6BG9
HYBRID NMR/CRYO-EM STRUCTURE OF THE HIV-1 RNA DIMERIZATION SIGNAL
Summary for 6BG9
| Entry DOI | 10.2210/pdb6bg9/pdb |
| EMDB information | 7080 |
| NMR Information | BMRB: 27289 |
| Descriptor | RNA dimerization signal (1 entity in total) |
| Functional Keywords | rna inernal loops, sheared ga pairs, gu wobble, s-turn thermodynamics, rna |
| Biological source | Homo sapiens (Human) |
| Total number of polymer chains | 2 |
| Total formula weight | 30718.48 |
| Authors | Summers, M.F. (deposition date: 2017-10-27, release date: 2018-02-21, Last modification date: 2024-05-01) |
| Primary citation | Zhang, K.,Keane, S.C.,Su, Z.,Irobalieva, R.N.,Chen, M.,Van, V.,Sciandra, C.A.,Marchant, J.,Heng, X.,Schmid, M.F.,Case, D.A.,Ludtke, S.J.,Summers, M.F.,Chiu, W. Structure of the 30 kDa HIV-1 RNA Dimerization Signal by a Hybrid Cryo-EM, NMR, and Molecular Dynamics Approach. Structure, 26:490-498.e3, 2018 Cited by PubMed Abstract: Cryoelectron microscopy (cryo-EM) and nuclear magnetic resonance (NMR) spectroscopy are routinely used to determine structures of macromolecules with molecular weights over 65 and under 25 kDa, respectively. We combined these techniques to study a 30 kDa HIV-1 dimer initiation site RNA ([DIS]; 47 nt/strand). A 9 Å cryo-EM map clearly shows major groove features of the double helix and a right-handed superhelical twist. Simulated cryo-EM maps generated from time-averaged molecular dynamics trajectories (10 ns) exhibited levels of detail similar to those in the experimental maps, suggesting internal structural flexibility limits the cryo-EM resolution. Simultaneous inclusion of the cryo-EM map and H-edited NMR-derived distance restraints during structure refinement generates a structure consistent with both datasets and supporting a flipped-out base within a conserved purine-rich bulge. Our findings demonstrate the power of combining global and local structural information from these techniques for structure determination of modest-sized RNAs. PubMed: 29398526DOI: 10.1016/j.str.2018.01.001 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (9 Å) SOLUTION NMR (9 Å) |
Structure validation
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