2D7G
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![BU of 2d7g by Molmil](/molmil-images/mine/2d7g) | Crystal structure of the aa complex of the N-terminal domain of PriA | 分子名称: | DNA (5'-D(P*AP*A)-3'), Primosomal protein N' | 著者 | Sasaki, K, Ose, T, Maenaka, K, Masai, H, Kohda, D. | 登録日 | 2005-11-21 | 公開日 | 2006-11-07 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (3.3 Å) | 主引用文献 | Structural basis of the 3'-end recognition of a leading strand in stalled replication forks by PriA. EMBO J., 26, 2007
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2DWN
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![BU of 2dwn by Molmil](/molmil-images/mine/2dwn) | Crystal structure of the PriA protein complexed with oligonucleotides | 分子名称: | DNA (5'-D(*A*G)-3'), Primosomal protein N' | 著者 | Sasaki, K, Ose, T, Tanaka, T, Masai, H, Maenaka, K, Kohda, D. | 登録日 | 2006-08-15 | 公開日 | 2006-11-07 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (3.35 Å) | 主引用文献 | Structural basis of the 3'-end recognition of a leading strand in stalled replication forks by PriA. EMBO J., 26, 2007
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2DWL
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![BU of 2dwl by Molmil](/molmil-images/mine/2dwl) | Crystal structure of the PriA protein complexed with oligonucleotides | 分子名称: | 5'-D(*AP*(DC))-3', Primosomal protein N | 著者 | Sasaki, K, Ose, T, Tanaka, T, Masai, H, Maenaka, K, Kohda, D. | 登録日 | 2006-08-15 | 公開日 | 2006-11-07 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | 主引用文献 | Structural basis of the 3'-end recognition of a leading strand in stalled replication forks by PriA. EMBO J., 26, 2007
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2DWM
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![BU of 2dwm by Molmil](/molmil-images/mine/2dwm) | Crystal structure of the PriA protein complexed with oligonucleotides | 分子名称: | 5'-D(*AP*T)-3', Primosomal protein N | 著者 | Sasaki, K, Ose, T, Tanaka, T, Masai, H, Maenaka, K, Kohda, D. | 登録日 | 2006-08-15 | 公開日 | 2006-11-07 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (3.15 Å) | 主引用文献 | Structural basis of the 3'-end recognition of a leading strand in stalled replication forks by PriA. EMBO J., 26, 2007
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6C4D
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![BU of 6c4d by Molmil](/molmil-images/mine/6c4d) | Structure based design of RIP1 kinase inhibitors | 分子名称: | (3S)-3-(2-benzyl-3-chloro-7-oxo-2,4,5,7-tetrahydro-6H-pyrazolo[3,4-c]pyridin-6-yl)-5-methyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-8-carbonitrile, Receptor-interacting serine/threonine-protein kinase 1 | 著者 | Saikatendu, K.S, Yoshikawa, M. | 登録日 | 2018-01-11 | 公開日 | 2018-03-21 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2.52 Å) | 主引用文献 | Discovery of 7-Oxo-2,4,5,7-tetrahydro-6 H-pyrazolo[3,4- c]pyridine Derivatives as Potent, Orally Available, and Brain-Penetrating Receptor Interacting Protein 1 (RIP1) Kinase Inhibitors: Analysis of Structure-Kinetic Relationships. J. Med. Chem., 61, 2018
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6C3E
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![BU of 6c3e by Molmil](/molmil-images/mine/6c3e) | CRYSTAL STRUCTURE OF RIP1 KINASE BOUND TO INHIBITOR | 分子名称: | 2-benzyl-5-nitro-1H-benzimidazole, Receptor-interacting serine/threonine-protein kinase 1 | 著者 | Saikatendu, K.S, Yoshikawa, M. | 登録日 | 2018-01-09 | 公開日 | 2018-03-21 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Discovery of 7-Oxo-2,4,5,7-tetrahydro-6 H-pyrazolo[3,4- c]pyridine Derivatives as Potent, Orally Available, and Brain-Penetrating Receptor Interacting Protein 1 (RIP1) Kinase Inhibitors: Analysis of Structure-Kinetic Relationships. J. Med. Chem., 61, 2018
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