Methylglutaconyl-CoA hydratase, mitochondrial
Definition:
References:
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[1]. T B Nga Ly, et al. Mutations in the AUH gene cause 3-methylglutaconic aciduria type I. Hum Mutat. 2003 Apr;21(4):401-7. [Content Brief]
[2]. Hongying Shen, et al. The Human Knockout Gene CLYBL Connects Itaconate to Vitamin B12. Cell. 2017 Nov 2;171(4):771-782.e11. [Content Brief]
[3]. Lodewijk IJlst, et al. 3-Methylglutaconic aciduria type I is caused by mutations in AUH. Am J Hum Genet. 2002 Dec;71(6):1463-6. [Content Brief]
[4]. K Kurimoto, et al. Crystal structure of human AUH protein, a single-stranded RNA binding homolog of enoyl-CoA hydratase. Structure. 2001 Dec;9(12):1253-63. [Content Brief]
[5]. Matthias Mack, et al. Biochemical characterization of human 3-methylglutaconyl-CoA hydratase and its role in leucine metabolism. FEBS J. 2006 May;273(9):2012-22. [Content Brief]
[6]. J Nakagawa, et al. AUH, a gene encoding an AU-specific RNA binding protein with intrinsic enoyl-CoA hydratase activity. Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):2051-5. [Content Brief]