1ry4

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(New page: 200px<br /><applet load="1ry4" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ry4" /> '''NMR Structure of the CRIB-PDZ module of Par-...)
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[[Image:1ry4.jpg|left|200px]]<br /><applet load="1ry4" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1ry4.jpg|left|200px]]<br /><applet load="1ry4" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1ry4" />
caption="1ry4" />
'''NMR Structure of the CRIB-PDZ module of Par-6'''<br />
'''NMR Structure of the CRIB-PDZ module of Par-6'''<br />
==Overview==
==Overview==
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Regulation of protein interaction domains is required for cellular, signaling dynamics. Here, we show that the PDZ protein interaction domain, from the cell polarity protein Par-6 is regulated by the Rho GTPase Cdc42., Cdc42 binds to a CRIB domain adjacent to the PDZ domain, increasing the, affinity of the Par-6 PDZ for its carboxy-terminal ligand by approximately, 13-fold. Par-6 PDZ regulation is required for function as mutational, disruption of Cdc42-Par-6 PDZ coupling leads to inactivation of Par-6 in, polarized MDCK epithelial cells. Structural analysis reveals that the free, PDZ domain has several deviations from the canonical PDZ conformation that, account for its low ligand affinity. Regulation results from a, Cdc42-induced conformational transition in the CRIB-PDZ module that causes, the PDZ to assume a canonical, high-affinity PDZ conformation. The coupled, CRIB and PDZ architecture of Par-6 reveals how simple binding domains can, be combined to yield complex regulation.
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Regulation of protein interaction domains is required for cellular signaling dynamics. Here, we show that the PDZ protein interaction domain from the cell polarity protein Par-6 is regulated by the Rho GTPase Cdc42. Cdc42 binds to a CRIB domain adjacent to the PDZ domain, increasing the affinity of the Par-6 PDZ for its carboxy-terminal ligand by approximately 13-fold. Par-6 PDZ regulation is required for function as mutational disruption of Cdc42-Par-6 PDZ coupling leads to inactivation of Par-6 in polarized MDCK epithelial cells. Structural analysis reveals that the free PDZ domain has several deviations from the canonical PDZ conformation that account for its low ligand affinity. Regulation results from a Cdc42-induced conformational transition in the CRIB-PDZ module that causes the PDZ to assume a canonical, high-affinity PDZ conformation. The coupled CRIB and PDZ architecture of Par-6 reveals how simple binding domains can be combined to yield complex regulation.
==About this Structure==
==About this Structure==
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1RY4 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Drosophila_melanogaster Drosophila melanogaster]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1RY4 OCA].
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1RY4 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Drosophila_melanogaster Drosophila melanogaster]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RY4 OCA].
==Reference==
==Reference==
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[[Category: Drosophila melanogaster]]
[[Category: Drosophila melanogaster]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Penkert, R.R.]]
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[[Category: Penkert, R R.]]
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[[Category: Peterson, F.C.]]
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[[Category: Peterson, F C.]]
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[[Category: Prehoda, K.E.]]
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[[Category: Prehoda, K E.]]
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[[Category: Volkman, B.F.]]
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[[Category: Volkman, B F.]]
[[Category: cdc-42]]
[[Category: cdc-42]]
[[Category: cell polarization]]
[[Category: cell polarization]]
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[[Category: polarity adaptor complex]]
[[Category: polarity adaptor complex]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sat Nov 24 23:29:53 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:55:54 2008''

Revision as of 12:55, 21 February 2008


1ry4

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NMR Structure of the CRIB-PDZ module of Par-6

Overview

Regulation of protein interaction domains is required for cellular signaling dynamics. Here, we show that the PDZ protein interaction domain from the cell polarity protein Par-6 is regulated by the Rho GTPase Cdc42. Cdc42 binds to a CRIB domain adjacent to the PDZ domain, increasing the affinity of the Par-6 PDZ for its carboxy-terminal ligand by approximately 13-fold. Par-6 PDZ regulation is required for function as mutational disruption of Cdc42-Par-6 PDZ coupling leads to inactivation of Par-6 in polarized MDCK epithelial cells. Structural analysis reveals that the free PDZ domain has several deviations from the canonical PDZ conformation that account for its low ligand affinity. Regulation results from a Cdc42-induced conformational transition in the CRIB-PDZ module that causes the PDZ to assume a canonical, high-affinity PDZ conformation. The coupled CRIB and PDZ architecture of Par-6 reveals how simple binding domains can be combined to yield complex regulation.

About this Structure

1RY4 is a Single protein structure of sequence from Drosophila melanogaster. Full crystallographic information is available from OCA.

Reference

Cdc42 regulates the Par-6 PDZ domain through an allosteric CRIB-PDZ transition., Peterson FC, Penkert RR, Volkman BF, Prehoda KE, Mol Cell. 2004 Mar 12;13(5):665-76. PMID:15023337

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