2MLI
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2MO5
| hIFABP-oleate complex | 分子名称: | Fatty acid-binding protein, intestinal, OLEIC ACID | 著者 | Patil, R, Mohanty, B, Headey, S, Porter, C, Scanlon, M. | 登録日 | 2014-04-17 | 公開日 | 2015-04-22 | 最終更新日 | 2024-05-01 | 実験手法 | SOLUTION NMR | 主引用文献 | Structure of oleate bound human intestinal fatty acid binding protein To be Published
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2MJN
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2MEF
| CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME | 分子名称: | LYSOZYME, SODIUM ION | 著者 | Funahashi, J, Takano, K, Yamagata, Y, Yutani, K. | 登録日 | 1998-05-04 | 公開日 | 1998-07-15 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Contribution of amino acid substitutions at two different interior positions to the conformational stability of human lysozyme Protein Eng., 12, 1999
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2LWI
| Solution structure of H-RasT35S mutant protein in complex with Kobe2601 | 分子名称: | 2-(2,4-dinitrophenyl)-N-(4-fluorophenyl)hydrazinecarbothioamide, GTPase HRas, MAGNESIUM ION, ... | 著者 | Araki, M, Tamura, A, Shima, F, Kataoka, T. | 登録日 | 2012-08-01 | 公開日 | 2013-05-22 | 最終更新日 | 2024-05-15 | 実験手法 | SOLUTION NMR | 主引用文献 | In silico discovery of small-molecule Ras inhibitors that display antitumor activity by blocking the Ras-effector interaction. Proc.Natl.Acad.Sci.USA, 110, 2013
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2MMG
| Structural Characterization of the Mengovirus Leader Protein Bound to Ran GTPase by Nuclear Magnetic Resonance | 分子名称: | GTP-binding nuclear protein Ran | 著者 | Bacot-Davis, V.R, Palmenberg, A.C, Cornilescu, C.C, Markley, J.L. | 登録日 | 2014-03-15 | 公開日 | 2014-10-15 | 最終更新日 | 2024-05-15 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structures of Mengovirus Leader protein, its phosphorylated derivatives, and in complex with nuclear transport regulatory protein, RanGTPase. Proc.Natl.Acad.Sci.USA, 111, 2014
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2M1D
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2M8H
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2MGH
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2MGE
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2MNU
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2MGB
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2MMY
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2MJH
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2MEG
| CHANGES IN CONFORMATIONAL STABILITY OF A SERIES OF MUTANT HUMAN LYSOZYMES AT CONSTANT POSITIONS. | 分子名称: | LYSOZYME, SODIUM ION | 著者 | Funahashi, J, Takano, K, Yamagata, Y, Yutani, K. | 登録日 | 1998-05-02 | 公開日 | 1998-07-15 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Contribution of amino acid substitutions at two different interior positions to the conformational stability of human lysozyme Protein Eng., 12, 1999
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2M99
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2LYV
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2MHN
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2M32
| Alpha-1 integrin I-domain in complex with GLOGEN triple helical peptide | 分子名称: | GLOGEN peptide, Integrin alpha-1, MAGNESIUM ION | 著者 | Chin, Y, Headey, S, Mohanty, B, McEwan, P, Swarbrick, J, Mulhern, T, Emsley, J, Simpson, J, Scanlon, M. | 登録日 | 2013-01-07 | 公開日 | 2013-11-06 | 最終更新日 | 2014-02-12 | 実験手法 | SOLUTION NMR | 主引用文献 | The Structure of Integrin alpha 1I Domain in Complex with a Collagen-mimetic Peptide. J.Biol.Chem., 288, 2013
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2M98
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2O3P
| Crystal structure of Pim1 with Quercetin | 分子名称: | 3,5,7,3',4'-PENTAHYDROXYFLAVONE, IMIDAZOLE, Proto-oncogene serine/threonine-protein kinase Pim-1 | 著者 | Holder, S, Zemskova, M, Zhang, C, Tabrizizad, M, Bremer, R, Neidigh, J.W, Lilly, M.B. | 登録日 | 2006-12-01 | 公開日 | 2007-02-13 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.24 Å) | 主引用文献 | Characterization of a potent and selective small-molecule inhibitor of the PIM1 kinase. Mol.Cancer Ther., 6, 2007
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2O52
| Crystal structure of human RAB4B in complex with GDP | 分子名称: | BETA-MERCAPTOETHANOL, GUANOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ... | 著者 | Zhu, H, Tempel, W, Wang, J, Shen, Y, Landry, R, Arrowsmith, C.H, Edwards, A.M, Sundstrom, M, Weigelt, J, Bochkarev, A, Park, H, Structural Genomics Consortium (SGC) | 登録日 | 2006-12-05 | 公開日 | 2006-12-19 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Crystal structure of human RAB4B in complex with GDP To be Published
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2O40
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2O65
| Crystal structure of Pim1 with Pentahydroxyflavone | 分子名称: | 5,7-DIHYDROXY-2-(3,4,5-TRIHYDROXYPHENYL)-4H-CHROMEN-4-ONE, IMIDAZOLE, Proto-oncogene serine/threonine-protein kinase Pim-1 | 著者 | Holder, S, Zemskova, M, Zhang, C, Tabrizizad, M, Bremer, R, Neidigh, J.W, Lilly, M.B. | 登録日 | 2006-12-06 | 公開日 | 2007-02-13 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.85 Å) | 主引用文献 | Characterization of a potent and selective small-molecule inhibitor of the PIM1 kinase. Mol.Cancer Ther., 6, 2007
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2O72
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