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Orthologous residues
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ACTN1 (human): Y12‑p, ACTN1 (mouse): Y12‑p, ACTN1 iso3 (mouse): Y12‑p, ACTN1 (rat): Y12‑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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Relevant cell lines - cell types - tissues:
COS (fibroblast), MEF (fibroblast) [PTP1B (mouse)]
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Cellular systems studied:
cell lines
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Species studied:
monkey, mouse
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Comments:
MEF PTP 1B -/-
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Downstream Regulation
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Effect of modification (function):
molecular association, regulation, phosphorylation
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Effect of modification (process):
cell motility, altered
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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
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Consequences (function)
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Consequences (process)
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Detection assays
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Src (human)
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Induces
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molecular association, regulation
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pull-down assay, co-immunoprecipitation
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Comments:
Phosphorylation of ACTN1 Y12 is required for PTP 1B to dephosphorylate FAK Y397. Y12F mutation or no expression of ACTN1 significantly decreases the FAK Y397 dephosphorylation by PTP 1B. Src's binding to phospho-Y12 ACTN1 competes with Src's binding to FAK.
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