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6P5C

Bacillus Fragment DNA polymerase mutant I716M

Summary for 6P5C
Entry DOI10.2210/pdb6p5c/pdb
DescriptorDNA (5'-D(*CP*GP*AP*TP*CP*AP*CP*GP*C)-3'), DNA (5'-D(P*GP*CP*GP*TP*GP*AP*TP*CP*G)-3'), DNA polymerase I, ... (5 entities in total)
Functional Keywordspolymerase, replication, transferase, replication-dna complex, replication/dna
Biological sourceGeobacillus stearothermophilus
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Total number of polymer chains3
Total formula weight72178.95
Authors
Wu, E.Y. (deposition date: 2019-05-30, release date: 2020-03-25, Last modification date: 2023-10-11)
Primary citationHamm, M.L.,Garcia, A.A.,Gilbert, R.,Johri, M.,Ricart, M.,Sholes, S.L.,Murray-Nerger, L.A.,Wu, E.Y.
The importance of Ile716 toward the mutagenicity of 8-Oxo-2'-deoxyguanosine with Bacillus fragment DNA polymerase.
DNA Repair (Amst.), 89:102826-102826, 2020
Cited by
PubMed Abstract: 8-oxo-2'-deoxyguanosine (OdG) is a prominent DNA lesion that can direct the incorporation of dCTP or dATP during replication. As the latter reaction can lead to mutation, the ratio of dCTP/dATP incorporation can significantly affect the mutagenic potential of OdG. Previous work with the A-family polymerase BF and seven analogues of OdG identified a major groove amino acid, Ile716, which likely influences the dCTP/dATP incorporation ratio opposite OdG. To further probe the importance of this amino acid, dCTP and dATP incorporations opposite the same seven analogues were tested with two BF mutants, I716M and I716A. Results from these studies support the presence of clashing interactions between Ile716 and the C8-oxygen and C2-amine during dCTP and dATP incorporations, respectively. Crystallographic analysis suggests that residue 716 alters the conformation of the template base prior to insertion into the active site, thereby affecting enzymatic efficiency. These results are also consistent with previous work with A-family polymerases, which indicate they have tight, rigid active sites that are sensitive to template perturbations.
PubMed: 32113909
DOI: 10.1016/j.dnarep.2020.102826
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

237735

數據於2025-06-18公開中

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