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1G2L

FACTOR XA INHIBITOR COMPLEX

1G2L の概要
エントリーDOI10.2210/pdb1g2l/pdb
分子名称COAGULATION FACTOR X, CALCIUM ION, [(1-{2[(4-CARBAMIMIDOYL-PHENYLAMINO)-METHYL]-1-METHYL-1H-BENZOIMIDAZOL-5-YL}-CYCLOPROPYL)-PYRIDIN-2-YL-METHYLENEAMINOOXY]-ACETIC ACID ETHYL ESTER, ... (5 entities in total)
機能のキーワードblood coagulation, factor xa, inhibitor complexes, serine proteinase, blood coagulation cascade, hydrolase
由来する生物種Homo sapiens (human)
詳細
細胞内の位置Secreted: P00742 P00742
タンパク質・核酸の鎖数2
化学式量合計37411.33
構造登録者
Nar, H. (登録日: 2000-10-20, 公開日: 2001-10-20, 最終更新日: 2024-11-20)
主引用文献Nar, H.,Bauer, M.,Schmid, A.,Stassen, J.M.,Wienen, W.,Priepke, H.W.,Kauffmann, I.K.,Ries, U.J.,Hauel, N.H.
Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors.
Structure, 9:29-38, 2001
Cited by
PubMed Abstract: A major current focus of pharmaceutical research is the development of selective inhibitors of the blood coagulation enzymes thrombin or factor Xa to be used as orally bioavailable anticoagulant drugs in thromboembolic disorders and in the prevention of venous and arterial thrombosis. Simultaneous direct inhibition of thrombin and factor Xa by synthetic proteinase inhibitors as a novel approach to antithrombotic therapy could result in potent anticoagulants with improved pharmacological properties.
PubMed: 11342132
DOI: 10.1016/S0969-2126(00)00551-7
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 1g2l
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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