Any feedback?
Literature summary extracted from
- Studies of enzyme stereochemistry. Elucidation of the stereochemistry of the reaction catalyzed by cob(I)alamin adenosyltransferase (1985), J. Am. Chem. Soc., 107, 2190-2191.
No PubMed abstract available
Natural Substrates/ Products (Substrates)
| EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 2.5.1.17 | ATP + cob(I)alamin | Clostridium tetanomorphum | - |
triphosphate + coenzyme B12 | - |
? |  |
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 2.5.1.17 | Clostridium tetanomorphum | - |
- |
- |
Substrates and Products (Substrate)
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 2.5.1.17 | ATP + cob(I)alamin | - |
Clostridium tetanomorphum | triphosphate + coenzyme B12 | - |
? | |
| 2.5.1.17 | ATP + cob(I)alamin | stereospecific process which proceeds with overall inversion of configuration at C-5' of the adenosyl moiety | Clostridium tetanomorphum | triphosphate + coenzyme B12 | adenosylcobalamin, B12-coenzyme or deoxyadenosyl-B12 | ? | |
| 2.5.1.17 | additional information | - |
Clostridium tetanomorphum | ? | - |
? | |
Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.
Release 2023.1 (January 2023)
Legal
Curated at
Member of
