ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
BABJCGNF_00001 | 8.1e-114 | K | Mga helix-turn-helix domain | |||
BABJCGNF_00002 | 5.4e-31 | S | Family of unknown function (DUF5322) | |||
BABJCGNF_00003 | 1e-64 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
BABJCGNF_00004 | 5.7e-109 | XK27_02070 | S | Nitroreductase family | ||
BABJCGNF_00005 | 6e-32 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
BABJCGNF_00006 | 2.4e-101 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
BABJCGNF_00007 | 4e-123 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
BABJCGNF_00008 | 9.5e-29 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
BABJCGNF_00009 | 7.3e-141 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
BABJCGNF_00010 | 4.5e-30 | pyrP | F | Permease | ||
BABJCGNF_00011 | 2.1e-34 | pyrP | F | Permease | ||
BABJCGNF_00012 | 4.5e-21 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
BABJCGNF_00013 | 3.3e-22 | pyrP | F | Permease | ||
BABJCGNF_00014 | 7.9e-36 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
BABJCGNF_00015 | 4.1e-22 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
BABJCGNF_00016 | 4.6e-17 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
BABJCGNF_00017 | 6.4e-176 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
BABJCGNF_00018 | 1.2e-58 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
BABJCGNF_00019 | 5.2e-30 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
BABJCGNF_00020 | 8.6e-73 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
BABJCGNF_00021 | 1.6e-33 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
BABJCGNF_00022 | 1.8e-19 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
BABJCGNF_00023 | 1.9e-14 | pfoS | S | Phosphotransferase system, EIIC | ||
BABJCGNF_00024 | 1.2e-39 | 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) | |
BABJCGNF_00025 | 4.8e-26 | 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) | |
BABJCGNF_00027 | 5.3e-33 | soj | D | Sporulation initiation inhibitor | ||
BABJCGNF_00028 | 4.5e-144 | spo0J | K | Belongs to the ParB family | ||
BABJCGNF_00029 | 3.7e-25 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
BABJCGNF_00030 | 2.6e-44 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
BABJCGNF_00031 | 3.5e-07 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
BABJCGNF_00032 | 1.6e-20 | FbpA | K | Fibronectin-binding protein | ||
BABJCGNF_00033 | 7.1e-32 | FbpA | K | Fibronectin-binding protein | ||
BABJCGNF_00034 | 5.4e-71 | degV | S | EDD domain protein, DegV family | ||
BABJCGNF_00035 | 3.1e-72 | degV | S | EDD domain protein, DegV family | ||
BABJCGNF_00037 | 7.4e-35 | 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 | |
BABJCGNF_00038 | 1.4e-18 | 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 | |
BABJCGNF_00039 | 3.7e-66 | |||||
BABJCGNF_00040 | 8.7e-14 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
BABJCGNF_00041 | 2.4e-110 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
BABJCGNF_00042 | 1.3e-85 | noc | K | Belongs to the ParB family | ||
BABJCGNF_00043 | 1.2e-15 | noc | K | Belongs to the ParB family | ||
BABJCGNF_00044 | 6.6e-19 | noc | K | Belongs to the ParB family | ||
BABJCGNF_00045 | 3.8e-54 | 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 | |
BABJCGNF_00046 | 8e-25 | 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 | |
BABJCGNF_00047 | 1e-113 | 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 | ||
BABJCGNF_00048 | 7.3e-68 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
BABJCGNF_00049 | 6.2e-30 | hisF | 3.5.4.19, 3.6.1.31 | 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 | |
BABJCGNF_00050 | 7e-40 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
BABJCGNF_00051 | 4.1e-41 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
BABJCGNF_00052 | 6.3e-45 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
BABJCGNF_00053 | 1.8e-36 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
BABJCGNF_00054 | 4.1e-11 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
BABJCGNF_00055 | 9.2e-44 | hisF | 3.5.4.19, 3.6.1.31 | 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 | |
BABJCGNF_00056 | 5.3e-27 | nfnB | 1.5.1.34 | C | Nitroreductase family | |
BABJCGNF_00057 | 1.3e-102 | Q | Fumarylacetoacetate (FAA) hydrolase family | |||
BABJCGNF_00058 | 2.7e-15 | K | Acetyltransferase (GNAT) domain | |||
BABJCGNF_00059 | 1.6e-20 | nfnB | 1.5.1.34 | C | Nitroreductase family | |
BABJCGNF_00060 | 9e-25 | msi198 | K | Acetyltransferase (GNAT) domain | ||
BABJCGNF_00061 | 6.7e-26 | EGP | Transmembrane secretion effector | |||
BABJCGNF_00062 | 3.5e-29 | S | Protein conserved in bacteria | |||
BABJCGNF_00063 | 2.5e-29 | |||||
BABJCGNF_00064 | 1.1e-60 | asp23 | S | Asp23 family, cell envelope-related function | ||
BABJCGNF_00065 | 7.9e-65 | asp2 | S | Asp23 family, cell envelope-related function | ||
BABJCGNF_00066 | 5.4e-129 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
BABJCGNF_00067 | 5.9e-77 | S | Protein of unknown function (DUF969) | |||
BABJCGNF_00068 | 6.9e-140 | S | Protein of unknown function (DUF979) | |||
BABJCGNF_00069 | 2.7e-117 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
BABJCGNF_00070 | 1.3e-79 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
BABJCGNF_00072 | 1.1e-122 | cobQ | S | glutamine amidotransferase | ||
BABJCGNF_00073 | 4.2e-12 | T | Histidine kinase-like ATPases | |||
BABJCGNF_00074 | 1.4e-26 | T | Transcriptional regulatory protein, C terminal | |||
BABJCGNF_00075 | 2.1e-64 | ysaB | V | FtsX-like permease family | ||
BABJCGNF_00076 | 1.6e-25 | ysaB | V | FtsX-like permease family | ||
BABJCGNF_00077 | 6e-65 | ysaB | V | FtsX-like permease family | ||
BABJCGNF_00078 | 1e-134 | XK27_05695 | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_00079 | 2.5e-45 | xerS | L | Belongs to the 'phage' integrase family | ||
BABJCGNF_00080 | 4.2e-55 | xerS | L | Belongs to the 'phage' integrase family | ||
BABJCGNF_00081 | 7.9e-64 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
BABJCGNF_00082 | 1.1e-34 | K | LysR substrate binding domain | |||
BABJCGNF_00083 | 4.4e-123 | K | LysR substrate binding domain | |||
BABJCGNF_00084 | 8.9e-80 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
BABJCGNF_00085 | 1.5e-42 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
BABJCGNF_00086 | 1.8e-46 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
BABJCGNF_00087 | 9.1e-71 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
BABJCGNF_00088 | 6.4e-38 | S | Transglycosylase associated protein | |||
BABJCGNF_00089 | 1e-32 | S | Protein conserved in bacteria | |||
BABJCGNF_00090 | 2.9e-27 | 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 | |
BABJCGNF_00091 | 2.1e-32 | 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 | |
BABJCGNF_00092 | 4.7e-52 | 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 | |
BABJCGNF_00093 | 6e-111 | 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 | |
BABJCGNF_00094 | 1.1e-46 | 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 | |
BABJCGNF_00095 | 6.3e-13 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
BABJCGNF_00096 | 3.9e-99 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
BABJCGNF_00097 | 4.3e-66 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
BABJCGNF_00098 | 3.3e-08 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
BABJCGNF_00099 | 1.9e-122 | 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 | ||
BABJCGNF_00100 | 4.6e-123 | 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 | ||
BABJCGNF_00101 | 9.6e-174 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
BABJCGNF_00102 | 5e-63 | 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 | |
BABJCGNF_00103 | 1.7e-22 | 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 | |
BABJCGNF_00104 | 1.2e-69 | 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 | |
BABJCGNF_00105 | 1.1e-47 | 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 | |
BABJCGNF_00106 | 9.1e-50 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
BABJCGNF_00107 | 3.6e-83 | |||||
BABJCGNF_00108 | 1.1e-75 | S | TPM domain | |||
BABJCGNF_00109 | 4.1e-78 | S | TPM domain | |||
BABJCGNF_00110 | 1.9e-23 | S | TPM domain | |||
BABJCGNF_00111 | 2.1e-18 | yxaA | S | Sulfite exporter TauE/SafE | ||
BABJCGNF_00112 | 5.1e-100 | yxaA | S | Sulfite exporter TauE/SafE | ||
BABJCGNF_00113 | 3.8e-55 | ywjH | S | Protein of unknown function (DUF1634) | ||
BABJCGNF_00115 | 6.5e-30 | |||||
BABJCGNF_00116 | 9.1e-29 | |||||
BABJCGNF_00117 | 1.3e-77 | fld | C | Flavodoxin | ||
BABJCGNF_00118 | 7.4e-167 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
BABJCGNF_00119 | 5.1e-80 | dprA | LU | DNA protecting protein DprA | ||
BABJCGNF_00120 | 2.9e-58 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
BABJCGNF_00121 | 6.7e-37 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
BABJCGNF_00122 | 1.2e-126 | S | Domain of unknown function (DUF4918) | |||
BABJCGNF_00130 | 1.5e-09 | S | Psort location Cytoplasmic, score 8.87 | |||
BABJCGNF_00131 | 3.1e-23 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
BABJCGNF_00132 | 1.8e-57 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
BABJCGNF_00133 | 2.2e-66 | msrA | 1.8.4.11, 1.8.4.12 | C | 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 | |
BABJCGNF_00134 | 1.8e-47 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
BABJCGNF_00135 | 1.8e-66 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
BABJCGNF_00136 | 6.3e-20 | hly | S | protein, hemolysin III | ||
BABJCGNF_00137 | 3.1e-152 | 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 | |
BABJCGNF_00138 | 6.9e-43 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
BABJCGNF_00139 | 4.1e-40 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
BABJCGNF_00140 | 1.8e-41 | hly | S | protein, hemolysin III | ||
BABJCGNF_00141 | 5.7e-133 | yfmR | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_00142 | 1e-30 | |||||
BABJCGNF_00143 | 2.5e-33 | |||||
BABJCGNF_00144 | 3e-25 | 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 | |
BABJCGNF_00145 | 3.8e-52 | 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 | |
BABJCGNF_00146 | 4e-156 | nox | 1.6.3.4 | C | NADH oxidase | |
BABJCGNF_00147 | 1.1e-65 | S | Tetratricopeptide repeat protein | |||
BABJCGNF_00148 | 1.2e-64 | S | Tetratricopeptide repeat protein | |||
BABJCGNF_00149 | 2e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
BABJCGNF_00150 | 1.5e-65 | S | Tetratricopeptide repeat protein | |||
BABJCGNF_00151 | 3.4e-98 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
BABJCGNF_00152 | 1.5e-65 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
BABJCGNF_00153 | 9.9e-53 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
BABJCGNF_00154 | 5.5e-11 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
BABJCGNF_00155 | 1e-15 | 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 | |
BABJCGNF_00156 | 1.6e-218 | fnq20 | 1.13.12.16 | S | FAD-NAD(P)-binding | |
BABJCGNF_00157 | 7.7e-51 | fnq20 | 1.13.12.16 | S | FAD-NAD(P)-binding | |
BABJCGNF_00158 | 2.9e-31 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
BABJCGNF_00159 | 3.6e-18 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
BABJCGNF_00160 | 5e-16 | 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 | |||
BABJCGNF_00161 | 1.7e-09 | 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 | ||
BABJCGNF_00162 | 7.5e-75 | 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 | ||
BABJCGNF_00163 | 3.4e-67 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
BABJCGNF_00164 | 2.9e-91 | xerD | D | recombinase XerD | ||
BABJCGNF_00165 | 6.5e-08 | |||||
BABJCGNF_00166 | 2.4e-85 | |||||
BABJCGNF_00167 | 3.7e-86 | |||||
BABJCGNF_00168 | 1.5e-86 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_00169 | 1.2e-74 | |||||
BABJCGNF_00170 | 3.7e-35 | S | NUDIX domain | |||
BABJCGNF_00171 | 5.7e-30 | S | NUDIX domain | |||
BABJCGNF_00172 | 8.8e-31 | S | nuclear-transcribed mRNA catabolic process, no-go decay | |||
BABJCGNF_00173 | 6e-84 | V | Best Blastp hit gi 7514214 pir G75157 'abc transporter, ATP-binding protein, puta tive PAB2069 - Pyrococcus abyssi (strain Orsay)' gi 5457852 emb CAB49342.1 '(AJ248284) ABC transporter, ATP-binding protein, puta tive Pyrococcus abyssi ', score 77, E-value 3.00E-13 | |||
BABJCGNF_00174 | 1.9e-66 | yeaL | S | Protein of unknown function (DUF441) | ||
BABJCGNF_00175 | 8.6e-128 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
BABJCGNF_00176 | 6.9e-31 | dnaE | 2.7.7.7 | L | DNA polymerase | |
BABJCGNF_00177 | 5e-174 | dnaE | 2.7.7.7 | L | DNA polymerase | |
BABJCGNF_00178 | 2.1e-16 | cpdB | 3.1.3.6, 3.1.4.16 | F | 5'-nucleotidase, C-terminal domain | |
BABJCGNF_00179 | 2.2e-107 | |||||
BABJCGNF_00180 | 1.6e-26 | |||||
BABJCGNF_00182 | 9e-08 | dnaE | 2.7.7.7 | L | DNA polymerase | |
BABJCGNF_00183 | 9.8e-49 | dnaE | 2.7.7.7 | L | DNA polymerase | |
BABJCGNF_00184 | 4.2e-144 | cpdB | 3.1.3.6, 3.1.4.16 | F | 5'-nucleotidase, C-terminal domain | |
BABJCGNF_00185 | 2.1e-27 | M1-874 | K | Domain of unknown function (DUF1836) | ||
BABJCGNF_00186 | 1.5e-40 | M1-874 | K | Domain of unknown function (DUF1836) | ||
BABJCGNF_00187 | 2.5e-50 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
BABJCGNF_00188 | 8.9e-69 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
BABJCGNF_00190 | 2.3e-11 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
BABJCGNF_00191 | 1.5e-24 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
BABJCGNF_00192 | 1.7e-119 | oatA | I | Acyltransferase | ||
BABJCGNF_00193 | 3.3e-83 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
BABJCGNF_00194 | 6.1e-50 | 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 | ||
BABJCGNF_00195 | 1.6e-33 | oatA | I | Acyltransferase | ||
BABJCGNF_00196 | 7.2e-203 | oppA | E | ABC transporter, substratebinding protein | ||
BABJCGNF_00197 | 6.4e-63 | fruR | K | DeoR C terminal sensor domain | ||
BABJCGNF_00198 | 7.9e-64 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
BABJCGNF_00199 | 7.6e-191 | 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 | ||
BABJCGNF_00200 | 8.7e-32 | 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 | ||
BABJCGNF_00201 | 8e-79 | 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 | ||
BABJCGNF_00202 | 1.6e-27 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BABJCGNF_00203 | 3.3e-11 | glnPH2 | P | ABC transporter permease | ||
BABJCGNF_00204 | 7.7e-53 | glnPH2 | P | ABC transporter permease | ||
BABJCGNF_00205 | 3.3e-40 | glnPH2 | P | ABC transporter permease | ||
BABJCGNF_00206 | 9.1e-43 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
BABJCGNF_00207 | 1e-47 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
BABJCGNF_00209 | 2e-163 | 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 | ||
BABJCGNF_00210 | 1.9e-56 | 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 | ||
BABJCGNF_00211 | 1.3e-44 | 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 | ||
BABJCGNF_00212 | 8.9e-66 | 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 | ||
BABJCGNF_00213 | 3.3e-22 | yknV | V | ABC transporter | ||
BABJCGNF_00214 | 3.5e-210 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
BABJCGNF_00215 | 4.2e-49 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
BABJCGNF_00216 | 2.7e-115 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
BABJCGNF_00217 | 4.5e-53 | oppA | E | ABC transporter, substratebinding protein | ||
BABJCGNF_00218 | 2.3e-31 | yknV | V | ABC transporter | ||
BABJCGNF_00219 | 1.3e-63 | cobB | K | Sir2 family | ||
BABJCGNF_00220 | 3.9e-50 | pcaC | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
BABJCGNF_00221 | 6.9e-30 | rmeD | K | helix_turn_helix, mercury resistance | ||
BABJCGNF_00222 | 1.4e-19 | yknV | V | ABC transporter | ||
BABJCGNF_00223 | 6.8e-67 | yknV | V | ABC transporter | ||
BABJCGNF_00224 | 3.5e-79 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
BABJCGNF_00225 | 9.2e-29 | M | Protein of unknown function (DUF3737) | |||
BABJCGNF_00226 | 1.4e-18 | M | Protein of unknown function (DUF3737) | |||
BABJCGNF_00227 | 2e-14 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
BABJCGNF_00228 | 4.1e-96 | S | Tetratricopeptide repeat | |||
BABJCGNF_00229 | 2.9e-213 | rnjB | J | 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 | ||
BABJCGNF_00230 | 2.9e-27 | rnjB | J | 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 | ||
BABJCGNF_00231 | 3e-11 | S | Tetratricopeptide repeat | |||
BABJCGNF_00232 | 6e-18 | |||||
BABJCGNF_00233 | 1.9e-39 | |||||
BABJCGNF_00234 | 9.9e-33 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
BABJCGNF_00235 | 9.2e-72 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
BABJCGNF_00236 | 7.4e-164 | ylbL | T | Belongs to the peptidase S16 family | ||
BABJCGNF_00237 | 7.9e-20 | ylbL | T | Belongs to the peptidase S16 family | ||
BABJCGNF_00238 | 1.6e-40 | comEA | L | Competence protein ComEA | ||
BABJCGNF_00239 | 9e-69 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
BABJCGNF_00240 | 6e-45 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
BABJCGNF_00241 | 8.2e-107 | 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 | |
BABJCGNF_00242 | 3.1e-72 | ftsW | D | Belongs to the SEDS family | ||
BABJCGNF_00243 | 0.0 | typA | T | GTP-binding protein TypA | ||
BABJCGNF_00244 | 5.5e-44 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
BABJCGNF_00245 | 1.4e-46 | yktA | S | Belongs to the UPF0223 family | ||
BABJCGNF_00246 | 3.1e-20 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
BABJCGNF_00247 | 1.2e-88 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
BABJCGNF_00248 | 3.6e-16 | |||||
BABJCGNF_00249 | 1.8e-37 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
BABJCGNF_00250 | 2.4e-43 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
BABJCGNF_00251 | 1.5e-83 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
BABJCGNF_00252 | 9.4e-181 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
BABJCGNF_00253 | 5.7e-63 | S | E1-E2 ATPase | |||
BABJCGNF_00254 | 6.7e-73 | |||||
BABJCGNF_00255 | 5.9e-08 | |||||
BABJCGNF_00256 | 3.8e-21 | |||||
BABJCGNF_00257 | 1.2e-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 | |
BABJCGNF_00258 | 4.2e-30 | rnjA | J | 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 | ||
BABJCGNF_00259 | 1.4e-138 | rnjA | J | 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 | ||
BABJCGNF_00260 | 4.4e-47 | rnjA | J | 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 | ||
BABJCGNF_00261 | 1.1e-29 | V | ATPase activity | |||
BABJCGNF_00263 | 3.4e-12 | els | S | Sterol carrier protein domain | ||
BABJCGNF_00264 | 2.7e-182 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
BABJCGNF_00265 | 7e-66 | 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 | |
BABJCGNF_00266 | 6.5e-56 | 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 | |
BABJCGNF_00267 | 1.1e-23 | 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 | |
BABJCGNF_00268 | 1.1e-19 | S | Repeat protein | |||
BABJCGNF_00270 | 1.2e-100 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
BABJCGNF_00271 | 2.8e-46 | S | Repeat protein | |||
BABJCGNF_00272 | 5.1e-44 | uvrA2 | L | ABC transporter | ||
BABJCGNF_00273 | 1.3e-218 | 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 | |
BABJCGNF_00274 | 2e-37 | uvrA2 | L | ABC transporter | ||
BABJCGNF_00277 | 1.2e-26 | |||||
BABJCGNF_00278 | 3.1e-12 | |||||
BABJCGNF_00279 | 2.6e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
BABJCGNF_00280 | 1.3e-17 | 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 | |
BABJCGNF_00281 | 6.6e-27 | 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 | |
BABJCGNF_00282 | 3.8e-22 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
BABJCGNF_00283 | 5.3e-23 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
BABJCGNF_00284 | 9e-33 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
BABJCGNF_00285 | 3.8e-96 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
BABJCGNF_00286 | 4.3e-09 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
BABJCGNF_00287 | 3.4e-08 | yaaN | P | Toxic anion resistance protein (TelA) | ||
BABJCGNF_00288 | 7e-56 | ydiC1 | EGP | Major facilitator Superfamily | ||
BABJCGNF_00289 | 4.9e-44 | 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) | |
BABJCGNF_00290 | 8.2e-37 | cspA | K | Cold shock protein | ||
BABJCGNF_00291 | 1.6e-51 | pstS | P | Phosphate | ||
BABJCGNF_00292 | 1.2e-21 | 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) | |
BABJCGNF_00293 | 1.2e-46 | bmr3 | EGP | Major facilitator Superfamily | ||
BABJCGNF_00295 | 2.7e-34 | 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) | |
BABJCGNF_00296 | 8.7e-42 | 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) | |
BABJCGNF_00297 | 1.6e-38 | divIVA | D | DivIVA protein | ||
BABJCGNF_00298 | 1.2e-08 | 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) | |
BABJCGNF_00299 | 2.3e-60 | ylmH | S | S4 domain protein | ||
BABJCGNF_00300 | 2.2e-55 | 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 | ||
BABJCGNF_00301 | 1.8e-102 | 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 | ||
BABJCGNF_00302 | 1.6e-20 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
BABJCGNF_00303 | 6.3e-181 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
BABJCGNF_00304 | 9.4e-43 | 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) |
BABJCGNF_00305 | 1e-23 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
BABJCGNF_00306 | 2e-40 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
BABJCGNF_00307 | 1.1e-22 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
BABJCGNF_00308 | 4.8e-51 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
BABJCGNF_00309 | 8.7e-161 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase superfamily domain | |
BABJCGNF_00310 | 3.8e-115 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
BABJCGNF_00311 | 3.8e-23 | bmr3 | EGP | Major facilitator Superfamily | ||
BABJCGNF_00312 | 6.1e-98 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
BABJCGNF_00313 | 6.2e-58 | ftsL | D | cell division protein FtsL | ||
BABJCGNF_00314 | 1.2e-83 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
BABJCGNF_00315 | 2.2e-37 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
BABJCGNF_00316 | 1.1e-07 | S | Protein of unknown function (DUF4044) | |||
BABJCGNF_00317 | 5e-26 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
BABJCGNF_00318 | 3.1e-50 | artQ | P | ABC transporter permease | ||
BABJCGNF_00319 | 2.9e-111 | glnQ | 3.6.3.21 | E | ABC transporter | |
BABJCGNF_00320 | 5e-29 | aatB | ET | ABC transporter substrate-binding protein | ||
BABJCGNF_00321 | 4.1e-68 | aatB | ET | ABC transporter substrate-binding protein | ||
BABJCGNF_00322 | 9.4e-29 | minD | D | Belongs to the ParA family | ||
BABJCGNF_00323 | 1.7e-35 | mreD | M | rod shape-determining protein MreD | ||
BABJCGNF_00324 | 1.3e-171 | sgaT | 2.7.1.194 | S | PTS system sugar-specific permease component | |
BABJCGNF_00325 | 2.9e-68 | mreC | M | Involved in formation and maintenance of cell shape | ||
BABJCGNF_00326 | 4e-23 | mreC | M | Involved in formation and maintenance of cell shape | ||
BABJCGNF_00327 | 8.6e-37 | S | Haloacid dehalogenase-like hydrolase | |||
BABJCGNF_00328 | 3.8e-61 | radC | L | DNA repair protein | ||
BABJCGNF_00329 | 1.2e-42 | radC | L | DNA repair protein | ||
BABJCGNF_00330 | 1.1e-40 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
BABJCGNF_00331 | 1.4e-32 | 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 | |
BABJCGNF_00332 | 2.1e-86 | 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 | |
BABJCGNF_00333 | 1.2e-99 | 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 | |
BABJCGNF_00334 | 1.3e-24 | 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 | |
BABJCGNF_00335 | 1e-30 | 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 | |
BABJCGNF_00336 | 3e-13 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BABJCGNF_00337 | 4.2e-40 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BABJCGNF_00338 | 4.7e-20 | K | DeoR C terminal sensor domain | |||
BABJCGNF_00339 | 8.1e-82 | K | DeoR C terminal sensor domain | |||
BABJCGNF_00340 | 8.9e-259 | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
BABJCGNF_00341 | 3.9e-12 | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
BABJCGNF_00342 | 1.2e-157 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
BABJCGNF_00343 | 6.6e-45 | 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 | |
BABJCGNF_00344 | 2.6e-161 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
BABJCGNF_00345 | 1.7e-169 | 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 | ||
BABJCGNF_00346 | 1.3e-29 | 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 | ||
BABJCGNF_00347 | 4e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
BABJCGNF_00350 | 1.7e-96 | |||||
BABJCGNF_00352 | 5.2e-121 | yqcC | S | WxL domain surface cell wall-binding | ||
BABJCGNF_00353 | 4.3e-136 | ynjC | S | Cell surface protein | ||
BABJCGNF_00355 | 2.2e-46 | L | Mga helix-turn-helix domain | |||
BABJCGNF_00356 | 1.8e-212 | L | Mga helix-turn-helix domain | |||
BABJCGNF_00357 | 5.4e-149 | yhaI | S | Protein of unknown function (DUF805) | ||
BABJCGNF_00358 | 6.1e-57 | |||||
BABJCGNF_00359 | 3.8e-82 | rarA | L | recombination factor protein RarA | ||
BABJCGNF_00360 | 1.2e-35 | rarA | L | recombination factor protein RarA | ||
BABJCGNF_00361 | 6.3e-102 | rarA | L | recombination factor protein RarA | ||
BABJCGNF_00362 | 1e-117 | KL | Helicase conserved C-terminal domain | |||
BABJCGNF_00363 | 2.4e-74 | dcm | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
BABJCGNF_00364 | 3.6e-38 | S | Domain of unknown function (DUF1998) | |||
BABJCGNF_00365 | 3.2e-29 | S | Domain of unknown function (DUF1998) | |||
BABJCGNF_00366 | 2.2e-26 | steT | E | Amino acid permease | ||
BABJCGNF_00367 | 8.1e-13 | puuD | S | peptidase C26 | ||
BABJCGNF_00368 | 2.9e-63 | yhgF | K | Tex-like protein N-terminal domain protein | ||
BABJCGNF_00369 | 1.2e-121 | yhgF | K | Tex-like protein N-terminal domain protein | ||
BABJCGNF_00370 | 8.6e-30 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
BABJCGNF_00371 | 1.7e-09 | |||||
BABJCGNF_00372 | 6.9e-29 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
BABJCGNF_00373 | 2.3e-66 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
BABJCGNF_00374 | 1.9e-44 | |||||
BABJCGNF_00375 | 2.3e-39 | |||||
BABJCGNF_00376 | 8e-21 | |||||
BABJCGNF_00377 | 4.4e-29 | |||||
BABJCGNF_00378 | 1.1e-49 | yvfR | V | ABC transporter | ||
BABJCGNF_00379 | 8.6e-17 | yvfS | V | ABC-2 type transporter | ||
BABJCGNF_00380 | 2.2e-22 | desK | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_00381 | 2e-65 | K | Acetyltransferase (GNAT) domain | |||
BABJCGNF_00382 | 5e-145 | S | Uncharacterised protein, DegV family COG1307 | |||
BABJCGNF_00383 | 8.1e-132 | pbuO | S | permease | ||
BABJCGNF_00384 | 2.4e-28 | S | DsrE/DsrF-like family | |||
BABJCGNF_00385 | 1e-78 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
BABJCGNF_00386 | 2.4e-25 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
BABJCGNF_00387 | 4.8e-16 | K | Transcriptional regulator | |||
BABJCGNF_00388 | 7.7e-45 | yphH | S | Cupin domain | ||
BABJCGNF_00389 | 1.9e-28 | S | ABC-2 family transporter protein | |||
BABJCGNF_00390 | 8.9e-56 | K | Transcriptional regulator | |||
BABJCGNF_00391 | 6.1e-24 | T | Transcriptional regulatory protein, C terminal | |||
BABJCGNF_00392 | 9.5e-26 | T | Transcriptional regulatory protein, C terminal | |||
BABJCGNF_00393 | 1.3e-82 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
BABJCGNF_00394 | 8.9e-102 | oppA | E | ABC transporter, substratebinding protein | ||
BABJCGNF_00395 | 2.3e-84 | oppA | E | ABC transporter, substratebinding protein | ||
BABJCGNF_00396 | 1.2e-40 | oppA | E | ABC transporter, substratebinding protein | ||
BABJCGNF_00397 | 6.1e-52 | T | GHKL domain | |||
BABJCGNF_00398 | 2.5e-54 | T | GHKL domain | |||
BABJCGNF_00399 | 3.2e-86 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
BABJCGNF_00400 | 8.1e-102 | pnuC | H | nicotinamide mononucleotide transporter | ||
BABJCGNF_00402 | 2.6e-45 | ypaA | S | Protein of unknown function (DUF1304) | ||
BABJCGNF_00403 | 4.4e-53 | S | Protein of unknown function (DUF1516) | |||
BABJCGNF_00404 | 2.2e-58 | IQ | NAD dependent epimerase/dehydratase family | |||
BABJCGNF_00405 | 4.4e-62 | 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 | |
BABJCGNF_00406 | 2.7e-37 | 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 | |
BABJCGNF_00407 | 8.3e-40 | IQ | NAD dependent epimerase/dehydratase family | |||
BABJCGNF_00408 | 1.4e-21 | G | Phosphoglycerate mutase family | |||
BABJCGNF_00409 | 2.8e-52 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
