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Capturing variation impact on molecular interactions in the IMEx Consortium mutations data set.
Del-Toro, N; Duesbury, M; Koch, M; Perfetto, L; Shrivastava, A; Ochoa, D; Wagih, O; Piñero, J; Kotlyar, M; Pastrello, C; Beltrao, P; Furlong, L I; Jurisica, I; Hermjakob, H; Orchard, S; Porras, P.
Afiliação
  • Del-Toro N; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Duesbury M; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Koch M; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Perfetto L; Novartis Institutes for BioMedical Research (NIBR), Maulbeerstrasse 66, 4058, Basel, Canton of Basel-Stadt, Switzerland.
  • Shrivastava A; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Ochoa D; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Wagih O; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Piñero J; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Kotlyar M; Deep Genomics, MaRS Centre, 661 University Ave, Suite 480, Toronto, ON, M5G 1M1, Canada.
  • Pastrello C; Research Programme on Biomedical Informatics (GRIB), Department of Experimental and Health Sciences (DCEXS), Hospital del Mar Medical Research Institute (IMIM), Universitat Pompeu Fabra (UPF), 08003, Barcelona, Spain.
  • Beltrao P; Krembil Research Institute, Data Science Discovery Centre for Chronic Diseases, University Health Network, 5KD-407, 60 Leonard Avenue, Toronto, ON, M5T 0S8, Canada.
  • Furlong LI; Krembil Research Institute, Data Science Discovery Centre for Chronic Diseases, University Health Network, 5KD-407, 60 Leonard Avenue, Toronto, ON, M5T 0S8, Canada.
  • Jurisica I; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Hermjakob H; Research Programme on Biomedical Informatics (GRIB), Department of Experimental and Health Sciences (DCEXS), Hospital del Mar Medical Research Institute (IMIM), Universitat Pompeu Fabra (UPF), 08003, Barcelona, Spain.
  • Orchard S; Krembil Research Institute, Data Science Discovery Centre for Chronic Diseases, University Health Network, 5KD-407, 60 Leonard Avenue, Toronto, ON, M5T 0S8, Canada.
  • Porras P; Departments of Medical Biophysics and Computer Science, University of Toronto, Toronto, M4B 1B5, Canada.
Nat Commun ; 10(1): 10, 2019 01 02.
Article em En | MEDLINE | ID: mdl-30602777
ABSTRACT
The current wealth of genomic variation data identified at nucleotide level presents the challenge of understanding by which mechanisms amino acid variation affects cellular processes. These effects may manifest as distinct phenotypic differences between individuals or result in the development of disease. Physical interactions between molecules are the linking steps underlying most, if not all, cellular processes. Understanding the effects that sequence variation has on a molecule's interactions is a key step towards connecting mechanistic characterization of nonsynonymous variation to phenotype. We present an open access resource created over 14 years by IMEx database curators, featuring 28,000 annotations describing the effect of small sequence changes on physical protein interactions. We describe how this resource was built, the formats in which the data is provided and offer a descriptive analysis of the data set. The data set is publicly available through the IntAct website and is enhanced with every monthly release.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Mutação Puntual / Substituição de Aminoácidos / Anotação de Sequência Molecular / Mapas de Interação de Proteínas Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Mutação Puntual / Substituição de Aminoácidos / Anotação de Sequência Molecular / Mapas de Interação de Proteínas Idioma: En Ano de publicação: 2019 Tipo de documento: Article