5WQE
 
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4JR7
 
 | Crystal structure of scCK2 alpha in complex with GMPPNP | 分子名称: | Casein kinase II subunit alpha, MAGNESIUM ION, PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER | 著者 | Liu, H. | 登録日 | 2013-03-21 | 公開日 | 2014-03-05 | 最終更新日 | 2024-03-20 | 実験手法 | X-RAY DIFFRACTION (1.48 Å) | 主引用文献 | The multiple nucleotide-divalent cation binding modes of Saccharomyces cerevisiae CK2 alpha indicate a possible co-substrate hydrolysis product (ADP/GDP) release pathway. Acta Crystallogr.,Sect.D, 70, 2014
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8XV4
 
 | Crystal structure of TTD-PHD domain of UHRF1 in complex with mStella peptide (residues 85-119) | 分子名称: | Developmental pluripotency-associated protein 3, E3 ubiquitin-protein ligase UHRF1, ZINC ION | 著者 | Du, X, Gan, Q, Xu, J, Liu, J. | 登録日 | 2024-01-14 | 公開日 | 2024-11-06 | 最終更新日 | 2025-02-19 | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | 主引用文献 | Defining ortholog-specific UHRF1 inhibition by STELLA for cancer therapy. Nat Commun, 16, 2025
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8XV6
 
 | Crystal structure of PHD domain of UHRF1 in complex with mStella peptide (residues 85-119) | 分子名称: | Developmental pluripotency-associated protein 3, E3 ubiquitin-protein ligase UHRF1, GLYCEROL, ... | 著者 | Du, X, Gan, Q, Xu, J, Liu, J. | 登録日 | 2024-01-14 | 公開日 | 2024-11-06 | 最終更新日 | 2025-02-19 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Defining ortholog-specific UHRF1 inhibition by STELLA for cancer therapy. Nat Commun, 16, 2025
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8XV7
 
 | Crystal structure of TTD-PHD domain of UHRF1 in complex with hStella peptide (residues 75-121) | 分子名称: | ACETIC ACID, Developmental pluripotency-associated protein 3, E3 ubiquitin-protein ligase UHRF1, ... | 著者 | Du, X, Gan, Q, Xu, J, Liu, J. | 登録日 | 2024-01-14 | 公開日 | 2024-11-06 | 最終更新日 | 2025-02-19 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Defining ortholog-specific UHRF1 inhibition by STELLA for cancer therapy. Nat Commun, 16, 2025
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5X8U
 
 | Crystal Structure of the wild Human ROR gamma Ligand Binding Domain. | 分子名称: | Nuclear receptor ROR-gamma, Nuclear receptor coactivator 1 | 著者 | Noguchi, M, Nomura, A, Murase, K, Doi, S, Yamaguchi, K, Adachi, T. | 登録日 | 2017-03-03 | 公開日 | 2017-06-07 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Ternary complex of human ROR gamma ligand-binding domain, inverse agonist and SMRT peptide shows a unique mechanism of corepressor recruitment Genes Cells, 22, 2017
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5X8Q
 
 | Crystal Structure of the mutant Human ROR gamma Ligand Binding Domain With rockogenin. | 分子名称: | (1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosane-6,2'-oxane]-10,16-diol, Nuclear receptor ROR-gamma, Nuclear receptor corepressor 2 | 著者 | Noguchi, M, Nomura, A, Murase, K, Doi, S, Yamaguchi, K, Adachi, T. | 登録日 | 2017-03-03 | 公開日 | 2017-06-07 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Ternary complex of human ROR gamma ligand-binding domain, inverse agonist and SMRT peptide shows a unique mechanism of corepressor recruitment Genes Cells, 22, 2017
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4K7F
 
 | Newly identified epitope V60 from HBV core protein complexed with HLA-A*0201 | 分子名称: | Beta-2-microglobulin, Core protein, HLA class I histocompatibility antigen, ... | 著者 | Meng, S.D, Zhang, Y, Wu, Y, Qi, J.X. | 登録日 | 2013-04-17 | 公開日 | 2013-06-05 | 最終更新日 | 2024-11-20 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | The L60V variation in hepatitis B virus core protein elicits new epitope-specific cytotoxic T lymphocytes and enhances viral replication. J.Virol., 87, 2013
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5V47
 
