Phenylketones include _____, phenyllactate, and phenylpyruvate
In addition to enzyme deficiencies, homocystinuria may be caused by decreased affinity of _____ for pyridoxal phosphate (B6, active form)
What are the 9 (10*) essential amino acids? _____ValineThreonineTryptophan IsoleucineMethionineHistidine Arginine* during periods of growthLysineLeucine
Creatine is synthesized from _____, arginine, and methionine (GAM)
What enzyme deficiencies may cause homocystinuria? _____ and methionine synthase deficiencies
In the muscle, glutamate transfers its NH3 group to _____, forming alanine and -ketoglutarate
_____ 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
Ornithine transcarbamylase (OTC) deficiency presents with _____ NH4+ and hyper-ammonemia
Pyruvate is converted to _____ via the enzyme alanine aminotransferase (ALT) (Cahill cycle)
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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