J Clin Endocrinol Metab 89 : 31313137 Reisch N et al
Interestingly, the residues at multiple positions (12, 16, 17, 20, 21, 24 and 28) of the multi-targeting agonists are highly solvent-accessible and of limited contact with GLP-1R, allowing them to employ distinct amino acids from GLP-1 without altering GLP-1R signaling profiles
Nygrd: None
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Here, we show that substitution of phenylalanine for leucine at position 973 in the IR decreases IRS-1/PI3K/Akt/mTORC1 signaling, upregulates Shc/Gab1/MAPK signaling and cell cyclerelated pathways, and decreases ligand-stimulated receptor internalization in vitro
