Evidence map›Paper›PMID 27565432›Full record

ArticleBMC genomics2016

G23D: Online tool for mapping and visualization of genomic variants on 3D protein structures.

Oz Solomon, Vered Kunik, Amos Simon, Nitzan Kol, Ortal Barel, Atar Lev, Ninette Amariglio, Raz Somech, Gidi Rechavi, Eran Eyal

Abstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Structural dynamics is a determinant of the functional significance of missense variants.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  10. Article
  11. 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

10 authors.

Oz SolomonCancer Research Center, Sheba Medical Center, Ramat-Gan, Israel.
Vered KunikCancer Research Center, Sheba Medical Center, Ramat-Gan, Israel.
Amos SimonPediatric Immunology Service, Jeffrey Modell Foundation, Sheba Medical Center, Ramat-Gan, Israel.
Nitzan KolCancer Research Center, Sheba Medical Center, Ramat-Gan, Israel.
Ortal BarelCancer Research Center, Sheba Medical Center, Ramat-Gan, Israel.
Atar LevPediatric Immunology Service, Jeffrey Modell Foundation, Sheba Medical Center, Ramat-Gan, Israel.
Ninette AmariglioCancer Research Center, Sheba Medical Center, Ramat-Gan, Israel.
Raz SomechEdmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat-Gan, Israel.
Gidi RechaviCancer Research Center, Sheba Medical Center, Ramat-Gan, Israel.
Eran EyalCancer Research Center, Sheba Medical Center, Ramat-Gan, Israel. eran.eyal@sheba.health.gov.il.ORCID 0000-0002-9505-6319

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvaluation of the possible implications of genomic variants is an increasingly important task in the current high throughput sequencing era. Structural information however is still not routinely exploited during this evaluation process. The main reasons can be attributed to the partial structural coverage of the human proteome and the lack of tools which conveniently convert genomic positions, which are the frequent output of genomic pipelines, to proteins and structure coordinates.

resultsWe present G23D, a tool for conversion of human genomic coordinates to protein coordinates and protein structures. G23D allows mapping of genomic positions/variants on evolutionary related (and not only identical) protein three dimensional (3D) structures as well as on theoretical models. By doing so it significantly extends the space of variants for which structural insight is feasible. To facilitate interpretation of the variant consequence, pathogenic variants, functional sites and polymorphism sites are displayed on protein sequence and structure diagrams alongside the input variants. G23D also provides modeling of the mutant structure, analysis of intra-protein contacts and instant access to functional predictions and predictions of thermo-stability changes. G23D is available at http://www.sheba-cancer.org.il/G23D .

conclusionsG23D extends the fraction of variants for which structural analysis is applicable and provides better and faster accessibility for structural data to biologists and geneticists who routinely work with genomic information.

Indexed as

Genetic VariationModels, MolecularProtein ConformationSoftwareGenomicsProteinsWeb BrowserProteinsMutationProteinStructureVariantVisualization

Identifiers

PMID27565432
PMCPMC5002099

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.