Exam 30: Amino Acid Degradation and the Urea Cycle
Exam 1: Biochemistry and the Unity of Life44 Questions
Exam 2: Water, Weak Bonds, and the Generation of Order Out of Chaos43 Questions
Exam 3: Amino Acids49 Questions
Exam 4: Protein Three-Dimensional Structure50 Questions
Exam 5: Techniques in Protein Biochemistry45 Questions
Exam 6: Basic Concepts of Enzyme Action50 Questions
Exam 7: Kinetics and Regulation47 Questions
Exam 8: Mechanisms and Inhibitors48 Questions
Exam 9: Hemoglobin: an Allosteric Protein47 Questions
Exam 10: Carbohydrates48 Questions
Exam 11: Lipids47 Questions
Exam 12: Membrane Structure and Function50 Questions
Exam 13: Signal Transduction Pathways49 Questions
Exam 14: Digestion: Turning a Meal Into Cellular Biochemicals50 Questions
Exam 15: Metabolism: Basic Concepts and Design47 Questions
Exam 16: Glycolysis50 Questions
Exam 17: Gluconeogenesis50 Questions
Exam 18: Preparation for the Cycle45 Questions
Exam 19: Harvesting Electrons From the Cycle48 Questions
Exam 20: The Electron Transport Chain43 Questions
Exam 21: The Proton-Motive Force45 Questions
Exam 22: The Light Reactions46 Questions
Exam 23: The Calvin Cycle48 Questions
Exam 24: Glycogen Degradation44 Questions
Exam 25: Glycogen Synthesis44 Questions
Exam 26: The Pentose Phosphate Pathway43 Questions
Exam 27: Fatty Acid Degredation46 Questions
Exam 28: Fatty Acid Synthesis44 Questions
Exam 29: Lipid Synthesis50 Questions
Exam 30: Amino Acid Degradation and the Urea Cycle47 Questions
Exam 31: Amino Acids Synthesis47 Questions
Exam 32: Nucleotide Metabolism48 Questions
Exam 33: The Structure of Informational Macromolecules: Dna and Rna45 Questions
Exam 34: DNA Replication45 Questions
Exam 35: DNA Repair and Recombination45 Questions
Exam 36: RNA Synthesis and Regulation in Prokaryotes45 Questions
Exam 37: Gene Expression in Eukaryotes45 Questions
Exam 38: RNA Processing in Eukaryotes44 Questions
Exam 39: The Genetic Code44 Questions
Exam 40: The Mechanism of Protein Synthesis44 Questions
Exam 41: Recombinant Dna Techniques45 Questions
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In the urea cycle, the carbon skeleton of aspartate is preserved as:
(Multiple Choice)
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In addition to increased fatty acid accumulation in the liver, excess consumption of ethanol can also induce two further stages of liver damage. What are they?
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Ketogenic amino acids are degraded to which of the following metabolites?
(Multiple Choice)
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___________________ is the prosthetic group used in deaminations by dehydratases.
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Why do you think that weight lifters take large amounts of branched-chain amino acids?
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The urea cycle is linked to gluconeogenesis via formation of ___________________, a precursor of glucose synthesis.
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Use the following to answer questions
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-_______________ is caused by defects in the urea cycle, which lead to an elevated level of ammonia in blood.
(Multiple Choice)
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-The cofactor required by phenylalanine hydroxylase is _______________.
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-The product _______________ results when aspartate is transaminated with ɑ-ketoglutarate.
(Multiple Choice)
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Which amino acids supply carbons for eventual entry into metabolism as succinyl CoA?
(Multiple Choice)
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Which amino acid(s) is/are metabolites in the urea cycle, but is/are not used as (a) building block(s) of proteins?
(Multiple Choice)
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In the degradation of amino acids, the amino nitrogens can eventually become the amino group of ___________________.
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-The ______________ enzymes transfer an ɑ-amino group from amino acids to ɑ-ketoglutarate.
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The hydrolysis of arginine by arginase produces ornithine and ___________________.
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In the urea cycle, free NH4+ is coupled with carboxyphosphate to form:
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In the first step of the urea cycle, CO2 and NH4+ are converted into ___________________.
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In adults, the urea cycle produces sufficient quantities of ___________________ so that it is not considered an essential amino acid.
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Nitrogen is transported from muscle to liver in the form of ___________________or _______________.
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