Leri: A web-server for identifying protein functional networks from evolutionary couplings

Information on the co-evolution of amino acid pairs in a protein can be used for endeavors such as protein engineering, mutation design, and structure prediction. Here we report a method that captures significant determinants of proteins using estimated co-evolution information to identify networks...

Full description

Bibliographic Details
Main Authors: Ngaam J. Cheung, Arun T. John Peter, Benoit Kornmann
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Computational and Structural Biotechnology Journal
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2001037021002300
id doaj-209267cafbb94ce3aa71b57f073879d3
record_format Article
spelling doaj-209267cafbb94ce3aa71b57f073879d32021-06-23T04:19:53ZengElsevierComputational and Structural Biotechnology Journal2001-03702021-01-011935563563Leri: A web-server for identifying protein functional networks from evolutionary couplingsNgaam J. Cheung0Arun T. John Peter1Benoit Kornmann2Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK; Leri Ltd, Oxford, UK; Corresponding author at: Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.Institute of Biochemistry, ETH Zürich, Zürich 8092, SwitzerlandDepartment of Biochemistry, University of Oxford, Oxford OX1 3QU, UKInformation on the co-evolution of amino acid pairs in a protein can be used for endeavors such as protein engineering, mutation design, and structure prediction. Here we report a method that captures significant determinants of proteins using estimated co-evolution information to identify networks of residues, termed ”residue communities”, relevant to protein function. On the benchmark dataset (67 proteins with both catalytic and allosteric residues), the Pearson’s correlation between the identified residues in the communities at functional sites is 0.53, and it is higher than 0.8 by taking account of conserved residues derived from the method. On the endoplasmic reticulum-mitochondria encounter structure complex, the results indicate three distinguishable residue communities that are relevant to functional roles in the protein family, suggesting that the residue communities could be general evolutionary signatures in proteins. Based on the method, we provide a webserver for the scientific community to explore the signatures in protein families, which establishes a powerful tool to analyze residue-level profiling for the discovery of functional sites and biological pathway identification. This web-server is freely available for non-commercial users at https://kornmann.bioch.ox.ac.uk/leri/services/ecs.html, neither login nor e-mail required.http://www.sciencedirect.com/science/article/pii/S2001037021002300Residue communityEvolutionary coupling analysisFunctional networkLeri
collection DOAJ
language English
format Article
sources DOAJ
author Ngaam J. Cheung
Arun T. John Peter
Benoit Kornmann
spellingShingle Ngaam J. Cheung
Arun T. John Peter
Benoit Kornmann
Leri: A web-server for identifying protein functional networks from evolutionary couplings
Computational and Structural Biotechnology Journal
Residue community
Evolutionary coupling analysis
Functional network
Leri
author_facet Ngaam J. Cheung
Arun T. John Peter
Benoit Kornmann
author_sort Ngaam J. Cheung
title Leri: A web-server for identifying protein functional networks from evolutionary couplings
title_short Leri: A web-server for identifying protein functional networks from evolutionary couplings
title_full Leri: A web-server for identifying protein functional networks from evolutionary couplings
title_fullStr Leri: A web-server for identifying protein functional networks from evolutionary couplings
title_full_unstemmed Leri: A web-server for identifying protein functional networks from evolutionary couplings
title_sort leri: a web-server for identifying protein functional networks from evolutionary couplings
publisher Elsevier
series Computational and Structural Biotechnology Journal
issn 2001-0370
publishDate 2021-01-01
description Information on the co-evolution of amino acid pairs in a protein can be used for endeavors such as protein engineering, mutation design, and structure prediction. Here we report a method that captures significant determinants of proteins using estimated co-evolution information to identify networks of residues, termed ”residue communities”, relevant to protein function. On the benchmark dataset (67 proteins with both catalytic and allosteric residues), the Pearson’s correlation between the identified residues in the communities at functional sites is 0.53, and it is higher than 0.8 by taking account of conserved residues derived from the method. On the endoplasmic reticulum-mitochondria encounter structure complex, the results indicate three distinguishable residue communities that are relevant to functional roles in the protein family, suggesting that the residue communities could be general evolutionary signatures in proteins. Based on the method, we provide a webserver for the scientific community to explore the signatures in protein families, which establishes a powerful tool to analyze residue-level profiling for the discovery of functional sites and biological pathway identification. This web-server is freely available for non-commercial users at https://kornmann.bioch.ox.ac.uk/leri/services/ecs.html, neither login nor e-mail required.
topic Residue community
Evolutionary coupling analysis
Functional network
Leri
url http://www.sciencedirect.com/science/article/pii/S2001037021002300
work_keys_str_mv AT ngaamjcheung leriawebserverforidentifyingproteinfunctionalnetworksfromevolutionarycouplings
AT aruntjohnpeter leriawebserverforidentifyingproteinfunctionalnetworksfromevolutionarycouplings
AT benoitkornmann leriawebserverforidentifyingproteinfunctionalnetworksfromevolutionarycouplings
_version_ 1721362574239334400