3igg
From Proteopedia
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| + | [[Image:3igg.jpg|left|200px]] | ||
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| + | The line below this paragraph, containing "STRUCTURE_3igg", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3igg| PDB=3igg | SCENE= }} | ||
| - | + | ===Novel CDK-5 inhibitors - crystal structure of inhibitor EFQ with CDK-2=== | |
| - | Description: Novel CDK-5 inhibitors -crystal structure of inhibitor EFQ with CDK-2 | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19700321}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19700321 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19700321}} | ||
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| + | ==About this Structure== | ||
| + | 3IGG is a 1 chain structure of 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=3IGG OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19700321</ref><references group="xtra"/> | ||
| + | [[Category: Cyclin-dependent kinase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Pandit, J.]] | ||
| + | [[Category: Atp-binding]] | ||
| + | [[Category: Cell cycle]] | ||
| + | [[Category: Cell division]] | ||
| + | [[Category: Inhibitor]] | ||
| + | [[Category: Kinase]] | ||
| + | [[Category: Mitosis]] | ||
| + | [[Category: Nucleotide-binding]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Protein kinase]] | ||
| + | [[Category: Serine/threonine protein kinase]] | ||
| + | [[Category: Serine/threonine-protein kinase]] | ||
| + | [[Category: Transferase]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 9 09:23:19 2009'' | ||
Revision as of 06:23, 9 September 2009
Novel CDK-5 inhibitors - crystal structure of inhibitor EFQ with CDK-2
Template:ABSTRACT PUBMED 19700321
About this Structure
3IGG is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Helal CJ, Kang Z, Lucas JC, Gant T, Ahlijanian MK, Schachter JB, Richter KE, Cook JM, Menniti FS, Kelly K, Mente S, Pandit J, Hosea N. Potent and cellularly active 4-aminoimidazole inhibitors of cyclin-dependent kinase 5/p25 for the treatment of Alzheimer's disease. Bioorg Med Chem Lett. 2009 Oct 1;19(19):5703-7. Epub 2009 Aug 8. PMID:19700321 doi:10.1016/j.bmcl.2009.08.019
Page seeded by OCA on Wed Sep 9 09:23:19 2009
