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LRRML: a conformational database and an XML description of leucine-rich repeats (LRRs)
BACKGROUND: Leucine-rich repeats (LRRs) are present in more than 6000 proteins. They are found in organisms ranging from viruses to eukaryotes and play an important role in protein-ligand interactions. To date, more than one hundred crystal structures of LRR containing proteins have been determined....
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2645405/ https://www.ncbi.nlm.nih.gov/pubmed/18986514 http://dx.doi.org/10.1186/1472-6807-8-47 |
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author | Wei, Tiandi Gong, Jing Jamitzky, Ferdinand Heckl, Wolfgang M Stark, Robert W Rössle, Shaila C |
author_facet | Wei, Tiandi Gong, Jing Jamitzky, Ferdinand Heckl, Wolfgang M Stark, Robert W Rössle, Shaila C |
author_sort | Wei, Tiandi |
collection | PubMed |
description | BACKGROUND: Leucine-rich repeats (LRRs) are present in more than 6000 proteins. They are found in organisms ranging from viruses to eukaryotes and play an important role in protein-ligand interactions. To date, more than one hundred crystal structures of LRR containing proteins have been determined. This knowledge has increased our ability to use the crystal structures as templates to model LRR proteins with unknown structures. Since the individual three-dimensional LRR structures are not directly available from the established databases and since there are only a few detailed annotations for them, a conformational LRR database useful for homology modeling of LRR proteins is desirable. DESCRIPTION: We developed LRRML, a conformational database and an extensible markup language (XML) description of LRRs. The release 0.2 contains 1261 individual LRR structures, which were identified from 112 PDB structures and annotated manually. An XML structure was defined to exchange and store the LRRs. LRRML provides a source for homology modeling and structural analysis of LRR proteins. In order to demonstrate the capabilities of the database we modeled the mouse Toll-like receptor 3 (TLR3) by multiple templates homology modeling and compared the result with the crystal structure. CONCLUSION: LRRML is an information source for investigators involved in both theoretical and applied research on LRR proteins. It is available at . |
format | Text |
id | pubmed-2645405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26454052009-02-20 LRRML: a conformational database and an XML description of leucine-rich repeats (LRRs) Wei, Tiandi Gong, Jing Jamitzky, Ferdinand Heckl, Wolfgang M Stark, Robert W Rössle, Shaila C BMC Struct Biol Database BACKGROUND: Leucine-rich repeats (LRRs) are present in more than 6000 proteins. They are found in organisms ranging from viruses to eukaryotes and play an important role in protein-ligand interactions. To date, more than one hundred crystal structures of LRR containing proteins have been determined. This knowledge has increased our ability to use the crystal structures as templates to model LRR proteins with unknown structures. Since the individual three-dimensional LRR structures are not directly available from the established databases and since there are only a few detailed annotations for them, a conformational LRR database useful for homology modeling of LRR proteins is desirable. DESCRIPTION: We developed LRRML, a conformational database and an extensible markup language (XML) description of LRRs. The release 0.2 contains 1261 individual LRR structures, which were identified from 112 PDB structures and annotated manually. An XML structure was defined to exchange and store the LRRs. LRRML provides a source for homology modeling and structural analysis of LRR proteins. In order to demonstrate the capabilities of the database we modeled the mouse Toll-like receptor 3 (TLR3) by multiple templates homology modeling and compared the result with the crystal structure. CONCLUSION: LRRML is an information source for investigators involved in both theoretical and applied research on LRR proteins. It is available at . BioMed Central 2008-11-05 /pmc/articles/PMC2645405/ /pubmed/18986514 http://dx.doi.org/10.1186/1472-6807-8-47 Text en Copyright © 2008 Wei et al; 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 | Database Wei, Tiandi Gong, Jing Jamitzky, Ferdinand Heckl, Wolfgang M Stark, Robert W Rössle, Shaila C LRRML: a conformational database and an XML description of leucine-rich repeats (LRRs) |
title | LRRML: a conformational database and an XML description of leucine-rich repeats (LRRs) |
title_full | LRRML: a conformational database and an XML description of leucine-rich repeats (LRRs) |
title_fullStr | LRRML: a conformational database and an XML description of leucine-rich repeats (LRRs) |
title_full_unstemmed | LRRML: a conformational database and an XML description of leucine-rich repeats (LRRs) |
title_short | LRRML: a conformational database and an XML description of leucine-rich repeats (LRRs) |
title_sort | lrrml: a conformational database and an xml description of leucine-rich repeats (lrrs) |
topic | Database |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2645405/ https://www.ncbi.nlm.nih.gov/pubmed/18986514 http://dx.doi.org/10.1186/1472-6807-8-47 |
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