PeroxisomeDB 2.0: an integrative view of the global peroxisomal metabolome. Export

@article{citeulike:6083170, abstract = {Peroxisomes are essential organelles that play a key role in redox signalling and lipid homeostasis. They contain a highly diverse enzymatic network among different species, mirroring the varied metabolic needs of the organisms. The previous PeroxisomeDB version organized the peroxisomal proteome of humans and Saccharomyces cerevisiae based on genetic and functional information into metabolic categories with a special focus on peroxisomal disease. The new release (http://www.peroxisomeDB.org) adds peroxisomal proteins from 35 newly sequenced eukaryotic genomes including fungi, yeasts, plants and lower eukaryotes. We searched these genomes for a core ensemble of 139 peroxisomal protein families and identified 2706 putative peroxisomal protein homologs. Approximately 37\% of the identified homologs contained putative peroxisome targeting signals (PTS). To help develop understanding of the evolutionary relationships among peroxisomal proteins, the new database includes phylogenetic trees for 2386 of the peroxisomal proteins. Additional new features are provided, such as a tool to capture kinetic information from Brenda, CheBI and Sabio-RK databases and more than 1400 selected bibliographic references. PeroxisomeDB 2.0 is a freely available, highly interactive functional genomics platform that offers an extensive view on the peroxisomal metabolome across lineages, thus facilitating comparative genomics and systems analysis of the organelle.}, author = {Schl\"{u}ter, Agatha and Real-Chicharro, Alejandro and Gabald\'{o}n, Toni and S\'{a}nchez-Jim\'{e}nez, Francisca and Pujol, Aurora}, citeulike-article-id = {6083170}, citeulike-linkout-0 = {http://dx.doi.org/10.1093/nar/gkp935}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/19892824}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=19892824}, day = {5}, doi = {10.1093/nar/gkp935}, issn = {1362-4962}, journal = {Nucleic acids research}, keywords = {cites-chebi}, month = {November}, posted-at = {2009-11-07 17:44:10}, priority = {2}, title = {PeroxisomeDB 2.0: an integrative view of the global peroxisomal metabolome.}, url = {http://dx.doi.org/10.1093/nar/gkp935}, year = {2009} }

TY - JOUR ID - citeulike:6083170 L3 - citeulike-article-id:6083170 N2 - Peroxisomes are essential organelles that play a key role in redox signalling and lipid homeostasis. They contain a highly diverse enzymatic network among different species, mirroring the varied metabolic needs of the organisms. The previous PeroxisomeDB version organized the peroxisomal proteome of humans and Saccharomyces cerevisiae based on genetic and functional information into metabolic categories with a special focus on peroxisomal disease. The new release (http://www.peroxisomeDB.org) adds peroxisomal proteins from 35 newly sequenced eukaryotic genomes including fungi, yeasts, plants and lower eukaryotes. We searched these genomes for a core ensemble of 139 peroxisomal protein families and identified 2706 putative peroxisomal protein homologs. Approximately 37% of the identified homologs contained putative peroxisome targeting signals (PTS). To help develop understanding of the evolutionary relationships among peroxisomal proteins, the new database includes phylogenetic trees for 2386 of the peroxisomal proteins. Additional new features are provided, such as a tool to capture kinetic information from Brenda, CheBI and Sabio-RK databases and more than 1400 selected bibliographic references. PeroxisomeDB 2.0 is a freely available, highly interactive functional genomics platform that offers an extensive view on the peroxisomal metabolome across lineages, thus facilitating comparative genomics and systems analysis of the organelle. JF - Nucleic acids research SN - 1362-4962 TI - PeroxisomeDB 2.0: an integrative view of the global peroxisomal metabolome. KW - cites-chebi AU - Schlüter, Agatha AU - Real-Chicharro, Alejandro AU - Gabaldón, Toni AU - Sánchez-Jiménez, Francisca AU - Pujol, Aurora PY - 2009/11/05/ UR - http://dx.doi.org/10.1093/nar/gkp935 ER -