Conformational effects in enzyme catalysis: Reaction via a high energy conformation in fatty acid amide hydrolase

80Citations
Citations of this article
62Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Quantum mechanics/molecular mechanics and molecular dynamics simulations of fatty acid amide hydrolase show that reaction (amide hydrolysis) occurs via a distinct, high energy conformation. This unusual finding has important implications for fatty acid amide hydrolase, a key enzyme in the endocannabinoid system. These results demonstrate the importance of structural fluctuations and the need to include them in the modeling of enzyme reactions. They also show that approaches based simply on studying enzyme-substrate complexes can be misleading for understanding biochemical reactivity. © 2007 by the Biophysical Society.

Cite

CITATION STYLE

APA

Lodola, A., Mor, M., Zurek, J., Tarzia, G., Piomelli, D., Harvey, J. N., & Mulholland, A. J. (2007). Conformational effects in enzyme catalysis: Reaction via a high energy conformation in fatty acid amide hydrolase. Biophysical Journal, 92(2). https://doi.org/10.1529/biophysj.106.098434

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free