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-Structure paper
タイトル | Design and Synthesis of Reversible Inhibitors of Cathepsin S: alpha,alpha-Disubstitution at the P1 Residue Provides Potent Inhibitors in Cellular Assays and In Vivo Models of Antigen Presentation |
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ジャーナル・号・ページ | To be Published |
掲載日 | 2007年9月13日 (構造データの登録日) |
![]() | Ward, Y.D. / Emmanuel, M.J. / Thomson, D.S. / Liu, W. / Bekkali, Y. / Frye, L.L. / Girardot, M. / Morwick, T. / Young, E.R.R. / Zindell, R. ...Ward, Y.D. / Emmanuel, M.J. / Thomson, D.S. / Liu, W. / Bekkali, Y. / Frye, L.L. / Girardot, M. / Morwick, T. / Young, E.R.R. / Zindell, R. / Hrapchak, M. / DeTuri, M. / White, A. / Crane, K.M. / White, D.M. / Wang, Y. / Hao, M.-H. / Grygon, C.A. / Labadia, M.E. / Wildeson, J. / Freeman, D. / Nelson, R. / Capolino, A. / Peterson, J.D. / Raymond, E.L. / Brown, M.L. / Spero, D.M. |
![]() | PubMedで検索 |
手法 | X線回折 |
解像度 | 1.97 - 2 Å |
構造データ | ![]() PDB-2r9m: ![]() PDB-2r9n: ![]() PDB-2r9o: |
化合物 | ![]() ChemComp-Y11: ![]() ChemComp-HOH: ![]() ChemComp-Y14: ![]() ChemComp-Y15: |
由来 |
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![]() | HYDROLASE / CATHEPSIN / PROTEASE / Glycoprotein / Lysosome / Polymorphism / Thiol protease / Zymogen |