Protein O-fucosyltransferase 1 (POFUT1) catalyzes the transfer of fucose to threonine or serine residues within epidermal growth factor-like domains (EGF-LDs) and is a therapeutic target for Notch-associated O-glycosylation disorders. Unlike classical inverting glycosyltransferases, POFUT1 employs a catalytic asparagine that tautomerizes to its imidic acid form during the reaction. How the enzyme subsequently restores the canonical amidic form of Asn51 has remained unclear. Here, quantum mechanics/molecular mechanics simulations reveal that active-site water molecules mediate Asn51 retautomerization through a Grotthuss-type proton relay involving a low free energy barrier (-1). This process can occur regardless of the presence of product molecules in the active site, although it is most favorable after product release. These findings elucidate how POFUT1 resets its catalytic machinery after turnover, underscore the essential role of water molecules in enzyme catalysis, and suggest that similar water-mediated strategies may operate in other enzymes in which catalytic residues undergo protonation changes during turnover.
Vidal-Gironès et al. (Fri,) studied this question.