Pfizer to release vaccine safety data in 20—

First will be the link to increased breast cancer potential found in the P.1 Gamma variant. The reader should see a red (Pro-Republican) flag every time they see a ‘N,’ which N can also stand for Dem/CDC stupidity and mandate arrogance:

Gamma Variant Hyperglycosylation Increases Breast Cancer Potential
’....wild type: TRT....alpha: TRT....beta: TRT....gamma: NRT.’

This N (positions 20-22) is one of the Ns that increase breast cancer potentials, so it’s a good thing not to get amnesia about the fact that Chinese communist women ride yaks in Yunnan.

Spike Positions 1-22

SARS-CoV-2 (before the P.1 Gamma variant occurred)
MFVFLVLLPLVSSQCVNLTTRT

Yak Coronavirus
MFLILLISLPTTFAVIGDLKCT

PHEV (porcine hemagglutinating encephalomyelitis [corona]virus)
MFFILLITLPSAFAVIGDLKCN

Notice the interchangeable N/T in the originally CDC published P.1 mutation: K417N/T. This is what the CDC changed on their webpage by removing the N, which then read ‘K417T.’ The CDC did not want the prisoners to notice that the N and T are indeed interchangeable. The virus can use either one. PHEV links to poliovirus. We’re not monkeying around.
 
badger2
I have zero idea what you just said
Can you give me simple explanations

Thx

I only got the N thing and yes I don’t like them either
 
PHEV Korea, 2011

In the above report, the original link is published at reference #5: 17649356

PHEV Canada, 1962
 
We are posting information about why Pfizer may want to block investigations and knowledge. Here we post two excerpts, one specifically linking to Pfizer’s pill that targets 3CLpro. Note that bovine coronavirus (BCoV) links to yak coronavirus:

’Early studies of coronaviruses and arteriviruses estimated the mutation rate to be 10(-3 ) to 10(-4) substitutions per site per year, the range that is typical for other RNA viruses, with (much) smaller genomes, whose replicase fidelity is known to be low. Most recently, these nubers were confirmed for SARS-CoV, HCoV-OC43, PHEV and HCoV-NL63. Using this rate and a (relaxed) molecular clock model, Vijgen et al estimated the time of the most recent common ancestors of BCoV and HCoV-OC43 and of PHEV, BCoV, and HCoV-OC43 to be in the late 19th century and not earlier than in the middle of the 16th century, respectively. Under a strict molecular clock model, the time of the most recent common ancestors pf HCoV-229E and HCoV-NL63 was estimated to be in the 11th century.

However, in contrast to the numbers cited above, it was also reported that SARS-CoV may have evolved at a lower mutation rate, approximating 0.1 replacement per genome per replication, and an unusually high genome stability was claimed for an isolate of HCoV-OC-43....corresponding to a mutation rate of 5.7 x 10(-6) substitutions per site per year.
....
It is common that the number of synonymous substitutions per synonymous site (dS) exceeds the number of nonsynonymous ones (dN), and an especially high and poorly understood dS/dN ratio was reported for the S protein of PHEV.
....
In the most conserved parts of the genome, nonsynonymous substitutions start to accumulate significantly only between the major nidovirus groups separated by relatively large evolutionary distances. In these viruses, replacements have sometimes been accepted at places of extraordinary conservation,e.g., in the active site of 3CLpro, which are not known to have been mutated in their DNA homologs. Although little is known about the absolute time scale of nidovirus evolution, it could have taken millions of years to generate the diversity observed in the most conserved enzymes.’
(Gorbalenya AE, Genomics and Evolution of the Nidovirales, in Nidoviruses, ASM Press, 2008)

This is in conjunction with the published probability that HCoV-OC43 jumped to Homo sapiens via bovine coronavirus (BCoV). Thus, the yak sequences we have posted also link a likely species crossover from yak to pig or vice versa.
 
Another excerpt links the Ns(asparagines), Ts(threonines) and Ks(lysines):

’Residues 82 to 84 comprise a glycosylation site on the rat receptor that is not present on the mouse, palm civet or human receptor. Residue 353 is a histidine in the mouse and rat receptors and a lysine in palm civet and human receptors Strikingly, alteration of histidine 353 of mouse ACE2 to the human lysine results in a receptor that supports infection as efficiently as human ACE2.
....
Two amino acids, residues 479 and 487, largely determined the much greater efficiency with which the TOR2 RBD bound human ACE2. Residue 479 is an asparagine or serine in all S proteins isolated from humans either during the 2002-3 epidemic or during the 2003-4 infections. However, most sequences isolated from palm civets and raccoon dogs encode a lysine at this position. This lysine is incompatible with human ACE2, but palm civet ACE2 can efficiently bind S proteins expressing either lysine or asparagine, without apparent preference for either. Palm civets may therefore be an important intermediate in the transfer of SARS-CoV to humans, permitting the emergence of viruses that express a small, uncharged amino acid at S protein residue 479.
....
Residue 487 is also of interest. Residue 487 is a threonine in all of the more than 100 S protein sequences obtained during the 2002-3 outbreak. It is a serine in S proteins from viruses isolated during the mild 2003-4 infections in all but one of the approximately 20 S-protein sequences obtained from palm civets and raccoon dogs. The relatively modest change of threonine in the TOR2 RBD to serine resulted in an approximately 20-fold decrease in binding to human ACE2. A corresponding increase was observed when a threonine was introduced into the SZ3 RBD. A threonine at position 487 also substantially increased association with palm civet ACE2. Notably, the single palm civet-derived S protein sequence that encoded a threonine at position 487 also encoded an asparagine at position 479 (Z. Hu, personal communication).’
(LiW, et al, Angiotensin-Converting Enzyme @, the Cellular Receptor for Severe Acute Respiratory Syndrome Coronavirus and Human Coronavirus NL63, in Nidoviruses, op cit)

Z. Hu is Wuhan Institute of Virology.
 
Folks, check out Bobby Kennedy Jr.'s book or his interviews on Fauci and the Big Pharma controlled agencies like the CDC, NIH, FDA, etc. My guess is no politician will draft legislation to shut them down and or demand prosecution of frauds like Fauci for weaponizing them against citizens.

Fraudi is now saying folks who foolishly took one Fauci Flu jab, now need a Fauci Flu jab (booster) every 6 months. :cry:
 
Folks, check out Bobby Kennedy Jr.'s book or his interviews on Fauci and the Big Pharma controlled agencies like the CDC, NIH, FDA, etc. My guess is no politician will draft legislation to shut them down and or demand prosecution of frauds like Fauci for weaponizing them against citizens.

Fraudi is now saying folks who foolishly took one Fauci Flu jab, now need a Fauci Flu jab (booster) every 6 months. :cry:
It can’t get here too soon for Badger. Ordered it yesterday after watching the video.
 

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