| 11. | Methylmalonyl-CoA mutase links the propionyl-CoA degradation byproduct of these macromolecules to the tricarboxylic acid cycle.
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| 12. | The enzymes that use as a built-in cofactor are methylmalonyl-CoA mutase ( PDB 1Q8J ).
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| 13. | The final product of methylmalonyl-CoA mutase activity is succinyl-CoA which is a tricarboxylic acid cycle substrate.
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| 14. | "' Bisphosphoglycerate mutase "'( BPGM ) is an enzyme unique to erythrocytes and placental cells.
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| 15. | "' Phosphoglycerate mutase "'( PGM ) is any enzyme that catalyzes step 8 of glycolysis.
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| 16. | Finally, mitochondrial methylmalonyl-CoA mutase with cofactor adenosylcobalamin produces succinyl-CoA which enters the citric acid cycle.
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| 17. | It is thought that this is due to the widespread presence of methylmalonyl-CoA mutase throughout the central nervous system.
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| 18. | This process is mediated by a phenylalanine ( PheA ) or tyrosine ( TyrA ) specific chorismate mutase-prephenate dehydrogenase.
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| 19. | Protein redesign has been used for protein simplification, creation of new quaternary structures, and topological redesign of a chorismate mutase.
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| 20. | Certain salts, such as KCl, are known to be competitive inhibitors in respect to 2-phosphoglycerate and mutase activity.
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