1UAO
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2RVD
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5AWL
| CRYSTAL STRUCTURE OF A MUTANT OF CHIGNOLIN, CLN025 | 分子名称: | A mutant of Chignolin, CLN025 | 著者 | Akiba, T, Ishimura, M, Odahara, T, Harata, K, Honda, S. | 登録日 | 2015-07-05 | 公開日 | 2015-08-12 | 最終更新日 | 2024-03-20 | 実験手法 | X-RAY DIFFRACTION (1.11 Å) | 主引用文献 | Crystal structure of a ten-amino acid protein J.Am.Chem.Soc., 130, 2008
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6KMC
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2RR7
| Microtubule Binding Domain of DYNEIN-C | 分子名称: | Dynein heavy chain 9 | 著者 | Kato, Y, Yagi, T, Ohki, S, Burgess, S, Honda, S, Kamiya, R, Tanokura, M. | 登録日 | 2010-06-04 | 公開日 | 2011-06-08 | 最終更新日 | 2024-05-01 | 実験手法 | SOLUTION NMR | 主引用文献 | Structure of the microtubule-binding domain of flagellar dynein Structure, 22, 2014
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2RT4
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5ZO6
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5GW9
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5VQG
| Crystal structure of the extended Tudor domain from BmPAPI | 分子名称: | Tudor and KH domain-containing protein homolog | 著者 | Hubbard, P.A, Pan, X, Ohtaki, A, McNally, R, Honda, S, Kirino, Y, Murali, R. | 登録日 | 2017-05-08 | 公開日 | 2017-06-14 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Structural studies of the Tudor domain from the Bombyx homolog of Drosophila PAPI: Implication to piRNA biogenesis To Be Published
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5VY1
| Crystal structure of the extended Tudor domain from BmPAPI | 分子名称: | Tudor and KH domain-containing protein homolog | 著者 | Hubbard, P.A, Pan, X, McNally, R, Ohtaki, A, Honda, S, Kirino, Y, Murali, R. | 登録日 | 2017-05-24 | 公開日 | 2017-06-14 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (3.05 Å) | 主引用文献 | Structural studies of the Tudor domain from the Bombyx homolog of Drosophila PAPI: Implication to piRNA biogenesis To Be Published
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5VQH
| Crystal structure of the extended Tudor domain from BmPAPI in complex with sDMA | 分子名称: | N3, N4-DIMETHYLARGININE, Tudor and KH domain-containing protein homolog | 著者 | Hubbard, P.A, Pan, X, Ohtaki, A, McNally, R, Honda, S, Kirino, Y, Murali, R. | 登録日 | 2017-05-08 | 公開日 | 2017-06-14 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Structural studies of the Tudor domain from the Bombyx homolog of Drosophila PAPI: Implication to piRNA biogenesis To Be Published
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2ZW0
| Crystal structure of a Streptococcal protein G B1 mutant | 分子名称: | Protein LG, SULFATE ION | 著者 | Watanabe, H, Matsumaru, H, Odahara, T, Suto, K, Honda, S. | 登録日 | 2008-11-26 | 公開日 | 2009-03-03 | 最終更新日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | Optimizing pH response of affinity between protein G and IgG Fc: how electrostatic modulations affect protein-protein interactions. J.Biol.Chem., 284, 2009
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2ZW1
| Crystal structure of a Streptococcal protein G B1 mutant | 分子名称: | Protein LG | 著者 | Watanabe, H, Matsumaru, H, Odahara, T, Suto, K, Honda, S. | 登録日 | 2008-11-26 | 公開日 | 2009-03-03 | 最終更新日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Optimizing pH response of affinity between protein G and IgG Fc: how electrostatic modulations affect protein-protein interactions. J.Biol.Chem., 284, 2009
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3WKN
