1h6h

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==Overview==
==Overview==
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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, ... [[http://ispc.weizmann.ac.il/pmbin/getpm?11684018 (full description)]]
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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.
==About this Structure==
==About this Structure==
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1H6H is a [[http://en.wikipedia.org/wiki/Single_protein Single protein]] structure of sequence from [[http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]] with PIB and GOL as [[http://en.wikipedia.org/wiki/ligands ligands]]. Structure known Active Site: PIB. Full crystallographic information is available from [[http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1H6H OCA]].
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1H6H is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with PIB and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Structure known Active Site: PIB. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1H6H OCA].
==Reference==
==Reference==
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[[Category: px domain]]
[[Category: px domain]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 15:30:32 2007''
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 5 13:19:13 2007''

Revision as of 11:13, 5 November 2007


1h6h, resolution 1.70Å

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STRUCTURE OF THE PX DOMAIN FROM P40PHOX BOUND TO PHOSPHATIDYLINOSITOL 3-PHOSPHATE

Overview

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.

About this Structure

1H6H is a Single protein structure of sequence from Homo sapiens with PIB and GOL as ligands. Structure known Active Site: PIB. Full crystallographic information is available from OCA.

Reference

The crystal structure of the PX domain from p40(phox) bound to phosphatidylinositol 3-phosphate., Bravo J, Karathanassis D, Pacold CM, Pacold ME, Ellson CD, Anderson KE, Butler PJ, Lavenir I, Perisic O, Hawkins PT, Stephens L, Williams RL, Mol Cell. 2001 Oct;8(4):829-39. PMID:11684018

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