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Collectively, these interlinked mechanisms demonstrate that the Nrf2-Keap1 and NLRP3 pathways form a dynamic regulatory axis in PD, in which redox balance mitochondrial integrity and inflammatory signaling are tightly coupled

We hypothesize that (i) the slow inhibition observed in the biochemical assay with the recombinant protein with some of the compounds is due to their preferential binding to a slowly populated conformer of the NADP + -TGR(H) complex and (ii) this conformer is already populated in the worm cell interior accounting for the more rapid inhibition of TGR observed in ex vivo worms with the slow inhibitors

Predicted aligned error plots (top) and predicted LDDT (local distance difference test) plots (bottom) of human (left) and yeast (right) AlphaFold models

Images of human body and cells was created using Microsoft Copilot AI