Evidence map›Paper›PMID 24047900›Full record

ArticleThe Journal of biological chemistry2013

Complexes of Trypanosoma cruzi sterol 14α-demethylase (CYP51) with two pyridine-based drug candidates for Chagas disease: structural basis for pathogen selectivity.

Tatiana Y Hargrove, Zdzislaw Wawrzak, Paul W Alexander, Jason H Chaplin, Martine Keenan, Susan A Charman, Catherine J Perez, Michael R Waterman, Eric Chatelain, Galina I Lepesheva

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Identification of Potent and Selective Inhibitors ofJournal of medicinal chemistry · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Current trends in the pharmacological management of Chagas disease.International journal for parasitology. Drugs and drug resistance · 2020
    Review
  14. A new chemotype with promise against Trypanosoma cruzi.Bioorganic & medicinal chemistry letters · 2020
    Article
  15. Review
  16. The Evolution of Azole Resistance inAntimicrobial agents and chemotherapy · 2019
    Article
  17. Article
  18. Review
  19. Article
  20. 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

10 authors at 5 institutions in 3 countries.

Tatiana Y HargroveFrom the Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, Tennessee 37232.
Zdzislaw Wawrzak
Paul W Alexander
Jason H Chaplin
Martine Keenan
Susan A Charman
Catherine J Perez
Michael R Waterman
Eric Chatelain
Galina I Lepesheva
Murdoch University · AUVanderbilt University · USDrugs for Neglected Diseases Initiative · CHMonash University · AUNorthwestern University · US

Funding

Structural Requirements for Sterol 14alpha-DemethylasesR01GM067871 · NIGMS · VANDERBILT UNIVERSITY · PI LEPESHEVA, GALINA I · 2004 to 2023
$7.2M
NIGMS NIH HHS GM 067871NIGMS NIH HHS R01 GM067871
6 · The paper itself

Abstract

Chagas disease, caused by the eukaryotic (protozoan) parasite Trypanosoma cruzi, is an alarming emerging global health problem with no clinical drugs available to treat the chronic stage. Azole inhibitors of sterol 14α-demethylase (CYP51) were proven effective against Chagas, and antifungal drugs posaconazole and ravuconazole have entered clinical trials in Spain, Bolivia, and Argentina. Here we present the x-ray structures of T. cruzi CYP51 in complexes with two alternative drug candidates, pyridine derivatives (S)-(4-chlorophenyl)-1-(4-(4-(trifluoromethyl)phenyl)-piperazin-1-yl)-2-(pyridin-3-yl)ethanone (UDO; Protein Data Bank code 3ZG2) and N-[4-(trifluoromethyl)phenyl]-N-[1-[5-(trifluoromethyl)-2-pyridyl]-4-piperi-dyl]pyridin-3-amine (UDD; Protein Data Bank code 3ZG3). These compounds have been developed by the Drugs for Neglected Diseases initiative (DNDi) and are highly promising antichagasic agents in both cellular and in vivo experiments. The binding parameters and inhibitory effects on sterol 14α-demethylase activity in reconstituted enzyme reactions confirmed UDO and UDD as potent and selective T. cruzi CYP51 inhibitors. Comparative analysis of the pyridine- and azole-bound CYP51 structures uncovered the features that make UDO and UDD T. cruzi CYP51-specific. The structures suggest that although a precise fit between the shape of the inhibitor molecules and T. cruzi CYP51 active site topology underlies their high inhibitory potency, a longer coordination bond between the catalytic heme iron and the pyridine nitrogen implies a weaker influence of pyridines on the iron reduction potential, which may be the basis for the observed selectivity of these compounds toward the target enzyme versus other cytochrome P450s, including human drug-metabolizing P450s. These findings may pave the way for the development of novel CYP51-targeted drugs with optimized metabolic properties that are very much needed for the treatment of human infections caused by eukaryotic microbial pathogens.

Indexed as

14-alpha Demethylase InhibitorsAntiprotozoal AgentsChagas DiseaseCrystallography, X-RayHumansProtozoan ProteinsSterol 14-DemethylaseThiazolesTriazolesTrypanosoma cruzi14-alpha Demethylase InhibitorsAntiprotozoal AgentsER 30346posaconazoleProtozoan ProteinsSterol 14-DemethylaseThiazolesTriazolesCytochrome P450Drug DiscoveryEnzyme InhibitorsInfectious DiseasesProtein ComplexesProtein StructureSterol 14α-DemethylaseTrypanosoma cruziX-ray Crystallography

Identifiers

PMID24047900
PMCPMC3814756
OpenAlexW2114104454

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.