7LXR
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1PX4
| E. COLI (LACZ) BETA-GALACTOSIDASE (G794A) WITH IPTG BOUND | 分子名称: | 1-methylethyl 1-thio-beta-D-galactopyranoside, DIMETHYL SULFOXIDE, MAGNESIUM ION, ... | 著者 | Juers, D.H, Hakda, S, Matthews, B.W, Huber, R.E. | 登録日 | 2003-07-02 | 公開日 | 2004-06-15 | 最終更新日 | 2023-08-16 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Structural Basis for the Altered Activity of Gly794 Variants of Escherichia coli Beta-Galactosidase Biochemistry, 42, 2003
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3ZKV
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4BL6
| Bicaudal-D uses a parallel, homodimeric coiled coil with heterotypic registry to co-ordinate recruitment of cargos to dynein | 分子名称: | ARGININE, PROTEIN BICAUDAL D | 著者 | Liu, Y, Salter, H.K, Holding, A.N, Johnson, C.M, Stephens, E, Lukavsky, P.J, Walshaw, J, Bullock, S.L. | 登録日 | 2013-05-02 | 公開日 | 2013-06-12 | 最終更新日 | 2017-07-12 | 実験手法 | X-RAY DIFFRACTION (2.18 Å) | 主引用文献 | Bicaudal-D Uses a Parallel, Homodimeric Coiled Coil with Heterotypic Registry to Coordinate Recruitment of Cargos to Dynein Genes Dev., 27, 2013
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4AXG
| Structure of eIF4E-Cup complex | 分子名称: | EUKARYOTIC TRANSLATION INITIATION FACTOR 4E, PROTEIN CUP | 著者 | Kinkelin, K, Veith, K, Gruenwald, M, Bono, F. | 登録日 | 2012-06-12 | 公開日 | 2012-08-29 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Crystal Structure of a Minimal Eif4E-Cup Complex Revelas a General Mechanism of Eif4E Regulation in Translational Repression RNA, 18, 2012
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8ZQF
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9B1E
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8YE0
| Crystal structure of KgpF prenyltransferase | 分子名称: | 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, LynF/TruF/PatF family peptide O-prenyltransferase, MAGNESIUM ION, ... | 著者 | Hamada, K, Inoue, S, Goto, Y, Suga, H, Ogata, K, Sengoku, T. | 登録日 | 2024-02-21 | 公開日 | 2024-06-19 | 最終更新日 | 2024-09-11 | 実験手法 | X-RAY DIFFRACTION (1.94 Å) | 主引用文献 | De Novo Discovery of Pseudo-Natural Prenylated Macrocyclic Peptide Ligands. Angew.Chem.Int.Ed.Engl., 63, 2024
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6NYV
| Structure of spastin AAA domain in complex with a quinazoline-based inhibitor | 分子名称: | (4S)-2-METHYL-2,4-PENTANEDIOL, N-(3-tert-butyl-1H-pyrazol-5-yl)-2-[(2R)-2-methylpiperazin-1-yl]quinazolin-4-amine, SULFATE ION, ... | 著者 | Pisa, R, Cupido, T, Kapoor, T.M. | 登録日 | 2019-02-12 | 公開日 | 2019-03-27 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (2.425 Å) | 主引用文献 | Designing Allele-Specific Inhibitors of Spastin, a Microtubule-Severing AAA Protein. J. Am. Chem. Soc., 141, 2019
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9C5E
| Covalent Complex Between Parkin Catalytic (Rcat) Domain and Ubiquitin | 分子名称: | E3 ubiquitin-protein ligase parkin, Polyubiquitin-B, ZINC ION | 著者 | Connelly, E.M, Rintala-Dempsey, A.C, Gundogdu, M, Freeman, E.A, Koszela, J, Aguirre, J.D, Zhu, G, Kamarainen, O, Tadayon, R, Walden, H, Shaw, G.S. | 登録日 | 2024-06-06 | 公開日 | 2024-08-14 | 最終更新日 | 2024-10-09 | 実験手法 | SOLUTION NMR | 主引用文献 | Capturing the catalytic intermediates of parkin ubiquitination. Proc.Natl.Acad.Sci.USA, 121, 2024
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9FTQ
| Drosophila golgi alpha-mannosidase II (dGMII) in complex with swainsonine-configured alkyl indolizidine | 分子名称: | Alpha-mannosidase 2, DI(HYDROXYETHYL)ETHER, ZINC ION, ... | 著者 | Bennett, M, Koemans, T, Overkleeft, H.S, Davies, G.J. | 登録日 | 2024-06-25 | 公開日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (2.47 Å) | 主引用文献 | Structure-guided design of C3-branched swainsonine as potent and selective human Golgi alpha-mannosidase (GMII) inhibitor. Chem.Commun.(Camb.), 2024
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9AT8
| Fab 77-stabilized MeV F ectodomain fragment | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Fusion glycoprotein F0, mAB 77 heavy chain, ... | 著者 | Zyla, D, Saphire, E.O. | 登録日 | 2024-02-26 | 公開日 | 2024-07-03 | 最終更新日 | 2024-07-24 | 実験手法 | ELECTRON MICROSCOPY (3.6 Å) | 主引用文献 | A neutralizing antibody prevents postfusion transition of measles virus fusion protein. Science, 384, 2024
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9FTR
| Drosophila golgi alpha-mannosidase II (dGMII) in complex with amide modified swainsonine-configured alkyl indolizidine | 分子名称: | 1,2-ETHANEDIOL, Alpha-mannosidase 2, ZINC ION, ... | 著者 | Bennett, M, Koemans, T, Overkleeft, H.S, Davies, G.J. | 登録日 | 2024-06-25 | 公開日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (2.14 Å) | 主引用文献 | Structure-guided design of C3-branched swainsonine as potent and selective human Golgi alpha-mannosidase (GMII) inhibitor. Chem.Commun.(Camb.), 2024
