(S)-N-acetyl-1-phenylethylamine hydrolase
| (S)-N-acetyl-1-phenylethylamine hydrolase | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| EC number | 3.5.1.85 | ||||||||
| CAS number | 192230-94-7 | ||||||||
| 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 / EGO | ||||||||
| |||||||||
In enzymology, a (S)-N-acetyl-1-phenylethylamine hydrolase (EC 3.5.1.85) is an enzyme that catalyzes the chemical reaction
- N-acetylphenylethylamine + H2O phenylethylamine + acetate
Thus, the two substrates of this enzyme are N-acetylphenylethylamine and H2O, whereas its two products are phenylethylamine and acetate.
This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. The systematic name of this enzyme class is (S)-N-acetylphenylethylamine:H2O hydrolase. At least one compound, Phenylmethanesulfonylfluoride is known to inhibit this enzyme.
References
- Brunella A, Graf M, Kittelmann M, Lauma K, Ghisalba O (1997). "Production, purification, and characterization of a highly enantioselective (S)-N-acetyl-1-phenylethyl amidohydrolase from Rhodococcus". Appl. Microbiol. Biotechnol. 47 (5): 515–520. doi:10.1007/s002530050965.
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