1elw

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{{STRUCTURE_1elw| PDB=1elw | SCENE= }}
{{STRUCTURE_1elw| PDB=1elw | SCENE= }}
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'''Crystal structure of the TPR1 domain of HOP in complex with a HSC70 peptide'''
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===Crystal structure of the TPR1 domain of HOP in complex with a HSC70 peptide===
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==Overview==
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The adaptor protein Hop mediates the association of the molecular chaperones Hsp70 and Hsp90. The TPR1 domain of Hop specifically recognizes the C-terminal heptapeptide of Hsp70 while the TPR2A domain binds the C-terminal pentapeptide of Hsp90. Both sequences end with the motif EEVD. The crystal structures of the TPR-peptide complexes show the peptides in an extended conformation, spanning a groove in the TPR domains. Peptide binding is mediated by electrostatic interactions with the EEVD motif, with the C-terminal aspartate acting as a two-carboxylate anchor, and by hydrophobic interactions with residues upstream of EEVD. The hydrophobic contacts with the peptide are critical for specificity. These results explain how TPR domains participate in the ordered assembly of Hsp70-Hsp90 multichaperone complexes.
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(as it appears on PubMed at http://www.pubmed.gov), where 10786835 is the PubMed ID number.
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{{ABSTRACT_PUBMED_10786835}}
==About this Structure==
==About this Structure==
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[[Category: Protein binding]]
[[Category: Protein binding]]
[[Category: Tpr-domain]]
[[Category: Tpr-domain]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 15:15:37 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 1 00:57:32 2008''

Revision as of 21:57, 30 June 2008

Image:1elw.png

Template:STRUCTURE 1elw

Crystal structure of the TPR1 domain of HOP in complex with a HSC70 peptide

Template:ABSTRACT PUBMED 10786835

About this Structure

1ELW is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structure of TPR domain-peptide complexes: critical elements in the assembly of the Hsp70-Hsp90 multichaperone machine., Scheufler C, Brinker A, Bourenkov G, Pegoraro S, Moroder L, Bartunik H, Hartl FU, Moarefi I, Cell. 2000 Apr 14;101(2):199-210. PMID:10786835

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