Mevalonate kinase is a cytosolic enzyme in humans
Author:
Affiliation:
1. Laboratory Genetic Metabolic Diseases, Department of Pediatrics, Emma Children's Hospital, Academic Medical Center, Amsterdam
2. Department of Anatomy, Embryology, Histology & Medical Physics, University of Gent, Belgium
Abstract
Publisher
The Company of Biologists
Subject
Cell Biology
Link
http://journals.biologists.com/jcs/article-pdf/117/4/631/1365461/631.pdf
Reference33 articles.
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2. Biardi, L., Sreedhar, A., Zokaei, A., Vartak, N. B., Bozeat, R. L., Shackelford, J. E., Keller, G. A. and Krisans, S. K. (1994). Mevalonate kinase is predominantly localized in peroxisomes and is defective in patients with peroxisome deficiency disorders. J. Biol. Chem.269, 1197-1205.
3. Bout, A., Teunissen, Y., Hashimoto, T., Benne, R. and Tager, J. M. (1988). Nucleotide sequence of human peroxisomal 3-oxoacyl-CoA thiolase. Nucleic Acids Res.16, 10369.
4. de Vet, E. C., van den Broek, B. T. and Van den, B. H. (1997). Nucleotide sequence of human alkyl-dihydroxyacetonephosphate synthase cDNA reveals the presence of a peroxisomal targeting signal 2. Biochim. Biophys. Acta1346, 25-29.
5. Espeel, M. and Van Limbergen, G. (1995). Immunocytochemical localization of peroxisomal proteins in human liver and kidney. J. Inherit. Metab. Dis.18 (Suppl. 1), 135-154.
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