EC Number | Activating Compound | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Bacillus subtilis | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Staphylococcus aureus | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Streptococcus pneumoniae | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Streptococcus mutans serotype c | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Streptococcus pyogenes serotype M2 | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Streptococcus equi subsp. zooepidemicus | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Enterococcus faecalis | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Bacillus amyloliquefaciens | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Bacillus licheniformis | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Bacillus anthracis | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Tetragenococcus halophilus | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Clostridium novyi | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Clostridium ljungdahlii | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Clostridium perfringens | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Clostridium botulinum | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Geobacter sulfurreducens | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Listeria monocytogenes EGD | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Lactococcus cremoris | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Lacticaseibacillus rhamnosus | |
2.7.7.85 | CdaR | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Lactobacillus acidophilus |
EC Number | Cloned (Comment) | Organism |
---|---|---|
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Bacillus subtilis |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Staphylococcus aureus |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Streptococcus pneumoniae |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Streptococcus mutans serotype c |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Streptococcus pyogenes serotype M2 |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Streptococcus equi subsp. zooepidemicus |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Enterococcus faecalis |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Bacillus amyloliquefaciens |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Bacillus licheniformis |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Bacillus anthracis |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Tetragenococcus halophilus |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Clostridium novyi |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Clostridium ljungdahlii |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Clostridium perfringens |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Clostridium botulinum |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Geobacter sulfurreducens |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Listeria monocytogenes EGD |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Lactococcus cremoris |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Lacticaseibacillus rhamnosus |
2.7.7.85 | gene cdaA, genetic organization of CdaA, CdaR, and GlmM encoding genes | Lactobacillus acidophilus |
EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Bacillus amyloliquefaciens | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Bacillus anthracis | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Bacillus licheniformis | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Bacillus subtilis | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Clostridium botulinum | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Clostridium ljungdahlii | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Clostridium novyi | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Clostridium perfringens | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Enterococcus faecalis | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Geobacter sulfurreducens | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Lacticaseibacillus rhamnosus | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Lactobacillus acidophilus | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate; cordycepin triphosphate | Lactococcus cremoris | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Listeria monocytogenes EGD | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Staphylococcus aureus | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Streptococcus equi subsp. zooepidemicus | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Streptococcus mutans serotype c | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Streptococcus pneumoniae | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Streptococcus pyogenes serotype M2 | |
