The content will be updated with new research and news at the end of this post.
28th of May 2022: important update, Monkeypox "MPXV-WRAIR7-61; Walter Reed 267" DNA polymerase related to Fauci’s research on HIV, and to SARS-Cov-2 spike protein, all leading to Monkeypox membrane glycoprotein AND its blood connection.
30st May 2022: improved sequence alignment between the universally injected Spike genetic code and Monkeypox DNA polymerase
1st June 2022: Dr. Mercola’s very revealing post today: “The Great Reset Snakes Are Slithering Together in Davos” at https://articles.mercola.com/sites/articles/archive/2022/06/01/the-great-reset-davos-meeting.aspx
6th June 2022: Duckduckgo search for my substack posts is censoring them, you will not find any hit for any of the topics I’m writing about. Strangely Quant, swisscow, even google works!!!
8th of June 2022: The top Nature journal continues spreading the CRIME: “Monkeypox vaccination begins — can the global outbreaks be contained? Some countries have begun to use smallpox vaccines to protect people exposed to the monkeypox virus. But researchers see challenges ahead.” https://www.nature.com/articles/d41586-022-01587-1
The African Green Monkeys, lived peacefully on the trees of West Africa for ages, until the science caught up with them and started experimenting with, without good intentions, for the monkeys.... This Old World animal, definitely must play some role in the New World transition of humanity, because it really goes viral right now (picture taken from https://nemosnewsnetwork.com/monkeypox-was-a-table-top-simulation-only-last-year/ ):
So much in fact, that the journal Nature just published that:
"Monkeypox goes global: why scientists are on alert."
https://www.nature.com/articles/d41586-022-01421-8
with the picture of that next invisible monster:
They 'just' got the genome sequence(!!) of the Monkeypox virus from the first case in Portugal: https://virological.org/t/first-draft-genome-sequence-of-monkeypox-virus-associated-with-the-suspected-multi-country-outbreak-may-2022-confirmed-case-in-portugal/799
As always the preparations were there, in advance, here a proof in this publication with the names of the involved institutions/companies (info from 28th May ‘22 ACU2020 hearings):
“The changing epidemiology of human monkeypox—A potential threat? A systematic review”
Eveline M. BungeID1, Bernard HoetID2*, Liddy Chen3, Florian LienertID2,
Heinz WeidenthalerID4, Lorraine R. Baer5, Robert SteffenID6,7
1 Pallas Health Research and Consultancy, Rotterdam, The Netherlands, 2 Bavarian Nordic AG, Zug, Switzerland, 3 Bavarian Nordic, Inc., Morrisville, North Carolina, United States of America, 4 Bavarian Nordic GmbH, Martinsried, Germany, 5 Baer PharMed Consulting, Ltd., Skokie, Illinois, United States of America,
6 Epidemiology, Biostatistics and Prevention Institute, WHO Collaborating Center on Travelers’ Health, University of Zurich, Zurich, Switzerland, 7 Department of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, Texas, United States of America
The name of Mrs. Baer is connected with: “delivering IBM mainframe system services” from the home page of the ‘consulting’ company…
Belgium has become the first country to introduce a mandatory 21-day monkeypox quarantine for those who contact the virus, after three cases were recorded in the country (zerohedge report on May 23rd). Children Health Defence just published more information about the preparations for this next pandemic: https://childrenshealthdefense.org/defender/monkeypox-gates-foundation-who-pharma-execs-monkeypox-pandemic-simulation/
and FDA in May 19, 2022, ‘just’ approved the intravenous (IV) formulation of TPOXX, which inhibits the viral maturation of the variola virus and other poxviruses by preventing the formation of a secondary viral envelope. In the absence of this envelope, viral particles remain inside the cell and cannot spread to and infect other cells ( information from https://www.precisionvaccinations.com/vaccines/tpoxx-smallpox-treatment )
Some of the disturbing bioinformatics results using NIH BLAST software, showing the relation between the Monkeypox viral proteins in comparison to SARS-CoV-2 Spike, are presented in the last section of this post, which should end with a question: why the take down of the humanity started with injections of genetic material with positive-sense synthetic mRNA (falsely called covid19 ‘vaccines’) and now it turns to the largest DNA viral monkeypox genome (mind, only from injections), which only works in nucleus?
Scientists with the support of their salaries and pensions, with the guidance of those who give them the money and their instructions, always prepare for the worst in advance, for all sorts of pests, for example:
https://www.cdc.gov/smallpox/bioterrorism/public/preparedness.html
https://www.who.int/news-room/feature-stories/detail/preparedness-in-the-event-of-a-smallpox-outbreak
https://www.gavi.org/vaccineswork/five-things-you-need-know-about-monkeypox
and some see it this time not as a threat, again, but rather another fearmongering:
So surely the PCR tests are ready, injection materials were ordered, and now what, count the cases, with the same fraudulent PCR tests just reformulated for another synthetic genetic sequence of this old exotic virus??
VAERS system supposedly erases the COVID injections and deaths data right now :
https://articles.mercola.com/sites/articles/archive/2022/05/21/vaers-reports-deleted.aspx
surely not to make more space on the computer disks for the next PLANDEMIC?
https://www.brighteon.com/a2940bf9-b0e8-40ac-86be-8ed5b747e171
Already in May 2020 scientists were fiddling with monkeys, turning them into a MODEL of COVID-19, here the publication:
"Establishment of an African green monkey model for COVID-19" By Courtney Woolsey et al. at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263506/
announcing full of proud that, quote:
"Here, we show that African green monkeys (AGM) support a high level of SARS-CoV-2 replication and develop pronounced respiratory disease that may be more substantial than reported for other NHP species including cynomolgus and rhesus macaques."
and also:
"Importantly, we show that virus replication and respiratory disease can be produced in African green monkeys using a much lower and more natural dose of SARS-CoV-2 than has been employed in other NHP studies."
Their pictures of the poor SARS-CoV-2 infected and slaughtered monkeys’ lungs are just unbearable! And although majority if not all of SARS-CoV-2 ‘cultures’ on this continent come from that one place:
"This study was supported by funds from the Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston, TX to TWG. Operations support of the Galveston National Laboratory was supported by NIAID/NIH grant UC7AI094660."
the samples for this AGM paper came from European Virus Archive goes Global (EVAg)...