BABJCGNF_00410 | 9.7e-49 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
BABJCGNF_00411 | 1.1e-53 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
BABJCGNF_00412 | 2.3e-72 | yueI | S | Protein of unknown function (DUF1694) | ||
BABJCGNF_00413 | 6.6e-53 | 6.3.2.2, 6.3.2.4 | M | Mur ligase middle domain protein | ||
BABJCGNF_00414 | 4.4e-17 | rarA | L | recombination factor protein RarA | ||
BABJCGNF_00415 | 3.5e-52 | K | UTRA | |||
BABJCGNF_00416 | 7.1e-14 | |||||
BABJCGNF_00417 | 8.5e-16 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
BABJCGNF_00418 | 1.9e-66 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
BABJCGNF_00419 | 5.1e-25 | |||||
BABJCGNF_00420 | 4.2e-08 | yueI | S | Protein of unknown function (DUF1694) | ||
BABJCGNF_00421 | 8.6e-50 | yueI | S | Protein of unknown function (DUF1694) | ||
BABJCGNF_00422 | 1.7e-34 | S | Protein of unknown function (DUF2785) | |||
BABJCGNF_00423 | 1.4e-14 | S | Protein of unknown function (DUF2785) | |||
BABJCGNF_00424 | 3.5e-117 | csdA | 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 | |
BABJCGNF_00425 | 2e-40 | nifU | C | SUF system FeS assembly protein, NifU family | ||
BABJCGNF_00426 | 7.5e-21 | nifU | C | SUF system FeS assembly protein, NifU family | ||
BABJCGNF_00427 | 1.2e-279 | sufB | O | assembly protein SufB | ||
BABJCGNF_00428 | 8.8e-106 | metI | P | ABC transporter permease | ||
BABJCGNF_00429 | 3.8e-63 | sufC | O | FeS assembly ATPase SufC | ||
BABJCGNF_00430 | 9.9e-70 | sufC | O | FeS assembly ATPase SufC | ||
BABJCGNF_00432 | 1.9e-43 | celD | 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 | |
BABJCGNF_00433 | 2.4e-28 | celD | 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 | |
BABJCGNF_00434 | 1.5e-128 | celD | 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 | |
BABJCGNF_00435 | 5.3e-28 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BABJCGNF_00436 | 4.8e-215 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BABJCGNF_00437 | 1.2e-96 | P | Belongs to the nlpA lipoprotein family | |||
BABJCGNF_00438 | 2.6e-86 | P | Belongs to the nlpA lipoprotein family | |||
BABJCGNF_00439 | 8.9e-156 | rodA | D | Belongs to the SEDS family | ||
BABJCGNF_00440 | 1.1e-47 | gcvH | E | glycine cleavage | ||
BABJCGNF_00441 | 2.4e-121 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
BABJCGNF_00442 | 2.2e-28 | rodA | D | Belongs to the SEDS family | ||
BABJCGNF_00443 | 1.4e-25 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
BABJCGNF_00444 | 1.6e-54 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
BABJCGNF_00445 | 1.3e-31 | S | Protein of unknown function (DUF2969) | |||
BABJCGNF_00446 | 7.3e-53 | mbl | D | Cell shape determining protein MreB Mrl | ||
BABJCGNF_00447 | 1.1e-47 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
BABJCGNF_00448 | 2.5e-29 | 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 | |
BABJCGNF_00449 | 6.5e-54 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
BABJCGNF_00450 | 7.6e-118 | 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 | |
BABJCGNF_00451 | 8.1e-64 | 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 | ||
BABJCGNF_00452 | 1.6e-81 | 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 | |
BABJCGNF_00453 | 3.6e-09 | 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 | |
BABJCGNF_00454 | 3.9e-88 | 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 | ||
BABJCGNF_00455 | 2.1e-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 | ||
BABJCGNF_00456 | 9.5e-16 | ogt | 2.1.1.63 | L | Methyltransferase | |
BABJCGNF_00457 | 6.6e-30 | ldhD3 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BABJCGNF_00458 | 6.6e-139 | ldhD3 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BABJCGNF_00459 | 1e-48 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
BABJCGNF_00460 | 3e-116 | 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 | |
BABJCGNF_00461 | 2e-77 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
BABJCGNF_00462 | 8.6e-23 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
BABJCGNF_00463 | 5.7e-146 | 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 | |
BABJCGNF_00464 | 2.6e-103 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
BABJCGNF_00465 | 4.3e-91 | tdk | 2.7.1.21 | F | thymidine kinase | |
BABJCGNF_00466 | 1.5e-88 | ampC | V | Beta-lactamase | ||
BABJCGNF_00467 | 4.8e-60 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
BABJCGNF_00468 | 2e-70 | 1.13.11.2 | S | glyoxalase | ||
BABJCGNF_00469 | 8.9e-98 | T | PhoQ Sensor | |||
BABJCGNF_00470 | 4.7e-120 | K | Transcriptional regulatory protein, C terminal | |||
BABJCGNF_00471 | 1.7e-36 | 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 | ||
BABJCGNF_00472 | 1.2e-14 | 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 | ||
BABJCGNF_00473 | 1.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
BABJCGNF_00474 | 1.5e-91 | yhbO | 3.5.1.124 | S | DJ-1/PfpI family | |
BABJCGNF_00475 | 3.7e-129 | cydA | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit I | |
BABJCGNF_00476 | 4.9e-13 | cydA | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit I | |
BABJCGNF_00477 | 1.3e-96 | cydA | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit I | |
BABJCGNF_00478 | 5.2e-100 | cydB | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit II | |
BABJCGNF_00479 | 2.2e-58 | cydB | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit II | |
BABJCGNF_00480 | 9.3e-29 | |||||
BABJCGNF_00481 | 5.2e-24 | S | CAAX protease self-immunity | |||
BABJCGNF_00483 | 1.9e-66 | yfiC | V | ABC transporter | ||
BABJCGNF_00484 | 2e-149 | yfiC | V | ABC transporter | ||
BABJCGNF_00485 | 7.8e-140 | S | NADPH-dependent FMN reductase | |||
BABJCGNF_00487 | 4.3e-75 | ycfI | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_00488 | 8.8e-19 | ycfI | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_00489 | 2e-25 | ycfI | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_00490 | 1.5e-28 | G | Phosphoglycerate mutase family | |||
BABJCGNF_00491 | 3.1e-22 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_00492 | 6.4e-19 | |||||
BABJCGNF_00493 | 8.3e-09 | |||||
BABJCGNF_00495 | 1.7e-259 | pipD | E | Dipeptidase | ||
BABJCGNF_00496 | 8.7e-22 | |||||
BABJCGNF_00497 | 1e-111 | |||||
BABJCGNF_00498 | 1.9e-199 | EGP | Major facilitator Superfamily | |||
BABJCGNF_00499 | 2.6e-17 | |||||
BABJCGNF_00501 | 2e-39 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
BABJCGNF_00502 | 4.1e-41 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
BABJCGNF_00503 | 2.8e-25 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
BABJCGNF_00504 | 2.6e-10 | wbbX | GT2,GT4 | M | Glycosyl transferases group 1 | |
BABJCGNF_00505 | 2e-42 | wbbX | GT2,GT4 | M | Glycosyl transferases group 1 | |
BABJCGNF_00506 | 1.7e-78 | wbbX | GT2,GT4 | M | Glycosyl transferases group 1 | |
BABJCGNF_00507 | 1.8e-22 | yttA | 2.7.13.3 | S | Pfam Transposase IS66 | |
BABJCGNF_00508 | 5.6e-46 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
BABJCGNF_00509 | 8.3e-37 | F | DNA/RNA non-specific endonuclease | |||
BABJCGNF_00510 | 2.6e-205 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
BABJCGNF_00511 | 8.1e-44 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
BABJCGNF_00512 | 1.3e-85 | glcU | U | sugar transport | ||
BABJCGNF_00513 | 2.2e-56 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
BABJCGNF_00514 | 1.1e-30 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
BABJCGNF_00515 | 5.7e-103 | |||||
BABJCGNF_00516 | 3.4e-32 | |||||
BABJCGNF_00517 | 3.1e-27 | |||||
BABJCGNF_00518 | 4.1e-99 | purK2 | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
BABJCGNF_00519 | 1.1e-62 | purK2 | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
BABJCGNF_00520 | 1.1e-18 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
BABJCGNF_00521 | 1e-75 | yveB | 2.7.4.29 | I | PAP2 superfamily | |
BABJCGNF_00522 | 1.3e-85 | yveB | 2.7.4.29 | I | PAP2 superfamily | |
BABJCGNF_00523 | 7.2e-166 | mccF | V | LD-carboxypeptidase | ||
BABJCGNF_00524 | 2.4e-15 | mccF | V | LD-carboxypeptidase | ||
BABJCGNF_00525 | 2.2e-26 | pbuX | F | xanthine permease | ||
BABJCGNF_00526 | 4.9e-42 | 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 | |
BABJCGNF_00527 | 7.9e-28 | 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 | |
BABJCGNF_00528 | 2.2e-64 | yvbK | 3.1.3.25 | K | GNAT family | |
BABJCGNF_00529 | 2e-12 | cspC | K | Cold shock protein | ||
BABJCGNF_00530 | 1.9e-27 | chpR | T | PFAM SpoVT AbrB | ||
BABJCGNF_00531 | 3.2e-57 | |||||
BABJCGNF_00533 | 5.7e-152 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
BABJCGNF_00534 | 1.3e-132 | S | Bacterial membrane protein YfhO | |||
BABJCGNF_00535 | 8.1e-60 | S | Bacterial membrane protein YfhO | |||
BABJCGNF_00536 | 3.9e-227 | S | Bacterial membrane protein YfhO | |||
BABJCGNF_00538 | 1.7e-148 | S | Psort location CytoplasmicMembrane, score | |||
BABJCGNF_00539 | 4e-71 | S | Psort location CytoplasmicMembrane, score | |||
BABJCGNF_00540 | 2.5e-89 | bglH | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
BABJCGNF_00541 | 1.1e-54 | bglH | G | phosphotransferase system | ||
BABJCGNF_00542 | 1.1e-44 | bglH | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
BABJCGNF_00543 | 5.6e-234 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
BABJCGNF_00544 | 2.6e-96 | N | domain, Protein | |||
BABJCGNF_00545 | 5.5e-46 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
BABJCGNF_00546 | 2e-39 | M | Glycosyltransferase like family 2 | |||
BABJCGNF_00548 | 4.5e-29 | |||||
BABJCGNF_00549 | 1.4e-191 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
BABJCGNF_00550 | 2.5e-75 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
BABJCGNF_00551 | 3.8e-75 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
BABJCGNF_00552 | 2.3e-46 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
BABJCGNF_00553 | 1.1e-110 | yihY | S | Belongs to the UPF0761 family | ||
BABJCGNF_00554 | 1.9e-80 | fld | C | Flavodoxin | ||
BABJCGNF_00555 | 2.2e-14 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
BABJCGNF_00556 | 1.5e-55 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
BABJCGNF_00558 | 3.3e-30 | yihY | S | Belongs to the UPF0761 family | ||
BABJCGNF_00559 | 7.2e-24 | S | Phospholipase_D-nuclease N-terminal | |||
BABJCGNF_00560 | 4.6e-79 | yxlF | V | ABC transporter | ||
BABJCGNF_00561 | 6.6e-11 | yxlF | V | ABC transporter | ||
BABJCGNF_00562 | 4.5e-103 | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | |||
BABJCGNF_00563 | 2.7e-111 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_00566 | 1.1e-35 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
BABJCGNF_00567 | 7.9e-19 | pepS | E | Thermophilic metalloprotease (M29) | ||
BABJCGNF_00570 | 2.3e-51 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
BABJCGNF_00571 | 2.6e-244 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
BABJCGNF_00572 | 7.4e-21 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
BABJCGNF_00573 | 6.9e-59 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
BABJCGNF_00574 | 8.3e-67 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
BABJCGNF_00575 | 8.6e-23 | mocA | S | Oxidoreductase | ||
BABJCGNF_00576 | 3.9e-12 | mocA | S | Oxidoreductase | ||
BABJCGNF_00577 | 6.3e-105 | lys | M | Glycosyl hydrolases family 25 | ||
BABJCGNF_00578 | 5.7e-19 | S | Protein of unknown function (DUF1093) | |||
BABJCGNF_00579 | 9.1e-60 | S | Domain of unknown function (DUF4828) | |||
BABJCGNF_00580 | 5e-12 | qmcA | O | prohibitin homologues | ||
BABJCGNF_00581 | 7e-30 | qmcA | O | prohibitin homologues | ||
BABJCGNF_00582 | 4.8e-33 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
BABJCGNF_00583 | 5.7e-17 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
BABJCGNF_00584 | 3.5e-17 | yttB | EGP | Major facilitator Superfamily | ||
BABJCGNF_00585 | 2.9e-130 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
BABJCGNF_00586 | 1.1e-21 | yttB | EGP | Major facilitator Superfamily | ||
BABJCGNF_00587 | 6.4e-33 | yttB | EGP | Major facilitator Superfamily | ||
BABJCGNF_00588 | 4e-78 | yttB | EGP | Major facilitator Superfamily | ||
BABJCGNF_00589 | 2.9e-22 | yegS | 2.7.1.107 | G | Lipid kinase | |
BABJCGNF_00590 | 8.9e-33 | yegS | 2.7.1.107 | G | Lipid kinase | |
BABJCGNF_00591 | 1.1e-25 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BABJCGNF_00592 | 2.8e-42 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BABJCGNF_00593 | 6.9e-26 | 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) | |
BABJCGNF_00594 | 1.1e-24 | 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) | |
BABJCGNF_00595 | 4.6e-174 | 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) | |
BABJCGNF_00596 | 2.3e-63 | yegS | 2.7.1.107 | G | Lipid kinase | |
BABJCGNF_00597 | 2.4e-69 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
BABJCGNF_00598 | 1.3e-54 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
BABJCGNF_00599 | 6.3e-11 | 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 | |
BABJCGNF_00600 | 2e-208 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
BABJCGNF_00601 | 1.2e-82 | 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 | |
BABJCGNF_00602 | 2.4e-129 | 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 | |
BABJCGNF_00603 | 1e-17 | yjgN | S | Bacterial protein of unknown function (DUF898) | ||
BABJCGNF_00604 | 1.1e-07 | S | response to antibiotic | |||
BABJCGNF_00605 | 1.6e-34 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
BABJCGNF_00606 | 1.4e-15 | |||||
BABJCGNF_00607 | 3.8e-82 | |||||
BABJCGNF_00608 | 8e-34 | K | response regulator | |||
BABJCGNF_00609 | 1e-111 | yclK | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_00610 | 1.1e-134 | yclK | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_00611 | 4.6e-73 | yhbS | S | acetyltransferase | ||
BABJCGNF_00612 | 7.6e-31 | |||||
BABJCGNF_00613 | 7.1e-60 | S | SdpI/YhfL protein family | |||
BABJCGNF_00614 | 7.2e-26 | K | response regulator | |||
BABJCGNF_00615 | 4.2e-211 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
BABJCGNF_00616 | 3.2e-59 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
BABJCGNF_00617 | 7.1e-22 | arbZ | I | Phosphate acyltransferases | ||
BABJCGNF_00618 | 2.8e-100 | arbY | M | family 8 | ||
BABJCGNF_00619 | 1.1e-141 | arbV | 2.3.1.51 | I | Phosphate acyltransferases | |
BABJCGNF_00620 | 9.7e-59 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
BABJCGNF_00621 | 4.7e-42 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
BABJCGNF_00622 | 8e-16 | |||||
BABJCGNF_00623 | 9.6e-80 | |||||
BABJCGNF_00624 | 2.6e-188 | 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 | |
BABJCGNF_00625 | 8.5e-13 | ssb_2 | L | Single-strand binding protein family | ||
BABJCGNF_00626 | 1e-34 | ssb_2 | L | Single-strand binding protein family | ||
BABJCGNF_00627 | 2.8e-29 | |||||
BABJCGNF_00629 | 6.1e-13 | yebC | K | Transcriptional regulatory protein | ||
BABJCGNF_00630 | 1e-15 | yebC | K | Transcriptional regulatory protein | ||
BABJCGNF_00631 | 7.3e-18 | comGB | NU | type II secretion system | ||
BABJCGNF_00632 | 3e-46 | S | VanZ like family | |||
BABJCGNF_00633 | 6.4e-173 | pepF2 | E | Oligopeptidase F | ||
BABJCGNF_00634 | 4.5e-138 | 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 | |
BABJCGNF_00635 | 5.7e-17 | pepF2 | E | Oligopeptidase F | ||
BABJCGNF_00636 | 1.2e-18 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
BABJCGNF_00637 | 2e-49 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
BABJCGNF_00638 | 6.4e-117 | K | Transcriptional regulator | |||
BABJCGNF_00639 | 5.2e-172 | V | ABC transporter | |||
BABJCGNF_00640 | 3.6e-126 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
BABJCGNF_00641 | 4.5e-23 | 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 | |
BABJCGNF_00642 | 4.8e-109 | 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 | |
BABJCGNF_00643 | 8.5e-35 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
BABJCGNF_00644 | 5.4e-53 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
BABJCGNF_00645 | 2e-21 | 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 | |
BABJCGNF_00646 | 7e-110 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
BABJCGNF_00647 | 1e-38 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
BABJCGNF_00649 | 1.3e-22 | potC | P | ABC transporter permease | ||
BABJCGNF_00650 | 2.4e-80 | potC | P | ABC transporter permease | ||
BABJCGNF_00651 | 7.7e-13 | potD | P | ABC transporter | ||
BABJCGNF_00652 | 8.4e-27 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
BABJCGNF_00653 | 1.9e-141 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
BABJCGNF_00654 | 1.3e-60 | potB | P | ABC transporter permease | ||
BABJCGNF_00655 | 6.8e-57 | yjcE | P | Sodium proton antiporter | ||
BABJCGNF_00656 | 5.5e-226 | yjcE | P | Sodium proton antiporter | ||
BABJCGNF_00657 | 9.9e-18 | puuR | K | Cupin domain | ||
BABJCGNF_00658 | 1.2e-11 | yjcE | P | Sodium proton antiporter | ||
BABJCGNF_00659 | 4.6e-29 | ysdA | CP | ABC-2 family transporter protein | ||
BABJCGNF_00660 | 1.3e-59 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
BABJCGNF_00661 | 1.3e-86 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
BABJCGNF_00662 | 4.3e-104 | ylbB | V | ABC transporter permease | ||
BABJCGNF_00663 | 3.5e-10 | 4.1.1.52 | S | Amidohydrolase | ||
BABJCGNF_00664 | 3e-65 | 4.1.1.52 | S | Amidohydrolase | ||
BABJCGNF_00665 | 2.4e-50 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
BABJCGNF_00666 | 4.6e-82 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
BABJCGNF_00667 | 9e-47 | natA | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_00668 | 2.5e-11 | natA | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_00669 | 1.1e-22 | natA | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_00670 | 1.3e-17 | ysdA | CP | ABC-2 family transporter protein | ||
BABJCGNF_00671 | 5.4e-23 | ysdA | CP | ABC-2 family transporter protein | ||
BABJCGNF_00672 | 2.3e-24 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
BABJCGNF_00673 | 2.8e-38 | 3.2.2.20 | K | Acetyltransferase (GNAT) domain | ||
BABJCGNF_00674 | 9e-45 | 3.2.2.20 | K | Acetyltransferase (GNAT) domain | ||
BABJCGNF_00675 | 2e-45 | yxjI | ||||
BABJCGNF_00676 | 6.9e-30 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
BABJCGNF_00677 | 1.5e-92 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
BABJCGNF_00678 | 5.3e-50 | malG | P | ABC-type sugar transport systems, permease components | ||
BABJCGNF_00679 | 5.6e-106 | YSH1 | S | Metallo-beta-lactamase superfamily | ||
BABJCGNF_00680 | 6.7e-75 | YSH1 | S | Metallo-beta-lactamase superfamily | ||
BABJCGNF_00681 | 7.8e-79 | malE | G | Bacterial extracellular solute-binding protein | ||
BABJCGNF_00682 | 1.7e-97 | malE | G | Bacterial extracellular solute-binding protein | ||
BABJCGNF_00683 | 2.9e-19 | malE | G | Bacterial extracellular solute-binding protein | ||
BABJCGNF_00684 | 1.7e-60 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
BABJCGNF_00685 | 1.3e-48 | |||||
BABJCGNF_00686 | 1e-59 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
BABJCGNF_00687 | 6.6e-51 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
BABJCGNF_00688 | 5.7e-77 | K | Helix-turn-helix domain, rpiR family | |||
BABJCGNF_00689 | 5.9e-29 | K | Helix-turn-helix domain, rpiR family | |||
BABJCGNF_00690 | 9.3e-15 | K | Transcriptional regulator C-terminal region | |||
BABJCGNF_00691 | 2.3e-52 | K | Transcriptional regulator C-terminal region | |||
BABJCGNF_00693 | 5.4e-127 | V | ABC transporter, ATP-binding protein | |||
BABJCGNF_00694 | 7.9e-143 | ylbB | V | ABC transporter permease | ||
BABJCGNF_00697 | 2e-72 | ylbB | V | ABC transporter permease | ||
BABJCGNF_00698 | 1.3e-27 | ylbB | V | ABC transporter permease | ||
BABJCGNF_00699 | 8.8e-40 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
BABJCGNF_00700 | 1.5e-19 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
BABJCGNF_00701 | 4.6e-137 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
BABJCGNF_00702 | 3.5e-296 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
BABJCGNF_00703 | 2.5e-125 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
BABJCGNF_00704 | 4e-54 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
BABJCGNF_00705 | 2.1e-25 | |||||
BABJCGNF_00706 | 9.7e-107 | 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 | |
BABJCGNF_00707 | 2.7e-43 | 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 | |
BABJCGNF_00708 | 7.4e-106 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
BABJCGNF_00709 | 2.9e-48 | 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 | |
BABJCGNF_00710 | 2.2e-63 | |||||
BABJCGNF_00711 | 2.9e-45 | 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 | |
BABJCGNF_00712 | 9.1e-101 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
BABJCGNF_00713 | 2.3e-25 | 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) | |
BABJCGNF_00714 | 1.8e-39 | 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) | |
BABJCGNF_00715 | 7.5e-58 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
BABJCGNF_00716 | 1.8e-33 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
BABJCGNF_00717 | 9.2e-136 | cggR | K | Putative sugar-binding domain | ||
BABJCGNF_00718 | 2.5e-101 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
BABJCGNF_00721 | 2.2e-16 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
BABJCGNF_00722 | 2.3e-23 | whiA | K | May be required for sporulation | ||
BABJCGNF_00723 | 2.2e-139 | |||||
BABJCGNF_00724 | 3.1e-49 | sacX | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
BABJCGNF_00725 | 3.5e-161 | sacX | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
BABJCGNF_00726 | 1.9e-130 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
BABJCGNF_00727 | 3.3e-42 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
BABJCGNF_00728 | 1.8e-11 | S | Short repeat of unknown function (DUF308) | |||
BABJCGNF_00729 | 3.6e-33 | S | Short repeat of unknown function (DUF308) | |||
BABJCGNF_00730 | 1.5e-22 | 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 | ||
BABJCGNF_00731 | 7.8e-29 | 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 | ||
BABJCGNF_00732 | 1.1e-64 | 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 | ||
BABJCGNF_00733 | 1.2e-57 | 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 | ||
BABJCGNF_00734 | 3.9e-25 | 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 | ||
BABJCGNF_00735 | 1e-28 | yfbR | S | HD containing hydrolase-like enzyme | ||
BABJCGNF_00736 | 8.2e-65 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
BABJCGNF_00737 | 5.2e-53 | |||||
BABJCGNF_00738 | 3.8e-90 | V | ABC transporter | |||
BABJCGNF_00739 | 9.8e-83 | T | Transcriptional regulatory protein, C terminal | |||
BABJCGNF_00740 | 1.2e-70 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
BABJCGNF_00741 | 6.3e-20 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
BABJCGNF_00742 | 1.4e-18 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
BABJCGNF_00743 | 5.1e-70 | rplI | J | Binds to the 23S rRNA | ||
BABJCGNF_00744 | 5.9e-57 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
BABJCGNF_00745 | 2e-37 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
BABJCGNF_00746 | 9.4e-58 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
BABJCGNF_00747 | 1.4e-104 | 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. Therefore, by controlling the phosphorylation state of HPr, 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 | ||
BABJCGNF_00748 | 2.2e-89 | yvlB | S | Putative adhesin | ||
BABJCGNF_00749 | 5.3e-90 | yvlB | S | Putative adhesin | ||
BABJCGNF_00751 | 1.3e-46 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
BABJCGNF_00752 | 1.1e-12 | 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 | |
BABJCGNF_00753 | 4.9e-39 | 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 | |
BABJCGNF_00754 | 8.1e-19 | 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 | |
BABJCGNF_00755 | 3.4e-36 | 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 | |
BABJCGNF_00756 | 6.8e-85 | 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 | |
BABJCGNF_00757 | 4.5e-109 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
BABJCGNF_00759 | 5.5e-90 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
BABJCGNF_00760 | 5.4e-66 | pstA | P | Phosphate transport system permease protein PstA | ||
BABJCGNF_00761 | 9.3e-27 | pstA | P | Phosphate transport system permease protein PstA | ||
BABJCGNF_00762 | 1.6e-100 | pstS | P | Phosphate | ||
BABJCGNF_00763 | 7.3e-114 | phoR | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_00764 | 2.1e-123 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
BABJCGNF_00765 | 4.3e-37 | K | response regulator | |||
BABJCGNF_00766 | 2.6e-31 | K | response regulator | |||
BABJCGNF_00767 | 4.5e-48 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
BABJCGNF_00768 | 6.6e-84 | ftsE | D | ABC transporter | ||
BABJCGNF_00769 | 1.9e-50 | 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 | ||
BABJCGNF_00770 | 1.8e-23 | 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 | ||
BABJCGNF_00771 | 1.2e-21 | 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 | ||
BABJCGNF_00772 | 1.8e-57 | 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 | ||
BABJCGNF_00773 | 1.3e-92 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
BABJCGNF_00774 | 3.8e-165 | comFA | L | Helicase C-terminal domain protein | ||
BABJCGNF_00775 | 2.5e-107 | rny | S | Endoribonuclease that initiates mRNA decay | ||
BABJCGNF_00776 | 1.6e-20 | yvyE | 3.4.13.9 | S | YigZ family | |
BABJCGNF_00777 | 2.7e-79 | yvyE | 3.4.13.9 | S | YigZ family | |
BABJCGNF_00778 | 6.3e-15 | 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 | ||
BABJCGNF_00779 | 4.4e-12 | 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 | ||
BABJCGNF_00780 | 5.9e-27 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
BABJCGNF_00781 | 1.8e-90 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
BABJCGNF_00782 | 1e-16 | ymfM | S | Helix-turn-helix domain | ||
BABJCGNF_00783 | 6.5e-09 | ymfM | S | Helix-turn-helix domain | ||
BABJCGNF_00784 | 1.5e-33 | ymfM | S | Helix-turn-helix domain | ||
BABJCGNF_00785 | 4.4e-46 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
BABJCGNF_00786 | 1.6e-52 | ymfF | S | Peptidase M16 inactive domain protein | ||
BABJCGNF_00787 | 8.6e-55 | ymfF | S | Peptidase M16 inactive domain protein | ||
BABJCGNF_00788 | 8.5e-34 | ymfF | S | Peptidase M16 inactive domain protein | ||
BABJCGNF_00789 | 3.3e-29 | ymfF | S | Peptidase M16 inactive domain protein | ||
BABJCGNF_00790 | 1.3e-65 | ymfH | S | Peptidase M16 | ||
BABJCGNF_00791 | 1.2e-68 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
BABJCGNF_00792 | 7.2e-27 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
BABJCGNF_00793 | 4.2e-08 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
BABJCGNF_00794 | 1.4e-21 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
BABJCGNF_00795 | 1.7e-42 | 3.6.1.55 | L | NUDIX domain | ||
BABJCGNF_00796 | 4.9e-47 | EG | EamA-like transporter family | |||
BABJCGNF_00797 | 6.3e-85 | EG | EamA-like transporter family | |||
BABJCGNF_00798 | 1.9e-192 | 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 | |
BABJCGNF_00799 | 4.8e-83 | 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 | |
BABJCGNF_00800 | 1.8e-36 | 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 | |
BABJCGNF_00801 | 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 | |
BABJCGNF_00802 | 1.2e-75 | rrmA | 2.1.1.187 | H | Methyltransferase | |
BABJCGNF_00803 | 7.8e-112 | corA | P | CorA-like Mg2+ transporter protein | ||
BABJCGNF_00804 | 1.8e-46 | 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 | |
BABJCGNF_00805 | 3.5e-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 | ||
BABJCGNF_00806 | 7.7e-79 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
BABJCGNF_00807 | 4.4e-112 | cutC | P | Participates in the control of copper homeostasis | ||
BABJCGNF_00808 | 1.4e-26 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
BABJCGNF_00809 | 3.9e-64 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
BABJCGNF_00810 | 9.7e-17 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
BABJCGNF_00811 | 1.7e-40 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
BABJCGNF_00812 | 2.9e-29 | |||||
BABJCGNF_00813 | 1.3e-64 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
BABJCGNF_00814 | 5.4e-77 | nadK | 2.7.1.23 | F | 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 | |
BABJCGNF_00815 | 7.1e-49 | nadK | 2.7.1.23 | F | 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 | |
BABJCGNF_00816 | 3e-26 | yjbH | Q | Thioredoxin | ||
BABJCGNF_00817 | 7.3e-45 | yjbK | S | CYTH | ||
BABJCGNF_00818 | 7.4e-19 | XK27_08635 | S | UPF0210 protein | ||
