The peroxin pex3p initiates membrane assembly in peroxisome biogenesis (Q24549973)

1

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S Tamura

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K Okumoto

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Y Matsuzono

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Y Fujiki

Molecular Biology of the Cell

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language of work or name

English

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publication date

June 2000

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published in

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volume

11

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issue

6

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page(s)

2085-102

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cites work

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Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

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Expression of PEX11beta mediates peroxisome proliferation in the absence of extracellular stimuli

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Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B

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Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders

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PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p

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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

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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

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PEX12 encodes an integral membrane protein of peroxisomes

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Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders

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Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways

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Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders

24 March 2017

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cDNA cloning and characterization of a constitutively expressed isoform of the human peroxin Pex11p

24 March 2017

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Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant

24 March 2017

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Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant

24 March 2017

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Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis

24 March 2017

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7 April 2017

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Biogenesis of peroxisomes

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Peroxisomes: Organelles at the crossroads

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Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris

27 September 2017

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Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals

27 September 2017

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Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders

27 September 2017

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Polypeptide and phospholipid composition of the membrane of rat liver peroxisomes: comparison with endoplasmic reticulum and mitochondrial membranes

27 September 2017

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Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes

27 September 2017

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Complete nucleotide sequence of cDNA and predicted amino acid sequence of rat acyl-CoA oxidase

27 September 2017

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Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus

27 September 2017

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27 September 2017

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27 September 2017

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

27 September 2017

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Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein

27 September 2017

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Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals

30 May 2018

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The endoplasmic reticulum plays an essential role in peroxisome biogenesis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=14905

Molecular defects in genetic diseases of peroxisomes

30 May 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=14905

Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=14905

Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.

30 May 2018

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The Hansenula polymorpha PER9 gene encodes a peroxisomal membrane protein essential for peroxisome assembly and integrity

30 May 2018

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Differential protein import deficiencies in human peroxisome assembly disorders

30 May 2018

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A possible role for plasmalogens in protecting animal cells against photosensitized killing

30 May 2018

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Structural analysis of cDNA for rat peroxisomal 3-ketoacyl-CoA thiolase

30 May 2018

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Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome

30 May 2018

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A rapid selection for animal cell mutants with defective peroxisomes.

30 May 2018

1 reference

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Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndrome

30 May 2018

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Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=14905

Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=14905

Isolation and characterization of Pas2p, a peroxisomal membrane protein essential for peroxisome biogenesis in the methylotrophic yeast Pichia pastoris.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=14905

Characterization of the signal peptide at the amino terminus of the rat peroxisomal 3-ketoacyl-CoA thiolase precursor.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=14905

Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group.

28 November 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=14905

Carboxyl-terminal consensus Ser-Lys-Leu-related tripeptide of peroxisomal proteins functions in vitro as a minimal peroxisome-targeting signal

28 November 2018

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12 December 2020

Peroxisome biogenesis

1 reference

12 December 2020

Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13

1 reference

12 December 2020

Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly

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12 December 2020

PEX genes on the rise

1 reference

12 December 2020

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

12 December 2020

Post-translational import of 3-ketoacyl-CoA thiolase into rat liver peroxisomes in vitro

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12 December 2020

Identifiers

DOI

10.1091/MBC.11.6.2085

1 reference

release_kr2zhzipf5cpliqnflp63jbqia

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/kr2zhzipf5cpliqnflp63jbqia

24 November 2022

mapped directly with Wikidata item

1 reference

1 reference

PubMed publication ID

10848631

1 reference