9wzv

Cryo-EM structure of Fks1 with intact active site

spinqualitylabelsall models 9wzv, resolution 3.35Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 9wzv is a 1 chain structure with sequence from Saccharomyces cerevisiae S288C. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: Electron Microscopy, Resolution 3.35Å Ligands: ERG, NAG, POV Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function FKS1_YEAST Alternate catalytic subunit of the 1,3-beta-glucan synthase (GS) complex. Synthesizes 1,3-beta-glucan, a major structural component of the yeast cell wall. Involved in cell wall synthesis, maintenance and remodeling. Publication Abstract from PubMed beta-1,3-glucan synthase is the molecular target for triterpenoid and echinocandin antifungal drugs in clinical. It catalyzes the formation of beta-1,3-glucan, which is the primary component of the fungal cell wall. However, the inhibition mechanism of beta-1,3-glucan synthase by triterpenoid drugs remains unclear. In this study, we report cryo-electron microscopy (cryo-EM) structures of Saccharomyces cerevisiae beta-1,3-glucan synthase Fks1 and Fks2 in the apo state, the triterpenoid drug enfumafungin-bound state, and an open state. Structural analysis along with mutagenesis reveals the enfumafungin binding site, and the mechanism of the clinical drug-resistant mutations of the beta-1,3-glucan synthases. Remarkably, the enfumafungin attaches on a single transmembrane helix TM5 of the beta-1,3-glucan synthases, reorganizes its nearby lipid environment, and stabilizes the enzyme in a specific basal state with intact active site. Moreover, we elucidate that both the basal state and the open state are essential for FKS's glycosyltransferase activity. Our research also shows that Fks2 is highly conserved with Fks1 in terms of structure, activity, and drug inhibition. These findings provide deep insights into the fungal cell wall synthesis, and will facilitate the development of antifungal drugs targeting beta-1,3-glucan synthase. Inhibition mechanism of the fungal beta-1,3-glucan synthases by triterpenoid antifungal drugs.,You ZL, Sun L, Wang LX, Ni YR, Lyu RQ, Chen DD, Yun CH, Song T, Song Y, Bai L Nat Commun. 2026 Feb 4. doi: 10.1038/s41467-026-69114-8. PMID:41639077 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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