Figure 5From: In silico characterization of a novel pathogenic deletion mutation identified in XPA gene in a Pakistani family with severe xeroderma pigmentosumSchematic presentation of XPA protein with distinct functional domains. Regions for binding to RPA, ERCC1, DDB2, TFIIH and location of the nuclear localization signal (NLS) and the zinc finger motif are shown. Numbers refer to amino acid numbers for the XPA protein. *Deletion mutation identified in this study. ** Predicted Coiled coil structure formation region.Back to article page