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Thr(649)Ala-AS160 knock-in mutation does not impair contraction/AICAR-induced glucose transport in mouse muscle

AS160 and its closely related protein TBC1D1 have emerged as key mediators for both insulin- and contraction-stimulated muscle glucose uptake through regulating GLUT4 trafficking. Insulin increases AS160 phosphorylation at multiple Akt/PKB consensus sites, including Thr(649), and promotes its bindin...

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Autori principali: Ducommun, Serge, Wang, Hong Yu, Sakamoto, Kei, MacKintosh, Carol, Chen, Shuai
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Physiological Society 2012
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3361978/
https://ncbi.nlm.nih.gov/pubmed/22318952
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpendo.00379.2011
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