2bdj

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[[Image:2bdj.png|left|200px]]
[[Image:2bdj.png|left|200px]]
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{{STRUCTURE_2bdj| PDB=2bdj | SCENE= }}
{{STRUCTURE_2bdj| PDB=2bdj | SCENE= }}
===Src kinase in complex with inhibitor AP23464===
===Src kinase in complex with inhibitor AP23464===
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{{ABSTRACT_PUBMED_16492148}}
{{ABSTRACT_PUBMED_16492148}}
==About this Structure==
==About this Structure==
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2BDJ is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2BDJ OCA].
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[[2bdj]] is a 1 chain structure of [[Proto-oncogene tyrosine-protein kinase]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2BDJ OCA].
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==See Also==
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*[[Proto-oncogene tyrosine-protein kinase|Proto-oncogene tyrosine-protein kinase]]
==Reference==
==Reference==
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<ref group="xtra">PMID:16492148</ref><references group="xtra"/>
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<ref group="xtra">PMID:016492148</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Transferase]]
[[Category: Transferase]]
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[[Category: Stehle, T.]]
[[Category: Stehle, T.]]
[[Category: Src kinase inhibitor]]
[[Category: Src kinase inhibitor]]
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[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 15:41:17 2009''
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Revision as of 21:42, 26 July 2012

Template:STRUCTURE 2bdj

Contents

Src kinase in complex with inhibitor AP23464

Template:ABSTRACT PUBMED 16492148

About this Structure

2bdj is a 1 chain structure of Proto-oncogene tyrosine-protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Dalgarno D, Stehle T, Narula S, Schelling P, van Schravendijk MR, Adams S, Andrade L, Keats J, Ram M, Jin L, Grossman T, MacNeil I, Metcalf C 3rd, Shakespeare W, Wang Y, Keenan T, Sundaramoorthi R, Bohacek R, Weigele M, Sawyer T. Structural basis of Src tyrosine kinase inhibition with a new class of potent and selective trisubstituted purine-based compounds. Chem Biol Drug Des. 2006 Jan;67(1):46-57. PMID:16492148 doi:10.1111/j.1747-0285.2005.00316.x

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