(Q51758002)

11 April 2018

title

Pex5p imports folded tetrameric catalase by interaction with Pex13p. (English)

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11 April 2018

author name string

Hidenori Otera

series ordinal

1

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11 April 2018

Yukio Fujiki

series ordinal

2

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11 April 2018

publication date

29 July 2012

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11 April 2018

published in

Traffic

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11 April 2018

volume

13

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11 April 2018

issue

10

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11 April 2018

page(s)

1364-1377

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11 April 2018

Biogenesis of peroxisomes

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PEX5 binds the PTS1 independently of Hsp70 and the peroxin PEX12

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PTS2 protein import into mammalian peroxisomes

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The peroxisomal matrix import of Pex8p requires only PTS receptors and Pex14p

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Peroxisomal catalase in the methylotrophic yeast Candida boidinii: transport efficiency and metabolic significance

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The synthesis and turnover of rat liver peroxisomes. V. Intracellular pathway of catalase synthesis

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Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders

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A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import

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Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders

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Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: conserved Pex5p WXXXF/Y motifs are critical for matrix protein import

21 January 2018

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Two independent peroxisomal targeting signals in catalase A of Saccharomyces cerevisiae

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Restoration of peroxisomal catalase import in a model of human cellular aging

21 January 2018

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21 January 2018

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Hypocatalasemic fibroblasts accumulate hydrogen peroxide and display age-associated pathologies

21 January 2018

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Pex5p binding affinities for canonical and noncanonical PTS1 peptides.

21 January 2018

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PEX5 protein binds monomeric catalase blocking its tetramerization and releases it upon binding the N-terminal domain of PEX14

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Abnormality in catalase import into peroxisomes leads to severe neurological disorder

21 January 2018

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21 January 2018

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The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes

21 January 2018

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Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p

21 January 2018

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Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants

21 January 2018

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Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-0854.2012.01391.X

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-0854.2012.01391.X

Quantitative Analysis of Peroxisomal Targeting Signal Type-1 Binding to Wild-type and Pathogenic Mutants of Pex5p Supports an Affinity Threshold for Peroxisomal Protein Targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2012.01391.X

10.1111/J.1600-0854.2012.01391.X

21 January 2018

Identifiers

DOI

1 reference

11 April 2018

1 reference

11 April 2018