Curated Information
Javascript is not enabled on this browser. This site will not work properly without Javascript.
PhosphoSitePlus Homepage PhosphoSitePlus® v6.7.5
Powered by Cell Signaling Technology
Home > Curated Information Page > PubMed Id: 23836560
Cramer-Morales K, et al. (2013) Personalized synthetic lethality induced by targeting RAD52 in leukemias identified by gene mutation and expression profile. Blood 122, 1293-304 23836560
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.
Click on the protein name to open the protein page, and on the RSD number to open the site page.
Download

Y104-p - RAD52 (human)
Modsite: DLNNGKFyVGVCAFV SwissProt Entrez-Gene
Orthologous residues
RAD52 (human): Y104‑p, RAD52 (mouse): Y105‑p
Characterization
Methods used to characterize site in vivo mutation of modification site, western blotting
Relevant cell lines - cell types - tissues:  bone marrow [RAD52 (mouse), homozygous knockout]
Cellular systems studied:  cell lines
Species studied:  mouse
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE BCR-ABL1 (human) co-immunoprecipitation
Downstream Regulation
Effect of modification (process):  DNA repair, induced
Comments:  single-strand annealing but not homologous recombination repair