Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 1.1.1.184 extracted from

  • Zhu, D.; Yang, Y.; Hua, L.
    Stereoselective enzymatic synthesis of chiral alcohols with the use of a carbonyl reductase from Candida magnoliae with anti-Prelog enantioselectivity (2006), J. Org. Chem., 71, 4202-4205.
    View publication on PubMed

Application

Application Comment Organism
synthesis the enzyme is useful for stereoselective enzymatic synthesis of chiral alcohols and chiral alcohol intermediates of pharmaceutical importance Starmerella magnoliae

Organism

Organism UniProt Comment Textmining
Starmerella magnoliae Q9C4B3 gene crs1
-

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
0.015 1.14 substrate specificity, overview Starmerella magnoliae

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information substrate specificity, detailed overview, the enzyme shows anti-Prelog enantioselectivity, the enzyme catalyzes the reduction of a series of ketones, alpha- and beta-ketoesters, synthesis of several chiral alcohol intermediates of pharmaceutical importance Starmerella magnoliae ?
-
?

Synonyms

Synonyms Comment Organism
carbonyl reductase S1
-
Starmerella magnoliae