Amino Acid Metabolism A glucogenic amino acid is one which is degraded to either acetyl CoA or acetoacetyl CoA keto-sugars pyruvate or citric acid cycle intermediates None of these either acetyl CoA or acetoacetyl CoA keto-sugars pyruvate or citric acid cycle intermediates None of these ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is glutamate = α-ketoglutarate + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + Oxaloacetate glutamate = α-ketoglutarate + NH3 aspartate + α-ketoglutarate = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + Oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism The most toxic compounds is lysine phenylalanine tyrosine phenylpyruvate lysine phenylalanine tyrosine phenylpyruvate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate phenylalanine to isoleucine tyrosine to phenylalanine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate phenylalanine to isoleucine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenol into ketones phenylalanine to tyrosine phenylalanine to lysine phenylalanine to isoleucine phenol into ketones phenylalanine to tyrosine phenylalanine to lysine phenylalanine to isoleucine ANSWER DOWNLOAD EXAMIANS APP
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