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The functional diversity of protein lysine methylation
- 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