Literature DB >> 28771691

Targeting HECT-type E3 ligases - insights from catalysis, regulation and inhibitors.

Valentina Fajner1, Elena Maspero1, Simona Polo1,2.   

Abstract

Ubiquitination plays a pivotal role in most cellular processes and is critical for protein degradation and signalling. E3 ligases are the matchmakers in the ubiquitination cascade, responsible for substrate recognition and modification with specific polyubiquitin chains. Until recently, it was not clear how the catalytic activity of E3s is modulated, but major recent studies on HECT E3 ligases is filling this void. These enzymes appear to be held in a closed, inactive conformation, which is relieved by biochemical manoeuvres unique to each member, thus ensuring exquisite regulation and specificity of the enzymes. The new advances and their significance to the function of HECT E3s are described here, with a particular focus on the Nedd4 family members.
© 2017 Federation of European Biochemical Societies.

Keywords:  HECT ubiquitin ligase; catalysis; regulation

Mesh:

Substances:

Year:  2017        PMID: 28771691     DOI: 10.1002/1873-3468.12775

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  23 in total

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