The PUA domain -: a structural and functional overview

被引:54
|
作者
Perez-Arellano, Isabel
Gallego, Jose
Cervera, Javier
机构
[1] Ctr Invest Principe Felipe, Mol Recognit Lab, E-46013 Valencia, Spain
[2] Ctr Invest Principe Felipe, Mol Struct & Simulat Lab, E-46013 Valencia, Spain
关键词
archaeosine tRNA transglycosylase; Cbf5; glutamate; 5-kinase; H/ACA box; MCT-1; methyltransferase; Nip7; pseudouridine synthase; PUA domain; translation initiation;
D O I
10.1111/j.1742-4658.2007.06031.x
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 pseudouridine synthase and archaeosine transglycosylase (PUA) domain is a compact and highly conserved RNA-binding motif that is widespread among diverse types of proteins from the three kingdoms of life. Its three-dimensional architecture is well established, and the structures of several PUA-RNA complexes reveal a common RNA recognition surface, but also some versatility in the way in which the motif binds to RNA. The PUA domain is often part of RNA modification enzymes and ribonucleoproteins, but it has also been unexpectedly found fused to enzymes involved in proline biosynthesis, where it plays an unknown role. The functional impact of the domain varies with the protein studied, ranging from minor to essential effects. PUA motifs are involved in dyskeratosis congenita and cancer, pointing to links between RNA metabolism and human diseases.
引用
收藏
页码:4972 / 4984
页数:13
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