6IC5
Human cathepsin-C in complex with dipeptidyl cyclopropyl nitrile inhibitor 2
6IC5 の概要
エントリーDOI | 10.2210/pdb6ic5/pdb |
分子名称 | Dipeptidyl peptidase 1, alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (8 entities in total) |
機能のキーワード | cathepsin-c, cysteine protease, structure-based drug design, arthritis, hydrolase |
由来する生物種 | Homo sapiens (Human) 詳細 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 41326.63 |
構造登録者 | Hakansson, M.,Logan, D.T.,Korkmaz, B.,Lesner, A.,Wysocka, M.,Gieldon, A.,Gauthier, F.,Jenne, D.,Lauritzen, C.,Pedersen, J. (登録日: 2018-12-02, 公開日: 2019-04-24, 最終更新日: 2020-07-29) |
主引用文献 | Korkmaz, B.,Lesner, A.,Wysocka, M.,Gieldon, A.,Hakansson, M.,Gauthier, F.,Logan, D.T.,Jenne, D.E.,Lauritzen, C.,Pedersen, J. Structure-based design and in vivo anti-arthritic activity evaluation of a potent dipeptidyl cyclopropyl nitrile inhibitor of cathepsin C. Biochem. Pharmacol., 164:349-367, 2019 Cited by PubMed: 30978322DOI: 10.1016/j.bcp.2019.04.006 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2 Å) |
構造検証レポート
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