SARS-CoV-2 Spike, engineered clots in human blood vessels, infertility, psychedelics, and the way to develop cancer after the covid genetically modifying injections, falsely called 'covid vaccines'.
SARS-CoV-2 Spike, psychedelics, and the way to develop cancer after the covid genetically modifying injections, falsely called 'covid vaccines'.
To read the main article please scroll down to the divider, which separates updates related to the post from the post itself.
UPDATE: 1/1/2023 Prof Arne Burkhardt now goes more into details of the clots and other foreign objects in the bodies of the deceased: https://report24.news/pathologe-dr-burkhardt-wir-fanden-gefaessveraenderungen-in-praktisch-jedem-gehirn/
UPDATE 11/22/2022: Stew Peters’ documentary “DIED SUDDENLY“ at: https://rumble.com/v1wac7i-world-premier-died-suddenly.html shows details about this horror happening right now in front of our eyes!
UPDATE: 11/11/2022 : The cancer rates AFTER covid injections increase significantly according to military data coming out from current lawsuits. But NOW there is a SOLUTION: https://www.nature.com/articles/d41586-022-03676-7 to it described in this article:”CRISPR cancer trial success paves the way for personalized treatments” ‘Most complicated therapy ever’ tailors bespoke, genome-edited immune cells to attack tumours.” !!!! MIT, at works as usual, the same criminal cabal who designed the Spike genes, Dr. Walensky included! That article states: “A small clinical trial has shown that researchers can use CRISPR gene editing to alter immune cells so that they will recognize mutated proteins specific to a person’s tumours. Those cells can then be safely set loose in the body to find and destroy their target.“
UPDATE: 11/1/2022 A renewed search for the similarities to the oldest traced patent similar to the Spike, described below, the so called peplomeric protein from 1987 at https://www.ncbi.nlm.nih.gov/protein/CAA01736.1, gives now a ‘strange’ result, an IDENTITY with the PIRBRIGHT Patent: Patent: US 8828407-B2 8 09-SEP-2014 for “Chimaeric protein“ AJN02361.1 (that’s the ncbi code). Slightly less homolog, but with equally very high score of identities is for AAE22284.1 protein from Patent: US 5853733-A 15 29-DEC-1998 for “Recombinant herpesvirus of turkeys and uses thereof“, having 52% sequence coverage (sc) with 38% identities with Spike2020 (score of 364 bits)!! Shall we expect infectious bronchitis viruses or herpesvirus outbreaks after covid injections, while never even touching any turkey???? Btw. https://www.gatesfoundation.org/about/committed-grants/2021/02/INV028944 shows how Gates supports that institution….. Just wonder for how long already? Slowly I’m getting the impression, that ALL vaccines, patented in the past and ‘implemented’ on humanity are the casue of never-ending chains of diseases plaguing this world’s people.
6/19/2002: A shock, to me, when hearing this from Dr. Jessica Rose at
, quote:”I’m fascinated. The concept is so cool. It’s just I have so many questions…” She is talking about applying GENE THERAPY ON LIVING HUMAN BODIES, laughing very frequently… What all the MD’s do actually think, they are? The new false gods??? The title of Dr. Rose post is:”When you hear BNT162c(2), run, don't walk, RUN away.” How about the countless deaths after the BNT162b1,2 billions of which were already distributed? How about genetically modifying humanity already, in a less cool way??? It is a CRIME of astronomic proportions, even by those who are apparently on the ‘other site’ of the establishment, unfortunately. Here I must add Mr. Kirsch himself who in the most recent interview with Greg Hunter at: https://usawatchdog.com/cv19-vax-lies-greatest-trust-destroyer-in-human-history-steve-kirsch/
states, that gene therapy is 'helpful technique'!!!??? I’m really worried, since he is injected, and to state something like this, is crazy, to me.
But going back to Dr. Rose post, reading the face expression of the young female scientist developing the self-replicating BNT162c series one can get actually a complete stomach turnover, an infinite anti-human arrogance.
URGENT update: 6/13/2022 Mike Adams from Natural News investigates the clots taken out of the deceased bodies of the victims after the covid19 gene therapy injections: https://forbiddenknowledgetv.net/microscopic-video-of-engineered-bio-structures-removed-from-blood-vessels/ and also at: https://banned.video/watch?id=62a7c513d3003e1cb464c25c
few sentences about it at the end of this post.
