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SUCLG1 encodes the alpha subunit of the heterodimeric enzyme succinate coenzyme A ligase. Additionally we are shipping Succinate-CoA Ligase, alpha Subunit Antibodies (24) and many more products for this protein.
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These abnormal phenotypes are rescued upon ectopic expression of wild-type SUCLG1 in the patient's fibroblasts, thus functionally confirming the pathogenic nature of the SUCLG1 VUS identified in this patient and expanding the phenotypic spectrum for SUCLG1 deficiency
Long survival, to age 20 years or older, was reported in 12% of SUCLA2 (show SUCLA2 Proteins) and in 10% of SUCLG1 patients.
First Chinese report of succinyl-CoA ligase (show SUCLG2 Proteins) deficiency caused by novel SUCLG1 mutations; five novel pathogenic mutations in SUCLG1 were identified
3 novel mutations have been identified in patients with the mitochondrial DNA depletion syndrome (c.1048G>A and c.1049G>T in SUCLA2 (show SUCLA2 Proteins) and c.531+4A>T in SUCLG1).
Our results suggest that SUCLG1 mutations that lead to complete absence of SUCLG1 protein are responsible for a very severe disorder with antenatal manifestations, whereas a SUCLA2 (show SUCLA2 Proteins)-like phenotype is found in patients with residual SUCLG1 protein.
This report enlarges the phenotypic spectrum of SUCLG1 mutations and confirms that a characteristic metabolic profile (presence of MMA (show MMD Proteins) and C4-DC carnitine in urines) and basal ganglia MRI (show C7ORF49 Proteins) lesions are the hallmarks of SCS (show TWIST1 Proteins) defects.
A novel mutation in the SUCLG1 gene was found in two newborns having lethal lactic acidosis, multi-organ failure and congenital malformations including interrupted aortic arch.
Pig GTP (show AK3 Proteins)-specific succinyl-CoA (show OXCT1 Proteins) synthetase was crystallized in the presence of succinate, magnesium ions and CoA, and the structure of the complex was determined by X-ray crystallography to 2.2 A resolution. Succinate binds in the carboxy-terminal domain of the beta-subunit (show POLG Proteins).
Structure of GTP-specific succinyl-CoA synthetase subunits in complex with CoA has been resolved.
succinyl-CoA (show OXCT1 Proteins) synthetase is able to protect GTP (show AK3 Proteins) from hydrolysis when the active-site histidine residue is not in position to be phosphorylated
ADP and GDP succinyl-CoA (show OXCT1 Proteins) synthetases have different expression patterns and specificity
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.
succinate-CoA ligase, GDP-forming, alpha subunit
, succinate-CoA ligase, GDP-forming alpha subunit
, succinyl-CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial
, succinyl-CoA ligase [GDP-forming] subunit alpha, mitochondrial
, succinyl-CoA synthetase subunit alpha
, succinyl-CoA synthetase alpha subunit