(Q40886599)

English

Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. Study with a novel Pex5-impaired Chinese hamster ovary cell mutant

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scholarly article

1 reference

Europe PubMed Central

24 September 2017

Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. Study with a novel Pex5-impaired Chinese hamster ovary cell mutant (English)

1 reference

Europe PubMed Central

24 September 2017

author name string

Matsumura T

1

1 reference

Europe PubMed Central

24 September 2017

Otera H

2

1 reference

Europe PubMed Central

24 September 2017

Fujiki Y

3

1 reference

Europe PubMed Central

24 September 2017

language of work or name

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publication date

1 July 2000

1 reference

Europe PubMed Central

24 September 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

24 September 2017

275

1 reference

Europe PubMed Central

24 September 2017

21715-21721

1 reference

Europe PubMed Central

24 September 2017

28

1 reference

Europe PubMed Central

24 September 2017

Molecular defects in genetic diseases of peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

A rapid selection for animal cell mutants with defective peroxisomes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

PEX12 encodes an integral membrane protein of peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

Synthesis of 3-ketoacyl-CoA thiolase of rat liver peroxisomes on free polyribosomes as a larger precursor. Induction of thiolase mRNA activity by clofibrate

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

Complete nucleotide sequence of cDNA and deduced amino acid sequence of rat liver catalase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

PEB1 (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intra-peroxisomal protein that is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p.PTS2 protein complex into peroxisomes via its initial docking site, Pex14p

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

PEX genes on the rise

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000721200

21 January 2018

Identifiers

10.1074/JBC.M000721200

1 reference

Europe PubMed Central

24 September 2017

1 reference

Europe PubMed Central

24 September 2017

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