Identification and structure solution of fragment hits against kinetoplastid N-myristoyltransferase

被引:3
|
作者
Robinson, David A. [1 ]
Wyatt, Paul G. [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Drug Discovery Unit, Dundee DD1 5EH, Scotland
基金
英国惠康基金;
关键词
N-myristoyltransferase; Trypanosoma brucei; African trypanosomiasis; POTENTIAL-DRUG TARGET; MYRISTOYL-COA; BINDING; RELAXATION; INHIBITORS; DISCOVERY; PROTEINS; AFFINITY;
D O I
10.1107/S2053230X15003040
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Trypanosoma bruceiN-myristoyltransferase (TbNMT) is an attractive therapeutic target for the treatment of human African trypanosomiasis. Pyrazole sulfonamide (DDD85646), a potent inhibitor of TbNMT, has been identified in previous studies; however, poor central nervous system exposure restricts its use to the haemolymphatic form (stage 1) of the disease. In order to identify new chemical matter, a fragment screen was carried out by ligand-observed NMR spectroscopy, identifying hits that occupy the DDD85646 binding site. Crystal structures of hits from this assay have been obtained in complex with the closely related NMT from Leishmania major, providing a structural starting point for the evolution of novel chemical matter.
引用
收藏
页码:586 / 593
页数:8
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