CUMING SOON!!!
This work remains ongoing... & I've done it again but got there in the end!
This Publication is a continuation of the publication DMT(+), Serotonin & Tryptophan(s) Brønsted Bondage, π-Systems, Quantum-Tunneling & Complete Reversible Hydrolytic Splicing: Coevolution of Group II Introns & RNA Viruses... OMG Filthy Little Whores!!! Which was abandon due to website limitations with it's poor structure providing organic learning process that in ways are beutifil in itself so after initially trying to delete and I think shifinf one lage paragraph have decided to include it as more of a mind map draft leading to the identification of irrefutable evidence of where DMT celular circuitary interface which` wasn't my intention but is of great enough significance to warrent minimal tidying up prior to remaining unchanged for historical purposes. If nothing else I've covered a fair few considerations regarding scientific analyses of stored samples associated with Universal Asylums dxperimental research Metabolic Implications of "Psychedelics / Forbidden Fruit" upon DRUG Saturation
Having unintentionally revealed the purpose of unaccounted for N terminals in SM domain [47] and oddly positioned C terminals within the LSM1 cellular complex which has had science baffled for at least 25years with all evidence indicating it completes the circuitry for N,N,Dimethyltryptamine to reconfigure the Peptidyl Transferase Center from a 5 to 6 member aromatic ring system capable of facilitating Cyclooctatetraene activity within the Ribosome to undertake Quantum level RNA genetic splicing this publication will hereby remain unchanged for historical purposes... To be continued in N,N-Dimethyltryptamine(s) & Tryptophan(annies) Hook-up at SM Domain & Spread their Aromatic Rings Connecting Cellular Matrix via Unexplained C Terminal in Lsm1 Complex for Hardcore Regular Servicing!
In addition to the above numerous reports confirm evidence of mirrored negative positive system which provides clear evidence of reverse configuration requiring DMT to potentially at times merely facilitate the reversal of standard amino acids basic actions which is likely the simplest example of the bare minimum of countless complex actions [48]. However, this is within the AMPA glutamate receptors (AMPARs) associated with dysfunctional RNA editing that additionally also include an aray of auxiliary subunits offering complex range of possible configurations [48, 49] which are dependant upon consciousness as critical component of DMTs stereochemically molecular facility. According to the US patent written by Manfredi et al. (2022) which provideds a neat 114pg collaboration of technical data combined by neat little legal definiations and easy to read explainations that regular consumption of DMT and most of the most significant included under the banner "forbidden fruit" fixes the above and basically lists every health condition and disease known to man particularly relting to RNA viruses. Yet they are claiming to be inventers of the solution to the one side effect being the "psychedelic effects" so they can maintian control for personal gain. This also provides evidence that the government are aware Vaccines are not necessary [50]. Universal Asylum as a global authority considered the US patent system a corrupt terrorist entity. Universal Asylum invented the concept that "consciousness as critical component of DMTs stereochemically molecular facility" warranting minimal interferance in terms of its consumption. Which due to it's ecological significance requires uninhibited efforts to proppergate and support regeneration with appropriate geological consideration of potentially invasive species, etc
If N,N-Dimethyltriptamine (DMT) is really the most invaluable asset to all forms of life on earth?.... Why doesn't everyone know?
Wang, Vidal, Sural, Loer, Aguilar, Merritt, Toker, Vogt, Cros & Hobert (2024) who must be the dumbest fucken scientists on the planet to have published "A neurotransmitter atlas of C. elegans males and hermaphrodites" which is currently claimed to provide "the most extensive whole-animal-wide map of neurotransmitter usage to date" and concisely provides everything anyone with half a brain needs to point them in the right direction of the "Unknown Neurotransmitter?" [1] yet they mysteriously failed to identify. Which fit's with whats problems within the Peptidyl Transferase Centre which has until recently accomodated intimate coevolutionary relationships with RNA viruses within the Ribsome which has remianed unchanged for 4 billion years [33].
Universal Asylum urgently advises that this is DMT and that the reason a "WTF's a Social Worker - A Brief Introduction." is advocating on behalf of the global scientific community is due to the fact that the most dangerous people in the world have gone to extreme lengths to burying any scientific evidence, undoubtedly including coutless scientists, polititians and anything else required to prevent this primitive centuries old form of social control from becoming public knowledge.
