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FIGURE: 1 / 1
Sequence of this protein is as follows: MTTMAAATLL RATPHFSGLA AGRTFLLQGL LRLLKAPALP LLCRGLAVEA KKTYVRDKPH VNVGTIGHVD HGKTTLTAAI TKILAEGGGA KFKKYEEIDN APEERARGIT INAAHVEYST AARHYAHTDC PGHADYVKNM ITGTAPLDGC ILVVAANDGP MPQTREHLLL ARQIGVEHVV VYVNKADAVQ DSEMVELVEL EIRELLTEFG YKGEETPVIV GSALCALEGR DPELGLKSVQ KLLDAVDTYI PVPARDLEKP FLLPVEAVYS VPGRGTVVTG TLERGILKKG DECELLGHSK NIRTVVTGIE MFHKSLERAE AGDNLGALVR GLKREDLRRG LVMVKPGSIK PHQKVEAQVY ILSKEEGGRH KPFVSHFMPV MFSLTWDMAC RIILPPEKEL AMPGEDLKFN LILRQPMILE KGQRFTLRDG NRTIGTGLVT NTLAMTEEEK NIKWG
This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: EF-Tu; Elongation factor Tu, mitochondrial; P43
Gene Aliases: COXPD4; EF-TuMT; EFTU; P43; TUFM
UniProt ID: (Human) P49411
Entrez Gene ID: (Human) 7284
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