How much HIV is in SARS-CoV-2? Fauci's 2018 patent, the NEW Synthetic SARS-CoV-2 Spike gene, with the OLD content.

URGENT: After sending out this post all email updates regarding it are NON-existend. Must have been the substack server or ‘something else’, and now it runs fine :) How surprising the Micro-soft products can be..

Btw., if the real Dr. Fauci’s name would be Dr. fAuIC, now read backwards the capital letters, then probably we could explain the incredible amount of tortures in all the experiments he participated in…

EXPERIMENTAL GENE MODIFICATIONS OF HUMANITY in EU, reactions of the few in parlament:

Update 10/29/2022: Prof. S. Bhakdi from Germany explains with simple words some of the details of immune response and resulting brain and heart damage after covid gene modifying injections: https://usawatchdog.com/cv19-vax-destroys-hearts-brains-of-billions-of-people-dr-sucharit-bhakdi/

Whoever can, please keep Prof. Bhakdi in your prayers. He is facing 5 years in prison and loosing his pension, all for speaking out the truth about covid injections! That’s Germany in 2022!!!

Update 12/14/2022 A link to Mod-E-RNA future plans, including their AI academy, AFTER ruining billions of HUMANS with their genetically modifying covid injections, at: https://s29.q4cdn.com/435878511/files/doc_presentations/2022/11/Moderna-Final-ESG-Day-Slides-11.10.22.pdf was send out by :

In case you didn't know...

Update 12/9/2023: Dr. David Martin uncoveres increidble important facts connecting AZT. HIV and SARS-CoV-2 : https://www.bitchute.com/video/MMXfRHgFybqK/

Clarification.

All my posts talking about the SARS-CoV-2 Spike protein, always refer to the NIH publicly accessible data base for the first OFFICIAL SARS-CoV-2 version at: https://www.ncbi.nlm.nih.gov/nuccore/NC_045512.2 with the code for the Spike: YP_009724390.1

The reason for that is the fact, that all the first covid19 injections, Pfizer and ModE-RNA in particular, should OFFICIALLY contain genetic material encoding the Spike described in these data bases. Any conclusions drawn from all the bioinformatics analysis, refer thus to facts about that genetic material of covid ILLEGAL genetically modifying injections.

The POST starts below, but if you read the above, that’s ok too, it will help in the long run:) THANK YOU for continuing:) And this post like others too, will be updated and changed when new insights flow in.

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For the last ~ 3 YEARS Dr. Fauci is flattening the curve, which at the begin of 2020 was not even there. He flattened many things in the meantime and that while for many, it almost looks like ‘fortune cookie game"‘ is the main feature of this man. Many think he does not know anything, including the late RIP Dr. Kary Mullis, who had to die right before the pandemic, and who also not only was the top specialist on the PCR technology, used so reckless during the covid pandemic, but who was also one of the first doing an extensive research on ACE receptors and alveolar hypoxia^8.

So does Fauci know ‘things’ or he does not? Whoever made the below caricature, THANK YOU.

Fact check: “SARS-CoV-2 was not created using genes from HIV, Fauci does not hold patents for an ‘HIV component’ to SARS-CoV-2. “

That comes from: https://www.reuters.com/article/uk-factcheck-hiv-covid-explained-idUSKBN29C26E

It’s hard to find any paper which would show how similar HIV gp160 actually is in comparison with the original Spike2020 (my own definition used bellow), from the original SARS-CoV-2 (ncbi entry: /protein_id="YP_009724390.1"). The one which was written by the indian team quickly disappeared from the horizon. Given that the 2008 Walensky’s patent from years back had already quite large pieces of the Spike2020 one ~100% of it and was officially intended to be for HIV treatment, including coronaviruses, how about US 9,896,509 B2 from Feb 2018 with Fauci as one of the inventors? The title of it is:”USE OF ANTAGONISTS OF THE INTERACTION BETWEEN HIV GP120 AND a4b7 INTEGRIN”.

Blast comparison of HIV-gp160 (gp160=gp120+gp41, its amino acid sequence in Query line, available at https://www.ncbi.nlm.nih.gov/protein/9629363 ) with Spike protein (Sbjct line), with the middle line showing the identical amino acids common for both proteins, gives the following fragments, starting with the most tryptophan rich sections:

