Stanford, Penn, MIT et al. dream, genetically modified world. More Spike2020 companions, with ADAM33, no EVE yet...
Imagine, all the sepsis cases could have been prevented by applying a super fast, huge dose of intravenous Vitamin C^18 and few other essential nutrients!!!
Change: Updates now will be attached at the very end of each post, except for this one, keep an eye on the good old Penn’s director Amy Gutmann (https://www.kla.tv/28574), Dr. Henry Daniell (https://www.dental.upenn.edu/faculty/henry-daniell/ ), Dr. Black’s lab (https://hosting.med.upenn.edu/blacklab/). THANK YOU.
This post is to honor all injured victims of covid gene based injections, in particular a teacher, who after loosing all extremities, still laughs, the story comes from Dr. Makis post:
and there are many more just unthinkably horrifying incidents, including multiple injuries and 3 deaths in my own family, all covid injections related plus personally witnessing just recently a man in shorts, supported by a female, barely walking towards the store, with both legs of dark purple color… A list of just newly deceased young people in connection with the covid gene modifications via the injections, can be found and translated at: https://report24.news/ploetzlich-und-unerwartet-das-sterben-hoert-nicht-auf/
There are too many injured people, alone on the streets! Just one quote from 2007 article^1: “Organ damage in sepsis involves an alteration in gene expression, making gene transfer a potential therapeutic modality.“ It is about using SV-40 vectors for pulmonary gene therapy..
The question is, to mutilate humanity to a point of no return, requires planning, precision and devotion, to do evil. This post will show just incredible flat admission of that precision (below the 3rd divider bar), while using NIH BLAST bioinformatics software for analysis of specific protein sequences and the universally injected Spike’s synthetic patented gene, expressing this toxic non-human protein. There are also many links for theme validation with clear words in the links title, so no need to read it all.. Also, Spike2020 as always, is the very first Spike version from the official NIH SARS-CoV-2 data base at https://www.ncbi.nlm.nih.gov/nuccore/NC_045512, the one which with tiny modification, was injected into billions of people..
Why is the contamination of the covid injections with the SV40 promoter now so popular (https://covid19criticalcare.com/covid-vaccines-genome-integration/)? Is it because the https://www.snapgene.com/plasmids/basic_cloning_vectors/SV40_promoter contains very special restriction enzyme called SexAI :
present in rCutSmart™ Buffer among 210 other DNA chopping dream tools of geneticists? Try to search SexAI with any engine, you will get everything else connected with the first 3 letters, but the SV40 promoter map.. SexAI can be purchased at https://www.neb.com/en-us/products/r0605-sexai . That is now in bodies of how many and it is all over the MSM, like https://expose-news.com/2024/03/17/sv40-a-dna-altering-carcinogenic-contaminant-found-in-pfizers-covid-19-vaccines/
Geneticists intentionally are sticking to FDA re-definitions of covid19 ‘vaccines’, which now include GENETIC MODIFICATIONS, because that’s their ‘daily bread’, money.
That SexAI insertion is on top of two examples of short amino acid strings inside of the expressed Spike toxin: ‘SSS-G-WTA-GAAAYY‘ or this one, from my first posts: ‘ALLAG-TITS-G-WTF-GAGAA‘ (sequences 254-266 and 886-893 from file https://www.ncbi.nlm.nih.gov/protein/1796318598). Dr Fauci, did the covid breeding bats attend some LBGT introduction course, in order to adjust to the global warm(n)ing changes with all these ‘biologically imprinted words’ (in form of single amino acid code) now so deep in human flesh?
Hands expression reflects the content of our intentions, some engage left, some right with few image examples below. First one is from a student from Stanford, the second well known Dark Act proponent https://www.huffpost.com/entry/obama-signs-dark-act-to-invalidate-vermonts-landmark_b_57a644c7e4b0ccb023727b2d, the one who chose Biden, who then chose himself, and the third one from other places. Links to the first one https://stanfordmag.org/contents/caption-this, and the last one from https://www.usatoday.com/story/news/nation/2023/05/03/satancon-boston-2023-convention/70168925007/)
They all say, these hands signs are just a gesture, to express love. Love?
Human heart is the place where love grows and also lot of blood flows, and that’s why Sherry Moody still laughs(!!), so thank YOU for that wonderful example of valuing what’s most important in life. What ‘they’ definitely do not like is, when YOU FORGIVE them their evil (ironically backwards live…), in particular, when intended..’They’ want you to be miserable, angry, crying for years, and some do indeed.
