4.8 Article

Interactome INSIDER: a structural interactome browser for genomic studies

期刊

NATURE METHODS
卷 15, 期 2, 页码 107-+

出版社

NATURE PORTFOLIO
DOI: 10.1038/nmeth.4540

关键词

-

资金

  1. National Institute of General Medical Sciences [R01 GM097358, R01 GM104424, R01 GM124559]
  2. National Cancer Institute [R01 CA167824]
  3. Eunice Kennedy Shriver National Institute of Child Health and Human Development grant [R01 HD082568]
  4. National Human Genome Research Institute [UM1 HG009393]
  5. National Science Foundation [DBI-1661380]
  6. Simons Foundation Autism Research Initiative [367561]
  7. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [R01HD082568] Funding Source: NIH RePORTER
  8. NATIONAL CANCER INSTITUTE [R01CA167824] Funding Source: NIH RePORTER
  9. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [UM1HG009393] Funding Source: NIH RePORTER
  10. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM097358, R01GM104424, R01GM124559] Funding Source: NIH RePORTER

向作者/读者索取更多资源

We present Interactome INSIDER, a tool to link genomic variant information with structural protein-protein interactomes. Underlying this tool is the application of machine learning to predict protein interaction interfaces for 185,957 protein interactions with previously unresolved interfaces in human and seven model organisms, including the entire experimentally determined human binary interactome. Predicted interfaces exhibit functional properties similar to those of known interfaces, including enrichment for disease mutations and recurrent cancer mutations. Through 2,164 de novo mutagenesis experiments, we show that mutations of predicted and known interface residues disrupt interactions at a similar rate and much more frequently than mutations outside of predicted interfaces. To spur functional genomic studies, Interactome INSIDER (http://interactomeinsider.yulab.org) enables users to identify whether variants or disease mutations are enriched in known and predicted interaction interfaces at various resolutions. Users may explore known population variants, disease mutations, and somatic cancer mutations, or they may upload their own set of mutations for this purpose.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据