Curated Information
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Curated Information Page
PubMed Id: 15299017 
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.
Qiao F, et al. (2004) Phosphorylation of fanconi anemia (FA) complementation group G protein, FANCG, at serine 7 is important for function of the FA pathway. J Biol Chem 279, 46035-45 15299017
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S7-p - FANCG (human)
Orthologous residues
FANCG (human): S7‑p, FANCG (mouse): P7‑p
Characterization
 Methods used to characterize site in vivo mass spectrometry, mutation of modification site, phospho-antibody
 Relevant cell lines - cell types - tissues:  HeLa (cervical) [FANCG (human)]
 Cellular systems studied:  cell lines
 Species studied:  human
Upstream Regulation
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
MMC increase
Associated Diseases
Diseases: Alterations: Comments:
Fanconi's anaemia


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