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Integrative visual analysis of protein sequence mutations.
Doncheva, Nadezhda T; Klein, Karsten; Morris, John H; Wybrow, Michael; Domingues, Francisco S; Albrecht, Mario.
Afiliación
  • Doncheva NT; Max Planck Institute for Informatics, 66123 Saarbücken, Germany ; University of California, San Francisco, 94143-2240 San Francisco, USA.
  • Klein K; The University of Sydney, 2006 Sydney, Australia.
  • Morris JH; University of California, San Francisco, 94143-2240 San Francisco, USA.
  • Wybrow M; Monash University, 3145 Melbourne, Australia.
  • Domingues FS; EURAC research, 39100 Bolzano, Italy.
  • Albrecht M; University Medicine Greifswald, 17475 Greifswald, Germany ; Graz University of Technology, 8010 Graz, Austria ; BioTechMed-Graz, 8010 Graz, Austria.
BMC Proc ; 8(Suppl 2 Proceedings of the 3rd Annual Symposium on Biologica): S2, 2014.
Article en En | MEDLINE | ID: mdl-25237389
BACKGROUND: An important aspect of studying the relationship between protein sequence, structure and function is the molecular characterization of the effect of protein mutations. To understand the functional impact of amino acid changes, the multiple biological properties of protein residues have to be considered together. RESULTS: Here, we present a novel visual approach for analyzing residue mutations. It combines different biological visualizations and integrates them with molecular data derived from external resources. To show various aspects of the biological information on different scales, our approach includes one-dimensional sequence views, three-dimensional protein structure views and two-dimensional views of residue interaction networks as well as aggregated views. The views are linked tightly and synchronized to reduce the cognitive load of the user when switching between them. In particular, the protein mutations are mapped onto the views together with further functional and structural information. We also assess the impact of individual amino acid changes by the detailed analysis and visualization of the involved residue interactions. We demonstrate the effectiveness of our approach and the developed software on the data provided for the BioVis 2013 data contest. CONCLUSIONS: Our visual approach and software greatly facilitate the integrative and interactive analysis of protein mutations based on complementary visualizations. The different data views offered to the user are enriched with information about molecular properties of amino acid residues and further biological knowledge.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BMC Proc Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BMC Proc Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos
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