Structural highlights
Disease
TIM22_HUMAN The disease is caused by variants affecting the gene represented in this entry.
Function
TIM22_HUMAN Essential core component of the TIM22 complex, a complex that mediates the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. In the TIM22 complex, it constitutes the voltage-activated and signal-gated channel. Forms a twin-pore translocase that uses the membrane potential as external driving force in 2 voltage-dependent steps (By similarity).[UniProtKB:Q12328]
See Also
