9E9H
 
 | Crystal structure of human KRAS G12C covalently bound to DEL triazine compound 5 | 分子名称: | (3S)-N,5-dimethyl-3-({4-[3-(morpholin-4-yl)phenyl]-6-(2-propanoyl-2,6-diazaspiro[3.4]octan-6-yl)-1,3,5-triazin-2-yl}amino)hexanamide, CALCIUM ION, GTPase KRas, ... | 著者 | Mohr, C. | 登録日 | 2024-11-08 | 公開日 | 2025-02-26 | 最終更新日 | 2025-03-05 | 実験手法 | X-RAY DIFFRACTION (1.65 Å) | 主引用文献 | Identification of Structurally Novel KRAS G12C Inhibitors through Covalent DNA-Encoded Library Screening. J.Med.Chem., 68, 2025
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9E9I
 
 | Crystal Structure of human KRAS G12C covalently bound to nopinone-derived naphthol compound 21 | 分子名称: | 1,2-ETHANEDIOL, 1-{6-[(4P,6R,8R)-3-fluoro-4-(3-hydroxynaphthalen-1-yl)-7,7-dimethyl-5,6,7,8-tetrahydro-6,8-methanoquinolin-2-yl]-2,6-diazaspiro[3.4]octan-2-yl}propan-1-one, GUANOSINE-5'-DIPHOSPHATE, ... | 著者 | Mohr, C. | 登録日 | 2024-11-08 | 公開日 | 2025-02-26 | 最終更新日 | 2025-03-05 | 実験手法 | X-RAY DIFFRACTION (1.18 Å) | 主引用文献 | Identification of Structurally Novel KRAS G12C Inhibitors through Covalent DNA-Encoded Library Screening. J.Med.Chem., 68, 2025
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4Z3D
 
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9DM3
 
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9B7A
 
 | Crystal structure of peroxiredoxin 1 with RA | 分子名称: | (2R)-3-(3,4-dihydroxyphenyl)-2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}propanoic acid, Peroxiredoxin-1 | 著者 | Wu, Y, Xu, H, Luo, C. | 登録日 | 2024-03-27 | 公開日 | 2025-01-22 | 実験手法 | X-RAY DIFFRACTION (1.71 Å) | 主引用文献 | Inhibited peroxidase activity of peroxiredoxin 1 by palmitic acid exacerbates nonalcoholic steatohepatitis in male mice. Nat Commun, 16, 2025
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9EQG
 
 | CryoEM structure of human full-length alpha1beta3gamma2L GABA(A)R in complex with GABA and puerarin | 分子名称: | (1R)-2-{[(S)-{[(2S)-2,3-dihydroxypropyl]oxy}(hydroxy)phosphoryl]oxy}-1-[(hexadecanoyloxy)methyl]ethyl (9Z)-octadec-9-enoate, 1,2-DILAUROYL-SN-GLYCERO-3-PHOSPHATE, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Kasaragod, V.B, Aricescu, A.R. | 登録日 | 2024-03-21 | 公開日 | 2024-09-18 | 最終更新日 | 2024-11-06 | 実験手法 | ELECTRON MICROSCOPY (2.4 Å) | 主引用文献 | A brain-to-gut signal controls intestinal fat absorption. Nature, 634, 2024
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5CI9
 
 | Crystal structure of human Tob in complex with inhibitor fragment 6 | 分子名称: | 1-(propan-2-yl)-1H-benzimidazole-5-carboxylic acid, Protein Tob1, SODIUM ION | 著者 | Bai, Y, Tashiro, S, Nagatoishi, S, Suzuki, T, Tsumoto, K, Bartlam, M, Yamamoto, T. | 登録日 | 2015-07-11 | 公開日 | 2015-11-18 | 最終更新日 | 2024-03-20 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Structural basis for inhibition of the Tob-CNOT7 interaction by a fragment screening approach Protein Cell, 6, 2015
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5CI8
 
 | Crystal structure of human Tob in complex with inhibitor fragment 1 | 分子名称: | Protein Tob1, pyrrolo[1,2-a]quinoxalin-4(5H)-one | 著者 | Bai, Y, Tashiro, S, Nagatoishi, S, Suzuki, T, Tsumoto, K, Bartlam, M, Yamamoto, T. | 登録日 | 2015-07-11 | 公開日 | 2015-11-18 | 最終更新日 | 2025-04-09 | 実験手法 | X-RAY DIFFRACTION (2.328 Å) | 主引用文献 | Structural basis for inhibition of the Tob-CNOT7 interaction by a fragment screening approach Protein Cell, 6, 2015
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5HH7
 
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4OAH
 
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4OAG
 
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4OAI
 
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4OAF
 
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5WQN
 
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7XDD
 
 | Cryo-EM structure of EDS1 and PAD4 | 分子名称: | Lipase-like PAD4, Protein EDS1 | 著者 | Huang, S.J, Jia, A.L, Sun, Y, Han, Z.F, Chai, J.J. | 登録日 | 2022-03-26 | 公開日 | 2022-07-13 | 最終更新日 | 2025-06-25 | 実験手法 | ELECTRON MICROSCOPY (2.93 Å) | 主引用文献 | Identification and receptor mechanism of TIR-catalyzed small molecules in plant immunity. Science, 377, 2022
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5WQP
 