So Stanford ‘lives’ from In-nova-t-I-on, researching/doing something what has to be new, not from non patentable nature made by the Creator. The overwrite of CREATION is well illustrated in this short abstract in one of the top scientific magazines, link at: https://www.nature.com/articles/nature16162 . The title: “Exploring the repeat protein universe through computational protein design“. There, Dr.’s John A. Tainer &David Baker et al. say: ”.. it is possible to design novel repeat proteins with precisely specified geometries, opening up a wide array of new possibilities for biomolecular engineering.” The end of that sentence should have been “new possibilities for biomolecular GENETIC engineering“. That was in 2015. Now ~10 years later, we have billions of human victims injected with genetically modifying materials, without consent (thus ILLEGAL!), containing synthetic genes of one and the same NON-human, toxic, patented Spike protein of the SARS-CoV2 coronavirus, whose only parts (not the entire active infectious virus) can be found in the Pdb Data Bank. The result of the covid tragedy called, mildly speaking, universal Spike gene therapy, until this day was not investigated properly, that’s why this illegal agenda explodes like the chinese balloons and now ends with just few recent announcements, like:
https://www.medicalcountermeasures.gov/BARDA “Project NextGen: Next Generation Medical Countermeasures“
https://www.statnews.com/2024/03/13/hemophilia-treatment-gene-therapy-use-of-hemgenix-roctavian/ “Hemophilia gene therapies arrived after 40 years of struggle. Where are the patients?“ 3/13/2024
https://www.wsj.com/health/pharma/doctors-can-now-edit-the-genes-inside-your-body-4c8e1aea “Doctors Can Now Edit the Genes Inside Your Body” It sounds like science fiction, but dozens of people have undergone gene editing for cardiovascular disease and other conditions“. 3/11/2024
https://www.technologyreview.com/2024/01/18/1086791/brain-dead-man-gene-edited-pig-liver/ 1/18/2024
that pure evil, comes from the top of the scientific establishment https://www.theguardian.com/environment/2024/jan/19/nobel-laureates-call-on-eu-to-relax-rules-on-genetic-modification “Nobel laureates call on EU to relax rules on genetic modification.“
with the explosion of cancers, in particular among the covid jabbed victims, the establishment is now keen on collecting the NEW genetic footprint of those victims, here their next trap: https://kffhealthnews.org/news/article/chemotherapy-drug-overdose-fluorouracil-common-gene-test-lifesaving/
A new documentary at https://brokentruth.com/epidemic-of-fraud/ (Truth is a bitter Pill HCQ) was pointed out by Steven Kirsch, the covid ninja fighter:
Due to brokentruth promotion of Wellness Company selling drugs, be it as great as HCQ or Ivermectin, but with Dr. McCullough not telling consistently the entire truth about covid genetically modifying injections, things should be questioned, as always. So let’s say, analysing part truths is still good, at some point lies will be filtered out.
Brokentruth movie mentions the congress woman Anne Eshoo, who established BARDA, the NO 1 decision maker in early 2020 covid response (directed by Rick Bright), crashing the Hydroxychloroquine based cure for the ‘new disease’. Just recently Mrs. Eshoo discussed the future of science in SLAC, the most unique Stanford project: https://www.flickr.com/photos/slaclab/albums/72177720314995447/ consuming lot of earth’s Helium supply, luckily still down to the earth..
Stanford is like a giant magnet attracting all the hummingbirds to a sweetest feeder. An example, caged guests (except for the one honorable James Baker III) at the memorial service for G.Shultz, who died at 100 in ‘21, with H. Kissinger in the front raw, who had no idea that he will be dead in 2 years too, equally at 100 ^2:
So the U.S. Rep. armenian Congress woman Anna Eshoo cares for Stanford a lot, it’s like her own child, which develops new things super fast for people in need, few examples:
https://news.stanford.edu/2024/02/21/new-rna-editing-tool-enhance-cancer-treatment/
https://med.stanford.edu/genetherapy.html (Program in Human Gene Therapy works on a variety of viral and non-viral vector systems, with major disease models of hemophilia, hepatitis C and B viral infections, and diabetes.)
https://online.stanford.edu/courses/xgen201-principles-and-practices-gene-therapy
https://stanmed.stanford.edu/scientists-are-refining-crispr-for-wider-applications/
https://biox.stanford.edu/research/seed-grants/interdisciplinary-initiatives-program-seed-grant-humanize-and-deimmunize (To increase the precision/efficacy of gene therapy and cell therapy, one promising approach is to use engineered intracellular proteins, such as transcription factors, to control cells.)
The entire research program https://biox.stanford.edu/research/research-projects, has NO organic carrots, red beets, grass fed beef, no Vit C, clean F-free water or raw milk, none of it, that’s history, instead, everything else unthinkable, which started with an initiative of just few people (https://biox.stanford.edu/about/biox-history). That was ~ quarter century ago with Condoleezza Rice et. al, Silicon valley money including the non-vanishing Bermuda-based entity, Atlantic Philanthropies... These days BioX endeavors include even taking into custody ‘free-flying’ birds (https://biox.stanford.edu/research/seed-grants/brain-activity-during-visual-motor-coordination-free-flying-birds), no one is spared. The final sentence of the birds imprisonment trial: ”In addition, the results will yield much-needed control strategies for search and rescue robots flying in turbulent wind.” Ha, here comes the wind, straight from the Stanford young global specialty: https://stanfordmag.org/contents/the-weather-man
The persistence of the money supply to ‘adjust’ any biological world into a synthetic man-made LAB product, later on patented, is just not only insane, but it is a HUGE issue of ethics, personal believes, to that level that in 2010 Dr. Fauci wife participated in 'Ethical' Committee initiated by Obama, it was about Synthetic Biology, which now includes HUMANS: https://bioethicsarchive.georgetown.edu/pcsbi/sites/default/files/PCSBI-Synthetic-Biology-Report-12.16.10_0.pdf
Let’s close with last example from Satnford: https://news.stanford.edu/2021/09/03/researchers-develop-hypercompact-crispr/
In the meantime, number of injured covid genetically affected takers of the injections is growing, with the newest:
And all that, while FDA secretly and illegally approves more and more of those, with their agents constantly migrating between their FDA homeland and corporation security:
with industry and academia, running the gov’s show, planning ahead:
https://www.nature.com/articles/s41587-024-02172-9 about genetic variants of p53..
https://www.science.org/doi/10.1126/scitranslmed.adj9283 “Genome-wide repeat landscapes in cancer and cell-free DNA“
https://www.thelancet.com/journals/lanmic/article/PIIS2666-5247(23)00378-6/ “Benchmarking CRISPR-BP34 for point-of-care melioidosis detection in low-income and middle-income countries: a molecular diagnostics study“
https://onlinelibrary.wiley.com/doi/10.1002/jgc4.1890 “Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis“
And this one, the 201 event organizer, JHI, gets it just one time, again:
https://www.hopkinsmedicine.org/news/newsroom/news-releases/2024/03/junk-dna-no-more-johns-hopkins-investigators-develop-method-of-identifying-cancers-from-repeat-elements-of-genetic-code
‘Junk DNA’ No More: Johns Hopkins Investigators Develop Method of Identifying Cancers from Repeat Elements of Genetic Code.
