11FC
E.Coli DNA Topoisomerase 3 in complex with an 8mer ssDNA oligo CTGAACTT
Summary for 11FC
| Entry DOI | 10.2210/pdb11fc/pdb |
| Descriptor | DNA topoisomerase 3, DNA (5'-D(P*CP*TP*GP*AP*AP*CP*TP*T)-3'), MALONATE ION, ... (5 entities in total) |
| Functional Keywords | ectopo3, ssdna complex, isomerase, isomerase-dna complex, isomerase/dna |
| Biological source | Escherichia coli More |
| Total number of polymer chains | 2 |
| Total formula weight | 75841.46 |
| Authors | Tan, K.,Tse Dinh, Y.C. (deposition date: 2026-02-20, release date: 2026-04-29, Last modification date: 2026-08-26) |
| Primary citation | Tan, K.,Annamalai, T.,Stols, L.,Bhuiyan, M.A.R.,Tse-Dinh, Y.C. New Insights into Binding of G-segment DNA to the Active Site of Escherichia coli Topoisomerase III. Sci Rep, 16:-, 2026 Cited by PubMed Abstract: Escherichia coli topoisomerase III (EcTopo3) is a type IA topoisomerase that binds single-stranded DNA (ssDNA) during DNA cleavage and strand passage. Here, we report five crystal structures of EcTopo3 in complex with distinct 8-base ssDNA oligonucleotides at 1.85-2.22 Å resolution. These structures reveal a previously unrecognized half-open ssDNA-binding mode. In this mode, EcTopo3 engages only the five 3'-terminal nucleotides of the oligonucleotide within the conserved D4/D1 DNA-binding groove, whereas the D1/D3 binding site near the active center remains closed. All five complex structures-three in the open form and two in the half-open form-clearly show that local base binding within the D4/D1 groove is adaptable and involves both direct and water-mediated contacts, consistent with limited sequence specificity. These findings suggest that ssDNA engagement by EcTopo3 may proceed in a stepwise manner, with partial binding in the D4/D1 groove preceding, or occurring independently of, full opening of the D1/D3 site. The half-open structures also identify a distinct metal-binding site on a glycine-rich loop near the active site, occupied by a metal cation coordinated by backbone carbonyls and conserved water molecules. Together, these results reveal greater conformational and mechanistic flexibility in EcTopo3-ssDNA binding than previously appreciated. PubMed: 42601361DOI: 10.1038/s41598-026-57834-2 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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