bioRxivBiophysics
Structure of a fungal 1,3-β-glucan synthase
C.-R. Zhao, Z.-L. You, D.-d. Chen, J. Hang, Z.-B. Wang, L.-X. Wang, P. Zhao, J. Qiao, C.-H. Yun, L. Bai
Abstract
1,3-{beta}-Glucan is the major component of the fungal cell wall and is synthesized by 1,3-{beta}-glucan synthase located in the plasma membrane, which is a molecular target of anti-fungal drugs echinocandins and the triterpenoid ibrexafungerp. In this study, we report the 3.0-[A] resolution cryo-EM structure of Saccharomyces cerevisiae 1,3-{beta}-glucan synthase, Fks1. The structure reveals a central catalytic region adopting a cellulose synthase fold with a cytosolic conserved GT-A type glycosyltransferase domain and a closed transmembrane glucan-transporting channel. We found that two extracellular disulfide bonds are crucial for Fks1 enzymatic activity. Structural comparison between Fks1 and cellulose synthases and structure-guided mutagenesis studies provided novel insights into the molecular mechanisms of the fungal 1,3-{beta}-glucan synthase.
- organism: yeast
- assay: cryo-EM
- research focus: protein structure prediction
- approach: experimental assay
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