Abstract
PAK1 plays an important role in proliferation and tumorigenesis, at least partially by promoting ERK phosphorylation of C-RAF (Ser-338) or MEK1 (Ser-298). We observed how that overexpression of a kinase-dead mutant form ofPAK1increased phosphorylation of MEK1/2 (Ser-217/Ser-221) and ERK (Thr- 202/Tyr-204), although phosphorylation of B-RAF (Ser-445) and C-RAF (Ser-338) remained unchanged. Furthermore, increased activation of the PAK1 activator Rac1 induced the formation of a triple complex of Rac1, PAK1, and MEK1 independent of the kinase activity of PAK1. These data suggest that PAK1 can stimulateMEKactivity in a kinase-independent manner, probably by serving as a scaffold to facilitate interaction of C-RAF.
Originalsprog | Engelsk |
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Tidsskrift | Journal of Biological Chemistry |
ISSN | 0021-9258 |
DOI | |
Status | Udgivet - 5 jul. 2013 |