9QHK image
Deposition Date 2025-03-15
Release Date 2026-03-11
Last Version Date 2026-04-08
Entry Detail
PDB ID:
9QHK
Title:
Nucleotide-free wild type Wzm-Wzt from Mycobacterium abscessus in nanodiscs
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
3.57 Å
Aggregation State:
PARTICLE
Reconstruction Method:
SINGLE PARTICLE
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:ABC transporter permease
Chain IDs:A, B
Chain Length:307
Number of Molecules:2
Biological Source:Mycobacteroides abscessus
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:ABC transporter ATP-binding p
Chain IDs:C, D
Chain Length:263
Number of Molecules:2
Biological Source:Mycobacteroides abscessus
Ligand Molecules
Primary Citation
Structural basis of lipid-linked galactan export by the mycobacterial ABC transporter Wzm-Wzt.
Nat Commun 17 ? ? (2026)
PMID: 41839883 DOI: 10.1038/s41467-026-70429-9

Abstact

Mycobacteria, including Mycobacterium tuberculosis, possess a unique cell envelope containing arabinogalactan, a heteropolysaccharide critical for cell wall integrity and target of several tuberculosis drugs. The cytosolic precursor of arabinogalactan, lipid-linked galactan (LLG), is translocated across the plasma membrane by the essential ABC transporter Wzm-Wzt through a molecular mechanism that is poorly understood. Here, we present a series of cryo-EM structures of Wzm-Wzt from Mycobacterium abscessus, representing different conformations of the transport cycle. Conserved residues lining the proposed LLG translocation pathway were investigated by three orthologous functional assays, revealing that the cytosolic gate helix (GH) plays a key functional role in polysaccharide transport. Our data suggests that the hydrophobic polyprenyl-moiety is translocated first, followed by the galactan-polysaccharide, which requires Wzm-Wzt to open a continuous channel through which the sugar chain is ratcheted at the expense of ATP hydrolysis. Our results provide a rational basis for the development of drugs that inhibit mycobacterial cell wall biosynthesis.

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Primary Citation of related structures
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