PEX6/YNL329C Literature Guide Help

Other names published for PEX6: PAS8, AAA family ATPase peroxin 6, YNL329C

PEX6 - Primary Literature (21)

ReferenceOther Genes Addressed
Saffian D, et al.  (2012) ATP-dependent assembly of the heteromeric Pex1p-Pex6p-complex of the peroxisomal matrix protein import machinery. J Struct Biol 179(2):126-32
van der Zand A, et al.  (2012) Biochemically distinct vesicles from the endoplasmic reticulum fuse to form peroxisomes. Cell 149(2):397-409
Debelyy MO, et al.  (2011) Ubp15p, a ubiquitin hydrolase associated with the peroxisomal export machinery. J Biol Chem 286(32):28223-34
Dziedzic SA and Caplan AB  (2011) Identification of autophagy genes participating in zinc-induced necrotic cell death in Saccharomyces cerevisiae. Autophagy 7(5):490-500
Saleem RA, et al.  (2010) Genome-wide analysis of effectors of peroxisome biogenesis.LID - e11953 [pii] PLoS One 5(8)
Jungwirth H, et al.  (2008) Loss of peroxisome function triggers necrosis. FEBS Lett 582(19):2882-6
Trzcinska-Danielewicz J, et al.  (2008) Yeast transcription factor Oaf1 forms homodimer and induces some oleate-responsive genes in absence of Pip2. Biochem Biophys Res Commun 374(4):763-6
Lockshon D, et al.  (2007) The sensitivity of yeast mutants to oleic Acid implicates the peroxisome and other processes in membrane function. Genetics 175(1):77-91
Seo JG, et al.  (2007) A novel role of peroxin PEX6: suppression of aging defects in mitochondria. Aging Cell 6(3):405-13
Rosenkranz K, et al.  (2006) Functional association of the AAA complex and the peroxisomal importomer. FEBS J 273(16):3804-15
Birschmann I, et al.  (2005) Structural and functional analysis of the interaction of the AAA-peroxins Pex1p and Pex6p. FEBS J 272(1):47-58
Kiel JA, et al.  (2005) Ubiquitination of the peroxisomal targeting signal type 1 receptor, Pex5p, suggests the presence of a quality control mechanism during peroxisomal matrix protein import. J Biol Chem 280(3):1921-30
Platta HW, et al.  (2005) Functional role of the AAA peroxins in dislocation of the cycling PTS1 receptor back to the cytosol. Nat Cell Biol 7(8):817-22
Birschmann I, et al.  (2003) Pex15p of Saccharomyces cerevisiae provides a molecular basis for recruitment of the AAA peroxin Pex6p to peroxisomal membranes. Mol Biol Cell 14(6):2226-36
Gurvitz A, et al.  (1998) Fate and role of peroxisomes during the life cycle of the yeast Saccharomyces cerevisiae: inheritance of peroxisomes during meiosis. Histochem Cell Biol 110(1):15-26
Lussier M, et al.  (1997) Large scale identification of genes involved in cell surface biosynthesis and architecture in Saccharomyces cerevisiae. Genetics 147(2):435-50
Swaffield JC and Purugganan MD  (1997) The evolution of the conserved ATPase domain (CAD): reconstructing the history of an ancient protein module. J Mol Evol 45(5):549-63
Fukuda S, et al.  (1996) Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans. Am J Hum Genet 59(6):1210-20
Yahraus T, et al.  (1996) The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor. EMBO J 15(12):2914-23
Voorn-Brouwer T, et al.  (1993) Sequence of the PAS8 gene, the product of which is essential for biogenesis of peroxisomes in Saccharomyces cerevisiae. Biochim Biophys Acta 1216(2):325-8
Van der Leij I, et al.  (1992) Isolation of peroxisome assembly mutants from Saccharomyces cerevisiae with different morphologies using a novel positive selection procedure. J Cell Biol 119(1):153-62