6JGX
| Crystal structure of the transcriptional regulator CadR from P. putida in complex with Cadmium(II) and DNA | 分子名称: | CADMIUM ION, CadR, DNA (5'-D(*CP*AP*CP*CP*CP*TP*AP*TP*AP*GP*TP*GP*GP*CP*TP*AP*CP*AP*GP*GP*GP*T)-3'), ... | 著者 | Liu, X.C, Gan, J.H, Chen, H. | 登録日 | 2019-02-15 | 公開日 | 2019-09-25 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.71 Å) | 主引用文献 | Selective cadmium regulation mediated by a cooperative binding mechanism in CadR. Proc.Natl.Acad.Sci.USA, 116, 2019
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6K1H
| Structure of membrane protein | 分子名称: | PTS mannose transporter subunit IID, PTS system mannose-specific EIIC component, alpha-D-mannopyranose | 著者 | Wang, J.W, Zeng, J.W. | 登録日 | 2019-05-10 | 公開日 | 2019-07-10 | 最終更新日 | 2024-03-27 | 実験手法 | ELECTRON MICROSCOPY (3.52 Å) | 主引用文献 | Structure of the mannose transporter of the bacterial phosphotransferase system. Cell Res., 29, 2019
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7W26
| monolignol ferulate transferase | 分子名称: | Ferulate monolignol transferase | 著者 | Xi, L, Shuliu, D, Yue, F, Yi, Z. | 登録日 | 2021-11-22 | 公開日 | 2022-03-30 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.43 Å) | 主引用文献 | Crystal structure of the plant feruloyl-coenzyme A monolignol transferase provides insights into the formation of monolignol ferulate conjugates. Biochem.Biophys.Res.Commun., 594, 2022
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7WUA
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7ECV
| The Csy-AcrIF14 complex | 分子名称: | AcrIF14, CRISPR type I-F/YPEST-associated protein Csy2, CRISPR-associated protein Csy3, ... | 著者 | Zhang, L.X, Feng, Y. | 登録日 | 2021-03-13 | 公開日 | 2021-11-17 | 最終更新日 | 2024-06-05 | 実験手法 | ELECTRON MICROSCOPY (3.43 Å) | 主引用文献 | Insights into the dual functions of AcrIF14 during the inhibition of type I-F CRISPR-Cas surveillance complex. Nucleic Acids Res., 49, 2021
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7DU0
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7ECW
| The Csy-AcrIF14-dsDNA complex | 分子名称: | 54-MER DNA, AcrIF14, CRISPR type I-F/YPEST-associated protein Csy2, ... | 著者 | Zhang, L.X, Feng, Y. | 登録日 | 2021-03-13 | 公開日 | 2021-11-17 | 最終更新日 | 2024-06-05 | 実験手法 | ELECTRON MICROSCOPY (3.1 Å) | 主引用文献 | Insights into the dual functions of AcrIF14 during the inhibition of type I-F CRISPR-Cas surveillance complex. Nucleic Acids Res., 49, 2021
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7XSQ
| Structure of the Craspase | 分子名称: | CHAT domain protein, RAMP superfamily protein, RNA (34-MER), ... | 著者 | Feng, Y, Zhang, L. | 登録日 | 2022-05-15 | 公開日 | 2022-11-09 | 最終更新日 | 2022-12-14 | 実験手法 | ELECTRON MICROSCOPY (2.88 Å) | 主引用文献 | Target RNA activates the protease activity of Craspase to confer antiviral defense. Mol.Cell, 82, 2022
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7XSP
| Structure of gRAMP-target RNA | 分子名称: | RAMP superfamily protein, RNA (35-MER), RNA (5'-R(P*GP*GP*GP*GP*CP*AP*GP*AP*AP*AP*AP*UP*UP*GP*G)-3'), ... | 著者 | Feng, Y, Zhang, L.X. | 登録日 | 2022-05-15 | 公開日 | 2022-11-09 | 最終更新日 | 2022-12-14 | 実験手法 | ELECTRON MICROSCOPY (2.89 Å) | 主引用文献 | Target RNA activates the protease activity of Craspase to confer antiviral defense. Mol.Cell, 82, 2022
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7XT4
