Evidence map›Paper›PMID 31302178›Full record

ArticleMethods (San Diego, Calif.)2020

Umbrella Visualization: A method of analysis dedicated to glycan flexibility with UnityMol.

Camille Besançon, Alexandre Guillot, Sébastien Blaise, Manuel Dauchez, Nicolas Belloy, Jessica Prévoteau-Jonquet, Stéphanie Baud

Open access · bronzeAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Three-Dimensional Structures of Carbohydrates and Where to Find Them.International journal of molecular sciences · 2020
    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

7 authors at 1 institution in 1 country.

Camille BesançonUniversité de Reims Champagne Ardenne, CNRS, MEDyC UMR 7369, 51097 Reims, France. Electronic address: camille.besancon@univ-reims.fr.
Alexandre GuillotUniversité de Reims Champagne Ardenne, CNRS, MEDyC UMR 7369, 51097 Reims, France.
Sébastien BlaiseUniversité de Reims Champagne Ardenne, CNRS, MEDyC UMR 7369, 51097 Reims, France.
Manuel DauchezUniversité de Reims Champagne Ardenne, CNRS, MEDyC UMR 7369, 51097 Reims, France; Université de Reims Champagne Ardenne, Plateau de Modélisation Moléculaire Multi-Echelle (P3M), Maison de la Simulation de Champagne Ardenne (MaSCA), 51097 Reims, France.
Nicolas BelloyUniversité de Reims Champagne Ardenne, CNRS, MEDyC UMR 7369, 51097 Reims, France; Université de Reims Champagne Ardenne, Plateau de Modélisation Moléculaire Multi-Echelle (P3M), Maison de la Simulation de Champagne Ardenne (MaSCA), 51097 Reims, France.
Jessica Prévoteau-JonquetUniversité de Reims Champagne Ardenne, CNRS, MEDyC UMR 7369, 51097 Reims, France.
Stéphanie BaudUniversité de Reims Champagne Ardenne, CNRS, MEDyC UMR 7369, 51097 Reims, France; Université de Reims Champagne Ardenne, Plateau de Modélisation Moléculaire Multi-Echelle (P3M), Maison de la Simulation de Champagne Ardenne (MaSCA), 51097 Reims, France.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N-glycosylation is a post-translational modification heavily impacting protein functions. Some alterations of glycosylation, such as sialic acid hydrolysis, are related to protein dysfunction. Because of their high flexibility and the many reactive groups of the glycan chains, studying glycans with in vitro methods is a challenging task. Molecular dynamics is a useful tool and probably the only one in biology able to overcome this problem and gives access to conformational information through exhaustive sampling. To better decipher the impact of N-glycans, the analysis and visualization of their influence over time on protein structure is a prerequisite. We developed the Umbrella Visualization, a graphical method that assigns the glycan intrinsic flexibility during a molecular dynamics trajectory. The density plot generated by this method brought relevant informations regarding glycans dynamics and flexibility, but needs further development in order to integrate an accurate description of the protein topology and its interactions. We propose here to transform this analysis method into a visualization mode in UnityMol. UnityMol is a molecular editor, viewer and prototyping platform, coded in C#. The new representation of glycan chains presented in this study takes into account both the main positions adopted by each antenna of a glycan and their statistical relevance. By displaying the collected data on the protein surface, one is then able to investigate the protein/glycan interactions.

Indexed as

Molecular Dynamics SimulationComputational BiologyGlycosylationMolecular ConformationPolysaccharidesProtein Processing, Post-TranslationalPolysaccharidesCovered surfaceGlycan flexibilityMolecular dynamicsUnityUnityMol

Identifiers

PMID31302178
PMCPMC7128144
OpenAlexW2958771624

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.