1uyg: Difference between revisions

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[[Image:1uyg.jpg|left|200px]]
[[Image:1uyg.jpg|left|200px]]


{{Structure
<!--
|PDB= 1uyg |SIZE=350|CAPTION= <scene name='initialview01'>1uyg</scene>, resolution 2.00&Aring;
The line below this paragraph, containing "STRUCTURE_1uyg", creates the "Structure Box" on the page.
|SITE= <scene name='pdbsite=AC1:Pu2+Binding+Site+For+Chain+A'>AC1</scene>
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=PU2:8-(2,5-DIMETHOXY-BENZYL)-2-FLUORO-9H-PURIN-6-YLAMINE'>PU2</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY=  
or leave the SCENE parameter empty for the default display.
|GENE=  
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|DOMAIN=
{{STRUCTURE_1uyg| PDB=1uyg  | SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1uyg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1uyg OCA], [http://www.ebi.ac.uk/pdbsum/1uyg PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1uyg RCSB]</span>
}}


'''HUMAN HSP90-ALPHA WITH 8-(2,5-DIMETHOXY-BENZYL)-2-FLUORO-9H-PURIN-6-YLAMINE'''
'''HUMAN HSP90-ALPHA WITH 8-(2,5-DIMETHOXY-BENZYL)-2-FLUORO-9H-PURIN-6-YLAMINE'''
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[[Category: Workman, P.]]
[[Category: Workman, P.]]
[[Category: Wright, L.]]
[[Category: Wright, L.]]
[[Category: atp-binding]]
[[Category: Atp-binding]]
[[Category: atpase]]
[[Category: Atpase]]
[[Category: chaperone]]
[[Category: Chaperone]]
[[Category: heat shock]]
[[Category: Heat shock]]
[[Category: hsp90]]
[[Category: Hsp90]]
[[Category: pu2]]
[[Category: Pu2]]
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:17:09 2008''

Revision as of 11:51, 3 May 2008

File:1uyg.jpg

Template:STRUCTURE 1uyg

HUMAN HSP90-ALPHA WITH 8-(2,5-DIMETHOXY-BENZYL)-2-FLUORO-9H-PURIN-6-YLAMINE


OverviewOverview

Inhibition of the ATPase activity of the chaperone protein HSP90 is a potential strategy for treatment of cancers. We have determined structures of the HSP90alpha N-terminal domain complexed with the purine-based inhibitor, PU3, and analogs with enhanced potency both in enzyme and cell-based assays. The compounds induce upregulation of HSP70 and downregulation of the known HSP90 client proteins Raf-1, CDK4, and ErbB2, confirming that the molecules inhibit cell growth by a mechanism dependent on HSP90 inhibition. We have also determined the first structure of the N-terminal domain of HSP90beta, complexed with PU3. The structures allow a detailed rationale to be developed for the observed affinity of the PU3 class of compounds for HSP90 and also provide a structural framework for design of compounds with improved binding affinity and drug-like properties.

About this StructureAbout this Structure

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

ReferenceReference

Structure-activity relationships in purine-based inhibitor binding to HSP90 isoforms., Wright L, Barril X, Dymock B, Sheridan L, Surgenor A, Beswick M, Drysdale M, Collier A, Massey A, Davies N, Fink A, Fromont C, Aherne W, Boxall K, Sharp S, Workman P, Hubbard RE, Chem Biol. 2004 Jun;11(6):775-85. PMID:15217611 Page seeded by OCA on Sat May 3 11:51:33 2008

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