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. 2015 Apr 8;290(22):13710–13724. doi: 10.1074/jbc.M115.646414

FIGURE 1.

FIGURE 1.

Structure and biosynthesis of representative capuramycin-type inhibitors of TL1. A, the CarU and α-d-mannopyranuronate components are found in all capuramycin-type antibiotics. SQ641 and SQ922 are semisynthetic leads prepared from 2b and 1c, respectively. B, prior results from isotopic enrichment studies using the indicated 13C-labeled precursors. The numerical value represents the -fold enrichment at the indicated site relative to a reference carbon.