Curated Information
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Curated Information Page
PubMed Id: 15557340 
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.
Yamamoto A, et al. (2005) Parkin phosphorylation and modulation of its E3 ubiquitin ligase activity. J Biol Chem 280, 3390-9 15557340
Only sites from this record are displayed on this page. Click on the protein name to open the protein page, and on the RSD number to open the site page. For the complete dataset, click the download button, on the right.
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S101-p - PARK2 (human)
Orthologous residues
PARK2 (human): S101‑p, PARK2 (mouse): S101‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, electrophoretic mobility shift, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  293 (epithelial), 293T (epithelial), SH-SY5Y (neural crest)
 Cellular systems studied:  cell lines
 Species studied:  human
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE CK1A (human)

S131-p - PARK2 (human)
Orthologous residues
PARK2 (human): S131‑p, PARK2 (mouse): S131‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, electrophoretic mobility shift, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  293 (epithelial), 293T (epithelial), SH-SY5Y (neural crest)
 Cellular systems studied:  cell lines
 Species studied:  human

S136-p - PARK2 (human)
Orthologous residues
PARK2 (human): S136‑p, PARK2 (mouse): G136‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, electrophoretic mobility shift, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  293 (epithelial), 293T (epithelial), SH-SY5Y (neural crest)
 Cellular systems studied:  cell lines
 Species studied:  human

S296-p - PARK2 (human)
Orthologous residues
PARK2 (human): S296‑p, PARK2 (mouse): S295‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, electrophoretic mobility shift, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  293 (epithelial), 293T (epithelial), SH-SY5Y (neural crest)
 Cellular systems studied:  cell lines
 Species studied:  human

S378-p - PARK2 (human)
Orthologous residues
PARK2 (human): S378‑p, PARK2 (mouse): D377‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, electrophoretic mobility shift, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  293 (epithelial), 293T (epithelial), SH-SY5Y (neural crest)
 Cellular systems studied:  cell lines
 Species studied:  human
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE CK1A (human)


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