This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
4lg6
From Proteopedia
Contents |
Crystal structure of ANKRA2-CCDC8 complex
Disease
[CCDC8_HUMAN] 3M syndrome. The disease is caused by mutations affecting the gene represented in this entry.
Function
[ANRA2_HUMAN] May facilitate endocytosis by linking megalin to components of the cytoskeleton or endocytic machinery.
About this Structure
4lg6 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
