Switching an active site helix in dihydrofolate reductase reveals limits to sub-domain modularity
V. Y. Zhao, J. V. Rodrigues, E. R. Lozovsky, D. L. Hartl, E. I. Shakhnovich
This study replaces a helical segment in DHFR with sequences from unrelated proteins, showing that while chimeras fold, their activity and stability are reduced, highlighting limits to sub-domain modularity.
bioRxiv · Jun 18, 2021Biophysics