These elements represent six families: transposable elements, SINes, satellites, LTRs, LINEs, and RNA elements, most of them were discussed in regard to the genetic changes by covid injections, some already in 2020. It was PREDICTABLE, and now it is official.
The global concentration on genes applications, modifications, tests, collections, is, as if the entire medical research suddenly cares about one thing only, genes related issues, which was already before but in particular AFTER the universal covid genes based agenda.
One of the previous posts:
mentioned a cross shaped protein, named LAMININ (https://www.uniprot.org/uniprotkb/P24043/entry), glycosylated, like Spike, and regulating integrin mediated signalling pathway. Since Spike contains the same signature motif of all integrins, the ‘RGD’ tripeptide, thus laminin must ‘somehow’ affect the covid19 condition. Indeed 2022 paper^3 observed quote:”Serum levels of laminin in COVID-19 survivors 6 months after discharge were significantly higher than those in the controls.” In short, more laminins, more ‘covid19’.. Please note here, the paper writes about COVID19, the virus, but the official NIH virus sequence has only 3 proteins with this motif, one of which is expressed by the injected Spike genome. Thus what generates more of the integrin motifs, natural infection on the mucus membranes or genetic construct with never ending Spike production in CELLS OF ALL POSSIBLE ORGANS?
Further laminin participates in 22 officially known fundamental biological processes, from cell membranes organization, to neuronal, embyo/brain development, which should have been a huge ‘STOP"‘ for anything Spike related in the global ‘covid rescue plan’. Yes, it should have been, but no, it wasn’t, NIH/CDC/FDA lead the dec-i-sion.
The now discussed Spike-laminin plot includes other covid country club proteins. For example, the LAMR1( https://www.uniprot.org/uniprotkb/P08865/entry), which binds laminin and is worse then the Khazars, it has 10 alternative names, not just 2, here few of its sections homologous with Spike:
Query 74 VSVIS--SRNTGQRAVLKFAAATGATPIA 100 LAM-R1
VSVI+ + + Q AVL P+A
Sbjct 595 VSVITPGTNTSNQVAVLYQDVNCTEVPVA 623 Spike2020
Query 11 KEEDVLKFLAAGTHLGGTNLDFQ----MEQYI 38 LAM-R1
KE D L +A +L + +D Q EQYI
Sbjct 1181 KEIDRLNEVA--KNLNESLIDLQELGKYEQYI 1210 Spike2020
Query 202 YFYRDPEE 209 LAM-R1
Y Y+ P++
Sbjct 421 YNYKLPDD 428 Spike
here quickly the LBGT section of Spike2020, manual alignment:
Query 272 ATEDWSAAPTAQATEWV-G 282 LAM-R1
++ W+A A ++ +
Sbjct 254 SSSGWTAGAAAYYVGYLQP 264 Spike2020
and here the Biden's singing bird:
DW-SAQPA---TEDWS-AAPTAQATEWVGATTDWS LAM-R1
+ SA A T W+ A +A + + ++
QYTSALLAGTITSGWTFGAGAALQIPF---AMQMA Spike2020
LAMR1 is not only part of ribosomes, it functions as receptor for many viruses, bacteria and pathogenic prion proteins, it is everywhere, in nucleus, cytosol, cytoplasm, exosomes.. Thus its binding to the for microvessel formation responsible antigenic, glycosylated laminin (40 glycans!), is just one of its tasks. The ‘sweet’ Lam-in-ins’ complicated network of interactions keeps the entire space between cell membranes and collagen matrix ‘in space’^5:
What else binds laminin proteins? Sounds religious, but it is not, or maybe, it is the LUTHERAN BLOOD GROUP Glycoprotein^6, which has a long history going back to the gene on the human X chromosome responsible for color blindness^7. It is a red blood cell receptor binding the laminin^8,^9 and is involved in vaso-occlusion in sickle cell disease, when body produces too much of it. That laminin very high affinity interaction with the Lutheran antigen contributes to many other processes, organogenesis, erythropoiesis, smooth muscle development, malignant transformation and tumor metastasis^10. The Lutheran antigen (https://www.uniprot.org/uniprotkb/P50895/entry) has again quite few homologies with SARS-CoV-2 Spike, using normal BLAST (Query is the Luther, Subjct the Spike2020, the lines inbetween are the identical parts) and manual alignment, to name just few:
Query 57 GTHDHYMLEWFLTDRSGARPRLASAEMQ----GSELQVTMHDTRGRSP--------PYQL 104
GTH WF+T R+ P++ + + ++ + + + P +L
Sbjct 1099 GTH------WFVTQRNFYEPQIITTDNTFVSGNCDVVIGIVNNTVYDPLQPELDSFKEEL 1152
Query 105 DSQGRLVLA-EAQVGDERDYVCVVRAGAAGTAEATARLNVFAK 146
D + + + +GD + + A + RLN AK
Sbjct 1153 DKYFKNHTSPDVDLGD----ISGINASVVNIQKEIDRLNEVAK 1191
Query 435 SRTQNFTLLVQGSPE---LKTAEIE-----------PKADGSWREGD 467
S+TQ +LL+ + +K E + K + SW E +
Sbjct 112 SKTQ--SLLIVNNATNVVIKVCEFQFCNDPFLGVYYHKNNKSWMESE 156
