Accessory proteins of SARS-CoV and other coronaviruses (Q38226293)

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scientific article published on July 2014

Language	Label	Description	Also known as
English	Accessory proteins of SARS-CoV and other coronaviruses	scientific article published on July 2014

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

2 references

13 July 2022

22 October 2022

Accessory proteins of SARS-CoV and other coronaviruses (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

0 references

Protein 3a [SARS-Cov]

1 reference

based on heuristic

inferred from abstract

Rolf Hilgenfeld

5

object named as

Rolf Hilgenfeld

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

author name string

Ding Xiang Liu

1

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

To Sing Fung

2

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

Kelvin Kian-Long Chong

3

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

Aditi Shukla

4

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

publication date

1 July 2014

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

1 September 2014

2 references

13 July 2022

22 October 2022

Antiviral Research

3 references

Europe PubMed Central

PubMed publication ID

31 August 2017

13 July 2022

22 October 2022

109

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

97-109

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

Inhibition of SARS-CoV replication cycle by small interference RNAs silencing specific SARS proteins, 7a/7b, 3a/3b and S.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Structural insights into SARS coronavirus proteins

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Identification of a noncanonically transcribed subgenomic mRNA of infectious bronchitis virus and other gammacoronaviruses

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Signals for sorting of transmembrane proteins to endosomes and lysosomes

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The HIV-1 Vpu protein: a multifunctional enhancer of viral particle release.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Folding of viral envelope glycoproteins in the endoplasmic reticulum

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus accessory proteins 6 and 9b interact in vivo.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Gene 5 of the avian coronavirus infectious bronchitis virus is not essential for replication

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The ion channel activity of the SARS-coronavirus 3a protein is linked to its pro-apoptotic function.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The protein X4 of severe acute respiratory syndrome-associated coronavirus is expressed on both virus-infected cells and lung tissue of severe acute respiratory syndrome patients and inhibits growth of Balb/c 3T3 cell line.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Open reading frame 8a of the human severe acute respiratory syndrome coronavirus not only promotes viral replication but also induces apoptosis

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

TreeDyn: towards dynamic graphics and annotations for analyses of trees

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Assembling an ion channel: ORF 3a from SARS-CoV

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Tracing SARS-coronavirus variant with large genomic deletion

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Alphacoronavirus protein 7 modulates host innate immune response

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The group-specific murine coronavirus genes are not essential, but their deletion, by reverse genetics, is attenuating in the natural host

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The role of accessory proteins in the replication of feline infectious peritonitis virus in peripheral blood monocytes

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

ORF7-encoded accessory protein 7a of feline infectious peritonitis virus as a counteragent against IFN-α-induced antiviral response

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Pathogenicity of severe acute respiratory coronavirus deletion mutants in hACE-2 transgenic mice.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Human coronavirus 229E encodes a single ORF4 protein between the spike and the envelope genes

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The first complete genome sequences of clinical isolates of human coronavirus 229E

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus protein 7a interacts with hSGT.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Characterization of a unique group-specific protein (U122) of the severe acute respiratory syndrome coronavirus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The internal open reading frame within the nucleocapsid gene of mouse hepatitis virus encodes a structural protein that is not essential for viral replication

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The open reading frame 3a protein of severe acute respiratory syndrome-associated coronavirus promotes membrane rearrangement and cell death

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Molecular determinants for subcellular localization of the severe acute respiratory syndrome coronavirus open reading frame 3b protein

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus ORF6 antagonizes STAT1 function by sequestering nuclear import factors on the rough endoplasmic reticulum/Golgi membrane

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The putative protein 6 of the severe acute respiratory syndrome-associated coronavirus: expression and functional characterization

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Isolation and characterization of viruses related to the SARS coronavirus from animals in southern China

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

A putative diacidic motif in the SARS-CoV ORF6 protein influences its subcellular localization and suppression of expression of co-transfected expression constructs.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS corona virus peptides recognized by antibodies in the sera of convalescent cases

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Live, attenuated coronavirus vaccines through the directed deletion of group-specific genes provide protection against feline infectious peritonitis

