Phosphate analogues in the dissection of mechanism.

Heidi J Korhonen, Louis P Conway, David R W Hodgson

Journal: Current opinion in chemical biology 2015;21():63-72

PMID: 24879389

Abstract

Phosphoryl group transfer is central to genetic replication, cellular signalling and many metabolic processes. Understanding the mechanisms of phosphorylation and phosphate ester and anhydride cleavage is key to efforts towards biotechnological and biomedical exploitation of phosphate-handling enzymes. Analogues of phosphate esters and anhydrides are indispensable tools, alongside protein mutagenesis and computational methods, for the dissection of phosphoryl transfer mechanisms. Hydrolysable and non-hydrolysable phosphate analogues have provided insight into the nature and sites of phosphoryl transfer processes. Kinetic isotope effects and crystallography using transition state analogues have painted more detailed pictures of transition states and how enzymes work to stabilise them.

Copyright © 2014 The Authors. Published by Elsevier Ltd.. All rights reserved.

Address: Department of Chemistry, Durham University Mountjoy Site, South Road, Durham DH1 3LE, UK; Department of Chemistry, University of Turku, Vatselankatu 2, 20014 Turku, Finland.; Department of Chemistry, Durham University Mountjoy Site, South Road, Durham DH1 3LE, UK.; Department of Chemistry, Durham University Mountjoy Site, South Road, Durham DH1 3LE, UK. Electronic address: [email protected].

Link outs

Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.