0000000000179174

AUTHOR

Mireia Garcia-viloca

0000-0001-5415-0248

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Critical Role of Substrate Conformational Change in the Proton Transfer Process Catalyzed by 4-Oxalocrotonate Tautomerase

2009

4-Oxalocrotonate tautomerase enzyme (4-OT) catalyzes the isomerization of 2-oxo-4-hexenedioate to 2-oxo-3-hexenedioate. The chemical process involves two proton transfers, one from a carbon of the substrate to the nitrogen of Pro1 and another from this nitrogen atom to a different carbon of the substrate. In this paper the isomerization has been studied using the combined quantum mechanical and molecular mechanical (QM/MM) method with a dual-level treatment of the quantum subsystem employing the MPW1BK density functional as the higher level. Exploration of the potential energy surface shows that the process is stepwise, with a stable intermediate state corresponding to the deprotonated subs…

Models MolecularConformational changeProtonMolecular ConformationProtonationCrystallography X-RayBiochemistryArticleCatalysisColloid and Surface ChemistryReaction rate constantIsomerismCatalytic DomainIsomerasesChemistrySubstrate (chemistry)Hydrogen BondingGeneral ChemistryChemical physicsCrotonatesPotential energy surface4-Oxalocrotonate tautomeraseQuantum TheoryThermodynamicsPhysical chemistryProtonsIsomerizationJournal of the American Chemical Society
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