DRACP00368 |
LL-III/2 |
NVWKKILGKIIKVVK |
15 |
Synthetic |
DRACP00369 |
LL-III/15 |
VNFKKLLGKLLKVVK |
15 |
Synthetic |
DRACP00370 |
LL-III/16 |
VNXKKLLGKLLKVVK |
15 |
Synthetic |
DRACP00371 |
LL-III/19 |
VNWKKXLGKXIKXVK |
15 |
Synthetic |
DRACP00372 |
LL-III/11 |
VNWKKIILGKIIKVVK |
16 |
Synthetic |
DRACP00373 |
LL-III/1 |
VNWKKILAKIIKVVK |
15 |
Synthetic |
DRACP00374 |
LL-III/36 |
VNWKKILAKIIKVVK |
15 |
Synthetic |
DRACP00375 |
LL-III |
VNWKKILGKIIKVVK |
15 |
Lasioglossin III and its analogs |
DRACP00376 |
LL-III/12 |
vnwkkilgkiikvvk |
15 |
Synthetic |
DRACP00377 |
LL-III/37 |
VNWKKVLAKIIKVVK |
15 |
Synthetic |
DRACP00378 |
LL-III/8 |
VNWKKILGKIIKVVK |
15 |
Synthetic |
DRACP00379 |
LL-III/9 |
VNWKKILGKIIKVVK |
15 |
Synthetic |
DRACP00380 |
LL-III/4 |
VNWKKILGKIKKVVK |
15 |
Synthetic |
DRACP00381 |
LL-III/3 |
VNWKKILKKIIKVVK |
15 |
Synthetic |
DRACP00382 |
LL-III/6 |
VNWKKILPKIIKVVK |
15 |
Synthetic |
DRACP00383 |
LL-III/23 |
VNWKKLLGKLLKVVK |
15 |
Synthetic |
DRACP00384 |
Cathelicidin-1, CATH-1, Fowlicidin-1 |
RVKRVWPLVIRTVIAGYNLYRAIKKK |
26 |
Gallus gallus |
DRACP00385 |
LL-III/25 |
vnwkkllgkllkvvk |
15 |
Synthetic |
DRACP00386 |
LL-III/27 |
VNWKKVLGKVVKVVK |
15 |
Synthetic |
DRACP00387 |
LL-III/24 |
VNWXXILGXIIXVVX |
15 |
Synthetic |
DRACP00388 |
LL-III/17 |
VNWRRILGRIIRVVR |
15 |
Synthetic |
DRACP00389 |
Cecropin-B |
KWKIFKKIEKVGRNIRNGIIKAGPAVAVLGEAKAL |
35 |
Antheraea pernyi (Chinese oak silk moth) |
DRACP00390 |
LL-III/26 |
VYWKKILGKIIKVVK |
15 |
Synthetic |
DRACP00412 |
N29D |
PDEDAINDALNKVCSTGRRQRSICKQLLKK |
30 |
Synthetic |
DRACP00413 |
N29N |
PDEDAINNALNKVCSTGRRQRSICKQLLKK |
30 |
Synthetic |
DRACP00449 |
Alliumin |
DDFLCAGGCL |
10 |
Allium sativum |
DRACP00450 |
Cupiennin-1a |
GFGALFKFLAKKVAKTVAKQAAKQGAKYVVNKQME |
35 |
Cupiennius salei |
DRACP00465 |
NRC-16 |
GWKKWLRKGAKHLGQAAIK |
19 |
Synthetic |
DRACP00477 |
KilerFLIP-E |
YGRKKRRQRRRREADFFWSLCTA |
23 |
The C-terminal domain of c-FLIP |
DRACP00478 |
Short α-helical peptides |
GIIKKIIKKI |
10 |
Alpha-helical proteins |