2.7.7.85 | 3'-deoxyATP | cordycepin triphosphate | Tetragenococcus halophilus | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Bacillus amyloliquefaciens | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Bacillus anthracis | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Bacillus licheniformis | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Bacillus subtilis | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Clostridium botulinum | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Clostridium ljungdahlii | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Clostridium novyi | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Clostridium perfringens | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Enterococcus faecalis | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Geobacter sulfurreducens | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Lacticaseibacillus rhamnosus | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Lactobacillus acidophilus | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine; 3'-deoxy adenosine | Lactococcus cremoris | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Listeria monocytogenes EGD | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Staphylococcus aureus | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Streptococcus equi subsp. zooepidemicus | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Streptococcus mutans serotype c | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Streptococcus pneumoniae | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Streptococcus pyogenes serotype M2 | |
2.7.7.85 | cordycepin | 3'-deoxy adenosine | Tetragenococcus halophilus | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Bacillus amyloliquefaciens | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Bacillus anthracis | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Bacillus licheniformis | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Bacillus subtilis | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Clostridium botulinum | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Clostridium ljungdahlii | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Clostridium novyi | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Clostridium perfringens | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Enterococcus faecalis | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Geobacter sulfurreducens | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Lacticaseibacillus rhamnosus | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Lactobacillus acidophilus | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex; binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Lactococcus cremoris | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Listeria monocytogenes EGD | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Staphylococcus aureus | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Streptococcus equi subsp. zooepidemicus | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Streptococcus mutans serotype c | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Streptococcus pneumoniae | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Streptococcus pyogenes serotype M2 | |
2.7.7.85 | GlmM | binds directly to enzyme CdaA in the CdaA-CdaR-GlmM protein complex | Tetragenococcus halophilus | |
2.7.7.85 | suramin | - |
Bacillus amyloliquefaciens | |
2.7.7.85 | suramin | - |
Bacillus anthracis | |
2.7.7.85 | suramin | - |
Bacillus licheniformis | |
2.7.7.85 | suramin | - |
Bacillus subtilis | |
2.7.7.85 | suramin | - |
Clostridium botulinum | |
2.7.7.85 | suramin | - |
Clostridium ljungdahlii | |
2.7.7.85 | suramin | - |
Clostridium novyi | |
2.7.7.85 | suramin | - |
Clostridium perfringens | |
2.7.7.85 | suramin | - |
Enterococcus faecalis | |
2.7.7.85 | suramin | - |
Geobacter sulfurreducens | |
2.7.7.85 | suramin | - |
Lacticaseibacillus rhamnosus | |
2.7.7.85 | suramin | - |
Lactobacillus acidophilus | |
2.7.7.85 | suramin | - |
Lactococcus cremoris | |
2.7.7.85 | suramin | - |
Listeria monocytogenes EGD | |
2.7.7.85 | suramin | - |
Staphylococcus aureus | |
2.7.7.85 | suramin | - |
Streptococcus equi subsp. zooepidemicus | |
2.7.7.85 | suramin | - |
Streptococcus mutans serotype c | |
2.7.7.85 | suramin | - |
Streptococcus pneumoniae | |
2.7.7.85 | suramin | - |
Streptococcus pyogenes serotype M2 | |
2.7.7.85 | suramin | - |
Tetragenococcus halophilus |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
2.7.7.85 | membrane | - |
Bacillus subtilis | 16020 | - |
2.7.7.85 | membrane | - |
Staphylococcus aureus | 16020 | - |
2.7.7.85 | membrane | - |
Streptococcus pneumoniae | 16020 | - |
2.7.7.85 | membrane | - |
Streptococcus mutans serotype c | 16020 | - |
2.7.7.85 | membrane | - |
Streptococcus pyogenes serotype M2 | 16020 | - |
2.7.7.85 | membrane | - |
Streptococcus equi subsp. zooepidemicus | 16020 | - |
2.7.7.85 | membrane | - |
Enterococcus faecalis | 16020 | - |
2.7.7.85 | membrane | - |
Bacillus amyloliquefaciens | 16020 | - |
2.7.7.85 | membrane | - |
Bacillus licheniformis | 16020 | - |
2.7.7.85 | membrane | - |
Bacillus anthracis | 16020 | - |
2.7.7.85 | membrane | - |
