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9YJZ

cryoEM structure of Apo Aspergillus fumigatus acetolactate synthase (ALS)

Summary for 9YJZ
Entry DOI10.2210/pdb9yjz/pdb
EMDB information73040
DescriptorAcetolactate synthase, MAGNESIUM ION, THIAMINE DIPHOSPHATE, ... (4 entities in total)
Functional Keywordsbranched-chain amino acid synthesis, antifungal target, herbicide target, anti fugal infection, plant protein
Biological sourceAspergillus fumigatus
Total number of polymer chains2
Total formula weight143085.96
Authors
Hu, Y. (deposition date: 2025-10-06, release date: 2026-03-18)
Primary citationPerlatti, B.,Vellanki, S.,Zhang, Y.,Chiang, Y.M.,Hu, Y.,Yuan, M.,Dunbar, K.,Fine, A.,Grau, M.F.,Li, S.,O'Donnell, T.,Shenoy, R.,Li, H.,Shi, H.,Xu, X.,Chen, Z.,Arvedson, T.,Tang, Y.,Cramer, R.A.,Cee, V.,Harvey, C.J.B.
An Antifungal with a Novel Mechanism of Action Discovered via Resistance Gene-Guided Genome Mining.
Acs Cent.Sci., 12:197-207, 2026
Cited by
PubMed Abstract: Invasive fungal infections claim over two million lives annually, a problem exacerbated by rising resistance to current antifungal treatments and an increasing population of immunocompromised individuals. Despite this, antifungal drug development has stagnated, with few novel agents and fewer novel targets explored in recent decades. Here, we validate acetolactate synthase (ALS), an enzyme critical for branched-chain amino acid biosynthesis and absent in humans, as a promising target for new therapeutics. Using resistance gene-guided genome mining, we discovered a biosynthetic gene cluster in encoding HB-35018 (1), a novel spiro-cis-decalin tetramic acid that potently inhibits ALS. Biochemical and antifungal assays demonstrate that surpasses existing ALS inhibitors in efficacy against and other pathogenic fungi. Structural studies via cryo-electron microscopy reveal a unique covalent binding interaction between compound and ALS, distinct from known inhibitors, and finally, we demonstrate that ALS is essential for virulence in a mouse model of invasive aspergillosis. These findings position ALS as a promising target for antifungal development and demonstrate the potential of resistance gene-guided genome mining for antifungal discovery.
PubMed: 41768770
DOI: 10.1021/acscentsci.5c02019
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.76 Å)
Structure validation

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PDB entries from 2026-03-18

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