1k9r: Difference between revisions

Revision as of 10:00, 2 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:1k9r.png

Template:STRUCTURE 1k9r

YAP65 WW domain complexed to Acetyl-PLPPYYAP65 WW domain complexed to Acetyl-PLPPY

Template:ABSTRACT PUBMED 11743730

About this StructureAbout this Structure

1K9R is a Protein complex structure. Full experimental information is available from OCA.

ReferenceReference

Solution structures of the YAP65 WW domain and the variant L30 K in complex with the peptides GTPPPPYTVG, N-(n-octyl)-GPPPY and PLPPY and the application of peptide libraries reveal a minimal binding epitope., Pires JR, Taha-Nejad F, Toepert F, Ast T, Hoffmuller U, Schneider-Mergener J, Kuhne R, Macias MJ, Oschkinat H, J Mol Biol. 2001 Dec 14;314(5):1147-56. PMID:11743730

Page seeded by OCA on Wed Jul 2 10:00:08 2008

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

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-[[Image:1k9r.gif|left|200px]]
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 {{STRUCTURE_1k9r|  PDB=1k9r  |  SCENE=  }}
-'''YAP65 WW domain complexed to Acetyl-PLPPY'''
+===YAP65 WW domain complexed to Acetyl-PLPPY===
-==Overview==
+<!--
-The single mutation L30 K in the Hu-Yap65 WW domain increased the stability of the complex with the peptide GTPPPPYTVG (K(d)=40(+/-5) microM). Here we report the refined solution structure of this complex by NMR spectroscopy and further derived structure-activity relationships by using ligand peptide libraries with truncated sequences and a substitution analysis that yielded acetyl-PPPPY as the smallest high-affinity binding peptide (K(d)=60 microM). The structures of two new complexes with weaker binding ligands chosen based on these results (N-(n-octyl)-GPPPYNH(2) and Ac-PLPPY) comprising the wild-type WW domain of Hu-Yap65 were determined. Comparison of the structures of the three complexes were useful for identifying the molecular basis of high-affinity: hydrophobic and specific interactions between the side-chains of Y28 and W39 and P5' and P4', respectively, and hydrogen bonds between T37 (donnor) and P5' (acceptor) and between W39 (donnor) and T2' (acceptor) stabilize the complex.The structure of the complex L30 K Hu-Yap65 WW domain/GTPPPPYTVG is compared to the published crystal structure of the dystrophin WW domain bound to a segment of the beta-dystroglycan protein and to the solution structure of the first Nedd4 WW domain and its prolin-rich ligand, suggesting that WW sequences bind proline-rich peptides in an evolutionary conserved fashion. The position equivalent to T22 in the Hu-Yap65 WW domain sequence is seen as responsible for differentiation in the binding mode among the WW domains of group I.
+The line below this paragraph, {{ABSTRACT_PUBMED_11743730}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 11743730 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_11743730}}
 ==About this Structure==
-K9R is a [[Protein complex]] structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1K9R OCA].
+K9R is a [[Protein complex]] structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1K9R OCA].
 ==Reference==
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 [[Category: Ww domain]]
 [[Category: Yap65]]
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