SUCLG1

Succinyl-CoA ligase [GDP-forming] subunit alpha, mitochondrial is an enzyme that in humans is encoded by the SUCLG1 gene.[5][6]

SUCLG1
Identifiers
AliasesSUCLG1, GALPHA, MTDPS9, SUCLA1, succinate-CoA ligase alpha subunit, succinate-CoA ligase GDP/ADP-forming subunit alpha
External IDsOMIM: 611224 MGI: 1927234 HomoloGene: 55785 GeneCards: SUCLG1
Gene location (Human)
Chr.Chromosome 2 (human)[1]
Band2p11.2Start84,423,528 bp[1]
End84,460,045 bp[1]
RNA expression pattern


More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

8802

56451

Ensembl

ENSG00000163541

ENSMUSG00000052738

UniProt

P53597

Q9WUM5

RefSeq (mRNA)

NM_003849

NM_019879

RefSeq (protein)

NP_003840

NP_063932

Location (UCSC)Chr 2: 84.42 – 84.46 MbChr 6: 73.25 – 73.28 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Structure

The enzyme encoded by SUCLG1 can exist in either a phosphorylated form or a dephosphorylated form. In the dephosphorylated structure, a phosphate ion works in coordination with a histidine residue in the active site and the two alpha helices, one contributed by each subunit of the alphabeta-dimer to stabilize the structure. One of the alpha helices contains amino acids, the modification of which result in conformational changes that accommodate either the bound phosphoryl group or the free phosphate ion.[7]

Function

This gene encodes the alpha subunit of the heterodimeric enzyme succinate coenzyme A ligase. This enzyme is targeted to the mitochondria and catalyzes the conversion of succinyl CoA and ADP or GDP to succinate and ATP or GTP. Mutations in this gene are the cause of the metabolic disorder fatal infantile lactic acidosis and mitochondrial DNA depletion.[8][9]

Clinical significance

Succinate-CoA ligase deficiency is responsible for encephalomyopathy with mitochondrial DNA depletion and mild methylmalonic aciduria. Mutations in SUCLG1 lead to complete absence of SUCLG1 protein and are responsible for a very severe disorder with antenatal manifestations. Furthermore, it is shown that in the absence of SUCLG1 protein, no SUCLA2 protein is found in fibroblasts by western blot analysis. This result is consistent with a degradation of SUCLA2 when its heterodimer partner, SUCLG1, is absent.[10] As mitochondrial DNA depletion in muscle is not a constant finding in SUCLG1 patients, diagnosis should not be based on it; additionally, it may be that alternative physiopathological mechanisms may be considered to explain the combined respiratory chain deficiency observed in these patients.[9]

Interactive pathway map

Click on genes, proteins and metabolites below to link to respective articles. [§ 1]

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|{{{bSize}}}px|alt=TCACycle_WP78 edit]]
TCACycle_WP78 edit
  1. The interactive pathway map can be edited at WikiPathways: "TCACycle_WP78".

References

  1. GRCh38: Ensembl release 89: ENSG00000163541 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000052738 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. James M, Man NT, Edwards YH, Morris GE (Apr 1997). "The molecular basis for cross-reaction of an anti-dystrophin antibody with alpha-actinin". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1360 (2): 169–76. doi:10.1016/s0925-4439(96)00076-2. PMID 9128182.
  6. "Entrez Gene: SUCLG1 succinate-CoA ligase, GDP-forming, alpha subunit".
  7. Fraser ME, James MN, Bridger WA, Wolodko WT (Jun 2000). "Phosphorylated and dephosphorylated structures of pig heart, GTP-specific succinyl-CoA synthetase". Journal of Molecular Biology. 299 (5): 1325–39. doi:10.1006/jmbi.2000.3807. PMID 10873456.
  8. Ostergaard E (Apr 2008). "Disorders caused by deficiency of succinate-CoA ligase". Journal of Inherited Metabolic Disease. 31 (2): 226–9. doi:10.1007/s10545-008-0828-7. PMID 18392745. S2CID 12722653.
  9. Valayannopoulos V, Haudry C, Serre V, Barth M, Boddaert N, Arnoux JB, Cormier-Daire V, Rio M, Rabier D, Vassault A, Munnich A, Bonnefont JP, de Lonlay P, Rötig A, Lebre AS (Jun 2010). "New SUCLG1 patients expanding the phenotypic spectrum of this rare cause of mild methylmalonic aciduria". Mitochondrion. 10 (4): 335–41. doi:10.1016/j.mito.2010.02.006. PMID 20197121.
  10. Rouzier C, Le Guédard-Méreuze S, Fragaki K, Serre V, Miro J, Tuffery-Giraud S, Chaussenot A, Bannwarth S, Caruba C, Ostergaard E, Pellissier JF, Richelme C, Espil C, Chabrol B, Paquis-Flucklinger V (Oct 2010). "The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein" (PDF). Journal of Medical Genetics. 47 (10): 670–6. doi:10.1136/jmg.2009.073445. PMID 20693550. S2CID 35860287.

Further reading

  • Overview of all the structural information available in the PDB for UniProt: P53597 (Human Succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial) at the PDBe-KB.
  • Overview of all the structural information available in the PDB for UniProt: O19069 (Pig Succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial) at the PDBe-KB.


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