phenylalanine hydroxylase
[ˌfenəlˈæləni:n haiˈdrɔksileis]

释义

[医]苯丙氨酸羟化酶；

英英释义

Phenylalanine hydroxylase

• 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.

以上来源于:Wikipedia

权威例句

Hyperphenylalaninemia: Phenylalanine Hydroxylase Deficiency
Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency ☆ ☆☆ ★
Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency, state of the art
Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Dutch neonates.
Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria.
Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency †
Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southe...
Crystal structure of the catalytic domain of human phenylalanine hydroxylase reveals the structural basis for phenylketonuria
Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.