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PDBsum entry 6btf

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Top Page protein dna_rna ligands metals links
Transferase,lyase/DNA PDB id
6btf
Contents
Protein chain
317 a.a.
DNA/RNA
Ligands
DUP
Metals
_NA ×3
_MG
Waters ×337

References listed in PDB file
Key reference
Title I260q DNA polymerase β highlights precatalytic conformational rearrangements critical for fidelity.
Authors C.Liptak, M.M.Mahmoud, B.E.Eckenroth, M.V.Moreno, K.East, K.S.Alnajjar, J.Huang, J.B.Towle-Weicksel, S.Doublié, J.P.Loria, J.B.Sweasy.
Ref. Nucleic Acids Res, 2018, 46, 10740-10756. [DOI no: 10.1093/nar/gky825]
PubMed id 30239932
Abstract
DNA polymerase β (pol β) fills single nucleotide gaps in DNA during base excision repair and non-homologous end-joining. Pol β must select the correct nucleotide from among a pool of four nucleotides with similar structures and properties in order to maintain genomic stability during DNA repair. Here, we use a combination of X-ray crystallography, fluorescence resonance energy transfer and nuclear magnetic resonance to show that pol β's ability to access the appropriate conformations both before and upon binding to nucleotide substrates is integral to its fidelity. Importantly, we also demonstrate that the inability of the I260Q mutator variant of pol β to properly navigate this conformational landscape results in error-prone DNA synthesis. Our work reveals that precatalytic conformational rearrangements themselves are an important underlying mechanism of substrate selection by DNA pol β.
PROCHECK
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 Headers

 

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