◀ Back to GAL
GAL — IKBKG
Text-mined interactions from Literome
Garbati et al., Gene Expr 2008
:
Ser484 and Ser494 in REL are the major sites of IKK phosphorylation in vitro : evidence that
IKK does not directly
enhance GAL4-REL transactivation ... We also show that the previously reported effects of overexpressed IKK and tumor necrosis factor treatment on
GAL4-REL transactivation are
due to
IKK mediated activation of the endogenous NF-kappa B pathway, which increases transcription from kappa B sites in the promoter of a commonly used GAL4 expression vector
Lu et al., Proc Natl Acad Sci U S A 2010
(Disease Models, Animal...) :
CYM2503 potentiated the
galanin stimulated
IP1 accumulation in HEK293 cells stably expressing GalR2 receptor, whereas it exhibited no detectable affinity for the ( 125 ) I galanin binding site of GalR2 receptor, an effect consistent with that of a positive allosteric modulator