It is really astonishing that the first outbreak of Monkeypox in US was in 2003:
https://stacks.cdc.gov/view/cdc/108095
exactly the same year of SARS-CoV outbreak:
https://www.cdc.gov/sars/about/fs-sars.html
And the answer to this gives as always, Dr. David Martin with his wife in their ‘Butterfly of the week’ lecture at:
I got this link from : THANK You for that!
So what Monkeypox and SARS coronaviruses have in common, besides of their sudden appearance in USA in 2003 and reappearance after 2020?? PCR tests for completely invisible ‘asymptomatic covid’ cases were a total fraud, but now with pox, you won’t need them, it’s visible, on the skin..
If SARS-CoV-2 comes from Wuhan lab, from which one comes the Monkeypox??? Ukraine?
https://www.planet-today.com/2022/05/ecdc-bombshell-monkeypox-outbreak.html
The pox double stranded DNA is supposedly packaged in a squarish box (that's why pox), and it replicates in the cytoplasm, exactly in the same cell location where the covid19 injected modified synthetic mRNA GENETIC MATERIAL was deposited via the injections in billions of human arms, causing explosion of deaths by now:
https://www.drrobertyoung.com/post/injuries-and-deaths-are-exploding
The in the Nature article mentioned Monkeypox genome (6x the size of SARS-CoV-2) is homolog with its Israel cousin deposited by Cohen Gihon et al. at the NIH at:
https://www.ncbi.nlm.nih.gov/nuccore/MN648051.1
There are hundreds of proteins in that file and going through each of them is impossible, so just catching here the few outstanding, due to their function. For example:
1. The 'RGD' motif (signature of integrins, snake venom proteins, synthetic biology) containing deoxyuridine 5'-triphosphate nucleotidohydrolase (code QGQ59755.1) has ~86% sequence homology with ~30% identities, when comparing with Spike2020 sequence from all the injections, using BLAST software from NIH. And here the furin site in the first 3 lines for the first homolog segment:
Query 4 NSPVRFVKETNRAKSPTRQS 23 ->Monkey Pox
NSP R RA+S QS ->IDENTITIES
Sbjct 679 NSP-R------RARSVASQS 691->Spike 2020
P R RAR <<<==FURIN site
Query 120 PEL----EEVQSLD 129 Monkey Pox
PEL EE LD IDENTITIES
Sbjct 1143 PELDSFKEE---LD 1153 Spike 2020
Query 25 GAAGYDLYSAY 35
GAA AY
Sbjct 261 GAA------AY 265
and many more homolog pieces. All further Queries represent Monkeypox proteins, and Subjct line the 2020 Spike sequence in the covid INJECTIONS! Next protein, threonine-protein kinase 2 (code QGQ59763.1):
Query 278 QYIK---FIFL 285 ->Monkey Pox
QYIK +I L ->IDENTITIES
Sbjct 1208 QYIKWPWYIWL 1218->Spike 2020
Query 409 YRL--KVSILHPISFLEKFIMRDI 430 Pox
YRL K S L P F E RDI -> IDENTITIES
Sbjct 453 YRLFRK-SNLKP--F-E----RDI 468 Spike 2020
Query 31 FNNIMSQLDLHQNWAPSVR-----LLNYFKNFNKETL 62 POX
FN SQ L PS R LL FNK TL ->IDENTITIES
Sbjct 800 FN--FSQI-LPDPSKPSKRSFIEDLL-----FNKVTL 828 Spike 2020
and many, many more examples. The last example is very ‘special’ since this fragment is not only part of everyones patent for the new covid19 injections, but that particular fragment KRSFIEDLLFNKV is also the content of the paper mentioned below, and in its homolog version was patented in 2009 by Eli Lilly, in a patent US 8,506,968 B2 (going back to first filing in 2001) “SARS VACCINE COMPOSITIONS AND METHODS OF MAKING AND USING THEM“ in its Table 4:
9704 149 ‘PLKPTKRSFIEDLLFNKV’ and seq 150 ‘FIEDLLFNKVTLADAGMP‘
These 2 peptides belong to ‘SARS Overlapping Peptide Array’ which ELi Lilly obtained from NIH Biodefense and Emerging Infections Research Repository, NIAID, NIH. The second above comparison contains majority of the Spike peptide 448YNYLYRLFRKSNLKP463 which some researchers claim^1, it binds to hemoglobin, leading to deposition of iron in tissues expressing the Spike after the injections. Most recent autopsy summary by Prof. Burkhardt found indeed extended iron deposits in the brains of the deceased after the covid gene therapy injection: https://report24.news/prof-burkhardt-einfluss-der-covid-impfungen-auf-das-sterben-von-menschen-muss-geklaert-werden/
Next protein, poly(A) polymerase catalytic subunit QGQ59772.1, which processes RNA while using ATP (remember, if you still have Pfizer/Mod-E-RNA injections in the body, they have the poly(A) section in the synthetic mod mRNA strings, possibly to be reused for the next virus??!!!)
Query 270 IDNIYIVDPT--FQLLNMIKMFSQIDRLEDLSKDPEK 304
+ IY P F N FSQI L D SK P K
Sbjct 785 VKQIYKTPPIKDFGGFN----FSQI--LPDPSK-PSK 814
hier the known HIV1 motiv, common for SARS-Cov-2 and now in MON(K)EYpox(!!):
Query 83 SKQTQTYNIGKLFTIIELQSVLVTTYTDILG----VLTIKAPNVISSKISYNVTSMEELA 138
S QTQT N + QS+ YT LG V I VT E L
Sbjct 673 SYQTQT-NSPRRARSVASQSII--AYTMSLGAENSVAYSNNSIAIPTNFTISVTT-EILP 728
the insertions seem literally obvious in this next case:
Query 281 QLLN-MIKMFS------------------------QIDRL 295
Q LN ++K S QIDRL
Sbjct 957 QALNTLVKQLSSNFGAISSVLNDILSRLDKVEAEVQIDRL 996
and many, many more sections. Next protein, DNA POLYMERASE QGQ59780.1, ~80% sequence coverage and 44% of IDENTITIES(!!), just few examples:
Query 758 EIDSQDVDKSIEIAKEL-ERLIN 779
EID + E+AK L E LI+
Sbjct 1182 EIDRLN-----EVAKNLNESLID 1199
Query 786 NFKI--EFEAVYKN 797
NFK EF V+KN
Sbjct 185 NFKNLREF--VFKN 196
Query 320 VNNNNGTIFFD-----LYSFIQKSEKLDSY 344
VNN T++ D L SF K E LD Y
Sbjct 1133 VNN---TVY-DPLQPELDSF--KEE-LDKY 1155
Next protein, telomere-binding protein I1 QGQ59785.1:
