6zm5 | pdb_00006zm5
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Human mitochondrial ribosome in complex with OXA1L, mRNA, A/A tRNA, P/P tRNA and nascent polypeptide
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Structural highlights
DiseaseRT16_HUMAN Combined oxidative phosphorylation defect type 2. The disease is caused by mutations affecting the gene represented in this entry. FunctionSee Also | ||||||||||||||||||||
This page was last modified 09:36, 16 September 2026.