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9G35

The HIV protease inhibitor lopinavir binding to the active site of Cryphonectria parasitica endothiapepsin

9G35 の概要
エントリーDOI10.2210/pdb9g35/pdb
関連するPDBエントリー9FVO 9G34
分子名称Endothiapepsin, N-{1-BENZYL-4-[2-(2,6-DIMETHYL-PHENOXY)-ACETYLAMINO]-3-HYDROXY-5-PHENYL-PENTYL}-3-METHYL-2-(2-OXO-TETRAHYDRO-PYRIMIDIN-1-YL)-BUTYRAMIDE, TRIETHYLENE GLYCOL, ... (6 entities in total)
機能のキーワードaspartic protease, drug development, inhibitor, x-ray crystallographic screening, chestnut blight fungus, protease model, hydrolase
由来する生物種Cryphonectria parasitica (chestnut blight fungus)
タンパク質・核酸の鎖数1
化学式量合計35105.42
構造登録者
Falke, S.,Senst, J.M.,Guenther, S.,Meents, A. (登録日: 2024-07-11, 公開日: 2024-07-24, 最終更新日: 2024-11-13)
主引用文献Falke, S.,Senst, J.M.,Guenther, S.,Meents, A.
The HIV protease inhibitor lopinavir binding to the active site of Cryphonectria parasitica endothiapepsin
To Be Published,
実験手法
X-RAY DIFFRACTION (1.5 Å)
構造検証レポート
Validation report summary of 9g35
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2026-04-22に公開中

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