# Glutaredoxin 5

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21103167](https://www.wikidata.org/wiki/Q21103167)  
**Source**: https://4ort.xyz/entity/glutaredoxin-5-q21103167


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q86SX6)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86SX6)
5. [Cochaperone Binding to LYR Motifs Confers Specificity of Iron Sulfur Cluster Delivery](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86SX6)
6. [A Single Adaptable Cochaperone-Scaffold Complex Delivers Nascent Iron-Sulfur Clusters to Mammalian Respiratory Chain Complexes I-III.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86SX6)
7. [A Single Adaptable Cochaperone-Scaffold Complex Delivers Nascent Iron-Sulfur Clusters to Mammalian Respiratory Chain Complexes I-III.](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q86SX6&geneProductId=UniProtKB:Q86SX6)
8. [Cochaperone Binding to LYR Motifs Confers Specificity of Iron Sulfur Cluster Delivery](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q86SX6&geneProductId=UniProtKB:Q86SX6)
9. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q86SX6&geneProductId=UniProtKB:Q86SX6)
10. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86SX6)
11. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q86SX6&geneProductId=UniProtKB:Q86SX6)
12. [Glutaredoxin 5 deficiency causes sideroblastic anemia by specifically impairing heme biosynthesis and depleting cytosolic iron in human erythroblasts](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q86SX6&geneProductId=UniProtKB:Q86SX6)
13. [Glutaredoxin 5 deficiency causes sideroblastic anemia by specifically impairing heme biosynthesis and depleting cytosolic iron in human erythroblasts](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86SX6)
14. [Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q86SX6)
15. Ensembl Release 99