Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a keto-gluco amino acid ketogenic and glucogenic amino acid ketogenic amino acid glucogenic amino acid keto-gluco amino acid ketogenic and glucogenic amino acid ketogenic amino acid glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transaminase enzymes are present in liver intestine none of these pancreas liver intestine none of these pancreas ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert phenylalanine to phenylpyruvate tyrosine to phenylalanine phenylalanine to isoleucine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate tyrosine to phenylalanine phenylalanine to isoleucine phenylpyruvate to phenylalanine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is aspartate + hexanoic acid = glutamate + Oxaloacetate 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 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to lysine fumarate phenylpuruvate tyrosine lysine fumarate phenylpuruvate tyrosine ANSWER DOWNLOAD EXAMIANS APP
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