Query  6     KYQHLWRWGWR-WGTMLLGMLMICSAT  31  >>>HIV-1 gp160
             KY+   +W W  W   + G++ I+  T      >>>IDENTITIES
Sbjct  1205  KYEQYIKWPWYIWLGFIAGLIAIVMVT  1231>>>Spike2020 
or extending it more 
Query  6     KYQHLWRWGW-RW-----GTMLLGM--LMICSAT  31   >>>HIV-1 gp160
             KY++  +W W  W     G + + M  +M+C  T       >>>IDENTITIES
Sbjct  1205  KYEQYIKWPWYIWLGFIAGLIAIVMVTIMLCCMT  1238 >>>Spike2020
Query  386  NSTQ-LF-----NSTWFNSTWSTEGSNNTEGSDTITLP  417>>>HIV-1 gp160
            +STQ LF     N TWF++   + G+N T   D   LP     >>>IDENTITIES
Sbjct  49   HSTQDLFLPFFSNVTWFHAIHVS-GTNGTKRFDNPVLP  85 >>>Spike2020 
here almost 100 residues in one string:
Query  158  SFNISTSIRGKVQKEYAFFYKLDIIPIDNDT-TS-YKL--TSCN-----------TSVIT
            S N+ + + G     Y  F K ++ P + D+ T  Y+   T CN            S   
Sbjct  438  SNNLDSKVGGNYNYLYRLFRKSNLKPFERDISTEIYQAGSTPCNGVEGFNCYFPLQSYGF
Query  203  QACPKVSFEPI------------PIHYCAPAGFAIL---KCNNKTFNG  235
            Q +  V ++P             P   C P   + L   KC N  FNG
Sbjct  498  QPTNGVGYQPYRVVVLSFELLHAPATVCGPKKSTNLVKNKCVNFNFNG  545
Query  791   EALKYWWNLLQYWSQELKNSAVSLLNATAIAVAEGTDRVIEVVQ  834
             E  KY+ N   + S ++    +S +NA+ + + + +DR+ EV++
Sbjct  1151  ELDKYFKN---HTSPDVDLGDISGINASVVNIQKEIDRLNEVAK  1191
Query  392  NSTWFNST-WSTEGSNNTEGSDTITLP  417
            N TWF ++   + G+N T+  D   LP
Sbjct  61   NVTWFHAI-HVS-GTNGTKRFDNPVLP  85
Query  208  VSFEPI--PIHYCAPAGFAIL---KCNNKTFNG  235
            +SFE +  P   C P   + L   KC N  FNG
Sbjct  513  LSFELLHAPATVCGPKKSTNLVKNKCVNFNFNG  545
Query  678   WLWYIKL------------FIMI  688
             W WYI L             IM+
Sbjct  1212  WPWYIWLGFIAGLIAIVMVTIML  1234
or better
Query  678   WLWYIKL-FIMIVGGLVGLRIV  698
             W WYI L FI    GL+ + +V
Sbjct  1212  WPWYIWLGFI---AGLIAIVMV  1230
Query  624  NHTTWMEWDREINNYTS  640
            N+ +WME   E   Y+S
Sbjct  148  NNKSWME--SEFRVYSS  162
Query  716  SFQTHLPTPR  725
            S+QT+  +PR
Sbjct  673  SYQTQTNSPR  682
Query  652  QQEKNEQELL  661
            +Q+KN QE+ 
Sbjct  773  EQDKNTQEVF  782
Query  458  GGNSNNESEIFR  469
            GGN N    +FR
Sbjct  446  GGNYNYLYRLFR  457
Query  495  GVAPTK  500
            GV+PTK
Sbjct  381  GVSPTK  386
Query  368   DPEIVT--HSF---NC  378
             +P+I+T  ++F   NC
Sbjct  1111  EPQIITTDNTFVSGNC  1126
Query  433  AMYAPPISGQIRCSSNITGLLL  454
            +MY   I G    S+  + LLL
Sbjct  739  TMY---ICGD---STECSNLLL  754
Query  377  NCGGEFFYCNSTQLFNSTWFNS  398
            NC  ++     + L+NS+ F++
Sbjct  360  NCVADY-----SVLYNSASFST  376
Query  705  VNRVR---QGYSPL-------------SFQTHLPTPR  725
            +N VR   QG+S L              FQT L   R
Sbjct  210  INLVRDLPQGFSALEPLVDLPIGINITRFQTLLALHR  246
Query  203  QACPKVSFEPI------------PIHYCAPAGFAIL---KCNNKTFNG  235
            Q    V ++P             P   C P   + L   KC N  FNG
Sbjct  498  QPTNGVGYQPYRVVVLSFELLHAPATVCGPKKSTNLVKNKCVNFNFNG  545
Query  235  GTGPCTNVSTVQCTHGIRPV--VSTQLLL--NGSLAEEEVVIRSVNFTDNAKTIIVQLNT
            G+G C++  T Q T+  R    V++Q ++    SL  E     SV +++N+ +I      
Sbjct  667  GAGICASYQT-Q-TNSPRRARSVASQSIIAYTMSLGAEN----SVAYSNNSIAIPTNFTI  
Query  291  SV--EI  294 HIV-1 gp160
            SV  EI
Sbjct  721  SVTTEI  726 Spike2020 (furin site start at 681 above)
Query  227  KCNNKTFN----------GTGPCTNV  242
            K N K F           G+ PC  V
Sbjct  458  KSNLKPFERDISTEIYQAGSTPCNGV  483
Query  197  NTS----VITQA--CPKVSFEPIPIH  216
            NTS    V+ Q   C  V   P+ IH
Sbjct  603  NTSNQVAVLYQDVNCTEV---PVAIH  625
and the comparison below is very special because it contains the homolog of the minimal essential epitope (mentioned in Fauci's patent), a SIMPLE TRIPEPTIDE LDT=Leucine-Aspartic Acid-Threonine(MadCAM), just THREE amino acids, or in case of fibronnectin it is LDV/LDI motif(integrin antagonist), with special function*, given that L,I,V can be substituted due to their molecular equivalence**.
Query  179  LDIIPIDNDTTSYKLTS--CNTS  199 HIV gp-160
            LDI P      S  +++  +NTS      IDENTITIES
Sbjct  585  LDITPCSFGGVS--VITPGTNTS  605 Spike2020
* quote from ^1:"Tenascins are extracellular matrix glycoproteins that act both as integrin ligands and as modifiers of fibronectin-integrin interactions to regulate cell adhesion, migration, proliferation and differentiation. In tetrapods, both tenascins and fibronectin bind to integrins via RGD and LDV-type tripeptide motifs found in exposed loops in their fibronectin-type III domains."
** Fauci's patent explains that:
Conservative amino acid substitutions providing functionally similar amino acids are well known in the art. The following six groups each contain amino acids that are conservative substitutions for one another:
        1) Alanine (A), Serine (S), Threonine (T);
        2) Aspartic acid (D), Glutamic acid (E);
        3) Asparagine (N), Glutamine (Q);
        4) Arginine (R), Lysine (K);
        5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); and
        6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W).
thus conforming: "Antagonists of α4 integrins are known, and include antibodies, peptide antagonists, LDV/LDI peptides, peptidomimetic antagonists, proteomimetic antagonists, and small molecule antagonists."

