1vyt: Difference between revisions

Revision as of 13:17, 29 July 2008

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:1vyt.png

Template:STRUCTURE 1vyt

BETA3 SUBUNIT COMPLEXED WITH AIDBETA3 SUBUNIT COMPLEXED WITH AID

Template:ABSTRACT PUBMED 15170217

About this StructureAbout this Structure

1VYT is a Protein complex structure of sequences from Rattus norvegicus. Full crystallographic information is available from OCA.

ReferenceReference

Structural basis of the alpha1-beta subunit interaction of voltage-gated Ca2+ channels., Chen YH, Li MH, Zhang Y, He LL, Yamada Y, Fitzmaurice A, Shen Y, Zhang H, Tong L, Yang J, Nature. 2004 Jun 10;429(6992):675-80. Epub 2004 May 30. PMID:15170217

Page seeded by OCA on Tue Jul 29 13:17:37 2008

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OCA

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 {{STRUCTURE_1vyt|  PDB=1vyt  |  SCENE=  }}
-'''BETA3 SUBUNIT COMPLEXED WITH AID'''
+===BETA3 SUBUNIT COMPLEXED WITH AID===
-==Overview==
+<!--
-High-voltage-activated Ca2+ channels are essential for diverse biological processes. They are composed of four or five subunits, including alpha1, alpha2-delta, beta and gamma (ref. 1). Their expression and function are critically dependent on the beta-subunit, which transports alpha1 to the surface membrane and regulates diverse channel properties. It is believed that the beta-subunit interacts with alpha1 primarily through the beta-interaction domain (BID), which binds directly to the alpha-interaction domain (AID) of alpha1; however, the molecular mechanism of the alpha1-beta interaction is largely unclear. Here we report the crystal structures of the conserved core region of beta3, alone and in complex with AID, and of beta4 alone. The structures show that the beta-subunit core contains two interacting domains: a Src homology 3 (SH3) domain and a guanylate kinase (GK) domain. The AID binds to a hydrophobic groove in the GK domain through extensive interactions, conferring extremely high affinity between alpha1 and beta-subunits. The BID is essential both for the structural integrity of and for bridging the SH3 and GK domains, but it does not participate directly in binding alpha1. The presence of multiple protein-interacting modules in the beta-subunit opens a new dimension to its function as a multi-functional protein.
+The line below this paragraph, {{ABSTRACT_PUBMED_15170217}}, adds the Publication Abstract to the page
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+{{ABSTRACT_PUBMED_15170217}}
 ==About this Structure==
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 [[Category: Sh3 domain]]
 [[Category: Voltage-gated channel]]
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