I'm gonna call polititions bluf with the statement "trust the science" strongly advise everyone to read the "Atlas" which is currently pending peer review which will be very interesting & trust the coultless sceintists soon to be sighted throughout Universal Asylums previous publishications many of which will soon be included here. The Scientific Community is invited to centre stage in the development of "Universal Asylums" "Global Leaderless System of Governance" which is designed to be as multifunctional as DMT including a Bioterrorism Intervention System to prevent the dangerously corpupt corporations giants, institutions and governments from consipring to commit genocide on a global scale as simple yet psychopathic means of avoiding ecological collapse. In fact Science, Social Work and Universal Asylum have a lot in common with "Mother Nature" in terms of in terms of the importance of maintaining equilibrium between stability adaptability to facilitate healthy evolution.
The neurotransmitter "Atlas" is written in manner that confirms the need for everything. The scientific significance of males and hermaphrodites "worms" raised in "the Atlas" confirms that DMT appears to be "male" with Tryptophan it's "female" equilibrial counterpart sharing intimate relationships with Serotonin with other sources identifying the "unidentified neurotransmittor [16]. The Atlas in addition to countless other scientits sighted supports previous work regarding DMT's role in facilitating complete and reverse transcripts hydrolytic splicing and therefore prolonged deprivation of DMT as a critically essential form of nutrition is contributing to countless health conditions and intergenerational genetic degeneration of Humans and other species. After abandoning my previous publication to serve as evidence of the organic learning process supporting this more adiquately infomed approach speaking matter of such complexity and significance .
DMT (and other tryptamines) in conjunction with Tryptophan are capable of facilitating the quantum mechanical actions within &/or otherwise surounding the Peptidyl Transferase Center (PTC) which is described as a dynamic peptide synthesis machine capable of such actions in the genetic splicing of RNA. This occurs within the Ribosome which can host 20 amino acids at least 9 of which are confirmed to be electro chemical with DMT the tenth catalytic counterpart to Tryptophan activating intense oscolation processess likely along the lines of Quantum Tunnelling within PTC [31, 33]. Within the ribsome a chain of Amino acids through which genetic splicing occurs are formed [34].
Reading [36] has left no uncertainty that under standard conditions splicing occurs at a relatively stable rate as via five member aromatic ring systems. However DMT and Tryptophan have got such great chemistry that only a fool would expect anything other than them to be all over one another spread their five mebered rings [37] to transition to either a 6 member aromatic ring or 8 member cyclooctane (also associated with peptides) [44, 45] configuration to get down and dirty with some hardcode RNA splicing. We'll start with 6 member ring systems.
Whilst some might consider that a presumptuous statement you'd be amazed what these filthy littly whores are capble of. Studies identified rates of 20- 50 and 80- 200 time tlower in various cell groups confirmed there is speace for such reconfigurations however despite evidence to suggest it possible were unable to identify pathways to achive them [34].
Other studies confirming evidence of variation of splice size and a range of often problematic other phenomenons includes an oddly positioned C terminal crossing an opening in the LSM1 [35, 36] celular complex is without question where DMT plugs in and is possibly the only fixed anchorage point to complete an otherwise highly divergent quantum circuitry system so advanced it could potentially crash a quantum computed system connected to equiptment capable of detecting all processes invilved. It's actually the obvious place due to it's significance and the fact that to create a stable quilibrium for such extreme splicing requires Tryptophan and DMT to be in appropriate forms. The following study demontrates what happens when the wrong amino is inserted [43]. Whilst considered something like Seretonin acting as a neautral which is entirely possibly. However, from memory there are two variations I'm aware of of DMT counting N,N-Dimethyltryptamine which I've been refering to as DMT+ which as opposed to DMT is considered a live major microspecie at pH of 7.3 and of possibly 5 Tryptophan variations I recally being confused by two being classed as live at the same pH though possibly only one considered "Major" presumably denoting dominant status. Functionally, this would make sense as far as precise coordination of such critical processes across and between a diverse range of interdependant cellular networks a 3rd perhaps transitional form of DMT would almost fit better with facilitating Cyclooctatetraenes. It also makes sense in terms of XX XY and I shouldn't risk starting WW3 by suggesting that in many ways women have more control than men weather they realise and/or like to admit it or not. But, I do my best to be an honest man and I'm kinda on a roll calling everyone cunts!
