2mkv | pdb_00002mkv
From Proteopedia
Structure of the NA,K-ATPASE regulatory protein FXYD2b in micelles
| ||||||||||||
Structural highlights
Disease[ATNG_HUMAN] Autosomal dominant primary hypomagnesemia with hypocalcuria. The disease is caused by mutations affecting the gene represented in this entry. Function[ATNG_HUMAN] May be involved in forming the receptor site for cardiac glycoside binding or may modulate the transport function of the sodium ATPase. Contents | ||||||||||||||||||||
This page was last modified 07:21, 14 May 2014.