ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
IJFNMBCI_00001 | 6e-59 | yugI | 5.3.1.9 | J | RNA binding protein (contains ribosomal protein S1 domain) | |
IJFNMBCI_00002 | 5.5e-209 | yugH | 2.6.1.1 | E | Aminotransferase | |
IJFNMBCI_00003 | 2e-83 | alaR | K | Transcriptional regulator | ||
IJFNMBCI_00004 | 1.4e-155 | yugF | I | Hydrolase | ||
IJFNMBCI_00005 | 2.7e-39 | yugE | S | Domain of unknown function (DUF1871) | ||
IJFNMBCI_00006 | 2.1e-224 | patB | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
IJFNMBCI_00007 | 1.8e-229 | T | PhoQ Sensor | |||
IJFNMBCI_00008 | 2.6e-67 | kapB | G | Kinase associated protein B | ||
IJFNMBCI_00009 | 4e-118 | kapD | L | the KinA pathway to sporulation | ||
IJFNMBCI_00010 | 6.5e-184 | yuxJ | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00011 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin-binding Protein |
IJFNMBCI_00012 | 2.2e-72 | yuxK | S | protein conserved in bacteria | ||
IJFNMBCI_00013 | 9.3e-74 | yufK | S | Family of unknown function (DUF5366) | ||
IJFNMBCI_00014 | 1.9e-292 | dcuS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
IJFNMBCI_00015 | 2.7e-126 | dcuR | T | COG4565 Response regulator of citrate malate metabolism | ||
IJFNMBCI_00016 | 7.1e-195 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
IJFNMBCI_00017 | 1.1e-286 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
IJFNMBCI_00018 | 1.1e-184 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
IJFNMBCI_00019 | 1.6e-169 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
IJFNMBCI_00020 | 1.8e-12 | |||||
IJFNMBCI_00021 | 0.0 | phaA | 1.6.5.3 | CP | COG1009 NADH ubiquinone oxidoreductase subunit 5 (chain L) Multisubunit Na H antiporter, MnhA subunit | |
IJFNMBCI_00022 | 9.2e-69 | mrpB | P | Subunit B of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
IJFNMBCI_00023 | 8.9e-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 | |
IJFNMBCI_00024 | 4.5e-264 | mrpD | CP | Subunit D of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
IJFNMBCI_00025 | 7.7e-77 | mrpE | P | Subunit E of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
IJFNMBCI_00026 | 1.5e-38 | phaF | P | Subunit F of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
IJFNMBCI_00027 | 5.2e-60 | phaG | P | COG1320 Multisubunit Na H antiporter, MnhG subunit | ||
IJFNMBCI_00028 | 1.6e-64 | ydiI | Q | protein, possibly involved in aromatic compounds catabolism | ||
IJFNMBCI_00029 | 8.5e-111 | comA | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
IJFNMBCI_00030 | 7.6e-255 | comP | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_00032 | 6.8e-66 | comQ | H | Polyprenyl synthetase | ||
IJFNMBCI_00034 | 9.5e-53 | yuzC | ||||
IJFNMBCI_00035 | 2e-230 | yuxH | 3.1.4.52 | T | signal transduction protein containing EAL and modified HD-GYP domains | |
IJFNMBCI_00036 | 7.2e-283 | 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 | |
IJFNMBCI_00037 | 1.1e-103 | pncA | Q | COG1335 Amidases related to nicotinamidase | ||
IJFNMBCI_00038 | 7.2e-68 | yueI | S | Protein of unknown function (DUF1694) | ||
IJFNMBCI_00039 | 2.8e-38 | yueH | S | YueH-like protein | ||
IJFNMBCI_00040 | 6.4e-34 | yueG | S | Spore germination protein gerPA/gerPF | ||
IJFNMBCI_00041 | 5.6e-187 | yueF | S | transporter activity | ||
IJFNMBCI_00042 | 8.7e-21 | S | Protein of unknown function (DUF2642) | |||
IJFNMBCI_00043 | 3.7e-96 | yueE | S | phosphohydrolase | ||
IJFNMBCI_00044 | 1.9e-130 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_00045 | 6.5e-76 | yueC | S | Family of unknown function (DUF5383) | ||
IJFNMBCI_00046 | 7.7e-196 | esaA | S | type VII secretion protein EsaA | ||
IJFNMBCI_00047 | 1e-230 | esaA | S | type VII secretion protein EsaA | ||
IJFNMBCI_00048 | 0.0 | essC | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | ||
IJFNMBCI_00049 | 8.1e-227 | essC | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | ||
IJFNMBCI_00050 | 1.8e-205 | essB | S | WXG100 protein secretion system (Wss), protein YukC | ||
IJFNMBCI_00051 | 3.9e-40 | yukD | S | WXG100 protein secretion system (Wss), protein YukD | ||
IJFNMBCI_00052 | 3.3e-46 | esxA | S | Belongs to the WXG100 family | ||
IJFNMBCI_00053 | 3.2e-228 | yukF | QT | Transcriptional regulator | ||
IJFNMBCI_00054 | 1e-204 | ald | 1.4.1.1 | E | Belongs to the AlaDH PNT family | |
IJFNMBCI_00055 | 2.8e-133 | yukJ | S | Uncharacterized conserved protein (DUF2278) | ||
IJFNMBCI_00056 | 6.2e-34 | mbtH | S | MbtH-like protein | ||
IJFNMBCI_00057 | 0.0 | dhbF | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | ||
IJFNMBCI_00058 | 6.5e-173 | entB | 3.3.2.1, 6.3.2.14 | Q | Isochorismatase family | |
IJFNMBCI_00059 | 0.0 | entE | 2.7.7.58, 6.3.2.14 | Q | 2,3-dihydroxybenzoate-AMP ligase | |
IJFNMBCI_00060 | 3.6e-224 | entC | 5.4.4.2 | HQ | Isochorismate synthase | |
IJFNMBCI_00061 | 7.1e-136 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
IJFNMBCI_00062 | 6.2e-165 | besA | S | Putative esterase | ||
IJFNMBCI_00063 | 4.1e-120 | yuiH | S | Oxidoreductase molybdopterin binding domain | ||
IJFNMBCI_00064 | 1.1e-101 | bioY | S | Biotin biosynthesis protein | ||
IJFNMBCI_00065 | 1.1e-208 | yuiF | S | antiporter | ||
IJFNMBCI_00066 | 5.8e-280 | 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 | |
IJFNMBCI_00067 | 9.1e-78 | yuiD | S | protein conserved in bacteria | ||
IJFNMBCI_00068 | 3.5e-117 | yuiC | S | protein conserved in bacteria | ||
IJFNMBCI_00069 | 9.9e-28 | yuiB | S | Putative membrane protein | ||
IJFNMBCI_00070 | 1.2e-235 | yumB | 1.6.99.3 | C | NADH dehydrogenase | |
IJFNMBCI_00071 | 1.5e-186 | yumC | 1.18.1.2, 1.19.1.1 | C | reductase | |
IJFNMBCI_00073 | 1.6e-185 | 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 | |
IJFNMBCI_00074 | 4.8e-29 | |||||
IJFNMBCI_00075 | 4.5e-70 | CP | Membrane | |||
IJFNMBCI_00076 | 3.1e-122 | V | ABC transporter | |||
IJFNMBCI_00078 | 2.9e-33 | S | Bacteriocin class IId cyclical uberolysin-like | |||
IJFNMBCI_00080 | 9e-72 | rimJ | 2.3.1.128 | J | Alanine acetyltransferase | |
IJFNMBCI_00081 | 8.5e-15 | rimJ | 2.3.1.128 | J | Alanine acetyltransferase | |
IJFNMBCI_00082 | 4e-136 | dltE | M | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
IJFNMBCI_00083 | 1.1e-62 | erpA | S | Belongs to the HesB IscA family | ||
IJFNMBCI_00084 | 1.6e-162 | 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 | |
IJFNMBCI_00085 | 8.5e-213 | yutK | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
IJFNMBCI_00086 | 2.4e-39 | yuzB | S | Belongs to the UPF0349 family | ||
IJFNMBCI_00087 | 2.7e-207 | yutJ | 1.6.99.3 | C | NADH dehydrogenase | |
IJFNMBCI_00088 | 9.7e-55 | yuzD | S | protein conserved in bacteria | ||
IJFNMBCI_00089 | 1.2e-35 | yutI | O | COG0694 Thioredoxin-like proteins and domains | ||
IJFNMBCI_00090 | 0.0 | yuxL | 3.4.14.5, 3.4.19.1 | EU | peptidase | |
IJFNMBCI_00091 | 2.6e-169 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
IJFNMBCI_00092 | 2.2e-196 | 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 | |
IJFNMBCI_00093 | 1e-240 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
IJFNMBCI_00094 | 1.2e-196 | yutH | S | Spore coat protein | ||
IJFNMBCI_00095 | 8.7e-85 | pgpA | 3.1.3.27 | I | COG1267 Phosphatidylglycerophosphatase A and related proteins | |
IJFNMBCI_00096 | 8.5e-142 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
IJFNMBCI_00097 | 9.5e-74 | yutE | S | Protein of unknown function DUF86 | ||
IJFNMBCI_00098 | 1.7e-47 | yutD | S | protein conserved in bacteria | ||
IJFNMBCI_00099 | 8e-168 | 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 | |
IJFNMBCI_00100 | 3.8e-195 | lytH | M | Peptidase, M23 | ||
IJFNMBCI_00101 | 4.8e-129 | yunB | S | Sporulation protein YunB (Spo_YunB) | ||
IJFNMBCI_00102 | 3.5e-191 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
IJFNMBCI_00103 | 5.2e-62 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
IJFNMBCI_00104 | 1.8e-145 | yunE | S | membrane transporter protein | ||
IJFNMBCI_00105 | 5.3e-169 | yunF | S | Protein of unknown function DUF72 | ||
IJFNMBCI_00106 | 1.5e-61 | 3.1.3.18, 3.8.1.2 | S | phosphoglycolate phosphatase activity | ||
IJFNMBCI_00107 | 3.8e-262 | 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 | |
IJFNMBCI_00108 | 4.4e-302 | pucR | QT | COG2508 Regulator of polyketide synthase expression | ||
IJFNMBCI_00110 | 5.3e-177 | S | Aspartate phosphatase response regulator | |||
IJFNMBCI_00111 | 1.2e-67 | |||||
IJFNMBCI_00112 | 4.1e-212 | blt | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00113 | 1.9e-236 | 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 | |
IJFNMBCI_00114 | 1.2e-233 | pucF | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
IJFNMBCI_00115 | 1.3e-167 | bsn | L | Ribonuclease | ||
IJFNMBCI_00116 | 3.1e-206 | msmX | P | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_00117 | 1.8e-133 | yurK | K | UTRA | ||
IJFNMBCI_00118 | 6.3e-162 | yurL | 2.7.1.218 | G | pfkB family carbohydrate kinase | |
IJFNMBCI_00119 | 2.5e-161 | yurM | P | COG0395 ABC-type sugar transport system, permease component | ||
IJFNMBCI_00120 | 7.8e-39 | yurN | G | Binding-protein-dependent transport system inner membrane component | ||
IJFNMBCI_00121 | 3.2e-104 | yurN | G | Binding-protein-dependent transport system inner membrane component | ||
IJFNMBCI_00122 | 3.1e-245 | yurO | G | COG1653 ABC-type sugar transport system, periplasmic component | ||
IJFNMBCI_00123 | 6.7e-184 | frlB | M | Catalyzes the conversion of a range of fructosamine 6- phosphates to glucose 6-phosphate and a free amino acid | ||
IJFNMBCI_00124 | 4.3e-164 | K | helix_turn_helix, mercury resistance | |||
IJFNMBCI_00125 | 3e-14 | |||||
IJFNMBCI_00126 | 3.4e-76 | |||||
IJFNMBCI_00127 | 2.1e-22 | S | Sporulation delaying protein SdpA | |||
IJFNMBCI_00129 | 3.1e-65 | yurQ | 2.7.7.7 | L | COG0322 Nuclease subunit of the excinuclease complex | |
IJFNMBCI_00130 | 2.5e-203 | yurR | 1.4.5.1 | E | COG0665 Glycine D-amino acid oxidases (deaminating) | |
IJFNMBCI_00131 | 1.1e-124 | Q | ubiE/COQ5 methyltransferase family | |||
IJFNMBCI_00132 | 5.4e-73 | yncE | S | Protein of unknown function (DUF2691) | ||
IJFNMBCI_00133 | 5.9e-157 | csn | 3.2.1.132 | M | Aids in the defense against invading fungal pathogens by degrading their cell wall chitosan | |
IJFNMBCI_00134 | 3e-270 | sufB | O | FeS cluster assembly | ||
IJFNMBCI_00135 | 8.5e-78 | nifU | C | COG0822 NifU homolog involved in Fe-S cluster formation | ||
IJFNMBCI_00136 | 4.6e-235 | 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 | |
IJFNMBCI_00137 | 1.2e-244 | sufD | O | assembly protein SufD | ||
IJFNMBCI_00138 | 1.2e-138 | sufC | O | COG0396 ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
IJFNMBCI_00139 | 7.6e-64 | 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 | |
IJFNMBCI_00140 | 1.1e-144 | metQ | P | Belongs to the NlpA lipoprotein family | ||
IJFNMBCI_00141 | 1.8e-95 | metI | P | COG2011 ABC-type metal ion transport system, permease component | ||
IJFNMBCI_00142 | 4.8e-185 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
IJFNMBCI_00143 | 5e-57 | yusD | S | SCP-2 sterol transfer family | ||
IJFNMBCI_00144 | 1.6e-54 | yusE | CO | Thioredoxin | ||
IJFNMBCI_00145 | 1.4e-62 | rnmV | 3.1.26.8 | L | COG1658 Small primase-like proteins (Toprim domain) | |
IJFNMBCI_00146 | 3.7e-40 | yusG | S | Protein of unknown function (DUF2553) | ||
IJFNMBCI_00147 | 2.4e-65 | gcvH | E | Is also involved in protein lipoylation via its role as an octanoyl lipoyl carrier protein intermediate | ||
IJFNMBCI_00148 | 2.1e-63 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
IJFNMBCI_00149 | 0.0 | fadE | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
IJFNMBCI_00150 | 4.2e-217 | fadA | 2.3.1.16 | I | Belongs to the thiolase family | |
IJFNMBCI_00151 | 0.0 | fadB | 1.1.1.35, 4.2.1.17, 5.1.2.3 | I | 3-hydroxyacyl-CoA dehydrogenase | |
IJFNMBCI_00152 | 3e-159 | fadM | E | Proline dehydrogenase | ||
IJFNMBCI_00153 | 2.6e-42 | |||||
IJFNMBCI_00154 | 1.1e-53 | yusN | M | Coat F domain | ||
IJFNMBCI_00155 | 5.7e-69 | yusO | K | Iron dependent repressor, N-terminal DNA binding domain | ||
IJFNMBCI_00156 | 8.1e-288 | yusP | P | Major facilitator superfamily | ||
IJFNMBCI_00157 | 3.7e-157 | ywbI2 | K | Transcriptional regulator | ||
IJFNMBCI_00158 | 3e-136 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
IJFNMBCI_00159 | 3.3e-189 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
IJFNMBCI_00160 | 3.4e-21 | yusU | S | Protein of unknown function (DUF2573) | ||
IJFNMBCI_00161 | 3.1e-150 | yusV | 3.6.3.34 | HP | ABC transporter | |
IJFNMBCI_00162 | 3.9e-43 | S | YusW-like protein | |||
IJFNMBCI_00163 | 7.1e-77 | pepF2 | E | COG1164 Oligoendopeptidase F | ||
IJFNMBCI_00164 | 2.4e-248 | pepF2 | E | COG1164 Oligoendopeptidase F | ||
IJFNMBCI_00165 | 3.2e-150 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
IJFNMBCI_00166 | 5.2e-78 | dps | P | Belongs to the Dps family | ||
IJFNMBCI_00167 | 2.5e-237 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
IJFNMBCI_00168 | 2.6e-126 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_00169 | 6.9e-248 | cssS | 2.7.13.3 | T | PhoQ Sensor | |
IJFNMBCI_00170 | 1.3e-23 | |||||
IJFNMBCI_00171 | 2.1e-152 | yuxN | K | Transcriptional regulator | ||
IJFNMBCI_00172 | 8.7e-262 | fumC | 1.1.1.38, 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
IJFNMBCI_00173 | 6.6e-24 | S | Protein of unknown function (DUF3970) | |||
IJFNMBCI_00174 | 1.4e-246 | gerAA | EG | Spore germination protein | ||
IJFNMBCI_00175 | 1.2e-178 | gerAB | E | Spore germination protein | ||
IJFNMBCI_00176 | 1.2e-197 | gerAC | S | Spore germination B3/ GerAC like, C-terminal | ||
IJFNMBCI_00177 | 5.6e-107 | vraR | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
IJFNMBCI_00178 | 4.3e-192 | vraS | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_00179 | 3.6e-126 | yvqF | S | Cell wall-active antibiotics response 4TMS YvqF | ||
IJFNMBCI_00180 | 1.3e-117 | liaG | S | Putative adhesin | ||
IJFNMBCI_00181 | 4e-87 | liaH | KT | COG1842 Phage shock protein A (IM30), suppresses sigma54-dependent transcription | ||
IJFNMBCI_00182 | 1.1e-44 | liaI | S | membrane | ||
IJFNMBCI_00183 | 3.6e-222 | yvqJ | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00184 | 5.2e-96 | yvqK | 2.5.1.17 | S | Adenosyltransferase | |
IJFNMBCI_00185 | 1.2e-211 | yvrA | 3.6.3.34 | HP | COG1120 ABC-type cobalamin Fe3 -siderophores transport systems, ATPase components | |
IJFNMBCI_00186 | 8.2e-180 | btuC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_00187 | 1.1e-167 | yvrC | P | ABC transporter substrate-binding protein | ||
IJFNMBCI_00188 | 9e-139 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
IJFNMBCI_00189 | 9.9e-171 | yvrE | G | SMP-30/Gluconolaconase/LRE-like region | ||
IJFNMBCI_00190 | 0.0 | T | PhoQ Sensor | |||
IJFNMBCI_00191 | 6.7e-133 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_00192 | 1.8e-34 | |||||
IJFNMBCI_00193 | 1e-99 | yvrI | K | RNA polymerase | ||
IJFNMBCI_00194 | 2.7e-15 | S | YvrJ protein family | |||
IJFNMBCI_00195 | 9.2e-233 | oxdC | 4.1.1.2 | G | Oxalate decarboxylase | |
IJFNMBCI_00196 | 7.1e-66 | yvrL | S | Regulatory protein YrvL | ||
IJFNMBCI_00197 | 1.4e-147 | fhuC | 3.6.3.34 | HP | ABC transporter | |
IJFNMBCI_00198 | 9e-176 | fhuG | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_00199 | 1.1e-182 | fhuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_00200 | 7.1e-175 | fhuD | P | ABC transporter | ||
IJFNMBCI_00201 | 2.6e-121 | Q | Exhibits S-adenosyl-L-methionine-dependent methyltransferase activity | |||
IJFNMBCI_00202 | 8.6e-233 | yvsH | E | Arginine ornithine antiporter | ||
IJFNMBCI_00203 | 5.2e-13 | S | Small spore protein J (Spore_SspJ) | |||
IJFNMBCI_00204 | 1.3e-84 | yvsG | S | LexA-binding, inner membrane-associated putative hydrolase | ||
IJFNMBCI_00205 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
IJFNMBCI_00206 | 2.3e-165 | yvgK | P | COG1910 Periplasmic molybdate-binding protein domain | ||
IJFNMBCI_00207 | 1.4e-139 | modA | P | COG0725 ABC-type molybdate transport system, periplasmic component | ||
IJFNMBCI_00208 | 2.3e-94 | modB | P | COG4149 ABC-type molybdate transport system, permease component | ||
IJFNMBCI_00209 | 2.4e-113 | yfiK | K | Regulator | ||
IJFNMBCI_00210 | 1.4e-32 | T | Histidine kinase | |||
IJFNMBCI_00211 | 9.6e-118 | T | Histidine kinase | |||
IJFNMBCI_00212 | 9.9e-169 | yfiL | V | COG1131 ABC-type multidrug transport system, ATPase component | ||
IJFNMBCI_00213 | 1.5e-184 | yfiM | V | ABC-2 type transporter | ||
IJFNMBCI_00214 | 6.4e-194 | yfiN | V | COG0842 ABC-type multidrug transport system, permease component | ||
IJFNMBCI_00215 | 5e-156 | yvgN | S | reductase | ||
IJFNMBCI_00216 | 3.2e-86 | yvgO | ||||
IJFNMBCI_00217 | 0.0 | yjcE | P | COG0025 NhaP-type Na H and K H antiporters | ||
IJFNMBCI_00218 | 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 | |
IJFNMBCI_00219 | 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 | |
IJFNMBCI_00220 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
IJFNMBCI_00221 | 3.1e-99 | yvgT | S | membrane | ||
IJFNMBCI_00222 | 9.7e-141 | S | Metallo-peptidase family M12 | |||
IJFNMBCI_00223 | 1.5e-71 | bdbC | O | Required for disulfide bond formation in some proteins | ||
IJFNMBCI_00224 | 1.2e-102 | bdbD | O | Thioredoxin | ||
IJFNMBCI_00225 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
IJFNMBCI_00226 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
IJFNMBCI_00227 | 3.2e-29 | copZ | P | Heavy-metal-associated domain | ||
IJFNMBCI_00228 | 3.7e-48 | csoR | S | transcriptional | ||
IJFNMBCI_00229 | 8.1e-196 | yvaA | 1.1.1.371 | S | Oxidoreductase | |
IJFNMBCI_00230 | 1.1e-118 | 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 | ||
IJFNMBCI_00231 | 3.1e-133 | moxC | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
IJFNMBCI_00232 | 6e-66 | moxC | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
IJFNMBCI_00233 | 1.1e-23 | ytnI | O | COG0695 Glutaredoxin and related proteins | ||
IJFNMBCI_00234 | 4.6e-180 | ytmO | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
IJFNMBCI_00235 | 6.2e-140 | tcyN | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
IJFNMBCI_00236 | 5.4e-119 | tcyM | U | Binding-protein-dependent transport system inner membrane component | ||
IJFNMBCI_00237 | 5.9e-121 | tcyL | P | Binding-protein-dependent transport system inner membrane component | ||
IJFNMBCI_00238 | 4.9e-148 | tcyK | M | Bacterial periplasmic substrate-binding proteins | ||
IJFNMBCI_00239 | 4.2e-74 | ytmJ | ET | Bacterial periplasmic substrate-binding proteins | ||
IJFNMBCI_00240 | 1.8e-39 | ytmJ | ET | Bacterial periplasmic substrate-binding proteins | ||
IJFNMBCI_00241 | 3.3e-100 | ytmI | K | Acetyltransferase (GNAT) domain | ||
IJFNMBCI_00242 | 5.2e-159 | ytlI | K | LysR substrate binding domain | ||
IJFNMBCI_00243 | 1.5e-138 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
IJFNMBCI_00244 | 3.2e-44 | yrdF | K | ribonuclease inhibitor | ||
IJFNMBCI_00246 | 1.6e-82 | 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 | ||
IJFNMBCI_00247 | 0.0 | rnr | K | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
IJFNMBCI_00248 | 4.8e-142 | est | 3.1.1.1 | S | Carboxylesterase | |
IJFNMBCI_00249 | 4.8e-24 | secG | U | Preprotein translocase subunit SecG | ||
IJFNMBCI_00250 | 6e-35 | yvzC | K | Transcriptional | ||
IJFNMBCI_00251 | 5.6e-68 | K | transcriptional | |||
IJFNMBCI_00252 | 9.8e-71 | yvaO | K | Cro/C1-type HTH DNA-binding domain | ||
IJFNMBCI_00253 | 2.6e-52 | yodB | K | transcriptional | ||
IJFNMBCI_00254 | 2e-242 | T | His Kinase A (phosphoacceptor) domain | |||
IJFNMBCI_00255 | 6e-120 | K | Transcriptional regulatory protein, C terminal | |||
IJFNMBCI_00256 | 3e-131 | mutG | S | ABC-2 family transporter protein | ||
IJFNMBCI_00257 | 2.1e-118 | spaE | S | ABC-2 family transporter protein | ||
IJFNMBCI_00258 | 1.5e-83 | mutF | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_00259 | 2.7e-24 | mutF | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_00260 | 6.8e-111 | opuCD | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
IJFNMBCI_00261 | 6.7e-170 | opuCC | M | COG1732 Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
IJFNMBCI_00262 | 1.6e-112 | opuCB | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
IJFNMBCI_00263 | 3.7e-210 | opuCA | 3.6.3.32 | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | |
IJFNMBCI_00264 | 4.3e-76 | yvbF | K | Belongs to the GbsR family | ||
IJFNMBCI_00265 | 1.1e-108 | opuCD | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
IJFNMBCI_00266 | 3.3e-169 | opuCC | M | COG1732 Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
IJFNMBCI_00267 | 4.5e-112 | opuCB | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
IJFNMBCI_00268 | 6.7e-212 | opuCA | 3.6.3.32 | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | |
IJFNMBCI_00269 | 4.6e-97 | yvbF | K | Belongs to the GbsR family | ||
IJFNMBCI_00270 | 7.5e-104 | yvbG | U | UPF0056 membrane protein | ||
IJFNMBCI_00271 | 1.3e-120 | exoY | M | Membrane | ||
IJFNMBCI_00272 | 0.0 | tcaA | S | response to antibiotic | ||
IJFNMBCI_00273 | 1.1e-80 | yvbK | 3.1.3.25 | K | acetyltransferase | |
IJFNMBCI_00277 | 2.2e-195 | 3.6.3.27 | V | Peptidase C39 family | ||
IJFNMBCI_00278 | 2.9e-190 | lcnDR2 | V | Lanthionine synthetase C-like protein | ||
IJFNMBCI_00280 | 8.2e-212 | lcnDR2 | V | Lanthionine synthetase C-like protein | ||
IJFNMBCI_00282 | 6.4e-243 | 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 | |
IJFNMBCI_00283 | 1.7e-298 | gpmI | 5.4.2.12 | G | Catalyzes the interconversion of 2-phosphoglycerate and | |
IJFNMBCI_00284 | 4.3e-138 | 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) | |
IJFNMBCI_00285 | 1.2e-216 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
IJFNMBCI_00286 | 1.2e-183 | gapA | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
IJFNMBCI_00287 | 6.3e-185 | cggR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
IJFNMBCI_00288 | 2e-223 | araE | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00289 | 1.4e-203 | araR | K | transcriptional | ||
IJFNMBCI_00290 | 1.1e-189 | yvbT | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
IJFNMBCI_00291 | 4.9e-125 | yvbU | K | Transcriptional regulator | ||
IJFNMBCI_00292 | 1.6e-34 | yvbV | EG | EamA-like transporter family | ||
IJFNMBCI_00293 | 3.2e-96 | yvbV | EG | EamA-like transporter family | ||
IJFNMBCI_00294 | 8.5e-214 | yvbW | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
IJFNMBCI_00296 | 8.5e-151 | ybbH_1 | K | RpiR family transcriptional regulator | ||
IJFNMBCI_00297 | 2.7e-296 | gntK | 2.7.1.12, 2.7.1.17, 2.7.1.189 | G | Belongs to the FGGY kinase family | |
IJFNMBCI_00298 | 3.1e-224 | gntP | EG | COG2610 H gluconate symporter and related permeases | ||
IJFNMBCI_00299 | 6.7e-133 | lutC | S | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
IJFNMBCI_00300 | 1.6e-271 | 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 | ||
IJFNMBCI_00301 | 9.3e-135 | lutA | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
IJFNMBCI_00302 | 3.5e-219 | EK | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |||
IJFNMBCI_00303 | 3e-120 | yvfI | K | COG2186 Transcriptional regulators | ||
IJFNMBCI_00304 | 3.2e-303 | yvfH | C | L-lactate permease | ||
IJFNMBCI_00305 | 4e-240 | rpoN | K | COG1508 DNA-directed RNA polymerase specialized sigma subunit, sigma54 homolog | ||
IJFNMBCI_00306 | 2.7e-32 | yvfG | S | YvfG protein | ||
IJFNMBCI_00307 | 3.2e-186 | yvfF | GM | Exopolysaccharide biosynthesis protein | ||
IJFNMBCI_00308 | 1.6e-221 | epsN | 2.6.1.102 | E | Belongs to the DegT DnrJ EryC1 family | |
IJFNMBCI_00309 | 3.5e-56 | epsM | GM | COG0110 Acetyltransferase (isoleucine patch superfamily) | ||
IJFNMBCI_00310 | 9.8e-109 | epsL | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
IJFNMBCI_00311 | 1e-271 | pglK | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
IJFNMBCI_00312 | 1.7e-193 | epsJ | GT2 | S | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
IJFNMBCI_00313 | 5.4e-203 | epsI | GM | pyruvyl transferase | ||
IJFNMBCI_00314 | 1.3e-193 | epsH | GT2 | S | Glycosyltransferase like family 2 | |
IJFNMBCI_00315 | 3.5e-205 | epsG | S | EpsG family | ||
IJFNMBCI_00316 | 1.4e-212 | epsF | GT4 | M | Glycosyl transferases group 1 | |
IJFNMBCI_00317 | 1.8e-161 | epsE | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
IJFNMBCI_00318 | 3.7e-218 | epsD | GT4 | M | Glycosyl transferase 4-like | |
IJFNMBCI_00319 | 0.0 | pglF | 4.2.1.115, 4.2.1.135, 4.2.1.46 | GM | Polysaccharide biosynthesis protein | |
IJFNMBCI_00320 | 2.4e-116 | epsB | 2.7.10.2 | D | COG0489 ATPases involved in chromosome partitioning | |
IJFNMBCI_00321 | 2.7e-118 | ywqC | M | biosynthesis protein | ||
IJFNMBCI_00322 | 5.7e-77 | slr | K | transcriptional | ||
IJFNMBCI_00323 | 7.1e-283 | pnbA | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
IJFNMBCI_00325 | 2.2e-96 | ywjB | H | RibD C-terminal domain | ||
IJFNMBCI_00326 | 1.5e-112 | yyaS | S | Membrane | ||
IJFNMBCI_00327 | 2.4e-92 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
IJFNMBCI_00328 | 5.8e-124 | L | Molecular Function DNA binding, Biological Process DNA recombination | |||
IJFNMBCI_00329 | 1.4e-45 | L | COG2963 Transposase and inactivated derivatives | |||
IJFNMBCI_00330 | 2.8e-146 | yerO | K | Transcriptional regulator | ||
IJFNMBCI_00331 | 0.0 | swrC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
IJFNMBCI_00332 | 1.6e-168 | yegS | 2.7.1.107 | I | COG1597 Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
IJFNMBCI_00333 | 7.5e-250 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
IJFNMBCI_00334 | 7.3e-199 | L | AAA ATPase domain | |||
IJFNMBCI_00335 | 9.8e-115 | 3.6.4.12 | L | AAA domain | ||
IJFNMBCI_00336 | 4.3e-67 | |||||
IJFNMBCI_00338 | 1.3e-28 | S | Colicin immunity protein / pyocin immunity protein | |||
IJFNMBCI_00340 | 3e-81 | S | Protein of unknown function, DUF600 | |||
IJFNMBCI_00341 | 0.0 | yobL | L | nucleic acid phosphodiester bond hydrolysis | ||
IJFNMBCI_00342 | 3.6e-126 | yeeN | K | transcriptional regulatory protein | ||
IJFNMBCI_00345 | 3.7e-109 | aadK | G | Streptomycin adenylyltransferase | ||
IJFNMBCI_00346 | 1.2e-44 | cotJA | S | Spore coat associated protein JA (CotJA) | ||
IJFNMBCI_00347 | 3.3e-45 | cotJB | S | CotJB protein | ||
IJFNMBCI_00348 | 8.9e-104 | cotJC | P | Spore Coat | ||
IJFNMBCI_00349 | 3e-93 | yesJ | K | Acetyltransferase (GNAT) family | ||
IJFNMBCI_00351 | 8.2e-120 | yetF | S | membrane | ||
IJFNMBCI_00352 | 5.7e-55 | isdI | 1.14.99.48, 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | |
IJFNMBCI_00353 | 2e-64 | yetH | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
IJFNMBCI_00354 | 4.1e-153 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
IJFNMBCI_00355 | 1.6e-135 | sbp | P | COG1613 ABC-type sulfate transport system, periplasmic component | ||
IJFNMBCI_00356 | 4.5e-112 | cysT | O | COG0555 ABC-type sulfate transport system, permease component | ||
IJFNMBCI_00357 | 1.3e-103 | cysW | P | COG4208 ABC-type sulfate transport system, permease component | ||
IJFNMBCI_00358 | 2e-80 | 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 | |
IJFNMBCI_00359 | 1.6e-36 | 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 | |
IJFNMBCI_00360 | 1.2e-22 | yezD | S | Uncharacterized small protein (DUF2292) | ||
IJFNMBCI_00361 | 1.2e-54 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase activity | |
IJFNMBCI_00362 | 8.2e-106 | yetJ | S | Belongs to the BI1 family | ||
IJFNMBCI_00363 | 1.3e-90 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
IJFNMBCI_00364 | 8.4e-207 | yetM | CH | FAD binding domain | ||
IJFNMBCI_00365 | 7.5e-197 | yetN | S | Protein of unknown function (DUF3900) | ||
IJFNMBCI_00366 | 0.0 | cypD | 1.14.14.1, 1.6.2.4 | C | Belongs to the cytochrome P450 family | |
IJFNMBCI_00368 | 3.4e-49 | MA20_23570 | K | Winged helix DNA-binding domain | ||
IJFNMBCI_00369 | 2.4e-164 | V | ATPases associated with a variety of cellular activities | |||
IJFNMBCI_00370 | 1.3e-126 | V | ABC-2 type transporter | |||
IJFNMBCI_00373 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
IJFNMBCI_00374 | 7.9e-148 | rfbF | 2.7.7.33 | JM | Nucleotidyl transferase | |
IJFNMBCI_00375 | 7.1e-172 | yfnG | 4.2.1.45 | M | dehydratase | |
IJFNMBCI_00376 | 3.2e-180 | yfnF | M | Nucleotide-diphospho-sugar transferase | ||
IJFNMBCI_00377 | 5.1e-223 | yfnE | 2.4.1.338 | GT2 | S | Glycosyltransferase like family 2 |
IJFNMBCI_00378 | 6.9e-186 | yfnD | M | Nucleotide-diphospho-sugar transferase | ||
IJFNMBCI_00379 | 3.4e-217 | fsr | P | COG0477 Permeases of the major facilitator superfamily | ||
IJFNMBCI_00380 | 1.1e-245 | yfnA | E | amino acid | ||
IJFNMBCI_00381 | 2.6e-277 | yfmT | 1.2.1.3, 1.2.1.67 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
IJFNMBCI_00382 | 6e-104 | yfmS | NT | chemotaxis protein | ||
IJFNMBCI_00383 | 5.2e-167 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
IJFNMBCI_00384 | 4.7e-207 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |||
IJFNMBCI_00385 | 0.0 | yfmR | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
IJFNMBCI_00386 | 2.4e-117 | pbuO_1 | S | permease | ||
IJFNMBCI_00387 | 4.1e-24 | cypA | Q | Cytochrome P450 | ||
IJFNMBCI_00388 | 1.1e-72 | S | haloacid dehalogenase-like hydrolase | |||
IJFNMBCI_00389 | 1.8e-69 | yfmP | K | transcriptional | ||
IJFNMBCI_00390 | 2.1e-208 | yfmO | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00391 | 1.1e-297 | yfmM | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
IJFNMBCI_00392 | 4.6e-205 | yfmL | 3.6.4.13 | L | COG0513 Superfamily II DNA and RNA helicases | |
IJFNMBCI_00393 | 6.4e-65 | yfmK | 2.3.1.128 | K | acetyltransferase | |
IJFNMBCI_00394 | 1.6e-188 | yfmJ | S | N-terminal domain of oxidoreductase | ||
IJFNMBCI_00395 | 1.2e-24 | S | Protein of unknown function (DUF3212) | |||
IJFNMBCI_00396 | 1.3e-57 | yflT | S | Heat induced stress protein YflT | ||
IJFNMBCI_00397 | 8.5e-240 | pel | 4.2.2.10, 4.2.2.2 | G | Pectate lyase | |
IJFNMBCI_00398 | 3.5e-234 | yflS | P | Sodium:sulfate symporter transmembrane region | ||
IJFNMBCI_00399 | 2.9e-145 | modF | 3.6.3.21, 3.6.3.34 | P | COG1119 ABC-type molybdenum transport system, ATPase component photorepair protein PhrA | |
IJFNMBCI_00400 | 3.6e-254 | argE | 3.5.1.16 | E | Acetylornithine deacetylase | |
IJFNMBCI_00401 | 2.2e-38 | ylmC | S | sporulation protein | ||
IJFNMBCI_00402 | 1.5e-160 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
IJFNMBCI_00403 | 6.1e-123 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
IJFNMBCI_00404 | 1.5e-61 | 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 | ||
IJFNMBCI_00405 | 5.2e-41 | yggT | S | membrane | ||
IJFNMBCI_00406 | 5.5e-141 | ylmH | 5.4.99.23, 5.4.99.24 | S | conserved protein, contains S4-like domain | |
IJFNMBCI_00407 | 8.9e-68 | divIVA | D | Cell division initiation protein | ||
IJFNMBCI_00408 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
IJFNMBCI_00409 | 3.8e-63 | dksA | T | COG1734 DnaK suppressor protein | ||
IJFNMBCI_00410 | 2.6e-77 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
IJFNMBCI_00411 | 2.5e-161 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
IJFNMBCI_00412 | 1e-93 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
IJFNMBCI_00413 | 5.2e-232 | pyrP | F | Xanthine uracil | ||
IJFNMBCI_00414 | 3.1e-167 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
IJFNMBCI_00415 | 9.5e-247 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
IJFNMBCI_00416 | 1.7e-207 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
IJFNMBCI_00417 | 0.0 | carB | 6.3.5.5 | F | Belongs to the CarB family | |
IJFNMBCI_00418 | 7.2e-141 | 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( ) | ||
IJFNMBCI_00419 | 4.6e-174 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
IJFNMBCI_00420 | 1e-125 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
IJFNMBCI_00421 | 8.6e-116 | 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) | |
IJFNMBCI_00423 | 3.8e-141 | cysH | 1.8.4.10, 1.8.4.8, 2.7.1.25 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
IJFNMBCI_00424 | 3.2e-179 | cysP | P | phosphate transporter | ||
IJFNMBCI_00425 | 3.8e-223 | sat | 2.7.7.4 | P | Belongs to the sulfate adenylyltransferase family | |
IJFNMBCI_00426 | 2.8e-108 | cysC | 2.7.1.25 | P | Catalyzes the synthesis of activated sulfate | |
IJFNMBCI_00427 | 8.2e-145 | hemD | 2.1.1.107, 4.2.1.75 | H | Belongs to the precorrin methyltransferase family | |
IJFNMBCI_00428 | 9.2e-144 | cbiX | 4.99.1.3, 4.99.1.4, 5.4.99.60, 5.4.99.61 | S | Sirohydrochlorin ferrochelatase | |
IJFNMBCI_00429 | 1.2e-77 | cysG | 1.3.1.76, 4.99.1.4 | H | Siroheme synthase | |
IJFNMBCI_00430 | 0.0 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
IJFNMBCI_00431 | 0.0 | yloB | 3.6.3.8 | P | COG0474 Cation transport ATPase | |
IJFNMBCI_00432 | 1e-154 | yloC | S | stress-induced protein | ||
IJFNMBCI_00433 | 1.5e-40 | ylzA | S | Belongs to the UPF0296 family | ||
IJFNMBCI_00434 | 8.1e-111 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
IJFNMBCI_00435 | 2.8e-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 | |
IJFNMBCI_00436 | 3.3e-225 | 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 | |
IJFNMBCI_00437 | 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 | ||
IJFNMBCI_00438 | 2.3e-84 | def | 2.1.2.9, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
IJFNMBCI_00439 | 1.1e-172 | 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 | |
IJFNMBCI_00440 | 1.5e-250 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
IJFNMBCI_00441 | 2.6e-205 | 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 | |
IJFNMBCI_00442 | 2.5e-138 | stp | 3.1.3.16 | T | phosphatase | |
IJFNMBCI_00443 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
IJFNMBCI_00444 | 2.2e-165 | 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 | |
IJFNMBCI_00445 | 1.2e-115 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
IJFNMBCI_00446 | 5.8e-120 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
IJFNMBCI_00447 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
IJFNMBCI_00448 | 5.5e-59 | asp | S | protein conserved in bacteria | ||
IJFNMBCI_00449 | 2.4e-303 | yloV | S | kinase related to dihydroxyacetone kinase | ||
IJFNMBCI_00450 | 1.4e-116 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
IJFNMBCI_00451 | 4.6e-155 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
IJFNMBCI_00452 | 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) | |
IJFNMBCI_00453 | 2e-92 | fapR | K | Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism | ||
IJFNMBCI_00454 | 3.6e-177 | 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 | |
IJFNMBCI_00455 | 7e-170 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
IJFNMBCI_00456 | 4.6e-129 | IQ | reductase | |||
IJFNMBCI_00457 | 2.8e-32 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
IJFNMBCI_00458 | 1.3e-134 | 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 | |
IJFNMBCI_00459 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
IJFNMBCI_00460 | 2.8e-174 | 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) | ||
IJFNMBCI_00461 | 3.2e-141 | S | Phosphotransferase enzyme family | |||
IJFNMBCI_00462 | 4.3e-50 | 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 | ||
IJFNMBCI_00463 | 1.8e-232 | 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 | |
IJFNMBCI_00464 | 1.4e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
IJFNMBCI_00465 | 1.7e-35 | ylqC | S | Belongs to the UPF0109 family | ||
IJFNMBCI_00466 | 1.3e-61 | ylqD | S | YlqD protein | ||
IJFNMBCI_00467 | 7.6e-94 | 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 | ||
IJFNMBCI_00468 | 5.4e-138 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
IJFNMBCI_00469 | 1.9e-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 | ||
IJFNMBCI_00470 | 6.4e-159 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
IJFNMBCI_00471 | 2.6e-127 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
IJFNMBCI_00472 | 3e-304 | ylqG | ||||
IJFNMBCI_00473 | 8.7e-44 | ylqH | S | homolog of the cytoplasmic domain of flagellar protein FhlB | ||
IJFNMBCI_00474 | 6.8e-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 | |
IJFNMBCI_00475 | 1.1e-167 | 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 | |
IJFNMBCI_00476 | 5.6e-169 | dprA | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | ||
IJFNMBCI_00477 | 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 | |
IJFNMBCI_00478 | 9.7e-247 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
IJFNMBCI_00479 | 7.2e-172 | xerC | L | tyrosine recombinase XerC | ||
IJFNMBCI_00480 | 3.3e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
IJFNMBCI_00481 | 4.5e-234 | 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 | ||
IJFNMBCI_00482 | 1.2e-135 | 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 | ||
IJFNMBCI_00483 | 3e-55 | flgB | N | Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body | ||
IJFNMBCI_00484 | 1.4e-75 | flgC | N | Belongs to the flagella basal body rod proteins family | ||
IJFNMBCI_00485 | 2.5e-31 | fliE | N | Flagellar hook-basal body | ||
IJFNMBCI_00486 | 1.4e-255 | fliF | N | The M ring may be actively involved in energy transduction | ||
IJFNMBCI_00487 | 1.3e-177 | 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 | ||
IJFNMBCI_00488 | 1.6e-89 | fliH | NU | COG1317 Flagellar biosynthesis type III secretory pathway protein | ||
IJFNMBCI_00489 | 1.5e-242 | fliI | 3.6.3.14 | NU | COG1157 Flagellar biosynthesis type III secretory pathway ATPase | |
IJFNMBCI_00490 | 4.5e-71 | fliJ | N | Flagellar biosynthesis chaperone | ||
IJFNMBCI_00491 | 1.3e-47 | ylxF | S | MgtE intracellular N domain | ||
IJFNMBCI_00492 | 7.2e-205 | fliK | N | Flagellar hook-length control protein | ||
IJFNMBCI_00493 | 5.3e-72 | flgD | N | Flagellar basal body rod modification protein | ||
IJFNMBCI_00494 | 4e-139 | flgG | N | Flagellar basal body rod | ||
