Nucleotide excision repair
| PAG Title | Nucleotide excision repair |
| PAG ID | WAG001001 |
| Type | P |
| Source Link |  KEGG |
| Publication Reference | NA |
| PAG Description | Nucleotide excision repair (NER) is a mechanism to recognize and repair bulky D damage caused by compounds, environmental carcinogens, and exposure to UV-light. In humans hereditary defects in the NER pathway are linked to at least three diseases: xeroderma pigmentosum (XP), Cockayne syndrome (CS), and trichothiodystrophy (TTD). The repair of damaged D involves at least 30 polypeptides within two different sub-pathways of NER known as transcription-coupled repair (TCR-NER) and global genome repair (GGR-NER). TCR refers to the expedited repair of lesions located in the actively transcribed strand of genes by R polymerase II (RP II). In GGR-NER the first step of damage recognition involves XPC-hHR23B complex together with XPE complex (in prokaryotes, uvrAB complex). The following steps of GGR-NER and TCR-NER are similar. |
| Species | Homo sapiens |
| nCoCo Score | 12,957 |
| Base PAG ID | WAG001001 |
| Human Phenotyte Annotation | |
| Curator | PAGER curation team |
| Curator Contact | PAGER-contact@googlegroups.com |
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