scholarly journals Graph Coverings for Investigating Non Local Structures in Proteins, Music and Poems

Sci ◽  
2021 ◽  
Vol 3 (4) ◽  
pp. 39
Author(s):  
Michel Planat ◽  
Raymond Aschheim ◽  
Marcelo M. Amaral ◽  
Fang Fang ◽  
Klee Irwin

We explore the structural similarities in three different languages, first in the protein language whose primary letters are the amino acids, second in the musical language whose primary letters are the notes, and third in the poetry language whose primary letters are the alphabet. For proteins, the non local (secondary) letters are the types of foldings in space (α-helices, β-sheets, etc.); for music, one is dealing with clear-cut repetition units called musical forms and for poems the structure consists of grammatical forms (names, verbs, etc.). We show in this paper that the mathematics of such secondary structures relies on finitely presented groups fp on r letters, where r counts the number of types of such secondary non local segments. The number of conjugacy classes of a given index (also the number of graph coverings over a base graph) of a group fp is found to be close to the number of conjugacy classes of the same index in the free group Fr−1 on r−1 generators. In a concrete way, we explore the group structure of a variant of the SARS-Cov-2 spike protein and the group structure of apolipoprotein-H, passing from the primary code with amino acids to the secondary structure organizing the foldings. Then, we look at the musical forms employed in the classical and contemporary periods. Finally, we investigate in much detail the group structure of a small poem in prose by Charles Baudelaire and that of the Bateau Ivre by Arthur Rimbaud.

Author(s):  
Michel Planat ◽  
Raymond Aschheim ◽  
Marcelo Amaral ◽  
Fang Fang ◽  
Klee Irwin

It is shown how the secondary structure of proteins, musical forms and verses of poems are approximately ruled by universal laws relying on graph coverings. In this direction, one explores the group structure of a variant of the SARS-Cov-2 spike protein and the group structure of apolipoprotein-H, passing from the primary code with amino acids to the secondary structures organizing the foldings. Then one look at the musical forms employed in the classical and contemporary periods. Finally, one investigates in much detail the group structure of a small poem in prose by Charles Baudelaire and that of the Bateau Ivre by Arthur Rimbaud.


Author(s):  
Michel Planat ◽  
Raymond Aschheim ◽  
Marcelo M Amaral ◽  
Fang Fang ◽  
Klee Irwin

It is shown how the secondary structure of proteins, musical forms and verses of poems are approximately ruled by universal laws relying on graph coverings. In this direction, one explores the group structure of a variant of the SARS-Cov-2 spike protein and the group structure of apolipoprotein-H, passing from the primary code with amino acids to the secondary structures organizing the foldings. Then one look at the musical forms employed in the classical and contemporary periods. Finally, one investigates in much detail the group structure of a small poem in prose by Charles Baudelaire and that of the Bateau Ivre by Arthur Rimbaud.


Quantum ◽  
2020 ◽  
Vol 4 ◽  
pp. 282 ◽  
Author(s):  
Andrea Coladangelo

We describe a two-player non-local game, with a fixed small number of questions and answers, such that an ϵ-close to optimal strategy requires an entangled state of dimension 2Ω(ϵ−1/8). Our non-local game is inspired by the three-player non-local game of Ji, Leung and Vidick \cite{ji2018three}. It reduces the number of players from three to two, as well as the question and answer set sizes. Moreover, it provides an (arguably) elementary proof of the non-closure of the set of quantum correlations, based on embezzlement and self-testing. In contrast, previous proofs \cite{slofstra2019set, dykema2017non, musat2018non} involved representation theoretic machinery for finitely-presented groups and C∗-algebras.


2013 ◽  
Vol 61 (1) ◽  
Author(s):  
A. M. Basri ◽  
N. H. Sarmin ◽  
N. M. Mohd Ali ◽  
J. R. Beuerle

In this paper, we develop appropriate programme using Groups, Algorithms and Programming (GAP) software enables performing different computations on various characteristics of all finite nonabelian metacyclic p–groups, p is prime, of nilpotency class 2. Such programme enables to compute structure of the group, order of the group, structure of the center, the number of conjugacy classes, structure of commutator subgroup, abelianization, Whitehead’s universal quadratic functor and other characteristics. In addition, structures of some other groups such as the nonabelian tensor square and various homological functors including Schur multiplier and exterior square can be computed using this programme. Furthermore, by computing the epicenter order or the exterior center order the capability can be determined. In our current article, we only compute the nonabelian tensor square of certain order groups, as an example, and give GAP codes for computing other characteristics and some subgroups.


Author(s):  
Robert A. Wilson

AbstractWe determine all conjugacy classes of maximal local subgroups of Thompson's sporadic simple group, and all maximal non-local subgroups except those with socle isomorphic to one of five particular small simple groups.


2011 ◽  
Vol 255-260 ◽  
pp. 2145-2149
Author(s):  
Lin Guo ◽  
Li Zhen Lian

A GST-driven spatially adaptive filter is developed in this paper based on the framework of non-local means (NLM) avoiding explicit motion estimation. Gradient Structure Tensor (GST) is introduced to express the underlying local image structural patterns, which drives the window function to yield adaptive scale and shape fitting for the local structure. This leads to patches with more similar gray-level and local structures being gathered for super-resolution estimation of image. Results on several test video sequences show that the proposed method is effective in providing super-resolution on general sequences and achieves improvement of performance on the compared method.