update 6/1/2022: CHD documentary “INFERTILITY: A DIABOLICAL AGENDA” => inspired by it, a check of a signal peptide from HUMAN CHORIONIC GONADOTROPIN (HCG). Looks like the begin of Spike genetic sequence, aligned BY NIH BLAST package first and also by HAND is quite similar to the HCG:
Query 3 MFQGLLLLLLLS 14 HCG
MF L LL L S
Sbjct 1 MFVFLVLLPLVS 12 Spike2020
by hand:
MEMFQGLLLLLLLSMGGTW--ASREMLRPR HCG
M F L+LL L+S + ++R L P
MFVF--LVLLPLVSSQ-CVNLTTRTQLPPAY SPIKE 2020the above confirmed by the recent data: https://principia-scientific.com/confidential-pfizer-docscovid-vax-depopulation/
8/8/2022: Cancer issues AFTER THE COVID GENE THERAPIES (falsely called ‘vaccines’) exploading: https://uncutnews.ch/turbo-krebs-wir-haben-ein-riesiges-problem/
Covid19 discrepancy between the official narrative and its UNIVERSAL GENE THERAPY solution, ends up with top professional specialists investigating the covid issues, being silenced, like Prof. Arne Burkhardt (https://report24.news/von-wegen-unwissenschaftlich-pathologe-prof-burkhardt-wir-arbeiten-absolut-in-einer-korrekten-art-und-weise/), or Prof. S. Bhakdi (https://newsrnd.com/life/2022-05-12-sucharit-bhakdi--attorney-general-s-office-files-charges-of-sedition.S1O2u5q85.html), or many professionals dealing with DEAD bodies (EXTREMELY IMPORTANT https://www.naturalnews.com/2022-06-12-blood-clots-microscopy-suddenly-died.html) including all the covid injected victims, like Mr. Kirsch himself (
). That’s why there is an urgent need to speak out, for every scientist who knows anything about the harm done to the entire HUMAN POPULATION, the harm done by the without consent enforced, thus unlawful and criminal, covid19 GENE THERAPY injections, one of the biggest crimes in human history. The irony in the official science paid frequently by criminals (NIH for example) is that it follows exactly the same strategy as politics. Example, create a problem first, like the one in the topic of this post and then create a solution, like this one:
from researchers of the University of North Carolina at Charlotte and Penn State (Biden’s financial paradise), who came up with these programmable RNA-DNA anticoagulant fibers which ‘communicate’ with thrombin in order to bind and inactivate it while dissolving the cloths.. And then a kill switch is applied and the fibers dissolve and are excreted:
The details can be found at: https://phys.org/news/2022-07-team-anticoagulant-platform-advances-heart.html
Strange, that all covid injections cause exactly the opposite to what this technology can supposedly fix… Just wonder, are there maybe the matching complementary sections in the Spike genomic synthetic mRNA sequence which will nicely match the above mentioned solution???? In the meantime, there are thousands of deaths after the covid gene therapies and millions over millions injuries..
Most of my previous posts describe some of the details of the Spike genome and the logical consequences which can be drawn from it. This one adds one more dimension, drugs. VAERS covid gene therapy deaths and injury reports show, that many of the deceased victims were already on few pharmaceutical drugs. An Apr 2020 publication by UNC Prof. Bryan L. Roth MD. and ~120 of other scientists (until then mainly particle physics papers were having this ‘load of participation’) titled:
“A SARS-CoV-2 protein interaction map reveals targets for drug repurposing.“ states in its abstract, quote:”Here we cloned, tagged and expressed 26 of the 29 SARS-CoV-2 proteins in human cells and identified the human proteins that physically associated with each of the SARS-CoV-2 proteins using affinity-purification mass spectrometry, identifying 332 high-confidence protein–protein interactions between SARS-CoV-2 and human proteins. Among these, we identify 66 druggable human proteins or host factors targeted by 69 compounds (of which, 29 drugs are approved by the US Food and Drug Administration, 12 are in clinical trials and 28 are preclinical compounds).”
Spike protein was included into this ‘interactome’ list, but only one single mention about the pathways the Spike (which was in preparations to be injected into millions) actually participates in was made, namely, quote:”lipid modification”. It is known for DECADES, the coronavirus Spike binds ACE2 receptor and the drugs list for inhibiting ACE receptors is long, but they found just one: “captopril modulates ACE2 indirectly via its direct interaction with angiotensin-converting enzyme, ACE)”. Their ‘drugs inhibition’ list included remdesivir (affecting RdRp), but no ivermectin, maybe because it was exactly around the same time when ivermectin was found to bind to the Spike, and thus affect the ‘covid19’ infection process? Or maybe because it was in the same Department of Pharmacology, University of North Carolina at Chapel Hill School of Medicine, where Dr. Ralf Baric also worked on remdesivir? Who knows, no, not WHO though.
So if Spike binds ACE2, and ACE2 list of molecular functions inside of every cell is really long, to be found at: https://www.uniprot.org/uniprot/Q9BYF1 , involving every single cardiovascular homeostasis process related to HUMAN BLOOD, why is the conclusion of >120 scientists, that Spike is only connected to lipids??? Strange, to say the least.
Dr. Bryan L. Roth is actually more known for his DREADD technology, quote from:
https://unclineberger.org/directory/bryan-roth/
“"I have studied molecular neuropharmacology for more than 30 years. Most recently, my lab invented the DREADD (Designer Receptor Exclusively Activated by Designer Drug) technology. DREADDs represent a novel synthetic biological tool-kit which enables the non-invasive remote control of neuronal signaling via orthologous ligand-receptor pairs.“
So why a neuropharmacologist, working on mildly speaking 'remote brain control', is also interested in repurposing of drugs for a SARS-CoV-2, very similar to SARS-CoV with the old flu like symptoms, we always knew? What if his most recent work on HTRA2 receptor and the SARS-CoV-2, including the Spike, in all covid genetically modifying injections, are actually somewhat related?
In Sep 2020, the most prestigious science journal Cell, published the 13 authors list paper: ”Structure of a Hallucinogen-Activated Gq-Coupled 5-HT2A Serotonin Receptor” with the summary, quote: ”Roth et al. reveal structurally how psychedelics, including LSD, psilocin, mescaline, and various N-BOH analogs, mediate their therapeutic and hallucinogenic effects by binding to and activating their molecular target, the serotonin (5-HT) 2A receptor coupled with G-protein Gaq.”
