3BM9
| Discovery of Benzisoxazoles as Potent Inhibitors of Chaperone Hsp90 | 分子名称: | 4-bromo-6-(6-hydroxy-1,2-benzisoxazol-3-yl)benzene-1,3-diol, Heat shock protein HSP 90-alpha | 著者 | Gopalsamy, A, Shi, M, Vogan, E.M, Golas, J, Jacob, J, Johnson, J, Lee, F, Nilakantan, R, Peterson, R, Svenson, K, Tam, M.S, Wen, Y, Chopra, R, Ellingboe, J, Arndt, K, Boschelli, F. | 登録日 | 2007-12-12 | 公開日 | 2008-07-08 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Discovery of benzisoxazoles as potent inhibitors of chaperone heat shock protein 90. J.Med.Chem., 51, 2008
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3BMY
| Discovery of Benzisoxazoles as Potent Inhibitors of Chaperone Hsp90 | 分子名称: | 4-chloro-6-{5-[(2-morpholin-4-ylethyl)amino]-1,2-benzisoxazol-3-yl}benzene-1,3-diol, Heat shock protein HSP 90-alpha | 著者 | Gopalsamy, A, Shi, M, Vogan, E.M, Golas, J, Jacob, J, Johnson, J, Lee, F, Nilakantan, R, Peterson, R, Svenson, K, Tam, M.S, Wen, Y, Chopra, R, Ellingboe, J, Arndt, K, Boschelli, F. | 登録日 | 2007-12-13 | 公開日 | 2008-07-08 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Discovery of benzisoxazoles as potent inhibitors of chaperone heat shock protein 90. J.Med.Chem., 51, 2008
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5ZYN
| Fumarate reductase | 分子名称: | FLAVIN MONONUCLEOTIDE, FLAVIN-ADENINE DINUCLEOTIDE, Fumarate reductase 2, ... | 著者 | Park, H.H, Kim, C.M. | 登録日 | 2018-05-25 | 公開日 | 2018-10-03 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.75 Å) | 主引用文献 | Molecular basis of maintaining an oxidizing environment under anaerobiosis by soluble fumarate reductase. Nat Commun, 9, 2018
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5EY0
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5EY1
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6T5I
| The Transcriptional Regulator PrfA from Listeria Monocytogenes in complex with inhibitor of WNT production (IWP)-2 | 分子名称: | DIMETHYL SULFOXIDE, Listeriolysin positive regulatory factor A, SODIUM ION, ... | 著者 | Oelker, M, Grundstrom, C, Blumenthal, A, Sauer-Eriksson, A.E. | 登録日 | 2019-10-16 | 公開日 | 2021-10-27 | 最終更新日 | 2024-01-24 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Inhibition of the master regulator of Listeria monocytogenes virulence enables bacterial clearance from spacious replication vacuoles in infected macrophages. Plos Pathog., 18, 2022
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3ZI0
| Structure of Mycobacterium tuberculosis DXR in complex with a fosmidomycin analogue | 分子名称: | 1-DEOXY-D-XYLULOSE 5-PHOSPHATE REDUCTOISOMERASE, MANGANESE (II) ION, [(1S)-1-(3,4-dichlorophenyl)-3-{hydroxy[2-(1H-1,2,4-triazol-1-ylmethyl)benzoyl]amino}propyl]phosphonic acid | 著者 | Bjorkelid, C, Jansson, A.M, Bergfors, T, Unge, T, Mowbray, S.L, Jones, T.A. | 登録日 | 2012-12-30 | 公開日 | 2013-10-09 | 最終更新日 | 2024-05-08 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Dxr Inhibition by Potent Mono- and Disubstituted Fosmidomycin Analogues. J.Med.Chem., 56, 2013
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6YVJ
| EED in complex with a triazolopyrimidine | 分子名称: | GLYCEROL, N-(2,3-dihydro-1-benzofuran-4-ylmethyl)-8-(4-methylsulfonylphenyl)-[1,2,4]triazolo[4,3-c]pyrimidin-5-amine, N-[(5-fluoranyl-2,3-dihydro-1-benzofuran-4-yl)methyl]-8-(2-methylpyridin-3-yl)-[1,2,4]triazolo[4,3-c]pyrimidin-5-amine, ... | 著者 | Read, J.A. | 登録日 | 2020-04-28 | 公開日 | 2021-05-12 | 最終更新日 | 2024-01-24 | 実験手法 | X-RAY DIFFRACTION (1.84 Å) | 主引用文献 | Free energy perturbation in the design of EED ligands as inhibitors of polycomb repressive complex 2 (PRC2) methyltransferase. Bioorg.Med.Chem.Lett., 39, 2021
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6YVI
| EED in complex with a cyano-benzofuran | 分子名称: | 5-fluoranyl-4-[[[8-(2-methylpyridin-3-yl)-[1,2,4]triazolo[4,3-c]pyrimidin-5-yl]amino]methyl]-2,3-dihydro-1-benzofuran-7-carbonitrile, CALCIUM ION, N-(2,3-dihydro-1-benzofuran-4-ylmethyl)-8-(4-methylsulfonylphenyl)-[1,2,4]triazolo[4,3-c]pyrimidin-5-amine, ... | 著者 | Read, J.A. | 登録日 | 2020-04-28 | 公開日 | 2021-05-12 | 最終更新日 | 2024-01-24 | 実験手法 | X-RAY DIFFRACTION (2.26 Å) | 主引用文献 | Free energy perturbation in the design of EED ligands as inhibitors of polycomb repressive complex 2 (PRC2) methyltransferase. Bioorg.Med.Chem.Lett., 39, 2021
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6D8E
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8ZVI
| Structure of the bacteriophage T5 capsid | 分子名称: | Decoration protein, Major capsid protein | 著者 | Peng, Y, Liu, H.R. | 登録日 | 2024-06-11 | 公開日 | 2024-09-04 | 実験手法 | ELECTRON MICROSCOPY (3.4 Å) | 主引用文献 | Structures of Mature and Urea-Treated Empty Bacteriophage T5: Insights into Siphophage Infection and DNA Ejection. Int J Mol Sci, 25, 2024
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9API
