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Functional analysis of human cytochrome P450 21A2 variants involved in congenital adrenal hyperplasia
Journal of Biological ChemistryVol. 292Issue 26p10767–10778Published online: May 24, 2017- Chunxue Wang
- Pradeep S. Pallan
- Wei Zhang
- Li Lei
- Francis K. Yoshimoto
- Michael R. Waterman
- and others
Cited in Scopus: 26Cytochrome P450 (P450, CYP) 21A2 is the major steroid 21-hydroxylase, converting progesterone to 11-deoxycorticosterone and 17α-hydroxyprogesterone (17α-OH-progesterone) to 11-deoxycortisol. More than 100 CYP21A2 variants give rise to congenital adrenal hyperplasia (CAH). We previously reported a structure of WT human P450 21A2 with bound progesterone and now present a structure bound to the other substrate (17α-OH-progesterone). We found that the 17α-OH-progesterone- and progesterone-bound complex structures are highly similar, with only some minor differences in surface loop regions.