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9KKV

Structure-guided interface engineering for modifying substrate binding and catalytic activity of 2-keto-3-deoxy-D-xylonate dehydratase

Summary for 9KKV
Entry DOI10.2210/pdb9kkv/pdb
DescriptorFumarylacetoacetate hydrolase family protein, DIHYDROGENPHOSPHATE ION, AMMONIUM ION, ... (4 entities in total)
Functional Keywordsapo, carbohydrate
Biological sourceCaulobacter vibrioides NA1000
Total number of polymer chains2
Total formula weight82775.22
Authors
Liang, B. (deposition date: 2024-11-14, release date: 2025-11-19, Last modification date: 2026-06-03)
Primary citationLiang, B.,Meng, C.,Wang, Q.,Du, Y.,Luo, Y.,Zhao, J.,Wu, D.,Liang, Y.,Lu, X.,Yang, J.
Structure-Guided Subunit Interface Engineering to Improve the Catalytic Efficiency of Dimeric Enzymes of FAH Family.
J.Agric.Food Chem., 73:32094-32106, 2025
Cited by
PubMed Abstract: The subunit interface plays a substantial role in the structures and functions of oligomeric enzymes, yet targeted mutations remain difficult to predict. Here, we targeted 2-keto-3-deoxy-d-xylonate dehydratase (XylX), the rate-limiting catalyst in the Weimberg pathway for d-xylose catabolism and a member of the fumarylacetoacetate hydrolase (FAH) family, which forms a compact homodimer. Guided by its crystal structure, we engineered the dimer interface and obtained triple mutant L210A/P181Q/Q308A, which showed a 6.04-fold increase in catalytic efficiency. Molecular dynamics simulations revealed that moderate enhancement of intersubunit flexibility accelerates substrate binding. When the mutant was coupled with other Weimberg enzymes in a one-pot process, 77% of d-xylose was converted to 56.05 ± 0.39 g/L α-ketoglutaric acid within 6 h. Moreover, this strategy is also applicable to other dimeric enzymes within the FAH family. This study highlights a promising strategy for engineering dimeric enzymes with a higher catalytic efficiency for producing valuable chemicals.
PubMed: 41339057
DOI: 10.1021/acs.jafc.5c09893
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.77 Å)
Structure validation

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