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In Giardia and Cryptosporidium sp., triosephosphate isomerase 52 , carbamate kinase 53 , and inosine 5-monophosphate dehydrogenase 54 were evaluated as antiprotozoal drug targets

MD simulations demonstrated that, compared to the wild-type PV2 (WT), PV2-C23pAcF exhibited a significantly higher total number of hydrogen bonds in replica 1approximately 80 morewhereas PV2-C96pAcF showed only a slight increase relative to WT (Fig

In general, our results are in line with the literature, finding support for a polysubstance class identification that is similar to, for example, the opioid use class of Votaw and colleagues (2020) 29 and the high past-month polysubstance use of Ellis and colleagues (2023) 59

PMID 28485121