(Q40760857)

23 September 2017

Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells (English)

1 reference

23 September 2017

Satoru Mukai

1

1 reference

23 September 2017

Kamran Ghaedi

series ordinal

2

1 reference

23 September 2017

Yukio Fujiki

series ordinal

3

1 reference

23 September 2017

language of work or name

English

0 references

publication date

27 December 2001

1 reference

Journal of Biological Chemistry

23 September 2017

1 reference

23 September 2017

277

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23 September 2017

9548-9561

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23 September 2017

11

1 reference

Molecular defects in genetic diseases of peroxisomes

23 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

A conserved tripeptide sorts proteins to peroxisomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Peroxisome biogenesis: from yeast to man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Peroxisomes: simple in function but complex in maintenance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Peroxisome biogenesis and peroxisome biogenesis disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Import of peroxisomal matrix and membrane proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Peroxisome biogenesis disorders: genetics and cell biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

The peroxin pex3p initiates membrane assembly in peroxisome biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

PEX12 encodes an integral membrane protein of peroxisomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Peb1p (Pas7p) is an intraperoxisomal receptor for the NH2-terminal, type 2, peroxisomal targeting sequence of thiolase: Peb1p itself is targeted to peroxisomes by an NH2-terminal peptide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

A mobile PTS2 receptor for peroxisomal protein import in Pichia pastoris.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Differential protein import deficiencies in human peroxisome assembly disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Acyl-Coa oxidase and hydratase-dehydrogenase, two enzymes of the peroxisomal beta-oxidation system, are synthesized on free polysomes of clofibrate-treated rat liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

A rapid selection for animal cell mutants with defective peroxisomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

The WD repeat: a common architecture for diverse functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

PTS2 protein import into mammalian peroxisomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a cycling receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

The human peroxisomal targeting signal receptor, Pex5p, is translocated into the peroxisomal matrix and recycled to the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

Hsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M108635200

21 January 2018

Identifiers

DOI

10.1074/JBC.M108635200

1 reference

release_oyny6qdzozgnbfod7iersfmxbm

23 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/oyny6qdzozgnbfod7iersfmxbm

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference