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Orthologous residues
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ASK1 (human): Y718‑p, ASK1 iso5 (human): Y798‑p, ASK1 (mouse): Y725‑p, ASK1 (rat): Y689‑p
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Characterization
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Enzymes shown to modify site in vitro:
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Upstream Regulation
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Potential in vivo enzymes for site:
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Type
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Enzyme
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Evidence
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Notes
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KINASE
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JAK2 (human)
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phospho-antibody, mutation in upstream enzyme recognition motif, co-immunoprecipitation, activation of upstream enzyme, transfection of wild-type enzyme
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PHOSPHATASE
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SHP-2 (human)
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co-immunoprecipitation, transfection of inactive enzyme, transfection of wild-type enzyme
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Comments:
"substrate trapping" mutant
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Treatments, proteins and their effect on site modification:
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Treatments
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Referenced Treatments
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Manipulated Protein
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Referenced Protein
|
Effect
|
Notes
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IFN-beta
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no change compared to control
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wild-type
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TNF
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|
|
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no change compared to control
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IFN-gamma
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|
|
|
increase
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|
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IFN-beta
|
|
|
|
no change compared to control
|
SOCS1 KO
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|
TNF
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|
|
|
increase
|
|
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IFN-gamma
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|
|
|
increase
|
|
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IFN-gamma
|
|
|
|
no change compared to control
|
SHP2-KO
|
|
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Downstream Regulation
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Effect of modification (function):
molecular association, regulation, protein degradation
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Modification regulates interactions with:
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|
Interacting molecule
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Interacting domains
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Effect
|
Consequences (function)
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Consequences (process)
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Detection assays
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SOCS1 (human)
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|
Induces
|
molecular association, regulation
|
|
co-immunoprecipitation
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|
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Comments:
SHP2 dephosphorylation of ASK1 Y798 disrupts binding of ASK1 to SOCS1 and induces apoptosis.
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