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Here, of note, this new Modigy [28] workflow with four missense mutations was only carried out for those key residue positions in semaglutides backbone and incomplete, because a complete Modigy [28] workflow here would require a total of 3,276,000,000 times of structural modeling by Modeller [29] and ligand-receptor binding affinity (K d ) calculations by Prodigy [30, 31], where the size of the computational task is too huge even for a traditional HPC facility [28]

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