8FDA

Human Cytochrome P450 17A1 in complex with steroidal isonitrile inhibitor

8FDA の概要

• エントリーDOI: 10.2210/pdb8fda/pdb
• 分子名称: Steroid 17-alpha-hydroxylase/17,20 lyase, PROTOPORPHYRIN IX CONTAINING FE, [(1~{R})-1-[(3~{S},5~{S},8~{R},9~{S},10~{S},13~{S},17~{R})-3-methanoyloxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,13,14,15,16,17-hexadecahydrocyclopenta[a]phenanthren-17-yl]ethyl]-methylidyne-azanium, ... (4 entities in total)
• 機能のキーワード: cytochrome p450 17a1, cytochrome p450 c17, 17-alpha hydroxylase, 17, 20 lyase, isonitrile, steroid, oxidoreductase
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 227571.69

構造登録者

Richard, A.M.,Scott, E.E. (登録日: 2022-12-02, 公開日: 2023-08-23, 最終更新日: 2023-09-13)

主引用文献

Richard, A.M.,Wong, N.R.,Harris, K.,Sundar, R.,Scott, E.E.,Pochapsky, T.C.
Selective steroidogenic cytochrome P450 haem iron ligation by steroid-derived isonitriles.
Commun Chem, 6:183-183, 2023

PubMed Abstract: Alkyl isonitriles, R-NC, have previously been shown to ligate the heme (haem) iron of cytochromes P450 in both accessible oxidation states (ferrous, Fe, and ferric, Fe). Herein, the preparation of four steroid-derived isonitriles and their interactions with several P450s, including the steroidogenic CYP17A1 and CYP106A2, as well as the more promiscuous drug metabolizers CYP3A4 and CYP2D6, is described. It was found that successful ligation of the heme iron by the isonitrile functionality for a given P450 depends on both the position and stereochemistry of the isonitrile on the steroid skeleton. Spectral studies indicate that isonitrile ligation of the ferric heme is stable upon reduction to the ferrous form, with reoxidation resulting in the original complex. A crystallographic structure of CYP17A1 with an isonitrile derived from pregnanalone further confirmed the interaction and identified the absolute stereochemistry of the bound species.

PubMed: 37660137
DOI: 10.1038/s42004-023-00994-3

実験手法

X-RAY DIFFRACTION (2.2 Å)