Evidence map›Paper›PMID 39960828›Full record

ArticleActa crystallographica. Section F, Structural biology communications2025

Crystal structure of dihydroorotate dehydrogenase from Helicobacter pylori with bound flavin mononucleotide.

Ashna A Agarwal, John D Georgiades, David M Dranow, Donald D Lorimer, Thomas Edwards, Kayleigh F Barrett, Justin K Craig, Wesley C Van Voorhis, Peter J Myler, Craig L Smith

Abstract read
In one paragraph

Article in Acta crystallographica. Section F, Structural biology communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Ashna A AgarwalDepartment of Biology, Washington University in St Louis School of Medicine, St Louis, MO 63114, USA.
John D GeorgiadesDepartment of Biology, Washington University in St Louis School of Medicine, St Louis, MO 63114, USA.ORCID 0009-0008-4783-1553
David M DranowBeryllium, 7869 NE Day Road West, Bainbridge Island, WA 98102, USA.
Donald D LorimerBeryllium, 7869 NE Day Road West, Bainbridge Island, WA 98102, USA.ORCID 0000-0002-9638-8083
Thomas EdwardsBeryllium, 7869 NE Day Road West, Bainbridge Island, WA 98102, USA.
Kayleigh F BarrettSeattle Structural Genomics Center for Infectious Disease (SSGCID), Seattle, Washington, USA.
Justin K CraigSeattle Structural Genomics Center for Infectious Disease (SSGCID), Seattle, Washington, USA.
Wesley C Van VoorhisSeattle Structural Genomics Center for Infectious Disease (SSGCID), Seattle, Washington, USA.
Peter J MylerSeattle Structural Genomics Center for Infectious Disease (SSGCID), Seattle, Washington, USA.ORCID 0000-0002-0056-0513
Craig L SmithDepartment of Biology, Washington University in St Louis School of Medicine, St Louis, MO 63114, USA.ORCID 0000-0003-3174-3053

Funding

Centers for Research on Structural Biology of Infectious Diseases: Universal Influenza Vaccine Research75N93022C00036 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI STAKER, BART · 2022 to 2025
$21.7M
Michigan Economic Development Corporation 085P1000817NIH HHS 75N93022C00036U.S. Department of Energy, Office of Science DE-AC02-06CH11357
6 · The paper itself

Abstract

Helicobacter pylori is the primary causative agent of peptic ulcer disease, among other gastrointestinal ailments, and currently affects over half of the global population. Although some treatments exist, growing resistance to these drugs has prompted efforts to develop novel approaches to fighting this pathogen. To generate many of the nucleotides essential to biochemical processes, H. pylori relies exclusively on the de novo biosynthesis of these molecules. Recent drug-discovery efforts have targeted the first committed step of this pathway, catalysed by a class 2 dihydroorotate dehydrogenase (DHODH). However, these initiatives have been limited by the lack of a crystal structure. Here, we detail the crystal structure of H. pylori DHODH (HpDHODH) at 2.25 Å resolution (PDB entry 6b8s). We performed a large-scale bioinformatics search to find evolutionary homologs. Our results indicate that HpDHODH shows high conservation of both sequence and structure in its active site. We identified key polar interactions between the HpDHODH protein and its requisite flavin mononucleotide (FMN) cofactor, identifying amino-acid residues that are critical to its function. Most notably, we found that HpDHODH maintains several structural features that allow it to associate with the inner membrane and utilize ubiquinone to achieve catalytic turnover. We discovered a hydrophobic channel that runs from the putative membrane interface on the N-terminal microdomain to the core of the protein. We predict that this channel establishes a connection between the ubiquinone pool in the membrane and the FMN in the active site. These findings provide a structural explanation for the competitive inhibition of ubiquinone by pyrazole-based compounds that was determined biochemically in other studies. Understanding this mechanism may facilitate the development of new drugs targeting this enzyme and push the effort to find a resistance-free treatment for H. pylori.

Indexed as

Bacterial ProteinsFlavin MononucleotideHelicobacter pyloriOxidoreductases Acting on CH-CH Group DonorsAmino Acid SequenceCatalytic DomainCrystallography, X-RayDihydroorotate DehydrogenaseEscherichia coliModels, MolecularProtein BindingBacterial ProteinsDihydroorotate DehydrogenaseFlavin MononucleotideOxidoreductases Acting on CH-CH Group Donorsdihydroorotate dehydrogenasesflavin mononucleotideHelicobacter pylorioxidoreductasesSeattle Structural Genomics Centre for Infectious Disease

Identifiers

PMID39960828
PMCPMC11866409

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.