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The Claisen Rearrangement of an Unusual Substrate in Chorismate Mutase

Published

Author(s)

S. E. Worthington, Morris Krauss

Abstract

The calculated reaction path for an unusual substrate of chorismate mutase (Bacillus.subtilis) is found to be completely comparable to that of the native chorismate. In the unusual substrate, the cyclohexadienyl ring in chorismate is replaced by dihydropyridine. Previous theoretical calculations of the native reaction path provide the basis for predicting that the interactions of the unusual reactant in the active site are electronically analogous to the native. Three unusual substrates are obtained by replacing each of the C-H moieties in the cyclohexadienyl ring by a nitrogen atom. This substitution does not substantially alter the electronic characteristics of the ring both with regard to the catalytic activation by the active site and the interaction with hydrophobic groups in the active site. The activation energies and optimized structures along the reaction path are obtained for the tautomers of the unusual reactant and product. The possibility of ultimately obtaining an unusual amino acid by this pathway is discussed.
Citation
Journal of Physical Chemistry B
Volume
105
Issue
29

Keywords

chorismate mutase, claisen rearrangement, effective fragment potentials, enzyme catalysis, quantum chemistry

Citation

Worthington, S. and Krauss, M. (2001), The Claisen Rearrangement of an Unusual Substrate in Chorismate Mutase, Journal of Physical Chemistry B (Accessed April 15, 2024)
Created June 30, 2001, Updated October 12, 2021