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1T8E

T7 DNA Polymerase Ternary Complex with dCTP at the Insertion Site.

1T8E の概要
エントリーDOI10.2210/pdb1t8e/pdb
分子名称5'-D(P*CP*GP*AP*AP*AP*AP*CP*GP*AP*CP*GP*GP*CP*CP*AP*GP*TP*GP*CP*CP*AP*(2DT))-3', 25-MER, DNA polymerase, ... (10 entities in total)
機能のキーワードprotein, dna, transferase, transferase-electron transport-dna complex, transferase/electron transport/dna
由来する生物種Enterobacteria phage T7
詳細
タンパク質・核酸の鎖数4
化学式量合計106552.31
構造登録者
Brieba, L.G.,Eichman, B.F.,Kokoska, R.J.,Doublie, S.,Kunkel, T.A.,Ellenberger, T. (登録日: 2004-05-12, 公開日: 2004-10-12, 最終更新日: 2024-02-14)
主引用文献Brieba, L.G.,Eichman, B.F.,Kokoska, R.J.,Doublie, S.,Kunkel, T.A.,Ellenberger, T.
Structural basis for the dual coding potential of 8-oxoguanosine by a high-fidelity DNA polymerase.
Embo J., 23:3452-3461, 2004
Cited by
PubMed Abstract: Accurate DNA replication involves polymerases with high nucleotide selectivity and proofreading activity. We show here why both fidelity mechanisms fail when normally accurate T7 DNA polymerase bypasses the common oxidative lesion 8-oxo-7, 8-dihydro-2'-deoxyguanosine (8oG). The crystal structure of the polymerase with 8oG templating dC insertion shows that the O8 oxygen is tolerated by strong kinking of the DNA template. A model of a corresponding structure with dATP predicts steric and electrostatic clashes that would reduce but not eliminate insertion of dA. The structure of a postinsertional complex shows 8oG(syn).dA (anti) in a Hoogsteen-like base pair at the 3' terminus, and polymerase interactions with the minor groove surface of the mismatch that mimic those with undamaged, matched base pairs. This explains why translesion synthesis is permitted without proofreading of an 8oG.dA mismatch, thus providing insight into the high mutagenic potential of 8oG.
PubMed: 15297882
DOI: 10.1038/sj.emboj.7600354
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.54 Å)
構造検証レポート
Validation report summary of 1t8e
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-13に公開中

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