9kkj
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Structure of Nectin-4 D1 domain in complex with the Fab fragment of 9MW2821 mAb
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Structural highlights
DiseaseNECT4_HUMAN Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionNECT4_HUMAN Seems to be involved in cell adhesion through trans-homophilic and -heterophilic interactions, the latter including specifically interactions with NECTIN1. Does not act as receptor for alpha-herpesvirus entry into cells. (Microbial infection) Acts as a receptor for measles virus.[1] [2] References
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This page was last modified 07:38, 19 November 2025.