9vbt

Cryo-EM structure of the multi-component acyltransferase complex MucABC from Streptococcus macacae at a stoichiometric ratio of 4:4:4

spinqualitylabelsall models 9vbt, resolution 2.32Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 9vbt is a 12 chain structure with sequence from Streptococcus. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: Electron Microscopy, Resolution 2.32Å Ligands: SCY, ZN Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function G5JW76_9STRE Publication Abstract from PubMed The functional diversification of biosynthetic enzymes underlies the chemical richness of natural products, yet how primary metabolic enzymes evolve to acquire specialized functions in secondary metabolism remains elusive. Here, we report a tripartite enzyme complex from oral Streptococcus species-comprising 3-hydroxy-3-methylglutaryl (HMG)-CoA synthase (HMGS), acetyl-CoA acetyltransferase (ACAT), and a DUF35 protein-that catalyzes an unusual Friedel-Crafts C-acetylation on a pyrrolidine-2,4-dione scaffold, completing the biosynthesis of the antibiotic reutericyclin A. Cryo-electron microscopy of the S. macacae-derived thiolase complex (SmaATase) reveals a conserved architecture resembling the archaeal HMGS/ACAT/DUF35 complex involved in the mevalonate pathway, yet with key catalytic residues rewired to reprogram substrate specificity. Biochemical characterization, molecular modeling, and evolutionary analysis confirmed that the ancestral activity of HMG-CoA synthesis has been lost, while the complex has been repurposed to mediate Friedel-Crafts C-acylation of small molecule acceptors. These findings reveal a rare example of thiolase complex neofunctionalization, shedding light on an underexplored trajectory in enzyme evolution and offering a template for engineering C-C bond-forming catalysts in synthetic biology. Evolutionary repurposing of a metabolic thiolase complex enables antibiotic biosynthesis.,Liao G, Sun R, Shen Z, Luo Z, Pang C, Shen Z, Wei A, Mi C, Wu G, Li F, Li YX, Hoi KK, Pan X, Tang X Nat Commun. 2026 Jan 30. doi: 10.1038/s41467-026-68910-6. PMID:41617701 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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