3lau
From Proteopedia
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- | The | + | <!-- |
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+ | {{STRUCTURE_3lau| PDB=3lau | SCENE= }} | ||
- | + | ===Crystal Structure of Aurora2 kinase in complex with a GSK3beta inhibitor=== | |
- | Description: Crystal Structure of Aurora2 kinase in complex with a GSK3beta inhibitor | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
+ | The line below this paragraph, {{ABSTRACT_PUBMED_20167481}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 20167481 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_20167481}} | ||
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+ | ==About this Structure== | ||
+ | 3LAU 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=3LAU OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:20167481</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Non-specific serine/threonine protein kinase]] | ||
+ | [[Category: Guilloteau, J P.]] | ||
+ | [[Category: Maignan, S.]] | ||
+ | [[Category: Pouzieux , S.]] | ||
+ | [[Category: Atp-binding]] | ||
+ | [[Category: Cell cycle]] | ||
+ | [[Category: Cytoplasm]] | ||
+ | [[Category: Cytoskeleton]] | ||
+ | [[Category: Kinase]] | ||
+ | [[Category: Kinase inhibitor complex]] | ||
+ | [[Category: Nucleotide-binding]] | ||
+ | [[Category: Phosphoprotein]] | ||
+ | [[Category: Polymorphism]] | ||
+ | [[Category: Serine/threonine-protein kinase]] | ||
+ | [[Category: Transferase]] | ||
+ | [[Category: Ubl conjugation]] | ||
+ | |||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 3 15:51:11 2010'' |
Revision as of 13:51, 3 March 2010
Crystal Structure of Aurora2 kinase in complex with a GSK3beta inhibitor
Template:ABSTRACT PUBMED 20167481
About this Structure
3LAU is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Lesuisse D, Dutruc-Rosset G, Tiraboschi G, Dreyer MK, Maignan S, Chevalier A, Halley F, Bertrand P, Burgevin MC, Quarteronet D, Rooney T. Rational design of potent GSK3beta inhibitors with selectivity for Cdk1 and Cdk2. Bioorg Med Chem Lett. 2010 Mar 15;20(6):1985-9. Epub 2010 Jan 25. PMID:20167481 doi:10.1016/j.bmcl.2010.01.114
Page seeded by OCA on Wed Mar 3 15:51:11 2010
Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Guilloteau, J P. | Maignan, S. | Pouzieux , S. | Atp-binding | Cell cycle | Cytoplasm | Cytoskeleton | Kinase | Kinase inhibitor complex | Nucleotide-binding | Phosphoprotein | Polymorphism | Serine/threonine-protein kinase | Transferase | Ubl conjugation