2c0t
From Proteopedia
(Difference between revisions)
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{{STRUCTURE_2c0t| PDB=2c0t | SCENE= }} | {{STRUCTURE_2c0t| PDB=2c0t | SCENE= }} | ||
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===SRC FAMILY KINASE HCK WITH BOUND INHIBITOR A-641359=== | ===SRC FAMILY KINASE HCK WITH BOUND INHIBITOR A-641359=== | ||
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==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID:016216497</ref><ref group="xtra">PMID:015109663</ref><references group="xtra"/> | + | <ref group="xtra">PMID:016216497</ref><ref group="xtra">PMID:015109663</ref><references group="xtra"/><references/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Transferase]] | [[Category: Transferase]] |
Revision as of 09:45, 24 March 2013
SRC FAMILY KINASE HCK WITH BOUND INHIBITOR A-641359
Template:ABSTRACT PUBMED 16216497
About this Structure
2c0t is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Burchat A, Borhani DW, Calderwood DJ, Hirst GC, Li B, Stachlewitz RF. Discovery of A-770041, a src-family selective orally active lck inhibitor that prevents organ allograft rejection. Bioorg Med Chem Lett. 2006 Jan 1;16(1):118-22. Epub 2005 Oct 10. PMID:16216497 doi:10.1016/j.bmcl.2005.09.039
- Borhani DW, Calderwood DJ, Friedman MM, Hirst GC, Li B, Leung AK, McRae B, Ratnofsky S, Ritter K, Waegell W. A-420983: a potent, orally active inhibitor of lck with efficacy in a model of transplant rejection. Bioorg Med Chem Lett. 2004 May 17;14(10):2613-6. PMID:15109663 doi:10.1016/j.bmcl.2004.02.101
Categories: Homo sapiens | Transferase | Borhani, D W. | Burchat, A. | Calderwood, D J. | Hirst, G C. | Li, B. | Loew, A. | Atp-binding | Kinase | Lipoprotein | Myristate | Nucleotide-binding | Palmitate | Sh2 domain | Sh3 domain