Dihydrolipoyl dehydrogenase, mitochondrial
Definition:
References:
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[1]. Yugang Wang, et al. KAT2A coupled with the α-KGDH complex acts as a histone H3 succinyltransferase. Nature. 2017 Dec 14;552(7684):273-277. [Content Brief]
[2]. Ngolela Esther Babady, et al. Cryptic proteolytic activity of dihydrolipoamide dehydrogenase. Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6158-63. [Content Brief]
[3]. Mulchand S Patel, et al. Interaction of E1 and E3 components with the core proteins of the human pyruvate dehydrogenase complex. J Mol Catal B Enzym. 2009 Nov 1;61(1-2):2-6. [Content Brief]
[4]. Jessie M Cameron, et al. Novel mutations in dihydrolipoamide dehydrogenase deficiency in two cousins with borderline-normal PDH complex activity. Am J Med Genet A. 2006 Jul 15;140(14):1542-52. [Content Brief]
[5]. Chad A Brautigam, et al. Structural insight into interactions between dihydrolipoamide dehydrogenase (E3) and E3 binding protein of human pyruvate dehydrogenase complex. Structure. 2006 Mar;14(3):611-21. [Content Brief]
[6]. Yun-Hee Park, et al. Characterization of interactions of dihydrolipoamide dehydrogenase with its binding protein in the human pyruvate dehydrogenase complex. Biochem Biophys Res Commun. 2010 May 7;395(3):416-9. [Content Brief]
[7]. Marie-Hélène Odièvre, et al. A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency. Hum Mutat. 2005 Mar;25(3):323-4. [Content Brief]
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