3lfq
From Proteopedia
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| + | [[Image:3lfq.jpg|left|200px]] | ||
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| + | {{STRUCTURE_3lfq| PDB=3lfq | SCENE= }} | ||
| - | + | ===Crystal structure of CDK2 with SAR60, an aminoindazole type inhibitor=== | |
| - | Description: Crystal structure of CDK2 with SAR60, an aminoindazole type 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== | ||
| + | 3LFQ 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=3LFQ OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:20167481</ref><references group="xtra"/> | ||
| + | [[Category: Cyclin-dependent kinase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Dreyer, M K.]] | ||
| + | [[Category: Loenze, P.]] | ||
| + | [[Category: Schimanski-Breves, S.]] | ||
| + | [[Category: Wendt, K U.]] | ||
| + | [[Category: Acetylation]] | ||
| + | [[Category: Atp-binding]] | ||
| + | [[Category: Cell cycle]] | ||
| + | [[Category: Cell division]] | ||
| + | [[Category: Kinase]] | ||
| + | [[Category: Mitosis]] | ||
| + | [[Category: Nucleotide-binding]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Protein kinase fold]] | ||
| + | [[Category: Serine/threonine-protein kinase]] | ||
| + | [[Category: Transferase]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 3 15:49:37 2010'' | ||
Revision as of 13:49, 3 March 2010
Crystal structure of CDK2 with SAR60, an aminoindazole type inhibitor
Template:ABSTRACT PUBMED 20167481
About this Structure
3LFQ 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 15:49:37 2010
Categories: Cyclin-dependent kinase | Homo sapiens | Dreyer, M K. | Loenze, P. | Schimanski-Breves, S. | Wendt, K U. | Acetylation | Atp-binding | Cell cycle | Cell division | Kinase | Mitosis | Nucleotide-binding | Phosphoprotein | Polymorphism | Protein kinase fold | Serine/threonine-protein kinase | Transferase
