6uqf | pdb_00006uqf
From Proteopedia
Human HCN1 channel in a hyperpolarized conformation
| ||||||||||||
Structural highlights
Disease[HCN1_HUMAN] Early infantile epileptic encephalopathy. The disease is caused by mutations affecting the gene represented in this entry. Function[HCN1_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
| ||||||||||||||||||
This page was last modified 15:25, 11 December 2019.