Curated Information
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Home > Curated Information Page > PubMed Id: 24829506
Schweikhard ES, Kempson SA, Ziegler C, Burckhardt BC (2014) Mutation of a single threonine in the cytoplasmic NH2 terminus disrupts trafficking of renal betaine-GABA transporter 1 during hypertonic stress. Am J Physiol Renal Physiol 307, F107-15 24829506
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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T40-p - SLC6A12 (dog)
Modsite: VKDRGQWtNKMEFVL SwissProt Entrez-Gene
Orthologous residues
SLC6A12 (human): T40‑p, SLC6A12 (mouse): T40‑p, SLC6A12 iso2 (mouse): T54‑p, SLC6A12 (rat): T40‑p, SLC6A12 (dog): T40‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mutation of modification site, phospho-antibody, western blotting
Relevant cell lines - cell types - tissues:  MDCK (epithelial)
Cellular systems studied:  cell lines
Species studied:  dog
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE PKCA (human) co-immunoprecipitation, activation of upstream enzyme, phospho-antibody
Downstream Regulation
Effect of modification (function):  activity, induced, intracellular localization
Comments:  important for trafficking and insertion of SLC6A12 in the plasma membrane