7sk2
Human wildtype GABA reuptake transporter 1 in complex with tiagabine, inward-open conformationHuman wildtype GABA reuptake transporter 1 in complex with tiagabine, inward-open conformation
Structural highlights
Disease[SC6A1_HUMAN] Myoclonic-astatic epilepsy. The disease is caused by variants affecting the gene represented in this entry. Function[SC6A1_HUMAN] Terminates the action of GABA by its high affinity sodium-dependent reuptake into presynaptic terminals. |
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