AdS5 Generated Generalized Chemical Block Systems on Chern-Simons φ∘ D∘
r2∘ S∘ r1 Topologies for the generation of the Roccustyrna Holomorphic
Ligand.
Abstract
SARS-CoV-2 variants with spike (S)-protein D614G mutations now
predominate globally and increase infectivity by assembling more
functional S protein into the virion. In this paper, I combine topology
geometric methods for the generation of novel drug designs by using
generalized k - nearest neighbors within a quantum computing chemical
context targeting in a atomistic level the S proteins with aspartic acid
(SD614) and glycine (SG614) at residue 614 protein apparatus. In this
effort, I propose powerful enough computer - aided rational drug design
strategies to achieve very high accuracy levels for the generation of AI
- Quantum designed molecules of GisitorviffirnaTM, Roccustyrna_
gs1_TM, and Roccustyrna_fr1_TM ligands targeting the SARS - COV - 2
SPIKE D614G mutation by unifying Eigenvalue Statements into Shannon
entropy quantities as composed on Tipping–Ogilvie driven Machine
Learning potentials for nonzero Christoffel symbols. For this model, I
find analytic black hole solutions relevant to address a vast variety of
small molecule modeling problems essential to describe pharmacophore
merging phenomena in the presence of chemical potentials among others at
the locally AdS5 spacetime. A boundary solution in five-dimensional
Chern-Simons supergravity is described in the form of a Quantum Circuit
which can carry U(1) charge provided the spacetime torsion is
non-vanishing. Thus, I analyze the most general configuration consistent
with the local AdS5 generated D614G Binding Site isometries in
Riemann-Cartan space. I also arrived at a new Zmatter derived finite ‐
dimensional state integral and a Schwarzschild (DFT) ℓneuron (ι) : =
φ∘D∘r2∘S∘r102 /3[T] Ψ0⋮Ψ0Ψ0e [r] (F ∧ F ∧ F) (1o∑ ∑ ∑ ) improver
for a Chern - Simons Topology and Euclidean symplectic ω =
(i~)− 1/2 F (ab)J(ab) o1 ℓ T (a)J(a) oF T1 (dx/x) ∧
(dy/y) model by computing the analytically continued “holomorphic
blocks” on an appropriate quantum Hilbert space H to put pharmacophoric
elements back together.