1H, 13C and 15N chemical shift assignment of the stem-loop 5a from the 5′-UTR of SARS-CoV-2

Author:

Schnieders Robbin,Peter Stephen A.,Banijamali Elnaz,Riad Magdalena,Altincekic Nadide,Bains Jasleen Kaur,Ceylan Betül,Fürtig Boris,Grün J. Tassilo,Hengesbach Martin,Hohmann Katharina F.,Hymon Daniel,Knezic Bozana,Oxenfarth Andreas,Petzold Katja,Qureshi Nusrat S.,Richter Christian,Schlagnitweit Judith,Schlundt Andreas,Schwalbe HaraldORCID,Stirnal Elke,Sudakov Alexey,Vögele Jennifer,Wacker Anna,Weigand Julia E.,Wirmer-Bartoschek Julia,Wöhnert Jens

Abstract

AbstractThe SARS-CoV-2 (SCoV-2) virus is the causative agent of the ongoing COVID-19 pandemic. It contains a positive sense single-stranded RNA genome and belongs to the genus of Betacoronaviruses. The 5′- and 3′-genomic ends of the 30 kb SCoV-2 genome are potential antiviral drug targets. Major parts of these sequences are highly conserved among Betacoronaviruses and contain cis-acting RNA elements that affect RNA translation and replication. The 31 nucleotide (nt) long highly conserved stem-loop 5a (SL5a) is located within the 5′-untranslated region (5′-UTR) important for viral replication. SL5a features a U-rich asymmetric bulge and is capped with a 5′-UUUCGU-3′ hexaloop, which is also found in stem-loop 5b (SL5b). We herein report the extensive 1H, 13C and 15N resonance assignment of SL5a as basis for in-depth structural studies by solution NMR spectroscopy.

Funder

Deutsche Forschungsgemeinschaft

Hessisches Ministerium für Wissenschaft und Kunst

Goethe-Universität Frankfurt am Main

Karolinska Institutet

Projekt DEAL

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry,Structural Biology

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