A structural overview of the zinc transporters in the cation diffusion facilitator family

被引:39
作者
Cotrim, Camila A. [1 ]
Jarrott, Russell J. [1 ]
Martin, Jennifer L. [1 ]
Drew, David [2 ]
机构
[1] Griffith Univ, Griffith Inst Drug Discovery, Nathan, Qld 4111, Australia
[2] Stockholm Univ, Dept Biochem & Biophys, SE-10691 Stockholm, Sweden
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2019年 / 75卷
基金
澳大利亚研究理事会;
关键词
cation diffusion facilitator; membrane proteins; zinc transporter; MULTIPLE SEQUENCE ALIGNMENT; METAL-ION-TRANSPORT; ANTIPORT MECHANISM; EFFLUX; PROTEINS; BINDING; ZNT-1; ZN2+; YIIP; IDENTIFICATION;
D O I
10.1107/S2059798319003814
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The cation diffusion facilitators (CDFs) are a family of membrane-bound proteins that maintain cellular homeostasis of essential metal ions. In humans, the zinc-transporter CDF family members (ZnTs) play important roles in zinc homeostasis. They do this by facilitating zinc efflux from the cytoplasm to the extracellular space across the plasma membrane or into intracellular organelles. Several ZnTs have been implicated in human health owing to their association with type 2 diabetes and neurodegenerative diseases. Although the structure determination of CDF family members is not trivial, recent advances in membrane-protein structural biology have resulted in two structures of bacterial YiiPs and several structures of their soluble C-terminal domains. These data reveal new insights into the molecular mechanism of ZnT proteins, suggesting a unique rocking-bundle mechanism that provides alternating access to the metal-binding site.
引用
收藏
页码:357 / 367
页数:11
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