Insight into the stereospecificity of short-chain Thermus thermophilus alcohol dehydrogenase showing pro-S hydride transfer and Prelog enantioselectivity

Protein and Peptide Letters

Volumn 17, Issue 4, 2010, Pages 437-443

  Pennacchio, Angela ^a   Giordano, Assunta ^a   Esposito, Luciana ^b   Langella, Emma ^b   Rossi, Mosè ^a   Raia, Carlo A ^a  

^a CNR   (Italy)

^b CNR   (Italy)

Author keywords

Bacillus stearothermophilus; Cofactor stereospecificity; Enantioselectivity; Prelog rule; Short chain dehydrogenase reductase; Thermus thermophilus

Indexed keywords

2 PROPANOL; ALCOHOL DEHYDROGENASE; BACTERIAL PROTEIN; DEUTERIUM; NICOTINAMIDE ADENINE DINUCLEOTIDE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; ENZYMOLOGY; METABOLISM; NUCLEAR MAGNETIC RESONANCE; PROTEIN CONFORMATION; STEREOISOMERISM; THERMUS THERMOPHILUS;

2-PROPANOL; ALCOHOL DEHYDROGENASE; BACTERIAL PROTEINS; DEUTERIUM; MODELS, MOLECULAR; NAD; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PROTEIN CONFORMATION; STEREOISOMERISM; THERMUS THERMOPHILUS;

GEOBACILLUS STEAROTHERMOPHILUS; THERMUS THERMOPHILUS;

EID: 77949957731     PISSN: 09298665     EISSN: None     Source Type: Journal    
DOI: 10.2174/092986610790963564     Document Type: Article

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