_____ is converted to dihydroxyphenylalanine (DOPA) via the enzyme tyrosine hydroxylase (with tetrahydrobiopterin as a cofactor)
In the muscle, glutamate transfers its NH3 group to _____, forming alanine and alpha-ketoglutarate
At the junction of the follicular cells and the follicular lumen, _____ residues of thyroglobulin react with I2 to form monoiodotyrosine (MIT) and diiodotyrosine (DIT)
Phenylketones include _____, phenyllactate, and phenylpyruvate
What enzyme deficiencies may cause homocystinuria? _____ and methionine synthase deficiencies
What are the 9 (10*) essential amino acids? _____, Valine, Threonine, Tryptophan, Isoleucine, Methionine, Histidine, Arginine*, Lysine, Leucine *Essential during periods of growth.
_____ is also called the 22nd amino acid and is encoded by UAG
In the kidney, glutamine may be broken down into _____ and glutamate via the enzyme glutaminase
Pyruvate is converted to _____ via the enzyme alanine aminotransferase (ALT) (Cahill cycle)
_____ urine is characteristically seen in multiple carboxylase deficiency.
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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