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In this study, we sought to use covalent ligand discovery approaches to identify unique ligandable sites within and functional inhibitors for GCL

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The alpha-helical content was 29% and 66% respectively for Cr FAP65AH1 and Cr FAP65AH2 which increased with the substitution of the valine at 2020 and 2231 positions, respectively with proline from 29% for Cr FAP65AH1 to 54% for the variant ( Cr FAP65AH1V12P)