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MmpL3 功能和抑制的分子机制。

Molecular Mechanisms of MmpL3 Function and Inhibition.

机构信息

Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.

出版信息

Microb Drug Resist. 2023 May;29(5):190-212. doi: 10.1089/mdr.2021.0424. Epub 2023 Feb 21.

Abstract

species include a large number of pathogenic organisms such as , , and various non-tuberculous mycobacteria. Mycobacterial membrane protein large 3 (MmpL3) is an essential mycolic acid and lipid transporter required for growth and cell viability. In the last decade, numerous studies have characterized MmpL3 with respect to protein function, localization, regulation, and substrate/inhibitor interactions. This review summarizes new findings in the field and seeks to assess future areas of research in our rapidly expanding understanding of MmpL3 as a drug target. An atlas of known MmpL3 mutations that provide resistance to inhibitors is presented, which maps amino acid substitutions to specific structural domains of MmpL3. In addition, chemical features of distinct classes of Mmpl3 inhibitors are compared to provide insights into shared and unique features of varied MmpL3 inhibitors.

摘要

物种包括大量的致病生物体,如、和各种非结核分枝杆菌。分枝杆菌膜蛋白大 3(MmpL3)是一种必需的分枝酸和脂类转运蛋白,对于生长和细胞活力是必需的。在过去的十年中,许多研究已经对 MmpL3 的蛋白质功能、定位、调节和底物/抑制剂相互作用进行了描述。本综述总结了该领域的新发现,并试图评估在我们对 MmpL3 作为药物靶点的快速扩展的理解中未来的研究领域。提供了对抑制剂耐药性的已知 MmpL3 突变的图谱,将氨基酸取代映射到 MmpL3 的特定结构域。此外,还比较了不同类别的 Mmpl3 抑制剂的化学特征,以深入了解不同的 MmpL3 抑制剂的共同和独特特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b4a/10171966/09e49f6efc41/mdr.2021.0424_figure1.jpg

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