Phosphorylation-dependent activation of TAK1 mitogen-activated protein kinase kinase kinase by TAB1

被引:154
作者
Sakurai, H [1 ]
Miyoshi, H [1 ]
Mizukami, J [1 ]
Sugita, T [1 ]
机构
[1] Tanabe Seiyaku Co Ltd, Discovery Res Lab, Yodogawa Ku, Osaka 5328505, Japan
关键词
TAK1; TAB1; MAP3K; IKK;
D O I
10.1016/S0014-5793(00)01588-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TAK1 is a mitogen-activated protein kinase kinase kinase (MAP3K) that is involved in the c-Jun N-terminal kinase/p38 MAPKs and NF-kappa B signaling pathways. Here, we characterized the molecular mechanisms of TAK1 activation by its specific activator TAB1. Autophosphorylation of two threonine residues in the activation loop of TAK1 was necessary for TAK1 activation. Association with TAK1 and induction of TAK1 autophosphorylation required the C-terminal 24 amino acids of TAB1, but full TAK1 activation required additional C-terminal Ser/Thr rich sequences, These results demonstrated that the association between the kinase domain of TAK1 and the C-terminal TAB1 triggered the phosphorylation-dependent TAK1 activation mechanism. (C) 2000 Federation of European Biochemical Societies.
引用
收藏
页码:141 / 145
页数:5
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