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Discovery of Lysine-Targeted eIF4E Inhibitors through Covalent Docking
分子名称:	3-{(1-oxo-1,2-dihydroisoquinolin-7-yl)[(pyridin-4-yl)methyl]sulfamoyl}benzene-1-sulfonyl fluoride, Eukaryotic translation initiation factor 4E
著者	Wan, X.B, Shoichet, B.K, Taunton, J.
登録日	2019-08-13
公開日	2019-10-23
最終更新日	2024-10-16
実験手法	X-RAY DIFFRACTION (1.79 Å)
主引用文献	Discovery of Lysine-Targeted eIF4E Inhibitors through Covalent Docking. J.Am.Chem.Soc., 142, 2020

Discovery of Lysine-Targeted eIF4E Inhibitors through Covalent Docking
分子名称:	3-{[(4-cyanophenyl)methyl](1-oxo-1,2-dihydroisoquinolin-7-yl)sulfamoyl}benzene-1-sulfonyl fluoride, Eukaryotic translation initiation factor 4E
著者	Wan, X.B, Shoichet, B.K, Taunton, J.
登録日	2019-08-13
公開日	2019-10-16
最終更新日	2024-10-23
実験手法	X-RAY DIFFRACTION (1.96 Å)
主引用文献	Discovery of Lysine-Targeted eIF4E Inhibitors through Covalent Docking. J.Am.Chem.Soc., 142, 2020

Reversible lysine-targeted probes reveal residence time-based kinase selectivity in vivo
分子名称:	6-[(5-cyclopropyl-1~{H}-pyrazol-3-yl)amino]-2-[4-[(3-methyl-4-oxidanyl-phenyl)methyl]piperazin-1-yl]-~{N}-prop-2-ynyl-pyrimidine-4-carboxamide, Aurora kinase A, CHLORIDE ION
著者	Craven, G.B, Wan, X.B, Taunton, J.
登録日	2021-07-31
公開日	2022-06-08
最終更新日	2024-10-09
実験手法	X-RAY DIFFRACTION (2.32 Å)
主引用文献	Reversible lysine-targeted probes reveal residence time-based kinase selectivity. Nat.Chem.Biol., 18, 2022

TssL periplasmic domain
分子名称:	GLYCEROL, Maltose/maltodextrin-binding periplasmic protein,TssL
著者	Ran, T.T, Wang, W.W, Wang, X.B, Xu, D.Q.
登録日	2018-08-06
公開日	2019-06-12
最終更新日	2024-03-27
実験手法	X-RAY DIFFRACTION (2.3 Å)
主引用文献	Crystal structure of the periplasmic domain of TssL, a key membrane component of Type VI secretion system. Int.J.Biol.Macromol., 120, 2018