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PMID: 11456876 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Triosephosphate isomerase: a theoretical comparison of alternative pathways.

Journal of the American Chemical Society ·Vol. 123 ·No. 10 ·2001-03-14 ·Pages 2284-90

Cui Q, Karplus M

Abstract

Three mechanisms proposed for the triosephosphate isomerase (TIM) catalyzed reactions were studied with the QM/MM approach using B3LYP/6-31+G(d,p) as the QM method. The two pathways that involve an enediol species were found to give similar values for the barriers and the calculated rates are in satisfactory agreement with experiment. By contrast, the mechanism that involves intramolecular proton transfer in the enediolate was found to be energetically unfavorable due to electrostatic interactions with His 95, a conserved residue in TIM from different organisms. A perturbation analysis was used to determine the residues that make the major contribution to catalysis.

MeSH Terms
Kinetics Static Electricity Triose-Phosphate Isomerase/metabolism
Chemicals
Triose-Phosphate Isomerase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cui Q
Contribution from the Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Karplus M
Article Info
Journal
Journal of the American Chemical Society
Abbr.
J Am Chem Soc
ISSN
0002-7863
Published
2001-03-14
Pages
2284-90
Language
English
Region
United States
NLM ID
7503056
Subset
IM
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