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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Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.Identification and characterization of the human orthologue of yeast Pex14pHuman PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assemblyPEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein importMolecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10pTopogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments. study using human membrane protein PMP34Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interactionIdentification of PEX5p-related novel peroxisome-targeting signal 1 (PTS1)-binding proteins in mammalsMutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complexFunctional studies on human Pex7p: subcellular localization and interaction with proteins containing a peroxisome-targeting signal type 2 and other peroxinsTwo proteases, trypsin domain-containing 1 (Tysnd1) and peroxisomal lon protease (PsLon), cooperatively regulate fatty acid β-oxidation in peroxisomal matrixDynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26pThe membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assemblyClofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12pMutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlationHsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: conserved Pex5p WXXXF/Y motifs are critical for matrix protein import.The peroxin pex3p initiates membrane assembly in peroxisome biogenesisHuman PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group ITissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndromeCrosstalk between mitochondria and peroxisomesThe similarity between N-terminal targeting signals for protein import into different organelles and its evolutionary relevanceCrystal structure of peroxisomal targeting signal-2 bound to its receptor complex Pex7p-Pex21pThe cytosolic DnaJ-like protein djp1p is involved specifically in peroxisomal protein import.Recognition of peroxisomal targeting signal type 1 by the import receptor Pex5p.The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysisYarrowia lipolytica Pex20p, Saccharomyces cerevisiae Pex18p/Pex21p and mammalian Pex5pL fulfil a common function in the early steps of the peroxisomal PTS2 import pathwayRab8b and its interacting partner TRIP8b are involved in regulated secretion in AtT20 cellsThe tetratricopeptide repeat: a structural motif mediating protein-protein interactionsTopogenesis and homeostasis of fatty acyl-CoA reductase 1Cysteine ubiquitination of PTS1 receptor Pex5p regulates Pex5p recycling.Interdependence of the peroxisome-targeting receptors in Arabidopsis thaliana: PEX7 facilitates PEX5 accumulation and import of PTS1 cargo into peroxisomesIdentification of a cytoplasmic targeting/retention signal in a retroviral Gag polyprotein.Yarrowia lipolytica cells mutant for the peroxisomal peroxin Pex19p contain structures resembling wild-type peroxisomesPeroxisome biogenesis and peroxisome biogenesis disorders.Localization of Protein Kinase NDR2 to Peroxisomes and Its Role in Ciliogenesis.A PEX7-centered perspective on the peroxisomal targeting signal type 2-mediated protein import pathway.Shuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export.The life cycle of the peroxisome.
P2860
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P2860
Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
name
Peroxisome targeting signal ty ...... EX5-defective CHO cell mutants
@nl
Peroxisome targeting signal ty ...... X5-defective CHO cell mutants.
@ast
Peroxisome targeting signal ty ...... X5-defective CHO cell mutants.
@en
type
label
Peroxisome targeting signal ty ...... EX5-defective CHO cell mutants
@nl
Peroxisome targeting signal ty ...... X5-defective CHO cell mutants.
@ast
Peroxisome targeting signal ty ...... X5-defective CHO cell mutants.
@en
prefLabel
Peroxisome targeting signal ty ...... EX5-defective CHO cell mutants
@nl
Peroxisome targeting signal ty ...... X5-defective CHO cell mutants.
@ast
Peroxisome targeting signal ty ...... X5-defective CHO cell mutants.
@en
P2093
P2860
P356
P1476
Peroxisome targeting signal ty ...... X5-defective CHO cell mutants.
@en
P2093
Nishimura M
Tateishi K
P2860
P304
P356
10.1128/MCB.18.1.388
P407
P577
1998-01-01T00:00:00Z