 =EUK+1 |
=PRO+1 |
||||||||
 |
 |
 |
 |
|
|
|
|
||
0 |
54 (α ≈ 10-9) |
22 |
32 |
0 |
59 (α ≈ 10-25) |
47 |
12 |
||
1 |
20 |
64 (α ≈ 10-120) |
44 |
1 |
20 |
51 (α ≈ 10-12) | 31 |
||
2 |
30 |
19 |
11 |
2 |
31 |
8 |
23 |
||
| =EUK−1 |
=PRO−1 |
||||||||
0 |
24 |
73 (α ≈ 10-198) |
49 |
0 |
13 |
47 (α ≈ 10-7) |
34 |
||
1 |
60 (α ≈ 10-64) |
13 |
47 |
1 |
81 (α ≈ 10-105) |
44 |
37 |
||
2 |
25 |
19 |
6 |
2 |
8 |
16 |
8 |
||
,a,b,) (in % rounded) of modulo 3 maxima in the three frames of the ranges [a,b] in the four studied frameshift gene populations . For each population , this probability is computed for two position intervals. The first interval is the region preceding the frameshift site and ranging from the minimum i position min = a (Table 2) of the populationF to the frameshift position b = 0. The second interval is the region following the frameshift site and ranging from the frameshift site a = 1 to the maximum i position max = b (Table 2) of the population . The values in bold indicate the identified reading frames. In all populations, the circular code periodic signals move in the same direction of translational frameshifting.