Table 3.
Gene |
Epitope sequence |
Genotype of epitope |
|
Class A- Alleles |
Class B- Alleles |
|||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
|
Supertypes |
A01 |
A02 |
A24 |
A01A03 |
A01A24 |
B07 |
B58 |
B27 |
|||||
Allele type | A*01:01 | A*02:01 | A*68:02 | A*23:01 | A*30:01 | A*29:02 | B*07:02 | B*35:01 | B*53:01 | B*57:01 | B*58:01 | B*15:03 | B*27:05 | |||
NS3 (A*02) |
CINGVCWTV |
1a |
|
17802 |
67 |
61 |
14908 |
15501 |
12611 |
23637 |
20927 |
25523 |
19827 |
13679 |
19257 |
23485 |
1073-1081 |
CVNGVCWTV |
1b |
|
16997 |
110 |
20 |
12228 |
13122 |
11766 |
21885 |
15696 |
13382 |
18288 |
12132 |
20367 |
23007 |
|
SISGVLWTV |
2a variant |
|
18961 |
11 |
16 |
21483 |
11417 |
11417 |
22455 |
22186 |
29702 |
18590 |
15055 |
15691 |
20667 |
|
TVGGVMWTV |
3a |
|
19940 |
64 |
8 |
12677 |
14750 |
9776 |
20729 |
21877 |
24623 |
16182 |
18054 |
26500 |
24303 |
|
AVNGVMWTV |
4a variant |
|
17734 |
23 |
14 |
24001 |
4015# |
12036 |
10753 |
20258 |
20595 |
17093 |
12996 |
13641 |
18882 |
|
CINGVLWTV |
5a |
|
15172 |
26 |
39 |
17548 |
13613 |
13865 |
23524 |
21854 |
15854 |
18628 |
11203 |
17516 |
21090 |
|
CINGVMWTL |
5a variant |
|
17922 |
140 |
101 |
10449 |
14413 |
11435 |
18947 |
13165 |
11237 |
2239 |
13165 |
13572 |
19956 |
NS3 (A*02) |
KLVALGINA |
1a |
|
22719 |
273 |
15048 |
32261 |
1830 |
18800 |
24242 |
25216 |
37253 |
23529 |
20557 |
4839 |
19019 |
1406-1415 |
KLSGLGLNA |
1b |
|
19133 |
475 |
21824 |
33559 |
2557 |
13152 |
20740 |
27147 |
37083 |
23891 |
19220 |
8973 |
18099 |
|
QLTSLGLNA |
4a |
|
20013 |
7051 |
15292 |
33674 |
12859 |
12517 |
26454 |
24440 |
37244 |
22168 |
26218 |
7165 |
19904 |
|
KLVALGINAV |
1a |
|
37929 |
52 |
8564 |
39134 |
NO VALUE |
31977 |
19547 |
42247 |
34339 |
NO VALUE |
NO VALUE |
NO VALUE |
26021 |
|
LTGLGINAV |
5a |
|
12100 |
5692 |
304 |
32426 |
10980 |
20519 |
21309 |
20981 |
33652 |
25012 |
21599 |
12577 |
26332 |
|
QLTGLGINA |
5a variant |
|
22408 |
6972 |
7419 |
34672 |
13389 |
17488 |
26117 |
23541 |
36968 |
25569 |
22283 |
15466 |
20054 |
NS4B (A*02) |
LLFNILGGW |
1a, 1b, 4, 5a |
|
22942 |
14359 |
17095 |
18086 |
17906 |
9175 |
24903 |
19854 |
17154 |
956# |
962# |
5918 |
23118 |
1807-1816 |
MFFNILGGWV |
3a |
|
24613 |
23482 |
19706 |
343 |
15640 |
1707# |
21757 |
11817 |
8151 |
10769 |
1251 |
13832 |
26621 |
|
LLFNILGGWV |
1a, 1b, 4, 5a |
|
32231 |
44 |
1159# |
38969 |
NO VALUE |
19453 |
32445 |
40287 |
25767 |
NO VALUE |
NO VALUE |
NO VALUE |
25868 |
NS4B (A*02) |
ILAGYGAGV |
1a, 1b, 5a |
|
20500 |
15 |
530# |
30882 |
15492 |
10120 |
11883 |
21134 |
37213 |
22934 |
20702 |
3735 |
20143 |
1851-1859 |
ILAGYGTGV |
5a variant |
|
20351 |
18 |
193 |
32028 |
17493 |
12563 |
11272 |
21994 |
36657 |
23555 |
20603 |
2196 |
19849 |
NS5B (B*15) |
MSYSWTGAL |
1a, 1b, 4 |
|
12612 |
1522 |
24 |
2924 |
2372 |
5457 |
1530# |
50 |
8456 |
10166 |
523# |
80 |
16876 |
2422-2433 |
MSYTWTGAL |
5a |
|
12133 |
2640 |
22 |
8602 |
2141# |
7606 |
2515# |
58 |
9150 |
10680 |
787# |
144 |
17267 |
|
YTWTGALIT |
5a variant |
|
15779 |
3000 |
13286 |
33166 |
13737 |
1561 |
18979 |
3920 |
27619 |
22480 |
17360 |
6553 |
18765 |
NS5B (A*02) |
GLQDCTMLV |
1a |
|
18371 |
8 |
5733 |
11972 |
13187 |
6275 |
20996 |
27015 |
35681 |
25282 |
22002 |
10687 |
17601 |
2727-2735 |
KLQDCTMLV |
1b |
|
17735 |
7 |
3878 |
6160 |
2071# |
9527 |
17308 |
26776 |
35038 |
23310 |
18296 |
3587 |
16634 |
|
KLRDCTLLV |
5a |
|
19744 |
13 |
14912 |
15150 |
10 |
5150 |
2800 |
27145 |
36627 |
21481 |
20362 |
1720# |
18071 |
ALRDCTMLV | 4a | 19976 | 19 | 4673 | 19836 | 29 | 9982 | 5384 | 26302 | 36740 | 24190 | 22343 | 1206# | 20027 |
<50 IC50nm, bold, high affinity.
>50 IC50nm, <500 IC50nm, italic, intermediate affinity.
>500 IC50nm, #, poor affinity.
No value indicates server produced no binding score.