BIOPEP-UWM: Peptide Data
ID
Name
Sequence
FKLFKKILKVLG
Chemical Mass
Number of residues
Monoisotopic Mass
EC50
IC50
µM
Additional Information
BIOPEP-UWM database of bioactive peptides SMILES: [H][C@](N)(Cc1ccccc1)C(=O)N[C@@]([H])(CCCCN)C(=O)N[C@@]([H])(CC(C)C)C(=O)N[C@@]([H])(Cc1ccccc1)C(=O)N[C@@]([H])(CCCCN)C(=O)N[C@@]([H])(CCCCN)C(=O)N[C@@]([H])([C@@H](C)CC)C(=O)N[C@@]([H])(CC(C)C)C(=O)N[C@@]([H])(CCCCN)C(=O)N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(CC(C)C)C(=O)NCC(O)=O InChI=1S/C73H124N16O13/c1-11-48(10)62(73(102)87-58(40-46(6)7)69(98)83-54(32-20-24-36-76)67(96)88-61(47(8)9)72(101)86-56(38-44(2)3)64(93)79-43-60(90)91)89-68(97)55(33-21-25-37-77)81-65(94)53(31-19-23-35-75)82-71(100)59(42-50-28-16-13-17-29-50)85-70(99)57(39-45(4)5)84-66(95)52(30-18-22-34-74)80-63(92)51(78)41-49-26-14-12-15-27-49/h12-17,26-29,44-48,51-59,61-62H,11,18-25,30-43,74-78H2,1-10H3,(H,79,93)(H,80,92)(H,81,94)(H,82,100)(H,83,98)(H,84,95)(H,85,99)(H,86,101)(H,87,102)(H,88,96)(H,89,97)(H,90,91)/t48-,51-,52-,53-,54-,55-,56-,57-,58-,59-,61-,62-/m0/s1 InChIKey: CXENRUVJCSPSPU-IYWWJOMXSA-N The active form is C-terminal amide group instead of C-terminal glycine residue. Peptide is the precursor of antifungal one (ID 9287 in BIOPEP-UWM database of bioactive peptides). Reviews concerning C-terminal amidation of peptides: Bradbury A. F., Smyth D. G., 1991, Peptide amidation. Trends Biochem. Sci., 16, 112-115 Merkler D. J., 1994, C-terminal amidated peptides: production by the in vitro enzymatic amidation of glycine-extended peptides and the importance of the amide to bioactivity. Enzyme Microb. Technol., 16, 450-456 Precursor of hemolytic peptide according to the BIOPEP-UWM database of bioactive peptides (ID 9306)
activity
references
function information
database references
screen and print peptide data
list of peptides