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9G98

Joint neutron and x-ray structure of alginate lyase PsAlg7C soaked with pentamannuronic acid

Replaces:  8RBN
Summary for 9G98
Entry DOI10.2210/pdb9g98/pdb
Related9G99
DescriptorAlginate lyase, 4-deoxy-alpha-L-erythro-hex-4-enopyranuronic acid-(1-4)-beta-D-mannopyranuronic acid, beta-D-mannopyranuronic acid-(1-4)-alpha-D-mannopyranuronic acid-(1-4)-beta-D-mannopyranuronic acid, ... (4 entities in total)
Functional Keywordsalginate lyase, complex, beta jellyroll, alginate, lyase
Biological sourceParadendryphiella salina
Total number of polymer chains1
Total formula weight26037.47
Authors
Wilkens, C.,Meilleur, F.,Morth, J.P. (deposition date: 2024-07-24, release date: 2025-07-30)
Primary citationRivas-Fernandez, J.P.,Vuillemin, M.,Pilgaard, B.,Klau, L.J.,Fredslund, F.,Lund-Hanssen, C.,Welner, D.H.,Meyer, A.S.,Morth, J.P.,Meilleur, F.,Aachmann, F.L.,Rovira, C.,Wilkens, C.
Unraveling the molecular mechanism of polysaccharide lyases for efficient alginate degradation.
Nat Commun, 16:2670-2670, 2025
Cited by
PubMed Abstract: Alginate lyases (ALs) catalyze the depolymerization of brown macroalgae alginates, widely used naturally occurring polysaccharides. Their molecular reaction mechanism remains elusive due to the lack of catalytically competent Michaelis-Menten-like complex structures. Here, we provide structural snapshots and dissect the mechanism of mannuronan-specific ALs from family 7 polysaccharide lyases (PL7), employing time-resolved NMR, X-ray, neutron crystallography, and QM/MM simulations. We reveal the protonation state of critical active site residues, enabling atomic-level analysis of the reaction coordinate. Our approach reveals an endolytic and asynchronous syn β-elimination reaction, with Tyr serving as both Brønsted base and acid, involving a carbanion-type transition state. This study not only reconciles previous structural and kinetic discrepancies, but also establishes a comprehensive PL reaction mechanism which is most likely applicable across all enzymes of the PL7 family as well as other PL families.
PubMed: 40102416
DOI: 10.1038/s41467-025-56754-5
PDB entries with the same primary citation
Experimental method
NEUTRON DIFFRACTION (2.15 Å)
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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