Literature DB >> 16317459

Dependence of enzyme reaction mechanism on protonation state of titratable residues and QM level description: lactate dehydrogenase.

Silvia Ferrer1, Estanislao Silla, Iñaki Tuñón, Mónica Oliva, Vicent Moliner, Ian H Williams.   

Abstract

We have studied the dependence of the chemical reaction mechanism of L-lactate dehydrogenase (LDH) on the protonation state of titratable residues and on the level of the quantum mechanical (QM) description by means of hybrid quantum-mechanical/molecular-mechanical (QM/MM) methods; this methodology has allowed clarification of the timing of the hydride transfer and proton transfer components that hitherto had not been possible to state definitively.

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Year:  2005        PMID: 16317459     DOI: 10.1039/b510735k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  4 in total

1.  Dynamic and Electrostatic Effects on the Reaction Catalyzed by HIV-1 Protease.

Authors:  Agnieszka Krzemińska; Vicent Moliner; Katarzyna Świderek
Journal:  J Am Chem Soc       Date:  2016-12-09       Impact factor: 15.419

2.  The protonation site of para-dimethylaminobenzoic acid using atmospheric pressure ionization methods.

Authors:  Yunfeng Chai; Guofeng Weng; Shanshan Shen; Cuirong Sun; Yuanjiang Pan
Journal:  J Am Soc Mass Spectrom       Date:  2015-01-28       Impact factor: 3.109

3.  Theoretical site-directed mutagenesis: Asp168Ala mutant of lactate dehydrogenase.

Authors:  Silvia Ferrer; Iñaki Tuñón; Vicent Moliner; Ian H Williams
Journal:  J R Soc Interface       Date:  2008-12-06       Impact factor: 4.118

4.  Dynamic mechanism of proton transfer in mannitol 2-dehydrogenase from Pseudomonas fluorescens: mobile GLU292 controls proton relay through a water channel that connects the active site with bulk solvent.

Authors:  Mario Klimacek; Michael Brunsteiner; Bernd Nidetzky
Journal:  J Biol Chem       Date:  2011-12-22       Impact factor: 5.157

  4 in total

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