Query 135 LKRSATQFNFNGHT 148 Monkeypox
K FNFNG T
Sbjct 534 VKNKCVNFNFNGLT 547 Spike2020
90 S1-90 535 KNKCVNFNFNGL 546 <<spike EPITOPE DESIGNED by chinese...
Here a short comparison of the above Spike2020 fragment with an epitope from a Table 1 of a 2020 publication by chinese team: "Linear epitopes of SARS-CoV-2 spike protein elicit neutralizing antibodies in COVID-19 patients”. (Cell Mol Immunol 2020 Oct;17(10):1095-1097. doi: 10.1038/s41423-020-00523-5. Epub 2020 Sep 7.). These pieces WERE DESIGNED, SYNTHETICALLY FABRICATED and TESTED on sera of covid19 patients!
Query 57 LVK--SSFVKKFGLCNYGGI 74 Monkeypox
LVK SS N+G I
Sbjct 962 LVKQLSS--------NFGAI 973 Spike 2020
and the neutralizing epitope from the above 2020 publication
161 S2-47 962 LVKQLSSNFGAI 973 !!!
Just wonder, how did the researchers know in advance, in what pieces to cut the Spike, what to synthesize in order to achieve such remarkable 'common ground’ between those totally different viruses???? Mind please, this is DNA polymerase, synthesizing DNA!!! And next example for the Ribonucleoside-diphosphate reductase large subunit (code QGQ59788.1) 82% sequence coverage and 'only' ~32% identities among the smaller fragments of that protein and SPike:
Query 262 ISGTNG 267
+SGTNG
Sbjct 70 VSGTNG 75
and the corresponding epitope: S1-12 67 AIHVSGTNGTKR 78
Query 5 KRNGYKENVMFDKIT 19
KR + E+ +F+K+T
Sbjct 814 KRS-FIEDLLFNKVT 827
S2-22 812 PSKRSFIEDLLF 823*
Query 429 CTEI---IQYAD 437
CTE+ I+ AD
Sbjct 617 CTEVPVAIH-AD 627
103 613 QDVNCTEVPVAI 624
Query 197 WF--THASPTLFNAGTTRHQMSSCFLLNMIDDSI----EGIY 232
WF H S T N GT R F D+ + +G+Y
Sbjct 64 WFHAIHVSGT--N-GTKR------F-----DNPVLPFNDGVY 91
14 S1-14 79 F DNPVLPFNDGV 90
The second example above overlaps almost entirely the 2 pieces of Monkeypox DNA polymerase and SARS-Cov-2 SPike, representing the very same by Eli Lilly patented fragment ‘KRS-FIEDLLFNKVT’! This piece is so prevalent that B. Robson in Jun 2020 published a revealing paper titled: ”COVID-19 Coronavirus spike protein analysis for synthetic vaccines, a peptidomimetic antagonist, and therapeutic drugs, and analysis of a proposed achilles’ heel conserved region to minimize probability of escape mutations and drug resistance” in Comp. in Biol. and Med. 121 (2020) 103749 with a short explanation of that sequence, quote:”Subsequence KRSFIEDLLFNKV of the S2′ spike glycoprotein proteolytic cleavage site continues to appear important. Here it is shown to be recognizable in the common cold coronaviruses, avian coronaviruses and possibly as traces in the nidoviruses of reptiles and fish.”
Next also really important one: DNA-directed RNA polymerase subunit 1 (code QGQ59813.1), 85% sequence coverage, 39% identities. Hier BLAST won't pick it up, but one see it with the naked eye:
LPD-SKDPEGRGYILNSLT-KG DNA-dir RNA pol
LPD SK P R +I L K
LPDPSK-PSKRSFIEDLLFNKV SPIKE 2020
and its homolog epitope
135 S2-21 806 LPDPSKPSKRSF 817
and other fragments found by BLAST:
Query DIHG--APVYGSIQDEIVAAYSLFRIQDLCLDEV---LN---I----LGKY 486
DI G A V IQ EI D L+EV LN I LGKY
Sbjct DISGINASV-VNIQKEI----------D-RLNEVAKNLNESLIDLQELGKY
3 different epitopes for this long segment:
S2-81 1166 LGDISGINASVV 1177
198 S2-84 1184 DRLNEVAKNLNE 1195
200 S2-86 1196 SLIDLQELGKYE 1207
next homolog segment:
Query 366 VEVAVQEYTSI---IFGRQPSLHRYNVIASSIRATE 398
VE VQ I I GR SL+ Y V IRA E
Sbjct 987 VEAEVQ----IDRLITGRLQSLQTY-VTQQLIRAAE 1017
and its matching epitope
66 S2-52 992 QIDRLITGRLQS 1003
Among the hundreds of poxvirus proteins, there are few which have the unique TRYPTOPHAN (in the single letter code it is W, in 3 letter code Trp) rich motif, also present in the 2020 Spike. These sequences are not very common in normal human proteins, BUT clearly in viral proteins, for example, without aligning them all:
-KYQHLWRWGWRWGT (HIV gp160 surface glycoprotein)
-EQYIKWPWYIWLGFIAG (SARS-CoV-2 SPike)
-EGTGWGLGGKWWTSDWG (Marburg Spike)
-GNHRREWSIAWVGDQVKVFEW (Parainfluenza, i.e. paramyxoviral VP2)
-DTIEVYNNRTYSWNIWDGMEW (Monkeypox Kelch protein F3)
-YDLWNVVPSDLWNWEPLKDK (Monkeypox ribonucleoside-diphosphate reductase large subunit)
These segments are frequently followed by the cysteine rich fragments, like in the Spike. For paramyxoviruses it is known that this portion blocks the TLR7/9 signaling pathway normally leading to the production of protective interferons^2. Remarkably many HIV patients are lacking tryptophan (largest aromatic amino acid) in their circulation^3, and one of the treatment protocols uses the simple nicotinamide, water soluble Vit B3 ^4. The connection between Tryptophan, Vit B3, human energy and LIVER is very well described in wiki, quote: “NAD+ is synthesized through two metabolic pathways. It is produced either in a de novo pathway from amino acids or in salvage pathways by recycling preformed components such as nicotinamide back to NAD+. Although most tissues synthesize NAD+ by the salvage pathway in mammals, much more de novo synthesis occurs in the liver from tryptophan, and in the kidney and macrophages from nicotinic acid.[26]“ The 1972 publication^5 “The control of nucleic acid and nicotinamide nucleotide synthesis in regenerating rat liver“ makes it clear, quote: “In regenerating liver the competition is normally in favour of the synthesis of nucleic acid precursors, at the expense of NAD synthesis. This situation may be reversed by the injection of nicotinamide with a subsequent inhibition of nucleic acid synthesis.“ Thus tryptophan indirectly is connected with the regeneration of GENETIC MATERIAL, very broadly speaking…