IJFNMBCI_00495 | 3.4e-32 | flbD | N | protein, possibly involved in motility | ||
IJFNMBCI_00496 | 2.3e-56 | fliL | N | Controls the rotational direction of flagella during chemotaxis | ||
IJFNMBCI_00497 | 5.4e-181 | 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 | ||
IJFNMBCI_00498 | 4.9e-186 | 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 | ||
IJFNMBCI_00499 | 1.2e-58 | cheB | 3.1.1.61, 3.5.1.44 | T | response regulator | |
IJFNMBCI_00500 | 5e-111 | fliZ | N | Flagellar biosynthesis protein, FliO | ||
IJFNMBCI_00501 | 1.6e-109 | fliP | N | Plays a role in the flagellum-specific transport system | ||
IJFNMBCI_00502 | 2e-37 | fliQ | N | Role in flagellar biosynthesis | ||
IJFNMBCI_00503 | 7.5e-130 | fliR | N | Flagellar biosynthetic protein FliR | ||
IJFNMBCI_00504 | 5.3e-190 | 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 | ||
IJFNMBCI_00505 | 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 | ||
IJFNMBCI_00506 | 7.9e-194 | flhF | N | Flagellar biosynthesis regulator FlhF | ||
IJFNMBCI_00507 | 3.5e-155 | flhG | D | Belongs to the ParA family | ||
IJFNMBCI_00508 | 1.3e-193 | 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 | |
IJFNMBCI_00509 | 0.0 | cheA | 2.7.13.3 | NT | COG0643 Chemotaxis protein histidine kinase and related kinases | |
IJFNMBCI_00510 | 8.8e-81 | cheW | NT | COG0835 Chemotaxis signal transduction protein | ||
IJFNMBCI_00511 | 3.7e-111 | cheC | NT | COG1776 Chemotaxis protein CheC, inhibitor of MCP methylation | ||
IJFNMBCI_00512 | 8.6e-87 | 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 | |
IJFNMBCI_00513 | 3.9e-139 | sigD | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
IJFNMBCI_00514 | 2e-53 | ylxL | ||||
IJFNMBCI_00515 | 3.8e-131 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
IJFNMBCI_00516 | 5.3e-156 | 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 | ||
IJFNMBCI_00517 | 9.4e-127 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
IJFNMBCI_00518 | 1.9e-90 | 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 | ||
IJFNMBCI_00519 | 2.9e-145 | uppS | 2.5.1.31 | I | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
IJFNMBCI_00520 | 6.9e-139 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
IJFNMBCI_00521 | 4.3e-214 | 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) | |
IJFNMBCI_00522 | 3.2e-231 | rasP | M | zinc metalloprotease | ||
IJFNMBCI_00523 | 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 | |
IJFNMBCI_00524 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
IJFNMBCI_00525 | 3.9e-81 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
IJFNMBCI_00526 | 6e-205 | nusA | K | Participates in both transcription termination and antitermination | ||
IJFNMBCI_00527 | 1.7e-36 | ylxR | K | nucleic-acid-binding protein implicated in transcription termination | ||
IJFNMBCI_00528 | 1.8e-47 | ylxQ | J | ribosomal protein | ||
IJFNMBCI_00529 | 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 | ||
IJFNMBCI_00530 | 3.9e-44 | ylxP | S | protein conserved in bacteria | ||
IJFNMBCI_00531 | 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 | ||
IJFNMBCI_00532 | 8.6e-173 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
IJFNMBCI_00533 | 3.5e-182 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
IJFNMBCI_00534 | 1e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
IJFNMBCI_00535 | 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 | |
IJFNMBCI_00536 | 8e-182 | ylxY | 3.5.1.104 | G | Sporulation protein, polysaccharide deacetylase | |
IJFNMBCI_00537 | 3.6e-235 | pepR | S | Belongs to the peptidase M16 family | ||
IJFNMBCI_00538 | 2.6e-42 | ymxH | S | YlmC YmxH family | ||
IJFNMBCI_00539 | 1.2e-160 | spoVFA | 1.1.1.29, 1.1.1.399, 1.1.1.95 | CH | Dipicolinate synthase subunit A | |
IJFNMBCI_00540 | 2e-106 | spoVFB | H | Together with DpaA, catalyzes the conversion of dihydrodipicolinate to dipicolinate (DPA) | ||
IJFNMBCI_00541 | 1.1e-192 | 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 | |
IJFNMBCI_00542 | 1.6e-219 | dapG | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
IJFNMBCI_00543 | 6.2e-157 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
IJFNMBCI_00544 | 5.7e-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 | ||
IJFNMBCI_00545 | 4.5e-129 | tepA | 3.4.21.92 | OU | COG0740 Protease subunit of ATP-dependent Clp proteases | |
IJFNMBCI_00546 | 6.3e-31 | S | YlzJ-like protein | |||
IJFNMBCI_00547 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
IJFNMBCI_00548 | 1.8e-133 | ymfC | K | Transcriptional regulator | ||
IJFNMBCI_00549 | 1.6e-228 | ymfD | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00550 | 6.2e-76 | K | helix_turn_helix multiple antibiotic resistance protein | |||
IJFNMBCI_00551 | 0.0 | ydgH | S | drug exporters of the RND superfamily | ||
IJFNMBCI_00552 | 8e-238 | ymfF | S | Peptidase M16 | ||
IJFNMBCI_00553 | 7.1e-242 | ymfH | S | zinc protease | ||
IJFNMBCI_00554 | 3e-128 | ymfI | 1.1.1.100, 1.3.1.28 | S | Catalyzes the first of the two reduction steps in the elongation cycle of fatty acid synthesis | |
IJFNMBCI_00555 | 9.7e-42 | ymfJ | S | Protein of unknown function (DUF3243) | ||
IJFNMBCI_00556 | 3.5e-143 | ymfK | S | Protein of unknown function (DUF3388) | ||
IJFNMBCI_00557 | 4.2e-124 | ymfM | S | protein conserved in bacteria | ||
IJFNMBCI_00558 | 1.1e-101 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
IJFNMBCI_00559 | 1.2e-230 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
IJFNMBCI_00560 | 6.2e-188 | 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 | ||
IJFNMBCI_00561 | 2e-182 | pbpX | V | Beta-lactamase | ||
IJFNMBCI_00562 | 4.2e-241 | rny | S | Endoribonuclease that initiates mRNA decay | ||
IJFNMBCI_00563 | 4.9e-153 | ymdB | S | protein conserved in bacteria | ||
IJFNMBCI_00564 | 1.2e-36 | spoVS | S | Stage V sporulation protein S | ||
IJFNMBCI_00565 | 8.7e-198 | tdh | 1.1.1.103 | C | Catalyzes the NAD( )-dependent oxidation of L-threonine to 2-amino-3-ketobutyrate | |
IJFNMBCI_00566 | 1.5e-214 | kbl | 2.3.1.29, 2.3.1.47 | H | Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide | |
IJFNMBCI_00567 | 2.2e-295 | 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 | |
IJFNMBCI_00568 | 3.5e-68 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
IJFNMBCI_00569 | 1.7e-88 | cotE | S | Spore coat protein | ||
IJFNMBCI_00570 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
IJFNMBCI_00571 | 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 | ||
IJFNMBCI_00572 | 1.7e-33 | S | Domain of unknown function (DUF4145) | |||
IJFNMBCI_00575 | 3.3e-129 | pksB | 3.1.2.6 | S | Polyketide biosynthesis | |
IJFNMBCI_00576 | 2.9e-162 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
IJFNMBCI_00577 | 2.5e-183 | pksD | Q | Acyl transferase domain | ||
IJFNMBCI_00578 | 0.0 | fabD | 1.13.12.16, 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
IJFNMBCI_00579 | 1.9e-34 | acpK | IQ | Phosphopantetheine attachment site | ||
IJFNMBCI_00580 | 1.8e-242 | pksG | 2.3.3.10 | I | synthase | |
IJFNMBCI_00581 | 1.2e-143 | pksH | 4.2.1.18 | I | enoyl-CoA hydratase | |
IJFNMBCI_00582 | 2.9e-139 | pksI | I | Belongs to the enoyl-CoA hydratase isomerase family | ||
IJFNMBCI_00583 | 0.0 | rhiB | IQ | polyketide synthase | ||
IJFNMBCI_00584 | 0.0 | Q | Polyketide synthase of type I | |||
IJFNMBCI_00585 | 0.0 | pfaA | 4.1.1.35 | GT4 | Q | Polyketide synthase of type I |
IJFNMBCI_00586 | 0.0 | dhbF | IQ | polyketide synthase | ||
IJFNMBCI_00587 | 0.0 | pks13 | HQ | Beta-ketoacyl synthase | ||
IJFNMBCI_00588 | 7.6e-230 | cypA | C | Cytochrome P450 | ||
IJFNMBCI_00589 | 3.2e-77 | nucB | M | Deoxyribonuclease NucA/NucB | ||
IJFNMBCI_00590 | 5.1e-117 | yoaK | S | Membrane | ||
IJFNMBCI_00591 | 1.4e-62 | ymzB | ||||
IJFNMBCI_00592 | 7.5e-255 | aprX | O | Belongs to the peptidase S8 family | ||
IJFNMBCI_00594 | 7.8e-126 | ymaC | S | Replication protein | ||
IJFNMBCI_00595 | 6e-79 | ymaD | O | redox protein, regulator of disulfide bond formation | ||
IJFNMBCI_00596 | 5.2e-54 | ebrB | P | Small Multidrug Resistance protein | ||
IJFNMBCI_00597 | 6.5e-48 | ebrA | P | Small Multidrug Resistance protein | ||
IJFNMBCI_00599 | 1.4e-47 | ymaF | S | YmaF family | ||
IJFNMBCI_00600 | 1.8e-170 | 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) | |
IJFNMBCI_00601 | 1.1e-33 | 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 | ||
IJFNMBCI_00602 | 9.4e-43 | |||||
IJFNMBCI_00603 | 1.8e-20 | ymzA | ||||
IJFNMBCI_00604 | 1.7e-66 | nrdI | 1.17.4.1 | F | Probably involved in ribonucleotide reductase function | |
IJFNMBCI_00605 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IJFNMBCI_00606 | 4.5e-188 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IJFNMBCI_00607 | 6.9e-110 | ymaB | S | MutT family | ||
IJFNMBCI_00608 | 1.6e-113 | cwlC | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
IJFNMBCI_00609 | 1.3e-176 | spoVK | O | stage V sporulation protein K | ||
IJFNMBCI_00610 | 2.7e-230 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
IJFNMBCI_00611 | 1.1e-242 | ynbB | 4.4.1.1 | P | COG4100 Cystathionine beta-lyase family protein involved in aluminum resistance | |
IJFNMBCI_00612 | 1.6e-67 | glnR | K | transcriptional | ||
IJFNMBCI_00613 | 1.9e-261 | glnA | 6.3.1.2 | E | glutamine synthetase | |
IJFNMBCI_00614 | 2.4e-153 | L | Belongs to the 'phage' integrase family | |||
IJFNMBCI_00615 | 3e-11 | |||||
IJFNMBCI_00616 | 3.8e-78 | yokF | 3.1.31.1 | L | RNA catabolic process | |
IJFNMBCI_00617 | 4.3e-227 | yobL | L | nucleic acid phosphodiester bond hydrolysis | ||
IJFNMBCI_00618 | 5.2e-60 | S | Protein of unknown function, DUF600 | |||
IJFNMBCI_00620 | 4.5e-127 | yunB | S | Sporulation protein YunB (Spo_YunB) | ||
IJFNMBCI_00621 | 6.9e-40 | S | YolD-like protein | |||
IJFNMBCI_00622 | 1.6e-222 | dinB2 | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
IJFNMBCI_00623 | 1.3e-207 | S | aspartate phosphatase | |||
IJFNMBCI_00626 | 2.3e-32 | S | Bacteriophage holin | |||
IJFNMBCI_00628 | 1.3e-79 | xlyA | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
IJFNMBCI_00629 | 2.9e-279 | M | Pectate lyase superfamily protein | |||
IJFNMBCI_00630 | 4.2e-91 | |||||
IJFNMBCI_00632 | 0.0 | S | Pfam Transposase IS66 | |||
IJFNMBCI_00633 | 3.2e-125 | S | Phage tail protein | |||
IJFNMBCI_00634 | 8.5e-228 | XK26_06135 | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
IJFNMBCI_00635 | 1.6e-47 | ypuD | ||||
IJFNMBCI_00636 | 1.4e-193 | 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 | |
IJFNMBCI_00637 | 1.9e-110 | ribE | 2.5.1.9 | H | Riboflavin synthase | |
IJFNMBCI_00638 | 2.5e-225 | 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 | |
IJFNMBCI_00639 | 2.5e-80 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
IJFNMBCI_00640 | 3.5e-64 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
IJFNMBCI_00641 | 1.4e-92 | ypuF | S | Domain of unknown function (DUF309) | ||
IJFNMBCI_00643 | 2.1e-129 | 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 | ||
IJFNMBCI_00644 | 7.8e-103 | 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 | ||
IJFNMBCI_00645 | 1.3e-84 | ypuI | S | Protein of unknown function (DUF3907) | ||
IJFNMBCI_00646 | 1.8e-212 | dacB | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
IJFNMBCI_00647 | 5.9e-103 | spmA | S | Spore maturation protein | ||
IJFNMBCI_00648 | 1.7e-88 | spmB | S | Spore maturation protein | ||
IJFNMBCI_00649 | 8.4e-131 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
IJFNMBCI_00650 | 1.6e-99 | 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 | ||
IJFNMBCI_00651 | 2.7e-307 | ccs1 | O | COG1333 ResB protein required for cytochrome c biosynthesis | ||
IJFNMBCI_00652 | 8.5e-194 | ccsA | O | 'COG0755 ABC-type transport system involved in cytochrome c biogenesis, permease component' | ||
IJFNMBCI_00653 | 8.8e-133 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_00654 | 0.0 | resE | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_00655 | 2.6e-103 | sigX | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
IJFNMBCI_00656 | 5.4e-198 | rsiX | ||||
IJFNMBCI_00657 | 9.7e-294 | serA | 1.1.1.399, 1.1.1.95 | E | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
IJFNMBCI_00658 | 1.9e-93 | fmnP | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
IJFNMBCI_00659 | 3.6e-41 | fer | C | Ferredoxin | ||
IJFNMBCI_00660 | 7e-195 | ypbB | 5.1.3.1 | S | protein conserved in bacteria | |
IJFNMBCI_00661 | 1.5e-272 | recQ | 3.6.4.12 | L | DNA helicase | |
IJFNMBCI_00662 | 9.9e-100 | ypbD | S | metal-dependent membrane protease | ||
IJFNMBCI_00663 | 6.8e-75 | ypbE | M | Lysin motif | ||
IJFNMBCI_00664 | 5.7e-85 | ypbF | S | Protein of unknown function (DUF2663) | ||
IJFNMBCI_00665 | 4e-147 | ypbG | S | Calcineurin-like phosphoesterase superfamily domain | ||
IJFNMBCI_00666 | 2e-106 | 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 | ||
IJFNMBCI_00667 | 1.4e-245 | gudB | 1.4.1.2, 1.4.1.3 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
IJFNMBCI_00668 | 4.5e-188 | ypdA | 1.18.1.2, 1.19.1.1, 1.8.1.9 | O | COG0492 Thioredoxin reductase | |
IJFNMBCI_00669 | 4.1e-121 | prsW | S | Involved in the degradation of specific anti-sigma factors | ||
IJFNMBCI_00670 | 7e-161 | sleB | 3.5.1.28 | M | Spore cortex-lytic enzyme | |
IJFNMBCI_00671 | 4.2e-253 | hemX | 2.1.1.107, 4.2.1.75 | H | sporulation protein | |
IJFNMBCI_00672 | 1.5e-62 | ypfA | M | Flagellar protein YcgR | ||
IJFNMBCI_00673 | 1.1e-12 | S | Family of unknown function (DUF5359) | |||
IJFNMBCI_00674 | 1e-111 | 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 | |
IJFNMBCI_00675 | 1.5e-206 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
IJFNMBCI_00676 | 4.2e-184 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
IJFNMBCI_00677 | 4.7e-08 | S | YpzI-like protein | |||
IJFNMBCI_00678 | 1.2e-103 | yphA | ||||
IJFNMBCI_00679 | 1.6e-249 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
IJFNMBCI_00680 | 1.9e-189 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
IJFNMBCI_00681 | 3.3e-16 | yphE | S | Protein of unknown function (DUF2768) | ||
IJFNMBCI_00682 | 1.1e-133 | yphF | ||||
IJFNMBCI_00683 | 6.4e-279 | spoIVA | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | ||
IJFNMBCI_00684 | 4.7e-42 | 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 | ||
IJFNMBCI_00685 | 5.4e-101 | folE | 3.5.4.16 | H | GTP cyclohydrolase | |
IJFNMBCI_00686 | 1.3e-34 | 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 | ||
IJFNMBCI_00687 | 6.9e-136 | hepS | 2.5.1.30 | H | Heptaprenyl diphosphate synthase (HEPPP synthase) subunit 1 | |
IJFNMBCI_00688 | 1.2e-131 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
IJFNMBCI_00689 | 7.4e-197 | hepT | 2.5.1.30, 2.5.1.83, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
IJFNMBCI_00690 | 2e-79 | 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 | |
IJFNMBCI_00691 | 1.1e-140 | cheR | 2.1.1.80 | NT | COG1352 Methylase of chemotaxis methyl-accepting proteins | |
IJFNMBCI_00692 | 9.4e-217 | 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 | |
IJFNMBCI_00693 | 1.1e-203 | 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) | |
IJFNMBCI_00694 | 2.4e-60 | 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 | |
IJFNMBCI_00695 | 2.1e-293 | 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 | |
IJFNMBCI_00696 | 1.6e-159 | 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) | |
IJFNMBCI_00697 | 8.6e-131 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
IJFNMBCI_00698 | 7.2e-118 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
IJFNMBCI_00699 | 6.4e-229 | 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 | |
IJFNMBCI_00700 | 7.2e-144 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
IJFNMBCI_00701 | 7.8e-202 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
IJFNMBCI_00702 | 1e-204 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
IJFNMBCI_00703 | 1.7e-235 | 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 | |
IJFNMBCI_00704 | 7e-234 | S | COG0457 FOG TPR repeat | |||
IJFNMBCI_00705 | 2.1e-99 | ypiB | S | Belongs to the UPF0302 family | ||
IJFNMBCI_00706 | 3.2e-77 | ypiF | S | Protein of unknown function (DUF2487) | ||
IJFNMBCI_00707 | 9.3e-97 | qcrA | C | Menaquinol-cytochrome c reductase | ||
IJFNMBCI_00708 | 6.7e-127 | petB | C | COG1290 Cytochrome b subunit of the bc complex | ||
IJFNMBCI_00709 | 6.7e-147 | qcrC | C | Menaquinol-cytochrome c reductase cytochrome b c subunit | ||
IJFNMBCI_00710 | 1.7e-102 | ypjA | S | membrane | ||
IJFNMBCI_00711 | 1.6e-140 | ypjB | S | sporulation protein | ||
IJFNMBCI_00712 | 2.9e-226 | oxdC | 4.1.1.2 | G | Oxalate decarboxylase | |
IJFNMBCI_00713 | 3.6e-157 | ypjC | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
IJFNMBCI_00714 | 1.8e-56 | ypjD | 2.5.1.19 | S | Nucleotide pyrophosphohydrolase | |
IJFNMBCI_00715 | 9.1e-147 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
IJFNMBCI_00716 | 1.4e-71 | mgsA | 2.7.1.24, 4.2.3.3 | G | methylglyoxal synthase | |
IJFNMBCI_00717 | 3.7e-131 | bshB1 | S | proteins, LmbE homologs | ||
IJFNMBCI_00718 | 1.8e-209 | bshA | GT4 | M | N-acetyl-alpha-D-glucosaminyl L-malate synthase | |
IJFNMBCI_00719 | 1.2e-219 | 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 | |
IJFNMBCI_00720 | 2.1e-182 | birA | 6.3.4.15 | K | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
IJFNMBCI_00721 | 6.3e-151 | 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 | |
IJFNMBCI_00722 | 5e-159 | 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 | |
IJFNMBCI_00723 | 2.3e-63 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
IJFNMBCI_00724 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
IJFNMBCI_00725 | 6.7e-23 | ypmA | S | Protein of unknown function (DUF4264) | ||
IJFNMBCI_00726 | 4e-81 | ypmB | S | protein conserved in bacteria | ||
IJFNMBCI_00727 | 1.3e-221 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
IJFNMBCI_00728 | 9.9e-252 | asnS | 6.1.1.22 | J | asparaginyl-tRNA | |
IJFNMBCI_00729 | 3e-130 | dnaD | L | DNA replication protein DnaD | ||
IJFNMBCI_00730 | 4.9e-122 | 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 | |
IJFNMBCI_00731 | 1.7e-90 | ypoC | ||||
IJFNMBCI_00732 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
IJFNMBCI_00733 | 6.8e-110 | 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 | ||
IJFNMBCI_00734 | 2.4e-186 | yppC | S | Protein of unknown function (DUF2515) | ||
IJFNMBCI_00737 | 1.3e-10 | yppE | S | Bacterial domain of unknown function (DUF1798) | ||
IJFNMBCI_00739 | 2.4e-30 | yppG | S | YppG-like protein | ||
IJFNMBCI_00740 | 6.5e-72 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
IJFNMBCI_00741 | 2.7e-88 | ypqE | 2.7.1.199 | G | COG2190 Phosphotransferase system IIA components | |
IJFNMBCI_00742 | 0.0 | yprA | L | COG1205 Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster | ||
IJFNMBCI_00743 | 1.7e-237 | yprB | L | RNase_H superfamily | ||
IJFNMBCI_00744 | 9.9e-33 | cotD | S | Inner spore coat protein D | ||
IJFNMBCI_00745 | 4.8e-99 | ypsA | S | Belongs to the UPF0398 family | ||
IJFNMBCI_00746 | 3.4e-46 | 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 | ||
IJFNMBCI_00747 | 4.2e-217 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
IJFNMBCI_00748 | 6.6e-22 | S | YpzG-like protein | |||
IJFNMBCI_00750 | 0.0 | ypvA | 3.6.4.12 | KL | COG1199 Rad3-related DNA helicases | |
IJFNMBCI_00751 | 3e-292 | 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 | |
IJFNMBCI_00752 | 2.2e-97 | 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 | |
IJFNMBCI_00753 | 1.6e-233 | pbuX | F | xanthine | ||
IJFNMBCI_00754 | 8.5e-99 | yrdC | 3.5.1.19 | Q | Isochorismatase family | |
IJFNMBCI_00756 | 6.2e-51 | ybaZ | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
IJFNMBCI_00757 | 3.8e-105 | J | Acetyltransferase (GNAT) domain | |||
IJFNMBCI_00758 | 5.3e-206 | bcsA | Q | Naringenin-chalcone synthase | ||
IJFNMBCI_00759 | 1.1e-89 | ypbQ | S | protein conserved in bacteria | ||
IJFNMBCI_00760 | 0.0 | ypbR | S | Dynamin family | ||
IJFNMBCI_00761 | 3.5e-39 | ypbS | S | Protein of unknown function (DUF2533) | ||
IJFNMBCI_00763 | 4.1e-164 | polA | 2.7.7.7 | L | 5'3' exonuclease | |
IJFNMBCI_00765 | 9.3e-68 | rnhA | 3.1.26.4 | L | Ribonuclease | |
IJFNMBCI_00766 | 3.1e-119 | ypdP | S | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | ||
IJFNMBCI_00767 | 2.4e-124 | ypeP | 3.1.26.4 | L | COG0328 Ribonuclease HI | |
IJFNMBCI_00768 | 1.5e-28 | ypeQ | S | Zinc-finger | ||
IJFNMBCI_00769 | 6.1e-36 | S | Protein of unknown function (DUF2564) | |||
IJFNMBCI_00770 | 4.4e-12 | degR | ||||
IJFNMBCI_00771 | 1e-30 | cspD | K | Cold-shock protein | ||
IJFNMBCI_00772 | 1.5e-214 | ugtP | 2.4.1.315 | GT28 | M | Processive glucosyltransferase involved in the biosynthesis of both the bilayer- and non-bilayer-forming membrane glucolipids. Is able to successively transfer up to three glucosyl residues to diacylglycerol (DAG), thereby catalyzing the formation of beta-monoglucosyl-DAG (3-O-(beta-D-glucopyranosyl)-1,2-diacyl- sn-glycerol), beta-diglucosyl-DAG (3-O-(beta-D-glucopyranosyl- beta-(1- 6)-D-glucopyranosyl)-1,2-diacyl-sn-glycerol) and beta- triglucosyl-DAG (3-O-(beta-D-glucopyranosyl-beta-(1- 6)-D- glucopyranosyl-beta-(1- 6)-D-glucopyranosyl)-1,2-diacyl-sn- glycerol). Beta-diglucosyl-DAG is the predominant glycolipid found in Bacillales and is also used as a membrane anchor for lipoteichoic acid (LTA) |
IJFNMBCI_00773 | 1.1e-177 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
IJFNMBCI_00774 | 1.3e-87 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
IJFNMBCI_00775 | 4.7e-49 | ypgQ | S | phosphohydrolase | ||
IJFNMBCI_00776 | 9.3e-31 | ypgQ | S | phosphohydrolase | ||
IJFNMBCI_00777 | 7.5e-155 | ypgR | C | COG0694 Thioredoxin-like proteins and domains | ||
IJFNMBCI_00778 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
IJFNMBCI_00779 | 1e-75 | yphP | S | Belongs to the UPF0403 family | ||
IJFNMBCI_00780 | 4.8e-129 | ypiP | 2.1.1.242 | AJ | Putative SAM-dependent methyltransferase | |
IJFNMBCI_00781 | 2.7e-114 | ypjP | S | YpjP-like protein | ||
IJFNMBCI_00782 | 8.7e-158 | 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 | |
IJFNMBCI_00783 | 1.3e-90 | 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 | |
IJFNMBCI_00784 | 1.4e-115 | ypkP | 2.3.1.40, 2.3.1.51, 6.2.1.20 | I | Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family | |
IJFNMBCI_00785 | 9.3e-110 | hlyIII | S | protein, Hemolysin III | ||
IJFNMBCI_00786 | 4.2e-178 | pspF | K | Transcriptional regulator | ||
IJFNMBCI_00787 | 2.2e-243 | 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 | |
IJFNMBCI_00788 | 2.6e-39 | ypmP | S | Protein of unknown function (DUF2535) | ||
IJFNMBCI_00789 | 3.3e-106 | ypmQ | S | protein SCO1 SenC PrrC, involved in biogenesis of respiratory and photosynthetic systems | ||
IJFNMBCI_00790 | 8.9e-136 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
IJFNMBCI_00791 | 1.6e-97 | ypmS | S | protein conserved in bacteria | ||
IJFNMBCI_00792 | 1.4e-66 | ypoP | K | transcriptional | ||
IJFNMBCI_00793 | 5.4e-103 | 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 | |
IJFNMBCI_00794 | 1.2e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
IJFNMBCI_00795 | 4e-104 | 4.2.1.115 | GM | Polysaccharide biosynthesis protein | ||
IJFNMBCI_00796 | 6.9e-306 | yokA | L | Recombinase | ||
IJFNMBCI_00799 | 7.8e-76 | yokF | 3.1.31.1 | L | RNA catabolic process | |
IJFNMBCI_00800 | 4.5e-19 | G | SMI1-KNR4 cell-wall | |||
IJFNMBCI_00801 | 9.5e-56 | G | SMI1-KNR4 cell-wall | |||
IJFNMBCI_00802 | 2.6e-239 | L | A nuclease of the HNH/ENDO VII superfamily with conserved LHH | |||
IJFNMBCI_00803 | 1.5e-85 | S | SMI1-KNR4 cell-wall | |||
IJFNMBCI_00804 | 3.2e-72 | S | SMI1-KNR4 cell-wall | |||
IJFNMBCI_00805 | 1.7e-89 | yokK | S | SMI1 / KNR4 family | ||
IJFNMBCI_00807 | 5.3e-53 | S | SMI1 / KNR4 family | |||
IJFNMBCI_00808 | 1.7e-70 | yoaW | ||||
IJFNMBCI_00814 | 8.9e-14 | S | Protein of unknown function (DUF4236) | |||
IJFNMBCI_00815 | 4.8e-08 | K | Putative DNA-binding domain | |||
IJFNMBCI_00816 | 5.4e-23 | K | Putative DNA-binding domain | |||
IJFNMBCI_00821 | 3.5e-241 | yobL | L | A nuclease of the HNH/ENDO VII superfamily with conserved LHH | ||
IJFNMBCI_00822 | 4e-62 | S | SMI1-KNR4 cell-wall | |||
IJFNMBCI_00825 | 2.5e-39 | 3.4.24.40 | S | amine dehydrogenase activity | ||
IJFNMBCI_00826 | 2.9e-62 | 3.4.24.40 | S | amine dehydrogenase activity | ||
IJFNMBCI_00827 | 1.3e-15 | 3.4.24.40 | S | amine dehydrogenase activity | ||
IJFNMBCI_00829 | 7.3e-195 | S | aspartate phosphatase | |||
IJFNMBCI_00830 | 6.9e-75 | yoqH | M | LysM domain | ||
IJFNMBCI_00833 | 4.4e-08 | |||||
IJFNMBCI_00834 | 6.2e-29 | S | DNA ligase (ATP) activity | |||
IJFNMBCI_00835 | 5.9e-78 | |||||
IJFNMBCI_00841 | 7.9e-73 | 4.2.1.115 | GM | Polysaccharide biosynthesis protein | ||
IJFNMBCI_00842 | 1.7e-218 | phy | 3.1.3.8 | I | Myo-inositol-hexaphosphate 3-phosphohydrolase | |
IJFNMBCI_00843 | 4.4e-180 | cgeB | S | Spore maturation protein | ||
IJFNMBCI_00844 | 2e-52 | cgeA | ||||
IJFNMBCI_00845 | 1.1e-41 | cgeC | ||||
IJFNMBCI_00846 | 1.7e-248 | cgeD | M | maturation of the outermost layer of the spore | ||
IJFNMBCI_00847 | 1.8e-144 | yiiD | K | acetyltransferase | ||
IJFNMBCI_00849 | 4.1e-64 | yosT | L | Bacterial transcription activator, effector binding domain | ||
IJFNMBCI_00850 | 3.4e-247 | yodT | H | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | ||
IJFNMBCI_00851 | 3.8e-125 | yodS | 2.8.3.8, 2.8.3.9 | I | COG1788 Acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
IJFNMBCI_00852 | 1.4e-122 | scoB | 2.8.3.5, 2.8.3.8, 2.8.3.9 | I | COG2057 Acyl CoA acetate 3-ketoacid CoA transferase, beta subunit | |
IJFNMBCI_00853 | 1.6e-254 | yodQ | 3.5.1.16 | E | Acetylornithine deacetylase | |
IJFNMBCI_00854 | 6.6e-159 | yodP | 2.3.1.264 | K | Acetyltransferase (GNAT) family | |
IJFNMBCI_00855 | 3.6e-279 | kamA | 5.4.3.2 | E | lysine 2,3-aminomutase | |
IJFNMBCI_00856 | 2e-45 | yokU | S | YokU-like protein, putative antitoxin | ||
IJFNMBCI_00857 | 2.6e-35 | yozE | S | Belongs to the UPF0346 family | ||
IJFNMBCI_00858 | 6.4e-11 | E | lactoylglutathione lyase activity | |||
IJFNMBCI_00859 | 4.9e-125 | yodN | ||||
IJFNMBCI_00861 | 6.2e-24 | yozD | S | YozD-like protein | ||
IJFNMBCI_00862 | 4e-102 | yodM | 3.6.1.27 | I | Acid phosphatase homologues | |
IJFNMBCI_00863 | 3.3e-55 | yodL | S | YodL-like | ||
IJFNMBCI_00865 | 3.5e-126 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
IJFNMBCI_00866 | 8.7e-145 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
IJFNMBCI_00867 | 1.1e-34 | yodI | ||||
IJFNMBCI_00868 | 3.7e-128 | yodH | Q | Methyltransferase | ||
IJFNMBCI_00869 | 7.9e-255 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
IJFNMBCI_00870 | 1.5e-132 | yydK | K | Transcriptional regulator | ||
IJFNMBCI_00871 | 7.8e-290 | bglA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
IJFNMBCI_00872 | 1.4e-278 | 3.2.1.45 | GH30 | M | Glycosyl hydrolase family 30 beta sandwich domain | |
IJFNMBCI_00873 | 4.6e-269 | yodF | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
IJFNMBCI_00874 | 1.4e-19 | S | Protein of unknown function (DUF3311) | |||
IJFNMBCI_00875 | 6.5e-173 | yodE | E | COG0346 Lactoylglutathione lyase and related lyases | ||
IJFNMBCI_00876 | 3.9e-110 | mhqD | S | Carboxylesterase | ||
IJFNMBCI_00877 | 4.5e-106 | yodC | C | nitroreductase | ||
IJFNMBCI_00878 | 3e-56 | yodB | K | transcriptional | ||
IJFNMBCI_00879 | 1.4e-70 | yoaQ | S | Evidence 4 Homologs of previously reported genes of | ||
IJFNMBCI_00880 | 1.6e-67 | yodA | S | tautomerase | ||
IJFNMBCI_00882 | 3.3e-80 | yozR | S | COG0071 Molecular chaperone (small heat shock protein) | ||
IJFNMBCI_00883 | 1.3e-92 | rarD | S | -transporter | ||
IJFNMBCI_00884 | 1.2e-55 | rarD | S | -transporter | ||
IJFNMBCI_00885 | 4.9e-23 | |||||
IJFNMBCI_00886 | 9.7e-61 | yojF | S | Protein of unknown function (DUF1806) | ||
IJFNMBCI_00887 | 7.4e-126 | yojG | S | deacetylase | ||
IJFNMBCI_00888 | 2.7e-149 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
IJFNMBCI_00889 | 1.3e-241 | norM | V | Multidrug efflux pump | ||
IJFNMBCI_00891 | 4.8e-111 | 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 | |
IJFNMBCI_00892 | 1.4e-223 | yojK | CG | UDP-glucoronosyl and UDP-glucosyl transferase | ||
IJFNMBCI_00893 | 5.2e-226 | sle1 | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
IJFNMBCI_00894 | 1.9e-109 | sodC | 1.15.1.1 | P | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | |
IJFNMBCI_00895 | 1.6e-163 | yojN | S | ATPase family associated with various cellular activities (AAA) | ||
IJFNMBCI_00896 | 0.0 | yojO | P | Von Willebrand factor | ||
IJFNMBCI_00897 | 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) | |
IJFNMBCI_00898 | 7.2e-183 | sucB | 2.3.1.61 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) | |
IJFNMBCI_00899 | 3.5e-140 | S | Metallo-beta-lactamase superfamily | |||
IJFNMBCI_00900 | 6e-161 | yocS | S | -transporter | ||
IJFNMBCI_00901 | 3.9e-235 | yocR | S | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family | ||
IJFNMBCI_00902 | 3.2e-166 | sodA | 1.15.1.1 | P | Superoxide dismutase | |
IJFNMBCI_00903 | 0.0 | sqhC | 4.2.1.137, 5.4.99.7 | I | COG1657 Squalene cyclase | |
IJFNMBCI_00904 | 6.4e-287 | dhaS | 1.2.1.3, 1.2.1.39 | C | Belongs to the aldehyde dehydrogenase family | |
IJFNMBCI_00905 | 4.7e-31 | yozC | ||||
IJFNMBCI_00907 | 2.4e-56 | yozO | S | Bacterial PH domain | ||
IJFNMBCI_00908 | 5.5e-36 | yocN | ||||
IJFNMBCI_00909 | 1.4e-43 | yozN | ||||
IJFNMBCI_00910 | 5.8e-88 | yocM | O | Belongs to the small heat shock protein (HSP20) family | ||
IJFNMBCI_00911 | 2.9e-08 | |||||
IJFNMBCI_00912 | 1e-09 | yocL | ||||
IJFNMBCI_00913 | 2.3e-60 | dksA | T | general stress protein | ||
IJFNMBCI_00915 | 8.2e-111 | 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 | ||
IJFNMBCI_00916 | 0.0 | recQ | 3.6.4.12 | L | DNA helicase | |
IJFNMBCI_00917 | 1e-114 | yocH | CBM50 | M | COG1388 FOG LysM repeat | |
IJFNMBCI_00919 | 1.5e-183 | yocD | 3.4.17.13 | V | peptidase S66 | |
IJFNMBCI_00920 | 1.9e-94 | yocC | ||||
IJFNMBCI_00921 | 9.6e-127 | yocB | J | Protein required for attachment to host cells | ||
IJFNMBCI_00922 | 6.9e-90 | yozB | S | membrane | ||
IJFNMBCI_00923 | 3.9e-119 | pvaA | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
IJFNMBCI_00924 | 1.7e-54 | czrA | K | transcriptional | ||
IJFNMBCI_00925 | 1.9e-92 | yobW | ||||
IJFNMBCI_00926 | 1.3e-136 | yobT | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
IJFNMBCI_00927 | 1.8e-93 | yobS | K | Transcriptional regulator | ||
IJFNMBCI_00928 | 2.1e-131 | yobQ | K | helix_turn_helix, arabinose operon control protein | ||
IJFNMBCI_00929 | 4.9e-54 | csaA | 6.1.1.10, 6.1.1.20, 6.1.1.6 | J | tRNA-binding protein | |
IJFNMBCI_00930 | 3.8e-250 | yobL | L | A nuclease of the HNH/ENDO VII superfamily with conserved LHH | ||
IJFNMBCI_00931 | 4.9e-44 | L | A nuclease of the HNH/ENDO VII superfamily with conserved LHH | |||
IJFNMBCI_00932 | 1.4e-75 | S | SMI1-KNR4 cell-wall | |||
IJFNMBCI_00933 | 1.3e-44 | |||||
IJFNMBCI_00934 | 4.8e-97 | hpr | K | helix_turn_helix multiple antibiotic resistance protein | ||
IJFNMBCI_00936 | 6.3e-26 | yoaF | ||||
IJFNMBCI_00937 | 0.0 | yoaE | C | belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
IJFNMBCI_00938 | 1.1e-192 | yoaD | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
IJFNMBCI_00939 | 1.8e-273 | yoaC | 2.7.1.12, 2.7.1.17, 2.7.1.189 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
IJFNMBCI_00940 | 6.5e-66 | yoaB | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00941 | 5e-121 | yoaB | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00942 | 5.8e-135 | yoxB | ||||
IJFNMBCI_00943 | 4.7e-43 | yoxC | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
IJFNMBCI_00944 | 5.2e-125 | fabG | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
IJFNMBCI_00945 | 9.5e-62 | rtp | K | Plays a role in DNA replication and termination (fork arrest mechanism). Two dimers of rtp bind to the two inverted repeat regions (IRI and IRII) present in the termination site. The binding of each dimer is centered on an 8 bp direct repeat | ||
IJFNMBCI_00946 | 3.7e-140 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
IJFNMBCI_00947 | 1.6e-197 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
IJFNMBCI_00948 | 1.3e-149 | gltC | K | Transcriptional regulator | ||
IJFNMBCI_00949 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase | |
IJFNMBCI_00950 | 3.3e-291 | gltD | 1.4.1.13, 1.4.1.14 | E | COG0493 NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
IJFNMBCI_00951 | 1.9e-50 | 1.16.3.1 | 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) | ||
IJFNMBCI_00952 | 9.3e-186 | yogA | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | ||
IJFNMBCI_00953 | 1.7e-154 | gltR1 | K | Transcriptional regulator | ||
IJFNMBCI_00954 | 1e-14 | 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) | |
IJFNMBCI_00955 | 6.7e-50 | ybzH | K | Helix-turn-helix domain | ||
IJFNMBCI_00956 | 1.8e-199 | ybcL | EGP | Major facilitator Superfamily | ||
IJFNMBCI_00957 | 0.0 | ggt | 2.3.2.2, 3.4.19.13 | E | gamma-glutamyltransferase | |
IJFNMBCI_00958 | 1.8e-34 | yoeD | G | Helix-turn-helix domain | ||
IJFNMBCI_00959 | 2.4e-20 | yngL | S | Protein of unknown function (DUF1360) | ||
IJFNMBCI_00960 | 1.4e-34 | yngL | S | Protein of unknown function (DUF1360) | ||
IJFNMBCI_00961 | 1.2e-301 | yngK | T | Glycosyl hydrolase-like 10 | ||
IJFNMBCI_00962 | 4.1e-209 | yngJ | 1.3.8.1, 1.3.99.12 | I | acyl-CoA dehydrogenase | |
IJFNMBCI_00963 | 0.0 | yngI | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
IJFNMBCI_00964 | 2.1e-252 | yngH | 6.3.4.14, 6.4.1.2, 6.4.1.3, 6.4.1.4 | I | Biotin carboxylase | |
IJFNMBCI_00965 | 2.4e-30 | pycB | 2.3.1.12, 6.4.1.1 | I | Biotin carboxyl carrier protein | |
IJFNMBCI_00966 | 1.4e-167 | mvaB | 4.1.3.4, 6.4.1.4 | E | Hydroxymethylglutaryl-CoA lyase | |
IJFNMBCI_00967 | 5.8e-138 | yngF | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
IJFNMBCI_00968 | 1.1e-289 | yngE | 2.1.3.15, 6.4.1.3 | I | COG4799 Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
IJFNMBCI_00969 | 2.7e-103 | yngC | S | SNARE associated Golgi protein | ||
IJFNMBCI_00970 | 1.6e-155 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
IJFNMBCI_00971 | 3.4e-65 | yngA | S | membrane | ||
IJFNMBCI_00972 | 2.3e-131 | bioW | 2.3.1.47, 6.2.1.14 | H | Catalyzes the transformation of pimelate into pimeloyl- CoA with concomitant hydrolysis of ATP to AMP | |
IJFNMBCI_00973 | 1.9e-253 | bioA | 2.6.1.105, 2.6.1.62 | H | Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor | |
IJFNMBCI_00974 | 1.2e-195 | bioF | 2.3.1.29, 2.3.1.47, 6.2.1.14 | H | Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide | |
IJFNMBCI_00975 | 2.3e-125 | bioD | 6.3.3.3 | H | Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring | |
IJFNMBCI_00976 | 3.7e-193 | bioB | 2.8.1.6 | H | Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism | |
IJFNMBCI_00977 | 9.9e-222 | bioI | 1.14.14.46 | C | Cytochrome P450 | |
IJFNMBCI_00978 | 2.9e-219 | yxjC | EG | COG2610 H gluconate symporter and related permeases | ||
IJFNMBCI_00979 | 1.6e-22 | yxjC | EG | COG2610 H gluconate symporter and related permeases | ||
IJFNMBCI_00980 | 8.4e-125 | scoA | 2.8.3.5 | I | COG1788 Acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
IJFNMBCI_00981 | 2.4e-121 | scoB | 2.8.3.5 | I | COG2057 Acyl CoA acetate 3-ketoacid CoA transferase, beta subunit | |
IJFNMBCI_00982 | 8.3e-137 | IQ | Catalyzes the formation of acetoacetate from 3-hydroxybutyrate | |||
IJFNMBCI_00983 | 7.3e-225 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
IJFNMBCI_00984 | 0.0 | nrsA | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | ||
IJFNMBCI_00985 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
IJFNMBCI_00986 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
IJFNMBCI_00987 | 1.4e-256 | xynD3 | 3.2.1.55 | CBM6,GH43 | G | Belongs to the glycosyl hydrolase 43 family |
IJFNMBCI_00988 | 2.1e-243 | xynC | 3.2.1.136 | GH5 | G | Glycosyl hydrolase family 30 beta sandwich domain |
IJFNMBCI_00989 | 3.8e-128 | T | Transcriptional regulatory protein, C terminal | |||
IJFNMBCI_00990 | 3.5e-234 | T | PhoQ Sensor | |||
IJFNMBCI_00991 | 1.3e-51 | S | Domain of unknown function (DUF4870) | |||
IJFNMBCI_00992 | 3.3e-291 | bglC5 | 3.2.1.4 | GH5,GH9 | G | PFAM glycoside hydrolase family 5 |
IJFNMBCI_00993 | 7.2e-214 | S | Platelet-activating factor acetylhydrolase, isoform II | |||
IJFNMBCI_00994 | 1.4e-11 | |||||
IJFNMBCI_00996 | 1.5e-64 | V | ABC transporter | |||
IJFNMBCI_00997 | 8.3e-86 | |||||
IJFNMBCI_00998 | 3.2e-300 | yndJ | S | YndJ-like protein | ||
IJFNMBCI_00999 | 3.1e-78 | yndH | S | Domain of unknown function (DUF4166) | ||
IJFNMBCI_01000 | 3.5e-154 | yndG | S | DoxX-like family | ||
IJFNMBCI_01001 | 8.6e-224 | exuT | G | Sugar (and other) transporter | ||
IJFNMBCI_01002 | 2.4e-181 | kdgR_1 | K | transcriptional | ||
IJFNMBCI_01003 | 2.3e-148 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
IJFNMBCI_01004 | 9.8e-213 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
IJFNMBCI_01005 | 1.3e-111 | eda | 4.1.2.14, 4.1.3.42 | G | 2-dehydro-3-deoxy-phosphogluconate aldolase | |
IJFNMBCI_01006 | 3.9e-187 | rspB | 1.1.1.380 | E | Alcohol dehydrogenase GroES-like domain | |
IJFNMBCI_01007 | 2.3e-181 | kdgK | 2.7.1.45 | G | COG0524 Sugar kinases, ribokinase family | |
IJFNMBCI_01008 | 1.6e-250 | agcS | E | Sodium alanine symporter | ||
IJFNMBCI_01009 | 5.1e-41 | ynfC | ||||
IJFNMBCI_01010 | 6e-13 | |||||
IJFNMBCI_01011 | 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 | |
IJFNMBCI_01012 | 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 | |
IJFNMBCI_01013 | 1.5e-68 | yccU | S | CoA-binding protein | ||
IJFNMBCI_01014 | 1.4e-93 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
IJFNMBCI_01015 | 1.3e-50 | yneR | S | Belongs to the HesB IscA family | ||
