Structural Insight into the Catalytic Mechanism of the Endoperoxide Synthase FtmOx1

The 2-oxoglutarate (2OG)-dependent non-heme enzyme FtmOx1 catalyzes the endoperoxide biosynthesis of verruculogen. Although several mechanistic studies have been carried out, the catalytic mechanism of FtmOx1 is not well determined owing to the lack of a reliable complex structure of FtmOx1 with fumitremorginB. Herein we provide the X-ray crystal structure of the ternary complex FtmOx1.2OG.fumitremorginB at a resolution of 1.22 angstrom. Our structures show that the binding of fumitremorginB induces significant compression of the active pocket and that Y68 is in close proximity to C26 of the substrate. Further MD simulation and QM/MM calculations support a CarC-like mechanism, in which Y68 acts as the Hatom donor for quenching the C26-centered substrate radical. Our results are consistent with all available experimental data and highlight the importance of accurate complex structures in the mechanistic study of enzymatic catalysis.

Automated summary

This study provides the complex structure of FtmOx1, revealing the interaction between fumitremorginB and the substrate. The results support a CarC-like catalytic mechanism and emphasize the importance of accurate complex structures in the mechanistic study of enzymatic catalysis.