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. 2020 Feb 10;10:2292. doi: 10.1038/s41598-020-59120-1

Figure 1.

Figure 1

Inhibition of rFAAH and its mutants by URB597 at different molar ratio. (a) Schematic model of rFAAH where the URB597 molecule is highlighted in balls and stick within the active site of one subunit of the enzyme; (b) from left to right: wild-type rFAAH, rFAAH F432A mutant, and rFAAH W445Y mutant specific activities in the presence of URB597 at 1:2 and 1:1 homodimer:inhibitor molar ratios. ***p < 0.0001.