Small multidrug resistance proteins: A multidrug transporter family that continues to grow

被引:206
作者
Bay, Denice C. [1 ]
Rommens, Kenton L. [1 ]
Turner, Raymond J. [1 ]
机构
[1] Univ Calgary, Dept Biol Sci, Calgary, AB T2N 1N4, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2008年 / 1778卷 / 09期
基金
加拿大自然科学与工程研究理事会;
关键词
small multidrug resistance (SMR); EmrE; SugE; paired SMR; dual topology; secondary drug transporter; drug binding; phylogenetic tree;
D O I
10.1016/j.bbamem.2007.08.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The small multidrug resistance (SMR) protein family is a bacterial multidrug transporter family. As suggested by their title, SMR proteins are composed Of four transmembrane alpha-helices of approximately 100-140 amino acids in length. Since their designation as a family, many homologues have been identified and characterized both structurally and functionally. In this review the topology, structure, drug resistance, drug binding, and transport mechanisms of the entire SMR protein family are examined. Additionally, updated bioinformatic analysis of predicted and characterized SMR protein family members was also conducted. Based on SMR sequence alignments and phylogenetic analysis of current members, we propose that this small multidrug resistance transporter family should be expanded into three subclasses: (i) the small multidrug pumps (SMP), (ii) suppressor of groEL mutation proteins (SUG), and a third group (iii) paired small multidrug resistance proteins (PSMR). The roles of these three SMR subclasses are examined, and the well-characterized members, such as Escherichia coli ErnrE and SugE, are described in terms of their function and structural organization. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1814 / 1838
页数:25
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