9x02 | pdb_00009x02
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Crystal structure of human type VII collagen vWFA2 domain in complex with homo-trimeric collagen model peptide.
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Structural highlights
DiseaseCO7A1_HUMAN Self-improving dystrophic epidermolysis bullosa;Localized dystrophic epidermolysis bullosa, nails only;Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form;Localized dystrophic epidermolysis bullosa, pretibial form;Autosomal dominant generalized dystrophic epidermolysis bullosa;Localized dystrophic epidermolysis bullosa, acral form;Dystrophic epidermolysis bullosa pruriginosa;Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form;Recessive dystrophic epidermolysis bullosa inversa. Epidermolysis bullosa acquisita (EBA) is an autoimmune acquired blistering skin disease resulting from autoantibodies to type VII collagen. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. FunctionCO7A1_HUMAN Stratified squamous epithelial basement membrane protein that forms anchoring fibrils which may contribute to epithelial basement membrane organization and adherence by interacting with extracellular matrix (ECM) proteins such as type IV collagen. Contents | ||||||||||||||||||||
This page was last modified 07:11, 7 October 2026.