Peroxisomal membrane protein PEX14 is a protein that in humans is encoded by the PEX14 gene.[5][6]
Peroxisomal membrane anchor protein (Pex14p) conserved region | |||||||||
---|---|---|---|---|---|---|---|---|---|
Identifiers | |||||||||
Symbol | Pex14_N | ||||||||
Pfam | PF04695 | ||||||||
InterPro | IPR006785 | ||||||||
|
Function
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.[6]
Interactions
PEX14 has been shown to interact with
References
Further reading
External links
- GeneReviews/NCBI/NIH/UW entry on Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum
- OMIM entries on Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum
- Eukaryotic Linear Motif resource motif class TRG_PEX_1
- Eukaryotic Linear Motif resource motif class TRG_PEX_2
- Overview of all the structural information available in the PDB for UniProt: O75381 (Peroxisomal membrane protein PEX14) at the PDBe-KB.
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