People with a genetic deficiency of _____ present with hypermethioninemia
Urea has two nitrogen molecules, one from _____ and one from aspartate
The treatment for propionic acidemia is a low _____ diet that does not include valine, methionine, isoleucine, or threonine
Glutathione is a tripeptide composed of _____, CystEine and Glycine
In the muscle, amino acids transfer their NH3 group to _____, forming glutamate and -ketoacids
An odour of _____ is diagnostic of type 1 tyrosinemia and hypermethioninemia
_____ may be converted to methionine via the enzyme methionine synthase (with methyl-THF and vitamin B12 as cofactors)
After release from iodinated thyroglobulin, MIT and DIT are _____ by the enzyme thyroid deiodinase, reproducing I- and tyrosine
_____ is a dipeptide that is a marker of meat consumption
_____ is a dipeptide that can be found in excitable tissues like brain and muscle.
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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