Pages that link to "Q22008838"
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The following pages link to Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly (Q22008838):
Displayed 50 items.
- Zellweger syndrome (Q189167) (← links)
- Peroxisomal biogenesis factor 19 (Q21140646) (← links)
- The human PICD gene encodes a cytoplasmic and peroxisomal NADP(+)-dependent isocitrate dehydrogenase (Q22010653) (← links)
- PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import (Q22010795) (← links)
- PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis (Q22253284) (← links)
- Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p (Q22253967) (← links)
- Molecular 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, Pex10p (Q22254195) (← links)
- Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients (Q22254302) (← links)
- Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G (Q24290144) (← links)
- Topogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments. study using human membrane protein PMP34 (Q24290647) (← links)
- Two different targeting signals direct human peroxisomal membrane protein 22 to peroxisomes (Q24291763) (← links)
- Two splice variants of human PEX19 exhibit distinct functions in peroxisomal assembly (Q24292418) (← links)
- In vitro transport of membrane proteins to peroxisomes by shuttling receptor Pex19p (Q24294471) (← links)
- Analysis of human Pex19p's domain structure by pentapeptide scanning mutagenesis (Q24294925) (← links)
- Role of Pex19p in the targeting of PMP70 to peroxisome (Q24298579) (← links)
- PEX19 is a predominantly cytosolic chaperone and import receptor for class 1 peroxisomal membrane proteins (Q24304129) (← links)
- Phosphomevalonate kinase is a cytosolic protein in humans (Q24305203) (← links)
- Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interaction (Q24305429) (← links)
- The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly (Q24306509) (← links)
- Structural basis for docking of peroxisomal membrane protein carrier Pex19p onto its receptor Pex3p (Q24307906) (← links)
- Human mevalonate pyrophosphate decarboxylase is localized in the cytosol (Q24309834) (← links)
- Peroxisomes are signaling platforms for antiviral innate immunity (Q24310723) (← links)
- The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway (Q24311655) (← links)
- PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins (Q24315009) (← links)
- The interaction between human PEX3 and PEX19 characterized by fluorescence resonance energy transfer (FRET) analysis (Q24316116) (← links)
- The peroxisomal receptor Pex19p forms a helical mPTS recognition domain (Q24318137) (← links)
- Mammalian Pex14p: membrane topology and characterisation of the Pex14p-Pex14p interaction (Q24337246) (← links)
- Interaction of a farnesylated protein with renal type IIa Na/Pi co-transporter in response to parathyroid hormone and dietary phosphate (Q24530634) (← links)
- PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G. (Q24538915) (← links)
- PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders (Q24540126) (← links)
- The peroxin pex3p initiates membrane assembly in peroxisome biogenesis (Q24549973) (← links)
- Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences (Q24550941) (← links)
- Peroxisomes in brain development and function (Q26774697) (← links)
- Peroxisome biogenesis in mammalian cells (Q26859014) (← links)
- Association between the intrinsically disordered protein PEX19 and PEX3 (Q27318204) (← links)
- Insights into Peroxisome Function from the Structure of PEX3 in Complex with a Soluble Fragment of PEX19 (Q27662365) (← links)
- Peroxins Pex30 and Pex29 Dynamically Associate with Reticulons to Regulate Peroxisome Biogenesis from the Endoplasmic Reticulum (Q27929790) (← links)
- The dynamin-like protein Vps1p of the yeast Saccharomyces cerevisiae associates with peroxisomes in a Pex19p-dependent manner (Q27932442) (← links)
- Saccharomyces cerevisiae PTS1 receptor Pex5p interacts with the SH3 domain of the peroxisomal membrane protein Pex13p in an unconventional, non-PXXP-related manner (Q27932676) (← links)
- Endoplasmic reticulum-associated secretory proteins Sec20p, Sec39p, and Dsl1p are involved in peroxisome biogenesis. (Q27936884) (← links)
- Pex30p, Pex31p, and Pex32p Form a Family of Peroxisomal Integral Membrane Proteins Regulating Peroxisome Size and Number inSaccharomyces cerevisiae (Q27937555) (← links)
- Yeast peroxisomes multiply by growth and division (Q27938051) (← links)
- Saccharomyces cerevisiae pex3p and pex19p are required for proper localization and stability of peroxisomal membrane proteins (Q27938108) (← links)
- Catalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorder (Q28144608) (← links)
- Potential role for Pex19p in assembly of PTS-receptor docking complexes (Q28238019) (← links)
- Domain architecture and activity of human Pex19p, a chaperone-like protein for intracellular trafficking of peroxisomal membrane proteins (Q28271907) (← links)
- The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum (Q28293113) (← links)
- 70-kDa peroxisomal membrane protein related protein (P70R/ABCD4) localizes to endoplasmic reticulum not peroxisomes, and NH2-terminal hydrophobic property determines the subcellular localization of ABC subfamily D proteins (Q28583012) (← links)
- The peroxisome: still a mysterious organelle (Q28754736) (← links)
- Topogenesis and homeostasis of fatty acyl-CoA reductase 1 (Q29871499) (← links)