5M1X
| Crystal structure of S. cerevisiae Rfa1 N-OB domain mutant (K45E) | 分子名称: | Replication factor A protein 1 | 著者 | Seeber, A, Hegnauer, A.M, Hustedt, N, Deshpande, I, Poli, J, Eglinger, J, Pasero, P, Gut, H, Shinohara, M, Hopfner, K.P, Shimada, K, Gasser, S.M. | 登録日 | 2016-10-11 | 公開日 | 2016-12-07 | 最終更新日 | 2016-12-14 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | RPA Mediates Recruitment of MRX to Forks and Double-Strand Breaks to Hold Sister Chromatids Together. Mol. Cell, 64, 2016
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5LZ1
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5LZ6
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5LZ3
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8P7A
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2N73
| Solution structure of the ACBD3:PI4KB complex | 分子名称: | Golgi resident protein GCP60, Phosphatidylinositol 4-kinase beta | 著者 | Veverka, V, Hexnerova, R. | 登録日 | 2015-09-02 | 公開日 | 2016-07-20 | 最終更新日 | 2024-05-15 | 実験手法 | SOLUTION NMR | 主引用文献 | Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein. Sci Rep, 6, 2016
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2N72
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5A53
| Crystal Structure of the Rpf2-Rrs1 complex | 分子名称: | REGULATOR OF RIBOSOME BIOSYNTHESIS, RIBOSOME BIOGENESIS PROTEIN RPF2, SULFATE ION | 著者 | Madru, C, Lebaron, S, Blaud, M, Delbos, L, Rety, S, Leulliot, N. | 登録日 | 2015-06-16 | 公開日 | 2015-10-21 | 最終更新日 | 2024-05-08 | 実験手法 | X-RAY DIFFRACTION (2.401 Å) | 主引用文献 | Chaperoning 5S RNA Assembly. Genes Dev., 29, 2015
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5MML
| HYL-20k | 分子名称: | GLY-ILE-LEU-SER-SER-LEU-TRP-LYS-LYS-LEU-LYS-LYS-ILE-ILE-ALA-LYS | 著者 | Hexnerova, R. | 登録日 | 2016-12-10 | 公開日 | 2017-09-06 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | How proteases from Enterococcus faecalis contribute to its resistance to short alpha-helical antimicrobial peptides. Pathog Dis, 75, 2017
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5MMK
| HYL-20 | 分子名称: | GLY-ILE-LEU-SER-SER-LEU-TRP-LYS-LYS-LEU-LYS-LYS-ILE-ILE-ALA-LYS | 著者 | Hexnerova, R. | 登録日 | 2016-12-10 | 公開日 | 2017-09-06 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | How proteases from Enterococcus faecalis contribute to its resistance to short alpha-helical antimicrobial peptides. Pathog Dis, 75, 2017
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6HM8
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6HLT
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6HLV
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6HLN
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6HMV
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6HLW
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3F8S
| Crystal structure of dipeptidyl peptidase IV in complex with inhibitor | 分子名称: | 2-(4-{(3S,5S)-5-[(3,3-difluoropyrrolidin-1-yl)carbonyl]pyrrolidin-3-yl}piperazin-1-yl)pyrimidine, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Ammirati, M.J, Liu, S, Piotrowski, D.W. | 登録日 | 2008-11-13 | 公開日 | 2009-06-23 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (2.43 Å) | 主引用文献 | (3,3-Difluoro-pyrrolidin-1-yl)-[(2S,4S)-(4-(4-pyrimidin-2-yl-piperazin-1-yl)-pyrrolidin-2-yl]-methanone: a potent, selective, orally active dipeptidyl peptidase IV inhibitor. Bioorg.Med.Chem.Lett., 19, 2009
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