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Solution structure of the X4 protein coded by the SARS related coronavirus reveals an immunoglobulin like fold and suggests a binding activity to integrin I domains

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS-CoV accessory protein 7a directly interacts with human LFA-1

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Molecular evolution of the SARS coronavirus during the course of the SARS epidemic in China

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

From SARS to MERS: 10 years of research on highly pathogenic human coronaviruses

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Neither the RNA nor the proteins of open reading frames 3a and 3b of the coronavirus infectious bronchitis virus are essential for replication

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus 7a accessory protein is a viral structural protein

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus 3a protein is released in membranous structures from 3a protein-expressing cells and infected cells

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus accessory protein 6 is a virion-associated protein and is released from 6 protein-expressing cells

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS-coronavirus protein 6 conformations required to impede protein import into the nucleus.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus protein 6 accelerates murine hepatitis virus infections by more than one mechanism.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus 3a protein is a viral structural protein

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Augmentation of chemokine production by severe acute respiratory syndrome coronavirus 3a/X1 and 7a/X4 proteins through NF-kappaB activation

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The human severe acute respiratory syndrome coronavirus (SARS-CoV) 8b protein is distinct from its counterpart in animal SARS-CoV and down-regulates the expression of the envelope protein in infected cells

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Over-expression of severe acute respiratory syndrome coronavirus 3b protein induces both apoptosis and necrosis in Vero E6 cells

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Coronavirus M proteins accumulate in the Golgi complex beyond the site of virion budding

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulum

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus open reading frame (ORF) 3b, ORF 6, and nucleocapsid proteins function as interferon antagonists

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

7a protein of severe acute respiratory syndrome coronavirus inhibits cellular protein synthesis and activates p38 mitogen-activated protein kinase

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Assembly of Viral Membrane Proteins

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The nonstructural protein 8 (nsp8) of the SARS coronavirus interacts with its ORF6 accessory protein.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The murine coronavirus hemagglutinin-esterase receptor-binding site: a major shift in ligand specificity through modest changes in architecture

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Kalign--an accurate and fast multiple sequence alignment algorithm

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Coexistence of different genotypes in the same bat and serological characterization of Rousettus bat coronavirus HKU9 belonging to a novel Betacoronavirus subgroup

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus-like virus in Chinese horseshoe bats

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Expression and functional characterization of the putative protein 8b of the severe acute respiratory syndrome-associated coronavirus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The 3a protein of severe acute respiratory syndrome-associated coronavirus induces apoptosis in Vero E6 cells

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Expression, post-translational modification and biochemical characterization of proteins encoded by subgenomic mRNA8 of the severe acute respiratory syndrome coronavirus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Upregulation of CHOP/GADD153 during coronavirus infectious bronchitis virus infection modulates apoptosis by restricting activation of the extracellular signal-regulated kinase pathway

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

A polycistronic mRNA specified by the coronavirus infectious bronchitis virus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Association of the infectious bronchitis virus 3c protein with the virion envelope

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Identification of two new polypeptides encoded by mRNA5 of the coronavirus infectious bronchitis virus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Internal entry of ribosomes on a tricistronic mRNA encoded by infectious bronchitis virus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Humoral and cellular immune responses induced by 3a DNA vaccines against severe acute respiratory syndrome (SARS) or SARS-like coronavirus in mice

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome-associated coronavirus 3a protein forms an ion channel and modulates virus release

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Infectious bronchitis viruses with a novel genomic organization

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The Genome sequence of the SARS-associated coronavirus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The molecular biology of coronaviruses

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The ORF4b-encoded accessory proteins of Middle East respiratory syndrome coronavirus and two related bat coronaviruses localize to the nucleus and inhibit innate immune signalling

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Detection of novel members, structure-function analysis and evolutionary classification of the 2H phosphoesterase superfamily

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Characterisation of a recent virulent transmissible gastroenteritis virus from Britain with a deleted ORF 3a.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The crystal structure of ORF-9b, a lipid binding protein from the SARS coronavirus.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The SARS Coronavirus 3a protein causes endoplasmic reticulum stress and induces ligand-independent downregulation of the type 1 interferon receptor