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BLAST output comparing the HIV-gp160 protein amino acid sequence NP_057856.1 with SARS-CoV-2 Spike results in ~89% of the entire sequence coverage of both with ~45% IDENTITIES. If the origin of HIV originated from non-human primates, how is it that the 2 outer proteins, i.e. Spikes coating HIV and the SARS-CoV-2 have so many common amino acid sections??? Two completely different origins of HIV and SARS-CoV-2 can’t end up with so many essential identities, unless the bats landed once in San Francisco and ended up with AIDS, if one believes in the ‘official narrative’! HIV is OLD, SARS-CoV-2 is NEW. Lets take the next toxic HIV tiny TAT protein, transcriptional activator; viral regulatory protein required for virus replication (https://www.ncbi.nlm.nih.gov/protein/9629358 ), protein which shares extremely important 3 common features with Spike2020: RGD motif, very unique cysteine cluster at the C-terminal of Spike, and part of the furin site, here the BLAST output, with Query being the HIV proteins, Subjct line the Spike, and in the middle the amino acids identical for both:

Query  20    TACTNCYCKKCCFHCQVC  37   <<<HIV TAT
             T+C  C C K C  C  C       <<<IDENTITIES 
Sbjct  1238  TSC--CSCLKGCCSCGSC  1253 <<<SPIKE2020
another way to align and extend the homolog section, by hand
C--TNC-YCKK-CCFHCQVC--F           HIV TAT  
C  T C  C K CC  C  C  F           IDENTITIES 
CCMTSCCSCLKGCCS-CGSCCKF Spike2020 SPIKE2020
The same Cys-rich TAT section compared with different Spike piece:
Query  23   TNCYCKKCCFH-CQVCFITKALGISYGRKKR  52  HIV TAT
            TN   K C F  C   F    LG+ Y +  +      IDENTITIES 
Sbjct  124  TNVVIKVCEFQFCNDPF----LGVYYHKNNK  150 SPIKE2020 
Query  46   SYGRKK  51   HIV TAT
            ++ RK+       IDENTITIES 
Sbjct  352  AWNRKR  357  SPIKE2020
this most important section is NOT found by BLAST, here by hand:
SY---GRKKRRQRRRAHQNSQTHQAS  HIV TAT
SY       RR R  A Q   +   S
SYQTQTNSPRRARSVASQSIIAYTMS  Spike2020 FURIN SITE
another section of Spike with the cys-rich
PGSQPKTACTNCYCKKCCFHCQV
P  ++     NCY    ++  Q
PC-NGVEGF-NCYFPLQSYGFQP
The integrin binding RGD motif by hand, since BLAST 'can't find it':
S-QPRGDPTGPKE  HIV TAT
S   RGD    ++  IDENTITIES
SFVIRGD--EVRQ  SPIKE
another section, by hand:
RAHQN-SQTHQASLSKQPT-SQPRG-DPT
RA    +   Q     Q    Q +    T
RALTGIAVE-QDKNT-QEVFAQVKQIYKT

What are the HIV TAT’s physiological consequences?

1. “Neonatal intrahippocampal injection of the HIV-1 proteins gp120
   and Tat: Differential effects on behavior and the relationship to
   stereological hippocampal measures“^2

2. “HIV-1 Proteins, Tat and gp120, Target the Developing Dopamine System“^3

3. “HIV-1 proteins gp120 and tat induce the epithelial–mesenchymal transition in oral and genital mucosal epithelial cells“^4

do we have similar issues within SARS infections? Here few citations mentioning similar pathological effects in covid infections:

Ad. 1 “SARS-CoV-2 spike protein induces cognitive deficit and anxiety-like behavior in mouse via non-cell autonomous hippocampal neuronal death“^5

Ad. 2 “SARS-CoV-2 Infection Causes Dopaminergic Neuron Senescence“*6

Ad. 3 “Epithelial-mesenchymal transition induced by SARS-CoV-2 required transcriptional upregulation of Snail“^7

These are just quick searches indicating few common features between HIV and SARS-CoV-2. A far more serious real live report on HIV and covid injections (encoding the Spike and producing it in billions), quite a while ago, by Dr. Nathan Thompson at: https://www.brighteon.com/fa58826c-654f-4d17-bc86-ee86364b2b54

“Dr Nathan Thompson test the blood of his Vaxxed patient!”

Natural Killer T-Cells, CD4, CD8 progression of HIV infection results in blood values which look very similar to the ones AFTER covid genetically modifying injections, NOT infections!!

Please recall, HIV ‘showed up’ in years when there was NO GRAPHENE yet, and yet, the HIV’s spike and SARS-CoV-2 spike are ‘macromolecularly’ RELATED. There is nothing without a purpose in a science paid by the richest!

