The crystal structure of the PX domain from p40phox bound to phosphatidylinositol 3-phosphate

被引:224
作者
Bravo, J
Karathanassis, D
Pacold, CM
Pacold, ME
Ellson, CD
Anderson, KE
Butler, PJG
Lavenir, I
Perisic, O
Hawkins, PT
Stephens, L
Williams, RL
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[2] Babraham Inst, Inositide Lab, Cambridge CB2 4AT, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/S1097-2765(01)00372-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Angstrom 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 Ptdlns(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 Ptdlns(3)P binding to the p40(phox) PX domain.
引用
收藏
页码:829 / 839
页数:11
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