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Enzymatic hydrolysis of the gycosidic linkage in thio-ADP-ribosylated peptide 19 and the O-ribose control. Enzymatic turnover of the peptide was assessed by measuring the AMP release directly (NudT16) or converting released thio-ADPr via NudT5 to AMP. AMP was measured using the AMP-Glo assay (Promega). Reactions were measured in triplicate ± the standard deviation.