 | Crystal structure of the SR1 domain of lizard sacsin | 分子名称: | Lizard sacsin, SULFATE ION | 著者 | Pan, T, Menade, M, Kozlov, G, Gehring, K. | 登録日 | 2017-03-08 | 公開日 | 2017-05-24 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (1.84 Å) | 主引用文献 | Structures of ubiquitin-like (Ubl) and Hsp90-like domains of sacsin provide insight into pathological mutations. J. Biol. Chem., 293, 2018
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6K1P
 
 | The complex of ISWI-nucleosome in the ADP.BeF-bound state | 分子名称: | ADENOSINE-5'-DIPHOSPHATE, BERYLLIUM TRIFLUORIDE ION, DNA (167-MER), ... | 著者 | Yan, L.J, Wu, H, Li, X.M, Gao, N, Chen, Z.C. | 登録日 | 2019-05-10 | 公開日 | 2019-05-29 | 最終更新日 | 2024-09-25 | 実験手法 | ELECTRON MICROSCOPY (3.87 Å) | 主引用文献 | Structures of the ISWI-nucleosome complex reveal a conserved mechanism of chromatin remodeling. Nat.Struct.Mol.Biol., 26, 2019
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5VSX
 
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7WW2
 
 | Structure of an Isocytosine specific deaminase Vcz | 分子名称: | 8-oxoguanine deaminase, ZINC ION | 著者 | Li, X.J, Wu, B.X. | 登録日 | 2022-02-12 | 公開日 | 2023-02-22 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Structural characterization of an isocytosine-specific deaminase VCZ reveals its application potential in the anti-cancer therapy. Iscience, 26, 2023
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5X8W
 
 | Crystal Structure of the mutant Human ROR gamma Ligand Binding Domain. | 分子名称: | Nuclear receptor ROR-gamma, Nuclear receptor coactivator 1 | 著者 | Noguchi, M, Nomura, A, Murase, K, Doi, S, Yamaguchi, K, Adachi, T. | 登録日 | 2017-03-03 | 公開日 | 2017-06-07 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Ternary complex of human ROR gamma ligand-binding domain, inverse agonist and SMRT peptide shows a unique mechanism of corepressor recruitment Genes Cells, 22, 2017
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6JYL
 
 | The crosslinked complex of ISWI-nucleosome in the ADP.BeF-bound state | 分子名称: | ADENOSINE-5'-DIPHOSPHATE, BERYLLIUM TRIFLUORIDE ION, DNA (167-MER), ... | 著者 | Yan, L.J, Wu, H, Li, X.M, Gao, N, Chen, Z.C. | 登録日 | 2019-04-26 | 公開日 | 2019-05-29 | 最終更新日 | 2024-03-27 | 実験手法 | ELECTRON MICROSCOPY (3.37 Å) | 主引用文献 | Structures of the ISWI-nucleosome complex reveal a conserved mechanism of chromatin remodeling. Nat.Struct.Mol.Biol., 26, 2019
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4K69
 
 | Crystal Structure of Human Chymase in Complex with Fragment Linked Benzimidazolone Inhibitor: (3S)-3-{3-[(6-bromo-2-oxo-2,3-dihydro-1H-indol-4-yl)methyl]-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl}hexanoic acid | 分子名称: | (3S)-3-{3-[(6-bromo-2-oxo-2,3-dihydro-1H-indol-4-yl)methyl]-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl}hexanoic acid, 2-acetamido-2-deoxy-beta-D-glucopyranose, Chymase, ... | 著者 | Collins, B.K, Padyana, A.K. | 登録日 | 2013-04-15 | 公開日 | 2013-05-29 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (1.5 Å) | 主引用文献 | Discovery of Potent, Selective Chymase Inhibitors via Fragment Linking Strategies. J.Med.Chem., 56, 2013
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5X8X
 
 | Crystal Structure of the mutant Human ROR gamma Ligand Binding Domain With Compound A. | 分子名称: | (3R,4R)-4-[4-cyclopropyl-5-[3-(2-methylpropyl)cyclobutyl]-1,2,4-triazol-3-yl]-N-(2,4-dimethylphenyl)-1-ethanoyl-pyrrolidine-3-carboxamide, Nuclear receptor ROR-gamma, Nuclear receptor corepressor 2 | 著者 | Noguchi, M, Nomura, A, Murase, K, Doi, S, Yamaguchi, K, Adachi, T. | 登録日 | 2017-03-03 | 公開日 | 2017-06-07 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Ternary complex of human ROR gamma ligand-binding domain, inverse agonist and SMRT peptide shows a unique mechanism of corepressor recruitment Genes Cells, 22, 2017
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4KR1
 
