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7ED5

A dual mechanism of action of AT-527 against SARS-CoV-2 polymerase

7ED5 の概要
エントリーDOI10.2210/pdb7ed5/pdb
EMDBエントリー31061
分子名称RNA-directed RNA polymerase, Non-structural protein 8, Non-structural protein 7, ... (8 entities in total)
機能のキーワードsars-cov-2, nsp12, niran, rdrp, at-9010, at-527, viral protein
由来する生物種Severe acute respiratory syndrome coronavirus 2
詳細
タンパク質・核酸の鎖数6
化学式量合計189253.30
構造登録者
主引用文献Shannon, A.,Fattorini, V.,Sama, B.,Selisko, B.,Feracci, M.,Falcou, C.,Gauffre, P.,El Kazzi, P.,Delpal, A.,Decroly, E.,Alvarez, K.,Eydoux, C.,Guillemot, J.C.,Moussa, A.,Good, S.S.,La Colla, P.,Lin, K.,Sommadossi, J.P.,Zhu, Y.,Yan, X.,Shi, H.,Ferron, F.,Canard, B.
A dual mechanism of action of AT-527 against SARS-CoV-2 polymerase.
Nat Commun, 13:621-621, 2022
Cited by
PubMed Abstract: The guanosine analog AT-527 represents a promising candidate against Severe Acute Respiratory Syndrome coronavirus type 2 (SARS-CoV-2). AT-527 recently entered phase III clinical trials for the treatment of COVID-19. Once in cells, AT-527 is converted into its triphosphate form, AT-9010, that presumably targets the viral RNA-dependent RNA polymerase (RdRp, nsp12), for incorporation into viral RNA. Here we report a 2.98 Å cryo-EM structure of the SARS-CoV-2 nsp12-nsp7-nsp8-RNA complex, showing AT-9010 bound at three sites of nsp12. In the RdRp active-site, one AT-9010 is incorporated at the 3' end of the RNA product strand. Its modified ribose group (2'-fluoro, 2'-methyl) prevents correct alignment of the incoming NTP, in this case a second AT-9010, causing immediate termination of RNA synthesis. The third AT-9010 is bound to the N-terminal domain of nsp12 - known as the NiRAN. In contrast to native NTPs, AT-9010 is in a flipped orientation in the active-site, with its guanine base unexpectedly occupying a previously unnoticed cavity. AT-9010 outcompetes all native nucleotides for NiRAN binding, inhibiting its nucleotidyltransferase activity. The dual mechanism of action of AT-527 at both RdRp and NiRAN active sites represents a promising research avenue against COVID-19.
PubMed: 35110538
DOI: 10.1038/s41467-022-28113-1
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.98 Å)
構造検証レポート
Validation report summary of 7ed5
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2026-02-04に公開中

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