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Mutation of key residues in the carnitine-binding site, R471A and Y358A resulted in no measurable currents, making further analysis untenable (Supplementary Table 3, Supplementary Fig
it is a natural byproduct of amino acid consumption
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Dowd CA et al
Additionally, the in silico ADME, pharmacokinetic, and toxicokinetic profiles of the compounds were predicted using computational platforms
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