The 5-hydroxytryptamine receptor 2A ( short HTR2A) is a GPCR protein receptor for serotonin but also functions as a receptor for various drugs and psychoactive substances described in that paper. The most essential fact about all GPCR's is that they all have a SINGLE tripeptide motif 'Asp-Arg-Tyr' (DRY)^1 or ERY, which is anchored in loops around the cell membrane and does the cellular signaling. I call this tripeptide ‘universal photonic dipole’ due to the negative-positive charge distribution of Asp-Arg and the photoreceptor Tyrosine reside. The HTR2A receptor has 2 SHORT stretches of 6 and 5 amino acids which bind the activating ligands (drugs), these are: residues 155 – 160 with the sequence ‘DVLFST’ and residues 336 – 340 ‘WCPFF’ according to uniprot entry P28223.2. Running the NIH BLAST amino acid comparison bioinformatics tool, with custom chosen parameters, one gets ‘only’ ~33% identities between the Spike and the HTR2A receptor. BLAST does NOT pick up the only ONE amino acids (AA) stretch in Spike, which has the PFF motif, it shows only 3 regions which do not match, so here they are and the rest done by hand:
Query 323 KVLGIVFFLFVVMWCPFFITNIMA 346 HTR2A
+V F V W I+N +A ===>>Identities of
Sbjct 340 EVFNATRFASVYAWNRKRISNCVA 363 Spike 2020
Query 326 GIVFFLFVVMWCPFFITNIMAV--ICKES 352 HTR1A
G+VF V + P N IC +
Sbjct 1059 GVVFLH--VTYVPAQEKNFTTAPAICHDG 1085 Spike 2020
Query 323 KVLGIVFFLFVVMWCPFFITNIMA 346
+V F V W I+N +A
Sbjct 340 EVFNATRFASVYAWNRKRISNCVA 363
the only segment in Spike with PFF aligned by hand:
KACKVL-GIVFFLFVVMWCPFFITNI-M--AVIKE HTRA2
KV V + PFF +N+ + A+ +
D--KVFRSSVLHSTQDLFLPFF-SNVTWFHAI-HV SPIKE 2020The above by hand made alignment covers actually both partly homolog stretches of the psycholigands binding residues WCPFF and DVLFST in that putative Spike side with its residues 57-59 string of the ‘PFF’ motif. Serotonin and melatonin are identical in their aromatic ring portion, usually bound by pi-pi stacking (identically to DNA/RNA binding with proteins), thus the WCPFF side binding serotonin, could be well this FLPFF proposed site in the Spike. That could explain WHY MELATONIN is such a precious help in ‘Spike’ remedies, because it possibly binds to it in that spot, not allowing to dock to ACE2, in addition to its rejuvenating features every night, without the light and 5G around… One has to realize these are the possible putative functions of ‘just’ the few amino acids out of ~1300 for every spike!!! The homologies between the HTR2A receptor and covid Spike, are even more alarming, when looking into a database of HTR2A MUTATIONS involved in human cancers. The ‘cosmic’=CATALOG OF SOMATIC MUTATIONS IN CANCER (!!!) for that receptor can be found at: https://cancer.sanger.ac.uk/cosmic/gene/samples and many of the overlapping segments of Spike and HTR2A are ‘covering’ those mutations, for example:
Query 262 QKEATLCVSDLGTRAKLASFSFLPQSSLSSEKL 294 HTR2A
+K + CV+D ASFS +S KL Identities
Sbjct 355 RKRISNCVADYSVLYNSASFSTFKCYGVSPTKL 387 Spike2020
^
HTR2A mutation S280Y (meaning serin S gets replaced with tyrosie Y) labelled with ^ is frequently involved in Caecum Carcinoma
Query 142 PLPSKLCAVWIYLDVLFSTASIMHLCAISLDRY--... HTR2A
P PSK D+LF+ ++ A + +Y +A ++ I
Sbjct 807 PDPSKPSKRSFIEDLLFNKVTLAD--AGFIKQY... SPIKE 2020
^
The L=147 in HTR2A can be mutated to anything.
Query 450 KQH-SEEASKDNSDGVNEKV 468
K H S + + G+N V
Sbjct 1157 KNHTSPDVDLGDISGINASV 1176
^
The p.H452Y was found in patients with Striated muscle NS Rhabdomyosarcoma
Query 462 DGVNE 466 HTR2A
D VN+
Sbjct 950 DVVNQ 954 Spike 2020
^^
D462= or G463R are found in patients with Large intestine Colon Descending Carcinoma
Query 9 TSLSSTTNSLMQLNDDTRL--------YSNDFNSGEANTSDAFNWTVDSENRTNLSCEGC 60
T+L S T SL+ +N+ T + + ND G + +W ++SE R S C
Sbjct 108 TTLDSKTQSLLIVNNATNVVIKVCEFQFCNDPFLGVYYHKNNKSW-MESEFRVYSSANNC 166
V47 or N33Y is a mutation found in BRAIN cancers!!
