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PHENYLALANINE METABOLISM
The genetic disorder phenylketonuria (PKU) is the inability to metabolize phenylalanine because of a...
The shikimate pathway was discovered as the biosynthetic route to the aromatic amino acids phenylala...
phenylalanine
Decarboxylation is the reaction by which CO2 is removed from the COOH group of an amino acid as a re...
This PPT contains topic related to Catabolism of Phenylalanine and Tyrosine, Disorders Of Tyrosine M...
Commonly known as its anionic form shikimate, is a cyclohexene, a cyclitol and a cyclohexanecarboxyl...
Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the a...
Phenylketonuria (PKU) : is a genetic disorder that is characterized by an inability of the body t...
Catecholamine, sympatho-mimetic monoamine, derived -phenylalanine and tyrosine. C9H13NO3 MOL WT:183....
Shikimic acid pathway is "metabolic pathway. " ,means metabolites are organic compounds s...
Aromatic amino acids (AAA)- are amino acids that include an aromatic ring. Examples include: Among...
Carboxypeptidase Y (CPY) catalyzes the following reaction: Peptidyl-L-amino acid + H2O ------> Pe...
The chosen amino acids were first dissolved in various aquatic solutions and then measured in a benc...
Alkaloids are basic (alkali-like), nitrogen-containing organic constituents found in some plants.Alk...
Porphyrias are a group of inherited or acquired metabolic disorders resulting from a defect in the h...
The slides gives you a complete information on the inborn error metabolic disease Phenylketonuria (P...
PhenylKetonuria ( PKU )
Phenylketonuria Metabolism subject Bio-chemistry
phenylketonuria
UNIT III_Amino acid Metabolism.pptx
Pleiotropism
DISORDERS DUE TO AMINO ACIDS
Inborn Errors of Metabolism 1) Phenylketonuria 2) Alkaptonuria