IJFNMBCI_01016 | 3.7e-53 | yneQ | ||||
IJFNMBCI_01017 | 1.6e-70 | yneP | S | Thioesterase-like superfamily | ||
IJFNMBCI_01018 | 2.7e-33 | tlp | S | Belongs to the Tlp family | ||
IJFNMBCI_01020 | 1.1e-92 | yneN | CO | alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen | ||
IJFNMBCI_01021 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
IJFNMBCI_01022 | 7.5e-15 | sspO | S | Belongs to the SspO family | ||
IJFNMBCI_01023 | 2.3e-19 | sspP | S | Belongs to the SspP family | ||
IJFNMBCI_01024 | 3.2e-62 | hspX | O | Spore coat protein | ||
IJFNMBCI_01025 | 8.5e-75 | yneK | S | Protein of unknown function (DUF2621) | ||
IJFNMBCI_01026 | 1.9e-75 | yneJ | O | COG4846 Membrane protein involved in cytochrome C biogenesis | ||
IJFNMBCI_01027 | 4.7e-58 | cheB | 3.1.1.61, 3.5.1.44 | T | cheY-homologous receiver domain | |
IJFNMBCI_01028 | 1.3e-125 | ccdA | O | cytochrome c biogenesis protein | ||
IJFNMBCI_01029 | 5.2e-23 | ynzD | S | Spo0E like sporulation regulatory protein | ||
IJFNMBCI_01030 | 2.3e-28 | yneF | S | UPF0154 protein | ||
IJFNMBCI_01031 | 1.6e-79 | yneE | S | Sporulation inhibitor of replication protein sirA | ||
IJFNMBCI_01032 | 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 | |
IJFNMBCI_01033 | 9.8e-33 | ynzC | S | UPF0291 protein | ||
IJFNMBCI_01034 | 8.5e-111 | yneB | L | resolvase | ||
IJFNMBCI_01035 | 9.3e-47 | yneA | D | Inhibits cell division during the SOS response. Affects a later stage of the cell division protein assembly, after the assembly of the Z ring, by probably suppressing recruitment of FtsL and or DivIC to the division machinery | ||
IJFNMBCI_01036 | 9e-110 | 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 | |
IJFNMBCI_01038 | 1e-11 | yoaW | ||||
IJFNMBCI_01039 | 3.2e-72 | yndM | S | Protein of unknown function (DUF2512) | ||
IJFNMBCI_01040 | 1.2e-138 | O | COG0330 Membrane protease subunits, stomatin prohibitin homologs | |||
IJFNMBCI_01041 | 1.6e-07 | |||||
IJFNMBCI_01042 | 8.2e-143 | yndL | S | Replication protein | ||
IJFNMBCI_01043 | 2.9e-78 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | Deoxyuridine 5'-triphosphate | |
IJFNMBCI_01044 | 6.1e-310 | yobO | M | Pectate lyase superfamily protein | ||
IJFNMBCI_01046 | 4.6e-94 | yvgO | ||||
IJFNMBCI_01048 | 1.2e-117 | AA10,CBM73 | S | Pfam:Chitin_bind_3 | ||
IJFNMBCI_01049 | 4.6e-202 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | |||
IJFNMBCI_01050 | 1.5e-117 | ynaE | S | Domain of unknown function (DUF3885) | ||
IJFNMBCI_01052 | 4.5e-35 | |||||
IJFNMBCI_01053 | 5e-22 | |||||
IJFNMBCI_01054 | 8e-63 | S | Acetyltransferase (GNAT) domain | |||
IJFNMBCI_01055 | 2.3e-94 | yokK | S | SMI1 / KNR4 family | ||
IJFNMBCI_01056 | 1.4e-51 | S | SMI1-KNR4 cell-wall | |||
IJFNMBCI_01057 | 1.2e-284 | yobL | L | A nuclease of the HNH/ENDO VII superfamily with conserved LHH | ||
IJFNMBCI_01058 | 1.2e-143 | yoaP | 3.1.3.18 | K | YoaP-like | |
IJFNMBCI_01060 | 5.6e-19 | yoaW | ||||
IJFNMBCI_01061 | 1.9e-16 | |||||
IJFNMBCI_01064 | 3.9e-187 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
IJFNMBCI_01065 | 2.2e-66 | S | DinB family | |||
IJFNMBCI_01066 | 1.7e-120 | K | WYL domain | |||
IJFNMBCI_01067 | 5.4e-17 | |||||
IJFNMBCI_01070 | 2.1e-76 | pps | 2.7.9.2 | GT | phosphoenolpyruvate synthase | |
IJFNMBCI_01071 | 0.0 | pps | 2.7.9.2 | GT | phosphoenolpyruvate synthase | |
IJFNMBCI_01072 | 1.8e-289 | xylB | 2.7.1.12, 2.7.1.17, 2.7.1.189 | G | xylulose kinase | |
IJFNMBCI_01073 | 3.7e-262 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
IJFNMBCI_01074 | 8.9e-212 | xylR | GK | ROK family | ||
IJFNMBCI_01075 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
IJFNMBCI_01076 | 2.8e-252 | xynT | G | MFS/sugar transport protein | ||
IJFNMBCI_01077 | 1.5e-39 | xerH | A | Belongs to the 'phage' integrase family | ||
IJFNMBCI_01080 | 8.4e-55 | |||||
IJFNMBCI_01081 | 2.4e-11 | S | peptidoglycan catabolic process | |||
IJFNMBCI_01083 | 1e-25 | |||||
IJFNMBCI_01084 | 5.2e-90 | 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 | ||
IJFNMBCI_01085 | 7.1e-10 | K | Cro/C1-type HTH DNA-binding domain | |||
IJFNMBCI_01096 | 1.9e-63 | |||||
IJFNMBCI_01098 | 1.1e-28 | folA | 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 | |
IJFNMBCI_01099 | 1.3e-130 | 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 | |
IJFNMBCI_01100 | 3.2e-09 | S | Protein of unknown function (DUF1643) | |||
IJFNMBCI_01105 | 3.9e-57 | ymaB | S | MutT family | ||
IJFNMBCI_01106 | 4.3e-48 | pth_2 | 3.1.1.29 | S | Peptidyl-tRNA hydrolase PTH2 | |
IJFNMBCI_01107 | 8.8e-32 | O | Glutaredoxin | |||
IJFNMBCI_01108 | 7.8e-63 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IJFNMBCI_01110 | 1.1e-102 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IJFNMBCI_01112 | 0.0 | S | ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor | |||
IJFNMBCI_01113 | 2.1e-56 | S | NrdI Flavodoxin like | |||
IJFNMBCI_01117 | 9.3e-13 | larC | 4.99.1.12 | FJ | Protein conserved in bacteria | |
IJFNMBCI_01125 | 1.2e-10 | |||||
IJFNMBCI_01130 | 5.1e-156 | dcm | 2.1.1.37 | L | DNA (cytosine-5-)-methyltransferase activity | |
IJFNMBCI_01133 | 6.4e-66 | tmk | 2.1.1.45, 2.7.4.9 | F | dTDP biosynthetic process | |
IJFNMBCI_01138 | 1.8e-51 | DR0488 | S | protein conserved in bacteria | ||
IJFNMBCI_01139 | 0.0 | S | Bacterial DNA polymerase III alpha subunit | |||
IJFNMBCI_01140 | 1.8e-272 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
IJFNMBCI_01141 | 6.1e-205 | L | DNA primase activity | |||
IJFNMBCI_01142 | 1.2e-272 | 3.6.4.12 | J | DnaB-like helicase C terminal domain | ||
IJFNMBCI_01143 | 3.3e-80 | |||||
IJFNMBCI_01144 | 9.4e-114 | L | AAA domain | |||
IJFNMBCI_01145 | 2.7e-155 | |||||
IJFNMBCI_01148 | 1.4e-221 | M | Parallel beta-helix repeats | |||
IJFNMBCI_01149 | 1.4e-89 | S | Pfam:DUF867 | |||
IJFNMBCI_01151 | 3.7e-36 | S | YopX protein | |||
IJFNMBCI_01152 | 3.6e-187 | |||||
IJFNMBCI_01154 | 7.5e-126 | yoqW | S | Belongs to the SOS response-associated peptidase family | ||
IJFNMBCI_01155 | 7.8e-138 | ligB | 6.5.1.1, 6.5.1.6, 6.5.1.7 | L | ATP-dependent DNA ligase | |
IJFNMBCI_01157 | 1.7e-08 | xtmA | L | phage terminase small subunit | ||
IJFNMBCI_01158 | 5.4e-62 | |||||
IJFNMBCI_01159 | 6.5e-54 | O | peptidyl-tyrosine sulfation | |||
IJFNMBCI_01160 | 6.5e-09 | |||||
IJFNMBCI_01169 | 8.8e-12 | S | Protein of unknown function (DUF2815) | |||
IJFNMBCI_01170 | 2.5e-263 | 3.1.3.16, 3.1.4.37 | T | phosphatase | ||
IJFNMBCI_01174 | 3.9e-64 | S | dUTPase | |||
IJFNMBCI_01179 | 1.8e-31 | K | Transcriptional regulator | |||
IJFNMBCI_01180 | 6.5e-155 | |||||
IJFNMBCI_01181 | 2.6e-226 | S | DNA-sulfur modification-associated | |||
IJFNMBCI_01182 | 1.8e-145 | L | Belongs to the 'phage' integrase family | |||
IJFNMBCI_01187 | 4e-103 | |||||
IJFNMBCI_01188 | 5.5e-39 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
IJFNMBCI_01194 | 1.3e-24 | |||||
IJFNMBCI_01199 | 8e-23 | K | Cro/C1-type HTH DNA-binding domain | |||
IJFNMBCI_01200 | 2.4e-69 | yoaW | ||||
IJFNMBCI_01202 | 1.1e-13 | I | Acyltransferase family | |||
IJFNMBCI_01205 | 1.9e-13 | K | Helix-turn-helix XRE-family like proteins | |||
IJFNMBCI_01207 | 1.1e-20 | kilA | K | SOS response | ||
IJFNMBCI_01209 | 1.9e-11 | |||||
IJFNMBCI_01210 | 1.3e-197 | 3.1.21.3 | L | Domain of unknown function (DUF4942) | ||
IJFNMBCI_01212 | 6.2e-219 | |||||
IJFNMBCI_01214 | 3.4e-59 | ftsZ | D | Tubulin/FtsZ family, GTPase domain | ||
IJFNMBCI_01218 | 0.0 | S | RNA-directed RNA polymerase activity | |||
IJFNMBCI_01219 | 2.3e-81 | |||||
IJFNMBCI_01220 | 6.5e-28 | 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 | ||
IJFNMBCI_01224 | 2.7e-219 | S | Calcineurin-like phosphoesterase superfamily domain | |||
IJFNMBCI_01228 | 1.9e-80 | |||||
IJFNMBCI_01229 | 4e-198 | |||||
IJFNMBCI_01230 | 1.2e-88 | |||||
IJFNMBCI_01231 | 2.8e-56 | |||||
IJFNMBCI_01233 | 3.1e-181 | |||||
IJFNMBCI_01234 | 2.8e-75 | |||||
IJFNMBCI_01235 | 7.4e-18 | |||||
IJFNMBCI_01236 | 5.7e-15 | |||||
IJFNMBCI_01237 | 5.6e-118 | |||||
IJFNMBCI_01238 | 7.4e-86 | |||||
IJFNMBCI_01239 | 2.3e-96 | |||||
IJFNMBCI_01240 | 6.6e-57 | |||||
IJFNMBCI_01242 | 4.4e-48 | |||||
IJFNMBCI_01243 | 1.6e-55 | S | Domain of unknown function (DUF2479) | |||
IJFNMBCI_01244 | 2e-13 | |||||
IJFNMBCI_01245 | 1.4e-84 | 3.1.4.46, 5.4.2.11 | C | glycerophosphoryl diester phosphodiesterase | ||
IJFNMBCI_01246 | 2e-56 | |||||
IJFNMBCI_01247 | 1.6e-49 | |||||
IJFNMBCI_01248 | 1.1e-66 | S | DNA integration | |||
IJFNMBCI_01250 | 7.9e-75 | |||||
IJFNMBCI_01251 | 0.0 | XK26_06135 | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
IJFNMBCI_01252 | 1.8e-104 | yxaF | K | Transcriptional regulator | ||
IJFNMBCI_01253 | 0.0 | yvnB | 3.1.4.53 | Q | Calcineurin-like phosphoesterase | |
IJFNMBCI_01254 | 1.5e-40 | yvlD | S | Membrane | ||
IJFNMBCI_01255 | 1.5e-23 | pspB | KT | PspC domain | ||
IJFNMBCI_01256 | 4.6e-165 | yvlB | S | Putative adhesin | ||
IJFNMBCI_01257 | 6.1e-49 | yvlA | ||||
IJFNMBCI_01258 | 2.2e-32 | yvkN | ||||
IJFNMBCI_01259 | 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 | ||
IJFNMBCI_01260 | 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 | ||
IJFNMBCI_01261 | 7.6e-33 | csbA | S | protein conserved in bacteria | ||
IJFNMBCI_01262 | 0.0 | yvkC | 2.7.9.2 | GT | Phosphotransferase | |
IJFNMBCI_01263 | 1.6e-109 | yvkB | K | Transcriptional regulator | ||
IJFNMBCI_01264 | 2.5e-226 | yvkA | EGP | Major facilitator Superfamily | ||
IJFNMBCI_01265 | 1.3e-49 | bacT | Q | Thioesterase domain | ||
IJFNMBCI_01266 | 9.5e-176 | S | Psort location CytoplasmicMembrane, score | |||
IJFNMBCI_01267 | 2.9e-221 | minJ | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | ||
IJFNMBCI_01268 | 1.5e-55 | swrA | S | Swarming motility protein | ||
IJFNMBCI_01269 | 6.1e-255 | ctpB | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
IJFNMBCI_01270 | 5e-225 | ywoF | P | Right handed beta helix region | ||
IJFNMBCI_01271 | 9.2e-156 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
IJFNMBCI_01272 | 1e-122 | ftsE | D | cell division ATP-binding protein FtsE | ||
IJFNMBCI_01273 | 2.8e-36 | cccB | C | COG2010 Cytochrome c, mono- and diheme variants | ||
IJFNMBCI_01274 | 9.3e-150 | yvjA | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
IJFNMBCI_01275 | 5.1e-176 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
IJFNMBCI_01276 | 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 | ||
IJFNMBCI_01277 | 3.7e-102 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
IJFNMBCI_01278 | 1.5e-67 | |||||
IJFNMBCI_01279 | 4.5e-10 | fliT | S | bacterial-type flagellum organization | ||
IJFNMBCI_01280 | 3e-66 | fliS | N | flagellar protein FliS | ||
IJFNMBCI_01281 | 6.2e-245 | 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 | ||
IJFNMBCI_01282 | 2.1e-100 | fliC | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
IJFNMBCI_01283 | 2.3e-31 | csrA | T | Could accelerate the degradation of some genes transcripts potentially through selective RNA binding | ||
IJFNMBCI_01284 | 8.5e-75 | fliW | S | Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum | ||
IJFNMBCI_01285 | 3.4e-79 | yviE | ||||
IJFNMBCI_01286 | 1.5e-161 | flgL | N | Belongs to the bacterial flagellin family | ||
IJFNMBCI_01287 | 2.8e-274 | flgK | N | flagellar hook-associated protein | ||
IJFNMBCI_01288 | 8.9e-81 | flgN | NOU | FlgN protein | ||
IJFNMBCI_01289 | 4.7e-39 | flgM | KNU | Negative regulator of flagellin synthesis | ||
IJFNMBCI_01290 | 9.2e-74 | yvyF | S | flagellar protein | ||
IJFNMBCI_01291 | 2e-77 | comFC | S | Phosphoribosyl transferase domain | ||
IJFNMBCI_01293 | 2e-40 | comFB | S | Late competence development protein ComFB | ||
IJFNMBCI_01294 | 9.8e-242 | comFA | L | COG4098 Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
IJFNMBCI_01295 | 1.4e-158 | degV | S | protein conserved in bacteria | ||
IJFNMBCI_01296 | 2e-126 | degU | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
IJFNMBCI_01297 | 1.7e-181 | 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 | |
IJFNMBCI_01298 | 2e-120 | yvyE | 3.4.13.9 | S | Domain of unknown function (DUF1949) | |
IJFNMBCI_01299 | 1.6e-167 | yvhJ | K | Transcriptional regulator | ||
IJFNMBCI_01300 | 3e-129 | V | ABC transporter transmembrane region | |||
IJFNMBCI_01301 | 1.9e-47 | Ogt | M | Glycosyl transferase, family 2 | ||
IJFNMBCI_01302 | 3e-42 | yaiS | S | GlcNAc-PI de-N-acetylase | ||
IJFNMBCI_01304 | 4.1e-19 | S | WbqC-like protein family | |||
IJFNMBCI_01305 | 1.1e-158 | tagO | 2.7.8.33, 2.7.8.35 | M | COG0472 UDP-N-acetylmuramyl pentapeptide phosphotransferase UDP-N-acetylglucosamine-1-phosphate transferase | |
IJFNMBCI_01306 | 2e-238 | tuaH | M | Teichuronic acid biosynthesis glycosyltransferase tuaH | ||
IJFNMBCI_01307 | 8.9e-144 | tuaG | GT2 | M | Glycosyltransferase like family 2 | |
IJFNMBCI_01308 | 3e-114 | tuaF | M | protein involved in exopolysaccharide biosynthesis | ||
IJFNMBCI_01309 | 7.7e-258 | tuaE | M | Teichuronic acid biosynthesis protein | ||
IJFNMBCI_01310 | 1.4e-248 | tuaD | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
IJFNMBCI_01311 | 8.3e-221 | tuaC | 2.4.1.21, 3.2.1.1 | GH13,GT4,GT5 | GM | Teichuronic acid |
IJFNMBCI_01312 | 2.5e-256 | wzxC | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
IJFNMBCI_01313 | 6.2e-117 | tuaA | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
IJFNMBCI_01314 | 6.8e-138 | 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) | ||
IJFNMBCI_01315 | 5.9e-184 | mnaA | 5.1.3.14 | M | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
IJFNMBCI_01316 | 3.7e-157 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
IJFNMBCI_01317 | 1.9e-180 | 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 | |
IJFNMBCI_01318 | 9.8e-136 | tagG | GM | Transport permease protein | ||
IJFNMBCI_01319 | 0.0 | tagF | 2.7.8.12 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
IJFNMBCI_01320 | 5.7e-246 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferase 1 domain A |
IJFNMBCI_01321 | 3.4e-70 | tagD | 2.7.7.15, 2.7.7.39 | IM | Cytidylyltransferase | |
IJFNMBCI_01322 | 2.2e-142 | tagA | 2.4.1.187 | GT26 | M | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
IJFNMBCI_01323 | 3.4e-211 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
IJFNMBCI_01324 | 1.4e-127 | atl | 3.2.1.96, 3.5.1.28 | GH73 | G | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase |
IJFNMBCI_01325 | 7.9e-182 | pmi | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
IJFNMBCI_01326 | 8.4e-260 | gerBA | EG | Spore germination protein | ||
IJFNMBCI_01327 | 1.5e-195 | gerBB | E | Spore germination protein | ||
IJFNMBCI_01328 | 9.7e-211 | gerAC | S | Spore germination protein | ||
IJFNMBCI_01329 | 3.1e-267 | GT2,GT4 | J | Glycosyl transferase family 2 | ||
IJFNMBCI_01330 | 1.3e-168 | ywtG | EGP | Major facilitator Superfamily | ||
IJFNMBCI_01331 | 8e-61 | ywtG | EGP | Major facilitator Superfamily | ||
IJFNMBCI_01332 | 1.4e-176 | ywtF | K | Transcriptional regulator | ||
IJFNMBCI_01333 | 5.5e-158 | ywtE | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
IJFNMBCI_01334 | 4.5e-36 | yttA | 2.7.13.3 | S | Pfam Transposase IS66 | |
IJFNMBCI_01335 | 4.9e-240 | pgdS | CBM50 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
IJFNMBCI_01336 | 1.3e-20 | ywtC | ||||
IJFNMBCI_01337 | 4.9e-218 | capA | M | enzyme of poly-gamma-glutamate biosynthesis (capsule formation) | ||
IJFNMBCI_01338 | 2.3e-70 | pgsC | S | biosynthesis protein | ||
IJFNMBCI_01339 | 1e-223 | murD | 6.3.2.9 | M | COG0769 UDP-N-acetylmuramyl tripeptide synthase | |
IJFNMBCI_01340 | 1e-183 | gerKA | EG | Spore germination protein | ||
IJFNMBCI_01341 | 5.7e-192 | gerKB | E | Spore germination protein | ||
IJFNMBCI_01342 | 3.3e-203 | gerKC | S | Spore germination B3/ GerAC like, C-terminal | ||
IJFNMBCI_01343 | 4.5e-180 | rbsR | K | transcriptional | ||
IJFNMBCI_01344 | 6.7e-151 | 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 | |
IJFNMBCI_01345 | 5.3e-63 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
IJFNMBCI_01346 | 3.2e-53 | 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 | |
IJFNMBCI_01347 | 1.6e-205 | 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 | |
IJFNMBCI_01348 | 8.7e-152 | rbsC | G | Belongs to the binding-protein-dependent transport system permease family | ||
IJFNMBCI_01349 | 4.1e-159 | rbsB | G | COG1879 ABC-type sugar transport system, periplasmic component | ||
IJFNMBCI_01350 | 6.4e-88 | batE | T | Sh3 type 3 domain protein | ||
IJFNMBCI_01351 | 2.8e-96 | ywrO | 1.6.5.2 | S | NADPH-quinone reductase (modulator of drug activity B) | |
IJFNMBCI_01352 | 7.9e-148 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
IJFNMBCI_01353 | 6.8e-309 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
IJFNMBCI_01354 | 9e-167 | alsR | K | LysR substrate binding domain | ||
IJFNMBCI_01356 | 6.2e-241 | ywrK | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
IJFNMBCI_01357 | 2.8e-125 | ywrJ | ||||
IJFNMBCI_01358 | 1.5e-129 | cotB | ||||
IJFNMBCI_01359 | 3.2e-211 | cotH | M | Spore Coat | ||
IJFNMBCI_01360 | 2.2e-09 | |||||
IJFNMBCI_01361 | 3.1e-110 | ywrF | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | ||
IJFNMBCI_01362 | 3.6e-07 | S | Domain of unknown function (DUF4181) | |||
IJFNMBCI_01363 | 1.1e-302 | ggt | 2.3.2.2, 3.4.19.13 | E | gamma-glutamyltransferase | |
IJFNMBCI_01364 | 1.9e-83 | ywrC | K | Transcriptional regulator | ||
IJFNMBCI_01365 | 5.9e-103 | ywrB | P | Chromate transporter | ||
IJFNMBCI_01366 | 3.8e-88 | ywrA | P | COG2059 Chromate transport protein ChrA | ||
IJFNMBCI_01368 | 1.4e-93 | ywqN | S | NAD(P)H-dependent | ||
IJFNMBCI_01369 | 1.8e-156 | K | Transcriptional regulator | |||
IJFNMBCI_01370 | 4.2e-127 | nfi | 3.1.21.7 | L | DNA repair enzyme involved in the repair of deaminated bases. Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA | |
IJFNMBCI_01371 | 6.6e-49 | S | MORN repeat variant | |||
IJFNMBCI_01372 | 0.0 | ywqJ | L | nucleic acid phosphodiester bond hydrolysis | ||
IJFNMBCI_01373 | 4.3e-37 | ywqI | S | Family of unknown function (DUF5344) | ||
IJFNMBCI_01374 | 1.9e-21 | S | Domain of unknown function (DUF5082) | |||
IJFNMBCI_01376 | 1.3e-148 | ywqG | S | Domain of unknown function (DUF1963) | ||
IJFNMBCI_01377 | 2.3e-248 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
IJFNMBCI_01378 | 1e-139 | ywqE | 3.1.3.48 | GM | COG4464 Capsular polysaccharide biosynthesis protein | |
IJFNMBCI_01379 | 5.7e-121 | ywqD | 2.7.10.1 | D | COG0489 ATPases involved in chromosome partitioning | |
IJFNMBCI_01380 | 5.2e-112 | ywqC | M | biosynthesis protein | ||
IJFNMBCI_01381 | 1.3e-14 | |||||
IJFNMBCI_01382 | 5.1e-306 | ywqB | S | SWIM zinc finger | ||
IJFNMBCI_01383 | 0.0 | ywqA | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
IJFNMBCI_01384 | 1.7e-154 | ywpJ | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
IJFNMBCI_01385 | 5.4e-128 | glcR | K | DeoR C terminal sensor domain | ||
IJFNMBCI_01386 | 2.3e-54 | ssbB | L | Single-stranded DNA-binding protein | ||
IJFNMBCI_01387 | 1.1e-56 | ywpG | ||||
IJFNMBCI_01388 | 7.6e-68 | ywpF | S | YwpF-like protein | ||
IJFNMBCI_01389 | 3.4e-37 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
IJFNMBCI_01390 | 4.9e-75 | 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 | |
IJFNMBCI_01391 | 2e-189 | S | aspartate phosphatase | |||
IJFNMBCI_01392 | 4.2e-139 | flhP | N | flagellar basal body | ||
IJFNMBCI_01393 | 1.6e-127 | flhO | N | flagellar basal body | ||
IJFNMBCI_01394 | 2.7e-180 | mbl | D | Rod shape-determining protein | ||
IJFNMBCI_01395 | 1.8e-44 | spoIIID | K | Stage III sporulation protein D | ||
IJFNMBCI_01396 | 1.6e-70 | ywoH | K | transcriptional | ||
IJFNMBCI_01397 | 1.4e-212 | ywoG | EGP | Major facilitator Superfamily | ||
IJFNMBCI_01398 | 1.6e-274 | ybbW | FH | COG1953 Cytosine uracil thiamine allantoin permeases | ||
IJFNMBCI_01399 | 6.1e-244 | ywoD | EGP | Major facilitator superfamily | ||
IJFNMBCI_01400 | 2.2e-102 | phzA | Q | Isochorismatase family | ||
IJFNMBCI_01401 | 9.3e-228 | amt | P | Ammonium transporter | ||
IJFNMBCI_01402 | 1.7e-57 | nrgB | K | Belongs to the P(II) protein family | ||
IJFNMBCI_01403 | 4.9e-210 | ftsW | D | Belongs to the SEDS family | ||
IJFNMBCI_01404 | 3.2e-101 | bcrC | 3.6.1.27 | I | COG0671 Membrane-associated phospholipid phosphatase | |
IJFNMBCI_01405 | 6.6e-72 | ywnJ | S | VanZ like family | ||
IJFNMBCI_01406 | 3.2e-121 | spoIIQ | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
IJFNMBCI_01407 | 1.2e-88 | ywnH | 2.3.1.183 | M | COG1247 Sortase and related acyltransferases | |
IJFNMBCI_01408 | 1.2e-10 | ywnC | S | Family of unknown function (DUF5362) | ||
IJFNMBCI_01409 | 1.2e-68 | ywnF | S | Family of unknown function (DUF5392) | ||
IJFNMBCI_01410 | 4.2e-275 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
IJFNMBCI_01411 | 1.2e-51 | ywnC | S | Family of unknown function (DUF5362) | ||
IJFNMBCI_01412 | 9e-121 | xlnB | 3.2.1.8 | G | Glycosyl hydrolases family 11 | |
IJFNMBCI_01413 | 1.8e-66 | ywnA | K | Transcriptional regulator | ||
IJFNMBCI_01414 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
IJFNMBCI_01415 | 5.5e-62 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
IJFNMBCI_01416 | 1.2e-49 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
IJFNMBCI_01418 | 2.1e-82 | ywmF | S | Peptidase M50 | ||
IJFNMBCI_01419 | 1.5e-94 | S | response regulator aspartate phosphatase | |||
IJFNMBCI_01420 | 7e-192 | 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 | |
IJFNMBCI_01421 | 3.8e-145 | 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 | ||
IJFNMBCI_01423 | 3e-122 | ywmD | S | protein containing a von Willebrand factor type A (vWA) domain | ||
IJFNMBCI_01424 | 1.2e-123 | ywmC | S | protein containing a von Willebrand factor type A (vWA) domain | ||
IJFNMBCI_01425 | 4e-187 | spoIID | D | Stage II sporulation protein D | ||
IJFNMBCI_01426 | 2.3e-240 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
IJFNMBCI_01427 | 7.4e-135 | ywmB | S | TATA-box binding | ||
IJFNMBCI_01428 | 1.3e-32 | ywzB | S | membrane | ||
IJFNMBCI_01429 | 3.5e-90 | ywmA | ||||
IJFNMBCI_01430 | 5.3e-63 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
IJFNMBCI_01431 | 1.2e-266 | 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 | |
IJFNMBCI_01432 | 5.9e-152 | 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 | ||
IJFNMBCI_01433 | 2.4e-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 | |
IJFNMBCI_01434 | 4.5e-89 | 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 | ||
IJFNMBCI_01435 | 1.3e-42 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
IJFNMBCI_01436 | 1.6e-26 | 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 | ||
IJFNMBCI_01437 | 9.3e-130 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
IJFNMBCI_01438 | 2.1e-61 | atpI | S | ATP synthase | ||
IJFNMBCI_01439 | 4e-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 | |
IJFNMBCI_01440 | 1.5e-233 | 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 | |
IJFNMBCI_01441 | 3.6e-94 | ywlG | S | Belongs to the UPF0340 family | ||
IJFNMBCI_01442 | 7e-80 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
IJFNMBCI_01443 | 4.3e-77 | ywlE | 3.1.3.48, 3.9.1.2, 5.3.1.6 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
IJFNMBCI_01444 | 1.2e-84 | mntP | P | Probably functions as a manganese efflux pump | ||
IJFNMBCI_01445 | 4.3e-189 | 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 | |
IJFNMBCI_01446 | 2.6e-74 | ywlB | 1.20.4.1, 2.3.1.1 | E | Belongs to the acetyltransferase family. ArgA subfamily | |
IJFNMBCI_01447 | 4.6e-99 | spoIIR | S | stage II sporulation protein R | ||
IJFNMBCI_01448 | 1.4e-60 | ywlA | S | Uncharacterised protein family (UPF0715) | ||
IJFNMBCI_01450 | 1.6e-157 | 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 | |
IJFNMBCI_01451 | 1.9e-192 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
IJFNMBCI_01452 | 5.8e-67 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
IJFNMBCI_01453 | 1.3e-94 | 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 | ||
IJFNMBCI_01454 | 6.1e-158 | ywkB | S | Membrane transport protein | ||
IJFNMBCI_01455 | 0.0 | sfcA | 1.1.1.38 | C | malic enzyme | |
IJFNMBCI_01456 | 1.4e-104 | tdk | 2.7.1.21 | F | thymidine kinase | |
IJFNMBCI_01457 | 1.1e-32 | rpmE | J | Binds the 23S rRNA | ||
IJFNMBCI_01458 | 4.3e-239 | 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 | ||
IJFNMBCI_01459 | 5.6e-175 | glpX | 3.1.3.11, 3.1.3.37 | G | fructose-1,6-bisphosphatase | |
IJFNMBCI_01460 | 6.6e-240 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
IJFNMBCI_01461 | 1.9e-110 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
IJFNMBCI_01462 | 5.5e-158 | fbaA | 4.1.2.13, 4.1.2.29 | G | Aldolase | |
IJFNMBCI_01463 | 8.5e-63 | spo0F | T | COG0784 FOG CheY-like receiver | ||
IJFNMBCI_01464 | 4.9e-93 | ywjG | S | Domain of unknown function (DUF2529) | ||
IJFNMBCI_01465 | 0.0 | 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 | |
IJFNMBCI_01466 | 2.4e-47 | 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 | ||
IJFNMBCI_01467 | 0.0 | fadF | C | COG0247 Fe-S oxidoreductase | ||
IJFNMBCI_01468 | 8.4e-205 | clsB | I | Belongs to the phospholipase D family. Cardiolipin synthase subfamily | ||
IJFNMBCI_01469 | 3.3e-175 | uvsE | L | Component in a DNA repair pathway. Removal of UV-light damaged nucleotides. Recognizes pyrimidine dimers and cleave a phosphodiester bond immediately 5' to the lesion | ||
IJFNMBCI_01470 | 4.2e-43 | ywjC | ||||
IJFNMBCI_01471 | 0.0 | ywjA | V | ABC transporter | ||
IJFNMBCI_01472 | 6.9e-300 | ywiE | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
IJFNMBCI_01473 | 4.1e-102 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
IJFNMBCI_01474 | 1.5e-123 | narI | 1.7.5.1 | C | nitrate reductase, gamma | |
IJFNMBCI_01475 | 1.6e-94 | narJ | 1.7.5.1 | C | nitrate reductase | |
IJFNMBCI_01476 | 2.8e-295 | narH | 1.7.5.1 | C | Nitrate reductase, beta | |
IJFNMBCI_01477 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
IJFNMBCI_01478 | 4.2e-83 | arfM | T | cyclic nucleotide binding | ||
IJFNMBCI_01479 | 1.8e-138 | ywiC | S | YwiC-like protein | ||
IJFNMBCI_01480 | 4.5e-129 | fnr | K | helix_turn_helix, cAMP Regulatory protein | ||
IJFNMBCI_01481 | 7.5e-214 | narK | P | COG2223 Nitrate nitrite transporter | ||
IJFNMBCI_01482 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
IJFNMBCI_01483 | 1.1e-42 | ywiB | S | protein conserved in bacteria | ||
IJFNMBCI_01484 | 1.1e-71 | S | aspartate phosphatase | |||
IJFNMBCI_01486 | 5.4e-169 | speB | 3.5.3.11 | E | Belongs to the arginase family | |
IJFNMBCI_01487 | 4.1e-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 | |
IJFNMBCI_01488 | 0.0 | pbpG | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
IJFNMBCI_01489 | 1.8e-80 | |||||
IJFNMBCI_01490 | 2.4e-95 | ywhD | S | YwhD family | ||
IJFNMBCI_01491 | 1.2e-117 | ywhC | S | Peptidase family M50 | ||
IJFNMBCI_01492 | 1.3e-24 | dmpI | 5.3.2.6 | G | 4-oxalocrotonate tautomerase | |
IJFNMBCI_01493 | 8e-70 | ywhA | K | Transcriptional regulator | ||
IJFNMBCI_01494 | 1.5e-246 | yhdG_1 | E | C-terminus of AA_permease | ||
IJFNMBCI_01495 | 9.2e-89 | ywgA | 2.1.1.72, 3.1.21.3 | |||
IJFNMBCI_01496 | 7.4e-255 | ywfO | S | COG1078 HD superfamily phosphohydrolases | ||
IJFNMBCI_01497 | 6.9e-36 | ywzC | S | Belongs to the UPF0741 family | ||
IJFNMBCI_01498 | 5.6e-109 | rsfA_1 | ||||
IJFNMBCI_01499 | 5.3e-50 | padR | K | PadR family transcriptional regulator | ||
IJFNMBCI_01500 | 4.4e-92 | S | membrane | |||
IJFNMBCI_01501 | 1.9e-164 | V | ABC transporter, ATP-binding protein | |||
IJFNMBCI_01502 | 2.9e-168 | yhcI | S | ABC transporter (permease) | ||
IJFNMBCI_01505 | 3.1e-167 | |||||
IJFNMBCI_01507 | 8.9e-156 | 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 | |
IJFNMBCI_01508 | 3e-159 | cysL | K | Transcriptional regulator | ||
IJFNMBCI_01509 | 1.5e-148 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
IJFNMBCI_01510 | 5.1e-176 | pta | 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | In Salmonella this enzyme is required for ethanolamine catabolism | |
IJFNMBCI_01511 | 2.5e-146 | ywfI | C | May function as heme-dependent peroxidase | ||
IJFNMBCI_01512 | 2.9e-78 | S | Iron-containing redox enzyme | |||
IJFNMBCI_01514 | 2.4e-64 | S | Putative stress-induced transcription regulator | |||
IJFNMBCI_01515 | 1.2e-70 | T | HPP family | |||
IJFNMBCI_01516 | 1.7e-78 | ytoQ | S | Nucleoside 2-deoxyribosyltransferase YtoQ | ||
IJFNMBCI_01517 | 1.6e-57 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
IJFNMBCI_01518 | 3.7e-148 | ytpQ | S | Belongs to the UPF0354 family | ||
IJFNMBCI_01519 | 7e-107 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
IJFNMBCI_01520 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
IJFNMBCI_01521 | 4.9e-251 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
IJFNMBCI_01522 | 2.8e-14 | ytxG | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
IJFNMBCI_01523 | 1.7e-16 | ytxH | S | COG4980 Gas vesicle protein | ||
IJFNMBCI_01524 | 1.7e-43 | ytxJ | O | Protein of unknown function (DUF2847) | ||
IJFNMBCI_01525 | 1.9e-195 | aroF | 2.5.1.54, 5.4.99.5 | E | Catalyzes the formation of 3-deoxy-D-aribino-hept-2-ulosonate 7-phosphate from phosphoenolpyruvate and D-erythrose 4-phosphate and the formation of prephenate from chorismate | |
IJFNMBCI_01526 | 6.4e-182 | ccpA | K | catabolite control protein A | ||
IJFNMBCI_01527 | 5.1e-145 | motA | N | flagellar motor | ||
IJFNMBCI_01528 | 3.7e-120 | motS | N | Flagellar motor protein | ||
IJFNMBCI_01529 | 5.6e-230 | acuC | BQ | histone deacetylase | ||
IJFNMBCI_01530 | 2.7e-117 | acuB | S | Domain in cystathionine beta-synthase and other proteins. | ||
IJFNMBCI_01531 | 3.4e-120 | 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 | ||
IJFNMBCI_01532 | 0.0 | acsA | 6.2.1.1 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
IJFNMBCI_01533 | 4.2e-239 | 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) | |
IJFNMBCI_01534 | 8.7e-48 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
IJFNMBCI_01535 | 2e-124 | azlC | E | AzlC protein | ||
IJFNMBCI_01536 | 4.4e-149 | K | Transcriptional regulator | |||
IJFNMBCI_01537 | 2.5e-150 | fieF | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
IJFNMBCI_01538 | 1.5e-138 | E | GDSL-like Lipase/Acylhydrolase family | |||
IJFNMBCI_01540 | 2.5e-89 | yhbO | 1.11.1.6, 3.5.1.124 | S | protease | |
IJFNMBCI_01541 | 7.3e-09 | |||||
IJFNMBCI_01542 | 2.6e-222 | 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 | |
IJFNMBCI_01543 | 3.3e-16 | |||||
IJFNMBCI_01544 | 1.5e-22 | S | Phage-like element PBSX protein XtrA | |||
IJFNMBCI_01545 | 5.5e-29 | wecC | 1.1.1.336 | M | ArpU family transcriptional regulator | |
IJFNMBCI_01546 | 1.4e-94 | resA | 3.1.21.5 | L | DEAD-like helicases superfamily | |
IJFNMBCI_01548 | 4.4e-66 | yokH | G | SMI1 / KNR4 family | ||
IJFNMBCI_01549 | 4.4e-258 | ywdH | 1.2.1.3 | C | Belongs to the aldehyde dehydrogenase family | |
IJFNMBCI_01550 | 2.5e-109 | 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 | ||
IJFNMBCI_01551 | 6.6e-283 | ytrP | 2.7.7.65 | T | COG2199 FOG GGDEF domain | |
IJFNMBCI_01552 | 1.1e-86 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
IJFNMBCI_01553 | 7.7e-109 | yttP | K | Transcriptional regulator | ||
IJFNMBCI_01554 | 1.7e-153 | hisK | 3.1.3.15 | E | COG1387 Histidinol phosphatase and related hydrolases of the PHP family | |
IJFNMBCI_01555 | 4.7e-262 | 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 | ||
IJFNMBCI_01556 | 5.3e-240 | braB | E | Component of the transport system for branched-chain amino acids | ||
IJFNMBCI_01557 | 2e-208 | iscS2 | 2.8.1.7 | E | Cysteine desulfurase | |
IJFNMBCI_01558 | 1.5e-225 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
IJFNMBCI_01559 | 3.9e-31 | sspB | S | spore protein | ||
IJFNMBCI_01560 | 1.1e-305 | acsA | 6.2.1.1, 6.2.1.2 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
IJFNMBCI_01561 | 0.0 | ytcJ | S | amidohydrolase | ||
IJFNMBCI_01562 | 5.7e-152 | 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 | |
IJFNMBCI_01563 | 6.4e-182 | sppA | OU | signal peptide peptidase SppA | ||
IJFNMBCI_01564 | 4.5e-88 | yteJ | S | RDD family | ||
IJFNMBCI_01565 | 6.5e-109 | ytfI | S | Protein of unknown function (DUF2953) | ||
IJFNMBCI_01566 | 4.6e-60 | ytfJ | S | Sporulation protein YtfJ | ||
IJFNMBCI_01567 | 4.9e-90 | 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 | |
IJFNMBCI_01568 | 2.2e-182 | ytxK | 2.1.1.72 | L | DNA methylase | |
IJFNMBCI_01569 | 3.1e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
IJFNMBCI_01570 | 2.1e-88 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
IJFNMBCI_01571 | 1.5e-233 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
IJFNMBCI_01572 | 5.9e-263 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
IJFNMBCI_01574 | 2.9e-142 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_01575 | 4.3e-129 | ytkL | S | Belongs to the UPF0173 family | ||
IJFNMBCI_01576 | 2.8e-238 | ytoI | K | transcriptional regulator containing CBS domains | ||
IJFNMBCI_01577 | 5.3e-47 | ytpI | S | YtpI-like protein | ||
IJFNMBCI_01578 | 2.7e-182 | nrnA | 3.1.13.3, 3.1.3.7 | S | COG0618 Exopolyphosphatase-related proteins | |
IJFNMBCI_01579 | 1.5e-23 | |||||
IJFNMBCI_01580 | 5.1e-87 | ytrI | ||||
IJFNMBCI_01581 | 9.2e-56 | ytrH | S | Sporulation protein YtrH | ||
IJFNMBCI_01582 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
IJFNMBCI_01583 | 9.8e-225 | ytsJ | 1.1.1.38 | C | Malate dehydrogenase | |
IJFNMBCI_01584 | 7.8e-160 | 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 | |
IJFNMBCI_01585 | 9e-181 | 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 | |
IJFNMBCI_01586 | 6.8e-181 | 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 | |
IJFNMBCI_01587 | 7e-293 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
IJFNMBCI_01588 | 4.6e-64 | fxsA | S | COG3030 Protein affecting phage T7 exclusion by the F plasmid | ||
IJFNMBCI_01589 | 3.6e-194 | ytvI | S | sporulation integral membrane protein YtvI | ||
IJFNMBCI_01590 | 1.1e-72 | yeaL | S | membrane | ||
IJFNMBCI_01591 | 2.5e-47 | yjdF | S | Protein of unknown function (DUF2992) | ||
IJFNMBCI_01592 | 8.1e-08 | S | Immunity protein 50 | |||
IJFNMBCI_01593 | 3.3e-132 | A | Pre-toxin TG | |||
IJFNMBCI_01594 | 3.2e-105 | S | aspartate phosphatase | |||
IJFNMBCI_01595 | 2.8e-210 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
IJFNMBCI_01596 | 3.1e-242 | icd | 1.1.1.42 | C | isocitrate | |
IJFNMBCI_01597 | 3.6e-171 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
IJFNMBCI_01598 | 5.3e-130 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_01599 | 0.0 | phoR | 2.7.13.3 | T | Signal transduction histidine kinase | |
IJFNMBCI_01600 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
IJFNMBCI_01601 | 5.9e-157 | 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 | |
IJFNMBCI_01602 | 1.6e-106 | ytaF | P | Probably functions as a manganese efflux pump | ||
IJFNMBCI_01603 | 6.4e-97 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
IJFNMBCI_01604 | 1.5e-160 | ytbE | S | reductase | ||
IJFNMBCI_01605 | 2.2e-205 | ytbD | EGP | Major facilitator Superfamily | ||
IJFNMBCI_01606 | 2e-67 | ytcD | K | Transcriptional regulator | ||
IJFNMBCI_01607 | 8.8e-195 | gapB | 1.2.1.12, 1.2.1.59 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
IJFNMBCI_01608 | 1.5e-67 | 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 | |
IJFNMBCI_01609 | 4.2e-80 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
IJFNMBCI_01610 | 2.9e-257 | dnaB | L | Membrane attachment protein | ||
IJFNMBCI_01611 | 4.3e-172 | dnaI | L | Primosomal protein DnaI | ||
IJFNMBCI_01612 | 2.7e-109 | ytxB | S | SNARE associated Golgi protein | ||
IJFNMBCI_01613 | 2.3e-153 | ytxC | S | YtxC-like family | ||
IJFNMBCI_01614 | 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) | |
IJFNMBCI_01615 | 1e-150 | ysaA | S | HAD-hyrolase-like | ||
IJFNMBCI_01616 | 0.0 | lytS | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_01617 | 1.1e-130 | lytT | T | COG3279 Response regulator of the LytR AlgR family | ||
IJFNMBCI_01618 | 9.1e-40 | lrgA | S | effector of murein hydrolase LrgA | ||
IJFNMBCI_01619 | 3.8e-109 | lrgB | M | Inhibits the expression or activity of extracellular murein hydrolases by interacting, possibly with LrgA, with the holin-like protein CidA. The LrgAB and CidA proteins may affect the proton motive force of the membrane. May be involved in programmed cell death (PCD), possibly triggering PCD in response to antibiotics and environmental stresses | ||
IJFNMBCI_01620 | 1.5e-86 | 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 | ||
IJFNMBCI_01621 | 3.1e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
IJFNMBCI_01622 | 4.6e-58 | 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 | ||
IJFNMBCI_01623 | 4.5e-42 | ysdA | S | Membrane | ||
IJFNMBCI_01624 | 1.7e-66 | ysdB | S | Sigma-w pathway protein YsdB | ||
IJFNMBCI_01625 | 8.1e-207 | ysdC | G | COG1363 Cellulase M and related proteins | ||
IJFNMBCI_01626 | 9.8e-188 | abnA | 3.2.1.99 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
IJFNMBCI_01627 | 2e-296 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
IJFNMBCI_01628 | 0.0 | araB | 2.7.1.16 | C | Belongs to the ribulokinase family | |
IJFNMBCI_01629 | 4.2e-132 | araD | 4.1.2.17, 4.2.1.109, 5.1.3.4 | G | COG0235 Ribulose-5-phosphate 4-epimerase and related epimerases and aldolases | |
IJFNMBCI_01630 | 3.5e-141 | araL | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
IJFNMBCI_01631 | 6.3e-221 | egsA | 1.1.1.261 | I | 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 | |
IJFNMBCI_01632 | 7.6e-252 | araN | G | carbohydrate transport | ||
IJFNMBCI_01633 | 5.5e-167 | araP | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
IJFNMBCI_01634 | 9.9e-144 | araQ | G | transport system permease | ||
IJFNMBCI_01635 | 3e-300 | abfA | 3.2.1.55 | GH51 | G | alpha-L-arabinofuranosidase activity |
IJFNMBCI_01636 | 0.0 | cstA | T | Carbon starvation protein | ||