Tetragenococcus halophilus | 16020 | - |
2.7.7.85 | membrane | - |
Clostridium novyi | 16020 | - |
2.7.7.85 | membrane | - |
Clostridium ljungdahlii | 16020 | - |
2.7.7.85 | membrane | - |
Clostridium perfringens | 16020 | - |
2.7.7.85 | membrane | - |
Clostridium botulinum | 16020 | - |
2.7.7.85 | membrane | - |
Geobacter sulfurreducens | 16020 | - |
2.7.7.85 | membrane | - |
Listeria monocytogenes EGD | 16020 | - |
2.7.7.85 | membrane | - |
Lactococcus cremoris | 16020 | - |
2.7.7.85 | membrane | - |
Lacticaseibacillus rhamnosus | 16020 | - |
2.7.7.85 | membrane | - |
Lactobacillus acidophilus | 16020 | - |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.7.85 | 2 ATP | Bacillus subtilis | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Staphylococcus aureus | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Streptococcus pneumoniae | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Streptococcus mutans serotype c | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Streptococcus pyogenes serotype M2 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Streptococcus equi subsp. zooepidemicus | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Enterococcus faecalis | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus amyloliquefaciens | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus licheniformis | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus anthracis | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Tetragenococcus halophilus | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium novyi | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium ljungdahlii | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium perfringens | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium botulinum | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Geobacter sulfurreducens | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Listeria monocytogenes EGD | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lactococcus cremoris | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lacticaseibacillus rhamnosus | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lactobacillus acidophilus | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Tetragenococcus halophilus JCM 20259 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Listeria monocytogenes EGD EGD-e | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lactococcus cremoris Sk11 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Staphylococcus aureus NCTC 8325 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus subtilis 168 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Tetragenococcus halophilus DSM 20338 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Tetragenococcus halophilus NCIMB 9735 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium ljungdahlii DSM 13528 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus licheniformis NCIMB 9375 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Enterococcus faecalis ERV62 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus licheniformis Gibson 46 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium novyi NT | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium perfringens NCIMB 6125 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium perfringens NCTC 8237 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium perfringens JCM 1290 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus licheniformis JCM 2505 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Streptococcus mutans serotype c ATCC 700610 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Tetragenococcus halophilus NBRC 12172 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lactococcus cremoris MG1363 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lactobacillus acidophilus NCFM | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Streptococcus pyogenes serotype M2 MGAS10270 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus licheniformis NRRL NRS-1264 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium perfringens type A | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lacticaseibacillus rhamnosus ATCC 8530 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Geobacter sulfurreducens PCA | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium ljungdahlii PETC | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Streptococcus pneumoniae ATCC 700669 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Listeria monocytogenes EGD ATCC BAA-679 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lactobacillus acidophilus ATCC 700396 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Geobacter sulfurreducens ATCC 51573 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lactobacillus acidophilus NCK56 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium perfringens DSM 756 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus licheniformis NBRC 12200 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Staphylococcus aureus PS 47 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus licheniformis ATCC 14580 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Lactobacillus acidophilus N2 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Streptococcus mutans serotype c UA159 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Bacillus licheniformis DSM 13 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Clostridium ljungdahlii ATCC 55383 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | Geobacter sulfurreducens DSM 12127 | - |
