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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

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Reducing the levels of proinflammatory molecules like mCRP and nnCRP (331, 332) will further reduce the detrimental effects of inflammaging