4ZO5

PDE10 complexed with 4-isopropoxy-2-(2-(3-(4-methoxyphenyl)-4-oxo-3,4-dihydroquinazolin-2-yl)ethyl)isoindoline-1,3-dione

4ZO5 の概要

• エントリーDOI: 10.2210/pdb4zo5/pdb
• 分子名称: cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A, ZINC ION, MAGNESIUM ION, ... (6 entities in total)
• 機能のキーワード: phosphodiesterase inhibitor, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
• 由来する生物種: Homo sapiens (Human)
• 細胞内の位置: Cytoplasm: Q9Y233
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 75873.63

構造登録者

Yan, Y. (登録日: 2015-05-06, 公開日: 2015-08-12, 最終更新日: 2023-09-27)

• 主引用文献: Cox, C.D.,Hostetler, E.D.,Flores, B.A.,Evelhoch, J.L.,Fan, H.,Gantert, L.,Holahan, M.,Eng, W.,Joshi, A.,McGaughey, G.,Meng, X.,Purcell, M.,Raheem, I.T.,Riffel, K.,Yan, Y.,Renger, J.J.,Smith, S.M.,Coleman, P.J.; Discovery of [(11)C]MK-8193 as a PET tracer to measure target engagement of phosphodiesterase 10A (PDE10A) inhibitors.; Bioorg.Med.Chem.Lett., 25:4893-4898, 2015; PubMed: 26077491; DOI: 10.1016/j.bmcl.2015.05.080

実験手法

X-RAY DIFFRACTION (2.5 Å)