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Completion of autobuilt protein models using a database of protein fragments
Two developments in the process of automated protein model building in the Buccaneer software are presented. A general-purpose library for protein fragments of arbitrary size is described, with a highly optimized search method allowing the use of a larger database than in previous work. The problem...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322592/ https://www.ncbi.nlm.nih.gov/pubmed/22505253 http://dx.doi.org/10.1107/S0907444911039655 |
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author | Cowtan, Kevin |
author_facet | Cowtan, Kevin |
author_sort | Cowtan, Kevin |
collection | PubMed |
description | Two developments in the process of automated protein model building in the Buccaneer software are presented. A general-purpose library for protein fragments of arbitrary size is described, with a highly optimized search method allowing the use of a larger database than in previous work. The problem of assembling an autobuilt model into complete chains is discussed. This involves the assembly of disconnected chain fragments into complete molecules and the use of the database of protein fragments in improving the model completeness. Assembly of fragments into molecules is a standard step in existing model-building software, but the methods have not received detailed discussion in the literature. |
format | Online Article Text |
id | pubmed-3322592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33225922012-04-16 Completion of autobuilt protein models using a database of protein fragments Cowtan, Kevin Acta Crystallogr D Biol Crystallogr Research Papers Two developments in the process of automated protein model building in the Buccaneer software are presented. A general-purpose library for protein fragments of arbitrary size is described, with a highly optimized search method allowing the use of a larger database than in previous work. The problem of assembling an autobuilt model into complete chains is discussed. This involves the assembly of disconnected chain fragments into complete molecules and the use of the database of protein fragments in improving the model completeness. Assembly of fragments into molecules is a standard step in existing model-building software, but the methods have not received detailed discussion in the literature. International Union of Crystallography 2012-04-01 2012-03-16 /pmc/articles/PMC3322592/ /pubmed/22505253 http://dx.doi.org/10.1107/S0907444911039655 Text en © Cowtan 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Research Papers Cowtan, Kevin Completion of autobuilt protein models using a database of protein fragments |
title | Completion of autobuilt protein models using a database of protein fragments |
title_full | Completion of autobuilt protein models using a database of protein fragments |
title_fullStr | Completion of autobuilt protein models using a database of protein fragments |
title_full_unstemmed | Completion of autobuilt protein models using a database of protein fragments |
title_short | Completion of autobuilt protein models using a database of protein fragments |
title_sort | completion of autobuilt protein models using a database of protein fragments |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322592/ https://www.ncbi.nlm.nih.gov/pubmed/22505253 http://dx.doi.org/10.1107/S0907444911039655 |
work_keys_str_mv | AT cowtankevin completionofautobuiltproteinmodelsusingadatabaseofproteinfragments |