No wonder, an old customer of mine, a retired biochemist, was buying out 12 bottles of niacinimide (no flush version of B3) every month! Yes, the little bricks inside of our human bodies are extremely important to feel good:)
Last example of a similarities between the Spike2020 and Monkeypox proteins, will be related to the in the post
mentioned Epstein-Barr nuclear antigen leader protein. This gammaherpesvirus entry https://www.ncbi.nlm.nih.gov/nuccore/82503188 alone by eye, super rich in furin sites(!!) and RGD motifs, very regularly spaced, looks extremely MAN MADE. It’s nearest similarity is Monkeypox putative membrane-associated glycoprotein (NIH entry AAY97189.1). Like for every virus, everything starts with the surface proteins, like the Spike, usually glycosylated (coated with SUGARS). So how similar is the Monkeypox membrane protein with Spike2020? 83% sequence coverage with ~80% identities, when searching for smaller fragments. These are among many:
Query 124 NYTIDYSTVITTEELQV 140 Monkeypox membrane glycoprot
N+TI S +TTE L V -> IDENTITIES
Sbjct 717 NFTI--S--VTTEILPV 729 SPike 2020
Query 983 NTSNLV--LEYQLKVAC 997
NTSN V L YQ V C
Sbjct 603 NTSNQVAVL-YQ-DVNC 617
Query 222 INNC---YNV---SVSDASF 235
I NC Y V S ASF
Sbjct 358 ISNCVADYSVLYNS---ASF 374
Query 118 YEPSIYNYTIDYSTVITTE 136
YEP I ITT+
Sbjct 1110 YEPQI----------ITTD 1118
Query 392 LYES--------YGVN----DDISHCF 406
LY S YGV +D CF
Sbjct 368 LYNSASFSTFKCYGVSPTKLNDL--CF 392
Query 1741 SYDYLESSG-------VVVLSCYEM 1758
SY + G VVVLS +E+
Sbjct 494 SYGFQPTNGVGYQPYRVVVLS-FEL 517
and of course the furing site:
Query 398 VND----DI-------------SHCFASPRRRRS 414 MPV glyco
VN+ DI SPRR RS
Sbjct 656 VNNSYECDIPIGAGICASYQTQTN---SPRRARS 686 Spike
Query 1569 WIESN--VLQQPPY------TFEFI 1585
W ES V Y TFE++
Sbjct 152 WMESEFRV-----YSSANNCTFEYV 171
The BLAST is not even finding the RGD motif, which should be in the output too, but the above is already enough to ask the question: if the Monkey pox is one among the oldest viruses out there, why does it have so many common features with just that ONE 2020 Spike, genome of which is being forcefully injected into billions of arms?
One could go on and on with these homologies, while using NIH BLAST and running it with custom chosen parameters. Without the last step, there is NO SIMILARITY found, Spike and Monkeypox proteins have nothing in common.. If so, why are there thousands cases of Herpes related infections, shingles in particular, after covid injections in VAERS? Anyone can distinguish the shingles wounds from the Monkeypox??? Every single line of the above comparisons can be verified by going to the above mentioned data base at NIH, which is https://www.ncbi.nlm.nih.gov/nuccore/NC_045512.2 for the Spike, and search for the residues string starting with the first number after the Query and ending with the number at the end of each line. And one more reminder, even something so simple as the tripeptide Aspartic Acid-Arginine-Tyrosine (DRY)^6, anywhere in the entire protein sequence, is decisive about its feature, which can get one a Nobel Prize^7…
There are so many similarities between the official NIH stored genome of the monkey virus and SARS-CoV-2 Spike from the coronavirus, despite of having totally different sizes, type and 'origin', that accepting any next injection, with the operating system of the current covid injections set in place, should end with that serious question:
Why all these similarities in the sequences made in labs, being the basics for now GENE THERAPIES falsely called ‘vaccines’?? Where all this is going to lead??? Warnings like this one, posted just few days ago, only confirms these data presented here:
In a easy going way, maybe it will lead to the first image created and posted by EMC2 just yesterday:
The more viral, SYNTHETIC parts (all from injection materials) made with some purpose(?), the higher probability of some sort of viral self assembly:
1. Viral self-assembly as a thermodynamic process. Phys Rev Lett. 2003 Jun 20;90(24):248101. doi: 10.1103/PhysRevLett.90.248101. Epub 2003 Jun 17.
2. https://www.sciencedaily.com/releases/2012/12/121217091334.htm
3. https://phys.org/news/2012-12-do-it-yourself-viruses.html
4. https://experts.umn.edu/en/publications/electrostatic-theory-of-viral-self-assembly
Viral parts are always electrostaticaly charged, like everything else inside of us and around us, but the ‘introduction’ of additional charges, via vaccines, now even genetically programmed into the human bodies by Pfizer/ModeRNA, maybe relates this to the very beginning of gathering the knowledge about the human immune system, hundreds of years ago, by a Nobel prize winner Dr. Karl Landsteiner. Strangely he didn’t get the prize for his most essential work, but rather for blood type discovery. Maybe the point of that move was to cover up the importance of charges of every organism born on this planet. I’ll leave that part for the next post..
