2e-149 | dppA | E | D-aminopeptidase | ||
NHNMODOO_03701 | 2.8e-152 | rarD | S | -transporter | ||
NHNMODOO_03702 | 1.8e-198 | pgl | 3.1.1.31 | G | 6-phosphogluconolactonase | |
NHNMODOO_03703 | 1.3e-194 | ald | 1.4.1.1 | E | Belongs to the AlaDH PNT family | |
NHNMODOO_03704 | 5.8e-225 | QT | Transcriptional regulator | |||
NHNMODOO_03705 | 3.4e-157 | sseA | 2.8.1.1, 2.8.1.2 | P | sulfurtransferase | |
NHNMODOO_03706 | 2.8e-247 | yeeF | E | Amino acid permease | ||
NHNMODOO_03707 | 1.2e-103 | cwlK | M | Peptidase M15B and M15C DD-carboxypeptidase VanY endolysin | ||
NHNMODOO_03708 | 3.4e-233 | K | Helix-turn-helix XRE-family like proteins | |||
NHNMODOO_03709 | 2.8e-197 | aprE | 3.4.21.62 | O | Belongs to the peptidase S8 family | |
NHNMODOO_03711 | 2.3e-224 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
NHNMODOO_03712 | 7.2e-169 | yfhM | S | Alpha beta hydrolase | ||
NHNMODOO_03713 | 1.9e-139 | P | COG0861 Membrane protein TerC, possibly involved in tellurium resistance | |||
NHNMODOO_03714 | 2.3e-09 | tnp | L | MULE transposase domain | ||
NHNMODOO_03715 | 4.4e-80 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
NHNMODOO_03716 | 2.3e-197 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
NHNMODOO_03717 | 4.8e-148 | vicX | 3.1.26.11 | S | COG1235 Metal-dependent hydrolases of the beta-lactamase superfamily I | |
NHNMODOO_03718 | 6e-155 | yycI | S | protein conserved in bacteria | ||
NHNMODOO_03719 | 6e-244 | yycH | S | protein conserved in bacteria | ||
NHNMODOO_03720 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
NHNMODOO_03721 | 5.1e-133 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_03725 | 4.3e-247 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
NHNMODOO_03726 | 2e-250 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
NHNMODOO_03727 | 4.2e-53 | rplI | J | binds to the 23S rRNA | ||
NHNMODOO_03728 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
NHNMODOO_03729 | 2.1e-144 | yybS | S | membrane | ||
NHNMODOO_03730 | 1.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
NHNMODOO_03731 | 4e-57 | 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 | ||
NHNMODOO_03732 | 6.1e-45 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
NHNMODOO_03733 | 4.5e-194 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
NHNMODOO_03734 | 1.8e-27 | yyzM | S | protein conserved in bacteria | ||
NHNMODOO_03735 | 3.6e-180 | yyaD | S | Membrane | ||
NHNMODOO_03736 | 1.8e-113 | yyaC | S | Sporulation protein YyaC | ||
NHNMODOO_03737 | 3.3e-214 | sufS | 2.8.1.7, 4.4.1.16 | E | Aminotransferase class-V | |
NHNMODOO_03738 | 3.9e-151 | spo0J | K | Belongs to the ParB family | ||
NHNMODOO_03739 | 1.3e-134 | soj | D | COG1192 ATPases involved in chromosome partitioning | ||
NHNMODOO_03740 | 8.8e-148 | 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 | ||
NHNMODOO_03741 | 1.4e-127 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of guanine in position 535 of 16S rRNA | |
NHNMODOO_03742 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
NHNMODOO_03743 | 5.1e-246 | 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 | ||
NHNMODOO_03744 | 1e-108 | jag | S | single-stranded nucleic acid binding R3H | ||
NHNMODOO_03745 | 2.5e-126 | 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 | ||
NHNMODOO_03746 | 1.7e-55 | 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 | |
NHNMODOO_03747 | 2.4e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
NHNMODOO_03748 | 4.5e-255 | 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 | ||
NHNMODOO_03749 | 2.5e-206 | 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 | |
NHNMODOO_03750 | 4.5e-32 | yaaA | S | S4 domain | ||
NHNMODOO_03751 | 1.5e-200 | 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 | ||
NHNMODOO_03752 | 3e-10 | yaaB | S | Domain of unknown function (DUF370) | ||
NHNMODOO_03753 | 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 | |
NHNMODOO_03754 | 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 | |
NHNMODOO_03755 | 1.3e-184 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_03756 | 1.1e-91 | bcrC | 3.6.1.27 | I | Bacitracin ABC transporter permease | |
NHNMODOO_03758 | 4.5e-137 | G | ABC transporter (permease) | |||
NHNMODOO_03759 | 6.1e-138 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03760 | 1.2e-194 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_03761 | 9.4e-208 | 2.7.13.3 | T | Histidine kinase | ||
NHNMODOO_03762 | 5.8e-153 | T | helix_turn_helix, arabinose operon control protein | |||
NHNMODOO_03763 | 4.2e-166 | 3.2.1.180 | GH88 | O | Glycosyl Hydrolase Family 88 | |
NHNMODOO_03764 | 5.8e-229 | S | Uncharacterized protein conserved in bacteria (DUF2264) | |||
NHNMODOO_03765 | 1.8e-195 | S | Heparinase II/III-like protein | |||
NHNMODOO_03766 | 0.0 | hylB | 3.2.1.55, 3.2.1.8, 4.2.2.1, 4.2.2.20, 4.2.2.21, 4.2.2.5 | CBM6,GH43,PL8 | M | Glycosyl hydrolase family 59 |
NHNMODOO_03767 | 5.3e-78 | yiaB | S | yiaA/B two helix domain | ||
NHNMODOO_03769 | 4.8e-261 | yeaV | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
NHNMODOO_03771 | 3.9e-124 | |||||
NHNMODOO_03772 | 6.7e-282 | S | Psort location Cytoplasmic, score 8.87 | |||
NHNMODOO_03773 | 7e-98 | L | RAMP superfamily | |||
NHNMODOO_03774 | 3.5e-151 | S | Psort location Cytoplasmic, score 8.87 | |||
NHNMODOO_03775 | 4.2e-107 | |||||
NHNMODOO_03776 | 1.4e-129 | S | CRISPR-associated endoribonuclease Cas6 | |||
NHNMODOO_03777 | 5.4e-124 | racX | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
NHNMODOO_03778 | 0.0 | cas3 | L | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NHNMODOO_03779 | 7.8e-134 | cas5d | S | CRISPR-associated protein (Cas_Cas5) | ||
NHNMODOO_03780 | 0.0 | csd1 | 3.5.1.28 | M | CRISPR-associated protein (Cas_Csd1) | |
NHNMODOO_03781 | 4.7e-157 | csd2 | L | CRISPR-associated protein Cas7 | ||
NHNMODOO_03782 | 1.5e-118 | cas4 | 3.1.12.1 | L | RecB family exonuclease | |
NHNMODOO_03783 | 5.7e-194 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
NHNMODOO_03784 | 9.6e-46 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
NHNMODOO_03785 | 4.5e-73 | L | HNH endonuclease | |||
NHNMODOO_03786 | 3.5e-220 | glcE | C | FAD binding domain | ||
NHNMODOO_03787 | 1.4e-251 | glcF | C | Glycolate oxidase | ||
NHNMODOO_03788 | 2e-272 | glcD | 1.1.2.4, 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
NHNMODOO_03789 | 0.0 | glcB | 2.3.3.9 | C | Involved in the glycolate utilization. Catalyzes the condensation and subsequent hydrolysis of acetyl-coenzyme A (acetyl-CoA) and glyoxylate to form malate and CoA | |
NHNMODOO_03790 | 3.9e-139 | Q | Domain of unknown function (DUF2437) | |||
NHNMODOO_03791 | 2.3e-136 | K | helix_turn_helix isocitrate lyase regulation | |||
NHNMODOO_03792 | 1.9e-47 | |||||
NHNMODOO_03793 | 7.3e-92 | MA20_21960 | FG | Domain of unknown function (DUF4269) | ||
NHNMODOO_03795 | 1e-212 | 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 | |
NHNMODOO_03797 | 2.7e-219 | yuxJ | EGP | Major facilitator Superfamily | ||
NHNMODOO_03798 | 2.6e-112 | 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 | |
NHNMODOO_03800 | 3.4e-115 | yneB | L | resolvase | ||
NHNMODOO_03801 | 4.2e-34 | ynzC | S | UPF0291 protein | ||
NHNMODOO_03802 | 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 | |
NHNMODOO_03803 | 2e-71 | yneE | S | Sporulation inhibitor of replication protein sirA | ||
NHNMODOO_03804 | 7.9e-29 | yneF | S | UPF0154 protein | ||
NHNMODOO_03805 | 0.0 | mdlA | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
NHNMODOO_03806 | 0.0 | mdlB | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
NHNMODOO_03807 | 3.9e-81 | yneK | S | Protein of unknown function (DUF2621) | ||
NHNMODOO_03808 | 9.4e-13 | |||||
NHNMODOO_03810 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
NHNMODOO_03813 | 1.2e-11 | sspN | S | Small acid-soluble spore protein N family | ||
