Curated Information
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Home > Curated Information Page > PubMed Id: 29519959
Kalogeropulou AF, et al. (2018) P62/SQSTM1 is a novel leucine-rich repeat kinase 2 (LRRK2) substrate that enhances neuronal toxicity. Biochem J 475, 1271-1293 29519959
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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T138-p - SQSTM1 (human)
Modsite: CNGPVVGtRYkCsVC SwissProt Entrez-Gene
Orthologous residues
SQSTM1 (human): T138‑p, SQSTM1 iso2 (human): T54‑p, SQSTM1 (mouse): T138‑p, SQSTM1 iso2 (mouse): T138‑p, SQSTM1 (rat): T135‑p, SQSTM1 iso2 (rat): T135‑p, SQSTM1 iso3 (rat): T135‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mass spectrometry, mutation of modification site, phospho-antibody, western blotting
Disease tissue studied:  lung cancer, non-small cell lung cancer, non-small cell lung adenocarcinoma
Relevant cell lines - cell types - tissues:  'neuron, cortical', 293 (epithelial), A549 (pulmonary)
Cellular systems studied:  cell lines
Species studied:  human, rat
Enzymes shown to modify site in vitro
Type Enzyme
KINASE LRRK2 (human)
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE LRRK2 (human) co-immunoprecipitation, pharmacological inhibitor of upstream enzyme, phospho-antibody, transfection of inactive enzyme, transfection of wild-type enzyme
Downstream Regulation
Effect of modification (process):  apoptosis, induced