BIOPEP-UWM: Peptide Data
ID
Name
Sequence
WKLFKKILKWLG
Chemical Mass
Number of residues
Monoisotopic Mass
EC50
IC50
µM
Additional Information
BIOPEP-UWM database of bioactive peptides SMILES: [H][C@@](C(N[C@](C(N[C@](C(N[C@](C(N[C@](C(N[C@](C(N[C@](C(N[C@](C(N[C@](C(N[C@](C(N[C@](C(NCC(=O)O)=O)(CC(C)C)[H])=O)(Cc1c2ccccc2[nH]c1)[H])=O)(CCCCN)[H])=O)(CC(C)C)[H])=O)([C@H](CC)C)[H])=O)(CCCCN)[H])=O)(CCCCN)[H])=O)(Cc1ccccc1)[H])=O)(CC(C)C)[H])=O)(CCCCN)[H])=O)(Cc1c2ccccc2[nH]c1)N InChI=1S/C81H126N18O13/c1-9-51(8)70(81(112)98-66(41-50(6)7)77(108)92-62(33-19-23-37-84)75(106)97-68(44-54-46-88-59-30-16-14-28-56(54)59)80(111)94-64(39-48(2)3)72(103)89-47-69(100)101)99-76(107)63(34-20-24-38-85)91-73(104)61(32-18-22-36-83)93-79(110)67(42-52-25-11-10-12-26-52)96-78(109)65(40-49(4)5)95-74(105)60(31-17-21-35-82)90-71(102)57(86)43-53-45-87-58-29-15-13-27-55(53)58/h10-16,25-30,45-46,48-51,57,60-68,70,87-88H,9,17-24,31-44,47,82-86H2,1-8H3,(H,89,103)(H,90,102)(H,91,104)(H,92,108)(H,93,110)(H,94,111)(H,95,105)(H,96,109)(H,97,106)(H,98,112)(H,99,107)(H,100,101)/t51-,57-,60-,61-,62-,63-,64-,65-,66-,67-,68-,70-/m0/s1 InChIKey: XTVXTDOQFBRQER-CGZBXLLSSA-N The active form is C-terminal amide group instead of C-terminal glycine residue. Peptide is the precursor of hemolytic one (ID 9295 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 antifungal peptide according to the BIOPEP-UWM database of bioactive peptides (ID 9315)
activity
references
function information
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