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4ZSC

Human Cyclophilin D Complexed with an Inhibitor at room temperature

4ZSC の概要
エントリーDOI10.2210/pdb4zsc/pdb
関連するPDBエントリー3RDC
分子名称Peptidyl-prolyl cis-trans isomerase F, mitochondrial, ethyl N-[(4-aminobenzyl)carbamoyl]glycinate (3 entities in total)
機能のキーワードisomerase inhibitor complex, isomerase
由来する生物種Homo sapiens (Human)
細胞内の位置Mitochondrion matrix : P30405
タンパク質・核酸の鎖数1
化学式量合計17903.41
構造登録者
Gelin, M.,Delfosse, V.,Allemand, F.,Hoh, F.,Sallaz-Damaz, Y.,Pirocchi, M.,Bourguet, W.,Ferrer, J.-L.,Labesse, G.,Guichou, J.-F. (登録日: 2015-05-13, 公開日: 2015-08-12, 最終更新日: 2024-05-08)
主引用文献Gelin, M.,Delfosse, V.,Allemand, F.,Hoh, F.,Sallaz-Damaz, Y.,Pirocchi, M.,Bourguet, W.,Ferrer, J.L.,Labesse, G.,Guichou, J.F.
Combining `dry' co-crystallization and in situ diffraction to facilitate ligand screening by X-ray crystallography.
Acta Crystallogr.,Sect.D, 71:1777-1787, 2015
Cited by
PubMed Abstract: X-ray crystallography is an established technique for ligand screening in fragment-based drug-design projects, but the required manual handling steps - soaking crystals with ligand and the subsequent harvesting - are tedious and limit the throughput of the process. Here, an alternative approach is reported: crystallization plates are pre-coated with potential binders prior to protein crystallization and X-ray diffraction is performed directly 'in situ' (or in-plate). Its performance is demonstrated on distinct and relevant therapeutic targets currently being studied for ligand screening by X-ray crystallography using either a bending-magnet beamline or a rotating-anode generator. The possibility of using DMSO stock solutions of the ligands to be coated opens up a route to screening most chemical libraries.
PubMed: 26249358
DOI: 10.1107/S1399004715010342
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.5 Å)
構造検証レポート
Validation report summary of 4zsc
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2025-06-18に公開中

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