3ezr
From Proteopedia
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| - | + | [[Image:3ezr.png|left|200px]] | |
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{{STRUCTURE_3ezr| PDB=3ezr | SCENE= }} | {{STRUCTURE_3ezr| PDB=3ezr | SCENE= }} | ||
===CDK-2 with indazole inhibitor 17 bound at its active site=== | ===CDK-2 with indazole inhibitor 17 bound at its active site=== | ||
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{{ABSTRACT_PUBMED_19097791}} | {{ABSTRACT_PUBMED_19097791}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[3ezr]] 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=3EZR 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:019097791</ref><references group="xtra"/> |
[[Category: Cyclin-dependent kinase]] | [[Category: Cyclin-dependent kinase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
[[Category: Pkc]] | [[Category: Pkc]] | ||
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[[Category: Protein kinase]] | [[Category: Protein 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 Wed Feb 4 11:36:51 2009'' | ||
Revision as of 09:40, 26 July 2012
Contents |
CDK-2 with indazole inhibitor 17 bound at its active site
Template:ABSTRACT PUBMED 19097791
About this Structure
3ezr 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
- Trujillo JI, Kiefer JR, Huang W, Thorarensen A, Xing L, Caspers NL, Day JE, Mathis KJ, Kretzmer KK, Reitz BA, Weinberg RA, Stegeman RA, Wrightstone A, Christine L, Compton R, Li X. 2-(6-Phenyl-1H-indazol-3-yl)-1H-benzo[d]imidazoles: design and synthesis of a potent and isoform selective PKC-zeta inhibitor. Bioorg Med Chem Lett. 2009 Feb 1;19(3):908-11. Epub 2008 Dec 6. PMID:19097791 doi:10.1016/j.bmcl.2008.11.105
Categories: Cyclin-dependent kinase | Homo sapiens | Caspers, N L. | Christine, L. | Compton, R. | Day, J E. | Huang, W. | Kiefer, J R. | Kretzmer, K K. | Li, X. | Mathis, K J. | Reitz, B A. | Stegeman, R A. | Thorarensen, A. | Trujillo, J I. | Weinberg, R A. | Wrightstone, A. | Xing, L. | Atp-binding | Cell cycle | Cell division | Inhibitor | Kinase | Mitosis | Nucleotide-binding | Phosphoprotein | Pkc | Protein kinase | Serine/threonine-protein kinase | Transferase
