1fbz: Difference between revisions
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New page: left|200px<br /> <applet load="1fbz" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fbz, resolution 2.40Å" /> '''Structure-based des... |
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[[Image:1fbz.gif|left|200px]]<br /> | [[Image:1fbz.gif|left|200px]]<br /><applet load="1fbz" size="350" color="white" frame="true" align="right" spinBox="true" | ||
<applet load="1fbz" size=" | |||
caption="1fbz, resolution 2.40Å" /> | caption="1fbz, resolution 2.40Å" /> | ||
'''Structure-based design of a novel, osteoclast-selective, nonpeptide Src SH2 inhibitor with in vivo anti-resorptive activity'''<br /> | '''Structure-based design of a novel, osteoclast-selective, nonpeptide Src SH2 inhibitor with in vivo anti-resorptive activity'''<br /> | ||
==Overview== | ==Overview== | ||
Targeted disruption of the pp60(src) (Src) gene has implicated this | Targeted disruption of the pp60(src) (Src) gene has implicated this tyrosine kinase in osteoclast-mediated bone resorption and as a therapeutic target for the treatment of osteoporosis and other bone-related diseases. Herein we describe the discovery of a nonpeptide inhibitor (AP22408) of Src that demonstrates in vivo antiresorptive activity. Based on a cocrystal structure of the noncatalytic Src homology 2 (SH2) domain of Src complexed with citrate [in the phosphotyrosine (pTyr) binding pocket], we designed 3',4'-diphosphonophenylalanine (Dpp) as a pTyr mimic. In addition to its design to bind Src SH2, the Dpp moiety exhibits bone-targeting properties that confer osteoclast selectivity, hence minimizing possible undesired effects on other cells that have Src-dependent activities. The chemical structure AP22408 also illustrates a bicyclic template to replace the post-pTyr sequence of cognate Src SH2 phosphopeptides such as Ac-pTyr-Glu-Glu-Ile (1). An x-ray structure of AP22408 complexed with Lck (S164C) SH2 confirmed molecular interactions of both the Dpp and bicyclic template of AP22408 as predicted from molecular modeling. Relative to the cognate phosphopeptide, AP22408 exhibits significantly increased Src SH2 binding affinity (IC(50) = 0.30 microM for AP22408 and 5.5 microM for 1). Furthermore, AP22408 inhibits rabbit osteoclast-mediated resorption of dentine in a cellular assay, exhibits bone-targeting properties based on a hydroxyapatite adsorption assay, and demonstrates in vivo antiresorptive activity in a parathyroid hormone-induced rat model. | ||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
1FBZ 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 CC1 as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 and 2.7.10.2 2.7.10.1 and 2.7.10.2] Full crystallographic information is available from [http:// | 1FBZ 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=CC1:'>CC1</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 and 2.7.10.2 2.7.10.1 and 2.7.10.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FBZ OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Pradeepan, S.]] | [[Category: Pradeepan, S.]] | ||
[[Category: Sawyer, T.]] | [[Category: Sawyer, T.]] | ||
[[Category: Schravendijk, M | [[Category: Schravendijk, M R.Van.]] | ||
[[Category: Shakespeare, W.]] | [[Category: Shakespeare, W.]] | ||
[[Category: Smith, J.]] | [[Category: Smith, J.]] | ||
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[[Category: sh2 domain]] | [[Category: sh2 domain]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:37:15 2008'' | ||