From Wikipedia, the free encyclopedia
NSP4 (rotavirus)
Identifiers
SymbolRota_NSP4
Pfam PF01452
InterPro IPR002107
CATH 1g1iA00
SCOP2 1g1i / SCOPe / SUPFAM
Available protein structures:
Pfam   structures / ECOD  
PDB RCSB PDB; PDBe; PDBj
PDBsum structure summary

The rotavirus nonstructural protein NSP4 was the first viral enterotoxin discovered. [1] It is a viroporin [2] and induces diarrhea and causes Ca2+-dependent transepithelial secretion. [3]

A transmembrane glycoprotein, NSP4 is organized into three main domains: a three-helical TM domain in the N-terminus (also a viroporin domain), a central cytoplasmic coiled-coil domain for multimerization, and a C-terminal flexible region. It can also be secreted out of the cell. As of 2019, only structures of the central domain, which is responsible for diarrhea, has been solved. It oligomerizes into dimeric, tetrameric, pentameric, and even higher-order forms. [4]

References

  1. ^ Dong Y, Zeng CQ, Ball JM, Estes MK, Morris AP (April 1997). "The rotavirus enterotoxin NSP4 mobilizes intracellular calcium in human intestinal cells by stimulating phospholipase C-mediated inositol 1,4,5-trisphosphate production". Proceedings of the National Academy of Sciences of the United States of America. 94 (8): 3960–5. Bibcode: 1997PNAS...94.3960D. doi: 10.1073/pnas.94.8.3960. PMC  20550. PMID  9108087.
  2. ^ Pham T, Perry JL, Dosey TL, Delcour AH, Hyser JM (March 2017). "The Rotavirus NSP4 Viroporin Domain is a Calcium-conducting Ion Channel". Scientific Reports. 7: 43487. Bibcode: 2017NatSR...743487P. doi: 10.1038/srep43487. PMC  5335360. PMID  28256607.
  3. ^ Gebert JT, Hyser J (May 2022). "Using Forward and Reverse Genetics to Understand Calcium Dysregulation in Enteric Viral Virulence". FASEB Journal. 36 (Suppl 1). doi: 10.1096/fasebj.2022.36.S1.R3214. PMID  35557094. S2CID  248633853.
  4. ^ Hu L, Crawford SE, Hyser JM, Estes MK, Prasad BV (August 2012). "Rotavirus non-structural proteins: structure and function". Current Opinion in Virology. 2 (4): 380–8. doi: 10.1016/j.coviro.2012.06.003. PMC  3422752. PMID  22789743.


From Wikipedia, the free encyclopedia
NSP4 (rotavirus)
Identifiers
SymbolRota_NSP4
Pfam PF01452
InterPro IPR002107
CATH 1g1iA00
SCOP2 1g1i / SCOPe / SUPFAM
Available protein structures:
Pfam   structures / ECOD  
PDB RCSB PDB; PDBe; PDBj
PDBsum structure summary

The rotavirus nonstructural protein NSP4 was the first viral enterotoxin discovered. [1] It is a viroporin [2] and induces diarrhea and causes Ca2+-dependent transepithelial secretion. [3]

A transmembrane glycoprotein, NSP4 is organized into three main domains: a three-helical TM domain in the N-terminus (also a viroporin domain), a central cytoplasmic coiled-coil domain for multimerization, and a C-terminal flexible region. It can also be secreted out of the cell. As of 2019, only structures of the central domain, which is responsible for diarrhea, has been solved. It oligomerizes into dimeric, tetrameric, pentameric, and even higher-order forms. [4]

References

  1. ^ Dong Y, Zeng CQ, Ball JM, Estes MK, Morris AP (April 1997). "The rotavirus enterotoxin NSP4 mobilizes intracellular calcium in human intestinal cells by stimulating phospholipase C-mediated inositol 1,4,5-trisphosphate production". Proceedings of the National Academy of Sciences of the United States of America. 94 (8): 3960–5. Bibcode: 1997PNAS...94.3960D. doi: 10.1073/pnas.94.8.3960. PMC  20550. PMID  9108087.
  2. ^ Pham T, Perry JL, Dosey TL, Delcour AH, Hyser JM (March 2017). "The Rotavirus NSP4 Viroporin Domain is a Calcium-conducting Ion Channel". Scientific Reports. 7: 43487. Bibcode: 2017NatSR...743487P. doi: 10.1038/srep43487. PMC  5335360. PMID  28256607.
  3. ^ Gebert JT, Hyser J (May 2022). "Using Forward and Reverse Genetics to Understand Calcium Dysregulation in Enteric Viral Virulence". FASEB Journal. 36 (Suppl 1). doi: 10.1096/fasebj.2022.36.S1.R3214. PMID  35557094. S2CID  248633853.
  4. ^ Hu L, Crawford SE, Hyser JM, Estes MK, Prasad BV (August 2012). "Rotavirus non-structural proteins: structure and function". Current Opinion in Virology. 2 (4): 380–8. doi: 10.1016/j.coviro.2012.06.003. PMC  3422752. PMID  22789743.



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