√π, x 10^3 = 1772.45 ~ 24 B-chains unbound
.
√π x10^3 = 56.05 ~ one B-chain
bound
.
√56 56 56 = 752.101 ~ half the R-chains
If these operations have sense, it remains for more advanced
mathematicians to explain. What kind of geometry could correspond
to the square root of π ?
—————————————————————————————
The similar parts of ams, the backbone (B) part, make up a separate
coordinate axis, not governed by codons. It gives a good reason
not to include them when studying differentiation of R-chains.
The B-chains appear in the ES-chain in groups of 6 (cf. the 4
codon type groups?).
R
|
B-chains: (H)NH2—CH—COO(H) =
74 A. Times 6 = 444.
Minus 1 H in the 4 ams Arg1,2 and Lys (charged), plus Pro gives
443.
Total sum 1776 - 4H = 1772.
Groups and condensations to bound B-chains are shown in figure
6-1:
Fig 6-1: Condensation of B-chains in groups of six
The division of the 6 unbound B-chains (444) in two intervals
around the middle of the ES-chain supports the recognition of
B-chains in this chain and connects R-chains with the middle step
Interval 544 to 367 = 177 = 6 x 29,5, the NH2(+H)-CH-part
of a B-chain, and 367 to 100 = 267 = 6 x 44,5, the COO(H)-part
of this chain as illustrated below. The decimal 0,5 may illustrate
the displacement of H in COOH to N-group, charging both ends of
B-chains. After condensation there is balance 28-28 between the
groups, times 6 = 168 - 168.
Fig 6-2: Division of interval 444 as 6 B-chains
(Interval 292 to 208, 5' - 3', = 84 = 1,5 x 56, the bound B-chain.
111, 1/4 of 444 = 1,5 x 74, the unbound B-chain. Perhaps an aspect
on why peptide bonds go on as if always a half was lacking?)
The number of B-chains from the exponent series was grouped in
6: Two of the number series giving the R-chains with the operation
below are not enough for the B-chains:
544 + 208, x 2 = 1504 = 24 R-chains
544 - 208, x 2 = 672 = 12 B-chains
bound
Should the first three steps in the exponent series eventually
be read both forward and backwards, (as in the “triplet
series 5-4-3 + 3-4-5 = 888, x 2 = 24 unbound B-chains à
74 A)? Eventually connected in some way with the opposite directions
of R-chains in proteins? More about this triplet series in file
II: 15.
It's often said that Asp - or Ala - constitute
the elementary form of an ams.
Whole mass of Asp R+B = 133 = interval 292
<—>159 in the ES-chain, its R-chain 59 is following
interval, 159 - 100, figure 6-3.
Number 74 for B-chains becomes a secondary
interval as Ala, R 15, the secondary interval 44 - 59. (Cf. that
origin of Ala can be both Pyruvate in glycolysis (2 x 44) and
Oxaloacetate (132) in citrate cycle.
Fig 6-3: Asp-Ala, R-chains 59, 15
A-base 135, /\ = 740740740...x10x: (Sign /\
here for inversion.)
At the protein synthesis it is the A-base as AMP that binds to
B-chains of ams and transports them to tRNAs. Square of this number
1/135 gives the "factor chain"
.
1 x 54 = 54
---> √ 54-86-96-84-50 = 74074,074074074...
2 x 43 = 86
3 x 32 = 96
370 / 5 = 74. Corresponding "factor chain" inwards =
235
4 x 21 = 84
= 5 x 47: 47 = R-chain of Cys which binds protein strings to more
5 x 10 = 50 complex
structures.
Sum 370
~ 5 x 74
Two times the inverted number of the C-base 111
A gives 18 (~ H2O) as periodic number,
180180180...and with one 10-power of displacement it gives
the difference* to inverted A-base 560560560..., the bound
B-chains à 56.
It looks like a connection with the common A-C-C-ends
of tRNAs at which the ams get attached, an intricate relation
between mass of codon bases and ams where inversions appear as
resonances in a complementary field? Only random associations?
*(Inversion of the G-base as bound (150A) to the period 66666..x10x
gives a difference to the inverted A-base that only is a displacement
of one 10-power in the period 740740... as if guiding the move
of tRNAs between positions on ribosomes?)
Another association about ACC-ends of tRNAs:
Sums of ams (R) with A- and C-contenting codons in 1st and/or
2nd position:
A = 888+1.= AA + AU + AG + AC + GA + CA + UA
C = 444 = CC + CG + CA + CU + GC + AC + UC,
These sums happen to approximate numbers for groups of B-chains.
A- plus two C-groups gives about the sum of 24 B-chains à
74 A. If the ACC-ends of tRNAs eventually should be part of a
reference system, it seems surely very intricate.
Keto-/amino polarity between bases:
Peptide bonds when O- and N-groups meet from two ams remind
of the keto-/amino polarity between the bases U + G versus
A + C. Two groups of codons divided by this polarity give sums
of ams R = 370, 5 x 74, -/+1 (Pair- + Cross-coded):
UU + GG + UG + GU = 370 - 1
AA + CC + AC + CA = 370 + 1.
370, corresponding to 5 B-chains à 74 A
Number of different atoms in the B-chains unbound:
C 48 = 576 = 3 x 192
O 48 = 768 = 4 x 192 ...(Note C+ O ~1344, sum
of bound B-chains.)
N 24 = 336
H = 96 -4 H (in Arg1, Arg2, Lys (charged) and in
Pro)
*
To N-Z-division
and H-atoms.