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Graphical analysis of pH-dependent properties of proteins predicted using PROPKA

BACKGROUND: Charge states of ionizable residues in proteins determine their pH-dependent properties through their pK(a )values. Thus, various theoretical methods to determine ionization constants of residues in biological systems have been developed. One of the more widely used approaches for predic...

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Autores principales: Rostkowski, Michał, Olsson, Mats HM, Søndergaard, Chresten R, Jensen, Jan H
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038139/
https://www.ncbi.nlm.nih.gov/pubmed/21269479
http://dx.doi.org/10.1186/1472-6807-11-6
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author Rostkowski, Michał
Olsson, Mats HM
Søndergaard, Chresten R
Jensen, Jan H
author_facet Rostkowski, Michał
Olsson, Mats HM
Søndergaard, Chresten R
Jensen, Jan H
author_sort Rostkowski, Michał
collection PubMed
description BACKGROUND: Charge states of ionizable residues in proteins determine their pH-dependent properties through their pK(a )values. Thus, various theoretical methods to determine ionization constants of residues in biological systems have been developed. One of the more widely used approaches for predicting pK(a )values in proteins is the PROPKA program, which provides convenient structural rationalization of the predicted pK(a )values without any additional calculations. RESULTS: The PROPKA Graphical User Interface (GUI) is a new tool for studying the pH-dependent properties of proteins such as charge and stabilization energy. It facilitates a quantitative analysis of pK(a )values of ionizable residues together with their structural determinants by providing a direct link between the pK(a )data, predicted by the PROPKA calculations, and the structure via the Visual Molecular Dynamics (VMD) program. The GUI also calculates contributions to the pH-dependent unfolding free energy at a given pH for each ionizable group in the protein. Moreover, the PROPKA-computed pK(a )values or energy contributions of the ionizable residues in question can be displayed interactively. The PROPKA GUI can also be used for comparing pH-dependent properties of more than one structure at the same time. CONCLUSIONS: The GUI considerably extends the analysis and validation possibilities of the PROPKA approach. The PROPKA GUI can conveniently be used to investigate ionizable groups, and their interactions, of residues with significantly perturbed pK(a )values or residues that contribute to the stabilization energy the most. Charge-dependent properties can be studied either for a single protein or simultaneously with other homologous structures, which makes it a helpful tool, for instance, in protein design studies or structure-based function predictions. The GUI is implemented as a Tcl/Tk plug-in for VMD, and can be obtained online at http://propka.ki.ku.dk/~luca/wiki/index.php/GUI_Web.
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spelling pubmed-30381392011-02-25 Graphical analysis of pH-dependent properties of proteins predicted using PROPKA Rostkowski, Michał Olsson, Mats HM Søndergaard, Chresten R Jensen, Jan H BMC Struct Biol Software BACKGROUND: Charge states of ionizable residues in proteins determine their pH-dependent properties through their pK(a )values. Thus, various theoretical methods to determine ionization constants of residues in biological systems have been developed. One of the more widely used approaches for predicting pK(a )values in proteins is the PROPKA program, which provides convenient structural rationalization of the predicted pK(a )values without any additional calculations. RESULTS: The PROPKA Graphical User Interface (GUI) is a new tool for studying the pH-dependent properties of proteins such as charge and stabilization energy. It facilitates a quantitative analysis of pK(a )values of ionizable residues together with their structural determinants by providing a direct link between the pK(a )data, predicted by the PROPKA calculations, and the structure via the Visual Molecular Dynamics (VMD) program. The GUI also calculates contributions to the pH-dependent unfolding free energy at a given pH for each ionizable group in the protein. Moreover, the PROPKA-computed pK(a )values or energy contributions of the ionizable residues in question can be displayed interactively. The PROPKA GUI can also be used for comparing pH-dependent properties of more than one structure at the same time. CONCLUSIONS: The GUI considerably extends the analysis and validation possibilities of the PROPKA approach. The PROPKA GUI can conveniently be used to investigate ionizable groups, and their interactions, of residues with significantly perturbed pK(a )values or residues that contribute to the stabilization energy the most. Charge-dependent properties can be studied either for a single protein or simultaneously with other homologous structures, which makes it a helpful tool, for instance, in protein design studies or structure-based function predictions. The GUI is implemented as a Tcl/Tk plug-in for VMD, and can be obtained online at http://propka.ki.ku.dk/~luca/wiki/index.php/GUI_Web. BioMed Central 2011-01-26 /pmc/articles/PMC3038139/ /pubmed/21269479 http://dx.doi.org/10.1186/1472-6807-11-6 Text en Copyright ©2011 Rostkowski et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Software
Rostkowski, Michał
Olsson, Mats HM
Søndergaard, Chresten R
Jensen, Jan H
Graphical analysis of pH-dependent properties of proteins predicted using PROPKA
title Graphical analysis of pH-dependent properties of proteins predicted using PROPKA
title_full Graphical analysis of pH-dependent properties of proteins predicted using PROPKA
title_fullStr Graphical analysis of pH-dependent properties of proteins predicted using PROPKA
title_full_unstemmed Graphical analysis of pH-dependent properties of proteins predicted using PROPKA
title_short Graphical analysis of pH-dependent properties of proteins predicted using PROPKA
title_sort graphical analysis of ph-dependent properties of proteins predicted using propka
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038139/
https://www.ncbi.nlm.nih.gov/pubmed/21269479
http://dx.doi.org/10.1186/1472-6807-11-6
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