Time to talk about one of my pet issues of concern: string theory.
Which begs two obvious questions: why doesn't string theory work? Why does it remain practically the only mainstream theory when it hasn't worked for decades?
You see, string theory presupposes a multiverse, and a multiverse seems to be the only way to make sense, from an atheist perspective, of the ...
(Anecdotally, certainly, the power of denial displayed by many atheists towards those coincidences of life that seem to suggest an organizing intelligence at work in the Universe is quite impressive.)
Again, mainstream physicists will admit this. The leading French cosmologist and philosopher Aurélien Barrau has said, essentially, yes, string theory doesn't work with the scientific ...
Again: when a scientist says, I have to choose between my theory and the scientific method, so I choose the theory, we have to conclude that ...
So why don't we?
In contrast to the Atheist Epicycles, a noteworthy thing I've noticed is that the few brave physicists who have put forward alternative theories to string theory...
This idea--that the most beautiful theory must also be the best theory--has for centuries guided the most brilliant scientific minds and has...
But this fruitful idea is also a dangerous idea since, logically, the idea that Beauty is convertible with Truth seems to imply that the Universe is ...
If it's true that this idea is particularly fruitful (which, certainly historically and empirically, it ...
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Keep dwelling on this:
Further Examination of the Motif near PRRA Reveals Close Structural Similarity to the SEB Superantigen as well as Sequence Similarities to Neurotoxins and a Viral SAg.
The insertion PRRA together with 7 sequentially preceding residues & succeeding R685 (conserved in β-CoVs) form a motif, Y674QTQTNSPRRAR685, homologous to those of neurotoxins from Ophiophagus (cobra) and Bungarus genera, as well as neurotoxin-like regions from three RABV strains
(20) (Fig. 2D). We further noticed that the same segment bears close similarity to the HIV-1 glycoprotein gp120 SAg motif F164 to V174.
https://t.co/EwwJOSa8RK
In (B), the segment S680PPRAR685 including the PRRA insert and highly conserved cleavage site *R685* is shown in van der Waals representation (black labels) and nearby CDR residues of the TCRVβ domain are labeled in blue/white
https://t.co/BsY8BAIzDa
Sequence Identity %
https://t.co/BsY8BAIzDa
Y674 - QTQTNSPRRA - R685
Similar to neurotoxins from Ophiophagus (cobra) & Bungarus genera & neurotoxin-like regions from three RABV strains
T678 - NSPRRA- R685
Superantigenic core, consistently aligned against bacterial or viral SAgs
Further Examination of the Motif near PRRA Reveals Close Structural Similarity to the SEB Superantigen as well as Sequence Similarities to Neurotoxins and a Viral SAg.
The insertion PRRA together with 7 sequentially preceding residues & succeeding R685 (conserved in β-CoVs) form a motif, Y674QTQTNSPRRAR685, homologous to those of neurotoxins from Ophiophagus (cobra) and Bungarus genera, as well as neurotoxin-like regions from three RABV strains
(20) (Fig. 2D). We further noticed that the same segment bears close similarity to the HIV-1 glycoprotein gp120 SAg motif F164 to V174.
https://t.co/EwwJOSa8RK
In (B), the segment S680PPRAR685 including the PRRA insert and highly conserved cleavage site *R685* is shown in van der Waals representation (black labels) and nearby CDR residues of the TCRVβ domain are labeled in blue/white
https://t.co/BsY8BAIzDa
Sequence Identity %
https://t.co/BsY8BAIzDa
Y674 - QTQTNSPRRA - R685
Similar to neurotoxins from Ophiophagus (cobra) & Bungarus genera & neurotoxin-like regions from three RABV strains
T678 - NSPRRA- R685
Superantigenic core, consistently aligned against bacterial or viral SAgs