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4J99
 
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6L7A
 
 | CsgFG complex in Curli biogenesis system | 分子名称: | CsgF, Curli production assembly/transport protein CsgG | 著者 | Yan, Z.F, Yin, M, Chen, J.N, Li, X.M. | 登録日 | 2019-11-01 | 公開日 | 2020-01-15 | 最終更新日 | 2024-03-27 | 実験手法 | ELECTRON MICROSCOPY (3.38 Å) | 主引用文献 | Assembly and substrate recognition of curli biogenesis system. Nat Commun, 11, 2020
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4QQ5
 
 | Crystal Structure of FGF Receptor (FGFR) 4 Kinase Harboring the V550L Gate-Keeper Mutation in Complex With FIIN-2, an Irreversible Tyrosine Kinase Inhibitor Capable of Overcoming FGFR Kinase Gate-Keeper Mutations | 分子名称: | Fibroblast growth factor receptor 4, N-(4-{[3-(3,5-dimethoxyphenyl)-7-{[4-(4-methylpiperazin-1-yl)phenyl]amino}-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl]methyl}phenyl)propanamide | 著者 | Huang, Z, Mohammadi, M. | 登録日 | 2014-06-26 | 公開日 | 2014-10-29 | 最終更新日 | 2024-11-20 | 実験手法 | X-RAY DIFFRACTION (2.203 Å) | 主引用文献 | DFG-out Mode of Inhibition by an Irreversible Type-1 Inhibitor Capable of Overcoming Gate-Keeper Mutations in FGF Receptors. Acs Chem.Biol., 10, 2015
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4JPO
 
 | 5A resolution structure of Proteasome Assembly Chaperone Hsm3 in complex with a C-terminal fragment of Rpt1 | 分子名称: | 26S protease regulatory subunit 7 homolog, DNA mismatch repair protein HSM3 | 著者 | Lovell, S, Battaile, K.P, Singh, R, Roelofs, J. | 登録日 | 2013-03-19 | 公開日 | 2013-04-10 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (5 Å) | 主引用文献 | Reconfiguration of the proteasome during chaperone-mediated assembly. Nature, 497, 2013
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4J96
 
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4HZ0
 
 | Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. | 分子名称: | 7-(1H-imidazol-1-yl)-2-(pyridin-3-yl)[1,3]thiazolo[5,4-d]pyrimidin-5-amine, DNA topoisomerase 4 subunit B, MAGNESIUM ION | 著者 | Bensen, D.C, Trzoss, M, Tari, L.W. | 登録日 | 2012-11-14 | 公開日 | 2013-02-13 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Pyrrolopyrimidine inhibitors of DNA gyrase B (GyrB) and topoisomerase IV (ParE). Part I: Structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. Bioorg.Med.Chem.Lett., 23, 2013
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7F2S
 
 | Crystal structure of anti S-gatifloxacin antibody Fab fragment apo form | 分子名称: | 1,2-ETHANEDIOL, Antibody Fab fragment heavy chain, Antibody Fab fragment light chain, ... | 著者 | Wang, L.T, Jiao, W.Y, Shen, X, Lei, H.T. | 登録日 | 2021-06-14 | 公開日 | 2021-12-29 | 最終更新日 | 2024-11-06 | 実験手法 | X-RAY DIFFRACTION (2.62 Å) | 主引用文献 | Conformational adaptability determining antibody recognition to distomer: structure analysis of enantioselective antibody against chiral drug gatifloxacin Rsc Adv, 11, 2021
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7F35
 
 | Crystal structure of anti S-gatifloxacin antibody Fab fragment in complex with S-gatifloxacin | 分子名称: | 1,2-ETHANEDIOL, 1-cyclopropyl-6-fluoro-8-methoxy-7-[(3S)-3-methylpiperazin-1-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, Antibody Fab fragment heavy chain, ... | 著者 | Wang, L.T, Jiao, W.Y, Shen, X, Lei, H.T. | 登録日 | 2021-06-15 | 公開日 | 2021-12-29 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Conformational adaptability determining antibody recognition to distomer: structure analysis of enantioselective antibody against chiral drug gatifloxacin Rsc Adv, 11, 2021
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