3du8
From Proteopedia
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{{STRUCTURE_3du8| PDB=3du8 | SCENE= }} | {{STRUCTURE_3du8| PDB=3du8 | SCENE= }} | ||
===Crystal structure of GSK-3 beta in complex with NMS-869553A=== | ===Crystal structure of GSK-3 beta in complex with NMS-869553A=== | ||
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{{ABSTRACT_PUBMED_19115845}} | {{ABSTRACT_PUBMED_19115845}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[3du8]] is a 2 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=3DU8 OCA]. | |
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| + | ==See Also== | ||
| + | *[[Glycogen synthase kinase 3|Glycogen synthase kinase 3]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:019115845</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Bossi, R T.]] | [[Category: Bossi, R T.]] | ||
| - | [[Category: Alternative splicing]] | ||
[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
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[[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 Mar 4 14:48:46 2009'' | ||
Revision as of 09:01, 9 January 2013
Contents |
Crystal structure of GSK-3 beta in complex with NMS-869553A
Template:ABSTRACT PUBMED 19115845
About this Structure
3du8 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
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
