- into dopamine. 17α-
Hydroxylase Cholesterol 7 alpha-
hydroxylase Dopamine β-
hydroxylase Phenylalanine hydroxylase Tyrosine hydroxylase One
example of non-biological...
-
Tyrosine hydroxylase or
tyrosine 3-monooxygenase is the
enzyme responsible for
catalyzing the
conversion of the
amino acid L-tyrosine to L-3,4-dihydroxyphenylalanine...
-
phenylalanine hydroxylase, and
tryptophan hydroxylase together constitute the
family of biopterin-dependent
aromatic amino acid
hydroxylases. TPH catalyzes...
-
Dopamine beta-
hydroxylase (DBH), also
known as
dopamine beta-monooxygenase, is an
enzyme (EC 1.14.17.1) that in
humans is
encoded by the DBH gene. Dopamine...
- (steroid 17α-monooxygenase, 17α-
hydroxylase, 17-alpha-
hydroxylase, 17,20-lyase, 17,20-desmolase) is an
enzyme of the
hydroxylase type that in
humans is encoded...
-
resulting in
corresponding activity changes in the ****ociated P450c21 (21-
hydroxylase)
enzyme which ultimately leads to
excessive androgen production. Other...
- of cases)involves the gene for 21-
hydroxylase,
which is
found on 6p21.3 as part of the HLA complex; 21-
hydroxylase deficiency results from a
unique mutation...
-
Phenylalanine hydroxylase (PAH) (EC 1.14.16.1) is an
enzyme that
catalyzes the
hydroxylation of the
aromatic side-chain of
phenylalanine to
generate tyrosine...
-
Congenital adrenal hyperplasia due to 21-
hydroxylase deficiency (CAH) is a
genetic disorder characterized by
impaired production of
cortisol in the adrenal...
- (+)-Camphor 6-exo-
hydroxylase (EC 1.14.13.161, (+)-camphor 6-
hydroxylase) is an
enzyme with
systematic name (+)-camphor,NADPH:oxygen
oxidoreductase (6-exo-hydroxylating)...