Yuan LL, et al. (2006) Acceleration of K+ channel inactivation by MEK inhibitor U0126. Am J Physiol Cell Physiol 290, C165-71 16135544

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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T602-p - Kv4.2 (rat) ▲
Modsite: TAIISIPtPPVTtPE SwissProt Orthologous residues Kv4.2 (human): T602‑p, Kv4.2 (mouse): T602‑p, Kv4.2 (rat): T602‑p Characterization Methods used to characterize site in vivo:  mutation of modification site Relevant cell lines - cell types - tissues:  CHO (fibroblast) Cellular systems studied:  cell lines Species studied:  hamster

T607-p - Kv4.2 (rat) ▲
Modsite: IPtPPVTtPEGDDRP SwissProt Orthologous residues Kv4.2 (human): T607‑p, Kv4.2 (mouse): T607‑p, Kv4.2 (rat): T607‑p Characterization Methods used to characterize site in vivo:  mutation of modification site Relevant cell lines - cell types - tissues:  CHO (fibroblast) Cellular systems studied:  cell lines Species studied:  hamster

S616-p - Kv4.2 (rat) ▲
Modsite: EGDDRPEsPEYSGGN SwissProt Orthologous residues Kv4.2 (human): S616‑p, Kv4.2 (mouse): S616‑p, Kv4.2 (rat): S616‑p Characterization Methods used to characterize site in vivo:  mutation of modification site Relevant cell lines - cell types - tissues:  CHO (fibroblast) Cellular systems studied:  cell lines Species studied:  hamster