脱氧鸟苷疟原虫途径的特殊性质作为代谢和药物发现研究的潜在领域。

Mahmoud Kandeel, Yoshiaki Kitamura, Yukio Kitade
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引用次数: 15

摘要

在恶性疟原虫中,脱氧鸟苷酸被发现是几种DNA代谢酶的底物。鸟苷酸激酶利用dGMP的特异性非常低,估计是已知的原核和真核酶中最低的。此外,胸苷激酶(thymidylate kinase)是一种嘧啶特异性酶,可以磷酸化dGMP,具有与天然底物相似的高特异性。上述差异是疟原虫原生动物所特有的,为在发育过程中追踪dGMP代谢提供了一种有趣的方法,也为药物开发提供了一个起点。
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The exceptional properties of Plasmodium deoxyguanylate pathways as a potential area for metabolic and drug discovery studies.

In Plasmodium falciparum, deoxyguanylate was found to be a substrate for several DNA metabolizing enzymes. Guanylate kinase utilizes dGMP with very low specificity, which is estimated to be the lowest among well-known prokaryotic and eukaryotic enzymes. Furthermore, thymidylate kinase, which is a pyrimidine specific enzyme, was found to phosphorylate dGMP with a surprisingly high specificity similar to that of the natural substrate. The above mentioned distinctions are specific for the Plasmodium protozoa and provide an interesting method for tracking dGMP metabolism during development and a starting point for drug development.

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Chemical methods to study protein-nucleic acid interactions. Development of novel chemical probes to detect abasic sites in DNA. Assessment of the DNA damage using the fluorescence microscope. Exciton-controlled fluorescence: application to hybridization-sensitive fluorescent DNA probe. Multiple activities of c-di-GMP in Pseudomonas aeruginosa.
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