| Crystal structure of the artificial protein AFFinger p17 (AF.p17) complexed with Fc fragment of human IgG | 分子名称: | AFFinger p17, Ig gamma-1 chain C region, beta-D-galactopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-2)-alpha-D-mannopyranose-(1-6)-[2-acetamido-2-deoxy-beta-D-glucopyranose-(1-2)-alpha-D-mannopyranose-(1-3)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose | 著者 | Watanabe, H, Honda, S. | 登録日 | 2013-10-29 | 公開日 | 2014-10-29 | 最終更新日 | 2022-08-24 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Adaptive Assembly: Maximizing the Potential of a Given Functional Peptide with a Tailor-Made Protein Scaffold. Chem.Biol., 22, 2015
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6KDZ
| Crystal structure of PDE10A in complex with a triazolopyrimidine inhibitor | 分子名称: | 4-[2-(5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)ethyl]-3,7,8,10-tetrazatricyclo[7.4.0.0^{2,7}]trideca-1,3,5,8,10,12-hexaen-6-ol, MAGNESIUM ION, ZINC ION, ... | 著者 | Amano, Y, Honbou, K. | 登録日 | 2019-07-03 | 公開日 | 2019-08-14 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (3.1 Å) | 主引用文献 | Synthesis, SAR study, and biological evaluation of novel 2,3-dihydro-1H-imidazo[1,2-a]benzimidazole derivatives as phosphodiesterase 10A inhibitors. Bioorg.Med.Chem., 27, 2019
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1BDD
| STAPHYLOCOCCUS AUREUS PROTEIN A, IMMUNOGLOBULIN-BINDING B DOMAIN, NMR, MINIMIZED AVERAGE STRUCTURE | 分子名称: | STAPHYLOCOCCUS AUREUS PROTEIN A | 著者 | Gouda, H, Torigoe, H, Saito, A, Sato, M, Arata, Y, Shimada, I. | 登録日 | 1996-06-28 | 公開日 | 1997-01-11 | 最終更新日 | 2024-05-22 | 実験手法 | SOLUTION NMR | 主引用文献 | Three-dimensional solution structure of the B domain of staphylococcal protein A: comparisons of the solution and crystal structures. Biochemistry, 31, 1992
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1BDC
| STAPHYLOCOCCUS AUREUS PROTEIN A, IMMUNOGLOBULIN-BINDING B DOMAIN, NMR, 10 STRUCTURES | 分子名称: | STAPHYLOCOCCUS AUREUS PROTEIN A | 著者 | Gouda, H, Torigoe, H, Saito, A, Sato, M, Arata, Y, Shimada, I. | 登録日 | 1996-06-28 | 公開日 | 1997-01-11 | 最終更新日 | 2024-05-22 | 実験手法 | SOLUTION NMR | 主引用文献 | Three-dimensional solution structure of the B domain of staphylococcal protein A: comparisons of the solution and crystal structures. Biochemistry, 31, 1992
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6KE0
| Crystal structure of PDE10A in complex with a triazolopyrimidine inhibitor | 分子名称: | 2-(5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-1-[(2S)-2-methyl-1,2-dihydroimidazo[1,2-a]benzimidazol-3-yl]ethanone, MAGNESIUM ION, ZINC ION, ... | 著者 | Amano, Y, Honbou, K. | 登録日 | 2019-07-03 | 公開日 | 2019-08-14 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.95 Å) | 主引用文献 | Synthesis, SAR study, and biological evaluation of novel 2,3-dihydro-1H-imidazo[1,2-a]benzimidazole derivatives as phosphodiesterase 10A inhibitors. Bioorg.Med.Chem., 27, 2019
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6KDX
| Crystal structure of PDE10A in complex with a triazolopyrimidine inhibitor | 分子名称: | MAGNESIUM ION, N-[2-(5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)ethyl]quinolin-2-amine, ZINC ION, ... | 著者 | Amano, Y, Honbou, K. | 登録日 | 2019-07-03 | 公開日 | 2019-08-14 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.44 Å) | 主引用文献 | Synthesis, SAR study, and biological evaluation of novel 2,3-dihydro-1H-imidazo[1,2-a]benzimidazole derivatives as phosphodiesterase 10A inhibitors. Bioorg.Med.Chem., 27, 2019
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