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phenylalanine hydroxylase中文是什么意思

  • 苯丙氨酸羟化酶

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  • 例句与用法
  • Phenylketonuria ( pku ) is an inherited metabolic disease that results in mental retardation and other neurological problems when treatment is not started within the first few weeks of life . the disease arises from the deficiency of a single enzyme , phenylalanine hydroxylase , which converts the essential amino acid , phenylalanine , to another amino acid , tyrosine . failure of the conversion to take place results in a buildup of phenylalanine in the body that then damages the central nervous system
    苯丙酮尿症( pku )是一种智力发育不全的先天性疾病,患者由于肝赃内苯丙氨酸羟化酶缺乏,苯丙氨酸不能正常代谢为酪氨酸,从而导致苯丙氨酸在肌体组织内积累,引起脑损伤和累进性精神障碍,临床表现为智力低下,头发颜色转黄,尿有异臭味,重者似鼠臭。
  • 百科解释
Phenylalanine hydroxylase (PheOH, alternatively PheH or PAH) () is an enzyme that catalyzes the hydroxylation of the aromatic side-chain of phenylalanine to generate tyrosine. PheOH is one of three members of the pterin-dependent amino acid hydroxylases, a class of monooxygenase that uses tetrahydrobiopterin (BH4, a pteridine cofactor) and a non-heme iron for catalysis.
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