NHNMODOO_03814 | 2.2e-139 | P | Copper resistance protein D | |||
NHNMODOO_03815 | 0.0 | spoVK | O | stage V sporulation protein K | ||
NHNMODOO_03816 | 2.9e-75 | S | thioesterase | |||
NHNMODOO_03817 | 9.4e-153 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
NHNMODOO_03818 | 1.7e-79 | S | Domain of unknown function (DUF4352) | |||
NHNMODOO_03819 | 2.3e-178 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
NHNMODOO_03820 | 3.6e-146 | I | Hydrolase | |||
NHNMODOO_03821 | 2.6e-233 | ykuI | T | Diguanylate phosphodiesterase | ||
NHNMODOO_03822 | 1e-22 | |||||
NHNMODOO_03823 | 1.9e-26 | S | YppG-like protein | |||
NHNMODOO_03824 | 2e-68 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
NHNMODOO_03825 | 2.6e-169 | 3.4.13.19 | E | COG2355 Zn-dependent dipeptidase, microsomal dipeptidase homolog | ||
NHNMODOO_03826 | 4.4e-158 | cheV | 2.7.13.3 | T | Chemotaxis protein CheV | |
NHNMODOO_03828 | 1.1e-49 | yneR | S | Belongs to the HesB IscA family | ||
NHNMODOO_03829 | 1.7e-87 | 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 | |
NHNMODOO_03830 | 6.5e-210 | I | COG0657 Esterase lipase | |||
NHNMODOO_03831 | 1.4e-57 | |||||
NHNMODOO_03833 | 6.8e-72 | L | Belongs to the 'phage' integrase family | |||
NHNMODOO_03835 | 4.3e-09 | |||||
NHNMODOO_03839 | 4.7e-67 | V | HNH endonuclease | |||
NHNMODOO_03840 | 2.3e-36 | L | phage terminase small subunit | |||
NHNMODOO_03841 | 1.4e-240 | S | Terminase | |||
NHNMODOO_03843 | 2.1e-81 | S | Phage portal protein | |||
NHNMODOO_03844 | 2e-68 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
NHNMODOO_03845 | 5.1e-79 | S | Phage capsid family | |||
NHNMODOO_03846 | 2.7e-17 | N | Bacterial Ig-like domain 2 | |||
NHNMODOO_03847 | 3.6e-128 | |||||
NHNMODOO_03848 | 2.3e-47 | S | Phage gp6-like head-tail connector protein | |||
NHNMODOO_03849 | 7.8e-58 | S | Phage head-tail joining protein | |||
NHNMODOO_03850 | 1e-16 | S | Bacteriophage HK97-gp10, putative tail-component | |||
NHNMODOO_03851 | 1.3e-50 | |||||
NHNMODOO_03852 | 8.9e-62 | N | phage major tail protein, phi13 family | |||
NHNMODOO_03853 | 6.3e-07 | |||||
NHNMODOO_03855 | 0.0 | D | phage tail tape measure protein | |||
NHNMODOO_03856 | 4.9e-151 | S | Phage tail protein | |||
NHNMODOO_03857 | 0.0 | M | Peptidase_G2, IMC autoproteolytic cleavage domain | |||
NHNMODOO_03858 | 8.8e-220 | |||||
NHNMODOO_03861 | 2.3e-31 | KLT | Protein tyrosine kinase | |||
NHNMODOO_03862 | 2.3e-201 | L | Prophage endopeptidase tail | |||
NHNMODOO_03863 | 2.1e-54 | S | Bacteriophage holin family | |||
NHNMODOO_03864 | 6.2e-96 | 3.5.1.28 | V | N-acetylmuramoyl-L-alanine amidase | ||
NHNMODOO_03865 | 4.7e-13 | |||||
NHNMODOO_03867 | 3.4e-14 | |||||
NHNMODOO_03869 | 1e-124 | ligB | 6.5.1.1, 6.5.1.6, 6.5.1.7 | L | ATP-dependent DNA ligase | |
NHNMODOO_03870 | 6.1e-58 | S | YolD-like protein | |||
NHNMODOO_03871 | 5.8e-23 | |||||
NHNMODOO_03874 | 1.2e-48 | 1.15.1.2 | E | Pfam:DUF955 | ||
NHNMODOO_03875 | 5e-13 | K | sequence-specific DNA binding | |||
NHNMODOO_03877 | 1.3e-60 | S | Phage regulatory protein Rha (Phage_pRha) | |||
NHNMODOO_03879 | 5.7e-44 | |||||
NHNMODOO_03881 | 1.8e-19 | |||||
NHNMODOO_03882 | 7e-82 | S | Bacteriophage Mu Gam like protein | |||
NHNMODOO_03883 | 5.7e-164 | tadZ | D | AAA domain | ||
NHNMODOO_03884 | 7.1e-77 | S | Protein of unknown function (DUF669) | |||
NHNMODOO_03885 | 9.8e-290 | S | D5 N terminal like | |||
NHNMODOO_03886 | 9.2e-61 | |||||
NHNMODOO_03887 | 1.8e-95 | L | ERCC4 domain | |||
NHNMODOO_03888 | 1.7e-44 | |||||
NHNMODOO_03889 | 5.2e-30 | S | Protein of unknwon function (DUF3310) | |||
NHNMODOO_03891 | 2.5e-69 | Q | DNA (cytosine-5-)-methyltransferase activity | |||
NHNMODOO_03893 | 3.1e-71 | GK | ROK family | |||
NHNMODOO_03894 | 4.6e-205 | G | ABC transporter substrate-binding protein | |||
NHNMODOO_03895 | 3.1e-133 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_03896 | 5.3e-130 | ypdA | G | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_03897 | 2e-102 | T | Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain | |||
NHNMODOO_03898 | 1.7e-121 | 2.7.13.3 | T | Histidine kinase | ||
NHNMODOO_03899 | 3.2e-27 | S | Protein of unknown function, DUF624 | |||
NHNMODOO_03900 | 9.2e-189 | S | Glycosyl hydrolase | |||
NHNMODOO_03901 | 1.1e-255 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain |
NHNMODOO_03902 | 1.9e-190 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
NHNMODOO_03903 | 0.0 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
NHNMODOO_03904 | 1.2e-210 | ydhP | 3.2.1.21, 3.2.1.86 | GT1 | G | Glycosyl hydrolase family 1 |
NHNMODOO_03905 | 3e-84 | |||||
NHNMODOO_03906 | 1.5e-80 | K | Bacterial transcription activator, effector binding domain | |||
NHNMODOO_03907 | 1.1e-98 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHNMODOO_03908 | 1.1e-59 | K | TetR family transcriptional regulator | |||
NHNMODOO_03909 | 0.0 | licR | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
NHNMODOO_03910 | 9.9e-274 | gmuD | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHNMODOO_03911 | 1.4e-48 | celC | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
NHNMODOO_03912 | 2.4e-234 | 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 | ||
NHNMODOO_03913 | 4.2e-44 | ydhM | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
NHNMODOO_03914 | 4.3e-112 | yybG | S | Pentapeptide repeat-containing protein | ||
NHNMODOO_03915 | 5.6e-147 | 3.4.16.4 | V | Beta-lactamase | ||
NHNMODOO_03916 | 1.5e-74 | K | Transcriptional regulator | |||
NHNMODOO_03917 | 4.4e-62 | cdd_2 | 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
NHNMODOO_03918 | 1.1e-204 | yeaN | P | COG2807 Cyanate permease | ||
NHNMODOO_03919 | 1.1e-113 | K | FCD | |||
NHNMODOO_03920 | 1.8e-119 | ycbG | K | FCD | ||
NHNMODOO_03921 | 3.2e-172 | kdgD | 4.2.1.41 | EM | 5-dehydro-4-deoxyglucarate dehydratase activity | |
NHNMODOO_03922 | 1.6e-255 | ycbD | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | ||
NHNMODOO_03923 | 7e-79 | S | Tripartite tricarboxylate transporter TctB family | |||
NHNMODOO_03924 | 3.9e-260 | S | Tripartite tricarboxylate transporter TctA family | |||
NHNMODOO_03925 | 3.7e-185 | S | Tripartite tricarboxylate transporter family receptor | |||
NHNMODOO_03926 | 7.2e-189 | uxuA | 4.2.1.8 | G | mannonate dehydratase activity | |
NHNMODOO_03927 | 2.1e-52 | |||||
NHNMODOO_03928 | 1.7e-43 | S | DNA alkylation repair protein | |||
NHNMODOO_03929 | 1.7e-177 | 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 | |
NHNMODOO_03930 | 0.0 | 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 | |
NHNMODOO_03931 | 5.2e-110 | qoxC | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
NHNMODOO_03932 | 4.8e-51 | qoxD | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
NHNMODOO_03933 | 9.6e-43 | ywcE | S | Required for proper spore morphogenesis. Important for spore germination | ||
NHNMODOO_03934 | 1.4e-38 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
NHNMODOO_03935 | 4.3e-245 | agcS | E | Sodium alanine symporter | ||
NHNMODOO_03936 | 1.7e-232 | ampS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
NHNMODOO_03937 | 2.8e-125 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
NHNMODOO_03938 | 4.5e-76 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
NHNMODOO_03939 | 1.9e-119 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
NHNMODOO_03940 | 1.5e-94 | queF | 1.7.1.13 | S | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
NHNMODOO_03941 | 5.2e-102 | KT | LuxR family transcriptional regulator | |||
NHNMODOO_03942 | 1.3e-183 | T | Histidine kinase | |||
NHNMODOO_03943 | 8.7e-114 | S | ABC-2 type transporter | |||
NHNMODOO_03944 | 6.4e-123 | V | ABC-2 type transporter | |||
NHNMODOO_03945 | 3.2e-167 | V | COG1131 ABC-type multidrug transport system, ATPase component | |||
NHNMODOO_03947 | 0.0 | topB1 | 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 | |