IJFNMBCI_01637 | 1.7e-254 | glcF | C | Glycolate oxidase | ||
IJFNMBCI_01638 | 8.2e-260 | glcD | 1.1.3.15 | C | FAD binding domain | |
IJFNMBCI_01639 | 3.9e-201 | ysfB | KT | regulator | ||
IJFNMBCI_01640 | 2e-32 | sspI | S | Belongs to the SspI family | ||
IJFNMBCI_01641 | 7e-133 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
IJFNMBCI_01642 | 1.4e-195 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
IJFNMBCI_01643 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
IJFNMBCI_01644 | 6.4e-168 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
IJFNMBCI_01645 | 9.1e-40 | 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 | ||
IJFNMBCI_01646 | 2.3e-82 | cvpA | S | membrane protein, required for colicin V production | ||
IJFNMBCI_01647 | 0.0 | polX | L | COG1796 DNA polymerase IV (family X) | ||
IJFNMBCI_01648 | 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 | ||
IJFNMBCI_01649 | 4.7e-67 | yshE | S | membrane | ||
IJFNMBCI_01650 | 2.7e-123 | ywbB | S | Protein of unknown function (DUF2711) | ||
IJFNMBCI_01651 | 0.0 | lcfA | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
IJFNMBCI_01652 | 9.2e-104 | fadR | K | Transcriptional regulator | ||
IJFNMBCI_01653 | 9.2e-136 | fadB | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
IJFNMBCI_01654 | 2e-138 | etfB | C | Electron transfer flavoprotein | ||
IJFNMBCI_01655 | 6.7e-176 | etfA | C | Electron transfer flavoprotein | ||
IJFNMBCI_01656 | 2.5e-299 | xsa | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus |
IJFNMBCI_01657 | 2.5e-52 | trxA | O | Belongs to the thioredoxin family | ||
IJFNMBCI_01658 | 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 | ||
IJFNMBCI_01659 | 2e-214 | lysC | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
IJFNMBCI_01660 | 1.2e-79 | yslB | S | Protein of unknown function (DUF2507) | ||
IJFNMBCI_01661 | 4.8e-108 | sdhC | C | succinate dehydrogenase | ||
IJFNMBCI_01662 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
IJFNMBCI_01663 | 1.3e-147 | sdhB | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
IJFNMBCI_01664 | 2.4e-77 | ybgC | 3.1.2.23, 3.1.2.28 | S | thioesterase | |
IJFNMBCI_01665 | 2e-30 | gerE | K | Transcriptional regulator | ||
IJFNMBCI_01666 | 4.8e-73 | ysmB | 2.4.2.28 | K | helix_turn_helix multiple antibiotic resistance protein | |
IJFNMBCI_01667 | 2.7e-154 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
IJFNMBCI_01668 | 8.1e-199 | gerM | S | COG5401 Spore germination protein | ||
IJFNMBCI_01669 | 6.9e-133 | 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 | |
IJFNMBCI_01670 | 1.5e-101 | 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 | |
IJFNMBCI_01671 | 1.6e-88 | ysnB | S | Phosphoesterase | ||
IJFNMBCI_01673 | 7.9e-90 | L | Phage integrase family | |||
IJFNMBCI_01676 | 7e-24 | |||||
IJFNMBCI_01680 | 5.8e-21 | |||||
IJFNMBCI_01681 | 1.1e-81 | |||||
IJFNMBCI_01683 | 5.6e-109 | L | DNA-dependent DNA replication | |||
IJFNMBCI_01684 | 4.9e-08 | yodN | ||||
IJFNMBCI_01686 | 5.2e-206 | 3.6.4.12 | L | DnaB-like helicase C terminal domain | ||
IJFNMBCI_01687 | 1.2e-135 | dnaG | L | Toprim-like | ||
IJFNMBCI_01688 | 5e-11 | K | Cro/C1-type HTH DNA-binding domain | |||
IJFNMBCI_01689 | 4.4e-08 | S | Cro/C1-type HTH DNA-binding domain | |||
IJFNMBCI_01690 | 1.2e-42 | |||||
IJFNMBCI_01695 | 4.2e-48 | |||||
IJFNMBCI_01696 | 2.1e-49 | |||||
IJFNMBCI_01697 | 2.1e-33 | |||||
IJFNMBCI_01698 | 3e-277 | 2.7.7.7 | L | DNA polymerase family A | ||
IJFNMBCI_01699 | 3.4e-165 | |||||
IJFNMBCI_01701 | 2.2e-30 | ruvC | 3.1.22.4 | L | Crossover junction endodeoxyribonuclease RuvC | |
IJFNMBCI_01702 | 2.4e-14 | S | Protein of unknown function (DUF1523) | |||
IJFNMBCI_01706 | 1.6e-42 | nrdI | 1.17.4.1 | F | Belongs to the NrdI family | |
IJFNMBCI_01707 | 1.5e-85 | yhdJ | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | |
IJFNMBCI_01708 | 3.1e-123 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IJFNMBCI_01709 | 3.1e-24 | L | GIY-YIG catalytic domain | |||
IJFNMBCI_01710 | 3.5e-209 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IJFNMBCI_01712 | 1.8e-152 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
IJFNMBCI_01713 | 5.3e-47 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | deoxyuridine 5'-triphosphate nucleotidohydrolase | |
IJFNMBCI_01714 | 4.9e-29 | S | AP2 domain | |||
IJFNMBCI_01716 | 3.2e-90 | thyX | 2.1.1.148 | H | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor, and NADPH and FADH(2) as the reductant | |
IJFNMBCI_01717 | 1.6e-36 | S | protein conserved in bacteria | |||
IJFNMBCI_01718 | 5.3e-67 | Q | Methyltransferase domain | |||
IJFNMBCI_01720 | 8.5e-40 | |||||
IJFNMBCI_01721 | 2.1e-68 | 2.7.1.24 | H | dephospho-CoA kinase activity | ||
IJFNMBCI_01723 | 8.7e-146 | L | the current gene model (or a revised gene model) may contain a | |||
IJFNMBCI_01724 | 9.5e-49 | K | Sigma-70, region 4 | |||
IJFNMBCI_01725 | 4.8e-50 | |||||
IJFNMBCI_01726 | 8.8e-134 | |||||
IJFNMBCI_01728 | 4e-118 | ligB | 6.5.1.1, 6.5.1.6, 6.5.1.7 | L | ATP-dependent DNA ligase | |
IJFNMBCI_01730 | 9.2e-23 | |||||
IJFNMBCI_01732 | 1.3e-46 | |||||
IJFNMBCI_01733 | 7.8e-60 | S | Protein of unknown function (DUF2786) | |||
IJFNMBCI_01737 | 6.7e-10 | K | Cro/C1-type HTH DNA-binding domain | |||
IJFNMBCI_01744 | 8.3e-67 | L | Phage integrase family | |||
IJFNMBCI_01745 | 2.4e-256 | S | TIGRFAM Phage | |||
IJFNMBCI_01746 | 1.2e-28 | S | Helix-turn-helix of insertion element transposase | |||
IJFNMBCI_01747 | 5.5e-167 | |||||
IJFNMBCI_01748 | 6.4e-79 | S | Phage minor capsid protein 2 | |||
IJFNMBCI_01749 | 1.9e-20 | |||||
IJFNMBCI_01750 | 5.1e-148 | S | Family of unknown function (DUF5309) | |||
IJFNMBCI_01752 | 1e-26 | |||||
IJFNMBCI_01753 | 2.7e-17 | |||||
IJFNMBCI_01754 | 4.6e-30 | |||||
IJFNMBCI_01755 | 4.3e-20 | |||||
IJFNMBCI_01756 | 4.6e-49 | eae | N | domain, Protein | ||
IJFNMBCI_01757 | 4.2e-22 | |||||
IJFNMBCI_01759 | 2.4e-276 | lytH | 3.5.1.28 | M | COG3103 SH3 domain protein | |
IJFNMBCI_01762 | 1.3e-243 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
IJFNMBCI_01763 | 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) | |
IJFNMBCI_01764 | 8.2e-137 | yrvM | H | COG1179 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 | ||
IJFNMBCI_01765 | 1.3e-235 | rarA | L | COG2256 ATPase related to the helicase subunit of the Holliday junction resolvase | ||
IJFNMBCI_01766 | 7.8e-64 | cymR | K | Transcriptional regulator | ||
IJFNMBCI_01767 | 1.8e-212 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
IJFNMBCI_01768 | 7e-222 | 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 | |
IJFNMBCI_01769 | 1.7e-18 | S | COG0457 FOG TPR repeat | |||
IJFNMBCI_01770 | 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 | |
IJFNMBCI_01771 | 1.8e-83 | yrrD | S | protein conserved in bacteria | ||
IJFNMBCI_01772 | 2.9e-30 | yrzR | ||||
IJFNMBCI_01773 | 2.1e-08 | S | Protein of unknown function (DUF3918) | |||
IJFNMBCI_01774 | 4.4e-107 | glnP | P | ABC transporter | ||
IJFNMBCI_01775 | 2.7e-109 | gluC | P | ABC transporter | ||
IJFNMBCI_01776 | 1.4e-145 | glnH | ET | Belongs to the bacterial solute-binding protein 3 family | ||
IJFNMBCI_01777 | 1.2e-129 | glnQ | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
IJFNMBCI_01778 | 2.4e-163 | yrrI | S | AI-2E family transporter | ||
IJFNMBCI_01779 | 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 | |
IJFNMBCI_01780 | 8.5e-41 | yrzL | S | Belongs to the UPF0297 family | ||
IJFNMBCI_01781 | 1.2e-70 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
IJFNMBCI_01782 | 7.1e-46 | yrzB | S | Belongs to the UPF0473 family | ||
IJFNMBCI_01783 | 5.2e-185 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
IJFNMBCI_01784 | 9.5e-118 | yrrM | 2.1.1.104 | S | O-methyltransferase | |
IJFNMBCI_01785 | 1.7e-173 | yegQ | O | Peptidase U32 | ||
IJFNMBCI_01786 | 2.7e-246 | yegQ | O | COG0826 Collagenase and related proteases | ||
IJFNMBCI_01787 | 1.1e-113 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
IJFNMBCI_01788 | 3.1e-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 | ||
IJFNMBCI_01789 | 0.0 | pbpI | 3.4.16.4 | M | Penicillin-binding Protein | |
IJFNMBCI_01790 | 1.5e-68 | yrrS | S | Protein of unknown function (DUF1510) | ||
IJFNMBCI_01791 | 4.1e-27 | yrzA | S | Protein of unknown function (DUF2536) | ||
IJFNMBCI_01792 | 8.4e-119 | yrrT | 4.4.1.21 | Q | Could be a S-adenosyl-L-methionine-dependent methyltransferase | |
IJFNMBCI_01793 | 3.6e-123 | 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 | |
IJFNMBCI_01794 | 1.4e-170 | mccA | 2.5.1.134, 2.5.1.47 | E | Cysteine synthase | |
IJFNMBCI_01795 | 3.7e-210 | mccB | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
IJFNMBCI_01796 | 4.6e-35 | yrhC | S | YrhC-like protein | ||
IJFNMBCI_01797 | 2.6e-80 | yrhD | S | Protein of unknown function (DUF1641) | ||
IJFNMBCI_01798 | 0.0 | fdhA | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase, alpha subunit | |
IJFNMBCI_01799 | 6e-61 | yrhF | S | Uncharacterized conserved protein (DUF2294) | ||
IJFNMBCI_01800 | 8e-143 | focA | P | Formate nitrite | ||
IJFNMBCI_01802 | 3.9e-93 | yrhH | Q | methyltransferase | ||
IJFNMBCI_01803 | 7.7e-100 | Z012_03230 | K | Tetracycline repressor, C-terminal all-alpha domain | ||
IJFNMBCI_01804 | 0.0 | MA20_16700 | 1.14.14.1, 1.6.2.4 | C | Belongs to the cytochrome P450 family | |
IJFNMBCI_01805 | 9.3e-212 | ynfM | EGP | Major facilitator Superfamily | ||
IJFNMBCI_01806 | 2.6e-163 | yybE | K | Transcriptional regulator | ||
IJFNMBCI_01807 | 3.6e-82 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
IJFNMBCI_01808 | 2.6e-182 | romA | S | Beta-lactamase superfamily domain | ||
IJFNMBCI_01809 | 0.0 | manR | 2.7.1.200, 2.7.1.202 | GKT | transcriptional antiterminator | |
IJFNMBCI_01810 | 0.0 | manP | 2.7.1.191, 2.7.1.202 | G | phosphotransferase system | |
IJFNMBCI_01811 | 3.5e-190 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
IJFNMBCI_01812 | 2e-129 | glvR | K | Helix-turn-helix domain, rpiR family | ||
IJFNMBCI_01813 | 6.5e-33 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | |
IJFNMBCI_01814 | 1.1e-95 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | |
IJFNMBCI_01815 | 1e-145 | S | hydrolase | |||
IJFNMBCI_01817 | 8.3e-90 | yrdA | S | DinB family | ||
IJFNMBCI_01818 | 3.8e-80 | yyaR | K | Acetyltransferase (GNAT) domain | ||
IJFNMBCI_01819 | 9.6e-221 | tetL | EGP | Major facilitator Superfamily | ||
IJFNMBCI_01820 | 3.6e-29 | yyaR | K | acetyltransferase | ||
IJFNMBCI_01821 | 1.3e-123 | yecA | E | amino acid | ||
IJFNMBCI_01822 | 9.7e-105 | K | Transcriptional regulator | |||
IJFNMBCI_01823 | 3.6e-149 | ydeE | K | AraC family transcriptional regulator | ||
IJFNMBCI_01825 | 2.9e-20 | S | SMI1-KNR4 cell-wall | |||
IJFNMBCI_01826 | 7.1e-195 | yobL | S | Bacterial EndoU nuclease | ||
IJFNMBCI_01827 | 2.1e-91 | K | Transcriptional regulator PadR-like family | |||
IJFNMBCI_01828 | 8.4e-159 | axeA | S | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
IJFNMBCI_01829 | 9.9e-124 | sigK | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
IJFNMBCI_01830 | 2e-212 | EGP | Major facilitator Superfamily | |||
IJFNMBCI_01832 | 7.2e-107 | yqeD | S | SNARE associated Golgi protein | ||
IJFNMBCI_01833 | 3.2e-138 | 3.5.1.104 | G | Polysaccharide deacetylase | ||
IJFNMBCI_01834 | 1.1e-138 | yqeF | E | GDSL-like Lipase/Acylhydrolase | ||
IJFNMBCI_01836 | 2e-94 | yqeG | S | hydrolase of the HAD superfamily | ||
IJFNMBCI_01837 | 5.9e-213 | yqeH | S | In Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
IJFNMBCI_01838 | 2.4e-158 | 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) | |
IJFNMBCI_01839 | 4.8e-45 | yhbY | J | RNA-binding protein containing KH domain, possibly ribosomal protein | ||
IJFNMBCI_01840 | 5e-107 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
IJFNMBCI_01841 | 3.3e-103 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
IJFNMBCI_01842 | 3.4e-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 | ||
IJFNMBCI_01843 | 2.2e-139 | yqeM | Q | Methyltransferase | ||
IJFNMBCI_01844 | 5e-148 | comER | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | ||
IJFNMBCI_01845 | 2.5e-104 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
IJFNMBCI_01846 | 8e-105 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
IJFNMBCI_01847 | 0.0 | comEC | S | Competence protein ComEC | ||
IJFNMBCI_01848 | 3.8e-182 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
IJFNMBCI_01849 | 2.2e-36 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
IJFNMBCI_01850 | 1.5e-203 | gpr | 3.4.24.78 | C | Initiates the rapid degradation of small, acid-soluble proteins during spore germination | |
IJFNMBCI_01851 | 3.2e-220 | spoIIP | M | stage II sporulation protein P | ||
IJFNMBCI_01852 | 3.8e-54 | yqxA | S | Protein of unknown function (DUF3679) | ||
IJFNMBCI_01853 | 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 | ||
IJFNMBCI_01854 | 5.3e-217 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
IJFNMBCI_01855 | 4e-187 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
IJFNMBCI_01856 | 3.5e-76 | 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 | ||
IJFNMBCI_01857 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
IJFNMBCI_01858 | 1.1e-198 | 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 | ||
IJFNMBCI_01859 | 4.6e-174 | prmA | J | Methylates ribosomal protein L11 | ||
IJFNMBCI_01860 | 7.9e-140 | 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 | |
IJFNMBCI_01861 | 1.2e-260 | yqeV | 2.8.4.5 | J | ribosomal protein S12 methylthiotransferase | |
IJFNMBCI_01862 | 1.6e-158 | yqeW | P | COG1283 Na phosphate symporter | ||
IJFNMBCI_01863 | 1.2e-19 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
IJFNMBCI_01864 | 1.2e-68 | yqeY | S | Yqey-like protein | ||
IJFNMBCI_01865 | 3.4e-231 | yqeZ | O | COG1030 Membrane-bound serine protease (ClpP class) | ||
IJFNMBCI_01866 | 1.2e-119 | yqfA | S | UPF0365 protein | ||
IJFNMBCI_01867 | 3.8e-54 | yqfB | ||||
IJFNMBCI_01868 | 9.3e-46 | yqfC | S | sporulation protein YqfC | ||
IJFNMBCI_01869 | 6.8e-215 | yqfD | 3.1.3.102, 3.1.3.104 | S | Stage IV sporulation | |
IJFNMBCI_01870 | 6.6e-176 | phoH | T | Phosphate starvation-inducible protein PhoH | ||
IJFNMBCI_01871 | 0.0 | yqfF | S | membrane-associated HD superfamily hydrolase | ||
IJFNMBCI_01872 | 2e-77 | 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 | |
IJFNMBCI_01873 | 1.3e-63 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
IJFNMBCI_01874 | 7.1e-71 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
IJFNMBCI_01875 | 4e-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 | ||
IJFNMBCI_01876 | 8.7e-16 | S | YqzL-like protein | |||
IJFNMBCI_01877 | 1.2e-143 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
IJFNMBCI_01878 | 5.1e-175 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
IJFNMBCI_01879 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
IJFNMBCI_01880 | 4.5e-112 | ccpN | K | CBS domain | ||
IJFNMBCI_01881 | 5.8e-149 | 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 | |
IJFNMBCI_01882 | 6.1e-88 | yaiI | S | Belongs to the UPF0178 family | ||
IJFNMBCI_01883 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
IJFNMBCI_01884 | 2.4e-201 | 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 | ||
IJFNMBCI_01885 | 3.1e-62 | cccA | C | COG2010 Cytochrome c, mono- and diheme variants | ||
IJFNMBCI_01886 | 5.4e-125 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
IJFNMBCI_01887 | 2.1e-210 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
IJFNMBCI_01888 | 1.9e-175 | 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 | |
IJFNMBCI_01889 | 6.2e-51 | yqfQ | S | YqfQ-like protein | ||
IJFNMBCI_01890 | 8.8e-240 | 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 | |
IJFNMBCI_01891 | 4.4e-166 | 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 | |
IJFNMBCI_01892 | 1.6e-36 | yqfT | S | Protein of unknown function (DUF2624) | ||
IJFNMBCI_01893 | 1.4e-156 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
IJFNMBCI_01894 | 2.9e-72 | zur | P | Belongs to the Fur family | ||
IJFNMBCI_01895 | 3.7e-105 | yqfW | S | Belongs to the 5'(3')-deoxyribonucleotidase family | ||
IJFNMBCI_01896 | 2.5e-51 | yqfX | S | membrane | ||
IJFNMBCI_01897 | 4.1e-201 | 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 | |
IJFNMBCI_01898 | 5.3e-47 | yqfZ | M | LysM domain | ||
IJFNMBCI_01899 | 9e-128 | yqgB | S | Protein of unknown function (DUF1189) | ||
IJFNMBCI_01900 | 2.9e-71 | yqgC | S | protein conserved in bacteria | ||
IJFNMBCI_01901 | 1.2e-114 | sodA | 1.15.1.1 | P | radicals which are normally produced within the cells and which are toxic to biological systems | |
IJFNMBCI_01902 | 2.5e-223 | yqgE | EGP | Major facilitator superfamily | ||
IJFNMBCI_01903 | 0.0 | pbpA | 3.4.16.4 | M | penicillin-binding protein | |
IJFNMBCI_01904 | 1.7e-157 | pstS | P | Phosphate | ||
IJFNMBCI_01905 | 5.2e-154 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
IJFNMBCI_01906 | 1.8e-156 | pstA | P | Phosphate transport system permease | ||
IJFNMBCI_01907 | 2.3e-145 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
IJFNMBCI_01908 | 1.9e-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 | |
IJFNMBCI_01909 | 1.6e-74 | yqzC | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
IJFNMBCI_01910 | 1.2e-50 | yqzD | ||||
IJFNMBCI_01911 | 9.4e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
IJFNMBCI_01912 | 4.1e-98 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
IJFNMBCI_01913 | 1.8e-07 | yqgO | ||||
IJFNMBCI_01914 | 4.1e-232 | nhaC | C | Na H antiporter | ||
IJFNMBCI_01915 | 1e-28 | yqgQ | S | Protein conserved in bacteria | ||
IJFNMBCI_01916 | 4.9e-179 | glcK | 2.7.1.2 | G | Glucokinase | |
IJFNMBCI_01917 | 9.3e-222 | yqgT | 3.4.19.11 | E | Gamma-D-glutamyl-L-diamino acid endopeptidase | |
IJFNMBCI_01918 | 3.5e-199 | yqgU | ||||
IJFNMBCI_01919 | 1.5e-49 | yqgV | S | Thiamine-binding protein | ||
IJFNMBCI_01920 | 5.4e-20 | yqgW | S | Protein of unknown function (DUF2759) | ||
IJFNMBCI_01921 | 7.3e-123 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
IJFNMBCI_01922 | 3.1e-37 | yqgY | S | Protein of unknown function (DUF2626) | ||
IJFNMBCI_01923 | 9.2e-65 | yqgZ | 1.20.4.1 | P | Belongs to the ArsC family | |
IJFNMBCI_01925 | 5.9e-149 | yqhA | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | ||
IJFNMBCI_01926 | 1.6e-238 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
IJFNMBCI_01927 | 1.5e-185 | corA | P | Mg2 transporter protein | ||
IJFNMBCI_01928 | 6.6e-201 | comGA | NU | COG2804 Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
IJFNMBCI_01929 | 3.5e-183 | comGB | NU | COG1459 Type II secretory pathway, component PulF | ||
IJFNMBCI_01930 | 4.9e-48 | comGC | U | Required for transformation and DNA binding | ||
IJFNMBCI_01931 | 5.8e-71 | gspH | NU | Tfp pilus assembly protein FimT | ||
IJFNMBCI_01932 | 3.4e-20 | comGE | ||||
IJFNMBCI_01933 | 4.3e-65 | comGF | U | Putative Competence protein ComGF | ||
IJFNMBCI_01934 | 2.5e-62 | S | ComG operon protein 7 | |||
IJFNMBCI_01935 | 2.3e-26 | yqzE | S | YqzE-like protein | ||
IJFNMBCI_01936 | 1.3e-54 | yqzG | S | Protein of unknown function (DUF3889) | ||
IJFNMBCI_01937 | 7.2e-121 | yqxM | ||||
IJFNMBCI_01938 | 3.5e-71 | sipW | 3.4.21.89 | U | Signal peptidase | |
IJFNMBCI_01939 | 1.6e-140 | tasA | S | Cell division protein FtsN | ||
IJFNMBCI_01940 | 7.8e-55 | sinR | K | transcriptional | ||
IJFNMBCI_01941 | 3.7e-21 | sinI | S | Anti-repressor SinI | ||
IJFNMBCI_01942 | 8.4e-153 | yqhG | S | Bacterial protein YqhG of unknown function | ||
IJFNMBCI_01943 | 0.0 | yqhH | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
IJFNMBCI_01944 | 3.3e-208 | gcvT | 1.4.4.2, 2.1.2.10 | E | The glycine cleavage system catalyzes the degradation of glycine | |
IJFNMBCI_01945 | 7.9e-252 | 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 | |
IJFNMBCI_01946 | 1.3e-284 | 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 | |
IJFNMBCI_01947 | 2.7e-64 | yqhL | P | COG0607 Rhodanese-related sulfurtransferase | ||
IJFNMBCI_01948 | 3.4e-160 | 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 | |
IJFNMBCI_01949 | 2.7e-73 | mntR | K | Involved in manganese homeostasis. Might activate the transcription of the mntABCD operon | ||
IJFNMBCI_01950 | 3.1e-164 | yqhO | S | esterase of the alpha-beta hydrolase superfamily | ||
IJFNMBCI_01951 | 3.4e-62 | yqhP | ||||
IJFNMBCI_01952 | 7e-167 | yqhQ | S | Protein of unknown function (DUF1385) | ||
IJFNMBCI_01953 | 4.9e-88 | yqhR | S | Conserved membrane protein YqhR | ||
IJFNMBCI_01954 | 2.3e-174 | yqhT | 3.4.11.9, 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
IJFNMBCI_01955 | 5.4e-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 | ||
IJFNMBCI_01956 | 1.5e-35 | yqhV | S | Protein of unknown function (DUF2619) | ||
IJFNMBCI_01957 | 9.4e-172 | spoIIIAA | S | stage III sporulation protein AA | ||
IJFNMBCI_01958 | 1.7e-85 | spoIIIAB | S | Stage III sporulation protein | ||
IJFNMBCI_01959 | 7.6e-29 | spoIIIAC | S | stage III sporulation protein AC | ||
IJFNMBCI_01960 | 2.5e-41 | spoIIIAD | S | Stage III sporulation protein AD | ||
IJFNMBCI_01961 | 4.1e-199 | spoIIIAE | S | stage III sporulation protein AE | ||
IJFNMBCI_01962 | 6.9e-102 | spoIIIAF | S | Stage III sporulation protein AF (Spore_III_AF) | ||
IJFNMBCI_01963 | 1e-117 | spoIIIAG | S | stage III sporulation protein AG | ||
IJFNMBCI_01964 | 9.6e-62 | spoIIIAH | S | SpoIIIAH-like protein | ||
IJFNMBCI_01965 | 4.9e-63 | 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 | |
IJFNMBCI_01966 | 1.2e-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 | |
IJFNMBCI_01967 | 8.1e-67 | yqhY | S | protein conserved in bacteria | ||
IJFNMBCI_01968 | 2.5e-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 | ||
IJFNMBCI_01969 | 4.3e-155 | 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 | |
IJFNMBCI_01970 | 1.8e-243 | 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 | |
IJFNMBCI_01971 | 2e-39 | 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 | |
IJFNMBCI_01972 | 3.6e-160 | 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 | |
IJFNMBCI_01973 | 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) | |
IJFNMBCI_01974 | 2.5e-155 | rrmJ | 2.1.1.226, 2.1.1.227 | J | rRNA methylase | |
IJFNMBCI_01975 | 3.9e-78 | argR | K | Regulates arginine biosynthesis genes | ||
IJFNMBCI_01976 | 1.2e-305 | recN | L | May be involved in recombinational repair of damaged DNA | ||
IJFNMBCI_01977 | 2.8e-238 | rseP | 3.4.21.116 | M | Stage IV sporulation protein B | |
IJFNMBCI_01978 | 3.2e-144 | 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 | |||
IJFNMBCI_01979 | 2.6e-214 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
IJFNMBCI_01982 | 2.3e-212 | yqiG | C | COG1902 NADH flavin oxidoreductases, Old Yellow Enzyme family | ||
IJFNMBCI_01984 | 1.6e-42 | yhjA | S | Excalibur calcium-binding domain | ||
IJFNMBCI_01985 | 3e-125 | yrpD | S | Domain of unknown function, YrpD | ||
IJFNMBCI_01986 | 1.4e-167 | els | S | Acetyltransferase, GNAT family | ||
IJFNMBCI_01987 | 5.3e-65 | frataxin | S | Domain of unknown function (DU1801) | ||
IJFNMBCI_01988 | 3.9e-68 | frataxin | S | Domain of unknown function (DU1801) | ||
IJFNMBCI_01989 | 1.9e-109 | comK | K | Competence transcription factor | ||
IJFNMBCI_01990 | 1.8e-31 | yhzC | S | IDEAL | ||
IJFNMBCI_01991 | 8.5e-159 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_01992 | 1.3e-298 | yhfW | CE | COG0665 Glycine D-amino acid oxidases (deaminating) | ||
IJFNMBCI_01993 | 8.2e-198 | hemAT | NT | chemotaxis protein | ||
IJFNMBCI_01994 | 9.3e-90 | bioY | S | BioY family | ||
IJFNMBCI_01995 | 6.8e-278 | yhfT | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | |
IJFNMBCI_01996 | 8.7e-201 | vraB | 2.3.1.9 | I | Belongs to the thiolase family | |
IJFNMBCI_01997 | 4.4e-103 | yhfR | 3.1.3.73 | G | Belongs to the phosphoglycerate mutase family | |
IJFNMBCI_01998 | 8.7e-151 | yhfQ | P | COG4594 ABC-type Fe3 -citrate transport system, periplasmic component | ||
IJFNMBCI_01999 | 5.2e-204 | aprE | 3.4.21.62 | O | Belongs to the peptidase S8 family | |
IJFNMBCI_02000 | 3.3e-236 | yhfN | 3.4.24.84 | O | Peptidase M48 | |
IJFNMBCI_02001 | 1.9e-65 | yhfM | ||||
IJFNMBCI_02002 | 8.9e-300 | fadD | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | |
IJFNMBCI_02003 | 1.7e-111 | yhfK | GM | NmrA-like family | ||
IJFNMBCI_02004 | 1.1e-186 | lplJ | 6.3.1.20 | H | Lipoate-protein ligase | |
IJFNMBCI_02005 | 3.2e-138 | yhfI | S | COG1234 Metal-dependent hydrolases of the beta-lactamase superfamily III | ||
IJFNMBCI_02006 | 7.9e-11 | yhfH | S | YhfH-like protein | ||
IJFNMBCI_02007 | 7.4e-223 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
IJFNMBCI_02008 | 1.6e-196 | yhfE | 3.2.1.4 | GH5,GH9 | G | peptidase M42 |
IJFNMBCI_02010 | 3.7e-182 | 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 | |
IJFNMBCI_02011 | 2.1e-276 | yhgE | S | YhgE Pip N-terminal domain protein | ||
IJFNMBCI_02012 | 3.2e-101 | yhgD | K | Transcriptional regulator | ||
IJFNMBCI_02013 | 2e-274 | 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 | |
IJFNMBCI_02014 | 7.3e-180 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
IJFNMBCI_02015 | 3.3e-203 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
IJFNMBCI_02016 | 0.0 | pbpF | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
IJFNMBCI_02017 | 6.4e-90 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
IJFNMBCI_02018 | 5.3e-243 | yhfA | C | membrane | ||
IJFNMBCI_02019 | 1.4e-223 | yhaA | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
IJFNMBCI_02020 | 1.1e-122 | ecsC | S | EcsC protein family | ||
IJFNMBCI_02021 | 8.5e-221 | ecsB | U | ABC transporter | ||
IJFNMBCI_02022 | 1.1e-135 | ecsA | V | transporter (ATP-binding protein) | ||
IJFNMBCI_02023 | 6.9e-80 | hit | FG | COG0537 Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
IJFNMBCI_02024 | 4.1e-203 | 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 | |
IJFNMBCI_02025 | 1.4e-76 | trpP | S | Tryptophan transporter TrpP | ||
IJFNMBCI_02026 | 2e-17 | |||||
IJFNMBCI_02027 | 6.2e-39 | yhaH | S | YtxH-like protein | ||
IJFNMBCI_02028 | 3.3e-112 | hpr | K | Negative regulator of protease production and sporulation | ||
IJFNMBCI_02029 | 2.2e-54 | yhaI | S | Protein of unknown function (DUF1878) | ||
IJFNMBCI_02030 | 7e-95 | yhaK | S | Putative zincin peptidase | ||
IJFNMBCI_02031 | 2.2e-119 | prsA | 5.2.1.8 | M | plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
IJFNMBCI_02032 | 1.6e-32 | yhaL | S | Sporulation protein YhaL | ||
IJFNMBCI_02033 | 2.6e-177 | yhaM | L | Shows a 3'-5' exoribonuclease activity | ||
IJFNMBCI_02034 | 0.0 | yhaN | L | AAA domain | ||
IJFNMBCI_02035 | 7.7e-238 | yhaO | L | DNA repair exonuclease | ||
IJFNMBCI_02036 | 2.3e-205 | yhaP | CP | COG1668 ABC-type Na efflux pump, permease component | ||
IJFNMBCI_02037 | 6.8e-167 | yhaQ | S | ABC transporter, ATP-binding protein | ||
IJFNMBCI_02038 | 7.3e-15 | S | YhzD-like protein | |||
IJFNMBCI_02039 | 2e-135 | yhaR | 5.3.3.18 | I | enoyl-CoA hydratase | |
IJFNMBCI_02041 | 7.8e-88 | yhaT | P | regulatory, ligand-binding protein related to C-terminal domains of K channels | ||
IJFNMBCI_02042 | 9.1e-207 | yhaU | P | COG0475 Kef-type K transport systems, membrane components | ||
IJFNMBCI_02043 | 7.1e-250 | iucD | 1.14.13.59 | Q | L-lysine 6-monooxygenase (NADPH-requiring) | |
IJFNMBCI_02044 | 4.6e-293 | hemZ | H | coproporphyrinogen III oxidase | ||
IJFNMBCI_02045 | 1.9e-158 | yhaX | S | haloacid dehalogenase-like hydrolase | ||
IJFNMBCI_02046 | 4e-196 | yhaZ | L | DNA alkylation repair enzyme | ||
IJFNMBCI_02047 | 4.4e-53 | yheA | S | Belongs to the UPF0342 family | ||
IJFNMBCI_02048 | 2.5e-198 | yheB | S | Belongs to the UPF0754 family | ||
IJFNMBCI_02049 | 2e-213 | yheC | HJ | YheC/D like ATP-grasp | ||
IJFNMBCI_02050 | 2.3e-259 | gshB | 6.3.2.2, 6.3.2.3 | HJ | YheC/D like ATP-grasp | |
IJFNMBCI_02051 | 1.7e-36 | yheE | S | Family of unknown function (DUF5342) | ||
IJFNMBCI_02052 | 2.9e-28 | sspB | S | spore protein | ||
IJFNMBCI_02054 | 6.2e-111 | yheG | GM | NAD(P)H-binding | ||
IJFNMBCI_02055 | 1.6e-14 | |||||
IJFNMBCI_02056 | 9.9e-81 | S | AAA ATPase domain | |||
IJFNMBCI_02057 | 0.0 | yheH | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
IJFNMBCI_02058 | 0.0 | yheI | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
IJFNMBCI_02060 | 2.1e-85 | T | universal stress protein | |||
IJFNMBCI_02061 | 1.8e-93 | ymcC | S | Membrane | ||
IJFNMBCI_02062 | 1.8e-87 | pksA | K | Transcriptional regulator | ||
IJFNMBCI_02063 | 6.3e-154 | 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 | |
IJFNMBCI_02064 | 1e-156 | yheN | G | deacetylase | ||
IJFNMBCI_02065 | 2.7e-137 | cobB | K | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form | ||
IJFNMBCI_02066 | 1.6e-205 | yhdY | M | Mechanosensitive ion channel | ||
IJFNMBCI_02068 | 1.1e-127 | yhdW | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
IJFNMBCI_02069 | 2.8e-64 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
IJFNMBCI_02070 | 8.5e-52 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
IJFNMBCI_02071 | 4.6e-255 | corC1 | P | COG1253 Hemolysins and related proteins containing CBS domains | ||
IJFNMBCI_02072 | 3.4e-233 | pksF | 2.3.1.179, 2.3.1.41 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
IJFNMBCI_02073 | 4.2e-225 | yhdR | 2.6.1.1 | E | Aminotransferase | |
IJFNMBCI_02074 | 4.3e-71 | cueR | K | transcriptional | ||
IJFNMBCI_02075 | 4.3e-242 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
IJFNMBCI_02076 | 5.1e-110 | plsC | 2.3.1.51 | I | Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family | |
IJFNMBCI_02077 | 4.2e-86 | sigM | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
IJFNMBCI_02078 | 6.6e-201 | yhdL | S | Sigma factor regulator N-terminal | ||
IJFNMBCI_02079 | 8.1e-45 | yhdK | S | Sigma-M inhibitor protein | ||
IJFNMBCI_02080 | 4.4e-199 | yhdH | S | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family | ||
IJFNMBCI_02081 | 2e-250 | yhdG | E | amino acid | ||
IJFNMBCI_02082 | 3e-159 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_02083 | 3.5e-205 | citA | 2.3.3.1 | C | Belongs to the citrate synthase family | |
IJFNMBCI_02084 | 2e-163 | citR | K | Transcriptional regulator | ||
IJFNMBCI_02085 | 2.2e-127 | lytE | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
IJFNMBCI_02086 | 1.3e-257 | phoB | 3.1.3.1 | P | Belongs to the alkaline phosphatase family | |
IJFNMBCI_02087 | 3.6e-271 | ycgB | S | Stage V sporulation protein R | ||
IJFNMBCI_02088 | 4.5e-256 | ygxB | M | Conserved TM helix | ||
IJFNMBCI_02089 | 5.6e-74 | nsrR | K | Transcriptional regulator | ||
IJFNMBCI_02090 | 4.7e-218 | sle1 | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
IJFNMBCI_02091 | 1.4e-50 | yhdC | S | Protein of unknown function (DUF3889) | ||
IJFNMBCI_02092 | 4.4e-36 | yhdB | S | YhdB-like protein | ||
IJFNMBCI_02093 | 7.2e-84 | azr | 1.7.1.6 | S | NADPH-dependent FMN reductase | |
IJFNMBCI_02094 | 1e-79 | yhcZ | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
IJFNMBCI_02095 | 7.6e-18 | yhcZ | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
IJFNMBCI_02096 | 2.5e-190 | yhcY | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_02097 | 0.0 | pmmB | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
IJFNMBCI_02098 | 0.0 | glpD | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
IJFNMBCI_02099 | 1.3e-292 | 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 | |
IJFNMBCI_02100 | 3.6e-146 | glpF | G | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
IJFNMBCI_02101 | 1.4e-101 | 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 | ||
IJFNMBCI_02102 | 3.1e-256 | yhxA | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | ||
IJFNMBCI_02103 | 9.5e-302 | yhcX | 3.5.1.3 | K | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
IJFNMBCI_02104 | 2.1e-120 | yhcW | 5.4.2.6 | S | hydrolase | |
IJFNMBCI_02105 | 3.8e-67 | yhcV | S | COG0517 FOG CBS domain | ||
IJFNMBCI_02106 | 1.6e-64 | yhcU | S | Family of unknown function (DUF5365) | ||
IJFNMBCI_02107 | 5.1e-162 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
IJFNMBCI_02108 | 1.7e-97 | yhcS | 3.4.22.70 | M | COG3764 Sortase (surface protein transpeptidase) | |
IJFNMBCI_02109 | 1.6e-304 | yhcR | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
IJFNMBCI_02110 | 1.1e-110 | yhcQ | M | Spore coat protein | ||
IJFNMBCI_02111 | 1.5e-153 | yhcP | ||||
IJFNMBCI_02112 | 3.3e-76 | yhcN | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
IJFNMBCI_02113 | 1.5e-40 | yhcM | ||||
IJFNMBCI_02114 | 2.7e-220 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
IJFNMBCI_02115 | 1.3e-185 | yhcK | 2.7.7.65 | T | COG2199 FOG GGDEF domain | |
IJFNMBCI_02116 | 8.5e-148 | metQ | M | Belongs to the nlpA lipoprotein family | ||
IJFNMBCI_02117 | 3.9e-30 | cspB | K | 'Cold-shock' DNA-binding domain | ||
IJFNMBCI_02118 | 1.7e-163 | yhcI | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | ||
IJFNMBCI_02119 | 3.4e-166 | yhcH | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_02120 | 3e-125 | yhcG | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_02121 | 2.5e-62 | yhcF | K | Transcriptional regulator | ||
IJFNMBCI_02122 | 4.3e-53 | |||||
IJFNMBCI_02123 | 6.5e-55 | yhcC | ||||
IJFNMBCI_02124 | 4.7e-99 | yhcB | 1.6.5.2 | S | NADPH-dependent FMN reductase | |
IJFNMBCI_02125 | 8.4e-285 | yhcA | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02126 | 8.1e-98 | yhbJ | V | COG1566 Multidrug resistance efflux pump | ||
IJFNMBCI_02127 | 4.6e-74 | yhbI | K | DNA-binding transcription factor activity | ||
IJFNMBCI_02128 | 1.4e-215 | yhbH | S | Belongs to the UPF0229 family | ||
IJFNMBCI_02129 | 0.0 | prkA | T | Ser protein kinase | ||
IJFNMBCI_02131 | 1.6e-62 | yhbF | M | COG1664 Integral membrane protein CcmA involved in cell shape determination | ||
IJFNMBCI_02132 | 8.9e-61 | yhbE | M | COG1664 Integral membrane protein CcmA involved in cell shape determination | ||
IJFNMBCI_02133 | 1e-108 | yhbD | K | Protein of unknown function (DUF4004) | ||
IJFNMBCI_02134 | 2e-85 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
IJFNMBCI_02135 | 1.5e-172 | yhbB | S | Putative amidase domain | ||
IJFNMBCI_02136 | 8.4e-226 | 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) | |
IJFNMBCI_02137 | 7.9e-114 | yhzB | S | B3/4 domain | ||
IJFNMBCI_02139 | 4.8e-23 | K | Transcriptional regulator | |||
IJFNMBCI_02140 | 6.6e-81 | ygaO | ||||
IJFNMBCI_02141 | 2.7e-42 | 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 | ||
IJFNMBCI_02142 | 7.9e-213 | ssuD | 1.14.14.5 | C | Catalyzes the desulfonation of aliphatic sulfonates | |
IJFNMBCI_02143 | 2e-144 | ssuC | P | ABC transporter (permease) | ||
IJFNMBCI_02144 | 1.7e-179 | ssuA | M | Sulfonate ABC transporter | ||
IJFNMBCI_02145 | 1.6e-140 | ssuB | P | COG1116 ABC-type nitrate sulfonate bicarbonate transport system, ATPase component | ||
IJFNMBCI_02146 | 4.1e-183 | S | Amidohydrolase | |||
IJFNMBCI_02147 | 3e-289 | katA | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
IJFNMBCI_02148 | 2.6e-106 | oppF3 | E | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_02149 | 2.1e-19 | oppF3 | E | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_02150 | 1.3e-134 | oppD3 | P | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_02151 | 2.4e-127 | appC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
IJFNMBCI_02152 | 9.2e-138 | appB | P | Binding-protein-dependent transport system inner membrane component | ||
IJFNMBCI_02153 | 5.7e-231 | oppA5 | E | PFAM extracellular solute-binding protein family 5 | ||
IJFNMBCI_02155 | 1.8e-264 | ygaK | C | Berberine and berberine like | ||
IJFNMBCI_02156 | 0.0 | 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 | |
IJFNMBCI_02157 | 5.2e-130 | pepE | 3.4.11.2, 3.4.13.21 | E | Belongs to the peptidase S51 family | |
IJFNMBCI_02158 | 2e-33 | C | Na+/H+ antiporter family | |||
IJFNMBCI_02159 | 3.3e-206 | C | Na+/H+ antiporter family | |||
IJFNMBCI_02163 | 1.6e-08 | |||||
IJFNMBCI_02166 | 4.6e-138 | ykuT | M | Mechanosensitive ion channel | ||
IJFNMBCI_02167 | 2.3e-78 | ykuV | CO | thiol-disulfide | ||
IJFNMBCI_02168 | 4.5e-98 | rok | K | Repressor of ComK | ||
IJFNMBCI_02169 | 2.5e-162 | yknT | ||||
IJFNMBCI_02170 | 8.8e-106 | 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 | |
IJFNMBCI_02171 | 1.9e-189 | moeB | 2.7.7.73, 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
IJFNMBCI_02172 | 7.1e-242 | moeA | 2.10.1.1 | H | molybdopterin | |
IJFNMBCI_02173 | 5.8e-94 | mobB | 2.10.1.1, 2.7.7.77 | H | molybdopterin-guanine dinucleotide biosynthesis protein | |
IJFNMBCI_02174 | 3.5e-82 | moaE | 2.8.1.12 | H | COG0314 Molybdopterin converting factor, large subunit | |
IJFNMBCI_02175 | 3.8e-32 | moaD | 2.8.1.12 | H | Involved in sulfur transfer in the conversion of molybdopterin precursor Z to molybdopterin | |
IJFNMBCI_02176 | 2.3e-106 | yknW | S | Yip1 domain | ||
IJFNMBCI_02177 | 7.5e-171 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
IJFNMBCI_02178 | 6.1e-123 | macB | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_02179 | 3.9e-210 | yknZ | V | ABC transporter (permease) | ||
IJFNMBCI_02180 | 4.6e-132 | fruR | K | Transcriptional regulator | ||
IJFNMBCI_02181 | 1.8e-167 | fruK | 2.7.1.11, 2.7.1.56 | G | Belongs to the carbohydrate kinase PfkB family | |
IJFNMBCI_02182 | 0.0 | fruA | 2.7.1.202 | GT | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
IJFNMBCI_02183 | 1.5e-106 | sipT | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
IJFNMBCI_02184 | 2.2e-36 | ykoA | ||||
IJFNMBCI_02185 | 2.2e-309 | ybiT | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
IJFNMBCI_02186 | 8.1e-168 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
IJFNMBCI_02187 | 1.3e-237 | ampS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
IJFNMBCI_02188 | 5.5e-12 | S | Uncharacterized protein YkpC | |||
