Curated Information
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Home > Curated Information Page > PubMed Id: 37456829
Wang B, et al. (2023) IDH1 K224 acetylation promotes colorectal cancer via miR-9-5p/NHE1 axis-mediated regulation of acidic microenvironment. iScience 26, 107206 37456829
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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K224-ac - IDH1 (human)
Modsite: KKyDGRFkDIFQEIy SwissProt Entrez-Gene
Orthologous residues
IDH1 (human): K224‑ac, IDH1 (mouse): K224‑ac, IDH1 (rat): K224‑ac
Characterization
Methods used to characterize site in vivo immunoprecipitation, mutation of modification site, western blotting
Disease tissue studied:  colorectal cancer, colorectal carcinoma
Relevant cell lines - cell types - tissues:  HCT116 (intestinal), SW480 (intestinal)
Cellular systems studied:  cell lines, tissue
Species studied:  human, mouse
Downstream Regulation
Effect of modification (process):  carcinogenesis, induced, cell growth, induced, cell motility, induced
Comments:  regulation of the acidic microenvironment of CRC cells; K224R cells had a significantly higher pH value than that of the WT cells; regulates expression of miRNA in CRC cells; correlated with NHE1 expression, enhancing hydroxylation; expression of Ago2 and NHE1 protein inCRC cells and tissues
Associated Diseases
Diseases Alterations Comments
colorectal carcinoma increased