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Acknowledgements Our work described in this article was supported by grants from the US Parkinson's Disease Foundation, the Swedish Parkinson's Disease Foundation and the Swedish Research Council, and by awards from the Swedish Society for the Neurologically Handicapped and the ke Wiberg Foundation

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The ANT crystal structures in both cytoplasmic-open (c-state) and matrix-open states (m-state) locked by two inhibitors bound at the solute binding site, carboxyatractyloside and bongkrekic acid respectively, highlighted a conserved alternating-access transport mechanism 5 enabled by the conformational change upon solute binding at the central cavity 6,7