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PDBsum entry 6is7

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Top Page protein dna_rna metals links
Transferase/DNA PDB id
6is7
Contents
Protein chains
757 a.a.
DNA/RNA
Metals
_CA ×7
Waters ×213

References listed in PDB file
Key reference
Title thermococcus sp. 9°n DNA polymerase exhibits 3'-Esterase activity that can be harnessed for DNA sequencing.
Authors S.W.Linwu, Y.H.Tu, T.Y.Tsai, M.Maestre-Reyna, M.S.Liu, W.J.Wu, J.Y.Huang, H.W.Chi, W.H.Chang, C.F.Chiou, A.H.Wang, J.Lee, M.D.Tsai.
Ref. Commun Biol, 2019, 2, 224. [DOI no: 10.1038/s42003-019-0458-7]
PubMed id 31240262
Abstract
It was reported in 1995 that T7 and Taq DNA polymerases possess 3'-esterase activity, but without follow-up studies. Here we report that the 3'-esterase activity is intrinsic to the Thermococcus sp. 9°N DNA polymerase, and that it can be developed into a continuous method for DNA sequencing with dNTP analogs carrying a 3'-ester with a fluorophore. We first show that 3'-esterified dNTP can be incorporated into a template-primer DNA, and solve the crystal structures of the reaction intermediates and products. Then we show that the reaction can occur continuously, modulated by active site residues Tyr409 and Asp542. Finally, we use 5'-FAM-labeled primer and esterified dNTP with a dye to show that the reaction can proceed to ca. 450 base pairs, and that the intermediates of many individual steps can be identified. The results demonstrate the feasibility of a 3'-editing based DNA sequencing method that could find practical applications after further optimization.
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