Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis (Q24300953)

4 July 2017

title

Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis (English)

1 reference

Peroxisomal biogenesis factor 26

4 July 2017

main subject

1 reference

protein import into peroxisome matrix

GOA release 2020-03-11

1 reference

alternative mRNA splicing, via spliceosome

GOA release 2020-03-11

1 reference

6

Stephen J Gould

1 reference

4 July 2017

Sabine Weller

1

1 reference

4 July 2017

Ivelisse Cajigas

2

1 reference

4 July 2017

James Morrell

3

1 reference

4 July 2017

Cassandra Obie

4

1 reference

4 July 2017

Gary Steel

5

1 reference

4 July 2017

David Valle

7

1 reference

4 July 2017

language of work or name

English

0 references

publication date

27 April 2005

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

76

1 reference

4 July 2017

issue

6

1 reference

4 July 2017

page(s)

987-1007

1 reference

Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene

4 July 2017

cites work

1 reference

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Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation

19 March 2017

1 reference

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Genomic disorders on 22q11

19 March 2017

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Multiple distinct targeting signals in integral peroxisomal membrane proteins

19 March 2017

1 reference

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Identification and characterization of HAOX1, HAOX2, and HAOX3, three human peroxisomal 2-hydroxy acid oxidases

19 March 2017

1 reference

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PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis

19 March 2017

1 reference

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The human PICD gene encodes a cytoplasmic and peroxisomal NADP( )-dependent isocitrate dehydrogenase

19 March 2017

1 reference

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PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders

19 March 2017

1 reference

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Identification of peroxisomal acyl-CoA thioesterases in yeast and humans

19 March 2017

1 reference

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

19 March 2017

1 reference

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Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

19 March 2017

1 reference

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Identification of PAHX, a Refsum disease gene

19 March 2017

1 reference

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Identification of a fourth half ABC transporter in the human peroxisomal membrane

19 March 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Structural and functional analysis of the interaction of the AAA-peroxins Pex1p and Pex6p

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Pex15p of Saccharomyces cerevisiae provides a molecular basis for recruitment of the AAA peroxin Pex6p to peroxisomal membranes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum

19 March 2017

1 reference

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Metabolic and molecular basis of peroxisomal disorders: a review

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Peroxisome biogenesis disorders

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome

19 March 2017

1 reference

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Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences

19 March 2017

1 reference

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A conserved tripeptide sorts proteins to peroxisomes

19 March 2017

1 reference

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Peroxisomes, lipid metabolism, and peroxisomal disorders

7 April 2017

1 reference

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Multiple binding proteins suggest diverse functions for the N-ethylmaleimide sensitive factor

27 September 2017

1 reference

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Phylogenetic analysis of AAA proteins

27 September 2017

1 reference

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NSF and p97/VCP: similar at first, different at last

27 September 2017

1 reference

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27 September 2017

1 reference

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Characterization of signal that directs C-tail-anchored proteins to mammalian mitochondrial outer membrane

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Opinion: peroxisomal-protein import: is it really that complex?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

The genetics of peroxisome biogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

The peroxisome biogenesis factors pex4p, pex22p, pex1p, and pex6p act in the terminal steps of peroxisomal matrix protein import

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Mitochondrial uncoupling proteins in energy expenditure

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Peroxisome biogenesis disorders: genetics and cell biology

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

AAA proteins. Lords of the ring

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Inhibitors of COPI and COPII do not block PEX3-mediated peroxisome synthesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

cDNA sequence coding for human kidney catalase

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Identification of peroxisomal targeting signals located at the carboxy terminus of four peroxisomal proteins

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

The N terminus of the peroxisomal cycling receptor, Pex5p, is required for redirecting the peroxisome-associated peroxin back to the cytosol

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Structure of the N-terminal domain of PEX1 AAA-ATPase. Characterization of a putative adaptor-binding domain

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

The energetics of Pex5p-mediated peroxisomal protein import.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Characterization of the peroxisomal cycling receptor, Pex5p, using a cell-free in vitro import system

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Hansenula polymorpha Pex1p and Pex6p are peroxisome-associated AAA proteins that functionally and physically interact

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Use of Pichia pastoris as a model eukaryotic system. Peroxisome biogenesis

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196456

Metabolic control of peroxisome abundance

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15858711

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15858711

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Biogenesis of peroxisomal proteins in vivo and in vitro

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15858711

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/430637

1 reference

4 July 2017

1 reference

4 July 2017

1 reference