It was good to have chicken pox as a child, and if not, will just continue protecting and detoxing body with nutrients, supplements, and if available, with some of the already well tested covid drugs, like ivermectin, and never ever any injection any more, in particular genetically modifying one!!! Most important: NOT to allow to turn ones own body into pharmaceutical drug factory.
The similarities between the monkeypox and chicken pox was very well summarized by a russian american team of experts in 2001:”Human monkeypox and smallpox viruses : genomic comparison” ( https://febs.onlinelibrary.wiley.com/doi/epdf/10.1016/S0014-5793(01)03144-1 ) showing that the essential anzymes and proteins are almost identical (96.3%), but the virulence and host-range factors differ. The american authors Peter B. Jahrling (USAMRIID) and the NIAID researcher https://www.niaid.nih.gov/research/bernard-moss-md-phd are still very active with todays’ covid19 issues, whereby the CDC’s Joseph J. Esposito died in 2014 (https://findingaids.library.emory.edu/documents/HS-MSS014/).
23rd May 2022: Dr. Richard Flemming is giving instructions to everyone how to indite the criminals responsible for this crime. Also he is giving more explanations about the already in Aug 2021 patented:
‘Recombinant poxvirus based vaccine against sars-cov-2 virus.’
Patent’s content is available at:
https://patents.google.com/patent/US20210260182A1/en
Dr. Flemming talk at: https://www.bitchute.com/video/Y28vBfwogy7Z/
24th May 2022: Dr. Jessica Rose summarized all the current pox related vaccines, currently on the market. A good read at:
https://principia-scientific.com/first-confirmed-monkeypox-cases-appear-on-exact-date-predicted-in-march-2021/
25 th of May 2022: first man in US lands in hospital with ‘monkeypox, a report at https://principia-scientific.com/u-s-buys-millions-of-monkeypox-vaccines-as-mass-man-infected/#comment-72074
Wisenox commenter from the above article, gave an interesting link to HIV https://www.uniprot.org/uniprot/P04601 small protein which alone in its description, sounds really bad. And of course its fragments are equally embedded into the Spike 2020 sequence, around 30% of identities. And of course the cover the above mentioned KRSFIED.. peptide and when you read its motifs description, these are JUST 2 amino acids in some cases, which are IMPORTANT to do the damage(!!!), for example:
62-65 ‘EEEE’ interacts with host PACS1 and PACS2; stabilizes the interaction of NEF/MHC-I with host AP1M1
69-78 ‘PVTPQVPLRP‘ SH3-binding; interaction with Src family tyrosine kinases
72–75 ‘PQVP’, or PxxP; stabilizes the interaction of NEF/MHC-I with host AP1M1; necessary for MHC-I internalization
164 – 165 ‘LL’ Dileucine internalization motif; necessary for CD4 internalization
174-175 ‘DD’ Diacidic; necessary for CD4 internalization
EXTREMELY IMPORTANT by Dr. Heiko Schoening, in German unfortunately:
https://uncutnews.ch/heiko-schoening-zu-affenpocken-impfstoff-es-sind-dieselben-verbrecher/
28th May 2022:
Aug 2018 Fauci et al. published an article titled: “Select gp120 V2 domain specific antibodies derived from HIV and SIV infection and vaccination inhibit gp120 binding to α4β7“ investigating the central role of gut in HIV pathogenesis directed by the envelope protein gp120. It is available at
https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1007278&type=printable
The α4β7 is an integrin belonging to receptors which bind fibronectins. Fig 3B of his work is presenting the short sequence of the HIV protein gp120 V2 (AA 168–181), which was identified in HIV vaccines trials and known to bind to the integrins. The HIV gp120 sequence: CSFNMTTELRDKKQKVHALFYKLDIVPIEDNTSSSEYRLINC (was turned into cyclic peptide by adding the cystein residues at the begin and end, one of Fauci’s patents) and was investigated for the binding to α4β7, in which the tripeptide ‘LDI’ is known to be critical. BLAST search for the same motif inside of the Spike, gives many fragments:
Query 12 KKQKVHALFYKLDIVPIEDNTSSSEYRL 35 HIV gp120 V2 dom
+ QK+ A + I I+D+ SS+ L
Sbjct 918 ENQKLIANQFNSAIGKIQDSLSSTASAL 941 Spike
Query 35 SEYRLI----NC 42 HIV gp120
SE+R+ NC
Sbjct 155 SEFRVYSSANNC 166 SPike
Query 29 EDNTS--SSEYRL 39 HIV gp120
+N S SE+R
Sbjct 147 KNNKSWMESEFRV 1 Spike
but none with the ‘LDI’ motif from Spike, which one can see with the naked eye, so aligning it here for you all by hand:
CSF----NMTTE-LRDKKQKVHALFYKLDIVPIEDNTSSSEYRLINC HIV gp120 V2
F TT +RD Q + + LDI+P S N
QQFGRDIADTTDAVRDP-QTLE-I---LDITPCSFGGVSVITPGTNT Spike SARSCoV2
Taking the very same HIV gp120 V2 fragment and now searching for homologs among pox viruses leads to few membrane glycoproteins from Monkypox virus (MPXV) but also strangely to "MPXV-WRAIR7-61; Walter Reed 267" Monkeypox DNA polymerase, with the latter sharing among 83% of sequence coverage 43% identities! Now just few example of the alignment between The Monekypox DNA polymerase AAU01261.1 with the SARS-CoV-2 SPike:
21.8 bits(44) 0.33 10/23(43%) 13/23(56%) 6/23(26%)
Query 758 EIDSQDVDKSIEIAKEL-ERLIN 779 MPXV-WRAIR051
EID + E+AK L E LI+
