What's so important about a Furin Cleaver being added to the "Spike Protein" sequence?
A "furin cleaver" supposedly attaches itself to ACE-2 receptors in the human body.
No longer believing in the pseudo-isolation process of any alleged “contagious viruses”, I still find it necessary to listen to “Virus Believing experts” in order to try to figure out what the intention behind using the toxic Spike Glycol Protein (SGP), allegedly emailed from “China”, actually is.
Virus believers are welcome to get their favorite “expert” to retrieve this money -
$1.2 M Reward Offered For Proof COVID-19 Virus Exists (here)
The experiment that shows that virology is bullshit, Tom Cowan, MD explains (here)
I would like the “No Virus” challengers to look into how the “ACE-2 furin cleaver” was “discovered”. I can’t talk to its genome sequence as being “meaningful”, but I do think that those who are modifying sequences to create “Gain-of-Function” toxins may be adding specific sequences based on their belief that their toxin will become more harmful. This following clip is very informative even though it is based in the perception (false belief) that genome sequences represent “real viruses”.
Our collective perspective requires a shift. We participate through believing a Scientism lie that is being compounded through false "data" built on top of a flawed foundation. The over-intellectualization of data that is fraudulent gives meaning to the lie.
Engineered Spike Protein Toxin (here)
This article includes content that shows the intent to incorporate a “computer sequence” into the Spike Protein (SP) “computer sequence” and thus shows an intent to do harm via marrying this toxin (SP) to an injectable biotech weapon.
There are scientific papers claiming to do experiments using the “SARS-CoV-2” virus, one has to wonder, how they are doing it? A multitude of evidence exists that this manmade computer, amino-acid, sequence/construct (Spike Protein) is toxic and has “gained” toxic attributes to compromise human health.
Dr. Robert Malone, a “SARS-CoV-2 virus believing expert” explains that the furin cleaver sequence currently added to the Spike Protein’s computer sequence was discovered close to 20 years ago. He says the furin cleaver is a key protein in how membrane proteins are clipped from their folding proteins starting point into smaller subunits which are activated into a variety of aspects in human biology.
From my previous more basic understandings, the reason this specific furin computer sequence was added, this time, to the toxic Spike Protein (SP) part of the “viruses” genetic computer sequence (previously added to SARS) is that the INTENTION, this time, is to ensure the synthetic toxic Spike Proteins, delivered using the LEAKY organ-bypassing Hydorgel, will allow these SP toxins to cleave to ACE-2 receptors throughout the jab recipient’s body. This alteration can ensure sterility, myocarditis, diabetes, and numerous other disease symptoms as well as sudden death. According to a French study, we have very few ACE-2 receptors in the lungs, i.e. this Lab Leak BS is mostly told by Germ Theory False Prophets. ACE-2 receptors are in the heart and dominant in the reproductive area.
Fallout with Robert Malone: The Disturbing Truth About COVID’s ‘Toxic Protein’, Episode 06 (here)
Involvement of Spike Protein, Furin, and ACE2 in SARS-CoV-2-Related Cardiovascular Complications (here)
Having a synthetic human ACE-2 furin clever computer sequence added to a fictitious SARS “virus” computer sequence means very little as this amino acid sequence is derived from biological “debris”/exosome… that’s sold as being representative of an actual “isolated virus”. Adding an amino acid sequence that functionalizes a toxic protein, injected into people, to connect onto the jab-recepients ACE-2 receptors is the real concern. The fact that the MASS MURDERING FDA never bothered to protect the American Military from being injected with a “Gain-of-Function” toxin requires investigation.
Furin Cleavage Sites Were Added to SARS –CoV – FOI Proof (here)
The problem with looking into “Gain-of-Function” research is that the terminology accepts the existence of a pathogenic “virus” and so is ultimately misleading. What really is occurring is the belief that particles believed to be a “cause of disease” are being modified through changes to the amino acid genetic sequence computer code. The initial human ACE-2 furin cleaver adaptation was orchestrated on the genetic sequence of the “coronavirus”. Hypothetically, this modification was likely done with the intent to roll out conventional vaxsins that would cause harm to humans, but with the invention of the mRNA biotechnology, this adaptation had to be performed on the toxic “Spike Protein” computer sequence poised to be Warpsped onto mankind.
The US Bioweapons effort is known to have introduced the Furin Cleavage site into Coronavirus in 2005. Has anyone found an earlier date for this weaponization?
Pfizer used Synthetic Life derived from US Bioweapons research for its mRNA trials (here)
It is and always has been about the “spike-protein” as the intention was always to inject a protein that could be replicated in the human body.
Spike Genes Have Patented DNA Sequences. This is Dangerous. Researchers have found a highly unusual presence of a proprietary DNA sequence in the spike protein genome.
We already know that the spike protein is dangerous for our cells and “immune” system. However, the presence of MSH3 protein can add dangerous outcomes for our cells. Let's review this hypothesis.
Spike Genes Have Patented DNA Sequences. This is Dangerous (here)
MSH3 Homology and Potential Recombination Link to SARS-CoV-2 Furin Cleavage Site (here)
Most Health Freedom Movement “experts” believe that the “full” SARS-CoV-2 sequence was “active” within the population, besides not a single RT-PCR test is capable of identifying it. Coupled with this is how the “original sequencing” was “qualified” i.e. it’s not a valid identification process.
Prof. Francis Boyle, a “Biological Warfare” expert, although good at exposing the modifications to the Spike Protein poised for the injections, does believe people “contagiously” spread “viruses”. In this interview with Alex Jones, he points out his concerns regarding sequence modifications to the “Spike Protein” within the “SARS-CoV-2” computer sequence. “The spike glycoprotein coronavirus contains a furin-like cleavage site absent in CoV of the same clade.” - Prof. Boyle.
