2OIY
Crystal structure of the duplex form of the HIV-1(LAI) RNA dimerization initiation site
Summary for 2OIY
Entry DOI | 10.2210/pdb2oiy/pdb |
Related | 1Y99 2OIJ 2OJ0 462D |
Descriptor | 5'-R(*CP*UP*UP*GP*CP*UP*GP*AP*AP*GP*CP*GP*CP*GP*CP*AP*CP*GP*GP*CP*AP*AP*G)-3', POTASSIUM ION, MAGNESIUM ION, ... (4 entities in total) |
Functional Keywords | hiv-1, dis, rna, dimerization |
Total number of polymer chains | 2 |
Total formula weight | 15000.88 |
Authors | Ennifar, E.,Walter, P.,Dumas, P. (deposition date: 2007-01-12, release date: 2007-12-25, Last modification date: 2023-12-27) |
Primary citation | Ennifar, E.,Walter, P.,Dumas, P. Cation-dependent cleavage of the duplex form of the subtype-B HIV-1 RNA dimerization initiation site. Nucleic Acids Res., 38:5807-5816, 2010 Cited by PubMed Abstract: The crystal structure of subtype-B HIV-1 genomic RNA Dimerization Initiation Site duplex revealed chain cleavage at a specific position resulting in 3'-phosphate and 5'-hydroxyl termini. A crystallographic analysis showed that Ba(2+), Mn(2+), Co(2+) and Zn(2+) bind specifically on a guanine base close to the cleaved position. The crystal structures also point to a necessary conformational change to induce an 'in-line' geometry at the cleavage site. In solution, divalent cations increased the rate of cleavage with pH/pKa compensation, indicating that a cation-bound hydroxide anion is responsible for the cleavage. We propose a 'Trojan horse' mechanism, possibly of general interest, wherein a doubly charged cation hosted near the cleavage site as a 'harmless' species is further transformed in situ into an 'aggressive' species carrying a hydroxide anion. PubMed: 20460458DOI: 10.1093/nar/gkq344 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.6 Å) |
Structure validation
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