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6VU1

Cap3G-TAR-F1 is an RNA hairpin. The 1H-1H NOESY data was collected at 308 K in 10 mM KH2PO4 pH 7.4.

Summary for 6VU1
Entry DOI10.2210/pdb6vu1/pdb
NMR InformationBMRB: 30723
DescriptorRNA (34-MER) (1 entity in total)
Functional Keywordsrna, virus, capped rna, viral, nucleotides, leader rna, hiv genome, genome, rna genome, start site exposed cap, free cap
Biological sourceHuman immunodeficiency virus 1
Total number of polymer chains1
Total formula weight11041.56
Authors
Summers, M.F.,Brown, J.D. (deposition date: 2020-02-14, release date: 2020-04-29, Last modification date: 2024-05-15)
Primary citationBrown, J.D.,Kharytonchyk, S.,Chaudry, I.,Iyer, A.S.,Carter, H.,Becker, G.,Desai, Y.,Glang, L.,Choi, S.H.,Singh, K.,Lopresti, M.W.,Orellana, M.,Rodriguez, T.,Oboh, U.,Hijji, J.,Ghinger, F.G.,Stewart, K.,Francis, D.,Edwards, B.,Chen, P.,Case, D.A.,Telesnitsky, A.,Summers, M.F.
Structural basis for transcriptional start site control of HIV-1 RNA fate.
Science, 368:413-417, 2020
Cited by
PubMed Abstract: Heterogeneous transcriptional start site usage by HIV-1 produces 5'-capped RNAs beginning with one, two, or three 5'-guanosines (1G, 2G, or 3G, respectively) that are either selected for packaging as genomes (1G) or retained in cells as translatable messenger RNAs (mRNAs) (2G and 3G). To understand how 5'-guanosine number influences fate, we probed the structures of capped HIV-1 leader RNAs by deuterium-edited nuclear magnetic resonance. The 1G transcript adopts a dimeric multihairpin structure that sequesters the cap, inhibits interactions with eukaryotic translation initiation factor 4E, and resists decapping. The 2G and 3G transcripts adopt an alternate structure with an elongated central helix, exposed splice donor residues, and an accessible cap. Extensive remodeling, achieved at the energetic cost of a G-C base pair, explains how a single 5'-guanosine modifies the function of a ~9-kilobase HIV-1 transcript.
PubMed: 32327595
DOI: 10.1126/science.aaz7959
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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