BABJCGNF_00819 | 4.1e-211 | coiA | 3.6.4.12 | S | Competence protein | |
BABJCGNF_00820 | 2.8e-43 | XK27_08635 | S | UPF0210 protein | ||
BABJCGNF_00821 | 1.6e-09 | XK27_08635 | S | UPF0210 protein | ||
BABJCGNF_00822 | 1.5e-37 | gcvR | T | Belongs to the UPF0237 family | ||
BABJCGNF_00823 | 4.4e-159 | cpdA | S | Calcineurin-like phosphoesterase | ||
BABJCGNF_00824 | 4.2e-52 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
BABJCGNF_00825 | 6.8e-128 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
BABJCGNF_00826 | 2.1e-85 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
BABJCGNF_00827 | 4.5e-48 | cpdA | S | Calcineurin-like phosphoesterase | ||
BABJCGNF_00828 | 5.2e-20 | ytgP | S | Polysaccharide biosynthesis protein | ||
BABJCGNF_00829 | 1.1e-129 | ytgP | S | Polysaccharide biosynthesis protein | ||
BABJCGNF_00830 | 6.9e-130 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
BABJCGNF_00831 | 3.3e-35 | yhcC | S | Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082) | ||
BABJCGNF_00832 | 3.9e-28 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme 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 | |
BABJCGNF_00833 | 5.5e-86 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme 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 | |
BABJCGNF_00834 | 2.9e-69 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BABJCGNF_00835 | 3.6e-28 | S | Domain of unknown function (DUF4811) | |||
BABJCGNF_00836 | 1.2e-45 | S | Domain of unknown function (DUF4811) | |||
BABJCGNF_00837 | 1.3e-37 | 3.6.1.27 | I | Acid phosphatase homologues | ||
BABJCGNF_00838 | 1.7e-70 | 3.6.1.27 | I | Acid phosphatase homologues | ||
BABJCGNF_00839 | 5.2e-147 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BABJCGNF_00840 | 1e-93 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BABJCGNF_00841 | 6e-63 | emrY | EGP | Major facilitator Superfamily | ||
BABJCGNF_00842 | 4.6e-121 | emrY | EGP | Major facilitator Superfamily | ||
BABJCGNF_00843 | 3.9e-44 | merR | K | MerR HTH family regulatory protein | ||
BABJCGNF_00844 | 3.6e-12 | merR | K | MerR HTH family regulatory protein | ||
BABJCGNF_00845 | 1.4e-85 | |||||
BABJCGNF_00846 | 7.3e-184 | 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 | |
BABJCGNF_00847 | 1.1e-17 | 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 | |
BABJCGNF_00849 | 5.6e-18 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
BABJCGNF_00850 | 6e-58 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
BABJCGNF_00851 | 7e-19 | 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 | |
BABJCGNF_00852 | 2.6e-132 | 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 | |
BABJCGNF_00854 | 1.2e-21 | perR | P | Belongs to the Fur family | ||
BABJCGNF_00855 | 1.4e-86 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
BABJCGNF_00856 | 3.9e-30 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
BABJCGNF_00857 | 1.6e-27 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
BABJCGNF_00858 | 5.9e-91 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
BABJCGNF_00859 | 5.7e-18 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
BABJCGNF_00860 | 9.4e-111 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
BABJCGNF_00861 | 5.9e-94 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
BABJCGNF_00862 | 8.5e-60 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
BABJCGNF_00863 | 8.8e-19 | ybeC | E | amino acid | ||
BABJCGNF_00864 | 2e-109 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
BABJCGNF_00866 | 2.5e-62 | sigH | K | Sigma-70 region 2 | ||
BABJCGNF_00867 | 2.7e-08 | sigH | K | Sigma-70 region 2 | ||
BABJCGNF_00890 | 5.6e-34 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
BABJCGNF_00891 | 2.6e-22 | yugI | 5.3.1.9 | J | general stress protein | |
BABJCGNF_00892 | 6.5e-46 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
BABJCGNF_00893 | 4e-43 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
BABJCGNF_00894 | 5.6e-30 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
BABJCGNF_00896 | 5.6e-115 | S | Protein of unknown function (DUF1461) | |||
BABJCGNF_00898 | 2.7e-14 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
BABJCGNF_00899 | 1.2e-93 | S | Calcineurin-like phosphoesterase | |||
BABJCGNF_00900 | 6.7e-77 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
BABJCGNF_00901 | 3.6e-48 | yibF | S | overlaps another CDS with the same product name | ||
BABJCGNF_00902 | 7.5e-56 | yibE | S | overlaps another CDS with the same product name | ||
BABJCGNF_00903 | 2.4e-29 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
BABJCGNF_00904 | 6.3e-28 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
BABJCGNF_00905 | 2.9e-53 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
BABJCGNF_00906 | 1.9e-63 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
BABJCGNF_00907 | 4e-30 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
BABJCGNF_00908 | 1.3e-93 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
BABJCGNF_00909 | 8.7e-18 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
BABJCGNF_00910 | 3.6e-188 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
BABJCGNF_00911 | 5.8e-16 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
BABJCGNF_00912 | 1.2e-70 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
BABJCGNF_00913 | 2.5e-25 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
BABJCGNF_00914 | 2.2e-23 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
BABJCGNF_00915 | 5.5e-217 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
BABJCGNF_00916 | 1.2e-36 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
BABJCGNF_00917 | 5.2e-36 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
BABJCGNF_00918 | 2.4e-170 | ccpA | K | catabolite control protein A | ||
BABJCGNF_00919 | 1.2e-51 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
BABJCGNF_00921 | 3e-84 | ykuL | S | CBS domain | ||
BABJCGNF_00922 | 2.9e-120 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
BABJCGNF_00923 | 4.4e-35 | S | Phosphoesterase | |||
BABJCGNF_00924 | 8.4e-125 | gla | U | Major intrinsic protein | ||
BABJCGNF_00925 | 4.9e-156 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
BABJCGNF_00926 | 3.3e-55 | yslB | S | Protein of unknown function (DUF2507) | ||
BABJCGNF_00927 | 7.3e-101 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
BABJCGNF_00928 | 4.8e-31 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
BABJCGNF_00929 | 1e-19 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
BABJCGNF_00930 | 5.8e-94 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
BABJCGNF_00931 | 2e-26 | S | Phosphoesterase | |||
BABJCGNF_00932 | 1.1e-101 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
BABJCGNF_00933 | 1.5e-22 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
BABJCGNF_00934 | 5.3e-62 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
BABJCGNF_00935 | 1.1e-107 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
BABJCGNF_00936 | 3e-215 | 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 | ||
BABJCGNF_00937 | 7.3e-66 | 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 | ||
BABJCGNF_00938 | 5e-184 | |||||
BABJCGNF_00939 | 2.1e-11 | yrzL | S | Belongs to the UPF0297 family | ||
BABJCGNF_00940 | 1.9e-17 | yrzL | S | Belongs to the UPF0297 family | ||
BABJCGNF_00941 | 2.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
BABJCGNF_00942 | 2.3e-53 | yrzB | S | Belongs to the UPF0473 family | ||
BABJCGNF_00943 | 2e-36 | 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 | ||
BABJCGNF_00944 | 4.6e-36 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
BABJCGNF_00945 | 3.6e-132 | 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 | |
BABJCGNF_00946 | 5.8e-93 | 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 | |
BABJCGNF_00947 | 4.4e-111 | |||||
BABJCGNF_00948 | 4.3e-33 | |||||
BABJCGNF_00950 | 4.1e-31 | ytoI | K | DRTGG domain | ||
BABJCGNF_00951 | 2.6e-175 | ytoI | K | DRTGG domain | ||
BABJCGNF_00952 | 2.5e-50 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
BABJCGNF_00953 | 3.2e-65 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
BABJCGNF_00954 | 8.3e-46 | 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 | |
BABJCGNF_00955 | 9.5e-32 | 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 | |
BABJCGNF_00956 | 2.1e-123 | 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 | |
BABJCGNF_00957 | 5.6e-208 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
BABJCGNF_00958 | 1.1e-130 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
BABJCGNF_00959 | 3.9e-116 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
BABJCGNF_00960 | 4.4e-101 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
BABJCGNF_00961 | 5.3e-27 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
BABJCGNF_00962 | 4.2e-35 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
BABJCGNF_00963 | 6.5e-96 | 1.1.1.133, 5.1.3.13 | M | dTDP-4-dehydrorhamnose 3,5-epimerase | ||
BABJCGNF_00964 | 1.2e-80 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
BABJCGNF_00965 | 1.2e-20 | yajC | U | Preprotein translocase | ||
BABJCGNF_00966 | 1.4e-116 | 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) | |
BABJCGNF_00967 | 7.3e-91 | 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) | |
BABJCGNF_00968 | 7.6e-88 | 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) | |
BABJCGNF_00969 | 8.5e-119 | 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 | |
BABJCGNF_00970 | 2.7e-18 | 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) | |
BABJCGNF_00971 | 4.5e-97 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
BABJCGNF_00972 | 7.9e-57 | norB | EGP | Major Facilitator | ||
BABJCGNF_00973 | 1.6e-111 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_00974 | 1e-57 | |||||
BABJCGNF_00975 | 1.1e-39 | |||||
BABJCGNF_00976 | 2.9e-31 | yaaA | S | S4 domain protein YaaA | ||
BABJCGNF_00977 | 4.3e-173 | 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 | ||
BABJCGNF_00978 | 3.5e-74 | S | Protein of unknown function (DUF3290) | |||
BABJCGNF_00979 | 3e-47 | S | Alpha beta hydrolase | |||
BABJCGNF_00980 | 6.2e-38 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
BABJCGNF_00981 | 3.9e-09 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
BABJCGNF_00982 | 1.9e-87 | gph | 3.1.3.18 | S | haloacid dehalogenase-like hydrolase | |
BABJCGNF_00983 | 5.6e-18 | gph | 3.1.3.18 | S | haloacid dehalogenase-like hydrolase | |
BABJCGNF_00984 | 3.7e-76 | K | Transcriptional regulator | |||
BABJCGNF_00985 | 9.7e-69 | D | Alpha beta | |||
BABJCGNF_00986 | 5.1e-39 | D | Alpha beta | |||
BABJCGNF_00987 | 2.2e-84 | nrdI | F | Belongs to the NrdI family | ||
BABJCGNF_00988 | 2.3e-120 | dkgB | S | reductase | ||
BABJCGNF_00989 | 3.5e-26 | |||||
BABJCGNF_00990 | 8.7e-15 | |||||
BABJCGNF_00991 | 6.8e-13 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
BABJCGNF_00992 | 1.9e-83 | yfgQ | P | E1-E2 ATPase | ||
BABJCGNF_00993 | 3.4e-94 | norB | EGP | Major Facilitator | ||
BABJCGNF_00994 | 1.1e-37 | yfgQ | P | E1-E2 ATPase | ||
BABJCGNF_00995 | 2.2e-141 | V | ABC transporter transmembrane region | |||
BABJCGNF_00996 | 4.8e-148 | pepF | E | Oligopeptidase F | ||
BABJCGNF_00997 | 6.7e-65 | pepF | E | Oligopeptidase F | ||
BABJCGNF_00998 | 3.4e-95 | pepF | E | Oligopeptidase F | ||
BABJCGNF_00999 | 8.3e-26 | V | ABC transporter transmembrane region | |||
BABJCGNF_01000 | 1.1e-64 | |||||
BABJCGNF_01001 | 2.5e-98 | K | sequence-specific DNA binding | |||
BABJCGNF_01002 | 1.8e-35 | mleP | S | Sodium Bile acid symporter family | ||
BABJCGNF_01003 | 1.1e-297 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
BABJCGNF_01004 | 6.7e-43 | mleR | K | LysR family | ||
BABJCGNF_01005 | 2.5e-172 | corA | P | CorA-like Mg2+ transporter protein | ||
BABJCGNF_01006 | 3.6e-34 | mleR | K | LysR family | ||
BABJCGNF_01007 | 2.9e-72 | |||||
BABJCGNF_01008 | 1e-104 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
BABJCGNF_01009 | 5.3e-42 | |||||
BABJCGNF_01010 | 2.6e-46 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
BABJCGNF_01011 | 1e-82 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
BABJCGNF_01012 | 3e-105 | ywrF | S | Flavin reductase like domain | ||
BABJCGNF_01013 | 2.1e-39 | |||||
BABJCGNF_01014 | 3.4e-80 | |||||
BABJCGNF_01015 | 1.5e-86 | yubA | S | AI-2E family transporter | ||
BABJCGNF_01016 | 1.4e-15 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
BABJCGNF_01017 | 1e-45 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
BABJCGNF_01018 | 4.7e-23 | K | Transcriptional regulator PadR-like family | |||
BABJCGNF_01019 | 7.6e-40 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
BABJCGNF_01020 | 2.5e-49 | |||||
BABJCGNF_01021 | 7.5e-71 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
BABJCGNF_01022 | 1.2e-58 | K | sequence-specific DNA binding | |||
BABJCGNF_01024 | 1.2e-25 | drgA | C | Nitroreductase family | ||
BABJCGNF_01025 | 2.3e-33 | drgA | C | Nitroreductase family | ||
BABJCGNF_01026 | 1.4e-119 | lctO | C | IMP dehydrogenase / GMP reductase domain | ||
BABJCGNF_01027 | 3.7e-44 | ciaH | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
BABJCGNF_01028 | 2.5e-67 | yqkB | S | Belongs to the HesB IscA family | ||
BABJCGNF_01029 | 1.2e-33 | K | cheY-homologous receiver domain | |||
BABJCGNF_01030 | 3.1e-83 | K | cheY-homologous receiver domain | |||
BABJCGNF_01031 | 8.7e-14 | ciaH | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
BABJCGNF_01032 | 2.4e-13 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
BABJCGNF_01033 | 2.2e-105 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
BABJCGNF_01034 | 3e-35 | S | GtrA-like protein | |||
BABJCGNF_01035 | 1.4e-40 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
BABJCGNF_01036 | 2.1e-61 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
BABJCGNF_01037 | 1e-125 | ykcC | GT2 | M | Glycosyl transferase family 2 | |
BABJCGNF_01038 | 2.7e-104 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
BABJCGNF_01039 | 1.8e-54 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
BABJCGNF_01040 | 8.7e-108 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
BABJCGNF_01041 | 8.8e-187 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
BABJCGNF_01042 | 1.1e-104 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
BABJCGNF_01043 | 2e-98 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
BABJCGNF_01044 | 2.9e-70 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
BABJCGNF_01045 | 1.2e-73 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
BABJCGNF_01046 | 8.3e-114 | cmpC | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_01047 | 3e-162 | yhfP | 1.1.1.1 | C | Zinc-binding dehydrogenase | |
BABJCGNF_01048 | 1e-31 | XK27_00670 | S | ABC transporter | ||
BABJCGNF_01050 | 4.3e-50 | XK27_00670 | S | ABC transporter substrate binding protein | ||
BABJCGNF_01051 | 2.7e-123 | bglB | 3.2.1.21 | GH3 | G | hydrolase, family 3 |
BABJCGNF_01055 | 1.8e-116 | ywnB | S | NmrA-like family | ||
BABJCGNF_01056 | 2.2e-137 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
BABJCGNF_01057 | 5.4e-87 | S | Short repeat of unknown function (DUF308) | |||
BABJCGNF_01058 | 5.5e-42 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
BABJCGNF_01059 | 2.3e-90 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
BABJCGNF_01060 | 6.4e-43 | |||||
BABJCGNF_01061 | 4.9e-57 | |||||
BABJCGNF_01063 | 3.1e-86 | hsp1 | O | Belongs to the small heat shock protein (HSP20) family | ||
BABJCGNF_01064 | 1e-127 | mutY | L | A G-specific adenine glycosylase | ||
BABJCGNF_01065 | 1.4e-65 | mutY | L | A G-specific adenine glycosylase | ||
BABJCGNF_01066 | 1.7e-20 | cytC6 | I | alpha/beta hydrolase fold | ||
BABJCGNF_01067 | 4.1e-30 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
BABJCGNF_01068 | 1.1e-78 | 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 | ||
BABJCGNF_01069 | 3.9e-42 | 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 | ||
BABJCGNF_01070 | 5.5e-30 | 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 | ||
BABJCGNF_01071 | 4.9e-51 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
BABJCGNF_01072 | 6e-58 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
BABJCGNF_01073 | 6.5e-102 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
BABJCGNF_01075 | 1.8e-24 | lacR | K | DeoR C terminal sensor domain | ||
BABJCGNF_01076 | 2.9e-19 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
BABJCGNF_01077 | 6.6e-72 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
BABJCGNF_01078 | 4.1e-48 | lacR | K | DeoR C terminal sensor domain | ||
BABJCGNF_01079 | 1.8e-19 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
BABJCGNF_01080 | 5.5e-77 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
BABJCGNF_01082 | 6.3e-72 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
BABJCGNF_01084 | 3.3e-70 | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01085 | 1.7e-48 | 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
BABJCGNF_01086 | 1.6e-169 | gatC | G | PTS system sugar-specific permease component | ||
BABJCGNF_01087 | 2.5e-75 | gatC | G | PTS system sugar-specific permease component | ||
BABJCGNF_01088 | 1.7e-28 | |||||
BABJCGNF_01089 | 1.5e-186 | V | Beta-lactamase | |||
BABJCGNF_01090 | 4.4e-70 | S | Domain of unknown function (DUF4867) | |||
BABJCGNF_01091 | 4.8e-76 | K | Transcriptional regulator | |||
BABJCGNF_01092 | 2.3e-31 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
BABJCGNF_01093 | 1e-25 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
BABJCGNF_01094 | 5.1e-167 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
BABJCGNF_01095 | 1.3e-20 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
BABJCGNF_01096 | 6.5e-90 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
BABJCGNF_01097 | 4e-92 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
BABJCGNF_01098 | 3.3e-35 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
BABJCGNF_01099 | 1.1e-16 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
BABJCGNF_01100 | 1.7e-45 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
BABJCGNF_01102 | 1.5e-46 | S | CAAX protease self-immunity | |||
BABJCGNF_01103 | 5e-45 | S | CAAX protease self-immunity | |||
BABJCGNF_01104 | 7.6e-18 | S | CAAX protease self-immunity | |||
BABJCGNF_01105 | 9.3e-23 | lacT | K | PRD domain | ||
BABJCGNF_01108 | 2e-39 | lacT | K | PRD domain | ||
BABJCGNF_01109 | 4.3e-50 | epsG | 2.4.1.293 | GT2 | M | Glycosyltransferase like family 2 |
BABJCGNF_01110 | 4.6e-28 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
BABJCGNF_01111 | 3.6e-269 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
BABJCGNF_01112 | 1.1e-146 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
BABJCGNF_01113 | 3.1e-117 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
BABJCGNF_01114 | 1.6e-78 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
BABJCGNF_01115 | 2.4e-48 | ybiT | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_01116 | 2.4e-43 | yhiD | S | MgtC family | ||
BABJCGNF_01117 | 2.3e-92 | F | DNA RNA non-specific endonuclease | |||
BABJCGNF_01118 | 1.2e-31 | F | DNA RNA non-specific endonuclease | |||
BABJCGNF_01121 | 6.6e-155 | ydgH | S | MMPL family | ||
BABJCGNF_01122 | 1.1e-159 | ydgH | S | MMPL family | ||
BABJCGNF_01123 | 1.3e-86 | ydgH | S | MMPL family | ||
BABJCGNF_01124 | 2e-106 | K | Tetracycline repressor, C-terminal all-alpha domain | |||
BABJCGNF_01125 | 5e-107 | S | Sulfite exporter TauE/SafE | |||
BABJCGNF_01126 | 6.6e-42 | 3.5.4.28, 3.5.4.31 | F | Amidohydrolase family | ||
BABJCGNF_01127 | 8.1e-82 | 3.5.4.28, 3.5.4.31 | F | Amidohydrolase family | ||
BABJCGNF_01128 | 2.8e-35 | 3.5.4.28, 3.5.4.31 | F | Amidohydrolase family | ||
BABJCGNF_01129 | 1.9e-69 | S | An automated process has identified a potential problem with this gene model | |||
BABJCGNF_01130 | 1e-148 | S | Protein of unknown function (DUF3100) | |||
BABJCGNF_01131 | 1.2e-107 | opuCD | P | Binding-protein-dependent transport system inner membrane component | ||
BABJCGNF_01132 | 1.1e-104 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BABJCGNF_01133 | 4.8e-58 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BABJCGNF_01134 | 4.2e-44 | opuCB | E | ABC transporter permease | ||
BABJCGNF_01135 | 2.3e-39 | opuCB | E | ABC transporter permease | ||
BABJCGNF_01136 | 1.3e-55 | opuCA | 2.7.7.7 | E | ABC transporter, ATP-binding protein | |
BABJCGNF_01137 | 1.1e-122 | opuCA | E | ABC transporter, ATP-binding protein | ||
BABJCGNF_01138 | 0.0 | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | ||
BABJCGNF_01139 | 1.9e-23 | copZ | P | Heavy-metal-associated domain | ||
BABJCGNF_01140 | 2.3e-28 | dps | P | Belongs to the Dps family | ||
BABJCGNF_01141 | 2.7e-61 | dps | P | Belongs to the Dps family | ||
BABJCGNF_01142 | 5.1e-11 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
BABJCGNF_01143 | 3.1e-72 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
BABJCGNF_01144 | 2.7e-71 | amt | P | ammonium transporter | ||
BABJCGNF_01145 | 1.5e-153 | yfeX | P | Peroxidase | ||
BABJCGNF_01146 | 5e-22 | amt | P | ammonium transporter | ||
BABJCGNF_01147 | 3.2e-78 | cylB | V | ABC-2 type transporter | ||
BABJCGNF_01148 | 3.4e-145 | cylA | V | ABC transporter | ||
BABJCGNF_01149 | 8.4e-72 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BABJCGNF_01150 | 3e-116 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
BABJCGNF_01151 | 1.2e-52 | ybjQ | S | Belongs to the UPF0145 family | ||
BABJCGNF_01153 | 2.5e-92 | nudC | 1.3.7.1, 3.6.1.22 | L | NUDIX domain | |
BABJCGNF_01154 | 8.8e-15 | 3.5.1.10 | C | nadph quinone reductase | ||
BABJCGNF_01156 | 8e-20 | S | Protein of unknown function (DUF3021) | |||
BABJCGNF_01157 | 1.6e-68 | K | LytTr DNA-binding domain | |||
BABJCGNF_01158 | 6.2e-134 | yjcE | P | Sodium proton antiporter | ||
BABJCGNF_01159 | 4e-54 | yjcE | P | Sodium proton antiporter | ||
BABJCGNF_01160 | 2.5e-36 | yjcE | P | Sodium proton antiporter | ||
BABJCGNF_01161 | 2.1e-21 | S | Protein of unknown function (DUF3800) | |||
BABJCGNF_01162 | 1.1e-56 | yifK | E | Amino acid permease | ||
BABJCGNF_01163 | 1.2e-121 | yifK | E | Amino acid permease | ||
BABJCGNF_01164 | 1.2e-65 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_01165 | 1.4e-59 | ylbE | GM | NAD(P)H-binding | ||
BABJCGNF_01166 | 2.4e-36 | ylbE | GM | NAD(P)H-binding | ||
BABJCGNF_01167 | 5e-67 | |||||
BABJCGNF_01168 | 4.3e-65 | O | OsmC-like protein | |||
BABJCGNF_01169 | 1.8e-47 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
BABJCGNF_01170 | 4.6e-31 | K | 'Cold-shock' DNA-binding domain | |||
BABJCGNF_01171 | 8.6e-122 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
BABJCGNF_01172 | 1.8e-176 | 3.1.1.83 | I | Alpha beta hydrolase | ||
BABJCGNF_01173 | 4.2e-164 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
BABJCGNF_01174 | 4e-68 | sstT | U | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
BABJCGNF_01175 | 2.9e-59 | sstT | U | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
BABJCGNF_01176 | 1.1e-113 | treR | K | UTRA | ||
BABJCGNF_01177 | 6e-60 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
BABJCGNF_01178 | 1.6e-157 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
BABJCGNF_01179 | 1.5e-79 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
BABJCGNF_01181 | 5.3e-25 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_01182 | 4.5e-21 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_01183 | 9.1e-19 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_01184 | 0.0 | V | ABC transporter | |||
BABJCGNF_01185 | 3.5e-20 | oxlT | P | Major Facilitator Superfamily | ||
BABJCGNF_01186 | 7e-105 | oxlT | P | Major Facilitator Superfamily | ||
BABJCGNF_01187 | 2.2e-39 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
BABJCGNF_01188 | 7.3e-61 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
BABJCGNF_01189 | 2.3e-116 | M | Glycosyl hydrolase family 59 | |||
BABJCGNF_01190 | 2e-177 | M | Glycosyl hydrolase family 59 | |||
BABJCGNF_01191 | 1.2e-57 | |||||
BABJCGNF_01192 | 7.2e-65 | S | pyridoxamine 5-phosphate | |||
BABJCGNF_01193 | 7.3e-33 | metF | 1.5.1.20 | C | Methylenetetrahydrofolate reductase | |
BABJCGNF_01194 | 8.6e-69 | metF | 1.5.1.20 | C | Methylenetetrahydrofolate reductase | |
BABJCGNF_01195 | 1.6e-112 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
BABJCGNF_01196 | 1.2e-225 | |||||
BABJCGNF_01197 | 4.2e-66 | |||||
BABJCGNF_01198 | 8.2e-21 | CcmA5 | V | ABC transporter | ||
BABJCGNF_01199 | 4.5e-101 | CcmA5 | V | ABC transporter | ||
BABJCGNF_01200 | 1.5e-60 | S | ECF-type riboflavin transporter, S component | |||
BABJCGNF_01201 | 1.3e-168 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
BABJCGNF_01202 | 9.8e-74 | yicL | EG | EamA-like transporter family | ||
BABJCGNF_01203 | 4.8e-51 | S | WxL domain surface cell wall-binding | |||
BABJCGNF_01204 | 2.3e-60 | |||||
BABJCGNF_01205 | 1.6e-112 | N | WxL domain surface cell wall-binding | |||
BABJCGNF_01206 | 5.2e-75 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
BABJCGNF_01208 | 3.5e-19 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
BABJCGNF_01209 | 3.7e-46 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
BABJCGNF_01210 | 1.1e-104 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
BABJCGNF_01211 | 1.9e-125 | S | Cell surface protein | |||
BABJCGNF_01212 | 8.1e-94 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
BABJCGNF_01213 | 2.3e-94 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
BABJCGNF_01214 | 5.2e-84 | tcyB | E | ABC transporter | ||
BABJCGNF_01215 | 6e-21 | tcyB | E | ABC transporter | ||
BABJCGNF_01216 | 8.4e-34 | |||||
BABJCGNF_01217 | 1.4e-48 | |||||
BABJCGNF_01218 | 2.6e-49 | metC | 4.4.1.8 | E | cystathionine | |
BABJCGNF_01219 | 1.2e-88 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
BABJCGNF_01220 | 5e-26 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
BABJCGNF_01221 | 2.3e-66 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
BABJCGNF_01222 | 3.8e-90 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
BABJCGNF_01224 | 2.6e-37 | |||||
BABJCGNF_01225 | 6.5e-87 | |||||
BABJCGNF_01226 | 2.1e-13 | G | MFS/sugar transport protein | |||
BABJCGNF_01227 | 4.3e-58 | S | Protein of unknown function (DUF1440) | |||
BABJCGNF_01229 | 1.7e-44 | kdgR | K | FCD domain | ||
BABJCGNF_01230 | 3.9e-21 | G | MFS/sugar transport protein | |||
BABJCGNF_01231 | 3.9e-11 | G | MFS/sugar transport protein | |||
BABJCGNF_01232 | 5.2e-11 | pepN | 3.4.11.2 | E | aminopeptidase | |
BABJCGNF_01233 | 5.5e-164 | pepN | 3.4.11.2 | E | aminopeptidase | |
BABJCGNF_01234 | 7e-38 | pepN | 3.4.11.2 | E | aminopeptidase | |
BABJCGNF_01235 | 1.8e-231 | ycaM | E | amino acid | ||
BABJCGNF_01236 | 6.3e-57 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
BABJCGNF_01237 | 4.3e-161 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_01238 | 8.1e-49 | |||||
BABJCGNF_01239 | 5e-117 | |||||
BABJCGNF_01240 | 1.1e-23 | |||||
BABJCGNF_01241 | 3.7e-39 | |||||
BABJCGNF_01242 | 3.6e-17 | XK27_12140 | V | ATPases associated with a variety of cellular activities | ||
BABJCGNF_01244 | 1.2e-280 | S | Psort location CytoplasmicMembrane, score | |||
BABJCGNF_01245 | 1.3e-125 | K | Transcriptional regulatory protein, C terminal | |||
BABJCGNF_01246 | 1e-07 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
BABJCGNF_01247 | 1.8e-131 | |||||
BABJCGNF_01248 | 1e-24 | G | Major Facilitator | |||
BABJCGNF_01249 | 2.8e-30 | S | membrane transporter protein | |||
BABJCGNF_01250 | 5.4e-14 | G | PTS system sugar-specific permease component | |||
BABJCGNF_01251 | 8e-49 | hxlR | K | Transcriptional regulator, HxlR family | ||
BABJCGNF_01252 | 4.9e-64 | S | membrane transporter protein | |||
BABJCGNF_01253 | 6.2e-24 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
BABJCGNF_01254 | 7.3e-19 | L | hmm pf00665 | |||
BABJCGNF_01257 | 1.4e-13 | V | ABC transporter | |||
BABJCGNF_01258 | 6.4e-49 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
BABJCGNF_01259 | 6e-13 | |||||
BABJCGNF_01260 | 3.1e-24 | N | Uncharacterized conserved protein (DUF2075) | |||
BABJCGNF_01261 | 2.7e-64 | morA2 | S | reductase | ||
BABJCGNF_01262 | 3.7e-51 | morA2 | S | reductase | ||
BABJCGNF_01263 | 6.6e-53 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
BABJCGNF_01264 | 3.8e-12 | M | 4-amino-4-deoxy-L-arabinose transferase activity | |||
BABJCGNF_01267 | 5.8e-15 | G | PTS system sugar-specific permease component | |||
BABJCGNF_01268 | 2.3e-12 | M | 4-amino-4-deoxy-L-arabinose transferase activity | |||
BABJCGNF_01269 | 5.5e-59 | K | helix_turn_helix, mercury resistance | |||
BABJCGNF_01270 | 1.9e-26 | |||||
BABJCGNF_01271 | 7.6e-12 | wbbI | M | transferase activity, transferring glycosyl groups | ||
