H H H HC00 C-CH2 H,0 C-Coo- -CH-C-CO0- -CH-C-CO0 NH NH NH NH2 H H Tryptophan N-Formylkynurenine Купurenine Og + NADPH H,0 + NADP+ H H20 H -CH,-C-CO0- H;C-C-Co0- NH NH2 NH2 NH OH он Alanine 3-Hydroxyanthranilate S-Hydroxykynurenine 5 reactions 7 reactions CH3-C-CH2-C00 +- O. Co CO2 a-Ketoadipate Acetoacetate
H H H HC00 C-CH2 H,0 C-Coo- -CH-C-CO0- -CH-C-CO0 NH NH NH NH2 H H Tryptophan N-Formylkynurenine Купurenine Og + NADPH H,0 + NADP+ H H20 H -CH,-C-CO0- H;C-C-Co0- NH NH2 NH2 NH OH он Alanine 3-Hydroxyanthranilate S-Hydroxykynurenine 5 reactions 7 reactions CH3-C-CH2-C00 +- O. Co CO2 a-Ketoadipate Acetoacetate
Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
Section: Chapter Questions
Problem 1P
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Draw the amino acid–Schiff base that forms in the breakdown of 3-hydroxykynurenine to yield 3-hydroxyanthranilate in the tryptophan degradation pathway (Fig.) and indicate which bond is to be cleaved.
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