Reaction Mechanism of Histone Demethylation in αKG-dependent Non-Heme Iron Enzymes

被引:15
作者
Singh, Warispreet [1 ,2 ]
Quinn, Derek [2 ]
Moody, Thomas S. [2 ,3 ]
Huang, Meilan [1 ]
机构
[1] Queens Univ Belfast, Sch Chem & Chem Engn, David Keir Bldg,Stranmillis Rd, Belfast BT9 5AG, Antrim, North Ireland
[2] Almac Sci, Dept Biocatalysis & Isotope Chem, Almac House,20 Seagoe Ind Estate, Craigavon BT63 5QD, North Ireland
[3] Arran Chem Co Ltd, Unit 1 Monksland Ind Estate, Athlone, Co Roscommon, Ireland
关键词
QUANTUM MECHANICS/MOLECULAR MECHANICS; ISOPENICILLIN-N-SYNTHASE; FERROUS ACTIVE-SITE; PARTICLE MESH EWALD; CLAVAMINATE SYNTHASE; CONTAINING PROTEINS; MOLECULAR-DYNAMICS; OXYGEN-ACTIVATION; HALOGENASE SYRB2; CATALYTIC CYCLE;
D O I
10.1021/acs.jpcb.9b06064
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Histone demethylases (KDMs) catalyze his tone lysine demethylation, an important epigenetic process that controls gene expression in eukaryotes, and represent important cancer drug targets for cancer treatment. Demethylation of histone is comprised of sequential reaction steps including oxygen activation, decarboxylation, and demethylation. The initial oxygen binding and activation steps have been studied. However, the information on the complete catalytic reaction cycle is limited, which has impeded the structure-based design of inhibitors targeting KDMs. Here we report the mechanism of the complete reaction steps catalyzed by a representative nonheme iron alpha KG-dependent KDM, PHF8 using QM/MM approaches. The atomic-level understanding on the complete reaction mechanism of PHF8 would shed light on the structure-based design of selective inhibitors targeting KDMs to intervene in cancer epigenetics.
引用
收藏
页码:7801 / 7811
页数:11
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