8TRJ
Cryo-EM structure of the rat P2X7 receptor in complex with the high-affinity agonist BzATP
This is a non-PDB format compatible entry.
Summary for 8TRJ
Entry DOI | 10.2210/pdb8trj/pdb |
Related | 8TR5 8TR6 8TR7 8TR8 8TRA 8TRB 8TRK |
EMDB information | 41570 41571 41572 41573 41575 41576 41581 41582 |
Descriptor | P2X purinoceptor 7, 3'-O-(4-benzoylbenzoyl)adenosine 5'-(tetrahydrogen triphosphate), GUANOSINE-5'-DIPHOSPHATE, ... (7 entities in total) |
Functional Keywords | membrane protein, ion channel, ligand-gate ion channel, p2x receptor, allosteric antagonist, high-affinity agonist |
Biological source | Rattus More |
Total number of polymer chains | 3 |
Total formula weight | 215122.85 |
Authors | Oken, A.C.,Lisi, N.E.,Krishnamurthy, I.,McCarthy, A.E.,Godsey, M.H.,Glasfeld, A.,Mansoor, S.E. (deposition date: 2023-08-09, release date: 2024-08-14, Last modification date: 2024-08-21) |
Primary citation | Oken, A.C.,Lisi, N.E.,Krishnamurthy, I.,McCarthy, A.E.,Godsey, M.H.,Glasfeld, A.,Mansoor, S.E. High-affinity agonism at the P2X 7 receptor is mediated by three residues outside the orthosteric pocket. Nat Commun, 15:6662-6662, 2024 Cited by PubMed: 39107314DOI: 10.1038/s41467-024-50771-6 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.78 Å) |
Structure validation
Download full validation report