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NMR analysis of four recombinant jerdostatin molecules was assessed to define the structural basis of two naturally occurring gain‐of‐function events: C‐terminal dipeptide processing and mutation of the active residue K21 to arginine. Removal of the highly mobile and a bulky C‐terminal dipeptide produced pronounced chemical shift changes in the sequentially unconnected but spatially nearby α1β1 inhibitory...
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