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Authordc.contributor.authorShani, N. 
Authordc.contributor.authorSapag, Amalia es_CL
Authordc.contributor.authorValle, David es_CL
Admission datedc.date.accessioned2011-06-30T13:02:41Z
Available datedc.date.available2011-06-30T13:02:41Z
Publication datedc.date.issued1996
Cita de ítemdc.identifier.citationThe Journal of Biological Chemistry 271 (15): 8725-8730es_CL
Identifierdc.identifier.issn0021-9258
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121362
General notedc.descriptionArtículo de publicación ISIes_CL
Abstractdc.description.abstractThe adrenoleukodystrophy protein (ALDP) and the 70-kDa peroxisomal membrane protein are half ATP-binding cassette (ABC) transporters in the human peroxisome membrane. Both are implicated in genetic disorders of peroxisome biogenesis and function. Proteins homologous to ALDP and the 70-KDa peroxisomal membrane protein have been discovered in other eukaryotic organisms and form a growing group of peroxisomal half ABC transporters. Amino acid sequence alignment of these and other ABC transporters reveals several protein motifs that are highly conserved both in sequence and location. Here we characyerize two of these, designated the EAA-like and the loop1 motiffs. We study them by introducing missense mutations in Pxa1p, a Saccharomyces cerevisiae ortholog of ALDP, and show that both motifs are important for Pxa1p function. Interestingly, missense mutations in corresponding amino acids in ALDP cause adrenoleukodystrophy in humans. We conclude that these motifs are important for ABC transporter function and that the yeast protein Pxa1p is a useful system for understanding the molecular basis of adrenoleukodystrophyes_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherThe American Society forBiochemistry and Molecular Biology, Inc.es_CL
Keywordsdc.subjectAdrenoleukodystrophy protein (ALDP)es_CL
Títulodc.titleCharacterization and analysis of conserved motifs in a peroxisomal ATP-binding cassette transporteres_CL
Document typedc.typeArtículo de revista


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