BABJCGNF_01273 | 1.5e-18 | |||||
BABJCGNF_01275 | 1.9e-10 | S | ABC-2 family transporter protein | |||
BABJCGNF_01277 | 1.4e-23 | 6.3.1.2 | E | Glutamine synthetase N-terminal domain | ||
BABJCGNF_01278 | 4.3e-163 | S | Amidohydrolase | |||
BABJCGNF_01279 | 2.3e-30 | S | Amidohydrolase | |||
BABJCGNF_01280 | 1.7e-27 | L | An automated process has identified a potential problem with this gene model | |||
BABJCGNF_01283 | 1.1e-13 | 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 | |
BABJCGNF_01284 | 3.7e-27 | 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 | |
BABJCGNF_01285 | 6e-29 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
BABJCGNF_01286 | 2.7e-71 | K | Psort location Cytoplasmic, score | |||
BABJCGNF_01287 | 5.3e-73 | G | Major Facilitator | |||
BABJCGNF_01289 | 4e-21 | D | Putative exonuclease SbcCD, C subunit | |||
BABJCGNF_01290 | 1.8e-33 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
BABJCGNF_01292 | 1.9e-138 | H | Protein of unknown function (DUF1698) | |||
BABJCGNF_01293 | 1.5e-139 | puuD | S | peptidase C26 | ||
BABJCGNF_01294 | 8.2e-28 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
BABJCGNF_01295 | 4.2e-10 | wbbI | M | transferase activity, transferring glycosyl groups | ||
BABJCGNF_01296 | 3.2e-11 | V | Beta-lactamase | |||
BABJCGNF_01297 | 4e-60 | V | Beta-lactamase | |||
BABJCGNF_01298 | 1.2e-45 | |||||
BABJCGNF_01299 | 2.4e-16 | S | PTS system sugar-specific permease component | |||
BABJCGNF_01301 | 1.6e-52 | 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) | |
BABJCGNF_01302 | 7e-150 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_01306 | 6.3e-11 | |||||
BABJCGNF_01308 | 4.5e-82 | tnpB | L | Putative transposase DNA-binding domain | ||
BABJCGNF_01309 | 2.3e-14 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
BABJCGNF_01310 | 1.4e-90 | yceJ | EGP | Major facilitator Superfamily | ||
BABJCGNF_01311 | 4.1e-95 | tag | 3.2.2.20 | L | glycosylase | |
BABJCGNF_01313 | 8.7e-12 | G | Major Facilitator | |||
BABJCGNF_01314 | 6.6e-27 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
BABJCGNF_01315 | 2.1e-11 | P | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
BABJCGNF_01316 | 2.9e-16 | S | PTS system sugar-specific permease component | |||
BABJCGNF_01317 | 3.2e-17 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
BABJCGNF_01318 | 3.9e-177 | L | Exonuclease | |||
BABJCGNF_01321 | 5.3e-77 | ohr | O | OsmC-like protein | ||
BABJCGNF_01322 | 3.8e-128 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
BABJCGNF_01324 | 9.6e-59 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
BABJCGNF_01327 | 1.6e-12 | |||||
BABJCGNF_01328 | 4.9e-110 | |||||
BABJCGNF_01329 | 3.1e-111 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
BABJCGNF_01330 | 3.6e-132 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
BABJCGNF_01331 | 8.7e-13 | wbbI | M | transferase activity, transferring glycosyl groups | ||
BABJCGNF_01332 | 5.4e-29 | U | Belongs to the binding-protein-dependent transport system permease family | |||
BABJCGNF_01333 | 3.3e-69 | pac | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
BABJCGNF_01334 | 6.4e-07 | |||||
BABJCGNF_01335 | 1.8e-34 | smoG | P | COG0395 ABC-type sugar transport system, permease component | ||
BABJCGNF_01336 | 1.2e-16 | |||||
BABJCGNF_01340 | 7.8e-19 | S | Phage-related minor tail protein | |||
BABJCGNF_01341 | 3e-94 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
BABJCGNF_01342 | 8.7e-13 | wbbI | M | transferase activity, transferring glycosyl groups | ||
BABJCGNF_01343 | 1.8e-27 | rfbD | 1.1.1.133 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
BABJCGNF_01344 | 4.1e-45 | S | hydrolase | |||
BABJCGNF_01345 | 2.6e-09 | S | hydrolase | |||
BABJCGNF_01346 | 1.5e-97 | npr | 1.11.1.1 | C | NADH oxidase | |
BABJCGNF_01347 | 1.8e-14 | G | PTS system sugar-specific permease component | |||
BABJCGNF_01349 | 4.9e-24 | licD3 | M | LicD family | ||
BABJCGNF_01350 | 8.5e-99 | gatC | G | PTS system sugar-specific permease component | ||
BABJCGNF_01351 | 9e-19 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
BABJCGNF_01352 | 8.9e-24 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
BABJCGNF_01353 | 1e-87 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
BABJCGNF_01354 | 1.2e-32 | S | YopX protein | |||
BABJCGNF_01359 | 3.6e-09 | S | Transcriptional regulator, RinA family | |||
BABJCGNF_01363 | 2.5e-45 | S | HNH endonuclease | |||
BABJCGNF_01364 | 1.5e-34 | P | ATPases associated with a variety of cellular activities | |||
BABJCGNF_01365 | 5.8e-49 | hrtB | V | ABC transporter permease | ||
BABJCGNF_01366 | 8.6e-49 | hrtB | V | ABC transporter permease | ||
BABJCGNF_01367 | 5.5e-101 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
BABJCGNF_01368 | 2e-42 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BABJCGNF_01369 | 4.3e-80 | G | PTS system sugar-specific permease component | |||
BABJCGNF_01370 | 1.5e-10 | V | ABC transporter, ATP-binding protein | |||
BABJCGNF_01371 | 2e-12 | |||||
BABJCGNF_01372 | 6.7e-13 | N | domain, Protein | |||
BABJCGNF_01373 | 2.3e-131 | M | Bacteriophage peptidoglycan hydrolase | |||
BABJCGNF_01374 | 1.1e-47 | K | sequence-specific DNA binding | |||
BABJCGNF_01376 | 4.4e-22 | gatY | G | Fructose-bisphosphate aldolase class-II | ||
BABJCGNF_01377 | 1.6e-56 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01378 | 1.3e-08 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01379 | 1.7e-25 | C | Iron-sulfur cluster-binding domain | |||
BABJCGNF_01380 | 2.4e-25 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01381 | 1.1e-23 | S | Sulfite exporter TauE/SafE | |||
BABJCGNF_01382 | 3.7e-27 | yqfZ | 3.2.1.17 | M | hydrolase, family 25 | |
BABJCGNF_01383 | 3.9e-87 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
BABJCGNF_01384 | 2.1e-15 | D | Putative exonuclease SbcCD, C subunit | |||
BABJCGNF_01385 | 7.9e-19 | 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 | |
BABJCGNF_01386 | 4.5e-11 | 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 | |
BABJCGNF_01388 | 2.4e-46 | P | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
BABJCGNF_01389 | 3.4e-16 | pnb | C | nitroreductase | ||
BABJCGNF_01390 | 3.8e-29 | pnb | C | nitroreductase | ||
BABJCGNF_01391 | 5.2e-67 | |||||
BABJCGNF_01395 | 1.3e-17 | S | YvrJ protein family | |||
BABJCGNF_01396 | 2.2e-19 | G | Phosphotransferase System | |||
BABJCGNF_01397 | 4.2e-28 | gatY | G | Fructose-bisphosphate aldolase class-II | ||
BABJCGNF_01399 | 2.8e-61 | 2.7.1.194, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | ||
BABJCGNF_01400 | 6.8e-116 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
BABJCGNF_01401 | 1e-176 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
BABJCGNF_01402 | 1.2e-279 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
BABJCGNF_01403 | 1.7e-29 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
BABJCGNF_01404 | 1.3e-126 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
BABJCGNF_01405 | 2.4e-22 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
BABJCGNF_01406 | 1.3e-212 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
BABJCGNF_01407 | 4.2e-80 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
BABJCGNF_01408 | 9.3e-62 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
BABJCGNF_01409 | 4.7e-08 | ydeA | S | intracellular protease amidase | ||
BABJCGNF_01411 | 3.1e-26 | |||||
BABJCGNF_01412 | 1.6e-33 | |||||
BABJCGNF_01413 | 2.8e-45 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_01414 | 1.9e-19 | |||||
BABJCGNF_01415 | 1.7e-25 | pkn1 | 1.8.3.7 | S | Sulfatase-modifying factor enzyme 1 | |
BABJCGNF_01416 | 3.5e-90 | S | Metal-independent alpha-mannosidase (GH125) | |||
BABJCGNF_01417 | 8.6e-09 | G | PTS system mannose/fructose/sorbose family IID component | |||
BABJCGNF_01418 | 7.6e-10 | G | PTS system sorbose-specific iic component | |||
BABJCGNF_01419 | 5.7e-36 | G | Phosphodiester glycosidase | |||
BABJCGNF_01420 | 5.8e-11 | srlE | 2.7.1.198 | G | COG3732 Phosphotransferase system sorbitol-specific component IIBC | |
BABJCGNF_01421 | 1.6e-88 | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | ||
BABJCGNF_01422 | 6.6e-58 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
BABJCGNF_01424 | 5.8e-14 | rfbN | GT2 | S | Glycosyl transferase family group 2 | |
BABJCGNF_01426 | 3.4e-16 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
BABJCGNF_01428 | 3e-31 | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
BABJCGNF_01429 | 1.3e-62 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
BABJCGNF_01430 | 1.5e-14 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
BABJCGNF_01431 | 8.9e-59 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
BABJCGNF_01432 | 8.3e-12 | G | PTS system sorbose-specific iic component | |||
BABJCGNF_01433 | 1.6e-13 | secY2 | U | SecY translocase | ||
BABJCGNF_01434 | 1.4e-07 | asp2 | 3.4.11.5 | S | Accessory Sec system GspB-transporter | |
BABJCGNF_01435 | 9.4e-68 | S | Sulphur transport | |||
BABJCGNF_01436 | 1.6e-106 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
BABJCGNF_01438 | 1.1e-11 | S | Acyltransferase family | |||
BABJCGNF_01440 | 2.1e-51 | kdsD | 5.3.1.13 | M | SIS domain | |
BABJCGNF_01442 | 2.4e-18 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01443 | 7.7e-52 | 2.7.1.194, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01444 | 5.3e-55 | 2.7.1.194, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01445 | 1.4e-11 | 2.7.1.194, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01446 | 4.3e-40 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
BABJCGNF_01447 | 2.8e-32 | |||||
BABJCGNF_01448 | 5.1e-44 | |||||
BABJCGNF_01449 | 2.7e-49 | dgoD | 4.2.1.6 | M | Mandelate racemase muconate lactonizing enzyme | |
BABJCGNF_01450 | 2.1e-95 | dgoD | 4.2.1.6 | M | Mandelate racemase muconate lactonizing enzyme | |
BABJCGNF_01451 | 5.7e-13 | dgoD | 4.2.1.6 | M | Mandelate racemase muconate lactonizing enzyme | |
BABJCGNF_01452 | 3.1e-22 | G | PTS system sugar-specific permease component | |||
BABJCGNF_01453 | 5.1e-57 | rpe | 5.1.3.1 | G | Psort location Cytoplasmic, score 8.87 | |
BABJCGNF_01454 | 1.5e-60 | hxlB | 4.1.2.43, 5.3.1.27 | G | SIS domain | |
BABJCGNF_01455 | 3.4e-21 | IQ | KR domain | |||
BABJCGNF_01456 | 3.1e-108 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
BABJCGNF_01457 | 1.2e-24 | manR | K | PRD domain | ||
BABJCGNF_01459 | 9.1e-38 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
BABJCGNF_01460 | 7.4e-108 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
BABJCGNF_01461 | 7.8e-48 | E | IrrE N-terminal-like domain | |||
BABJCGNF_01462 | 2.7e-76 | L | Helix-turn-helix domain | |||
BABJCGNF_01463 | 1.5e-80 | mngB | 3.2.1.170 | GH38 | G | hydrolase, family 38 |
BABJCGNF_01464 | 3.2e-132 | mngB | 3.2.1.170 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
BABJCGNF_01465 | 7.6e-37 | mngB | 3.2.1.170 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
BABJCGNF_01466 | 8e-09 | 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 | ||
BABJCGNF_01467 | 1.4e-19 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
BABJCGNF_01468 | 1.5e-30 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01469 | 3e-33 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01470 | 6.1e-35 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
BABJCGNF_01471 | 5.4e-30 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
BABJCGNF_01472 | 3.9e-29 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
BABJCGNF_01473 | 3.2e-111 | hchA | S | DJ-1/PfpI family | ||
BABJCGNF_01475 | 3.3e-32 | malY | 4.4.1.8 | E | Aminotransferase class I and II | |
BABJCGNF_01476 | 2.1e-09 | malY | 4.4.1.8 | E | Aminotransferase class I and II | |
BABJCGNF_01477 | 3.4e-25 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01478 | 2.5e-63 | S | Prophage endopeptidase tail | |||
BABJCGNF_01479 | 4.6e-52 | S | phage tail | |||
BABJCGNF_01482 | 1.5e-26 | D | Phage-related minor tail protein | |||
BABJCGNF_01483 | 3e-28 | yjdF | S | Protein of unknown function (DUF2992) | ||
BABJCGNF_01484 | 1.1e-38 | |||||
BABJCGNF_01486 | 4.3e-18 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase | |
BABJCGNF_01487 | 3.5e-143 | S | Phage portal protein, SPP1 Gp6-like | |||
BABJCGNF_01488 | 3.1e-117 | frvB | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BABJCGNF_01489 | 7e-20 | S | CAAX protease self-immunity | |||
BABJCGNF_01490 | 2.1e-09 | |||||
BABJCGNF_01492 | 6.2e-40 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
BABJCGNF_01498 | 5.5e-17 | 2.7.1.194, 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
BABJCGNF_01500 | 8.5e-30 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01501 | 1.2e-09 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01502 | 2.3e-09 | S | Calcineurin-like phosphoesterase | |||
BABJCGNF_01503 | 8e-60 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01504 | 4.7e-09 | S | 40-residue YVTN family beta-propeller | |||
BABJCGNF_01505 | 5e-23 | G | Transmembrane secretion effector | |||
BABJCGNF_01506 | 1.5e-08 | G | MFS/sugar transport protein | |||
BABJCGNF_01507 | 4.9e-18 | licD4 | M | O-Antigen ligase | ||
BABJCGNF_01509 | 4.7e-46 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BABJCGNF_01510 | 1.1e-99 | gadR | K | Transcriptional activator, Rgg GadR MutR family | ||
BABJCGNF_01511 | 6.5e-26 | L | Winged helix-turn helix | |||
BABJCGNF_01512 | 5.3e-89 | L | hmm pf00665 | |||
BABJCGNF_01513 | 1.1e-42 | cps2I | S | Psort location CytoplasmicMembrane, score | ||
BABJCGNF_01514 | 0.0 | M | Glycosyl hydrolase family 59 | |||
BABJCGNF_01515 | 7.2e-21 | M | Glycosyl hydrolase family 59 | |||
BABJCGNF_01516 | 7.8e-20 | M | Bacteriophage peptidoglycan hydrolase | |||
BABJCGNF_01517 | 2.4e-23 | wbbI | M | transferase activity, transferring glycosyl groups | ||
BABJCGNF_01520 | 6.5e-50 | K | UbiC transcription regulator-associated domain protein | |||
BABJCGNF_01521 | 1.2e-59 | |||||
BABJCGNF_01523 | 5.2e-214 | S | phage terminase, large subunit | |||
BABJCGNF_01526 | 1.7e-120 | S | Phage capsid family | |||
BABJCGNF_01528 | 2.7e-36 | S | Phage protein Gp19/Gp15/Gp42 | |||
BABJCGNF_01529 | 7.4e-22 | |||||
BABJCGNF_01530 | 1.1e-12 | |||||
BABJCGNF_01531 | 5.3e-32 | |||||
BABJCGNF_01532 | 1.4e-14 | |||||
BABJCGNF_01533 | 3.9e-32 | eae | N | domain, Protein | ||
BABJCGNF_01534 | 3.9e-19 | |||||
BABJCGNF_01535 | 1.8e-28 | S | Family of unknown function (DUF5361) | |||
BABJCGNF_01536 | 1.5e-13 | N | phage tail tape measure protein | |||
BABJCGNF_01537 | 2.8e-45 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
BABJCGNF_01538 | 4e-52 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
BABJCGNF_01539 | 8.6e-33 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
BABJCGNF_01540 | 1.3e-52 | epsB | M | biosynthesis protein | ||
BABJCGNF_01541 | 1.4e-21 | epsB | M | biosynthesis protein | ||
BABJCGNF_01543 | 4.3e-32 | |||||
BABJCGNF_01544 | 1.5e-30 | |||||
BABJCGNF_01545 | 7e-18 | cotH | M | CotH kinase protein | ||
BABJCGNF_01546 | 3.4e-21 | cotH | M | CotH kinase protein | ||
BABJCGNF_01547 | 2.7e-14 | |||||
BABJCGNF_01548 | 2.7e-56 | 3.5.1.28 | M | N-Acetylmuramoyl-L-alanine amidase | ||
BABJCGNF_01549 | 1e-47 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BABJCGNF_01550 | 3.5e-10 | glvR | K | DNA-binding transcription factor activity | ||
BABJCGNF_01551 | 1e-08 | K | Transcriptional regulator | |||
BABJCGNF_01552 | 6.5e-185 | S | hydrolase activity | |||
BABJCGNF_01553 | 3.2e-34 | S | Phage plasmid primase, P4 | |||
BABJCGNF_01554 | 1.3e-83 | S | hydrolase activity | |||
BABJCGNF_01555 | 9.7e-59 | S | Phage plasmid primase, P4 | |||
BABJCGNF_01556 | 1.6e-72 | S | Protein of unknown function (DUF669) | |||
BABJCGNF_01557 | 4.7e-176 | S | helicase activity | |||
BABJCGNF_01558 | 2.8e-29 | S | AAA domain | |||
BABJCGNF_01559 | 3.4e-52 | S | Siphovirus Gp157 | |||
BABJCGNF_01565 | 1.7e-50 | wcaJ | M | Bacterial sugar transferase | ||
BABJCGNF_01566 | 8.7e-33 | wcaJ | M | Bacterial sugar transferase | ||
BABJCGNF_01567 | 1e-41 | G | PTS system mannose/fructose/sorbose family IID component | |||
BABJCGNF_01568 | 5.6e-19 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
BABJCGNF_01569 | 8.2e-40 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
BABJCGNF_01570 | 1.1e-141 | tauC | P | Binding-protein-dependent transport system inner membrane component | ||
BABJCGNF_01572 | 1.6e-22 | |||||
BABJCGNF_01573 | 1.2e-43 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_01574 | 7.6e-32 | G | PTS system enzyme II sorbitol-specific factor | |||
BABJCGNF_01575 | 9.5e-41 | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | ||
BABJCGNF_01576 | 3.1e-07 | S | CAAX protease self-immunity | |||
BABJCGNF_01577 | 4.1e-70 | K | ORF6N domain | |||
BABJCGNF_01579 | 1.1e-32 | 1.15.1.2 | CE | Pfam:DUF955 | ||
BABJCGNF_01580 | 1.5e-65 | |||||
BABJCGNF_01581 | 9.4e-19 | L | Belongs to the 'phage' integrase family | |||
BABJCGNF_01582 | 4.8e-25 | L | Belongs to the 'phage' integrase family | |||
BABJCGNF_01583 | 1.4e-25 | 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01586 | 1.5e-104 | 5.3.1.15 | S | Pfam:DUF1498 | ||
BABJCGNF_01587 | 4.3e-21 | xylB | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
BABJCGNF_01589 | 4.5e-13 | 1.1.1.14 | C | PFAM Alcohol dehydrogenase | ||
BABJCGNF_01590 | 1.7e-09 | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | ||
BABJCGNF_01592 | 1e-78 | G | PTS system sugar-specific permease component | |||
BABJCGNF_01593 | 2.5e-83 | thrA | E | SAF | ||
BABJCGNF_01594 | 3.6e-39 | thrA | E | SAF | ||
BABJCGNF_01595 | 7.1e-12 | |||||
BABJCGNF_01596 | 4.3e-31 | K | LysR substrate binding domain | |||
BABJCGNF_01597 | 7e-147 | L | PFAM Integrase catalytic region | |||
BABJCGNF_01598 | 2.2e-42 | L | Helix-turn-helix domain | |||
BABJCGNF_01599 | 1.2e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
BABJCGNF_01600 | 1.3e-137 | jag | S | R3H domain protein | ||
BABJCGNF_01601 | 2.4e-64 | 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 | ||
BABJCGNF_01602 | 1.9e-47 | 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 | ||
BABJCGNF_01603 | 3.6e-51 | 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 | |
BABJCGNF_01604 | 9.2e-64 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
BABJCGNF_01605 | 2.6e-80 | S | Threonine/Serine exporter, ThrE | |||
BABJCGNF_01606 | 3.2e-133 | thrE | S | Putative threonine/serine exporter | ||
BABJCGNF_01608 | 6.4e-137 | V | ABC transporter transmembrane region | |||
BABJCGNF_01609 | 2.5e-92 | V | ABC transporter transmembrane region | |||
BABJCGNF_01610 | 3.6e-82 | 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 | ||
BABJCGNF_01611 | 2.8e-271 | 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 | ||
BABJCGNF_01612 | 6.1e-97 | 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 | ||
BABJCGNF_01613 | 8.6e-105 | 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 | ||
BABJCGNF_01614 | 1.6e-12 | 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 | ||
BABJCGNF_01615 | 3.3e-68 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
BABJCGNF_01616 | 8e-121 | gldA | 1.1.1.1, 1.1.1.6 | C | dehydrogenase | |
BABJCGNF_01617 | 4.1e-42 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
BABJCGNF_01618 | 1.6e-54 | glvC | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
BABJCGNF_01619 | 7.6e-39 | glvC | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
BABJCGNF_01621 | 6.6e-142 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
BABJCGNF_01622 | 3.9e-32 | M | NLPA lipoprotein | |||
BABJCGNF_01624 | 8.2e-19 | M | Leucine rich repeats (6 copies) | |||
BABJCGNF_01625 | 6.8e-104 | M | Leucine rich repeats (6 copies) | |||
BABJCGNF_01626 | 3.2e-168 | M | Leucine rich repeats (6 copies) | |||
BABJCGNF_01627 | 5.4e-130 | |||||
BABJCGNF_01628 | 1.3e-26 | M | Leucine rich repeats (6 copies) | |||
BABJCGNF_01629 | 8.7e-151 | M | Leucine rich repeats (6 copies) | |||
BABJCGNF_01630 | 8.1e-47 | bacI | V | MacB-like periplasmic core domain | ||
BABJCGNF_01631 | 8e-11 | V | ABC transporter | |||
BABJCGNF_01632 | 2.9e-41 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
BABJCGNF_01633 | 9e-17 | |||||
BABJCGNF_01634 | 2e-14 | |||||
BABJCGNF_01635 | 6.6e-41 | |||||
BABJCGNF_01636 | 1e-82 | |||||
BABJCGNF_01637 | 1.6e-21 | spiA | K | IrrE N-terminal-like domain | ||
BABJCGNF_01638 | 4.4e-77 | spiA | K | IrrE N-terminal-like domain | ||
BABJCGNF_01639 | 4e-40 | spiA | K | IrrE N-terminal-like domain | ||
BABJCGNF_01640 | 1.3e-285 | mtlR | K | Mga helix-turn-helix domain | ||
BABJCGNF_01641 | 9.4e-133 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BABJCGNF_01642 | 1.6e-97 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BABJCGNF_01643 | 4.2e-62 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BABJCGNF_01644 | 1.5e-101 | 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 | |
BABJCGNF_01645 | 7.3e-172 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
BABJCGNF_01646 | 1.1e-24 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
BABJCGNF_01647 | 2.1e-42 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
BABJCGNF_01648 | 1.2e-22 | ulaG | S | Beta-lactamase superfamily domain | ||
BABJCGNF_01649 | 2.2e-184 | lipA | I | Carboxylesterase family | ||
BABJCGNF_01650 | 1.8e-179 | D | Alpha beta | |||
BABJCGNF_01651 | 1.5e-169 | O | protein-N(PI)-phosphohistidine-lactose phosphotransferase system transporter activity | |||
BABJCGNF_01653 | 1.6e-73 | 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) | |
BABJCGNF_01654 | 2.7e-149 | 1.1.1.31 | I | NAD binding domain of 6-phosphogluconate dehydrogenase | ||
BABJCGNF_01655 | 1.1e-67 | |||||
BABJCGNF_01656 | 4.5e-52 | yfeJ | 6.3.5.2 | F | Glutamine amidotransferase class-I | |
BABJCGNF_01657 | 2.3e-78 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
BABJCGNF_01658 | 3.3e-162 | maeN | C | 2-hydroxycarboxylate transporter family | ||
BABJCGNF_01659 | 2.6e-27 | maeN | C | 2-hydroxycarboxylate transporter family | ||
BABJCGNF_01660 | 2.1e-23 | dcuS | 2.7.13.3 | T | Single cache domain 3 | |
BABJCGNF_01661 | 1.5e-65 | dcuS | 2.7.13.3 | T | Single cache domain 3 | |
BABJCGNF_01662 | 2.9e-88 | dcuS | 2.7.13.3 | T | Single cache domain 3 | |
BABJCGNF_01663 | 6e-55 | dpiA | KT | cheY-homologous receiver domain | ||
BABJCGNF_01664 | 2.2e-35 | dpiA | KT | cheY-homologous receiver domain | ||
BABJCGNF_01665 | 4.5e-45 | |||||
BABJCGNF_01667 | 3.8e-145 | yebA | E | Transglutaminase/protease-like homologues | ||
BABJCGNF_01668 | 1.7e-27 | lsgC | M | Glycosyl transferases group 1 | ||
BABJCGNF_01669 | 5.8e-143 | lsgC | M | Glycosyl transferases group 1 | ||
BABJCGNF_01670 | 8.5e-128 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
BABJCGNF_01671 | 3.8e-104 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
BABJCGNF_01672 | 2e-20 | yeaD | S | Protein of unknown function DUF58 | ||
BABJCGNF_01673 | 2.2e-42 | yeaD | S | Protein of unknown function DUF58 | ||
BABJCGNF_01674 | 9.4e-65 | yebA | E | Transglutaminase/protease-like homologues | ||
BABJCGNF_01675 | 8.1e-85 | yebA | E | Transglutaminase/protease-like homologues | ||
BABJCGNF_01676 | 5.5e-131 | S | PTS system sugar-specific permease component | |||
BABJCGNF_01677 | 1.9e-25 | 2.7.1.194 | G | protein-N(PI)-phosphohistidine-sugar phosphotransferase activity | ||
BABJCGNF_01678 | 1.3e-66 | ydaF | J | Acetyltransferase (GNAT) domain | ||
BABJCGNF_01679 | 3.5e-40 | S | Stage II sporulation protein M | |||
BABJCGNF_01680 | 2e-41 | S | Stage II sporulation protein M | |||
BABJCGNF_01681 | 3.7e-97 | yeaC | S | ATPase family associated with various cellular activities (AAA) | ||
BABJCGNF_01682 | 6.2e-55 | yeaC | S | ATPase family associated with various cellular activities (AAA) | ||
BABJCGNF_01683 | 4e-265 | glnP | P | ABC transporter | ||
BABJCGNF_01684 | 1.3e-48 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BABJCGNF_01685 | 2.6e-22 | glnP | P | ABC transporter | ||
BABJCGNF_01686 | 2.3e-36 | glnP | P | ABC transporter | ||
BABJCGNF_01687 | 4.8e-111 | ydbT | S | Bacterial PH domain | ||
BABJCGNF_01688 | 2.6e-86 | S | AAA ATPase domain | |||
BABJCGNF_01689 | 2.5e-99 | yniA | G | Phosphotransferase enzyme family | ||
BABJCGNF_01690 | 3.5e-54 | yniA | G | Phosphotransferase enzyme family | ||
BABJCGNF_01691 | 9.1e-33 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BABJCGNF_01692 | 1.9e-44 | S | Bacterial PH domain | |||
BABJCGNF_01693 | 2.3e-20 | S | Bacterial PH domain | |||
BABJCGNF_01694 | 6.8e-14 | ydbT | S | Bacterial PH domain | ||
BABJCGNF_01695 | 1.5e-27 | ydbT | S | Bacterial PH domain | ||
BABJCGNF_01696 | 6.1e-57 | yqkB | S | Iron-sulphur cluster biosynthesis | ||
BABJCGNF_01697 | 3.3e-46 | |||||
BABJCGNF_01699 | 5.8e-222 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
BABJCGNF_01700 | 1.4e-79 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
BABJCGNF_01702 | 3.1e-154 | glnP | P | ABC transporter permease | ||
BABJCGNF_01703 | 2.5e-100 | glnP | P | ABC transporter permease | ||
BABJCGNF_01704 | 4.1e-133 | glnQ | E | ABC transporter, ATP-binding protein | ||
BABJCGNF_01705 | 1.2e-22 | |||||
BABJCGNF_01706 | 1.3e-235 | malE | G | Bacterial extracellular solute-binding protein | ||
BABJCGNF_01707 | 8.8e-53 | S | Protein of unknown function (DUF975) | |||
BABJCGNF_01708 | 1.2e-19 | EGP | Major facilitator Superfamily | |||
BABJCGNF_01709 | 6.2e-149 | EGP | Major facilitator Superfamily | |||
BABJCGNF_01710 | 5.2e-187 | K | Helix-turn-helix XRE-family like proteins | |||
BABJCGNF_01711 | 3.3e-46 | K | Helix-turn-helix XRE-family like proteins | |||
BABJCGNF_01712 | 1.8e-93 | K | Helix-turn-helix XRE-family like proteins | |||
BABJCGNF_01713 | 1.3e-119 | K | sequence-specific DNA binding | |||
BABJCGNF_01717 | 2.8e-140 | manN | G | system, mannose fructose sorbose family IID component | ||
BABJCGNF_01718 | 1.6e-122 | manY | G | PTS system | ||
BABJCGNF_01719 | 1.3e-182 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
BABJCGNF_01720 | 5.1e-31 | 2.7.1.194, 2.7.1.197, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_01721 | 5.6e-172 | iolS | C | Aldo keto reductase | ||
BABJCGNF_01722 | 4.4e-64 | manO | S | Domain of unknown function (DUF956) | ||
BABJCGNF_01723 | 1.2e-37 | ycaC | Q | Isochorismatase family | ||
BABJCGNF_01724 | 8.2e-24 | ycaC | Q | Isochorismatase family | ||
BABJCGNF_01725 | 3.1e-193 | ydiC1 | EGP | Major Facilitator Superfamily | ||
BABJCGNF_01726 | 1.3e-37 | ydiC1 | EGP | Major Facilitator Superfamily | ||
BABJCGNF_01727 | 3.8e-92 | yeaN | P | Transporter, major facilitator family protein | ||
BABJCGNF_01728 | 1.4e-47 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
BABJCGNF_01729 | 1e-26 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
BABJCGNF_01730 | 9e-57 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
BABJCGNF_01731 | 4.3e-25 | S | Bacterial protein of unknown function (DUF871) | |||
BABJCGNF_01732 | 1.1e-83 | S | Bacterial protein of unknown function (DUF871) | |||
BABJCGNF_01733 | 9e-43 | S | Bacterial protein of unknown function (DUF871) | |||
BABJCGNF_01734 | 1.4e-71 | S | Domain of unknown function (DUF3284) | |||
BABJCGNF_01735 | 2.7e-223 | 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 | |
BABJCGNF_01736 | 4.8e-60 | K | UbiC transcription regulator-associated domain protein | |||
BABJCGNF_01737 | 8.1e-31 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
BABJCGNF_01738 | 8.4e-40 | arpJ | P | ABC transporter permease | ||
BABJCGNF_01739 | 2.9e-73 | arpJ | P | ABC transporter permease | ||
BABJCGNF_01740 | 4.4e-55 | arpJ | P | ABC transporter permease | ||
BABJCGNF_01741 | 1.1e-36 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
BABJCGNF_01742 | 1.1e-40 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
BABJCGNF_01743 | 8.3e-56 | gntR | K | rpiR family | ||
BABJCGNF_01744 | 6.8e-95 | S | Alpha/beta hydrolase family | |||
BABJCGNF_01745 | 6.1e-20 | yycH | S | YycH protein | ||
BABJCGNF_01746 | 6e-19 | yycH | S | YycH protein | ||
BABJCGNF_01747 | 6.3e-142 | vicK | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_01748 | 1.6e-75 | vicK | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_01749 | 3.8e-29 | vicK | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_01750 | 4.8e-56 | vicK | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_01751 | 2.9e-96 | K | response regulator | |||
BABJCGNF_01752 | 2.7e-76 | hsp3 | O | Hsp20/alpha crystallin family | ||
BABJCGNF_01753 | 8.7e-69 | S | Iron-sulphur cluster biosynthesis | |||
BABJCGNF_01754 | 1.5e-78 | htrA | 3.4.21.107 | O | serine protease | |
BABJCGNF_01755 | 1.8e-43 | htrA | 3.4.21.107 | O | serine protease | |
BABJCGNF_01756 | 1.8e-39 | htrA | 3.4.21.107 | O | serine protease | |
