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Analyzing the symmetrical arrangement of structural repeats in proteins with CE-Symm

View ORCID ProfileSpencer E Bliven, View ORCID ProfileAleixa Lafita, View ORCID ProfilePeter W Rose, Guido Capitani, View ORCID ProfileAndreas Prlić, View ORCID ProfilePhilip E Bourne
doi: https://doi.org/10.1101/297960
Spencer E Bliven
1Laboratory of Biomolecular Research, Paul Scherrer Institute, Villigen, Switzerland
2National Center for Biotechnology Information, National Library of Medicine,National Institutes of Health, Bethesda, MD, USA
3Institute of Applied Simulation, Zurich University of Applied Science, Wäadenswil,Switzerland
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  • For correspondence: mailto:spencer.bliven@zhaw.ch mailto:aleixlafita@ebi.ac.uk
Aleixa Lafita
1Laboratory of Biomolecular Research, Paul Scherrer Institute, Villigen, Switzerland
4Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland
5European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus,Hinxton, Cambridgeshire, UK
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  • For correspondence: mailto:spencer.bliven@zhaw.ch mailto:aleixlafita@ebi.ac.uk
Peter W Rose
6RCSB Protein Data Bank, San Diego Supercomputing Center, University of California San Diego, La Jolla, CA, USA
7Structural Bioinformatics Laboratory, San Diego Supercomputing Center, University of California San Diego, La Jolla, CA, USA
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Guido Capitani
1Laboratory of Biomolecular Research, Paul Scherrer Institute, Villigen, Switzerland
8Department of Biology, ETH Zurich, Zurich, Switzerland
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Andreas Prlić
6RCSB Protein Data Bank, San Diego Supercomputing Center, University of California San Diego, La Jolla, CA, USA
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Philip E Bourne
2National Center for Biotechnology Information, National Library of Medicine,National Institutes of Health, Bethesda, MD, USA
9Department of Biomedical Engineering, University of Virginia, Charlottesville, VA,USA
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Abstract

Many proteins fold into highly regular and repetitive three dimensional structures. The analysis of structural patterns and repeated elements is fundamental to understand protein function and evolution. We present recent improvements to the CE-Symm tool for systematically detecting and analyzing the internal symmetry and structural repeats in proteins. In addition to the accurate detection of internal symmetry, the tool is now capable of i) reporting the type of symmetry, ii) identifying the smallest repeating unit, iii) describing the arrangement of repeats with transformation operations and symmetry axes, and iv) comparing the similarity of all the internal repeats at the residue level. CE-Symm 2.0 helps the user investigate proteins with a robust and intuitive sequence-to-structure analysis, with many applications in protein classification, functional annotation and evolutionary studies. We describe the algorithmic extensions of the method and demonstrate its applications to the study of interesting cases of protein evolution.

Availabilit: CE-Symm is an open source tool integrated into the BioJava library(www.biojava.org)and freely available at https://github.com/rcsb/symmetry.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted October 30, 2018.
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Analyzing the symmetrical arrangement of structural repeats in proteins with CE-Symm
Spencer E Bliven, Aleixa Lafita, Peter W Rose, Guido Capitani, Andreas Prlić, Philip E Bourne
bioRxiv 297960; doi: https://doi.org/10.1101/297960
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Analyzing the symmetrical arrangement of structural repeats in proteins with CE-Symm
Spencer E Bliven, Aleixa Lafita, Peter W Rose, Guido Capitani, Andreas Prlić, Philip E Bourne
bioRxiv 297960; doi: https://doi.org/10.1101/297960

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