NHNMODOO_03948 | 9.8e-74 | osmC | O | redox protein, regulator of disulfide bond formation | ||
NHNMODOO_03950 | 1e-116 | M | lytic transglycosylase activity | |||
NHNMODOO_03951 | 3.7e-185 | 2.1.1.163, 2.1.1.201 | Q | O-methyltransferase | ||
NHNMODOO_03953 | 0.0 | sucA | 1.2.4.2, 4.1.1.71 | 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) | |
NHNMODOO_03954 | 6e-177 | sucB | 2.3.1.61 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) | |
NHNMODOO_03955 | 5.4e-32 | yozC | ||||
NHNMODOO_03956 | 4.4e-302 | ybiT | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
NHNMODOO_03957 | 2.2e-156 | S | reductase | |||
NHNMODOO_03958 | 0.0 | recQ | 3.6.4.12 | L | DNA helicase | |
NHNMODOO_03959 | 5e-54 | ytxJ | O | Protein of unknown function (DUF2847) | ||
NHNMODOO_03960 | 4.7e-90 | yocC | ||||
NHNMODOO_03961 | 5.4e-103 | speG | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_03962 | 6.4e-165 | polA | 2.7.7.7 | L | Helix-hairpin-helix class 2 (Pol1 family) motifs | |
NHNMODOO_03963 | 8.2e-125 | bshB2 | S | deacetylase | ||
NHNMODOO_03964 | 1.3e-60 | yojF | S | Protein of unknown function (DUF1806) | ||
NHNMODOO_03965 | 9.2e-112 | mucD | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
NHNMODOO_03966 | 3.3e-68 | ydaT | S | Uncharacterized protein conserved in bacteria (DUF2188) | ||
NHNMODOO_03968 | 1.2e-211 | ydbM | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
NHNMODOO_03969 | 5.4e-157 | S | membrane | |||
NHNMODOO_03970 | 9.6e-50 | xlyA | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
NHNMODOO_03971 | 8.2e-182 | hsk | 2.7.1.39 | S | Phosphotransferase enzyme family | |
NHNMODOO_03972 | 9.2e-144 | 2.1.1.144, 2.1.1.197 | S | Methyltransferase domain | ||
NHNMODOO_03973 | 2.6e-224 | adhB | 1.1.1.1, 1.1.1.14, 1.1.1.284 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
NHNMODOO_03974 | 1.1e-172 | fhuD | P | Periplasmic binding protein | ||
NHNMODOO_03975 | 6.7e-171 | fhuG | 3.6.3.34 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | |
NHNMODOO_03976 | 6.9e-53 | isdG | 1.14.99.48, 1.14.99.57 | C | Allows bacterial pathogens to use the host heme as an iron source. Catalyzes the oxidative degradation of the heme macrocyclic porphyrin ring to the biliverdin in the presence of a suitable electron donor such as ascorbate or NADPH--cytochrome P450 reductase, with subsequent release of free iron | |
NHNMODOO_03977 | 3.3e-105 | isdC | M | NEAr Transporter domain | ||
NHNMODOO_03978 | 0.0 | M | Cell surface protein | |||
NHNMODOO_03979 | 5.5e-156 | isdE | P | ABC transporter substrate-binding protein | ||
NHNMODOO_03980 | 2.6e-167 | fhuB11 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHNMODOO_03981 | 1.6e-132 | fhuC | 3.6.3.28, 3.6.3.34 | HP | ABC transporter, ATP-binding protein | |
NHNMODOO_03982 | 3.7e-137 | srtB | 3.4.22.70 | S | Sortase family | |
NHNMODOO_03983 | 6.7e-240 | yhdP | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
NHNMODOO_03984 | 2.7e-157 | opuAC | E | Glycine betaine ABC transporter | ||
NHNMODOO_03985 | 3.2e-256 | S | Predicted membrane protein (DUF2254) | |||
NHNMODOO_03986 | 2.2e-173 | P | Catalase | |||
NHNMODOO_03987 | 3.4e-168 | yflN | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
NHNMODOO_03988 | 1.8e-220 | adhB | 1.1.1.1, 1.1.1.14, 1.1.1.284 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
NHNMODOO_03990 | 2.3e-140 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
NHNMODOO_03991 | 4.4e-109 | Q | Methyltransferase domain | |||
NHNMODOO_03992 | 6.6e-60 | gntR1 | K | helix_turn_helix gluconate operon transcriptional repressor | ||
NHNMODOO_03993 | 2.2e-162 | V | ATPases associated with a variety of cellular activities | |||
NHNMODOO_03994 | 2.3e-125 | |||||
NHNMODOO_03995 | 1.3e-151 | acrR_2 | K | Transcriptional regulator | ||
NHNMODOO_03997 | 0.0 | swrC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NHNMODOO_03998 | 5.7e-29 | sspB | S | spore protein | ||
NHNMODOO_03999 | 1.8e-27 | sspB | S | spore protein | ||
NHNMODOO_04000 | 7.3e-121 | S | membrane | |||
NHNMODOO_04001 | 1.8e-86 | ypmQ | S | protein SCO1 SenC PrrC, involved in biogenesis of respiratory and photosynthetic systems | ||
NHNMODOO_04002 | 3.4e-258 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
NHNMODOO_04003 | 7.1e-164 | gltC | K | Transcriptional regulator | ||
NHNMODOO_04004 | 5.7e-49 | czrA | K | transcriptional | ||
NHNMODOO_04005 | 7.8e-150 | czcD | P | COG1230 Co Zn Cd efflux system component | ||
NHNMODOO_04006 | 4.1e-150 | 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 | |
NHNMODOO_04007 | 1.5e-109 | 1.15.1.1 | P | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | ||
NHNMODOO_04008 | 2.1e-169 | K | WYL domain | |||
NHNMODOO_04009 | 8.7e-170 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_04010 | 2.2e-21 | S | Fur-regulated basic protein B | |||
NHNMODOO_04013 | 1e-145 | yfkD | S | YfkD-like protein | ||
NHNMODOO_04014 | 4.7e-218 | yfkA | S | YfkB-like domain | ||
NHNMODOO_04015 | 4.1e-113 | gpmB | 5.4.2.11 | G | Belongs to the phosphoglycerate mutase family | |
NHNMODOO_04016 | 7.5e-242 | yhdP | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
NHNMODOO_04017 | 5.9e-141 | S | Domain of unknown function (DUF368) | |||
NHNMODOO_04018 | 7.2e-149 | pdaA | G | deacetylase | ||
NHNMODOO_04020 | 2.1e-148 | thiC | 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
NHNMODOO_04021 | 9.7e-84 | thiC | 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
NHNMODOO_04022 | 2.4e-164 | ahpF | 1.8.1.9 | O | Pyridine nucleotide-disulphide oxidoreductase | |
NHNMODOO_04023 | 6.2e-70 | ywgB | K | Transcriptional regulator | ||
NHNMODOO_04024 | 1.3e-84 | G | Xylose isomerase-like TIM barrel | |||
NHNMODOO_04025 | 1.3e-113 | surE | 3.1.3.5 | S | Survival protein SurE | |
NHNMODOO_04026 | 1.5e-136 | afuA | P | Bacterial extracellular solute-binding protein | ||
NHNMODOO_04027 | 1.1e-189 | afuB2 | P | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_04028 | 1.5e-136 | 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 | ||
NHNMODOO_04029 | 1.6e-61 | |||||
NHNMODOO_04030 | 2.6e-269 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NHNMODOO_04031 | 1.6e-191 | mccF | 3.4.17.13 | V | LD-carboxypeptidase | |
NHNMODOO_04032 | 1.2e-48 | |||||
NHNMODOO_04033 | 1.1e-164 | yfhF | S | nucleoside-diphosphate sugar epimerase | ||
NHNMODOO_04034 | 5e-140 | recX | 2.4.1.337 | GT4 | S | Modulates RecA activity |
NHNMODOO_04035 | 7.6e-52 | yfhH | S | Protein of unknown function (DUF1811) | ||
NHNMODOO_04036 | 1.2e-21 | S | YpzG-like protein | |||
NHNMODOO_04037 | 4.2e-186 | yfhP | S | membrane-bound metal-dependent | ||
NHNMODOO_04038 | 1.3e-201 | mutY | L | A G-specific | ||
NHNMODOO_04039 | 1.7e-126 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_04040 | 9.1e-59 | |||||
NHNMODOO_04041 | 4e-19 | yfhS | ||||
NHNMODOO_04042 | 1.3e-131 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NHNMODOO_04043 | 6e-15 | S | Small, acid-soluble spore protein, gamma-type | |||
NHNMODOO_04044 | 1.5e-102 | ygaC | J | Belongs to the UPF0374 family | ||
NHNMODOO_04045 | 0.0 | ygaD | V | ABC transporter | ||
NHNMODOO_04046 | 7e-187 | ygaE | S | Membrane | ||
NHNMODOO_04047 | 8.2e-246 | gsaB | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
NHNMODOO_04048 | 8.1e-87 | bcp | 1.11.1.15 | O | Peroxiredoxin | |
NHNMODOO_04049 | 7.5e-172 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NHNMODOO_04050 | 2.7e-48 | S | Cyclic-di-AMP receptor | |||
NHNMODOO_04051 | 1.5e-79 | perR | P | Belongs to the Fur family | ||
NHNMODOO_04052 | 5.2e-57 | ygzB | S | UPF0295 protein | ||
NHNMODOO_04053 | 1.4e-182 | ywtF | K | Transcriptional regulator | ||
NHNMODOO_04054 | 3.2e-80 | asnC | K | helix_turn_helix ASNC type | ||
NHNMODOO_04055 | 1.2e-146 | oppD | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_04056 | 1.3e-133 | oppF | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_04057 | 5.4e-138 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHNMODOO_04058 | 1.3e-117 | oppC | EP | binding-protein-dependent transport systems inner membrane component | ||
