Suppr超能文献

与磷脂酰肌醇3-磷酸结合的p40(吞噬细胞氧化酶)PX结构域的晶体结构。

The crystal structure of the PX domain from p40(phox) bound to phosphatidylinositol 3-phosphate.

作者信息

Bravo J, Karathanassis D, Pacold C M, Pacold M E, Ellson C D, Anderson K E, Butler P J, Lavenir I, Perisic O, Hawkins P T, Stephens L, Williams R L

机构信息

Laboratory of Molecular Biology, Medical Research Council, Hills Road, Cambridge CB2 2QH, United Kingdom.

出版信息

Mol Cell. 2001 Oct;8(4):829-39. doi: 10.1016/s1097-2765(01)00372-0.

Abstract

More than 50 human proteins with a wide range of functions have a 120 residue phosphoinositide binding module known as the PX domain. The 1.7 A X-ray crystal structure of the PX domain from the p40(phox) subunit of NADPH oxidase bound to PtdIns(3)P shows that the PX domain embraces the 3-phosphate on one side of a water-filled, positively charged pocket and reveals how 3-phosphoinositide specificity is achieved. A chronic granulomatous disease (CGD)-associated mutation in the p47(phox) PX domain that abrogates PtdIns(3)P binding maps to a conserved Arg that does not directly interact with the phosphoinositide but instead appears to stabilize a critical lipid binding loop. The SH3 domain present in the full-length protein does not affect soluble PtdIns(3)P binding to the p40(phox) PX domain.

摘要

超过50种具有广泛功能的人类蛋白质拥有一个由120个残基组成的磷酸肌醇结合模块,称为PX结构域。来自NADPH氧化酶p40(phox)亚基的PX结构域与磷脂酰肌醇-3-磷酸(PtdIns(3)P)结合的1.7埃X射线晶体结构表明,PX结构域在一个充满水的带正电荷口袋的一侧包围着3-磷酸基团,并揭示了如何实现3-磷酸肌醇特异性。p47(phox) PX结构域中一个与慢性肉芽肿病(CGD)相关的突变消除了PtdIns(3)P结合,该突变定位到一个保守的精氨酸,该精氨酸不直接与磷酸肌醇相互作用,而是似乎稳定了一个关键的脂质结合环。全长蛋白中存在的SH3结构域不影响可溶性PtdIns(3)P与p40(phox) PX结构域的结合。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验