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Intracellular localization of the SARS coronavirus protein 9b: evidence of active export from the nucleus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Differential maturation and subcellular localization of severe acute respiratory syndrome coronavirus surface proteins S, M and E.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS coronavirus accessory proteins.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Structure and intracellular targeting of the SARS-coronavirus Orf7a accessory protein

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Enhancement of murine coronavirus replication by severe acute respiratory syndrome coronavirus protein 6 requires the N-terminal hydrophobic region but not C-terminal sorting motifs

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Middle East respiratory syndrome coronavirus accessory protein 4a is a type I interferon antagonist

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

A di-acidic signal required for selective export from the endoplasmic reticulum

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Analysis of nonessential gene function in recombinant MHV-JHM. Gene 4 knockout recombinant virus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Glycosylation of the severe acute respiratory syndrome coronavirus triple-spanning membrane proteins 3a and M.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The 29-nucleotide deletion present in human but not in animal severe acute respiratory syndrome coronaviruses disrupts the functional expression of open reading frame 8.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus 3a protein activates the mitochondrial death pathway through p38 MAP kinase activation.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus Orf3a protein interacts with caveolin

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Pathogenicity and sequence analysis studies suggest potential role of gene 3 in virulence of swine enteric and respiratory coronaviruses

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The severe acute respiratory syndrome

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Structure, expression, and intracellular localization of the SARS-CoV accessory proteins 7a and 7b.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

A severe acute respiratory syndrome-associated coronavirus-specific protein enhances virulence of an attenuated murine coronavirus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Reverse genetic characterization of the natural genomic deletion in SARS-Coronavirus strain Frankfurt-1 open reading frame 7b reveals an attenuating function of the 7b protein in-vitro and in-vivo

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Antibody responses to individual proteins of SARS coronavirus and their neutralization activities

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Full-length genome sequences of two SARS-like coronaviruses in horseshoe bats and genetic variation analysis

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Characterization of a novel coronavirus associated with severe acute respiratory syndrome

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Assembly in vitro of a spanning membrane protein of the endoplasmic reticulum: the E1 glycoprotein of coronavirus mouse hepatitis virus A59.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Predicted membrane topology of the coronavirus protein E1

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

A contemporary view of coronavirus transcription.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The transmembrane domain of the severe acute respiratory syndrome coronavirus ORF7b protein is necessary and sufficient for its retention in the Golgi complex

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The ORF7b protein of severe acute respiratory syndrome coronavirus (SARS-CoV) is expressed in virus-infected cells and incorporated into SARS-CoV particles

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus gene 7 products contribute to virus-induced apoptosis

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Isolated HE-protein from hemagglutinating encephalomyelitis virus and bovine coronavirus has receptor-destroying and receptor-binding activity

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS-CoV 9b protein diffuses into nucleus, undergoes active Crm1 mediated nucleocytoplasmic export and triggers apoptosis when retained in the nucleus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The 3a accessory protein of SARS coronavirus specifically interacts with the 5'UTR of its genomic RNA, Using a unique 75 amino acid interaction domain.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The severe acute respiratory syndrome coronavirus 3a is a novel structural protein.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Emergence of a coronavirus infectious bronchitis virus mutant with a truncated 3b gene: functional characterization of the 3b protein in pathogenesis and replication

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Atomic structure of a Na+- and K+-conducting channel

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Viral encounters with 2',5'-oligoadenylate synthetase and RNase L during the interferon antiviral response

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Middle east respiratory syndrome coronavirus 4a protein is a double-stranded RNA-binding protein that suppresses PACT-induced activation of RIG-I and MDA5 in the innate antiviral response.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

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

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Inhibition of Beta interferon induction by severe acute respiratory syndrome coronavirus suggests a two-step model for activation of interferon regulatory factor 3.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The 8ab protein of SARS-CoV is a luminal ER membrane-associated protein and induces the activation of ATF6.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The Severe Acute Respiratory Syndrome (SARS)-coronavirus 3a protein may function as a modulator of the trafficking properties of the spike protein

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Genetic lesions within the 3a gene of SARS-CoV.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Overexpression of 7a, a protein specifically encoded by the severe acute respiratory syndrome coronavirus, induces apoptosis via a caspase-dependent pathway

