Brooks-Wilson A R, Ball E, Pawson T
Division of Molecular and Developmental Biology, Mount Sinai Hospital Research Institute, Toronto, Ontario, Canada.
Mol Cell Biol. 1989 May;9(5):2214-9. doi: 10.1128/mcb.9.5.2214-2219.1989.
The P130gag-fps protein-tyrosine kinase of Fujinami sarcoma virus contains an N-terminal fps-specific domain (Nfps) that is important for oncogenicity. The N-terminal 14 amino acids of p60v-src, which direct myristylation and membrane association, can replace the gag-Nfps sequences of P130gag-fps (residues 1 to 635), producing a highly transforming src-fps polypeptide. Conversely, gag-Nfps can restore modest transforming activity to a nonmyristylated v-src polypeptide. These results emphasize the modular construction of protein-tyrosine kinases and indicate that Nfps, possibly in conjunction with gag, functions in the subcellular localization of P130gag-fps.
藤浪肉瘤病毒的P130gag-fps蛋白酪氨酸激酶含有一个对致癌性很重要的N端fps特异性结构域(Nfps)。p60v-src的N端14个氨基酸可指导肉豆蔻酰化和膜结合,它能取代P130gag-fps的gag-Nfps序列(第1至635位氨基酸),产生一种具有高度转化能力的src-fps多肽。相反,gag-Nfps可恢复非肉豆蔻酰化v-src多肽的适度转化活性。这些结果强调了蛋白酪氨酸激酶的模块化结构,并表明Nfps可能与gag协同作用,在P130gag-fps的亚细胞定位中发挥作用。