Sbjct 1182 EIDRLN-----EVAKNLNESLID 1199 Spike
Query 753 DSVFTEIDSQDVD---------KSIEIAKELERL 777
D F S DVD + I KE++RL
Sbjct 1153 DKYFKNHTSPDVDLGDISGINASVVNIQKEIDRL 1186
Query 98 SIQNATMDEFL----NISWF 113
S+ T D FL N+ WF
Sbjct 46 SVLHSTQDLFLPFFSNVTWF 65
Query 786 NFKI--EFEAVYKN 797
NFK EF V+KN
Sbjct 185 NFKNLREF--VFKN 196
Query 909 YLVTEYNKNNPETIELGERYY 929
+L Y+KNN +E R Y
Sbjct 140 FLGVYYHKNNKSWMESEFRVY 160
Query 319 HVNNNNGTIFFD 330
HV+ NGT FD
Sbjct 69 HVSGTNGTKRFD 80
Query 499 STIIKGPLLKLLLETKT 515
S II+G + L++KT
Sbjct 98 SNIIRGWIFGTTLDSKT 114
the 2 sections below are all one continuous string from each of the proteins, Query being the MOnekeypox polymerase, Sbjct the Spike2020
Query 481 AGAATYVL----PQSMVFEYRASTIIKGPL---LKLLLETKTILVRSETKQKFPYEGGKV
AGAA Y + P++ + +Y + I + L L ETK L +S T +K Y+
Sbjct 260 AGAAAYYVGYLQPRTFLLKYNENGTITDAVDCALDPLSETKCTL-KSFTVEKGIYQ----
Query 534 FAPKQKMFSNNVLIFDYNSL--YPNV---CIFGNLSPETLVGVVVSTNR 577
++N + S+ +PN+ C FG + T V + NR
Sbjct 315 --------TSNFRVQPTESIVRFPNITNLCPFGEVFNATRFASVYAWNR 355
and another one:
Query 648 TEKAIYDSMQYTYKIVANSVYGLMGFRNSALYSYASAKSCTSIGRRMILYLESVLNGAEL 707
T+ +Y++ K++AN +G +L S ASA +G+ L+ V+N
Sbjct 912 TQNVLYENQ----KLIANQFNSAIGKIQDSLSSTASA-----LGK-----LQDVVN---- 953
Query 708 SNGMLRFANTLSNPFYMDDRDINPIVKTSLPIDYRFRFRSVYGDTDSVFTEIDSQDVDKS 767
+ + +N +VK + S +G SV +I S+ +DK
Sbjct 954 ----------------QNAQALNTLVK---------QLSSNFGAISSVLNDILSR-LDK- 986
Query 768 IEIAKELERLINSRV 782
+E +++RLI R+
Sbjct 987 VEAEVQIDRLITGRL 1001
Query 96 KRSIQNATMDEFL----NISWFYISNGISPDGCYSLDEQYLTKINNGCYHCDDP 145
+ S+ ++T D FL N++WF+ I G NG D+P
Sbjct 44 RSSVLHSTQDLFLPFFSNVTWFH---AIHVSG------------TNGTKRFDNP 82
Query 785 NNFKIEFEAVYKNL 798
NFK E V+KN+
Sbjct 184 GNFKNLREFVFKNI 197
Query 433 FGKDDIDLAQMYKD 446
FG+D D +D
Sbjct 565 FGRDIADTTDAVRD 578
Query 322 NNNGTI 327
N NGTI
Sbjct 280 NENGTI 285
Query 340 KLDSYK--LDSISKN 352
+LDS+K LD KN
Sbjct 1144 ELDSFKEELDKYFKN 1158
and so many more, which clearly shows, this can’t be just a ‘coincidence’! One has to remember, according to the definition of DNA polymerase, it performs following function :
deoxynucleoside triphosphate + DNAn ⇌ pyrophosphate + DNAn+1.
thus, why is that an infectious, toxic Spike protein has so many identical segments with completely different protein, shared among many organisms and regenerating the DNA genetic material???
The biggest surprise though one gets when looking ‘just’ for the MPXV homologs among snakes proteins. The score of 68 bits(154) results in homologies with segments overlapping HUNDREDS of amino acids, most related to BLOOD proteins, like: von Willebrand factor type A, coagulation factor XIII B chain, complement factor H-like, all with that one feature overlaps in the tryptophan sections! Tryptophan, the largest aromatic ring among all 20 amino acids, like DNA… Here just two, out of many homologs between the Monkeypox membrane glycoprotein (QNI38932.1) and the snake complement receptor XP_039176015.1, sorry for the format, this editor is not optimal for the BLAST output:
68.5 bits(154) 3e-16 Compositional matrix adjust. 70/250(28%) 82/250(32%) 35/250(14%)
Query 347 CPAPIIENGKV-DAEDDVRLGGSVTFSCVPGFRLIGEATRKCILKDGKVDWNSALPHCEH 405
C P N K E VTF C G+ + C W E
Sbjct 21 CTVPTMNNAKLTSTETSFNDKQKVTFTCDSGYHSL-DPNAVC----ETDKWK-----YEN 70
Query 406 IPCERPVSI---LNGQYDPDPKDEYYVGSVVIYRCKGDFSLIGNSTITCITAEDGVNGRW 462
PC + YD K Y V S C G+ C E N W
Sbjct 71 -PCKKMCTVSDYVSELYD---KPLYEVNSTMTLSCNGE-----TKYFRC--EEKNGNTSW 119
Query 463 NFPAPECKQVKCDQPEVENGKITNLPKPSYTYNEAISIECNSGYSAVGSLHIKCGANSSW 522
N C C + E G K Y + E I C+ GY +G I C NS
Sbjct 120 N-DTVTCPNAECQPLQLEHGSCQPV-KEKYSFGEYMTINCDVGYEVIGVSYISCTDNSWN 177
Query 523 VPAIPKCVKEVKCDQPEVENGKITDLSKPSYSYNESISFECNSGYSAVGSLHITCGANSL 582
V IP C + KCD P NG I S +S I C SG+ GS TC +
Sbjct 178 V--IPSC--QQKCDIPSLSNGLI---SGSTFSIGGVIHLSCKSGFTLTGSPSSTC-IDGK 229
Query 583 WLPAIPKCVK 592
W P P CV
Sbjct 230 WNPILPTCVR 239
and the second fragment:
62.1 bits(139) 3e-14 Compositional matrix adjust. 65/250(26%) 79/250(31%) 36/250(14%)
Query 308 NLTYHCITGYEYIPGINPSVTCLNTSKWTEIS---ELCQGKKCPAPIIENGKVDAEDDVR 364
T+ C GY +P C T KW +C + +
Sbjct 43 KVTFTCDSGY---HSLDPNAVC-ETDKWKYENPCKKMCTVSDYVSELYDKPLYE------ 92
Query 365 LGGSVTFSCVPGFRLIGEAT-RKCILKDGKVDWNSALPHCEHIPCERPVSILNGQYDPDP 423
T SC GE C K+G WN C C+ P G P
Sbjct 93 VNSTMTLSC------NGETKYFRCEEKNGNTSWNDTVT-CPNAECQ-PLQLEHGSCQP-V 143
Query 424 KDEYYVGSVVIYRCKGDFSLIGNSTITCITAEDGVNGRWNFPAPECKQVKCDQPEVENGK 483
K+ Y G C + IG S I C + WN P C Q KCD P NG
Sbjct 144 KEKYSFGEYMTINCDVGYEVIGVSYISCT------DNSWN-VIPSCQQ-KCDIPSLSNGL 195
Query 484 ITNLPKPSYTYNEAISIECNSGYSAVGSLHIKCGANSSWVPAIPKCVK-EVKCDQPEVEN 542
I + I C SG+ GS C + W P P CV D +
Sbjct 196 ISG---STFSIGGVIHLSCKSGFTLTGSPSSTC-IDGKWNPILPTCVRSNEEFDPVDDGP 251
Query 543 GKITDLSKPS 552
TDLSK S
Sbjct 252 DDETDLSKLS 261
Doesn’t it look like the Monkleypox surface glycoprotein, clearly related to Covid spike, a surface glycoprotein from SARS-CoV-2 (in all the mandatory injections), is completely dervied from other proteins, as an example of this snake secreted complement-binding protein??? The question would be what was discovered first?