IJFNMBCI_02189 | 2.6e-183 | mreB | D | Rod-share determining protein MreBH | ||
IJFNMBCI_02190 | 1.8e-44 | abrB | K | of stationary sporulation gene expression | ||
IJFNMBCI_02191 | 6.3e-246 | kinC | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
IJFNMBCI_02192 | 2.6e-149 | ykqA | P | Gamma-glutamyl cyclotransferase, AIG2-like | ||
IJFNMBCI_02193 | 2e-115 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
IJFNMBCI_02194 | 0.0 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
IJFNMBCI_02195 | 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 | ||
IJFNMBCI_02196 | 8.2e-31 | ykzG | S | Belongs to the UPF0356 family | ||
IJFNMBCI_02197 | 3.9e-147 | ykrA | S | hydrolases of the HAD superfamily | ||
IJFNMBCI_02198 | 5.8e-100 | 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 | |
IJFNMBCI_02200 | 5.9e-104 | recN | L | Putative cell-wall binding lipoprotein | ||
IJFNMBCI_02201 | 0.0 | fabD | 1.13.12.16, 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
IJFNMBCI_02202 | 0.0 | Q | Polyketide synthase of type I | |||
IJFNMBCI_02203 | 0.0 | Q | polyketide synthase | |||
IJFNMBCI_02204 | 0.0 | Q | Polyketide synthase of type I | |||
IJFNMBCI_02205 | 0.0 | Q | Polyketide synthase of type I | |||
IJFNMBCI_02206 | 0.0 | Q | Polyketide synthase of type I | |||
IJFNMBCI_02207 | 0.0 | Q | Polyketide synthase of type I | |||
IJFNMBCI_02208 | 0.0 | bioH | 2.1.1.197, 3.1.1.85, 4.2.99.20 | IQ | Phosphopantetheine attachment site | |
IJFNMBCI_02209 | 2.7e-210 | V | Beta-lactamase | |||
IJFNMBCI_02210 | 2.7e-205 | pdhA | 1.2.4.1, 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
IJFNMBCI_02211 | 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 | |
IJFNMBCI_02212 | 2.9e-230 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
IJFNMBCI_02213 | 5e-241 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
IJFNMBCI_02214 | 1.2e-45 | slp | CO | COG0526, thiol-disulfide isomerase and thioredoxins | ||
IJFNMBCI_02215 | 9.1e-139 | pdaA_2 | 3.5.1.104 | G | Polysaccharide deacetylase | |
IJFNMBCI_02216 | 8.5e-276 | speA | 4.1.1.19 | E | Arginine | |
IJFNMBCI_02217 | 1.6e-42 | yktA | S | Belongs to the UPF0223 family | ||
IJFNMBCI_02218 | 1.8e-118 | yktB | S | Belongs to the UPF0637 family | ||
IJFNMBCI_02219 | 1e-21 | ykzI | ||||
IJFNMBCI_02220 | 6.1e-151 | suhB | 3.1.3.25 | G | Inositol monophosphatase | |
IJFNMBCI_02221 | 1.2e-82 | ykzC | S | Acetyltransferase (GNAT) family | ||
IJFNMBCI_02222 | 2.7e-296 | mpl | 3.4.24.28, 3.4.24.29 | E | Peptidase M4 | |
IJFNMBCI_02223 | 2.8e-13 | sigC | S | Putative zinc-finger | ||
IJFNMBCI_02224 | 4.9e-39 | ylaE | ||||
IJFNMBCI_02225 | 8.7e-24 | S | Family of unknown function (DUF5325) | |||
IJFNMBCI_02226 | 0.0 | typA | T | GTP-binding protein TypA | ||
IJFNMBCI_02227 | 1.7e-48 | ylaH | S | YlaH-like protein | ||
IJFNMBCI_02228 | 6.3e-31 | ylaI | S | protein conserved in bacteria | ||
IJFNMBCI_02229 | 2.8e-95 | ylaJ | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
IJFNMBCI_02230 | 1.3e-243 | phoH | T | ATPase related to phosphate starvation-inducible protein PhoH | ||
IJFNMBCI_02231 | 2.2e-84 | 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 | ||
IJFNMBCI_02232 | 1.9e-172 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
IJFNMBCI_02233 | 8.7e-44 | ylaN | S | Belongs to the UPF0358 family | ||
IJFNMBCI_02234 | 9.4e-212 | ftsW | D | Belongs to the SEDS family | ||
IJFNMBCI_02235 | 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 | |
IJFNMBCI_02236 | 1.9e-164 | ctaA | 2.5.1.141 | O | Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group | |
IJFNMBCI_02237 | 3.2e-164 | 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 | |
IJFNMBCI_02238 | 8.9e-190 | 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) | |
IJFNMBCI_02239 | 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 | |
IJFNMBCI_02240 | 2.4e-110 | cyoC | 1.10.3.12, 1.9.3.1 | C | COG1845 Heme copper-type cytochrome quinol oxidase, subunit 3 | |
IJFNMBCI_02241 | 2.7e-52 | ctaF | 1.10.3.12, 1.9.3.1 | C | COG3125 Heme copper-type cytochrome quinol oxidase, subunit 4 | |
IJFNMBCI_02242 | 4.8e-165 | ctaG | S | cytochrome c oxidase | ||
IJFNMBCI_02243 | 4.6e-80 | L | Molecular Function DNA binding, Biological Process DNA recombination | |||
IJFNMBCI_02244 | 1.1e-40 | L | transposase activity | |||
IJFNMBCI_02245 | 1.9e-59 | ylbA | S | YugN-like family | ||
IJFNMBCI_02246 | 2.2e-73 | ylbB | T | COG0517 FOG CBS domain | ||
IJFNMBCI_02247 | 3.9e-198 | ylbC | S | protein with SCP PR1 domains | ||
IJFNMBCI_02248 | 1.3e-56 | ylbD | S | Putative coat protein | ||
IJFNMBCI_02249 | 8.8e-37 | ylbE | S | YlbE-like protein | ||
IJFNMBCI_02250 | 6e-71 | ylbF | S | Belongs to the UPF0342 family | ||
IJFNMBCI_02251 | 7.2e-43 | ylbG | S | UPF0298 protein | ||
IJFNMBCI_02253 | 8.5e-90 | rsmD | 2.1.1.171 | L | Methyltransferase | |
IJFNMBCI_02254 | 3.6e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
IJFNMBCI_02255 | 1.7e-216 | ylbJ | S | Sporulation integral membrane protein YlbJ | ||
IJFNMBCI_02256 | 2e-138 | ylbK | S | esterase of the alpha-beta hydrolase superfamily | ||
IJFNMBCI_02257 | 3.6e-188 | ylbL | T | Belongs to the peptidase S16 family | ||
IJFNMBCI_02258 | 2.5e-228 | ylbM | S | Belongs to the UPF0348 family | ||
IJFNMBCI_02259 | 8.7e-90 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
IJFNMBCI_02260 | 1.2e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
IJFNMBCI_02261 | 7.6e-71 | ylbO | S | SANT SWI3, ADA2, N-CoR and TFIIIB'' DNA-binding domains | ||
IJFNMBCI_02262 | 3.1e-89 | ylbP | K | n-acetyltransferase | ||
IJFNMBCI_02263 | 2.6e-161 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
IJFNMBCI_02264 | 1.5e-308 | 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 | ||
IJFNMBCI_02265 | 1.2e-77 | mraZ | K | Belongs to the MraZ family | ||
IJFNMBCI_02266 | 5.6e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
IJFNMBCI_02267 | 1.4e-51 | ftsL | D | Essential cell division protein | ||
IJFNMBCI_02268 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
IJFNMBCI_02269 | 0.0 | ftsI | 3.4.16.4 | M | stage V sporulation protein D | |
IJFNMBCI_02270 | 7.5e-280 | murE | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
IJFNMBCI_02271 | 1.7e-171 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
IJFNMBCI_02272 | 1.3e-254 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
IJFNMBCI_02273 | 2.2e-185 | spoVE | D | Belongs to the SEDS family | ||
IJFNMBCI_02274 | 2.1e-202 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
IJFNMBCI_02275 | 5.6e-169 | murB | 1.3.1.98 | M | cell wall formation | |
IJFNMBCI_02276 | 3e-134 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
IJFNMBCI_02277 | 2e-228 | 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 | ||
IJFNMBCI_02278 | 1.2e-203 | 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 | ||
IJFNMBCI_02279 | 0.0 | bpr | O | COG1404 Subtilisin-like serine proteases | ||
IJFNMBCI_02280 | 2.2e-160 | 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 | ||
IJFNMBCI_02281 | 6.8e-117 | sigE | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
IJFNMBCI_02282 | 1.1e-139 | sigG | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
IJFNMBCI_02283 | 1.2e-62 | S | Peptidase propeptide and YPEB domain | |||
IJFNMBCI_02284 | 2.9e-93 | K | PFAM response regulator receiver | |||
IJFNMBCI_02285 | 1.2e-250 | phoR3 | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
IJFNMBCI_02286 | 3.8e-190 | 2.7.7.73, 2.7.7.80 | H | ThiF family | ||
IJFNMBCI_02287 | 2.7e-252 | |||||
IJFNMBCI_02288 | 5.8e-198 | S | Major Facilitator Superfamily | |||
IJFNMBCI_02289 | 4.1e-303 | S | ABC transporter | |||
IJFNMBCI_02290 | 2.5e-143 | 1.14.11.27 | P | peptidyl-arginine hydroxylation | ||
IJFNMBCI_02291 | 6.3e-260 | rocR | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | ||
IJFNMBCI_02292 | 1.5e-233 | rocD | 2.6.1.11, 2.6.1.13, 2.6.1.17 | E | Catalyzes the interconversion of ornithine to glutamate semialdehyde | |
IJFNMBCI_02293 | 5e-257 | rocE | E | amino acid | ||
IJFNMBCI_02294 | 6.7e-167 | rocF | 3.5.3.1, 3.5.3.11 | E | Belongs to the arginase family | |
IJFNMBCI_02295 | 1.7e-199 | S | Histidine kinase | |||
IJFNMBCI_02297 | 4.9e-15 | yycN | 2.3.1.128 | K | Acetyltransferase | |
IJFNMBCI_02298 | 1.1e-55 | yycN | 2.3.1.128 | K | Acetyltransferase | |
IJFNMBCI_02299 | 2.3e-184 | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | |||
IJFNMBCI_02300 | 1.9e-130 | yycO | S | Permuted papain-like amidase enzyme, YaeF/YiiX, C92 family | ||
IJFNMBCI_02301 | 1.2e-208 | yycP | ||||
IJFNMBCI_02303 | 2.1e-08 | S | YyzF-like protein | |||
IJFNMBCI_02304 | 8.9e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
IJFNMBCI_02305 | 0.0 | L | reverse transcriptase | |||
IJFNMBCI_02306 | 2.7e-27 | T | intracellular signal transduction | |||
IJFNMBCI_02307 | 1.4e-168 | S | Fusaric acid resistance protein-like | |||
IJFNMBCI_02308 | 8.4e-190 | pucA | 1.17.1.4 | O | COG1975 Xanthine and CO dehydrogenases maturation factor, XdhC CoxF family | |
IJFNMBCI_02309 | 4.3e-96 | pucB | 1.1.1.328, 1.17.1.4, 2.7.7.76 | S | MobA-like NTP transferase domain | |
IJFNMBCI_02310 | 0.0 | C | COG1529 Aerobic-type carbon monoxide dehydrogenase, large subunit CoxL CutL homologs | |||
IJFNMBCI_02311 | 3.1e-153 | 1.2.5.3 | C | COG1319 Aerobic-type carbon monoxide dehydrogenase, middle subunit CoxM CutM homologs | ||
IJFNMBCI_02312 | 9.7e-85 | pucE | 1.2.5.3, 1.3.99.16 | C | COG2080 Aerobic-type carbon monoxide dehydrogenase, small subunit CoxS CutS homologs | |
IJFNMBCI_02313 | 0.0 | fbp | 3.1.3.11 | G | Firmicute fructose-1,6-bisphosphatase | |
IJFNMBCI_02314 | 2.1e-244 | aapA | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
IJFNMBCI_02315 | 1.6e-227 | XK27_00240 | S | Fic/DOC family | ||
IJFNMBCI_02316 | 2.5e-286 | ahpF | O | Alkyl hydroperoxide reductase | ||
IJFNMBCI_02317 | 3.2e-106 | ahpC | 1.11.1.15 | O | Alkyl hydroperoxide reductase | |
IJFNMBCI_02318 | 2e-126 | E | Ring-cleavage extradiol dioxygenase | |||
IJFNMBCI_02319 | 7.6e-74 | yxaI | S | membrane protein domain | ||
IJFNMBCI_02320 | 6.3e-67 | EGP | Major facilitator Superfamily | |||
IJFNMBCI_02321 | 3.5e-89 | EGP | Major facilitator Superfamily | |||
IJFNMBCI_02322 | 5.1e-50 | arsR3 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
IJFNMBCI_02323 | 8.6e-64 | S | Family of unknown function (DUF5391) | |||
IJFNMBCI_02324 | 2.8e-142 | S | PQQ-like domain | |||
IJFNMBCI_02325 | 5.1e-251 | alkH | 1.2.1.3 | C | Belongs to the aldehyde dehydrogenase family | |
IJFNMBCI_02326 | 6.2e-109 | M | HlyD family secretion protein | |||
IJFNMBCI_02327 | 4.6e-233 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
IJFNMBCI_02332 | 6.1e-16 | ygzD | K | transcriptional | ||
IJFNMBCI_02333 | 2e-24 | alkH | 1.2.1.3 | C | Belongs to the aldehyde dehydrogenase family | |
IJFNMBCI_02334 | 1e-215 | yxbF | K | Bacterial regulatory proteins, tetR family | ||
IJFNMBCI_02335 | 1.3e-198 | des | 1.14.19.23, 1.14.19.45 | I | fatty acid desaturase | |
IJFNMBCI_02336 | 5e-199 | desK | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_02337 | 1e-102 | desR | T | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
IJFNMBCI_02338 | 3.4e-149 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
IJFNMBCI_02340 | 0.0 | htpG | O | Molecular chaperone. Has ATPase activity | ||
IJFNMBCI_02341 | 8.7e-246 | csbC | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02342 | 4.9e-176 | iolS | C | Aldo keto reductase | ||
IJFNMBCI_02343 | 3.1e-136 | iolR | K | COG1349 Transcriptional regulators of sugar metabolism | ||
IJFNMBCI_02344 | 6.1e-282 | 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 | |
IJFNMBCI_02345 | 2.2e-156 | 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) | |
IJFNMBCI_02346 | 8.3e-182 | 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) | |
IJFNMBCI_02347 | 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) | |
IJFNMBCI_02348 | 1.5e-174 | iolE | 4.2.1.44 | H | 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) | |
IJFNMBCI_02349 | 3.3e-231 | iolF | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02350 | 8.9e-195 | 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 | |
IJFNMBCI_02351 | 1.1e-166 | iolH | G | Xylose isomerase-like TIM barrel | ||
IJFNMBCI_02352 | 1.7e-148 | 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) | |
IJFNMBCI_02353 | 2.1e-160 | 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) | |
IJFNMBCI_02354 | 1.9e-124 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_02355 | 3.9e-176 | T | PhoQ Sensor | |||
IJFNMBCI_02356 | 2.4e-19 | yxdL | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_02357 | 7.3e-44 | yxdL | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_02358 | 0.0 | yxdM | V | ABC transporter (permease) | ||
IJFNMBCI_02359 | 1.3e-57 | yxeA | S | Protein of unknown function (DUF1093) | ||
IJFNMBCI_02360 | 4.1e-178 | fhuD | P | Periplasmic binding protein | ||
IJFNMBCI_02361 | 1.3e-34 | |||||
IJFNMBCI_02362 | 8.4e-23 | yxeD | ||||
IJFNMBCI_02363 | 6.4e-13 | yxeE | ||||
IJFNMBCI_02366 | 4e-150 | yidA | S | hydrolases of the HAD superfamily | ||
IJFNMBCI_02367 | 1.6e-171 | deoR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
IJFNMBCI_02368 | 7.9e-112 | 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 | |
IJFNMBCI_02369 | 2.3e-207 | nupC | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
IJFNMBCI_02370 | 5.1e-232 | pdp | 2.4.2.2, 2.4.2.4 | F | phosphorylase | |
IJFNMBCI_02371 | 3.7e-252 | lysP | E | amino acid | ||
IJFNMBCI_02372 | 4.5e-177 | hutG | 3.5.3.11, 3.5.3.8 | E | Catalyzes the conversion of N-formimidoyl-L-glutamate to L-glutamate and formamide | |
IJFNMBCI_02373 | 2e-236 | hutI | 3.5.2.7 | Q | Imidazolone-5-propionate hydrolase | |
IJFNMBCI_02374 | 0.0 | hutU | 4.2.1.49 | E | Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate | |
IJFNMBCI_02375 | 5.1e-287 | hutH | 4.3.1.3 | E | Histidine ammonia-lyase | |
IJFNMBCI_02376 | 1.1e-77 | hutP | K | Antiterminator that binds to cis-acting regulatory sequences on the mRNA in the presence of histidine, thereby suppressing transcription termination and activating the hut operon for histidine utilization | ||
IJFNMBCI_02377 | 3.6e-211 | yxiA | 3.2.1.99 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
IJFNMBCI_02378 | 3e-23 | yxiA | 3.2.1.99 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
IJFNMBCI_02379 | 3.1e-60 | nudG | 3.6.1.55, 3.6.1.65 | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
IJFNMBCI_02380 | 0.0 | L | HKD family nuclease | |||
IJFNMBCI_02381 | 9.8e-74 | yxiE | T | Belongs to the universal stress protein A family | ||
IJFNMBCI_02382 | 3.6e-147 | yxxF | EG | EamA-like transporter family | ||
IJFNMBCI_02383 | 5.9e-202 | pelB | 4.2.2.10, 4.2.2.2 | G | Pectate lyase | |
IJFNMBCI_02384 | 0.0 | wapA | M | COG3209 Rhs family protein | ||
IJFNMBCI_02385 | 1.6e-87 | |||||
IJFNMBCI_02386 | 1.6e-36 | |||||
IJFNMBCI_02387 | 4.6e-07 | |||||
IJFNMBCI_02389 | 2.1e-70 | yxxG | ||||
IJFNMBCI_02390 | 1.3e-72 | yxiG | ||||
IJFNMBCI_02394 | 5.1e-15 | S | YxiJ-like protein | |||
IJFNMBCI_02395 | 5.1e-17 | |||||
IJFNMBCI_02397 | 1.2e-261 | dbpA | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in the assembly of the 50S ribosomal subunit. Has an RNA-dependent ATPase activity, which is specific for 23S rRNA, and a 3' to 5' RNA helicase activity that uses the energy of ATP hydrolysis to destabilize and unwind short rRNA duplexes | |
IJFNMBCI_02398 | 3.5e-222 | yxiO | S | COG2270 Permeases of the major facilitator superfamily | ||
IJFNMBCI_02399 | 3e-62 | licT | K | transcriptional antiterminator | ||
IJFNMBCI_02400 | 7.2e-71 | licT | K | transcriptional antiterminator | ||
IJFNMBCI_02401 | 1.5e-143 | exoK | GH16 | M | licheninase activity | |
IJFNMBCI_02402 | 2.1e-222 | citH | C | Citrate transporter | ||
IJFNMBCI_02403 | 0.0 | katE | 1.11.1.6, 3.5.1.124 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
IJFNMBCI_02404 | 1.5e-49 | yxiS | ||||
IJFNMBCI_02405 | 2.7e-75 | T | Domain of unknown function (DUF4163) | |||
IJFNMBCI_02406 | 1.1e-210 | nupG | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
IJFNMBCI_02407 | 2.5e-161 | rlmA | 2.1.1.187 | Q | Methyltransferase domain | |
IJFNMBCI_02408 | 5.3e-217 | yxjG | 2.1.1.14 | E | Methionine synthase | |
IJFNMBCI_02409 | 9.1e-86 | yxjI | S | LURP-one-related | ||
IJFNMBCI_02412 | 1e-234 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
IJFNMBCI_02413 | 1.3e-195 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
IJFNMBCI_02414 | 3.8e-87 | yxkC | S | Domain of unknown function (DUF4352) | ||
IJFNMBCI_02415 | 6.4e-143 | yxkD | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
IJFNMBCI_02416 | 8.3e-165 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
IJFNMBCI_02417 | 1e-204 | msmK | P | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_02418 | 6e-157 | yxkH | G | Polysaccharide deacetylase | ||
IJFNMBCI_02419 | 1.5e-215 | cimH | C | COG3493 Na citrate symporter | ||
IJFNMBCI_02420 | 1.4e-267 | cydA | 1.10.3.14 | C | oxidase, subunit | |
IJFNMBCI_02421 | 5.5e-189 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase, subunit II | |
IJFNMBCI_02422 | 6.8e-309 | cydD | V | ATP-binding | ||
IJFNMBCI_02423 | 1.2e-292 | cydD | V | ATP-binding protein | ||
IJFNMBCI_02424 | 7.7e-157 | 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 | |
IJFNMBCI_02425 | 3.9e-251 | yxlA | F | Belongs to the purine-cytosine permease (2.A.39) family | ||
IJFNMBCI_02426 | 1.4e-192 | yxeI | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
IJFNMBCI_02427 | 0.0 | katX | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
IJFNMBCI_02428 | 4.7e-96 | gmuG | 3.2.1.78 | GH26 | G | Belongs to the glycosyl hydrolase 26 family |
IJFNMBCI_02429 | 7.5e-58 | gmuG | 3.2.1.78 | GH26 | G | Belongs to the glycosyl hydrolase 26 family |
IJFNMBCI_02430 | 1.7e-184 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
IJFNMBCI_02431 | 4.8e-165 | gmuE | 2.7.1.2, 2.7.1.4 | GK | COG1940 Transcriptional regulator sugar kinase | |
IJFNMBCI_02432 | 4.3e-285 | ydhP | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
IJFNMBCI_02433 | 7.6e-130 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IJFNMBCI_02434 | 7.6e-89 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IJFNMBCI_02435 | 3.9e-48 | ydhN3 | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
IJFNMBCI_02436 | 4.5e-49 | ydhM | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
IJFNMBCI_02437 | 4.2e-226 | arsB | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
IJFNMBCI_02438 | 2e-58 | arsR | K | transcriptional | ||
IJFNMBCI_02439 | 4e-167 | cbrA3 | P | Periplasmic binding protein | ||
IJFNMBCI_02440 | 1.3e-179 | fhuG1 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_02441 | 5.6e-173 | fhuB3 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_02442 | 1.8e-107 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
IJFNMBCI_02444 | 0.0 | licR | 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
IJFNMBCI_02445 | 1.2e-49 | licB | 2.7.1.196, 2.7.1.205 | G | transporter subunit IIB | |
IJFNMBCI_02446 | 2.8e-249 | licC | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IJFNMBCI_02447 | 1.7e-51 | licA | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
IJFNMBCI_02448 | 1.2e-252 | licH | 3.2.1.86 | GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
IJFNMBCI_02449 | 7.6e-205 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
IJFNMBCI_02450 | 1.8e-228 | dltD | M | COG3966 Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
IJFNMBCI_02451 | 1.5e-36 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
IJFNMBCI_02452 | 1.4e-228 | dltB | M | membrane protein involved in D-alanine export | ||
IJFNMBCI_02453 | 9.3e-294 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
IJFNMBCI_02454 | 6.1e-12 | S | D-Ala-teichoic acid biosynthesis protein | |||
IJFNMBCI_02455 | 3.8e-168 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
IJFNMBCI_02456 | 7.8e-117 | ywaC | 2.7.6.5 | S | protein conserved in bacteria | |
IJFNMBCI_02457 | 3.3e-163 | gspA | M | General stress | ||
IJFNMBCI_02458 | 3.1e-264 | epr | 3.4.21.62 | O | Belongs to the peptidase S8 family | |
IJFNMBCI_02459 | 2.4e-245 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IJFNMBCI_02460 | 9e-68 | ywbC | 4.4.1.5 | E | glyoxalase | |
IJFNMBCI_02461 | 8.8e-223 | ywbD | 2.1.1.191 | J | Methyltransferase | |
IJFNMBCI_02462 | 6.6e-170 | yjfC | O | Predicted Zn-dependent protease (DUF2268) | ||
IJFNMBCI_02463 | 2.2e-142 | mta | K | transcriptional | ||
IJFNMBCI_02464 | 1.8e-27 | ywbE | S | Uncharacterized conserved protein (DUF2196) | ||
IJFNMBCI_02465 | 3.4e-110 | ywbG | M | effector of murein hydrolase | ||
IJFNMBCI_02466 | 2.5e-57 | ywbH | 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 | ||
IJFNMBCI_02467 | 8.2e-152 | ywbI | K | Transcriptional regulator | ||
IJFNMBCI_02468 | 3.7e-135 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
IJFNMBCI_02469 | 5e-114 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | 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) | |
IJFNMBCI_02470 | 7.1e-239 | ywbN | P | Dyp-type peroxidase family protein | ||
IJFNMBCI_02471 | 2.7e-111 | ywbO | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
IJFNMBCI_02472 | 1.1e-132 | S | Streptomycin biosynthesis protein StrF | |||
IJFNMBCI_02473 | 9.5e-129 | H | Methionine biosynthesis protein MetW | |||
IJFNMBCI_02475 | 4.3e-112 | ywcC | K | Bacterial regulatory proteins, tetR family | ||
IJFNMBCI_02476 | 1.9e-60 | gtcA | S | GtrA-like protein | ||
IJFNMBCI_02477 | 6.9e-170 | 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) | |
IJFNMBCI_02478 | 1.5e-283 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
IJFNMBCI_02479 | 8.4e-27 | ywzA | S | membrane | ||
IJFNMBCI_02480 | 8.3e-179 | 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 | |
IJFNMBCI_02481 | 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 | |
IJFNMBCI_02482 | 8.1e-111 | qoxC | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
IJFNMBCI_02483 | 9.9e-64 | qoxD | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
IJFNMBCI_02484 | 3e-38 | ywcE | S | Required for proper spore morphogenesis. Important for spore germination | ||
IJFNMBCI_02485 | 2.1e-75 | ysnE | K | acetyltransferase | ||
IJFNMBCI_02487 | 1.6e-155 | rodA | D | Belongs to the SEDS family | ||
IJFNMBCI_02488 | 2.7e-137 | nfrA | 1.5.1.38, 1.5.1.39 | C | Oxidoreductase | |
IJFNMBCI_02489 | 1.5e-183 | ywcH | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
IJFNMBCI_02490 | 0.0 | vpr | O | Belongs to the peptidase S8 family | ||
IJFNMBCI_02492 | 8.3e-151 | sacT | K | transcriptional antiterminator | ||
IJFNMBCI_02493 | 3.6e-252 | scrA | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IJFNMBCI_02494 | 4.7e-287 | scrB | 3.2.1.26, 3.2.1.65 | GH32 | G | invertase |
IJFNMBCI_02495 | 9.7e-20 | ywdA | ||||
IJFNMBCI_02496 | 1.7e-145 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
IJFNMBCI_02497 | 1.8e-56 | pex | K | Transcriptional regulator PadR-like family | ||
IJFNMBCI_02498 | 9.9e-88 | ywdD | ||||
IJFNMBCI_02500 | 4.2e-152 | ywdF | GT2,GT4 | S | Glycosyltransferase like family 2 | |
IJFNMBCI_02501 | 8.3e-133 | 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 | |
IJFNMBCI_02502 | 3.4e-39 | ywdI | S | Family of unknown function (DUF5327) | ||
IJFNMBCI_02503 | 5.4e-229 | ywdJ | F | Xanthine uracil | ||
IJFNMBCI_02504 | 4.2e-46 | ywdK | S | small membrane protein | ||
IJFNMBCI_02505 | 4e-61 | 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 | ||
IJFNMBCI_02506 | 8.5e-142 | spsA | M | Spore Coat | ||
IJFNMBCI_02507 | 1.7e-273 | spsB | M | Capsule polysaccharide biosynthesis protein | ||
IJFNMBCI_02508 | 9.6e-222 | spsC | E | Belongs to the DegT DnrJ EryC1 family | ||
IJFNMBCI_02509 | 7.7e-160 | spsD | 2.3.1.210 | K | Spore Coat | |
IJFNMBCI_02510 | 9.3e-214 | spsE | 2.5.1.56 | M | acid synthase | |
IJFNMBCI_02511 | 4.1e-133 | spsF | M | Spore Coat | ||
IJFNMBCI_02512 | 3.4e-183 | spsG | M | Spore Coat | ||
IJFNMBCI_02513 | 1.2e-137 | spsI | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
IJFNMBCI_02514 | 3e-181 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
IJFNMBCI_02515 | 1.5e-160 | spsK | 1.1.1.133 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
IJFNMBCI_02516 | 3e-86 | spsL | 5.1.3.13 | M | Spore Coat | |
IJFNMBCI_02517 | 2.1e-58 | |||||
IJFNMBCI_02518 | 2.5e-247 | rocG | 1.4.1.2, 1.4.1.3 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
IJFNMBCI_02519 | 2.3e-295 | putA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
IJFNMBCI_02520 | 0.0 | rocB | E | arginine degradation protein | ||
IJFNMBCI_02521 | 1.8e-259 | lysP | E | amino acid | ||
IJFNMBCI_02522 | 2.4e-207 | tcaB | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02523 | 7.1e-223 | ywfA | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02524 | 1.1e-112 | pheA | 1.1.1.3, 1.3.1.12, 4.1.1.100, 4.2.1.51, 5.4.99.5 | E | Part of the bacABCDEF operon responsible for the biosynthesis of the nonribosomally synthesized dipeptide antibiotic bacilysin, composed of L-alanine and L-anticapsin. Bacilysin is an irreversible inactivator of the glutaminase domain of glucosamine synthetase. BacA is an unusual prephenate decarboxylase that avoids the typical aromatization of the cyclohexadienol ring of prephenate. BacA catalyzes the protonation of prephenate (1-carboxy-4-hydroxy-alpha-oxo-2,5-cyclohexadiene-1- propanoic acid) at C6 position, followed by a decarboxylation to produce the endocyclic-delta(4),delta(8)-7R-dihydro- hydroxyphenylpyruvate (en-H2HPP). En-H2HPP is able to undergo a slow nonenzymatic isomerization to produce the exocyclic- delta(3),delta(5)-dihydro-hydroxyphenylpyruvate (ex-H2HPP). BacA isomerizes only the pro-R double bond in prephenate | |
IJFNMBCI_02525 | 1.5e-137 | bacB | 5.3.3.19, 5.4.99.5 | S | Part of the bacABCDEF operon responsible for the biosynthesis of the nonribosomally synthesized dipeptide antibiotic bacilysin, composed of L-alanine and L-anticapsin. Bacilysin is an irreversible inactivator of the glutaminase domain of glucosamine synthetase. BacB catalyzes the allylic isomerization of the | |
IJFNMBCI_02526 | 3e-139 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_02527 | 2.2e-268 | purD | 6.3.2.49, 6.3.4.13 | F | Part of the bacABCDEFG operon responsible for the biosynthesis of bacilysin, an irreversible inactivator of the glutaminase domain of glucosamine synthetase. Catalyzes the formation of alpha-dipeptides from various L-amino acids in the presence of ATP. In vivo catalyzes the ligation of L-alanine and L-anticapsin (epoxycyclohexanonyl-Ala) to produce the final bacilysin antibiotic (L-Ala-L-4S-cyclohexenonyl-Ala dipeptide) | |
IJFNMBCI_02528 | 4.7e-208 | bacE | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02529 | 1.7e-234 | ywfG | 2.6.1.83 | E | Aminotransferase class I and II | |
IJFNMBCI_02530 | 1.4e-139 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
IJFNMBCI_02531 | 9.1e-18 | bdbA | CO | Thioredoxin | ||
IJFNMBCI_02532 | 7.6e-18 | mauE | S | Methylamine utilisation protein MauE | ||
IJFNMBCI_02533 | 1.3e-06 | |||||
IJFNMBCI_02534 | 1.7e-07 | |||||
IJFNMBCI_02535 | 7.8e-15 | K | Helix-turn-helix XRE-family like proteins | |||
IJFNMBCI_02536 | 1.8e-37 | ykuS | S | Belongs to the UPF0180 family | ||
IJFNMBCI_02537 | 8.7e-212 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
IJFNMBCI_02538 | 9.7e-76 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
IJFNMBCI_02539 | 6.2e-76 | fld | C | Flavodoxin | ||
IJFNMBCI_02540 | 5.7e-158 | ykuO | ||||
IJFNMBCI_02541 | 4.1e-86 | fld | C | Flavodoxin | ||
IJFNMBCI_02542 | 5.6e-166 | ccpC | K | Transcriptional regulator | ||
IJFNMBCI_02543 | 1e-75 | ykuL | S | CBS domain | ||
IJFNMBCI_02544 | 7.3e-26 | ykzF | S | Antirepressor AbbA | ||
IJFNMBCI_02545 | 7.1e-92 | ykuK | S | Ribonuclease H-like | ||
IJFNMBCI_02546 | 3.9e-37 | ykuJ | S | protein conserved in bacteria | ||
IJFNMBCI_02547 | 3.3e-233 | ykuI | T | Diguanylate phosphodiesterase | ||
IJFNMBCI_02549 | 1.8e-139 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_02550 | 1.9e-145 | ykuE | S | Metallophosphoesterase | ||
IJFNMBCI_02551 | 7.1e-89 | ykuD | S | protein conserved in bacteria | ||
IJFNMBCI_02552 | 6.4e-235 | ykuC | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02553 | 7e-83 | ykyB | S | YkyB-like protein | ||
IJFNMBCI_02554 | 7.6e-166 | cheV | 2.7.13.3 | T | Chemotaxis protein CheV | |
IJFNMBCI_02555 | 2.3e-09 | |||||
IJFNMBCI_02556 | 3.9e-215 | patA | 2.6.1.1 | E | Aminotransferase | |
IJFNMBCI_02557 | 1.5e-290 | pilS | 2.1.1.80, 2.7.13.3, 3.1.1.61 | T | Histidine kinase | |
IJFNMBCI_02558 | 0.0 | mrdA | 3.4.16.4 | M | Penicillin-binding Protein | |
IJFNMBCI_02559 | 2e-93 | ykwD | J | protein with SCP PR1 domains | ||
IJFNMBCI_02560 | 1.1e-46 | |||||
IJFNMBCI_02561 | 8.6e-159 | glxR | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
IJFNMBCI_02562 | 8.7e-250 | mcpC | NT | chemotaxis protein | ||
IJFNMBCI_02563 | 1.9e-189 | splB | 4.1.99.14 | L | Spore photoproduct lyase | |
IJFNMBCI_02564 | 6.1e-38 | splA | S | Transcriptional regulator | ||
IJFNMBCI_02565 | 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) | |
IJFNMBCI_02566 | 2.1e-39 | ptsH | G | phosphocarrier protein HPr | ||
IJFNMBCI_02567 | 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 | |
IJFNMBCI_02568 | 5.1e-156 | glcT | K | antiterminator | ||
IJFNMBCI_02569 | 2.5e-175 | ykvZ | 5.1.1.1 | K | Transcriptional regulator | |
IJFNMBCI_02571 | 1.8e-206 | pepQ | 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
IJFNMBCI_02572 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
IJFNMBCI_02573 | 7.7e-88 | stoA | CO | thiol-disulfide | ||
IJFNMBCI_02574 | 1.1e-240 | ykvU | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
IJFNMBCI_02575 | 1.2e-109 | ykvT | 3.5.1.28 | M | Cell Wall Hydrolase | |
IJFNMBCI_02576 | 7.9e-28 | |||||
IJFNMBCI_02577 | 7.8e-25 | ykvS | S | protein conserved in bacteria | ||
IJFNMBCI_02578 | 1e-44 | ykvR | S | Protein of unknown function (DUF3219) | ||
IJFNMBCI_02579 | 1.3e-131 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
IJFNMBCI_02580 | 5.8e-61 | ykvN | K | Transcriptional regulator | ||
IJFNMBCI_02581 | 7.8e-96 | queF | 1.7.1.13 | S | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
IJFNMBCI_02582 | 1.2e-134 | 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 | |
IJFNMBCI_02583 | 1.3e-78 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
IJFNMBCI_02584 | 1.5e-126 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
IJFNMBCI_02585 | 9.6e-187 | |||||
IJFNMBCI_02586 | 6e-183 | ykvI | S | membrane | ||
IJFNMBCI_02587 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
IJFNMBCI_02588 | 1.1e-136 | motA | N | flagellar motor | ||
IJFNMBCI_02589 | 4.6e-127 | motB | N | Flagellar motor protein | ||
IJFNMBCI_02590 | 5.5e-77 | ykvE | K | transcriptional | ||
IJFNMBCI_02591 | 2.1e-274 | kinD | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
IJFNMBCI_02592 | 3.4e-10 | S | Spo0E like sporulation regulatory protein | |||
IJFNMBCI_02593 | 6.4e-96 | mtnD | 1.13.11.53, 1.13.11.54 | S | Catalyzes 2 different reactions between oxygene and the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) depending upon the metal bound in the active site. Fe-containing acireductone dioxygenase (Fe-ARD) produces formate and 2-keto-4- methylthiobutyrate (KMTB), the alpha-ketoacid precursor of methionine in the methionine recycle pathway. Ni-containing acireductone dioxygenase (Ni-ARD) produces methylthiopropionate, carbon monoxide and formate, and does not lie on the methionine recycle pathway | |
IJFNMBCI_02594 | 4.2e-115 | mtnB | 3.1.3.87, 4.1.2.17, 4.2.1.109, 5.1.3.4 | E | Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) | |
IJFNMBCI_02595 | 1.2e-134 | mtnX | 3.1.3.87, 4.2.1.109 | E | Dephosphorylates 2-hydroxy-3-keto-5-methylthiopentenyl- 1-phosphate (HK-MTPenyl-1-P) yielding 1,2-dihydroxy-3-keto-5- methylthiopentene (DHK-MTPene) | |
IJFNMBCI_02596 | 6.7e-226 | 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) | |
IJFNMBCI_02597 | 3.2e-228 | mtnE | 2.6.1.83 | E | Aminotransferase | |
IJFNMBCI_02598 | 7.7e-151 | mtnU | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
IJFNMBCI_02599 | 1.2e-224 | mtnK | 2.7.1.100 | F | Catalyzes the phosphorylation of methylthioribose into methylthioribose-1-phosphate | |
IJFNMBCI_02600 | 1.8e-195 | mtnA | 5.3.1.23 | E | Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1- P) | |
IJFNMBCI_02602 | 1.6e-85 | ogt | 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 | |
IJFNMBCI_02603 | 0.0 | kinE | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_02604 | 1e-187 | ykrP | G | COG3594 Fucose 4-O-acetylase and related acetyltransferases | ||
IJFNMBCI_02605 | 7.9e-24 | ykzE | ||||
IJFNMBCI_02606 | 3e-44 | ydfR | S | Protein of unknown function (DUF421) | ||
IJFNMBCI_02607 | 1.3e-52 | ydfR | S | Protein of unknown function (DUF421) | ||
IJFNMBCI_02608 | 1.3e-241 | ktrB | P | COG0168 Trk-type K transport systems, membrane components | ||
IJFNMBCI_02609 | 4.1e-156 | htpX | O | Belongs to the peptidase M48B family | ||
IJFNMBCI_02610 | 3.9e-125 | ykrK | S | Domain of unknown function (DUF1836) | ||
IJFNMBCI_02611 | 2.5e-26 | sspD | S | small acid-soluble spore protein | ||
IJFNMBCI_02612 | 2.2e-117 | rsgI | S | Anti-sigma factor N-terminus | ||
IJFNMBCI_02613 | 1.7e-126 | sigI | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
IJFNMBCI_02614 | 4.6e-135 | ykoY | P | COG0861 Membrane protein TerC, possibly involved in tellurium resistance | ||
IJFNMBCI_02615 | 4.1e-101 | ykoX | S | membrane-associated protein | ||
IJFNMBCI_02616 | 1.4e-153 | 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 | ||
IJFNMBCI_02617 | 0.0 | ligD | 6.5.1.1 | L | ATP-dependent DNA ligase | |
IJFNMBCI_02618 | 3.7e-99 | ykoP | G | polysaccharide deacetylase | ||
IJFNMBCI_02619 | 5e-81 | ykoM | K | transcriptional | ||
IJFNMBCI_02620 | 1.2e-25 | ykoL | ||||
IJFNMBCI_02621 | 1.9e-16 | |||||
IJFNMBCI_02622 | 1.6e-52 | tnrA | K | transcriptional | ||
IJFNMBCI_02623 | 5e-238 | mgtE | P | Acts as a magnesium transporter | ||
IJFNMBCI_02625 | 1e-245 | ydhD | M | Glycosyl hydrolase | ||
IJFNMBCI_02626 | 4.5e-98 | ykoE | S | ABC-type cobalt transport system, permease component | ||
IJFNMBCI_02627 | 1.2e-305 | P | ABC transporter, ATP-binding protein | |||
IJFNMBCI_02628 | 1e-131 | ykoC | P | Cobalt transport protein | ||
IJFNMBCI_02629 | 3.4e-144 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
IJFNMBCI_02630 | 1.1e-175 | isp | O | Belongs to the peptidase S8 family | ||
IJFNMBCI_02631 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
IJFNMBCI_02632 | 2.6e-121 | yeiL | T | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
IJFNMBCI_02633 | 1.2e-216 | hcaT | 1.5.1.2 | EGP | Major facilitator Superfamily | |
IJFNMBCI_02634 | 3.1e-120 | 3.2.1.4 | GH5,GH9 | K | Collagen triple helix repeat | |
IJFNMBCI_02635 | 4.9e-215 | M | Glycosyl transferase family 2 | |||
IJFNMBCI_02637 | 9e-56 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
IJFNMBCI_02638 | 4.2e-71 | ohrB | O | Organic hydroperoxide resistance protein | ||
IJFNMBCI_02639 | 1.5e-86 | ohrR | K | COG1846 Transcriptional regulators | ||
IJFNMBCI_02640 | 2.8e-70 | ohrA | O | Organic hydroperoxide resistance protein | ||
IJFNMBCI_02641 | 3.6e-227 | 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 | |
IJFNMBCI_02642 | 6e-205 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
IJFNMBCI_02643 | 3e-170 | purU | 2.7.7.72, 3.5.1.10 | F | Catalyzes the hydrolysis of 10-formyltetrahydrofolate (formyl-FH4) to formate and tetrahydrofolate (FH4) | |
IJFNMBCI_02644 | 3.4e-49 | ykkD | P | Multidrug resistance protein | ||
IJFNMBCI_02645 | 2.7e-52 | ykkC | P | Multidrug resistance protein | ||
IJFNMBCI_02646 | 5.1e-101 | ykkB | 2.3.1.128 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
IJFNMBCI_02647 | 1.2e-91 | ykhA | 3.1.2.20 | I | Acyl-CoA hydrolase | |
IJFNMBCI_02648 | 6.2e-154 | ykgA | E | Amidinotransferase | ||
IJFNMBCI_02649 | 1.3e-206 | pgl | 3.1.1.31 | G | 6-phosphogluconolactonase | |
IJFNMBCI_02650 | 8.2e-165 | ygxA | S | Nucleotidyltransferase-like | ||
IJFNMBCI_02651 | 1.5e-56 | ygzB | S | UPF0295 protein | ||
IJFNMBCI_02652 | 1.8e-80 | perR | P | Belongs to the Fur family | ||
IJFNMBCI_02653 | 3.1e-86 | bcp | 1.11.1.15 | O | Peroxiredoxin | |
IJFNMBCI_02654 | 6.2e-246 | gsaB | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
IJFNMBCI_02655 | 3.2e-179 | ygaE | S | Membrane | ||
IJFNMBCI_02656 | 4.2e-306 | ygaD | V | ABC transporter | ||
IJFNMBCI_02657 | 2.2e-104 | ygaC | J | Belongs to the UPF0374 family | ||
IJFNMBCI_02658 | 3.3e-37 | ygaB | S | YgaB-like protein | ||
IJFNMBCI_02660 | 5.8e-135 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_02661 | 8.2e-37 | yfhS | ||||
IJFNMBCI_02662 | 7.4e-208 | mutY | L | A G-specific | ||
IJFNMBCI_02663 | 1.5e-183 | yfhP | S | membrane-bound metal-dependent | ||
IJFNMBCI_02664 | 0.0 | yfhO | S | Bacterial membrane protein YfhO | ||
IJFNMBCI_02665 | 4.6e-185 | csbB | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
IJFNMBCI_02666 | 1.8e-169 | yfhM | S | Alpha/beta hydrolase family | ||
IJFNMBCI_02667 | 5.7e-34 | yfhL | S | SdpI/YhfL protein family | ||
IJFNMBCI_02668 | 4.5e-94 | batE | T | Bacterial SH3 domain homologues | ||
IJFNMBCI_02669 | 2.9e-44 | yfhJ | S | WVELL protein | ||
IJFNMBCI_02670 | 1.5e-166 | mpr | 3.4.21.19 | M | Belongs to the peptidase S1B family | |
IJFNMBCI_02672 | 1.5e-206 | yfhI | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02673 | 8.8e-53 | yfhH | S | Protein of unknown function (DUF1811) | ||
IJFNMBCI_02674 | 9.6e-141 | recX | 2.4.1.337 | GT4 | S | Modulates RecA activity |
IJFNMBCI_02675 | 3.1e-167 | yfhF | S | nucleoside-diphosphate sugar epimerase | ||
IJFNMBCI_02677 | 3.1e-24 | yfhD | S | YfhD-like protein | ||
IJFNMBCI_02678 | 9.7e-106 | yfhC | C | nitroreductase | ||
