Sanada K, et al. (2004) Serine phosphorylation of mCRY1 and mCRY2 by mitogen-activated protein kinase. Genes Cells 9, 697-708 15298678

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.

Click on the protein name to open the protein page, and on the RSD number to open the site page.

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S247-p - CRY1 (mouse) ▲

Modsite: NANSLLAsPtGLSPY SwissProt Entrez-Gene Orthologous residues CRY1 (human): S247‑p, CRY1 (mouse): S247‑p, CRY1 (rat): S247‑p Characterization Methods used to characterize site in vivo:  phospho-antibody Relevant cell lines - cell types - tissues:  COS (fibroblast) [CRY1 (mouse)], COS (fibroblast) [ERK2 (chicken)], COS (fibroblast) [MEK2 (chicken)] Cellular systems studied:  cell lines Species studied:  green monkey Enzymes shown to modify site in vitro:  Type Enzyme KINASE ERK2 (chicken) Upstream Regulation Potential in vivo enzymes for site:  Type Enzyme Evidence Notes KINASE ERK2 (chicken) co-immunoprecipitation

S265-p - CRY2 (mouse) ▲

Modsite: NANSLLAsPTGLSPY SwissProt Entrez-Gene Orthologous residues CRY2 (human): S266‑p, CRY2 (mouse): S265‑p, CRY2 (rat): S265‑p Characterization Methods used to characterize site in vivo:  phospho-antibody Relevant cell lines - cell types - tissues:  COS (fibroblast) [CRY2 (mouse)], COS (fibroblast) [ERK2 (chicken)], COS (fibroblast) [MEK2 (chicken)] Enzymes shown to modify site in vitro:  Type Enzyme KINASE ERK2 (chicken) Upstream Regulation Potential in vivo enzymes for site:  Type Enzyme Evidence Notes KINASE ERK2 (chicken) co-immunoprecipitation