and the list of homologies is long, despite of the just 33% of identities in 'small peptides' sections between Spike and HTR2A:
Query 10 SLSSTTNSLMQLND 23 HTR2A
SLSST L L D
Sbjct 937 SLSSTASALGKLQD 950 Spike
Query 127 VMPVSM 132 HTR2A
++PVSM
Sbjct 726 ILPVSM 731 Spike
Query 123 LGF------LVMPVS-ML 133
LGF VM V ML
Sbjct 1218 LGFIAGLIAIVM-VTIML 1234
Query 365 FVWIGYLSSAVNPLVYTL 382
++W+G+++ + ++ T+
Sbjct 1215 YIWLGFIAGLIAIVMVTI 1232
Query 188 SRTKAFLKIIAVWTISVG 205 HTR2A
+R+ A IIA +T+S+G
Sbjct 684 ARSVASQSIIA-YTMSLG 700 Spike
and many,many more!!!The second example in the above table contains the sequence ‘PDPSKPSKRSFIEDLLFNKVT’ with the rest after the 2x(PSK) motif. Just recently the ‘KRSFIEDLLFNKVT‘ peptide is being associated by J. Rose and wmcresearch here on substack with a quote, ‘weaponized amyloidosis’, whereby the paper they cite to base their assumption, has actually a different sequence:’ RSAIEDLLFDK(V)’, with high homolgy though. I was writing about the KRSFIEDLLFNKV peptide since 2020, because it is really unique, based on the literature and the chains of patents containing that sequence in regard to ‘vaccines development’ first for ‘Receptor binding polypeptides’ (US 7491397-A 17-FEB-2009), then inside of the early Eli Lilly “SARS vaccine compositions and methods of making and using them’ US 8506968-B2 13-AUG-2013, then in ‘Ii-key/antigenic epitope hybrid peptide vaccines’ US 8815249-B2 1149 26-AUG-2014, then in "Vaccines for porcine epidemic diarrhea virus infections." US 10143739-B2 3 04-DEC-2018, and now in ALL the 2020 corona virus synthetic mRNA ‘vaccines’, and finding it right now, going actually all the way back to 1987! That patent “New antigenically active proteins and peptides, and infectious bronchitis virus (IBV) vaccines“ EP 0221609-A1 13-MAY-1987 was assigned to DUPHAR INTERNATIONAL RESEARCH B.V which operates as a subsidiary of Abbott Laboratories. Btw. The IBV was derived from monkies, not bats… And here that N-terminus of the 1987 patented ‘peplomeric protein’ from the Infectious bronchitis virus
Query 1 MLVTPLLLVTLL---CV-LCSAALYDSSS-Y 1987 peplomeric IBV
M V L+L+ L+ CV L ++ + Y IDENTITIES
Sbjct 1 MFVF-LVLLPLVSSQCVNL--TTRTQLPPAY Spike 2020And now the very KRSF… SARS-CoV-2 Spike motif aligned with the 1987 patented IBV protein:
Query PSSPRRRSFIEDLLFTSVE 702 1987 peplomeric IBV
PS P +RSFIEDLLF V IDENTITIES
Sbjct PSKPSKRSFIEDLLFNKVT 827 Spike2020In the above example one can actually see the ‘shortened’ version of the furin site ‘PRR_RS’ placed at different spot in the Spike2020. Actually when running BLAST search with DEFAULT parameters between the 1987 patented peplomeric protein CAA01736.1 at https://www.ncbi.nlm.nih.gov/protein/CAA01736.1 [Infectious bronchitis virus] and the Spike, one gets 38% IDENTITIES!!!! One can clearly see that the entire ACE2 RBD domain parts of S1 and the entire S2 domain of 2020 Spike was derived from that 1987 protein! Here a BLAST output, Query line is the 1987 protein and Subjct line is the Spike:
358 bits(838) 8e-103 Compositional matrix adjust. 205/550(37%) 245/550(44%) 26/550(4%)
Query 583 NVLIPNSFNLTVTDEYIQTRMDKVQINCLQYVCGNSLDCRDLFQQYGPVCDNILSVVNSI 642
+ IP F VT E M K ++C Y+CG+S +C +L QYG C I
Sbjct 711 SIAIPTNFTISVTTEILPVSMTKTSVDCTMYICGDSTECSNLLLQYGSFCTQLNRALTGI 770
Query 643 GQKEDMELLNFYSSTKPAGFNTPFLSNVSTGEFNISLLLTTPSSPRRRSFIEDLLFTSVE 702
+D + K + TP + G FN S L PS P RSFIEDLLF V
Sbjct 771 AVEQDKNTQEVFAQVKQI-YKTPPIKDF--GGFNFSQILPDPSKPSKRSFIEDLLFNKVT 827
Query 703 SVGLPTDDAYKNCTAGPLGFLKDLACAREYNGLLVLPPIITAEMQTLYTSSLVASMAFGG 762
