6KDZ
Crystal structure of PDE10A in complex with a triazolopyrimidine inhibitor
Summary for 6KDZ
Entry DOI | 10.2210/pdb6kdz/pdb |
Related | 6KDX |
Descriptor | cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A, ZINC ION, MAGNESIUM ION, ... (4 entities in total) |
Functional Keywords | inhibitor, hydrolase |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 2 |
Total formula weight | 79752.66 |
Authors | Amano, Y.,Honbou, K. (deposition date: 2019-07-03, release date: 2019-08-14, Last modification date: 2023-11-22) |
Primary citation | Chino, A.,Honda, S.,Morita, M.,Yonezawa, K.,Hamaguchi, W.,Amano, Y.,Moriguchi, H.,Yamazaki, M.,Aota, M.,Tomishima, M.,Masuda, N. Synthesis, SAR study, and biological evaluation of novel 2,3-dihydro-1H-imidazo[1,2-a]benzimidazole derivatives as phosphodiesterase 10A inhibitors. Bioorg.Med.Chem., 27:3692-3706, 2019 Cited by PubMed: 31301949DOI: 10.1016/j.bmc.2019.07.010 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.1 Å) |
Structure validation
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