# Peroxisomal biogenesis factor 1

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21122485](https://www.wikidata.org/wiki/Q21122485)  
**Source**: https://4ort.xyz/entity/peroxisomal-biogenesis-factor-1-q21122485


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O43933)
3. Q20641742
4. [Swiss-Prot](http://www.uniprot.org/uniprot/Q5BL07.txt?version=101)
5. [Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43933&geneProductId=UniProtKB:O43933)
6. [Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
7. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
8. [Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
9. [A Cytoplasmic AAA Family Peroxin, Pex1p, Interacts with Pex6p](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
10. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
11. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43933&geneProductId=UniProtKB:O43933)
12. [PEX14 is required for microtubule-based peroxisome motility in human cells](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43933&geneProductId=UniProtKB:O43933)
13. [Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43933&geneProductId=UniProtKB:O43933)
14. [Proteomic analysis of exosomes from human neural stem cells by flow field-flow fractionation and nanoflow liquid chromatography-tandem mass spectrometry](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43933&geneProductId=UniProtKB:O43933)
15. [Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
16. [PEX14 is required for microtubule-based peroxisome motility in human cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
17. [Proteomic analysis of exosomes from human neural stem cells by flow field-flow fractionation and nanoflow liquid chromatography-tandem mass spectrometry](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
18. [Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
19. [Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43933&geneProductId=UniProtKB:O43933)
20. [Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43933)
21. Ensembl Release 99
22. Transporter Classification database