Y +C DL CA +NGL VLPP T EM YTS L A G
Sbjct 828 LADAGFIKQYGDCLGDIAA--RDLICAQKFNGLTVLPPLLTDEMIAQYTSALLAGTITSG 885
Query 763 IT-AAGA---IPFATQLQARINHLGITQSLLLKNQEKIAASFNKAIGRMQEGFRSTSLAL 818
T AGA IPFA Q+ R N G+TQ L NQ IA FN AIG Q+ ST AL
Sbjct 886 WTFGAGAALQIPFAMQMAYRFNGIGVTQNVLYENQKLIANQFNSAIGKIQDSLSSTASAL 945
Query 819 QQIQDVVNKQSAILTETMASLNKNFGAISSVIQEIYQQLDAIQANAQVDRLITGRLSSLS 878
QDVVN L L NFGAISSV +I LD ++A Q+DRLITGRL SL
Sbjct 946 GKLQDVVNQNAQALNTLVKQLSSNFGAISSVLNDILSRLDKVEAEVQIDRLITGRLQSLQ 1005
Query 879 VLASAK--QAEHIRVSQQRELATQKINECVKSQSIRYSFCGNGRHVLTIPQNAPNGIVFI 936
A IR S LA K ECV QS R FCG G H + PQ AP G+VF
Sbjct 1006 TYVTQQLIRAAEIRASA--NLAATKMSECVLGQSKRVDFCGKGYHLMSFPQSAPHGVVFL 1063
Query 937 HFSYTPDSFVNVTAIVGFCVKPANASQYAIVPANGRGIFIQVNGSYYITARDMYMPRAIT 996
H Y P N T C ++ G+F+ ++T R+ Y P IT
Sbjct 1064 HVTYVPAQEKNFTTAPAIC--HDGKAHFPRE-----GVFVSNGTHWFVTQRNFYEPQIIT 1116
Query 997 AGDIVTLTSCQANYVSVNKTVITTFVDNDDFDFNDELSKWWND---TKHELPDFDKFNYT 1053
+ C VN TV D F +EL K + +L D N
Sbjct 1117 TDNTFVSGNCDVVIGIVNNTVYDPLQPELD-SFKEELDKYFKNHTSPDVDLGDISGINAS 1175
Query 1054 VPILDIDSEIDRIQGVIQGLNDSLIDLEKLSILKTYIKWPWYVWLAIAFATIIFILILGW 1113
V +I EIDR V LN+SLIDL+ L YIKWPWY+WL I +++
Sbjct 1176 V--VNIQKEIDRLNEVAKNLNESLIDLQELGKYEQYIKWPWYIWLGFIAGLIAIVMVTIM 1233
Query 1114 VFFMTGCCGC 1123
MT CC C
Sbjct 1234 LCCMTSCCSC 1243
and the N-terminal portion:
17.6 bits(34) 7.0 Compositional matrix adjust. 47/190(25%) 57/190(30%) 42/190(22%)
Query 633 DNILSVVNSIGQKEDME-LLNFYSSTKPAGF---NTPFLSNVSTGEFNISLLLTTPSSPR 688
D L V K ME YSS F PFL + + N L
Sbjct 138 DPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFLMDLEGKQGNFKNL-------- 189
Query 689 RRSFIEDLLFTSVESVGLPTDDAYKNCTAGPLGFLKDLACAREYNGL--LVLPPI---IT 743
R F+ F ++ Y T P DL + L LV PI IT
Sbjct 190 -REFV----FKNIDGYF----KIYSKHT--PINLVRDL--PQGFSALEPLVDLPIGINIT 236
Query 744 --AEMQTLYTSSLVASMAFGGITAAGAIPFATQLQARINHLGITQSLLLKNQEK--IAAS 799
+ L S L G TA A + LQ R LLK E I
Sbjct 237 RFQTLLALHRSYLTPGDSSSGWTAGAAAYYVGYLQPR--------TFLLKYNENGTITDA 288
Query 800 FNKAIGRMQE 809
+ A + E
Sbjct 289 VDCALDPLSE 298And when we get to the furin site portion:
10.8 bits(18) 918 Compositional matrix adjust. 6/31(19%) 9/31(29%) 1/31(3%)
Query 820 QIQ-DVVNKQ-SAILTETM-ASLNKNFGAISSV 849
Q+Q + + S + + + A GA SV
Sbjct 675 QTQTNSPRRARS-VASQSIIA-YTMSLGAENSV 705there is a VERY TROUBLING issue at the begin of this section, the ‘QTQT’.. All it started with searching across the https://www.ncbi.nlm.nih.gov/nuccore/CP000672.1 entry for Haemophilus Influenzae total genome data. One protein is EXTRAORDINARY:
/protein_id="ABQ99175.1" /db_xref="CDD:30856"/translation="MQSINQSINQSINQSINQSINQSINQSINQSINQSINQSINQSINQSINQSINQSINQSINQSINQSINQIVGFVKTCYKPEEVFHFLHQNSIPFSSIGGMTNQNVLLNISGIKFVLRIPNAVNLSLINREYEAFNNAQAYRAGLNVETPVLDAKSGVKLTRYLENSKPLSQIQLNEQSCLSQVVNNLYRLHNSEFVFRNVFSVFDEFRQYFSLLENKSAFYQADSKMDKLSAVFWQFEEINKEIILRPCHNDLVPENMLLQDDRLFFIDWEYSGLNDPLFDIATIIEEAHLSKEAADFLLETYCNQTNKYHKTEFQIAHKRLKIHRFCQNVLWFLWTKVKEEHGENFGDYALKRLDAAFKLLEELP"The ‘SINQ’ section REPEATED SO MANY times looks really ‘not normal’.. On top of it, take the biblical meaning of a ‘SIN’!!! So now, when starting with that Haemophilus Influenzae sinful protein ABQ99175.1 (phospho-2-dehydro-3-heoxyheptonate aldolase) and search for similar to it PATENTED proteins, you will end up chasing your own tail, that 37% with Spike 2020 identical 1987 peplomeric protein comes up again, and its ‘SINQ’ alignment sections are:
16.3 bits(31) 99 10/26(38%) 11/26(42%) 9/26(34%)
Query 8 INQ-SINQSI---NQ-----SINQSI 24 Haem. Infl.
