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Furthermore, roGFP2 fusion constructs with wild-type and mutant enzymes allow the intracellular analysis of enzyme mechanisms and structure-function relationships 15,34,35,75

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Various structural alterations were made at the N-terminal such as substitution of D-norleucine for L-norleucine, N-acetylation of norleucine, and replacement of norleucine with GABA in order to improve overall stability by reducing susceptibility to aminopeptidases