NHNMODOO_04059 | 2.5e-248 | oppA1 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | ||
NHNMODOO_04060 | 1.8e-102 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
NHNMODOO_04061 | 4e-113 | yvyE | 3.4.13.9 | S | Domain of unknown function (DUF1949) | |
NHNMODOO_04062 | 4.1e-201 | 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 | |
NHNMODOO_04063 | 1.1e-147 | degV | S | protein conserved in bacteria | ||
NHNMODOO_04064 | 6.7e-251 | comFA | L | COG4098 Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
NHNMODOO_04065 | 1.2e-123 | comFC | S | Phosphoribosyl transferase domain | ||
NHNMODOO_04066 | 1.7e-75 | yvyF | S | flagellar protein | ||
NHNMODOO_04067 | 3.6e-39 | N | Anti-sigma-28 factor, FlgM | |||
NHNMODOO_04069 | 2.8e-280 | flgK | N | flagellar hook-associated protein | ||
NHNMODOO_04070 | 1.7e-185 | flgL | N | Belongs to the bacterial flagellin family | ||
NHNMODOO_04071 | 8.2e-73 | fliW | S | Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum | ||
NHNMODOO_04072 | 7.7e-33 | csrA | T | Could accelerate the degradation of some genes transcripts potentially through selective RNA binding | ||
NHNMODOO_04073 | 5.7e-47 | flaG | N | flagellar protein FlaG | ||
NHNMODOO_04074 | 1.6e-289 | 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 | ||
NHNMODOO_04075 | 6.7e-66 | fliS | N | flagellar protein FliS | ||
NHNMODOO_04077 | 6.3e-146 | |||||
NHNMODOO_04078 | 3.8e-30 | cspB | K | cold-shock protein | ||
NHNMODOO_04079 | 1.2e-97 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
NHNMODOO_04080 | 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 | ||
NHNMODOO_04081 | 2.6e-183 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
NHNMODOO_04082 | 3.8e-146 | yvjA | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
NHNMODOO_04083 | 2.7e-123 | ftsE | D | cell division ATP-binding protein FtsE | ||
NHNMODOO_04084 | 8.8e-151 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
NHNMODOO_04085 | 2.2e-100 | D | peptidase | |||
NHNMODOO_04086 | 5.1e-265 | ctpB | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
NHNMODOO_04087 | 5.5e-201 | minJ | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | ||
NHNMODOO_04088 | 1e-146 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_04089 | 2.3e-151 | G | Binding-protein-dependent transport system inner membrane component | |||
NHNMODOO_04090 | 4e-199 | T | helix_turn_helix, arabinose operon control protein | |||
NHNMODOO_04091 | 7.1e-280 | 2.7.13.3 | T | Cache domain | ||
NHNMODOO_04092 | 1.5e-228 | G | Bacterial extracellular solute-binding protein | |||
NHNMODOO_04093 | 8.1e-210 | mtnW | 5.3.2.5 | G | Catalyzes the enolization of 2,3-diketo-5- methylthiopentyl-1-phosphate (DK-MTP-1-P) into 2-hydroxy-3-keto-5- methylthiopentenyl-1-phosphate (HK-MTPenyl-1-P) | |
NHNMODOO_04094 | 1.4e-90 | S | UPF0316 protein | |||
NHNMODOO_04095 | 7.3e-78 | ypqE | 2.7.1.199 | G | COG2190 Phosphotransferase system IIA components | |
NHNMODOO_04096 | 1.9e-95 | yvbF | K | Belongs to the GbsR family | ||
NHNMODOO_04097 | 9.5e-52 | ybaZ | 2.1.1.63 | L | Methyltransferase | |
NHNMODOO_04098 | 1.1e-72 | V | COG4767 Glycopeptide antibiotics resistance protein | |||
NHNMODOO_04099 | 5e-184 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
NHNMODOO_04100 | 0.0 | asnO | 6.3.5.4 | E | Asparagine synthase | |
NHNMODOO_04101 | 1.3e-202 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
NHNMODOO_04102 | 1.9e-223 | 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 | |
NHNMODOO_04103 | 8.8e-140 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
NHNMODOO_04104 | 2.9e-121 | P | Polycystin cation channel | |||
NHNMODOO_04105 | 4.7e-244 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
NHNMODOO_04107 | 3.2e-49 | |||||
NHNMODOO_04108 | 3.4e-46 | tnrA | K | transcriptional | ||
NHNMODOO_04109 | 9.1e-139 | yibQ | S | protein conserved in bacteria | ||
NHNMODOO_04110 | 0.0 | apr | O | Belongs to the peptidase S8 family | ||
NHNMODOO_04111 | 2.7e-41 | |||||
NHNMODOO_04112 | 2e-74 | ykuL | S | CBS domain | ||
NHNMODOO_04113 | 2.3e-78 | 3.6.1.55 | S | Pfam Polyketide cyclase dehydrase and lipid transport | ||
NHNMODOO_04114 | 7.1e-69 | yaaR | S | protein conserved in bacteria | ||
NHNMODOO_04116 | 2.1e-95 | 3.5.1.104 | G | Polysaccharide deacetylase | ||
NHNMODOO_04117 | 6.2e-194 | yqjE | 3.4.11.4 | E | COG2195 Di- and tripeptidases | |
NHNMODOO_04118 | 1.3e-67 | 5.1.99.1 | E | COG0346 Lactoylglutathione lyase and related lyases | ||
NHNMODOO_04120 | 4.4e-94 | yqjB | S | protein conserved in bacteria | ||
NHNMODOO_04121 | 3.9e-168 | yqjA | S | Putative aromatic acid exporter C-terminal domain | ||
NHNMODOO_04122 | 3.3e-167 | pilS | 2.7.13.3 | F | GHKL domain | |
NHNMODOO_04123 | 4.4e-20 | pbuO_1 | S | Permease | ||
NHNMODOO_04124 | 4.1e-67 | pbuO_1 | S | permease | ||
NHNMODOO_04125 | 2.1e-91 | 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 | |
NHNMODOO_04126 | 2e-79 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
NHNMODOO_04127 | 1.4e-259 | fumC | 1.1.1.38, 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
NHNMODOO_04128 | 1.4e-19 | bofA | S | Sigma-K factor-processing regulatory protein BofA | ||
NHNMODOO_04129 | 3.4e-30 | S | Protein of unknown function (DUF2508) | |||
NHNMODOO_04130 | 3.9e-110 | 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 | ||
NHNMODOO_04131 | 1.8e-34 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
NHNMODOO_04132 | 8.2e-307 | 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 | |
NHNMODOO_04133 | 1.3e-94 | K | Sigma-70, region 4 | |||
NHNMODOO_04134 | 3.2e-101 | 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 | |
NHNMODOO_04135 | 4.3e-83 | tadA | 3.5.4.1, 3.5.4.3, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
NHNMODOO_04136 | 5.1e-290 | gsiB_4 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | ||
NHNMODOO_04137 | 3.4e-158 | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | |||
NHNMODOO_04138 | 5.9e-169 | EP | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | |||
NHNMODOO_04139 | 2.4e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
NHNMODOO_04140 | 4.9e-190 | E | Belongs to the ABC transporter superfamily | |||
NHNMODOO_04141 | 4.2e-127 | glnQ2 | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
NHNMODOO_04142 | 4.2e-110 | glnP | E | Polar amino acid ABC transporter, inner membrane subunit | ||
NHNMODOO_04143 | 4.7e-143 | glnH | ET | Ligated ion channel L-glutamate- and glycine-binding site | ||
NHNMODOO_04144 | 5.5e-61 | S | Bacterial PH domain | |||
NHNMODOO_04145 | 1.1e-262 | gabD_2 | 1.2.1.9 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
NHNMODOO_04146 | 6.1e-191 | hom2 | 1.1.1.3 | E | Homoserine dehydrogenase | |
NHNMODOO_04147 | 1.5e-225 | amaA | 3.5.1.47 | E | Peptidase dimerisation domain | |
NHNMODOO_04148 | 3e-226 | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.2, 4.4.1.8 | E | cystathionine | ||
NHNMODOO_04149 | 8.5e-234 | eutD | 3.4.13.9, 3.5.4.44 | E | Creatinase/Prolidase N-terminal domain | |
NHNMODOO_04150 | 1.2e-242 | nhaC | C | Na H antiporter | ||
NHNMODOO_04151 | 3.3e-191 | rocG | 1.4.1.2, 1.4.1.3 | E | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase | |
NHNMODOO_04152 | 1.9e-228 | rocD | 2.6.1.11, 2.6.1.13, 2.6.1.17 | E | Catalyzes the interconversion of ornithine to glutamate semialdehyde | |
NHNMODOO_04153 | 2.2e-249 | rocR | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | ||
NHNMODOO_04154 | 2.3e-309 | QT | COG2508 Regulator of polyketide synthase expression | |||
NHNMODOO_04155 | 1.7e-145 | mtnU | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
NHNMODOO_04156 | 3.9e-216 | 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) | |
