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Breaking the chains: structure and function of the deubiquitinases

Journal

NATURE REVIEWS MOLECULAR CELL BIOLOGY
Volume 10, Issue 8, Pages 550-563

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrm2731

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Funding

  1. Medical Research Council [MC_U105192732] Funding Source: researchfish
  2. Medical Research Council [MC_U105192732] Funding Source: Medline
  3. MRC [MC_U105192732] Funding Source: UKRI

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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.

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