A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p (Q24316346)

1

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N Shimozawa

2

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Y Suzuki

3

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T Tsukamoto

4

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T Osumi

5

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Y Fujiki

Biochemical and Biophysical Research Communications

6

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language of work or name

English

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publication date

28 April 1998

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published in

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volume

245

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issue

3

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page(s)

883-6

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cites work

A 200‐amino acid ATPase module in search of a basic function

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

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

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Molecular defects in genetic diseases of peroxisomes

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

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PEX12 encodes an integral membrane protein of peroxisomes

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

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

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Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

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

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Role of the PAS1 gene of Pichia pastoris in peroxisome biogenesis

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A human gene responsible for Zellweger syndrome that affects peroxisome assembly

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

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

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Identifiers

DOI

10.1006/BBRC.1998.8522

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2639900

OpenCitations bibliographic resource ID

2639900

1 reference