398D
3'-DNA-RNA-5' JUNCTION FORMED DURING INITIATION OF MINUS-STRAND SYNTHESIS OF HIV REPLICATION
Summary for 398D
| Entry DOI | 10.2210/pdb398d/pdb |
| Descriptor | RNA (5'-R(*GP*CP*AP*GP*UP*GP*GP*C)-3'), DNA/RNA (5'-R(*GP*CP*CP*AP)-D(*CP*TP*GP*C)-3') (3 entities in total) |
| Functional Keywords | a-dna/rna, double helix, dna-rna hybrid |
| Total number of polymer chains | 4 |
| Total formula weight | 10066.36 |
| Authors | Mueller, U.,Meier, G.,Mochi-Onori, A.,Cellai, L.,Heumann, H. (deposition date: 1998-05-04, release date: 1998-10-06, Last modification date: 2024-04-03) |
| Primary citation | Mueller, U.,Maier, G.,Mochi Onori, A.,Cellai, L.,Heumann, H.,Heinemann, U. Crystal structure of an eight-base pair duplex containing the 3'-DNA-RNA-5' junction formed during initiation of minus-strand synthesis of HIV replication. Biochemistry, 37:12005-12011, 1998 Cited by PubMed Abstract: During initiation of minus-strand synthesis by HIV-1 reverse transcriptase, a 3'-DNA-RNA-5' junction is formed involving the 3'-end of tRNAlys,3. The HIV-RT-associated RNase H cleaves the RNA template strand specifically, opposite the newly synthesized DNA strand. We have determined the crystal structure at 1.9 A resolution of an eight-base pair hybrid duplex representing the junction to identify global or local structural perturbations which may be recognized by HIV-RT RNase H. The junction octamer is in a global A-type conformation throughout. A base pair step with distinct stacking geometry and variable backbone conformation is located next to the main endonucleolytic cleavage site. This base pair step may serve as a recognition site for HIV-RT RNase H. PubMed: 9724510DOI: 10.1021/bi981152y PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.94 Å) |
Structure validation
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