3lfs: Difference between revisions
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[[Image:3lfs.png|left|200px]] | [[Image:3lfs.png|left|200px]] | ||
{{STRUCTURE_3lfs| PDB=3lfs | SCENE= }} | {{STRUCTURE_3lfs| PDB=3lfs | SCENE= }} | ||
===Crystal structure of CDK2 with SAR37, an aminoindazole type inhibitor=== | ===Crystal structure of CDK2 with SAR37, an aminoindazole type inhibitor=== | ||
{{ABSTRACT_PUBMED_20167481}} | {{ABSTRACT_PUBMED_20167481}} | ||
==About this Structure== | ==About this Structure== | ||
[[3lfs]] is a 1 chain structure of [[Cell Division Protein Kinase 2]] 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=3LFS OCA]. | |||
==See Also== | |||
*[[Cell Division Protein Kinase 2|Cell Division Protein Kinase 2]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:020167481</ref><references group="xtra"/> | ||
[[Category: Cyclin-dependent kinase]] | [[Category: Cyclin-dependent kinase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Schimanski-Breves, S.]] | [[Category: Schimanski-Breves, S.]] | ||
[[Category: Wendt, K U.]] | [[Category: Wendt, K U.]] | ||
[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: Cell cycle]] | [[Category: Cell cycle]] | ||
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[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
[[Category: Protein kinase fold]] | [[Category: Protein kinase fold]] | ||
[[Category: Serine/threonine-protein kinase]] | [[Category: Serine/threonine-protein kinase]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
Revision as of 13:33, 25 July 2012
Crystal structure of CDK2 with SAR37, an aminoindazole type inhibitor
Template:ABSTRACT PUBMED 20167481
About this Structure
3lfs is a 1 chain structure of Cell Division Protein Kinase 2 with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
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
