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Assignment of PolyProline II Conformation and Analysis of Sequence – Structure Relationship
BACKGROUND: Secondary structures are elements of great importance in structural biology, biochemistry and bioinformatics. They are broadly composed of two repetitive structures namely α-helices and β-sheets, apart from turns, and the rest is associated to coil. These repetitive secondary structures...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069088/ https://www.ncbi.nlm.nih.gov/pubmed/21483785 http://dx.doi.org/10.1371/journal.pone.0018401 |
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author | Mansiaux, Yohann Joseph, Agnel Praveen Gelly, Jean-Christophe de Brevern, Alexandre G. |
author_facet | Mansiaux, Yohann Joseph, Agnel Praveen Gelly, Jean-Christophe de Brevern, Alexandre G. |
author_sort | Mansiaux, Yohann |
collection | PubMed |
description | BACKGROUND: Secondary structures are elements of great importance in structural biology, biochemistry and bioinformatics. They are broadly composed of two repetitive structures namely α-helices and β-sheets, apart from turns, and the rest is associated to coil. These repetitive secondary structures have specific and conserved biophysical and geometric properties. PolyProline II (PPII) helix is yet another interesting repetitive structure which is less frequent and not usually associated with stabilizing interactions. Recent studies have shown that PPII frequency is higher than expected, and they could have an important role in protein – protein interactions. METHODOLOGY/PRINCIPAL FINDINGS: A major factor that limits the study of PPII is that its assignment cannot be carried out with the most commonly used secondary structure assignment methods (SSAMs). The purpose of this work is to propose a PPII assignment methodology that can be defined in the frame of DSSP secondary structure assignment. Considering the ambiguity in PPII assignments by different methods, a consensus assignment strategy was utilized. To define the most consensual rule of PPII assignment, three SSAMs that can assign PPII, were compared and analyzed. The assignment rule was defined to have a maximum coverage of all assignments made by these SSAMs. Not many constraints were added to the assignment and only PPII helices of at least 2 residues length are defined. CONCLUSIONS/SIGNIFICANCE: The simple rules designed in this study for characterizing PPII conformation, lead to the assignment of 5% of all amino as PPII. Sequence – structure relationships associated with PPII, defined by the different SSAMs, underline few striking differences. A specific study of amino acid preferences in their N and C-cap regions was carried out as their solvent accessibility and contact patterns. Thus the assignment of PPII can be coupled with DSSP and thus opens a simple way for further analysis in this field. |
format | Text |
id | pubmed-3069088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30690882011-04-11 Assignment of PolyProline II Conformation and Analysis of Sequence – Structure Relationship Mansiaux, Yohann Joseph, Agnel Praveen Gelly, Jean-Christophe de Brevern, Alexandre G. PLoS One Research Article BACKGROUND: Secondary structures are elements of great importance in structural biology, biochemistry and bioinformatics. They are broadly composed of two repetitive structures namely α-helices and β-sheets, apart from turns, and the rest is associated to coil. These repetitive secondary structures have specific and conserved biophysical and geometric properties. PolyProline II (PPII) helix is yet another interesting repetitive structure which is less frequent and not usually associated with stabilizing interactions. Recent studies have shown that PPII frequency is higher than expected, and they could have an important role in protein – protein interactions. METHODOLOGY/PRINCIPAL FINDINGS: A major factor that limits the study of PPII is that its assignment cannot be carried out with the most commonly used secondary structure assignment methods (SSAMs). The purpose of this work is to propose a PPII assignment methodology that can be defined in the frame of DSSP secondary structure assignment. Considering the ambiguity in PPII assignments by different methods, a consensus assignment strategy was utilized. To define the most consensual rule of PPII assignment, three SSAMs that can assign PPII, were compared and analyzed. The assignment rule was defined to have a maximum coverage of all assignments made by these SSAMs. Not many constraints were added to the assignment and only PPII helices of at least 2 residues length are defined. CONCLUSIONS/SIGNIFICANCE: The simple rules designed in this study for characterizing PPII conformation, lead to the assignment of 5% of all amino as PPII. Sequence – structure relationships associated with PPII, defined by the different SSAMs, underline few striking differences. A specific study of amino acid preferences in their N and C-cap regions was carried out as their solvent accessibility and contact patterns. Thus the assignment of PPII can be coupled with DSSP and thus opens a simple way for further analysis in this field. Public Library of Science 2011-03-31 /pmc/articles/PMC3069088/ /pubmed/21483785 http://dx.doi.org/10.1371/journal.pone.0018401 Text en Mansiaux et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Mansiaux, Yohann Joseph, Agnel Praveen Gelly, Jean-Christophe de Brevern, Alexandre G. Assignment of PolyProline II Conformation and Analysis of Sequence – Structure Relationship |
title | Assignment of PolyProline II Conformation and Analysis of Sequence – Structure Relationship |
title_full | Assignment of PolyProline II Conformation and Analysis of Sequence – Structure Relationship |
title_fullStr | Assignment of PolyProline II Conformation and Analysis of Sequence – Structure Relationship |
title_full_unstemmed | Assignment of PolyProline II Conformation and Analysis of Sequence – Structure Relationship |
title_short | Assignment of PolyProline II Conformation and Analysis of Sequence – Structure Relationship |
title_sort | assignment of polyproline ii conformation and analysis of sequence – structure relationship |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069088/ https://www.ncbi.nlm.nih.gov/pubmed/21483785 http://dx.doi.org/10.1371/journal.pone.0018401 |
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