2 diphosphate + cyclic di-3',5'-adenylate | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.7.7.85 | Bacillus amyloliquefaciens | A0A0D7XMK3 | - |
- |
2.7.7.85 | Bacillus anthracis | A0A2A8KZ47 | - |
- |
2.7.7.85 | Bacillus licheniformis | Q65P49 | - |
- |
2.7.7.85 | Bacillus licheniformis ATCC 14580 | Q65P49 | - |
- |
2.7.7.85 | Bacillus licheniformis DSM 13 | Q65P49 | - |
- |
2.7.7.85 | Bacillus licheniformis Gibson 46 | Q65P49 | - |
- |
2.7.7.85 | Bacillus licheniformis JCM 2505 | Q65P49 | - |
- |
2.7.7.85 | Bacillus licheniformis NBRC 12200 | Q65P49 | - |
- |
2.7.7.85 | Bacillus licheniformis NCIMB 9375 | Q65P49 | - |
- |
2.7.7.85 | Bacillus licheniformis NRRL NRS-1264 | Q65P49 | - |
- |
2.7.7.85 | Bacillus subtilis | Q45589 | - |
- |
2.7.7.85 | Bacillus subtilis 168 | Q45589 | - |
- |
2.7.7.85 | Clostridium botulinum | A0A0C2N691 | - |
- |
2.7.7.85 | Clostridium ljungdahlii | D8GIJ7 | - |
- |
2.7.7.85 | Clostridium ljungdahlii ATCC 55383 | D8GIJ7 | - |
- |
2.7.7.85 | Clostridium ljungdahlii DSM 13528 | D8GIJ7 | - |
- |
2.7.7.85 | Clostridium ljungdahlii PETC | D8GIJ7 | - |
- |
2.7.7.85 | Clostridium novyi | A0PXZ3 | - |
- |
2.7.7.85 | Clostridium novyi NT | A0PXZ3 | - |
- |
2.7.7.85 | Clostridium perfringens | A0A0H2YU52 | - |
- |
2.7.7.85 | Clostridium perfringens DSM 756 | A0A0H2YU52 | - |
- |
2.7.7.85 | Clostridium perfringens JCM 1290 | A0A0H2YU52 | - |
- |
2.7.7.85 | Clostridium perfringens NCIMB 6125 | A0A0H2YU52 | - |
- |
2.7.7.85 | Clostridium perfringens NCTC 8237 | A0A0H2YU52 | - |
- |
2.7.7.85 | Clostridium perfringens type A | A0A0H2YU52 | - |
- |
2.7.7.85 | Enterococcus faecalis | A0A2Z6BU13 | - |
- |
2.7.7.85 | Enterococcus faecalis ERV62 | A0A2Z6BU13 | - |
- |
2.7.7.85 | Geobacter sulfurreducens | Q74EU1 | - |
- |
2.7.7.85 | Geobacter sulfurreducens ATCC 51573 | Q74EU1 | - |
- |
2.7.7.85 | Geobacter sulfurreducens DSM 12127 | Q74EU1 | - |
- |
2.7.7.85 | Geobacter sulfurreducens PCA | Q74EU1 | - |
- |
2.7.7.85 | Lacticaseibacillus rhamnosus | A0A2A5L6R6 | - |
- |
2.7.7.85 | Lacticaseibacillus rhamnosus ATCC 8530 | A0A2A5L6R6 | - |
- |
2.7.7.85 | Lactobacillus acidophilus | Q5FL37 | - |
- |
2.7.7.85 | Lactobacillus acidophilus ATCC 700396 | Q5FL37 | - |
- |
2.7.7.85 | Lactobacillus acidophilus N2 | Q5FL37 | - |
- |
2.7.7.85 | Lactobacillus acidophilus NCFM | Q5FL37 | - |
- |
2.7.7.85 | Lactobacillus acidophilus NCK56 | Q5FL37 | - |
- |
2.7.7.85 | Lactococcus cremoris | A2RIF7 | - |
- |
2.7.7.85 | Lactococcus cremoris | Q031P4 | - |
- |
2.7.7.85 | Lactococcus cremoris MG1363 | A2RIF7 | - |
- |
2.7.7.85 | Lactococcus cremoris Sk11 | Q031P4 | - |
- |
2.7.7.85 | Listeria monocytogenes EGD | Q8Y5E4 | - |
- |
2.7.7.85 | Listeria monocytogenes EGD ATCC BAA-679 | Q8Y5E4 | - |
- |
2.7.7.85 | Listeria monocytogenes EGD EGD-e | Q8Y5E4 | - |
- |
2.7.7.85 | Staphylococcus aureus | Q2FW92 | - |
- |
2.7.7.85 | Staphylococcus aureus NCTC 8325 | Q2FW92 | - |
- |
2.7.7.85 | Staphylococcus aureus PS 47 | Q2FW92 | - |
- |
2.7.7.85 | Streptococcus equi subsp. zooepidemicus | A0A2X3T317 | - |
- |
2.7.7.85 | Streptococcus mutans serotype c | Q8DTC4 | - |
- |
2.7.7.85 | Streptococcus mutans serotype c ATCC 700610 | Q8DTC4 | - |
- |
2.7.7.85 | Streptococcus mutans serotype c UA159 | Q8DTC4 | - |
- |
2.7.7.85 | Streptococcus pneumoniae | A0A0B7L730 | - |
- |
2.7.7.85 | Streptococcus pneumoniae ATCC 700669 | A0A0B7L730 | - |
- |
2.7.7.85 | Streptococcus pyogenes serotype M2 | Q1JH51 | - |
- |
2.7.7.85 | Streptococcus pyogenes serotype M2 MGAS10270 | Q1JH51 | - |
- |
2.7.7.85 | Tetragenococcus halophilus | G4L7W3 | Pediococcus halophilus | - |
2.7.7.85 | Tetragenococcus halophilus DSM 20338 | G4L7W3 | Pediococcus halophilus | - |
2.7.7.85 | Tetragenococcus halophilus JCM 20259 | G4L7W3 | Pediococcus halophilus | - |
2.7.7.85 | Tetragenococcus halophilus NBRC 12172 | G4L7W3 | Pediococcus halophilus | - |
2.7.7.85 | Tetragenococcus halophilus NCIMB 9735 | G4L7W3 | Pediococcus halophilus | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.7.85 | 2 ATP | - |
