3bz3

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[[Image:3bz3.png|left|200px]]
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{{STRUCTURE_3bz3| PDB=3bz3 | SCENE= }}
{{STRUCTURE_3bz3| PDB=3bz3 | SCENE= }}
===Crystal Structure Analysis of Focal Adhesion Kinase with a Methanesulfonamide Diaminopyrimidine Inhibitor===
===Crystal Structure Analysis of Focal Adhesion Kinase with a Methanesulfonamide Diaminopyrimidine Inhibitor===
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{{ABSTRACT_PUBMED_18339875}}
{{ABSTRACT_PUBMED_18339875}}
==About this Structure==
==About this Structure==
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3BZ3 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=3BZ3 OCA].
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[[3bz3]] is a 1 chain structure of [[Focal adhesion 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=3BZ3 OCA].
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==See Also==
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*[[Focal adhesion kinase|Focal adhesion kinase]]
==Reference==
==Reference==
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<ref group="xtra">PMID:18339875</ref><references group="xtra"/>
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<ref group="xtra">PMID:018339875</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Non-specific protein-tyrosine kinase]]
[[Category: Non-specific protein-tyrosine kinase]]
[[Category: Marr, E.]]
[[Category: Marr, E.]]
[[Category: Vajdos, F.]]
[[Category: Vajdos, F.]]
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[[Category: Acetylation]]
 
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[[Category: Alternative splicing]]
 
[[Category: Atp-binding]]
[[Category: Atp-binding]]
[[Category: Cell junction]]
[[Category: Cell junction]]
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[[Category: Transferase]]
[[Category: Transferase]]
[[Category: Tyrosine-protein kinase]]
[[Category: Tyrosine-protein kinase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 09:56:35 2009''
 

Revision as of 13:29, 26 July 2012

Template:STRUCTURE 3bz3

Contents

Crystal Structure Analysis of Focal Adhesion Kinase with a Methanesulfonamide Diaminopyrimidine Inhibitor

Template:ABSTRACT PUBMED 18339875

About this Structure

3bz3 is a 1 chain structure of Focal adhesion kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Roberts WG, Ung E, Whalen P, Cooper B, Hulford C, Autry C, Richter D, Emerson E, Lin J, Kath J, Coleman K, Yao L, Martinez-Alsina L, Lorenzen M, Berliner M, Luzzio M, Patel N, Schmitt E, LaGreca S, Jani J, Wessel M, Marr E, Griffor M, Vajdos F. Antitumor activity and pharmacology of a selective focal adhesion kinase inhibitor, PF-562,271. Cancer Res. 2008 Mar 15;68(6):1935-44. PMID:18339875 doi:68/6/1935

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