VarQ: A Tool for the Structural and Functional Analysis of Human Protein Variants

Files in This Item:
File Description SizeFormat 
VarQ A Tool for the Structural and Functional Analysis of Human Protein Variants.pdf2.2 MBAdobe PDFDownload
Title: VarQ: A Tool for the Structural and Functional Analysis of Human Protein Variants
Authors: Radusky, LeandroModenutti, CarlosDelgado, JavierKiel, Christinaet al.
Permanent link:
Date: 6-Dec-2018
Online since: 2021-01-25T07:53:49Z
Abstract: Understanding the functional effect of Single Amino acid Substitutions (SAS), derived from the occurrence of single nucleotide variants (SNVs), and their relation to disease development is a major issue in clinical genomics. Despite the existence of several bioinformatic algorithms and servers that predict if a SAS is pathogenic or not, they give little or no information at all on the reasons for pathogenicity prediction and on the actual predicted effect of the SAS on the protein function. Moreover, few actual methods take into account structural information when available for automated analysis. Moreover, many of these algorithms are able to predict an effect that no necessarily translates directly into pathogenicity. VarQ is a bioinformatic pipeline that incorporates structural information for the detailed analysis and prediction of SAS effect on protein function. It is an online tool which uses UniProt id and automatically analyzes known and user provided SAS for their effect on protein activity, folding, aggregation and protein interactions, among others. We show that structural information, when available, can improve the SAS pathogenicity diagnosis and more important explain its causes. We show that VarQ is able to correctly reproduce previous analysis of RASopathies related mutations, saving extensive and time consuming manual curation. VarQ assessment was performed over a set of previously manually curated RASopathies (diseases that affects the RAS/MAPK signaling pathway) related variants, showing its ability to correctly predict the phenotypic outcome and its underlying cause. This resource is available online at Supporting Information & Tutorials may be found in the webpage of the tool.
Funding Details: European Commission - European Regional Development Fund
European Commission - Seventh Framework Programme (FP7)
Funding Details: Spanish Ministerio de Economía y Competitividad
Type of material: Journal Article
Publisher: Frontiers Media
Journal: Frontiers in Genetics
Volume: 9
Copyright (published version): 2018 the Authors
Keywords: Variation diagnosisBioinformaticsWeb serverSingle amino acid substitutionsSingle amino acid substitutions classificationFoldX
DOI: 10.3389/fgene.2018.00620
Language: en
Status of Item: Peer reviewed
ISSN: 1664-8021
This item is made available under a Creative Commons License:
Appears in Collections:Medicine Research Collection

Show full item record

Page view(s)

Last Week
Last month
checked on Feb 25, 2021


checked on Feb 25, 2021

Google ScholarTM



If you are a publisher or author and have copyright concerns for any item, please email and the item will be withdrawn immediately. The author or person responsible for depositing the article will be contacted within one business day.