6X8O
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![BU of 6x8o by Molmil](/molmil-images/mine/6x8o) | BimBH3 peptide tetramer | 分子名称: | Bcl-2-like protein 11, THIOCYANATE ION | 著者 | Robin, A.Y, Westphal, D, Uson, I, Czabotar, P.E. | 登録日 | 2020-06-01 | 公開日 | 2020-09-09 | 最終更新日 | 2021-02-17 | 実験手法 | X-RAY DIFFRACTION (1.31 Å) | 主引用文献 | Biophysical Characterization of Pro-apoptotic BimBH3 Peptides Reveals an Unexpected Capacity for Self-Association. Structure, 29, 2021
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6UVW
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6UWK
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6UWJ
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6UWH
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6UWG
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6UW0
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8G5B
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8G5A
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1JPS
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![BU of 1jps by Molmil](/molmil-images/mine/1jps) | Crystal structure of tissue factor in complex with humanized Fab D3h44 | 分子名称: | immunoglobulin Fab D3H44, heavy chain, light chain, ... | 著者 | Faelber, K, Kirchhofer, D, Presta, L, Kelley, R.F, Muller, Y.A. | 登録日 | 2001-08-03 | 公開日 | 2002-02-03 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | The 1.85 A resolution crystal structures of tissue factor in complex with humanized Fab D3h44 and of free humanized Fab D3h44: revisiting the solvation of antigen combining sites. J.Mol.Biol., 313, 2001
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1JPT
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![BU of 1jpt by Molmil](/molmil-images/mine/1jpt) | Crystal Structure of Fab D3H44 | 分子名称: | immunoglobulin Fab D3H44, heavy chain, immunoglobulin Fab D3h44, ... | 著者 | Faelber, K, Kirchhofer, D, Presta, L, Kelley, R.F, Muller, Y.A. | 登録日 | 2001-08-03 | 公開日 | 2002-02-03 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | The 1.85 A resolution crystal structures of tissue factor in complex with humanized Fab D3h44 and of free humanized Fab D3h44: revisiting the solvation of antigen combining sites. J.Mol.Biol., 313, 2001
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3LE6
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![BU of 3le6 by Molmil](/molmil-images/mine/3le6) | The structure of cyclin dependent kinase 2 (CKD2) with a pyrazolobenzodiazepine inhibitor | 分子名称: | 5-(2-chlorophenyl)-3-methyl-7-nitropyrazolo[3,4-b][1,4]benzodiazepine, Cell division protein kinase 2 | 著者 | Lukacs, C.M, Swain, A, Crowther, R.L, Kammlott, R.U, Liu, J.J. | 登録日 | 2010-01-14 | 公開日 | 2010-11-17 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Pyrazolobenzodiazepines: part I. Synthesis and SAR of a potent class of kinase inhibitors. Bioorg.Med.Chem.Lett., 20, 2010
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