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5TPY

Crystal structure of an exonuclease resistant RNA from Zika virus

Summary for 5TPY
Entry DOI10.2210/pdb5tpy/pdb
DescriptorRNA (71-MER), MAGNESIUM ION, HEXANE-1,6-DIOL, ... (4 entities in total)
Functional Keywordszika rna exonuclease resistance, rna
Biological sourceZika virus
Total number of polymer chains1
Total formula weight23160.25
Authors
Akiyama, B.M.,Laurence, H.M.,Massey, A.R.,Costantino, D.A.,Xie, X.,Yang, Y.,Shi, P.-Y.,Nix, J.C.,Beckham, J.D.,Kieft, J.S. (deposition date: 2016-10-21, release date: 2016-12-14, Last modification date: 2023-10-04)
Primary citationAkiyama, B.M.,Laurence, H.M.,Massey, A.R.,Costantino, D.A.,Xie, X.,Yang, Y.,Shi, P.Y.,Nix, J.C.,Beckham, J.D.,Kieft, J.S.
Zika virus produces noncoding RNAs using a multi-pseudoknot structure that confounds a cellular exonuclease.
Science, 354:1148-1152, 2016
Cited by
PubMed Abstract: The outbreak of Zika virus (ZIKV) and associated fetal microcephaly mandates efforts to understand the molecular processes of infection. Related flaviviruses produce noncoding subgenomic flaviviral RNAs (sfRNAs) that are linked to pathogenicity in fetal mice. These viruses make sfRNAs by co-opting a cellular exonuclease via structured RNAs called xrRNAs. We found that ZIKV-infected monkey and human epithelial cells, mouse neurons, and mosquito cells produce sfRNAs. The RNA structure that is responsible for ZIKV sfRNA production forms a complex fold that is likely found in many pathogenic flaviviruses. Mutations that disrupt the structure affect exonuclease resistance in vitro and sfRNA formation during infection. The complete ZIKV xrRNA structure clarifies the mechanism of exonuclease resistance and identifies features that may modulate function in diverse flaviviruses.
PubMed: 27934765
DOI: 10.1126/science.aah3963
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.805 Å)
Structure validation

226707

数据于2024-10-30公开中

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