https://d1py7umku9kunm.cloudfront.net/assets/1715661/amino_acid_structures.pngHemoglobin aggregates in sickle cell disease due to a mutation that changes a specific glutamate (Glu) to a valine (Val), . What would you expect in the case of a Glu to aspartate (Asp) mutation? The structures of these amino acids are shown below: A. A change in primary structure B. Aggregation similar to sickle cell C. Large-scale disruption of tertiary structureD. Large-scale disruption of quaternary structureE. Little or no effect on three-dimensional structureF. None of the above

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