Xiao T, Towb P, Wasserman S A, Sprang S R
The Howard Hughes Medical Institute and Department of Biochemistry, The University of Texas Southwestern Medical Center, Dallas 75235-9050, USA.
Cell. 1999 Nov 24;99(5):545-55. doi: 10.1016/s0092-8674(00)81542-1.
The interaction of the serine/threonine kinase Pelle and adaptor protein Tube through their N-terminal death domains leads to the nuclear translocation of the transcription factor Dorsal and activation of zygotic patterning genes during Drosophila embryogenesis. Crystal structure of the Pelle and Tube death domain heterodimer reveals that the two death domains adopt a six-helix bundle fold and are arranged in an open-ended linear array with plastic interfaces mediating their interactions. The Tube death domain has an insertion between helices 2 and 3, and a C-terminal tail making significant and indispensable contacts in the heterodimer. In vivo assays of Pelle and Tube mutants confirmed that the integrity of the major heterodimer interface is critical to the activity of these molecules.
在果蝇胚胎发育过程中,丝氨酸/苏氨酸激酶Pelle与衔接蛋白Tube通过它们的N端死亡结构域相互作用,导致转录因子Dorsal的核转位以及合子模式基因的激活。Pelle和Tube死亡结构域异二聚体的晶体结构表明,这两个死亡结构域采用六螺旋束折叠,以开放式线性阵列排列,具有介导它们相互作用的可塑性界面。Tube死亡结构域在螺旋2和螺旋3之间有一个插入序列,以及一个在异二聚体中形成重要且不可或缺接触的C端尾巴。对Pelle和Tube突变体的体内试验证实,主要异二聚体界面的完整性对这些分子的活性至关重要。