Now a jump to recent developments. According to an DoD investigation by Tod Callender at:

https://principia-scientific.com/marburg-virus-will-be-activated-in-the-vaxxed-via-5g/

the next ‘coming crisis’ is supposedly related to Marburg virus. Lets’ try the NIH entry for it at: https://www.ncbi.nlm.nih.gov/nuccore/OL702894.1 Is it much different from the above analysis? Keeping all the NIH’s BLAST search parameters identical, targeted for the smaller sections (epitopes connections), the comparison between Marburg glycoprotein UFZ14320.1 and the original SARS-CoV2 Spike glycoprotein shows that they are 62% IDENTICAL, in particular when taking the smaller fragments. Here few examples with Query being Marburg and Sbjct Spike2020:

Query  364  YNTQSTATENEQTSAPSK----TTLLPTENPTTAKSTNSTKSPTT-TVPNTT  410
            Y TQ+ +    ++ A       T  L  EN + A S NS   PT  T+  TT
Sbjct  674  YQTQTNSPRRARSVASQSIIAYTMSLGAEN-SVAYSNNSIAIPTNFTISVTT  724
Query  191  LTSTNK-YWTSSNGTQTNDTGC  211 <<<Marburg SPike
            LT T + Y T SN  QT  +GC      <<<IDENTITIES
Sbjct  629  LTPTWRVYSTGSNVFQTR-AGC  649 <<<SARS-CoV-2 SPike2020
Query  7     LISIILI  13            <<< Marburg SPike
             LI+I+++                <<<IDENTITIES
Sbjct  1224  LIAIVMV  1230          <<<SARS-CoV-2 SPike2020
Query  429  VYFRRKRNILWREGD  443 
            VY+  K N  W E +
Sbjct  143  VYY-HKNNKSWMESE  156
Query  519   WSVQEDDLAAGLSWIPFFGPGIEGLYTAGLI  549 MARBURG
             W +          W+ F          AGLI
Sbjct  1214  WYI----------WLGFI---------AGLI  1225 Spike
Query  318  VVTEPGKTNTTAQ  330
            V+T PG TNT+ Q
Sbjct  597  VIT-PG-TNTSNQ  607
Query  242  VKLTSTSTDATELNTTDTNS  261
            V LT+     T+L  + TNS
Sbjct  16   VNLTTR----TQLPPAYTNS  31
Query  390  PTTA----KSTN  397
            P+T     KSTN
Sbjct  521  PATVCGPKKSTN  532
Query  226  CAPPKKPSPL  235
            C+ PKK + L
Sbjct  525  CG-PKKSTNL  533
Query  300  PQPSTPQQ  307
            P PS P +
Sbjct  807  PDPSKPSK  814
Query  141  GAFFLYDRIAST---TMYRGKVF  160
            G +F     AST    + RG +F
Sbjct  89   GVYF-----ASTEKSNIIRGWIF  106 
Query  304  TPQQGGNNTNHSQGV-VTEPGKTNTTAQ  330
            TP   G       GV V  PG TNT+ Q
Sbjct  588  TPCSFG-------GVSVITPG-TNTSNQ  607

although the tryptophan rich section is at the C-terminal of MarburgVirus glycopprtein, it does not come up within the alignment, so here by hand: 
 KEGTGWGLGGKW-WTSDWGVLTNL  <<< Marburg GLycoprotein
  E   +    KW W   W   +
 QELGKYEQYIKWPWYI-WLGFIAG  <<< SARS-CoV-2 Spike
or now shifted section
Query  643   KW-WTSDWGVLTNLGILLLLSIAVLIALSCI-C  673
             KW W    G +  L  +++++I +    SC  C
Sbjct  1211  KWPWYIWLGFIAGLIAIVMVTIMLCCMTSCCSC  1243
Query  533  IPFFGPGIEGLYTAGLIKNQNNLVCRLRRLANQT  566
            IP  G GI   Y     + Q N   R R +A Q+
Sbjct  664  IPI-GAGICASY-----QTQTNSPRRARSVASQS  691 <<<Furin in Spike
Query  255  NTTDTNSDDE-----DLT  267 Marburg glycoprotein
            +TTD   D +     D+T
Sbjct  571  DTTDAVRDPQTLEILDIT  588 <<Spike homolog with Fauci's epitope
 
note that the non-overlapping segments sometimes are containing exactly the same pool of amino acids, but arranged in different way, frequently backwards, RNA interference???

Is this all just random phenomenon??? I DO NOT THINK SO. Molecular biologists learn how to cut and paste pieces of all different organisms, how to change single amino acids to completely change the characteristics of the ‘outcome’. Again and again, every single amino acids counts, a single tripeptide like ‘RGD’ or ‘DRY’ already characterizes the entire feature of a specific protein. If Spike is so similar with other viral proteins, is it also similar with HUMAN proteins?? Almost every post of mine touched that issue, but here once again, some completely random tests on few of them.

