Short peptides derived from the interaction domain of SARS coronavirus nonstructural protein nsp10 can suppress the 2'-O-methyltransferase activity of nsp10/nsp16 complex (Q84279534)

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scientific article published on 29 May 2012

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English	Short peptides derived from the interaction domain of SARS coronavirus nonstructural protein nsp10 can suppress the 2'-O-methyltransferase activity of nsp10/nsp16 complex	scientific article published on 29 May 2012

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3 February 2020

Short peptides derived from the interaction domain of SARS coronavirus nonstructural protein nsp10 can suppress the 2'-O-methyltransferase activity of nsp10/nsp16 complex (English)

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3 February 2020

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Min Ke

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Yu Chen

2

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Andong Wu

3

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Ying Sun

4

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Ceyang Su

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Hao Wu

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Xu Jin

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Jiali Tao

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Yi Wang

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Xiao Ma

10

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Ji-An Pan

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Deyin Guo

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publication date

29 May 2012

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322-328

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3 February 2020

Update on SARS research and other possibly zoonotic coronaviruses

1 reference

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In vitro reconstitution of SARS-coronavirus mRNA cap methylation

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Biochemical characterization of exoribonuclease encoded by SARS coronavirus

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Functional screen reveals SARS coronavirus nonstructural protein nsp14 as a novel cap N7 methyltransferase

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Biochemical and Structural Insights into the Mechanisms of SARS Coronavirus RNA Ribose 2′-O-Methylation by nsp16/nsp10 Protein Complex

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2'-O methylation of the viral mRNA cap evades host restriction by IFIT family members

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Crystallization and diffraction analysis of the SARS coronavirus nsp10-nsp16 complex

1 reference

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7 January 2021

Crystal Structure and Functional Analysis of the SARS-Coronavirus RNA Cap 2′-O-Methyltransferase nsp10/nsp16 Complex

1 reference

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7 January 2021

Coronavirus nonstructural protein 16 is a cap-0 binding enzyme possessing (nucleoside-2'O)-methyltransferase activity

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Flavivirus methyltransferase: a novel antiviral target

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Programmed -1 ribosomal frameshifting in the SARS coronavirus

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Potent and selective inhibition of SARS coronavirus replication by aurintricarboxylic acid

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The SARS-Coronavirus PLnc domain of nsp3 as a replication/transcription scaffolding protein

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Crystal structure of nonstructural protein 10 from the severe acute respiratory syndrome coronavirus reveals a novel fold with two zinc-binding motifs

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Molecular mapping of the RNA Cap 2'-O-methyltransferase activation interface between severe acute respiratory syndrome coronavirus nsp10 and nsp16.

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Unique and conserved features of genome and proteome of SARS-coronavirus, an early split-off from the coronavirus group 2 lineage

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Dodecamer structure of severe acute respiratory syndrome coronavirus nonstructural protein nsp10.

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Therapies for coronaviruses. Part 2: Inhibitors of intracellular life cycle.

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Therapies for coronaviruses. Part I of II -- viral entry inhibitors

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SARS-coronavirus replication/transcription complexes are membrane-protected and need a host factor for activity in vitro

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Analysis of intraviral protein-protein interactions of the SARS coronavirus ORFeome

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Ribose 2'-O-methylation provides a molecular signature for the distinction of self and non-self mRNA dependent on the RNA sensor Mda5.

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12 December 2020

based on heuristic

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The RNA capping machinery as an anti-infective target

1 reference

https://pubmed.ncbi.nlm.nih.gov/22659295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Critical residues of Semliki Forest virus RNA capping enzyme involved in methyltransferase and guanylyltransferase-like activities

1 reference

https://pubmed.ncbi.nlm.nih.gov/22659295

12 December 2020

based on heuristic

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10.1016/J.VIRUSRES.2012.05.017

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Europe PubMed Central

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3 February 2020

1 reference

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3 February 2020

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