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2XDW

Inhibition of Prolyl Oligopeptidase with a Synthetic Unnatural Dipeptide

2XDW の概要
エントリーDOI10.2210/pdb2xdw/pdb
関連するPDBエントリー1E5T 1E8M 1E8N 1H2W 1H2X 1H2Y 1H2Z 1O6F 1O6G 1QFM 1QFS 1UOO 1UOP 1UOQ 1VZ2 1VZ3
関連するBIRD辞書のPRD_IDPRD_000694
分子名称Prolyl endopeptidase, SYNTHETIC PEPTIDE PHQ-PRO-YCP, TRIS(HYDROXYETHYL)AMINOMETHANE, ... (5 entities in total)
機能のキーワードalpha/beta-hydrolase, amnesia, beta-propeller, hydrolase, inhibitor
由来する生物種Sus scrofa (pig)
詳細
細胞内の位置Cytoplasm: P23687
タンパク質・核酸の鎖数2
化学式量合計82235.26
構造登録者
Racys, D.T.,Rea, D.,Fulop, V.,Wills, M. (登録日: 2010-05-09, 公開日: 2010-06-23, 最終更新日: 2024-11-06)
主引用文献Racys, D.T.,Rea, D.,Fulop, V.,Wills, M.
Inhibition of Prolyl Oligopeptidase with a Synthetic Unnatural Dipeptide
Bioorg.Med.Chem., 18:4775-, 2010
Cited by
PubMed Abstract: A new inhibitor, containing a linked proline-piperidine structure, for the enzyme prolyl oligopeptidase (POP) has been synthesised and demonstrated to bind covalently with the enzyme at the active site. This provides evidence that covalent inhibitors of POP do not have to be limited to structures containing five-membered N-containing heterocyclic rings.
PubMed: 20627594
DOI: 10.1016/J.BMC.2010.05.012
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.35 Å)
構造検証レポート
Validation report summary of 2xdw
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2026-02-04に公開中

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