NADH dehydrogenase [Homo sapiens]

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Most mitochondrial dGTP is tightly bound to respiratory complex I through the NDUFA10 subunit. [Commun Biol. 2022]
Most mitochondrial dGTP is tightly bound to respiratory complex I through the NDUFA10 subunit.
Molina-Granada D, González-Vioque E, Dibley MG, Cabrera-Pérez R, Vallbona-Garcia A, Torres-Torronteras J, Sazanov LA, Ryan MT, Cámara Y, Martí R. Commun Biol. 2022 Jun 23; 5(1):620. Epub 2022 Jun 23.
NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. [Eur J Hum Genet. 2011]
NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease.
Hoefs SJ, van Spronsen FJ, Lenssen EW, Nijtmans LG, Rodenburg RJ, Smeitink JA, van den Heuvel LP. Eur J Hum Genet. 2011 Mar; 19(3):270-4. Epub 2010 Dec 8.
Mass spectrometric characterization of mitochondrial complex I NDUFA10 variants. [Proteomics. 2008]
Mass spectrometric characterization of mitochondrial complex I NDUFA10 variants.
Muñoz J, Fernández-Irigoyen J, Santamaría E, Parbel A, Obeso J, Corrales FJ. Proteomics. 2008 May; 8(9):1898-908.

RefSeq genomic sequence
See the genomic reference sequence for the NDUFA10 gene (NG_031855.2).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the NDUFA10 gene.

Nucleotide
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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