Metzger Meredith B, Pruneda Jonathan N, Klevit Rachel E, Weissman Allan M
Laboratory of Protein Dynamics and Signaling, Center for Cancer Research, National Cancer Institute, 1050 Boyles Street, Frederick, MD 21702, USA.
Biochim Biophys Acta. 2014 Jan;1843(1):47-60. doi: 10.1016/j.bbamcr.2013.05.026. Epub 2013 Jun 6.
RING finger domain and RING finger-like ubiquitin ligases (E3s), such as U-box proteins, constitute the vast majority of known E3s. RING-type E3s function together with ubiquitin-conjugating enzymes (E2s) to mediate ubiquitination and are implicated in numerous cellular processes. In part because of their importance in human physiology and disease, these proteins and their cellular functions represent an intense area of study. Here we review recent advances in RING-type E3 recognition of substrates, their cellular regulation, and their varied architecture. Additionally, recent structural insights into RING-type E3 function, with a focus on important interactions with E2s and ubiquitin, are reviewed. This article is part of a Special Issue entitled: Ubiquitin-Proteasome System. Guest Editors: Thomas Sommer and Dieter H. Wolf.
环状结构域和类环状结构域泛素连接酶(E3),如U-box蛋白,构成了绝大多数已知的E3。环状结构域型E3与泛素结合酶(E2)共同发挥作用,介导泛素化过程,并参与众多细胞进程。部分由于它们在人类生理学和疾病中的重要性,这些蛋白质及其细胞功能成为了一个热门研究领域。在此,我们综述了环状结构域型E3在底物识别、细胞调控及其多样结构方面的最新进展。此外,还综述了环状结构域型E3功能的最新结构见解,重点关注其与E2和泛素的重要相互作用。本文是名为《泛素-蛋白酶体系统》特刊的一部分。客座编辑:托马斯·索默和迪特尔·H·沃尔夫。