9F8V

Structure of the mouse 8-oxoguanine DNA Glycosylase mOGG1 in complex with ligand TH7420

これはPDB形式変換不可エントリーです。

9F8V の概要

• エントリーDOI: 10.2210/pdb9f8v/pdb
• 分子名称: N-glycosylase/DNA lyase, 2-azanyl-8-propyl-3,7-dihydropurine-6-thione, NICKEL (II) ION, ... (4 entities in total)
• 機能のキーワード: ogg1, dna binding protein
• 由来する生物種: Mus musculus (house mouse)
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 108136.46

構造登録者

Scaletti, E.,Kosenina, S.,Stenmark, P. (登録日: 2024-05-07, 公開日: 2025-05-21, 最終更新日: 2026-01-28)

主引用文献

Hank, E.C.,D'Arcy-Evans, N.D.,Scaletti, E.R.,Benitez-Buelga, C.,Wallner, O.,Ortis, F.,Zhou, K.,Meng, L.,Del Prado, A.,Calvo, P.,Almlof, I.,Wiita, E.,Nierlin, K.,Kosenina, S.,Kramer, A.,Eddershaw, A.,Kehler, M.,Long, M.,Jemth, A.S.,Dawson, H.,Stewart, J.,Dickey, A.,Astorga, M.E.,Varga, M.,Homan, E.J.,Scobie, M.,Knapp, S.,Sastre, L.,Stenmark, P.,de Vega, M.,Helleday, T.,Michel, M.
Nucleobase catalysts for the enzymatic activation of 8-oxoguanine DNA glycosylase 1.
Rsc Chem Biol, 7:169-181, 2026

PubMed Abstract: Bifunctional DNA glycosylases employ an active site lysine or the N-terminus to form a Schiff base with an abasic (AP) site base excision repair intermediate. For 8-oxoguanine DNA glycosylase 1 (OGG1), cleaving this reversible structure is the rate-determining step in the initiation of 8-oxoguanine (8-oxoG) repair in DNA. Evolution has led OGG1 to use a product-assisted catalysis approach, where the excised 8-oxoG acts as a Brønsted base for cleavage of a Schiff base intermediate. However, the physicochemical properties of 8-oxoG significantly limit the inherent enzymatic turnover leading to a weak, cellularly absent, AP lyase activity. We hypothesized that chemical synthesis of purine analogues enables access to complex structures that are suitable as product-like catalysts. Herein, the nucleobase landscape is profiled for its potential to increase OGG1 Schiff base cleavage. 8-Substituted 6-thioguanines emerge as potent and selective scaffolds enabling OGG1 to cleave AP sites opposite any canonical nucleobase by β-elimination. This effectively broadens the enzymatic substrate scope of OGG1, shaping a complete, artificial AP-lyase function. In addition, a second class of compounds, 6-substituted pyrazolo-[3,4-]-pyrimidines, stimulate OGG1 function at high pH, while thioguanines govern enzymatic control at acidic pH. This enables up to 20-fold increased enzyme turnover and a OGG1 β-elimination in conditions commonly not tolerated. The tool compounds employed here are non-toxic in cells and stimulate the repair of AP sites through a natural, APE1 dependent pathway, as opposed to previously reported β,δ-lyase stimulator TH10785.

PubMed: 41195166
DOI: 10.1039/d4cb00323c

実験手法

X-RAY DIFFRACTION (2.4 Å)