| 31. | Pyruvate carboxylase deficiency is a rare condition, with an estimated incidence of 1 in 250, 000 births worldwide.
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| 32. | It inhibits carboxylase, the enzyme that activates clotting factors and also shuts them down before they get out of hand.
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| 33. | However, it is also possible for pyruvate to be carboxylated by pyruvate carboxylase to form " oxaloacetate ".
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| 34. | Organic prosthetic groups can be covalently bound ( e . g ., biotin in enzymes such as pyruvate carboxylase ).
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| 35. | These genes are responsible for the formation of the enzyme propionyl-CoA carboxylase ( ), referred to as PCC.
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| 36. | It interacts with both the large and small subunits of the ribulose-1, 5-bisphosphate carboxylase / oxygenase.
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| 37. | "' Propionyl-CoA carboxylase "'catalyses the carboxylation reaction of propionyl CoA in the mitochondrial matrix.
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| 38. | As of late 2007, 3 D-alanine : D-alanine ligase, biotin carboxylase, and glutathione synthetase.
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| 39. | By controlling the activity of the pyruvate dehydrogenase and the acetyl-CoA carboxylase enzymes, insulin promotes unsaturated fatty acid synthesis.
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| 40. | Another tether is biotin-lysine residue complex associated with pyruvate carboxylase, an enzyme which plays an important role in gluconeogenesis.
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