Evidence map›Paper›PMID 33925823›Full record

ArticleInternational journal of molecular sciences2021

Methods for Identifying Microbial Natural Product Compounds that Target Kinetoplastid RNA Structural Motifs by Homology and De Novo Modeled 18S rRNA.

Harrison Ndung'u Mwangi, Edward Kirwa Muge, Peter Waiganjo Wagacha, Albert Ndakala, Francis Jackim Mulaa

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

5 authors at 1 institution in 1 country.

Harrison Ndung'u MwangiDepartment of Biochemistry, University of Nairobi, Nairobi 00200-30197, Kenya.ORCID 0000-0002-6678-566X
Edward Kirwa MugeDepartment of Biochemistry, University of Nairobi, Nairobi 00200-30197, Kenya.
Peter Waiganjo WagachaDepartment of Computing and Informatics, University of Nairobi, Nairobi 00200-30197, Kenya.
Albert NdakalaDepartment of Chemistry, University of Nairobi, Nairobi 00200-30197, Kenya.
Francis Jackim MulaaDepartment of Biochemistry, University of Nairobi, Nairobi 00200-30197, Kenya.
University of Nairobi · KE

Funding

Medicines for Malaria Venture PO 15/01083(02)
6 · The paper itself

Abstract

The development of novel anti-infectives against Kinetoplastids pathogens targeting proteins is a big problem occasioned by the antigenic variation in these parasites. This is also a global concern due to the zoonosis of these parasites, as they infect both humans and animals. Therefore, we need not only to create novel antibiotics, but also to speed up the development pipeline for these antibiotics. This may be achieved by using novel drug targets for Kinetoplastids drug discovery. In this study, we focused our attention on motifs of rRNA molecules that have been created using homology modeling. The RNA is the most ambiguous biopolymer in the kinetoplatid, which carries many different functions. For instance, tRNAs, rRNAs, and mRNAs are essential for gene expression both in the pro-and eukaryotes. However, all these types of RNAs have sequences with unique 3D structures that are specific for kinetoplastids only and can be used to shut down essential biochemical processes in kinetoplastids only. All these features make RNA very potent targets for antibacterial drug development. Here, we combine in silico methods combined with both computational biology and structure prediction tools to address our hypothesis. In this study, we outline a systematic approach for identifying kinetoplastid rRNA-ligand interactions and, more specifically, techniques that can be used to identify small molecules that target particular RNA. The high-resolution optimized model structures of these kineoplastids were generated using RNA 123, where all the stereochemical conflicts were solved and energies minimized to attain the best biological qualities. The high-resolution optimized model's structures of these kinetoplastids were generated using RNA 123 where all the stereochemical conflicts were solved and energies minimized to attain the best biological qualities. These models were further analyzed to give their docking assessment reliability. Docking strategies, virtual screening, and fishing approaches successfully recognized novel and myriad macromolecular targets for the myxobacterial natural products with high binding affinities to exploit the unmet therapeutic needs. We demonstrate a sensible exploitation of virtual screening strategies to 18S rRNA using natural products interfaced with classical maximization of their efficacy in phamacognosy strategies that are well established. Integration of these virtual screening strategies in natural products chemistry and biochemistry research will spur the development of potential interventions to these tropical neglected diseases.

Indexed as

AnimalsBiological ProductsChagas DiseaseComputational BiologyDrug DiscoveryGenes, ProtozoanHumansKinetoplastidaLeishmaniasisLigandsMolecular Docking SimulationMolecular Dynamics SimulationProtein Interaction MappingProtozoan ProteinsRNA, RibosomalRNA, Ribosomal, 18SBiological ProductsLigandsProtozoan ProteinsRNA, RibosomalRNA, Ribosomal, 18S18S rRNAhomology and de novo modelingkinetoplastidsmolecular dockingnatural productsvirtual screening

Identifiers

PMID33925823
PMCPMC8123475
OpenAlexW3158771058

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.