| Literature DB >> 11134046 |
R Meijers1, R J Morris, H W Adolph, A Merli, V S Lamzin, E S Cedergren-Zeppezauer.
Abstract
Atomic (1 A) resolution x-ray structures of horse liver alcohol dehydrogenase in complex with NADH revealed the formation of an adduct in the active site between a metal-bound water and NADH. Furthermore, a pronounced distortion of the pyridine ring of NADH was observed. A series of quantum chemical calculations on the water-nicotinamide adduct showed that the puckering of the pyridine ring in the crystal structures can only be reproduced when the water is considered a hydroxide ion. These observations provide fundamental insight into the enzymatic activation of NADH for hydride transfer.Entities:
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Year: 2000 PMID: 11134046 DOI: 10.1074/jbc.M010870200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157