Amino Acid Metabolism A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of tyrosine phenylalanine phenylpyruvate isoleucine tyrosine phenylalanine phenylpyruvate isoleucine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is aspartate + hexanoic acid = glutamate + oxaloacetate aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is 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 aspartate + hexanoic acid = glutamate + Oxaloacetate glutamate = α-ketoglutarate + NH3 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to lysine tyrosine phenylpuruvate fumarate lysine tyrosine phenylpuruvate fumarate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert phenylalanine to isoleucine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate tyrosine to phenylalanine phenylalanine to isoleucine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate tyrosine to phenylalanine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transaminase enzymes are present in liver pancreas intestine none of these liver pancreas intestine none of these ANSWER DOWNLOAD EXAMIANS APP
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