Curated Information
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Home > Curated Information Page > PubMed Id: 21414324
Henkels KM, et al. (2011) Cell Invasion of Highly Metastatic MTLn3 Cancer Cells Is Dependent on Phospholipase D2 (PLD2) and Janus Kinase 3 (JAK3). J Mol Biol 408, 850-62 21414324
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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Y415-p - PLD2 (human)
Modsite: ALGINSGysKRALML SwissProt Entrez-Gene
Orthologous residues
PLD2 (human): Y415‑p, PLD2 (mouse): Y415‑p, PLD2 (rat): Y415‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Disease tissue studied:  breast cancer, lung cancer, non-small cell lung cancer
Relevant cell lines - cell types - tissues:  MCF-7 (breast cell), MDA-MB-231 (breast cell), MTLn3 (breast cell), NCI-H1299 (pulmonary)
Cellular systems studied:  cell lines
Species studied:  human, rat
Enzymes shown to modify site in vitro
Type Enzyme
KINASE JAK3 (human)
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE JAK3 (human) siRNA inhibition of enzyme
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
siRNA decrease JAK3 siRNA
Downstream Regulation
Effect of modification (function):  enzymatic activity, induced
Effect of modification (process):  carcinogenesis, induced, cell motility, induced