European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
Novartis Institutes for BioMedical Research (NIBR), Maulbeerstrasse 66, 4058, Basel, Canton of Basel-Stadt, Switzerland.
Nat Commun. 2019 Jan 2;10(1):10. doi: 10.1038/s41467-018-07709-6.
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.
目前在核苷酸水平上确定的基因组变异数据的丰富程度提出了一个挑战,即需要了解氨基酸变异通过哪些机制影响细胞过程。这些影响可能表现为个体之间明显的表型差异,或者导致疾病的发展。分子之间的物理相互作用是大多数(如果不是全部)细胞过程的基础连接步骤。了解序列变异对分子相互作用的影响是将非同义变异的机制特征与表型联系起来的关键步骤。我们提供了一个由 14 年来 IMEx 数据库管理员创建的开放获取资源,其中包含 28000 个注释,描述了小序列变化对物理蛋白质相互作用的影响。我们描述了如何构建这个资源,提供了数据的格式,并对数据集进行了描述性分析。该数据集可通过 IntAct 网站公开获取,并在每月发布时进行增强。