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5EHO

Rapid Discovery of Pyrido[3,4-d]pyrimidine Inhibitors of Monopolar Spindle kinase 1 (MPS1) Using a Structure-Based Hydridization Approach

5EHO の概要
エントリーDOI10.2210/pdb5eho/pdb
関連するPDBエントリー5EH0
分子名称Dual specificity protein kinase TTK, ~{N}8-cyclohexyl-~{N}2-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]pyrido[3,4-d]pyrimidine-2,8-diamine, DIMETHYL SULFOXIDE, ... (4 entities in total)
機能のキーワードspindle assembly checkpoint (sac), oncology target pyrido[3, 4-d]pyrimidine based inhibitors selective against mps1, transferase
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数1
化学式量合計36622.91
構造登録者
主引用文献Innocenti, P.,Woodward, H.L.,Solanki, S.,Naud, N.,Westwood, I.M.,Cronin, N.,Hayes, A.,Roberts, J.,Henley, A.T.,Baker, R.,Faisal, A.,Mak, G.,Box, G.,Valenti, M.,De Haven Brandon, A.,O'Fee, L.,Saville, J.,Schmitt, J.,Burke, R.,van Montfort, R.L.M.,Raymaud, F.I.,Eccles, S.A.,Linardopoulos, S.,Blagg, J.,Hoelder, S.
Rapid Discovery of Pyrido[3,4-d]pyrimidine Inhibitors of Monopolar Spindle kinase 1 (MPS1) Using a Structure-Based Hydridization Approach
To Be Published,
実験手法
X-RAY DIFFRACTION (2.18 Å)
構造検証レポート
Validation report summary of 5eho
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-04-17に公開中

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