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Updated: Apr 28, 2026

Nucleoside Triphosphates - From Synthesis to Biochemical Characterization
Published on: April 3, 2014
Phosphate analogues in the dissection of mechanism
Heidi J Korhonen1, Louis P Conway2, David R W Hodgson2
1Department of Chemistry, Durham University Mountjoy Site, South Road, Durham DH1 3LE, UK; Department of Chemistry, University of Turku, Vatselankatu 2, 20014 Turku, Finland.
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.
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