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10.1016/j.bbrc.2020.03.047

http://scihub22266oqcxt.onion/10.1016/j.bbrc.2020.03.047
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32201080!7102515!32201080
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suck abstract from ncbi


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pmid32201080      Biochem+Biophys+Res+Commun 2020 ; 526 (1): 165-169
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  • Spike protein recognition of mammalian ACE2 predicts the host range and an optimized ACE2 for SARS-CoV-2 infection #MMPMID32201080
  • Luan J; Lu Y; Jin X; Zhang L
  • Biochem Biophys Res Commun 2020[May]; 526 (1): 165-169 PMID32201080show ga
  • SARS-CoV-2 causes the recent global COVID-19 public health emergency. ACE2 is the receptor for both SARS-CoV-2 and SARS-CoV. To predict the potential host range of SARS-CoV-2, we analyzed the key residues of ACE2 for recognizing S protein. We found that most of the selected mammals including pets (dog and cat), pangolin and Circetidae mammals remained the most of key residues for association with S protein from SARS-CoV and SARS-CoV-2. The interaction interface between cat/dog/pangolin/Chinese hamster ACE2 and SARS-CoV/SARS-CoV-2 S protein was simulated through homology modeling. We identified that N82 in ACE2 showed a closer contact with SARS-CoV-2 S protein than M82 in human ACE2. Our finding will provide important insights into the host range of SARS-CoV-2 and a new strategy to design an optimized ACE2 for SARS-CoV-2 infection.
  • |*Viral Tropism[MESH]
  • |Amino Acid Sequence[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Animals[MESH]
  • |Betacoronavirus/*physiology[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/metabolism/transmission/virology[MESH]
  • |Humans[MESH]
  • |Mammals/classification/metabolism[MESH]
  • |Models, Molecular[MESH]
  • |Pandemics[MESH]
  • |Peptidyl-Dipeptidase A/chemistry/*metabolism[MESH]
  • |Pneumonia, Viral/metabolism/transmission/virology[MESH]
  • |SARS-CoV-2[MESH]
  • |Sequence Alignment[MESH]


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