| acetoxybutynylbithiophene deacetylase | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| EC no. | 3.1.1.54 | ||||||||
| CAS no. | 82346-63-2 | ||||||||
| Databases | |||||||||
| IntEnz | IntEnz view | ||||||||
| BRENDA | BRENDA entry | ||||||||
| ExPASy | NiceZyme view | ||||||||
| KEGG | KEGG entry | ||||||||
| MetaCyc | metabolic pathway | ||||||||
| PRIAM | profile | ||||||||
| PDB structures | RCSB PDB PDBe PDBsum | ||||||||
| Gene Ontology | AmiGO / QuickGO | ||||||||
| |||||||||
The enzyme acetoxybutynylbithiophene deacetylase (EC 3.1.1.54) catalyzes the reaction
- 5-(4-acetoxybut-1-ynyl)-2,2′-bithiophene + H2O 5-(4-hydroxybut-1-ynyl)-2,2′-bithiophene + acetate
This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. The systematic name is 5-(4-acetoxybut-1-ynyl)-2,2′-bithiophene O-acetylhydrolase. Other names in common use include acetoxybutynylbithiophene esterase, and 5-(4-acetoxy-1-butynyl)-2,2′-bithiophene:acetate esterase.
- Granander J, Sott R, Hilmersson G (2006). "Correlation between the 6Li,15N coupling constant and the coordination number at lithium". Chemistry: A European Journal. 12 (15): 4191–7. doi: 10.1002/chem.200501371. PMID 16526078.
| acetoxybutynylbithiophene deacetylase | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| EC no. | 3.1.1.54 | ||||||||
| CAS no. | 82346-63-2 | ||||||||
| Databases | |||||||||
| IntEnz | IntEnz view | ||||||||
| BRENDA | BRENDA entry | ||||||||
| ExPASy | NiceZyme view | ||||||||
| KEGG | KEGG entry | ||||||||
| MetaCyc | metabolic pathway | ||||||||
| PRIAM | profile | ||||||||
| PDB structures | RCSB PDB PDBe PDBsum | ||||||||
| Gene Ontology | AmiGO / QuickGO | ||||||||
| |||||||||
The enzyme acetoxybutynylbithiophene deacetylase (EC 3.1.1.54) catalyzes the reaction
- 5-(4-acetoxybut-1-ynyl)-2,2′-bithiophene + H2O 5-(4-hydroxybut-1-ynyl)-2,2′-bithiophene + acetate
This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. The systematic name is 5-(4-acetoxybut-1-ynyl)-2,2′-bithiophene O-acetylhydrolase. Other names in common use include acetoxybutynylbithiophene esterase, and 5-(4-acetoxy-1-butynyl)-2,2′-bithiophene:acetate esterase.
- Granander J, Sott R, Hilmersson G (2006). "Correlation between the 6Li,15N coupling constant and the coordination number at lithium". Chemistry: A European Journal. 12 (15): 4191–7. doi: 10.1002/chem.200501371. PMID 16526078.