H, C and N chemical shift assignment for stem-loop 5a from the 5’UTR of HCoV-229E.

Publication date: Jul 31, 2025

Due to the emergence of the SARS-CoV-2 virus, research on coronaviruses has been massively accelerated. In addition to SARS-CoV-2, there are other human coronaviruses, including HCoV-229E. In all coronaviruses, secondary structure predictions indicate the presence of conserved structural elements in the 5′-untranslated region (5′-UTR). These conserved elements play crucial roles in RNA translation and replication. Stem-loop 5 (SL5), consisting of three substructures (5a, 5b, 5c), is highly conserved and harbours the start codon for translation. SL5 has repetitive structural motifs (RSMs), 5′-UUYYGU-3′, which are conserved in many alpha- and betacoronaviruses. In the following, we present the H, C and N NMR resonance assignment of the SL5a RNA element from HCoV-229E and variations in the RSMs to show the effect of loop mutations on the structure of the hexaloop, revealing the different impact of each loop nucleotide on RNA dynamics.

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Concepts Keywords
229e 5‘-UTR
Accelerated Coronaviruses
Coronaviruses HCoV-229E
Mutations SL5a
Nucleotide Solution NMR spectroscopy

Semantics

Type Source Name
pathway REACTOME Translation
disease IDO replication
pathway KEGG Viral replication
drug DRUGBANK Sodium lauryl sulfate
disease MESH COVID 19
disease IDO host
drug DRUGBANK Edetic Acid
drug DRUGBANK Peracetic acid
disease MESH shock
drug DRUGBANK Acetate ion
drug DRUGBANK Flunarizine
drug DRUGBANK Potassium Chloride
drug DRUGBANK Monopotassium phosphate
drug DRUGBANK Phosphate ion
disease IDO production
drug DRUGBANK Cysteamine
drug DRUGBANK Cinacalcet
drug DRUGBANK Tretamine
drug DRUGBANK Guanosine
drug DRUGBANK Coenzyme M
drug DRUGBANK Water
drug DRUGBANK Activated charcoal
drug DRUGBANK Uridine
drug DRUGBANK Cytidine
drug DRUGBANK Fenamole
drug DRUGBANK Ezogabine
pathway REACTOME Reproduction
drug DRUGBANK Nitrogen
drug DRUGBANK Amino acids

Original Article

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