5UKH
| Structure of TelC from Streptococcus intermedius B196 | 分子名称: | CALCIUM ION, Uncharacterized protein | 著者 | Whitney, J.C, Ching, M.Q, Bryant, D, Mougous, J.D. | 登録日 | 2017-01-22 | 公開日 | 2017-07-26 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (1.98 Å) | 主引用文献 | A broadly distributed toxin family mediates contact-dependent antagonism between gram-positive bacteria. Elife, 6, 2017
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5FRN
| Crystal structure of the Prototype Foamy Virus (PFV) intasome in complex with magnesium and the INSTI XZ419 (compound 4c) | 分子名称: | 4-azanyl-N-[[2,4-bis(fluoranyl)phenyl]methyl]-1-oxidanyl-2-oxidanylidene-6-(5-oxidanylpentyl)-1,8-naphthyridine-3-carboxamide, 5'-D(*AP*TP*TP*GP*TP*CP*AP*TP*GP*GP*AP*AP*TP*TP *TP*CP*GP*CP*A)-3', 5'-D(*TP*GP*CP*GP*AP*AP*AP*TP*TP*CP*CP*AP*TP*GP *AP*CP*A)-3', ... | 著者 | Maskell, D.P, Pye, V.E, Cherepanov, P. | 登録日 | 2015-12-18 | 公開日 | 2016-02-17 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (2.85 Å) | 主引用文献 | HIV-1 Integrase Strand Transfer Inhibitors with Reduced Susceptibility to Drug Resistant Mutant Integrases. Acs Chem.Biol., 11, 2016
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8S3X
| LIM Domain Kinase 2 (LIMK2) bound to compound 52 | 分子名称: | 4-(5-cyclopropyl-7~{H}-pyrrolo[2,3-d]pyrimidin-4-yl)-~{N}-[3-(3-methoxyphenyl)phenyl]-3,6-dihydro-2~{H}-pyridine-1-carboxamide, LIM domain kinase 2 | 著者 | Mathea, S, Chatterjee, D, Preuss, F, Ple, K, Knapp, S. | 登録日 | 2024-02-20 | 公開日 | 2024-03-06 | 最終更新日 | 2024-09-18 | 実験手法 | X-RAY DIFFRACTION (2.59 Å) | 主引用文献 | Tetrahydropyridine LIMK inhibitors: Structure activity studies and biological characterization. Eur.J.Med.Chem., 271, 2024
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5LNQ
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5UNR
| Structure of rat neuronal nitric oxide synthase heme domain in complex with 3-[(2-aminoquinolin-7-yl)methoxy]-5-((methylamino)methyl)benzonitrile | 分子名称: | 3-[(2-aminoquinolin-7-yl)methoxy]-5-[(methylamino)methyl]benzonitrile, 5,6,7,8-TETRAHYDROBIOPTERIN, ACETATE ION, ... | 著者 | Li, H, Poulos, T.L. | 登録日 | 2017-01-31 | 公開日 | 2017-05-03 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Nitrile in the Hole: Discovery of a Small Auxiliary Pocket in Neuronal Nitric Oxide Synthase Leading to the Development of Potent and Selective 2-Aminoquinoline Inhibitors. J. Med. Chem., 60, 2017
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5LOL
| Glutathione-bound Dehydroascorbate Reductase 2 of Arabidopsis thaliana | 分子名称: | GLUTATHIONE, GLYCEROL, Glutathione S-transferase DHAR2, ... | 著者 | Young, D.R, Pallo, A, Bodra, N, Messens, J. | 登録日 | 2016-08-09 | 公開日 | 2017-06-07 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Arabidopsis thaliana dehydroascorbate reductase 2: Conformational flexibility during catalysis. Sci Rep, 7, 2017
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5LPF
| Kallikrein-related peptidase 10 | 分子名称: | Kallikrein-10, SULFATE ION | 著者 | Goettig, P, Debela, M, Magdolen, V, Bode, W, Brandstetter, H. | 登録日 | 2016-08-12 | 公開日 | 2016-10-05 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Structural basis for the Zn2+ inhibition of the zymogen-like kallikrein-related peptidase 10. Biol.Chem., 397, 2016
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5UO5
| Structure of human neuronal nitric oxide synthase heme domain in complex with (RS)-3-[(2-amino-4-methylquinolin-7-yl)methoxy]-5-(2-(methylamino)propyl)benzonitrile | 分子名称: | 3-[(2-amino-4-methylquinolin-7-yl)methoxy]-5-[(2R)-2-(methylamino)propyl]benzonitrile, 3-[(2-amino-4-methylquinolin-7-yl)methoxy]-5-[(2S)-2-(methylamino)propyl]benzonitrile, 5,6,7,8-TETRAHYDROBIOPTERIN, ... | 著者 | Li, H, Poulos, T.L. | 登録日 | 2017-01-31 | 公開日 | 2017-05-03 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Nitrile in the Hole: Discovery of a Small Auxiliary Pocket in Neuronal Nitric Oxide Synthase Leading to the Development of Potent and Selective 2-Aminoquinoline Inhibitors. J. Med. Chem., 60, 2017
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5FW3
| Crystal structure of SpCas9 variant VRER bound to sgRNA and TGCG PAM target DNA | 分子名称: | CRISPR-ASSOCIATED ENDONUCLEASE CAS9/CSN1, MAGNESIUM ION, NON-TARGET DNA STRAND, ... | 著者 | Anders, C, Bargsten, K, Jinek, M. | 登録日 | 2016-02-11 | 公開日 | 2016-06-15 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Structural Plasticity of Pam Recognition by Engineered Variants of the RNA-Guided Endonuclease Cas9. Mol.Cell, 61, 2016
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6LG7
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7UZ0