IJFNMBCI_02679 | 1.4e-164 | yfhB | 5.3.3.17 | S | PhzF family | |
IJFNMBCI_02680 | 0.0 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
IJFNMBCI_02681 | 9.5e-83 | yfiV | K | transcriptional | ||
IJFNMBCI_02682 | 3.6e-288 | yfiU | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02683 | 1.8e-56 | yfiT | S | Belongs to the metal hydrolase YfiT family | ||
IJFNMBCI_02684 | 1.5e-25 | yfiT | S | Belongs to the metal hydrolase YfiT family | ||
IJFNMBCI_02685 | 9.9e-45 | yrdF | K | ribonuclease inhibitor | ||
IJFNMBCI_02686 | 0.0 | 2.7.9.2 | GT | phosphoenolpyruvate synthase | ||
IJFNMBCI_02687 | 1.1e-112 | 1.6.5.2 | S | NADPH-dependent FMN reductase | ||
IJFNMBCI_02688 | 6.6e-96 | padR | K | transcriptional | ||
IJFNMBCI_02689 | 4.2e-167 | cyoE | 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 | |
IJFNMBCI_02690 | 2.9e-159 | yfiE | 1.13.11.2 | S | glyoxalase | |
IJFNMBCI_02691 | 2.4e-63 | mhqP | S | DoxX | ||
IJFNMBCI_02692 | 0.0 | yfiC | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
IJFNMBCI_02693 | 0.0 | yfiB3 | V | ABC transporter | ||
IJFNMBCI_02694 | 1.2e-291 | glvC | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IJFNMBCI_02695 | 5.6e-138 | glvR | F | Helix-turn-helix domain, rpiR family | ||
IJFNMBCI_02696 | 1.9e-261 | 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 |
IJFNMBCI_02697 | 4.2e-15 | sspH | S | Belongs to the SspH family | ||
IJFNMBCI_02698 | 0.0 | acoR | KQ | COG3284 Transcriptional activator of acetoin glycerol metabolism | ||
IJFNMBCI_02699 | 1.2e-255 | acoL | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
IJFNMBCI_02700 | 3.7e-213 | acoC | 2.3.1.12, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
IJFNMBCI_02701 | 2.1e-188 | acoB | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | ||
IJFNMBCI_02702 | 7.5e-191 | acoA | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | ||
IJFNMBCI_02703 | 2.1e-90 | yfjM | S | Psort location Cytoplasmic, score | ||
IJFNMBCI_02704 | 2.7e-193 | yfjN | 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 | ||
IJFNMBCI_02705 | 1.4e-47 | S | YfzA-like protein | |||
IJFNMBCI_02706 | 6.2e-268 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
IJFNMBCI_02707 | 7e-161 | yfjP | 3.2.2.21 | L | COG0122 3-methyladenine DNA glycosylase 8-oxoguanine DNA glycosylase | |
IJFNMBCI_02708 | 2.5e-183 | corA | P | Mediates influx of magnesium ions | ||
IJFNMBCI_02709 | 6e-32 | |||||
IJFNMBCI_02710 | 5.2e-148 | yfjR | 1.1.1.31 | I | NAD-binding of NADP-dependent 3-hydroxyisobutyrate dehydrogenase | |
IJFNMBCI_02711 | 3.4e-154 | pdaA | G | deacetylase | ||
IJFNMBCI_02712 | 4.9e-27 | yfjT | ||||
IJFNMBCI_02713 | 3e-220 | yfkA | S | YfkB-like domain | ||
IJFNMBCI_02714 | 4.7e-146 | yfkC | M | Mechanosensitive ion channel | ||
IJFNMBCI_02715 | 1.6e-143 | yfkD | S | YfkD-like protein | ||
IJFNMBCI_02716 | 5.5e-184 | cax | P | COG0387 Ca2 H antiporter | ||
IJFNMBCI_02717 | 6.5e-218 | ycaD | EGP | COG0477 Permeases of the major facilitator superfamily | ||
IJFNMBCI_02719 | 1.3e-143 | yihY | S | Belongs to the UPF0761 family | ||
IJFNMBCI_02720 | 3.5e-52 | yfkI | S | gas vesicle protein | ||
IJFNMBCI_02721 | 4.1e-86 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
IJFNMBCI_02722 | 2.7e-29 | yfkK | S | Belongs to the UPF0435 family | ||
IJFNMBCI_02723 | 9.6e-193 | ydiM | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02724 | 1.7e-134 | 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 | |
IJFNMBCI_02725 | 5.3e-164 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | 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) | |
IJFNMBCI_02726 | 1.7e-185 | K | helix_turn _helix lactose operon repressor | |||
IJFNMBCI_02727 | 6e-91 | yfkM | 1.11.1.6, 3.5.1.124 | S | protease | |
IJFNMBCI_02728 | 0.0 | cpdB | 3.1.3.5, 3.1.3.6, 3.1.4.16 | F | COG0737 5'-nucleotidase 2',3'-cyclic phosphodiesterase and related esterases | |
IJFNMBCI_02729 | 6.5e-199 | yibE | S | YibE/F-like protein | ||
IJFNMBCI_02730 | 9.3e-125 | yibF | S | YibE/F-like protein | ||
IJFNMBCI_02731 | 1.2e-123 | yfkO | C | nitroreductase | ||
IJFNMBCI_02732 | 1.1e-127 | treR | K | transcriptional | ||
IJFNMBCI_02733 | 0.0 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
IJFNMBCI_02734 | 4.7e-239 | treP | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IJFNMBCI_02735 | 1.2e-39 | ydgB | S | Spore germination protein gerPA/gerPF | ||
IJFNMBCI_02736 | 3.6e-38 | ydgA | S | Spore germination protein gerPA/gerPF | ||
IJFNMBCI_02737 | 9.8e-79 | cotP | O | Belongs to the small heat shock protein (HSP20) family | ||
IJFNMBCI_02738 | 2.3e-63 | yhdN | S | Domain of unknown function (DUF1992) | ||
IJFNMBCI_02739 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
IJFNMBCI_02740 | 3.7e-73 | yfmQ | S | Uncharacterised protein from bacillus cereus group | ||
IJFNMBCI_02741 | 6.4e-241 | 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 | |
IJFNMBCI_02742 | 1.4e-136 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
IJFNMBCI_02743 | 3.1e-50 | yflH | S | Protein of unknown function (DUF3243) | ||
IJFNMBCI_02744 | 7e-19 | yflI | ||||
IJFNMBCI_02745 | 1.5e-14 | yflJ | S | Protein of unknown function (DUF2639) | ||
IJFNMBCI_02746 | 4.1e-121 | yflK | S | protein conserved in bacteria | ||
IJFNMBCI_02747 | 4.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
IJFNMBCI_02748 | 2.1e-218 | nos | 1.14.14.47 | C | Belongs to the NOS family. Bacterial NOS oxygenase subfamily | |
IJFNMBCI_02749 | 2.1e-148 | yflN | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
IJFNMBCI_02750 | 1.4e-226 | citM | C | Citrate transporter | ||
IJFNMBCI_02751 | 8.3e-179 | yflP | S | Tripartite tricarboxylate transporter family receptor | ||
IJFNMBCI_02752 | 4e-119 | citT | T | response regulator | ||
IJFNMBCI_02753 | 1.5e-273 | citS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
IJFNMBCI_02754 | 1.8e-73 | M1-820 | Q | Collagen triple helix repeat (20 copies) | ||
IJFNMBCI_02755 | 4.6e-28 | Q | PFAM Collagen triple helix | |||
IJFNMBCI_02756 | 9.1e-11 | NU | Prophage endopeptidase tail | |||
IJFNMBCI_02757 | 2.4e-30 | S | KTSC domain | |||
IJFNMBCI_02760 | 8.2e-57 | |||||
IJFNMBCI_02761 | 1e-279 | yobL | S | Bacterial EndoU nuclease | ||
IJFNMBCI_02762 | 2e-84 | yqjL | S | Alpha beta hydrolase | ||
IJFNMBCI_02763 | 2.8e-49 | FG | Scavenger mRNA decapping enzyme C-term binding | |||
IJFNMBCI_02764 | 2.3e-73 | XK27_05370 | 5.3.1.24 | E | phosphoribosylanthranilate isomerase activity | |
IJFNMBCI_02767 | 2e-27 | S | Protein of unknown function (DUF2971) | |||
IJFNMBCI_02769 | 2.5e-09 | S | YjcQ protein | |||
IJFNMBCI_02771 | 6.2e-11 | yqaS | L | DNA packaging | ||
IJFNMBCI_02772 | 1.6e-147 | bla | 3.5.2.6 | V | beta-lactamase | |
IJFNMBCI_02773 | 1.2e-45 | yjcS | S | Antibiotic biosynthesis monooxygenase | ||
IJFNMBCI_02774 | 7.7e-250 | yfjF | EGP | Belongs to the major facilitator superfamily | ||
IJFNMBCI_02775 | 5.1e-81 | napB | K | helix_turn_helix multiple antibiotic resistance protein | ||
IJFNMBCI_02776 | 1.5e-219 | ganA | 3.2.1.89 | G | arabinogalactan | |
IJFNMBCI_02777 | 9.9e-288 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
IJFNMBCI_02778 | 3.6e-185 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
IJFNMBCI_02779 | 7.4e-214 | 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) | |
IJFNMBCI_02780 | 1.1e-306 | lacE | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
IJFNMBCI_02781 | 9.1e-50 | lacF | 2.7.1.207 | G | phosphotransferase system | |
IJFNMBCI_02782 | 6.9e-283 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
IJFNMBCI_02783 | 3.3e-138 | lacR | K | COG1349 Transcriptional regulators of sugar metabolism | ||
IJFNMBCI_02784 | 2.1e-123 | 5.4.2.6 | S | Haloacid dehalogenase-like hydrolase | ||
IJFNMBCI_02786 | 8.1e-106 | yhiD | S | MgtC SapB transporter | ||
IJFNMBCI_02787 | 7.5e-22 | yjfB | S | Putative motility protein | ||
IJFNMBCI_02788 | 4.2e-68 | T | PhoQ Sensor | |||
IJFNMBCI_02789 | 2.9e-99 | yjgB | S | Domain of unknown function (DUF4309) | ||
IJFNMBCI_02790 | 0.0 | yjgC | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase, alpha subunit | |
IJFNMBCI_02791 | 1e-245 | yjgC | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase, alpha subunit | |
IJFNMBCI_02792 | 4.3e-92 | yjgD | S | Protein of unknown function (DUF1641) | ||
IJFNMBCI_02793 | 5.7e-225 | yjiB | 1.14.13.154, 1.14.15.8 | C | Cytochrome P450 | |
IJFNMBCI_02794 | 1.4e-220 | oleD | GT1 | CG | COG1819 Glycosyl transferases, related to UDP-glucuronosyltransferase | |
IJFNMBCI_02795 | 6.8e-29 | |||||
IJFNMBCI_02796 | 1e-145 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
IJFNMBCI_02797 | 1.5e-122 | ybbM | S | transport system, permease component | ||
IJFNMBCI_02798 | 1.3e-128 | pstB | 3.6.3.27 | P | Belongs to the ABC transporter superfamily | |
IJFNMBCI_02799 | 4.4e-175 | yjlA | EG | Putative multidrug resistance efflux transporter | ||
IJFNMBCI_02800 | 2.2e-90 | yjlB | S | Cupin domain | ||
IJFNMBCI_02801 | 7e-66 | yjlC | S | Protein of unknown function (DUF1641) | ||
IJFNMBCI_02802 | 1.3e-218 | yjlD | 1.6.99.3 | C | NADH dehydrogenase | |
IJFNMBCI_02803 | 2.5e-277 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
IJFNMBCI_02804 | 6.7e-254 | yjmB | G | symporter YjmB | ||
IJFNMBCI_02805 | 1.7e-182 | exuR | K | transcriptional | ||
IJFNMBCI_02806 | 2.5e-280 | uxaB | 1.1.1.17, 1.1.1.58 | G | tagaturonate reductase activity | |
IJFNMBCI_02807 | 2.7e-285 | uxaA | 4.2.1.7, 4.4.1.24 | G | Altronate | |
IJFNMBCI_02808 | 3.9e-131 | MA20_18170 | S | membrane transporter protein | ||
IJFNMBCI_02809 | 3.1e-78 | yjoA | S | DinB family | ||
IJFNMBCI_02810 | 4.9e-215 | S | response regulator aspartate phosphatase | |||
IJFNMBCI_02812 | 9.4e-167 | xlyA | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
IJFNMBCI_02813 | 1e-60 | yjqA | S | Bacterial PH domain | ||
IJFNMBCI_02814 | 1.8e-110 | yjqB | S | phage-related replication protein | ||
IJFNMBCI_02816 | 3.8e-110 | xkdA | E | IrrE N-terminal-like domain | ||
IJFNMBCI_02817 | 1.1e-56 | xre | K | Helix-turn-helix XRE-family like proteins | ||
IJFNMBCI_02819 | 6.9e-09 | xkdB | K | sequence-specific DNA binding | ||
IJFNMBCI_02820 | 8.5e-153 | xkdC | L | Bacterial dnaA protein | ||
IJFNMBCI_02823 | 2e-10 | yqaO | S | Phage-like element PBSX protein XtrA | ||
IJFNMBCI_02824 | 1.4e-84 | xpf | K | COG1595 DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog | ||
IJFNMBCI_02825 | 1.8e-110 | xtmA | L | phage terminase small subunit | ||
IJFNMBCI_02826 | 6.1e-209 | xtmB | S | phage terminase, large subunit | ||
IJFNMBCI_02827 | 3e-241 | yqbA | S | portal protein | ||
IJFNMBCI_02828 | 4.8e-90 | xkdF | 2.1.1.72 | L | Putative phage serine protease XkdF | |
IJFNMBCI_02829 | 1e-157 | xkdG | S | Phage capsid family | ||
IJFNMBCI_02830 | 7.4e-46 | yqbG | S | Protein of unknown function (DUF3199) | ||
IJFNMBCI_02831 | 4.6e-42 | yqbH | S | Domain of unknown function (DUF3599) | ||
IJFNMBCI_02832 | 4.1e-60 | xkdI | S | Bacteriophage HK97-gp10, putative tail-component | ||
IJFNMBCI_02833 | 8.3e-57 | xkdJ | ||||
IJFNMBCI_02834 | 9.1e-14 | |||||
IJFNMBCI_02835 | 1e-225 | xkdK | S | Phage tail sheath C-terminal domain | ||
IJFNMBCI_02836 | 2e-74 | xkdM | S | Phage tail tube protein | ||
IJFNMBCI_02837 | 1.7e-73 | S | Phage XkdN-like tail assembly chaperone protein, TAC | |||
IJFNMBCI_02838 | 3.4e-19 | |||||
IJFNMBCI_02839 | 1e-189 | xkdO | L | Transglycosylase SLT domain | ||
IJFNMBCI_02840 | 1.5e-110 | xkdP | S | Lysin motif | ||
IJFNMBCI_02841 | 7.2e-162 | xkdQ | 3.2.1.96 | G | NLP P60 protein | |
IJFNMBCI_02842 | 1.2e-31 | xkdR | S | Protein of unknown function (DUF2577) | ||
IJFNMBCI_02843 | 1e-56 | xkdS | S | Protein of unknown function (DUF2634) | ||
IJFNMBCI_02844 | 1.5e-165 | xkdT | S | Evidence 3 Function proposed based on presence of conserved amino acid motif, structural feature or limited homology | ||
IJFNMBCI_02845 | 1.4e-85 | xkdU | S | Uncharacterised protein conserved in bacteria (DUF2313) | ||
IJFNMBCI_02846 | 1.2e-26 | |||||
IJFNMBCI_02847 | 6.1e-187 | |||||
IJFNMBCI_02849 | 6.5e-30 | xkdX | ||||
IJFNMBCI_02850 | 8.1e-137 | xepA | ||||
IJFNMBCI_02851 | 8.7e-38 | xhlA | S | Haemolysin XhlA | ||
IJFNMBCI_02852 | 1.3e-38 | xhlB | S | SPP1 phage holin | ||
IJFNMBCI_02853 | 6.4e-170 | xlyA | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
IJFNMBCI_02854 | 8.7e-23 | spoIISB | S | Stage II sporulation protein SB | ||
IJFNMBCI_02855 | 1.4e-133 | spoIISA | S | Toxin SpoIISA, type II toxin-antitoxin system | ||
IJFNMBCI_02856 | 5.8e-175 | pit | P | phosphate transporter | ||
IJFNMBCI_02857 | 6.9e-110 | ykaA | P | COG1392 Phosphate transport regulator (distant homolog of PhoU) | ||
IJFNMBCI_02858 | 3.8e-243 | steT | E | amino acid | ||
IJFNMBCI_02859 | 6.7e-181 | mhqA | E | COG0346 Lactoylglutathione lyase and related lyases | ||
IJFNMBCI_02860 | 3.5e-302 | ykcB | M | COG1807 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
IJFNMBCI_02861 | 1.2e-177 | ykcC | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
IJFNMBCI_02863 | 1.8e-203 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
IJFNMBCI_02864 | 1e-279 | yubD | P | Major Facilitator Superfamily | ||
IJFNMBCI_02866 | 6.5e-156 | dppA | E | D-aminopeptidase | ||
IJFNMBCI_02867 | 2.4e-159 | dppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
IJFNMBCI_02868 | 1.1e-175 | dppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
IJFNMBCI_02869 | 2.2e-190 | dppD | P | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_02870 | 0.0 | dppE | E | ABC transporter substrate-binding protein | ||
IJFNMBCI_02871 | 2.9e-176 | ykfA | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | |
IJFNMBCI_02872 | 4.1e-198 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
IJFNMBCI_02873 | 1.1e-169 | ykfC | 3.4.14.13 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
IJFNMBCI_02874 | 8.2e-182 | ykfD | E | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_02875 | 3.8e-13 | S | Domain of unknown function (DUF4367) | |||
IJFNMBCI_02876 | 3e-74 | S | response regulator aspartate phosphatase | |||
IJFNMBCI_02879 | 1.1e-227 | proP | EGP | Transporter | ||
IJFNMBCI_02880 | 5e-57 | S | Domain of unknown function with cystatin-like fold (DUF4467) | |||
IJFNMBCI_02881 | 1.2e-73 | maoC | I | N-terminal half of MaoC dehydratase | ||
IJFNMBCI_02882 | 1e-62 | yyaQ | S | YjbR | ||
IJFNMBCI_02883 | 1.8e-66 | ywnA | K | Transcriptional regulator | ||
IJFNMBCI_02884 | 3.8e-111 | ywnB | S | NAD(P)H-binding | ||
IJFNMBCI_02885 | 1.4e-30 | cspL | K | Cold shock | ||
IJFNMBCI_02886 | 2e-77 | carD | K | Transcription factor | ||
IJFNMBCI_02887 | 4.6e-39 | yrkD | S | protein conserved in bacteria | ||
IJFNMBCI_02888 | 1.6e-82 | yrkE | O | DsrE/DsrF/DrsH-like family | ||
IJFNMBCI_02889 | 2.1e-58 | P | Rhodanese Homology Domain | |||
IJFNMBCI_02890 | 9.2e-93 | yrkF | OP | Belongs to the sulfur carrier protein TusA family | ||
IJFNMBCI_02891 | 1.6e-197 | yrkH | P | Rhodanese Homology Domain | ||
IJFNMBCI_02892 | 1.2e-35 | yrkI | O | Belongs to the sulfur carrier protein TusA family | ||
IJFNMBCI_02893 | 7.8e-119 | yrkJ | S | membrane transporter protein | ||
IJFNMBCI_02894 | 7e-124 | racX | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
IJFNMBCI_02895 | 3.8e-99 | S | Protein of unknown function (DUF2812) | |||
IJFNMBCI_02896 | 4.9e-51 | K | Transcriptional regulator PadR-like family | |||
IJFNMBCI_02897 | 3.4e-180 | S | Patatin-like phospholipase | |||
IJFNMBCI_02898 | 6.3e-79 | S | DinB superfamily | |||
IJFNMBCI_02899 | 5e-117 | ygeX | 4.3.1.15, 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
IJFNMBCI_02900 | 2.7e-67 | K | COG1802 Transcriptional regulators | |||
IJFNMBCI_02901 | 1.7e-39 | yabJ | 3.5.99.10 | J | Endoribonuclease L-PSP | |
IJFNMBCI_02902 | 9.3e-141 | sdaC | E | Serine transporter | ||
IJFNMBCI_02903 | 4.5e-163 | E | Peptidase dimerisation domain | |||
IJFNMBCI_02904 | 6.4e-125 | rhaS5 | K | helix_turn_helix, arabinose operon control protein | ||
IJFNMBCI_02905 | 9.4e-175 | amaB | 3.5.1.6, 3.5.1.87 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
IJFNMBCI_02906 | 6.5e-233 | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |||
IJFNMBCI_02907 | 1.2e-191 | ydeG | EGP | Major facilitator superfamily | ||
IJFNMBCI_02908 | 1.3e-51 | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | ||
IJFNMBCI_02911 | 1.3e-267 | ygaK | C | COG0277 FAD FMN-containing dehydrogenases | ||
IJFNMBCI_02912 | 6.3e-38 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
IJFNMBCI_02913 | 3.3e-164 | czcD | P | COG1230 Co Zn Cd efflux system component | ||
IJFNMBCI_02914 | 1.3e-198 | trkA | P | Oxidoreductase | ||
IJFNMBCI_02916 | 1.8e-98 | yrkC | G | Cupin domain | ||
IJFNMBCI_02917 | 3.8e-85 | ykkA | S | Protein of unknown function (DUF664) | ||
IJFNMBCI_02918 | 1.2e-138 | dapA_5 | 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
IJFNMBCI_02920 | 6.2e-196 | rlmN | 2.1.1.192, 2.1.1.224 | J | Specifically methylates position 8 of adenine 2503 in 23S rRNA. Confers resistance to some classes of antibiotics | |
IJFNMBCI_02921 | 3.4e-51 | ydeH | ||||
IJFNMBCI_02922 | 3.6e-166 | S | Sodium Bile acid symporter family | |||
IJFNMBCI_02923 | 1.6e-199 | adhA | 1.1.1.1 | C | alcohol dehydrogenase | |
IJFNMBCI_02924 | 4e-66 | yraB | K | helix_turn_helix, mercury resistance | ||
IJFNMBCI_02925 | 2.3e-224 | mleN_2 | C | antiporter | ||
IJFNMBCI_02926 | 1.7e-257 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
IJFNMBCI_02927 | 2.3e-113 | paiB | K | Transcriptional regulator | ||
IJFNMBCI_02929 | 6.7e-178 | ydeR | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02930 | 3.8e-102 | ydeS | K | Transcriptional regulator | ||
IJFNMBCI_02931 | 1.7e-157 | ydeK | EG | -transporter | ||
IJFNMBCI_02932 | 5.2e-267 | ydeL | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
IJFNMBCI_02933 | 4.7e-48 | yraD | M | Spore coat protein | ||
IJFNMBCI_02934 | 5.1e-25 | yraE | ||||
IJFNMBCI_02935 | 4.2e-222 | adhB | 1.1.1.1, 1.1.1.14, 1.1.1.284 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
IJFNMBCI_02936 | 2.2e-63 | yraF | M | Spore coat protein | ||
IJFNMBCI_02937 | 4.5e-36 | yraG | ||||
IJFNMBCI_02938 | 2.3e-216 | ydfH | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_02939 | 8.3e-111 | ydfI | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
IJFNMBCI_02940 | 0.0 | ydfJ | S | drug exporters of the RND superfamily | ||
IJFNMBCI_02941 | 1.2e-132 | puuD | S | Peptidase C26 | ||
IJFNMBCI_02942 | 3.6e-299 | expZ | S | ABC transporter | ||
IJFNMBCI_02943 | 1.8e-98 | ynaD | J | Acetyltransferase (GNAT) domain | ||
IJFNMBCI_02944 | 7.2e-150 | S | Uncharacterized protein conserved in bacteria (DUF2179) | |||
IJFNMBCI_02945 | 1.1e-93 | gldA | 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
IJFNMBCI_02946 | 1.5e-89 | gldA | 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
IJFNMBCI_02947 | 3.9e-210 | tcaB | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02948 | 4.4e-225 | fabF_1 | 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 | |
IJFNMBCI_02949 | 1.1e-155 | K | Helix-turn-helix XRE-family like proteins | |||
IJFNMBCI_02950 | 9.4e-122 | ydhB | S | membrane transporter protein | ||
IJFNMBCI_02951 | 5.3e-78 | bltD | 2.3.1.57 | K | FR47-like protein | |
IJFNMBCI_02952 | 2.6e-149 | bltR | K | helix_turn_helix, mercury resistance | ||
IJFNMBCI_02953 | 1.2e-147 | ydzE | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
IJFNMBCI_02954 | 1.3e-113 | yjhB | 3.6.1.13, 3.6.1.55 | F | ADP-ribose pyrophosphatase | |
IJFNMBCI_02955 | 1.7e-145 | ycgJ_1 | Q | ubiE/COQ5 methyltransferase family | ||
IJFNMBCI_02956 | 3.6e-167 | ycsA | 1.1.1.83, 1.1.1.93, 4.1.1.73 | CE | Isocitrate/isopropylmalate dehydrogenase | |
IJFNMBCI_02957 | 2.4e-119 | ydhC | K | FCD | ||
IJFNMBCI_02958 | 2.4e-228 | ydhE | CG | COG1819 Glycosyl transferases, related to UDP-glucuronosyltransferase | ||
IJFNMBCI_02961 | 6.5e-262 | pbpE | V | Beta-lactamase | ||
IJFNMBCI_02963 | 1.2e-97 | ydhK | M | Protein of unknown function (DUF1541) | ||
IJFNMBCI_02964 | 1.2e-195 | pbuE | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02965 | 6.7e-133 | ydhQ | K | UTRA | ||
IJFNMBCI_02966 | 5.3e-119 | K | FCD | |||
IJFNMBCI_02967 | 7.4e-217 | yeaN | P | COG2807 Cyanate permease | ||
IJFNMBCI_02968 | 2.6e-49 | sugE | P | Small Multidrug Resistance protein | ||
IJFNMBCI_02969 | 2.3e-51 | ykkC | P | Small Multidrug Resistance protein | ||
IJFNMBCI_02970 | 5.3e-104 | yvdT | K | Transcriptional regulator | ||
IJFNMBCI_02971 | 3.5e-296 | yveA | E | amino acid | ||
IJFNMBCI_02972 | 7.2e-166 | ydhU | P | Catalase | ||
IJFNMBCI_02973 | 1.7e-81 | yndB | S | Activator of Hsp90 ATPase homolog 1-like protein | ||
IJFNMBCI_02974 | 1e-177 | yhfP | 1.1.1.1 | C | Quinone oxidoreductase | |
IJFNMBCI_02975 | 1e-249 | iolT | EGP | Major facilitator Superfamily | ||
IJFNMBCI_02978 | 2.9e-60 | S | Phage tail protein | |||
IJFNMBCI_02979 | 2.2e-79 | L | Prophage endopeptidase tail | |||
IJFNMBCI_02980 | 0.0 | S | Peptidase_G2, IMC autoproteolytic cleavage domain | |||
IJFNMBCI_02981 | 1.1e-97 | S | Domain of unknown function (DUF2479) | |||
IJFNMBCI_02982 | 1.6e-21 | |||||
IJFNMBCI_02984 | 4.5e-29 | S | BhlA holin family | |||
IJFNMBCI_02985 | 1.2e-145 | xlyB | 3.5.1.28 | CBM50 | MT | N-acetylmuramoyl-L-alanine amidase |
IJFNMBCI_02986 | 3.7e-33 | S | Bacteriophage A118-like holin, Hol118 | |||
IJFNMBCI_02989 | 4.8e-21 | S | protein disulfide oxidoreductase activity | |||
IJFNMBCI_02991 | 5.2e-127 | ftsK | D | FtsK/SpoIIIE family | ||
IJFNMBCI_02992 | 1.2e-64 | |||||
IJFNMBCI_02993 | 5.3e-14 | K | Transcriptional regulator | |||
IJFNMBCI_02994 | 3.2e-99 | K | Helix-turn-helix domain | |||
IJFNMBCI_02997 | 0.0 | ilvB | 2.2.1.6 | E | Acetolactate synthase | |
IJFNMBCI_02998 | 4.6e-83 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
IJFNMBCI_02999 | 1.2e-191 | 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 | |
IJFNMBCI_03000 | 1.8e-287 | 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) | |
IJFNMBCI_03001 | 4.8e-199 | 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 | |
IJFNMBCI_03002 | 3.1e-275 | 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 | |
IJFNMBCI_03003 | 6.2e-116 | 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 | |
IJFNMBCI_03004 | 1.3e-187 | ysoA | H | Tetratricopeptide repeat | ||
IJFNMBCI_03005 | 4.7e-214 | 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 | ||
IJFNMBCI_03006 | 7.7e-233 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
IJFNMBCI_03007 | 6e-310 | lonB | 2.7.7.7, 3.4.21.53 | LO | Belongs to the peptidase S16 family | |
IJFNMBCI_03008 | 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 | |
IJFNMBCI_03009 | 8.8e-107 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
IJFNMBCI_03010 | 8.5e-87 | ysxD | ||||
IJFNMBCI_03011 | 4.5e-247 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
IJFNMBCI_03012 | 3.6e-146 | hemX | O | cytochrome C | ||
IJFNMBCI_03013 | 2.4e-175 | 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 | |
IJFNMBCI_03014 | 5e-142 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
IJFNMBCI_03015 | 3.9e-184 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
IJFNMBCI_03016 | 1.8e-245 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
IJFNMBCI_03017 | 7.3e-129 | spoVID | M | stage VI sporulation protein D | ||
IJFNMBCI_03018 | 3.3e-197 | 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 | ||
IJFNMBCI_03019 | 2.1e-25 | |||||
IJFNMBCI_03020 | 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 | |
IJFNMBCI_03021 | 1.6e-230 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
IJFNMBCI_03022 | 2.8e-121 | comC | 3.4.23.43 | NOU | COG1989 Type II secretory pathway, prepilin signal peptidase PulO and related peptidases | |
IJFNMBCI_03023 | 2e-127 | spoIIB | S | Sporulation related domain | ||
IJFNMBCI_03024 | 2.3e-99 | maf | D | septum formation protein Maf | ||
IJFNMBCI_03025 | 1.8e-127 | radC | E | Belongs to the UPF0758 family | ||
IJFNMBCI_03026 | 4e-184 | mreB | D | Rod shape-determining protein MreB | ||
IJFNMBCI_03027 | 1.2e-157 | mreC | M | Involved in formation and maintenance of cell shape | ||
IJFNMBCI_03028 | 5.4e-84 | mreD | M | shape-determining protein | ||
IJFNMBCI_03029 | 1.5e-97 | 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 | ||
IJFNMBCI_03030 | 2.3e-142 | minD | D | Belongs to the ParA family | ||
IJFNMBCI_03031 | 1.9e-144 | spoIVFA | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
IJFNMBCI_03032 | 7.8e-160 | spoIVFB | S | Stage IV sporulation protein | ||
IJFNMBCI_03033 | 9.2e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
IJFNMBCI_03034 | 3.2e-56 | ysxB | J | ribosomal protein | ||
IJFNMBCI_03035 | 5.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
IJFNMBCI_03036 | 4.8e-105 | spo0B | T | Sporulation initiation phospho-transferase B, C-terminal | ||
IJFNMBCI_03037 | 7.6e-236 | 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 | ||
IJFNMBCI_03038 | 4.8e-73 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
IJFNMBCI_03039 | 7.7e-160 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
IJFNMBCI_03040 | 1.1e-95 | niaR | S | small molecule binding protein (contains 3H domain) | ||
IJFNMBCI_03041 | 2.3e-223 | nifS | 2.8.1.7 | E | Cysteine desulfurase | |
IJFNMBCI_03042 | 1e-298 | nadB | 1.3.5.4, 1.4.3.16 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
IJFNMBCI_03043 | 2.6e-152 | nadC | 1.4.3.16, 2.4.2.19 | H | Belongs to the NadC ModD family | |
IJFNMBCI_03044 | 5.5e-211 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
IJFNMBCI_03045 | 5.7e-145 | safA | M | spore coat assembly protein SafA | ||
IJFNMBCI_03046 | 1.4e-46 | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | |||
IJFNMBCI_03048 | 1.1e-92 | bofC | S | BofC C-terminal domain | ||
IJFNMBCI_03049 | 5.9e-106 | 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 | |
IJFNMBCI_03050 | 2.1e-185 | 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 | |
IJFNMBCI_03051 | 1.6e-20 | yrzS | S | Protein of unknown function (DUF2905) | ||
IJFNMBCI_03052 | 2.4e-192 | 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) | |
IJFNMBCI_03053 | 4e-228 | 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) | |
IJFNMBCI_03054 | 5.6e-37 | yajC | U | Preprotein translocase subunit YajC | ||
IJFNMBCI_03055 | 2.4e-60 | yrzE | S | Protein of unknown function (DUF3792) | ||
IJFNMBCI_03056 | 9.5e-110 | yrbG | S | membrane | ||
IJFNMBCI_03057 | 7.2e-273 | spoVB | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
IJFNMBCI_03058 | 8.5e-50 | yrzD | S | Post-transcriptional regulator | ||
IJFNMBCI_03059 | 0.0 | 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 | ||
IJFNMBCI_03060 | 9.5e-86 | yrvC | P | regulatory, ligand-binding protein related to C-terminal domains of K channels | ||
IJFNMBCI_03061 | 1.4e-40 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
IJFNMBCI_03062 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
IJFNMBCI_03063 | 7.7e-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 | |
IJFNMBCI_03064 | 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 | |
IJFNMBCI_03065 | 1.8e-75 | 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 | ||
IJFNMBCI_03066 | 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 | |
IJFNMBCI_03067 | 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 | |
IJFNMBCI_03068 | 8.1e-38 | yaaB | S | Domain of unknown function (DUF370) | ||
IJFNMBCI_03069 | 9.2e-206 | 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 | ||
IJFNMBCI_03070 | 2.4e-33 | yaaA | S | S4 domain | ||
IJFNMBCI_03071 | 1.6e-205 | 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 | |
IJFNMBCI_03072 | 1.5e-250 | 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 | ||
IJFNMBCI_03073 | 5.2e-54 | 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 | |
IJFNMBCI_03074 | 1.9e-133 | 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 | ||
IJFNMBCI_03075 | 3.9e-108 | jag | S | single-stranded nucleic acid binding R3H | ||
IJFNMBCI_03076 | 5.2e-251 | 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 | ||
IJFNMBCI_03077 | 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 | ||
IJFNMBCI_03078 | 4.2e-127 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of guanine in position 535 of 16S rRNA | |
IJFNMBCI_03079 | 1.1e-150 | 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 | ||
IJFNMBCI_03080 | 9.2e-136 | soj | D | COG1192 ATPases involved in chromosome partitioning | ||
IJFNMBCI_03081 | 7.9e-149 | spo0J | K | Belongs to the ParB family | ||
IJFNMBCI_03082 | 1.4e-110 | yyaC | S | Sporulation protein YyaC | ||
IJFNMBCI_03083 | 1.5e-175 | yyaD | S | Membrane | ||
IJFNMBCI_03084 | 6.6e-33 | yyzM | S | protein conserved in bacteria | ||
IJFNMBCI_03085 | 0.0 | yyaE | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
IJFNMBCI_03086 | 2.6e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
IJFNMBCI_03087 | 7.3e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
IJFNMBCI_03088 | 3.8e-69 | 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 | ||
IJFNMBCI_03089 | 3e-37 | 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 | ||
IJFNMBCI_03090 | 9.7e-106 | adaA | 3.2.2.21 | K | Transcriptional regulator | |
IJFNMBCI_03091 | 1.1e-98 | adaB | 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 | |
IJFNMBCI_03092 | 8.1e-145 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
IJFNMBCI_03093 | 9.6e-180 | ccpB | 3.5.1.4, 5.1.1.1 | K | Transcriptional regulator | |
IJFNMBCI_03094 | 2.1e-64 | yyaH | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
IJFNMBCI_03095 | 6.8e-248 | ydjK | G | Sugar (and other) transporter | ||
IJFNMBCI_03096 | 3.5e-163 | yyaK | S | CAAX protease self-immunity | ||
IJFNMBCI_03097 | 0.0 | yyaL | O | COG1331 Highly conserved protein containing a thioredoxin domain | ||
IJFNMBCI_03098 | 8e-131 | ydfC | EG | EamA-like transporter family | ||
IJFNMBCI_03099 | 4e-246 | ydfD | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
IJFNMBCI_03100 | 7.7e-67 | isp | O | Subtilase family | ||
IJFNMBCI_03101 | 3.5e-18 | |||||
IJFNMBCI_03102 | 1e-65 | S | Leucine-rich repeat (LRR) protein | |||
IJFNMBCI_03103 | 4.5e-97 | |||||
IJFNMBCI_03104 | 1.8e-14 | S | Psort location Cytoplasmic, score | |||
IJFNMBCI_03105 | 1.7e-46 | mutT | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | |
IJFNMBCI_03106 | 4.2e-41 | 3.1.3.18 | S | glycolate biosynthetic process | ||
IJFNMBCI_03107 | 2.6e-55 | eaeH | M | Domain of Unknown Function (DUF1259) | ||
IJFNMBCI_03108 | 5.8e-94 | eaeH | M | Domain of Unknown Function (DUF1259) | ||
IJFNMBCI_03109 | 1e-75 | yjcF | S | Acetyltransferase (GNAT) domain | ||
IJFNMBCI_03110 | 1.3e-76 | yybA | 2.3.1.57 | K | transcriptional | |
IJFNMBCI_03111 | 1.1e-153 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
IJFNMBCI_03112 | 3.2e-69 | ydgJ | K | Winged helix DNA-binding domain | ||
IJFNMBCI_03113 | 9.6e-115 | drgA | C | nitroreductase | ||
IJFNMBCI_03114 | 2.1e-53 | ypaA | S | Protein of unknown function (DUF1304) | ||
IJFNMBCI_03115 | 1.1e-164 | gltC | K | Transcriptional regulator | ||
IJFNMBCI_03116 | 7.3e-217 | ynfM | EGP | Major facilitator Superfamily | ||
IJFNMBCI_03117 | 4.3e-100 | E | LysE type translocator | |||
IJFNMBCI_03118 | 1.4e-161 | yfiE | K | LysR substrate binding domain | ||
IJFNMBCI_03119 | 2.6e-161 | G | Major Facilitator Superfamily | |||
IJFNMBCI_03120 | 5.4e-76 | dinB | S | PFAM DinB family protein | ||
IJFNMBCI_03121 | 1.1e-113 | K | FCD domain | |||
IJFNMBCI_03122 | 0.0 | levB | 3.2.1.26, 3.2.1.64, 3.2.1.65 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
IJFNMBCI_03123 | 7.2e-272 | sacB | 2.4.1.10 | GH68 | M | levansucrase activity |
IJFNMBCI_03124 | 1.7e-154 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
IJFNMBCI_03125 | 3.9e-165 | ppaC | 3.6.1.1 | C | Inorganic pyrophosphatase | |
IJFNMBCI_03126 | 2.8e-66 | ydeP3 | K | Transcriptional regulator | ||
IJFNMBCI_03127 | 6.5e-85 | cotF | M | Spore coat protein | ||
IJFNMBCI_03129 | 2.7e-158 | yybS | S | membrane | ||
IJFNMBCI_03130 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
IJFNMBCI_03131 | 4.9e-73 | rplI | J | binds to the 23S rRNA | ||
IJFNMBCI_03132 | 4.9e-122 | KLT | COG0515 Serine threonine protein kinase | |||
IJFNMBCI_03133 | 1.1e-121 | S | GlcNAc-PI de-N-acetylase | |||
IJFNMBCI_03134 | 1.3e-238 | M | Glycosyltransferase Family 4 | |||
IJFNMBCI_03135 | 9.1e-236 | S | Carbamoyl-phosphate synthase L chain, ATP binding domain | |||
IJFNMBCI_03136 | 3.4e-202 | S | Ecdysteroid kinase | |||
IJFNMBCI_03137 | 9.6e-239 | M | Glycosyltransferase Family 4 | |||
IJFNMBCI_03138 | 2.8e-140 | yycA | M | COG1807 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
IJFNMBCI_03139 | 2.1e-106 | yycA | M | COG1807 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
IJFNMBCI_03140 | 4.6e-17 | yycC | K | YycC-like protein | ||
IJFNMBCI_03142 | 5.7e-26 | yycD | S | Uncharacterized protein conserved in bacteria (DUF2188) | ||
IJFNMBCI_03143 | 8e-252 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
IJFNMBCI_03144 | 1e-69 | yycE | 3.4.21.26, 5.3.1.24 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
IJFNMBCI_03145 | 3e-248 | 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 | |
IJFNMBCI_03150 | 1.1e-132 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_03151 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_03152 | 2.7e-260 | yycH | S | protein conserved in bacteria | ||
IJFNMBCI_03153 | 1.9e-150 | yycI | S | protein conserved in bacteria | ||
IJFNMBCI_03154 | 1.8e-150 | vicX | 3.1.26.11 | S | COG1235 Metal-dependent hydrolases of the beta-lactamase superfamily I | |
IJFNMBCI_03155 | 6e-219 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
IJFNMBCI_03164 | 1.2e-77 | tspO | T | membrane | ||
IJFNMBCI_03165 | 1.7e-131 | dksA | T | COG1734 DnaK suppressor protein | ||
IJFNMBCI_03166 | 4.2e-272 | menF | 5.4.4.2 | HQ | Isochorismate synthase | |
IJFNMBCI_03167 | 0.0 | menD | 2.2.1.9 | H | Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) | |
IJFNMBCI_03168 | 3.6e-154 | menH | 4.2.99.20 | S | Catalyzes a proton abstraction reaction that results in 2,5-elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6- hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) | |
IJFNMBCI_03169 | 2.1e-154 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
IJFNMBCI_03170 | 1.1e-275 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
IJFNMBCI_03171 | 1e-212 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
IJFNMBCI_03172 | 1.5e-122 | troA | P | Belongs to the bacterial solute-binding protein 9 family | ||
IJFNMBCI_03173 | 3.3e-122 | mntB | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
IJFNMBCI_03174 | 2.6e-159 | mntC | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
IJFNMBCI_03175 | 4.1e-124 | troD | P | 'COG1108 ABC-type Mn2 Zn2 transport systems, permease components' | ||
IJFNMBCI_03176 | 2.3e-24 | S | Domain of Unknown Function (DUF1540) | |||
IJFNMBCI_03177 | 5.8e-186 | cydB | 1.10.3.14 | C | COG1294 Cytochrome bd-type quinol oxidase, subunit 2 | |
IJFNMBCI_03178 | 2.6e-239 | cydA | 1.10.3.14 | C | oxidase, subunit | |
IJFNMBCI_03179 | 7.9e-41 | rpmE2 | J | Ribosomal protein L31 | ||
IJFNMBCI_03180 | 3.6e-105 | ytiB | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
IJFNMBCI_03181 | 6.2e-40 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
IJFNMBCI_03182 | 5.7e-88 | 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) | |
IJFNMBCI_03183 | 1.6e-76 | ytkA | S | YtkA-like | ||
IJFNMBCI_03185 | 1.6e-76 | dps | P | Belongs to the Dps family | ||
IJFNMBCI_03186 | 1.7e-61 | ytkC | S | Bacteriophage holin family | ||
IJFNMBCI_03187 | 1.7e-87 | ytkD | 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
IJFNMBCI_03188 | 3.4e-125 | ytlD | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
IJFNMBCI_03189 | 1.2e-143 | ytlC | P | ABC transporter | ||
IJFNMBCI_03190 | 8.1e-185 | ytlA | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
IJFNMBCI_03191 | 1.4e-147 | ytmA | E | COG1506 Dipeptidyl aminopeptidases acylaminoacyl-peptidases | ||
IJFNMBCI_03192 | 1.6e-38 | ytmB | S | Protein of unknown function (DUF2584) | ||
IJFNMBCI_03193 | 4.8e-309 | 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 | |
IJFNMBCI_03194 | 1.5e-225 | 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 | |
IJFNMBCI_03195 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
IJFNMBCI_03196 | 7.4e-261 | ytnA | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
IJFNMBCI_03197 | 1.9e-57 | ytoA | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
IJFNMBCI_03198 | 2.9e-150 | ytpA | 3.1.1.5 | I | Alpha beta hydrolase | |
IJFNMBCI_03199 | 6e-210 | ytpB | 4.2.3.130 | S | Tetraprenyl-beta-curcumene synthase | |
IJFNMBCI_03200 | 4.7e-143 | glpQ | 3.1.4.46, 5.4.2.11 | C | glycerophosphoryl diester phosphodiesterase | |
IJFNMBCI_03202 | 3.3e-106 | ytqB | J | Putative rRNA methylase | ||
IJFNMBCI_03203 | 4.7e-190 | yhcC | S | Fe-S oxidoreductase | ||
IJFNMBCI_03204 | 1e-285 | norB | EGP | COG0477 Permeases of the major facilitator superfamily | ||
IJFNMBCI_03205 | 1.6e-189 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
IJFNMBCI_03206 | 7.4e-40 | ytzC | S | Protein of unknown function (DUF2524) | ||
IJFNMBCI_03207 | 3.9e-66 | ytrA | K | GntR family transcriptional regulator | ||
IJFNMBCI_03208 | 6e-160 | ytrB | P | abc transporter atp-binding protein | ||
IJFNMBCI_03209 | 5.4e-165 | S | ABC-2 family transporter protein | |||
IJFNMBCI_03210 | 3e-168 | P | ABC-2 family transporter protein | |||
IJFNMBCI_03211 | 1.2e-151 | |||||
IJFNMBCI_03212 | 2.9e-125 | ytrE | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_03213 | 6.3e-222 | ytrF | V | COG0577 ABC-type antimicrobial peptide transport system, permease component | ||
IJFNMBCI_03214 | 5.7e-129 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_03215 | 2.6e-164 | T | PhoQ Sensor | |||
