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The crystal structure of the PX domain from p40(phox) bound to phosphatidylinositol 3-phosphate.
- 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.
- Subjects :
- Amino Acid Sequence
Binding Sites
Calorimetry
Crystallography, X-Ray
Humans
Models, Molecular
Molecular Sequence Data
NADPH Oxidases chemistry
Phosphatidylinositol Phosphates chemistry
Phosphoproteins metabolism
Protein Binding
Protein Subunits
Sequence Alignment
Ultracentrifugation
Phosphatidylinositol Phosphates metabolism
Phosphoproteins chemistry
Protein Structure, Tertiary
Subjects
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