Peroxisomes: simple in function but complex in maintenance. (Q33747044)

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31 October 2019

review article

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title

Peroxisomes: simple in function but complex in maintenance (English)

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31 October 2019

2

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31 October 2019

author name string

H F Tabak

series ordinal

1

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31 October 2019

B Distel

series ordinal

3

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31 October 2019

publication date

1 November 1999

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31 October 2019

published in

Trends in Cell Biology

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31 October 2019

volume

9

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31 October 2019

page(s)

447-453

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31 October 2019

issue

11

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Peroxisomes (microbodies and related particles)

31 October 2019

cites work

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The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein

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Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

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PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene

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Peroxisomes: Organelles at the crossroads

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Peroxisomal and mitochondrial carnitine acetyltransferases of Saccharomyces cerevisiae are encoded by a single gene.

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Peroxisomal beta-oxidation of polyunsaturated fatty acids in Saccharomyces cerevisiae: isocitrate dehydrogenase provides NADPH for reduction of double bonds at even positions

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The Saccharomyces cerevisiae peroxisomal 2,4-dienoyl-CoA reductase is encoded by the oleate-inducible gene SPS19.

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Molecular characterization of Saccharomyces cerevisiae Delta3, Delta2-enoyl-CoA isomerase

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Human mitochondrial transmembrane metabolite carriers: tissue distribution and its implication for mitochondrial disorders.

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Peroxisomal lipid metabolism.

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The peroxisome proliferator activated receptors (PPARS) and their effects on lipid metabolism and adipocyte differentiation

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A heterodimer of the Zn2Cys6 transcription factors Pip2p and Oaf1p controls induction of genes encoding peroxisomal proteins in Saccharomyces cerevisiae

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Purification, identification, and properties of a Saccharomyces cerevisiae oleate-activated upstream activating sequence-binding protein that is involved in the activation of POX1.

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Comparison of the complete protein sets of worm and yeast: orthology and divergence

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Recombinant human peroxisomal targeting signal receptor PEX5. Structural basis for interaction of PEX5 with PEX14.

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Import of proteins into peroxisomes

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Characterization of intermediates in the process of plant peroxisomal protein import

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In vitro insertion of the 22-kD peroxisomal membrane protein into isolated rat liver peroxisomes

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The sorting sequence of the peroxisomal integral membrane protein PMP47 is contained within a short hydrophilic loop

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The endoplasmic reticulum plays an essential role in peroxisome biogenesis.

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Biogenesis of peroxisomes

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Peroxisome synthesis in the absence of preexisting peroxisomes

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7 January 2021

Brefeldin A interferes with peroxisomal protein sorting in the yeast Hansenula polymorpha

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Enlarged peroxisomes are present in oleic acid-grown Yarrowia lipolytica overexpressing the PEX16 gene encoding an intraperoxisomal peripheral membrane peroxin

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Peroxisome biogenesis: involvement of ARF and coatomer

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Two AAA family peroxins, PpPex1p and PpPex6p, interact with each other in an ATP-dependent manner and are associated with different subcellular membranous structures distinct from peroxisomes

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7 January 2021

The cytosolic DnaJ-like protein djp1p is involved specifically in peroxisomal protein import

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Cytosol-dependent peroxisomal protein import in a permeabilized cell system

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Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene

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Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor

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7 January 2021

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

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7 January 2021

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor

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7 January 2021

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

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Identifiers

DOI

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31 October 2019

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