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Scharfe, C.* ; Zaccaria, P. ; Hoertnagel, K.* ; Jaksch, M.* ; Klopstock, T.* ; Dembowski, M.* ; Lill, R.* ; Prokisch, H.* ; Gerbitz, K.D.* ; Neupert, W.* ; Mewes, H.-W. ; Meitinger, T.*

MITOP, the mitochondrial proteome database: 2000 update.

Nucleic Acids Res. 28, 155-158 (2000)
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MITOP (http://www.mips.biochem.mpg.de/proj/medgen/mitop/) is a comprehensive database for genetic and functional information on both nuclear- and mitochondrial-encoded proteins and their genes. The five species files--Saccharomyces cerevisiae, Mus musculus, Caenorhabditis elegans, Neurospora crassa and Homo sapiens--include annotated data derived from a variety of online resources and the literature. A wide spectrum of search facilities is given in the overlapping sections 'Gene catalogues', 'Protein catalogues', 'Homologies', 'Pathways and metabolism' and 'Human disease catalogue' including extensive references and hyperlinks to other databases. Central features are the results of various homology searches, which should facilitate the investigations into interspecies relationships. Precomputed FASTA searches using all the MITOP yeast protein entries and a list of the best human EST hits with graphical cluster alignments related to the yeast reference sequence are presented. The orthologue tables with cross-listings to all the protein entries for each species in MITOP have been expanded by adding the genomes of Rickettsia prowazeckii and Escherichia coli. To find new mitochondrial proteins the complete yeast genome has been analyzed using the MITOPROT program which identifies mitochondrial targeting sequences. The 'Human disease catalogue' contains tables with a total of 110 human diseases related to mitochondrial protein abnormalities, sorted by clinical criteria and age of onset. MITOP should contribute to the systematic genetic characterization of the mitochondrial proteome in relation to human disease.
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Publication type Article: Journal article
Document type Scientific Article
Keywords CYTOCHROME-C-OXIDASE; NUCLEAR; GENOME; DEFICIENCY; MUTATIONS; SEQUENCE; DISEASE
Language english
Publication Year 2000
HGF-reported in Year 0
ISSN (print) / ISBN 0305-1048
e-ISSN 1362-4962
Quellenangaben Volume: 28, Issue: 1, Pages: 155-158 Article Number: , Supplement: ,
Publisher Oxford University Press
Reviewing status Peer reviewed
PubMed ID 10592209
Erfassungsdatum 2000-12-31