PEX5 Products

Antibodies
PEX5 Antibody
PEX5 Antibody
NBP1-87185
Species: Hu, Mu, Rt
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
PEX5 Antibody
PEX5 Antibody
NBP2-38443
Species: Hu, Mouse, Rat
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
PEX5 Antibody
PEX5 Antibody
NBP2-19781
Species: Hu
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
Lysates
PEX5 Overexpression Lysate (N ...
PEX5 Overexpression Lysate (Native)
NBL1-14304
Applications: WB
Proteins
PEX5 Recombinant Protein
PEX5 Recombinant Protein
H00005830-P01
Species: Hu
Applications: WB, ELISA, PA
PEX5 Recombinant Protein Anti ...
PEX5 Recombinant Protein Antigen
NBP1-87185PEP
Species: Hu
Applications: AC
PEX5 Recombinant Protein Anti ...
PEX5 Recombinant Protein Antigen
NBP2-38443PEP
Species: Hu
Applications: AC
RNAi
PEX5 RNAi
PEX5 RNAi
H00005830-R02
Species: Hu

Description

The product of the PEX5 gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified. (provided by RefSeq)

Bioinformatics

Uniprot Human
Human
Human
Human
Product By Gene ID 5830
Alternate Names
  • Peroxin-5
  • FLJ50634
  • peroxisomal targeting signal receptor 1
  • PTS1 receptor
  • peroxisomal targeting signal import receptor
  • PTS1-BP
  • peroxisomal targeting signal 1 receptor
  • Peroxisomal C-terminal targeting signal import receptor
  • PXR1peroxisomal targeting signal 1 (SKL type) receptor
  • Peroxisome receptor 1peroxin-5
  • PTS1RFLJ51948
  • FLJ50721
  • peroxisomal biogenesis factor 5

PTMs for PEX5

Learn more about PTMs related to PEX5.

Oxidation
Ubiquitination
Phosphorylation
Reduction
Cleavage

Bioinformatics Tool for PEX5

Discover related pathways, diseases and genes to PEX5. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
Vizit™, under license from BioVista Inc.