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Orthologous residues
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FOXO1A (human): S256‑p, FOXO1A (mouse): S253‑p, FOXO1A (rat): S250‑p
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Characterization
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Methods used to characterize site in vivo:
mutation of modification site
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Disease tissue studied:
liver cancer
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Relevant cell lines - cell types - tissues:
HepG2 (hepatic)
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Cellular systems studied:
cell lines
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Species studied:
human
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Downstream Regulation
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Effect of modification (function):
inhibition
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Effect of modification (process):
transcription, altered
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Comments:
Phosphorylation of FKHR at Ser256 is required to disrupt IRS-dependent transactivation by FOXO1A.
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