this corrected manually:
Query 361 LDPLELSEGKV-L-SLPL 376
LDPL SE K+ L S +
Sbjct 293 LDPL--SETKCTLKSFTV 308
BLAST alignment of the integrin motif 'RGD' in LUTHER
Query 290 LCRGDGSPSPEYTLF 304 LUTHER
+C+ + P +F
Sbjct 1081 ICHDGKAHFPREGVF 1095 Spike2020
and here the same RGD manually, since BLAST won't do it
QLLCRGDG----SPSPEYT LUTHER
++ RGD +P ++
FVI-RGDEVRQIAP-GQTG Spike
or also the special ACE2 RBD Spike fragment with larger piece of Luther
VQLLCRGDGS-PSPE-YTLFRLQDEQ Luther
Q+L +D+S PS ++ L +
SQIL--PDPSKPSKRSFIEDLLFNKV Spike
The above first “RGD’ Luther motif overlaps with ‘HDG’, where the GD→DG inversion is an example of a frequent phenomenon in the Spike homologus insertions. The complexity of the invisible micro-world in our bodies goes beyond astronomy atlas, here another actor on the Luther scene, again blood related, and it is called spectrin^11, the heaviest part in red blood cells membranes. A 2001 publication^12 described how the erythroid alpha-spectrin gene mutation caused by exon skipping resulted in a amino acids deletion which in turn changed multimer formation stability and lead to thrombosis. There are 2 types of spectrin, alpha and beta chains (only ~27% seq ID) which have following homologies with Spike2020 (Sbjct lines), beta first (https://www.uniprot.org/uniprotkb/P11277/entry), heavily phosphorylated, thus lot of charge:
Query 422 QLARRFDRKAAMRETWLSENQRLVA 446 Spectrin Beta
Q+A RF+ + L ENQ+L+A
Sbjct 901 QMAYRFN-GIGVTQNVLYENQKLIA 924 Spike2020
Query 1542 QQLVEAAEI 1550
QQL+ AAEI
Sbjct 1010 QQLIRAAEI 1018
Query 1412 TSVNRMLAKLKRVEDQVNVRKEELGELFAQV 1442 Spectrin Beta
T NR L + VE N + E FAQV
Sbjct 761 TQLNRALTGIA-VEQDKNTQ-----EVFAQV 785
Query 1917 SWMESIIR 1924 Spectrin Beta
SWMES R
Sbjct 151 SWMESEFR 158
Query 623 SNMAAGRKAQ--LEQSKR 638 Spectrin Beta
+N+AA + ++ L QSKR
Sbjct 1022 ANLAATKMSECVLGQSKR 1039
Query 1567 DRLREAAAGRLQRLR 1581 Spectrin Beta
DRL GRLQ L+
Sbjct 994 DRL---ITGRLQSLQ 1005
also manual
FDEDDSEPVLKGVKLHYT C-terminus of SPike2020
PQEEEGE--TAG Spectrin
according to uniprot:
Spectrin is cleaved in Malaria infection in 2 spots:
Site 165-166 (Microbial infection) Cleavage; by P.falciparum SERA6 'QT'
Site 167-168 (Microbial infection) Cleavage; by P.falciparum SERA6 'QE'
both sites span the Spike furin site section
------------>.-.>
150-WTIILRFQIQDIVVQTQEG--RETRSAKDALL-170 --->Spectrin Beta
GAGICASYQTQTNSPRRARSVAS --->Spike2020
also the 'RGD' motif in Spike has high homolog section in spectrin:
Query 556 FGKHLLEVEDLLQKHKLMEADIAIQGDKVKAI 587 Spectrin Beta
+G + DL + ++ I GD V+ I
Sbjct 380 YGVSPTKLNDLCFTNVYADS-FVIRGDEVRQI 410 Spike
and now the alpha chain of spectrin, with lot of bound Ca+2, few phosphors and metals, all at https://www.uniprot.org/uniprotkb/P02549/entry
Query 1716 FQFFQDL-------DDEESWIEEKLIRVSS----------QDYGRDLQGVQNLLKK---- 1754
FQF D + +SW+E + SS Q + DL+G Q K
Sbjct 133 FQFCNDPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFLMDLEGKQGNFKNLREF 192
Query 1755 -HKRLEGEL---VAHEPAIQNVLDMAEKLKDKAAVGQEEIQLRLAQF----VEHWEKLKE 1806
K ++G H P I V D+ + + I + + +F H L
Sbjct 193 VFKNIDGYFKIYSKHTP-INLVRDLPQGFSALEPLVDLPIGINITRFQTLLALHRSYLTP 251
Query 1807 LAKARGLKLEESLEYLQFMQNAEEEEAWINEKNALAVRGDCG-DTLAATQSLLMKHEALE 1865
+ G + Y+ ++Q + NE + DC D L+ T+ L +
Sbjct 252 GDSSSGWTAGAAAYYVGYLQPRTFLLKY-NENGTITDAVDCALDPLSETKCTLKSFTVEK 310
Query 1866 NDFAVHETRVQ------------NVCAQGE 1883
+ RVQ N+C GE
Sbjct 311 GIYQTSNFRVQPTESIVRFPNITNLCPFGE 340
Query 1489 LIDERTKLGDYANLKQF-YRDLEELEEWISEMLP 1521
L+D K G++ NL++F +++++ + S+ P
Sbjct 176 LMDLEGKQGNFKNLREFVFKNIDGYFKIYSKHTP 209
Query 264 ANLQRFKRDVTEAI 277
+NL+ F+RD++ I
Sbjct 459 SNLKPFERDISTEI 472
Query 1402 GNCDQVESWMVARENSLRSDDKSSLDSLEALMKKRDDLDKAI---TAQEGKITDLEHFAE 1458
GNCD V + N++ + LDS +++LDK T+ + + D+
Sbjct 1124 GNCDVVIGIV---NNTVYDPLQPELDSF------KEELDKYFKNHTSPDVDLGDISGINA 1174
Query 1459 SLIADEHYAKEEIATRLQRVLDRWKALKAQLIDERTKLGDY 1499
S++ I + R+ + K L LID + +LG Y
Sbjct 1175 SVV--------NIQKEIDRLNEVAKNLNESLIDLQ-ELGKY 1206
Both RGD motifs by hand, BLAST won't do it:
EKNALAVRGDCGDTLAATQSLLMK spectrin alpha
++ ++RGD +A Q+
YADSFVIRGDEVRQIAPGQTGKIA Spike2020
when looking at spectrin a and b chains, it seems Spike2020 has more similarities to one or the other, than both chains on their own. It is also known that the first Arginine in ‘RGD’ motif in Spike suppose to bind ivermectin (https://www.futuremedicine.com/doi/10.2217/fvl-2020-0342), implying a possibly similar binding scheme in the above investigated malaria related proteins.
