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. 2024 Sep 16;16(12):1989–1998. doi: 10.1038/s41557-024-01603-z

Extended Data Fig. 5. Mass spectra of the nitrile product when AetD reaction was performed with 13C-labelled isotopologues of 5,7-dibromo-L-tryptophan.

Extended Data Fig. 5

a, AetD + 5,7-dibromo-L-tryptophan. b, AetD + [2-13C1]-5,7-dibromo-L-tryptophan. c, AetD + [3-13C1]-5,7-dibromo-L-tryptophan. d, AetD + [1,2,3-13C3]-5,7-dibromo-L-tryptophan. A 1 Da increase in the mass of the nitrile product was observed only when [3-13C1]-5,7-dibromo-L-tryptophan and [1,2,3-13C3]-5,7-dibromo-L-tryptophan were used as substrates, confirming the β-carbon C-3 is retained in the product.