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首页> 外文期刊>Journal of molecular recognition: JMR >Identification of ligand binding activity and DNA recognition by RhlR protein from opportunistic pathogen Pseudomonas aeruginosa Pseudomonas aeruginosa —a molecular dynamic simulation approach
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Identification of ligand binding activity and DNA recognition by RhlR protein from opportunistic pathogen Pseudomonas aeruginosa Pseudomonas aeruginosa —a molecular dynamic simulation approach

机译:来自机会理性病原体的RHLR蛋白的配体结合活性和DNA识别的鉴定来自机会理性病原体假单胞菌铜绿假单胞菌铜绿假单胞菌-A分子动态模拟方法

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Abstract RhlR protein from opportunistic pathogen Pseudomonas aeruginosa is involved in the transcription of virulence genes of the organism. The RhlR protein functions as a dimer and binds to the cognate promoter DNA with the help of an autoinducer ligand BHL to initiate the transcription of the virulence genes. Till date, there are no reports that detail the mechanism of virulence gene expression by RhlR protein in P. aeruginosa . In this work, we tried to analyse the molecular aspects of the various binding interactions of the RhlR protein while formimg the dimmer as well as with the promoter DNA. We analysed the mode of dimerisation of the RhlR protein and its binding interactions with the autoinducer BHL ligand. From our analyses, we could identify the potential amino acid residues which are involved in the binding interactions. We also predicted how the autoinducer BHL would help in making contacts with the DNA as well as with itself. Thus, the autoinducer BHL would serve as an important mediator of molecular interactions involved in binding the RhlR protein to itself as well as with the promoter DNA. Therefore, any other molecule which would be able to compete with the autoinducer ligand BHL to bind to RhlR protein but would not let the RhlR protein bind the promoter DNA would be an ideal drug candidate to prevent the transcription process of the virulence genes in P. aeruginosa . Our future aim is to predict suitable ligands which would compete with BHL to thwart the transcription process.
机译:摘要来自机会主义病原体假单胞菌铜绿假单胞菌的RHLR蛋白参与了生物体的毒力基因的转录。 RHLR蛋白用作二聚体并借助于自动挤出机配体BHL与同源启动子DNA结合,以引发毒力基因的转录。迄今为止,没有报告详细介绍了铜绿假单胞菌中RHLR蛋白的毒力基因表达的机制。在这项工作中,我们尝试分析RHLR蛋白的各种结合相互作用的分子方面,同时形成调光器以及促进剂DNA。我们分析了rhlR蛋白的二聚化模式及其与自动挤出机BHL配体的结合相互作用。从我们的分析中,我们可以识别参与结合相互作用的潜在氨基酸残基。我们还预测了AutoInuceer BHL如何有助于与DNA以及其自身进行接触。因此,自动挤出机BHL将作为将RHLR蛋白与启动子DNA结合到其自身和启动子的分子相互作用的重要介体。因此,任何其他能够与AutoInucucer配体BHL竞争的任何其他分子以结合RHLR蛋白,但不会让RHLR蛋白结合启动子DNA是一种理想的药物候选者,以防止毒力基因的转录过程。铜绿假单胞菌。我们未来的目的是预测合适的配体,这些配体将与BHL竞争以挫败转录过程。

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