Evidence map›Paper›PMID 33760815›Full record

ArticlePloS one2021

Naegleria fowleri: Protein structures to facilitate drug discovery for the deadly, pathogenic free-living amoeba.

Logan Tillery, Kayleigh Barrett, Jenna Goldstein, Jared W Lassner, Bram Osterhout, Nathan L Tran, Lily Xu, Ryan M Young, Justin Craig, Ian Chun and 21 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 11% of its field
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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. In Silico Structural Analysis of Serine CarboxypeptidaseInternational journal of molecular sciences · 2022
    Article
  10. Article
  11. Differential Growth Rates andMicrobiology spectrum · 2022
    Article
  12. Infections Caused by Free-Living Amoebae.Journal of clinical microbiology · 2022
    Article
  13. The therapeutic potential of novel isobenzofuranones against Naegleria fowleri.International journal for parasitology. Drugs and drug resistance · 2021
    Article
  14. Naphthyridine Derivatives Induce Programmed Cell Death inPharmaceuticals (Basel, Switzerland) · 2021
    Article
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

31 authors at 6 institutions in 1 country.

Logan TilleryDepartment of Medicine, Division Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Disease (CERID) University of Washington, Seattle, Washington, United States of America.ORCID 0000-0002-5431-3489
Kayleigh BarrettDepartment of Medicine, Division Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Disease (CERID) University of Washington, Seattle, Washington, United States of America.
Jenna GoldsteinDepartment of Biology, Washington University, St. Louis, Missouri, United States of America.ORCID 0000-0002-3989-1002
Jared W LassnerDepartment of Biology, Washington University, St. Louis, Missouri, United States of America.ORCID 0000-0003-1933-7458
Bram OsterhoutDepartment of Biology, Washington University, St. Louis, Missouri, United States of America.
Nathan L TranDepartment of Biology, Washington University, St. Louis, Missouri, United States of America.ORCID 0000-0002-7917-3945
Lily XuDepartment of Biology, Washington University, St. Louis, Missouri, United States of America.
Ryan M YoungDepartment of Biology, Washington University, St. Louis, Missouri, United States of America.
Justin CraigDepartment of Medicine, Division Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Disease (CERID) University of Washington, Seattle, Washington, United States of America.
Ian ChunDepartment of Medicine, Division Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Disease (CERID) University of Washington, Seattle, Washington, United States of America.
David M DranowSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0003-1871-2455
Jan AbendrothSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0002-8229-3243
Silvia L DelkerSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0001-6858-3431
Douglas R DaviesSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0002-3729-3463
Stephen J MayclinSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0002-1600-4554
Brandy CalhounSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.
Madison J BolejackSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.
Bart StakerSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0001-9570-5086
Sandhya SubramanianSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.
Isabelle PhanSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0001-6873-3401
Donald D LorimerSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0002-9638-8083
Peter J MylerSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.ORCID 0000-0002-0056-0513
Thomas E EdwardsSeattle Structural Genomics Center for Infectious Diseases, Seattle, Washington, United States of America.
Dennis E KyleCenter for Tropical and Emerging Global Diseases, University of Georgia, Athens, Georgia, United States of America.ORCID 0000-0002-0238-965X
Christopher A RiceCenter for Tropical and Emerging Global Diseases, University of Georgia, Athens, Georgia, United States of America.ORCID 0000-0003-0672-9604
James C MorrisEukaryotic Pathogens Innovation Center, Department of Genetics and Biochemistry, Clemson University, Clemson, South Carolina, United States of America.ORCID 0000-0003-2515-5714
James W LeahyDepartment of Chemistry, University of South Florida, Tampa, Florida, United States of America.ORCID 0000-0003-3647-4489
Roman ManetschDepartment of Chemistry and Chemical Biology and Department of Pharmaceutical Sciences, Northeastern University, Boston, Massachusetts, United States of America.ORCID 0000-0001-7038-6867
Lynn K BarrettDepartment of Medicine, Division Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Disease (CERID) University of Washington, Seattle, Washington, United States of America.
Craig L SmithDepartment of Biology, Washington University, St. Louis, Missouri, United States of America.
Wesley C Van VoorhisDepartment of Medicine, Division Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Disease (CERID) University of Washington, Seattle, Washington, United States of America.ORCID 0000-0001-6141-2015
Center for Infectious Disease Research · USWashington University in St. Louis · USUniversity of Georgia · USClemson University · USNortheastern University · USUniversity of South Florida · US

Funding

NIAID NIH HHS HHSN272201200025CNIAID NIH HHS HHSN272201700059C
6 · The paper itself

Abstract

Naegleria fowleri is a pathogenic, thermophilic, free-living amoeba which causes primary amebic meningoencephalitis (PAM). Penetrating the olfactory mucosa, the brain-eating amoeba travels along the olfactory nerves, burrowing through the cribriform plate to its destination: the brain's frontal lobes. The amoeba thrives in warm, freshwater environments, with peak infection rates in the summer months and has a mortality rate of approximately 97%. A major contributor to the pathogen's high mortality is the lack of sensitivity of N. fowleri to current drug therapies, even in the face of combination-drug therapy. To enable rational drug discovery and design efforts we have pursued protein production and crystallography-based structure determination efforts for likely drug targets from N. fowleri. The genes were selected if they had homology to drug targets listed in Drug Bank or were nominated by primary investigators engaged in N. fowleri research. In 2017, 178 N. fowleri protein targets were queued to the Seattle Structural Genomics Center of Infectious Disease (SSGCID) pipeline, and to date 89 soluble recombinant proteins and 19 unique target structures have been produced. Many of the new protein structures are potential drug targets and contain structural differences compared to their human homologs, which could allow for the development of pathogen-specific inhibitors. Five of the structures were analyzed in more detail, and four of five show promise that selective inhibitors of the active site could be found. The 19 solved crystal structures build a foundation for future work in combating this devastating disease by encouraging further investigation to stimulate drug discovery for this neglected pathogen.

Indexed as

Drug DiscoveryAdenosylhomocysteinaseBinding SitesEnzyme InhibitorsMolecular Dynamics SimulationNaegleria fowleriPhosphoglycerate MutaseProtein-Arginine N-MethyltransferasesProtein Structure, QuaternaryProteomeProtozoan ProteinsAdenosylhomocysteinaseEnzyme InhibitorsPhosphoglycerate MutaseProtein-Arginine N-MethyltransferasesProteomeProtozoan Proteins

Identifiers

PMID33760815
PMCPMC7990177
OpenAlexW3139376637

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.