Capturing variation impact on molecular interactions: the IMEx Consortium mutations data set
J. Khadake, Birgit MeldaliD, Simona PanniiD, David Thorneycroft, K. Van Roey, Sara Abbani, Łukasz SalwińskiiD, Matteo A. PellegriniiD, Marta IannuccelliiD, Luana LicataiD, G. Cesareni, Bernd Roechert, Alan James BridgeiD, Mais G. Ammari, Fiona McCarthyiD, F. Broackes-Carter, Nancy H. CampbelliD, Anna N. MelidoniiD, M. Rodríguez-LópeziD, Ruth C. LoveringiD, S. Jagannathan, Carol C. L. CheniD, David John LynniD, Sylvie Ricard‐BlumiD, U. Mahadevan, , Pablo PorrasiD
Abstract
The current wealth of genomic variation data identified at the nucleotide level has provided us with 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 amino acid variation of a molecules sequence has on its molecular interactions is a key step towards connecting a full mechanistic characterization of nonsynonymous variation to cellular phenotype. Here we present an open access resource created by IMEx database curators over 14 years, featuring 28,000 annotations fully describing the effect of individual point sequence changes on physical protein interactions. We describe how this resource was built, the formats in which the data content is provided and offer a descriptive analysis of the data set. The data set is publicly available through the IntAct website at www.ebi.ac.uk/intact/resources/datasets#mutationDs and is being enhanced with every monthly release.
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