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首页> 外文期刊>Nucleic Acids Research >Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways
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Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways

机译:由GE81112停滞的30S预发起复合物的结构显示细菌和真核蛋白质合成起始途径中的结构状瓣膜

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In bacteria, the start site and the reading frame of the messenger RNA are selected by the small ribosomal subunit (30S) when the start codon, typically an AUG, is decoded in the P-site by the initiator tRNA in a process guided and controlled by three initiation factors. This process can be efficiently inhibited by GE81112, a natural tetrapeptide antibiotic that is highly specific toward bacteria. Here GE81112 was used to stabilize the 30S pre-initiation complex and obtain its structure by cryo-electron microscopy. The results obtained reveal the occurrence of changes in both the ribosome conformation and initiator tRNA position that may play a critical role in controlling translational fidelity. Furthermore, the structure highlights similarities with the early steps of initiation in eukaryotes suggesting that shared structural features guide initiation in all kingdoms of life.
机译:在细菌中,当启动密码子(30s)在引导和控制的过程中,当起始密码子在P-Pain中解码开始密码子(通常是八月)时,通过小核糖体亚基(30s)选出所述信使RNA的读取框。 通过三个启动因素。 通过GE81112可以有效地抑制该方法,这是对细菌具有高度特异性的天然四肽抗生素。 这里使用GE81112稳定30S预发起复合物并通过冷冻电子显微镜获得其结构。 得到的结果揭示了核糖体兼容性和引发剂TRNA位置的变化的发生,这可能在控制平移保真度方面发挥关键作用。 此外,该结构突出了与真核生物开始的早期步骤的相似性,这表明共享结构特征指南在所有界的所有王国中启动。

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