On the Enzymatic Activation of NADH

Rob Meijers, Richard J Morris, Hans W Adolph, Angelo Merli, Victor S Lamzin, Eila Cedergren

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)9316-9321
JournalJournal of Biological Chemistry
Volume276
Issue number12
DOIs
Publication statusPublished - 2001

Subject classification (UKÄ)

  • Biological Sciences

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