3R7X
Crystal Structure Analysis of a Quinazolinedione sulfonamide bound to human GluR2: A Novel Class of Competitive AMPA Receptor Antagonists with Oral Activity
Summary for 3R7X
Entry DOI | 10.2210/pdb3r7x/pdb |
Related | 2CMO |
Descriptor | Glutamate receptor 2, N-[6-(1H-imidazol-1-yl)-7-nitro-2,4-dioxo-1,4-dihydroquinazolin-3(2H)-yl]methanesulfonamide, GLUTAMIC ACID, ... (4 entities in total) |
Functional Keywords | ion channel, ionic channel, postsynaptic membrane, transmembrane, transport protein |
Biological source | Homo sapiens (human) More |
Cellular location | Cell membrane ; Multi-pass membrane protein : P42262 |
Total number of polymer chains | 2 |
Total formula weight | 59209.17 |
Authors | Kallen, J. (deposition date: 2011-03-23, release date: 2011-05-18, Last modification date: 2017-07-26) |
Primary citation | Koller, M.,Lingenhoehl, K.,Schmutz, M.,Vranesic, I.T.,Kallen, J.,Auberson, Y.P.,Carcache, D.A.,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., 21:3358-3361, 2011 Cited by PubMed: 21531559DOI: 10.1016/j.bmcl.2011.04.017 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
Download full validation report