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对促凋亡蛋白ASPP2的结构及蛋白质-蛋白质相互作用的见解。

Insights into the structure and protein-protein interactions of the pro-apoptotic protein ASPP2.

作者信息

Rotem S, Katz C, Friedler A

机构信息

Department of Organic Chemistry, The Hebrew University of Jerusalem, Givat Ram, Jerusalem 91904, Israel.

出版信息

Biochem Soc Trans. 2007 Nov;35(Pt 5):966-9. doi: 10.1042/BST0350966.

Abstract

ASPP (apoptosis-stimulating protein of p53) 2 is a pro-apoptotic protein that stimulates the p53-mediated apoptotic response. Here, we provide an overview of the structure and protein-protein interactions of ASPP2. The C-terminus of ASPP2 contains Ank (ankyrin) repeats and an SH3 domain (Src homology 3 domain). The Ank-SH3 domains mediate interactions between ASPP2 and numerous proteins involved in apoptosis such as p53 and Bcl-2. The proline-rich domain of ASPP2 is unfolded in its native state, but was not shown to mediate intermolecular interactions. Instead, it makes an intramolecular domain-domain interaction with the Ank-SH3 C-terminal domains of ASPP2. This intramolecular interaction between the unstructured proline-rich domain and the structured Ank-SH3 domains in ASPP2, which is possible due to the unfolded nature of the proline-rich domain, is proposed to have an important role in regulating the intermolecular interactions of ASPP2 with its partner proteins.

摘要

ASPP(p53凋亡刺激蛋白)2是一种促凋亡蛋白,可刺激p53介导的凋亡反应。在此,我们概述ASPP2的结构和蛋白质-蛋白质相互作用。ASPP2的C末端包含锚蛋白(ankyrin)重复序列和一个SH3结构域(Src同源3结构域)。锚蛋白-SH3结构域介导ASPP2与众多参与凋亡的蛋白质(如p53和Bcl-2)之间的相互作用。ASPP2富含脯氨酸的结构域在其天然状态下是展开的,但未显示其介导分子间相互作用。相反,它与ASPP2的锚蛋白-SH3 C末端结构域形成分子内结构域-结构域相互作用。由于富含脯氨酸结构域的展开性质,ASPP2中无结构的富含脯氨酸结构域与有结构的锚蛋白-SH3结构域之间的这种分子内相互作用,被认为在调节ASPP2与其伴侣蛋白的分子间相互作用中起重要作用。

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