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Reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures

BACKGROUND: Electron cryomicroscopy is a fast developing technique aiming at the determination of the 3-dimensional structures of large protein complexes. Using this technique, protein density maps can be generated with 6 to 10 Å resolution. At such resolutions, the secondary structure elements such...

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Autores principales: Sun, Weitao, He, Jing
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648730/
https://www.ncbi.nlm.nih.gov/pubmed/19208142
http://dx.doi.org/10.1186/1471-2105-10-S1-S40
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author Sun, Weitao
He, Jing
author_facet Sun, Weitao
He, Jing
author_sort Sun, Weitao
collection PubMed
description BACKGROUND: Electron cryomicroscopy is a fast developing technique aiming at the determination of the 3-dimensional structures of large protein complexes. Using this technique, protein density maps can be generated with 6 to 10 Å resolution. At such resolutions, the secondary structure elements such as helices and β-strands appear to be skeletons and can be computationally detected. However, it is not known which segment of the protein sequence corresponds to which of the skeletons. The topology in this paper refers to the linear order and the directionality of the secondary structures. For a protein with N helices and M strands, there are (N!2(N))(M!2(M)) different topologies, each of which maps N helix segments and M strand segments on the protein sequence to N helix and M strand skeletons. Since the backbone position is not available in the skeleton, each topology of the skeletons corresponds to additional freedom to position the atoms in the skeletons. RESULTS: We have developed a method to construct the possible atomic structures for the helix skeletons by sampling the solution space of all the possible topologies of the skeletons. Our method also ranks the possible structures based on the contact energy formed by the secondary structures, rather than the entire chain. If we assume that the backbone atomic positions are known for the skeletons, then the native topology of the secondary structures can be found in the top 30% of the ranked list of all possible topologies for all the 30 proteins tested, and within the top 5% for most of the 30 proteins. Without assuming the backbone location of the skeletons, the possible atomic structures of the skeletons can be constructed using the axis of the skeleton and the sequence segments. The best constructed structure for the skeletons has RMSD to native between 4 and 5 Å for the four tested α-proteins. These best constructed structures were ranked the 17(th), 31(st), 16(th )and 5(th )respectively for the four proteins out of 32066, 391833, 98755 and 192935 possible assignments in the pool. CONCLUSION: Our work suggested that the direct estimation of the contact energy formed by the secondary structures is quite effective in reducing the topological space to a small subset that includes a near native structure for the skeletons.
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spelling pubmed-26487302009-03-03 Reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures Sun, Weitao He, Jing BMC Bioinformatics Research BACKGROUND: Electron cryomicroscopy is a fast developing technique aiming at the determination of the 3-dimensional structures of large protein complexes. Using this technique, protein density maps can be generated with 6 to 10 Å resolution. At such resolutions, the secondary structure elements such as helices and β-strands appear to be skeletons and can be computationally detected. However, it is not known which segment of the protein sequence corresponds to which of the skeletons. The topology in this paper refers to the linear order and the directionality of the secondary structures. For a protein with N helices and M strands, there are (N!2(N))(M!2(M)) different topologies, each of which maps N helix segments and M strand segments on the protein sequence to N helix and M strand skeletons. Since the backbone position is not available in the skeleton, each topology of the skeletons corresponds to additional freedom to position the atoms in the skeletons. RESULTS: We have developed a method to construct the possible atomic structures for the helix skeletons by sampling the solution space of all the possible topologies of the skeletons. Our method also ranks the possible structures based on the contact energy formed by the secondary structures, rather than the entire chain. If we assume that the backbone atomic positions are known for the skeletons, then the native topology of the secondary structures can be found in the top 30% of the ranked list of all possible topologies for all the 30 proteins tested, and within the top 5% for most of the 30 proteins. Without assuming the backbone location of the skeletons, the possible atomic structures of the skeletons can be constructed using the axis of the skeleton and the sequence segments. The best constructed structure for the skeletons has RMSD to native between 4 and 5 Å for the four tested α-proteins. These best constructed structures were ranked the 17(th), 31(st), 16(th )and 5(th )respectively for the four proteins out of 32066, 391833, 98755 and 192935 possible assignments in the pool. CONCLUSION: Our work suggested that the direct estimation of the contact energy formed by the secondary structures is quite effective in reducing the topological space to a small subset that includes a near native structure for the skeletons. BioMed Central 2009-01-30 /pmc/articles/PMC2648730/ /pubmed/19208142 http://dx.doi.org/10.1186/1471-2105-10-S1-S40 Text en Copyright © 2009 Sun and He; 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 Research
Sun, Weitao
He, Jing
Reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures
title Reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures
title_full Reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures
title_fullStr Reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures
title_full_unstemmed Reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures
title_short Reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures
title_sort reduction of the secondary structure topological space through direct estimation of the contact energy formed by the secondary structures
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648730/
https://www.ncbi.nlm.nih.gov/pubmed/19208142
http://dx.doi.org/10.1186/1471-2105-10-S1-S40
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