A check for homologies with Dipeptidyl peptidase DPP4, membrane glycoprotein (https://www.uniprot.org/uniprotkb/P27487/entry), 92% sc and 37% identities, among others, when searched for smaller fragments:

Query  1     MKTPWKVLLGLLGAAALVTIITVPVVL  27
             +K PW + LG +  A L+ I+ V + L
Sbjct  1210  IKWPWYIWLGFI--AGLIAIVMVTIML  1234
Query  558  VFRLNWATYLASTE--NII  574
            V   N   Y ASTE  NII
Sbjct  83   VLPFNDGVYFASTEKSNII  101
Query  153   QWVTWSPVGHKLAYVW  168
             Q++ W P      Y+W
Sbjct  1208  QYIKW-PW-----YIW  1217
Query  177  EPNLPSYRITWTGKEDIIYNGIT  199
            +P  PS R   +  ED+++N +T
Sbjct  808  DPSKPSKR---SFIEDLLFNKVT  827

or Spike2020 VERSUS human integrin beta3 (https://www.uniprot.org/uniprotkb/P05106/entry) 87% sc, 50% identities(!!):

24.7 bits(50) 0.035 13/26(50%) 16/26(61%) 4/26(15%)

Query  371  VDAYGKIRSK---VELEVRDLPEELS  393 <<<Human integrin beta3 
            +D Y KI SK   + L VRDLP+  S      <<<IDENTITIES
Sbjct  197  IDGYFKIYSKHTPINL-VRDLPQGFS  221 <<<Spike2020
Query  593   CMSSNGLLCSG-RGKCECGSC  612
             CM+S    CS  +G C CGSC
Sbjct  1236  CMTS---CCSCLKGCCSCGSC  1253
Query  566   GQCSCGDCLCDSD  578
             G CSCG C C  D
Sbjct  1246  GCCSCGSC-CKFD  1257
Query  484   GVCRCGPGWLGSQCECSEEDYRP  506
             G C C     GS C   E+D  P
Sbjct  1246  GCCSC-----GSCCKFDEDDSEP  1263
Query  336  VTENVVNLYQN  346
            VT+NV  LY+N
Sbjct  911  VTQNV--LYEN  919
Query  513  SPREGQPVCSQ  523 <<<human integrin beta3 
            SPR    V SQ      <<<IDENTITIES
Sbjct  680  SPRRARSVASQ  690 <<<Spike2020 FURIN site, again!!!
Query  338  ENVVNLYQNYSELIPGTTVGVLSMDSSNVLQLIVDAYGKIRSKVELEVR  386
            ++VVN  QN   L   T V  LS +   +   + D   ++  KVE EV+
Sbjct  949  QDVVN--QNAQAL--NTLVKQLSSNFGAISSVLNDILSRL-DKVEAEVQ  992
Query  627   CPTCPDACTFKKECVECKKFD  647
             C +C   C     C  C KFD
Sbjct  1240  CCSCLKGCC---SCGSCCKFD  1257
Query  674  TGKDAVNCTYKNEDD---CVV  691
            TGK A +  YK  DD   CV+
Sbjct  415  TGKIA-DYNYKLPDDFTGCVI  434
Query  585  NCTTRT  590
            N TTRT
Sbjct  17   NLTTRT  22
Query  328  KNINLIFAVTENVVNLYQ----------NYSELIP  352
            KN   +FA    V  +Y+          N+S+++P
Sbjct  776  KNTQEVFA---QVKQIYKTPPIKDFGGFNFSQILP  807
Query  334  FAVTENVVNLYQNYSELIPGTTVGVLSMDSSNVLQLIVD  372
            FA TE   N+ + +   I GTT     +DS     LIV+
Sbjct  92   FASTEKS-NIIRGW---IFGTT-----LDSKTQSLLIVN  121

The above is extremely disturbing and serious! So how about the Spike comparison with the very same Integrin alpha-4/beta-7 from Fauci’s patent (https://www.uniprot.org/uniprotkb/P26010/entry)? Here few comparisons:

Query  686  GWCKERTLDNQLFFFLVEDDARGTVV  711 Integrin in Fauci's patent
            GW    TLD++    L+ ++A   V+
Sbjct  103  GWIFGTTLDSKTQSLLIVNNATNVVI  128 SPike2020
over 80 amino acid long entire segment:
Query  2    VALPMVLVL-----LLVLSRGESELDAKIPSTGDATEWRNPHLSMLGSCQPAPSCQKCIL  
            +A+P    +     +L +S  ++ +D  +   GD+TE                 C   +L
Sbjct  712  IAIPTNFTISVTTEILPVSMTKTSVDCTMYICGDSTE-----------------CSNLLL 
Query  57   SHPSCAWCKQLNFTASGEAEARRCARREELLAR  89
             + S  +C QLN   +G A   +    +E+ A+
Sbjct  755  QYGS--FCTQLNRALTGIA-VEQDKNTQEVFAQ  784
Query  278   RNVSRLLVFTSDDTF  292
             RN     + T+D+TF
Sbjct  1107  RNFYEPQIITTDNTF  1121
Query  602   MDSCISPEGGLCSGHGRCK  620
             M SC S   G CS    CK
Sbjct  1237  MTSCCSCLKGCCSCGSCCK  1255
Query  503  APGRLGRLCECSVAELSSPDLESGC  527
            APG+ G++ + +      PD  +GC
Sbjct  411  APGQTGKIADYNY---KLPDDFTGC  432
Query  572   ILCGGFGRCQC--GVCHCHANRTGRACECSGD  601
             +LC     C C  G C C     G  C+   D
Sbjct  1233  MLCCMTSCCSCLKGCCSC-----GSCCKFDED  1259
or the above with better shifting
Query  536   LCSGKGHCQCGRCSCSGQSSGHLCECDDASCE  567
             LC     C C +  C   S G  C+ D+   E
Sbjct  1234  LCCMTSCCSCLKGCC---SCGSCCKFDEDDSE  1262
Query  366  SAVGELSEDSSNVVQLIMDAYNSLSS  391
            SA+G+L +  +   Q +      LSS
Sbjct  943  SALGKLQDVVNQNAQALNTLVKQLSS  968
Query  193  FGSFVDKTVLPFVSTVPSK  211
            FG F    +LP  S  PSK
Sbjct  797  FGGFNFSQILPDPSK-PSK  814
Query  157   LMDLS------YSMKDDLERVRQLGHAL---LVRLQEV  185
             L D+S       +++ +++R+ ++   L   L+ LQE+
Sbjct  1166  LGDISGINASVVNIQKEIDRLNEVAKNLNESLIDLQEL  1203
Query  251   VSGNLD  256
             VSGN D
Sbjct  1122  VSGNCD  1127
and also the biggest fragment covering the Spike's ACE2 binding domain:
Query  695  NQLFFFLVEDDA---RGTVVLRVRPQEKG--ADHTQAIVLGCVGGIVA---------VGL 
            N L F  V  D+   RG  V ++ P + G  AD+   +     G ++A         VG 
Sbjct  388  NDLCFTNVYADSFVIRGDEVRQIAPGQTGKIADYNYKLPDDFTGCVIAWNSNNLDSKVGG 
Query  741  GLVLAYRLSVEIYDRREYSRFEKEQQQLNWKQDSNP  776
                 YRL    + +     FE++     ++  S P
Sbjct  448  NYNYLYRL----FRKSNLKPFERDISTEIYQAGSTP  479