| AntiT-tRNA flip UCCA | 分子名称: | AntiT-tRNA flip UCCA, MAGNESIUM ION, STRONTIUM ION | 著者 | Price, I.R, Grigg, J.C, Ke, A. | 登録日 | 2022-05-07 | 公開日 | 2022-06-08 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (3.03 Å) | 主引用文献 | tRNA Fusion to Streamline RNA Structure Determination: Case Studies in Probing Aminoacyl-tRNA Sensing Mechanisms by the T-Box Riboswitch Crystals, 12, 2022
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5FK6
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5LQM
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5UN1
| Crystal structure of GluN1/GluN2B delta-ATD NMDA receptor | 分子名称: | (5S,10R)-5-methyl-10,11-dihydro-5H-5,10-epiminodibenzo[a,d][7]annulene, 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Song, X, Gouaux, E. | 登録日 | 2017-01-30 | 公開日 | 2018-02-07 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (3.6 Å) | 主引用文献 | Mechanism of NMDA receptor channel block by MK-801 and memantine. Nature, 556, 2018
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7U9U
| Crystal structure of human D-amino acid oxidase in complex with inhibitor | 分子名称: | (3R)-3-(5,6-dioxo-1,4,5,6-tetrahydropyrazin-2-yl)-2,3-dihydro-1,4-benzoxathiine-7-carbonitrile, BENZOIC ACID, D-amino-acid oxidase, ... | 著者 | Skene, R.J, Bell, J.A. | 登録日 | 2022-03-11 | 公開日 | 2022-06-08 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (1.66 Å) | 主引用文献 | Discovery of a Novel Class of d-Amino Acid Oxidase Inhibitors Using the Schrodinger Computational Platform. J.Med.Chem., 65, 2022
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5LOH
| Kinase domain of human Greatwall | 分子名称: | 1,2-ETHANEDIOL, CHLORIDE ION, STAUROSPORINE, ... | 著者 | Rajasekaran, M.B, Pearl, L.H, Oliver, A.W. | 登録日 | 2016-08-09 | 公開日 | 2016-09-07 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (3.1 Å) | 主引用文献 | A first generation inhibitor of human Greatwall kinase, enabled by structural and functional characterisation of a minimal kinase domain construct. Oncotarget, 7, 2016
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7U9S
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5UQ2
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5LPE
| Kallikrein-related peptidase 10 complex with Zn2+ | 分子名称: | Kallikrein-10, SULFATE ION, ZINC ION | 著者 | Goettig, P, Debela, M, Magdolen, V, Bode, W, Brandstetter, H. | 登録日 | 2016-08-12 | 公開日 | 2016-10-05 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.65 Å) | 主引用文献 | Structural basis for the Zn2+ inhibition of the zymogen-like kallikrein-related peptidase 10. Biol.Chem., 397, 2016
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5USS
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5LU3
| The Structure of Spirochaeta thermophila CBM64 | 分子名称: | 3,6,9,12,15-pentaoxaoctadecan-17-amine, 4-oxobutanoic acid, CALCIUM ION, ... | 著者 | Correia, M.A.S, Romao, M.J, Carvalho, A.L. | 登録日 | 2016-09-07 | 公開日 | 2017-02-15 | 最終更新日 | 2024-05-08 | 実験手法 | X-RAY DIFFRACTION (1.5 Å) | 主引用文献 | Stability and Ligand Promiscuity of Type A Carbohydrate-binding Modules Are Illustrated by the Structure of Spirochaeta thermophila StCBM64C. J. Biol. Chem., 292, 2017
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7UE9
| Structure of anti-C3d Fab(3d8b) in complex with C3d | 分子名称: | Complement C3dg fragment, Fab heavy chain, Fab light chain, ... | 著者 | Olland, A.M, White, A, Suto, R.K. | 登録日 | 2022-03-21 | 公開日 | 2022-06-08 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (1.75 Å) | 主引用文献 | Development and Optimization of Bifunctional Fusion Proteins to Locally Modulate Complement Activation in Diseased Tissue. Front Immunol, 13, 2022
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6LJI
| X-ray structure of synthetic GB1 domain with mutations K10(DVA), T11V | 分子名称: | Immunoglobulin G-binding protein G | 著者 | Penmatsa, A, Chatterjee, J, Majumder, P, Khatri, B. | 登録日 | 2019-12-16 | 公開日 | 2020-08-12 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (1.843 Å) | 主引用文献 | Increasing protein stability by engineering the n -> pi * interaction at the beta-turn. Chem Sci, 11, 2020
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5LV2
| Crystal structure of mouse CARM1 in complex with inhibitor LH1246 | 分子名称: | 1,2-DIMETHOXYETHANE, 1,2-ETHANEDIOL, 1-METHOXY-2-(2-METHOXYETHOXY)ETHANE, ... | 著者 | Cura, V, Marechal, N, Troffer-Charlier, N, Halby, L, Arimondo, P, Bonnefond, L, Cavarelli, J. | 登録日 | 2016-09-12 | 公開日 | 2017-09-20 | 最終更新日 | 2024-01-17 | 実験手法 | X-RAY DIFFRACTION (2.29 Å) | 主引用文献 | Hijacking DNA methyltransferase transition state analogues to produce chemical scaffolds for PRMT inhibitors. Philos.Trans.R.Soc.Lond.B Biol.Sci., 373, 2018
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5FQN
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