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3I5Z

Crystal structure of ERK2 bound to (S)-N-(2-hydroxy-1-phenylethyl)-4-(5-methyl-2-(phenylamino)pyrimidin-4-yl)-1H-pyrrole-2-carboxamide

3I5Z の概要
エントリーDOI10.2210/pdb3i5z/pdb
関連するPDBエントリー3I60
分子名称Mitogen-activated protein kinase 1, SULFATE ION, N-[(1S)-2-hydroxy-1-phenylethyl]-4-[5-methyl-2-(phenylamino)pyrimidin-4-yl]-1H-pyrrole-2-carboxamide, ... (4 entities in total)
機能のキーワードkinase, inhibitor, atp-binding, cell cycle, host-virus interaction, nucleotide-binding, phosphoprotein, serine/threonine-protein kinase, transferase
由来する生物種Homo sapiens (human)
細胞内の位置Cytoplasm, cytoskeleton, spindle : P28482
タンパク質・核酸の鎖数1
化学式量合計44413.73
構造登録者
Jacobs, M.D.,Xie, X. (登録日: 2009-07-06, 公開日: 2010-01-12, 最終更新日: 2024-04-03)
主引用文献Aronov, A.M.,Tang, Q.,Martinez-Botella, G.,Bemis, G.W.,Cao, J.,Chen, G.,Ewing, N.P.,Ford, P.J.,Germann, U.A.,Green, J.,Hale, M.R.,Jacobs, M.,Janetka, J.W.,Maltais, F.,Markland, W.,Namchuk, M.N.,Nanthakumar, S.,Poondru, S.,Straub, J.,ter Haar, E.,Xie, X.
Structure-guided design of potent and selective pyrimidylpyrrole inhibitors of extracellular signal-regulated kinase (ERK) using conformational control.
J.Med.Chem., 52:6362-6368, 2009
Cited by
PubMed: 19827834
DOI: 10.1021/jm900630q
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.2 Å)
構造検証レポート
Validation report summary of 3i5z
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2024-07-24に公開中

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