Curated Information
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Curated Information Page
PubMed Id: 12239280 
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.
Grønborg M, et al. (2002) A mass spectrometry-based proteomic approach for identification of serine/threonine-phosphorylated proteins by enrichment with phospho-specific antibodies: identification of a novel protein, Frigg, as a protein kinase A substrate. Mol Cell Proteomics 1, 517-27 12239280
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.
Download Sites

S12-p - SUN2 (human) ▲
Orthologous residues
SUN2 (human): S12‑p, SUN2 iso3 (human): S12‑p, SUN2 (mouse): S12‑p, SUN2 (rat): S12‑p
Characterization
 Methods used to characterize site in vivo:  immunoprecipitation, mass spectrometry
 Relevant cell lines - cell types - tissues:  HeLa (cervical)
 Cellular systems studied:  cell lines
 Species studied:  human
 Enzymes shown to modify site in vitro: 
Type Enzyme
KINASE PKACa (human)

S54-p - SUN2 (human) ▲
Orthologous residues
SUN2 (human): S54‑p, SUN2 iso3 (human): S54‑p, SUN2 (mouse): S55‑p, SUN2 (rat): S54‑p
Characterization
 Methods used to characterize site in vivo:  immunoprecipitation, mass spectrometry
 Relevant cell lines - cell types - tissues:  HeLa (cervical)
 Cellular systems studied:  cell lines
 Species studied:  human
 Enzymes shown to modify site in vitro: 
Type Enzyme
KINASE PKACa (human)

S116-p - SUN2 (human) ▲
Orthologous residues
SUN2 (human): S116‑p, SUN2 iso3 (human): S116‑p, SUN2 (mouse): N126‑p, SUN2 (rat): N125‑p
Characterization
 Methods used to characterize site in vivo:  immunoprecipitation, mass spectrometry
 Relevant cell lines - cell types - tissues:  HeLa (cervical)
 Cellular systems studied:  cell lines
 Species studied:  human
 Enzymes shown to modify site in vitro: 
Type Enzyme
KINASE PKACa (human)


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