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VSGdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins
BACKGROUND: Trypanosomes are coated with a variant surface glycoprotein (VSG) that is so densely packed that it physically protects underlying proteins from effectors of the host immune system. Periodically cells expressing a distinct VSG arise in a population and thereby evade immunity. The main st...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1868767/ https://www.ncbi.nlm.nih.gov/pubmed/17474977 http://dx.doi.org/10.1186/1471-2105-8-143 |
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author | Marcello, Lucio Menon, Suraj Ward, Pauline Wilkes, Jonathan M Jones, Nicola G Carrington, Mark Barry, J David |
author_facet | Marcello, Lucio Menon, Suraj Ward, Pauline Wilkes, Jonathan M Jones, Nicola G Carrington, Mark Barry, J David |
author_sort | Marcello, Lucio |
collection | PubMed |
description | BACKGROUND: Trypanosomes are coated with a variant surface glycoprotein (VSG) that is so densely packed that it physically protects underlying proteins from effectors of the host immune system. Periodically cells expressing a distinct VSG arise in a population and thereby evade immunity. The main structural feature of VSGs are two long α-helices that form a coiled coil, and sets of relatively unstructured loops that are distal to the plasma membrane and contain most or all of the protective epitopes. The primary structure of different VSGs is highly variable, typically displaying only ~20% identity with each other. The genome has nearly 2000 VSG genes, which are located in subtelomeres. Only one VSG gene is expressed at a time, and switching between VSGs primarily involves gene conversion events. The archive of silent VSGs undergoes diversifying evolution rapidly, also involving gene conversion. The VSG family is a paradigm for α helical coiled coil structures, epitope variation and GPI-anchor signals. At the DNA level, the genes are a paradigm for diversifying evolutionary processes and for the role of subtelomeres and recombination mechanisms in generation of diversity in multigene families. To enable ready availability of VSG sequences for addressing these general questions, and trypanosome-specific questions, we have created VSGdb, a database of all known sequences. DESCRIPTION: VSGdb contains fully annotated VSG sequences from the genome sequencing project, with which it shares all identifiers and annotation, and other available sequences. The database can be queried in various ways. Sequence retrieval, in FASTA format, can deliver protein or nucleotide sequence filtered by chromosomes or contigs, gene type (functional, pseudogene, etc.), domain and domain sequence family. Retrieved sequences can be stored as a temporary database for BLAST querying, reports from which include hyperlinks to the genome project database (GeneDB) CDS Info and to individual VSGdb pages for each VSG, containing annotation and sequence data. Queries (text search) with specific annotation terms yield a list of relevant VSGs, displayed as identifiers leading again to individual VSG web pages. CONCLUSION: VSGdb is a freely available, web-based platform enabling easy retrieval, via various filters, of sets of VSGs that will enable detailed analysis of a number of general and trypanosome-specific questions, regarding protein structure potential, epitope variability, sequence evolution and recombination events. |
format | Text |
id | pubmed-1868767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18687672007-05-15 VSGdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins Marcello, Lucio Menon, Suraj Ward, Pauline Wilkes, Jonathan M Jones, Nicola G Carrington, Mark Barry, J David BMC Bioinformatics Database BACKGROUND: Trypanosomes are coated with a variant surface glycoprotein (VSG) that is so densely packed that it physically protects underlying proteins from effectors of the host immune system. Periodically cells expressing a distinct VSG arise in a population and thereby evade immunity. The main structural feature of VSGs are two long α-helices that form a coiled coil, and sets of relatively unstructured loops that are distal to the plasma membrane and contain most or all of the protective epitopes. The primary structure of different VSGs is highly variable, typically displaying only ~20% identity with each other. The genome has nearly 2000 VSG genes, which are located in subtelomeres. Only one VSG gene is expressed at a time, and switching between VSGs primarily involves gene conversion events. The archive of silent VSGs undergoes diversifying evolution rapidly, also involving gene conversion. The VSG family is a paradigm for α helical coiled coil structures, epitope variation and GPI-anchor signals. At the DNA level, the genes are a paradigm for diversifying evolutionary processes and for the role of subtelomeres and recombination mechanisms in generation of diversity in multigene families. To enable ready availability of VSG sequences for addressing these general questions, and trypanosome-specific questions, we have created VSGdb, a database of all known sequences. DESCRIPTION: VSGdb contains fully annotated VSG sequences from the genome sequencing project, with which it shares all identifiers and annotation, and other available sequences. The database can be queried in various ways. Sequence retrieval, in FASTA format, can deliver protein or nucleotide sequence filtered by chromosomes or contigs, gene type (functional, pseudogene, etc.), domain and domain sequence family. Retrieved sequences can be stored as a temporary database for BLAST querying, reports from which include hyperlinks to the genome project database (GeneDB) CDS Info and to individual VSGdb pages for each VSG, containing annotation and sequence data. Queries (text search) with specific annotation terms yield a list of relevant VSGs, displayed as identifiers leading again to individual VSG web pages. CONCLUSION: VSGdb is a freely available, web-based platform enabling easy retrieval, via various filters, of sets of VSGs that will enable detailed analysis of a number of general and trypanosome-specific questions, regarding protein structure potential, epitope variability, sequence evolution and recombination events. BioMed Central 2007-05-02 /pmc/articles/PMC1868767/ /pubmed/17474977 http://dx.doi.org/10.1186/1471-2105-8-143 Text en Copyright © 2007 Marcello 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 Marcello, Lucio Menon, Suraj Ward, Pauline Wilkes, Jonathan M Jones, Nicola G Carrington, Mark Barry, J David VSGdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins |
title | VSGdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins |
title_full | VSGdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins |
title_fullStr | VSGdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins |
title_full_unstemmed | VSGdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins |
title_short | VSGdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins |
title_sort | vsgdb: a database for trypanosome variant surface glycoproteins, a large and diverse family of coiled coil proteins |
topic | Database |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1868767/ https://www.ncbi.nlm.nih.gov/pubmed/17474977 http://dx.doi.org/10.1186/1471-2105-8-143 |
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