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Profiles of antibody responses against severe acute respiratory syndrome coronavirus recombinant proteins and their potential use as diagnostic markers

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Understanding the accessory viral proteins unique to the severe acute respiratory syndrome (SARS) coronavirus.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus protein 6 accelerates murine coronavirus infections

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Induction of apoptosis by the severe acute respiratory syndrome coronavirus 7a protein is dependent on its interaction with the Bcl-XL protein

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

A novel severe acute respiratory syndrome coronavirus protein, U274, is transported to the cell surface and undergoes endocytosis

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The severe acute respiratory syndrome coronavirus 3a protein up-regulates expression of fibrinogen in lung epithelial cells

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Mechanisms and enzymes involved in SARS coronavirus genome expression

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Signal-dependent membrane protein trafficking in the endocytic pathway

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The 9-kDa hydrophobic protein encoded at the 3' end of the porcine transmissible gastroenteritis coronavirus genome is membrane-associated

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Genomic characterization of a newly discovered coronavirus associated with acute respiratory distress syndrome in humans

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS coronavirus 3b accessory protein modulates transcriptional activity of RUNX1b

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS-CoV accessory protein 3b induces AP-1 transcriptional activity through activation of JNK and ERK pathways

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The E3 protein of bovine coronavirus is a receptor-destroying enzyme with acetylesterase activity

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

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

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Identification of Hepta- and Octo-Uridine stretches as sole signals for programmed +1 and -1 ribosomal frameshifting during translation of SARS-CoV ORF 3a variants

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Coronavirus genomics and bioinformatics analysis

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Comparative analysis of twelve genomes of three novel group 2c and group 2d coronaviruses reveals unique group and subgroup features

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Civets are equally susceptible to experimental infection by two different severe acute respiratory syndrome coronavirus isolates

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus accessory protein 9b is a virion-associated protein

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The structural and accessory proteins M, ORF 4a, ORF 4b, and ORF 5 of Middle East respiratory syndrome coronavirus (MERS-CoV) are potent interferon antagonists

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

A SARS-CoV protein, ORF-6, induces caspase-3 mediated, ER stress and JNK-dependent apoptosis

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus group-specific open reading frames encode nonessential functions for replication in cell cultures and mice

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Subcellular localization and membrane association of SARS-CoV 3a protein.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Mitochondrial location of severe acute respiratory syndrome coronavirus 3b protein

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

G0/G1 arrest and apoptosis induced by SARS-CoV 3b protein in transfected cells

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Nucleolar localization of non-structural protein 3b, a protein specifically encoded by the severe acute respiratory syndrome coronavirus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

SARS coronavirus 7a protein blocks cell cycle progression at G0/G1 phase via the cyclin D3/pRb pathway

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

G1 phase cell cycle arrest induced by SARS-CoV 3a protein via the cyclin D3/pRb pathway

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Structure of coronavirus hemagglutinin-esterase offers insight into corona and influenza virus evolution

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Characterization of the 3a protein of SARS-associated coronavirus in infected vero E6 cells and SARS patients

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Homologous 2',5'-phosphodiesterases from disparate RNA viruses antagonize antiviral innate immunity

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The hemagglutinin/esterase gene of human coronavirus strain OC43: phylogenetic relationships to bovine and murine coronaviruses and influenza C virus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Cell-type-specific activation of the oligoadenylate synthetase-RNase L pathway by a murine coronavirus.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Severe acute respiratory syndrome coronavirus protein 6 is required for optimal replication

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Antagonism of the interferon-induced OAS-RNase L pathway by murine coronavirus ns2 protein is required for virus replication and liver pathology

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Cell-type-specific type I interferon antagonism influences organ tropism of murine coronavirus

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Amino terminus of the SARS coronavirus protein 3a elicits strong, potentially protective humoral responses in infected patients

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

The N-terminal region of severe acute respiratory syndrome coronavirus protein 6 induces membrane rearrangement and enhances virus replication.

1 reference

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113789

13 September 2020

Identifiers

10.1016/J.ANTIVIRAL.2014.06.013

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

PMC publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 August 2017

ResearchGate publication ID

0 references

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