作者: H Varmus , D Morgan , J M Bishop , J Kaplan , H Hirai
DOI:
关键词: ASK1 、 MAP2K7 、 Serine/threonine-specific protein kinase 、 Biology 、 SH3 domain 、 Proto-oncogene tyrosine-protein kinase Src 、 c-Raf 、 Integrin-linked kinase 、 Biochemistry 、 Cyclin-dependent kinase 2
摘要: The physiological roles, precise locations, and relevant targets of the 60 kD protein-tyrosine kinase encoded by viral cellular src genes p60src are not known, despite intensive study. We describe recent work that bears upon these unresolved problems: (i) p60c-src is phosphorylated during mitosis on threonine serine residues protein mammalian homologue cdc2, suggesting c-src may contribute to phenotype mitotic cells; (ii) multiple regions in amino-terminal portion required for its proper intracellular localization--a short signal myristylation signals association with cytoplasmic granules perinuclear plasma membranes; (iii) (called SH3 SH2) upstream domain modulate behavior complex ways, some mutations SH2 rendering p60 host-dependent transformation. latter mutants prove be powerful tools identifying proteins modify or serve as src-encoded kinases.