 | Crystal structure of a carbonyl reductase from Pseudomonas aeruginosa PAO1 in complex with NADP (condition II) | 分子名称: | NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, NICOTINAMIDE, PHOSPHATE ION, ... | 著者 | Li, S, Wang, Y, Bartlam, M. | 登録日 | 2016-11-27 | 公開日 | 2017-10-04 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Structure and characterization of a NAD(P)H-dependent carbonyl reductase from Pseudomonas aeruginosa PAO1. FEBS Lett., 591, 2017
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5WQO
 
 | Crystal structure of a carbonyl reductase from Pseudomonas aeruginosa PAO1 in complex with NADP (condition I) | 分子名称: | 1,2-ETHANEDIOL, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, Probable dehydrogenase, ... | 著者 | Li, S, Wang, Y, Bartlam, M. | 登録日 | 2016-11-27 | 公開日 | 2017-10-04 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (1.78 Å) | 主引用文献 | Structure and characterization of a NAD(P)H-dependent carbonyl reductase from Pseudomonas aeruginosa PAO1. FEBS Lett., 591, 2017
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5WQM
 
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7XEY
 
 | EDS1-PAD4 complexed with pRib-ADP | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, 5-O-phosphono-beta-D-ribofuranose, ADENOSINE-5'-DIPHOSPHATE, ... | 著者 | Huang, S, Jia, A, Xiao, Y. | 登録日 | 2022-03-31 | 公開日 | 2022-07-13 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.29 Å) | 主引用文献 | Identification and receptor mechanism of TIR-catalyzed small molecules in plant immunity. Science, 377, 2022
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4F3I
 
 | Crystal structure of the first bromodomain of human BRD4 in complex with MS417 inhibitor | 分子名称: | 1,2-ETHANEDIOL, Bromodomain-containing protein 4, methyl [(6S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl]acetate | 著者 | Joshua, J, Zhou, M.-M, Plotnikov, A.N. | 登録日 | 2012-05-09 | 公開日 | 2012-09-12 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | Down-regulation of NF-{kappa}B Transcriptional Activity in HIV-associated Kidney Disease by BRD4 Inhibition. J.Biol.Chem., 287, 2012
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4NY9
 
 | Crystal Structure Of the Human PXR-LBD In Complex With N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-3-hydroxy-3-methylbutanamide | 分子名称: | GLYCEROL, N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-3-hydroxy-3-methylbutanamide, Nuclear receptor subfamily 1 group I member 2 | 著者 | Khan, J.A, Camac, D.M. | 登録日 | 2013-12-10 | 公開日 | 2014-08-27 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Discovery of the CCR1 antagonist, BMS-817399, for the treatment of rheumatoid arthritis. J.Med.Chem., 57, 2014
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7BZJ
 
 | The Discovery of Benzhydrol-Oxaborole Hybrid Derivatives as Leucyl-tRNA Synthetase Inhibitors | 分子名称: | Leucine--tRNA ligase, [(1~{R},5~{R},6~{S},8~{R})-8-(6-aminopurin-9-yl)-4'-[(~{R})-oxidanyl-[4-(2-oxidanylidenepropylsulfanyl)phenyl]methyl]spiro[2,4,7-trioxa-3-boranuidabicyclo[3.3.0]octane-3,7'-7-boranuidabicyclo[4.3.0]nona-1(6),2,4-triene]-6-yl]methoxy-tris(oxidanyl)phosphanium | 著者 | Liu, R.J, Li, H, Wang, E.D, Zhou, H. | 登録日 | 2020-04-28 | 公開日 | 2020-12-09 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Discovery of benzhydrol-oxaborole derivatives as Streptococcus pneumoniae leucyl-tRNA synthetase inhibitors. Bioorg.Med.Chem., 29, 2021
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6IR2
 
 | Crystal structure of red fluorescent protein mCherry complexed with the nanobody LaM2 at 1.4 Angstron resolution | 分子名称: | MCherry fluorescent protein, mCherry's nanobody LaM2 | 著者 | Ding, Y, Wang, Z.Y, Hu, R.T, Chen, X. | 登録日 | 2018-11-09 | 公開日 | 2019-11-13 | 最終更新日 | 2024-11-06 | 実験手法 | X-RAY DIFFRACTION (1.393 Å) | 主引用文献 | Structural insights into the binding of nanobodies LaM2 and LaM4 to the red fluorescent protein mCherry. Protein Sci., 30, 2021
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7DB7
 
 | Crystal structure of Mycobacterium tuberculosis phenylalanyl-tRNA synthetase in complex with compound GDI05-001 | 分子名称: | 1-[3-[2-(1H-indol-3-yl)ethylsulfamoyl]phenyl]-3-(1,3-thiazol-2-yl)urea, Phenylalanine--tRNA ligase alpha subunit, Phenylalanine--tRNA ligase beta subunit, ... | 著者 | Xu, M, Zhang, X, Xu, L, Chen, S. | 登録日 | 2020-10-19 | 公開日 | 2021-01-13 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.71 Å) | 主引用文献 | Re-discovery of PF-3845 as a new chemical scaffold inhibiting phenylalanyl-tRNA synthetase in Mycobacterium tuberculosis . J.Biol.Chem., 2021
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6IR1
 
 | Crystal structure of red fluorescent protein mCherry complexed with the nanobody LaM4 at 1.9 Angstron resolution | 分子名称: | MCherry fluorescent protein, mCherry's nanobody LaM4 | 著者 | Ding, Y, Wang, Z.Y, Hu, R.T, Chen, X. | 登録日 | 2018-11-09 | 公開日 | 2019-11-13 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.919 Å) | 主引用文献 | Structural insights into the binding of nanobodies LaM2 and LaM4 to the red fluorescent protein mCherry. Protein Sci., 30, 2021
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