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Network-based prediction of protein interactions.
Kovács, István A; Luck, Katja; Spirohn, Kerstin; Wang, Yang; Pollis, Carl; Schlabach, Sadie; Bian, Wenting; Kim, Dae-Kyum; Kishore, Nishka; Hao, Tong; Calderwood, Michael A; Vidal, Marc; Barabási, Albert-László.
Afiliação
  • Kovács IA; Network Science Institute and Department of Physics, Northeastern University, Boston, MA, 02115, USA. i.kovacs@northeastern.edu.
  • Luck K; Center for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, 02115, USA. i.kovacs@northeastern.edu.
  • Spirohn K; Wigner Research Centre for Physics, Institute for Solid State Physics and Optics, H-1525, Budapest, P.O.Box 49, Hungary. i.kovacs@northeastern.edu.
  • Wang Y; Center for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, 02115, USA.
  • Pollis C; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, 02115, USA.
  • Schlabach S; Center for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, 02115, USA.
  • Bian W; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, 02115, USA.
  • Kim DK; Center for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, 02115, USA.
  • Kishore N; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, 02115, USA.
  • Hao T; Center for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, 02115, USA.
  • Calderwood MA; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, 02115, USA.
  • Vidal M; Center for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, 02115, USA.
  • Barabási AL; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, 02115, USA.
Nat Commun ; 10(1): 1240, 2019 03 18.
Article em En | MEDLINE | ID: mdl-30886144
Despite exceptional experimental efforts to map out the human interactome, the continued data incompleteness limits our ability to understand the molecular roots of human disease. Computational tools offer a promising alternative, helping identify biologically significant, yet unmapped protein-protein interactions (PPIs). While link prediction methods connect proteins on the basis of biological or network-based similarity, interacting proteins are not necessarily similar and similar proteins do not necessarily interact. Here, we offer structural and evolutionary evidence that proteins interact not if they are similar to each other, but if one of them is similar to the other's partners. This approach, that mathematically relies on network paths of length three (L3), significantly outperforms all existing link prediction methods. Given its high accuracy, we show that L3 can offer mechanistic insights into disease mechanisms and can complement future experimental efforts to complete the human interactome.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article