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6WEN

Crystal Structure of ADP ribose phosphatase of NSP3 from SARS-CoV-2 in the apo form

6WEN の概要
エントリーDOI10.2210/pdb6wen/pdb
関連するPDBエントリー6WCF 6vxs 6w02 6w6y
分子名称Non-structural protein 3, CHLORIDE ION (3 entities in total)
機能のキーワードsars coronavirus, structural genomics, center for structural genomics of infectious diseases, csgid, viral protein, hydrolase
由来する生物種Severe acute respiratory syndrome coronavirus 2 (2019-nCoV)
タンパク質・核酸の鎖数1
化学式量合計18311.22
構造登録者
主引用文献Michalska, K.,Kim, Y.,Jedrzejczak, R.,Maltseva, N.I.,Stols, L.,Endres, M.,Joachimiak, A.
Crystal structures of SARS-CoV-2 ADP-ribose phosphatase: from the apo form to ligand complexes.
Iucrj, 7:814-824, 2020
Cited by
PubMed Abstract: Among 15 nonstructural proteins (Nsps), the newly emerging Severe Acute Respiratory Syndrome coronavirus 2 (SARS-CoV-2) encodes a large, multidomain Nsp3. One of its units is the ADP-ribose phosphatase domain (ADRP; also known as the macrodomain, MacroD), which is believed to interfere with the host immune response. Such a function appears to be linked to the ability of the protein to remove ADP-ribose from ADP-ribosylated proteins and RNA, yet the precise role and molecular targets of the enzyme remain unknown. Here, five high-resolution (1.07-2.01 Å) crystal structures corresponding to the apo form of the protein and its complexes with 2-(-morpholino)ethanesulfonic acid (MES), AMP and ADP-ribose have been determined. The protein is shown to undergo conformational changes to adapt to the ligand in the manner previously observed in close homologues from other viruses. A conserved water molecule is also identified that may participate in hydrolysis. This work builds foundations for future structure-based research on ADRP, including the search for potential antiviral therapeutics.
PubMed: 32939273
DOI: 10.1107/S2052252520009653
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.35 Å)
構造検証レポート
Validation report summary of 6wen
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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