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3P22

Crystal structure of the ENE, a viral RNA stability element, in complex with A9 RNA

Summary for 3P22
Entry DOI10.2210/pdb3p22/pdb
DescriptorCore ENE hairpin from KSHV PAN RNA, oligo(A)9 RNA (3 entities in total)
Functional Keywordsmajor groove triple helix, viral non-coding rna, stability element, nucleus, rna
Total number of polymer chains8
Total formula weight63293.34
Authors
Mitton-Fry, R.M.,DeGregorio, S.J.,Wang, J.,Steitz, T.A.,Steitz, J.A. (deposition date: 2010-10-01, release date: 2010-12-08, Last modification date: 2024-02-21)
Primary citationMitton-Fry, R.M.,DeGregorio, S.J.,Wang, J.,Steitz, T.A.,Steitz, J.A.
Poly(A) tail recognition by a viral RNA element through assembly of a triple helix.
Science, 330:1244-1247, 2010
Cited by
PubMed Abstract: Kaposi's sarcoma-associated herpesvirus produces a highly abundant, nuclear noncoding RNA, polyadenylated nuclear (PAN) RNA, which contains an element that prevents its decay. The 79-nucleotide expression and nuclear retention element (ENE) was proposed to adopt a secondary structure like that of a box H/ACA small nucleolar RNA (snoRNA), with a U-rich internal loop that hybridizes to and protects the PAN RNA poly(A) tail. The crystal structure of a complex between the 40-nucleotide ENE core and oligo(A)(9) RNA at 2.5 angstrom resolution reveals that unlike snoRNAs, the U-rich loop of the ENE engages its target through formation of a major-groove triple helix. A-minor interactions extend the binding interface. Deadenylation assays confirm the functional importance of the triple helix. Thus, the ENE acts as an intramolecular RNA clamp, sequestering the PAN poly(A) tail and preventing the initiation of RNA decay.
PubMed: 21109672
DOI: 10.1126/science.1195858
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.501 Å)
Structure validation

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