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In HpGGT, mutation of the same threonine residue at position 398 to serine (T398S) and alanine (T398A) resulted in comparable processing rates with respect to native HpGGT ( FIGURE 3 The role of residues present in the immediate vicinity of the cleavage site during autoprocessing was also explored

Watson-Crick base pairing probabilities for each nucleotide were obtained by computing the partition function with ViennaRNA default parameters

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