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9C0O
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9C1U
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8HLS
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6NPW
| SSu72/Sympk in complex with Ser2/Ser5 phosphorylated peptide | 分子名称: | PHOSPHATE ION, Ser2/Ser5 phosphorylated peptide, Ssu72 ortholog, ... | 著者 | Irani, S, Zhang, Y. | 登録日 | 2019-01-18 | 公開日 | 2019-04-24 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (2.486 Å) | 主引用文献 | Structural determinants for accurate dephosphorylation of RNA polymerase II by its cognate C-terminal domain (CTD) phosphatase during eukaryotic transcription. J.Biol.Chem., 294, 2019
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1JYX
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6NRX
| Crystal structure of DIP-eta IG1 homodimer | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Dpr-interacting protein eta, isoform B, ... | 著者 | Cheng, S, Park, Y.J, Kurleto, J.D, Ozkan, E. | 登録日 | 2019-01-24 | 公開日 | 2019-02-06 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Molecular basis of synaptic specificity by immunoglobulin superfamily receptors in Drosophila. Elife, 8, 2019
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6NRQ
| Crystal structure of Dpr10 IG1 bound to DIP-alpha IG1 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Defective proboscis extension response 10, isoform A, ... | 著者 | Cheng, S, Park, Y.J, Kurleto, J.D, Ozkan, E. | 登録日 | 2019-01-24 | 公開日 | 2019-02-06 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Molecular basis of synaptic specificity by immunoglobulin superfamily receptors in Drosophila. Elife, 8, 2019
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6NS1
| Crystal structure of DIP-gamma IG1+IG2 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, Dpr-interacting protein gamma | 著者 | Cheng, S, Park, Y.J, Kurleto, J.D, Ozkan, E. | 登録日 | 2019-01-24 | 公開日 | 2019-02-06 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | Molecular basis of synaptic specificity by immunoglobulin superfamily receptors in Drosophila. Elife, 8, 2019
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6NYW
| Structure of spastin AAA domain N527C mutant in complex with 8-fluoroquinazoline-based inhibitor | 分子名称: | (4S)-2-METHYL-2,4-PENTANEDIOL, ACETATE ION, N-(5-tert-butyl-1H-pyrazol-3-yl)-8-fluoro-2-[(2R)-2-methylpiperazin-1-yl]quinazolin-4-amine, ... | 著者 | Pisa, R, Cupido, T, Kapoor, T.M. | 登録日 | 2019-02-12 | 公開日 | 2019-03-27 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (2.189 Å) | 主引用文献 | Designing Allele-Specific Inhibitors of Spastin, a Microtubule-Severing AAA Protein. J. Am. Chem. Soc., 141, 2019
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6NZV
| Crystal structure of HCV NS3/4A protease in complex with compound 12 | 分子名称: | (1aR,5S,8S,9S,10R,22aR)-5-tert-butyl-N-[(1R,2R)-2-(difluoromethyl)-1-{[(1-methylcyclopropyl)sulfonyl]carbamoyl}cyclopropyl]-9-ethyl-14-methoxy-3,6-dioxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocyclopropa[18,19][1,10,3,6]dioxadiazacyclononadecino[11,12-b]quinoxaline-8-carboxamide, HCV NS3/4A protease, SULFATE ION, ... | 著者 | Appleby, T.C, Taylor, J.G. | 登録日 | 2019-02-14 | 公開日 | 2019-07-10 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.55 Å) | 主引用文献 | Discovery of the pan-genotypic hepatitis C virus NS3/4A protease inhibitor voxilaprevir (GS-9857): A component of Vosevi®. Bioorg.Med.Chem.Lett., 29, 2019
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6NWZ
| Crystal structure of Agd3 a novel carbohydrate deacetylase | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CHLORIDE ION, ... | 著者 | Bamford, N.C, Howell, P.L. | 登録日 | 2019-02-07 | 公開日 | 2020-02-12 | 最終更新日 | 2020-08-26 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Structural and biochemical characterization of the exopolysaccharide deacetylase Agd3 required for Aspergillus fumigatus biofilm formation. Nat Commun, 11, 2020
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6WML
| Human TLR8 bound to the potent agonist, GS-9688 (Selgantolimod) | 分子名称: | (2R)-2-[(2-amino-7-fluoropyrido[3,2-d]pyrimidin-4-yl)amino]-2-methylhexan-1-ol, 2-acetamido-2-deoxy-beta-D-glucopyranose, Toll-like receptor 8, ... | 著者 | Appleby, T.C, Perry, J.K, Mish, M, Villasenor, A.G, Mackman, R.L. | 登録日 | 2020-04-21 | 公開日 | 2021-02-03 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Discovery of GS-9688 (Selgantolimod) as a Potent and Selective Oral Toll-Like Receptor 8 Agonist for the Treatment of Chronic Hepatitis B. J.Med.Chem., 63, 2020
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