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Thus, ASD is characterized by an imbalance of the processes of mitochondrial fusion, fission, and mitophagy that leads to contamination of the brain with dysfunctional mitochondrial fragments, insufficient energy supply to the brain tissues, and as a result, impairments of memory and synaptic function [187] contributing to ASD pathogenesis

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The secondary structure analysis of the predicted structures (except DrugBank peptides) revealed that the peptide residues frequently belong to loop regions (~32%), followed by helix (~30%), turns (~17%) and bends (~19%)

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