Evidence map›Paper›PMID 29042405›Full record

ArticleJournal of lipid research2017

Sterol methyltransferase a target for anti-amoeba therapy: towards transition state analog and suicide substrate drug design.

Medhanie E Kidane, Boden H Vanderloop, Wenxu Zhou, Crista D Thomas, Emilio Ramos, Ujjal Singha, Minu Chaudhuri, W David Nes

Abstract read
In one paragraph

Article in Journal of lipid research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Identification of Potent and Selective Inhibitors ofJournal of medicinal chemistry · 2024
    Article
  3. Review
  4. InhibitingPharmaceuticals (Basel, Switzerland) · 2023
    Article
  5. Steroidal Antimetabolites Protect Mice againstMolecules (Basel, Switzerland) · 2022
    Article
  6. Homology Modeling,Frontiers in cellular and infection microbiology · 2022
    Article
  7. Article
  8. Article
  9. Inhibition of Phytosterol Biosynthesis by Azasterols.Molecules (Basel, Switzerland) · 2020
    Article
  10. Article
  11. Article
  12. Review
  13. Microbial Sterolomics as a Chemical Biology Tool.Molecules (Basel, Switzerland) · 2018
    Review
  14. Functional importance for developmental regulation of sterol biosynthesis in Acanthamoeba castellanii.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2018
    Article
  15. Review
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

8 authors.

Medhanie E KidaneDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409.
Boden H VanderloopDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409.
Wenxu ZhouDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409.
Crista D ThomasDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409.
Emilio RamosDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409.
Ujjal SinghaDepartment of Microbiology and Immunology, Meharry Medical College, Nashville, TN 37208.
Minu ChaudhuriDepartment of Microbiology and Immunology, Meharry Medical College, Nashville, TN 37208.
W David NesDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409 wdavid.nes@ttu.edu.

Funding

The RCMI Program in Health Disparities Research at Meharry Medical College - SupplementU54MD007586 · NIMHD · MEHARRY MEDICAL COLLEGE · PI Samuel Evans Adunyah · 2017 to 2026
$48.2M
Discovery of New Anti-amoeba TherapeuticsR33AI119782 · NIAID · TEXAS TECH UNIVERSITY · PI NES, WILLIAM DAVID · 2017 to 2019
$881k
Discovery of New Anti-amoeba TherapeuticsR21AI119782 · NIAID · TEXAS TECH UNIVERSITY · PI NES, WILLIAM DAVID · 2015 to 2016
$447k
NIAID NIH HHS R21 AI119782NIAID NIH HHS R33 AI119782NIMHD NIH HHS U54 MD007586
6 · The paper itself

Abstract

Ergosterol biosynthesis pathways essential to pathogenic protozoa growth and absent from the human host offer new chokepoint targets. Here, we present characterization and cell-based interference of Acanthamoeba spp sterol 24-/28-methylases (SMTs) that catalyze the committed step in C

Indexed as

AcanthamoebaAmino Acid SequenceCell LineCell SurvivalCholestadienolsDrug DesignEpithelial CellsGene ExpressionHumansKidneyKineticsLanosterolMethyltransferasesPhytosterolsProtein BindingProtozoan Proteins24,25-iminolanosterol24-methylenelophenolCholestadienolscycloartenolLanosterolMethyltransferasesPhytosterolsProtozoan ProteinsRecombinant ProteinsSterolsTriterpenesAcanthamoebaanti-amoeba drugsergosterol biosynthesis inhibitorsphytosterol biosynthesissterol C24-methyltransferase

Identifiers

PMID29042405
PMCPMC5711494

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.