BIOPEP-UWM: Peptide Data
ID
Name
Sequence
APSGFLGMRG
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)N1CCC[C@@]1([H])C(=O)N[C@@]([H])(CO)C(=O)NCC(=O)N[C@@]([H])(Cc1ccccc1)C(=O)N[C@@]([H])(CC(C)C)C(=O)NCC(=O)N[C@@]([H])(CCSC)C(=O)N[C@@]([H])(CCCNC(N)=N)C(=O)NCC(O)=O InChI=1S/C43H69N13O12S/c1-24(2)18-29(37(63)48-20-33(58)51-28(14-17-69-4)39(65)53-27(12-8-15-47-43(45)46)36(62)50-22-35(60)61)54-40(66)30(19-26-10-6-5-7-11-26)52-34(59)21-49-38(64)31(23-57)55-41(67)32-13-9-16-56(32)42(68)25(3)44/h5-7,10-11,24-25,27-32,57H,8-9,12-23,44H2,1-4H3,(H,48,63)(H,49,64)(H,50,62)(H,51,58)(H,52,59)(H,53,65)(H,54,66)(H,55,67)(H,60,61)(H4,45,46,47)/t25-,27-,28-,29-,30-,31-,32-/m0/s1 InChIKey: UPAJFDNABZANJN-CXZRMZRFSA-N The active form is C-terminal amide group instead of C-terminal glycine residue. Peptide is the precursor of neuropeptide (ID 2604 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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