ArticleBMC genomics2016
G23D: Online tool for mapping and visualization of genomic variants on 3D protein structures.
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.
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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.
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Who cites it
11 citing papers in PubMed.
- Biallelic PIGM Coding Variant Causes Intractable Epilepsy and Intellectual Disability Without Thrombotic Events.Clinical genetics · 2025Article
- PSnpBind: a database of mutated binding site protein-ligand complexes constructed using a multithreaded virtual screening workflow.Journal of cheminformatics · 2022Article
- Swiss-PO: a new tool to analyze the impact of mutations on protein three-dimensional structures for precision oncology.NPJ precision oncology · 2021Article
- TGPred: a tumor gene prediction webserver for analyzing structural and functional impacts of variants.Journal of molecular cell biology · 2020Article
- VarMap: a web tool for mapping genomic coordinates to protein sequence and structure and retrieving protein structural annotations.Bioinformatics (Oxford, England) · 2019Article
- Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients WithFrontiers in immunology · 2019Article
- Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy.American journal of human genetics · 2018Article
- G2S: a web-service for annotating genomic variants on 3D protein structures.Bioinformatics (Oxford, England) · 2018Article
- 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 · 2018Article
- A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter Horses.Skeletal muscle · 2018Article
- GenProBiS: web server for mapping of sequence variants to protein binding sites.Nucleic acids research · 2017Article
Corrections and comments
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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