• DRAMP ID

    • DRAMP18343
    • Peptide Name

    • BI-32169(Bacteriocin)
    • Source

    • Streptomyces sp. (DSM 14996)
    • Family

    • Belongs to the class I bacteriocin
    • Gene

    • Not found
    • Sequence

    • GLPWGCPSDIPGWNTPWAC
    • Sequence Length

    • 19
    • UniProt Entry

    • No entry found
    • Protein Existence

    • Biological Activity

    • Antidiabetic
    • Target Organism

    • No MICs found in DRAMP database
    • Hemolytic Activity

      • No hemolysis information or data found in the reference(s) presented in this entry
    • Cytotoxicity

      • Not included yet
    • Binding Target

    • Not found
    • Linear/Cyclic

    • Not included yet
    • N-terminal Modification

    • Not included yet
    • C-terminal Modification

    • Not included yet
    • Nonterminal Modifications and Unusual Amino Acids

    • Not included yet
    • Stereochemistry

    • Not included yet
    • Structure

    • Not found
    • Structure Description

    • BI-32169 consists exclusively of protein amino acids and is cyclized from the side chain of Asp9 to the N-terminus of Gly1. One disulfide bond between Cys6 and Cys19 forms a bicyclic structure.
    • Helical Wheel Diagram

    • DRAMP18343 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP18343.
    • Formula

    • C95H129N23O25S2
    • Absent Amino Acids

    • EFHKMQRVY
    • Common Amino Acids

    • P
    • Mass

    • 2057.33
    • PI

    • 3.8
    • Basic Residues

    • 0
    • Acidic Residues

    • 1
    • Hydrophobic Residues

    • 6
    • Net Charge

    • -1
    • Boman Index

    • 269
    • Hydrophobicity

    • -0.195
    • Aliphatic Index

    • 46.32
    • Half Life

      • Mammalian:30 hour
      • Yeast:>20 hour
      • E.coli:>10 hour
    • Extinction Coefficient Cystines

    • 16625
    • Absorbance 280nm

    • 923.61
    • Polar Residues

    • 8

DRAMP18343

DRAMP18343 chydropathy plot
    • BI-32169 and its methyl ester derivative (2) showed potent inhibitory activity against the human glucagon receptor (IC50 440 and 320 nM, respectively) in a functional cell-based assay.

  • ·Literature 1
    • Title

    • BI-32169, a bicyclic 19-peptide with strong glucagon receptor antagonist activity from Streptomyces sp.
    • Reference

    • J Nat Prod. 2004 Sep;67(9):1528-31.
    • Author

    • Potterat O, Wagner K, Gemmecker G, Mack J, Puder C, Vettermann R, Streicher R.