An Accurate Model for Biomolecular Helices and Its Application to Helix Visualization.

Helices are the most abundant secondary structural elements in proteins and the structural forms assumed by double stranded DNAs (dsDNA). Though the mathematical expression for a helical curve is simple, none of the previous models for the biomolecular helices in either proteins or DNAs use a genuin...

Full description

Bibliographic Details
Main Authors: Lincong Wang, Hui Qiao, Chen Cao, Shutan Xu, Shuxue Zou
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4488352?pdf=render
id doaj-c7e5993a1b174262a27b610b75dd0a08
record_format Article
spelling doaj-c7e5993a1b174262a27b610b75dd0a082020-11-24T21:58:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01106e012965310.1371/journal.pone.0129653An Accurate Model for Biomolecular Helices and Its Application to Helix Visualization.Lincong WangHui QiaoChen CaoShutan XuShuxue ZouHelices are the most abundant secondary structural elements in proteins and the structural forms assumed by double stranded DNAs (dsDNA). Though the mathematical expression for a helical curve is simple, none of the previous models for the biomolecular helices in either proteins or DNAs use a genuine helical curve, likely because of the complexity of fitting backbone atoms to helical curves. In this paper we model a helix as a series of different but all bona fide helical curves; each one best fits the coordinates of four consecutive backbone Cα atoms for a protein or P atoms for a DNA molecule. An implementation of the model demonstrates that it is more accurate than the previous ones for the description of the deviation of a helix from a standard helical curve. Furthermore, the accuracy of the model makes it possible to correlate deviations with structural and functional significance. When applied to helix visualization, the ribbon diagrams generated by the model are less choppy or have smaller side chain detachment than those by the previous visualization programs that typically model a helix as a series of low-degree splines.http://europepmc.org/articles/PMC4488352?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Lincong Wang
Hui Qiao
Chen Cao
Shutan Xu
Shuxue Zou
spellingShingle Lincong Wang
Hui Qiao
Chen Cao
Shutan Xu
Shuxue Zou
An Accurate Model for Biomolecular Helices and Its Application to Helix Visualization.
PLoS ONE
author_facet Lincong Wang
Hui Qiao
Chen Cao
Shutan Xu
Shuxue Zou
author_sort Lincong Wang
title An Accurate Model for Biomolecular Helices and Its Application to Helix Visualization.
title_short An Accurate Model for Biomolecular Helices and Its Application to Helix Visualization.
title_full An Accurate Model for Biomolecular Helices and Its Application to Helix Visualization.
title_fullStr An Accurate Model for Biomolecular Helices and Its Application to Helix Visualization.
title_full_unstemmed An Accurate Model for Biomolecular Helices and Its Application to Helix Visualization.
title_sort accurate model for biomolecular helices and its application to helix visualization.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Helices are the most abundant secondary structural elements in proteins and the structural forms assumed by double stranded DNAs (dsDNA). Though the mathematical expression for a helical curve is simple, none of the previous models for the biomolecular helices in either proteins or DNAs use a genuine helical curve, likely because of the complexity of fitting backbone atoms to helical curves. In this paper we model a helix as a series of different but all bona fide helical curves; each one best fits the coordinates of four consecutive backbone Cα atoms for a protein or P atoms for a DNA molecule. An implementation of the model demonstrates that it is more accurate than the previous ones for the description of the deviation of a helix from a standard helical curve. Furthermore, the accuracy of the model makes it possible to correlate deviations with structural and functional significance. When applied to helix visualization, the ribbon diagrams generated by the model are less choppy or have smaller side chain detachment than those by the previous visualization programs that typically model a helix as a series of low-degree splines.
url http://europepmc.org/articles/PMC4488352?pdf=render
work_keys_str_mv AT lincongwang anaccuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT huiqiao anaccuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT chencao anaccuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT shutanxu anaccuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT shuxuezou anaccuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT lincongwang accuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT huiqiao accuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT chencao accuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT shutanxu accuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
AT shuxuezou accuratemodelforbiomolecularhelicesanditsapplicationtohelixvisualization
_version_ 1725850943022432256