3faa
From Proteopedia
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==About this Structure== | ==About this Structure== | ||
- | 3FAA is a | + | 3FAA is a 5 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=3FAA OCA]. |
==Reference== | ==Reference== | ||
- | + | <ref group="xtra">PMID:19135364</ref><references group="xtra"/> | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Receptor protein serine/threonine kinase]] | [[Category: Receptor protein serine/threonine kinase]] | ||
- | [[Category: | + | [[Category: Boriack-Sjodin, P A.]] |
- | [[Category: | + | [[Category: Fitch, C.]] |
[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: Craniosynostosis]] | [[Category: Craniosynostosis]] | ||
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[[Category: Transmembrane]] | [[Category: Transmembrane]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 15 08:48:13 2009'' |
Revision as of 06:48, 15 February 2009
Contents |
Crystal structure of TGFbRI complexed with a 2-aminoimidazole inhibitor
Template:ABSTRACT PUBMED 19135364
Disease
Known disease associated with this structure: Loeys-Dietz syndrome, type 1A OMIM:[190181], Loeys-Dietz syndrome, type 2A OMIM:[190181]
About this Structure
3FAA is a 5 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Bonafoux D, Chuaqui C, Boriack-Sjodin PA, Fitch C, Hankins G, Josiah S, Black C, Hetu G, Ling L, Lee WC. 2-Aminoimidazoles inhibitors of TGF-beta receptor 1. Bioorg Med Chem Lett. 2009 Feb 1;19(3):912-6. Epub 2008 Dec 11. PMID:19135364 doi:10.1016/j.bmcl.2008.11.119
Page seeded by OCA on Sun Feb 15 08:48:13 2009
Categories: Homo sapiens | Receptor protein serine/threonine kinase | Boriack-Sjodin, P A. | Fitch, C. | Atp-binding | Craniosynostosis | Disease mutation | Glycoprotein | Kinase | Magnesium | Manganese | Membrane | Metal-binding | Nucleotide-binding | Phosphoprotein | Polymorphism | Protein-inhibitor complex | Receptor | Serine/threonine-protein kinase | Structure-based drug design | Tgfbeta | Transferase | Transmembrane