Both integrins P05106 and P26010 are related, belong to the same family of proteins(that’s why the name), 40% identity and a BLAST score:

568 bits(1465) 0.0 304/757(40%) 434/757(57%) 31/757(4%)

Query  50   SCQKCILSHPSCAWCKQLNFTASGEAEARRCARREELLARGCPLEELEEPRGQQEVLQDQ  
            SCQ+C+   P CAWC              RC  +E LL   C  E +E P  +  VL+D+
Sbjct  38   SCQQCLAVSPMCAWCSDEALPLGSP----RCDLKENLLKDNCAPESIEFPVSEARVLEDR  
Query  110  PLSQGARGEGA--TQLAPQRVRVTLRPGEPQQLQVRFLRAEGYPVDLYYLMDLSYSMKDD  
            PLS    G+ +  TQ++PQR+ + LRP + +   ++  + E YPVD+YYLMDLSYSMKDD
Sbjct  94   PLSDKGSGDSSQVTQVSPQRIALRLRPDDSKNFSIQVRQVEDYPVDIYYLMDLSYSMKDD  

To speed up the detective work, let’s stick with official scientific titles and associations.. When we read “HIV-1 Tat Protein Enters Dysfunctional Endothelial Cells via Integrins and Renders Them Permissive to Virus Replication“ (https://pubmed.ncbi.nlm.nih.gov/33396807/)

and then

“SARS-CoV-2 Mediated Endothelial Dysfunction: The Potential Role of Chronic Oxidative Stress“ (https://pubmed.ncbi.nlm.nih.gov/33519510/)

then we would need to ask, do integrins have anything to do with the known ACE2 affinity for Sars-Cov-2? Only recently (https://pubmed.ncbi.nlm.nih.gov/35150743/) new admission states that:

”Integrin mediates cell entry of the SARS-CoV-2 virus independent of cellular receptor ACE2”.

And then we get 2012 paper (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3327712/) :

”Angiotensin Converting Enzyme (ACE) and ACE2 Bind Integrins and ACE2 Regulates Integrin Signalling”…

With a quote from it:”These results suggest that ACE2 plays a role in cell-cell interactions, possibly acting to fine-tune integrin signalling. Hence the expression and cleavage of ACE2 at the plasma membrane may influence cell-extracellular matrix interactions and the signalling that mediates cell survival and proliferation. As such, ectodomain shedding of ACE2 may play a role in the process of pathological cardiac remodelling.”

So if the first HIV paper states: “Tat protein of Human Immunodeficiency Virus (HIV)-1 is released by acutely infected cells in a biologically active form and enters dendritic cells upon the binding of its arginine-glycine-aspartic acid (RGD) domain to the α5β1, αvβ3, and αvβ5 integrins.“ and then we suddenly get the very same binding RGD motif in the very first ‘NEW’ SARS-CoV-2 Spike, sharing the extremely unique cystein cluster, part of the furin site, with that ‘RGD’not even present in Spikes of OLD coronaviruses, shall we believe that, all that is random???

Is that why Fauci, the HIV expert warned in 2017 Of ‘Surprise Outbreak’ During Trump Administration, a YEAR BEFORE he got his patent??? Fauci’s solution to HIV was: “In several examples, the α4 integrin antagonist is a monoclonal antibody that specifically binds to a α4, β1 or β7 integrin subunit or a cyclic hexapeptide with the amino acid sequence of CWLDVC.“ Here most recent research on: “Discovery of Cyclic Peptide Ligands to the SARS-CoV-2 Spike Protein Using mRNA Display” with a picture displaying the sequences:

The above cyclic peptides, containig the terminal cysteins, bind the receptor binding domain of ACE2 on Spike2020, Fauci’s cyclic peptide binds to the integrins!! Arent’ they all sharing the above similarities?? Does Fauci know all this? If something needs to be ‘fact-checked’ involving BIG names it almost instantaneously implies: check it once again! Just to show once again, how many times Fauci’s octapeptide CxxxxC aligns with the C-terminal part of the Spike, injected into billions:

           
Sbjct  1235  CCMTSCCSCLKGCCSCGSCCK  1244 SPIKE 2020
Query  2     CWLDVC  8   Fauci's patented cyclic 'HIV-octapeptide'
Query  3      CWLDVC  8  
Query  4             CWLDVC  8  
Query  5                  CWLDVC  8  

