6IPF

Post-catalytic Complex of Human DNA Polymerase Mu with Templating Cytosine and Mn-8oxodGMP

6IPF の概要

• エントリーDOI: 10.2210/pdb6ipf/pdb
• 分子名称: DNA-directed DNA/RNA polymerase mu, 1,2-ETHANEDIOL, DNA (5'-D(*CP*GP*GP*CP*CP*TP*AP*CP*G)-3'), ... (11 entities in total)
• 機能のキーワード: dna polymerase mu, dna break repair, transferase-dna complex, 8-oxo-dgtp, transferase/dna
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 46703.12

構造登録者

Chang, Y.K.,Wu, W.J.,Tsai, M.D. (登録日: 2018-11-03, 公開日: 2019-05-29, 最終更新日: 2024-03-27)

主引用文献

Chang, Y.K.,Huang, Y.P.,Liu, X.X.,Ko, T.P.,Bessho, Y.,Kawano, Y.,Maestre-Reyna, M.,Wu, W.J.,Tsai, M.D.
Human DNA Polymerase mu Can Use a Noncanonical Mechanism for Multiple Mn2+-Mediated Functions.
J.Am.Chem.Soc., 141:8489-8502, 2019

PubMed Abstract: Recent research on the structure and mechanism of DNA polymerases has continued to generate fundamentally important features, including a noncanonical pathway involving "prebinding" of metal-bound dNTP (MdNTP) in the absence of DNA. While this noncanonical mechanism was shown to be a possible subset for African swine fever DNA polymerase X (Pol X) and human Pol λ, it remains unknown whether it could be the primary pathway for a DNA polymerase. Pol μ is a unique member of the X-family with multiple functions and with unusual Mn preference. Here we report that Pol μ not only prebinds MdNTP in a catalytically active conformation but also exerts a Mn over Mg preference at this early stage of catalysis, for various functions: incorporation of dNTP into a single nucleotide gapped DNA, incorporation of rNTP in the nonhomologous end joining (NHEJ) repair, incorporation of dNTP to an ssDNA, and incorporation of an 8-oxo-dGTP opposite template dA (mismatched) or dC (matched). The structural basis of this noncanonical mechanism and Mn over Mg preference in these functions was analyzed by solving 19 structures of prebinding binary complexes, precatalytic ternary complexes, and product complexes. The results suggest that the noncanonical pathway is functionally relevant for the multiple functions of Pol μ. Overall, this work provides the structural and mechanistic basis for the long-standing puzzle in the Mn preference of Pol μ and expands the landscape of the possible mechanisms of DNA polymerases to include both mechanistic pathways.

PubMed: 31067051
DOI: 10.1021/jacs.9b01741

実験手法

X-RAY DIFFRACTION (1.77 Å)