8csx | pdb_00008csx
From Proteopedia
Local refinement of RhAG/CE trimer in class 2 of erythrocyte ankyrin-1 complex
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Structural highlights
DiseaseRHCE_HUMAN Rh deficiency syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionRHCE_HUMAN May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane. Contents | ||||||||||||||||||||
This page was last modified 09:40, 14 February 2024.