5P5J
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5P1L
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5P20
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5P2G
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1I09
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1WVN
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3FDN
| Structure-based drug design of novel Aurora kinase A inhibitors: Structure basis for potency and specificity | 分子名称: | N-[3-(acetylamino)phenyl]-5-{(2E)-2-[(4-methoxyphenyl)methylidene]hydrazino}-3-methyl-1H-pyrazole-4-carboxamide, Serine/threonine-protein kinase 6 | 著者 | Leou, J.S, Wu, J.S, Coumar, M.S, Shukla, P, Hsieh, H.P, Wu, S.Y. | 登録日 | 2008-11-26 | 公開日 | 2009-09-15 | 最終更新日 | 2023-11-01 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Structure-based drug design of novel Aurora kinase A inhibitors: structural basis for potency and specificity J.Med.Chem., 52, 2009
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3TZM
| TGF-beta Receptor type 1 in complex with SB431542 | 分子名称: | 4-[5-(1,3-benzodioxol-5-yl)-4-(pyridin-2-yl)-1H-imidazol-2-yl]benzamide, TGF-beta receptor type-1 | 著者 | Ogunjimi, A.A, Zeqiraj, E, Ceccarelli, D.F, Sicheri, F. | 登録日 | 2011-09-27 | 公開日 | 2012-05-23 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Structural Basis for Specificity of TGFbeta Family Receptor Small Molecule Inhibitors Cell Signal, 24, 2012
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5P2U
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5P39
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5P3M
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5OZQ
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5P41
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2D09
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5P01
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5P4M
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1WWG
| NMR Structure Determined for MLV NC Complex with RNA Sequence UAUCUG | 分子名称: | 5'-R(P*UP*AP*UP*CP*UP*G)-3', Nucleoprotein p10, ZINC ION | 著者 | Dey, A, York, D, Smalls-Mantey, A, Summers, M.F. | 登録日 | 2005-01-05 | 公開日 | 2005-04-05 | 最終更新日 | 2024-05-29 | 実験手法 | SOLUTION NMR | 主引用文献 | Composition and sequence-dependent binding of RNA to the nucleocapsid protein of Moloney murine leukemia virus(,) Biochemistry, 44, 2005
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5P52
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5P0E
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5P5F
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5P0S
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5P5U
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2CUE
| Solution structure of the homeobox domain of the human paired box protein Pax-6 | 分子名称: | Paired box protein Pax6 | 著者 | Ohnishi, S, Kigawa, T, Tochio, N, Tomizawa, T, Koshiba, S, Inoue, M, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI) | 登録日 | 2005-05-26 | 公開日 | 2005-11-26 | 最終更新日 | 2024-05-29 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of the homeobox domain of the human paired box protein Pax-6 To be Published
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1SQO
| Substituted 2-Naphthamidine Inhibitors of Urokinase | 分子名称: | 8-(PYRIMIDIN-2-YLAMINO)NAPHTHALENE-2-CARBOXIMIDAMIDE, SULFATE ION, Urokinase-type plasminogen activator | 著者 | Wendt, M.D, Geyer, A, McClellan, W.J, Rockway, T.W, Weitzberg, M, Zhao, X, Mantei, R, Stewart, K, Nienaber, V, Klinghofer, V, Giranda, V.L. | 登録日 | 2004-03-19 | 公開日 | 2004-04-27 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (1.84 Å) | 主引用文献 | Interaction with the S1beta-pocket of urokinase: 8-heterocycle substituted and 6,8-disubstituted 2-naphthamidine urokinase inhibitors. Bioorg.Med.Chem.Lett., 14, 2004
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5P18
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