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MODBASE: a database of annotated comparative protein structure models and associated resources
MODBASE () is a database of annotated comparative protein structure models for all available protein sequences that can be matched to at least one known protein structure. The models are calculated by MODPIPE, an automated modeling pipeline that relies on MODELLER for fold assignment, sequence–struc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347422/ https://www.ncbi.nlm.nih.gov/pubmed/16381869 http://dx.doi.org/10.1093/nar/gkj059 |
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author | Pieper, Ursula Eswar, Narayanan Davis, Fred P. Braberg, Hannes Madhusudhan, M. S. Rossi, Andrea Marti-Renom, Marc Karchin, Rachel Webb, Ben M. Eramian, David Shen, Min-Yi Kelly, Libusha Melo, Francisco Sali, Andrej |
author_facet | Pieper, Ursula Eswar, Narayanan Davis, Fred P. Braberg, Hannes Madhusudhan, M. S. Rossi, Andrea Marti-Renom, Marc Karchin, Rachel Webb, Ben M. Eramian, David Shen, Min-Yi Kelly, Libusha Melo, Francisco Sali, Andrej |
author_sort | Pieper, Ursula |
collection | PubMed |
description | MODBASE () is a database of annotated comparative protein structure models for all available protein sequences that can be matched to at least one known protein structure. The models are calculated by MODPIPE, an automated modeling pipeline that relies on MODELLER for fold assignment, sequence–structure alignment, model building and model assessment (). MODBASE is updated regularly to reflect the growth in protein sequence and structure databases, and improvements in the software for calculating the models. MODBASE currently contains 3 094 524 reliable models for domains in 1 094 750 out of 1 817 889 unique protein sequences in the UniProt database (July 5, 2005); only models based on statistically significant alignments and models assessed to have the correct fold despite insignificant alignments are included. MODBASE also allows users to generate comparative models for proteins of interest with the automated modeling server MODWEB (). Our other resources integrated with MODBASE include comprehensive databases of multiple protein structure alignments (DBAli, ), structurally defined ligand binding sites and structurally defined binary domain interfaces (PIBASE, ) as well as predictions of ligand binding sites, interactions between yeast proteins, and functional consequences of human nsSNPs (LS-SNP, ). |
format | Text |
id | pubmed-1347422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-13474222006-01-25 MODBASE: a database of annotated comparative protein structure models and associated resources Pieper, Ursula Eswar, Narayanan Davis, Fred P. Braberg, Hannes Madhusudhan, M. S. Rossi, Andrea Marti-Renom, Marc Karchin, Rachel Webb, Ben M. Eramian, David Shen, Min-Yi Kelly, Libusha Melo, Francisco Sali, Andrej Nucleic Acids Res Article MODBASE () is a database of annotated comparative protein structure models for all available protein sequences that can be matched to at least one known protein structure. The models are calculated by MODPIPE, an automated modeling pipeline that relies on MODELLER for fold assignment, sequence–structure alignment, model building and model assessment (). MODBASE is updated regularly to reflect the growth in protein sequence and structure databases, and improvements in the software for calculating the models. MODBASE currently contains 3 094 524 reliable models for domains in 1 094 750 out of 1 817 889 unique protein sequences in the UniProt database (July 5, 2005); only models based on statistically significant alignments and models assessed to have the correct fold despite insignificant alignments are included. MODBASE also allows users to generate comparative models for proteins of interest with the automated modeling server MODWEB (). Our other resources integrated with MODBASE include comprehensive databases of multiple protein structure alignments (DBAli, ), structurally defined ligand binding sites and structurally defined binary domain interfaces (PIBASE, ) as well as predictions of ligand binding sites, interactions between yeast proteins, and functional consequences of human nsSNPs (LS-SNP, ). Oxford University Press 2006-01-01 2005-12-28 /pmc/articles/PMC1347422/ /pubmed/16381869 http://dx.doi.org/10.1093/nar/gkj059 Text en © The Author 2006. Published by Oxford University Press. All rights reserved |
spellingShingle | Article Pieper, Ursula Eswar, Narayanan Davis, Fred P. Braberg, Hannes Madhusudhan, M. S. Rossi, Andrea Marti-Renom, Marc Karchin, Rachel Webb, Ben M. Eramian, David Shen, Min-Yi Kelly, Libusha Melo, Francisco Sali, Andrej MODBASE: a database of annotated comparative protein structure models and associated resources |
title | MODBASE: a database of annotated comparative protein structure models and associated resources |
title_full | MODBASE: a database of annotated comparative protein structure models and associated resources |
title_fullStr | MODBASE: a database of annotated comparative protein structure models and associated resources |
title_full_unstemmed | MODBASE: a database of annotated comparative protein structure models and associated resources |
title_short | MODBASE: a database of annotated comparative protein structure models and associated resources |
title_sort | modbase: a database of annotated comparative protein structure models and associated resources |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347422/ https://www.ncbi.nlm.nih.gov/pubmed/16381869 http://dx.doi.org/10.1093/nar/gkj059 |
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