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9N9A

Crystal structure of Class-3 OPX WzaB from Myxococcus xanthus

Summary for 9N9A
Entry DOI10.2210/pdb9n9a/pdb
DescriptorPolysaccharide export protein, GLYCEROL (3 entities in total)
Functional Keywordspolysaccharide secretion, lipoprotein, opx protein, transport, translocase
Biological sourceMyxococcus xanthus DZ2
Total number of polymer chains1
Total formula weight20228.86
Authors
Mellouk, A.,Calmettes, C. (deposition date: 2025-02-10, release date: 2026-01-28, Last modification date: 2026-02-04)
Primary citationMellouk, A.,Ngo, K.,Kezzo, A.A.,Martini, C.,Franca, T.C.C.,Laplante, S.R.,Islam, S.T.,Calmettes, C.
Mechanism of trans-envelope bacterial polysaccharide secretion in Class-3 outer-membrane polysaccharide export (OPX) protein systems.
Nat Commun, 17:732-732, 2026
Cited by
PubMed Abstract: Bacterial secretion of extracellular polysaccharides is essential for surface colonization, biofilm formation, and pathogenesis. In diderm bacteria, such polymers traverse the periplasm and outer membrane (OM) through outer-membrane polysaccharide export (OPX) proteins that form secretion pores. Among them, Class-3 OPX proteins are the most widespread but lack an OM-spanning pore domain, leaving their mechanisms poorly understood. Here, we characterize WzaB from Myxococcus xanthus as a model for Class-3 OPX-mediated secretion. Structural and molecular dynamics analyses reveal that WzaB exists as a rigid monomer in solution, in contrast to the constitutive octamerization observed in Class-1 OPX proteins. Biochemical, biophysical, and in vivo analyses show that WzaB oligomerizes in a lipidation-dependent manner and directly interacts with the OM porin WzpB and the inner-membrane co-polymerase WzcB, with binding determinants mapped for both partners. Together, these proteins assemble into a trans-envelope polysaccharide secretion complex, redefining OPX function and revealing a distinct translocon architecture for Class-3 OPX systems.
PubMed: 41545361
DOI: 10.1038/s41467-025-67321-3
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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