A single line often inverts meaning once you see what it
answers, so neighbouring messages are always shown.
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So, the Proline at 681 is important for the O-glycans. S at 681 changes the prediction from three to only one O-linked glycan - as @Kristian Andersen has pointed out this likely is involved in regulation of cleavage - rather than any "glycan shielding." [shared file(s): image.png]
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Interestingly this is actually a R681S mutation
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(i.e., a Delta)
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2021-09-14 06:27
Robert F. Garry
Of course N501 is the a key residue for cross-species transmission. N501T is a key mutation for minks and ferrets. Serine is chemically similar to Threonine.
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Mutation of two amino acids (K479N and S487T) in palm civet SARS-CoV RBD allows this virus to infect humans (Li, 2008). These changes overcome the species barrier between civets and humans and enable favorable interactions between the RBD and contact residues on human ACE2. Q493 and N501 are the two SARS-CoV-2 residues that have similar interactions with ACE2 as SARS-CoV residues N479 and T487.
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R681S - That is interesting - hard to predict the effect on cleavage. The fsc is still there of course, but cleavage could be improved (the S might be a better landing site than the R) or decreased. And, the wild-card of the O-glycans not being there.
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These are the mutations we are seeing (we are not sure how they are linked as they are environmental samples). The last column is me looking outside the SARS-CoV-2 to the bats/pangolins ```S:R102T (21867:G>C) conserved S:D442N (22886:G>A) conserved S:Y449H (22907:T>C) 449F 449G S:N450T (22911:A>C) 450S (RaTG13), 450G S:P499S (23057:C>T) 499S (Cambodian bats) S:N501D (23063:A>G) 501D (RaTG13), 501T, 501V S:N501S (23064:A>G) S:Q506P (23079:A>C) conserved S:P681S (23603:C>T) missing S:V772A (23877:T>C) conserved S:Q779L (23898:A>T) conserved S:L828I (24044:C>A) conserved S:G932D (24357:G>A) conserved S:S937A (24371:T>G) conserved```
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question is - does any of this spike profile make you think it might be in a non-human host?