Curated Information
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Home > Curated Information Page > PubMed Id: 29703898
Shah N, et al. (2018) TAK1 activation of alpha-TAT1 and microtubule hyperacetylation control AKT signaling and cell growth. Nat Commun 9, 1696 29703898
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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S237-p - ATAT1 (human)
Modsite: GDIkPYSsSDREFLK SwissProt Entrez-Gene
Orthologous residues
ATAT1 (human): S237‑p, ATAT1 (mouse): S237‑p, ATAT1 iso2 (mouse): S214‑p, ATAT1 (rat): S237‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mutation of modification site, phospho-antibody, western blotting
Relevant cell lines - cell types - tissues:  COS7 (fibroblast), HeLa (cervical), MEF (fibroblast)
Cellular systems studied:  cell lines
Species studied:  human
Enzymes shown to modify site in vitro
Type Enzyme
KINASE TAK1 (human)
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE TAK1 (human) co-immunoprecipitation, phospho-antibody, pharmacological inhibitor of upstream enzyme, activation of upstream enzyme
Downstream Regulation
Effect of modification (function):  acetylation, enzymatic activity, induced
Effect of modification (process):  cell growth, inhibited