Analysis of <i>Burkholderia pseudomallei</i> IspF in complex with sulfapyridine, sulfamonomethoxine, ethoxzolamide and acetazolamide

The methylerythritol phosphate (MEP) pathway is a metabolic pathway that produces the isoprenoids isopentyl pyrophosphate and dimethylallyl pyrophosphate. Notably, the MEP pathway is present in bacteria and not in mammals, which makes the enzymes of the MEP pathway attractive targets for the discovery of new anti-infective agents due to the reduced chances of off-target interactions leading to side effects. There are seven enzymes in the MEP pathway, the fifth of which is IspF. Crystal structures of Burkholderia pseudomallei IspF were determined with five different sulfonamide ligands bound. The sulfonamide-containing ligands were ethoxzolamide, acetazolamide, sulfapyridine and sulfamonomethoxine. The fifth bound ligand was a synthetic analog of acetazolamide. All ligands coordinated to the active-site Zn<sup>+2</sup> ion through the sulfonamide group, although sulfapyridine and sulfamonomethoxine, both of which are known antibacterial agents, possess similar binding interactions that are distinct from the other three sulfonamides. These structural data will aid in the discovery of new IspF inhibitors.

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Journal
Acta Crystallographica Section F Structural Biology Communications
Published
2025-02-28
DOI
https://doi.org/10.1107/s2053230x25001414
Citations
1
Primary Topic
Burkholderia infections and melioidosis
Type
article
Field-Weighted Citation Impact
1.35

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article

Analysis of Burkholderia pseudomallei IspF in complex with sulfapyridine, sulfamonomethoxine, ethoxzolamide and acetazolamide

David M. Dranow, Thomas E. Edwards, Phillip G. Pierce, Dakota L. Grote et al.
1 citations
Acta Crystallographica Section F Structural Biology Communications
Burkholderia infections and melioidosis
1.35
article

Analysis of Burkholderia pseudomallei IspF in complex with sulfapyridine, sulfamonomethoxine, ethoxzolamide and acetazolamide

David M. Dranow, Thomas E. Edwards, Phillip G. Pierce, Dakota L. Grote, Cary C. Stewart, Timothy J. Hagen, Parisa Enayati, Jan Abendroth, Peter J. Myler, Bart L. Staker, Jason K. Yano, Donald D. Lorimer, James R. Horn, P.S. Horanyi, Drashti G. Daraji, Madison Bolejack, Kristina N Braverman, CeAnn Romanaggi
article en
1 citations

Abstract

The methylerythritol phosphate (MEP) pathway is a metabolic pathway that produces the isoprenoids isopentyl pyrophosphate and dimethylallyl pyrophosphate. Notably, the MEP pathway is present in bacteria and not in mammals, which makes the enzymes of the MEP pathway attractive targets for the discovery of new anti-infective agents due to the reduced chances of off-target interactions leading to side effects. There are seven enzymes in the MEP pathway, the fifth of which is IspF. Crystal structures of Burkholderia pseudomallei IspF were determined with five different sulfonamide ligands bound. The sulfonamide-containing ligands were ethoxzolamide, acetazolamide, sulfapyridine and sulfamonomethoxine. The fifth bound ligand was a synthetic analog of acetazolamide. All ligands coordinated to the active-site Zn<sup>+2</sup> ion through the sulfonamide group, although sulfapyridine and sulfamonomethoxine, both of which are known antibacterial agents, possess similar binding interactions that are distinct from the other three sulfonamides. These structural data will aid in the discovery of new IspF inhibitors.

Acta Crystallographica Section F Structural Biology CommunicationsVol. 81(4)
Northern Illinois University (US), Center for Infectious Disease Research (US), Virginia Mason Bainbridge Island Medical Center (US)
National Science Foundation, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 22%
Burkholderia infections and melioidosis
1.35
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