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PHENYLKETONURIA & OTHER DISEASES CAUSED BY DEFECTS IN BIOPTERIN-DEPENDENT ENZYMES

PHENYLKETONURIA & OTHER DISEASES CAUSED BY DEFECTS IN BIOPTERIN-DEPENDENT ENZYMES
苯丙酮尿症
批准号：
3759384
负责人：
S KAUFMAN
金额：
$0.0万
依托单位：
NATIONAL INSTITUTE OF MENTAL HEALTH
依托单位国家：
美国
项目类别：
财政年份：
--
资助国家：
美国
项目状态：
未结题
起止时间：
至
来源：
https://reporter.nih.gov/project-details/3759384
关键词：
aminoacid metabolism carbon oxygen lyase cofactor enzyme activity enzyme deficiency enzyme mechanism genetic regulation genetic transcription hydroxylation hyperphenylalaninemia phenylalanine phenylalanine 4 monooxygenase phenylketonurias pteridine analog

项目摘要

项目成果

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相关文献

中文摘要
翻译
一种轻度高苯丙氨酸血症的遗传特征是 由于4a-甲醇胺脱水酶缺乏，4a-甲醇胺脱水酶是一种必需的酶， 4 α-羟基四氢生物蝶呤快速转化为喹蝶呤 二氢生物蝶呤。 这些是多组分的中间体 苯丙氨酸羟基化系统。
英文摘要
A form of mild hyperphenylalaninemia has been genetically characterized as a deficiency in 4a-carbinolamine dehydratase, an enzyme necessary for the rapid conversion of 4a-hydroxytetrahydrobiopterin to quinonoid dihydrobiopterin. These are intermediates in the multicomponent phenylalanine hydroxylation system.
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SYNTHESIS AND RELEASE OF BIOGENIC AMINES
BIOSYNTHESIS OF CATECHOLAMINES
THE CONVERSION OF PHENYLALANINE TO TYROSINE
PHENYLKETONURIA & OTHER DISEASES CAUSED BY DEFECTS IN BIOPTERIN-DEPENDENT ENZYMES