2xng
From Proteopedia
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- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_2xng", creates the "Structure Box" on the page. | ||
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+ | {{STRUCTURE_2xng| PDB=2xng | SCENE= }} | ||
- | + | ===STRUCTURE OF AURORA-A BOUND TO A SELECTIVE IMIDAZOPYRAZINE INHIBITOR=== | |
- | Description: Structure of Aurora-A bound to a selective imidazopyrazine inhibitor | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
+ | The line below this paragraph, {{ABSTRACT_PUBMED_20833547}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 20833547 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_20833547}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | 2XNG is a 1 chain structure 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=2XNG OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:20833547</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Non-specific serine/threonine protein kinase]] | ||
+ | [[Category: Bayliss, R.]] | ||
+ | [[Category: Kosmopoulou, M.]] | ||
+ | [[Category: Cell cycle]] | ||
+ | [[Category: Cell division]] | ||
+ | [[Category: Cytoskeleton]] | ||
+ | [[Category: Kinase]] | ||
+ | [[Category: Microtubule]] | ||
+ | [[Category: Mitosis]] | ||
+ | [[Category: Proto-oncogene]] | ||
+ | [[Category: Ser-thr protein kinase complex]] | ||
+ | [[Category: Transferase]] | ||
+ | |||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 22 14:43:30 2010'' |
Revision as of 11:34, 22 September 2010
STRUCTURE OF AURORA-A BOUND TO A SELECTIVE IMIDAZOPYRAZINE INHIBITOR
Template:ABSTRACT PUBMED 20833547
About this Structure
2XNG is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Bouloc N, Large JM, Kosmopoulou M, Sun C, Faisal A, Matteucci M, Reynisson J, Brown N, Atrash B, Blagg J, McDonald E, Linardopoulos S, Bayliss R, Bavetsias V. Structure-based design of imidazo[1,2-a]pyrazine derivatives as selective inhibitors of Aurora-A kinase in cells. Bioorg Med Chem Lett. 2010 Oct 15;20(20):5988-93. Epub 2010 Aug 21. PMID:20833547 doi:10.1016/j.bmcl.2010.08.091
Page seeded by OCA on Wed Sep 22 14:43:30 2010