Bacillus subtilis | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Staphylococcus aureus | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Streptococcus pneumoniae | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Streptococcus mutans serotype c | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Streptococcus pyogenes serotype M2 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Streptococcus equi subsp. zooepidemicus | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Enterococcus faecalis | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus amyloliquefaciens | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus licheniformis | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus anthracis | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Tetragenococcus halophilus | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium novyi | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium ljungdahlii | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium perfringens | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium botulinum | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Geobacter sulfurreducens | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Listeria monocytogenes EGD | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lactococcus cremoris | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lacticaseibacillus rhamnosus | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lactobacillus acidophilus | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Tetragenococcus halophilus JCM 20259 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Listeria monocytogenes EGD EGD-e | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lactococcus cremoris Sk11 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Staphylococcus aureus NCTC 8325 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus subtilis 168 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Tetragenococcus halophilus DSM 20338 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Tetragenococcus halophilus NCIMB 9735 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium ljungdahlii DSM 13528 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus licheniformis NCIMB 9375 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Enterococcus faecalis ERV62 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus licheniformis Gibson 46 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium novyi NT | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium perfringens NCIMB 6125 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium perfringens NCTC 8237 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium perfringens JCM 1290 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus licheniformis JCM 2505 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Streptococcus mutans serotype c ATCC 700610 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Tetragenococcus halophilus NBRC 12172 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lactococcus cremoris MG1363 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lactobacillus acidophilus NCFM | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Streptococcus pyogenes serotype M2 MGAS10270 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus licheniformis NRRL NRS-1264 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium perfringens type A | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lacticaseibacillus rhamnosus ATCC 8530 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Geobacter sulfurreducens PCA | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium ljungdahlii PETC | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Streptococcus pneumoniae ATCC 700669 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Listeria monocytogenes EGD ATCC BAA-679 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lactobacillus acidophilus ATCC 700396 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Geobacter sulfurreducens ATCC 51573 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lactobacillus acidophilus NCK56 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium perfringens DSM 756 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus licheniformis NBRC 12200 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Staphylococcus aureus PS 47 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus licheniformis ATCC 14580 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Lactobacillus acidophilus N2 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Streptococcus mutans serotype c UA159 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Bacillus licheniformis DSM 13 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Clostridium ljungdahlii ATCC 55383 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? | |
2.7.7.85 | 2 ATP | - |
Geobacter sulfurreducens DSM 12127 | 2 diphosphate + cyclic di-3',5'-adenylate | - |
? |
EC Number | Subunits | Comment | Organism |
---|---|---|---|
