5BUU
Crystal structure of the GluA2 ligand-binding domain (L483Y-N754S) in complex with glutamate and BPAM-321 at 2.07 A resolution
Summary for 5BUU
Entry DOI | 10.2210/pdb5buu/pdb |
Related | 3il1 4n07 |
Descriptor | Glutamate receptor 2,Glutamate receptor 2, (3R)-7-chloro-2,3,4-trimethyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide, GLUTAMIC ACID, ... (6 entities in total) |
Functional Keywords | ampa receptor ligand-binding domain, glua2 l483y-n754s, bpam-321 positive allosteric modulation, membrane protein |
Biological source | Rattus norvegicus (Norway Rat) More |
Cellular location | Cell membrane ; Multi-pass membrane protein : P19491 |
Total number of polymer chains | 2 |
Total formula weight | 60095.75 |
Authors | Larsen, A.P.,Tapken, D.,Frydenvang, K.,Kastrup, J.S. (deposition date: 2015-06-04, release date: 2016-02-17, Last modification date: 2024-01-10) |
Primary citation | Larsen, A.P.,Francotte, P.,Frydenvang, K.,Tapken, D.,Goffin, E.,Fraikin, P.,Caignard, D.H.,Lestage, P.,Danober, L.,Pirotte, B.,Kastrup, J.S. Synthesis and Pharmacology of Mono-, Di-, and Trialkyl-Substituted 7-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-Dioxides Combined with X-ray Structure Analysis to Understand the Unexpected Structure-Activity Relationship at AMPA Receptors. Acs Chem Neurosci, 7:378-390, 2016 Cited by PubMed: 26771108DOI: 10.1021/acschemneuro.5b00318 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.07 Å) |
Structure validation
Download full validation report