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RBR 连接酶介导的泛素转移:一个充满曲折的故事。

RBR ligase-mediated ubiquitin transfer: a tale with many twists and turns.

机构信息

Institute of Molecular Cell and Systems Biology, University of Glasgow, Glasgow, Scotland, UK.

Molecular Structure of Cell Signalling Laboratory, The Francis Crick Institute, London, UK.

出版信息

Nat Struct Mol Biol. 2018 Jun;25(6):440-445. doi: 10.1038/s41594-018-0063-3. Epub 2018 May 7.

Abstract

RBR ligases are an enigmatic class of E3 ubiquitin ligases that combine properties of RING and HECT-type E3s and undergo multilevel regulation through autoinhibition, post-translational modifications, multimerization and interaction with binding partners. Here, we summarize recent progress in RBR structures and function, which has uncovered commonalities in the mechanisms by which different family members transfer ubiquitin through a multistep process. However, these studies have also highlighted clear differences in the activity of different family members, suggesting that each RBR ligase has evolved specific properties to fit the biological process it regulates.

摘要

RBR 连接酶是一类神秘的 E3 泛素连接酶,它们结合了 RING 和 HECT 型 E3 的特性,并通过自身抑制、翻译后修饰、多聚化以及与结合伙伴相互作用等多种方式进行多层次调节。在这里,我们总结了 RBR 结构和功能的最新进展,这些进展揭示了不同家族成员通过多步过程转移泛素的机制具有共同性。然而,这些研究也突出了不同家族成员活性的明显差异,表明每个 RBR 连接酶都进化出了特定的性质,以适应其调节的生物学过程。

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