Serotonin is still likely in some way involved due to evidence of accompanying, l-tryptophan, and tryptamine binding to and inhibiting transport function but not being carried by the proton-coupled amino acid transporter PAT1 inhibiting transport function but are not transported by this carrier protein [35]. PAT1 contributes to the RNA binding activity and rather than motifs feature oppositional terminals and substrate with the C-terminal segments contain the polypeptide regions that are necessary for supporting decay, mediating interaction with other decay factors and that closest to N terminus of Pat1 proteins is sufficient for interaction with Dhh1 orthologs in yeast, Drosophila, and humans (Braun et al. 2010; Haas et al. 2010; Ozgur et al. 2010; Sharif et al. 2013) via [35}. Interestingly the C terminal ends aren't being used by the Lsm1-7 complex, which provides additional evidence supporting DMT and other tryptamines Essential Primary Amino of hydrolytic splicing in 3' of 5' splice sites [36] previously identified as unable to complete and reversable hyrdolific splicing in the previously described in the abandonded draft publication. Pat1 has also been implicated in nuclear functions with both Lsm1 and Pat1 are both nucleocytoplasmic shuttling proteins & is apparently "a substrate of cAMP-dependent protein kinase (PKA)–mediated phosphorylation, and such phosphorylation affects its ability to promote p-body formation" [36]. The former of which fits with the quantum mechanical atomic processes raised previously and whilst I'm not entire sure I fully comprehend the latter form what I recall DMT is pretty handy with phosphorus which it requires for various purposes, and if there's nothing else to do might even help clean up about the place.
Additionally, "A unique feature of the Lsm1-7 complex is that the extended C-terminal domain of Lsm1 forms a long α-helix that crosses the entire diameter of the doughnut and partially blocks the central hole" [36]. Lsm1 forms the interface of the celular matrix running back to complete the circuitry with the following which can be considered the equivelent to the master diagnostic and maintence terminal."The crystal structures of two Sm dimers, namely, D1D2 and BD3, revealed that the Sm motif represents an autonomously folding domain consisting of an N-terminal -helix followed by five -sheets (21). In both crystal structures, dimerization is brought about by an interaction of the 4 sheet of one Sm protein with 5 of the other, in line with biochemical and genetic evidence that the Sm domain is necessary and sufficient for the Sm proteins to form heteromers. Extrapolation of the Sm BD3 and Sm D1D2 structures, in conjunction with known interac- tions between the other Sm proteins, allowed the modeling of the Sm proteins into a seven-member ring (21). Although this ring still remains a model, it agrees both in size and shape with the Sm and LSm images obtained by electron microscopy (6, 20)." [47]. This will be explored in the following publication.
According to Chowdhury, Kalurupalle and Tharun (2014) as a direct result of Lsm1 complex not being able to achive not being able to achieve the 6 figure ring congigure right configuration it was designed to facilitate 4 billion years ago which are confirmed the broad range of problem I've been refering to as Hypo Cellular Divergence create problems in other areas due a combination of lack of peptidal expression resulting in buildups of unsured phospherous, glutames etc caunding dommino efects of congenstion in other earas, contributing to genetic degradation associaed with the above result mRNA stability turns out to be as significant a determinant of global changes [34, 39] in mRNA abundance as transcription rate [36]. This is is refleced by apromlems in nd the countless other scientific references supporting an extensive portfolio is why I don't for a second believe countless scientists haven't figured this out before me. Universal Asylum was always slapped together 10years behing schedual in a race against time with deadlines, including several real actual people I personal knew who might still be alive if someone had listened or the UN and WHO both of which I have only recently learned who they are and what they do not belive for one second believe they are unaware of the above and due to knowingly creating the circumstances above can already be considered Terrorism by their own definitions having bioweaponised Humans, in a manipulative attempt to commit genocide on a global scale via a bioweaponised vaccine Universal Asylum's Global Bioterrorism Intervention: A System Capable of Ensuring the Corporate Giants, the World Health Organisation, United Nations & World Governments Cannot Commit Global Genocide.
From Gradual compaction of the nascent peptide during cotranslational folding on the ribosome [39] providing evdence of genetitic digression in peptide expression which although on the opposite end of the spectrum as far as cell groups reflects the equal opposite problem to whats described in the draft publication. This could be due to such combination of not having whatever the completely stalled splice make out of the PAT1 that's not being used or imbalances caused by lack of processes associated with it not being used. Some are also said to be due to hydrolytic splicing covered in the draft publication.
The Ribosomal Peptidyl Transferase [46]
Exploring 5 and 6 ring configurations which I expect to incorporate 8 member cyclooctanes will require some consideration looking at the nature of the P, A and E sights. I was going to do some maths and considerations of the 5-6 / 6-8 system and in relation to forward reverse transcription particularly in relation to that left over PAT1. However, I just learned my Cousin is having a blood transfusion so my hearts with him and the family right now and I have a headache so think I’ll leave it here for now.
I wrote the above after my computer crashed loosing hundreds of windows of referencing material. The reason was by being trying to find a reference for a couple Gatekeepers of psychedelic community who until they prove otherwise I consider to dangerous for the positions they are in. The reference was in relation to contextual information which was beside the point of the two reasonable questions in the following fb post which I had hoped would provide some positive human connection but resulted in the closest thing I’ve had to a nervous break down since finding my father in a pool of blood and having Rosie screaming in my face how fucking great it was and pretending she was the victim.
