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1H, 13C, and 15N backbone chemical shift assignments of coronavirus-2 non-structural protein Nsp10

Authors :
Kubatova, Nina
Qureshi, Nusrat
Altınçekiç, Nadide
Abele, Rupert
Bains, Jasleen Kaur
Ceylan, Betül
Ferner, Jan
Fuks, Christin
Hargittay, Bruno
Hutchison, Marie
de Jesus, Vanessa
Kutz, Felicitas
Wirtz Martin, Maria Alexandra
Meiser, Nathalie
Linhard, Verena
Pyper, Dennis Joshua
Trucks, Sven
Fürtig, Boris
Hengesbach, Martin
Löhr, Frank
Richter, Christian
Saxena, Krishna
Schlundt, Andreas
Schwalbe, Harald
Sreeramulu, Sridhar
Wacker, Anna
Weigand, Julia
Wirmer-Bartoschek, Julia
Wöhnert, Jens
Kubatova, Nina
Qureshi, Nusrat
Altınçekiç, Nadide
Abele, Rupert
Bains, Jasleen Kaur
Ceylan, Betül
Ferner, Jan
Fuks, Christin
Hargittay, Bruno
Hutchison, Marie
de Jesus, Vanessa
Kutz, Felicitas
Wirtz Martin, Maria Alexandra
Meiser, Nathalie
Linhard, Verena
Pyper, Dennis Joshua
Trucks, Sven
Fürtig, Boris
Hengesbach, Martin
Löhr, Frank
Richter, Christian
Saxena, Krishna
Schlundt, Andreas
Schwalbe, Harald
Sreeramulu, Sridhar
Wacker, Anna
Weigand, Julia
Wirmer-Bartoschek, Julia
Wöhnert, Jens
Publication Year :
2020

Abstract

The international Covid19-NMR consortium aims at the comprehensive spectroscopic characterization of SARS-CoV-2 RNA elements and proteins and will provide NMR chemical shift assignments of the molecular components of this virus. The SARS-CoV-2 genome encodes approximately 30 different proteins. Four of these proteins are involved in forming the viral envelope or in the packaging of the RNA genome and are therefore called structural proteins. The other proteins fulfill a variety of functions during the viral life cycle and comprise the so-called non-structural proteins (nsps). Here, we report the near-complete NMR resonance assignment for the backbone chemical shifts of the non-structural protein 10 (nsp10). Nsp10 is part of the viral replication-transcription complex (RTC). It aids in synthesizing and modifying the genomic and subgenomic RNAs. Via its interaction with nsp14, it ensures transcriptional fidelity of the RNA-dependent RNA polymerase, and through its stimulation of the methyltransferase activity of nsp16, it aids in synthesizing the RNA cap structures which protect the viral RNAs from being recognized by the innate immune system. Both of these functions can be potentially targeted by drugs. Our data will aid in performing additional NMR-based characterizations, and provide a basis for the identification of possible small molecule ligands interfering with nsp10 exerting its essential role in viral replication.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1417379847
Document Type :
Electronic Resource