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

Authors :
Bravo J
Karathanassis D
Pacold CM
Pacold ME
Ellson CD
Anderson KE
Butler PJ
Lavenir I
Perisic O
Hawkins PT
Stephens L
Williams RL
Source :
Molecular cell [Mol Cell] 2001 Oct; Vol. 8 (4), pp. 829-39.
Publication Year :
2001

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.

Details

Language :
English
ISSN :
1097-2765
Volume :
8
Issue :
4
Database :
MEDLINE
Journal :
Molecular cell
Publication Type :
Academic Journal
Accession number :
11684018
Full Text :
https://doi.org/10.1016/s1097-2765(01)00372-0