8uc8 | pdb_00008uc8
From Proteopedia
Structural highlights
DiseaseHCN1_HUMAN Early infantile epileptic encephalopathy. The disease is caused by mutations affecting the gene represented in this entry. FunctionHCN1_HUMAN Hyperpolarization-activated ion channel exhibiting weak selectivity for potassium over sodium ions. Contributes to the native pacemaker currents in heart (If) and in neurons (Ih). May mediate responses to sour stimuli.[1] References
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This page was last modified 06:06, 31 July 2024.