BABJCGNF_01757 | 9.5e-13 | |||||
BABJCGNF_01758 | 9.1e-115 | vicX | 3.1.26.11 | S | domain protein | |
BABJCGNF_01759 | 1.9e-23 | vicX | 3.1.26.11 | S | domain protein | |
BABJCGNF_01760 | 2.5e-74 | yycI | S | YycH protein | ||
BABJCGNF_01761 | 4.1e-51 | yycI | S | YycH protein | ||
BABJCGNF_01762 | 1.3e-48 | yycH | S | YycH protein | ||
BABJCGNF_01763 | 2.2e-202 | cadA | P | P-type ATPase | ||
BABJCGNF_01764 | 8.3e-52 | cadA | P | P-type ATPase | ||
BABJCGNF_01765 | 8e-139 | |||||
BABJCGNF_01767 | 2.7e-46 | E | ABC transporter, substratebinding protein | |||
BABJCGNF_01768 | 3e-63 | E | ABC transporter, substratebinding protein | |||
BABJCGNF_01769 | 8.4e-131 | ybiR | P | Citrate transporter | ||
BABJCGNF_01770 | 1.1e-68 | |||||
BABJCGNF_01771 | 9.6e-23 | |||||
BABJCGNF_01773 | 3.4e-219 | E | Peptidase dimerisation domain | |||
BABJCGNF_01774 | 3.7e-25 | frdC | 1.3.5.4 | C | HI0933-like protein | |
BABJCGNF_01775 | 6.8e-37 | 4.1.2.17 | G | Class II Aldolase and Adducin N-terminal domain | ||
BABJCGNF_01776 | 9.5e-34 | 4.1.2.17 | G | Class II Aldolase and Adducin N-terminal domain | ||
BABJCGNF_01777 | 3e-142 | 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 | ||
BABJCGNF_01778 | 1.4e-39 | K | Acetyltransferase (GNAT) domain | |||
BABJCGNF_01779 | 7.4e-47 | |||||
BABJCGNF_01780 | 4e-60 | |||||
BABJCGNF_01781 | 5.1e-29 | |||||
BABJCGNF_01783 | 1.5e-36 | |||||
BABJCGNF_01784 | 7.5e-101 | S | alpha beta | |||
BABJCGNF_01785 | 3.2e-81 | MA20_25245 | K | FR47-like protein | ||
BABJCGNF_01786 | 1.5e-57 | hisB | 2.7.7.71, 3.1.3.15, 3.1.3.82, 3.1.3.83, 4.2.1.19, 5.3.1.28, 6.3.2.10 | GT9 | E | HAD-hyrolase-like |
BABJCGNF_01787 | 1.9e-13 | hisB | 2.7.7.71, 3.1.3.15, 3.1.3.82, 3.1.3.83, 4.2.1.19, 5.3.1.28, 6.3.2.10 | GT9 | E | HAD-hyrolase-like |
BABJCGNF_01788 | 1.3e-102 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
BABJCGNF_01789 | 2.9e-51 | sugE | U | Multidrug resistance protein | ||
BABJCGNF_01790 | 9.1e-37 | G | PTS system mannose/fructose/sorbose family IID component | |||
BABJCGNF_01791 | 5.9e-77 | G | PTS system mannose/fructose/sorbose family IID component | |||
BABJCGNF_01792 | 2.2e-127 | G | PTS system sorbose-specific iic component | |||
BABJCGNF_01793 | 2.3e-45 | S | endonuclease exonuclease phosphatase family protein | |||
BABJCGNF_01794 | 1.2e-77 | S | endonuclease exonuclease phosphatase family protein | |||
BABJCGNF_01795 | 1.7e-38 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
BABJCGNF_01796 | 6.4e-39 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
BABJCGNF_01797 | 8.8e-40 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
BABJCGNF_01798 | 4.9e-146 | 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 | |
BABJCGNF_01799 | 1.7e-70 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
BABJCGNF_01800 | 2.2e-69 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
BABJCGNF_01801 | 2.6e-22 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
BABJCGNF_01802 | 7.3e-138 | EGP | Major facilitator Superfamily | |||
BABJCGNF_01803 | 1.3e-13 | EGP | Major facilitator Superfamily | |||
BABJCGNF_01804 | 1.1e-147 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
BABJCGNF_01805 | 2.4e-59 | ugpE | G | ABC transporter permease | ||
BABJCGNF_01806 | 2.8e-163 | ugpA | P | ABC-type sugar transport systems, permease components | ||
BABJCGNF_01807 | 3.2e-112 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
BABJCGNF_01808 | 2.6e-142 | ugpB | G | Bacterial extracellular solute-binding protein | ||
BABJCGNF_01809 | 2.6e-10 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
BABJCGNF_01810 | 1.2e-13 | ugpB | G | Bacterial extracellular solute-binding protein | ||
BABJCGNF_01811 | 2.2e-124 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
BABJCGNF_01813 | 9.4e-132 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
BABJCGNF_01814 | 9.9e-108 | pncA | Q | Isochorismatase family | ||
BABJCGNF_01815 | 3.4e-65 | sca1 | G | Belongs to the glycosyl hydrolase 31 family | ||
BABJCGNF_01816 | 2e-95 | sca1 | G | Belongs to the glycosyl hydrolase 31 family | ||
BABJCGNF_01817 | 1.4e-220 | sca1 | G | Belongs to the glycosyl hydrolase 31 family | ||
BABJCGNF_01818 | 1.7e-62 | sca1 | G | Belongs to the glycosyl hydrolase 31 family | ||
BABJCGNF_01819 | 7.1e-22 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
BABJCGNF_01820 | 1.2e-77 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
BABJCGNF_01822 | 1.7e-53 | K | Helix-turn-helix domain | |||
BABJCGNF_01823 | 2.3e-79 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
BABJCGNF_01824 | 2.6e-20 | frdC | 1.3.5.4 | C | HI0933-like protein | |
BABJCGNF_01825 | 3.8e-15 | uhpT | EGP | Major facilitator Superfamily | ||
BABJCGNF_01826 | 9.2e-167 | uhpT | EGP | Major facilitator Superfamily | ||
BABJCGNF_01827 | 7.3e-32 | 3.5.1.18 | E | Peptidase family M20/M25/M40 | ||
BABJCGNF_01828 | 1.4e-77 | aspG | 3.4.19.5, 3.5.1.1, 3.5.1.26 | E | Asparaginase | |
BABJCGNF_01829 | 9.5e-68 | aspG | 3.4.19.5, 3.5.1.1, 3.5.1.26 | E | Asparaginase | |
BABJCGNF_01830 | 1.9e-115 | O | Belongs to the peptidase S8 family | |||
BABJCGNF_01831 | 2.2e-41 | |||||
BABJCGNF_01832 | 7.2e-301 | O | Belongs to the peptidase S8 family | |||
BABJCGNF_01833 | 1.3e-44 | O | Belongs to the peptidase S8 family | |||
BABJCGNF_01834 | 9.1e-28 | O | Belongs to the peptidase S8 family | |||
BABJCGNF_01835 | 4.8e-114 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
BABJCGNF_01836 | 6.7e-41 | sgaB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BABJCGNF_01837 | 7e-70 | ulaA | S | PTS system sugar-specific permease component | ||
BABJCGNF_01838 | 2.7e-149 | ulaA | S | PTS system sugar-specific permease component | ||
BABJCGNF_01839 | 2.9e-35 | ulaA | S | PTS system sugar-specific permease component | ||
BABJCGNF_01840 | 1.8e-19 | cmtB | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01841 | 8.4e-51 | cmtB | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01842 | 1.2e-213 | ulaG | S | Beta-lactamase superfamily domain | ||
BABJCGNF_01843 | 4.8e-75 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
BABJCGNF_01844 | 4.6e-28 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
BABJCGNF_01845 | 7.7e-45 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
BABJCGNF_01846 | 2.3e-44 | repA | K | DeoR C terminal sensor domain | ||
BABJCGNF_01847 | 1.1e-136 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
BABJCGNF_01848 | 4.5e-51 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
BABJCGNF_01849 | 1.3e-122 | tal | 2.2.1.2 | H | Pfam:Transaldolase | |
BABJCGNF_01850 | 1.2e-64 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
BABJCGNF_01851 | 1.2e-161 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
BABJCGNF_01852 | 1.8e-21 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
BABJCGNF_01853 | 2.2e-102 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
BABJCGNF_01854 | 1.5e-86 | gutM | K | Glucitol operon activator protein (GutM) | ||
BABJCGNF_01855 | 8.5e-11 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
BABJCGNF_01856 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
BABJCGNF_01857 | 5.5e-43 | IQ | NAD dependent epimerase/dehydratase family | |||
BABJCGNF_01858 | 2.6e-101 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
BABJCGNF_01859 | 4.8e-137 | 4.1.2.14 | S | KDGP aldolase | ||
BABJCGNF_01860 | 4.9e-105 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
BABJCGNF_01861 | 3.5e-61 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
BABJCGNF_01862 | 9.9e-17 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
BABJCGNF_01863 | 4e-40 | dho | 3.5.2.3 | S | Amidohydrolase family | |
BABJCGNF_01864 | 1.4e-50 | dho | 3.5.2.3 | S | Amidohydrolase family | |
BABJCGNF_01865 | 1.8e-29 | dho | 3.5.2.3 | S | Amidohydrolase family | |
BABJCGNF_01866 | 7.8e-46 | S | Domain of unknown function (DUF4310) | |||
BABJCGNF_01867 | 1.7e-100 | S | Domain of unknown function (DUF4311) | |||
BABJCGNF_01868 | 1.2e-61 | S | Glycine-rich SFCGS | |||
BABJCGNF_01869 | 4.8e-34 | S | PRD domain | |||
BABJCGNF_01870 | 0.0 | K | Mga helix-turn-helix domain | |||
BABJCGNF_01872 | 3.3e-43 | K | Helix-turn-helix domain, rpiR family | |||
BABJCGNF_01873 | 2.5e-55 | K | Helix-turn-helix domain, rpiR family | |||
BABJCGNF_01874 | 2.1e-56 | V | ABC-type multidrug transport system, ATPase and permease components | |||
BABJCGNF_01875 | 4.3e-65 | V | ABC-type multidrug transport system, ATPase and permease components | |||
BABJCGNF_01876 | 8.4e-11 | V | ABC-type multidrug transport system, ATPase and permease components | |||
BABJCGNF_01877 | 1.2e-47 | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
BABJCGNF_01878 | 6.6e-41 | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
BABJCGNF_01880 | 8.5e-08 | rliB | K | helix_turn_helix gluconate operon transcriptional repressor | ||
BABJCGNF_01881 | 1.1e-25 | araR | K | helix_turn_helix gluconate operon transcriptional repressor | ||
BABJCGNF_01882 | 3e-96 | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain | |
BABJCGNF_01883 | 1.3e-238 | G | Major Facilitator | |||
BABJCGNF_01884 | 4.1e-21 | G | PTS system mannose/fructose/sorbose family IID component | |||
BABJCGNF_01885 | 3.5e-20 | G | PTS system mannose/fructose/sorbose family IID component | |||
BABJCGNF_01888 | 7e-10 | rafA | 3.2.1.22 | G | Melibiase | |
BABJCGNF_01889 | 2.8e-55 | CP_0954 | 4.2.2.1 | PL8 | N | Polysaccharide lyase family 8, N terminal alpha-helical domain |
BABJCGNF_01890 | 8.3e-63 | K | Bacterial transcriptional regulator | |||
BABJCGNF_01891 | 6.2e-48 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
BABJCGNF_01892 | 2.5e-58 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
BABJCGNF_01893 | 1e-137 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BABJCGNF_01894 | 1.1e-86 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
BABJCGNF_01895 | 4.9e-153 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
BABJCGNF_01896 | 2.9e-40 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
BABJCGNF_01897 | 1.2e-66 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
BABJCGNF_01899 | 7.4e-30 | CP_0954 | 4.2.2.1 | PL8 | N | Polysaccharide lyase family 8, N terminal alpha-helical domain |
BABJCGNF_01900 | 5.8e-22 | agaV | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
BABJCGNF_01901 | 6.8e-42 | agaV | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
BABJCGNF_01902 | 2.8e-41 | ugl | 3.2.1.180 | GH88 | S | Glycosyl Hydrolase Family 88 |
BABJCGNF_01903 | 3e-55 | ugl | 3.2.1.180 | GH88 | S | Glycosyl Hydrolase Family 88 |
BABJCGNF_01904 | 1.6e-45 | ugl | 3.2.1.180 | GH88 | S | Glycosyl Hydrolase Family 88 |
BABJCGNF_01905 | 6.6e-14 | Z012_03480 | S | Psort location Cytoplasmic, score | ||
BABJCGNF_01906 | 9.7e-119 | agaD | G | PTS system mannose/fructose/sorbose family IID component | ||
BABJCGNF_01908 | 3.5e-09 | G | PTS system fructose IIA component | |||
BABJCGNF_01909 | 7.3e-95 | |||||
BABJCGNF_01910 | 7.3e-20 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
BABJCGNF_01911 | 3.8e-243 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
BABJCGNF_01913 | 2.8e-185 | plyA3 | M | Right handed beta helix region | ||
BABJCGNF_01914 | 3.3e-26 | |||||
BABJCGNF_01915 | 3.9e-35 | |||||
BABJCGNF_01916 | 3.5e-33 | M | Heparinase II/III N-terminus | |||
BABJCGNF_01918 | 2.7e-09 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
BABJCGNF_01919 | 4.6e-64 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
BABJCGNF_01920 | 1.4e-59 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
BABJCGNF_01921 | 9.7e-42 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
BABJCGNF_01922 | 5e-40 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
BABJCGNF_01923 | 1.5e-24 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
BABJCGNF_01924 | 1.3e-66 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
BABJCGNF_01925 | 7.1e-65 | S | Protein of unknown function (DUF1093) | |||
BABJCGNF_01926 | 5.1e-123 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
BABJCGNF_01927 | 1.6e-13 | rhaB | 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
BABJCGNF_01928 | 2.3e-39 | iolF | EGP | Major facilitator Superfamily | ||
BABJCGNF_01929 | 6.6e-34 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
BABJCGNF_01930 | 1.6e-38 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
BABJCGNF_01931 | 4.7e-45 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
BABJCGNF_01932 | 9.6e-64 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
BABJCGNF_01933 | 1e-36 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
BABJCGNF_01934 | 3.3e-29 | cbiQ | P | cobalt transport | ||
BABJCGNF_01935 | 1.1e-43 | pts36A | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01936 | 4.9e-241 | pts36C | G | PTS system sugar-specific permease component | ||
BABJCGNF_01937 | 6.5e-33 | ypiB | EGP | Major facilitator Superfamily | ||
BABJCGNF_01938 | 5.1e-25 | ypiB | EGP | Major facilitator Superfamily | ||
BABJCGNF_01939 | 3.5e-118 | ypiB | EGP | Major facilitator Superfamily | ||
BABJCGNF_01941 | 6.6e-136 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
BABJCGNF_01942 | 1.1e-79 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01943 | 8.9e-37 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
BABJCGNF_01944 | 1.4e-69 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
BABJCGNF_01945 | 2.3e-37 | pfkB | 2.7.1.11, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
BABJCGNF_01946 | 2.6e-39 | rpl | K | Helix-turn-helix domain, rpiR family | ||
BABJCGNF_01947 | 5.3e-56 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01948 | 3.4e-66 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01949 | 3e-75 | fruA | 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_01950 | 8.7e-106 | 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 | ||
BABJCGNF_01951 | 2.7e-61 | ydfK | S | Protein of unknown function (DUF554) | ||
BABJCGNF_01952 | 4.5e-71 | |||||
BABJCGNF_01953 | 5.8e-55 | 3.6.3.24 | P | ATP-binding cassette cobalt transporter | ||
BABJCGNF_01954 | 2.6e-46 | 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 | ||
BABJCGNF_01955 | 8.5e-122 | EK | Aminotransferase, class I | |||
BABJCGNF_01956 | 2.9e-45 | |||||
BABJCGNF_01957 | 1.7e-91 | yoaK | S | Protein of unknown function (DUF1275) | ||
BABJCGNF_01958 | 4.9e-66 | yjhF | G | Phosphoglycerate mutase family | ||
BABJCGNF_01959 | 5.8e-50 | yjhF | G | Phosphoglycerate mutase family | ||
BABJCGNF_01960 | 1.4e-150 | yitU | 3.1.3.104 | S | hydrolase | |
BABJCGNF_01961 | 8.1e-90 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
BABJCGNF_01962 | 1.4e-54 | K | LysR substrate binding domain | |||
BABJCGNF_01963 | 1e-82 | K | LysR substrate binding domain | |||
BABJCGNF_01965 | 7.2e-72 | uvrA3 | L | excinuclease ABC | ||
BABJCGNF_01966 | 5.5e-71 | uvrA3 | L | excinuclease ABC | ||
BABJCGNF_01967 | 2.4e-130 | yghZ | C | Aldo keto reductase family protein | ||
BABJCGNF_01968 | 1.4e-40 | yghZ | C | Aldo keto reductase family protein | ||
BABJCGNF_01969 | 1.1e-30 | salL | 2.5.1.63, 2.5.1.94 | K | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
BABJCGNF_01970 | 3.5e-77 | salL | 2.5.1.63, 2.5.1.94 | K | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
BABJCGNF_01971 | 3.5e-97 | S | UPF0397 protein | |||
BABJCGNF_01972 | 8.4e-64 | 3.6.3.24 | P | ATP-binding cassette cobalt transporter | ||
BABJCGNF_01973 | 4.3e-39 | 3.6.3.24 | P | ATP-binding cassette cobalt transporter | ||
BABJCGNF_01974 | 1.2e-25 | 3.6.3.24 | P | ATP-binding cassette cobalt transporter | ||
BABJCGNF_01975 | 1.1e-68 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
BABJCGNF_01976 | 6.6e-12 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
BABJCGNF_01977 | 3.8e-147 | V | ABC transporter transmembrane region | |||
BABJCGNF_01978 | 1.2e-109 | S | CAAX protease self-immunity | |||
BABJCGNF_01980 | 1.3e-130 | nodJ | V | ABC-2 type transporter | ||
BABJCGNF_01981 | 3.9e-19 | nodI | V | ABC transporter | ||
BABJCGNF_01982 | 3.2e-93 | nodI | V | ABC transporter | ||
BABJCGNF_01983 | 6e-46 | ydfF | K | Transcriptional | ||
BABJCGNF_01984 | 5.2e-20 | ydfF | K | Transcriptional | ||
BABJCGNF_01985 | 2.4e-153 | shetA | P | Voltage-dependent anion channel | ||
BABJCGNF_01986 | 3.1e-301 | helD | 3.6.4.12 | L | DNA helicase | |
BABJCGNF_01987 | 5.7e-92 | helD | 3.6.4.12 | L | DNA helicase | |
BABJCGNF_01988 | 2.6e-16 | rlrG | K | Transcriptional regulator | ||
BABJCGNF_01989 | 3.7e-61 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BABJCGNF_01990 | 2.5e-60 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BABJCGNF_01991 | 6.9e-28 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BABJCGNF_01992 | 6.6e-251 | gshR | 1.8.1.7 | C | Glutathione reductase | |
BABJCGNF_01993 | 1e-84 | proV | E | ABC transporter, ATP-binding protein | ||
BABJCGNF_01994 | 5.1e-70 | proV | E | ABC transporter, ATP-binding protein | ||
BABJCGNF_01996 | 4.9e-35 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BABJCGNF_01997 | 3.2e-12 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
BABJCGNF_01998 | 7.3e-110 | S | TPM domain | |||
BABJCGNF_01999 | 5.1e-41 | lemA | S | LemA family | ||
BABJCGNF_02001 | 4.8e-134 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BABJCGNF_02002 | 4.6e-45 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BABJCGNF_02003 | 3.9e-11 | EGP | Major Facilitator Superfamily | |||
BABJCGNF_02004 | 4.9e-12 | G | Major facilitator Superfamily | |||
BABJCGNF_02005 | 3.3e-40 | dinF | V | MatE | ||
BABJCGNF_02006 | 3.2e-145 | dinF | V | MatE | ||
BABJCGNF_02007 | 1e-20 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
BABJCGNF_02008 | 3.4e-34 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
BABJCGNF_02009 | 1.9e-135 | S | Aldo keto reductase | |||
BABJCGNF_02010 | 2.5e-76 | bioC | 2.1.1.187, 2.1.1.197 | Q | Protein-L-isoaspartate(D-aspartate) O-methyltransferase (PCMT) | |
BABJCGNF_02011 | 5.3e-26 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
BABJCGNF_02012 | 3.2e-66 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
BABJCGNF_02013 | 4.2e-40 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
BABJCGNF_02014 | 1.4e-37 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
BABJCGNF_02015 | 6.5e-108 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
BABJCGNF_02017 | 1.5e-29 | ypuA | S | Protein of unknown function (DUF1002) | ||
BABJCGNF_02018 | 1.2e-61 | ypuA | S | Protein of unknown function (DUF1002) | ||
BABJCGNF_02019 | 2.7e-152 | yunF | F | Protein of unknown function DUF72 | ||
BABJCGNF_02020 | 4.9e-33 | 3.6.1.55 | F | NUDIX domain | ||
BABJCGNF_02021 | 1.4e-134 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
BABJCGNF_02022 | 5.5e-80 | yiiE | S | Protein of unknown function (DUF1211) | ||
BABJCGNF_02023 | 1e-116 | cobB | K | Sir2 family | ||
BABJCGNF_02025 | 2.8e-17 | |||||
BABJCGNF_02026 | 1.5e-141 | |||||
BABJCGNF_02027 | 1.1e-15 | |||||
BABJCGNF_02028 | 1.8e-33 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
BABJCGNF_02029 | 1.4e-173 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
BABJCGNF_02030 | 6e-20 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
BABJCGNF_02031 | 5.1e-90 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
BABJCGNF_02032 | 8.4e-19 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
BABJCGNF_02033 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
BABJCGNF_02034 | 1.3e-28 | K | Transcriptional | |||
BABJCGNF_02035 | 7.1e-133 | V | ABC transporter | |||
BABJCGNF_02036 | 3.1e-16 | V | ABC transporter | |||
BABJCGNF_02037 | 1.5e-27 | T | LytTr DNA-binding domain | |||
BABJCGNF_02038 | 3.4e-55 | T | LytTr DNA-binding domain | |||
BABJCGNF_02039 | 1.2e-166 | 2.7.13.3 | T | GHKL domain | ||
BABJCGNF_02040 | 1.6e-91 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
BABJCGNF_02041 | 2.6e-67 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
BABJCGNF_02042 | 2.1e-31 | yqhA | G | Aldose 1-epimerase | ||
BABJCGNF_02043 | 3.4e-19 | manR | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | |
BABJCGNF_02044 | 7.1e-34 | ptxB | 2.7.1.194, 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BABJCGNF_02045 | 2e-204 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
BABJCGNF_02046 | 6.7e-48 | |||||
BABJCGNF_02047 | 1.1e-90 | 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 | |
BABJCGNF_02048 | 3.4e-49 | 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 | |
BABJCGNF_02049 | 1.1e-121 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
BABJCGNF_02050 | 1.3e-24 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
BABJCGNF_02051 | 1.1e-37 | veg | S | Biofilm formation stimulator VEG | ||
BABJCGNF_02052 | 1.4e-69 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
BABJCGNF_02053 | 2.5e-89 | ybbL | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_02054 | 2.3e-18 | ysaA | V | RDD family | ||
BABJCGNF_02055 | 6.7e-47 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
BABJCGNF_02056 | 4.4e-213 | 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 | |
BABJCGNF_02057 | 1.9e-44 | nudA | S | ASCH | ||
BABJCGNF_02058 | 1.4e-68 | S | DUF218 domain | |||
BABJCGNF_02059 | 2.2e-51 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
BABJCGNF_02060 | 2.8e-42 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
BABJCGNF_02061 | 1.7e-161 | ywfO | S | HD domain protein | ||
BABJCGNF_02062 | 5.1e-67 | ywfO | S | HD domain protein | ||
BABJCGNF_02063 | 2.4e-15 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
BABJCGNF_02064 | 4.7e-43 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
BABJCGNF_02065 | 1.5e-77 | S | Protein of unknown function (DUF1211) | |||
BABJCGNF_02066 | 2.3e-57 | S | Protein of unknown function (DUF1211) | |||
BABJCGNF_02067 | 2.9e-61 | 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 | ||
BABJCGNF_02068 | 7.3e-25 | ywiB | S | Domain of unknown function (DUF1934) | ||
BABJCGNF_02069 | 1.5e-18 | ywiB | S | Domain of unknown function (DUF1934) | ||
BABJCGNF_02070 | 9.2e-22 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
BABJCGNF_02073 | 1.1e-236 | 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 | |
BABJCGNF_02074 | 1.5e-36 | 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 | |
BABJCGNF_02075 | 3.7e-91 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
BABJCGNF_02076 | 2.5e-13 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
BABJCGNF_02077 | 1.3e-25 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
BABJCGNF_02078 | 1.8e-238 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
BABJCGNF_02079 | 4.1e-127 | |||||
BABJCGNF_02080 | 7.2e-83 | S | Tetratricopeptide repeat | |||
BABJCGNF_02081 | 5.9e-123 | |||||
BABJCGNF_02082 | 4e-27 | |||||
BABJCGNF_02083 | 3.3e-42 | rpmE2 | J | Ribosomal protein L31 | ||
BABJCGNF_02084 | 9.1e-37 | |||||
BABJCGNF_02085 | 2.6e-216 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
BABJCGNF_02086 | 1.7e-63 | 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 | |
BABJCGNF_02087 | 6.9e-46 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
BABJCGNF_02088 | 1.8e-11 | |||||
BABJCGNF_02089 | 1.3e-28 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
BABJCGNF_02090 | 7.1e-49 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1, 2.1.1.21 | E | GXGXG motif | |
BABJCGNF_02091 | 4.6e-23 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1, 2.1.1.21 | E | GXGXG motif | |
BABJCGNF_02092 | 2.2e-36 | S | QueT transporter | |||
BABJCGNF_02093 | 6.1e-194 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1, 2.1.1.21 | E | GXGXG motif | |
BABJCGNF_02094 | 7.7e-141 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1, 2.1.1.21 | E | GXGXG motif | |
BABJCGNF_02095 | 5e-84 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1, 2.1.1.21 | E | GXGXG motif | |
BABJCGNF_02096 | 5.7e-89 | gltD | 1.4.1.13, 1.4.1.14 | E | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
BABJCGNF_02097 | 7.8e-53 | gltD | 1.4.1.13, 1.4.1.14 | E | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
BABJCGNF_02098 | 9.9e-84 | XK27_06930 | S | ABC-2 family transporter protein | ||
BABJCGNF_02099 | 8.9e-23 | 1.6.5.2 | S | Flavodoxin-like fold | ||
BABJCGNF_02100 | 4.7e-43 | 1.6.5.2 | S | Flavodoxin-like fold | ||
BABJCGNF_02101 | 3.6e-94 | S | (CBS) domain | |||
BABJCGNF_02102 | 1.6e-89 | yciB | M | ErfK YbiS YcfS YnhG | ||
BABJCGNF_02103 | 6e-94 | padR | K | Transcriptional regulator PadR-like family | ||
BABJCGNF_02104 | 9.9e-39 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
BABJCGNF_02105 | 3.9e-129 | S | Putative peptidoglycan binding domain | |||
BABJCGNF_02106 | 2.4e-101 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
BABJCGNF_02107 | 2e-55 | 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 | ||
BABJCGNF_02108 | 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 | ||
BABJCGNF_02109 | 1.1e-24 | 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 | ||
BABJCGNF_02110 | 1.8e-52 | divIC | D | cell cycle | ||
BABJCGNF_02111 | 1.8e-38 | yabO | J | S4 domain protein | ||
BABJCGNF_02112 | 3.2e-63 | yabM | S | Polysaccharide biosynthesis protein | ||
BABJCGNF_02113 | 5.9e-97 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
BABJCGNF_02114 | 9.3e-220 | tilS | 6.3.4.19 | J | 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 | |
BABJCGNF_02115 | 2.5e-16 | 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 | ||
BABJCGNF_02116 | 1.2e-39 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
BABJCGNF_02117 | 5.9e-23 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
BABJCGNF_02118 | 3.1e-19 | 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 | ||
BABJCGNF_02119 | 1.1e-145 | 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 | ||
BABJCGNF_02120 | 2.4e-59 | 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 | ||
BABJCGNF_02121 | 1.1e-33 | 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 | ||
BABJCGNF_02122 | 4.9e-22 | 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 | ||
BABJCGNF_02123 | 5.9e-209 | 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 | ||
BABJCGNF_02124 | 6.1e-28 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
BABJCGNF_02125 | 4.6e-29 | |||||
BABJCGNF_02126 | 8.6e-45 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
BABJCGNF_02134 | 4.8e-280 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
BABJCGNF_02135 | 1.7e-38 | ctsR | K | Belongs to the CtsR family | ||
BABJCGNF_02136 | 2.9e-47 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BABJCGNF_02137 | 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 | |
BABJCGNF_02138 | 1.6e-55 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BABJCGNF_02139 | 3.3e-59 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BABJCGNF_02140 | 5.5e-86 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BABJCGNF_02141 | 3.3e-63 | 3.4.23.43 | ||||
BABJCGNF_02142 | 5.6e-14 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BABJCGNF_02143 | 3.6e-70 | 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 | ||
BABJCGNF_02144 | 4.5e-67 | 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 | ||
BABJCGNF_02145 | 4.9e-15 | 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 | ||
BABJCGNF_02146 | 5.7e-14 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BABJCGNF_02147 | 1.5e-166 | 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 | ||
BABJCGNF_02148 | 2.5e-114 | yfjR | K | WYL domain | ||
BABJCGNF_02149 | 4.1e-73 | yfjR | K | WYL domain | ||
BABJCGNF_02150 | 4.2e-37 | psiE | S | Phosphate-starvation-inducible E | ||
BABJCGNF_02151 | 1.1e-71 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
BABJCGNF_02152 | 1.2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
BABJCGNF_02153 | 8.1e-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 | ||
BABJCGNF_02154 | 5.7e-26 | rplD | J | Forms part of the polypeptide exit tunnel | ||
BABJCGNF_02155 | 2.3e-72 | rplD | J | Forms part of the polypeptide exit tunnel | ||
BABJCGNF_02156 | 8.6e-81 | 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 | ||
BABJCGNF_02157 | 2.4e-28 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
BABJCGNF_02158 | 9e-36 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
BABJCGNF_02159 | 5.8e-11 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
BABJCGNF_02160 | 1.4e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
BABJCGNF_02161 | 1.1e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
BABJCGNF_02162 | 2.3e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
BABJCGNF_02163 | 3.7e-109 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
BABJCGNF_02164 | 1.1e-54 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
BABJCGNF_02165 | 2.2e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
