Institute of Neuroanatomy, Medical Faculty Manheim, University of Heidelberg, 68167 Mannheim, Germany.
College of Life and Environmental Sciences, Biosciences, University of Exeter, Exeter EX4 4QD, Devon, UK.
Biochim Biophys Acta Mol Cell Res. 2020 May;1867(5):118675. doi: 10.1016/j.bbamcr.2020.118675. Epub 2020 Feb 8.
Members of the large multigene family of acyl-CoA binding domain containing proteins (ACBDs) share a conserved motif required for binding of Coenzyme A esterified fatty acids of various chain length. These proteins are present in the three kingdoms of life, and despite their predicted roles in cellular lipid metabolism, knowledge about the precise functions of many ACBD proteins remains scarce. Interestingly, several ACBD proteins are now suggested to function at organelle contact sites, and are recognized as host interaction proteins for different pathogens including viruses and bacteria. Here, we present a thorough phylogenetic analysis of the ACBD family and discuss their structure and evolution. We summarize recent findings on the various functions of animal and fungal ACBDs with particular focus on peroxisomes, the role of ACBD proteins at organelle membranes, and their increasing recognition as targets for pathogens.
酰基辅酶 A 结合域蛋白(ACBD)大家族的成员都含有一个保守基序,该基序对于结合不同链长的辅酶 A 酯化脂肪酸是必需的。这些蛋白存在于生命的三个领域,尽管它们被预测在细胞脂质代谢中发挥作用,但对于许多 ACBD 蛋白的确切功能仍然知之甚少。有趣的是,现在有几种 ACBD 蛋白被认为在细胞器接触部位发挥作用,并被认为是不同病原体(包括病毒和细菌)的宿主相互作用蛋白。在这里,我们对 ACBD 家族进行了全面的系统发育分析,并讨论了它们的结构和进化。我们总结了最近关于动物和真菌 ACBD 的各种功能的发现,特别关注过氧化物酶体,ACBD 蛋白在细胞器膜上的作用,以及它们作为病原体靶标的日益被认可。