NHNMODOO_04157 | 6.4e-238 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NHNMODOO_04158 | 7.4e-272 | 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 | |
NHNMODOO_04159 | 1e-144 | yaaC | S | YaaC-like Protein | ||
NHNMODOO_04160 | 1.5e-84 | |||||
NHNMODOO_04161 | 2.1e-67 | 3.6.1.55 | F | NUDIX domain | ||
NHNMODOO_04162 | 5.4e-98 | S | Tetratricopeptide repeat | |||
NHNMODOO_04163 | 4e-26 | |||||
NHNMODOO_04164 | 2.1e-236 | V | MatE | |||
NHNMODOO_04165 | 1.9e-242 | NT | chemotaxis protein | |||
NHNMODOO_04166 | 5e-219 | C | Citrate transporter | |||
NHNMODOO_04167 | 1.1e-52 | |||||
NHNMODOO_04168 | 2e-234 | E | Acyclic terpene utilisation family protein AtuA | |||
NHNMODOO_04169 | 2e-250 | KT | Transcriptional regulator | |||
NHNMODOO_04170 | 9.1e-104 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
NHNMODOO_04171 | 3e-159 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
NHNMODOO_04172 | 4e-267 | gabR | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NHNMODOO_04174 | 4.1e-92 | 5.3.1.15 | S | Cupin 2, conserved barrel domain protein | ||
NHNMODOO_04175 | 3.3e-168 | fruA2 | G | Phosphotransferase System | ||
NHNMODOO_04176 | 1.1e-47 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHNMODOO_04177 | 4.4e-77 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NHNMODOO_04178 | 2.3e-159 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
NHNMODOO_04179 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | K | transcriptional regulator, MtlR | ||
NHNMODOO_04180 | 2.1e-293 | uxaB | 1.1.1.17, 1.1.1.58 | G | tagaturonate reductase activity | |
NHNMODOO_04181 | 6.2e-290 | uxaA | 4.2.1.7 | G | Altronate | |
NHNMODOO_04182 | 2.1e-222 | G | Tripartite ATP-independent periplasmic transporter, DctM component | |||
NHNMODOO_04183 | 6.8e-81 | G | Tripartite ATP-independent periplasmic transporters, DctQ component | |||
NHNMODOO_04184 | 2.1e-188 | dctP | G | Bacterial extracellular solute-binding protein, family 7 | ||
NHNMODOO_04185 | 2.5e-186 | yjjN | E | Alcohol dehydrogenase GroES-like domain | ||
NHNMODOO_04186 | 1.2e-157 | K | AraC-like ligand binding domain | |||
NHNMODOO_04188 | 9.6e-247 | bxlD | G | Bacterial extracellular solute-binding protein | ||
NHNMODOO_04189 | 4.3e-164 | bxlC | G | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_04190 | 2.4e-142 | bxlB | G | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_04191 | 3.9e-62 | S | Putative zinc- or iron-chelating domain | |||
NHNMODOO_04192 | 2.6e-244 | metY | 2.5.1.49 | E | O-acetylhomoserine | |
NHNMODOO_04193 | 1.8e-87 | M | FR47-like protein | |||
NHNMODOO_04195 | 2.9e-35 | S | membrane | |||
NHNMODOO_04196 | 7e-90 | S | Peptidase M50 | |||
NHNMODOO_04197 | 8.3e-235 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
NHNMODOO_04198 | 2.4e-113 | ypgQ | S | phosphohydrolase | ||
NHNMODOO_04199 | 7.6e-26 | |||||
NHNMODOO_04200 | 1.2e-272 | apc3 | 3.5.2.9 | EQ | Hydantoinase/oxoprolinase | |
NHNMODOO_04201 | 2.9e-204 | S | Protein of unknown function (DUF917) | |||
NHNMODOO_04202 | 4e-213 | codB_1 | F | cytosine purines uracil thiamine allantoin | ||
NHNMODOO_04203 | 6.6e-102 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_04204 | 2.1e-135 | K | acetyltransferase | |||
NHNMODOO_04205 | 9.4e-81 | S | Stage II sporulation protein P (SpoIIP) | |||
NHNMODOO_04206 | 9.3e-63 | KLT | Protein kinase domain | |||
NHNMODOO_04207 | 1.2e-83 | KLT | Protein kinase domain | |||
NHNMODOO_04208 | 1.4e-56 | FG | HIT domain | |||
NHNMODOO_04209 | 1.2e-164 | ydhJ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NHNMODOO_04210 | 6.8e-41 | S | Histidine kinase | |||
NHNMODOO_04211 | 1.1e-87 | |||||
NHNMODOO_04213 | 4.1e-178 | S | COG1073 Hydrolases of the alpha beta superfamily | |||
NHNMODOO_04214 | 1.7e-230 | S | protein conserved in bacteria | |||
NHNMODOO_04215 | 4.3e-250 | 3.5.4.28, 3.5.4.31 | F | Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine | ||
NHNMODOO_04216 | 6.4e-219 | amaB | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
NHNMODOO_04217 | 4.4e-239 | hutI | 3.5.2.7 | Q | Imidazolone-5-propionate hydrolase | |
NHNMODOO_04218 | 0.0 | hutU | 4.2.1.49 | E | Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate | |
NHNMODOO_04219 | 8.9e-281 | T | COG4753 Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain | |||
NHNMODOO_04220 | 8.5e-216 | G | Transmembrane secretion effector | |||
NHNMODOO_04221 | 5.3e-185 | desK | 2.7.13.3 | T | Histidine kinase | |
NHNMODOO_04222 | 1.5e-104 | K | helix_turn_helix, Lux Regulon | |||
NHNMODOO_04223 | 3.5e-112 | |||||
NHNMODOO_04224 | 4.4e-152 | licT | K | antiterminator | ||
NHNMODOO_04225 | 1.3e-268 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | COG1263 Phosphotransferase system IIC components, glucose maltose N-acetylglucosamine-specific | |
NHNMODOO_04226 | 8.2e-176 | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | ||
NHNMODOO_04227 | 5.7e-79 | M | Protein of unknown function (DUF1541) | |||
NHNMODOO_04228 | 1.5e-44 | |||||
NHNMODOO_04229 | 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) | |
NHNMODOO_04230 | 8.1e-290 | glpK | 2.7.1.30 | C | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
NHNMODOO_04231 | 1e-117 | glpF | G | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHNMODOO_04232 | 1.5e-199 | cebE | G | PFAM extracellular solute-binding protein family 1 | ||
NHNMODOO_04233 | 3.3e-156 | P | PFAM binding-protein-dependent transport systems inner membrane component | |||
NHNMODOO_04234 | 1.4e-145 | P | PFAM binding-protein-dependent transport systems inner membrane component | |||
NHNMODOO_04235 | 3.5e-191 | purR11 | K | helix_turn _helix lactose operon repressor | ||
NHNMODOO_04236 | 0.0 | DSE4 | M | glycoside hydrolase family 81 | ||
NHNMODOO_04237 | 2.2e-113 | 4.4.1.3, 5.3.1.15 | S | Cupin | ||
NHNMODOO_04238 | 4.5e-29 | |||||
NHNMODOO_04240 | 5.5e-102 | |||||
NHNMODOO_04241 | 1.5e-124 | yvqF | S | Cell wall-active antibiotics response 4TMS YvqF | ||
NHNMODOO_04242 | 8.9e-182 | vraS | 2.7.13.3 | T | Histidine kinase | |
NHNMODOO_04243 | 1.6e-106 | vraR | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
NHNMODOO_04244 | 9.7e-110 | modB | P | COG4149 ABC-type molybdate transport system, permease component | ||
NHNMODOO_04245 | 1.1e-130 | modA | P | COG0725 ABC-type molybdate transport system, periplasmic component | ||
NHNMODOO_04246 | 5.1e-300 | xsa | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus |
NHNMODOO_04248 | 1.5e-283 | yxiA | 3.2.1.99 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
NHNMODOO_04249 | 0.0 | 3.6.3.8 | P | COG0474 Cation transport ATPase | ||
NHNMODOO_04250 | 1.3e-137 | S | GNAT acetyltransferase | |||
NHNMODOO_04251 | 1.9e-144 | tagG | GM | Transport permease protein | ||
NHNMODOO_04252 | 7.7e-165 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
NHNMODOO_04253 | 2.6e-52 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
NHNMODOO_04254 | 4.1e-41 | S | Membrane | |||
NHNMODOO_04255 | 5.2e-198 | frvX | 3.2.1.4 | GH5,GH9 | G | M42 glutamyl aminopeptidase |
NHNMODOO_04256 | 3.6e-157 | spoVID | M | stage VI sporulation protein D | ||
NHNMODOO_04257 | 2.4e-156 | |||||
NHNMODOO_04258 | 1.9e-186 | 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 | ||
NHNMODOO_04259 | 1.7e-102 | |||||
NHNMODOO_04260 | 1.1e-27 | |||||
NHNMODOO_04261 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
NHNMODOO_04262 | 9.4e-234 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
NHNMODOO_04263 | 2.7e-49 | comC | 3.4.23.43 | NOU | COG1989 Type II secretory pathway, prepilin signal peptidase PulO and related peptidases | |
NHNMODOO_04264 | 2e-50 | comC | 3.4.23.43 | NOU | COG1989 Type II secretory pathway, prepilin signal peptidase PulO and related peptidases | |
NHNMODOO_04265 | 2.1e-194 | |||||
NHNMODOO_04266 | 0.0 | yuxL | 3.4.19.1 | EU | peptidase | |
NHNMODOO_04267 | 2.1e-100 | maf | D | septum formation protein Maf | ||
NHNMODOO_04268 | 2.8e-120 | radC | E | Belongs to the UPF0758 family | ||
