BIOPEP-UWM: Peptide Data
ID
Name
Sequence
ASFSPWGG
Chemical Mass
Number of residues
Monoisotopic Mass
EC50
IC50
µM
Additional Information
BIOPEP-UWM database of bioactive peptides SMILES: [H][C@@](C)(N)C(=O)N[C@@]([H])(CO)C(=O)N[C@@]([H])(Cc1ccccc1)C(=O)N[C@@]([H])(CO)C(=O)N1CCC[C@@]1([H])C(=O)N[C@@]([H])(Cc1c[nH]c2ccccc12)C(=O)NCC(=O)NCC(O)=O InChI=1S/C38H49N9O11/c1-21(39)33(53)45-28(19-48)36(56)43-26(14-22-8-3-2-4-9-22)35(55)46-29(20-49)38(58)47-13-7-12-30(47)37(57)44-27(34(54)42-17-31(50)41-18-32(51)52)15-23-16-40-25-11-6-5-10-24(23)25/h2-6,8-11,16,21,26-30,40,48-49H,7,12-15,17-20,39H2,1H3,(H,41,50)(H,42,54)(H,43,56)(H,44,57)(H,45,53)(H,46,55)(H,51,52)/t21-,26-,27-,28-,29-,30-/m0/s1 InChIKey: CPGSPLSRQMQJKK-RSGBUPOYSA-N The active form is C-terminal amide group instead of C-terminal glycine residue. Peptide is the precursor of neuropeptide (ID 2602 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
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