Search results for SUCLG2

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Protein (1 results from a total of 1)

Identifier: R-HSA-156628
Species: Homo sapiens
Compartment: mitochondrial matrix
Primary external reference: UniProt: SUCLG2: Q96I99

Complex (2 results from a total of 2)

Identifier: R-HSA-156627
Species: Homo sapiens
Compartment: mitochondrial matrix
Identifier: R-HSA-9853492
Species: Homo sapiens
Compartment: mitochondrial matrix

Reaction (1 results from a total of 1)

Identifier: R-HSA-71775
Species: Homo sapiens
Compartment: mitochondrial matrix
Mitochondrial succinate CoA ligase (GDP-forming) catalyzes the reversible conversion of succinyl CoA to succinate plus Coenzyme A, coupled to the conversion of GDP and orthophosphate to GTP. The enzyme is a heterodimer containing SUCLG1 and SUCLG2 monomers.

The enzyme catalyzing the reaction in vertebrates is a heterodimer that occurs in two isoforms. The enzymes have been purified from pigeon and rat tissue and characterized in detail. Both isoforms, an alpha:betaA heterodimer and an alpha:betaG heterodimer, catalyze the reversible conversion of succinyl CoA to succinate plus Coenzyme A. The alpha:betaA heterodimer couples this conversion to the synthesis of ATP from ADP and orthophosphate, while the alpha:betaG heterodimer couples it to the synthesis of GTP from GDP and orthophosphate (Johnson et al. 1998a,b; Lambeth et al. 2004). Consistent with these results in model systems, patients homozygous for a mutant allele of the gene encoding the ADP enzyme beta subunit, SUCLA2, are deficient in succinyl CoA ligase activity (Elpeleg et al. 2005).

Both isoforms are found in vivo, and appear to be expressed at different levels in various tissues. Their relative contributions to the flux of carbon atoms through the TCA cycle are unknown. Genetic and biochemical data suggest that the alpha:betaA isoform may be required to catalyze the reverse reaction, conversion of succinate, Coenzyme A, and ATP to succinyl CoA, ADP, and orthophosphate for heme biosynthesis (Furuyama and Sassa 2000).

Mutations in SUCLG1 are the cause of the infantile metabolic disease named mitochondrial DNA depletion syndrome 9 (MTDPS9; MIM:245400; reviewed by Molaei Ramsheh et al., 2020).

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