BIO 360 Chapter Notes - Chapter 18: Phenylalanine Hydroxylase, Normal Route, Alpha-Ketoglutaric Acid
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Chapter /81-11 1 problems : aspartate, glutamate a- ketoglutarate -1 aspartate oxaloacetate a- ketoglutarate -1 glutamate a- ketoglutarate. C - coo: alanine a- ketoglutarate -1 alanine pyruvate if. % - coo: phenylalanine a- ketoglutarate -1 phenylalanine phenylpyruvate. F-chi%- ooo: phenylalanine hydroxylase ; alow - phenylalanine diet, normal route of phenylalanine metabolism lyla hydroxylation -10 tyrosine) is blocked . This causes phenylalanine -10 accumulate : phenylalanine transformed tophenylpy. ru/atebytransaminat1on+phenyi1actate by reduction . Transom/nation reaction has an equilibrium constant 01-1. 0 + phenylpyruvate. Is formed insignificant amounts when phenylalanine accumulates: deficiency in production of tyrosine (precursor of melanin . "snh , i: citralline r - nh - c - " " coo : ornithine no labeled n in ornithine, arginine . R - mh - -15mhz: aspartate 15mhz. Transfer of nitrogen from nh> to carbon skeletons can be catalyzed by 1 glutamine synthetase and 2 glutamate dehydrogenase .