IN+ I QS NQ S N I
Sbjct 779 INHLGITQSLLLKNQEKIAASFNKAI 804 1987 patent
SEVEN of those, and more... Now look where is Spike sinful section overlapping with the above, aligning 'by hand':
GICAS-YQT--QT-N-SPRRARSVASQSIIAYT >>> 2020covid SPIKE
S Q+ Q+ N S S+ QSI + IDENTITIES
MQSINQSINQSINQSINQ--SIN-QSINQ-SINQSINQSINQ >>>1987 PATENT
that's the FURIN site of the Spike!Paraphrasing the above: one has the feeling that the 2020 Spike GENOME, injected into bodies of billions, has really NOTHING to do with any in the skies flying bats, but rather from the SINs of the 80-ies and experiments on the best human friends, canine, i.e. dog, since the even better matching sequences to this SINQ chain are sequences for canine corona vaccines…. On the molecular level S, i.e. serines, are frequently phosphorylated, and N glycosylated… Thus do we need to wonder why we have so much glyphosate and sugar everywhere?? Also the above peplomeric protein delivers another confirmation of the early 2020 retracted publication by the indian researchers (“Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag“), who found HIV-1 insertions in the 2020 Spike genome. When searching for HIV-1 similarities to that 1987 peoplomeric protein, there are mainly two proteins which pop out in the search, the gp160 HIV1 protein and the gag-pol (otherwise known as Reverse transcriptase/ribonuclease!), with the following homolog segments, for the gp160:
29.3 bits(64) 0.22 Compositional matrix adjust. 30/124(24%) 51/124(41%) 12/124(9%)
Query 976 IQVNGSYYITARDMYMPRAITAGDIVTLTSCQANYVSVNKTVITTFVdnddfdfndELSK 1035
+ V G + AR + + R + ++ + C K + TT V + N L +
Sbjct 566 LTVWGIKQLQARILAVERYLKDQQLLGIWGCSG------KLICTTAVPWNASWSNKSLEQ 619
Query 1036 WWNDTKHELPDFDKFNYTVPILDIDSEIDRIQGVIQGLNDSLIDLEKLSILKTYI---KW 1092
+WN+ D + NYT I S ID Q + L++L+K + L + W
Sbjct 620 FWNNMTWMEWDREINNYTSL---IHSLIDESQNQQEKNEQELLELDKWASLWNWFNITNW 676
Query 1093 PWYV 1096
WY+
Sbjct 677 LWYI 680
and
18.5 bits(36) 413 Compositional matrix adjust. 14/61(23%) 26/61(42%) 7/61(11%)
Query 1017 VITTFVdnddfdfndELSKWWNDTKHELPDFDKFNYTVPILD-----IDSEIDRIQGVIQ 1071
++T V+ + L WWN ++ + N V +L+ + DR+ V+Q
Sbjct 775 IVTRIVELLGRRGWEALKYWWNLLQYWSQELK--NSAVSLLNATAIAVAEGTDRVIEVVQ 832
Query 1072 G 1072
G
Sbjct 833 G 833
and
18.5 bits(36) 445 Compositional matrix adjust. 16/50(32%) 25/50(50%) 3/50(6%)
Query 577 LLNVTENVLIPNSFNLTVTDEYIQTRMDKVQINCLQY--VCGNSLDCRDL 624
L+NVTEN + + + E I + D+ C++ +C N L C DL
Sbjct 86 LVNVTENFDMWKNDMVEQMHEDIISLWDQSLKPCVKLTPLCVN-LKCTDL 134and the homologies with the gag-pol:
18.5 bits(36) 436 Compositional matrix adjust. 9/18(50%) 12/18(66%) 0/18(0%)
Query 199 KVMRKVKALAYFVNGTAQ 216
K++R VKAL V TA+
Sbjct 863 KLLRGVKALTDIVPLTAE 880
Query 969 ANGRGIFIQ-VNGSYYITARDM 989
A R I + V+G YY ++D+
Sbjct 886 AENREILKEPVHGVYYDPSKDL 907
Query 884 KQAEHIRVSQQ 894
+QAEH++ + Q
Sbjct 1309 EQAEHLKTAVQ 1319
16.2 bits(30) 2006 Compositional matrix adjust. 6/7(86%) 7/7(100%) 0/7(0%)
Query 499 VVSGGKL 505
V+SGGKL
Sbjct 7 VLSGGKL 13
and many more segments.
The gp160(gp41+gp120) and the gag HIV-1 proteins similar to the 1987 peplomeric patented protein from the Infectious bronchitis virus are the very same, the indian researchers were talking about. Is it maybe that the HIV-1 origin, like SARS-CoV-2, are actually stemming from those first avian coronaviruses? Going back to the very homolog KRSF.. motif from 1987 and also in the present Spike, the question about the by Dr. Rose claimed ‘weaponized amyloidosis‘, why first NOW prions, when that motif was out there for DECADES??? Listening to the Nobel lecture from Dr. Prusiner could help…
With all the above, imagine a cell which exactly in the same time have to produce HTR2A and now gets a new genetic synthetic HUGE in size mRNA message to start producing the very same stretches of amino acids for a different protein. A question to anyone who wants the covid Spike genome human body reprogramming injection, what do you prefer your body shall produce, the synthetic viral-bacterial-human chimera or the HUMAN HTR2A receptor which regulates your behavior, including responses to anxiogenic situations and psychoactive substances??? Think infinite amount of times, when you even dream to inject the Spike genome into children!!! Consider that work in this case: “Possible association of serotonin 2A receptor gene (HTR2A) regulatory variants with severity of depression symptoms in children with autism spectrum disorder“ (Cogn Behav Neurol. 2014 Jun; 27(2): 107–116.) To genetically reprogram the children for the rest of their lives is SO INHUMANE, that those who are making these decisions should never get out of GUNATANAMO, in my opinion! For those reading this and didn’t check out the post:
Please do so, it explains little bit more the cancer connections. Lot of the mentioned cancer mutations translate to specific DNA/RNA elements, in particular C and T nucleotides in DNA. A patent for “Method for regulating genes with electromagnetic response elements“ by Martin Blank and Reba Goodman at https://patents.justia.com/patent/6919207 describes the essence, quote:
“In the present invention, exogenously introduced genes, in gene therapy, are regulated by the introduction of electromagnetic response elements (EMREs) into the gene promoters that do not have them to serve as “switches.” Exposure to electromagnetic fields of 8 μT 60 Hz for 30 minutes induces gene expression, because the switches make the gene now responsive to EM fields. The electromagnetic field response elements, therefore, are the “switches.” The present invention therefore provides a non-invasive technique in gene therapy.“
Also the publication of the BioInitiative Reports authors:
“DNA is a fractal antenna in electromagnetic fields” by Martin Blank 1 , Reba Goodman and any of the publications added to the search at: https://pubmed.ncbi.nlm.nih.gov/21457072/
adds more to the topic.
