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
相关论文
共 50 条
  • [41] Design and synthesis of novel imidazole-substituted dipeptide amides as potent and selective inhibitors of Candida albicans myristoylCoA:protein N-myristoyltransferase and identification of related tripeptide inhibitors with mechanism-based antifungal activity
    Devadas, B
    Freeman, SK
    Zupec, ME
    Lu, HF
    Nagarajan, SR
    Kishore, NS
    Lodge, JK
    Kuneman, DW
    McWherter, CA
    Vinjamoori, DV
    Getman, DP
    Gordon, JI
    Sikorski, JA
    JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (16) : 2609 - 2625
  • [42] Structure-based virtual screening against SARS-3CLpro: Identification of hits and insights into the process of lead development
    Mukherjee, Prasenjit
    Desai, Prashant V.
    Ross, Larry
    White, Lucile
    Avery, Mitchell A.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 234
  • [43] Structure guided modification of 2-chloro-5-(ethyl-phenyl-sulfamoyl)-N-[2-(2-oxo-pyrrolidin-1-yl)-phenyl]-benzamide to afford selective inhibitors of Cryptosporidium parvum N-myristoyltransferase
    Sigalapalli, Dilep K.
    Groustra, Sophia
    Fenwick, Michael K.
    Zigweid, Rachael
    Hulverson, Matthew A.
    Owsley, Eric
    Khim, Monique
    Shibata, Sayaka
    Van Voorhis, Wesley C.
    Staker, Bart L.
    Fan, Erkang
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2025, 119
  • [44] Calmodulin modulation of the olfactory CNG channel: Solution structure by NMR of a complex between a fragment of the N-terminal domain and calmodulin.
    Orsale, MV
    Melino, S
    Contessa, GM
    Torre, V
    Paci, M
    Desideri, A
    Cicero, DO
    BIOPHYSICAL JOURNAL, 2003, 84 (02) : 137A - 137A
  • [45] Structure and molecular lability of N-(thio)phosphoryl(thio)amides: XVII. Intramolecular transformations of N,N′-bis(thio)phosphoryl(thio)ureas with the open-chain fragment in DMSO solution
    F. Kh. Karataeva
    Russian Journal of General Chemistry, 2013, 83 : 274 - 278
  • [46] Structure and molecular lability of N-(thio)phosphoryl(thio)amides: XVII. Intramolecular transformations of N,N′-bis(thio)phosphoryl(thio)ureas with the open-chain fragment in DMSO solution
    Karataeva, F. Kh.
    RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2013, 83 (02) : 274 - 278
  • [47] SUBSTRATE-SPECIFICITY OF SACCHAROMYCES-CEREVISIAE MYRISTOYL-COA-PROTEIN N-MYRISTOYLTRANSFERASE - ANALYSIS OF FATTY-ACID ANALOGS CONTAINING CARBONYL GROUPS, NITROGEN HETEROATOMS, AND NITROGEN-HETEROCYCLES IN AN INVITRO ENZYME ASSAY AND SUBSEQUENT IDENTIFICATION OF INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS-I REPLICATION
    DEVADAS, B
    LU, TB
    KATOH, A
    KISHORE, NS
    WADE, AC
    MEHTA, PP
    RUDNICK, DA
    BRYANT, ML
    ADAMS, SP
    LI, Q
    GOKEL, GW
    GORDON, JI
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1992, 267 (11) : 7224 - 7239
  • [48] Identification of ligand efficient, fragment-like hits from an HTS library: structure-based virtual screening and docking investigations of 2H- and 3H-pyrazolo tautomers for Aurora kinase A selectivity
    Sarvagalla, Sailu
    Singh, Vivek Kumar
    Ke, Yi-Yu
    Shiao, Hui-Yi
    Lin, Wen-Hsing
    Hsieh, Hsing-Pang
    Hsu, John T. A.
    Coumar, Mohane Selvaraj
    JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 2015, 29 (01) : 89 - 100
  • [49] Identification of ligand efficient, fragment-like hits from an HTS library: structure-based virtual screening and docking investigations of 2H- and 3H-pyrazolo tautomers for Aurora kinase A selectivity
    Sailu Sarvagalla
    Vivek Kumar Singh
    Yi-Yu Ke
    Hui-Yi Shiao
    Wen-Hsing Lin
    Hsing-Pang Hsieh
    John T. A. Hsu
    Mohane Selvaraj Coumar
    Journal of Computer-Aided Molecular Design, 2015, 29 : 89 - 100
  • [50] Solution structure and dynamics of the CX3C chemokine domain of fractalkine and its interaction with an N-terminal fragment of CX3CR1
    Mizoue, LS
    Bazan, JF
    Johnson, EC
    Handel, TM
    BIOCHEMISTRY, 1999, 38 (05) : 1402 - 1414