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8RSJ

Crystal structure of Methanobrevibacter oralis macrodomain in complex with ADPr in open conformation

8RSJ の概要
エントリーDOI10.2210/pdb8rsj/pdb
分子名称O-acetyl-ADP-ribose deacetylase, ZINC ION, [[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] [(2~{R},3~{S},4~{S})-2,3,4,5-tetrakis(oxidanyl)pentyl] hydrogen phosphate, ... (5 entities in total)
機能のキーワードadp-ribosylation, adp-ribose, adp-ribosylhydrolase, lipoylation, metalloenzyme, hydrolase
由来する生物種Methanobrevibacter oralis
タンパク質・核酸の鎖数2
化学式量合計60689.13
構造登録者
Ariza, A. (登録日: 2024-01-24, 公開日: 2024-09-25, 最終更新日: 2024-10-16)
主引用文献Ariza, A.,Liu, Q.,Cowieson, N.P.,Ahel, I.,Filippov, D.V.,Rack, J.G.M.
Evolutionary and molecular basis of ADP-ribosylation reversal by zinc-dependent macrodomains.
J.Biol.Chem., 300:107770-107770, 2024
Cited by
PubMed Abstract: Dynamic ADP-ribosylation signalling is a crucial pathway that controls fundamental cellular processes, in particular, the response to cellular stresses such as DNA damage, reactive oxygen species and infection. In some pathogenic microbes the response to oxidative stress is controlled by a SirTM/zinc-containing macrodomain (Zn-Macro) pair responsible for establishment and removal of the modification, respectively. Targeting this defence mechanism against the host's innate immune response may lead to novel approaches to support the fight against emerging antimicrobial resistance. Earlier studies suggested that Zn-Macros play a key role in the activation of this defence. Therefore, we used phylogenetic, biochemical, and structural approaches to elucidate the functional properties of these enzymes. Using the substrate mimetic asparagine-ADP-ribose as well as the ADP-ribose product, we characterise the catalytic role of the zinc ion in the removal of the ADP-ribosyl modification. Furthermore, we determined structural properties that contribute to substrate selectivity within the different Zn-Macro branches. Together, our data not only give new insights into the Zn-Macro family but also highlight their distinct features that may be exploited for the development of future therapies.
PubMed: 39270823
DOI: 10.1016/j.jbc.2024.107770
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.66 Å)
構造検証レポート
Validation report summary of 8rsj
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2024-11-06に公開中

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