Breaking the chains: structure and function of the deubiquitinases

被引:1619
作者
Komander, David [1 ]
Clague, Michael J. [2 ]
Urbe, Sylvie [2 ]
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 0QH, England
[2] Univ Liverpool, Physiol Lab, Sch Biomed Sci, Liverpool L69 3BX, Merseyside, England
基金
英国医学研究理事会;
关键词
NF-KAPPA-B; UBIQUITIN-BINDING; CRYSTAL-STRUCTURE; ENZYME; PROTEIN; DOMAIN; SPECIFICITY; PROTEASOME; COMPLEX; A20;
D O I
10.1038/nrm2731
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ubiquitylation is a reversible protein modification that is implicated in many cellular functions. Recently, much progress has been made in the characterization of a superfamily of isopeptidases that remove ubiquitin: the deubiquitinases (DUBs; also known as deubiquitylating or deubiquitinating enzymes). Far from being uniform in structure and function, these enzymes display a myriad of distinct mechanistic features. The small number (< 100) of DUBs might at first suggest a low degree of selectivity; however, DUBs are subject to multiple layers of regulation that modulate both their activity and their specificity. Due to their wide-ranging involvement in key regulatory processes, these enzymes might provide new therapeutic targets.
引用
收藏
页码:550 / 563
页数:14
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