Skip to main content
. 2012 Jun 22;13:277. doi: 10.1186/1471-2164-13-277

Table 3.

The number of CD-epitope cores in γ-gliadin transcripts ofT. aestivum

epitope
Gli-A1
Gli-A1
Gli-B1
Gli-B1
Gli-B1
Gli-D1
Gli-D1

Group 6 Group 7 Group 3 Group 5 Group 8 Group 9 Group 10  
DQ2-γ-VIIb3*
701
144
72
230
57
1257
50
2511
DQ2-γ-VI3
224
0
0
0
38
678
50
990
DQ2-glia-γ2a6
140
30
36
59
38
684
0
987
DQ2-γ-II(Glia γ30)3,4
136
0
41
125
0
293
61
656
DQ2-γ-I (Glia-γ1)2
120
38
41
115
19
293
61
567
DQ2-γ-VIIa3
0
0
0
115
19
0
0
134
DQ2-γ-IV5
0
0
0
0
0
0
61
61
DQ2-γ-III5*
0
0
0
0
0
0
50
50
DQ2-glia-γ2b6
0
0
0
0
0
0
50
50
Nepitopes
1321
212
190
644
171
3205
383
6006
Ntranscripts
140
38
41
125
19
293
61
717
Nepitopes/Ntranscripts
9.4
5.6
4.6
5.2
9.0
10.9
6.3
8.4
Nepitopes/Ntranscripts 8.6 (1533/178) 5.4 (1005/185) 10.1 (3588/354)  

The number of T-cell stimulating sequences involved in CD (9 mer epitope cores) found in a set of 717 γ-gliadin transcripts from T. aestivum (genome ABD) attributed to respectively Gli-A1 (topology group 6 and 7), Gli-B1 (topology group 3, 5, and 8) and Gli-D1 (topology group 9 and10). The sequence topology was obtained by Neighbor joining analysis (see Figure 2). The frequency of T-cell epitopes in γ- gliadin transcripts (Nepitopes/Ntranscripts) is calculated.