| During normal catabolism, protease enzymes break down carboxylase enzymes and reclaim the associated amino acids and biocytin for recycling. |
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| Phosphoenolpyruvate carboxylase catalyses the carboxylation of PEP to form oxaloacetate. |
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| Within skeletal muscle and heart activation of AMPK leads to the phosphorylation and inhibition of acetyl-CoA carboxylase. |
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| Depending on ratios of CO 2 to O 2 at binding sites of ribulose bisphosphate carboxylase, ribulose bisphosphate is either carboxylated or oxygenated. |
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| The carboxylation reaction is catalyzed by acetyl CoA carboxylase, an enzyme whose prosthetic group is the vitamin biotin. |
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| Propionic acidemia is caused by a deficiency of the enzyme propionyl-CoA carboxylase, which results in an accumulation of propionic acid. |
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| Comparison of rbcL genes for the large subunit of ribulose-bisphosphate carboxylase from closely related C3 and C4 plant species. |
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| During the dark reactions, carbon dioxide is bound to ribulose bisphosphate, a 5-carbon sugar with two attached phosphate groups, by the enzyme ribulose bisphosphate carboxylase. |
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| Ribulose bisphosphate carboxylase and proteolytic activity in wheat leaves from anthesis through senescence. |
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| Large doses of supplemental vitamin A and vitamin E have been found to antagonize with vitamin K. Vitamin A prevents absorptions, whereas one form of vitamin E inhibits vitamin K carboxylase enzymes. |
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| Role of the propeptide and gamma-glutamic acid domain of factor IX for in vitro carboxylation by the vitamin K-dependent carboxylase. |
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| It is an important cofactor to several enzymes, including acetyl CoA carboxylase and other carboxylases. |
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| Phosphorylation of both acetyl CoA carboxylase and AMP-activated protein kinase was increased, thus explaining the increase in fatty acid oxidation. |
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