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3fz1
From Proteopedia
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{{STRUCTURE_3fz1| PDB=3fz1 | SCENE= }} | {{STRUCTURE_3fz1| PDB=3fz1 | SCENE= }} | ||
===Crystal structure of a benzthiophene inhibitor bound to human Cyclin-dependent Kinase-2 (CDK-2)=== | ===Crystal structure of a benzthiophene inhibitor bound to human Cyclin-dependent Kinase-2 (CDK-2)=== | ||
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{{ABSTRACT_PUBMED_19616942}} | {{ABSTRACT_PUBMED_19616942}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[3fz1]] 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=3FZ1 OCA]. | |
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| + | ==See Also== | ||
| + | *[[Cell Division Protein Kinase 2|Cell Division Protein Kinase 2]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:019616942</ref><references group="xtra"/> |
[[Category: Cyclin-dependent kinase]] | [[Category: Cyclin-dependent kinase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
| - | [[Category: Polymorphism]] | ||
[[Category: Ser/thr kinase]] | [[Category: Ser/thr kinase]] | ||
[[Category: Serine/threonine-protein kinase]] | [[Category: Serine/threonine-protein kinase]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Sep 21 20:15:54 2009'' | ||
Revision as of 11:12, 26 July 2012
Contents |
Crystal structure of a benzthiophene inhibitor bound to human Cyclin-dependent Kinase-2 (CDK-2)
Template:ABSTRACT PUBMED 19616942
About this Structure
3fz1 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
- Anderson DR, Meyers MJ, Kurumbail RG, Caspers N, Poda GI, Long SA, Pierce BS, Mahoney MW, Mourey RJ, Parikh MD. Benzothiophene inhibitors of MK2. Part 2: improvements in kinase selectivity and cell potency. Bioorg Med Chem Lett. 2009 Aug 15;19(16):4882-4. Epub 2009 Feb 8. PMID:19616942 doi:10.1016/j.bmcl.2009.02.017
Categories: Cyclin-dependent kinase | Homo sapiens | Caspers, N. | Kurumbail, R G. | Atp-binding | Benzothiophene | Cdk-2 | Cell cycle | Cell division | Cell divison kinase-2 | Cyclin | Kinase | Mapkap kinase-2 | Mitosis | Mk-2 | Mk2 | Nucleotide-binding | Phosphoprotein | Ser/thr kinase | Serine/threonine-protein kinase | Transferase
