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NEDD8 在调节 Cullin-RING 连接酶中的作用。

NEDD8-its role in the regulation of Cullin-RING ligases.

机构信息

Plant Systems Biology, Emil-Ramann-Strasse 8, Technical University of Munich, 85354 Freising, Germany.

出版信息

Curr Opin Plant Biol. 2018 Oct;45(Pt A):112-119. doi: 10.1016/j.pbi.2018.05.017. Epub 2018 Jun 15.

Abstract

The ubiquitin-related protein NEDD8 is conjugated and deconjugated to and from proteins in processes related to ubiquitin conjugation and deconjugation. Neddylation is a well-studied posttranslational modification of Cullin-RING E3 ligases (CRLs). Biochemical and structural studies aiming at understanding the role of NEDD8 in CRL function have now resulted in a convincing model of how neddylation and deneddylation antagonistically regulate CRL stability, conformation, activity as well as degradation substrate receptor exchange. Studies of the Arabidopsis thaliana deneddylation-deficient den1 mutant led to the identification of many low abundant, non-Cullin NEDD8 conjugates. Examination of neddylated AUXIN RESISTANT1 (AXR1), a prominent neddylated protein in den1, suggests, however, that AXR1 neddylation may be an auto-catalytic side-reaction of Cullin-targeted neddylation and that DEN1 may serve to antagonize non-productive, auto-neddylation from substrates to provide free NEDD8 for CRL regulation.

摘要

泛素相关蛋白 NEDD8 与蛋白质结合和去结合,与泛素结合和去结合过程有关。Neddylation 是 Cullin-RING E3 连接酶(CRLs)的一种研究得很好的翻译后修饰。旨在了解 NEDD8 在 CRL 功能中的作用的生化和结构研究,现在已经提出了一个令人信服的模型,说明 neddylation 和 deneddylation 如何拮抗调节 CRL 的稳定性、构象、活性以及降解底物受体交换。对拟南芥去 neddylation 缺陷突变体 den1 的研究导致了许多低丰度、非 Cullin NEDD8 缀合物的鉴定。然而,对 neddylated AUXIN RESISTANT1(AXR1)的研究表明,AXR1 的 neddylation 可能是 Cullin 靶向 neddylation 的自动催化副反应,而 DEN1 可能用于拮抗非生产性的、来自底物的自动 neddylation,从而为 CRL 调节提供游离的 NEDD8。

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