And probably not for nothing Prof. Bryan L. Roth’s ‘non-invasive remote control of neuronal signaling’ has such a large amount of tax payers supportive grants dollars
https://neurotree.org/beta/grants.php?pid=16803
Today, 6/11/2022 Children’s Health Defense just published an article:
”CHD Films Presents — Infertility: A Diabolical Agenda” with the documentary available for free at: https://live.childrenshealthdefense.org/infertility-a-diabolical-agenda
Already in 2020 I posted MANY summaries touching the two human proteins related to fertility, Human Chorionic Gonadotropin (HSG) AND Follicle-stimulating hormone receptor (FSHR). In the 2021 letter to FDA
after the same analysis as presented above, the ‘content’ of the injected Spike genome was equally terrifying (with ‘sc’ meaning amino acid sequence coverage and ‘id’ identities in that sequence) in terms of homologies with these fertility proteins:
- HCG (68% sc, 29% id), infertility
- FSHR (94% sc, 44% id), pregnancy, menstruation
The signal peptide of each protein at its N-terminus is the very begin of translational process, and it carries information about the protein secretion^2. Here the signal peptide of the FSHR protein overlapping the injected Spike 2020:
Query 1 M-A-LLLVSLLAFLSLG-SGCH FSHR
M + L+L+ L++ + + ++ IDENTITIES
Sbjct 1 MFVFLVLLPLVSSQCVNLT-TR Spike2020And just to throw it in, the overlaps of the N-termina of the 2 ESSENTIAL digestive enzymes and human HEMOGLOBIN with Spike2020:
Query 1 MN--LLLI-L-TF--V-AAAVAA-P--F Trypsin-2(P07478)
M L+L+ L + V ++ + P + IDENTITIES
Sbjct 1 MFVFLVLLPLVSSQCVNLTTRTQLPPAY Spike2020
and
Query 1 MNP-LLILTFVAA---ALAA----P--F SERINE PROTEASE
M L++L V++ L++ P + IDENTITIES
Sbjct 1 MFVFLVLLPLVSSQCVNLTTRTQLPPAY Spike2020
and gamma-1 subunit from hemoglobin (uniprot P69891)
Query 1 MGHFTEEDKATITSLWGKVNVEDAGGET H.Hemoglobin P69891
M F +S + + IDENTITIES
Sbjct 1 MFVFLVLLPLV-SSQCVNLTTRTQLPPAY Spike2020 Imagine your HUMAN body, in case of a women, needs to start producing HCG, or FSHR, and now, it CAN‘T do it the same way as it used to any more, because it is reprogrammed by Pfizer and Mod-E-RNA genetic codes, which now steal your human building blocks like HUMAN t-RNA, amino acids, ATP’s, minerals to produce NON-HUMAN toxic, synthetic Spike! Imagine the same synthetic genetic fragments are landing now in MEN’S body??? I don’t know yet the consequences, just can imagine, they will be HUMILIATING. After posting many comments to substack MD’s (some do not even allow posting comments, they want the money for that, like Jessica Rose), trying to remind them that covid GENE THERAPY should NOT be called ‘vaccines’ and here is what I received today as a response (from one who allows to comment):
“I thought your point over for a while and I made the decision to continue call them vaccines because the other vaccines are also dangerous, and I have no issue with guilt by association dripping over to the rest of the vaccine program.“
The very same ‘good doctors’ which suppose to save your life, see no difference between GENE MODIFICATION INJECTION and old style vaccines, as if they didn’t see the VAERS reports!!! And then it takes them 1.5 years to analyze the deaths and injuries graphs from VAERS system in order to even start speaking about ‘dangerous vaccines’???? It is a CRIME, and I do believe it is intentional, from the very begin, and hopefully many readers here know it too, and warn others, INDEPENDENTLY from the Rockefellers ‘guided’ MD’s!!!