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Bacillus subtilis |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Staphylococcus aureus |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Streptococcus pneumoniae |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Streptococcus mutans serotype c |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Streptococcus pyogenes serotype M2 |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Streptococcus equi subsp. zooepidemicus |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Enterococcus faecalis |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Bacillus amyloliquefaciens |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Bacillus licheniformis |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Bacillus anthracis |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Tetragenococcus halophilus |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Clostridium novyi |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Clostridium ljungdahlii |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Clostridium perfringens |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Clostridium botulinum |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Geobacter sulfurreducens |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Listeria monocytogenes EGD |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Lactococcus cremoris |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Lacticaseibacillus rhamnosus |
2.7.7.85 | homodimer | the dimer-forming CdaA contains three transmembrane domains with the DAC domain (Dis_N Pfam PF02457) located intracellularly, while CdaR contains one transmembrane domain and several YbbR domains (Pfam PF07949) predicted to be located extracellularly | Lactobacillus acidophilus |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Bacillus subtilis |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Staphylococcus aureus |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Streptococcus pneumoniae |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Streptococcus mutans serotype c |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Streptococcus pyogenes serotype M2 |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Streptococcus equi subsp. zooepidemicus |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Enterococcus faecalis |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Bacillus amyloliquefaciens |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Bacillus licheniformis |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Bacillus anthracis |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Tetragenococcus halophilus |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Clostridium novyi |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Clostridium ljungdahlii |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Clostridium perfringens |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Clostridium botulinum |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Geobacter sulfurreducens |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Listeria monocytogenes EGD |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Lactococcus cremoris |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Lacticaseibacillus rhamnosus |
2.7.7.85 | More | the DAC enzyme is organized in the CdaA-CdaR-GlmM protein complex | Lactobacillus acidophilus |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
2.7.7.85 | CdaA | - |
Bacillus subtilis |
2.7.7.85 | CdaA | - |
Staphylococcus aureus |
2.7.7.85 | CdaA | - |
Streptococcus pneumoniae |
2.7.7.85 | CdaA | - |
Streptococcus mutans serotype c |
2.7.7.85 | CdaA | - |
Streptococcus pyogenes serotype M2 |
2.7.7.85 | CdaA | - |
Streptococcus equi subsp. zooepidemicus |
2.7.7.85 | CdaA | - |
Enterococcus faecalis |
2.7.7.85 | CdaA | - |
Bacillus amyloliquefaciens |
2.7.7.85 | CdaA | - |
Bacillus licheniformis |
2.7.7.85 | CdaA | - |
Bacillus anthracis |
2.7.7.85 | CdaA | - |
Tetragenococcus halophilus |
2.7.7.85 | CdaA | - |
Clostridium novyi |
2.7.7.85 | CdaA | - |
Clostridium ljungdahlii |
2.7.7.85 | CdaA | - |
Clostridium perfringens |
2.7.7.85 | CdaA | - |
Clostridium botulinum |
2.7.7.85 | CdaA | - |
Geobacter sulfurreducens |
2.7.7.85 | CdaA | - |
Listeria monocytogenes EGD |
2.7.7.85 | CdaA | - |
Lactococcus cremoris |
2.7.7.85 | CdaA | - |
Lacticaseibacillus rhamnosus |
2.7.7.85 | CdaA | - |
Lactobacillus acidophilus |
2.7.7.85 | Cyclic di-AMP synthase | - |
Bacillus subtilis |
2.7.7.85 | Dac | - |
Bacillus subtilis |
2.7.7.85 | Dac | - |
Staphylococcus aureus |
2.7.7.85 | Dac | - |
Streptococcus pneumoniae |
2.7.7.85 | Dac | - |
Streptococcus mutans serotype c |
2.7.7.85 | Dac | - |
Streptococcus pyogenes serotype M2 |
2.7.7.85 | Dac | - |
Streptococcus equi subsp. zooepidemicus |
2.7.7.85 | Dac | - |
Enterococcus faecalis |
2.7.7.85 | Dac | - |
Bacillus amyloliquefaciens |
2.7.7.85 | Dac | - |
Bacillus licheniformis |
2.7.7.85 | Dac | - |
Bacillus anthracis |
2.7.7.85 | Dac | - |
Tetragenococcus halophilus |
2.7.7.85 | Dac | - |
Clostridium novyi |
2.7.7.85 | Dac | - |
Clostridium ljungdahlii |
2.7.7.85 | Dac | - |
Clostridium perfringens |
2.7.7.85 | Dac | - |
Clostridium botulinum |
2.7.7.85 | Dac | - |
Geobacter sulfurreducens |
2.7.7.85 | Dac | - |
Listeria monocytogenes EGD |
2.7.7.85 | Dac | - |
Lactococcus cremoris |
2.7.7.85 | Dac | - |
Lacticaseibacillus rhamnosus |
2.7.7.85 | Dac | - |
Lactobacillus acidophilus |
2.7.7.85 | dacA | - |
Bacillus subtilis |
