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靶向HECT型E3连接酶——来自催化、调控及抑制剂的见解

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

作者信息

Fajner Valentina, Maspero Elena, Polo Simona

机构信息

IFOM, Fondazione Istituto FIRC di Oncologia Molecolare, Milan, Italy.

DiPO, Dipartimento di Oncologia ed Emato-Oncologia, Università degli Studi di Milano, Italy.

出版信息

FEBS Lett. 2017 Sep;591(17):2636-2647. doi: 10.1002/1873-3468.12775. Epub 2017 Aug 20.

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.

摘要

泛素化在大多数细胞过程中起着关键作用,对蛋白质降解和信号传导至关重要。E3 连接酶是泛素化级联反应中的“媒人”,负责底物识别以及用特定的多聚泛素链进行修饰。直到最近,E3 酶的催化活性是如何被调节的仍不清楚,但近期关于 HECT E3 连接酶的主要研究正在填补这一空白。这些酶似乎以一种封闭的、无活性的构象存在,每个成员特有的生化操作可缓解这种构象,从而确保酶的精确调控和特异性。本文描述了这些新进展及其对 HECT E3 酶功能的意义,特别关注 Nedd4 家族成员。

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