Sienna who runs the Patch put up a post regarding bullying playing the victim presumably for the reasons stated in the following post the response I am going to give upon sealing this publication for historical purposes. Thereafter it’s up to them. This is groundbreaking. But so was earlier work which apparently doesn’t suit her agenda. Turns out it was because I said I hoped Torsten get hit by a car after he bullied me then deleted my the following post.
Thereafter is my earlier attempts to once again be stupid enough to leading in in a more structured manner whilst juggling countless references some of the material I never got around to looking at in context to other work. Perhaps I was good as if I didn’t start from fresh. I have squeezed in a nice ending though.
These transitional metals are in plants and do form nanotubes with amines which I hopefully have referenced somewhere but fuck it if I haven’t. Also the implied question regarding “TRYPT” is fair too. So to get bullied bullied over gramma, and typos. Perhaps I could have said I am certain Pt stands for Platinum. Yes would have been better wording. I am sure I had at least one reference confirming platinum in DMT or Tryptamines.
Last thing I needed was to be bullied off topic by a gang of CUNTS who unable to answer either of questions arguably relevant in an entheo-botanical group!.
Ha, I even stated I didn’t have time to waste so yeah I wished the CUNT got hit by a car. Sorry about that!
This was whats I'd previously written before loosing my reference material anyways...
N,N-Dimethyltryptamine (DMT) in it's most commonly recognised chemical structure and written form depicted in Figure 1 will be broken down using brackets to provide a basic introducion to its basic individual eliments. However, prior to doing so it should be noted that in it's alternate form of N,N-Dimethyltriptaminium, "DMT" is scientifically recognised as a "Live" "Major Microspecies at pH 7.3".
[N,N] = a Nitrogen Atom [-] Linking [Di][Methyl] 2x Methyl Groups. Until recently I've interpreted "N,N" as representing each of DMT's two nitrogen atoms rather than having two methly groups stemming from one nitrogen atom [2]. Apparently "a methyl group consists of three hydrogen atoms surrounding one carbon atom, symbolized as CH3 and are capable of attaching directly to DNA by forming a chemical bond with cytosine to form 5-methylcytosine" [3]. OMFG and DMT has two, but wiat there's more... Five- and Six-membered aromatic rings bearing a methyl group are important molecular fragments, as the methyl group can play a pivotal role in improving the biological activities due to its capability in modulating the molecular conformation as well as the physical and chemical properties [4]. The aromatic nature of the rings is of great significance which at this point in time will be identified as represented by the three lines within the Hexagonal ring and one within the Pentagonal ring.
After exploring countless plausable possiblilities I expect its no accident that [Trypt] isn't proving easy to get a clear answer on. However, after leaning towards [T] which according to Professor Emeritusas via LibraTexts Chemistry (2024) could represent: "Terra, 10+12" [5] (Which I possibly read the chat wrong but later dodiscared regardless) as a formula prefix to [R] presumably being the R Group side chain of Amino Acids. Interestingly there are claimed to be 21 Amino Acids with only Tryptophan the only of which mirrors the structure of DMT and configured as if its designed to facilitate equilibrial opposition [6]. Tryptophan is also one sharing the "Trypt" componant of it's name. Based on the amouont of research required to get this far in the puzzle I understand science has very specific rules on naming substances and principles to understanding shit my impression of the scientific community is they are generally more than happy to share. However, for some reason it's almost as if those those who keep saying "trust the science" wan't this one particular thing to remain a secret language the majority of the population to understand.
I'm actually finally confident in having peiced together the mysterious puzzle of [TR] and [YPT] after exploring yet another deadend possibility of potentially valuable reference at some point after unpacking [YPT].
Assuming the above is correct it would make sense for [Y] to represent: "Yota, 10+24" as the "Decimal Multiples and Submultiple" [5] one would roughly expect to prefix [PT] representing Platinum #78 as the transitional metal at the centre of the periodic table [7] which has been detected in 9 amino acids including Tryptophan [31] (with DMT excluded due to politics forcing science to pretend it's not an amino acid group).
I'm yet to attempt double checking the complex mathamatical equations associated with this which would be a great excuse to go see Grandpa who'd love this yet might struggle to grasp quantum tunnelling. But probably not as much as he does with my use of expletives.
