7cgp
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Cryo-EM structure of the human mitochondrial translocase TIM22 complex at 3.7 angstrom.
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Structural highlights
DiseaseTIM22_HUMAN The disease is caused by variants affecting the gene represented in this entry. FunctionTIM22_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 | ||||||||||||||||||||
This page was last modified 09:27, 9 April 2025.