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aminopeptidases such APN, ERAP1, ERAP2, and LTA4H, exerted a cognitive-enhancing effect in rodents after icv administration similar to that of Ang IV 1 and LVV-H7 3 ( Figure 9 As deduced from computational docking the S -isomer is the preferred binding mode of the inhibitors although alternative binding conformations were suggested ( 37 , 38 , and 39 into the IRAP structure demonstrated that these inhibitors all bind in the same orientation relative to the active site (Hermans et al., 2015), in contrast to conclusions drawn in previous modeling studies
