3du8
From Proteopedia
(Difference between revisions)
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+ | [[Image:3du8.jpg|left|200px]] | ||
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3du8", creates the "Structure Box" on the page. | ||
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+ | {{STRUCTURE_3du8| PDB=3du8 | SCENE= }} | ||
- | + | ===Crystal structure of GSK-3 beta in complex with NMS-869553A=== | |
- | Description: Crystal structure of GSK-3 beta in complex with NMS-869553A | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
+ | The line below this paragraph, {{ABSTRACT_PUBMED_19115845}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 19115845 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_19115845}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | 3DU8 is a 2 chains structure of sequences 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=3DU8 OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:19115845</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Bossi, R T.]] | ||
+ | [[Category: Alternative splicing]] | ||
+ | [[Category: Atp-binding]] | ||
+ | [[Category: Nucleotide-binding]] | ||
+ | [[Category: Phosphoprotein]] | ||
+ | [[Category: Protein kinase]] | ||
+ | [[Category: Serine/threonine-protein kinase]] | ||
+ | [[Category: Transferase]] | ||
+ | |||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 4 14:48:46 2009'' |
Revision as of 12:48, 4 March 2009
Crystal structure of GSK-3 beta in complex with NMS-869553A
Template:ABSTRACT PUBMED 19115845
About this Structure
3DU8 is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Menichincheri M, Bargiotti A, Berthelsen J, Bertrand JA, Bossi R, Ciavolella A, Cirla A, Cristiani C, Croci V, D'Alessio R, Fasolini M, Fiorentini F, Forte B, Isacchi A, Martina K, Molinari A, Montagnoli A, Orsini P, Orzi F, Pesenti E, Pezzetta D, Pillan A, Poggesi I, Roletto F, Scolaro A, Tato M, Tibolla M, Valsasina B, Varasi M, Volpi D, Santocanale C, Vanotti E. First Cdc7 kinase inhibitors: pyrrolopyridinones as potent and orally active antitumor agents. 2. Lead discovery. J Med Chem. 2009 Jan 22;52(2):293-307. PMID:19115845 doi:10.1021/jm800977q
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