3bz3: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
[[Image:3bz3.png|left|200px]] | [[Image:3bz3.png|left|200px]] | ||
{{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=== | ||
{{ABSTRACT_PUBMED_18339875}} | {{ABSTRACT_PUBMED_18339875}} | ||
==About this Structure== | ==About this Structure== | ||
[[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]. | |||
==See Also== | |||
*[[Focal adhesion kinase|Focal adhesion kinase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <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.]] | ||
[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: Cell junction]] | [[Category: Cell junction]] | ||
| Line 38: | Line 27: | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
[[Category: Tyrosine-protein kinase]] | [[Category: Tyrosine-protein kinase]] | ||
Revision as of 13:29, 26 July 2012
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