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Strategies for Structural Genomics Target Selection
We have developed a protein sequence analysis pipeline that ranks proteins as targets for high throughput structure determination. The ranking is designed to maximize both the biological and informational impact of new 3D protein structures solved through the structural genomics initiative. The anal...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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TheScientificWorldJOURNAL
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009347/ https://www.ncbi.nlm.nih.gov/pubmed/29973807 http://dx.doi.org/10.1100/tsw.2002.33 |
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author | Gaasterland, Teri |
author_facet | Gaasterland, Teri |
author_sort | Gaasterland, Teri |
collection | PubMed |
description | We have developed a protein sequence analysis pipeline that ranks proteins as targets for high throughput structure determination. The ranking is designed to maximize both the biological and informational impact of new 3D protein structures solved through the structural genomics initiative. The analysis system accepts proteins from multiple genomes as input, builds sequence families based on remote homology, identifies families with one or more solved structures, and ranks the remaining families according to criteria designed to maximize structure determination efficacy, increase the likelihood of a novel fold, and maximize the number of new protein structure models that can be built from a solved structure. |
format | Online Article Text |
id | pubmed-6009347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | TheScientificWorldJOURNAL |
record_format | MEDLINE/PubMed |
spelling | pubmed-60093472018-07-04 Strategies for Structural Genomics Target Selection Gaasterland, Teri ScientificWorldJournal Short Report We have developed a protein sequence analysis pipeline that ranks proteins as targets for high throughput structure determination. The ranking is designed to maximize both the biological and informational impact of new 3D protein structures solved through the structural genomics initiative. The analysis system accepts proteins from multiple genomes as input, builds sequence families based on remote homology, identifies families with one or more solved structures, and ranks the remaining families according to criteria designed to maximize structure determination efficacy, increase the likelihood of a novel fold, and maximize the number of new protein structure models that can be built from a solved structure. TheScientificWorldJOURNAL 2002-03-05 /pmc/articles/PMC6009347/ /pubmed/29973807 http://dx.doi.org/10.1100/tsw.2002.33 Text en Copyright © 2002 Teri Gaasterland. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Gaasterland, Teri Strategies for Structural Genomics Target Selection |
title | Strategies for Structural Genomics Target Selection |
title_full | Strategies for Structural Genomics Target Selection |
title_fullStr | Strategies for Structural Genomics Target Selection |
title_full_unstemmed | Strategies for Structural Genomics Target Selection |
title_short | Strategies for Structural Genomics Target Selection |
title_sort | strategies for structural genomics target selection |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009347/ https://www.ncbi.nlm.nih.gov/pubmed/29973807 http://dx.doi.org/10.1100/tsw.2002.33 |
work_keys_str_mv | AT gaasterlandteri strategiesforstructuralgenomicstargetselection |