1yet

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[[Image:1yet.jpg|left|200px]]
[[Image:1yet.jpg|left|200px]]
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{{Structure
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|PDB= 1yet |SIZE=350|CAPTION= <scene name='initialview01'>1yet</scene>, resolution 1.90&Aring;
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The line below this paragraph, containing "STRUCTURE_1yet", creates the "Structure Box" on the page.
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|SITE=
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|LIGAND= <scene name='pdbligand=GDM:GELDANAMYCIN'>GDM</scene>
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{{STRUCTURE_1yet| PDB=1yet | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1yet FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1yet OCA], [http://www.ebi.ac.uk/pdbsum/1yet PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1yet RCSB]</span>
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'''GELDANAMYCIN BOUND TO THE HSP90 GELDANAMYCIN-BINDING DOMAIN'''
'''GELDANAMYCIN BOUND TO THE HSP90 GELDANAMYCIN-BINDING DOMAIN'''
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[[Category: Russo, A A.]]
[[Category: Russo, A A.]]
[[Category: Stebbins, C E.]]
[[Category: Stebbins, C E.]]
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[[Category: chaperone protein]]
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[[Category: Chaperone protein]]
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[[Category: geldanamycin]]
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[[Category: Geldanamycin]]
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[[Category: heat shock]]
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[[Category: Heat shock]]
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[[Category: signal transduction]]
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[[Category: Signal transduction]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 16:14:03 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 01:05:09 2008''
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Revision as of 13:14, 3 May 2008

Template:STRUCTURE 1yet

GELDANAMYCIN BOUND TO THE HSP90 GELDANAMYCIN-BINDING DOMAIN


Overview

The Hsp90 chaperone is required for the activation of several families of eukaryotic protein kinases and nuclear hormone receptors, many of which are protooncogenic and play a prominent role in cancer. The geldanamycin antibiotic has antiproliferative and antitumor effects, as it binds to Hsp90, inhibits the Hsp90-mediated conformational maturation/refolding reaction, and results in the degradation of Hsp90 substrates. The structure of the geldanamycin-binding domain of Hsp90 (residues 9-232) reveals a pronounced pocket, 15 A deep, that is highly conserved across species. Geldanamycin binds inside this pocket, adopting a compact structure similar to that of a polypeptide chain in a turn conformation. This, and the pocket's similarity to substrate-binding sites, suggest that the pocket binds a portion of the polypeptide substrate and participates in the conformational maturation/refolding reaction.

About this Structure

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

Reference

Crystal structure of an Hsp90-geldanamycin complex: targeting of a protein chaperone by an antitumor agent., Stebbins CE, Russo AA, Schneider C, Rosen N, Hartl FU, Pavletich NP, Cell. 1997 Apr 18;89(2):239-50. PMID:9108479 Page seeded by OCA on Sat May 3 16:14:03 2008

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