Title : CYP17 mutation E305G causes isolated 17,20-lyase deficiency by selectively altering substrate binding.

Pub. Date : 2003 Dec 5

PMID : 14504283






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Cytochrome p450c17 (CYP17) converts the C21 steroids pregnenolone and progesterone to the C19 androgen precursors dehydroepiandrosterone (DHEA) and androstenedione, respectively, via sequential 17alpha-hydroxylase and 17,20-lyase reactions. Androstenedione cytochrome P450 family 17 subfamily A member 1 Homo sapiens
2 Cytochrome p450c17 (CYP17) converts the C21 steroids pregnenolone and progesterone to the C19 androgen precursors dehydroepiandrosterone (DHEA) and androstenedione, respectively, via sequential 17alpha-hydroxylase and 17,20-lyase reactions. Androstenedione cytochrome P450 family 17 subfamily A member 1 Homo sapiens
3 In contrast, mutation E305G exhibits 11-fold greater catalytic efficiency (kcat/Km) for the cleavage of 17alpha-hydroxyprogesterone to androstenedione compared with wild-type CYP17. Androstenedione cytochrome P450 family 17 subfamily A member 1 Homo sapiens