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The functional diversity of protein lysine methylation

Authors :
Sylvain Lanouette
Vanessa Mongeon
Daniel Figeys
Jean‐François Couture
Source :
Molecular Systems Biology, Vol 10, Iss 4, Pp 1-26 (2014)
Publication Year :
2014
Publisher :
Springer Nature, 2014.

Abstract

Abstract Large‐scale characterization of post‐translational modifications (PTMs), such as phosphorylation, acetylation and ubiquitination, has highlighted their importance in the regulation of a myriad of signaling events. While high‐throughput technologies have tremendously helped cataloguing the proteins modified by these PTMs, the identification of lysine‐methylated proteins, a PTM involving the transfer of one, two or three methyl groups to the ε‐amine of a lysine side chain, has lagged behind. While the initial findings were focused on the methylation of histone proteins, several studies have recently identified novel non‐histone lysine‐methylated proteins. This review provides a compilation of all lysine methylation sites reported to date. We also present key examples showing the impact of lysine methylation and discuss the circuitries wired by this important PTM.

Details

Language :
English
ISSN :
17444292
Volume :
10
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Molecular Systems Biology
Publication Type :
Academic Journal
Accession number :
edsdoj.3bde2bd8de554055bd9f038d74c6e7d8
Document Type :
article
Full Text :
https://doi.org/10.1002/msb.134974