It all ABSOLUTELY DOES NOT LOOK RANDOM. Spectrin is also involved in hemolytic anemia, exactly the same symptoms reported in Dec ‘21 and in ‘22, only after introduction of the Spike gene therapies^13. A 2004 publication^14 with overlapping coauthor (J Aura Gimm) pointed to yet another Blood group antigen and Host cell receptor for virus entry, Glycophorin-A (https://www.uniprot.org/uniprotkb/P02724/entry), which binds sialic acid, it is a major intrinsic membrane protein of the erythrocyte. Like Luther antigen, it has high sequence homology with Spike, not only in the integrin ‘RGD’ motif section, but again at the ACE2 RBD domain:
Query 27 MHTSTSSSVTKSYISSQT--NDTHKRDTYAAT--PRAHEVSEIS 66 Glycophorin-A
++ S+S S K Y S T ND + YA + R EV +I+
Sbjct 368 LYNSASFSTFKCYGVSPTKLNDLCFTNVYADSFVIRGDEVRQIA 411 Spike's RGD motif
or even better, overlap with even longer Spike section:
Query 27 MHTSTSSSVTKSYISSQT--NDTHKRDTYAATP--RAHEVSEISVRTVYPPEEETGERV- 81
++ S+S S K Y S T ND + YA + R EV +I +TG
Sbjct 368 LYNSASFSTFKCYGVSPTKLNDLCFTNVYADSFVIRGDEVRQI-------APGQTGKIAD 420
Query 82 ---QLAHHFSEPEITLIIFGVMAGVIGTILLISYGIRRLIKKSPSDVKPL 128
L F+ I+ + V G Y + RL +K S+ KP
Sbjct 421 YNYKLPDDFTGCVIAWNSNNLDSKVGGNY---NY-LYRLFRK--SNLKPF 464
and more overlapping sections:
Query 13 EIVSISASSTTGVAM---HTSTSSSVTKSY 39
EI+ I+ S GV+ T TS V+ Y
Sbjct 583 EILDITPCSFGGVSVITPGTNTSNQVAVLY 612
by hand few special sections, ACE2 RBD domain:
SPSDVKPLPS-PDTDVPLSSV Glycophorin
NFSQILPDPSKPSKRSFIEDL Spike2020
The LBGT section of Spike2020:
VAMHTST-----SSSV-TKSYISSQTN
LALHRSYLTPGDSSSGWT-AGAAAYYVG
the furin site:
TSSSVTKSYISSQTNDTHKRDTYAATPRAH
PIGAGICASYQTQTNSPRRARSVASQ
and expression signal:
MYGKIIFVLLL---SEIVSISAS
MF---VFLVLLPLVSSQCVNLTT
Glycoporin-A, is a receptor for HepatitisA Virus, it is a receptor for P.falciparum erythrocyte-binding antigen 175,
in MALARIA. With its countless sugars and linked phosphors, has more interaction partners than amino acids, and with its genetic polymorphism in P.falciparum infection, it allows for resistance to malaria…
Malaria? again? HCQ OR Ivermectin anyone? Red blood cells explosions all over?
Well, Glycoporin is also used for SARS-COV2 detection, quote (https://www.nature.com/articles/s41467-021-22045-y#Sec2): “We have adapted this approach for detection of antibodies to SARS-CoV-2 by linking the RBD of the SARS-CoV-2 spike protein to IH4 via a short (GSG)2 linker to produce the fusion protein IH4-RBD-6H.” The same was done with antibodies to HIV p24, which when present in serum, crosslinked the p24 and agglutinated the red cells.
Sounds like a real war against human blood, in particular the red cells.… Stay calm, just go down the food chain pyramid, who eats/degrades what.
So what ‘eats’/degrades laminin, and even takes apart the collagen matrix on all organs?? MMP-9, Matrix Metalloproteinase-9, full of bound Ca2+ and Zn+2 ions, one of the latter inhibits the munching, the same protease which is also ESSENTIAL in malaria development: https://ncbi.nlm.nih.gov/pmc/articles/PMC7123976/ “Etiopathogenesis and Pathophysiology of Malaria“, and in cardiovascular disease^16. This MMP-9 monster (https://www.uniprot.org/uniprotkb/P14780/entry) degrades collagen and more, but it is actually produced by the best human friends, the so normal alveolar macrophages and granulocytes, fighting the enemies. And what regulates that MMP-9 super soldier?
A protein called RECK_HUMAN, yes that’s right, its link is at https://www.uniprot.org/uniprotkb/O95980/entry and is stands for the mouthful “Reversion-inducing cysteine-rich protein with 3 Kazal motifs”! It suppresses MMP9 secretion and directly inhibits its enzymatic activity (PubMed:9789069, PubMed:18194466), thus negatively regulating the soldier.
