MITOP, the mitochondrial proteome database: 2000 update
Open Access
- 1 January 2000
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 28 (1) , 155-158
- https://doi.org/10.1093/nar/28.1.155
Abstract
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.Keywords
This publication has 19 references indexed in Scilit:
- SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndromeNature Genetics, 1998
- Mutations of SURF-1 in Leigh Disease Associated with Cytochrome c Oxidase DeficiencyAmerican Journal of Human Genetics, 1998
- The genome sequence of Rickettsia prowazekii and the origin of mitochondriaNature, 1998
- A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy.Journal of Medical Genetics, 1998
- The yeast genome and clinical geneticsClinical Genetics, 1998
- Nuclear power and mitochondrial diseaseNature Genetics, 1998
- Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial MetalloproteaseCell, 1998
- Localization of the Wilson’s disease protein product to mitochondriaProceedings of the National Academy of Sciences, 1998
- Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxinNature Genetics, 1997
- SHY1, the Yeast Homolog of the MammalianSURF-1 Gene, Encodes a Mitochondrial Protein Required for RespirationJournal of Biological Chemistry, 1997