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PeroxisomeDB: a database for the peroxisomal proteome, functional genomics and disease
Peroxisomes are essential organelles of eukaryotic origin, ubiquitously distributed in cells and organisms, playing key roles in lipid and antioxidant metabolism. Loss or malfunction of peroxisomes causes more than 20 fatal inherited conditions. We have created a peroxisomal database (http://www.per...
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Published in: | Nucleic acids research 2007-01, Vol.35 (suppl-1), p.D815-D822 |
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creator | Schlüter, Agatha Fourcade, Stéphane Domènech-Estévez, Enric Gabaldón, Toni Huerta-Cepas, Jaime Berthommier, Guillaume Ripp, Raymond Wanders, Ronald J.A Poch, Olivier Pujol, Aurora |
description | Peroxisomes are essential organelles of eukaryotic origin, ubiquitously distributed in cells and organisms, playing key roles in lipid and antioxidant metabolism. Loss or malfunction of peroxisomes causes more than 20 fatal inherited conditions. We have created a peroxisomal database (http://www.peroxisomeDB.org) that includes the complete peroxisomal proteome of Homo sapiens and Saccharomyces cerevisiae, by gathering, updating and integrating the available genetic and functional information on peroxisomal genes. PeroxisomeDB is structured in interrelated sections 'Genes', 'Functions', 'Metabolic pathways' and 'Diseases', that include hyperlinks to selected features of NCBI, ENSEMBL and UCSC databases. We have designed graphical depictions of the main peroxisomal metabolic routes and have included updated flow charts for diagnosis. Precomputed BLAST, PSI-BLAST, multiple sequence alignment (MUSCLE) and phylogenetic trees are provided to assist in direct multispecies comparison to study evolutionary conserved functions and pathways. Highlights of the PeroxisomeDB include new tools developed for facilitating (i) identification of novel peroxisomal proteins, by means of identifying proteins carrying peroxisome targeting signal (PTS) motifs, (ii) detection of peroxisomes in silico, particularly useful for screening the deluge of newly sequenced genomes. PeroxisomeDB should contribute to the systematic characterization of the peroxisomal proteome and facilitate system biology approaches on the organelle. |
doi_str_mv | 10.1093/nar/gkl935 |
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Loss or malfunction of peroxisomes causes more than 20 fatal inherited conditions. We have created a peroxisomal database (http://www.peroxisomeDB.org) that includes the complete peroxisomal proteome of Homo sapiens and Saccharomyces cerevisiae, by gathering, updating and integrating the available genetic and functional information on peroxisomal genes. PeroxisomeDB is structured in interrelated sections 'Genes', 'Functions', 'Metabolic pathways' and 'Diseases', that include hyperlinks to selected features of NCBI, ENSEMBL and UCSC databases. We have designed graphical depictions of the main peroxisomal metabolic routes and have included updated flow charts for diagnosis. Precomputed BLAST, PSI-BLAST, multiple sequence alignment (MUSCLE) and phylogenetic trees are provided to assist in direct multispecies comparison to study evolutionary conserved functions and pathways. Highlights of the PeroxisomeDB include new tools developed for facilitating (i) identification of novel peroxisomal proteins, by means of identifying proteins carrying peroxisome targeting signal (PTS) motifs, (ii) detection of peroxisomes in silico, particularly useful for screening the deluge of newly sequenced genomes. PeroxisomeDB should contribute to the systematic characterization of the peroxisomal proteome and facilitate system biology approaches on the organelle.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkl935</identifier><identifier>PMID: 17135190</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Animals ; Biochemistry, Molecular Biology ; Databases, Protein ; Genomics ; Humans ; Internet ; Life Sciences ; Mice ; Molecular biology ; Peroxisomal Disorders ; Peroxisomal Disorders - genetics ; Peroxisomes ; Peroxisomes - metabolism ; Protein Sorting Signals ; Proteome ; Proteome - chemistry ; Proteome - genetics ; Proteome - physiology ; Rats ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae Proteins ; Saccharomyces cerevisiae Proteins - genetics ; Saccharomyces cerevisiae Proteins - physiology ; Software ; User-Computer Interface</subject><ispartof>Nucleic acids research, 2007-01, Vol.35 (suppl-1), p.D815-D822</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2006 The Author(s) 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c530t-e526d0c5430dec3d00e470d08d0f902d91ff3cec0c7fa49a3097ac33868244993</citedby><orcidid>0000-0001-6732-1528 ; 0000-0002-7134-3217 ; 0000-0002-9606-0600</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1747181/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1747181/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17135190$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00166257$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Schlüter, Agatha</creatorcontrib><creatorcontrib>Fourcade, Stéphane</creatorcontrib><creatorcontrib>Domènech-Estévez, Enric</creatorcontrib><creatorcontrib>Gabaldón, Toni</creatorcontrib><creatorcontrib>Huerta-Cepas, Jaime</creatorcontrib><creatorcontrib>Berthommier, Guillaume</creatorcontrib><creatorcontrib>Ripp, Raymond</creatorcontrib><creatorcontrib>Wanders, Ronald J.A</creatorcontrib><creatorcontrib>Poch, Olivier</creatorcontrib><creatorcontrib>Pujol, Aurora</creatorcontrib><title>PeroxisomeDB: a database for the peroxisomal proteome, functional genomics and disease</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>Peroxisomes are essential organelles of eukaryotic origin, ubiquitously distributed in cells and organisms, playing key roles in lipid and antioxidant metabolism. 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Loss or malfunction of peroxisomes causes more than 20 fatal inherited conditions. We have created a peroxisomal database (http://www.peroxisomeDB.org) that includes the complete peroxisomal proteome of Homo sapiens and Saccharomyces cerevisiae, by gathering, updating and integrating the available genetic and functional information on peroxisomal genes. PeroxisomeDB is structured in interrelated sections 'Genes', 'Functions', 'Metabolic pathways' and 'Diseases', that include hyperlinks to selected features of NCBI, ENSEMBL and UCSC databases. We have designed graphical depictions of the main peroxisomal metabolic routes and have included updated flow charts for diagnosis. Precomputed BLAST, PSI-BLAST, multiple sequence alignment (MUSCLE) and phylogenetic trees are provided to assist in direct multispecies comparison to study evolutionary conserved functions and pathways. 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subjects | Animals Biochemistry, Molecular Biology Databases, Protein Genomics Humans Internet Life Sciences Mice Molecular biology Peroxisomal Disorders Peroxisomal Disorders - genetics Peroxisomes Peroxisomes - metabolism Protein Sorting Signals Proteome Proteome - chemistry Proteome - genetics Proteome - physiology Rats Saccharomyces cerevisiae Saccharomyces cerevisiae Proteins Saccharomyces cerevisiae Proteins - genetics Saccharomyces cerevisiae Proteins - physiology Software User-Computer Interface |
title | PeroxisomeDB: a database for the peroxisomal proteome, functional genomics and disease |
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