Probing stereoselectivity and pro-chirality of hydride transfer during short-chain alcohol dehydrogenase activity: A combined quantitative 2H NMR and computational approach

Archives of Biochemistry and Biophysics

Volumn 482, Issue 1-2, 2009, Pages 42-51

  Kwiecień, Renata A ^a   Ayadi, Farouk ^a   Nemmaoui, Youssef ^a   Silvestre, Virginie ^a   Zhang, Ben Li ^a   Robins, Richard J ^a  

^a UNIVERSITÉ DE NANTES   (France)

Author keywords

Alcohol dehydrogenase; Enantioselectivity; Ethanol; Hybrid QM MM computation; Quantitative isotopic 2H NMR

Indexed keywords

ALCOHOL DEHYDROGENASE; ALDEHYDE DERIVATIVE; ISOTOPE; PROTON; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE DEHYDROGENASE;

ARTICLE; CHIRALITY; CONTROLLED STUDY; ENANTIOSELECTIVITY; ENZYME ACTIVE SITE; ENZYME ACTIVITY; LACTOBACILLUS BREVIS; MOLECULAR MODEL; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTITATIVE ANALYSIS; SACCHAROMYCES CEREVISIAE; STEREOCHEMISTRY;

AMINO ACIDS; BACTERIAL PROTEINS; BUTYRYL-COA DEHYDROGENASE; CALORIMETRY; CATALYTIC DOMAIN; ETHANOL; KINETICS; LACTOBACILLUS BREVIS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; NAD; NADP; PROTEIN CONFORMATION; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SUBSTRATE SPECIFICITY; THERMODYNAMICS;

LACTOBACILLUS BREVIS; SACCHAROMYCES CEREVISIAE;

EID: 59249100026     PISSN: 00039861     EISSN: 10960384     Source Type: Journal    
DOI: 10.1016/j.abb.2008.11.019     Document Type: Article

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