RecName: Full=Atypical kinase COQ8A, mitochondrial; AltName: Full=Chap - Protein

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Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy. [Mitochondrion. 2010]
Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy.
Gerards M, van den Bosch B, Calis C, Schoonderwoerd K, van Engelen K, Tijssen M, de Coo R, van der Kooi A, Smeets H. Mitochondrion. 2010 Aug; 10(5):510-5. Epub 2010 May 23.
Mitochondrial ADCK3 employs an atypical protein kinase-like fold to enable coenzyme Q biosynthesis. [Mol Cell. 2015]
Mitochondrial ADCK3 employs an atypical protein kinase-like fold to enable coenzyme Q biosynthesis.
Stefely JA, Reidenbach AG, Ulbrich A, Oruganty K, Floyd BJ, Jochem A, Saunders JM, Johnson IE, Minogue CE, Wrobel RL, et al. Mol Cell. 2015 Jan 8; 57(1):83-94. Epub 2014 Dec 11.
Cerebellar Ataxia and Coenzyme Q Deficiency through Loss of Unorthodox Kinase Activity. [Mol Cell. 2016]
Cerebellar Ataxia and Coenzyme Q Deficiency through Loss of Unorthodox Kinase Activity.
Stefely JA, Licitra F, Laredj L, Reidenbach AG, Kemmerer ZA, Grangeray A, Jaeg-Ehret T, Minogue CE, Ulbrich A, Hutchins PD, et al. Mol Cell. 2016 Aug 18; 63(4):608-620. Epub 2016 Aug 4.

RefSeq protein isoforms
See 2 reference sequence protein isoforms for the Coq8a gene.

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Protein