Chapter 14: Problem 5
What is the primary mechanism by which metabolic flux is regulated in the pentose phosphate pathway?
Chapter 14: Problem 5
What is the primary mechanism by which metabolic flux is regulated in the pentose phosphate pathway?
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Get started for freeDefects in essentially every enzyme required for human glycogen metabolism have been identified and are collectively called glycogen storage diseases. Explain why Andersen disease, caused by a defect in glycogen branching enzyme, is fatal, whereas Cori disease, caused by a defect in glycogen debranching enzyme, only manifests in mild hypoglycemia.
Glycogen contains an \(\alpha-1,6\) -glycosidic bond about once every 10 glucose residues, thereby creating a branch point and a corresponding non reducing end for the removal and addition of glucose molecules. If a glycogen particle contains a total of 50,000 glucose residues, how many nonreducing ends are most likely to be found: \(\sim 25,000\) ends, \(\sim 2,500\) ends, or \(\sim 250\) ends? Explain your answer.
The product of the glycogen phosphorylase reaction is glucose-1-P. Is there a difference in glycolytic ATP yield comparing the yield from the metabolism of glucose-1-P derived from glycogen degradation with the yield from the metabolism of dietary glucose? Explain.
What are the chemical and functional differences between NADH and NADPH?
Explain why the Cori cycle has a net cost of \(4 \mathrm{ATP}\) equivalents per glucose to the organism.
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