9z6t
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Human HCN1 in complex with cAMP in nanodisc
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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 11:51, 24 May 2026.