5m6c | pdb_00005m6c
From Proteopedia
CRYSTAL STRUCTURE OF T71N MUTANT OF HUMAN HIPPOCALCIN
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Structural highlights
Disease[HPCA_HUMAN] The disease is caused by mutations affecting the gene represented in this entry. Function[HPCA_HUMAN] May be involved in the calcium-dependent regulation of rhodopsin phosphorylation. Binds two calcium ions. Contents | ||||||||||||||||||
This page was last modified 11:45, 12 April 2017.