Evidence map›Paper›PMID 31067280›Full record

ArticlePloS one2019

Identification of a potential allosteric site of Golgi α-mannosidase II using computer-aided drug design.

Lina Irsheid, Thomas Wehler, Christoph Borek, Werner Kiefer, Ruth Brenk, Maria Elena Ortiz-Soto, Jürgen Seibel, Tanja Schirmeister

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. 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

8 authors at 3 institutions in 2 countries.

Lina IrsheidInstitute of Pharmacy and Biochemistry, University of Mainz, Mainz, Germany.ORCID 0000-0002-4587-5076
Thomas WehlerInstitute of Pharmacy and Biochemistry, University of Mainz, Mainz, Germany.
Christoph BorekInstitute of Pharmacy and Biochemistry, University of Mainz, Mainz, Germany.
Werner KieferInstitute of Pharmacy and Biochemistry, University of Mainz, Mainz, Germany.
Ruth BrenkDepartment of Biomedicine, University of Bergen, Bergen, Norway.ORCID 0000-0002-6204-5488
Maria Elena Ortiz-SotoInstitute of Organic Chemistry, University of Würzburg, Würzburg, Germany.
Jürgen SeibelInstitute of Organic Chemistry, University of Würzburg, Würzburg, Germany.
Tanja SchirmeisterInstitute of Pharmacy and Biochemistry, University of Mainz, Mainz, Germany.
Johannes Gutenberg University Mainz · DEUniversity of Würzburg · DEUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Golgi α-mannosidase II (GMII) is a glycoside hydrolase playing a crucial role in the N-glycosylation pathway. In various tumour cell lines, the distribution of N-linked sugars on the cell surface is modified and correlates with the progression of tumour metastasis. GMII therefore is a possible molecular target for anticancer agents. Here, we describe the identification of a non-competitive GMII inhibitor using computer-aided drug design methods including identification of a possible allosteric binding site, pharmacophore search and virtual screening.

Indexed as

Drug DesignAllosteric Sitealpha-MannosidaseAnimalsBinding SitesCloning, MolecularDrosophila melanogasterGolgi ApparatusMolecular Docking SimulationProtein Structure, QuaternaryRecombinant Proteinsalpha-MannosidaseRecombinant Proteins

Identifiers

PMID31067280
PMCPMC6505943
OpenAlexW2944661266

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.