Chapter 14: Problem 9
What is the metabolic logic of reciprocal regulation of the glycolytic and gluconeogenic pathways by citrate?
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Chapter 14: Problem 9
What is the metabolic logic of reciprocal regulation of the glycolytic and gluconeogenic pathways by citrate?
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Defects 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.
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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.
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