# ERCC excision repair 8, CSA ubiquitin ligase complex subunit

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21112346](https://www.wikidata.org/wiki/Q21112346)  
**Source**: https://4ort.xyz/entity/ercc-excision-repair-8-csa-ubiquitin-ligase-complex-subunit


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q13216)
3. Q20641742
4. [Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
5. [The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q13216&geneProductId=UniProtKB:Q13216)
6. [Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
7. [A family of diverse Cul4-Ddb1-interacting proteins includes Cdt2, which is required for S phase destruction of the replication factor Cdt1](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
8. [The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
9. [XAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcription](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
10. [Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
11. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
12. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
13. [Translocation of Cockayne syndrome group A protein to the nuclear matrix: Possible relevance to transcription-coupled DNA repair](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
14. [The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q13216&geneProductId=UniProtKB:Q13216)
15. [CSA-dependent degradation of CSB by the ubiquitin-proteasome pathway establishes a link between complementation factors of the Cockayne syndrome](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q13216&geneProductId=UniProtKB:Q13216)
16. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q13216&geneProductId=UniProtKB:Q13216)
17. [Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q13216&geneProductId=UniProtKB:Q13216)
18. [The role of CSA in the response to oxidative DNA damage in human cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
19. [CSA-dependent degradation of CSB by the ubiquitin-proteasome pathway establishes a link between complementation factors of the Cockayne syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13216)
20. Ensembl Release 99