Published in

Annual Reviews, Annual Review of Biochemistry, 1(85), p. 405-429, 2016

DOI: 10.1146/annurev-biochem-060815-014537

Links

Tools

Export citation

Search in Google Scholar

The Substrate Specificity of Sirtuins

Journal article published in 2015 by Poonam Bheda, Hui Jing, Cynthia Wolberger ORCID, Hening Lin
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Red circle
Postprint: archiving forbidden
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

Sirtuins are NAD+-dependent enzymes universally present in all organisms, where they play central roles in regulating numerous biological processes. Although early studies showed that sirtuins deacetylated lysines in a reaction that consumes NAD+, more recent studies have revealed that these enzymes can remove a variety of acyl-lysine modifications. The specificities for varied acyl modifications may thus underlie the distinct roles of the different sirtuins within a given organism. This review summarizes the structure, chemistry, and substrate specificity of sirtuins with a focus on how different sirtuins recognize distinct substrates and thus carry out specific functions.