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PEX5 information


PEX5
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPEX5, peroxisomal biogenesis factor 5, RCDP5, PTS1R, PBD2B, PTS1-BP, PXR1, PBD2A
External IDsOMIM: 600414; MGI: 1098808; HomoloGene: 270; GeneCards: PEX5; OMA:PEX5 - orthologs
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: 124.37 – 124.39 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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

PTS1R is a peroxisomal targeting sequence involved in the specific transport of molecules for oxidation inside the peroxisome. SKL 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.

  1. ^ a b c ENSG00000288217 GRCh38: Ensembl release 89: ENSG00000139197, ENSG00000288217 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000005069 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: PEX5 Peroxisomal biogenesis factor 5".

and 20 Related for: PEX5 information

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PEX5

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signal 1 receptor (PTS1R) is a protein that in humans is encoded by the PEX5 gene. PTS1R is a peroxisomal targeting sequence involved in the specific...

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Tetratricopeptide repeat

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kinase R (PKR), the major receptor for peroxisomal matrix protein import PEX5, protein arginine methyltransferase 9 (PRMT9), and mitochondrial import proteins...

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Peroxisome

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the peroxisome lumen. The matrix protein import receptors, the peroxins PEX5 and PEX7, accompany their cargoes (containing a PTS1 or a PTS2 amino acid...

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Peroxisomal targeting signal

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is encoded by the PEX5 gene. PEX5 imports folded proteins into the peroxisome, shuttling between the peroxisome and cytosol. PEX5 interacts with a large...

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Peroxisomal disorder

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PEX3, PEX5, PEX6, PEX12, PEX14, PEX26 Q87.82 Infantile Refsum disease 266510 PEX1, PEX2, PEX26 E80.3 Neonatal adrenoleukodystrophy 202370 PEX5, PEX1,...

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Protein targeting

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protein called pex5 (peroxin 5). Once bound, pex5 interacts with a peroxisomal membrane protein pex14 to form a complex. When the pex5 protein with bound...

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Zellweger syndrome

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peroxisomes. Most commonly, patients have mutations in the PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, or PEX26 genes. In almost...

Word Count : 1403

Peroxin

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transmembrane proteins, for example Peroxisomal biogenesis factor 11. PEX1 PEX2 PEX3 PEX5 PEX6 PEX7 PEX10 PEX11A, PEX11B, PEX11G PEX12 PEX13 PEX14 PEX16 PEX19 PEX26...

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List of genetic disorders

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XYYYY syndrome (49,XYYYY) Y 1:1,000,000 males Zellweger syndrome PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX26 recessive...

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Heimler syndrome

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mechanism that shuttles the peroxisome targeting signal receptor protein PEX5 back to the cytosol after release of its protein cargo within the peroxisomal...

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PEX12

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complementation groups (CGs). PEX12 has been shown to interact with PEX10, PEX5 and PEX19. GRCh38: Ensembl release 89: ENSG00000108733 – Ensembl, May 2017...

Word Count : 1168

PEX13

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chromosome 2 next to KIAA1841 PEX13 has been shown to interact with PEX14, PEX5 and PEX19. GRCh38: Ensembl release 89: ENSG00000162928 – Ensembl, May 2017...

Word Count : 1069

SCP2

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SCP2 has been shown to interact with Caveolin 1 and peroxisomal receptor PEX5. GRCh38: Ensembl release 89: ENSG00000116171 – Ensembl, May 2017 GRCm38:...

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TMEM267

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indicates that TMEM267 could be involved in the interaction of Pex14 with Pex5 proteins. Overall, TMEM267 is most likely found in the cytoplasm. The TMEM267...

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PEX14

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in one form of Zellweger syndrome. PEX14 has been shown to interact with PEX5, PEX7, and PEX13. GRCh38: Ensembl release 89: ENSG00000142655 – Ensembl,...

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PEX6

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verified function of PEX6; PEX6 (and PEX1) removes PEX5 from the peroxisomal membrane so that PEX5 may do additional rounds of peroxisomal import. Human...

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Tetratricopeptide repeat domain 16 isoform 1

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motifs and has 16 exons. Other notable TPR containing peptides include HOP, PEX5, and neutrophil cytosolic factor 2. TTC16 is highly conserved among species...

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PEX10

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Warren DS, Sacksteder KA, Gould SJ (November 1999). "PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein...

Word Count : 975

C18orf63

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Erdmann R (January 2014). "A novel Pex14 protein-interacting site of human Pex5 is critical for matrix protein import into peroxisomes". The Journal of Biological...

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List of OMIM disorder codes

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Adrenoleukodystrophy, neonatal; 202370; PEX26 Adrenoleukodystrophy, neonatal; 202370; PEX5 Adrenomyeloneuropathy; 300100; ABCD1 Adult i phenotype with congenital cataract;...

Word Count : 18877

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