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Crystal structure of human ERK2 complexed with a pyrazolo[3,4-c]pyridazine derivative
Authors:Kinoshita Takayoshi  Warizaya Masaichi  Ohori Makoto  Sato Kentaro  Neya Masahiro  Fujii Takashi
Institution:Exploratory Research Laboratories, Fujisawa Pharmaceutical Co., Ltd, 5-2-3 Tokodai, Tsukuba, Ibaraki 300-2698, Japan. kinotk@b.s.osakafu-u.ac.jp
Abstract:A series of pyrazolopyridazine compounds were briefly investigated as ERK2 inhibitors. The crystal structure of ERK2 complexed with an allyl derivative was determined. The compound induces structural change including movement of the glycine-rich loop and peptide flip between Met108-Glu109. As a result, the newly formed subsite can recognize small hydrophobic substituents but not hydrophilic ones.
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