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Potential DNA binding and nuclease functions of ComEC domains characterized in silico

Bacterial competence, which can be natural or induced, allows the uptake of exogenous double stranded DNA (dsDNA) into a competent bacterium. This process is known as transformation. A multiprotein assembly binds and processes the dsDNA to import one strand and degrade another yet the underlying mol...

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Autores principales: Baker, James A., Simkovic, Felix, Taylor, Helen M.C., Rigden, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031224/
https://www.ncbi.nlm.nih.gov/pubmed/27318187
http://dx.doi.org/10.1002/prot.25088
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author Baker, James A.
Simkovic, Felix
Taylor, Helen M.C.
Rigden, Daniel J.
author_facet Baker, James A.
Simkovic, Felix
Taylor, Helen M.C.
Rigden, Daniel J.
author_sort Baker, James A.
collection PubMed
description Bacterial competence, which can be natural or induced, allows the uptake of exogenous double stranded DNA (dsDNA) into a competent bacterium. This process is known as transformation. A multiprotein assembly binds and processes the dsDNA to import one strand and degrade another yet the underlying molecular mechanisms are relatively poorly understood. Here distant relationships of domains in Competence protein EC (ComEC) of Bacillus subtilis (Uniprot: P39695) were characterized. DNA‐protein interactions were investigated in silico by analyzing models for structural conservation, surface electrostatics and structure‐based DNA binding propensity; and by data‐driven macromolecular docking of DNA to models. Our findings suggest that the DUF4131 domain contains a cryptic DNA‐binding OB fold domain and that the β‐lactamase‐like domain is the hitherto cryptic competence nuclease. Proteins 2016; 84:1431–1442. © 2016 The Authors Proteins: Structure, Function, and Bioinformatics Published by Wiley Periodicals, Inc.
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spelling pubmed-50312242016-10-03 Potential DNA binding and nuclease functions of ComEC domains characterized in silico Baker, James A. Simkovic, Felix Taylor, Helen M.C. Rigden, Daniel J. Proteins Articles Bacterial competence, which can be natural or induced, allows the uptake of exogenous double stranded DNA (dsDNA) into a competent bacterium. This process is known as transformation. A multiprotein assembly binds and processes the dsDNA to import one strand and degrade another yet the underlying molecular mechanisms are relatively poorly understood. Here distant relationships of domains in Competence protein EC (ComEC) of Bacillus subtilis (Uniprot: P39695) were characterized. DNA‐protein interactions were investigated in silico by analyzing models for structural conservation, surface electrostatics and structure‐based DNA binding propensity; and by data‐driven macromolecular docking of DNA to models. Our findings suggest that the DUF4131 domain contains a cryptic DNA‐binding OB fold domain and that the β‐lactamase‐like domain is the hitherto cryptic competence nuclease. Proteins 2016; 84:1431–1442. © 2016 The Authors Proteins: Structure, Function, and Bioinformatics Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2016-07-01 2016-10 /pmc/articles/PMC5031224/ /pubmed/27318187 http://dx.doi.org/10.1002/prot.25088 Text en © 2016 The Authors Proteins: Structure, Function, and Bioinformatics Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Baker, James A.
Simkovic, Felix
Taylor, Helen M.C.
Rigden, Daniel J.
Potential DNA binding and nuclease functions of ComEC domains characterized in silico
title Potential DNA binding and nuclease functions of ComEC domains characterized in silico
title_full Potential DNA binding and nuclease functions of ComEC domains characterized in silico
title_fullStr Potential DNA binding and nuclease functions of ComEC domains characterized in silico
title_full_unstemmed Potential DNA binding and nuclease functions of ComEC domains characterized in silico
title_short Potential DNA binding and nuclease functions of ComEC domains characterized in silico
title_sort potential dna binding and nuclease functions of comec domains characterized in silico
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031224/
https://www.ncbi.nlm.nih.gov/pubmed/27318187
http://dx.doi.org/10.1002/prot.25088
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