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Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces
BACKGROUND: Many newly detected point mutations are located in protein-coding regions of the human genome. Knowledge of their effects on the protein's 3D structure provides insight into the protein's mechanism, can aid the design of further experiments, and eventually can lead to the devel...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992548/ https://www.ncbi.nlm.nih.gov/pubmed/21059217 http://dx.doi.org/10.1186/1471-2105-11-548 |
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author | Venselaar, Hanka te Beek, Tim AH Kuipers, Remko KP Hekkelman, Maarten L Vriend, Gert |
author_facet | Venselaar, Hanka te Beek, Tim AH Kuipers, Remko KP Hekkelman, Maarten L Vriend, Gert |
author_sort | Venselaar, Hanka |
collection | PubMed |
description | BACKGROUND: Many newly detected point mutations are located in protein-coding regions of the human genome. Knowledge of their effects on the protein's 3D structure provides insight into the protein's mechanism, can aid the design of further experiments, and eventually can lead to the development of new medicines and diagnostic tools. RESULTS: In this article we describe HOPE, a fully automatic program that analyzes the structural and functional effects of point mutations. HOPE collects information from a wide range of information sources including calculations on the 3D coordinates of the protein by using WHAT IF Web services, sequence annotations from the UniProt database, and predictions by DAS services. Homology models are built with YASARA. Data is stored in a database and used in a decision scheme to identify the effects of a mutation on the protein's 3D structure and function. HOPE builds a report with text, figures, and animations that is easy to use and understandable for (bio)medical researchers. CONCLUSIONS: We tested HOPE by comparing its output to the results of manually performed projects. In all straightforward cases HOPE performed similar to a trained bioinformatician. The use of 3D structures helps optimize the results in terms of reliability and details. HOPE's results are easy to understand and are presented in a way that is attractive for researchers without an extensive bioinformatics background. |
format | Text |
id | pubmed-2992548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29925482010-11-27 Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces Venselaar, Hanka te Beek, Tim AH Kuipers, Remko KP Hekkelman, Maarten L Vriend, Gert BMC Bioinformatics Methodology Article BACKGROUND: Many newly detected point mutations are located in protein-coding regions of the human genome. Knowledge of their effects on the protein's 3D structure provides insight into the protein's mechanism, can aid the design of further experiments, and eventually can lead to the development of new medicines and diagnostic tools. RESULTS: In this article we describe HOPE, a fully automatic program that analyzes the structural and functional effects of point mutations. HOPE collects information from a wide range of information sources including calculations on the 3D coordinates of the protein by using WHAT IF Web services, sequence annotations from the UniProt database, and predictions by DAS services. Homology models are built with YASARA. Data is stored in a database and used in a decision scheme to identify the effects of a mutation on the protein's 3D structure and function. HOPE builds a report with text, figures, and animations that is easy to use and understandable for (bio)medical researchers. CONCLUSIONS: We tested HOPE by comparing its output to the results of manually performed projects. In all straightforward cases HOPE performed similar to a trained bioinformatician. The use of 3D structures helps optimize the results in terms of reliability and details. HOPE's results are easy to understand and are presented in a way that is attractive for researchers without an extensive bioinformatics background. BioMed Central 2010-11-08 /pmc/articles/PMC2992548/ /pubmed/21059217 http://dx.doi.org/10.1186/1471-2105-11-548 Text en Copyright ©2010 Venselaar et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Venselaar, Hanka te Beek, Tim AH Kuipers, Remko KP Hekkelman, Maarten L Vriend, Gert Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces |
title | Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces |
title_full | Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces |
title_fullStr | Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces |
title_full_unstemmed | Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces |
title_short | Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces |
title_sort | protein structure analysis of mutations causing inheritable diseases. an e-science approach with life scientist friendly interfaces |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992548/ https://www.ncbi.nlm.nih.gov/pubmed/21059217 http://dx.doi.org/10.1186/1471-2105-11-548 |
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