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Fast Tree Search for A Triangular Lattice Model of Protein Folding

Using a triangular lattice model to study the designability of protein folding, we overcame the parity problem of previous cubic lattice model and enumerated all the sequences and compact structures on a simple two-dimensional triangular lattice model of size 4+5+6+5+4. We used two types of amino ac...

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Detalles Bibliográficos
Autores principales: Li, Xiaomei, Wang, Nengchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5187417/
https://www.ncbi.nlm.nih.gov/pubmed/15901253
http://dx.doi.org/10.1016/S1672-0229(04)02031-5
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author Li, Xiaomei
Wang, Nengchao
author_facet Li, Xiaomei
Wang, Nengchao
author_sort Li, Xiaomei
collection PubMed
description Using a triangular lattice model to study the designability of protein folding, we overcame the parity problem of previous cubic lattice model and enumerated all the sequences and compact structures on a simple two-dimensional triangular lattice model of size 4+5+6+5+4. We used two types of amino acids, hydrophobic and polar, to make up the sequences, and achieved 2(23)+2(12) different sequences excluding the reverse symmetry sequences. The total string number of distinct compact structures was 219,093, excluding reflection symmetry in the self-avoiding path of length 24 triangular lattice model. Based on this model, we applied a fast search algorithm by constructing a cluster tree. The algorithm decreased the computation by computing the objective energy of non-leaf nodes. The parallel experiments proved that the fast tree search algorithm yielded an exponential speed-up in the model of size 4+5+6+5+4. Designability analysis was performed to understand the search result.
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spelling pubmed-51874172017-01-03 Fast Tree Search for A Triangular Lattice Model of Protein Folding Li, Xiaomei Wang, Nengchao Genomics Proteomics Bioinformatics Letter Using a triangular lattice model to study the designability of protein folding, we overcame the parity problem of previous cubic lattice model and enumerated all the sequences and compact structures on a simple two-dimensional triangular lattice model of size 4+5+6+5+4. We used two types of amino acids, hydrophobic and polar, to make up the sequences, and achieved 2(23)+2(12) different sequences excluding the reverse symmetry sequences. The total string number of distinct compact structures was 219,093, excluding reflection symmetry in the self-avoiding path of length 24 triangular lattice model. Based on this model, we applied a fast search algorithm by constructing a cluster tree. The algorithm decreased the computation by computing the objective energy of non-leaf nodes. The parallel experiments proved that the fast tree search algorithm yielded an exponential speed-up in the model of size 4+5+6+5+4. Designability analysis was performed to understand the search result. Elsevier 2004-11 2016-11-28 /pmc/articles/PMC5187417/ /pubmed/15901253 http://dx.doi.org/10.1016/S1672-0229(04)02031-5 Text en . http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Letter
Li, Xiaomei
Wang, Nengchao
Fast Tree Search for A Triangular Lattice Model of Protein Folding
title Fast Tree Search for A Triangular Lattice Model of Protein Folding
title_full Fast Tree Search for A Triangular Lattice Model of Protein Folding
title_fullStr Fast Tree Search for A Triangular Lattice Model of Protein Folding
title_full_unstemmed Fast Tree Search for A Triangular Lattice Model of Protein Folding
title_short Fast Tree Search for A Triangular Lattice Model of Protein Folding
title_sort fast tree search for a triangular lattice model of protein folding
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5187417/
https://www.ncbi.nlm.nih.gov/pubmed/15901253
http://dx.doi.org/10.1016/S1672-0229(04)02031-5
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