NHNMODOO_04269 | 1.5e-186 | mreB | D | Rod shape-determining protein MreB | ||
NHNMODOO_04270 | 2.1e-160 | mreC | M | Involved in formation and maintenance of cell shape | ||
NHNMODOO_04271 | 8.8e-74 | mreD | M | shape-determining protein | ||
NHNMODOO_04272 | 4.3e-121 | 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 | ||
NHNMODOO_04273 | 1.6e-140 | minD | D | Belongs to the ParA family | ||
NHNMODOO_04274 | 4.1e-92 | yfkM | 3.5.1.124 | S | protease | |
NHNMODOO_04275 | 3.4e-74 | moaC | 4.6.1.17 | H | MoaC family | |
NHNMODOO_04276 | 2.9e-91 | bioY | S | BioY family | ||
NHNMODOO_04277 | 2.4e-167 | yqkF | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | ||
NHNMODOO_04278 | 1.2e-126 | spoIVFA | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
NHNMODOO_04279 | 1.8e-133 | spoIVFB | S | Stage IV sporulation protein | ||
NHNMODOO_04280 | 1.8e-265 | rng | J | ribonuclease, Rne Rng family | ||
NHNMODOO_04281 | 2.2e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
NHNMODOO_04282 | 5.3e-56 | ysxB | J | ribosomal protein | ||
NHNMODOO_04283 | 1.7e-44 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
NHNMODOO_04284 | 2.8e-79 | S | Domain of unknown function (DUF4188) | |||
NHNMODOO_04285 | 1.7e-90 | padR | K | Virulence activator alpha C-term | ||
NHNMODOO_04286 | 2.7e-152 | ydeE | K | AraC family transcriptional regulator | ||
NHNMODOO_04287 | 2e-72 | S | Activator of Hsp90 ATPase homolog 1-like protein | |||
NHNMODOO_04288 | 5.8e-124 | |||||
NHNMODOO_04289 | 4.6e-44 | |||||
NHNMODOO_04290 | 1.4e-210 | blt9 | EGP | Major facilitator Superfamily | ||
NHNMODOO_04291 | 1.6e-43 | |||||
NHNMODOO_04292 | 1.5e-70 | |||||
NHNMODOO_04293 | 1.8e-106 | C | Zinc-binding dehydrogenase | |||
NHNMODOO_04294 | 1.3e-276 | metP | S | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family | ||
NHNMODOO_04296 | 4.5e-55 | yitW | S | metal-sulfur cluster biosynthetic enzyme | ||
NHNMODOO_04298 | 1.1e-140 | ywfM | EG | EamA-like transporter family | ||
NHNMODOO_04299 | 2.7e-126 | yeeN | K | transcriptional regulatory protein | ||
NHNMODOO_04300 | 3.3e-146 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
NHNMODOO_04301 | 2.7e-244 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
NHNMODOO_04302 | 2.2e-96 | gmhB | 3.1.3.82, 3.1.3.83 | E | D,D-heptose 1,7-bisphosphate phosphatase | |
NHNMODOO_04303 | 1.9e-155 | asbF | 4.2.1.118 | G | Xylose isomerase-like TIM barrel | |
NHNMODOO_04304 | 6.9e-181 | asbE | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
NHNMODOO_04305 | 6.5e-41 | asbD | IQ | Phosphopantetheine attachment site | ||
NHNMODOO_04306 | 2.1e-219 | asbC | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | |
NHNMODOO_04307 | 0.0 | asbB | Q | IucA / IucC family | ||
NHNMODOO_04308 | 0.0 | iucA | 6.3.2.38 | Q | Siderophore biosynthesis protein | |
NHNMODOO_04309 | 7.5e-58 | isdI | 1.14.99.48, 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | |
NHNMODOO_04310 | 5.2e-256 | aglB | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
NHNMODOO_04311 | 5.7e-294 | glvC | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NHNMODOO_04312 | 2.5e-138 | glvR | K | Helix-turn-helix domain, rpiR family | ||
NHNMODOO_04313 | 1.9e-70 | S | Protein of unknown function (DUF1648) | |||
NHNMODOO_04314 | 1.9e-75 | |||||
NHNMODOO_04315 | 8.2e-09 | |||||
NHNMODOO_04316 | 2e-37 | yqjY | K | Acetyltransferase (GNAT) domain | ||
NHNMODOO_04317 | 6.7e-173 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | G | Belongs to the carbohydrate kinase PfkB family | |
NHNMODOO_04318 | 6.2e-140 | K | COG1349 Transcriptional regulators of sugar metabolism | |||
NHNMODOO_04319 | 1.8e-78 | pts36A | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
NHNMODOO_04320 | 3.9e-41 | gatB | 2.7.1.194, 2.7.1.200 | G | COG3414 Phosphotransferase system, galactitol-specific IIB component | |
NHNMODOO_04321 | 5.9e-239 | gatC | G | COG3775 Phosphotransferase system, galactitol-specific IIC component | ||
NHNMODOO_04322 | 3.8e-193 | gatD | 1.1.1.14, 1.1.1.251 | C | Alcohol dehydrogenase GroES-like domain | |
NHNMODOO_04323 | 1.4e-156 | kbaY | 4.1.2.13, 4.1.2.40 | G | in enteric bacteria there are two D-tagatose 1,6-bisphosphate-specific aldolases KbaY (also called AgaY), involved in catabolism of N-acetyl-galactosamine and D-galactosamine, and GatY which is part of the galactitol catabolism pathway | |
NHNMODOO_04324 | 6.2e-55 | yyaQ | S | Protein conserved in bacteria | ||
NHNMODOO_04325 | 3.7e-104 | folE2 | 3.5.4.16 | S | Converts GTP to 7,8-dihydroneopterin triphosphate | |
NHNMODOO_04326 | 7.8e-61 | yoaS | S | membrane | ||
NHNMODOO_04327 | 2.2e-29 | K | Transcriptional regulator | |||
NHNMODOO_04328 | 2.9e-137 | yoaT | S | Protein of unknown function (DUF817) | ||
NHNMODOO_04330 | 5.2e-24 | uppS | 2.5.1.31, 2.5.1.89 | H | Catalyzes the sequential condensation of isopentenyl diphosphate (IPP) with geranylgeranyl diphosphate (GGPP) to yield (2Z,6Z,10Z,14Z,18Z,22Z,26Z,30E,34E,38E)-undecaprenyl diphosphate (tritrans,heptacis-UPP). It is probably the precursor of glycosyl carrier lipids | |
NHNMODOO_04331 | 1.1e-90 | K | Helix-turn-helix domain | |||
NHNMODOO_04332 | 5.1e-157 | rspA | 4.2.1.8 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
NHNMODOO_04333 | 1.2e-98 | 3.4.22.70 | M | Sortase family | ||
NHNMODOO_04334 | 3.1e-18 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
NHNMODOO_04335 | 0.0 | yebA | E | COG1305 Transglutaminase-like enzymes | ||
NHNMODOO_04336 | 3.9e-207 | yeaD | S | conserved protein (some members contain a von Willebrand factor type A (vWA) domain) | ||
NHNMODOO_04337 | 5.4e-170 | yeaC | S | COG0714 MoxR-like ATPases | ||
NHNMODOO_04338 | 2.1e-97 | CO | Thioredoxin | |||
NHNMODOO_04339 | 6e-182 | 3.1.4.53 | Q | Calcineurin-like phosphoesterase | ||
NHNMODOO_04342 | 0.0 | pbpC | 3.4.16.4 | M | Penicillin-binding Protein | |
NHNMODOO_04343 | 5e-107 | C | nitroreductase | |||
NHNMODOO_04344 | 4e-115 | cwlC | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
NHNMODOO_04345 | 6e-62 | S | Bacteriophage holin family | |||
NHNMODOO_04347 | 0.0 | L | Phage minor structural protein | |||
NHNMODOO_04348 | 2.2e-136 | S | Phage tail protein | |||
NHNMODOO_04349 | 2.2e-116 | D | Phage tail tape measure protein, TP901 family | |||
NHNMODOO_04350 | 8.2e-76 | |||||
NHNMODOO_04351 | 1.3e-70 | |||||
NHNMODOO_04352 | 8.7e-55 | S | Short C-terminal domain | |||
NHNMODOO_04353 | 1e-210 | mez_1 | 1.1.1.38 | C | Malate dehydrogenase | |
NHNMODOO_04354 | 8.7e-243 | maeN | C | COG3493 Na citrate symporter | ||
NHNMODOO_04355 | 2.5e-292 | expZ | S | ABC transporter | ||
NHNMODOO_04356 | 7.8e-210 | gatD | 1.1.1.14 | C | Alcohol dehydrogenase GroES-like domain | |
NHNMODOO_04357 | 7.3e-21 | |||||
NHNMODOO_04358 | 1.3e-193 | gutB | 1.1.1.1, 1.1.1.14 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
NHNMODOO_04359 | 9.4e-215 | gatC | G | COG3775 Phosphotransferase system, galactitol-specific IIC component | ||
NHNMODOO_04360 | 4.8e-42 | gatB_1 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHNMODOO_04361 | 1.9e-75 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NHNMODOO_04362 | 0.0 | licR | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | COG3711 Transcriptional antiterminator | |
NHNMODOO_04363 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
NHNMODOO_04364 | 2.9e-185 | |||||
NHNMODOO_04365 | 1.7e-103 | hxlA | 4.1.2.43 | G | 3-hexulose-6-phosphate synthase | |
NHNMODOO_04366 | 1.4e-175 | kdgK | 2.7.1.45 | G | COG0524 Sugar kinases, ribokinase family | |
NHNMODOO_04367 | 2e-102 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
NHNMODOO_04368 | 1.7e-88 | hxlB | 4.1.2.14, 4.1.2.43, 4.1.3.42, 5.3.1.27 | M | SIS domain | |
NHNMODOO_04369 | 2.8e-198 | MA20_17100 | G | COG1593 TRAP-type C4-dicarboxylate transport system, large permease component | ||
