Loading Pathway...
Error: Pathway image not found.
Hide
Pathway Description
Tyrosine Metabolism
Arabidopsis thaliana
Metabolic Pathway
The biosynthesis of tyrosine begins with chorismate interacting with chorismate mutase resulting in a prephenate. Prephenate reacts with a hydrogen ion through a prephenate dehydratase resulting in the release of NADPH, carbon dioxide and 4-hydroxyphenylpyruvate. The latter compound can be turn into tyrosine through two different reversible reactions a) 4-hydroxyphenylpyruvate reacts with alanine through a aromatic amino acid aminotransferase 2 resulting in the release of pyruvate and phenylalanine. b) 4-hydroxyphenylpyruvatereacts with glutamic acid through a amino aci aminotransferase 1 resulting in the release of oxoglutaric acid and phenylalanine. The degradation of phenylalanine begins with the two previous reactions turning phenylalanine back into 4-hydroxyphenylpyruvate. The latter compound reacts with a phenylpyruvate carboxy lyase resulting in the release of phenylacetaldehyde. This latter compound reacts with a alcohol dehydrogenase resulting in the release of tyrosol.
References
Tyrosine Metabolism References
Highlighted elements will appear in red.
Highlight Compounds
Highlight Proteins
Enter relative concentration values (without units). Elements will be highlighted in a color gradient where red = lowest concentration and green = highest concentration. For the best results, view the pathway in Black and White.
Visualize Compound Data
Visualize Protein Data
Downloads
Settings