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-Structure paper
タイトル | Structure Based Drug Design: Development of Potent and Selective Factor IXa (FIXa) Inhibitors. |
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ジャーナル・号・ページ | J. Med. Chem., Vol. 53, Page 1473-1482, Year 2010 |
掲載日 | 2010年1月9日 (構造データの登録日) |
![]() | Wang, S. / Beck, R. / Burd, A. / Blench, T. / Marlin, F. / Ayele, T. / Buxton, S. / Dagostin, C. / Malic, M. / Joshi, R. ...Wang, S. / Beck, R. / Burd, A. / Blench, T. / Marlin, F. / Ayele, T. / Buxton, S. / Dagostin, C. / Malic, M. / Joshi, R. / Barry, J. / Sajad, M. / Cheung, C. / Shaikh, S. / Chahwala, S. / Chander, C. / Baumgartner, C. / Holthoff, H.P. / Murray, E. / Blackney, M. / Giddings, A. |
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手法 | X線回折 |
解像度 | 2.62 Å |
構造データ | ![]() PDB-3lc5: |
化合物 | ![]() ChemComp-CA: ![]() ChemComp-IZX: ![]() ChemComp-HOH: |
由来 |
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![]() | Hydrolase/Hydrolase Inhibitor / Protein-Inhibitor complex / Peptidase S1 / Blood coagulation / Calcium / Cleavage on pair of basic residues / Disease mutation / Disulfide bond / EGF-like domain / Gamma-carboxyglutamic acid / Glycoprotein / Hemophilia / Hydrolase / Hydroxylation / Pharmaceutical / Phosphoprotein / Polymorphism / Protease / Secreted / Serine protease / Sulfation / Zymogen / Hydrolase-Hydrolase Inhibitor complex |