Author(s):  
David Cavanaugh ◽  
Krishnan Chittur

In a previous paper we have introduced a new hydrophobicity proclivity scale and justified its superior performance characteristics, particularly in the context of a scale for protein alignments, but also for its strong correlation with many other amino-acid physico-chemical properties. Within that paper, we calculated a corrected free energy of residue burial of each amino-acid in folded proteins from a linear regression of amino-acid free energy of transfer from water to n-Octanol (F&P octanol scale dGow, Y axis) and our Hydrophobicity Proclivity Scale<br>(HPS, X axis). In this present paper we pursue the latter general findings in more detail by considering the relationship of hydrophobicity and other physico-amino-<br>acid scales with the molecular geometry of amino-acids and secondary group structure/surface chemistry, with a concommitant discussion of the dimensions/geometry<br>of the caveties that amino-acids make in water. We identify a series of molecular physico-chemical properties that uniquely define the natural selection and geometry of the 20 natural amino-acids. We use the corrected free energy of amino-acid burials in proteins (Y axis) and a multiple linear regression to identify the AA molecular physico-chemical properties (X1, X2, ...) that explain the energetics of amino-<br>acid water contacts in an unfolded protein state to that of the folded protein state by modeling these two states as a solvent-solvent transfer, thus, providing a thermodynamical model for the initial stages of protein folding. Between our previous paper and the current paper we can greatly simplify and reduce the very large number of amino-acid scales in the literature to a small number of amino-acid property scales. Finally, we explore the numerical relationship between the structure of the genetic code and molecular physico-chemical properties of AA’s that in turn can be related directly to hydrophobicity. We validate and explain our novel models we describe herein with extensive data from the literature.<br>


Author(s):  
Michael A. Persinger ◽  
Nirosha J. Murugan ◽  
Lukasz M. Karbowski

The duality of matter-energy as particle-waves was applied to the classic ERK-MAP signaling pathways between the plasma cell membrane and the nucleus and was tested with Cosic’s Resonance Recognition Method. Spectral analyses of sequences of pseudopotentials that reflect de-localized electrons of amino acids for the 11 proteins in the pathway were computed. The spectral power density of the terminal protein (cFOS) was shown to be the average of the profiles of the precursor proteins. The results demonstrated that in addition to minute successive alterations in molecular structure wave-functions and resonant patterns can also describe complex molecular signaling pathways in cells. Different pathways may be defined by a single resonance profile. The separations between the peaks of wavelengths from Cosic’s predictions for photon emissions in the visible spectrum that define the ERK-MAP pathway were within the range of 10-20 J. This quantity has been shown to be a fundamental unit of energy within the universe. The involvement of photon patterns indicates that non-local effects could accompany the serial causality (locality) assumed to connect molecular pathways.


2020 ◽  
Author(s):  
David Cavanaugh ◽  
Krishnan Chittur

In a previous paper we have introduced a new hydrophobicity proclivity scale and justified its superior performance characteristics, particularly in the context of a scale for protein alignments, but also for its strong correlation with many other amino-acid physico-chemical properties. Within that paper, we calculated a corrected free energy of residue burial of each amino-acid in folded proteins from a linear regression of amino-acid free energy of transfer from water to n-Octanol (F&P octanol scale dGow, Y axis) and our Hydrophobicity Proclivity Scale<br>(HPS, X axis). In this present paper we pursue the latter general findings in more detail by considering the relationship of hydrophobicity and other physico-amino-<br>acid scales with the molecular geometry of amino-acids and secondary group structure/surface chemistry, with a concommitant discussion of the dimensions/geometry<br>of the caveties that amino-acids make in water. We identify a series of molecular physico-chemical properties that uniquely define the natural selection and geometry of the 20 natural amino-acids. We use the corrected free energy of amino-acid burials in proteins (Y axis) and a multiple linear regression to identify the AA molecular physico-chemical properties (X1, X2, ...) that explain the energetics of amino-<br>acid water contacts in an unfolded protein state to that of the folded protein state by modeling these two states as a solvent-solvent transfer, thus, providing a thermodynamical model for the initial stages of protein folding. Between our previous paper and the current paper we can greatly simplify and reduce the very large number of amino-acid scales in the literature to a small number of amino-acid property scales. Finally, we explore the numerical relationship between the structure of the genetic code and molecular physico-chemical properties of AA’s that in turn can be related directly to hydrophobicity. We validate and explain our novel models we describe herein with extensive data from the literature.<br>


2017 ◽  
Vol 21 (2) ◽  
pp. 819-826 ◽  
Author(s):  
Derya Avci ◽  
Eroglu Iskender ◽  
Necati Ozdemir

The conformable heat equation is defined in terms of a local and limit-based definition called conformable derivative which provides some basic properties of integer order derivative such that conventional fractional derivatives lose some of them due to their non-local structures. In this paper, we aim to find the fundamental solution of a conformable heat equation acting on a radial symmetric plate. Moreover, we give a comparison between the new conformable and the existing Grunwald-Letnikov solutions of heat equation. The computational results show that conformable formulation is quite successful to show the sub-behaviors of heat process. In addition, conformable solution can be obtained by a analytical method without the need of a numerical scheme and any restrictions on the problem formulation. This is surely a significant advantageous compared to the Grunwald-Letnikov solution.


Sign in / Sign up

Export Citation Format

Share Document