IJFNMBCI_03216 | 9.8e-135 | bceA | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_03217 | 0.0 | bceB | V | ABC transporter (permease) | ||
IJFNMBCI_03218 | 8e-126 | ywaF | S | Integral membrane protein | ||
IJFNMBCI_03219 | 1.5e-206 | yttB | EGP | Major facilitator Superfamily | ||
IJFNMBCI_03220 | 2.1e-138 | pfyP | T | Motif C-terminal to PAS motifs (likely to contribute to PAS structural domain) | ||
IJFNMBCI_03221 | 1.2e-52 | ytvB | S | Protein of unknown function (DUF4257) | ||
IJFNMBCI_03222 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
IJFNMBCI_03223 | 3.6e-51 | ytwF | P | Sulfurtransferase | ||
IJFNMBCI_03224 | 1.6e-85 | M | Acetyltransferase (GNAT) domain | |||
IJFNMBCI_03225 | 1.7e-251 | melA | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase |
IJFNMBCI_03226 | 1.4e-142 | amyC | P | ABC transporter (permease) | ||
IJFNMBCI_03227 | 1.1e-164 | amyD | G | Binding-protein-dependent transport system inner membrane component | ||
IJFNMBCI_03228 | 2.6e-244 | msmE | G | Bacterial extracellular solute-binding protein | ||
IJFNMBCI_03229 | 4.8e-185 | msmR | K | Transcriptional regulator | ||
IJFNMBCI_03230 | 9e-26 | yteV | S | Sporulation protein Cse60 | ||
IJFNMBCI_03231 | 9.5e-278 | opuD | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
IJFNMBCI_03232 | 3.6e-230 | ytfP | S | HI0933-like protein | ||
IJFNMBCI_03233 | 2.8e-291 | ytgP | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
IJFNMBCI_03234 | 2e-124 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
IJFNMBCI_03235 | 2.4e-33 | ytzE | K | COG1349 Transcriptional regulators of sugar metabolism | ||
IJFNMBCI_03236 | 1.1e-127 | ythP | V | ABC transporter | ||
IJFNMBCI_03237 | 1.9e-154 | ythQ | U | Bacterial ABC transporter protein EcsB | ||
IJFNMBCI_03238 | 5.3e-229 | pbuO | S | permease | ||
IJFNMBCI_03239 | 6.6e-270 | pepV | 3.5.1.18 | E | Dipeptidase | |
IJFNMBCI_03240 | 1.3e-173 | ytkP | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
IJFNMBCI_03241 | 3e-101 | ligT | 3.1.4.58, 3.5.1.42 | J | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | |
IJFNMBCI_03242 | 3.1e-170 | ytlQ | ||||
IJFNMBCI_03243 | 2.9e-176 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
IJFNMBCI_03244 | 6.3e-156 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
IJFNMBCI_03245 | 3.5e-45 | ytzH | S | YtzH-like protein | ||
IJFNMBCI_03246 | 8e-125 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
IJFNMBCI_03247 | 6.7e-218 | glcP | G | Major Facilitator Superfamily | ||
IJFNMBCI_03248 | 1.9e-247 | dat | 2.6.1.19 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
IJFNMBCI_03249 | 2e-180 | suhB | 3.1.3.25, 3.1.3.7 | G | inositol monophosphate 1-phosphatase activity | |
IJFNMBCI_03250 | 1.5e-202 | 1.1.1.14, 1.1.1.303, 1.1.1.4 | E | alcohol dehydrogenase | ||
IJFNMBCI_03251 | 1.9e-224 | ybaR | P | COG0659 Sulfate permease and related transporters (MFS superfamily) | ||
IJFNMBCI_03252 | 2.2e-174 | ybaS | 1.1.1.58 | S | Na -dependent transporter | |
IJFNMBCI_03253 | 2e-111 | ybbA | S | Putative esterase | ||
IJFNMBCI_03254 | 2.3e-179 | feuC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_03255 | 1.8e-176 | feuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_03256 | 2e-172 | feuA | P | Iron-uptake system-binding protein | ||
IJFNMBCI_03257 | 7.5e-310 | ybbB | K | COG2207 AraC-type DNA-binding domain-containing proteins | ||
IJFNMBCI_03258 | 1e-237 | ybbC | 3.2.1.52 | S | protein conserved in bacteria | |
IJFNMBCI_03259 | 0.0 | ybbD | 3.2.1.52 | G | Belongs to the glycosyl hydrolase 3 family | |
IJFNMBCI_03260 | 2e-244 | yfeW | 3.4.16.4 | V | Belongs to the UPF0214 family | |
IJFNMBCI_03261 | 4.8e-236 | ybbF | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
IJFNMBCI_03262 | 2.6e-161 | 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 | |
IJFNMBCI_03263 | 9.1e-86 | ybbJ | J | acetyltransferase | ||
IJFNMBCI_03264 | 8.7e-78 | ybbK | 2.4.2.1, 6.3.2.4 | S | Protein of unknown function (DUF523) | |
IJFNMBCI_03270 | 7.2e-98 | sigW | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
IJFNMBCI_03271 | 1.3e-116 | 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 | ||
IJFNMBCI_03272 | 1e-145 | 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 | |
IJFNMBCI_03273 | 2.8e-223 | ybbR | S | protein conserved in bacteria | ||
IJFNMBCI_03274 | 3.5e-252 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
IJFNMBCI_03275 | 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 | |
IJFNMBCI_03276 | 1e-140 | hincIIM | 2.1.1.72 | L | DNA restriction-modification system | |
IJFNMBCI_03277 | 5.3e-232 | T | Histidine kinase | |||
IJFNMBCI_03278 | 5.3e-15 | 2.7.13.3 | KT | response regulator, receiver | ||
IJFNMBCI_03279 | 2.9e-60 | L | HNH nucleases | |||
IJFNMBCI_03280 | 1.8e-57 | ybdO | S | Domain of unknown function (DUF4885) | ||
IJFNMBCI_03281 | 2.8e-162 | dkgB | S | Aldo/keto reductase family | ||
IJFNMBCI_03282 | 1e-93 | yxaC | M | effector of murein hydrolase | ||
IJFNMBCI_03283 | 6.9e-52 | S | LrgA family | |||
IJFNMBCI_03284 | 5.2e-72 | yxaD | K | helix_turn_helix multiple antibiotic resistance protein | ||
IJFNMBCI_03285 | 4e-259 | yifK | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
IJFNMBCI_03286 | 9.4e-95 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
IJFNMBCI_03287 | 5.3e-201 | T | COG4585 Signal transduction histidine kinase | |||
IJFNMBCI_03288 | 1.1e-110 | KT | LuxR family transcriptional regulator | |||
IJFNMBCI_03289 | 1.1e-167 | V | COG1131 ABC-type multidrug transport system, ATPase component | |||
IJFNMBCI_03290 | 8.3e-205 | V | COG0842 ABC-type multidrug transport system, permease component | |||
IJFNMBCI_03291 | 1.5e-198 | V | ABC-2 family transporter protein | |||
IJFNMBCI_03292 | 8.3e-24 | |||||
IJFNMBCI_03293 | 2.3e-65 | S | Domain of unknown function (DUF4879) | |||
IJFNMBCI_03294 | 3.7e-38 | csgA | S | Sigma-G-dependent sporulation-specific SASP protein | ||
IJFNMBCI_03295 | 2.3e-106 | yqeB | ||||
IJFNMBCI_03296 | 9.2e-40 | ybyB | ||||
IJFNMBCI_03297 | 1.5e-289 | ybeC | E | amino acid | ||
IJFNMBCI_03298 | 3.5e-48 | M | PFAM Glycosyl transferase family 2 | |||
IJFNMBCI_03299 | 4.1e-13 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
IJFNMBCI_03301 | 4e-53 | |||||
IJFNMBCI_03302 | 2.6e-15 | S | Protein of unknown function (DUF2651) | |||
IJFNMBCI_03303 | 9.7e-166 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
IJFNMBCI_03304 | 6.7e-226 | glpT | G | -transporter | ||
IJFNMBCI_03305 | 1.3e-16 | S | Protein of unknown function (DUF2651) | |||
IJFNMBCI_03306 | 8.6e-212 | hpaB | 1.14.14.9 | Q | COG2368 Aromatic ring hydroxylase | |
IJFNMBCI_03308 | 0.0 | ybfG | 3.2.1.132 | M | Domain of unknown function (DUF1906) | |
IJFNMBCI_03309 | 8.6e-30 | |||||
IJFNMBCI_03310 | 1.2e-82 | K | Helix-turn-helix XRE-family like proteins | |||
IJFNMBCI_03311 | 5.6e-200 | gldA | 1.1.1.1, 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
IJFNMBCI_03312 | 1.1e-212 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
IJFNMBCI_03313 | 5e-93 | pssA | 2.7.8.8 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
IJFNMBCI_03314 | 1.9e-86 | ybfM | S | SNARE associated Golgi protein | ||
IJFNMBCI_03315 | 2.5e-152 | psd | 4.1.1.65 | I | Catalyzes the formation of phosphatidylethanolamine (PtdEtn) from phosphatidylserine (PtdSer) | |
IJFNMBCI_03316 | 2.3e-41 | ybfN | ||||
IJFNMBCI_03317 | 8.6e-192 | yceA | S | Belongs to the UPF0176 family | ||
IJFNMBCI_03318 | 1.9e-215 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
IJFNMBCI_03319 | 8.6e-201 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
IJFNMBCI_03320 | 1.3e-99 | sipT | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
IJFNMBCI_03321 | 2.4e-81 | ccdC1 | O | Protein of unknown function (DUF1453) | ||
IJFNMBCI_03322 | 3.7e-78 | 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 | |
IJFNMBCI_03323 | 3e-154 | ypuA | S | Secreted protein | ||
IJFNMBCI_03324 | 1e-256 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
IJFNMBCI_03325 | 1.2e-269 | spoVAF | EG | Stage V sporulation protein AF | ||
IJFNMBCI_03326 | 5.2e-110 | spoVAEA | S | stage V sporulation protein | ||
IJFNMBCI_03327 | 3.8e-57 | spoVAEB | S | stage V sporulation protein | ||
IJFNMBCI_03328 | 1.4e-189 | spoVAD | I | Stage V sporulation protein AD | ||
IJFNMBCI_03329 | 1.3e-78 | spoVAC | S | stage V sporulation protein AC | ||
IJFNMBCI_03330 | 3.9e-60 | spoVAB | S | Stage V sporulation protein AB | ||
IJFNMBCI_03331 | 4.8e-111 | spoVAA | S | Stage V sporulation protein AA | ||
IJFNMBCI_03332 | 6.9e-136 | sigF | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
IJFNMBCI_03333 | 1.8e-75 | 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 | |
IJFNMBCI_03334 | 7.8e-58 | spoIIAA | T | Belongs to the anti-sigma-factor antagonist family | ||
IJFNMBCI_03335 | 1.1e-212 | dacF | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
IJFNMBCI_03336 | 2.2e-148 | 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 | |
IJFNMBCI_03337 | 2.3e-231 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
IJFNMBCI_03338 | 3.7e-165 | xerD | L | recombinase XerD | ||
IJFNMBCI_03339 | 3.7e-37 | S | Protein of unknown function (DUF4227) | |||
IJFNMBCI_03340 | 1.9e-80 | fur | P | Belongs to the Fur family | ||
IJFNMBCI_03341 | 5.5e-110 | 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 | ||
IJFNMBCI_03342 | 1.7e-34 | yqkK | ||||
IJFNMBCI_03343 | 5.7e-22 | |||||
IJFNMBCI_03344 | 7.7e-244 | mleA | 1.1.1.38 | C | malic enzyme | |
IJFNMBCI_03345 | 4.7e-239 | mleN | C | Na H antiporter | ||
IJFNMBCI_03346 | 1.3e-268 | aspA | 4.2.1.2, 4.3.1.1 | E | Aspartate ammonia-lyase | |
IJFNMBCI_03347 | 2.9e-187 | ansA | 3.5.1.1 | EJ | L-asparaginase | |
IJFNMBCI_03348 | 1e-57 | ansR | K | Transcriptional regulator | ||
IJFNMBCI_03349 | 3.6e-221 | yqxK | 3.6.4.12 | L | DNA helicase | |
IJFNMBCI_03350 | 1.6e-94 | nudF | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | |
IJFNMBCI_03352 | 8.2e-168 | yqkF | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | ||
IJFNMBCI_03354 | 1.4e-175 | yqkD | S | COG1073 Hydrolases of the alpha beta superfamily | ||
IJFNMBCI_03355 | 3.2e-39 | yqkC | S | Protein of unknown function (DUF2552) | ||
IJFNMBCI_03356 | 1.7e-60 | yqkB | S | Belongs to the HesB IscA family | ||
IJFNMBCI_03357 | 1.2e-174 | yqkA | K | GrpB protein | ||
IJFNMBCI_03358 | 1.2e-60 | yqjZ | 2.3.1.128, 2.5.1.18 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
IJFNMBCI_03359 | 1.9e-88 | yqjY | K | acetyltransferase | ||
IJFNMBCI_03360 | 3.6e-235 | 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 | |
IJFNMBCI_03361 | 7.6e-58 | S | YolD-like protein | |||
IJFNMBCI_03363 | 2.5e-184 | yueF | S | transporter activity | ||
IJFNMBCI_03365 | 1.2e-72 | yqjT | 3.1.26.4 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
IJFNMBCI_03366 | 2e-177 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
IJFNMBCI_03367 | 1.8e-256 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
IJFNMBCI_03368 | 1.9e-141 | yqjQ | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
IJFNMBCI_03369 | 9.5e-175 | yqjP | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
IJFNMBCI_03370 | 3.6e-146 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
IJFNMBCI_03371 | 7.5e-135 | pksI | I | Belongs to the enoyl-CoA hydratase isomerase family | ||
IJFNMBCI_03372 | 1.6e-238 | pksG | 2.3.3.10 | I | synthase | |
IJFNMBCI_03373 | 3.1e-220 | eryK | 1.14.13.154 | C | Cytochrome P450 | |
IJFNMBCI_03374 | 0.0 | pks13 | 1.6.5.5 | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | |
IJFNMBCI_03375 | 0.0 | Q | Polyketide synthase of type I | |||
IJFNMBCI_03376 | 0.0 | pfaA | Q | Polyketide synthase of type I | ||
IJFNMBCI_03377 | 0.0 | pksJ | Q | Polyketide synthase of type I | ||
IJFNMBCI_03378 | 4.4e-77 | yclD | ||||
IJFNMBCI_03379 | 2e-38 | bsdD | 4.1.1.61 | S | response to toxic substance | |
IJFNMBCI_03380 | 1.8e-283 | yclC | 4.1.1.61 | H | Decarboxylase involved in the decarboxylation and detoxification of phenolic derivatives under both aerobic and anaerobic conditions. It is able to catalyze the reversible decarboxylation of 4-hydroxybenzoate | |
IJFNMBCI_03381 | 3.2e-36 | 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 | |
IJFNMBCI_03382 | 1e-48 | 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 | |
IJFNMBCI_03383 | 1.6e-157 | bsdA | K | LysR substrate binding domain | ||
IJFNMBCI_03384 | 1.6e-143 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
IJFNMBCI_03385 | 4.1e-119 | tcyB | P | COG0765 ABC-type amino acid transport system, permease component | ||
IJFNMBCI_03386 | 1.5e-132 | tcyC | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
IJFNMBCI_03387 | 2e-109 | yczE | S | membrane | ||
IJFNMBCI_03388 | 1.5e-129 | acpT | 2.7.8.7 | H | Belongs to the P-Pant transferase superfamily | |
IJFNMBCI_03389 | 2.3e-248 | bamJ | E | Aminotransferase class I and II | ||
IJFNMBCI_03390 | 3e-136 | srfAD | Q | thioesterase | ||
IJFNMBCI_03391 | 0.0 | srfAC | Q | COG1020 Non-ribosomal peptide synthetase modules and related proteins | ||
IJFNMBCI_03392 | 0.0 | srfAB | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | ||
IJFNMBCI_03393 | 0.0 | srfAA | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | ||
IJFNMBCI_03394 | 6.3e-63 | hxlR | K | transcriptional | ||
IJFNMBCI_03395 | 2.8e-106 | hxlA | 4.1.2.43 | G | 3-hexulose-6-phosphate synthase | |
IJFNMBCI_03396 | 6.2e-94 | hxlB | 4.1.2.43, 5.3.1.27 | G | SIS domain | |
IJFNMBCI_03397 | 2.4e-77 | nucA | M | Deoxyribonuclease NucA/NucB | ||
IJFNMBCI_03398 | 2.9e-69 | nin | S | Competence protein J (ComJ) | ||
IJFNMBCI_03399 | 2.8e-295 | yckE | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
IJFNMBCI_03400 | 2.2e-51 | S | Protein of unknown function (DUF2680) | |||
IJFNMBCI_03401 | 1.1e-72 | yckC | S | membrane | ||
IJFNMBCI_03402 | 4.6e-221 | adhB | 1.1.1.1, 1.1.1.14, 1.1.1.284 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
IJFNMBCI_03403 | 5.4e-228 | yciC | S | GTPases (G3E family) | ||
IJFNMBCI_03404 | 2.4e-223 | nasA | P | COG2223 Nitrate nitrite transporter | ||
IJFNMBCI_03405 | 0.0 | nirB | 1.7.1.15 | C | Assimilatory nitrate reductase (electron transfer subunit) | |
IJFNMBCI_03406 | 0.0 | nasC | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
IJFNMBCI_03407 | 0.0 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
IJFNMBCI_03408 | 3.5e-57 | nirD | 1.7.1.15 | P | Nitrite reductase | |
IJFNMBCI_03409 | 1.4e-275 | cobA | 2.1.1.107, 4.2.1.75 | H | Belongs to the precorrin methyltransferase family | |
IJFNMBCI_03410 | 2.3e-187 | ycgT | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
IJFNMBCI_03411 | 6.2e-227 | ycgP | QT | COG2508 Regulator of polyketide synthase expression | ||
IJFNMBCI_03412 | 2.2e-244 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
IJFNMBCI_03413 | 1.3e-290 | rocA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
IJFNMBCI_03414 | 6.7e-170 | ycgM | E | Proline dehydrogenase | ||
IJFNMBCI_03415 | 2e-146 | ycgL | S | Predicted nucleotidyltransferase | ||
IJFNMBCI_03416 | 1.7e-184 | cah | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
IJFNMBCI_03417 | 8.7e-104 | 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 | |
IJFNMBCI_03418 | 2.3e-232 | G | COG0477 Permeases of the major facilitator superfamily | |||
IJFNMBCI_03419 | 3.9e-150 | 4.2.1.118 | G | Xylose isomerase-like TIM barrel | ||
IJFNMBCI_03420 | 1.8e-107 | tmrB | S | AAA domain | ||
IJFNMBCI_03422 | 7.9e-36 | |||||
IJFNMBCI_03423 | 0.0 | yjcD | 3.6.4.12 | L | DNA helicase | |
IJFNMBCI_03424 | 3.8e-38 | spoVIF | S | Stage VI sporulation protein F | ||
IJFNMBCI_03428 | 7.3e-56 | yjcA | S | Protein of unknown function (DUF1360) | ||
IJFNMBCI_03429 | 9.7e-54 | cotV | S | Spore Coat Protein X and V domain | ||
IJFNMBCI_03430 | 8e-22 | cotW | ||||
IJFNMBCI_03431 | 1.5e-70 | cotX | S | Spore Coat Protein X and V domain | ||
IJFNMBCI_03432 | 4.6e-93 | cotY | S | Spore coat protein Z | ||
IJFNMBCI_03433 | 6.7e-83 | cotZ | S | Spore coat protein | ||
IJFNMBCI_03434 | 5e-89 | yjbX | S | Spore coat protein | ||
IJFNMBCI_03435 | 4e-139 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
IJFNMBCI_03436 | 3.7e-148 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
IJFNMBCI_03437 | 8.4e-190 | thiF | 2.7.7.73, 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
IJFNMBCI_03438 | 2.6e-135 | 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 | |
IJFNMBCI_03439 | 1.4e-30 | thiS | H | Thiamine biosynthesis | ||
IJFNMBCI_03440 | 2.9e-212 | thiO | 1.4.3.19 | E | Glycine oxidase | |
IJFNMBCI_03441 | 7.1e-107 | tenI | 2.5.1.3, 5.3.99.10 | H | Transcriptional regulator TenI | |
IJFNMBCI_03442 | 5.2e-138 | 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 | |
IJFNMBCI_03443 | 0.0 | yjbQ | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
IJFNMBCI_03444 | 1.4e-144 | prpE | 3.1.3.16, 3.6.1.41 | T | Asymmetrically hydrolyzes Ap4p to yield AMP and ATP | |
IJFNMBCI_03445 | 1.5e-161 | yjbO | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
IJFNMBCI_03446 | 2.1e-151 | 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 | |
IJFNMBCI_03447 | 1.1e-107 | yjbM | 2.7.6.5 | S | GTP pyrophosphokinase | |
IJFNMBCI_03448 | 1.6e-61 | yjbL | S | Belongs to the UPF0738 family | ||
IJFNMBCI_03449 | 4.6e-100 | yjbK | S | protein conserved in bacteria | ||
IJFNMBCI_03450 | 1.9e-113 | yjbJ | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
IJFNMBCI_03451 | 4.8e-72 | yjbI | S | Bacterial-like globin | ||
IJFNMBCI_03452 | 2.3e-170 | yjbH | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
IJFNMBCI_03453 | 5.8e-19 | |||||
IJFNMBCI_03454 | 0.0 | pepF | E | oligoendopeptidase F | ||
IJFNMBCI_03455 | 1.2e-219 | yjbF | S | Competence protein | ||
IJFNMBCI_03456 | 2e-116 | 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 | ||
IJFNMBCI_03457 | 6.2e-109 | yjbE | P | Integral membrane protein TerC family | ||
IJFNMBCI_03458 | 1.6e-67 | 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 | |
IJFNMBCI_03459 | 1.3e-98 | yjbC | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
IJFNMBCI_03460 | 5.2e-231 | S | Putative glycosyl hydrolase domain | |||
IJFNMBCI_03461 | 2.1e-171 | oppF | E | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_03462 | 2.7e-202 | oppD | P | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_03463 | 1.7e-165 | oppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
IJFNMBCI_03464 | 2.7e-166 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
IJFNMBCI_03465 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
IJFNMBCI_03466 | 3e-184 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
IJFNMBCI_03467 | 5.5e-146 | yjbA | S | Belongs to the UPF0736 family | ||
IJFNMBCI_03468 | 3.6e-155 | appC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
IJFNMBCI_03469 | 7e-170 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
IJFNMBCI_03470 | 8.9e-250 | appA | E | COG0747 ABC-type dipeptide transport system, periplasmic component | ||
IJFNMBCI_03471 | 8.5e-187 | appF | E | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_03472 | 9.7e-183 | appD | P | Belongs to the ABC transporter superfamily | ||
IJFNMBCI_03473 | 1.8e-147 | yjaZ | O | Zn-dependent protease | ||
IJFNMBCI_03474 | 2.9e-232 | 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 | |
IJFNMBCI_03475 | 1.1e-172 | 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 | |
IJFNMBCI_03476 | 5.9e-32 | yjzB | ||||
IJFNMBCI_03477 | 2.5e-26 | comZ | S | ComZ | ||
IJFNMBCI_03478 | 1.9e-166 | med | S | Transcriptional activator protein med | ||
IJFNMBCI_03479 | 3.6e-105 | yjaV | ||||
IJFNMBCI_03480 | 8.8e-62 | yjaU | I | carboxylic ester hydrolase activity | ||
IJFNMBCI_03481 | 2e-62 | yjaU | I | carboxylic ester hydrolase activity | ||
IJFNMBCI_03482 | 1.5e-23 | yjzD | S | Protein of unknown function (DUF2929) | ||
IJFNMBCI_03483 | 1.2e-27 | yjzC | S | YjzC-like protein | ||
IJFNMBCI_03484 | 3.5e-177 | 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 | |
IJFNMBCI_03485 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase ammonia chain | |
IJFNMBCI_03486 | 6.3e-204 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
IJFNMBCI_03487 | 4.9e-218 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
IJFNMBCI_03488 | 3.3e-133 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
IJFNMBCI_03489 | 4.6e-227 | 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 | |
IJFNMBCI_03490 | 2.5e-197 | 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 | |
IJFNMBCI_03491 | 1.2e-89 | norB | G | Major Facilitator Superfamily | ||
IJFNMBCI_03492 | 2.7e-272 | yitY | C | D-arabinono-1,4-lactone oxidase | ||
IJFNMBCI_03493 | 6.9e-80 | 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 | |
IJFNMBCI_03494 | 4.7e-51 | yitW | S | metal-sulfur cluster biosynthetic enzyme | ||
IJFNMBCI_03495 | 1.1e-144 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
IJFNMBCI_03496 | 1.3e-153 | yitU | 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
IJFNMBCI_03497 | 3.5e-07 | |||||
IJFNMBCI_03498 | 4.4e-26 | S | Protein of unknown function (DUF3813) | |||
IJFNMBCI_03499 | 2.5e-133 | pdaB | 3.5.1.104 | G | Polysaccharide deacetylase | |
IJFNMBCI_03500 | 1.3e-102 | kbaA | 2.7.8.43 | S | Involved in the activation of the KinB signaling pathway of sporulation | |
IJFNMBCI_03501 | 7.6e-76 | gerD | ||||
IJFNMBCI_03502 | 5.7e-197 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
IJFNMBCI_03503 | 2.5e-132 | cwlD | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
IJFNMBCI_03504 | 5.6e-77 | ybaK | S | Protein of unknown function (DUF2521) | ||
IJFNMBCI_03505 | 1.6e-43 | yizA | S | Damage-inducible protein DinB | ||
IJFNMBCI_03506 | 3e-139 | ybaJ | Q | Methyltransferase domain | ||
IJFNMBCI_03507 | 1.6e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
IJFNMBCI_03508 | 1.9e-77 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
IJFNMBCI_03509 | 1.2e-137 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
IJFNMBCI_03510 | 1.2e-138 | 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 | ||
IJFNMBCI_03511 | 6.4e-146 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
IJFNMBCI_03512 | 2.1e-154 | cbiO | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
IJFNMBCI_03513 | 4.7e-58 | rplQ | J | Ribosomal protein L17 | ||
IJFNMBCI_03514 | 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 | |
IJFNMBCI_03515 | 2.8e-64 | 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 | ||
IJFNMBCI_03516 | 4e-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 | ||
IJFNMBCI_03517 | 4.2e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
IJFNMBCI_03518 | 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 | ||
IJFNMBCI_03519 | 4.8e-142 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
IJFNMBCI_03520 | 2.6e-123 | 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 | |
IJFNMBCI_03521 | 1.3e-232 | 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 | ||
IJFNMBCI_03522 | 4.1e-72 | rplO | J | binds to the 23S rRNA | ||
IJFNMBCI_03523 | 1.9e-23 | rpmD | J | Ribosomal protein L30 | ||
IJFNMBCI_03524 | 2.4e-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 | ||
IJFNMBCI_03525 | 1.2e-56 | 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 | ||
IJFNMBCI_03526 | 7.9e-94 | 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 | ||
IJFNMBCI_03527 | 2.3e-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 | ||
IJFNMBCI_03528 | 3.4e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
IJFNMBCI_03529 | 6e-94 | 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 | ||
IJFNMBCI_03530 | 6.2e-51 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
IJFNMBCI_03531 | 2.3e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
IJFNMBCI_03532 | 1.3e-38 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
IJFNMBCI_03533 | 1.7e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
IJFNMBCI_03534 | 1.3e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
IJFNMBCI_03535 | 8e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
IJFNMBCI_03536 | 4.3e-53 | 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 | ||
IJFNMBCI_03537 | 3.7e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
IJFNMBCI_03538 | 1.5e-155 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
IJFNMBCI_03539 | 1.2e-43 | 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 | ||
IJFNMBCI_03540 | 2e-104 | rplD | J | Forms part of the polypeptide exit tunnel | ||
IJFNMBCI_03541 | 9.8e-112 | 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 | ||
IJFNMBCI_03542 | 7.5e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
IJFNMBCI_03543 | 1.3e-171 | ybaC | 3.4.11.5 | S | Alpha/beta hydrolase family | |
IJFNMBCI_03544 | 1.8e-223 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
IJFNMBCI_03545 | 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 | ||
IJFNMBCI_03546 | 7.9e-82 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
IJFNMBCI_03547 | 6.5e-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 | ||
IJFNMBCI_03548 | 2.6e-31 | ybxF | J | Belongs to the eukaryotic ribosomal protein eL8 family | ||
IJFNMBCI_03549 | 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 | |
IJFNMBCI_03550 | 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 | |
IJFNMBCI_03551 | 1.8e-107 | rsmC | 2.1.1.172 | J | Methyltransferase | |
IJFNMBCI_03552 | 1.3e-42 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
IJFNMBCI_03553 | 2.5e-78 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
IJFNMBCI_03554 | 4.2e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
IJFNMBCI_03555 | 2.8e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
IJFNMBCI_03556 | 3.2e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
IJFNMBCI_03557 | 7.8e-22 | 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 | ||
IJFNMBCI_03558 | 8.9e-116 | sigH | K | Belongs to the sigma-70 factor family | ||
IJFNMBCI_03559 | 4.2e-89 | yacP | S | RNA-binding protein containing a PIN domain | ||
IJFNMBCI_03560 | 9.8e-135 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
IJFNMBCI_03561 | 1e-72 | 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) | ||
IJFNMBCI_03562 | 1.1e-267 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
IJFNMBCI_03563 | 1.6e-117 | cysE | 2.3.1.30 | E | Serine acetyltransferase | |
IJFNMBCI_03564 | 5.3e-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) | |
IJFNMBCI_03565 | 7e-86 | 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) | |
IJFNMBCI_03566 | 1.5e-124 | 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) | |
IJFNMBCI_03567 | 9.4e-195 | yacL | S | COG4956 Integral membrane protein (PIN domain superfamily) | ||
IJFNMBCI_03568 | 1.9e-195 | 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 | |
IJFNMBCI_03569 | 7e-256 | 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 | ||
IJFNMBCI_03570 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
IJFNMBCI_03571 | 7.2e-203 | 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 | |
IJFNMBCI_03572 | 6e-64 | mcsA | 2.7.14.1 | S | protein with conserved CXXC pairs | |
IJFNMBCI_03573 | 7.5e-77 | ctsR | K | Belongs to the CtsR family | ||
IJFNMBCI_03574 | 8.8e-257 | mmuP | E | amino acid | ||
IJFNMBCI_03575 | 1.6e-179 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine | |
IJFNMBCI_03576 | 3.9e-257 | agcS | E | Sodium alanine symporter | ||
IJFNMBCI_03577 | 1.4e-189 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
IJFNMBCI_03578 | 5.9e-212 | phoQ | 2.7.13.3 | T | Histidine kinase | |
IJFNMBCI_03579 | 6.7e-173 | glnL | T | Regulator | ||
IJFNMBCI_03580 | 8e-85 | ycbJ | S | Macrolide 2'-phosphotransferase | ||
IJFNMBCI_03581 | 8.2e-26 | rtpA | K | Tryptophan RNA-binding attenuator protein inhibitory protein | ||
IJFNMBCI_03582 | 5.6e-62 | ycbP | S | Protein of unknown function (DUF2512) | ||
IJFNMBCI_03583 | 5.3e-77 | sleB | 3.5.1.28 | M | Cell wall | |
IJFNMBCI_03584 | 1.4e-253 | phoD | 3.1.3.1 | P | COG3540 Phosphodiesterase alkaline phosphatase D | |
IJFNMBCI_03585 | 2.9e-81 | phoD | 3.1.3.1 | P | COG3540 Phosphodiesterase alkaline phosphatase D | |
IJFNMBCI_03586 | 4.4e-26 | 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 | ||
IJFNMBCI_03587 | 1.2e-124 | 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 | ||
IJFNMBCI_03588 | 8.5e-119 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
IJFNMBCI_03589 | 3.8e-207 | ycbU | E | Selenocysteine lyase | ||
IJFNMBCI_03590 | 6.7e-241 | lmrB | EGP | the major facilitator superfamily | ||
IJFNMBCI_03591 | 1.2e-100 | yxaF | K | Transcriptional regulator | ||
IJFNMBCI_03592 | 1.7e-199 | ansB | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
IJFNMBCI_03593 | 5.9e-112 | lip | 3.1.1.3 | S | acetyltransferases and hydrolases with the alpha beta hydrolase fold | |
IJFNMBCI_03594 | 7.8e-194 | yccF | K | DNA-templated transcriptional preinitiation complex assembly | ||
IJFNMBCI_03595 | 1e-71 | yccK | C | Aldo keto reductase | ||
IJFNMBCI_03596 | 6.1e-76 | yccK | C | Aldo keto reductase | ||
IJFNMBCI_03597 | 1.1e-173 | ycdA | S | Domain of unknown function (DUF5105) | ||
IJFNMBCI_03598 | 1.3e-252 | ycdB | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
IJFNMBCI_03599 | 1.4e-264 | ycdC | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
IJFNMBCI_03600 | 2.4e-89 | cwlK | M | D-alanyl-D-alanine carboxypeptidase | ||
IJFNMBCI_03601 | 2.3e-188 | S | response regulator aspartate phosphatase | |||
IJFNMBCI_03602 | 4.7e-140 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
IJFNMBCI_03603 | 0.0 | ycdG | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
IJFNMBCI_03604 | 1e-163 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
IJFNMBCI_03605 | 7.2e-132 | adcC | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
IJFNMBCI_03606 | 3.4e-136 | adcB | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
IJFNMBCI_03607 | 1.4e-184 | yceB | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
IJFNMBCI_03608 | 2.8e-108 | yceC | 3.5.4.33 | T | proteins involved in stress response, homologs of TerZ and | |
IJFNMBCI_03609 | 6.3e-105 | yceD | T | proteins involved in stress response, homologs of TerZ and | ||
IJFNMBCI_03610 | 1e-107 | yceE | T | proteins involved in stress response, homologs of TerZ and | ||
IJFNMBCI_03611 | 9.7e-138 | terC | P | Protein of unknown function (DUF475) | ||
IJFNMBCI_03612 | 0.0 | yceG | S | Putative component of 'biosynthetic module' | ||
IJFNMBCI_03613 | 2.3e-193 | yceH | P | Belongs to the TelA family | ||
IJFNMBCI_03614 | 2.4e-215 | naiP | P | Uncharacterised MFS-type transporter YbfB | ||
IJFNMBCI_03615 | 3.9e-229 | proV | 3.6.3.32 | E | glycine betaine | |
IJFNMBCI_03616 | 1.6e-138 | opuAB | P | glycine betaine | ||
IJFNMBCI_03617 | 3.4e-163 | opuAC | E | glycine betaine | ||
IJFNMBCI_03618 | 3.1e-209 | amhX | S | amidohydrolase | ||
IJFNMBCI_03619 | 4.5e-229 | ycgA | S | Membrane | ||
IJFNMBCI_03620 | 3.1e-81 | ycgB | ||||
IJFNMBCI_03621 | 4.4e-269 | amyE | 3.2.1.1 | GH13 | G | alpha-amylase |
IJFNMBCI_03622 | 1.7e-24 | amyE | 3.2.1.1 | GH13 | G | alpha-amylase |
IJFNMBCI_03623 | 3.7e-179 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
IJFNMBCI_03624 | 8.1e-261 | mdr | EGP | Major facilitator Superfamily | ||
IJFNMBCI_03625 | 1.8e-75 | emrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
IJFNMBCI_03626 | 1.4e-113 | ycgF | E | Lysine exporter protein LysE YggA | ||
IJFNMBCI_03627 | 5.8e-151 | yqcI | S | YqcI/YcgG family | ||
IJFNMBCI_03628 | 1.7e-241 | ycgH | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
IJFNMBCI_03629 | 7.6e-114 | ycgI | S | Domain of unknown function (DUF1989) | ||
IJFNMBCI_03630 | 3.1e-150 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
IJFNMBCI_03631 | 1.1e-133 | yvoA | K | transcriptional | ||
IJFNMBCI_03632 | 8e-134 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
IJFNMBCI_03633 | 6.8e-223 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
IJFNMBCI_03634 | 3.4e-169 | 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 | ||
IJFNMBCI_03635 | 2.6e-149 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
IJFNMBCI_03636 | 2.8e-114 | 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 | |
IJFNMBCI_03637 | 4.3e-81 | yvoF | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | ||
IJFNMBCI_03638 | 9.1e-138 | yvpB | NU | protein conserved in bacteria | ||
IJFNMBCI_03639 | 1e-207 | 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 | |
IJFNMBCI_03640 | 5.6e-115 | 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 | |
IJFNMBCI_03641 | 1.6e-233 | 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 | |
IJFNMBCI_03642 | 3.3e-106 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
IJFNMBCI_03643 | 9.6e-115 | 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 | ||
IJFNMBCI_03644 | 2.9e-131 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
IJFNMBCI_03645 | 4.7e-137 | 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 | ||
IJFNMBCI_03646 | 5.6e-112 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | belongs to the PRA-CH family | |
IJFNMBCI_03647 | 0.0 | msbA2 | 3.6.3.44 | V | ABC transporter | |
IJFNMBCI_03648 | 6.1e-58 | |||||
IJFNMBCI_03649 | 2.5e-121 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_03650 | 8e-191 | sasA | T | Histidine kinase | ||
IJFNMBCI_03651 | 1.3e-273 | S | COG0457 FOG TPR repeat | |||
IJFNMBCI_03652 | 5e-124 | usp | CBM50 | M | protein conserved in bacteria | |
IJFNMBCI_03653 | 3.5e-177 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
IJFNMBCI_03654 | 6.5e-87 | yvcI | 3.6.1.55 | F | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
IJFNMBCI_03655 | 1.1e-166 | rapZ | S | Displays ATPase and GTPase activities | ||
IJFNMBCI_03656 | 1.7e-176 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
IJFNMBCI_03657 | 3.1e-170 | whiA | K | May be required for sporulation | ||
IJFNMBCI_03658 | 1.2e-36 | crh | G | Phosphocarrier protein Chr | ||
IJFNMBCI_03659 | 1.3e-142 | nhoA | 2.3.1.118 | Q | Belongs to the arylamine N-acetyltransferase family | |
IJFNMBCI_03660 | 1.6e-79 | M | Ribonuclease | |||
IJFNMBCI_03661 | 4.3e-183 | 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 | |
IJFNMBCI_03662 | 7.4e-106 | ytiB | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
IJFNMBCI_03663 | 1.2e-280 | sulP | P | COG0659 Sulfate permease and related transporters (MFS superfamily) | ||
IJFNMBCI_03664 | 3.4e-52 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
IJFNMBCI_03665 | 3.4e-103 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
IJFNMBCI_03666 | 1.6e-161 | yvdE | K | Transcriptional regulator | ||
IJFNMBCI_03667 | 1.1e-309 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Alpha amylase, N-terminal ig-like domain |
IJFNMBCI_03668 | 2.7e-206 | mdxE | G | COG2182 Maltose-binding periplasmic proteins domains | ||
IJFNMBCI_03669 | 9.1e-221 | malC | P | COG1175 ABC-type sugar transport systems, permease components | ||
IJFNMBCI_03670 | 2.3e-140 | malD | P | transport | ||
IJFNMBCI_03671 | 2.2e-109 | malA | S | Protein of unknown function (DUF1189) | ||
IJFNMBCI_03672 | 0.0 | yvdK | 2.4.1.8 | GH65 | G | Glycoside hydrolase, family 65 |
IJFNMBCI_03673 | 0.0 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
IJFNMBCI_03674 | 1.5e-97 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
IJFNMBCI_03675 | 2.4e-104 | 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 | |
IJFNMBCI_03676 | 1.9e-183 | scrR | K | transcriptional | ||
IJFNMBCI_03677 | 1.6e-219 | rafB | P | LacY proton/sugar symporter | ||
IJFNMBCI_03678 | 1.1e-296 | cscA | 3.2.1.26, 3.2.1.65 | GH32 | G | invertase |
IJFNMBCI_03680 | 8.5e-15 | |||||
IJFNMBCI_03681 | 8.9e-262 | I | Pfam Lipase (class 3) | |||
IJFNMBCI_03682 | 2.9e-16 | S | Protein of unknown function (DUF1433) | |||
IJFNMBCI_03683 | 1.1e-47 | I | Pfam Lipase (class 3) | |||
IJFNMBCI_03684 | 2.4e-40 | S | Protein of unknown function (DUF1433) | |||
IJFNMBCI_03685 | 5e-15 | S | Protein of unknown function (DUF1433) | |||
IJFNMBCI_03686 | 2.3e-54 | MA20_18690 | S | Protein of unknown function (DUF3237) | ||
IJFNMBCI_03687 | 1.6e-93 | padC | Q | Phenolic acid decarboxylase | ||
IJFNMBCI_03688 | 8.4e-287 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
IJFNMBCI_03689 | 1.9e-189 | 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 | ||
IJFNMBCI_03690 | 4.5e-29 | yazB | K | transcriptional | ||
IJFNMBCI_03691 | 9.9e-91 | 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 | |
IJFNMBCI_03692 | 7e-62 | 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 | |
IJFNMBCI_03693 | 6.7e-156 | 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 | |
IJFNMBCI_03694 | 9.4e-161 | pabC | 2.6.1.42, 4.1.3.38 | EH | 4-amino-4-deoxychorismate lyase | |
IJFNMBCI_03695 | 2.3e-107 | pabA | 2.6.1.85, 4.1.3.27 | EH | Anthranilate synthase | |
IJFNMBCI_03696 | 1.2e-269 | 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 | |
IJFNMBCI_03697 | 1.7e-168 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
IJFNMBCI_03698 | 8.5e-154 | yacD | 5.2.1.8 | O | peptidyl-prolyl isomerase | |
IJFNMBCI_03699 | 1.1e-161 | 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 | ||
IJFNMBCI_03700 | 4.8e-145 | coaX | 2.7.1.33 | F | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
IJFNMBCI_03701 | 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 | ||
IJFNMBCI_03702 | 5.1e-93 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
IJFNMBCI_03703 | 7.2e-272 | 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 | |
IJFNMBCI_03704 | 1.1e-184 | KLT | serine threonine protein kinase | |||
IJFNMBCI_03705 | 1.1e-122 | yabS | S | protein containing a von Willebrand factor type A (vWA) domain | ||
IJFNMBCI_03706 | 0.0 | spoIIE | 3.1.3.16, 3.1.3.3 | KT | stage II sporulation protein E | |
IJFNMBCI_03709 | 1.1e-57 | yabR | J | RNA binding protein (contains ribosomal protein S1 domain) | ||
IJFNMBCI_03710 | 1.8e-52 | divIC | D | Septum formation initiator | ||
IJFNMBCI_03711 | 1.4e-102 | yabQ | S | spore cortex biosynthesis protein | ||
IJFNMBCI_03712 | 1.9e-49 | yabP | S | Sporulation protein YabP | ||
