Carbamoyl phosphate synthetase I deficiency presents with _____ NH4+ and hyper-ammonemia
Vitamins required for the conversion of serine to glycine are _____ and folic acid
_____ is eventually broken down into acetyl-CoA via the enzyme branched-chain α-ketoacid dehydrogenase
Hartnup disease is treated with a high-_____ diet and nicotinic acid (niacin)
In the liver, alanine transfers its NH3 group to _____, forming glutamate and pyruvate
_____ may be converted to melanin via the enzyme tyrosinase
Arginine may be broken down into _____ and urea via the enzyme arginase
_____ may be converted to epinephrine via the enzyme phenylethanolamine-N-methyltransferase (with SAM as a cofactor) and stimulated by cortisol
_____ may be converted to dopamine via the enzyme DOPA decarboxylase (with vitamin B6 as a cofactor)
The urea cycle begins with _____, CO2, and 2 ATP
Protein Digestion and Absorption
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Transamination and Deamination
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Urea Cycle
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Disorders of Urea Cycle
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Metabolism of Individual Amino Acids
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Inborn Errors of Amino Acid Metabolism
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Phenylketonuria and Alkaptonuria
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Homocystinuria and Methionine Metabolism
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Synthesis of Biologically Important Compounds from Amino Acids
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Nitrogen Balance
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Ammonia Metabolism and Toxicity
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One-Carbon Transfer Reactions
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