7WCC

Oxidase ChaP-D49L/Q91C mutant

Summary for 7WCC

• Entry DOI: 10.2210/pdb7wcc/pdb
• Descriptor: ChaP, FE (III) ION (3 entities in total)
• Functional Keywords: chap, oxidative rearrangement steps, mycobacterium tuberculosis, biosynthetic protein
• Biological source: Streptomyces chartreusis
• Total number of polymer chains: 4
• Total formula weight: 57888.37

Authors

Sun, M.X.,Zheng, W.,Wang, Y.S.,Zhu, J.P.,Tan, R.X. (deposition date: 2021-12-19, release date: 2023-05-24, Last modification date: 2024-12-18)

Primary citation

Wang, Y.S.,Zheng, W.,Jiang, N.,Jin, Y.X.,Meng, Z.K.,Sun, M.X.,Zong, Y.L.,Xu, T.,Zhu, J.,Tan, R.X.
Alteration of the Catalytic Reaction Trajectory of a Vicinal Oxygen Chelate Enzyme by Directed Evolution.
Angew.Chem.Int.Ed.Engl., 61:e202201321-e202201321, 2022

PubMed Abstract: The vicinal oxygen chelate (VOC) metalloenzyme superfamily catalyzes a highly diverse set of reactions with the mechanism characterized by the bidentate coordination of vicinal oxygen atoms to metal ion centers, but there remains a lack of a platform to steer the reaction trajectories, especially for o-quinone metabolizing pathways. Herein, we present the directed-evolution-enabled bifunctional turnover of ChaP, which is a homotetramer and represents an unprecedented VOC enzyme class. Unlike the ChaP catalysis of extradiol-like o-quinone cleavage and concomitant α-keto acid decarboxylation, a group of ChaP variants (CVs) catalyze intradiol-like o-quinone deconstruction and CO liberation from the resulting o-hydroxybenzoic acid scaffolds with high regioselectivity. Enzyme crystal structures, labeling experiments and computational simulations corroborated that the D49L mutation allows the metal ion to change its coordination with the tyrosine phenoxy atoms in different monomers, thereby altering the reaction trajectory with the regiospecificity further improved by the follow-up replacement of the Y92 residue with any of alanine, glycine, threonine, and serine. The study highlights the unpredicted catalytic versatility and enzymatic plasticity of VOC enzymes with biotechnological significance.

PubMed: 35415958
DOI: 10.1002/anie.202201321

Experimental method

X-RAY DIFFRACTION (1.5 Å)