Sameena Khan, Arvind Sharma, Hassan Belrhali, Manickam Yogavel, Amit Sharma
{"title":"克拉多菌素抑制疟原虫赖氨酸- trna合成酶的结构基础。","authors":"Sameena Khan, Arvind Sharma, Hassan Belrhali, Manickam Yogavel, Amit Sharma","doi":"10.1007/s10969-014-9182-1","DOIUrl":null,"url":null,"abstract":"<p><p>Malaria parasites inevitably develop drug resistance to anti-malarials over time. Hence the immediacy for discovering new chemical scaffolds to include in combination malaria drug therapy. The desirable attributes of new chemotherapeutic agents currently include activity against both liver and blood stage malaria parasites. One such recently discovered compound called cladosporin abrogates parasite growth via inhibition of Plasmodium falciparum lysyl-tRNA synthetase (PfKRS), an enzyme central to protein translation. Here, we present crystal structure of ternary PfKRS-lysine-cladosporin (PfKRS-K-C) complex that reveals cladosporin's remarkable ability to mimic the natural substrate adenosine and thereby colonize PfKRS active site. The isocoumarin fragment of cladosporin sandwiches between critical adenine-recognizing residues while its pyran ring fits snugly in the ribose-recognizing cavity. PfKRS-K-C structure highlights ample space within PfKRS active site for further chemical derivatization of cladosporin. Such derivatives may be useful against additional human pathogens that retain high conservation in cladosporin chelating residues within their lysyl-tRNA synthetase. </p>","PeriodicalId":73957,"journal":{"name":"Journal of structural and functional genomics","volume":"15 2","pages":"63-71"},"PeriodicalIF":0.0000,"publicationDate":"2014-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s10969-014-9182-1","citationCount":"53","resultStr":"{\"title\":\"Structural basis of malaria parasite lysyl-tRNA synthetase inhibition by cladosporin.\",\"authors\":\"Sameena Khan, Arvind Sharma, Hassan Belrhali, Manickam Yogavel, Amit Sharma\",\"doi\":\"10.1007/s10969-014-9182-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Malaria parasites inevitably develop drug resistance to anti-malarials over time. Hence the immediacy for discovering new chemical scaffolds to include in combination malaria drug therapy. The desirable attributes of new chemotherapeutic agents currently include activity against both liver and blood stage malaria parasites. One such recently discovered compound called cladosporin abrogates parasite growth via inhibition of Plasmodium falciparum lysyl-tRNA synthetase (PfKRS), an enzyme central to protein translation. Here, we present crystal structure of ternary PfKRS-lysine-cladosporin (PfKRS-K-C) complex that reveals cladosporin's remarkable ability to mimic the natural substrate adenosine and thereby colonize PfKRS active site. The isocoumarin fragment of cladosporin sandwiches between critical adenine-recognizing residues while its pyran ring fits snugly in the ribose-recognizing cavity. PfKRS-K-C structure highlights ample space within PfKRS active site for further chemical derivatization of cladosporin. Such derivatives may be useful against additional human pathogens that retain high conservation in cladosporin chelating residues within their lysyl-tRNA synthetase. </p>\",\"PeriodicalId\":73957,\"journal\":{\"name\":\"Journal of structural and functional genomics\",\"volume\":\"15 2\",\"pages\":\"63-71\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/s10969-014-9182-1\",\"citationCount\":\"53\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of structural and functional genomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s10969-014-9182-1\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2014/6/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of structural and functional genomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s10969-014-9182-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2014/6/17 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 53
摘要
随着时间的推移,疟疾寄生虫不可避免地对抗疟疾药物产生耐药性。因此,发现新的化学支架用于联合疟疾药物治疗迫在眉睫。目前,新的化疗药物的理想特性包括对肝期和血期疟疾寄生虫的活性。最近发现的一种化合物cladosporin通过抑制恶性疟原虫赖基- trna合成酶(PfKRS)来抑制寄生虫的生长,PfKRS是一种蛋白质翻译的核心酶。在这里,我们展示了PfKRS-赖氨酸-克拉多菌素(PfKRS- k -c)复合物的晶体结构,揭示了克拉多菌素模拟天然底物腺苷的卓越能力,从而定殖PfKRS活性位点。cladosporin的异香豆素片段夹在关键的腺嘌呤识别残基之间,而其吡喃环则紧贴在核糖识别腔中。PfKRS- k - c结构突出了PfKRS活性位点内的充足空间,用于进一步化学衍生cladosporin。这种衍生物可能对其他人类病原体有用,这些病原体在其赖氨酸- trna合成酶中保留了高度保守的克拉霉素螯合残基。
Structural basis of malaria parasite lysyl-tRNA synthetase inhibition by cladosporin.
Malaria parasites inevitably develop drug resistance to anti-malarials over time. Hence the immediacy for discovering new chemical scaffolds to include in combination malaria drug therapy. The desirable attributes of new chemotherapeutic agents currently include activity against both liver and blood stage malaria parasites. One such recently discovered compound called cladosporin abrogates parasite growth via inhibition of Plasmodium falciparum lysyl-tRNA synthetase (PfKRS), an enzyme central to protein translation. Here, we present crystal structure of ternary PfKRS-lysine-cladosporin (PfKRS-K-C) complex that reveals cladosporin's remarkable ability to mimic the natural substrate adenosine and thereby colonize PfKRS active site. The isocoumarin fragment of cladosporin sandwiches between critical adenine-recognizing residues while its pyran ring fits snugly in the ribose-recognizing cavity. PfKRS-K-C structure highlights ample space within PfKRS active site for further chemical derivatization of cladosporin. Such derivatives may be useful against additional human pathogens that retain high conservation in cladosporin chelating residues within their lysyl-tRNA synthetase.