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PDB: 78 件

4BI2
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BU of 4bi2 by Molmil
Scaffold Focused Virtual Screening: Prospective Application to the Discovery of TTK Inhibitor
分子名称: 1,2-ETHANEDIOL, 2-(2-(2-(2-(2-(2-ETHOXYETHOXY)ETHOXY)ETHOXY)ETHOXY)ETHOXY)ETHANOL, DUAL SPECIFICITY PROTEIN KINASE TTK, ...
著者Langdon, S.R, Westwood, I.M, van Montfort, R.L.M, Brown, N, Blagg, J.
登録日2013-04-09
公開日2013-05-22
最終更新日2023-12-20
実験手法X-RAY DIFFRACTION (3.11 Å)
主引用文献Scaffold-Focused Virtual Screening: Prospective Application to the Discovery of Ttk Inhibitors.
J.Chem.Inf.Model, 53, 2013
2ZMC
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Crystal structure of human mitotic checkpoint kinase Mps1 catalytic domain apo form
分子名称: 2-(2-(2-(2-(2-(2-ETHOXYETHOXY)ETHOXY)ETHOXY)ETHOXY)ETHOXY)ETHANOL, Dual specificity protein kinase TTK
著者Chu, M.L.H, Chavas, L.M.G, Douglas, K.T, Eyers, P.A, Tabernero, L.
登録日2008-04-16
公開日2008-05-13
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (3.14 Å)
主引用文献Crystal structure of the catalytic domain of the mitotic checkpoint kinase Mps1 in complex with SP600125.
J.Biol.Chem., 283, 2008
5O91
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Crystal structure of human Mps1 (TTK) C604W mutant in complex with Cpd-5
分子名称: 1,2-ETHANEDIOL, Dual specificity protein kinase TTK, ~{N}-(2,6-diethylphenyl)-8-[[2-methoxy-4-(4-methylpiperazin-1-yl)phenyl]amino]-1-methyl-4,5-dihydropyrazolo[4,3-h]quinazoline-3-carboxamide
著者Hiruma, Y, Joosten, R.P, Perrakis, A.
登録日2017-06-15
公開日2017-07-26
最終更新日2024-01-17
実験手法X-RAY DIFFRACTION (3.2 Å)
主引用文献Understanding inhibitor resistance in Mps1 kinase through novel biophysical assays and structures.
J. Biol. Chem., 292, 2017
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件を2024-07-10に公開中

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