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The FoldX web server: an online force field

FoldX is an empirical force field that was developed for the rapid evaluation of the effect of mutations on the stability, folding and dynamics of proteins and nucleic acids. The core functionality of FoldX, namely the calculation of the free energy of a macromolecule based on its high-resolution 3D...

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Autores principales: Schymkowitz, Joost, Borg, Jesper, Stricher, Francois, Nys, Robby, Rousseau, Frederic, Serrano, Luis
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1160148/
https://www.ncbi.nlm.nih.gov/pubmed/15980494
http://dx.doi.org/10.1093/nar/gki387
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author Schymkowitz, Joost
Borg, Jesper
Stricher, Francois
Nys, Robby
Rousseau, Frederic
Serrano, Luis
author_facet Schymkowitz, Joost
Borg, Jesper
Stricher, Francois
Nys, Robby
Rousseau, Frederic
Serrano, Luis
author_sort Schymkowitz, Joost
collection PubMed
description FoldX is an empirical force field that was developed for the rapid evaluation of the effect of mutations on the stability, folding and dynamics of proteins and nucleic acids. The core functionality of FoldX, namely the calculation of the free energy of a macromolecule based on its high-resolution 3D structure, is now publicly available through a web server at . The current release allows the calculation of the stability of a protein, calculation of the positions of the protons and the prediction of water bridges, prediction of metal binding sites and the analysis of the free energy of complex formation. Alanine scanning, the systematic truncation of side chains to alanine, is also included. In addition, some reporting functions have been added, and it is now possible to print both the atomic interaction networks that constitute the protein, print the structural and energetic details of the interactions per atom or per residue, as well as generate a general quality report of the pdb structure. This core functionality will be further extended as more FoldX applications are developed.
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spelling pubmed-11601482005-06-29 The FoldX web server: an online force field Schymkowitz, Joost Borg, Jesper Stricher, Francois Nys, Robby Rousseau, Frederic Serrano, Luis Nucleic Acids Res Article FoldX is an empirical force field that was developed for the rapid evaluation of the effect of mutations on the stability, folding and dynamics of proteins and nucleic acids. The core functionality of FoldX, namely the calculation of the free energy of a macromolecule based on its high-resolution 3D structure, is now publicly available through a web server at . The current release allows the calculation of the stability of a protein, calculation of the positions of the protons and the prediction of water bridges, prediction of metal binding sites and the analysis of the free energy of complex formation. Alanine scanning, the systematic truncation of side chains to alanine, is also included. In addition, some reporting functions have been added, and it is now possible to print both the atomic interaction networks that constitute the protein, print the structural and energetic details of the interactions per atom or per residue, as well as generate a general quality report of the pdb structure. This core functionality will be further extended as more FoldX applications are developed. Oxford University Press 2005-07-01 2005-06-27 /pmc/articles/PMC1160148/ /pubmed/15980494 http://dx.doi.org/10.1093/nar/gki387 Text en © The Author 2005. Published by Oxford University Press. All rights reserved
spellingShingle Article
Schymkowitz, Joost
Borg, Jesper
Stricher, Francois
Nys, Robby
Rousseau, Frederic
Serrano, Luis
The FoldX web server: an online force field
title The FoldX web server: an online force field
title_full The FoldX web server: an online force field
title_fullStr The FoldX web server: an online force field
title_full_unstemmed The FoldX web server: an online force field
title_short The FoldX web server: an online force field
title_sort foldx web server: an online force field
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1160148/
https://www.ncbi.nlm.nih.gov/pubmed/15980494
http://dx.doi.org/10.1093/nar/gki387
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