A QM/MM study of the reaction mechanism of human beta-ketoacyl reductase

• Type: Article in International Scientific Journal
• Date: 2017

Authors

Medina, FE (Author) Other; Neves, RPP (Author) FCUP; Ramos, MJ (Author) FCUP; Pedro A Fernandes (Author) FCUP

Journal

Title: Physical Chemistry Chemical Physics

Vol. 19 No. 2

Pages: 347-355

ISSN: 1463-9076

Publisher: Royal Society of Chemistry

Indexing

ISI Web of Knowledge - 16 Citations

Scopus - 16 Citations

Other information

Authenticus ID: P-00M-DJR

DOI: 10.1039/c6cp07014k

Abstract (EN): Human fatty acid synthase (hFAS) is a multifunctional enzyme involved in a wide diversity of biological functions. For instance, it is a precursor of phospholipids and other complex processes such as the de novo synthesis of long chain fatty acid. Human FAS is also a component of biological membranes and it is implicated in the overexpression of several types of cancers. In this work, we describe the catalytic mechanism of beta-ketoreductase (KR), which is a catalytic domain of the hFAS enzyme that catalyzes the reduction of beta-ketoacyl to beta-hydroxyacyl with the concomitant oxidation of the NADPH cofactor. The catalysis by KR is an intermediate step in the cycle of reactions that elongate the substrate's carbon chain until the final product is obtained. We study and propose the catalytic mechanism of the KR domain determined using the hybrid QM/MM methodology, at the ONIOM(B3LYP/6-311+G(2d,2p): AMBER) level of theory. The results indicate that the reaction mechanism occurs in two stages: (i) nucleophilic attack by a NADPH hydride to the beta-carbon of the substrate, together with an asynchronous deprotonation of the Tyr2034 by the oxygen of the beta-alkoxide to hold the final alcohol product; and (ii) an asynchronous deprotonation of the hydroxyl in the NADP+'s ribose by Tyr2034, and of the Lys1995 by the resulting alkoxide in the former ribose to restore the protonation state of Tyr2034. The reduction step occurs with a Gibbs energy barrier of 11.7 kcal mol(-1) and a Gibbs reaction energy of -10.6 kcal mol(-1). These results have provided an understanding of the catalytic mechanism of the KR hFAS domain, a piece of the heavy hFAS biosynthetic machinery.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 9