Abstract
Atomic (1 Å) 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.
Original language | English |
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Pages (from-to) | 9316-9321 |
Journal | Journal of Biological Chemistry |
Volume | 276 |
Issue number | 12 |
DOIs | |
Publication status | Published - 2001 |
Subject classification (UKÄ)
- Biological Sciences