1yrs: Difference between revisions
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'''Crystal structure of KSP in complex with inhibitor 1'''<br /> | '''Crystal structure of KSP in complex with inhibitor 1'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
1YRS 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 MG, ADP and L47 as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http:// | 1YRS 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=MG:'>MG</scene>, <scene name='pdbligand=ADP:'>ADP</scene> and <scene name='pdbligand=L47:'>L47</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1YRS OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: cell cycle]] | [[Category: cell cycle]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:12:24 2008'' | ||
Revision as of 18:12, 15 February 2008
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Crystal structure of KSP in complex with inhibitor 1
OverviewOverview
Optimization of high-throughput screening (HTS) hits resulted in the, discovery of 3,5-diaryl-4,5-dihydropyrazoles as potent and selective, inhibitors of KSP. Dihydropyrazole 15 is a potent, cell-active KSP, inhibitor that induces apoptosis and generates aberrant mitotic spindles, in human ovarian carcinoma cells at low nanomolar concentrations. X-ray, crystallographic evidence is presented which demonstrates that these, inhibitors bind in an allosteric pocket of KSP distant from the nucleotide, and microtubule binding sites.
About this StructureAbout this Structure
1YRS is a Single protein structure of sequence from Homo sapiens with , and as ligands. Full crystallographic information is available from OCA.
ReferenceReference
Kinesin spindle protein (KSP) inhibitors. Part 1: The discovery of 3,5-diaryl-4,5-dihydropyrazoles as potent and selective inhibitors of the mitotic kinesin KSP., Cox CD, Breslin MJ, Mariano BJ, Coleman PJ, Buser CA, Walsh ES, Hamilton K, Huber HE, Kohl NE, Torrent M, Yan Y, Kuo LC, Hartman GD, Bioorg Med Chem Lett. 2005 Apr 15;15(8):2041-5. PMID:15808464
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