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7U34

The structure of phosphoglucose isomerase from Aspergillus fumigatus

Summary for 7U34
Entry DOI10.2210/pdb7u34/pdb
Related7OYL
DescriptorGlucose-6-phosphate isomerase, GLYCEROL, CITRATE ANION, ... (6 entities in total)
Functional Keywordsphosphoglucose isomerase, aspergillus fumigatus, antifungal, isomerase
Biological sourceAspergillus fumigatus
Total number of polymer chains1
Total formula weight62485.92
Authors
Yan, K.,Kowalski, B.,Fang, W.,van Aalten, D. (deposition date: 2022-02-25, release date: 2022-08-17, Last modification date: 2023-10-18)
Primary citationZhou, Y.,Yan, K.,Qin, Q.,Raimi, O.G.,Du, C.,Wang, B.,Ahamefule, C.S.,Kowalski, B.,Jin, C.,van Aalten, D.M.F.,Fang, W.
Phosphoglucose Isomerase Is Important for Aspergillus fumigatus Cell Wall Biogenesis.
Mbio, 13:e0142622-e0142622, 2022
Cited by
PubMed Abstract: Aspergillus fumigatus is a devastating opportunistic fungal pathogen causing hundreds of thousands of deaths every year. Phosphoglucose isomerase (PGI) is a glycolytic enzyme that converts glucose-6-phosphate to fructose-6-phosphate, a key precursor of fungal cell wall biosynthesis. Here, we demonstrate that the growth of A. fumigatus is repressed by the deletion of , which can be rescued by glucose and fructose supplementation in a 1:10 ratio. Even under these optimized growth conditions, the Δ mutant exhibits severe cell wall defects, retarded development, and attenuated virulence in Caenorhabditis elegans and Galleria mellonella infection models. To facilitate exploitation of A. fumigatus PGI as an antifungal target, we determined its crystal structure, revealing potential avenues for developing inhibitors, which could potentially be used as adjunctive therapy in combination with other systemic antifungals. Aspergillus fumigatus is an opportunistic fungal pathogen causing deadly infections in immunocompromised patients. Enzymes essential for fungal survival and cell wall biosynthesis are considered potential drug targets against A. fumigatus. PGI catalyzes the second step of the glycolysis pathway, linking glycolysis and the pentose phosphate pathway. As such, PGI has been widely considered as a target for metabolic regulation and therefore a therapeutic target against hypoxia-related diseases. Our study here reveals that PGI is important for A. fumigatus survival and exhibit pleiotropic functions, including development, cell wall glucan biosynthesis, and virulence. We also solved the crystal structure of PGI, thus providing the genetic and structural groundwork for the exploitation of PGI as a potential antifungal target.
PubMed: 35913157
DOI: 10.1128/mbio.01426-22
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.56 Å)
Structure validation

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