首页> 美国卫生研究院文献>Molecular Cellular Proteomics : MCP >aKMT Catalyzes Extensive Protein Lysine Methylation in the Hyperthermophilic Archaeon Sulfolobus islandicus but is Dispensable for the Growth of the Organism
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aKMT Catalyzes Extensive Protein Lysine Methylation in the Hyperthermophilic Archaeon Sulfolobus islandicus but is Dispensable for the Growth of the Organism

机译:aKMT催化超嗜热古细菌Sulfolobus islandicus中广泛的蛋白质赖氨酸甲基化但对于有机体的生长是必不可少的

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摘要

Protein methylation is believed to occur extensively in creanarchaea. Recently, aKMT, a highly conserved crenarchaeal protein lysine methyltransferase, was identified and shown to exhibit broad substrate specificity in vitro. Here, we have constructed an aKMT deletion mutant of the hyperthermophilic crenarchaeon Sulfolobus islandicus. The mutant was viable but showed a moderately slower growth rate than the parental strain under non-optimal growth conditions. Consistent with the moderate effect of the lack of aKMT on the growth of the cell, expression of a small number of genes, which encode putative functions in substrate transportation, energy metabolism, transcriptional regulation, stress response proteins, etc, was differentially regulated by more than twofold in the mutant strain, as compared with that in the parental strain. Analysis of the methylation of total cellular protein by mass spectrometry revealed that methylated proteins accounted for ∼2/3 (1,158/1,751) and ∼1/3 (591/1,757) of the identified proteins in the parental and the mutant strains, respectively, indicating that there is extensive protein methylation in S. islandicus and that aKMT is a major protein methyltransferase in this organism. No significant sequence preference was detected at the sites of methylation by aKMT. Methylated lysine residues, when visible in the structure, are all located on the surface of the proteins. The crystal structure of aKMT in complex with S-adenosyl-l-methionine (SAM) or S-adenosyl homocysteine (SAH) reveals that the protein consists of four α helices and seven β sheets, lacking a substrate recognition domain found in PrmA, a bacterial homolog of aKMT, in agreement with the broad substrate specificity of aKMT. Our results suggest that aKMT may serve a role in maintaining the methylation status of cellular proteins required for the efficient growth of the organism under certain non-optimal conditions.
机译:据信蛋白质甲基化广泛地存在于颅骨古菌中。最近,鉴定了高度保守的crenarchaeal蛋白赖氨酸甲基转移酶aKMT,并显示出其在体外具有广泛的底物特异性。在这里,我们已经构建了一个超嗜热的克氏变种Sulfolobus islandicus的aKMT缺失突变体。该突变体是可行的,但在非最佳生长条件下,其生长速度比亲本菌株慢。与缺乏aKMT对细胞生长的中等作用相一致,少量的基因表达在底物转运,能量代谢,转录调节,应激反应蛋白等方面编码假定的功能,并受到更多的差异调节。与亲本菌株相比,突变体菌株的抗性要高两倍。通过质谱分析总细胞蛋白的甲基化表明,在亲本和突变菌株中,甲基化蛋白分别占所鉴定蛋白的约2/3(1,158 / 1,751)和约1/3(591 / 1,757),这表明在岛链球菌中存在广泛的蛋白质甲基化,而aKMT是该生物中的主要蛋白质甲基转移酶。通过aKMT在甲基化位点未检测到明显的序列偏好。当在结构中可见时,甲基化的赖氨酸残基都位于蛋白质的表面上。 aKMT与S-腺苷-1-蛋氨酸(SAM)或S-腺苷高半胱氨酸(SAH)的复合物的晶体结构表明,该蛋白由4个α螺旋和7个β折叠组成,缺少PrmA中发现的底物识别域。与aKMT具有广泛的底物特异性相一致的aKMT细菌同源物。我们的结果表明,aKMT可能在维持生物体在某些非最佳条件下有效生长所需的细胞蛋白质的甲基化状态中起作用。

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