BAlaS: fast, interactive and accessible computational alanine-scanning using BudeAlaScan.


Journal

Bioinformatics (Oxford, England)
ISSN: 1367-4811
Titre abrégé: Bioinformatics
Pays: England
ID NLM: 9808944

Informations de publication

Date de publication:
01 05 2020
Historique:
received: 07 11 2019
accepted: 09 01 2020
pubmed: 14 1 2020
medline: 10 10 2020
entrez: 14 1 2020
Statut: ppublish

Résumé

In experimental protein engineering, alanine-scanning mutagenesis involves the replacement of selected residues with alanine to determine the energetic contribution of each side chain to forming an interaction. For example, it is often used to study protein-protein interactions. However, such experiments can be time-consuming and costly, which has led to the development of programmes for performing computational alanine-scanning mutagenesis (CASM) to guide experiments. While programmes are available for this, there is a need for a real-time web application that is accessible to non-expert users. Here, we present BAlaS, an interactive web application for performing CASM via BudeAlaScan and visualizing its results. BAlaS is interactive and intuitive to use. Results are displayed directly in the browser for the structure being interrogated enabling their rapid inspection. BAlaS has broad applications in areas, such as drug discovery and protein-interface design. BAlaS works on all modern browsers and is available through the following website: https://balas.app. The project is open source, distributed using an MIT license and is available on GitHub (https://github.com/wells-wood-research/balas).

Identifiants

pubmed: 31930404
pii: 5701649
doi: 10.1093/bioinformatics/btaa026
doi:

Substances chimiques

Alanine OF5P57N2ZX

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2917-2919

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/L01386X/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/R00661X/1
Pays : United Kingdom

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Christopher W Wood (CW)

School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FF, UK.

Amaurys A Ibarra (AA)

School of Biochemistry, University of Bristol, Medical Sciences Building, University Walk, Bristol BS8 1TD, UK.

Gail J Bartlett (GJ)

School of Chemistry, University of Bristol, Bristol BS8 1TS, UK.

Andrew J Wilson (AJ)

School of Chemistry.
Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.

Derek N Woolfson (DN)

School of Biochemistry, University of Bristol, Medical Sciences Building, University Walk, Bristol BS8 1TD, UK.
School of Chemistry, University of Bristol, Bristol BS8 1TS, UK.
BrisSynBio, University of Bristol, Life Sciences Building, Bristol BS8 1TQ, UK.

Richard B Sessions (RB)

School of Biochemistry, University of Bristol, Medical Sciences Building, University Walk, Bristol BS8 1TD, UK.
BrisSynBio, University of Bristol, Life Sciences Building, Bristol BS8 1TQ, UK.

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Classifications MeSH