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10.1016/j.jmb.2004.06.016

http://scihub22266oqcxt.onion/10.1016/j.jmb.2004.06.016
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suck abstract from ncbi


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pmid15312778      J+Mol+Biol 2004 ; 341 (1): 271-9
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  • Characterization of the 3a protein of SARS-associated coronavirus in infected vero E6 cells and SARS patients #MMPMID15312778
  • Zeng R; Yang RF; Shi MD; Jiang MR; Xie YH; Ruan HQ; Jiang XS; Shi L; Zhou H; Zhang L; Wu XD; Lin Y; Ji YY; Xiong L; Jin Y; Dai EH; Wang XY; Si BY; Wang J; Wang HX; Wang CE; Gan YH; Li YC; Cao JT; Zuo JP; Shan SF; Xie E; Chen SH; Jiang ZQ; Zhang X; Wang Y; Pei G; Sun B; Wu JR
  • J Mol Biol 2004[Jul]; 341 (1): 271-9 PMID15312778show ga
  • Proteomics was used to identify a protein encoded by ORF 3a in a SARS-associated coronavirus (SARS-CoV). Immuno-blotting revealed that interchain disulfide bonds might be formed between this protein and the spike protein. ELISA indicated that sera from SARS patients have significant positive reactions with synthesized peptides derived from the 3a protein. These results are concordant with that of a spike protein-derived peptide. A tendency exists for co-mutation between the 3a protein and the spike protein of SARS-CoV isolates, suggesting that the function of the 3a protein correlates with the spike protein. Taken together, the 3a protein might be tightly correlated to the spike protein in the SARS-CoV functions. The 3a protein may serve as a new clinical marker or drug target for SARS treatment.
  • |Animals[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Disulfides/metabolism[MESH]
  • |Humans[MESH]
  • |Membrane Glycoproteins/metabolism[MESH]
  • |Phylogeny[MESH]
  • |Proteomics[MESH]
  • |Sequence Analysis, Protein[MESH]
  • |Severe acute respiratory syndrome-related coronavirus/chemistry/genetics/*metabolism[MESH]
  • |Spike Glycoprotein, Coronavirus[MESH]
  • |Vero Cells[MESH]
  • |Viral Envelope Proteins/metabolism[MESH]
  • |Viral Proteins/chemistry/genetics/*metabolism[MESH]


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