Interestingly, Moderna’s CEO knew the “Spike Protein” was ideal for their bioweapon injections. They can manufacture super quickly, so fast that the FDA doesn’t even need to question if the “protein”, emailed from another country, would be toxic to Military personnel (?). So fast that even Donald Trump can’t brag about “pushing the FDA as they’ve never been pushed before”. So! ideally future Jab All PLANdemics can be rolled out within a week, it’s not like the FDA will allow Actual Risk Reduction treatments to be used or that they will challenge the corrupt Liable Free Pharmakeia Killers about all their bullshit “efficacy manipulation tricks”.
Reminder: Moderna CEO Stéphane Bancel Says Their mRNA Jab Was Made in TWO Days | 2020 (here)
“Here’s where it gets interesting. Different organisms have different codon preferences. Human cells like to designate arginine with codons CGT, CGC or CGG. But CGG is coronavirus’s last popular codon for arginine. Keep that in mind when looking at how the amino acids in the furin cleavage site are encoded in the SARS2 genome.
Now the functional reason why “SARS2” (computer sequence) has a furin cleavage site, and its cousin viruses don’t, can be seen by lining up (in a computer) the string of nearly 30,000 nucleotides in its genome with those of its cousin coronaviruses, of which the closest so far known is one called RAtg13. Compared with RAtg13, SARS2 has a 12-nucleotide insert right at the S1/2 junction. The insert is the sequence T-CCT-CGG-CGG-GC. The CCT codes for proline, the two CGG’s for two arginine.
There are several curious features about this insert, but the oddest is that of the two side-by-side CGG codons. Only 5 percent of SARS2’s arginine codons are CGG, and the double codon CGG-CGG has not been found in any other beta-coronavirus. So how did SARS acquire a pair of arginine codons that are favored by human cells but not by coronaviruses?” - Nicolas Wade
Part II delves deeply into the genetic alteration of humanity and the players that brought that to the fore. An investigation into the virus, that was engineered, and then, propagandized to bring humanity ultimately to heel before its amoral global masters. Those masters see us as a useless impediment to their grander designs and visions.
The short history of the 2020’s Or how to takeover the world (here)
Bear in mind that we are talking about a COMPUTER SEQUENCE i.e. it can be added to and subtracted from i.e. AI editing is possible. The first organic biological particle, the first (non-edited computer amino acid sequence) was NEVER PROVEN to Cause the Disease it allegedly Causes i.e. the “isolation” method regarding the “discovery process” has been openly accused of faulty pseudo-scientific non-Scientific method practices that call into question all of virology i.e. it’s a “Fear Thy Neighbour’s Invisible Virus” IDEOLOGICAL Cult followed by the bulk of mankind i.e. all the Priests are deceived, as too are All Nations. This does not mean that the “furin cleaver” sequence doesn’t represent a biological clever, that has been successfully modified as to attach itself to human ACE-2 receptor binding domains, which are predominantly in the reproductive system. Thanks to the all-organ bypassing Lipid Nanoparticle Hydrogel the (AI) Spike-Glycol-Protein (toxin) is distributed all over the body. Karen Kingston believes the content is Electromagnetically sensitive and could be used to stage the next PLANdemic.
Electromagnetic Programable Lipid Nanoparticles (LNPs) & Bio-Synthetic Life Forms (Spike Glycol-Proteins) - Karen Kingston & Dr. Ana Maria Mihalcea (here)
Okay, forgive me, Moderna’s CEO thinks they can, using an emailed sequence, be injecting people’s children in just over 2 months.
Moderna CEO 2019 Plan to Use a Computer Sequence to kick-start an mRNA vaccine campaign – Diabolical (here)
So! Modified a FULL-computer “Gnome” sequence BELIEVED to represent an existing alleged “isolated virus’s gnome”.
Use one that has a protein ideal for mRNA bioweapon injections.
Add numerous potentially toxic sequences (don’t worry about the FDA) to that FULL-sequence’s protein sequence.
When ready, introduce a new EMF pulse that ensures a novel detox experience.
Use the new FULL sequence to qualify if a patient’s detox sample is a “sequence match” (magically it will be). Don’t use the old pseudo-isolation process.
Email the FULL “Gnome sequence” PLUS the Protein’s Gnome sequence to the disease-causing Jab Manufacturers for mandated “immunization” production.
Ensure the “Gold Standard” Regulatory Agencies and controlled media outlets are happy and ready to “serve” the “Greater Good”.
Moderna CEO gets called out for having the same genetic sequence patented 3 years before the pandemic (here)
Nikolai Petrovsky - Furin Cleavage Site Is KEY To Covid's Origin (here)
I saw some stories claiming that Fauci held the patent for the HIV-gp120 sequence added to the SP and Moderna owned the patent to the furin-cleaver sequence. This would be worth casing up. I don’t know if this interview was referring to the furin-cleaver, it likely was.
Moderna CEO gets called out for having the same genetic sequence patented 3 years before pandemic (here)
Additional information pertaining to the adaptation of the SGP amino acid computer sequence -
Adaptations to the "Spike Glycol Protein" Computer Sequence were Ignored during Operation WarpSpeed (here)
It seems that all investigations into the “furin clever sequence” within the “Spike-Glycol-Protein” (toxin) amino acid computer sequence being connected to Moderna have ended. If Karen Kingston is right about the SGP being AI created with the potential shape shifting because of EMFs, then the longer this toxin remains in the body, the worse it is for the jab recipient.
Long-lasting, biochemical modified mRNA, and its frameshifted recombinant spike proteins in human tissues and circulation after COVID-19 vaccination (here)
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