Some might say, the biological world consists of 4 basic nucleotides, encoding 20 basic amino acids, thus all their sequences will be to some extend similar. I’d like to ask a good mathematician, please calculate the probability of the composition similarities like the above, between a snake protein and a Monkeypox virus. To close this, here the comparison between Python polymerase XP_007423155.1 and the above mentioned MPXV-WRAIR051 Walter Reed 267 Monkeypox DNA Polymerase, submitted to NIH data base among others by R.I.P. Dr. Buller, R.M.L., yes the bioterrorism expert on poxviruses, who was killed in 2017 while riding his byke. Clearly all DNA polymerases are related.
100 bits(249) 3e-20 Compositional matrix adjust. 103/401(26%) 164/401(40%) 69/401(17%)
Query 518 VRSETKQKFPYEGGKVFAPKQKMFSNNVLIFDYNSLYPNVCIFGNLSPETLVGVVVSTNR 577
V+SE + Y G V P + + + D++SLYP++ + NL TL+
Sbjct 583 VKSEGGED--YAGATVIEPLKGYYDVPIATLDFSSLYPSIMMAHNLCYTTLL-------- 632
Query 578 leeeinnqlllqKYPPPRYITVHCEPRLPNLISEIAIFDRSIEGTIPRLLRTFLAERARY 637
+ P ++I R P + + +G +P +L LA R R
Sbjct 633 ----QQGAVERYGLSPEQFI------RTPT--GDHFVKASVCKGLLPEILENLLAARKRA 680
Query 638 KKMLKQATSSTEKAIYDSMQYTYKIVANSVYGLMGFRNSALYSYASAKSCTSIGRRMILY 697
K LKQ T ++ + D Q K+ ANSVYG G + L ++S T GR+MI
Sbjct 681 KLELKQETDPFKRQVLDGRQLALKVSANSVYGFTGAQVGKLPCLEISQSVTGFGRQMI-- 738
Query 698 LESVLNGAELSNGMLRFANTLSNPFYMDDRDINPIVKTSLPIDYRFRFRSVYGDTDSVFT 757
E + ++ T++N + D + I YGDTDSV
Sbjct 739 --------EKTKQLVESKYTVANGYSADAKVI-------------------YGDTDSVMC 771
Query 758 EIDSQDVDKSIEIAKELERLINSRVLFNNFKIEFEAVYKNLIMQSKKKYTTMKYSASSNS 817
+ Q V +++EI KE ++S + K+EFE VY ++ +KK+Y + + SSNS
Sbjct 772 RLGVQSVAEAMEIGKEAAAWVSSHFI-PPIKLEFEKVYFPYLLINKKRYAGLYF--SSNS 828
Query 818 KSVPERINKGTSETRRDVSKFHKNMIKTYKTRL-------------SEMLSEGRMNSNQV 864
+ KG RRD N+I T +L E++S+ N +
Sbjct 829 DMHDKMDCKGIETVRRDNCPLVANLINTCLEKLLIDRDPAGAVAHAKEVISDLLCNRVDI 888
Query 865 CIDILRSLETDLRSEFDSRSSPLELFMLSRMHHSNYKSADN 905
++ T E+ R + +EL RM + SA N
Sbjct 889 SQLVITKELTRTADEYAGRQAHVEL--AERMRRRDPGSAPN 927
The amino scid sequence identity between a Python coagulation factor VIII B chain and the same human isoform is 43% with the 529 bits(1241), just for a comparison to what is shown above.
As of May 29 2022, the Monkeypox ‘cases’ statistics from
https://report24.news/angstporno-statistik-seite-our-world-in-data-fuegt-affenpocken-als-pandemie-hinzu/
and also new involvements, from Mike Adams: https://www.naturalnews.com/2022-05-28-biden-crime-family-reap-massive-profits-monkeypox-vaccines.html
and the copy of PennU contract at: https://nationalfile.com/exclusive-fauci-funded-monkeypox-vaccine-maker-paid-bidens-host-university-for-clinical-trial-of-monkeypox-vaccine/
which is directly linked to : https://markets.businessinsider.com/news/stocks/metabiota-gains-government-momentum-with-black-veatch-sub-contracts-for-defense-threat-reduction-programs-1027442834 with a title “Metabiota Gains Government Momentum with Black & Veatch Sub-Contracts for Defense Threat Reduction Programs“.