BABJCGNF_02166 | 2.7e-48 | 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 | ||
BABJCGNF_02167 | 1.2e-83 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
BABJCGNF_02168 | 4.6e-58 | 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 | ||
BABJCGNF_02169 | 6.5e-93 | 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 | ||
BABJCGNF_02170 | 1.5e-46 | 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 | ||
BABJCGNF_02171 | 3.2e-26 | 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 | ||
BABJCGNF_02172 | 5.4e-229 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
BABJCGNF_02173 | 6.1e-50 | rplO | J | Binds to the 23S rRNA | ||
BABJCGNF_02174 | 1.1e-54 | 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 | ||
BABJCGNF_02175 | 6.6e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
BABJCGNF_02177 | 3.1e-60 | rplQ | J | Ribosomal protein L17 | ||
BABJCGNF_02178 | 6.7e-27 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BABJCGNF_02179 | 9.8e-49 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BABJCGNF_02180 | 7.9e-65 | ydiC1 | EGP | Major facilitator Superfamily | ||
BABJCGNF_02181 | 8.2e-59 | |||||
BABJCGNF_02182 | 2.8e-38 | |||||
BABJCGNF_02183 | 8.2e-27 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
BABJCGNF_02184 | 3e-84 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
BABJCGNF_02185 | 1e-93 | ecfT | U | 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 | ||
BABJCGNF_02186 | 1.6e-38 | ecfT | U | 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 | ||
BABJCGNF_02187 | 2.7e-73 | 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 | |
BABJCGNF_02188 | 3.1e-19 | 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 | |
BABJCGNF_02189 | 1.5e-127 | tipA | K | TipAS antibiotic-recognition domain | ||
BABJCGNF_02190 | 9.3e-29 | |||||
BABJCGNF_02191 | 1.1e-27 | yxeA | V | FtsX-like permease family | ||
BABJCGNF_02192 | 7.4e-49 | devA | 3.6.3.25 | V | ATPases associated with a variety of cellular activities | |
BABJCGNF_02193 | 7.2e-38 | devA | 3.6.3.25 | V | ATPases associated with a variety of cellular activities | |
BABJCGNF_02194 | 1.1e-24 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_02195 | 6.9e-16 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_02196 | 5.3e-50 | yxeA | V | FtsX-like permease family | ||
BABJCGNF_02197 | 3.2e-70 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_02198 | 2.7e-40 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_02199 | 6.1e-23 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_02200 | 2.3e-48 | EGP | Transmembrane secretion effector | |||
BABJCGNF_02201 | 2.6e-144 | EGP | Transmembrane secretion effector | |||
BABJCGNF_02202 | 1.1e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
BABJCGNF_02203 | 7e-80 | 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 | ||
BABJCGNF_02204 | 1.2e-72 | V | ABC transporter | |||
BABJCGNF_02205 | 2.1e-13 | |||||
BABJCGNF_02206 | 6.2e-123 | V | ABC transporter | |||
BABJCGNF_02207 | 2e-20 | ydiC1 | EGP | Major facilitator Superfamily | ||
BABJCGNF_02208 | 2.3e-25 | ydiC1 | EGP | Major facilitator Superfamily | ||
BABJCGNF_02209 | 1e-16 | S | B3/4 domain | |||
BABJCGNF_02210 | 6.5e-69 | S | B3/4 domain | |||
BABJCGNF_02211 | 3.8e-11 | S | B3/4 domain | |||
BABJCGNF_02212 | 7.3e-53 | ssuB | P | ATPases associated with a variety of cellular activities | ||
BABJCGNF_02213 | 6.5e-31 | 6.2.1.3, 6.2.1.8 | IQ | AMP-binding enzyme C-terminal domain | ||
BABJCGNF_02214 | 8e-67 | yfiQ | I | Acyltransferase family | ||
BABJCGNF_02215 | 6.9e-63 | yfiQ | I | Acyltransferase family | ||
BABJCGNF_02216 | 6.6e-30 | 6.2.1.3, 6.2.1.8 | IQ | AMP-binding enzyme C-terminal domain | ||
BABJCGNF_02217 | 2.7e-100 | 6.2.1.3, 6.2.1.8 | IQ | AMP-binding enzyme C-terminal domain | ||
BABJCGNF_02218 | 1.3e-17 | ssuA | P | NMT1-like family | ||
BABJCGNF_02219 | 9.3e-112 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase concanavalin-like domain | ||
BABJCGNF_02221 | 1.8e-22 | |||||
BABJCGNF_02222 | 8e-46 | |||||
BABJCGNF_02223 | 5.3e-151 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase concanavalin-like domain | ||
BABJCGNF_02224 | 4.5e-36 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
BABJCGNF_02225 | 1.1e-66 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
BABJCGNF_02227 | 3.5e-266 | G | MFS/sugar transport protein | |||
BABJCGNF_02228 | 1.7e-82 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
BABJCGNF_02229 | 1.9e-16 | |||||
BABJCGNF_02230 | 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 | ||
BABJCGNF_02231 | 2.2e-60 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
BABJCGNF_02232 | 2.1e-117 | GM | NmrA-like family | |||
BABJCGNF_02233 | 2.4e-85 | |||||
BABJCGNF_02234 | 2e-31 | mtsB | U | ABC 3 transport family | ||
BABJCGNF_02235 | 4.3e-16 | mtsB | U | ABC 3 transport family | ||
BABJCGNF_02236 | 1.8e-128 | mntB | 3.6.3.35 | P | ABC transporter | |
BABJCGNF_02237 | 1.3e-47 | 2.5.1.105 | P | Cation efflux family | ||
BABJCGNF_02238 | 1.5e-50 | czrA | K | Transcriptional regulator, ArsR family | ||
BABJCGNF_02239 | 8.8e-201 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
BABJCGNF_02240 | 7.9e-29 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
BABJCGNF_02241 | 6.4e-84 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
BABJCGNF_02242 | 4.3e-36 | |||||
BABJCGNF_02243 | 8.4e-87 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
BABJCGNF_02244 | 9.1e-22 | |||||
BABJCGNF_02245 | 7.2e-113 | azlC | E | branched-chain amino acid | ||
BABJCGNF_02246 | 4.6e-20 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
BABJCGNF_02247 | 2.6e-12 | mco | Q | Multicopper oxidase | ||
BABJCGNF_02248 | 2.6e-244 | mco | Q | Multicopper oxidase | ||
BABJCGNF_02249 | 1e-24 | |||||
BABJCGNF_02251 | 2.6e-32 | pacL | P | P-type ATPase | ||
BABJCGNF_02252 | 2.9e-19 | |||||
BABJCGNF_02253 | 1.9e-44 | EGP | Major Facilitator Superfamily | |||
BABJCGNF_02254 | 5.8e-63 | EGP | Major Facilitator Superfamily | |||
BABJCGNF_02255 | 3e-159 | pacL | P | P-type ATPase | ||
BABJCGNF_02256 | 1.2e-15 | pacL | P | P-type ATPase | ||
BABJCGNF_02257 | 3.7e-10 | |||||
BABJCGNF_02258 | 2.3e-18 | |||||
BABJCGNF_02259 | 3.3e-113 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BABJCGNF_02260 | 2.4e-31 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BABJCGNF_02261 | 5.3e-83 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BABJCGNF_02262 | 1.1e-71 | |||||
BABJCGNF_02263 | 3e-218 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
BABJCGNF_02264 | 1.9e-22 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
BABJCGNF_02265 | 1.6e-28 | yqiG | C | Oxidoreductase | ||
BABJCGNF_02266 | 2.9e-76 | yqiG | C | Oxidoreductase | ||
BABJCGNF_02267 | 4.4e-28 | yqiG | C | Oxidoreductase | ||
BABJCGNF_02268 | 8.5e-109 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BABJCGNF_02270 | 3.6e-52 | S | Enterocin A Immunity | |||
BABJCGNF_02271 | 6.6e-51 | S | CAAX protease self-immunity | |||
BABJCGNF_02272 | 1.3e-71 | S | CAAX protease self-immunity | |||
BABJCGNF_02273 | 9.5e-40 | K | Transcriptional regulator | |||
BABJCGNF_02274 | 4e-17 | K | Transcriptional regulator | |||
BABJCGNF_02275 | 4.5e-121 | EGP | Major Facilitator Superfamily | |||
BABJCGNF_02276 | 1.7e-112 | EGP | Major Facilitator Superfamily | |||
BABJCGNF_02279 | 6.4e-24 | spiA | S | Enterocin A Immunity | ||
BABJCGNF_02280 | 5.7e-45 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
BABJCGNF_02281 | 1.2e-84 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
BABJCGNF_02282 | 4.1e-50 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
BABJCGNF_02283 | 2.7e-26 | mesE | M | Transport protein ComB | ||
BABJCGNF_02284 | 1.2e-45 | mesE | M | Transport protein ComB | ||
BABJCGNF_02285 | 4.7e-40 | S | Protein of unknown function (DUF2785) | |||
BABJCGNF_02286 | 7e-59 | |||||
BABJCGNF_02287 | 1e-23 | yjjP | S | Putative threonine/serine exporter | ||
BABJCGNF_02288 | 1.7e-42 | S | Enterocin A Immunity | |||
BABJCGNF_02289 | 2.7e-186 | tas | C | Aldo/keto reductase family | ||
BABJCGNF_02290 | 2.3e-25 | K | Transcriptional regulator PadR-like family | |||
BABJCGNF_02291 | 8.5e-15 | |||||
BABJCGNF_02292 | 5.2e-111 | |||||
BABJCGNF_02293 | 6.8e-90 | |||||
BABJCGNF_02294 | 3.6e-96 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
BABJCGNF_02295 | 1.9e-83 | N | Uncharacterized conserved protein (DUF2075) | |||
BABJCGNF_02296 | 4.9e-107 | N | Uncharacterized conserved protein (DUF2075) | |||
BABJCGNF_02297 | 1.8e-19 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
BABJCGNF_02298 | 9.6e-103 | |||||
BABJCGNF_02300 | 2.5e-30 | M | domain protein | |||
BABJCGNF_02301 | 3.3e-43 | M | domain protein | |||
BABJCGNF_02302 | 2.5e-287 | M | domain protein | |||
BABJCGNF_02303 | 2.9e-55 | M | Cna protein B-type domain | |||
BABJCGNF_02304 | 1.9e-77 | 3.4.22.70 | M | Sortase family | ||
BABJCGNF_02305 | 1.4e-20 | macB | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_02312 | 1.2e-45 | |||||
BABJCGNF_02313 | 1.3e-24 | |||||
BABJCGNF_02315 | 2.9e-28 | proA | 1.2.1.41 | 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 | |
BABJCGNF_02316 | 2.7e-138 | proA | 1.2.1.41 | 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 | |
BABJCGNF_02317 | 5.4e-150 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
BABJCGNF_02318 | 2.5e-95 | pimH | EGP | Major facilitator Superfamily | ||
BABJCGNF_02319 | 8.8e-72 | pimH | EGP | Major facilitator Superfamily | ||
BABJCGNF_02320 | 1.9e-29 | |||||
BABJCGNF_02321 | 5.4e-08 | |||||
BABJCGNF_02322 | 3e-09 | udp | 2.4.2.3, 3.2.2.4 | F | Phosphorylase superfamily | |
BABJCGNF_02323 | 2.1e-120 | EGP | Major facilitator Superfamily | |||
BABJCGNF_02324 | 1.6e-172 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
BABJCGNF_02325 | 7.2e-46 | |||||
BABJCGNF_02326 | 1.5e-96 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
BABJCGNF_02327 | 2.8e-88 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
BABJCGNF_02328 | 8.8e-09 | yhjA | S | CsbD-like | ||
BABJCGNF_02329 | 1.9e-39 | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | ||
BABJCGNF_02330 | 4.9e-82 | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | ||
BABJCGNF_02331 | 6.9e-180 | EGP | Major facilitator Superfamily | |||
BABJCGNF_02332 | 1.3e-90 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
BABJCGNF_02333 | 4.2e-53 | ccpN | K | Domain in cystathionine beta-synthase and other proteins. | ||
BABJCGNF_02334 | 2.3e-151 | ppdK | 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
BABJCGNF_02335 | 2.5e-36 | kup | P | Transport of potassium into the cell | ||
BABJCGNF_02336 | 1.9e-30 | ppdK | 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
BABJCGNF_02337 | 2.5e-58 | kup | P | Transport of potassium into the cell | ||
BABJCGNF_02338 | 1.1e-33 | S | ABC-2 family transporter protein | |||
BABJCGNF_02339 | 1.1e-73 | S | ABC-2 family transporter protein | |||
BABJCGNF_02340 | 4.3e-87 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_02341 | 7.5e-64 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_02342 | 1e-114 | kup | P | Transport of potassium into the cell | ||
BABJCGNF_02343 | 1.4e-59 | |||||
BABJCGNF_02344 | 1.1e-96 | |||||
BABJCGNF_02345 | 1.2e-23 | S | ABC-2 family transporter protein | |||
BABJCGNF_02346 | 6.3e-72 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
BABJCGNF_02347 | 6.9e-15 | rbsK | 2.7.1.15 | 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 | |
BABJCGNF_02348 | 2.9e-123 | rbsK | 2.7.1.15 | 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 | |
BABJCGNF_02349 | 5.1e-40 | K | DNA-binding helix-turn-helix protein | |||
BABJCGNF_02350 | 5.4e-34 | |||||
BABJCGNF_02353 | 4.2e-49 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
BABJCGNF_02354 | 6.7e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
BABJCGNF_02355 | 1e-26 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
BABJCGNF_02356 | 2.3e-32 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTPase | |
BABJCGNF_02357 | 9.8e-35 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTPase | |
BABJCGNF_02358 | 1.1e-30 | yacL | S | domain protein | ||
BABJCGNF_02359 | 2.1e-41 | 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 | ||
BABJCGNF_02360 | 4.5e-33 | 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 | ||
BABJCGNF_02361 | 6.7e-49 | 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 | ||
BABJCGNF_02362 | 3.1e-19 | 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 | ||
BABJCGNF_02363 | 1e-51 | yacL | S | domain protein | ||
BABJCGNF_02364 | 2.5e-43 | inlJ | M | MucBP domain | ||
BABJCGNF_02365 | 6.8e-126 | inlJ | M | MucBP domain | ||
BABJCGNF_02366 | 1.1e-44 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
BABJCGNF_02367 | 4.7e-56 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
BABJCGNF_02368 | 6.2e-70 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
BABJCGNF_02369 | 3e-64 | rbsA | 3.6.3.17 | G | ABC transporter | |
BABJCGNF_02370 | 5.4e-37 | rbsA | 3.6.3.17 | G | ABC transporter | |
BABJCGNF_02371 | 4.5e-142 | rbsC | U | Belongs to the binding-protein-dependent transport system permease family | ||
BABJCGNF_02372 | 3.9e-69 | rbsB | G | Periplasmic binding protein domain | ||
BABJCGNF_02373 | 3.7e-59 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
BABJCGNF_02374 | 3.7e-44 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BABJCGNF_02375 | 4.5e-70 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
BABJCGNF_02376 | 6.1e-22 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BABJCGNF_02377 | 1.2e-38 | 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) | ||
BABJCGNF_02378 | 3e-51 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BABJCGNF_02379 | 9.3e-08 | yacP | S | YacP-like NYN domain | ||
BABJCGNF_02380 | 1.6e-18 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BABJCGNF_02381 | 2.6e-24 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BABJCGNF_02382 | 7.4e-11 | 1.5.1.40 | S | Rossmann-like domain | ||
BABJCGNF_02383 | 4.9e-162 | XK27_00915 | C | Luciferase-like monooxygenase | ||
BABJCGNF_02384 | 4.1e-36 | 1.5.1.40 | S | Rossmann-like domain | ||
BABJCGNF_02385 | 1.5e-27 | |||||
BABJCGNF_02386 | 9.9e-153 | |||||
BABJCGNF_02387 | 3.3e-31 | |||||
BABJCGNF_02388 | 8.4e-25 | |||||
BABJCGNF_02389 | 8.4e-28 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_02390 | 3.2e-31 | V | ATPases associated with a variety of cellular activities | |||
BABJCGNF_02391 | 1.7e-24 | |||||
BABJCGNF_02392 | 4e-74 | |||||
BABJCGNF_02393 | 7.1e-44 | |||||
BABJCGNF_02394 | 2.6e-154 | T | Calcineurin-like phosphoesterase superfamily domain | |||
BABJCGNF_02395 | 1.6e-95 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
BABJCGNF_02396 | 1.7e-81 | ynhH | S | NusG domain II | ||
BABJCGNF_02397 | 6.2e-50 | tnpB | L | Putative transposase DNA-binding domain | ||
BABJCGNF_02398 | 4.1e-30 | cad | S | FMN_bind | ||
BABJCGNF_02399 | 2.5e-50 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
BABJCGNF_02400 | 1.2e-169 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
BABJCGNF_02401 | 1.5e-83 | menA | 2.5.1.74 | M | UbiA prenyltransferase family | |
BABJCGNF_02402 | 1.7e-51 | menA | 2.5.1.74 | M | UbiA prenyltransferase family | |
BABJCGNF_02403 | 1.5e-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 | ||
BABJCGNF_02404 | 5.9e-79 | F | nucleoside 2-deoxyribosyltransferase | |||
BABJCGNF_02405 | 3.5e-157 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BABJCGNF_02406 | 1.3e-17 | E | Amino acid permease | |||
BABJCGNF_02407 | 9.3e-175 | E | Amino acid permease | |||
BABJCGNF_02408 | 1.1e-57 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
BABJCGNF_02409 | 2.2e-99 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
BABJCGNF_02410 | 3.7e-61 | S | Domain of unknown function (DUF4430) | |||
BABJCGNF_02411 | 7.2e-106 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
BABJCGNF_02412 | 5.6e-129 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
BABJCGNF_02413 | 2.8e-55 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Cobalamin adenosyltransferase | |
BABJCGNF_02414 | 8e-11 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Cobalamin adenosyltransferase | |
BABJCGNF_02415 | 2.2e-48 | S | ECF transporter, substrate-specific component | |||
BABJCGNF_02416 | 1.6e-21 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
BABJCGNF_02417 | 1e-114 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
BABJCGNF_02418 | 6.4e-61 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
BABJCGNF_02419 | 1.3e-44 | yqaB | S | Acetyltransferase (GNAT) domain | ||
BABJCGNF_02420 | 4.3e-32 | yqaB | S | Acetyltransferase (GNAT) domain | ||
BABJCGNF_02421 | 1.3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
BABJCGNF_02423 | 3.6e-30 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
BABJCGNF_02424 | 1.1e-14 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
BABJCGNF_02425 | 6.1e-51 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
BABJCGNF_02426 | 1e-83 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
BABJCGNF_02427 | 2.5e-73 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
BABJCGNF_02429 | 2.1e-96 | |||||
BABJCGNF_02431 | 1.3e-44 | mdtG | EGP | Major facilitator Superfamily | ||
BABJCGNF_02432 | 1.4e-21 | K | acetyltransferase | |||
BABJCGNF_02433 | 4.2e-96 | K | acetyltransferase | |||
BABJCGNF_02434 | 4.6e-27 | |||||
BABJCGNF_02435 | 1.2e-17 | |||||
BABJCGNF_02436 | 9.8e-16 | |||||
BABJCGNF_02437 | 1.2e-53 | yceI | G | Sugar (and other) transporter | ||
BABJCGNF_02438 | 3.8e-55 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
BABJCGNF_02439 | 3.2e-56 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
BABJCGNF_02440 | 8.9e-62 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
BABJCGNF_02441 | 3.5e-51 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
BABJCGNF_02442 | 1.3e-89 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
BABJCGNF_02443 | 6.8e-13 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
BABJCGNF_02444 | 6.2e-125 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
BABJCGNF_02445 | 1.4e-102 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
BABJCGNF_02446 | 2.7e-94 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
BABJCGNF_02447 | 6.8e-59 | ccpB | 5.1.1.1 | K | lacI family | |
BABJCGNF_02448 | 1.2e-39 | ccpB | 5.1.1.1 | K | lacI family | |
BABJCGNF_02449 | 3.4e-18 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
BABJCGNF_02450 | 3.4e-91 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
BABJCGNF_02451 | 1.5e-53 | |||||
BABJCGNF_02452 | 2.6e-07 | ccpB | 5.1.1.1 | K | lacI family | |
BABJCGNF_02453 | 1.4e-20 | 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 | |
BABJCGNF_02454 | 4.7e-55 | 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 | |
BABJCGNF_02455 | 2.3e-29 | 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 | |
BABJCGNF_02457 | 6.1e-49 | |||||
BABJCGNF_02458 | 3.8e-62 | rsmC | 2.1.1.172 | J | Methyltransferase | |
BABJCGNF_02459 | 2.1e-14 | rsmC | 2.1.1.172 | J | Methyltransferase | |
BABJCGNF_02460 | 1.7e-28 | 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 | |
BABJCGNF_02461 | 7.4e-115 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
BABJCGNF_02462 | 8.7e-38 | S | Protein of unknown function (DUF2508) | |||
BABJCGNF_02463 | 1.2e-65 | 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 | ||
BABJCGNF_02464 | 8.4e-34 | 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 | ||
BABJCGNF_02465 | 1.5e-33 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
BABJCGNF_02466 | 5.8e-66 | 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 | |
BABJCGNF_02467 | 4.7e-43 | 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 | |
BABJCGNF_02468 | 1.4e-167 | 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 | |
BABJCGNF_02469 | 2.5e-25 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
BABJCGNF_02470 | 4.7e-97 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
BABJCGNF_02471 | 1.4e-37 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
BABJCGNF_02472 | 1.7e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
BABJCGNF_02473 | 7.2e-90 | holB | 2.7.7.7 | L | DNA polymerase III | |
BABJCGNF_02474 | 2.8e-70 | holB | 2.7.7.7 | L | DNA polymerase III | |
BABJCGNF_02475 | 1.2e-21 | yaaQ | S | Cyclic-di-AMP receptor | ||
BABJCGNF_02476 | 2.8e-74 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
BABJCGNF_02477 | 3.1e-12 | ansA | 3.5.1.1 | EJ | Asparaginase | |
BABJCGNF_02478 | 7.7e-146 | ansA | 3.5.1.1 | EJ | Asparaginase | |
BABJCGNF_02479 | 1.3e-53 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
BABJCGNF_02480 | 1.6e-82 | P | cobalt transport | |||
BABJCGNF_02481 | 4.7e-42 | 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 | |
BABJCGNF_02482 | 4.2e-71 | 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 | |
BABJCGNF_02483 | 4.2e-81 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
BABJCGNF_02484 | 1.6e-69 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
BABJCGNF_02485 | 1e-49 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
BABJCGNF_02486 | 6.1e-45 | |||||
BABJCGNF_02487 | 3.8e-188 | uup | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_02488 | 7.2e-37 | uup | S | ABC transporter, ATP-binding protein | ||
BABJCGNF_02489 | 1.6e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
BABJCGNF_02490 | 2.7e-45 | tsaD | 2.3.1.234 | 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. 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 | |
BABJCGNF_02491 | 2e-103 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
BABJCGNF_02492 | 1.1e-32 | ytrB | V | ABC transporter | ||
BABJCGNF_02493 | 3.4e-34 | ytrB | V | ABC transporter | ||
BABJCGNF_02494 | 6.1e-61 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BABJCGNF_02495 | 5.9e-45 | |||||
BABJCGNF_02496 | 1.3e-77 | |||||
BABJCGNF_02497 | 6.7e-102 | ydiL | S | CAAX protease self-immunity | ||
BABJCGNF_02498 | 1.2e-16 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BABJCGNF_02499 | 1.1e-125 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
BABJCGNF_02500 | 1.7e-40 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
BABJCGNF_02501 | 8.4e-88 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
BABJCGNF_02502 | 9.1e-117 | ydaO | E | amino acid | ||
BABJCGNF_02503 | 1.1e-43 | S | Domain of unknown function (DUF1827) | |||
BABJCGNF_02504 | 2.2e-185 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
BABJCGNF_02505 | 8.1e-192 | 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 | ||
BABJCGNF_02506 | 1.3e-137 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
BABJCGNF_02507 | 1.1e-31 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
BABJCGNF_02508 | 3.9e-54 | lmrB | EGP | Major facilitator Superfamily | ||
BABJCGNF_02509 | 8.8e-84 | S | Domain of unknown function (DUF4811) | |||
BABJCGNF_02510 | 1.4e-86 | maf | D | nucleoside-triphosphate diphosphatase activity | ||
BABJCGNF_02511 | 2e-96 | lmrB | EGP | Major facilitator Superfamily | ||
BABJCGNF_02512 | 4.7e-46 | S | Alpha beta hydrolase | |||
BABJCGNF_02513 | 7.8e-196 | I | Acyltransferase | |||
BABJCGNF_02514 | 8e-112 | yhdP | S | Transporter associated domain | ||
BABJCGNF_02515 | 2.3e-26 | yhdP | S | Transporter associated domain | ||
BABJCGNF_02516 | 6.3e-69 | S | Alpha beta hydrolase | |||
BABJCGNF_02518 | 5.7e-106 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
BABJCGNF_02519 | 2.3e-20 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
BABJCGNF_02520 | 1.7e-41 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
BABJCGNF_02521 | 4e-34 | |||||
BABJCGNF_02522 | 1.3e-27 | |||||
BABJCGNF_02524 | 1.9e-81 | S | ABC-type cobalt transport system, permease component | |||
BABJCGNF_02525 | 1e-24 | P | ABC transporter | |||
BABJCGNF_02526 | 2.1e-74 | P | ABC transporter | |||
BABJCGNF_02528 | 6.3e-11 | Q | methyltransferase | |||
BABJCGNF_02529 | 4.1e-62 | |||||
BABJCGNF_02530 | 1.6e-51 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
BABJCGNF_02531 | 6.2e-48 | K | Helix-turn-helix XRE-family like proteins | |||
BABJCGNF_02532 | 2.5e-76 | usp5 | T | universal stress protein | ||
BABJCGNF_02533 | 1.1e-68 | tag | 3.2.2.20 | L | glycosylase | |
BABJCGNF_02534 | 8e-30 | tag | 3.2.2.20 | L | glycosylase | |
BABJCGNF_02535 | 5.7e-24 | yicL | EG | EamA-like transporter family | ||
BABJCGNF_02536 | 2.9e-24 | |||||
BABJCGNF_02537 | 2.2e-43 | nisT | V | ABC transporter | ||
BABJCGNF_02538 | 4.9e-87 | |||||
BABJCGNF_02539 | 2.7e-35 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
BABJCGNF_02540 | 1.5e-178 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
BABJCGNF_02541 | 3.5e-110 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
BABJCGNF_02542 | 3.4e-191 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
BABJCGNF_02543 | 4e-131 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
BABJCGNF_02544 | 2.7e-71 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
BABJCGNF_02545 | 5e-25 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
BABJCGNF_02546 | 2.6e-17 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
BABJCGNF_02547 | 6.3e-108 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
BABJCGNF_02548 | 3.7e-58 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
BABJCGNF_02549 | 1.3e-28 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
BABJCGNF_02550 | 1.7e-75 | ynhH | S | NusG domain II | ||
BABJCGNF_02551 | 1.2e-59 | M | Peptidoglycan-binding domain 1 protein | |||
BABJCGNF_02552 | 1.1e-110 | nisT | V | ABC transporter | ||
BABJCGNF_02553 | 0.0 | cydD | CO | ABC transporter transmembrane region | ||
BABJCGNF_02554 | 5.1e-63 | cydC | V | ABC transporter transmembrane region | ||
BABJCGNF_02555 | 4.3e-30 | licT | K | CAT RNA binding domain | ||
BABJCGNF_02556 | 1.6e-132 | bglP | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
BABJCGNF_02557 | 7.4e-89 | VPA0052 | I | ABC-2 family transporter protein | ||
BABJCGNF_02558 | 1.1e-104 | IQ | reductase | |||
BABJCGNF_02559 | 3.3e-19 | IQ | reductase | |||
BABJCGNF_02560 | 4.2e-93 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BABJCGNF_02561 | 3.2e-36 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BABJCGNF_02562 | 2.1e-23 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BABJCGNF_02563 | 1.4e-17 | ysdA | CP | ABC-2 family transporter protein | ||
BABJCGNF_02564 | 1e-72 | ysdA | CP | ABC-2 family transporter protein | ||
BABJCGNF_02565 | 2.8e-22 | ysdA | CP | ABC-2 family transporter protein | ||
BABJCGNF_02566 | 6.1e-26 | natA | S | ABC transporter | ||
BABJCGNF_02567 | 1.2e-80 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BABJCGNF_02568 | 2.3e-30 | natA | S | ABC transporter | ||
BABJCGNF_02569 | 1.9e-62 | S | Acetyltransferase (GNAT) family | |||
BABJCGNF_02571 | 1.2e-36 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BABJCGNF_02573 | 5.2e-93 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
BABJCGNF_02574 | 8.2e-57 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
BABJCGNF_02575 | 5.1e-60 | S | Calcineurin-like phosphoesterase | |||
BABJCGNF_02576 | 4.2e-42 | asnB | 6.3.5.4 | E | Asparagine synthase | |
BABJCGNF_02577 | 5.9e-14 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
BABJCGNF_02578 | 3.4e-81 | XK27_06930 | V | domain protein | ||
BABJCGNF_02579 | 4.4e-172 | E | ABC transporter, substratebinding protein | |||
BABJCGNF_02580 | 2.4e-30 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
BABJCGNF_02581 | 2.5e-80 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
BABJCGNF_02582 | 9.9e-146 | S | Alpha/beta hydrolase family | |||
BABJCGNF_02583 | 3.1e-47 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_02584 | 7.6e-31 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_02585 | 6.5e-30 | XK27_06930 | V | domain protein | ||
BABJCGNF_02586 | 3.6e-117 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
BABJCGNF_02587 | 1.5e-56 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BABJCGNF_02588 | 4.4e-68 | |||||
BABJCGNF_02589 | 9.3e-83 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
BABJCGNF_02590 | 9.6e-69 | yclM | 2.7.2.4 | E | Belongs to the aspartokinase family | |
BABJCGNF_02591 | 2.2e-148 | yclM | 2.7.2.4 | E | Belongs to the aspartokinase family | |
BABJCGNF_02592 | 5.5e-26 | thrC | 4.2.3.1 | E | Threonine synthase | |
BABJCGNF_02593 | 1.7e-08 | thrC | 4.2.3.1 | E | Threonine synthase | |
BABJCGNF_02594 | 2.3e-135 | thrB | 2.7.1.39, 4.2.3.1 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
BABJCGNF_02595 | 1.5e-80 | thrC | 4.2.3.1 | E | Threonine synthase | |
BABJCGNF_02596 | 2.7e-34 | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | ||
BABJCGNF_02597 | 1.8e-53 | E | ABC transporter, substratebinding protein | |||
