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Orthologous residues
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rictor (human): T1135‑p, rictor (mouse): T1135‑p, rictor (rat): T1120‑p
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Characterization
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Methods used to characterize site in vivo:
mass spectrometry, mutation of modification site, phospho-antibody, western blotting
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Disease tissue studied:
liver cancer
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Relevant cell lines - cell types - tissues:
293 (epithelial), 3T3-L1 (fibroblast), C2C12 (myoblast), HepG2 (hepatic)
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Cellular systems studied:
cell lines
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Species studied:
human, mouse
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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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p70S6K (human)
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siRNA inhibition of enzyme
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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
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Effect
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Notes
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insulin
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increase
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rapamycin
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insulin
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|
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inhibit treatment-induced increase
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Downstream Regulation
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Effect of modification (function):
molecular association, regulation, phosphorylation
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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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|
14-3-3 beta (human)
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Induces
|
|
|
pull-down assay, co-immunoprecipitation
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Comments:
cells expressing Rictor T1135A exhibit an increase in insulin-stimulated Akt-S473 and TSC2-T1462 phosphorylation
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