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5SFH

Crystal Structure of human phosphodiesterase 10 in complex with N-cyclopropyl-5-[2-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)ethyl]-N,1-dimethyl-1,2,4-triazol-3-amine

5SFH の概要
エントリーDOI10.2210/pdb5sfh/pdb
Group depositionExploiting Structural Data for Improved On-Target Prediction in Lead Optimization (G_1002226)
分子名称cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A, ZINC ION, MAGNESIUM ION, ... (5 entities in total)
機能のキーワードphosphodiesterase, pde10, hydrolase, schizophrenia, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数4
化学式量合計159317.26
構造登録者
Joseph, C.,Flohr, A.,Benz, J.,Schlatter, D.,Rudolph, M.G. (登録日: 2022-01-21, 公開日: 2022-10-12, 最終更新日: 2024-04-03)
主引用文献Tosstorff, A.,Rudolph, M.G.,Cole, J.C.,Reutlinger, M.,Kramer, C.,Schaffhauser, H.,Nilly, A.,Flohr, A.,Kuhn, B.
A high quality, industrial data set for binding affinity prediction: performance comparison in different early drug discovery scenarios.
J.Comput.Aided Mol.Des., 36:753-765, 2022
Cited by
PubMed: 36153472
DOI: 10.1007/s10822-022-00478-x
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.29 Å)
構造検証レポート
Validation report summary of 5sfh
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-07-17に公開中

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