Curated Information
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Home > Curated Information Page > PubMed Id: 22975325
Christoforides C, et al. (2012) PKD Controls αvβ3 Integrin Recycling and Tumor Cell Invasive Migration through Its Substrate Rabaptin-5. Dev Cell 23, 560-72 22975325
This page summarizes selected information from the record referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2015, 43:D512-20). To learn more about the scope of PhosphoSitePlus®, click here.
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S407-p - RABEP1 (human)
Modsite: DGLRRAQstDsLGts SwissProt Entrez-Gene
Orthologous residues
RABEP1 (human): S407‑p, RABEP1 iso2 (human): S407‑p, RABEP1 (mouse): S407‑p, RABEP1 (rat): S407‑p
Characterization
Methods used to characterize site in vivo mutation of modification site, western blotting
Disease tissue studied:  breast cancer
Relevant cell lines - cell types - tissues:  293 (epithelial), 3T3 (fibroblast), MDA-MB-231 (breast cell)
Cellular systems studied:  cell lines
Species studied:  human
Enzymes shown to modify site in vitro
Type Enzyme
KINASE PRKD1 (human)
Downstream Regulation
Effect of modification (function):  receptor recycling, induced
Effect of modification (process):  cell motility, induced
Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
Rab4 (human) Induces cell motility, induced microscopy-colocalization, co-immunoprecipitation
Comments:  EGFR and integrin recycling; persistent directional migration; invasion into Matrigel