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Politics : The Trump Presidency

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i-node
To: J_F_Shepard who wrote (225105)2/7/2022 10:19:09 AM
From: Thomas M.1 Recommendation  Read Replies (2) of 361484
 
Ivermectin Mechanism #1

Ivermectin blocks the virus from entering cells.
ivermectin docked in the region of leucine 91 of the SARS-CoV-2 spike protein and histidine 378 of the host cell ACE-2 receptor blocking its entry into the host cell

pubmed.ncbi.nlm.nih.gov

Ivermectin showed 5 important docking properties:

  • Highest binding affinity to the predicted active site of the S glycoprotein (Moldock score -140.584) and protein–ligand interactions (Moldock score -139.371).

  • Considerable binding affinity to the predicted active site of the SARS-CoV-2 RdRp protein (Moldock score -149.9900) and protein–ligand interactions (Moldock score -147.608), it formed H-bonds with only two amino acids: Cys622 and Asp760.

  • Highest binding affinity (Moldock score -212.265) to the predicted active site of nsp14.

  • The highest binding affinity to the active site of the TMPRSS2 protein (Moldock score -174.971) and protein–ligand interactions (Moldock score -180.548). Moreover, it formed five H-bonds with Cys297, Glu299, Gln438, Gly462, and Gly464 amino acid residues present at the predicted active site of the TMPRSS protein.

  • The free binding energy of the spike protein (open) was higher in ivermectin (-398.536?kJ/mol) than remdesivir (-232.973?kJ/mol).


  • frontiersin.org

    Tom
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