Curated Information
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Curated Information Page
PubMed Id: 16775013 
This page summarizes selected information from the article referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2012,40:D261-70). To learn more about the scope of PhosphoSitePlus®, click here.
Ducharme NA, et al. (2006) MARK2/EMK1/Par-1Balpha phosphorylation of Rab11-family interacting protein 2 is necessary for the timely establishment of polarity in Madin-Darby canine kidney cells. Mol Biol Cell 17, 3625-37 16775013
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S227-p - Rab11FIP2 (human)
Orthologous residues
Rab11FIP2 (human): S227‑p, Rab11FIP2 (mouse): S227‑p, Rab11FIP2 (rat): S227‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, immunoprecipitation
 Relevant cell lines - cell types - tissues:  MDCK (epithelial)
 Cellular systems studied:  cell lines
 Species studied:  human
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE MARK2 (human)
Downstream Regulation
 Effect of modification (process):  cytoskeletal reorganization
 Comments:  important for formation of junctional complexes and cell polarity


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