Curated Information

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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

S227-p - Rab11FIP2 (human)

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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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