3BJY
Catalytic core of Rev1 in complex with DNA (modified template guanine) and incoming nucleotide
3BJY の概要
| エントリーDOI | 10.2210/pdb3bjy/pdb |
| 関連するPDBエントリー | 2AQ4 |
| 分子名称 | DNA repair protein REV1, DNA (5'-D(*DTP*DAP*DAP*(P)P*DGP*DTP*DAP*DGP*DGP*DGP*DGP*DAP*DGP*DGP*DAP*DT)-3'), DNA (5'-D(*DAP*DTP*DCP*DCP*DTP*DCP*DCP*DCP*DCP*DTP*DAP*(DOC))-3'), ... (6 entities in total) |
| 機能のキーワード | dna polymerase, protein-dna complex, adduct, bypass, dna damage, dna repair, dna synthesis, dna-binding, magnesium, metal-binding, nucleotidyltransferase, nucleus, transferase, transferase-dna complex, transferase/dna |
| 由来する生物種 | Saccharomyces cerevisiae (yeast) |
| 細胞内の位置 | Nucleus: P12689 |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 58578.40 |
| 構造登録者 | Nair, D.T.,Johnson, R.E.,Prakash, L.,Prakash, S.,Aggarwal, A.K. (登録日: 2007-12-05, 公開日: 2008-10-28, 最終更新日: 2025-06-04) |
| 主引用文献 | Nair, D.T.,Johnson, R.E.,Prakash, L.,Prakash, S.,Aggarwal, A.K. Protein-template-directed synthesis across an acrolein-derived DNA adduct by yeast Rev1 DNA polymerase Structure, 16:239-245, 2008 Cited by PubMed Abstract: Acrolein is generated as the end product of lipid peroxidation and is also a ubiquitous environmental pollutant. Its reaction with the N2 of guanine leads to a cyclic gamma-HOPdG adduct that presents a block to normal replication. We show here that yeast Rev1 incorporates the correct nucleotide C opposite a permanently ring-closed form of gamma-HOPdG (PdG) with nearly the same efficiency as opposite an undamaged G. The structural basis of this action lies in the eviction of the PdG adduct from the Rev1 active site, and the pairing of incoming dCTP with a "surrogate" arginine residue. We also show that yeast Polzeta can carry out the subsequent extension reaction. Together, our studies reveal how the exocyclic PdG adduct is accommodated in a DNA polymerase active site, and they show that the combined action of Rev1 and Polzeta provides for accurate and efficient synthesis through this potentially carcinogenic DNA lesion. PubMed: 18275815DOI: 10.1016/j.str.2007.12.009 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.41 Å) |
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