ORF7a

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Betacoronavirus NS7A protein
Structure of the SARS-coronavirus ORF7a accessory protein
Identifiers
SymbolbCoV_NS7A
PfamPF08779
InterProIPR014888
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

ORF7a (also known by several other names, including SARS coronavirus X4, SARS-X4, ORF7a, or U122)

sequence identity to the SARS-CoV protein.[3]

Function

A number of possible functions for the ORF7a protein have been described. The primary function is thought to be immunomodulation and interferon antagonism. The protein is not essential for viral replication.[1]

Viral protein interactions

Studies in SARS-CoV suggest that the protein forms

virions, making it a minor viral structural protein.[1][4] It is unclear if this occurs in SARS-CoV-2.[5] It may have a role in viral assembly.[1]

Host effects

A number of interactions with host proteins and effects on

binding activity to integrin I domains.[6]

It has also been reported to induce apoptosis via a caspase dependent pathway.[1][7] Also, it contains a motif which has been demonstrated to mediate COPII dependent transport out of the endoplasmic reticulum, and the protein is targeted to the Golgi apparatus.[8]

In SARS-CoV-2, ORF7a protein has been described as an effective

immunomodulatory effects through interaction with monocytes.[5]

Structure

The ORF7a protein is a

Post-translational modifications

The SARS-CoV-2 ORF7a protein has been reported to be

ubiquitination. Polyubiquitin chains attached to lysine 119 may be related to the protein's reported interferon antagonism.[3][9]

Expression and localization

Genomic information
Genomic organisation of isolate Wuhan-Hu-1, the earliest sequenced sample of SARS-CoV-2, indicating the location of ORF7a
NCBI genome ID86693
Genome size29,903 bases
Year of completion2020
Genome browser (UCSC)

Along with the genes for other

5' end of the coronavirus RNA genome.[3] ORF7a is an overlapping gene that overlaps ORF7b.[10] In SARS-CoV, subcellular localization to the endoplasmic reticulum, Golgi apparatus, and ERGIC has been reported,[1] with similar Golgi localization described for SARS-CoV-2.[11]

Evolution

Structural superposition of the Ig domains of ORF8 (blue, PDB: 7JTL[12]) and ORF7a (orange, PDB: 7CI3[5]) illustrating the similarity of their beta-sandwich topologies.

It is thought that

deltacoronaviruses.[16][14] The beta and alpha Ig domains may be independent acquisitions, where ORF8 and ORF7a may have been acquired from host proteins.[16]

Many SARS-CoV-2 genomes have been sequenced throughout the

References

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