| Structure of Craspase-NTR | 分子名称: | CHAT domain protein, RAMP superfamily protein, RNA (34-MER), ... | 著者 | Feng, Y, Zhang, L. | 登録日 | 2022-05-16 | 公開日 | 2022-11-09 | 最終更新日 | 2022-12-14 | 実験手法 | ELECTRON MICROSCOPY (3.08 Å) | 主引用文献 | Target RNA activates the protease activity of Craspase to confer antiviral defense. Mol.Cell, 82, 2022
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7XSR
| Structure of Craspase-target RNA | 分子名称: | CHAT domain protein, RAMP superfamily protein, RNA (34-MER), ... | 著者 | Feng, Y, Zhang, L. | 登録日 | 2022-05-15 | 公開日 | 2022-11-09 | 最終更新日 | 2022-12-14 | 実験手法 | ELECTRON MICROSCOPY (2.97 Å) | 主引用文献 | Target RNA activates the protease activity of Craspase to confer antiviral defense. Mol.Cell, 82, 2022
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7XSS
| Structure of Craspase-CTR | 分子名称: | CHAT domain protein, RAMP superfamily protein, RNA (34-MER), ... | 著者 | Feng, Y, Zang, L.X. | 登録日 | 2022-05-15 | 公開日 | 2022-11-09 | 最終更新日 | 2022-12-14 | 実験手法 | ELECTRON MICROSCOPY (3.2 Å) | 主引用文献 | Target RNA activates the protease activity of Craspase to confer antiviral defense. Mol.Cell, 82, 2022
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7XSO
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1MKS
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6DQ4
| LINKED KDM5A JMJ DOMAIN BOUND TO THE INHIBITOR GSK-J1 | 分子名称: | 3-[[2-pyridin-2-yl-6-(1,2,4,5-tetrahydro-3-benzazepin-3-yl)pyrimidin-4-yl]amino]propanoic acid, DIMETHYL SULFOXIDE, GLYCEROL, ... | 著者 | Horton, J.R, Cheng, X. | 登録日 | 2018-06-10 | 公開日 | 2018-11-21 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.392 Å) | 主引用文献 | Structure-Based Engineering of Irreversible Inhibitors against Histone Lysine Demethylase KDM5A. J. Med. Chem., 61, 2018
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6DQ9
| Linked KDM5A JMJ Domain Bound to the Covalent Inhibitor N69 i.e. [2-((3-acrylamidophenyl)(2-(piperidin-1-yl)ethoxy)methyl)thieno[3,2-b]pyridine-7-carboxylic acid] | 分子名称: | 1,2-ETHANEDIOL, 2-{(R)-[3-(acryloylamino)phenyl][2-(piperidin-1-yl)ethoxy]methyl}thieno[3,2-b]pyridine-7-carboxylic acid, DIMETHYL SULFOXIDE, ... | 著者 | Horton, J.R, Cheng, X. | 登録日 | 2018-06-10 | 公開日 | 2018-11-21 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.748 Å) | 主引用文献 | Structure-Based Engineering of Irreversible Inhibitors against Histone Lysine Demethylase KDM5A. J. Med. Chem., 61, 2018
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6DQ5
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6DQ7
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6DQE
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6DQD
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6R9G
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5IVE
| Linked KDM5A Jmj Domain Bound to the Inhibitor N8 ( 5-methyl-7-oxo-6-(propan-2-yl)-4,7-dihydropyrazolo[1,5-a]pyrimidine-3-carbonitrile) | 分子名称: | 5-methyl-7-oxo-6-(propan-2-yl)-4,7-dihydropyrazolo[1,5-a]pyrimidine-3-carbonitrile, Lysine-specific demethylase 5A, MANGANESE (II) ION | 著者 | Horton, J.R, Cheng, X. | 登録日 | 2016-03-20 | 公開日 | 2016-07-27 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (1.783 Å) | 主引用文献 | Structural Basis for KDM5A Histone Lysine Demethylase Inhibition by Diverse Compounds. Cell Chem Biol, 23, 2016
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5IW0
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7YW5
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5J87
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