6AR4
Crystal structure of PICK1 in complex with the small molecule inhibitor 1o
Summary for 6AR4
Entry DOI | 10.2210/pdb6ar4/pdb |
Descriptor | PRKCA-binding protein, N-[4-(4-bromophenyl)-1-{[2-(trifluoromethyl)phenyl]methyl}piperidine-4-carbonyl]-3-cyclopropyl-L-alanine (3 entities in total) |
Functional Keywords | pdz domain pdz inhibitor, actin binding protein |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 2 |
Total formula weight | 28187.63 |
Authors | Marcotte, D. (deposition date: 2017-08-21, release date: 2018-08-22, Last modification date: 2023-10-04) |
Primary citation | Lin, E.Y.S.,Silvian, L.F.,Marcotte, D.J.,Banos, C.C.,Jow, F.,Chan, T.R.,Arduini, R.M.,Qian, F.,Baker, D.P.,Bergeron, C.,Hession, C.A.,Huganir, R.L.,Borenstein, C.F.,Enyedy, I.,Zou, J.,Rohde, E.,Wittmann, M.,Kumaravel, G.,Rhodes, K.J.,Scannevin, R.H.,Dunah, A.W.,Guckian, K.M. Potent PDZ-Domain PICK1 Inhibitors that Modulate Amyloid Beta-Mediated Synaptic Dysfunction. Sci Rep, 8:13438-13438, 2018 Cited by PubMed: 30194389DOI: 10.1038/s41598-018-31680-3 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.69 Å) |
Structure validation
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