2c0t

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==Reference==
==Reference==
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<ref group="xtra">PMID:16216497</ref><ref group="xtra">PMID:15109663</ref><references group="xtra"/>
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<ref group="xtra">PMID:016216497</ref><ref group="xtra">PMID:015109663</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Transferase]]
[[Category: Transferase]]
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[[Category: Li, B.]]
[[Category: Li, B.]]
[[Category: Loew, A.]]
[[Category: Loew, A.]]
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[[Category: Alternative initiation]]
 
[[Category: Atp-binding]]
[[Category: Atp-binding]]
[[Category: Kinase]]
[[Category: Kinase]]
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[[Category: Nucleotide-binding]]
[[Category: Nucleotide-binding]]
[[Category: Palmitate]]
[[Category: Palmitate]]
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[[Category: Phosphorylation]]
 
[[Category: Sh2 domain]]
[[Category: Sh2 domain]]
[[Category: Sh3 domain]]
[[Category: Sh3 domain]]
[[Category: Transferase]]
[[Category: Transferase]]
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[[Category: Tyrosine-protein kinase]]
 

Revision as of 05:59, 24 August 2011

Template:STRUCTURE 2c0t

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

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