Hang on. Fuck this is tricky.... Given DMT's classed as 'LIVE" [TRY] Could also represent the Encoding Gene - Transcription factor TRY (thale cress) [27] which is titled under "GENE SUMMARY: on a seperate page as: TRY - Homeodomain-like superfamily proton (thale cress)" [28]. However before going into that. [TR] Could also represent represent the "Gene group: Cytoplasmic transfer RNAs (TR)" [30] in which case [Y] could either represent Yotta or Yttrium followed By [Pt] Platnum. Which a both rare transitional metal associated with photosynthesic, or hologenic, nucular energetic and other sysergenic qualilities combined with amino acids and likely to have both once been regularly consumed via plants before cowardice cunts fucked up the entire world tring to control everything [31, 32].
Now for the genetic definition of [TRY] "Transcription factor. Involved in epidermal cell fate specification. Negative regulator of trichome development, including endoreplication, by lateral inhibition involving intercellular interactions. Promotes the formation of hair developing cells (trichoblasts) in H position in root epidermis, probably by inhibiting non-hair cell (atrichoblasts) formation." [27] with a synomyn of TRIPTYCHON [28] "Trichomes in Arabidopsis are single-celled hairs that exhibit a regular spacing pattern. Here, the role of TRIPTYCHON (TRY) in the generation of this spacing pattern is studied. By using genetic mosaics, we demonstrate that the formation of trichome clusters in try mutants is not correlated with cell lineage, indicating that TRY is required to single out trichome cells in a process involving cellular interactions. The genetic interactions of TRY, GLABRA1 (GL1), and TRANSPARENT TESTA GLABRA (T TG) in trichome patterning are assessed by determining the cluster frequency in various genetic combinations. It is shown that TRY acts as a negative regulator of GL1- and TTG-dependent pathways. Furthermore, it is demonstrated that trichome initiation in ttg-1, a strong ttg allele, is rescued almost to wild-type levels in a try background in which GL1 is expressed under the control of the cauliflower mosaic virus 35S promoter, indicating that T TG acts upstream of GL1 and TRY. These findings are incorporated into a model to explain the generation of a trichome spacing pattern from a homogeneous population of epidermal cells." [29]
Either way [Trypt] it doesn't matter as [PT] Platinum #78 is certain and both fit with the biomolecular science that proves where DMT belongs.
However, based on consistency in the nature of platinum in term of its stability, solubility, conductivity, nuclear magnetic resonance spectroscopy, mass spectrometer with direct sample inlet, ultraviolet/visible molecular absorption spectrometry, thermodynamics, and powerfulful chemical shifts [13, 24] particularly in response to reactions to Water, Carbon and Oxygen, along side the thought of DMT bringing a couple of methyl's haning off one of two nitrogen atoms the other of which is attach to one of two aromatic rings and it's platnum cock to party with Tryptophan and all their their favourite third wheel fuck buddy friend like Serotonin - I bet they know all kinds of crazy positions most have never even considered. Not a wonder they populated the planet with such crazy kids!?!. This fits with concepts such as π-Systems, Quantum-Tunnelling, complete hydrolytic splicing with reverse transcription, along with providing scientifically plausible explainations for the coulntless clues associated with the identified 'unknown neurotransmittor" in the Atlas and Universal Asylums work supporting its advocacy that DMT is invaluable to all life on earth as reflected by centuries of deprivation contributing to the genetic degeneration of our species. Medical industry is recogoing the value of platnum and in relations to hydrgen, nitrogen, and carbon along with peptide binding which has been assocaited with improved cancer treatmetns [18, 20, 22, 24] and general imporing the regulation of the system which remins limited to their insessnt need to want to control things they don't understand [17]. In adition to peptidesome of the limited improvements noted where due the acivation of amine groups to systhisise appropriate acide groups associated with the metabolism of glutamates being associated by the AAtlas and others as a resous faror relanting to many helth conditions [19, 1], Despite plantum being all the rage some critic publications are noting dysregulative problems [21] which I propose is due to the fact that the sytem remains incomple with DMT and it's full kit and kaboodle.
Oh, it's also entirely possible DMT is Tryptophan plays more of a gateway role in some kind of quantum cycle DMT through space and time into "our" World via plants and cycles it back through us and other creatures whilst exchanging information in either direction through space and time. This fits with scientific evidence of that Platinum based phosphoric derivative proteins being found in reproductive componants of humans including semen [23] and plants which I believe both seeds and flowers. Now I have litterally 100's of pages of scientific literature confirming most of the above and that such combinations solve the problems highlighted in the Atlas cause by the "unknown neurotransmitter". Everything form To solve such complex equasions accuratly and efficiently would require the quantum computer linked into a global system desigfned to apply state of the art scientific tecnolgy to scientific research across the global scal merging all feilds of science rather than becuase it's aboviously the right fucken thing to do and only fucken hope we have of avioding WW3, Genocide or Ecological Collapse. Just like the one I've was originally inspiredd to desing in 2008 and have been banging my head agaist a brick wall for years suggesting is a better idea that trusting the wrong cowardice cunts with slightly dressed up a 2000year old system of governance and military system we should be working collectively towards dismantling. I'm working on a 2013 iMac that keeps crashing with not cunt to help me becuase they all think the greedy cunts with money are all about helping people - so I'll do my best to get onto referencing the above ASAP before some cowardous cunt either accidentially or delliberatelyget us all killed.
