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Volumn 16, Issue 7, 2015, Pages 1052-1059

Structure, activity and stereoselectivity of NADPH-dependent oxidoreductases catalysing the S-selective reduction of the imine substrate 2-methylpyrroline

(8) Man, Henry a Wells, Elizabeth a Hussain, Shahed b Leipold, Friedemann b Hart, Sam a Turkenburg, Johan P a Turner, Nicholas J b Grogan, Gideon a

a UNIVERSITY OF YORK (United Kingdom)

b UNIVERSITY OF MANCHESTER (United Kingdom)

Author keywords

amines; asymmetric catalysis; imines; IREDs; NADPH; oxidoreductases

Indexed keywords

2 METHYLPYRROLINE; IMINE; OXIDOREDUCTASE; PYRROLINE DERIVATIVE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; UNCLASSIFIED DRUG; 2-METHYLPYRROLIDINE; PYRROLIDINE DERIVATIVE;

ARTICLE; BIOTRANSFORMATION; CATALYSIS; CONTROLLED STUDY; COWORKER; CRYSTAL STRUCTURE; DRUG STRUCTURE; NONHUMAN; PRIORITY JOURNAL; SEQUENCE ALIGNMENT; STEREOCHEMISTRY; X RAY CRYSTALLOGRAPHY; BIOCATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; ENZYME ACTIVE SITE; ENZYME SPECIFICITY; ENZYMOLOGY; GRAM POSITIVE BACTERIUM; METABOLISM; OXIDATION REDUCTION REACTION; SEQUENCE HOMOLOGY;

BACILLUS CEREUS; NOCARDIOPSIS HALOPHILA; STREPTOMYCES SP.;

BIOCATALYSIS; CATALYTIC DOMAIN; GRAM-POSITIVE BACTERIA; IMINES; MODELS, MOLECULAR; NADH, NADPH OXIDOREDUCTASES; OXIDATION-REDUCTION; PYRROLIDINES; SEQUENCE HOMOLOGY, AMINO ACID; SUBSTRATE SPECIFICITY;

EID: 84928487130 PISSN: 14394227 EISSN: 14397633 Source Type: Journal
DOI: 10.1002/cbic.201402625 Document Type: Article

Times cited : (59)

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