BABJCGNF_02598 | 1e-102 | M | Peptidoglycan-binding domain 1 protein | |||
BABJCGNF_02599 | 2.1e-36 | M | Peptidoglycan-binding domain 1 protein | |||
BABJCGNF_02600 | 1.5e-23 | usp1 | T | Universal stress protein family | ||
BABJCGNF_02601 | 1.6e-10 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
BABJCGNF_02602 | 9.3e-225 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
BABJCGNF_02603 | 2.3e-30 | sfsA | S | Belongs to the SfsA family | ||
BABJCGNF_02604 | 2.1e-55 | gbuA | 3.6.3.32 | E | glycine betaine | |
BABJCGNF_02605 | 1.5e-104 | gbuA | 3.6.3.32 | E | glycine betaine | |
BABJCGNF_02606 | 1.4e-101 | gbuC | E | glycine betaine | ||
BABJCGNF_02607 | 1.2e-54 | proW | E | glycine betaine | ||
BABJCGNF_02608 | 4.9e-51 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02609 | 4.5e-65 | gtcA | S | Teichoic acid glycosylation protein | ||
BABJCGNF_02610 | 7e-127 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02611 | 3.3e-26 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02612 | 1.4e-37 | srtA | 3.4.22.70 | M | Sortase family | |
BABJCGNF_02613 | 6.1e-28 | srtA | 3.4.22.70 | M | Sortase family | |
BABJCGNF_02614 | 5.2e-79 | S | zinc-ribbon domain | |||
BABJCGNF_02615 | 2.3e-23 | pbpX1 | V | Beta-lactamase | ||
BABJCGNF_02616 | 2.1e-152 | pbpX1 | V | Beta-lactamase | ||
BABJCGNF_02617 | 2.2e-138 | K | AI-2E family transporter | |||
BABJCGNF_02618 | 2.9e-33 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_02619 | 1.4e-98 | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | ||
BABJCGNF_02621 | 6.6e-81 | rmaB | K | Transcriptional regulator, MarR family | ||
BABJCGNF_02622 | 2.9e-12 | rmaB | K | Transcriptional regulator, MarR family | ||
BABJCGNF_02623 | 8.8e-83 | F | NUDIX domain | |||
BABJCGNF_02624 | 3.5e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
BABJCGNF_02625 | 5.8e-32 | S | Putative esterase | |||
BABJCGNF_02626 | 3e-24 | |||||
BABJCGNF_02627 | 1.7e-83 | |||||
BABJCGNF_02629 | 4.6e-77 | nox | C | NADH oxidase | ||
BABJCGNF_02630 | 4.9e-79 | nox | C | NADH oxidase | ||
BABJCGNF_02631 | 3.6e-44 | 2.7.7.65 | T | diguanylate cyclase | ||
BABJCGNF_02632 | 2.1e-43 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
BABJCGNF_02633 | 4e-34 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_02634 | 3.6e-160 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_02635 | 1.5e-24 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_02636 | 1.2e-32 | S | Protein conserved in bacteria | |||
BABJCGNF_02638 | 4e-22 | |||||
BABJCGNF_02640 | 1.9e-16 | |||||
BABJCGNF_02642 | 6.1e-23 | ydaM | M | Glycosyltransferases, probably involved in cell wall biogenesis | ||
BABJCGNF_02643 | 1.4e-88 | ydaN | S | Bacterial cellulose synthase subunit | ||
BABJCGNF_02644 | 4.8e-50 | 2.7.7.65 | T | diguanylate cyclase activity | ||
BABJCGNF_02646 | 3.6e-32 | bdhA | C | Iron-containing alcohol dehydrogenase | ||
BABJCGNF_02647 | 8.2e-31 | P | Rhodanese-like domain | |||
BABJCGNF_02648 | 8.5e-28 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
BABJCGNF_02649 | 2.6e-97 | bdhA | C | Iron-containing alcohol dehydrogenase | ||
BABJCGNF_02650 | 9e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
BABJCGNF_02652 | 1.9e-43 | 2.7.1.207 | U | 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 | ||
BABJCGNF_02653 | 6.4e-112 | 2.7.1.207 | U | 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 | ||
BABJCGNF_02654 | 4.6e-65 | 2.7.1.207 | U | 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 | ||
BABJCGNF_02655 | 1.8e-59 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
BABJCGNF_02656 | 1.9e-47 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
BABJCGNF_02657 | 7.3e-32 | ypdE | E | M42 glutamyl aminopeptidase | ||
BABJCGNF_02658 | 4.5e-33 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
BABJCGNF_02659 | 2e-46 | 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 | |
BABJCGNF_02660 | 1.3e-77 | 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 | |
BABJCGNF_02661 | 1.4e-34 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
BABJCGNF_02662 | 5.1e-24 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
BABJCGNF_02663 | 9.7e-124 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
BABJCGNF_02664 | 9.4e-15 | 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 | |
BABJCGNF_02665 | 9.8e-47 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
BABJCGNF_02666 | 8.1e-120 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
BABJCGNF_02667 | 9.5e-53 | 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 | |
BABJCGNF_02668 | 1.1e-28 | 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 | |
BABJCGNF_02669 | 6.3e-31 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
BABJCGNF_02670 | 1.6e-117 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
BABJCGNF_02671 | 4e-231 | 4.4.1.8 | E | Aminotransferase, class I | ||
BABJCGNF_02672 | 1e-69 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
BABJCGNF_02673 | 1.2e-85 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
BABJCGNF_02674 | 4.3e-27 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
BABJCGNF_02675 | 2.1e-39 | scrB | 3.2.1.26 | GH32 | G | invertase |
BABJCGNF_02677 | 8.9e-26 | azoB | GM | NmrA-like family | ||
BABJCGNF_02678 | 1.7e-31 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
BABJCGNF_02679 | 1.4e-67 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
BABJCGNF_02680 | 1.1e-30 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
BABJCGNF_02681 | 4.5e-140 | scrB | 3.2.1.26 | GH32 | G | invertase |
BABJCGNF_02682 | 1.8e-95 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
BABJCGNF_02683 | 4e-75 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
BABJCGNF_02684 | 1.6e-75 | pip | V | domain protein | ||
BABJCGNF_02685 | 3.3e-83 | pip | V | domain protein | ||
BABJCGNF_02686 | 7.9e-72 | pip | V | domain protein | ||
BABJCGNF_02687 | 3.1e-212 | ykiI | ||||
BABJCGNF_02688 | 1.4e-54 | |||||
BABJCGNF_02689 | 1.1e-48 | |||||
BABJCGNF_02690 | 3.1e-45 | S | Protein of unknown function (DUF917) | |||
BABJCGNF_02691 | 4.9e-78 | S | Protein of unknown function (DUF917) | |||
BABJCGNF_02692 | 4.3e-156 | F | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
BABJCGNF_02693 | 1e-252 | apc3 | 3.5.2.9 | EQ | Hydantoinase/oxoprolinase N-terminal region | |
BABJCGNF_02695 | 4.9e-21 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
BABJCGNF_02696 | 5.8e-61 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
BABJCGNF_02697 | 1e-73 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
BABJCGNF_02698 | 7.4e-55 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
BABJCGNF_02699 | 4.8e-43 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
BABJCGNF_02700 | 3.9e-34 | |||||
BABJCGNF_02701 | 1.3e-46 | S | Belongs to the UPF0246 family | |||
BABJCGNF_02702 | 5e-56 | XK27_05520 | S | Uncharacterized protein conserved in bacteria (DUF2087) | ||
BABJCGNF_02703 | 2.6e-61 | XK27_05520 | S | Uncharacterized protein conserved in bacteria (DUF2087) | ||
BABJCGNF_02704 | 5.6e-68 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
BABJCGNF_02705 | 1.4e-40 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
BABJCGNF_02706 | 6.9e-26 | 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 | |
BABJCGNF_02707 | 2.3e-119 | lutB | C | 4Fe-4S dicluster domain | ||
BABJCGNF_02708 | 8e-123 | lutA | C | Cysteine-rich domain | ||
BABJCGNF_02709 | 1.3e-34 | |||||
BABJCGNF_02710 | 1.9e-46 | |||||
BABJCGNF_02711 | 2.8e-21 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
BABJCGNF_02713 | 8.6e-113 | S | Bacterial protein of unknown function (DUF871) | |||
BABJCGNF_02714 | 3.1e-90 | S | Bacterial protein of unknown function (DUF871) | |||
BABJCGNF_02715 | 1.9e-49 | S | Domain of unknown function (DUF3284) | |||
BABJCGNF_02716 | 4.8e-111 | yrjD | S | LUD domain | ||
BABJCGNF_02717 | 1.4e-131 | lutB | C | 4Fe-4S dicluster domain | ||
BABJCGNF_02718 | 1.3e-116 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
BABJCGNF_02719 | 7e-16 | 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 | ||
BABJCGNF_02720 | 4e-134 | EGP | Major facilitator Superfamily | |||
BABJCGNF_02721 | 5.6e-22 | oppA | E | ABC transporter, substratebinding protein | ||
BABJCGNF_02722 | 4.9e-17 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
BABJCGNF_02723 | 1.9e-197 | oppD | P | Belongs to the ABC transporter superfamily | ||
BABJCGNF_02724 | 2.3e-11 | oppF | P | Belongs to the ABC transporter superfamily | ||
BABJCGNF_02725 | 8.4e-27 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
BABJCGNF_02726 | 1.8e-09 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
BABJCGNF_02727 | 5e-48 | K | Cro/C1-type HTH DNA-binding domain | |||
BABJCGNF_02728 | 1.6e-70 | gpm5 | 3.1.3.3, 5.4.2.11 | G | Phosphoglycerate mutase family | |
BABJCGNF_02729 | 1.1e-61 | E | lipolytic protein G-D-S-L family | |||
BABJCGNF_02730 | 5.3e-47 | ccl | S | QueT transporter | ||
BABJCGNF_02731 | 7.9e-26 | ccl | S | QueT transporter | ||
BABJCGNF_02733 | 1.7e-26 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
BABJCGNF_02734 | 3.7e-97 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
BABJCGNF_02735 | 4.2e-68 | clpL | O | associated with various cellular activities | ||
BABJCGNF_02736 | 4.8e-54 | clpL | O | associated with various cellular activities | ||
BABJCGNF_02737 | 5.7e-65 | nrp | 1.20.4.1 | P | ArsC family | |
BABJCGNF_02738 | 9e-27 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
BABJCGNF_02739 | 6.4e-48 | manZ_1 | G | PTS system mannose/fructose/sorbose family IID component | ||
BABJCGNF_02740 | 3.5e-83 | manZ_1 | G | PTS system mannose/fructose/sorbose family IID component | ||
BABJCGNF_02741 | 7.8e-64 | XK27_08465 | 2.7.1.191 | G | PTS system fructose IIA component | |
BABJCGNF_02742 | 9.2e-118 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
BABJCGNF_02743 | 1.9e-19 | fbp | 3.1.3.11 | G | phosphatase activity | |
BABJCGNF_02744 | 8.8e-38 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
BABJCGNF_02745 | 1.1e-86 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
BABJCGNF_02746 | 3.4e-35 | ylcC | 3.4.22.70 | M | Sortase family | |
BABJCGNF_02747 | 8.4e-26 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
BABJCGNF_02748 | 1.5e-59 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
BABJCGNF_02749 | 5.4e-81 | manX_1 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
BABJCGNF_02750 | 1.3e-30 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
BABJCGNF_02751 | 4.1e-29 | |||||
BABJCGNF_02753 | 5.5e-49 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
BABJCGNF_02754 | 1.8e-28 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
BABJCGNF_02755 | 2.5e-31 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
BABJCGNF_02756 | 7.9e-57 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
BABJCGNF_02757 | 1.4e-53 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
BABJCGNF_02758 | 2.4e-68 | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | ||
BABJCGNF_02759 | 6.5e-75 | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | ||
BABJCGNF_02760 | 8.5e-100 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
BABJCGNF_02761 | 1.4e-162 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
BABJCGNF_02762 | 5.5e-10 | 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) | |
BABJCGNF_02764 | 9.4e-61 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
BABJCGNF_02765 | 3.6e-163 | 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) | |
BABJCGNF_02766 | 4.8e-117 | bgaC | 3.2.1.23 | G | Glycosyl hydrolases family 35 | |
BABJCGNF_02768 | 6.5e-78 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
BABJCGNF_02769 | 2.4e-19 | K | Acetyltransferase (GNAT) domain | |||
BABJCGNF_02770 | 8.9e-37 | K | Acetyltransferase (GNAT) domain | |||
BABJCGNF_02771 | 1.1e-96 | |||||
BABJCGNF_02773 | 2.5e-58 | zur | P | Belongs to the Fur family | ||
BABJCGNF_02774 | 1.5e-07 | |||||
BABJCGNF_02775 | 1.5e-37 | glnH | ET | ABC transporter substrate-binding protein | ||
BABJCGNF_02776 | 6.6e-90 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BABJCGNF_02777 | 2.3e-17 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BABJCGNF_02778 | 6.8e-31 | glnP | P | ABC transporter permease | ||
BABJCGNF_02779 | 3.3e-47 | glnP | P | ABC transporter permease | ||
BABJCGNF_02780 | 3.3e-105 | gluC | P | ABC transporter permease | ||
BABJCGNF_02781 | 2.2e-60 | glnH | ET | ABC transporter substrate-binding protein | ||
BABJCGNF_02782 | 1.2e-65 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
BABJCGNF_02783 | 3.7e-38 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
BABJCGNF_02784 | 1.9e-90 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
BABJCGNF_02785 | 1.1e-98 | E | amino acid | |||
BABJCGNF_02786 | 2.1e-14 | E | Amino acid permease | |||
BABJCGNF_02787 | 5.8e-30 | bgaC | 3.2.1.23 | G | Glycosyl hydrolases family 35 | |
BABJCGNF_02788 | 1.6e-18 | V | FtsX-like permease family | |||
BABJCGNF_02789 | 1.5e-106 | pgm3 | G | Phosphoglycerate mutase family | ||
BABJCGNF_02790 | 7.2e-39 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
BABJCGNF_02791 | 1.9e-51 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
BABJCGNF_02792 | 1.6e-55 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
BABJCGNF_02793 | 8e-41 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
BABJCGNF_02794 | 4.2e-32 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
BABJCGNF_02795 | 3.5e-82 | yjhE | S | Phage tail protein | ||
BABJCGNF_02796 | 4.3e-50 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BABJCGNF_02797 | 6.8e-60 | yjbQ | P | TrkA C-terminal domain protein | ||
BABJCGNF_02798 | 2.7e-14 | yjbQ | P | TrkA C-terminal domain protein | ||
BABJCGNF_02799 | 5.4e-20 | yjbQ | P | TrkA C-terminal domain protein | ||
BABJCGNF_02800 | 1.2e-51 | helD | 3.6.4.12 | L | DNA helicase | |
BABJCGNF_02801 | 2.2e-17 | helD | 3.6.4.12 | L | DNA helicase | |
BABJCGNF_02802 | 4.7e-73 | helD | 3.6.4.12 | L | DNA helicase | |
BABJCGNF_02803 | 1.6e-34 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
BABJCGNF_02804 | 2.7e-82 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
BABJCGNF_02806 | 9.8e-114 | pipD | E | Dipeptidase | ||
BABJCGNF_02807 | 6.4e-18 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
BABJCGNF_02808 | 7e-51 | |||||
BABJCGNF_02809 | 6e-14 | |||||
BABJCGNF_02810 | 3.6e-25 | pipD | E | Dipeptidase | ||
BABJCGNF_02812 | 2.7e-140 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
BABJCGNF_02814 | 3.5e-08 | K | Cro/C1-type HTH DNA-binding domain | |||
BABJCGNF_02815 | 2e-13 | L | Belongs to the 'phage' integrase family | |||
BABJCGNF_02816 | 1e-172 | manP | 2.7.1.191, 2.7.1.202 | G | phosphotransferase system | |
BABJCGNF_02817 | 6.1e-40 | manP | 2.7.1.191, 2.7.1.202 | G | phosphotransferase system | |
BABJCGNF_02818 | 8.3e-195 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
BABJCGNF_02819 | 2.1e-23 | XK27_08435 | K | UTRA | ||
BABJCGNF_02820 | 7e-65 | XK27_08435 | K | UTRA | ||
BABJCGNF_02821 | 9.8e-09 | agaS | G | SIS domain | ||
BABJCGNF_02822 | 3.9e-185 | agaS | G | SIS domain | ||
BABJCGNF_02824 | 3.6e-22 | lytN | 3.5.1.104 | M | LysM domain | |
BABJCGNF_02825 | 2.4e-123 | lytN | 3.5.1.104 | M | LysM domain | |
BABJCGNF_02826 | 3.2e-68 | S | Iron-sulphur cluster biosynthesis | |||
BABJCGNF_02827 | 7.8e-129 | 2.7.1.39 | S | Phosphotransferase enzyme family | ||
BABJCGNF_02828 | 2.5e-114 | zmp3 | O | Zinc-dependent metalloprotease | ||
BABJCGNF_02829 | 2.2e-228 | V | ABC transporter transmembrane region | |||
BABJCGNF_02830 | 2.1e-88 | V | ABC transporter transmembrane region | |||
BABJCGNF_02831 | 2e-94 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_02832 | 2.7e-116 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BABJCGNF_02833 | 1.9e-28 | frvA | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
BABJCGNF_02834 | 2.5e-53 | oppB | P | Binding-protein-dependent transport system inner membrane component | ||
BABJCGNF_02835 | 6.7e-69 | oppB | P | Binding-protein-dependent transport system inner membrane component | ||
BABJCGNF_02836 | 1e-125 | amiD | P | N-terminal TM domain of oligopeptide transport permease C | ||
BABJCGNF_02837 | 3.4e-11 | |||||
BABJCGNF_02838 | 1.2e-118 | oppD | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
BABJCGNF_02839 | 1.1e-19 | oppD | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
BABJCGNF_02841 | 2e-27 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
BABJCGNF_02842 | 2.8e-61 | skfE | V | ATPases associated with a variety of cellular activities | ||
BABJCGNF_02843 | 6.1e-48 | skfE | V | ATPases associated with a variety of cellular activities | ||
BABJCGNF_02844 | 1.1e-50 | S | membrane transporter protein | |||
BABJCGNF_02845 | 6.8e-135 | K | Helix-turn-helix domain | |||
BABJCGNF_02846 | 6.9e-68 | S | Alpha beta hydrolase | |||
BABJCGNF_02848 | 2e-10 | |||||
BABJCGNF_02849 | 5.2e-139 | ypiB | EGP | Major facilitator Superfamily | ||
BABJCGNF_02850 | 1.8e-12 | EGP | Major facilitator Superfamily | |||
BABJCGNF_02851 | 1.1e-17 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
BABJCGNF_02852 | 2.1e-88 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
BABJCGNF_02853 | 1.3e-57 | yjjC | V | ABC transporter | ||
BABJCGNF_02854 | 7e-24 | citM | C | Citrate transporter | ||
BABJCGNF_02855 | 2.1e-33 | |||||
BABJCGNF_02857 | 1.2e-115 | malE | G | Bacterial extracellular solute-binding protein | ||
BABJCGNF_02858 | 6.7e-23 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
BABJCGNF_02859 | 2.2e-48 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
BABJCGNF_02860 | 3.1e-63 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
BABJCGNF_02861 | 8.9e-34 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
BABJCGNF_02863 | 5.3e-23 | oadB | 4.1.1.3 | C | Na+-transporting oxaloacetate decarboxylase beta subunit | |
BABJCGNF_02864 | 1.7e-50 | oadB | 4.1.1.3 | C | Na+-transporting oxaloacetate decarboxylase beta subunit | |
BABJCGNF_02865 | 4.9e-235 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
BABJCGNF_02866 | 4.3e-17 | citR | K | FCD | ||
BABJCGNF_02867 | 3.2e-38 | citR | K | FCD | ||
BABJCGNF_02868 | 2.2e-87 | oadA | 2.1.3.1, 4.1.1.3, 6.4.1.1, 6.4.1.7 | C | Conserved carboxylase domain | |
BABJCGNF_02869 | 3.9e-49 | oadA | 2.1.3.1, 4.1.1.3, 6.4.1.1, 6.4.1.7 | C | Conserved carboxylase domain | |
BABJCGNF_02870 | 2e-50 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
BABJCGNF_02871 | 2e-64 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
BABJCGNF_02872 | 7.9e-46 | |||||
BABJCGNF_02873 | 6.3e-15 | |||||
BABJCGNF_02874 | 8e-08 | |||||
BABJCGNF_02875 | 5.1e-60 | malE | G | Bacterial extracellular solute-binding protein | ||
BABJCGNF_02876 | 2.1e-87 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
BABJCGNF_02877 | 1.2e-32 | |||||
BABJCGNF_02878 | 1.1e-110 | S | Bacterial protein of unknown function (DUF916) | |||
BABJCGNF_02879 | 2.2e-89 | |||||
BABJCGNF_02880 | 5.8e-38 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
BABJCGNF_02881 | 9.1e-151 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02882 | 3e-24 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02883 | 5.1e-19 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02884 | 5.1e-22 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02885 | 2.7e-28 | sepS16B | ||||
BABJCGNF_02886 | 9.8e-81 | sepS16B | ||||
BABJCGNF_02887 | 2e-118 | |||||
BABJCGNF_02888 | 5.8e-152 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
BABJCGNF_02889 | 3.8e-94 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
BABJCGNF_02890 | 2.3e-21 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
BABJCGNF_02891 | 1.4e-78 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
BABJCGNF_02892 | 8.5e-28 | |||||
BABJCGNF_02893 | 3.9e-11 | |||||
BABJCGNF_02894 | 9.6e-24 | frvR | K | Mga helix-turn-helix domain | ||
BABJCGNF_02895 | 3.5e-46 | frvR | K | Mga helix-turn-helix domain | ||
BABJCGNF_02896 | 3.5e-67 | frvR | K | Mga helix-turn-helix domain | ||
BABJCGNF_02897 | 1.4e-201 | lysP | E | amino acid | ||
BABJCGNF_02898 | 1.6e-56 | frvR | K | Mga helix-turn-helix domain | ||
BABJCGNF_02899 | 6.2e-37 | frvR | K | Mga helix-turn-helix domain | ||
BABJCGNF_02900 | 4.2e-36 | frvR | K | Mga helix-turn-helix domain | ||
BABJCGNF_02901 | 3.1e-65 | 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) | |
BABJCGNF_02903 | 1.8e-15 | |||||
BABJCGNF_02904 | 7.2e-71 | ywnB | S | NAD(P)H-binding | ||
BABJCGNF_02905 | 5.1e-37 | E | AAA domain | |||
BABJCGNF_02906 | 5.4e-18 | feoA | P | FeoA | ||
BABJCGNF_02907 | 9.3e-31 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
BABJCGNF_02908 | 1.1e-28 | alfA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
BABJCGNF_02909 | 3.3e-40 | alfA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
BABJCGNF_02910 | 1.5e-88 | alfA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
BABJCGNF_02911 | 1e-56 | |||||
BABJCGNF_02912 | 8.6e-237 | pckG | 4.1.1.32, 4.1.1.49 | C | Phosphoenolpyruvate carboxykinase | |
BABJCGNF_02913 | 7.5e-18 | pckG | 4.1.1.32, 4.1.1.49 | C | Phosphoenolpyruvate carboxykinase | |
BABJCGNF_02914 | 1.6e-24 | S | Virus attachment protein p12 family | |||
BABJCGNF_02915 | 8.5e-243 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
BABJCGNF_02916 | 3.6e-45 | G | MFS/sugar transport protein | |||
BABJCGNF_02917 | 1.7e-130 | G | MFS/sugar transport protein | |||
BABJCGNF_02918 | 1.7e-12 | |||||
BABJCGNF_02919 | 8.7e-40 | S | function, without similarity to other proteins | |||
BABJCGNF_02920 | 1.3e-42 | macB_3 | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_02921 | 1e-91 | macB_3 | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_02923 | 5.3e-46 | yjjH | S | Calcineurin-like phosphoesterase | ||
BABJCGNF_02924 | 6.6e-47 | yjjH | S | Calcineurin-like phosphoesterase | ||
BABJCGNF_02925 | 2.1e-55 | mga | K | Mga helix-turn-helix domain | ||
BABJCGNF_02926 | 5.4e-13 | mga | K | Mga helix-turn-helix domain | ||
BABJCGNF_02927 | 8.5e-55 | mga | K | Mga helix-turn-helix domain | ||
BABJCGNF_02928 | 4.8e-18 | sprD | D | Domain of Unknown Function (DUF1542) | ||
BABJCGNF_02929 | 8e-232 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
BABJCGNF_02930 | 1.9e-127 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
BABJCGNF_02931 | 1.8e-143 | p75 | M | NlpC P60 family protein | ||
BABJCGNF_02932 | 1.6e-20 | sprD | D | Domain of Unknown Function (DUF1542) | ||
BABJCGNF_02933 | 8.6e-50 | sprD | D | Domain of Unknown Function (DUF1542) | ||
BABJCGNF_02935 | 1.2e-08 | sprD | D | Domain of Unknown Function (DUF1542) | ||
BABJCGNF_02936 | 3.8e-79 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
BABJCGNF_02937 | 1.5e-19 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
BABJCGNF_02938 | 5e-47 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
BABJCGNF_02939 | 7.4e-72 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
BABJCGNF_02940 | 2.8e-35 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
BABJCGNF_02941 | 4.9e-09 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
BABJCGNF_02942 | 1.2e-15 | V | Beta-lactamase | |||
BABJCGNF_02943 | 1.4e-30 | V | Beta-lactamase | |||
BABJCGNF_02944 | 5.1e-37 | V | Beta-lactamase | |||
BABJCGNF_02945 | 2.7e-70 | V | Beta-lactamase | |||
BABJCGNF_02946 | 7.5e-81 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BABJCGNF_02947 | 9.2e-96 | 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 | |
BABJCGNF_02948 | 2.8e-94 | pacL | 3.6.3.8 | P | P-type ATPase | |
BABJCGNF_02949 | 2.6e-65 | XK27_08835 | S | ABC transporter | ||
BABJCGNF_02950 | 9.2e-25 | |||||
BABJCGNF_02951 | 1.7e-17 | XK27_08835 | S | ABC transporter | ||
BABJCGNF_02953 | 8.9e-53 | yodP | 2.3.1.264 | K | FR47-like protein | |
BABJCGNF_02954 | 4.4e-101 | S | ECF transporter, substrate-specific component | |||
BABJCGNF_02955 | 5.6e-14 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
BABJCGNF_02956 | 2.4e-158 | 5.1.3.3 | G | Aldose 1-epimerase | ||
BABJCGNF_02957 | 3.6e-48 | |||||
BABJCGNF_02958 | 8.1e-93 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
BABJCGNF_02959 | 5.9e-51 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
BABJCGNF_02960 | 3.7e-35 | V | Restriction endonuclease | |||
BABJCGNF_02961 | 3.5e-18 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
BABJCGNF_02962 | 2.4e-21 | mvaA | 1.1.1.34, 1.1.1.88 | C | Belongs to the HMG-CoA reductase family | |
BABJCGNF_02963 | 3.4e-08 | F | Nucleoside 2-deoxyribosyltransferase | |||
BABJCGNF_02964 | 6.8e-110 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02965 | 3.2e-127 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
BABJCGNF_02966 | 1.9e-29 | livG | E | Branched-chain amino acid ATP-binding cassette transporter | ||
BABJCGNF_02967 | 1.9e-46 | livG | E | Branched-chain amino acid ATP-binding cassette transporter | ||
BABJCGNF_02968 | 2.8e-13 | livF | E | ABC transporter | ||
BABJCGNF_02969 | 6.8e-96 | livF | E | ABC transporter | ||
BABJCGNF_02970 | 7.9e-103 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BABJCGNF_02971 | 1.9e-34 | |||||
BABJCGNF_02972 | 3.1e-107 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BABJCGNF_02973 | 5.2e-85 | frvR | K | Mga helix-turn-helix domain | ||
BABJCGNF_02974 | 9.2e-136 | frvR | K | Mga helix-turn-helix domain | ||
BABJCGNF_02975 | 3.8e-30 | ygaC | J | Belongs to the UPF0374 family | ||
BABJCGNF_02976 | 1.5e-47 | yueF | S | AI-2E family transporter | ||
BABJCGNF_02977 | 1.4e-22 | yueF | S | AI-2E family transporter | ||
BABJCGNF_02978 | 8.6e-63 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
BABJCGNF_02979 | 1e-73 | livM | E | Branched-chain amino acid transport system / permease component | ||
BABJCGNF_02980 | 2.2e-87 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
BABJCGNF_02981 | 7.1e-56 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
BABJCGNF_02982 | 2.4e-41 | clpE | O | Belongs to the ClpA ClpB family | ||
BABJCGNF_02983 | 8.9e-48 | clpE | O | Belongs to the ClpA ClpB family | ||
BABJCGNF_02984 | 7.9e-46 | 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) | |
BABJCGNF_02985 | 2.7e-39 | ptsH | G | phosphocarrier protein HPR | ||
BABJCGNF_02986 | 2.5e-74 | 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) | |
BABJCGNF_02987 | 2.7e-77 | 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) | |
BABJCGNF_02989 | 1.9e-181 | iolT | EGP | Major facilitator Superfamily | ||
BABJCGNF_02990 | 9.1e-75 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
BABJCGNF_02991 | 6.4e-41 | 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 | |
BABJCGNF_02992 | 3.8e-69 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
BABJCGNF_02993 | 6.3e-60 | 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 | |
BABJCGNF_02994 | 2.1e-61 | livJ | E | Receptor family ligand binding region | ||
BABJCGNF_02995 | 8.1e-35 | macB | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_02996 | 3e-96 | K | transcriptional regulator | |||
BABJCGNF_02997 | 6.5e-72 | supH | G | Sucrose-6F-phosphate phosphohydrolase | ||
BABJCGNF_02998 | 5.8e-70 | supH | G | Sucrose-6F-phosphate phosphohydrolase | ||
BABJCGNF_02999 | 7.4e-40 | |||||
BABJCGNF_03000 | 4.1e-128 | S | membrane transporter protein | |||
BABJCGNF_03001 | 4.2e-34 | S | Protein of unknown function (DUF1211) | |||
BABJCGNF_03002 | 5.4e-23 | S | Protein of unknown function (DUF1211) | |||
BABJCGNF_03003 | 4.3e-15 | S | Protein of unknown function (DUF1211) | |||
BABJCGNF_03004 | 1.7e-113 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
BABJCGNF_03005 | 6.6e-53 | |||||
BABJCGNF_03006 | 1.5e-166 | pipD | E | Dipeptidase | ||
BABJCGNF_03007 | 3.3e-91 | pipD | E | Dipeptidase | ||
BABJCGNF_03008 | 9.6e-104 | S | Membrane | |||
BABJCGNF_03009 | 7.4e-74 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
BABJCGNF_03010 | 1e-87 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
BABJCGNF_03011 | 3.8e-87 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
BABJCGNF_03012 | 1.3e-54 | 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 | |
BABJCGNF_03013 | 3.1e-19 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
BABJCGNF_03014 | 9e-26 | 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 | |
BABJCGNF_03015 | 2.4e-25 | 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 | |
BABJCGNF_03016 | 8.6e-26 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
BABJCGNF_03017 | 8.6e-19 | copB | 3.6.3.4 | P | P-type ATPase | |
BABJCGNF_03018 | 2.1e-72 | livJ | E | Receptor family ligand binding region | ||
BABJCGNF_03019 | 6.4e-193 | T | PhoQ Sensor | |||
BABJCGNF_03020 | 1.6e-27 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
BABJCGNF_03021 | 5.6e-176 | copB | 3.6.3.4 | P | P-type ATPase | |
BABJCGNF_03022 | 2e-16 | K | response regulator | |||