I spent some time considering the possiblity of [R] being in reference DMT's "Stereochemical Configureation" trything to understand chiral centres wondering if perhabs DMT mirrored Tryptophan as R confirurates and perhaps S was associated with Serotonin perhaps the evulvelant of hermathrodite thirswheel sexual partner where they grabed what felt best and sterioinverted the fuck outa one other [9]. However, in my futile attempts to understand enough language to speak to the countless ways the three or parhas more if DMT had a buddy I'm yet to come across work functionally opperate are the chilral centre whilst examining the plain variation of the chart below it seemed as with R/S confiruration was limited to direction presumable suject to all kinds of domenant force within a 3D space. Now Imaging adding the dimention of space and time to being able to turn those basic representations inside out and abackwardsand forars through space and time.
"Quantumed-uped" chart from [9]
The following qoute from my draft provides an example of what DMT does and how it does it. work Contrary to the chiral inversion known in amines, the stereoinversion in corresponding aminiums is considered highly unlikely because of a high reaction barrier. However, high-level quantum mechanical computations, indicate that in gaseous state as well as in the presence of single water molecule acting as a catalyst, and also in a water solvated environment - the reaction barrier is reduced making the aminium cation prone to inversion. Interestingly, in contrast to molecules with a carbon atom stereocenter, stereoinversion with a nitrogen stereocenter was observed as a three multi-step process with quite high, or perhaps particular, reaction barrier. Although "gas-phase stereoinversion in the aminium cation is predicted to be infeasible, even along the proton transfer pathway which involves significant quantum tunneling" (Kaur, Ramanpreet & Vikas,. 2017) - DMT and Tryptophan appear to be biophysiologically equipped to facilitate the precision femto-scale actions required to create such conditions in order to achieve the processes above involved in stereoinversion. It is also not only possibly but highly likely that this same three multi step process is required to lariat the intron and complete hydrolytic splicing. As introns and exon include a range of metals of different compositions including Ca2+∼Mg2+<Mn2+ <Fe2+<Cu2+≥Zn2+ such processes irequire extreme particular and cordinated approach es to splicing to aviod dysfunctional splicing with harmful genetic. Comparitive analysis comparing the strongest and weakest of these found close-to-constitutive splicing in multiple tissues was contrasted by amino acids ability to coordinate of splicing being inhibited for Za+ (the stronger). Apparently this could sometimes be "compensated by stronger splice sites and uridine-richer polypyrimidine tracts, except for position –3 relative to 3′ splice junctions". [26]. This is of great interest being identified as a disregulative splice sight in the darft publication which will possibly both become crossover works in progress
As both DMT and Tryptophan are consider Live Major Mirospecies at pH 7.3 in particular forms it's possible they alternate shared control of equal and opposite mechinisms. As sthis can countless negitively and positively charged configurations the nature of DMTs polypyrimidine structures being removed from the equasion are likely responsible for dysfunction at the 3' splicing site. Considering DMTs skill set is at least the sum of [T]"Terra, 10+12" [5] [R] R Group Amino Acid Side Chain [Y] "Yota, 10+24" [PT] Platinum #78. Potentially mirroed by Tryptophan which I'm unsure includes the aromatic identifying the precice confiuration would be like finding a needele in a heystack except for DMT who could probably have the job done in a nanosecond. Additional studies making reference to various bonds strength under different conditions and the phenyl rings ability to provide epitaxial coordination with the facet, strongly contributing to its facet specificity [25]. This is to suggest that DMT and Trypt concisely work together in facilitating procise quantum mechanical molecular processes making gas stage sterioinversion not only feesable but a peice of cake with the right "micro-mechanics" on the job for the right reasons such as looking after the least deserving of their otherwise eternally great grandchildren.
