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DOI | 10.2210/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 | Michalska, K.,Stols, L.,Jedrzejczak, R.,Endres, M.,Babnigg, G.,Kim, Y.,Joachimiak, A.,Center for Structural Genomics of Infectious Diseases (CSGID) (登録日: 2020-04-02, 公開日: 2020-04-15, 最終更新日: 2023-10-18) |
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: 32939273DOI: 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) |
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