One of the very kind readers, Sally Gold, pointed out in the comment section to another extremely important fact I didn’t know, namely that Sars-Cov2 infection depends stronly on the expression level of cathepsin peptidase^9. That cysteine protease according to MEROPS database, contributes to the generation of anigenic peptides for the MHC II system. A licensed anti-influenza drug, amantadine, inhibiting that protease, prevented SARS-CoV-2 infection. Also Teicoplanin^10, an antibacterial drug previously used to treat virus infections caused by influenza virus, hepatitis C virus, HIV, Ebola, flavivirus, as well as MERS-CoV and SARS-CoV, works equally for SARS-CoV-2. Teicoplanin acts as a CatL inhibitor, blocking the S protein cleavage (Zhou et al., 2016; Yousefi et al., 2020). Doesn’t is sound that one and the same drug is capable of inhibiting ALL THE Spikes of all the most infectious diseases??? What does the cathepsin L does in HIV infection? “HIV Infection Induces Extracellular Cathepsin B Uptake and Damage to Neurons“^12, exactly like SARS-CoV-2 Spike. And if “HIV Protease Inhibitor-Induced Cathepsin Modulation Alters Antigen Processing and Cross-Presentation”^12 and this process by which pathogen Ags are internalized, degraded, and presented by MHC class I, is crucial to prime CD8 T cell responses, than that’s exactly the same what happens in SARS-CoV-2. BUT if the degardation pieces are very similar, due to high homology of all the sequences between the Spikes, then we’ll end up with similar drugs blocking the same targeting family of proteases.. Last example “Cathepsins and Their Endogenous Inhibitors in Host Defense During Mycobacterium tuberculosis and HIV Infection“ ^13 with its quote:”The moment a very old bacterial pathogen met a young virus from the 80’s defined the beginning of a tragic syndemic for humanity.” indicates all these common pathways leading to specific dis-eases, where one and the same immune system consisting of the very same T cells, B cells, CD4, CD8, etc. has to deal with an EXTERNAL foreign intruder, clearly always RECOGNIZED as such. NO MORE NOW, with covid genetically modifying injections. NOW Humans are the intruders themselves, literally, by expressing the very pathogenic injected agent they should avoid!

The main point of these comparisons is to point out the fact, that in order to propagate for example viral SARS-CoV-2 infection with a big pool of identical building blocks common with HIV-1, with Marburg, with all the other viruses mentioned in previous posts, incredible large portions of HUMAN proteins, any genetic re-programming of the human body for synthetic SARS Spikes production will automatically affect infections with other even more lethal or maybe even benign viruses.

Craig Venter, the ‘genetics genius’, expressed in few simple examples^13 the importance of the NATURAL mRNA content of every single cell:

-”CCR5 mRNA is significantly increased in a woman with STDs (sexually transmitted diseases) and inflammatory conditions, so the bacterial environment in conjunction with a woman’s genetics could determine her susceptibility to HIV.”^13

-in vivo “knockdown” of TRIM30a mRNA by small interfering RNA impaired LPS-induced tolerance.

-Intracellular components create myriad metabolites that can interfere and alter the
correct transcription of human proteins. Some of these metabolites can also disrupt
cellular repair mechanisms, resulting in the accumulation of “junk” (e.g., proteins,
enzymes, and mRNA) in the cytosol.

With one word, the mRNA status in every cell mirrors its health, or disease. Venter investigated mRNA profiling of thousands of traditionally HEP vaccinated people, in 2020 (right on time), all realted to human disease, and yet, Fauci didn’t seem to have from him the same information on Spike mod mRNA before changing that profiling in billions of covid injected HUMAN victims starting on global scale in 2021!?

The oldest protein in which I can find traces related to Spike, carrying actully the furin site, just shifted in the sequence, is the s.c. peplomeric protein, filed for a patent in 1986 (https://www.ncbi.nlm.nih.gov/nuccore/A24863.1). The alignment of the 2020 SPike and the 1986 furin site from the Infectious bronchitis virus spike looks following:

20.4 bits(41) 6e-04 Compositional matrix adjust. 12/34(35%) 15/34(44%) 1/34(2%)

Query  22  TTPSSPRR-RSFIEDLLFTSVESVGLPTDDAYKN  54 Spike 1986 furin site
           T  +SPRR RS     +     S+G     AY N
Sbjct  25  TQTNSPRRARSVASQSIIAYTMSLGAENSVAYSN  58 Spike 2020 furin site

Patent: EP 0221609-A1 13-MAY-1987; DUPHAR INTERNATIONAL RESEARCH B.V

The score of the alignment of the entire 1986 Spike with the 2020 Spike, with 100% overlap and ~37% identities is 364, here just first 3 raws of the alignment:

364 bits(935) 7e-111 Compositional matrix adjust. 202/548(37%) 299/548(54%) 22/548(4%)

NVLIPNSFNLTVTDEYIQTRMDKVQINCLQYVCGNSLDCRDLFQQYGPVCDNILSVVNSI  642 1987
++ IP +F ++VT E +   M K  ++C  Y+CG+S +C +L  QYG  C  +   +  I
SIAIPTNFTISVTTEILPVSMTKTSVDCTMYICGDSTECSNLLLQYGSFCTQLNRALTGI  770 2020

