Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus.
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Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assemblyMolecular 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 interactionTwo proteases, trypsin domain-containing 1 (Tysnd1) and peroxisomal lon protease (PsLon), cooperatively regulate fatty acid β-oxidation in peroxisomal matrixIdentification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disordersOverexpression and characterization of the human peroxisomal acyl-CoA oxidase in insect cellsClofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11Subcellular localisation and processing of non-specific lipid transfer protein are not aberrant in Rhizomelic Chondrodysplasia Punctata fibroblastsHuman peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codonPEX12, 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 PTS1Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.Peroxisomal 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 ICrystal structures of nitroalkane oxidase: insights into the reaction mechanism from a covalent complex of the flavoenzyme trapped during turnoverMultiple 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 receptorPeroxisomes in Saccharomyces cerevisiae: immunofluorescence analysis and import of catalase A into isolated peroxisomesSaccharomyces cerevisiae acyl-CoA oxidase follows a novel, non-PTS1, import pathway into peroxisomes that is dependent on Pex5p.Citrate synthase encoded by the CIT2 gene of Saccharomyces cerevisiae is peroxisomal.The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysisCatalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorderPeroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutantAWP1/ZFAND6 functions in Pex5 export by interacting with cys-monoubiquitinated Pex5 and Pex6 AAA ATPasePeroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysisA conserved tripeptide sorts proteins to peroxisomesIdentification of a consensus motif for retention of transmembrane proteins in the endoplasmic reticulumCysteine ubiquitination of PTS1 receptor Pex5p regulates Pex5p recycling.Soybean Nodule-Specific Uricase (Nodulin-35) Is Expressed and Assembled into a Functional Tetrameric Holoenzyme in Escherichia coli.Pumpkin malate synthase. Cloning and sequencing of the cDNA and northern blot analysis.Peroxisomal protein import is conserved between yeast, plants, insects and mammalsTransformation of mammalian cells by overexpressing H2O2-generating peroxisomal fatty acyl-CoA oxidaseShuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export.Plant peroxisomes: recent studies on function and biosynthesis.A genetic approach to the biogenesis of peroxisomes in the yeast Saccharomyces cerevisiae.Targeting signals for protein import into peroxisomes.Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome
P2860
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P2860
Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Peroxisome targeting signal of ...... sides at the carboxy terminus.
@en
type
label
Peroxisome targeting signal of ...... sides at the carboxy terminus.
@en
prefLabel
Peroxisome targeting signal of ...... sides at the carboxy terminus.
@en
P2093
P2860
P356
P1476
Peroxisome targeting signal of ...... sides at the carboxy terminus.
@en
P2093
P2860
P356
10.1128/MCB.9.1.83
P407
P577
1989-01-01T00:00:00Z