Sicheri F, Kuriyan J
Laboratory of Molecular Biophysics, Howard Hughes Medical Institute, Rockefeller University, New York, NY 10021, USA.
Curr Opin Struct Biol. 1997 Dec;7(6):777-85. doi: 10.1016/s0959-440x(97)80146-7.
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.
最近已确定了三种Src家族酪氨酸激酶的晶体结构。Lck催化结构域的结构已在活性自磷酸化状态下确定。c-Src和Hck更大构建体的结构,包括SH3、SH2和催化结构域以及C末端调节尾巴,已在下调状态下确定,C末端尾巴发生了磷酸化。对这些结构的比较揭示了一种意想不到的机制,即通过SH2、SH3和催化结构域之间的协同相互作用来调节催化活性。