1yc3: Difference between revisions

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New page: left|200px<br /> <applet load="1yc3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1yc3, resolution 2.12Å" /> '''Crystal Structure o...
 
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[[Image:1yc3.gif|left|200px]]<br />
[[Image:1yc3.gif|left|200px]]<br /><applet load="1yc3" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1yc3" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1yc3, resolution 2.12&Aring;" />
caption="1yc3, resolution 2.12&Aring;" />
'''Crystal Structure of human HSP90alpha complexed with dihydroxyphenylpyrazoles'''<br />
'''Crystal Structure of human HSP90alpha complexed with dihydroxyphenylpyrazoles'''<br />


==Overview==
==Overview==
A series of dihydroxyphenylpyrazole compounds were identified as a unique, class of reversible Hsp90 inhibitors. The crystal structures for two of, the identified compounds complexed with the N-terminal ATP binding domain, of human Hsp90alpha were determined. The dihydroxyphenyl ring of the, compounds fits deeply into the adenine binding pocket with the C2 hydroxyl, group forming a direct hydrogen bond with the side chain of Asp93. The, pyrazole ring forms hydrogen bonds to the backbone carbonyl of Gly97, the, hydroxyl group of Thr184 and to a water molecule, which is present in all, of the published HSP90 structures. One of the identified compounds (G3130), demonstrated cellular activities (in Her-2 degradation and activation of, Hsp70 promoter) consistent with the inhibition of cellular Hsp90, functions.
A series of dihydroxyphenylpyrazole compounds were identified as a unique class of reversible Hsp90 inhibitors. The crystal structures for two of the identified compounds complexed with the N-terminal ATP binding domain of human Hsp90alpha were determined. The dihydroxyphenyl ring of the compounds fits deeply into the adenine binding pocket with the C2 hydroxyl group forming a direct hydrogen bond with the side chain of Asp93. The pyrazole ring forms hydrogen bonds to the backbone carbonyl of Gly97, the hydroxyl group of Thr184 and to a water molecule, which is present in all of the published HSP90 structures. One of the identified compounds (G3130) demonstrated cellular activities (in Her-2 degradation and activation of Hsp70 promoter) consistent with the inhibition of cellular Hsp90 functions.


==About this Structure==
==About this Structure==
1YC3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with 4BC as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1YC3 OCA].  
1YC3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=4BC:'>4BC</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1YC3 OCA].  


==Reference==
==Reference==
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[[Category: He, Y.]]
[[Category: He, Y.]]
[[Category: Kreusch, A.]]
[[Category: Kreusch, A.]]
[[Category: Lesley, S.A.]]
[[Category: Lesley, S A.]]
[[Category: Zhou, V.]]
[[Category: Zhou, V.]]
[[Category: 4BC]]
[[Category: 4BC]]
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[[Category: drug design]]
[[Category: drug design]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:17:43 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:03:49 2008''