Layers of DUB regulation

被引:110
作者
Sahtoe, Danny D.
Sixma, Titia K. [1 ]
机构
[1] Netherlands Canc Inst, Div Biochem, NL-1066 CX Amsterdam, Netherlands
基金
欧洲研究理事会;
关键词
deubiquitinating enzyme; isopeptidase; allosteric; ubiquitin; regulation; mechanism; UCH37 DEUBIQUITINATING ENZYME; DNA-DAMAGE; CRYSTAL-STRUCTURE; UBIQUITIN LIGASE; STRUCTURAL BASIS; BINDING DOMAIN; ACTIVE-SITE; ACTIVATION; PROTEASOME; MECHANISM;
D O I
10.1016/j.tibs.2015.05.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteolytic enzymes, such as (iso-)peptidases, are potentially hazardous for cells. To neutralize their potential danger, tight control of their activities has evolved. Deubiquitylating enzymes (DUBs) are isopeptidases involved in eukaryotic ubiquitylation. They reverse ubiquitin signals by hydrolyzing ubiquitin adducts, giving them control over all aspects of ubiquitin biology. The importance of DUB function is underscored by their frequent deregulation in human disease, making these enzymes potential drug targets. Here, we review the different layers of DUB enzyme regulation. We discuss how post-translational modification (PTM), regulatory domains within DUBs, and incorporation of DUBs into macromolecular complexes contribute to their activity. We conclude that most DUBs are likely to use a combination of these basic regulatory mechanisms.
引用
收藏
页码:456 / 467
页数:12
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