Here's an absract supporting that under controled conditions along the line of the above Platnum is capable of what I'm suggesting. I'll try to find the reference on triptamines tying this both together but I'm unsure i haven't lost it in a computer crash. "Abstract: The water gas shift (WGS) reaction is an important step in many industrial processes and has thus stimulated various investigations focusing on optimising its catalysts. Previous studies comparing the reactivity of pure and doped-metallic nanotubes towards the catalysis of water dissociation, the key rate-limiting step for the WGS reaction on copper surfaces, suggest that platinum nanotubes stand up as being probably the most active catalysts for the water gas shift reaction. Therefore, we present here a detailed analysis of the performance of platinum nanotubes in the catalysis of the WGS reaction, by employing the Pt(5,3) nanotube as catalyst model and periodic density functional theory calculations. To do so, several reaction pathways were considered on the faces of the Pt(5,3) nanotube and then, energetic balances for the elementary steps on each pathway were determined. This allowed us to conclude that the most feasible reaction route for the WGS reaction on this nanotube follows an associative mechanism through the carboxyl intermediary. The results of this study revealed also that the Pt(5,3) nanotube is an adequate system for the catalysis of the WGS reaction, apart from avoiding the sintering problem intrinsic to catalysts based on nanoparticles dispersed on a support" [10]. Personally, I'm thinking of the couless potential ways such nanno tubles acts in supporting the therapeautic actions associated with the profound resulsts of my experimental rapid opiod detoxification treatment model and associated experimental research.
Another one... "The effect of sulfuric acid (SA) concentrations on heterogeneous reactions of amines such as methylamine (MA), dimethylamine (DMA), and trimethylamine (TMA) at the air–particle interface is investigated using combined classical molecular dynamics, Born–Oppenheimer molecular dynamics, and quantum chemical calculations. The results show that the mixtures of these amine vapors can accumulate at the air–particle interface and then participate in two types of heterogeneous reactions depending on the SA concentrations in the aqueous particles. At high SA concentrations, amines are neutralized by H3O+ and form ammonium salts within only a few picoseconds. At low SA concentrations, amines mainly proceed by hydrolysis reactions and produce ionic pairs of ammonium and OH–. However, the formed ionic pair is extremely unstable, and the reverse reaction takes place. Considering that the salt conversion time scales of amines at high SA concentrations are 2.5–15 times faster than those at low SA concentration, amine accumulation at high acidity particles is more favored" [14]. I'm unsure that sharp shift necesserally equate to instability. Sharp powerful and reversabile quantum scale shits under such conditions are exactly what hydrolythic splicing and reverse transcriptioin requires. Other similar studies into Ammonium ionic response across ranges of NH repeated similar sharp response which also maintained euliberal opposite responce which consistently increased or deceased based on thermodynamics [15]. In my oppinion that's stability and to state one condition is favorable over the other without understanding its purose is questionable itself. The fact of the matter is DMT and Triptophan are the best pair of biophysists in the history of anything which was going just find for millions of years until the stupided of men arrogant as to pretent they were obove everythignn else started fucking with shit they don't understand for the word reasons,
He's a great one from 30years ago which I actually should invest money i don't have to buy the full veriosion given it's nature and direct relevance toall over the above "Abstract: This article reviews all the known Pt(II) and Pt(IV) complexes with amino acids, peptides and their analogues referred in the literature. It gives details on the work done after 1975 since excellent reviews on the subject before that date have been published previously. The compounds described have been classified, in the first place, according to the metal ion oxidation state and in the second according to the binding site(s) of the ligand(s). Section 1 refers briefly to the reasons for studying platinum complexes with amino acids and similar molecules and gives the orientation of the research on the topic in recent years. In Sect. 2, the known Pt(II) complexes are reviewed in four sub-sections. The first describes the complexes with the metal ion binding to the terminal amino group or/and to a ring nitrogen of a side chain of the amino acid. This coordination mode is easily achieved and results in various products when the ligand contains more than one nitrogen donor atom. The second sub-section describes the complexes with the metal simultaneously binding to a nitrogen and one or more oxygen donor atoms of the ligand. A large number of stable chelates are thus formed. In contrast, binding of an amino acid or analogue through only an oxygen donor atom is not easily achieved. The third sub-section describes the complexes formed with sulphur-containing ligands. In such complexes, coordination of sulphur, which is the primary binding site, may result in bridged or oligomeric complexes. The fourth sub-section refers to the organometallic Pt(II) complexes which contain an amino acid or analogue coordinated through an amino terminal group or chelated through nitrogen and oxygen donor atoms. In Sect. 3, the known Pt(IV) complexes are reviewed in four sub-sections corresponding to those in Sect. 2. The same amino acid coordination modes are also found here. Finally, Sect. 4 summarizes the conclusions drawn from the previous three sections and emphasizes their most important features" [11].