2.7.7.85 | dacA | - |
Staphylococcus aureus |
2.7.7.85 | dacA | - |
Streptococcus pneumoniae |
2.7.7.85 | dacA | - |
Streptococcus mutans serotype c |
2.7.7.85 | dacA | - |
Streptococcus pyogenes serotype M2 |
2.7.7.85 | dacA | - |
Streptococcus equi subsp. zooepidemicus |
2.7.7.85 | dacA | - |
Enterococcus faecalis |
2.7.7.85 | dacA | - |
Bacillus amyloliquefaciens |
2.7.7.85 | dacA | - |
Bacillus licheniformis |
2.7.7.85 | dacA | - |
Bacillus anthracis |
2.7.7.85 | dacA | - |
Tetragenococcus halophilus |
2.7.7.85 | dacA | - |
Clostridium novyi |
2.7.7.85 | dacA | - |
Clostridium ljungdahlii |
2.7.7.85 | dacA | - |
Clostridium perfringens |
2.7.7.85 | dacA | - |
Clostridium botulinum |
2.7.7.85 | dacA | - |
Geobacter sulfurreducens |
2.7.7.85 | dacA | - |
Lactococcus cremoris |
2.7.7.85 | dacA | - |
Lactobacillus acidophilus |
2.7.7.85 | dacA_1 | - |
Lacticaseibacillus rhamnosus |
2.7.7.85 | ybbP | - |
Streptococcus pneumoniae |
2.7.7.85 | ybbP | - |
Bacillus licheniformis |
2.7.7.85 | ybbP | - |
Bacillus anthracis |
2.7.7.85 | yedA | - |
Listeria monocytogenes EGD |
EC Number | General Information | Comment | Organism |
---|---|---|---|
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Bacillus subtilis |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Staphylococcus aureus |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Streptococcus pneumoniae |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Streptococcus mutans serotype c |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Streptococcus pyogenes serotype M2 |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Streptococcus equi subsp. zooepidemicus |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Enterococcus faecalis |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Bacillus amyloliquefaciens |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Bacillus licheniformis |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Bacillus anthracis |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Tetragenococcus halophilus |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Clostridium novyi |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Clostridium ljungdahlii |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Clostridium perfringens |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Clostridium botulinum |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Geobacter sulfurreducens |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Listeria monocytogenes EGD |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Lactococcus cremoris |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Lacticaseibacillus rhamnosus |
2.7.7.85 | metabolism | regulation of diadenylate cyclase activity in bacteria, replenishing the cyclic-di-AMP pool, overview. The intracellular pool of c-di-AMP is maintained by the activities of diadenylate cyclase (DAC) and phosphodiesterase (PDE) enzymes, as well as possibly via c-di-AMP export. Transient regulation of DAC enzyme in the CdaA-CdaR-GlmM protein complex | Lactobacillus acidophilus |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Bacillus subtilis |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Staphylococcus aureus |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Streptococcus pneumoniae |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Streptococcus mutans serotype c |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Streptococcus pyogenes serotype M2 |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Streptococcus equi subsp. zooepidemicus |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Enterococcus faecalis |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Bacillus amyloliquefaciens |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Bacillus licheniformis |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Bacillus anthracis |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Tetragenococcus halophilus |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Clostridium novyi |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Clostridium ljungdahlii |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Clostridium perfringens |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Clostridium botulinum |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Geobacter sulfurreducens |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Listeria monocytogenes EGD |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Lactococcus cremoris |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Lacticaseibacillus rhamnosus |
2.7.7.85 | physiological function | a broadly conserved second messenger is cyclic-di-AMP (c-di-AMP) which regulates a range of processes including cell wall homeostasis, potassium uptake, DNA repair, fatty acid synthesis, biofilm formation and central metabolism in bacteria. Regulators of the membrane-bound enzyme CdaA are the membrane-bound CdaR and the phosphoglucosamine mutase GlmM which both bind directly to the DAC | Lactobacillus acidophilus |