With that, we got the picture of the disaster painted on the wall, based on official data. In nutshell, and I kid you not: an aged armenian congress woman, very Stanford friendly, trailblazer, a true problem solver, indirectly contributes to a suppression of malaria wonder (BARDA’s fault to cut out Ivermectin/HQC) right at the begin of covid19 disaster so that only gene therapies will be allowed as the ‘cure’, while the only enzyme regulating the disaster got its name RECK_HUMAN and it has 3 Kazal-iam motifs, each of which has some homology with Spike2020, which now is all in human blood… Here the sequences of the 3 K(h)azal-ian motifs and how they overlap with Spike2020, using automated BLAST, not perfect (because the real BLAST is in Mod-E-RNA hands…), but still:
Kazal-like 1
627-673 TFTGLPCNCADQFVPVCGQNGRTYPSACIARCVGLQDHQFEFGSCMS
Query 592 TSFSIDCNVCSCFAGNLVCSTRLCLSEHSSEDDRRTFTGLPCNCADQFVPVCGQNGRTYP 651
T S+DC + C + CS L R+ TG+ V Q + Y
Sbjct 732 TKTSVDCTMYIC-GDSTECSNLLLQYGSFCTQLNRALTGIAVEQDKNTQEVFAQVKQIYK 790
Query 652 SACIARCVGLQDHQFEFGSCMSKDPCNPN 680
+ I G F F + DP P+
Sbjct 791 TPPIKDFGG-----FNFSQILP-DPSKPS 813
2. Kazal-like 2 (part only, no time to fit it all…)
698-752 TFDKFGCSQYECVPRQLACDQVQDPVCDTDHMEHNNLCTLYQRGKSLSYKGPCQP
Query 738 YQRGKSLSYKGPCQPFCR 755
Y L K +PF R
Sbjct 449 YNYLYRLFRKSNLKPFER 466
Kazal-like 3
753-789 FCRATEPVCGHNGETYSSVCAAYSDRVAVDYYGDCQA
Query 733 NLCTLYQRGKSLSYKGPCQPFCRATEPVCGHNGETYSSVCAAYSDRVAVDYYGDCQAVGV 792
N TL G Y G C A + +C + + +D ++ Y A G
Sbjct 824 NKVTLADAGFIKQY-GDCLGDIAARDLICAQKFNGLTVLPPLLTDEMIAQYTSALLA-GT 881
Those who speak japanese would probably assume, it is a Khazar-motif…. Molecular biology, full of history, and fight.
It all goes back to 1901, and a military general from WWI, named Karl LANDsteiner, Nobel Prize winner for Blood groups types. He also discovered, that addition of iodo-diazo group into serum albumins, causes that the original species specificity disappear. Rockefellers enjoyed the solutions of his brilliant mind. He also implied, there are so many blood types as there are humans… Every one of us is unique, every electron counts. Well, he is dead too, of course.
That’s not all, one more special name, by the molecular biologists, who ignore the Creator, but use a biblical name (no wonder there are projects out there like Mockingbird..) , ADAM33, another munching machine, from the title. Why not Adolf, or Barack, or Joe or even Donald, NO, it has to be ADAM33.
Officially it is a disintegrin and metalloproteinase domain-containing protein 33. Even in ‘pre-covid’ times it was heavily involved is severity of asthma. Lot of literature on it, for example showing how it chops down other important membrane proteins:
It almost looks like a snake, crawling down and eating all the eggs on the ground. Is it why, for environmental reasons, no eggs in White House this ‘24 Easter, they will paint the potatoes for the children…?
Take the ADAM33 sequence from https://www.uniprot.org/uniprotkb/Q9BZ11/entry, and run BLAST, its active site E346, nicely conserved in the first BLAST output, right next to the completely conserved tripeptide PIGA, with the letter ‘I’ being Isoleucine, the 666-th residue is the Spike amino acide sequence:
*<== ADAM's33 ACTIVE SITE E346
Query 334 ELPIGAAATMAHE 346 ADAM33
++PIGA +++
Sbjct 663 DIPIGAGICASYQ 675 Spike2020
* that I=isoleucine, in the middle of the 'PIG' tripeptide is the 666-th residue in the Spike sequence (https://www.ncbi.nlm.nih.gov/protein/YP_009724390.1)
Query 380 PFPRVFSACSRRQLRAFFRKGGGACLSN 407
PF+ VF+A + A+ RK C+++
Sbjct 337 PFGEVFNATRFASVYAWNRKRISNCVAD 364
expression signal from Spike2020
Query 706 MLLSVLLPLL 715 ADAM33
+ VLLPL+
Sbjct 2 FVFLVLLPLV 11 Spike2020
COMPLETE furin site conservation(!!), being part of expression signal in ADAM33
Query 1 MGWPRRARGT 11 ADAM33
PRRAR
Sbjct 681 QTQTNSPRRARSV 687 SPike2020
ADAM33, like Spike2020, is heavily ‘sugar coated’ and has that cysteine switch 131-CTCSGMSG-138, equally conserved in Spike2020. That motif in collaboration with the catalytic Zn+2 ions, inhibits its munching. Here some of the essential functional parts of ADAM33 and and their SIMILARITY within the Spike2020:
Disintegrin part:
Query 26 LCCFAHNCS 34 <<<---ADAM33
LCC + CS <<<---IDENTITIES
Sbjct 1234 LCCMTSCCS 12 <<<---Spike2020
Query 3 LCGNGFVEAGEECDCGPGQECRDLCC 28
L GF++ + DC + RDL C
Sbjct 828 LADAGFIK--QYGDCLGDIAARDLIC 851
Query 11 AGEECDCGPGQECR-DLCCFAHNCSLRPGAQCAHGDCCVRCLLKPA 55
A + +C GQ R D C ++ P + HG + PA
Sbjct 1026 ATKMSECVLGQSKRVDFCGKGYHLMSFPQS-APHGVVFLHVTYVPA 1070
Peptidase part:
Query 237 LLEVANYVDQLLRTLDIQVALTGLEVWTERDRSRVTQDANA 277
LL+ + QL R ALTG+ V E+D+ TQ+ A
Sbjct 753 LLQYGSFCTQLNR------ALTGIAV--EQDKN--TQEVFA 783
Cysteine switch:
Query 131 CTCSGMSGLITLSRNAS 147
C+ G S IT N S
Sbjct 590 CSFGGVS-VITPGTNTS 605
Query 181 HRDPGNKAGMTS 192
H++ NK+ M S
Sbjct 146 HKN--NKSWMES 155
Query 75 QELLLELEKNHRLLA-PGYIETHYG 98
++LL N+ LA G+I +YG
Sbjct 819 EDLLF----NKVTLADAGFIK-QYG 838
manualy the LBGT SPike2020 section:
DHSELPIGAAATMAHEIGHS <<<-ADAM33
SSSGWTAGAAAYYVGYLQPR <<<-Spike2020
Query 146 ASYYLRPW-PPR 156
A+YY+ + PR
Sbjct 263 AAYYVG-YLQPR 273
ADAM33's cystein switch with Zn+2 binding to the last cysteine CTC*:
*
VVLCT----CSGM----SGLITLSRN
IMLCCMTSCCSCLKGCCSCGSCCKFD
The above is not all. A section of 100 residues in ADAM33 overlap quite well with Spike2020:
Query 146 ASYYLRPWPPRGSKDFSTHEIFRMEQLLTWKGTCGHRD-----PGNKAGMTSLPGGPQSR 200
ASY + PR ++ ++ I L + ++ + + P N + + P S
Sbjct 672 ASYQTQTNSPRRARSVASQSIIAYTMSLGAENSVAYSNNSIAIPTNFTISVTTEILPVSM 731
Query 201 GRREARRTRKYLELYIVADHTLFLTRHRNLNHTKQRLLEVANYVDQLLRTLDIQVALTGL 260
+ T +YI D T LL+ ++ QL R ALTG+
Sbjct 732 TKTSVDCT-----MYICGDST----------ECSNLLLQYGSFCTQLNR------ALTGI 770
Query 261 EVWTERDRSRV 271
V +++ V
Sbjct 771 AVEQDKNTQEV 781
AND this below, unprecedented, is defined as part of disintegrin in ADAM33, but in Spike2020 it is said to be all S-palmitoyl cysteines, in one publication^17, only..
