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Protein Name: DNA excision repair protein ERCC-8

UniprotKB/SwissProt ID: ERCC8_HUMAN (Q13216)

Gene Name: ERCC8

Synonyms: CKN1, CSA

Organism: Homo sapiens (Human).

Function: Substrate-recognition component of the CSA complex, a DCX (DDB1-CUL4-X-box) E3 ubiquitin-protein ligase complex, involved in transcription-coupled nucleotide excision repair. The CSA complex (DCX(ERCC8) complex) promotes the ubiquitination and subsequent proteasomal degradation of ERCC6 in a UV-dependent manner; ERCC6 degradation is essential for the recovery of RNA synthesis after transcription-coupled repair. It is required for the recruitment of XAB2, HMGN1 and TCEA1/TFIIS to a transcription- coupled repair complex which removes RNA polymerase II-blocking lesions from the transcribed strand of active genes.

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Nucleus (Probable).

PDB :
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Graphical Visualization of Ubiquitination Sites:
Overview of Protein Ubiquitination Sites with Functional and Structural Information
InterPro ID Domain
IPR001680
IPR011046
IPR015943


The ubiquitination sites of ERCC8_HUMAN

No. Position Ubiquitinated Peptide Secondary Structure Solvent Accessibility Substrate Motifs PubMed ID
1233DQHNGK K SQAVES ECCCCC C CEEEEE 49.55%2190698

The interacting network mediated by proteins: ERCC8_HUMAN


Disease:
Disease database Database Entry Disease information
HPRD07523Cockayne syndrome, type A
Metabolic pathway:
Kegg map ID Pathway
map03008Ribosome biogenesis in eukaryotes