PEX5

 Peroxisomal targeting signal 1 receptor (PTS1R) is a protein that in humans is encoded by the PEX5 gene.[5]

PEX5
Protein PEX5 PDB 1fch.png
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPEX5, PBD2A, PBD2B, PTS1-BP, PTS1R, PXR1, RCDP5, peroxisomal biogenesis factor 5
External IDsOMIM: 600414 MGI: 1098808 HomoloGene: 270 GeneCards: PEX5
Gene location (Human)
Chromosome 12 (human)
Chr.Chromosome 12 (human)[1]
Chromosome 12 (human)
Genomic location for PEX5
Genomic location for PEX5
Band12p13.31Start7,188,685 bp[1]
End7,218,574 bp[1]
RNA expression pattern
PBB GE PEX5 215481 s at fs.png

PBB GE PEX5 203244 at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001277330
NM_001277805
NM_008995
NM_175933
NM_001360570

RefSeq (protein)

NP_001264259
NP_001264734
NP_033021
NP_787947
NP_001347499

Location (UCSC)Chr 12: 7.19 – 7.22 MbChr 6: 124.4 – 124.42 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

PTS1R is a peroxisomal targeting sequence involved in the specific transport of molecules for oxidation inside the peroxisomeSKL binds to PTS1R in the cytosol followed by binding to the Pex14p receptor allowing importation of the peroxisomal protein through the pexsubunit transporter.

Diseases associated with dysfunctional PTS1R receptors include X-linked adrenoleukodystrophy and Zellweger syndrome.

InteractionsEdit

PEX5 has been shown to interact with PEX12,[6][7] PEX13[8][9] and PEX14.[7][9



This article uses material from the Wikipedia article
 Metasyntactic variable, which is released under the 
Creative Commons
Attribution-ShareAlike 3.0 Unported License
.