Evidence map›Paper›PMID 38693166›Full record

ArticleScientific reports2024

Structural investigation of Trypanosoma cruzi Akt-like kinase as drug target against Chagas disease.

Karina A Stadler, Lesly J Ortiz-Joya, Amit Singh Sahrawat, Christoph Buhlheller, Karl Gruber, Tea Pavkov-Keller, Treasa B O'Hagan, Alba Guarné, Sergio Pulido, Marcel Marín-Villa and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. 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
0.8field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

12 authors at 5 institutions in 3 countries.

Karina A Stadler *Institute of Chemistry/Organic and Bioorganic Chemistry, University of Graz, Graz, Austria.
Lesly J Ortiz-Joya *Institute of Chemistry/Organic and Bioorganic Chemistry, University of Graz, Graz, Austria.
Amit Singh SahrawatInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Christoph BuhlhellerInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Karl GruberInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Tea Pavkov-KellerInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Treasa B O'HaganDepartment of Biochemistry, McGill University, Montreal, Canada.
Alba GuarnéDepartment of Biochemistry, McGill University, Montreal, Canada.
Sergio PulidoPrograma de Estudio y Control de Enfermedades Tropicales (PECET), Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Marcel Marín-VillaPrograma de Estudio y Control de Enfermedades Tropicales (PECET), Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Klaus ZanggerInstitute of Chemistry/Organic and Bioorganic Chemistry, University of Graz, Graz, Austria. klaus.zangger@uni-graz.at.
Nina GubensäkInstitute of Molecular Biosciences, University of Graz, Graz, Austria. nina.gubensaek@uni-graz.at.
University of Graz · ATMcGill University · CABioTechMed-Graz · ATUniversidad Católica de Oriente · COUniversidad de Antioquia · CO

Funding

CIHR PJT-155941
6 · The paper itself

Abstract

According to the World Health Organization, Chagas disease (CD) is the most prevalent poverty-promoting neglected tropical disease. Alarmingly, climate change is accelerating the geographical spreading of CD causative parasite, Trypanosoma cruzi, which additionally increases infection rates. Still, CD treatment remains challenging due to a lack of safe and efficient drugs. In this work, we analyze the viability of T. cruzi Akt-like kinase (TcAkt) as drug target against CD including primary structural and functional information about a parasitic Akt protein. Nuclear Magnetic Resonance derived information in combination with Molecular Dynamics simulations offer detailed insights into structural properties of the pleckstrin homology (PH) domain of TcAkt and its binding to phosphatidylinositol phosphate ligands (PIP). Experimental data combined with Alpha Fold proposes a model for the mechanism of action of TcAkt involving a PIP-induced disruption of the intramolecular interface between the kinase and the PH domain resulting in an open conformation enabling TcAkt kinase activity. Further docking experiments reveal that TcAkt is recognized by human inhibitors PIT-1 and capivasertib, and TcAkt inhibition by UBMC-4 and UBMC-6 is achieved via binding to TcAkt kinase domain. Our in-depth structural analysis of TcAkt reveals potential sites for drug development against CD, located at activity essential regions.

Indexed as

Chagas DiseaseMolecular Docking SimulationMolecular Dynamics SimulationTrypanosoma cruziHumansProtein BindingProtein Kinase InhibitorsProto-Oncogene Proteins c-aktProtozoan ProteinsProtein Kinase InhibitorsProto-Oncogene Proteins c-aktProtozoan ProteinsAkt/PKBAmerican trypanosomiasisNMRParasitic diseasePH domain

Identifiers

PMID38693166
PMCPMC11063076
OpenAlexW4396598949

What Socratic 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 Socratic graph.