1v1t

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Revision as of 20:25, 29 October 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="1v1t" size="450" color="white" frame="true" align="right" spinBox="true" caption="1v1t, resolution 1.80Å" /> '''CRYSTAL STRUCTURE O...)
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File:1v1t.gif


1v1t, resolution 1.80Å

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CRYSTAL STRUCTURE OF THE PDZ TANDEM OF HUMAN SYNTENIN IN COMPLEX WITH TNEYKV PEPTIDE

OverviewOverview

PDZ domains are among the most abundant protein modules in the known, genomes. Their main function is to provide scaffolds for, membrane-associated protein complexes by binding to the cytosolic, C-terminal fragments of receptors, channels, and other integral membrane, proteins. Here, using both heteronuclear NMR and single crystal X-ray, diffraction, we show how peptides with different sequences, including, those corresponding to the C-termini of syndecan, neurexin, and ephrin B, can simultaneously bind to both PDZ domains of the scaffolding protein, syntenin. The PDZ2 domain binds these peptides in the canonical fashion, and an induced fit mechanism allows for the accommodation of a range of, side chains in the P(0) and P(-)(2) positions. However, binding to the, PDZ1 domain requires ... [(full description)]

About this StructureAbout this Structure

1V1T is a [Single protein] structure of sequence from [Homo sapiens] with BEZ as [ligand]. Full crystallographic information is available from [OCA].

ReferenceReference

The binding of the PDZ tandem of syntenin to target proteins., Grembecka J, Cierpicki T, Devedjiev Y, Derewenda U, Kang BS, Bushweller JH, Derewenda ZS, Biochemistry. 2006 Mar 21;45(11):3674-83. PMID:16533050

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