NHNMODOO_04370 | 3e-84 | G | Tripartite ATP-independent periplasmic transporters, DctQ component | |||
NHNMODOO_04371 | 7.9e-164 | dctP_1 | G | Bacterial extracellular solute-binding protein, family 7 | ||
NHNMODOO_04372 | 5.6e-178 | kdgR | K | transcriptional | ||
NHNMODOO_04373 | 4.5e-52 | K | Transcriptional regulator PadR-like family | |||
NHNMODOO_04374 | 7.9e-73 | |||||
NHNMODOO_04375 | 2.1e-55 | trpG | 2.6.1.85, 4.1.3.27 | EH | TIGRFAM glutamine amidotransferase of anthranilate synthase | |
NHNMODOO_04376 | 2e-75 | 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 | |
NHNMODOO_04377 | 4.2e-167 | K | LysR substrate binding domain | |||
NHNMODOO_04378 | 1.3e-185 | ord | 1.4.1.12, 1.4.1.16, 1.4.1.26 | S | Dihydrodipicolinate reductase, N-terminus | |
NHNMODOO_04379 | 1.8e-235 | C | Na+/H+ antiporter family | |||
NHNMODOO_04380 | 1.2e-76 | S | glyoxalase bleomycin resistance protein dioxygenase | |||
NHNMODOO_04381 | 0.0 | S | AAA-like domain | |||
NHNMODOO_04382 | 0.0 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
NHNMODOO_04383 | 6.5e-182 | yddH | M | Lysozyme-like | ||
NHNMODOO_04384 | 3.9e-159 | S | Conjugative transposon protein TcpC | |||
NHNMODOO_04385 | 3.3e-22 | K | transcriptional regulator | |||
NHNMODOO_04386 | 7.3e-138 | MA20_20400 | 3.4.11.5 | S | Alpha/beta hydrolase family | |
NHNMODOO_04388 | 2.1e-110 | L | PFAM transposase IS4 family protein | |||
NHNMODOO_04389 | 2.4e-75 | L | Transposase | |||
NHNMODOO_04390 | 2.1e-103 | pksA | K | BetI-type transcriptional repressor, C-terminal | ||
NHNMODOO_04391 | 2.5e-116 | S | Sap, sulfolipid-1-addressing protein | |||
NHNMODOO_04392 | 3.5e-32 | |||||
NHNMODOO_04393 | 3.9e-161 | I | Acyltransferase family | |||
NHNMODOO_04394 | 5.3e-31 | phyR | K | Sigma-70, region 4 | ||
NHNMODOO_04395 | 3e-31 | phyR | K | Sigma-70, region 4 | ||
NHNMODOO_04396 | 1.5e-39 | S | Helix-turn-helix domain | |||
NHNMODOO_04397 | 2e-25 | K | Helix-turn-helix domain | |||
NHNMODOO_04398 | 6.7e-56 | yqjZ | 2.3.1.128, 2.5.1.18 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
NHNMODOO_04399 | 4.1e-50 | padR | K | Transcriptional regulator PadR-like family | ||
NHNMODOO_04400 | 2.2e-115 | S | Protein of unknown function (DUF2812) | |||
NHNMODOO_04401 | 1.1e-191 | EGP | MFS/sugar transport protein | |||
NHNMODOO_04402 | 7.2e-134 | KT | PFAM sigma-54 factor interaction domain-containing protein | |||
NHNMODOO_04403 | 2.3e-191 | MA20_01110 | 4.2.1.81 | M | Mandelate racemase / muconate lactonizing enzyme, C-terminal domain | |
NHNMODOO_04404 | 2.1e-160 | K | Acetyltransferase (GNAT) family | |||
NHNMODOO_04405 | 1.5e-141 | K | MerR family transcriptional regulator | |||
NHNMODOO_04406 | 1.2e-71 | |||||
NHNMODOO_04407 | 8e-115 | O | Sap, sulfolipid-1-addressing protein | |||
NHNMODOO_04408 | 4.6e-86 | aacA-aphD | 2.7.1.190 | S | Protein of unknown function (DUF1679) | |
NHNMODOO_04409 | 7.8e-11 | aacA-aphD | 2.7.1.190 | S | Protein of unknown function (DUF1679) | |
NHNMODOO_04410 | 3.8e-28 | aacA-aphD | 2.7.1.190 | S | Protein of unknown function (DUF1679) | |
NHNMODOO_04411 | 5.6e-79 | K | helix_turn_helix, mercury resistance | |||
NHNMODOO_04412 | 4.6e-171 | L | Endonuclease/Exonuclease/phosphatase family | |||
NHNMODOO_04414 | 4.7e-87 | ydcK | S | Belongs to the SprT family | ||
NHNMODOO_04415 | 3.9e-08 | |||||
NHNMODOO_04416 | 0.0 | yhgF | K | COG2183 Transcriptional accessory protein | ||
NHNMODOO_04417 | 1.1e-65 | E | lactoylglutathione lyase activity | |||
NHNMODOO_04418 | 1.4e-150 | 3.5.1.28 | M | COG3103 SH3 domain protein | ||
NHNMODOO_04419 | 4.3e-110 | K | LysR substrate binding domain | |||
NHNMODOO_04420 | 5.3e-122 | pkn1 | 1.8.3.7 | S | Sulfatase-modifying factor enzyme 1 | |
NHNMODOO_04421 | 1.3e-102 | 5.1.3.9 | G | Putative N-acetylmannosamine-6-phosphate epimerase | ||
NHNMODOO_04422 | 4.9e-47 | 2.7.1.201 | G | PTS system, glucose subfamily, IIA | ||
NHNMODOO_04423 | 1.9e-205 | atsG | P | Type I phosphodiesterase / nucleotide pyrophosphatase | ||
NHNMODOO_04424 | 3e-218 | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | ||
NHNMODOO_04425 | 7.3e-87 | K | Regulates the succiny-lCoA synthetase operon | |||
NHNMODOO_04426 | 3.6e-79 | S | Sulfite exporter TauE/SafE | |||
NHNMODOO_04427 | 1.6e-155 | htpX | O | Belongs to the peptidase M48B family | ||
NHNMODOO_04428 | 6e-24 | mcbG | S | Pentapeptide repeats (9 copies) | ||
NHNMODOO_04429 | 4.9e-148 | araQ | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
NHNMODOO_04430 | 2.4e-159 | lacF | G | Binding-protein-dependent transport system inner membrane component | ||
NHNMODOO_04431 | 1.1e-239 | araN | G | ABC transporter substrate-binding protein | ||
NHNMODOO_04432 | 3.9e-48 | S | Branched-chain amino acid transport protein (AzlD) | |||
NHNMODOO_04433 | 2.5e-116 | azlC | E | AzlC protein | ||
NHNMODOO_04434 | 3.5e-67 | 2.3.1.128 | J | L-PSP family endoribonuclease | ||
NHNMODOO_04435 | 4.9e-92 | 3.1.3.41, 3.6.1.55 | F | Belongs to the Nudix hydrolase family | ||
NHNMODOO_04436 | 1.5e-115 | 3.1.3.41, 3.6.1.55 | F | Belongs to the Nudix hydrolase family | ||
NHNMODOO_04437 | 1e-52 | GM | NmrA-like family | |||
NHNMODOO_04438 | 4e-71 | phnB5 | S | 3-demethylubiquinone-9 3-methyltransferase | ||
NHNMODOO_04439 | 2.3e-72 | BH1582 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
NHNMODOO_04440 | 5.1e-125 | azlC | E | AzlC protein | ||
NHNMODOO_04441 | 4.7e-49 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
NHNMODOO_04442 | 5.8e-64 | frataxin | S | Domain of unknown function (DU1801) | ||
NHNMODOO_04443 | 3.4e-55 | smtB | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
NHNMODOO_04444 | 4.3e-73 | yndB | K | Activator of Hsp90 ATPase homolog 1-like protein | ||
NHNMODOO_04445 | 0.0 | L | ABC transporter | |||
NHNMODOO_04446 | 1.7e-109 | 1.14.12.17 | C | Oxidoreductase NAD-binding domain | ||
NHNMODOO_04447 | 1.2e-63 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
NHNMODOO_04448 | 2.7e-199 | ycsA | 1.1.1.83, 1.1.1.93, 4.1.1.73 | CE | Tartrate dehydrogenase | |
NHNMODOO_04449 | 5.7e-110 | ydhC | K | FCD | ||
NHNMODOO_04451 | 9.5e-161 | catE | 1.13.11.2 | S | glyoxalase | |
NHNMODOO_04452 | 4.1e-22 | |||||
NHNMODOO_04453 | 4.7e-16 | yheE | S | Family of unknown function (DUF5342) | ||
NHNMODOO_04454 | 4.4e-203 | yheB | S | Belongs to the UPF0754 family | ||
NHNMODOO_04455 | 1.4e-54 | yheA | S | Belongs to the UPF0342 family | ||
NHNMODOO_04456 | 1.3e-156 | yhaX | S | hydrolases of the HAD superfamily | ||
NHNMODOO_04458 | 1.3e-40 | |||||
NHNMODOO_04459 | 1.4e-124 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NHNMODOO_04460 | 8.5e-257 | T | PhoQ Sensor | |||
NHNMODOO_04461 | 8e-182 | yhaM | L | Shows a 3'-5' exoribonuclease activity | ||
NHNMODOO_04462 | 4.4e-43 | yhaL | S | Sporulation protein YhaL | ||
NHNMODOO_04463 | 2.2e-161 | prsA | 5.2.1.8 | M | plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
NHNMODOO_04465 | 1.1e-102 | S | Protein conserved in bacteria | |||
NHNMODOO_04466 | 2.8e-21 | ydcG | K | Helix-turn-helix domain | ||
NHNMODOO_04467 | 1.6e-38 | |||||
NHNMODOO_04468 | 2.7e-198 | L | Transposase | |||
NHNMODOO_04469 | 0.0 | V | ABC transporter (permease) | |||
NHNMODOO_04470 | 1.2e-135 | V | ABC transporter, ATP-binding protein | |||
NHNMODOO_04471 | 4.5e-123 | T | Transcriptional regulatory protein, C terminal | |||
NHNMODOO_04472 | 3.1e-176 | T | PhoQ Sensor | |||
NHNMODOO_04473 | 1.2e-25 | S | Helix-turn-helix domain | |||
NHNMODOO_04474 | 1.4e-26 | S | Domain of unknown function (DUF3173) | |||
NHNMODOO_04475 | 1e-107 | hpr | K | Negative regulator of protease production and sporulation | ||
NHNMODOO_04476 | 1.8e-49 | yhaH | D | gas vesicle protein | ||
NHNMODOO_04477 | 7.7e-205 | 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 | |
NHNMODOO_04478 | 1.2e-73 | hit | FG | COG0537 Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
NHNMODOO_04479 | 7.1e-138 | ecsA | V | transporter (ATP-binding protein) | ||