Query 442 LCCFAHNCS-LRPGAQCAHGDCC 463 ADAM33
LCC + CS L+ G C+ G CC
Sbjct 1234 LCCMTSCCSCLK-GC-CSCGSCC 1254 Spike2020
What that very C-terminal part of Spike actually represents is a cysteine cluster, like in ADAM33, where most probably metals bind, and not only fats… This cysteine rich Spike motif in earlier posts, was also related to venoms, something what was shared for the first time by Dr. Richard Bartlett (featured at 2:31 in https://rumble.com/v1hu7xr-the-truth-about-ivermectin-a-new-short-documentary-by-plandemic-filmmaker-m.html).
Isn’t somebody laughing wickedly right now, while watching the humanity to get literally disintegrated by ADAM33-like Spike2020, while buying out all lands, homes, animals, and offering worms for the rest??? Or even better, snakes: https://www.scientificamerican.com/article/snake-steak-could-be-a-climate-friendly-source-of-protein/
And wasn’t it Congress woman Eshoo who on January 30, 2008 (right on time before the collapse), endorsed the equally Stanford friendly, U.S. Senator Barack Obama for president? The same who in 2022 in a speech at Stanford, admitted:
"We've essentially clinically tested the vaccine on billions of people worldwide"
https://www.c-span.org/video/?519625-1/president-obama-speaks-threat-disinformation (source at 29.32). Oh, the humanity mutilating Stanford, takes something else from this speech: https://news.stanford.edu/2022/04/21/disinformation-weakening-democracy-barack-obama-said/ for promotions of its greatness. Lot of the world establishment was featured on the cover of Economist’s Christmas edition in 2012 with Barack Obama floating in a canoe right into the EURO sign:
It is a great pity, that Stanford, a place on this planet, once geographically breathtakingly beautiful, turned into a death pit.
So far, it’s all a complicated net of no coincidences of actions in the right place and the right time, even on the microscopic level.
One more thought, inspired by an old article in Proc R Soc Med. from 1923 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2103460/pdf/procrsmed01359-0005.pdf, which makes a very interesting comparison of loosened teeth with a " Dental Sepsis", all preventable with the right living conditions, including proper living plant food with LOT of vitamin C..
This post needs to end, too long for email already, so no EVE yet..;)))
STAY HEALTHY with LOT of good organic food, VitD3, VitC and LOVE. And stay tuned for the next episode, if time allows. And THANK YOU for checking in, without the boarding pass…
Update 3/21/2024 : “There is a new most expensive drug in the world. Price tag: $4.25 million“ https://www.technologyreview.com/2024/03/20/1089996/there-is-a-new-most-expensive-drug-in-the-world-price-tag-4-25-million/ The deception of this title from MIT news is explained in the first sentence: “There is a new most expensive drug ever—a gene therapy that costs as much as a Brooklyn brownstone or a Miami mansion, and more than the average person will earn in a lifetime.“ So we not only have deception in term of gene therapies called now ‘vaccines’, they are basically ‘drugs’!??
Repetition of an old but very important info from post titled “The 20 years of 'genomic medicine'. JP Morgan, is it about money or health?“
Update: 1/29/2024 The title “Cell-free DNA and RNA—measurement and applications in clinical diagnostics with focus on metabolic disorders” in Physiol Genomics 53: 33–46, 2021, implies, to what extend the medial cartel planned their future, while forcing the genetically modifying covid injections on billions of clueless citizens, ever since the end of 2020, the begin of that universal therapy, which started with changing the RNA pools of the human genome. The medical genocide goes that far, that SATNFORD, sorry Stanford, publishes proudly an article titled ‘The beat goes on’, in which since 2022 cardiothoracic surgeries are being performed with still beating hearts form cardiac arrest patients (the ones caused by the covid injections?) with astonishing success!!! A new field of ‘morpholome’ was invented, also in Satnford, sorry, stanford, which refers to variety of cell shapes taken on by an organism. Euan Ashley, Maddison Masaeli and Mahyar Salek (google AI expert) while analyzing the HEART CELL MORPHOLOME, want to differentiate deceased cells from others that have been ‘cured’(????) by gene-editing technology (Stanford Medicine, Issue 3, 2023). Between Apr 2023 and the print out date of that Stanford magazine (begin of ‘24), the amount of this sort of heart transplants, more than DOUBLED (https://med.stanford.edu/news/all-news/2023/04/beating-heart-transplant.html)
Another Stanford hero, https://profiles.stanford.edu/michael-ma, published in ‘22 statistics on infants heart transplants, https://pubmed.ncbi.nlm.nih.gov/35835207/, strangely covering the years 1994 to Sep 2019, and avoiding anything AFTER 2020 (WHY????), together 2552 infant heart transplants reported to UNOS.. If there is anyone who could help the embalmers to decipher the terrible clot issues, it would be this person specializing on multilevel obstruction of systemic and pulmonic arterial systems… Straight from Chemical Engineering to medicine, what an ideal transformation, unfortunately with ZERO input for the embalmers struggling with dead bodies of covid injected victims!!!
