3r7x
From Proteopedia
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===Crystal Structure Analysis of a Quinazolinedione sulfonamide bound to human GluR2: A Novel Class of Competitive AMPA Receptor Antagonists with Oral Activity=== | ===Crystal Structure Analysis of a Quinazolinedione sulfonamide bound to human GluR2: A Novel Class of Competitive AMPA Receptor Antagonists with Oral Activity=== | ||
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{{ABSTRACT_PUBMED_21531559}} | {{ABSTRACT_PUBMED_21531559}} | ||
==About this Structure== | ==About this Structure== | ||
| - | [[3r7x]] 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=3R7X OCA]. | + | [[3r7x]] is a 2 chain structure of [[Ionotropic Glutamate Receptors]] 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=3R7X OCA]. |
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| + | ==See Also== | ||
| + | *[[Ionotropic Glutamate Receptors|Ionotropic Glutamate Receptors]] | ||
==Reference== | ==Reference== | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Kallen, J.]] | [[Category: Kallen, J.]] | ||
| + | [[Category: Ion channel]] | ||
| + | [[Category: Ionic channel]] | ||
| + | [[Category: Postsynaptic membrane]] | ||
| + | [[Category: Transmembrane]] | ||
| + | [[Category: Transport protein]] | ||
Revision as of 01:35, 27 July 2012
Contents |
Crystal Structure Analysis of a Quinazolinedione sulfonamide bound to human GluR2: A Novel Class of Competitive AMPA Receptor Antagonists with Oral Activity
Template:ABSTRACT PUBMED 21531559
About this Structure
3r7x is a 2 chain structure of Ionotropic Glutamate Receptors with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Koller M, Lingenhoehl K, Schmutz M, Vranesic IT, Kallen J, Auberson YP, Carcache DA, Mattes H, Ofner S, Orain D, Urwyler S. Quinazolinedione sulfonamides: A novel class of competitive AMPA receptor antagonists with oral activity. Bioorg Med Chem Lett. 2011 Apr 8. PMID:21531559 doi:10.1016/j.bmcl.2011.04.017
