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. 2016 May 4;12(5):e1005585. doi: 10.1371/journal.ppat.1005585

Fig 8. Tunicamycin inhibits MnaA in a concentration-dependent manner.

Fig 8

Representative electropherograms of the MnaA-catalyzed conversion of UDP-ManNAc to UDP-GlcNAc in the absence of tunicamycin (A), in the presence of 100 μM (B) and 200 μM tunicamycin (C). Substrate concentration is 100 μM. Peaks: 1 UDP-ManNAc; 2 UDP-GlcNAc.