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[靶向polo样激酶1的底物结合结构域:PBD1抑制剂的研究进展]

[Targeting the substrate binding domain of polo-like kinase 1: advances in the study of PBD1 inhibitors].

作者信息

Zhang Liang, Cao Yan-Hua, Lu Shuai, Sun Shan-Liang, Liu Hai-Chun, Lu Tao

机构信息

Department of Organic Chemistry, China Pharmaceutical University, Nanjing 210009, China.

出版信息

Yao Xue Xue Bao. 2013 Mar;48(3):315-24.

Abstract

Polo-box domain 1 (PBD1) is a characteristic domain of polo-like kinase 1 (PLK1), which locates in C-terminal and can influence the catalytic activity and specific subcellular locations of PLK1. At present, most PLK1 inhibitors are developed to occupy the ATP pocket or its close sites. However, this kind of PLK1 inhibitors is difficult to pursue target selectivity and may encounter cross drug resistance with other kinase inhibitors due to the conserved sequence of ATP pocket. Recently, PBD1, with aberrant specificity in sequence and structure, has attracted enormous interests as the alternative target to the discovery of corresponding inhibitors for anti-tumor drugs. The structure and function of PBD1 as well as the advances of its inhibitors are reviewed in this paper.

摘要

Polo-box结构域1(PBD1)是polo样激酶1(PLK1)的一个特征性结构域,位于C末端,可影响PLK1的催化活性和特定亚细胞定位。目前,大多数PLK1抑制剂是为占据ATP口袋或其附近位点而开发的。然而,这类PLK1抑制剂难以实现靶点选择性,并且由于ATP口袋序列保守,可能会与其他激酶抑制剂产生交叉耐药性。近年来,PBD1在序列和结构上具有独特的特异性,作为抗肿瘤药物相应抑制剂发现的替代靶点引起了广泛关注。本文综述了PBD1的结构与功能及其抑制剂的研究进展。

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