Search Thermo Fisher Scientific
Peptide sequence: FESPFTISDG IYGSTFFVAT GFHGLHVIIG STFLTICFIR QLMFHFTSKH
Sequence homology: Human: 100%
COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Co3; Cytochrome c oxidase polypeptide III; Cytochrome c oxidase subunit 3
基因别名: COIII; COX3; COXIII; MT-CO3; MTCO3
UniProt ID: (Human) P00414
Entrez Gene ID: (Human) 4514