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2ONC

Crystal structure of human DPP-4

2ONC の概要
エントリーDOI10.2210/pdb2onc/pdb
分子名称Dipeptidyl peptidase 4, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
機能のキーワードdpp4 protein-inhibitor complex, hydrolase
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346989.81
構造登録者
主引用文献Feng, J.,Zhang, Z.,Wallace, M.B.,Stafford, J.A.,Kaldor, S.W.,Kassel, D.B.,Navre, M.,Shi, L.,Skene, R.J.,Asakawa, T.,Takeuchi, K.,Xu, R.,Webb, D.R.,Gwaltney, S.L.
Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV.
J.Med.Chem., 50:2297-2300, 2007
Cited by
PubMed Abstract: Alogliptin is a potent, selective inhibitor of the serine protease dipeptidyl peptidase IV (DPP-4). Herein, we describe the structure-based design and optimization of alogliptin and related quinazolinone-based DPP-4 inhibitors. Following an oral dose, these noncovalent inhibitors provide sustained reduction of plasma DPP-4 activity and a lowering of blood glucose in animal models of diabetes. Alogliptin is currently undergoing phase III trials in patients with type 2 diabetes.
PubMed: 17441705
DOI: 10.1021/jm070104l
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.55 Å)
構造検証レポート
Validation report summary of 2onc
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2024-10-30に公開中

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