IJFNMBCI_03713 | 5.6e-37 | yabO | J | COG1188 Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
IJFNMBCI_03714 | 7.3e-275 | mazG | 3.6.1.66, 3.6.1.9 | S | COG3956 Protein containing tetrapyrrole methyltransferase domain and MazG-like | |
IJFNMBCI_03715 | 5e-282 | yabM | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
IJFNMBCI_03716 | 6.2e-91 | spoVT | K | stage V sporulation protein | ||
IJFNMBCI_03717 | 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 | ||
IJFNMBCI_03718 | 3.7e-40 | yabK | S | Peptide ABC transporter permease | ||
IJFNMBCI_03719 | 4.2e-106 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
IJFNMBCI_03720 | 1.7e-105 | 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 | ||
IJFNMBCI_03721 | 9.4e-175 | 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) | |
IJFNMBCI_03722 | 9.2e-248 | 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 | |
IJFNMBCI_03723 | 1.8e-47 | spoVG | D | Essential for sporulation. Interferes with or is a negative regulator of the pathway leading to asymmetric septation | ||
IJFNMBCI_03724 | 5.1e-63 | yabJ | 3.5.99.10 | J | translation initiation inhibitor, yjgF family | |
IJFNMBCI_03725 | 1.6e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
IJFNMBCI_03726 | 1e-159 | 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 | |
IJFNMBCI_03727 | 2.9e-27 | sspF | S | DNA topological change | ||
IJFNMBCI_03728 | 7.8e-39 | veg | S | protein conserved in bacteria | ||
IJFNMBCI_03729 | 8.4e-146 | yabG | S | peptidase | ||
IJFNMBCI_03730 | 3e-159 | 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 | |
IJFNMBCI_03731 | 2.1e-97 | 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 | |
IJFNMBCI_03732 | 1.8e-232 | rpfB | GH23 | T | protein conserved in bacteria | |
IJFNMBCI_03733 | 3.8e-142 | tatD | L | hydrolase, TatD | ||
IJFNMBCI_03734 | 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 | |
IJFNMBCI_03735 | 8.8e-44 | abrB | K | COG2002 Regulators of stationary sporulation gene expression | ||
IJFNMBCI_03736 | 8.4e-162 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
IJFNMBCI_03737 | 4.7e-48 | yazA | L | endonuclease containing a URI domain | ||
IJFNMBCI_03738 | 1.9e-138 | yabB | 2.1.1.223 | S | Conserved hypothetical protein 95 | |
IJFNMBCI_03739 | 7.7e-37 | yabA | L | Involved in initiation control of chromosome replication | ||
IJFNMBCI_03740 | 8.8e-145 | yaaT | S | stage 0 sporulation protein | ||
IJFNMBCI_03741 | 1.3e-182 | holB | 2.7.7.7 | L | DNA polymerase III | |
IJFNMBCI_03742 | 1.2e-71 | yaaR | S | protein conserved in bacteria | ||
IJFNMBCI_03743 | 7.5e-55 | yaaQ | S | protein conserved in bacteria | ||
IJFNMBCI_03744 | 1.5e-112 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
IJFNMBCI_03745 | 2.2e-268 | adiA | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | Orn Lys Arg decarboxylase | |
IJFNMBCI_03746 | 1e-188 | yaaN | P | Belongs to the TelA family | ||
IJFNMBCI_03747 | 3e-105 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
IJFNMBCI_03748 | 2.2e-30 | csfB | S | Inhibitor of sigma-G Gin | ||
IJFNMBCI_03749 | 1.8e-128 | IQ | reductase | |||
IJFNMBCI_03750 | 2e-247 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |||
IJFNMBCI_03753 | 0.0 | fabD | 1.13.12.16, 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
IJFNMBCI_03754 | 1.6e-94 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
IJFNMBCI_03755 | 2.9e-31 | S | GlpM protein | |||
IJFNMBCI_03756 | 1.6e-193 | namA | 1.6.99.1 | 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 | |
IJFNMBCI_03757 | 1.1e-146 | yqjL | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | ||
IJFNMBCI_03758 | 2.1e-171 | 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 | |
IJFNMBCI_03759 | 2.5e-291 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
IJFNMBCI_03760 | 1.7e-265 | 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 | |
IJFNMBCI_03761 | 1.5e-236 | 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 | |
IJFNMBCI_03762 | 2.4e-25 | yqzJ | ||||
IJFNMBCI_03763 | 4.6e-149 | 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 | ||
IJFNMBCI_03764 | 4.7e-202 | yqjE | 3.4.11.4 | E | COG2195 Di- and tripeptidases | |
IJFNMBCI_03765 | 2.8e-290 | mmdA | 2.1.3.15, 6.4.1.3 | I | COG4799 Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
IJFNMBCI_03766 | 4.2e-74 | mce | 4.4.1.5, 5.1.99.1, 5.4.99.2 | E | COG0346 Lactoylglutathione lyase and related lyases | |
IJFNMBCI_03768 | 3.1e-95 | yqjB | S | protein conserved in bacteria | ||
IJFNMBCI_03769 | 6.3e-171 | yqjA | S | Putative aromatic acid exporter C-terminal domain | ||
IJFNMBCI_03770 | 6.5e-128 | artM | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
IJFNMBCI_03771 | 3.8e-106 | artQ | E | COG0765 ABC-type amino acid transport system, permease component | ||
IJFNMBCI_03772 | 1.2e-135 | artP | ET | Belongs to the bacterial solute-binding protein 3 family | ||
IJFNMBCI_03773 | 1.7e-75 | yqiW | S | Belongs to the UPF0403 family | ||
IJFNMBCI_03774 | 7.7e-171 | yegS | 2.7.1.107 | I | COG1597 Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
IJFNMBCI_03775 | 1.1e-202 | bfmBB | 2.3.1.168, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
IJFNMBCI_03776 | 1e-184 | bfmBAB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
IJFNMBCI_03777 | 8.6e-163 | bfmBAA | 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
IJFNMBCI_03778 | 5.4e-267 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
IJFNMBCI_03779 | 5.7e-208 | buk | 2.7.2.7 | C | Belongs to the acetokinase family | |
IJFNMBCI_03780 | 2e-205 | ldh | 1.4.1.9 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
IJFNMBCI_03781 | 4.3e-153 | pta | 2.3.1.19, 2.3.1.8 | C | phosphate butyryltransferase | |
IJFNMBCI_03782 | 0.0 | bkdR | 2.7.13.3 | KT | Transcriptional regulator | |
IJFNMBCI_03783 | 7e-34 | yqzF | S | Protein of unknown function (DUF2627) | ||
IJFNMBCI_03784 | 3.1e-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 | |
IJFNMBCI_03785 | 7.5e-277 | prpD | 4.2.1.79 | S | 2-methylcitrate dehydratase | |
IJFNMBCI_03786 | 1.5e-205 | prpC | 2.3.3.1, 2.3.3.5 | C | Belongs to the citrate synthase family | |
IJFNMBCI_03787 | 6.1e-205 | mmgC | I | acyl-CoA dehydrogenase | ||
IJFNMBCI_03788 | 1.2e-152 | hbdA | 1.1.1.157 | I | Dehydrogenase | |
IJFNMBCI_03789 | 2.2e-213 | mmgA | 2.3.1.9 | I | Belongs to the thiolase family | |
IJFNMBCI_03790 | 3.7e-134 | yqiK | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
IJFNMBCI_03791 | 1.5e-104 | amiC | 3.5.1.28 | M | Cell wall hydrolase autolysin | |
IJFNMBCI_03792 | 2.5e-17 | |||||
IJFNMBCI_03793 | 2.6e-101 | ytaF | P | Probably functions as a manganese efflux pump | ||
IJFNMBCI_03794 | 1.2e-112 | K | Protein of unknown function (DUF1232) | |||
IJFNMBCI_03796 | 3.3e-183 | 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 | |
IJFNMBCI_03797 | 2e-85 | ydiB | 2.7.1.221, 5.1.1.1 | S | ATPase or kinase | |
IJFNMBCI_03798 | 1.3e-125 | yeaZ | 2.3.1.234 | O | COG1214 Inactive homolog of metal-dependent proteases | |
IJFNMBCI_03799 | 2.4e-83 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
IJFNMBCI_03800 | 3e-190 | 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 | |
IJFNMBCI_03801 | 0.0 | ydiF | S | ABC transporter | ||
IJFNMBCI_03802 | 1.2e-88 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
IJFNMBCI_03803 | 3e-116 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
IJFNMBCI_03804 | 1.7e-18 | 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 | ||
IJFNMBCI_03805 | 1.4e-125 | 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 | ||
IJFNMBCI_03806 | 1.7e-27 | ydiK | S | Domain of unknown function (DUF4305) | ||
IJFNMBCI_03807 | 2.5e-127 | ydiL | S | CAAX protease self-immunity | ||
IJFNMBCI_03808 | 1.3e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
IJFNMBCI_03809 | 7.5e-281 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
IJFNMBCI_03810 | 3.5e-82 | soj | D | AAA domain | ||
IJFNMBCI_03813 | 0.0 | K | NB-ARC domain | |||
IJFNMBCI_03814 | 5.5e-200 | gutB | 1.1.1.14 | E | Dehydrogenase | |
IJFNMBCI_03815 | 8.4e-185 | gutA | G | MFS/sugar transport protein | ||
IJFNMBCI_03816 | 1.7e-48 | gutA | G | MFS/sugar transport protein | ||
IJFNMBCI_03817 | 1.9e-170 | ydjE | 2.7.1.4 | G | pfkB family carbohydrate kinase | |
IJFNMBCI_03818 | 4.3e-31 | yjdJ | S | Domain of unknown function (DUF4306) | ||
IJFNMBCI_03819 | 9.6e-113 | pspA | KT | Phage shock protein A | ||
IJFNMBCI_03820 | 6.8e-179 | ydjG | 3.6.4.12 | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | |
IJFNMBCI_03821 | 2.6e-119 | ydjH | S | COG1512 Beta-propeller domains of methanol dehydrogenase type | ||
IJFNMBCI_03822 | 1.1e-149 | ydjI | S | virion core protein (lumpy skin disease virus) | ||
IJFNMBCI_03823 | 0.0 | yrhL | I | Acyltransferase family | ||
IJFNMBCI_03824 | 5e-143 | rsiV | S | Protein of unknown function (DUF3298) | ||
IJFNMBCI_03825 | 1.6e-85 | sigV | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
IJFNMBCI_03826 | 4e-195 | bdhA | 1.1.1.303, 1.1.1.4 | E | Dehydrogenase | |
IJFNMBCI_03827 | 7.1e-62 | ydjM | M | Lytic transglycolase | ||
IJFNMBCI_03828 | 2.7e-135 | ydjN | U | Involved in the tonB-independent uptake of proteins | ||
IJFNMBCI_03830 | 7.2e-35 | ydjO | S | Cold-inducible protein YdjO | ||
IJFNMBCI_03831 | 0.0 | cotA | 1.10.3.4, 1.16.3.3 | Q | multicopper oxidases | |
IJFNMBCI_03832 | 5.6e-245 | gabP | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
IJFNMBCI_03833 | 4.9e-154 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
IJFNMBCI_03834 | 1.7e-176 | yeaC | S | COG0714 MoxR-like ATPases | ||
IJFNMBCI_03835 | 6.7e-207 | yeaD | S | conserved protein (some members contain a von Willebrand factor type A (vWA) domain) | ||
IJFNMBCI_03836 | 0.0 | yebA | E | COG1305 Transglutaminase-like enzymes | ||
IJFNMBCI_03837 | 2.9e-306 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
IJFNMBCI_03838 | 8.9e-204 | ydbM | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
IJFNMBCI_03839 | 6.1e-52 | ydbL | ||||
IJFNMBCI_03840 | 7.4e-130 | ydbK | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | ||
IJFNMBCI_03841 | 1.1e-172 | ydbJ | V | ABC transporter, ATP-binding protein | ||
IJFNMBCI_03842 | 5.7e-157 | ydbI | S | AI-2E family transporter | ||
IJFNMBCI_03843 | 5e-224 | dctA | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
IJFNMBCI_03844 | 3.9e-119 | dctR | T | COG4565 Response regulator of citrate malate metabolism | ||
IJFNMBCI_03845 | 5.5e-300 | dctS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
IJFNMBCI_03846 | 2.2e-201 | dctB | G | COG1638 TRAP-type C4-dicarboxylate transport system, periplasmic component | ||
IJFNMBCI_03847 | 5.5e-155 | ydbD | P | Catalase | ||
IJFNMBCI_03848 | 4.5e-61 | ydbC | S | Domain of unknown function (DUF4937 | ||
IJFNMBCI_03849 | 3.7e-57 | ydbB | G | Cupin domain | ||
IJFNMBCI_03851 | 1.8e-142 | ydbA | 3.6.3.4, 3.6.3.54 | P | EcsC protein family | |
IJFNMBCI_03852 | 4.1e-54 | yvaE | P | Small Multidrug Resistance protein | ||
IJFNMBCI_03853 | 3.2e-71 | yvaD | S | Family of unknown function (DUF5360) | ||
IJFNMBCI_03854 | 6.5e-34 | ydaT | ||||
IJFNMBCI_03856 | 3.2e-226 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
IJFNMBCI_03857 | 2.1e-39 | |||||
IJFNMBCI_03858 | 2.4e-99 | |||||
IJFNMBCI_03859 | 5.7e-79 | |||||
IJFNMBCI_03861 | 1.6e-11 | |||||
IJFNMBCI_03863 | 8.8e-119 | S | Histidine kinase | |||
IJFNMBCI_03865 | 5.9e-68 | |||||
IJFNMBCI_03866 | 5.3e-48 | xlyA | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
IJFNMBCI_03867 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
IJFNMBCI_03868 | 1.8e-75 | mutT | 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
IJFNMBCI_03869 | 0.0 | ydaO | E | amino acid | ||
IJFNMBCI_03870 | 0.0 | ydaN | S | Bacterial cellulose synthase subunit | ||
IJFNMBCI_03871 | 1e-229 | ydaM | M | Glycosyl transferase family group 2 | ||
IJFNMBCI_03872 | 0.0 | ydaL | S | Uncharacterized protein conserved in bacteria (DUF2334) | ||
IJFNMBCI_03873 | 1.3e-146 | ydaK | T | Diguanylate cyclase, GGDEF domain | ||
IJFNMBCI_03874 | 1.8e-198 | ydaJ | M | Belongs to the glycosyl hydrolase 8 (cellulase D) family | ||
IJFNMBCI_03875 | 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 | |
IJFNMBCI_03876 | 1.5e-74 | lrpC | K | Transcriptional regulator | ||
IJFNMBCI_03877 | 1.3e-47 | ydzA | EGP | Major facilitator Superfamily | ||
IJFNMBCI_03878 | 5.4e-139 | amj | U | Involved in peptidoglycan biosynthesis. Transports lipid-linked peptidoglycan precursors from the inner to the outer leaflet of the cytoplasmic membrane | ||
IJFNMBCI_03879 | 1.4e-77 | ydaG | 1.4.3.5 | S | general stress protein | |
IJFNMBCI_03880 | 2.3e-113 | rimL | 1.1.1.25 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
IJFNMBCI_03881 | 1.3e-93 | MA20_27600 | 5.3.1.15 | S | Cupin 2, conserved barrel domain protein | |
IJFNMBCI_03882 | 4.5e-160 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_03883 | 5.3e-96 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
IJFNMBCI_03884 | 4.2e-177 | yuaG | 3.4.21.72 | S | protein conserved in bacteria | |
IJFNMBCI_03885 | 5.6e-84 | yuaF | OU | Membrane protein implicated in regulation of membrane protease activity | ||
IJFNMBCI_03886 | 2.2e-82 | yuaE | S | DinB superfamily | ||
IJFNMBCI_03887 | 5.5e-109 | yuaD | S | MOSC domain | ||
IJFNMBCI_03888 | 7.1e-228 | gbsB | 1.1.1.1 | C | alcohol dehydrogenase | |
IJFNMBCI_03889 | 8e-282 | gbsA | 1.2.1.8 | C | Belongs to the aldehyde dehydrogenase family | |
IJFNMBCI_03890 | 2.7e-97 | yuaC | K | Belongs to the GbsR family | ||
IJFNMBCI_03891 | 2.1e-94 | yuaB | ||||
IJFNMBCI_03892 | 5.5e-121 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
IJFNMBCI_03893 | 2.5e-147 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
IJFNMBCI_03894 | 4.1e-220 | 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 | |
IJFNMBCI_03895 | 6.2e-122 | G | Cupin | |||
IJFNMBCI_03896 | 8.9e-53 | yjcN | ||||
IJFNMBCI_03898 | 2.3e-145 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
IJFNMBCI_03899 | 4.9e-194 | yubA | S | transporter activity | ||
IJFNMBCI_03900 | 2.1e-185 | ygjR | S | Oxidoreductase | ||
IJFNMBCI_03901 | 4.3e-97 | pfpI | 1.11.1.6, 3.5.1.124 | S | DJ-1/PfpI family | |
IJFNMBCI_03902 | 6.2e-237 | mcpA | NT | chemotaxis protein | ||
IJFNMBCI_03903 | 3.9e-223 | mcpA | NT | chemotaxis protein | ||
IJFNMBCI_03904 | 7.3e-238 | mcpA | NT | chemotaxis protein | ||
IJFNMBCI_03905 | 1.8e-220 | mcpA | NT | chemotaxis protein | ||
IJFNMBCI_03906 | 1.3e-139 | tgl | 2.3.2.13 | S | protein-glutamine gamma-glutamyltransferase activity | |
IJFNMBCI_03907 | 2.5e-17 | |||||
IJFNMBCI_03908 | 1.3e-190 | yrpB | 1.13.12.16 | S | COG2070 Dioxygenases related to 2-nitropropane dioxygenase | |
IJFNMBCI_03909 | 1.5e-76 | yugU | S | Uncharacterised protein family UPF0047 | ||
IJFNMBCI_03910 | 0.0 | yugT | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | COG0366 Glycosidases |
IJFNMBCI_03911 | 3e-232 | yugS | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
IJFNMBCI_03912 | 8.3e-117 | yugP | S | Zn-dependent protease | ||
IJFNMBCI_03913 | 1e-17 | |||||
IJFNMBCI_03914 | 3.9e-27 | mstX | S | Membrane-integrating protein Mistic | ||
IJFNMBCI_03915 | 1.8e-181 | yugO | P | COG1226 Kef-type K transport systems | ||
IJFNMBCI_03916 | 1.7e-72 | yugN | S | YugN-like family | ||
IJFNMBCI_03918 | 8.7e-259 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
IJFNMBCI_03919 | 1.2e-95 | S | NADPH-dependent FMN reductase | |||
IJFNMBCI_03920 | 9.3e-118 | ycaC | Q | Isochorismatase family | ||
IJFNMBCI_03921 | 7.4e-230 | yugK | C | Dehydrogenase | ||
IJFNMBCI_03922 | 3.8e-226 | yugJ | C | oxidoreductases, Fe-dependent alcohol dehydrogenase family | ||
IJFNMBCI_03923 | 1.8e-34 | yuzA | S | Domain of unknown function (DUF378) | ||
IJFNMBCI_03925 | 2e-43 | S | Domain of unknown function with cystatin-like fold (DUF4467) | |||
IJFNMBCI_03926 | 2.7e-56 | yddI | ||||
IJFNMBCI_03927 | 5.9e-159 | yddH | CBM50 | M | Lysozyme-like | |
IJFNMBCI_03928 | 3.6e-207 | yddG | S | maturation of SSU-rRNA | ||
IJFNMBCI_03929 | 3.7e-35 | S | Domain of unknown function (DUF1874) | |||
IJFNMBCI_03930 | 0.0 | yddE | S | AAA-like domain | ||
IJFNMBCI_03931 | 3.6e-75 | yddD | S | TcpE family | ||
IJFNMBCI_03932 | 6.8e-24 | yddC | ||||
IJFNMBCI_03933 | 5.8e-125 | yddB | S | Conjugative transposon protein TcpC | ||
IJFNMBCI_03935 | 6.8e-39 | yddA | ||||
IJFNMBCI_03941 | 9.7e-162 | nicK | L | Replication initiation factor | ||
IJFNMBCI_03942 | 2.5e-243 | ydcQ | D | Ftsk spoiiie family protein | ||
IJFNMBCI_03943 | 8.4e-39 | S | Bacterial protein of unknown function (DUF961) | |||
IJFNMBCI_03945 | 4.1e-13 | |||||
IJFNMBCI_03946 | 1.2e-43 | yvaO | K | Transcriptional | ||
IJFNMBCI_03947 | 8.2e-56 | immA | E | IrrE N-terminal-like domain | ||
IJFNMBCI_03948 | 5.6e-147 | L | Belongs to the 'phage' integrase family | |||
IJFNMBCI_03956 | 1.9e-58 | ydcK | S | Belongs to the SprT family | ||
IJFNMBCI_03957 | 8.4e-14 | |||||
IJFNMBCI_03958 | 0.0 | yhgF | K | COG2183 Transcriptional accessory protein | ||
IJFNMBCI_03959 | 2.4e-107 | rsbX | 3.1.3.16, 3.1.3.3 | KT | Sigma factor PP2C-like phosphatases | |
IJFNMBCI_03960 | 1.4e-139 | sigB | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
IJFNMBCI_03961 | 2.1e-85 | rsbW | 2.7.11.1 | F | 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) | |
IJFNMBCI_03962 | 5.4e-53 | rsbV | T | Belongs to the anti-sigma-factor antagonist family | ||
IJFNMBCI_03963 | 1.7e-187 | rsbU | 3.1.3.3 | KT | phosphatase | |
IJFNMBCI_03964 | 3.8e-69 | rsbT | 2.7.11.1 | T | COG2172 Anti-sigma regulatory factor (Ser Thr protein kinase) | |
IJFNMBCI_03965 | 6.8e-57 | rsbS | T | antagonist | ||
IJFNMBCI_03966 | 1.3e-145 | rsbR | T | Positive regulator of sigma-B | ||
IJFNMBCI_03967 | 2.5e-56 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
IJFNMBCI_03968 | 8.1e-42 | ndoAI | K | transcriptional regulators containing the CopG Arc MetJ DNA-binding domain and a metal-binding domain | ||
IJFNMBCI_03969 | 6.9e-220 | 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 | |
IJFNMBCI_03970 | 2.6e-183 | ydcC | M | COG2834 Outer membrane lipoprotein-sorting protein | ||
IJFNMBCI_03971 | 6.8e-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 | |
IJFNMBCI_03972 | 5.3e-107 | ydcA | 3.4.21.105 | S | membrane protein (homolog of Drosophila rhomboid) | |
IJFNMBCI_03973 | 7.5e-264 | ydbT | S | Membrane | ||
IJFNMBCI_03974 | 4.3e-59 | ydbS | S | Bacterial PH domain | ||
IJFNMBCI_03975 | 2.9e-247 | 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 | |
IJFNMBCI_03976 | 3.1e-256 | 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 | |
IJFNMBCI_03977 | 1e-201 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
IJFNMBCI_03978 | 8.5e-56 | ydbP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
IJFNMBCI_03979 | 8.1e-120 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
IJFNMBCI_03980 | 4.4e-09 | S | Fur-regulated basic protein A | |||
IJFNMBCI_03981 | 1.5e-10 | S | Fur-regulated basic protein B | |||
IJFNMBCI_03982 | 3.2e-270 | dtpT | E | amino acid peptide transporter | ||
IJFNMBCI_03983 | 2.8e-281 | yclG | M | Pectate lyase superfamily protein | ||
IJFNMBCI_03985 | 1.6e-294 | gerKA | EG | Spore germination protein | ||
IJFNMBCI_03986 | 1.7e-232 | gerKC | S | spore germination | ||
IJFNMBCI_03987 | 3.3e-195 | gerKB | F | Spore germination protein | ||
IJFNMBCI_03988 | 4.8e-254 | yxeK | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
IJFNMBCI_03989 | 1.8e-92 | yxeL | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
IJFNMBCI_03990 | 1.8e-142 | yxeM | M | Belongs to the bacterial solute-binding protein 3 family | ||
IJFNMBCI_03991 | 3.5e-115 | yxeN | P | COG0765 ABC-type amino acid transport system, permease component | ||
IJFNMBCI_03992 | 5.4e-133 | yxeO | 3.6.3.21 | P | ABC transporter, ATP-binding protein | |
IJFNMBCI_03993 | 1.9e-217 | yxeP | 3.5.1.47 | E | hydrolase activity | |
IJFNMBCI_03994 | 5.1e-251 | yxeQ | S | MmgE/PrpD family | ||
IJFNMBCI_03995 | 1.7e-122 | yclH | P | ABC transporter | ||
IJFNMBCI_03996 | 1.3e-231 | yclI | V | ABC transporter (permease) YclI | ||
IJFNMBCI_03997 | 5.2e-127 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
IJFNMBCI_03998 | 3e-257 | T | PhoQ Sensor | |||
IJFNMBCI_03999 | 2.3e-79 | S | aspartate phosphatase | |||
IJFNMBCI_04001 | 1e-251 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
IJFNMBCI_04002 | 6.8e-165 | yclN | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_04003 | 1.1e-164 | fatC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
IJFNMBCI_04004 | 6.8e-136 | yclP | 3.6.3.34 | P | ABC transporter, ATP-binding protein | |
IJFNMBCI_04005 | 1.2e-174 | yclQ | P | COG4607 ABC-type enterochelin transport system, periplasmic component | ||
IJFNMBCI_04006 | 6.6e-249 | ycnB | EGP | Major facilitator Superfamily | ||
IJFNMBCI_04007 | 1.2e-152 | ycnC | K | Transcriptional regulator | ||
IJFNMBCI_04008 | 1.4e-133 | nfrA2 | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
IJFNMBCI_04009 | 1.8e-44 | ycnE | S | Monooxygenase | ||
IJFNMBCI_04010 | 8.8e-53 | yczG | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
IJFNMBCI_04011 | 1e-198 | gabR | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
IJFNMBCI_04012 | 3.2e-50 | gabR | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
IJFNMBCI_04013 | 2.5e-218 | gabT | 2.6.1.19, 2.6.1.22 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
IJFNMBCI_04014 | 1.4e-264 | 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 | |
IJFNMBCI_04015 | 1.2e-184 | abrB | S | membrane | ||
IJFNMBCI_04016 | 1e-202 | blt | EGP | Major facilitator Superfamily | ||
IJFNMBCI_04017 | 1.3e-108 | K | QacR-like protein, C-terminal region | |||
IJFNMBCI_04018 | 1.4e-92 | yhjR | S | Rubrerythrin | ||
IJFNMBCI_04019 | 4.3e-124 | ydfS | S | Protein of unknown function (DUF421) | ||
IJFNMBCI_04020 | 0.0 | addB | 3.1.21.3, 3.6.4.12 | L | ATP-dependent helicase deoxyribonuclease subunit B | |
IJFNMBCI_04021 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
IJFNMBCI_04022 | 8.7e-223 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
IJFNMBCI_04023 | 0.0 | sbcC | L | COG0419 ATPase involved in DNA repair | ||
IJFNMBCI_04024 | 1.1e-49 | yisB | V | COG1403 Restriction endonuclease | ||
IJFNMBCI_04025 | 5.9e-32 | gerPF | S | Spore germination protein gerPA/gerPF | ||
IJFNMBCI_04026 | 2.2e-61 | gerPE | S | Spore germination protein GerPE | ||
IJFNMBCI_04027 | 3.1e-23 | gerPD | S | Spore germination protein | ||
IJFNMBCI_04028 | 1.2e-58 | gerPC | S | Spore germination protein | ||
IJFNMBCI_04029 | 5.2e-34 | gerPB | S | cell differentiation | ||
IJFNMBCI_04030 | 8.4e-34 | gerPA | S | Spore germination protein | ||
IJFNMBCI_04031 | 5e-07 | yisI | S | Spo0E like sporulation regulatory protein | ||
IJFNMBCI_04032 | 3.5e-171 | yisK | Q | COG0179 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) | ||
IJFNMBCI_04033 | 3.2e-59 | yisL | S | UPF0344 protein | ||
IJFNMBCI_04034 | 1.5e-97 | yisN | S | Protein of unknown function (DUF2777) | ||
IJFNMBCI_04035 | 0.0 | asnO | 6.3.5.4 | E | Asparagine synthase | |
IJFNMBCI_04036 | 2.1e-129 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | phytoene | |
IJFNMBCI_04037 | 1.5e-245 | yisQ | V | Mate efflux family protein | ||
IJFNMBCI_04038 | 5e-159 | yisR | K | Transcriptional regulator | ||
IJFNMBCI_04039 | 4.1e-144 | purR | K | helix_turn _helix lactose operon repressor | ||
IJFNMBCI_04040 | 1.8e-155 | yisS | 1.1.1.370 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
IJFNMBCI_04042 | 3e-08 | |||||
IJFNMBCI_04045 | 2.4e-211 | D | Ftsk spoiiie family protein | |||
IJFNMBCI_04046 | 1.6e-69 | |||||
IJFNMBCI_04047 | 1.6e-167 | L | Replication initiation factor | |||
IJFNMBCI_04048 | 4e-30 | S | Domain of unknown function (DUF3173) | |||
IJFNMBCI_04049 | 3.6e-209 | L | Phage integrase family | |||
IJFNMBCI_04051 | 8.1e-91 | sigV | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
IJFNMBCI_04052 | 2.3e-257 | S | Domain of unknown function (DUF4179) | |||
IJFNMBCI_04053 | 1.4e-208 | pbuG | S | permease | ||
IJFNMBCI_04054 | 1.2e-122 | yebC | M | Membrane | ||
IJFNMBCI_04056 | 2e-92 | yebE | S | UPF0316 protein | ||
IJFNMBCI_04057 | 6.1e-28 | yebG | S | NETI protein | ||
IJFNMBCI_04058 | 2.5e-83 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
IJFNMBCI_04059 | 6.7e-223 | 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) | |
IJFNMBCI_04060 | 1.6e-246 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
IJFNMBCI_04061 | 2.5e-127 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
IJFNMBCI_04062 | 2.2e-38 | 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 | |
IJFNMBCI_04063 | 3.4e-126 | 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 | |
IJFNMBCI_04064 | 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 | |
IJFNMBCI_04065 | 2.8e-271 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
IJFNMBCI_04066 | 1e-182 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
IJFNMBCI_04067 | 8.3e-105 | 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 | |
IJFNMBCI_04068 | 5.6e-286 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
IJFNMBCI_04069 | 7.7e-233 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
IJFNMBCI_04070 | 2.7e-285 | ydaB | IQ | acyl-CoA ligase | ||
IJFNMBCI_04071 | 0.0 | mtlR | K | transcriptional regulator, MtlR | ||
IJFNMBCI_04072 | 7.5e-174 | ydhF | S | Oxidoreductase | ||
IJFNMBCI_04073 | 0.0 | pbpC | 3.4.16.4 | M | Penicillin-binding Protein | |
IJFNMBCI_04074 | 5.1e-56 | yczJ | S | biosynthesis | ||
IJFNMBCI_04076 | 4.6e-117 | ycsK | E | anatomical structure formation involved in morphogenesis | ||
IJFNMBCI_04077 | 1.5e-130 | kipR | K | Transcriptional regulator | ||
IJFNMBCI_04078 | 1.1e-189 | kipA | 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
IJFNMBCI_04079 | 3.9e-136 | kipI | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
IJFNMBCI_04080 | 7.5e-146 | ycsI | S | Belongs to the D-glutamate cyclase family | ||
IJFNMBCI_04081 | 1e-210 | ycsG | P | COG1914 Mn2 and Fe2 transporters of the NRAMP family | ||
IJFNMBCI_04082 | 6e-140 | ycsF | S | Belongs to the UPF0271 (lamB) family | ||
IJFNMBCI_04083 | 2.3e-136 | ycsE | 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
IJFNMBCI_04084 | 3.5e-67 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
IJFNMBCI_04085 | 7.6e-208 | mtlD | 1.1.1.17 | G | COG0246 Mannitol-1-phosphate altronate dehydrogenases | |
IJFNMBCI_04086 | 1.4e-72 | mtlF | 2.7.1.197 | G | COG4668 Mannitol fructose-specific phosphotransferase system, IIA domain | |
IJFNMBCI_04087 | 2.5e-227 | mtlA | 2.7.1.197 | G | COG2213 Phosphotransferase system, mannitol-specific IIBC component | |
IJFNMBCI_04088 | 6e-55 | |||||
IJFNMBCI_04089 | 1.9e-106 | ycnK | K | COG1349 Transcriptional regulators of sugar metabolism | ||
IJFNMBCI_04090 | 9.4e-300 | ycnJ | P | protein, homolog of Cu resistance protein CopC | ||
IJFNMBCI_04091 | 1.3e-97 | ycnI | S | protein conserved in bacteria | ||
IJFNMBCI_04092 | 1.1e-144 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
IJFNMBCI_04093 | 3.6e-149 | glcU | U | Glucose uptake | ||
IJFNMBCI_04094 | 0.0 | pksJ | Q | Polyketide synthase of type I | ||
IJFNMBCI_04095 | 0.0 | 1.1.1.320 | Q | Polyketide synthase of type I | ||
IJFNMBCI_04096 | 0.0 | Q | Polyketide synthase of type I | |||
IJFNMBCI_04097 | 1e-56 | mpr | S | SprT-like family | ||
IJFNMBCI_04099 | 7.3e-98 | |||||
IJFNMBCI_04100 | 2.3e-51 | repE | K | Primase C terminal 1 (PriCT-1) | ||
IJFNMBCI_04101 | 2.4e-170 | S | COG0433 Predicted ATPase | |||
IJFNMBCI_04102 | 7.1e-47 | S | Replication-relaxation | |||
IJFNMBCI_04104 | 4.1e-10 | S | Conjugative transposon protein TcpC | |||
IJFNMBCI_04107 | 2.9e-90 | yddE | S | AAA-like domain | ||
IJFNMBCI_04109 | 6.5e-17 | M | Psort location CytoplasmicMembrane, score | |||
IJFNMBCI_04110 | 1.2e-21 | |||||
IJFNMBCI_04111 | 1.6e-14 | M | lytic transglycosylase activity | |||
IJFNMBCI_04112 | 9.9e-26 | S | Protein of unknown function (DUF2892) | |||
IJFNMBCI_04113 | 0.0 | yerA | 3.5.4.2 | F | adenine deaminase | |
IJFNMBCI_04114 | 1.7e-187 | yerB | S | Protein of unknown function (DUF3048) C-terminal domain | ||
IJFNMBCI_04115 | 2.4e-50 | yerC | S | protein conserved in bacteria | ||
IJFNMBCI_04116 | 8e-288 | yerD | 1.4.7.1 | E | Belongs to the glutamate synthase family | |
IJFNMBCI_04117 | 3.1e-127 | 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 | ||
IJFNMBCI_04118 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
IJFNMBCI_04119 | 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 | |
IJFNMBCI_04120 | 2.6e-222 | camS | S | COG4851 Protein involved in sex pheromone biosynthesis | ||
IJFNMBCI_04121 | 3e-192 | yerI | S | homoserine kinase type II (protein kinase fold) | ||
IJFNMBCI_04122 | 1.7e-120 | sapB | S | MgtC SapB transporter | ||
IJFNMBCI_04123 | 1.1e-262 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
IJFNMBCI_04124 | 1.6e-45 | 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) | |
IJFNMBCI_04125 | 1.6e-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) | |
IJFNMBCI_04126 | 7.5e-269 | 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) | |
IJFNMBCI_04127 | 1e-136 | L | Tn3 transposase DDE domain | |||
IJFNMBCI_04128 | 0.0 | Q | D-alanine [D-alanyl carrier protein] ligase activity | |||
IJFNMBCI_04129 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
IJFNMBCI_04130 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
IJFNMBCI_04131 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
IJFNMBCI_04132 | 8.9e-273 | dacC | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | |
IJFNMBCI_04133 | 3.8e-187 | yoxA | 5.1.3.3 | G | Aldose 1-epimerase | |
IJFNMBCI_04134 | 7.9e-247 | yoeA | V | MATE efflux family protein | ||
IJFNMBCI_04135 | 1.1e-95 | yoeB | S | IseA DL-endopeptidase inhibitor | ||
IJFNMBCI_04137 | 3.5e-97 | L | Integrase | |||
IJFNMBCI_04138 | 4.2e-16 | |||||
IJFNMBCI_04140 | 2.7e-57 | L | Phage integrase family | |||
IJFNMBCI_04144 | 5.7e-16 | S | Repressor of ComK | |||
IJFNMBCI_04145 | 2.5e-21 | |||||
IJFNMBCI_04149 | 4.9e-77 | S | Histidine kinase | |||
IJFNMBCI_04151 | 1.7e-14 | |||||
IJFNMBCI_04152 | 4.5e-34 | |||||
IJFNMBCI_04153 | 5.4e-26 | padR | K | PadR family transcriptional regulator | ||
IJFNMBCI_04154 | 7e-26 | S | membrane | |||
IJFNMBCI_04155 | 4.9e-07 | |||||
IJFNMBCI_04156 | 1.6e-84 | S | Protein of unknown function (DUF1430) | |||
IJFNMBCI_04157 | 5.7e-64 | V | ABC transporter | |||
IJFNMBCI_04160 | 1.9e-74 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
IJFNMBCI_04161 | 1.1e-92 | yjcG | J | Belongs to the 2H phosphoesterase superfamily. YjcG family | ||
IJFNMBCI_04162 | 7.2e-127 | yjcH | P | COG2382 Enterochelin esterase and related enzymes | ||
IJFNMBCI_04163 | 6.2e-210 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
IJFNMBCI_04164 | 7.7e-211 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
IJFNMBCI_04166 | 6e-191 | L | Belongs to the 'phage' integrase family | |||
IJFNMBCI_04167 | 5.1e-104 | S | Helix-turn-helix domain | |||
IJFNMBCI_04168 | 3.4e-96 | L | Belongs to the 'phage' integrase family | |||
IJFNMBCI_04169 | 1.8e-28 | K | Cro/C1-type HTH DNA-binding domain | |||
IJFNMBCI_04171 | 1.5e-08 | |||||
IJFNMBCI_04173 | 2.4e-15 | K | Cro/C1-type HTH DNA-binding domain | |||
IJFNMBCI_04176 | 1.1e-13 | |||||
IJFNMBCI_04179 | 1.6e-82 | |||||
IJFNMBCI_04180 | 9.3e-139 | |||||
IJFNMBCI_04181 | 3.3e-33 | K | Helix-turn-helix XRE-family like proteins | |||
IJFNMBCI_04182 | 1.8e-10 | |||||
IJFNMBCI_04187 | 1.4e-10 | |||||
IJFNMBCI_04189 | 2.5e-37 | bofA | S | Sigma-K factor-processing regulatory protein BofA | ||
IJFNMBCI_04190 | 3.6e-32 | yaaL | S | Protein of unknown function (DUF2508) | ||
IJFNMBCI_04191 | 2.3e-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 | ||
IJFNMBCI_04192 | 1e-35 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
IJFNMBCI_04193 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
IJFNMBCI_04194 | 3.5e-85 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
IJFNMBCI_04195 | 1.1e-98 | yaaI | Q | COG1335 Amidases related to nicotinamidase | ||
IJFNMBCI_04196 | 1e-208 | yaaH | M | Glycoside Hydrolase Family | ||
IJFNMBCI_04197 | 6.1e-114 | dgk | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxyguanosine kinase | |
IJFNMBCI_04198 | 5.4e-121 | dck | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxycytidine kinase | |
IJFNMBCI_04199 | 1.3e-09 | |||||
IJFNMBCI_04200 | 1.6e-22 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
IJFNMBCI_04201 | 1.8e-165 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
IJFNMBCI_04202 | 1.6e-206 | 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) | |
IJFNMBCI_04203 | 6.1e-108 | 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 | |
IJFNMBCI_04204 | 5.7e-158 | 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 | |
IJFNMBCI_04205 | 2.3e-248 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
IJFNMBCI_04206 | 1.8e-273 | 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 | |
IJFNMBCI_04207 | 2e-183 | yaaC | S | YaaC-like Protein | ||
IJFNMBCI_04208 | 9.1e-71 | M | Transglycosylase SLT domain | |||
IJFNMBCI_04211 | 1.2e-43 | nucA | M | Deoxyribonuclease NucA/NucB | ||
IJFNMBCI_04221 | 3e-30 | radC | L | RadC-like JAB domain | ||
IJFNMBCI_04229 | 3.2e-27 | abrB | K | toxin-antitoxin pair type II binding | ||
IJFNMBCI_04232 | 9.7e-26 | |||||
IJFNMBCI_04235 | 1.3e-26 | traI | 2.5.1.15 | U | relaxase mobilization nuclease domain protein | |
IJFNMBCI_04236 | 3.3e-08 | |||||
IJFNMBCI_04239 | 2.7e-180 | L | Replication protein | |||
IJFNMBCI_04240 | 8.2e-98 | S | COG0457 FOG TPR repeat | |||
IJFNMBCI_04246 | 5e-26 | traI | 2.5.1.15 | U | relaxase mobilization nuclease domain protein | |
IJFNMBCI_04248 | 4.4e-178 | L | Replication protein | |||
IJFNMBCI_04249 | 7.9e-91 | L | Transposase and inactivated derivatives, TnpA family | |||
IJFNMBCI_04250 | 7.1e-85 | L | resolvase | |||
IJFNMBCI_04251 | 6.6e-78 | |||||
IJFNMBCI_04252 | 1.4e-18 | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | ||
IJFNMBCI_04253 | 1.8e-26 | EG | Spore germination protein | |||
IJFNMBCI_04254 | 9e-67 | S | TIGRFAM germination protein, Ger(x)C family | |||
IJFNMBCI_04255 | 1.4e-118 | EG | Spore germination protein | |||
IJFNMBCI_04256 | 6e-26 | S | Protein of unknown function (DUF1657) | |||
IJFNMBCI_04257 | 4.1e-78 | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | |||
IJFNMBCI_04258 | 4.4e-80 | spoVAC | S | stage V sporulation protein AC | ||
IJFNMBCI_04259 | 3.9e-195 | spoVAD | I | Stage V sporulation protein AD | ||
IJFNMBCI_04260 | 6.5e-57 | spoVAE | S | stage V sporulation protein | ||
IJFNMBCI_04261 | 5.8e-29 | S | Protein of unknown function (DUF1657) | |||
IJFNMBCI_04262 | 1.6e-149 | yetF1 | S | membrane | ||
IJFNMBCI_04263 | 1.2e-70 | S | Protein of unknown function (DUF421) | |||
IJFNMBCI_04264 | 5.4e-286 | clsA_1 | I | PLD-like domain | ||
IJFNMBCI_04265 | 1.4e-98 | S | Protein of unknown function (DUF421) | |||
IJFNMBCI_04266 | 3.2e-80 | ipi | S | Intracellular proteinase inhibitor | ||
IJFNMBCI_04267 | 6.6e-148 | yitT | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
IJFNMBCI_04268 | 4.9e-159 | yitS | S | protein conserved in bacteria | ||
IJFNMBCI_04270 | 4e-242 | cypC | 1.11.2.4, 1.14.14.1 | Q | Cytochrome P450 | |
IJFNMBCI_04271 | 1.6e-99 | yvaQ | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | ||
IJFNMBCI_04272 | 3.5e-119 | yvaQ | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | ||
IJFNMBCI_04273 | 1.3e-28 | yufN | S | ABC transporter substrate-binding protein PnrA-like | ||
IJFNMBCI_04274 | 1.5e-125 | yufN | S | ABC transporter substrate-binding protein PnrA-like | ||
IJFNMBCI_04275 | 2.4e-161 | cvfB | S | protein conserved in bacteria | ||
IJFNMBCI_04276 | 4.3e-54 | yajQ | S | Belongs to the UPF0234 family | ||
IJFNMBCI_04277 | 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 | |
IJFNMBCI_04278 | 1.1e-80 | yjcF | S | Acetyltransferase (GNAT) domain | ||
IJFNMBCI_04279 | 4.9e-71 | mcbG | S | Pentapeptide repeats (9 copies) | ||
IJFNMBCI_04280 | 1e-84 | yisT | S | DinB family | ||
IJFNMBCI_04281 | 9.6e-23 | |||||
IJFNMBCI_04284 | 9.9e-37 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
IJFNMBCI_04285 | 1.9e-26 | |||||
IJFNMBCI_04287 | 4.1e-59 | yhcS | 3.4.22.70 | M | COG3764 Sortase (surface protein transpeptidase) | |
IJFNMBCI_04288 | 3.2e-113 | M | Psort location Cellwall, score | |||
IJFNMBCI_04289 | 1.7e-136 | S | Domain of unknown function (DUF5068) | |||
IJFNMBCI_04291 | 2.7e-91 | yhjH | K | helix_turn_helix multiple antibiotic resistance protein | ||
IJFNMBCI_04292 | 1.5e-259 | yhjG | CH | FAD binding domain | ||
IJFNMBCI_04294 | 2.3e-90 | sipV | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
IJFNMBCI_04295 | 9.4e-107 | yhjE | S | SNARE associated Golgi protein | ||
IJFNMBCI_04296 | 1.9e-59 | yhjD | ||||
IJFNMBCI_04297 | 1.4e-27 | yhjC | S | Protein of unknown function (DUF3311) | ||
IJFNMBCI_04298 | 3.2e-267 | yhjB | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
IJFNMBCI_04299 | 3.3e-47 | S | Belongs to the UPF0145 family | |||
IJFNMBCI_04300 | 7.1e-166 | ytnP | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
IJFNMBCI_04301 | 0.0 | sfcA | 1.1.1.38 | C | Malate dehydrogenase | |
IJFNMBCI_04302 | 1.7e-51 | ytzB | S | small secreted protein | ||
IJFNMBCI_04303 | 7.5e-205 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
IJFNMBCI_04304 | 2.1e-35 | K | SpoVT / AbrB like domain | |||
IJFNMBCI_04305 | 5.8e-132 | nodI | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
IJFNMBCI_04306 | 1.2e-124 | S | ABC-2 type transporter | |||
IJFNMBCI_04307 | 1.1e-141 | blm | 3.5.2.6 | S | Belongs to the metallo-beta-lactamase superfamily. Class-B beta-lactamase family | |
IJFNMBCI_04308 | 1.1e-203 | ltrA | L | DNA polymerase | ||
IJFNMBCI_04311 | 1.6e-08 | |||||
IJFNMBCI_04313 | 2.8e-32 | L | Transposase DDE domain |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)