Update 3/26/2024: An old lecture by Rob Skiba, explaining the historical/religious background of the goals of the elites:
and also this one:
where he ends, quote: ”I stand alone on the word of GOD, because in the sea of lies, that is our only compass.” Rob Skiba died of ‘covid’ in hospital on the 13-th of Oct 2021…
Literature.
Luminita Eid et al. “Simian virus 40 vectors for pulmonary gene therapy.“ Respir Res. 2007; 8(1): 74. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2238754/
Mahsa Khoramipour et al. “Evaluation of the association between clinical parameters and ADAM33 and ORMDL3 asthma gene single-nucleotide polymorphisms with the severity of COVID-19” International Immunopharmacology, Volume 123, October 2023, 110707https://www.sciencedirect.com/science/article/abs/pii/S1567576923010329
https://stanforddaily.com/2021/10/07/secretaries-of-state-politicians-remember-george-shultz-at-memorial-service/
Hongwei Li et al. “Serum levels of laminin and von Willebrand factor in COVID-19 survivors 6 months after discharge“ Int J Infect Dis. 2022 Feb; 115: 134–141. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626146/
https://www.omim.org/entry/303800#47
Wilson, E. B. The sex chromosomes. Arch. Mikrosk. Anat. Enwicklungsmech. 77: 249-271, 1911
https://www.jbc.org/article/S0021-9258(18)80596-8/pdf with “The Lutheran Blood Group Glycoproteins, the Erythroid Receptors for Laminin, Are Adhesion Molecules“
https://www.researchgate.net/publication/12194734_Lutheran_blood_group_glycoprotein_and_its_newly_characterized_mouse_homologue_specifically_bind_a5_chain-containing_human_laminin_with_high_affinity
C. Eyler & M. Telen “The Lutheran glycoprotein: a multifunctional adhesion receptor“ Transfusion. 2006 Apr;46(4):668-77. https://pubmed.ncbi.nlm.nih.gov/16584446/
Xiuli An et al. “Adhesive activity of Lu glycoproteins is regulated by interaction with spectrin”. Blood. 2008 Dec 15; 112(13): 5212–5218. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2597615/
N J Wandersee et al. “Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis“ Blood. 2001 Jan 15;97(2):543-50. https://pubmed.ncbi.nlm.nih.gov/11154235/
Tyler A Finkenthal et al. “Autoimmune Hemolytic Anemia Exacerbation Associated With COVID-19 Infection and Markedly Elevated Inflammatory Markers“ Cureus. 2021 Dec; 13(12): e20416. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759712/ AND Hayder M. Al-kuraishy et al. “Hemolytic anemia in COVID-19“ Ann Hematol. 2022; 101(9): 1887–1895. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9263052/
James C-M Lee et al. “Mechanism of protein sorting during erythroblast enucleation: role of cytoskeletal connectivity” Blood 2004 Mar 1:103(5) 1912-9.
Mauro Prato “Etiopathogenesis and Pathophysiology of Malaria“ Human and Mosquito Lysozymes. 2014 Sep 22 : 1–18. https://ncbi.nlm.nih.gov/pmc/articles/PMC7123976/
“Matrix Metalloproteinase-9: Many Shades of Function in Cardiovascular Disease” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3858212/
https://www.cell.com/action/showPdf?pii=S1534-5807%2821%2900734-6
Paul E Marik et al. “Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Severe Sepsis and Septic Shock: A Retrospective Before-After Study“ Chest. 2017 Jun;151(6):1229-1238.https://pubmed.ncbi.nlm.nih.gov/27940189/
P. E. Marik was severely prosecuted for applications of VitC protocol in covid19 times to a level where he CRIED in front of one of the covid19 crimes hearings…
Thanks again, I have no words to add
Your level of research detail - I could never imagine this is what things are in the laboratory of the most dedicated minds.
The ignorance and ego defies my imagination
Billions of people have become guinea pigs for experiments. and "experiment" seems to me too much said, because no one follows its results. they just know that serums and drugs can cause misfortune and money and that is their greatest satisfaction in experiments.
On the other hand, being just a spectator in a stand, as much as my intuition tells me, otherwise I don't know, I don't believe in the veracity, efficiency and supernatural powers of computational biology.
by chance I read Michael Conrad's (if i remember well the name) theorem which kind of confirms my intuitions and which says that three desired characteristics of a computer, programmability, efficiency and the ability to adapt and learn are contradictory. there is no computer that can possess them all at the same time. I think, even if I may be wrong, I'm not a scientist, nothing has convinced me otherwise so far, that computational biology as well as other sciences based on models, algorithms and other things are modern tricks from which only those who use them profit. when science will be able to demonstrate that it knows how life appeared on earth, not through all kinds of assumptions, then it will be something else, it means that science has understood the life and behavior of each individual organism in all circumstances.
But "science" today is too busy with inventing master’s degrees in lgbtq+, new vocabulary, new definitions and so many others tricks and lies....
https://www.europarl.europa.eu/news/en/press-room/20200706IPR82731/parliament-to-allow-covid-19-vaccines-to-be-developed-more-quickly