| THE S VARIANT OF HUMAN ALPHA1-ANTITRYPSIN, STRUCTURE AND IMPLICATIONS FOR FUNCTION AND METABOLISM | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-2)-alpha-D-mannopyranose-(1-6)-[alpha-D-mannopyranose-(1-3)]alpha-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ALPHA 1-ANTITRYPSIN, ... | 著者 | Loebermann, H, Tokuoka, R, Deisenhofer, J, Huber, R. | 登録日 | 1988-09-08 | 公開日 | 1990-10-15 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (3 Å) | 主引用文献 | The S variant of human alpha 1-antitrypsin, structure and implications for function and metabolism. Protein Eng., 2, 1989
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2QCY
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8V4I
| Structure of bovine anti-HIV Fab ElsE1 | 分子名称: | ElsE1 Fab heavy chain, ElsE1 Fab light chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-11-29 | 公開日 | 2024-09-04 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.81 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultra-long CDRH3 repertoire To Be Published
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8VBR
| Structure of bovine anti-HIV Fab ElsE11 | 分子名称: | Bovine Fab ElsE11 light chain, Bovine Fab Else11 heavy chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.65 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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8VBM
| Structure of bovine anti-HIV Fab ElsE7 | 分子名称: | Bovine Fab ElsE7 heavy chain, Bovine Fab ElsE7 light chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.54 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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8VBK
| Structure of bovine anti-HIV Fab ElsE5 | 分子名称: | Bovine Fab ElsE5 heavy chain, Bovine Fab ElsE5 light chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-09-25 | 実験手法 | X-RAY DIFFRACTION (1.89 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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8VBJ
| Structure of bovine anti-HIV Fab ElsE2 | 分子名称: | Bovine Fab ElsE2 heavy chain, Bovine Fab ElsE2 light chain, POTASSIUM ION, ... | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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8VBN
| Structure of bovine anti-HIV Fab ElsE8 | 分子名称: | Bovine Fab ElsE8 heavy chain, Bovine Fab ElsE8 light chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (1.83 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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8VBP
| Structure of bovine anti-HIV Fab Bess4 | 分子名称: | Bovine Fab Bess4 heavy chain, Bovine Fab Bess4 light chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-09-25 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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8VBQ
| Structure of bovine anti-HIV Fab Bess7 | 分子名称: | Bovine Fab Bess7 heavy chain, Bovine Fab Bess7 light chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-09-25 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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8VBO
| Structure of bovine anti-HIV Fab ElsE9 | 分子名称: | Bovine Fab ElsE9 heavy chain, Bovine Fab ElsE9 light chain, GLYCEROL, ... | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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8VBL
| Structure of bovine anti-HIV Fab ElsE6 | 分子名称: | Bovine Fab ElsE6 heavy chain, Bovine Fab ElsE6 light chain | 著者 | Stanfield, R.L, Wilson, I.A. | 登録日 | 2023-12-12 | 公開日 | 2024-09-04 | 最終更新日 | 2024-09-25 | 実験手法 | X-RAY DIFFRACTION (2.35 Å) | 主引用文献 | Immunization of cows with HIV envelope trimers generates broadly neutralizing antibodies to the V2-apex from the ultralong CDRH3 repertoire. Plos Pathog., 20, 2024
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7LTY
| Bruton's tyrosine kinase in complex with compound 23 | 分子名称: | DIMETHYL SULFOXIDE, Isoform BTK-C of Tyrosine-protein kinase BTK, ~{N}-[(5~{R})-2-[2-[(1-methylpyrazol-4-yl)amino]pyrimidin-4-yl]-6,7,8,9-tetrahydro-5~{H}-benzo[7]annulen-5-yl]-3-propan-2-yloxy-azetidine-1-carboxamide | 著者 | Metrick, C.M, Marcotte, D.J. | 登録日 | 2021-02-20 | 公開日 | 2022-01-12 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (1.69 Å) | 主引用文献 | Discovery and Preclinical Characterization of BIIB091, a Reversible, Selective BTK Inhibitor for the Treatment of Multiple Sclerosis. J.Med.Chem., 65, 2022
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7LTZ
| Bruton's tyrosine kinase in complex with compound 51 | 分子名称: | 1-~{tert}-butyl-~{N}-[(5~{R})-8-[2-[(1-methylpyrazol-4-yl)amino]pyrimidin-4-yl]-2-(oxetan-3-yl)-1,3,4,5-tetrahydro-2-benzazepin-5-yl]-1,2,3-triazole-4-carboxamide, 2,3-DIHYDROXY-1,4-DITHIOBUTANE, ACETATE ION, ... | 著者 | Metrick, C.M, Marcotte, D.J. | 登録日 | 2021-02-20 | 公開日 | 2022-01-12 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (1.53 Å) | 主引用文献 | Discovery and Preclinical Characterization of BIIB091, a Reversible, Selective BTK Inhibitor for the Treatment of Multiple Sclerosis. J.Med.Chem., 65, 2022
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