BABJCGNF_03023 | 1.3e-61 | bceA | V | ABC transporter | ||
BABJCGNF_03024 | 1.9e-72 | V | ABC transporter (permease) | |||
BABJCGNF_03025 | 5.8e-19 | V | ABC transporter (permease) | |||
BABJCGNF_03026 | 1.6e-41 | V | ABC transporter (permease) | |||
BABJCGNF_03027 | 5.8e-89 | traP | 1.14.99.57, 6.2.1.3 | S | Antibiotic biosynthesis monooxygenase | |
BABJCGNF_03028 | 1.2e-65 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
BABJCGNF_03029 | 2e-39 | 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 | |
BABJCGNF_03030 | 6.6e-99 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
BABJCGNF_03031 | 1.2e-21 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
BABJCGNF_03032 | 6.5e-22 | thrE | S | Putative threonine/serine exporter | ||
BABJCGNF_03033 | 4.2e-61 | thrE | S | Putative threonine/serine exporter | ||
BABJCGNF_03034 | 6e-33 | S | Threonine/Serine exporter, ThrE | |||
BABJCGNF_03035 | 9.5e-34 | S | Threonine/Serine exporter, ThrE | |||
BABJCGNF_03036 | 4.3e-41 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
BABJCGNF_03038 | 5.2e-69 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
BABJCGNF_03039 | 9e-32 | argR | K | Regulates arginine biosynthesis genes | ||
BABJCGNF_03040 | 2.2e-44 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
BABJCGNF_03041 | 3.8e-33 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BABJCGNF_03042 | 1.4e-80 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BABJCGNF_03043 | 3.5e-18 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BABJCGNF_03044 | 1.2e-67 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BABJCGNF_03045 | 1.6e-35 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
BABJCGNF_03046 | 1.9e-18 | yhaH | S | YtxH-like protein | ||
BABJCGNF_03047 | 6.1e-57 | ecsB | U | ABC transporter | ||
BABJCGNF_03048 | 5e-48 | ecsA | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_03049 | 1.3e-28 | ecsA | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_03050 | 1.2e-38 | ecsB | U | ABC transporter | ||
BABJCGNF_03051 | 2.7e-49 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
BABJCGNF_03052 | 3.1e-25 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
BABJCGNF_03053 | 7e-86 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
BABJCGNF_03054 | 1.2e-154 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
BABJCGNF_03055 | 2.8e-28 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
BABJCGNF_03056 | 7.2e-50 | K | Mga helix-turn-helix domain | |||
BABJCGNF_03057 | 3.4e-53 | N | domain, Protein | |||
BABJCGNF_03058 | 7e-23 | N | domain, Protein | |||
BABJCGNF_03059 | 8.3e-70 | N | domain, Protein | |||
BABJCGNF_03060 | 3.6e-55 | S | WxL domain surface cell wall-binding | |||
BABJCGNF_03061 | 4.1e-65 | S | Cell surface protein | |||
BABJCGNF_03062 | 3.2e-10 | ybhL | S | Inhibitor of apoptosis-promoting Bax1 | ||
BABJCGNF_03063 | 3.7e-23 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
BABJCGNF_03064 | 1.3e-88 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
BABJCGNF_03066 | 2.3e-44 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
BABJCGNF_03067 | 1.5e-58 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
BABJCGNF_03068 | 8.8e-57 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
BABJCGNF_03069 | 6.6e-13 | S | ABC transporter | |||
BABJCGNF_03070 | 9.1e-127 | S | ABC transporter | |||
BABJCGNF_03071 | 6.6e-82 | dnaB | L | replication initiation and membrane attachment | ||
BABJCGNF_03072 | 2.8e-48 | dnaI | L | Primosomal protein DnaI | ||
BABJCGNF_03073 | 2.5e-56 | dnaB | L | replication initiation and membrane attachment | ||
BABJCGNF_03074 | 3.3e-36 | 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) | |
BABJCGNF_03075 | 1.4e-69 | dnaI | L | Primosomal protein DnaI | ||
BABJCGNF_03076 | 1.7e-30 | 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) | |
BABJCGNF_03077 | 3.1e-93 | 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) | |
BABJCGNF_03078 | 3.5e-78 | S | SseB protein N-terminal domain | |||
BABJCGNF_03079 | 4.9e-12 | S | SseB protein N-terminal domain | |||
BABJCGNF_03080 | 3.7e-38 | |||||
BABJCGNF_03081 | 4.9e-51 | 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 | ||
BABJCGNF_03082 | 1.6e-109 | 3.5.1.10 | C | Alcohol dehydrogenase GroES-like domain | ||
BABJCGNF_03083 | 1e-99 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
BABJCGNF_03084 | 1.1e-56 | 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 | ||
BABJCGNF_03085 | 9e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
BABJCGNF_03086 | 1.3e-164 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
BABJCGNF_03087 | 1.6e-100 | mhqD | S | Dienelactone hydrolase family | ||
BABJCGNF_03088 | 6.1e-12 | S | ABC transporter | |||
BABJCGNF_03089 | 5.1e-40 | ykcA | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
BABJCGNF_03090 | 4.4e-59 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
BABJCGNF_03091 | 7.4e-42 | yqeG | S | HAD phosphatase, family IIIA | ||
BABJCGNF_03092 | 8.4e-37 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
BABJCGNF_03093 | 1.9e-38 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
BABJCGNF_03094 | 4e-94 | yqeM | Q | Methyltransferase | ||
BABJCGNF_03095 | 5.4e-19 | yqeM | Q | Methyltransferase | ||
BABJCGNF_03096 | 3.4e-16 | 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 | ||
BABJCGNF_03097 | 6.5e-24 | 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 | ||
BABJCGNF_03098 | 2e-100 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
BABJCGNF_03099 | 1.1e-83 | yceD | S | Uncharacterized ACR, COG1399 | ||
BABJCGNF_03101 | 2.8e-38 | ylbM | S | Belongs to the UPF0348 family | ||
BABJCGNF_03102 | 2e-35 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
BABJCGNF_03103 | 6.6e-96 | draG | O | ADP-ribosylglycohydrolase | ||
BABJCGNF_03104 | 1.3e-57 | draG | O | ADP-ribosylglycohydrolase | ||
BABJCGNF_03105 | 3.3e-61 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
BABJCGNF_03106 | 3.6e-30 | arlS | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_03107 | 1.2e-32 | 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 | ||
BABJCGNF_03108 | 2e-65 | arlS | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_03109 | 7.7e-31 | arlS | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_03110 | 5.5e-45 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
BABJCGNF_03111 | 2e-104 | 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 | ||
BABJCGNF_03112 | 5.3e-22 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BABJCGNF_03113 | 4.5e-34 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
BABJCGNF_03116 | 1.3e-23 | |||||
BABJCGNF_03117 | 4.5e-18 | |||||
BABJCGNF_03118 | 4.9e-17 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BABJCGNF_03119 | 1.3e-62 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
BABJCGNF_03120 | 4.9e-45 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
BABJCGNF_03121 | 5.4e-72 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BABJCGNF_03123 | 4.2e-59 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BABJCGNF_03124 | 3.8e-16 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BABJCGNF_03125 | 5.8e-65 | 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 | ||
BABJCGNF_03126 | 2e-17 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
BABJCGNF_03127 | 2.2e-21 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
BABJCGNF_03128 | 1e-48 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
BABJCGNF_03129 | 1.9e-89 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
BABJCGNF_03130 | 4.2e-30 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
BABJCGNF_03131 | 1.2e-44 | vraS | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_03132 | 1.9e-58 | yvqF | S | Cell wall-active antibiotics response 4TMS YvqF | ||
BABJCGNF_03133 | 4.2e-17 | vraR | K | helix_turn_helix, Lux Regulon | ||
BABJCGNF_03134 | 3.4e-49 | vraR | K | helix_turn_helix, Lux Regulon | ||
BABJCGNF_03135 | 6.1e-28 | vraS | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_03136 | 4.6e-97 | S | Bacterial membrane protein YfhO | |||
BABJCGNF_03137 | 2.2e-81 | S | Bacterial membrane protein YfhO | |||
BABJCGNF_03138 | 6.4e-16 | usp | 3.5.1.28 | CBM50 | D | CHAP domain |
BABJCGNF_03139 | 0.0 | ylbB | V | ABC transporter permease | ||
BABJCGNF_03140 | 1.1e-40 | macB | V | ABC transporter, ATP-binding protein | ||
BABJCGNF_03143 | 5.8e-40 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
BABJCGNF_03144 | 3.1e-68 | glk | 2.7.1.2 | G | Glucokinase | |
BABJCGNF_03145 | 2.6e-163 | miaA | 2.5.1.75 | F | 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) | |
BABJCGNF_03146 | 9.2e-47 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
BABJCGNF_03147 | 1.5e-91 | glnA | 6.3.1.2 | E | glutamine synthetase | |
BABJCGNF_03148 | 4.8e-41 | glnR | K | Transcriptional regulator | ||
BABJCGNF_03149 | 5.1e-40 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
BABJCGNF_03150 | 7.1e-117 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
BABJCGNF_03151 | 1.3e-14 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
BABJCGNF_03152 | 4.2e-150 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
BABJCGNF_03153 | 8.3e-19 | V | ABC transporter transmembrane region | |||
BABJCGNF_03154 | 2.4e-59 | ywhK | S | Membrane | ||
BABJCGNF_03156 | 7.3e-44 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
BABJCGNF_03157 | 1.3e-32 | |||||
BABJCGNF_03158 | 1.2e-13 | |||||
BABJCGNF_03159 | 4.3e-26 | 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 | ||
BABJCGNF_03160 | 6.8e-26 | 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 | ||
BABJCGNF_03161 | 4.3e-26 | 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 | ||
BABJCGNF_03162 | 6.4e-87 | ypdF | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
BABJCGNF_03163 | 7.7e-74 | ypdF | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
BABJCGNF_03164 | 1.7e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
BABJCGNF_03165 | 2.3e-93 | 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 | |
BABJCGNF_03166 | 1e-14 | 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 | |
BABJCGNF_03167 | 4e-63 | 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 | |
BABJCGNF_03168 | 8.1e-129 | 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 | |
BABJCGNF_03170 | 1.6e-32 | 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 | |
BABJCGNF_03171 | 7.8e-33 | 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 | |
BABJCGNF_03172 | 4.8e-34 | |||||
BABJCGNF_03173 | 2.2e-35 | recN | L | May be involved in recombinational repair of damaged DNA | ||
BABJCGNF_03174 | 6.5e-25 | rssA | S | Patatin-like phospholipase | ||
BABJCGNF_03175 | 1.5e-49 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
BABJCGNF_03176 | 2.4e-49 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
BABJCGNF_03177 | 4.5e-70 | T | Sh3 type 3 domain protein | |||
BABJCGNF_03179 | 3e-15 | 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 | |
BABJCGNF_03180 | 4e-46 | 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 | |
BABJCGNF_03181 | 2.6e-35 | 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 | ||
BABJCGNF_03182 | 4.9e-35 | 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 | ||
BABJCGNF_03183 | 2.3e-34 | 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 | ||
BABJCGNF_03184 | 1.3e-105 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
BABJCGNF_03185 | 3.1e-53 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
BABJCGNF_03186 | 4.3e-52 | 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 | |
BABJCGNF_03187 | 6.7e-18 | stp | 3.1.3.16 | T | phosphatase | |
BABJCGNF_03188 | 3.7e-23 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
BABJCGNF_03189 | 9.8e-86 | KLT | serine threonine protein kinase | |||
BABJCGNF_03190 | 6.2e-76 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BABJCGNF_03191 | 2.4e-153 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
BABJCGNF_03192 | 2.4e-46 | 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 | |
BABJCGNF_03193 | 8.2e-19 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
BABJCGNF_03194 | 4.2e-63 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
BABJCGNF_03195 | 3.1e-63 | 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 | |
BABJCGNF_03196 | 9.4e-32 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
BABJCGNF_03197 | 3.7e-31 | asp | S | Asp23 family, cell envelope-related function | ||
BABJCGNF_03198 | 4.6e-16 | 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) | |
BABJCGNF_03199 | 5.4e-43 | 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) | |
BABJCGNF_03200 | 4.2e-92 | 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 | |
BABJCGNF_03201 | 4.4e-45 | fhuC | 3.6.3.35 | P | ABC transporter | |
BABJCGNF_03202 | 4e-60 | fhuC | 3.6.3.35 | P | ABC transporter | |
BABJCGNF_03203 | 5.2e-134 | znuB | U | ABC 3 transport family | ||
BABJCGNF_03204 | 1.2e-159 | T | Calcineurin-like phosphoesterase superfamily domain | |||
BABJCGNF_03205 | 3.3e-52 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
BABJCGNF_03206 | 9.8e-72 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
BABJCGNF_03207 | 4.9e-84 | pepF | E | oligoendopeptidase F | ||
BABJCGNF_03208 | 9e-178 | pepF | E | oligoendopeptidase F | ||
BABJCGNF_03209 | 2.1e-53 | pepF | E | oligoendopeptidase F | ||
BABJCGNF_03210 | 1e-49 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BABJCGNF_03211 | 3.7e-13 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BABJCGNF_03212 | 7.3e-13 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
BABJCGNF_03213 | 4.2e-66 | oppD | P | Belongs to the ABC transporter superfamily | ||
BABJCGNF_03214 | 1.2e-45 | oppF | P | Belongs to the ABC transporter superfamily | ||
BABJCGNF_03215 | 1.3e-65 | oppF | P | Belongs to the ABC transporter superfamily | ||
BABJCGNF_03216 | 1.1e-20 | 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 | |
BABJCGNF_03217 | 1.2e-55 | 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 | |
BABJCGNF_03218 | 1e-30 | oppA1 | E | ABC transporter substrate-binding protein | ||
BABJCGNF_03219 | 7.8e-46 | smc | D | Required for chromosome condensation and partitioning | ||
BABJCGNF_03220 | 4.3e-23 | smc | D | AAA ATPase domain | ||
BABJCGNF_03221 | 8.3e-35 | smc | D | AAA ATPase domain | ||
BABJCGNF_03222 | 2.1e-23 | smc | D | Required for chromosome condensation and partitioning | ||
BABJCGNF_03223 | 7.6e-58 | |||||
BABJCGNF_03224 | 1.9e-26 | 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) | ||
BABJCGNF_03225 | 1.7e-35 | 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) | ||
BABJCGNF_03227 | 6.4e-31 | 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 | ||
BABJCGNF_03228 | 2.1e-45 | 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 | |
BABJCGNF_03229 | 9.7e-27 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
BABJCGNF_03230 | 1e-20 | 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 | |
BABJCGNF_03231 | 2.8e-27 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
BABJCGNF_03232 | 9.1e-80 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
BABJCGNF_03233 | 2.1e-23 | 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 | ||
BABJCGNF_03234 | 9.5e-55 | 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 | ||
BABJCGNF_03235 | 1.1e-30 | ylqC | S | Belongs to the UPF0109 family | ||
BABJCGNF_03236 | 3.7e-83 | gntP | EG | Gluconate | ||
BABJCGNF_03237 | 1.4e-18 | yneF | S | UPF0154 protein | ||
BABJCGNF_03238 | 1.5e-25 | |||||
BABJCGNF_03239 | 3.7e-29 | mdlA | V | ABC transporter | ||
BABJCGNF_03240 | 3.6e-84 | mdlB | V | ABC transporter | ||
BABJCGNF_03241 | 5.6e-21 | mdlA | V | ABC transporter | ||
BABJCGNF_03242 | 1.9e-22 | mdlB | V | ABC transporter | ||
BABJCGNF_03243 | 7.9e-36 | yejC | S | Protein of unknown function (DUF1003) | ||
BABJCGNF_03244 | 8.3e-94 | yejC | S | Protein of unknown function (DUF1003) | ||
BABJCGNF_03245 | 1.4e-104 | plsC | 2.3.1.51 | I | Acyltransferase | |
BABJCGNF_03246 | 1.1e-13 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
BABJCGNF_03247 | 5.8e-18 | 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 | ||
BABJCGNF_03248 | 6.5e-123 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
BABJCGNF_03250 | 1.9e-86 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
BABJCGNF_03251 | 4.6e-49 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
BABJCGNF_03252 | 2.4e-78 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
BABJCGNF_03253 | 5.1e-84 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
BABJCGNF_03254 | 2.3e-88 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
BABJCGNF_03255 | 2.7e-144 | 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 | |
BABJCGNF_03256 | 4.3e-53 | 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 | |
BABJCGNF_03257 | 7.5e-34 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BABJCGNF_03258 | 7.1e-30 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BABJCGNF_03259 | 2.8e-44 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BABJCGNF_03260 | 2.2e-54 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BABJCGNF_03261 | 3.7e-51 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
BABJCGNF_03262 | 9.8e-13 | nusA | K | Participates in both transcription termination and antitermination | ||
BABJCGNF_03263 | 6.7e-31 | ylxQ | J | ribosomal protein | ||
BABJCGNF_03264 | 4.1e-185 | 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 | ||
BABJCGNF_03265 | 1.9e-132 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
BABJCGNF_03266 | 5.2e-165 | amtB | P | Ammonium Transporter Family | ||
BABJCGNF_03267 | 4.5e-213 | P | Pyridine nucleotide-disulphide oxidoreductase | |||
BABJCGNF_03268 | 8.2e-72 | usp | 3.5.1.28 | CBM50 | D | CHAP domain |
BABJCGNF_03269 | 2.7e-31 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
BABJCGNF_03270 | 4.2e-94 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
BABJCGNF_03271 | 1.8e-08 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
BABJCGNF_03272 | 2.8e-73 | terC | P | membrane | ||
BABJCGNF_03273 | 3.4e-30 | terC | P | membrane | ||
BABJCGNF_03274 | 4.6e-58 | 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 | ||
BABJCGNF_03275 | 2.6e-21 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
BABJCGNF_03276 | 2.4e-81 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
BABJCGNF_03277 | 1.1e-11 | 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 | ||
BABJCGNF_03278 | 1.7e-33 | 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 | ||
BABJCGNF_03279 | 1e-99 | 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 | ||
BABJCGNF_03280 | 1.2e-26 | 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 | ||
BABJCGNF_03281 | 1e-08 | 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 | ||
BABJCGNF_03282 | 9.4e-16 | dnaK | O | Hsp70 protein | ||
BABJCGNF_03283 | 9.5e-89 | 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 | ||
BABJCGNF_03284 | 5.9e-32 | |||||
BABJCGNF_03285 | 3.1e-64 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
BABJCGNF_03286 | 2.7e-46 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
BABJCGNF_03287 | 2.1e-42 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
BABJCGNF_03289 | 9.1e-33 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
BABJCGNF_03290 | 5.2e-31 | hutG | 3.5.3.8 | E | N-formylglutamate amidohydrolase | |
BABJCGNF_03291 | 7.8e-62 | hutG | 3.5.3.8 | E | N-formylglutamate amidohydrolase | |
BABJCGNF_03292 | 1.8e-32 | K | Bacterial regulatory proteins, tetR family | |||
BABJCGNF_03293 | 1.7e-31 | |||||
BABJCGNF_03295 | 1.1e-34 | |||||
BABJCGNF_03296 | 9.9e-14 | prmA | J | Ribosomal protein L11 methyltransferase | ||
BABJCGNF_03297 | 1.1e-15 | |||||
BABJCGNF_03298 | 1.4e-54 | 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 | |
BABJCGNF_03299 | 5.1e-27 | 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 | |
BABJCGNF_03300 | 9.4e-37 | prmA | J | Ribosomal protein L11 methyltransferase | ||
BABJCGNF_03301 | 1.6e-22 | gntR | K | rpiR family | ||
BABJCGNF_03302 | 8.5e-51 | gntR | K | rpiR family | ||
BABJCGNF_03303 | 3e-133 | 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 | |
BABJCGNF_03304 | 1.9e-47 | 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 | |
BABJCGNF_03305 | 1e-26 | 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 | |
BABJCGNF_03306 | 1e-60 | 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 | ||
BABJCGNF_03307 | 1.6e-49 | lytH | 3.5.1.28, 6.1.1.12 | M | N-acetylmuramoyl-L-alanine amidase | |
BABJCGNF_03308 | 1.2e-38 | 3.1.3.18 | J | HAD-hyrolase-like | ||
BABJCGNF_03309 | 2.3e-63 | lytH | 3.5.1.28, 6.1.1.12 | M | N-acetylmuramoyl-L-alanine amidase | |
BABJCGNF_03310 | 2.5e-50 | FG | adenosine 5'-monophosphoramidase activity | |||
BABJCGNF_03311 | 8.8e-73 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
BABJCGNF_03312 | 1.5e-127 | iolI | 5.3.99.11 | G | Xylose isomerase-like TIM barrel | |
BABJCGNF_03313 | 1.2e-14 | iolH | G | Xylose isomerase-like TIM barrel | ||
BABJCGNF_03314 | 7.9e-32 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
BABJCGNF_03315 | 2.1e-36 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
BABJCGNF_03316 | 5.9e-51 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
BABJCGNF_03317 | 5.7e-35 | 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 | |
BABJCGNF_03318 | 7e-37 | 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 | |
BABJCGNF_03319 | 5.1e-47 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
BABJCGNF_03320 | 5.5e-29 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
BABJCGNF_03321 | 6.1e-25 | yqeY | S | YqeY-like protein | ||
BABJCGNF_03322 | 1.9e-17 | yqeY | S | YqeY-like protein | ||
BABJCGNF_03323 | 2.9e-21 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
BABJCGNF_03324 | 2.4e-59 | phoH | T | phosphate starvation-inducible protein PhoH | ||
BABJCGNF_03325 | 7.9e-64 | 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 | ||
BABJCGNF_03326 | 3.9e-13 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
BABJCGNF_03327 | 7.7e-18 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
BABJCGNF_03328 | 1.6e-25 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
BABJCGNF_03329 | 6.2e-52 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
BABJCGNF_03330 | 8.7e-57 | iolJ | 4.1.2.13, 4.1.2.29 | G | Fructose-bisphosphate aldolase class-II | |
BABJCGNF_03331 | 2.8e-63 | iolJ | 4.1.2.13, 4.1.2.29 | G | Fructose-bisphosphate aldolase class-II | |
BABJCGNF_03332 | 6.9e-11 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
BABJCGNF_03333 | 5.6e-29 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
BABJCGNF_03334 | 9.3e-55 | |||||
BABJCGNF_03336 | 1.1e-21 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
BABJCGNF_03337 | 3e-17 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
BABJCGNF_03338 | 3.3e-27 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
BABJCGNF_03339 | 2e-59 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
BABJCGNF_03340 | 9.9e-39 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
BABJCGNF_03341 | 3.7e-180 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
BABJCGNF_03342 | 1.5e-46 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
BABJCGNF_03343 | 1.1e-250 | iolA | 1.2.1.18, 1.2.1.27 | C | Belongs to the aldehyde dehydrogenase family | |
BABJCGNF_03344 | 8.4e-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) | |
BABJCGNF_03345 | 3.5e-177 | iolC | 2.7.1.92 | H | 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) | |
BABJCGNF_03346 | 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) | |
BABJCGNF_03347 | 4.1e-192 | iolG | 1.1.1.18, 1.1.1.369 | C | 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 | |
BABJCGNF_03348 | 1.4e-192 | iolG2 | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
BABJCGNF_03349 | 1.2e-35 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
BABJCGNF_03350 | 4.2e-59 | 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 | ||
BABJCGNF_03351 | 7.6e-146 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
BABJCGNF_03352 | 9.7e-18 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
BABJCGNF_03353 | 2.2e-86 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
BABJCGNF_03354 | 1.6e-59 | V | ABC transporter transmembrane region | |||
BABJCGNF_03355 | 5.2e-37 | V | ABC transporter transmembrane region | |||
BABJCGNF_03356 | 6.3e-24 | V | (ABC) transporter | |||
BABJCGNF_03357 | 5.6e-134 | V | (ABC) transporter | |||
BABJCGNF_03358 | 9.7e-61 | yitW | S | Iron-sulfur cluster assembly protein | ||
BABJCGNF_03359 | 1.9e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
BABJCGNF_03360 | 3e-26 | |||||
BABJCGNF_03361 | 7.8e-51 | |||||
BABJCGNF_03362 | 1.3e-52 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
BABJCGNF_03363 | 6.9e-84 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
BABJCGNF_03364 | 6.6e-47 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
BABJCGNF_03365 | 2e-135 | |||||
BABJCGNF_03366 | 4e-215 | iolT | EGP | Major facilitator Superfamily | ||
BABJCGNF_03367 | 1.1e-116 | 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) | |
BABJCGNF_03368 | 1.2e-46 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
BABJCGNF_03369 | 7.3e-217 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
BABJCGNF_03370 | 1.4e-47 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
BABJCGNF_03371 | 5e-90 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
BABJCGNF_03372 | 5.4e-134 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
BABJCGNF_03373 | 3.5e-83 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
BABJCGNF_03374 | 7.9e-23 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
BABJCGNF_03375 | 2.8e-154 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
BABJCGNF_03376 | 3.9e-81 | iolR | K | DeoR C terminal sensor domain | ||
BABJCGNF_03377 | 3.5e-45 | iolR | K | DeoR C terminal sensor domain | ||
BABJCGNF_03378 | 3.3e-86 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
BABJCGNF_03379 | 6.6e-57 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
BABJCGNF_03380 | 6.2e-89 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
BABJCGNF_03381 | 4.2e-92 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
BABJCGNF_03382 | 1.5e-118 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
BABJCGNF_03383 | 3.5e-38 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
BABJCGNF_03384 | 1.9e-26 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
BABJCGNF_03385 | 9.5e-14 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
BABJCGNF_03386 | 6.4e-35 | ypmB | S | Protein conserved in bacteria | ||
BABJCGNF_03387 | 1.2e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
BABJCGNF_03388 | 2.2e-114 | 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 | |
BABJCGNF_03389 | 3e-44 | dnaD | L | DnaD domain protein | ||
BABJCGNF_03390 | 2e-29 | dnaD | L | DnaD domain protein | ||
BABJCGNF_03391 | 7.7e-84 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
BABJCGNF_03392 | 3.5e-56 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
BABJCGNF_03393 | 4.6e-24 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
BABJCGNF_03394 | 2.7e-73 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
BABJCGNF_03396 | 6.3e-11 | ypsA | S | Belongs to the UPF0398 family | ||
BABJCGNF_03399 | 1.1e-113 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
BABJCGNF_03400 | 1.6e-69 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
BABJCGNF_03401 | 7.6e-150 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
BABJCGNF_03402 | 8e-82 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BABJCGNF_03403 | 1.1e-84 | 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 | ||
BABJCGNF_03404 | 3.7e-157 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
BABJCGNF_03405 | 3.7e-79 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
BABJCGNF_03406 | 7.2e-52 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
BABJCGNF_03407 | 3e-47 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BABJCGNF_03408 | 1.4e-80 | K | Transcriptional regulator | |||
BABJCGNF_03409 | 1.8e-33 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BABJCGNF_03410 | 9.2e-22 | nrdH | O | Glutaredoxin | ||
BABJCGNF_03411 | 2.9e-107 | guaB | 1.1.1.205 | 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 | |
BABJCGNF_03412 | 1.8e-49 | guaB | 1.1.1.205 | 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 | |
BABJCGNF_03413 | 9.4e-70 | |||||
BABJCGNF_03415 | 1.1e-98 | K | response regulator | |||
BABJCGNF_03416 | 5.9e-219 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
BABJCGNF_03417 | 3.1e-23 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BABJCGNF_03418 | 8.4e-54 | 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 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)