|
Orthologous residues
|
|
JunD (human): S100‑p, JunD (mouse): S100‑p, JunD (rat): S100‑p
|
|
Characterization
|
|
Methods used to characterize site in vivo:
mutation of modification site, phospho-antibody, western blotting
|
|
Relevant cell lines - cell types - tissues:
'granulosa, luteal'
|
|
Cellular systems studied:
primary cells
|
|
Species studied:
rat
|
|
Upstream Regulation
|
|
Potential in vivo enzymes for site:
|
|
Type
|
Enzyme
|
Evidence
|
Notes
|
|
KINASE
|
ERK1 (rat)
|
phospho-antibody, pharmacological activator of upstream enzyme, pharmacological inhibitor of upstream enzyme
|
|
|
KINASE
|
ERK2 (rat)
|
phospho-antibody, pharmacological activator of upstream enzyme, pharmacological inhibitor of upstream enzyme
|
|
|
|
Treatments, proteins and their effect on site modification:
|
|
Treatments
|
Referenced Treatments
|
Manipulated Protein
|
Referenced Protein
|
Effect
|
Notes
|
|
PGE2a
|
|
|
|
increase
|
|
|
BAPTA-AM
|
PGE2a
|
|
|
inhibit treatment-induced increase
|
|
|
W-7
|
PGE2a
|
|
|
inhibit treatment-induced increase
|
|
|
PD98059
|
PGE2a
|
|
|
inhibit treatment-induced increase
|
|
|
SB203580
|
PGE2a
|
|
|
augment treatment-induced increase
|
|
|
|
Downstream Regulation
|
|
Effect of modification (function):
activation
|
|
Effect of modification (process):
transcription, altered
|