NHNMODOO_04480 | 1.2e-209 | ecsB | U | ABC transporter | ||
NHNMODOO_04481 | 2.3e-125 | ecsC | S | EcsC protein family | ||
NHNMODOO_04482 | 4.1e-122 | ccdA | O | cytochrome c biogenesis protein | ||
NHNMODOO_04483 | 0.0 | pbpF | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NHNMODOO_04486 | 1.2e-26 | |||||
NHNMODOO_04488 | 8.5e-96 | |||||
NHNMODOO_04489 | 4.1e-161 | aadK | G | Streptomycin adenylyltransferase | ||
NHNMODOO_04490 | 0.0 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
NHNMODOO_04491 | 1.8e-156 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
NHNMODOO_04492 | 0.0 | K | transcriptional regulator, MtlR | |||
NHNMODOO_04493 | 7.8e-166 | mviM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
NHNMODOO_04494 | 1.3e-28 | cspL | K | 'Cold-shock' DNA-binding domain | ||
NHNMODOO_04495 | 8.3e-76 | carD | K | Transcription factor | ||
NHNMODOO_04496 | 5.9e-49 | arsR | K | ArsR family transcriptional regulator | ||
NHNMODOO_04497 | 1.2e-64 | cadI | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
NHNMODOO_04498 | 3.3e-53 | arsR | K | transcriptional | ||
NHNMODOO_04499 | 7.9e-217 | arsB | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
NHNMODOO_04500 | 1.9e-74 | arsC | 1.20.4.1 | T | Catalyzes the reduction of arsenate As(V) to arsenite As(III) | |
NHNMODOO_04502 | 4.9e-234 | oxdD | 4.1.1.2 | G | Oxalate decarboxylase | |
NHNMODOO_04503 | 1e-113 | rsbX | 3.1.3.16, 3.1.3.3 | KT | Sigma factor PP2C-like phosphatases | |
NHNMODOO_04504 | 4.3e-141 | sigB | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
NHNMODOO_04505 | 1.1e-81 | rsbW | 2.7.11.1 | T | Negative regulator of sigma-B activity. Phosphorylates and inactivates its specific antagonist protein, RsbV. Upon phosphorylation of RsbV, RsbW is released and binds to sigma-B, thereby blocking its ability to form an RNA polymerase holoenzyme (E-sigma-B) | |
NHNMODOO_04506 | 3.2e-53 | rsbV | T | Belongs to the anti-sigma-factor antagonist family | ||
NHNMODOO_04507 | 9e-184 | rsbU | 3.1.3.3 | KT | phosphatase | |
NHNMODOO_04508 | 1.4e-72 | rsbT | 2.7.11.1 | T | COG2172 Anti-sigma regulatory factor (Ser Thr protein kinase) | |
NHNMODOO_04509 | 1.3e-52 | rsbS | T | antagonist | ||
NHNMODOO_04510 | 5.8e-141 | rsbR | T | Positive regulator of sigma-B | ||
NHNMODOO_04511 | 1.3e-55 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
NHNMODOO_04512 | 8e-25 | ndoAI | K | transcriptional regulators containing the CopG Arc MetJ DNA-binding domain and a metal-binding domain | ||
NHNMODOO_04513 | 8.3e-224 | 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 | |
NHNMODOO_04514 | 4.7e-115 | |||||
NHNMODOO_04515 | 1.5e-34 | ptsH | G | PTS HPr component phosphorylation site | ||
NHNMODOO_04516 | 9e-234 | thrA | E | SAF | ||
NHNMODOO_04517 | 6.4e-67 | K | Glucitol operon activator protein (GutM) | |||
NHNMODOO_04518 | 5.6e-89 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
NHNMODOO_04519 | 1e-179 | srlE | 2.7.1.198 | G | PTS system glucitol sorbitol-specific transporter subunit IIB | |
NHNMODOO_04520 | 4.2e-59 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
NHNMODOO_04521 | 1.9e-167 | K | Putative sugar-binding domain | |||
NHNMODOO_04524 | 1.4e-98 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
NHNMODOO_04525 | 1.1e-27 | copP | P | Heavy-metal-associated domain | ||
NHNMODOO_04526 | 9.9e-46 | csoR | S | transcriptional | ||
NHNMODOO_04527 | 1.9e-29 | |||||
NHNMODOO_04528 | 1.7e-145 | ykrA | S | hydrolases of the HAD superfamily | ||
NHNMODOO_04529 | 6.7e-70 | S | Transcriptional regulator | |||
NHNMODOO_04530 | 4e-22 | |||||
NHNMODOO_04531 | 6.2e-64 | XK27_03185 | S | Phosphoribosyl-ATP pyrophosphohydrolase | ||
NHNMODOO_04532 | 7.2e-146 | L | Phage integrase, N-terminal SAM-like domain | |||
NHNMODOO_04533 | 3.6e-69 | S | Protein of unknown function (DUF418) | |||
NHNMODOO_04534 | 6.2e-88 | yqeB | ||||
NHNMODOO_04535 | 6.5e-81 | K | Bacterial regulatory proteins, tetR family | |||
NHNMODOO_04536 | 1.9e-177 | sthIM | 2.1.1.72 | L | DNA methylase | |
NHNMODOO_04538 | 3.3e-95 | yokH | G | SMI1 / KNR4 family | ||
NHNMODOO_04539 | 1.5e-59 | Q | ubiE/COQ5 methyltransferase family | |||
NHNMODOO_04540 | 2.5e-97 | yrkC | G | Cupin domain | ||
NHNMODOO_04541 | 2.2e-61 | S | TraX protein | |||
NHNMODOO_04542 | 3.9e-37 | |||||
NHNMODOO_04543 | 1e-145 | U | AAA domain | |||
NHNMODOO_04544 | 1.3e-48 | L | Mu transposase, C-terminal | |||
NHNMODOO_04545 | 1.2e-08 | S | nuclease activity | |||
NHNMODOO_04546 | 2.3e-07 | |||||
NHNMODOO_04547 | 4.6e-88 | |||||
NHNMODOO_04548 | 3.1e-07 | |||||
NHNMODOO_04550 | 3.1e-129 | K | TIGRFAM RNA polymerase sigma factor, sigma-70 family | |||
NHNMODOO_04551 | 1.3e-36 | S | Carboxymuconolactone decarboxylase family | |||
NHNMODOO_04553 | 3.5e-51 | |||||
NHNMODOO_04554 | 6.3e-111 | K | Bacterial transcriptional repressor C-terminal | |||
NHNMODOO_04555 | 3e-249 | EGP | Major facilitator Superfamily | |||
NHNMODOO_04556 | 2.6e-141 | L | PFAM Integrase catalytic region | |||
NHNMODOO_04557 | 1.7e-31 | L | COG2963 Transposase and inactivated derivatives | |||
NHNMODOO_04558 | 3.2e-10 | L | transposase activity | |||
NHNMODOO_04559 | 3.9e-168 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
NHNMODOO_04560 | 1.1e-231 | 2.7.7.49 | L | RNA-directed DNA polymerase (reverse transcriptase) | ||
NHNMODOO_04561 | 4.5e-47 | L | Transposase | |||
NHNMODOO_04562 | 1.1e-95 | L | COG3385 FOG Transposase and inactivated derivatives | |||
NHNMODOO_04563 | 1.1e-71 | L | transposase activity | |||
NHNMODOO_04564 | 1.7e-87 | L | COG2801 Transposase and inactivated derivatives | |||
NHNMODOO_04565 | 1.9e-133 | L | IstB-like ATP binding protein | |||
NHNMODOO_04566 | 4.3e-70 | L | Transposase | |||
NHNMODOO_04567 | 2.3e-213 | |||||
NHNMODOO_04568 | 1.7e-33 | L | COG3666 Transposase and inactivated derivatives | |||
NHNMODOO_04569 | 1.7e-100 | L | HTH-like domain | |||
NHNMODOO_04570 | 2.4e-36 | L | Transposase | |||
NHNMODOO_04571 | 7.8e-24 | L | Transposase and inactivated derivatives | |||
NHNMODOO_04572 | 1.2e-77 | res_1 | 3.1.21.5 | S | Type III restriction | |
NHNMODOO_04573 | 2.5e-168 | L | reverse transcriptase | |||
NHNMODOO_04576 | 6e-149 | L | COG3385 FOG Transposase and inactivated derivatives | |||
NHNMODOO_04577 | 1.5e-86 | S | Erythromycin esterase | |||
NHNMODOO_04579 | 2.2e-79 | L | Transposase IS200 like | |||
NHNMODOO_04580 | 9.1e-68 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
NHNMODOO_04581 | 1.2e-91 | L | Molecular Function DNA binding, Biological Process DNA recombination | |||
NHNMODOO_04582 | 3.5e-25 | phnM | 3.6.1.63 | P | Amidohydrolase family | |
NHNMODOO_04586 | 4.8e-22 | S | membrane | |||
NHNMODOO_04587 | 3e-22 | L | Transposase | |||
NHNMODOO_04588 | 2.7e-39 | 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) | |
NHNMODOO_04589 | 3.8e-22 | cwlK | M | Peptidase M15B and M15C DD-carboxypeptidase VanY endolysin | ||
NHNMODOO_04590 | 2.9e-45 | rsbR | T | Positive regulator of sigma-B | ||
NHNMODOO_04591 | 1.1e-19 | P | Ion transport | |||
NHNMODOO_04592 | 1.3e-44 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
NHNMODOO_04593 | 1.7e-31 | istA | L | Integrase core domain | ||
NHNMODOO_04594 | 3.8e-39 | E | COG1177 ABC-type spermidine putrescine transport system, permease component II | |||
NHNMODOO_04595 | 2.9e-31 | nifS | 2.8.1.7 | E | Cysteine desulfurase | |
NHNMODOO_04598 | 1.5e-07 | |||||
NHNMODOO_04603 | 1.4e-18 | spoVID | M | stage VI sporulation protein D | ||
NHNMODOO_04606 | 4.5e-19 | 3.5.1.28 | M | Ami_2 | ||
NHNMODOO_04609 | 4.2e-17 | 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 | ||
NHNMODOO_04610 | 1.7e-07 | |||||
NHNMODOO_04612 | 8.7e-22 | |||||
NHNMODOO_04615 | 3.7e-14 | S | MMPL domain protein | |||
NHNMODOO_04616 | 7e-16 | G | isomerase | |||
NHNMODOO_04617 | 6.1e-14 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)