6/13/2022 : A day when more embalmers samples were analyzed by Mike Adams (Natural News). In the march’22 post:
I mentioned there one of the human blood proteins: complement factor B being one of the predictive biomarkers of cardiovascular disease (CVD), https://www.uniprot.or/uniprot/P01024 . There are few more complementary factors, all in blood plasma, among others C3, which functions among others are amyloid-beta clearance, and more than 30 other essential tasks, including:
G protein-coupled receptor signaling pathway Source: ProtInc
immune response Source: ProtInc
inflammatory response Source: UniProtKB-KW
fatty acid metabolic process Source: UniProtKB-KW
The BLAST search for the homologies of C3 with Spike, genome of which is injected into billions, gives following results, for 96% sequence coverage ~33% identities, with examples of few substantial ones, Query is the HUMAN complementary protein and Subjct is the Spike2020:
24.4 bits(50) 0.10 Compositional matrix adjust. 20/62(32%) 25/62(40%) 6/62(9%)
Query 974 TESETRIL-LQ--GTPVAQMTEDAVDAERLKHLIVTPSGCGEQNMIGM---TPTVIAVHY 1027
TES L Q G +A T+ D + L L +TP G I T +AV Y
Sbjct 553 TESNKKFLPFQQFGRDIADTTDAVRDPQTLEILDITPCSFGGVSVITPGTNTSNQVAVLY 612
Query 1028 LD 1029
D
Sbjct 613 QD 614
20.6 bits(41) 1.3 Compositional matrix adjust. 18/66(27%) 23/66(34%) 18/66(27%)
Query 1501 KLNKLCRDELCRCAEENCFIQKSDDKVTLEERLDKACEPG--VDYVYKTRLVKVQLSNDF 1558
KLN LC + F+ D E R + G DY YK L +DF
Sbjct 386 KLNDLCFTNVY----ADSFVIRGD-----EVRQIAPGQTGKIADYNYK-------LPDDF 429
Query 1559 DEYIMA 1564
+ A
Sbjct 430 TGCVIA 435
19.3 bits(38) 3.0 Compositional matrix adjust. 10/19(53%) 11/19(57%) 1/19(5%)
Query 798 SITTWEILAVSMSDKKGIC 816 HUMAN C3
S+TT EIL VSM C IDENTITIES
Sbjct 721 SVTT-EILPVSMTKTSVDC 738 Spike
16.3 bits(31) 24 Compositional matrix adjust. 13/33(39%) 16/33(48%) 2/33(6%)
Query 1549 LVKVQLSNDFDEYIMAIEQTIKSGSDEVQVGQQ 1581
LVK QLS +F I + I S D V+ Q
Sbjct 962 LVK-QLSSNFGA-ISSVLNDILSRLDKVEAEVQ 992
Query 172 GIPVKQDSLSS-QNQLGVL 189
I QDSLSS LG L
Sbjct 930 AIGKIQDSLSSTASALGKL 948
Query 1066 FAAFVKRAPSTWLTAYVVKVFS-LAVNLIAI 1095
+ ++K WL +A LIAI
Sbjct 1206 YEQYIKWPWYIWL--------GFIA-GLIAI 1227
and in particular these 2, furin site:
Query 657 RAELQCPQPAARRRRSV 673 Human C3
A Q RR RSV
Sbjct 671 CASYQTQTNSPRRARSV 687 Spike
or also in other segments
Query 663 PQPAARRRRS 672
P P+ +RS
Sbjct 807 PDPSKPSKRS 816
and the integrin binding site motif RGD:
Query 1393 RGDQ 1396
RGD+
Sbjct 403 RGDE 406With any disturbance of that protein function, including removing amyloids out of the body via blood, there are going to be consequences. This could be one possible scenario, without trying to interpret the regular repetitive wire structures seen by Mike. Genetic sequencing, atom force spectroscopy, mass spectroscopy and Raman spectroscopy (graphene detection) will definitely help. The larger the amount of the genetic reprogramming material, injected into human bodies, the higher the probability that some of the human stem cells will get reprogrammed for good. The by Dr. Jane Ruby cited paper from the Scripps Research Institute got the following NIH funding, quote:
“Funding: This work was funded by NIH grants AI129698 and AI140844 (to J.Z.), Ufovax/SFP-2018-0416, Ufovax/SFP-2018-1013, and Ufovax/SFP-2020-0111 (to J.Z.).“
It is available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7978432/pdf/abf1591.pdf and it is NOT A JOKE! One of Mike’s images showing the wire structure looked almost as a distinct neuronal repeatable myelin insulation around the central portion of the wire. It is possible that the blood vessels are being reprogrammed into becoming neuronal tissue????? It’s completely crazy idea though.
But the most important, what are all the MD’s talking about ‘vaccines’ (total deception) are waiting for????? TIME TO ACT IS NOW and it should have been ~2.5 years ago!
This post like many others, is not finished. We learn every single day, and still die so clueless, unfortunately. So checking now and then for new hints and connections might be of interest, since it might end up all with this one logo:
since every day brings more terrible stuff. like:
https://phys.org/news/2022-06-crispr-technology-tying-human-gene.html
but also a good stuff like:
https://www.brighteon.com/ae8f879f-3ce2-4379-af6d-21ae021c594e
talking about Highpowerheart.com .
Thank you for getting that far. In case of suggestions, corrections, please leave a comment.
post from March 2022:
2.Hajar Owji et al. “A comprehensive review of signal peptides: Structure, roles, and applications” Eur J Cell Biol. 2018 Aug:97(6):422-441
Man another UNC Deepstater I just want to ⚰ RIP up my diploma, so ashamed of my alma mater 👣..I'm so much less technical & more creatively punitive, here's what I got: https://www.tiktok.com/t/ZTd3poyC7/?k=1
I like your MODǝRNA 🔌 btw!
beginning to suspect that c19 injectables are not the first ones to contain these toxins... and fascinating (in a evil way) about the non-invasive EM gene therapy... culling & control are the clear objectives... gitmo would be too lenient.