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As expected, mutagenesis of H182 to phenylalanine (FabX H182F) abolished the FabX dehydrogenation ability without significantly interfering with FMN binding (the FMN content remains ~80%) or protein stability (Figs
The other issue was the Aortic defect, that while stable, could be made worse
Schneider C, Okun JG, Schwarz KV, et al
10 , bpaf038 (2025)
Eu 3+ -Eu 2+ can shuttle electrons and recover lead and iodine ions to suppress the formation of defects in PSCs under aging conditions
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