GQKEDMELLNFYSSTKPAGFNTPFLSNVSTGEFNISLLLTTPSSPRRRSFIEDLLFTSVE  702 1987
  ++D      ++  K   + TP + +   G FN S +L  PS P +RSFIEDLLF  V 
AVEQDKNTQEVFAQVKQI-YKTPPIKDF--GGFNFSQILPDPSKPSKRSFIEDLLFNKVT  827 2020

SVGLPTDDAYKNCTAGPLGFLKDLACAREYNGLLVLPPIITAEMQTLYTSSLVASMAFGG  762 1987
         Y +C        +DL CA+++NGL VLPP++T EM   YTS+L+A     G
LADAGFIKQYGDCLGDIAA--RDLICAQKFNGLTVLPPLLTDEMIAQYTSALLAGTITSG  885 2020

Few clarifications: the entire SARS-CoV-2 3D model exists as a genetic sequence, Pdb Data Bank does NOT have SARS-CoV-2 three dimentional structure of all componds (usually determined by X-Ray crystallography or Electron Microscopy). The OFFICIALLY known SARS-CoV-2 3D parts are some of the viral sub-components, like the Spike, with all its mutations.

For those who claim all is just graphene, frequencies, I have this counterargument: molecular biologists, geneticists created your GMO food, where mixed species (bugs+viruses+plants) were produced and served on people’s tables withut their consent, for the last ~25 YEARS! Do you think they will stop doing the same with the entire human body with incredible wonderful properties?? If you apply JUST graphene to a mixture of proteins/DNA/RNA you get a RANDOM cutting events without too much intelligence behind (my believe). YOU NEED THE WONDER of being a HUMAN and having a great HEART and BRAIN in order to function as such. In order to negate all the HUMAN BEAUTY, you need to be Dr. Fauci. Here a quote from him from the ‘Real Anthony Fauci.“ Part2:

“The worst bioterrorist is nature itself. The chances of Nature creating something really bad is much better the we near mortal humans doing it” « what a bunch of crap!!!

The Real Anthony Fauci-The Movie: Part Two, #2

Dr. Fauci, look into the mirror and find the nature’s error in your creation.

For those interested, Optogenetics will continue.. Right now, FAuCI comes first.

LITERATURE.

1. Josephine C Adams et al. “The evolution of tenascins and fibronectin“ Cell Adh Migr. 2015;9(1-2):22-33. https://pubmed.ncbi.nlm.nih.gov/25482621/

2. Sylvia Fitting et al. Brain Res. 2008 September 26; 1232: 139–154.

3. Sylvia Fitting et. al. Curr HIV Res. 2015; 13(1): 21–42. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467793/

4. Kathy Lien et al. PLoS One. 2019; 14(12): e0226343. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927651/

5. Junyoung Oh et al. Sci Rep. 2022 Mar 31;12(1):5496. https://pubmed.ncbi.nlm.nih.gov/35361832/

6. Shuibing Chen et al. Res Sq. 2021 May 21;rs.3.rs-513461. https://pubmed.ncbi.nlm.nih.gov/34031650/

7. Yun-Ju Lai et al. Am J Cancer Res. 2021 May 15;11(5):2278-2290. https://pubmed.ncbi.nlm.nih.gov/34094684/

8. https://academictree.org/chemistry/publications.php?pid=52415
   with following titles:

   Molteni A, Zakheim RM, Mullis KB, Mattioli L. The effect of chronic alveolar hypoxia on lung and serum angiotensin I converting enzyme activity. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 147: 263-5. PMID 4373751

   Zakheim RM, Molteni A, Mattioli L, Mullis KB. Angiotensin I-converting enzyme and angiotensin II levels in women receiving an oral contraceptive. The Journal of Clinical Endocrinology and Metabolism. 42: 588-9. PMID 176173 DOI: 10.1210/Jcem-42-3-588 

   Mattioli L, Zakheim RM, Mullis K, Molteni A. Angiotensin-I-converting enzyme activity in idiopathic respiratory distress syndrome of the newborn infant and in experimental alveolar hypoxia in mice. The Journal of Pediatrics. 87: 97-101. PMID 168336

   Molteni A, Mullis KB, Zakheim RM, Mattioli L. The effect of changes in dietary sodium on lung and serum angiotensin I converting enzyme in the rat Laboratory Investigation. 35: 569-573. PMID 186664 

   Zakheim RM, Mattioli L, Molteni A, Mullis KB, Bartley J. Prevention of pulmonary vascular changes of chronic alveolar hypoxia by inhibition of angiotensin I-converting enzyme in the rat. Laboratory Investigation; a Journal of Technical Methods and Pathology. 33: 57-61. PMID 167232 

9. Miao-Miao Zhao et al. “Cathepsin L plays a key role in SARS-CoV-2 infection in humans and humanized mice and is a promising target for new drug development“ Signal Transduct Target Ther. 2021 Mar 27;6(1):134.

10. Caio P. Gomes et al. “Cathepsin L in COVID-19: From Pharmacological Evidences to Genetics” Front Cell Infect Microbiol. 2020; 10: 589505.

    Published online 2020 Dec 8. doi: 10.3389/fcimb.2020.589505

11. Yisel M Cantres-Rosario et al. Sci Rep. 2019 May 29;9(1):8006. https://pubmed.ncbi.nlm.nih.gov/31142756/

12. Georgio Kourjianet al. J Immunol. 2016 May 1;196(9):3595-607. https://pubmed.ncbi.nlm.nih.gov/27009491/

13. “Metagenomics of the Human Body” by Craig VEnter