酪氨酸蛋白激酶
原癌基因酪氨酸蛋白激酶Src
SH2域
SH3域
激酶
酪氨酸激酶
磷酸化
酪氨酸
化学
细胞生物学
生物化学
生物
信号转导
作者
Frank Sicheri,John Kuriyan
标识
DOI:10.1016/s0959-440x(97)80146-7
摘要
The crystal structures of three Src-family tyrosine kinases have been determined recently. The structure of the catalytic domain of Lck has been determined in the active autophosphorylated state. The structures of larger constructs of c-Src and Hck, containing the SH3, SH2 and catalytic domains, as well as a C-terminal regulatory tail, have been determined in the down-regulated state, phosphorylated in the C-terminal tail. A comparison of these structures leads to an unanticipated mechanism for the regulation of catalytic activity by cooperative interactions between the SH2, SH3 and catalytic domains.
科研通智能强力驱动
Strongly Powered by AbleSci AI