According to these scientist "phosphorylation substantially contributes to proper functioning of sperm proteins. Hence, phosphorylated sperm proteins might be considered as prime candidates for diagnosis and treatment of reduced male fertility." They're on the money right up until tyhe last sentence "treatment". At some point I'll try and reference the scientic evidence of how handy DMT is with phosphorylation when I come across them. but even if I don't get around to that it supports claim of genetic degeneration. Supporting the above and associting phophorylation and Platnum and intergenerations isuuse associated with semen, which I'm bite my tonge on the conluding solutions are [23]
Ramakrishnan et al further elucidated the binding contributions from other amino acids in the S7 peptide using constant valence force field parameters [42]. It was further verified that the presence of water and buffering ions is important for the peptide adsorption process [42]. For the S7 peptide, the F residue has the highest affinity toward the Pt-{111} facet. In addition, glutamine (Q), asparagine (N), and proline (P) have higher adsorption energy toward Pt-{111} as opposed to Pt-{100} [42]. The hydrophilic nature of Q, the polar nature of N, the hydroxyl group in serine (S), and the added structural constraint from P contribute to the specific adhesion of the S7 peptide to the Pt-{111} surface [25]
Because proteins are flexible, steric selection of metals is imperfect, especially by nascent polypeptides first emerging from the ribosome (7). Under such conditions the relative affinities of divalent metals for proteins have a tendency to follow ligand field stabilization energies of metals themselves, creating a universal order of binding preferences known as the Irving–Williams series (7–9), first proposed for a subset of transition metals 75 years ago (10). For essential divalent metals abundant in humans [ppm > 50 (9)], this order is Ca2+∼Mg2+<Mn2+ <Fe2+<Cu2+≥Zn2+, with Ca2+and Mg2+ forming the weakest and Cu2+ and Zn2+ forming the tightest complexes with organic ligands (1,5,7,8,11). In equimolar mixtures of these and other divalent metals in the series (Co2+ and Ni2+), proteins that require weaker binding ions preferentially bind tighter metals. Although metalloproteins can bind incorrect metals in vitro, metalation in vivo is usually accurate (12,13), implying that cells evolved efficient strategies to overcome or reduce these constraints and avoid binding by tight non-cognate metals (mismetalation) to safeguard selective metal-binding properties of their polymers (7,14,15). Harmful mismetalation events can distort geometry of cognate metal-binding sites, recruit undesired ligands or exploit only a subset of native ligands (1). Hence, it is essential to understand how protein-coding genes and their products manage metal acquisition to avoid mismetalation. [26]
The ESE/ESS profiles have been recently linked to amino acid frequencies at binding sites for divalent metals (28). The weakest binders of the Irving–Williams series (Ca2+, Mg2+) were shown to preferentially bind residues encoded by splice-enhancing codons, whereas the tight binders (Cu2+, Zn2+) are coordinated to amino acids encoded by splice-repressing codons, with moderate binders in the series (Mn2+, Fe2+) exhibiting intermediate codon-specific ESE/ESS values (28) (Figure 1A). This splicing dichotomy suggested that protein-binding sites for weak divalent metals may have been promoted during evolution at the exon level, whereas sites for competitive metals may have been repressed, potentially reducing mismetalation [26]
that codons coding for amino acids coordinating the two divalent metals in human proteins have the capacity to confer a significantly lower exon inclusion for tight Zn2+ than for weak Ca2+ [26].
Splicing reporters containing pyrimidine transitions at posi- tion –3 of 3′ss were first tested for three human genes: F8 (56), UBE2F (57) and HGD (58). [26]
Such Quantum tunnelling is so powerful that 'Hyper' is an insult as although difficult to comprehend it would seem more along the lines of quantum tunnelling through to an alternate dimension and exchanging information between space and time with some for of collective consciousness. If I’m correct about Tryptophan being the equivalent of a quantum cunt who only gets wet hot enough for the right type of quantum cocks such cycling them enough of presumably both of them into this realm via plants etc and back through us the DMT traces aren’t exactly endogenous, whilst they could be the equivalent to cum dripping off her lips. It’s also possible that we always need to attain one or more molecules to to maintain life. But theres an ever scaried throught...
According to Chowdhury, Kalurupalle and Tharun (2014) as a direct result of Lsm1 complex not being able to achive not being able to achieve the 6 figure ring configuration it was designed to facilitate 4 billion years ago contributing to genetic degradation associated with the above result mRNA stability turns out to be as significant a determinant of global changes [34, 39] in mRNA abundance as transcription rate [36]. If we his possibility cycling degenerative RNA through such a system, which as hard as it is to comprehend despite the fact fits with many mysteries of the world, and they are comming back into this one genocide of nearly 8billion people pumping defective RNA into the other side, would be likely to result in something like Jurasic park. Now this is in countless
Knowing that despite the fact everyone knows our outdated social structure the greatest liability to life on earth as I'm just a Social Worker - No cunt's likely to take me seriously anyway!!!
To be Continued...
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