Abstract
Members of the YcaO superfamily are among the most common post-translational modification enzymes in natural product biosynthesis, with wide usage in biotechnology and synthetic biology applications. Here, we use domain-swapped chimeras and discovered unstructured regions in cyanobactin YcaOs that guide interactions with the substrates, governing access to interior amino acids in the substrates and explaining the chemoselectivity between PatD and TruD. These results define how the cyanobactin heterocyclases modify exceptionally sequence diverse substrates, yet with a high degree of positional and nucleophile selectivity. (Equation present).
Original language | English (US) |
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Pages (from-to) | 1215–1225 |
Number of pages | 11 |
Journal | ACS chemical biology |
Volume | 17 |
Issue number | 5 |
Early online date | Apr 14 2022 |
DOIs | |
State | Published - May 20 2022 |
ASJC Scopus subject areas
- Biochemistry
- Molecular Medicine