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PEX14 encodes an essential component of the peroxisomal import machinery. Additionally we are shipping PEX14 Antibodies (65) and PEX14 Proteins (8) and many more products for this protein.
PEX5 (show PEX5 ELISA Kits) binding to the PEX14N-terminal domain (PEX14N) has no effect on the affinity of PEX5 (show PEX5 ELISA Kits) for a PTS1 containing peptides.
PEX14 facilitates peroxisomal matrix protein import in plants.
The novel Pex14-binding site may represent the initial tethering site of Pex5 (show PEX5 ELISA Kits) from which the cargo-loaded receptor is further processed in a sequential manner.
interaction of PEX5 (show PEX5 ELISA Kits) with catalase (show CAT ELISA Kits) and PEX14
PEX14 is a multi-tasking protein that not only facilitates peroxisomal protein (show FNDC5 ELISA Kits) import but is also required for peroxisome motility by serving as membrane anchor for microtubules.
peroxisomal localization of Pex14p is affected by Pex13p (show PEX13 ELISA Kits)
a new complementation group of the peroxisome biogenesis disorders with PEX14 as the defective gene
This report represents the second PEX14-deficiency associated with Zellweger syndrome (show PEX1 ELISA Kits) and the first documentation of a PEX14-deficient patient with detailed clinical follow-up and biochemical, morphological, and radiological data.
N-terminal domain of Pex14, Pex14(N), adopts a three-helical fold. Pex5 (show PEX5 ELISA Kits) and Pex19 (show PEX19 ELISA Kits) ligand helices bind competitively to the same surface in Pex14(N) albeit with opposite directionality.
analysis of the human Pex5 (show PEX5 ELISA Kits).Pex14.PTS1 protein complex structure obtained by small angle X-ray scattering
This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal. The protein also functions as a transcriptional corepressor and interacts with a histone deacetylase. A mutation in this gene results in one form of Zellweger syndrome.
peroxisomal membrane protein PEX14
, NF-E2 associated polypeptide 2
, PTS1 receptor docking protein
, PTS1 receptor-docking protein
, peroxisomal membrane anchor protein PEX14
, peroxisomal membrane anchor protein Pex14p
, peroxisomal protein Pex14