8XK9
ternary complex of DNA polymerase SFM4-3 recognizing C2 methyoxy nucleotide
This is a non-PDB format compatible entry.
Summary for 8XK9
| Entry DOI | 10.2210/pdb8xk9/pdb |
| Related | 8XJR 8XK7 |
| Descriptor | DNA (5'-D(*GP*AP*CP*CP*AP*CP*GP*GP*CP*GP*CP*(DOC))-3'), DNA (5'-D(*AP*AP*CP*GP*GP*CP*GP*CP*CP*GP*TP*GP*GP*TP*C)-R(P*(OMG))-3'), DNA polymerase I, thermostable, ... (8 entities in total) |
| Functional Keywords | dna polymerase, dna binding protein |
| Biological source | Thermus aquaticus More |
| Total number of polymer chains | 6 |
| Total formula weight | 140391.28 |
| Authors | |
| Primary citation | Wen, C.,Wang, G.,Yang, L.,Chen, T.,Liu, H.,Gong, W. Structural Basis for C2'-methoxy Recognition by DNA Polymerases and Function Improvement. J.Mol.Biol., 436:168744-168744, 2024 Cited by PubMed Abstract: DNA modified with C2'-methoxy (C2'-OMe) greatly enhances its resistance to nucleases, which is beneficial for the half-life of aptamers and DNA nanomaterials. Although the unnatural DNA polymerases capable of incorporating C2'-OMe modified nucleoside monophosphates (C2'-OMe-NMPs) were engineered via directed evolution, the detailed molecular mechanism by which an evolved DNA polymerase recognizes C2'-OMe-NTPs remains poorly understood. Here, we present the crystal structures of the evolved Stoffel fragment of Taq DNA polymerase SFM4-3 processing the C2'-OMe-GTP in different states. Our results reveal the structural basis for recognition of C2'-methoxy by SFM4-3. Based on the analysis of other mutated residues in SFM4-3, a new Stoffel fragment variant with faster catalytic rate and stronger inhibitor-resistance was obtained. In addition, the capture of a novel pre-insertion co-existing with template 5'-overhang stacking conformation provides insight into the catalytic mechanism of Taq DNA polymerase. PubMed: 39147125DOI: 10.1016/j.jmb.2024.168744 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.4 Å) |
Structure validation
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