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Results 1 - 9 of 9 for "Succinyl-CoA"
  1. Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is an inherited disorder that impairs the body's ability ... gene provides instructions for making an enzyme called succinyl-CoA:3-ketoacid CoA transferase (SCOT). The SCOT enzyme ...
  2. ... gene provides instruction for making an enzyme called succinyl-CoA:3-ketoacid CoA transferase, often abbreviated as SCOT. ... transferase 1 OXCT SCOT SCOT1_HUMAN somatic-type succinyl CoA:3-oxoacid CoA-transferase somatic-type succinyl-CoA: ...
  3. ... About This Health Condition A-BETA ATP-specific succinyl-CoA synthetase, beta subunit renal carcinoma antigen NY-REN- ... S, Saada A. Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial ...
  4. ... beta cell: evidence for its complexation with mitochondrial succinyl-CoA synthetase. Arch Biochem Biophys. 2002 Feb 15;398( ... S, Frohlich D, Milavetz BI. Expression of two succinyl-CoA synthetases with different nucleotide specificities in mammalian tissues. ...
  5. ... pathway that converts the molecule propionyl-CoA to succinyl-CoA. This pathway is important in the breakdown of ... pathway for the conversion of propionyl-CoA to succinyl-CoA that does not involve methylmalonyl CoA epimerase, so ...
  6. ... mutase converts methylmalonyl CoA to a compound called succinyl-CoA. Other enzymes break down succinyl-CoA into molecules that are later used for energy. ...
  7. Mitochondrial Diseases (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
  8. ... S, Saada A. Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial ...
  9. ... molecule called α-ketoglutarate to another molecule called succinyl-CoA. Further steps in this process generate ATP for ...