Todays new article on the 2nd of Oct 2022 at:
indicates even more detailed involvents of Metabiota in the entire pandemic scheme and its connection to the newest terrifying Biden’s executive order described in:
30st May 2022: Running NIH BLAST session (with different parameters then in the above trials) on AAU01261.1 and YP_009724390.1 results in overlaps of section with more than 150 reidues, spanning both S1 and S2 domain of Spike 2020. Here the examples, with Query being the Monkeypox protein and Subjct the Spike2020 in the bodies of all the covid jabbed:
18.9 bits(37) 2.7 Compositional matrix adjust. 31/135(23%) 57/135(42%) 45/135(33%)
Query 648 TEKAIYDSMQYTYKIVANSVYGLMGFRNSALYSYASAKSCTSIGRRMILYLESVLNGAEL
T+ +Y++ K++AN +G +L S ASA +G+ L+ V+N
Sbjct 912 TQNVLYENQ----KLIANQFNSAIGKIQDSLSSTASA-----LGK-----LQDVVN---- 953
Query 708 SNGMLRFANTLSNPFYMDDRDINPIVKTSLPIDYRFRFRSVYGDTDSVFTEIDSQDVDKS
+ + +N +VK + S +G SV +I S+ +DK
Sbjct 954 ----------------QNAQALNTLVK---------QLSSNFGAISSVLNDILSR-LDK- 986
Query 768 IEIAKELERLINSRV 782
+E +++RLI R+
Sbjct 987 VEAEVQIDRLITGRL 1001
AND
18.5 bits(36) 3.6 Compositional matrix adjust. 29/109(27%) 47/109(43%) 25/109(22%)
Query 481 AGAATYVL----PQSMVFEYRASTIIKGPL---LKLLLETKTILVRSETKQKFPYEGGKV 533
AGAA Y + P++ + +Y + I + L L ETK L +S T +K Y+
Sbjct 260 AGAAAYYVGYLQPRTFLLKYNENGTITDAVDCALDPLSETKCTL-KSFTVEKGIYQ---- 314
Query 534 FAPKQKMFSNNVLIFDYNSL--YPNV---CIFGNLSPETLVGVVVSTNR 577
++N + S+ +PN+ C FG + T V + NR
Sbjct 315 --------TSNFRVQPTESIVRFPNITNLCPFGEVFNATRFASVYAWNR 355
AND
18.1 bits(35) 4.2 Compositional matrix adjust. 17/67(25%) 29/67(43%) 20/67(29%)
Query 744 RFRSVYGDTDSVFTEIDSQDVDKSIEIAKELERLINSRVLFNNFKIEFEAVYKNLIMQSK 803
+ S +G SV +I S+ +DK +E +++RLI R +QS
Sbjct 965 QLSSNFGAISSVLNDILSR-LDK-VEAEVQIDRLITGR------------------LQSL 1004
Query 804 KKYTTMK 810
+ Y T +
Sbjct 1005 QTYVTQQ 1011
AND
16.5 bits(31) 12 Compositional matrix adjust. 14/54(26%) 22/54(40%) 19/54(35%)
Query 96 KRSIQNATMDEFL----NISWFYISNGISPDGCYSLDEQYLTKINNGCYHCDDP 145
+ S+ ++T D FL N++WF+ I G NG D+P
Sbjct 44 RSSVLHSTQDLFLPFFSNVTWFH---AIHVSG------------TNGTKRFDNP 82
AND
Query 753 DSVFTEIDSQDVD---------KSIEIAKELERL 777
D F S DVD + I KE++RL
Sbjct 1153 DKYFKNHTSPDVDLGDISGINASVVNIQKEIDRL 1186
AND
Query 909 YLVTEYNKNNPETIELGERYY 929
+L Y+KNN +E R Y
Sbjct 140 FLGVYYHKNNKSWMESEFRVY 160
AND
Query 564 SPETLVGVVVSTNRLEEEINN 584
+P T+ G STN ++ + N
Sbjct 520 APATVCGPKKSTNLVKNKCVN 540
Query 322 NNNGTI 327
N NGTI
Sbjct 280 NENGTI 285
and many, many more sections. What is not good, at all, is that, once again, this is the injected Spike genome, compared with the Monkleypox DNA polymerase, belonging to the conserved family of poxviridae PHA03036 (https://www.ncbi.nlm.nih.gov/Structure/cdd/PHA03036), which promotes DNA pairing and strand-transfer reactions => genetic modifications!!! A surface glycoprotein from an RNA coronavirus similar to 6x the size polymerase of a DNA virus????? At least in many fragments.
G.C.Lechuga et al. “SARS-CoV-2 Proteins Bind to Hemoglobin and Its Metabolites“ Int J Mol Sci. 2021 Aug; 22(16): 9035. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396565/
Yoshinori Kitagawa et al. “A Tryptophan-Rich Motif in the Human Parainfluenza Virus Type 2 V Protein Is Critical for the Blockade of Toll-Like Receptor 7 (TLR7)- and TLR9-Dependent Signaling“ JOURNAL OF VIROLOGY, May 2011, p. 4606–4611
M. F. Murray “Tryptophan depletion and HIV infection: a metabolic link to pathogenesis“ THE LANCET Infectious Diseases Vol 3 October 2003, p.644.
M. F. Murray et al. “Increased Plasma Tryptophan in HIV-Infected Patients Treated With Pharmacologic Doses of Nicotinamide”. Nutrition 17:654 – 656, 2001.
G.M. Ferris & J.B.Clark “The control of nucleic acid and nicotinamide nucleotide synthesis in regenerating rat liver“ Biochem J. 1972 Jul; 128(4): 869–877.
G.E.Rovati et al. “The highly conserved DRY motif of class A G protein-coupled receptors: beyond the ground state“ Mol Pharmacol. 2007 Apr;71(4):959-64. doi: 10.1124/mol.106.029470
https://www.nobelprize.org/prizes/chemistry/2012/press-release/
Count me in as vaccinated against smallpox - twice! I was 5 years old and the first injection did not "take" - it left no scar on my left shoulder. So I was vaccinated a second time and the characteristic scar resulted. Then in the first grade, 1953, I had red measles, mumps, chicken pox, tonsillitis, and German measles. Survived all that just fine. Unfortunately, only 2-3 years later I received both the Injectable polio vaccine (2 injections) and the oral polio vaccine (3 sugar cubes)...so carrying that Monkey SIV for sure!
Thank you for your work!