• DRAMP ID

    • DRAMP18666
    • Peptide Name

    • P1 (Pilosulin-1 1-20; Ant, insects, arthropods, invertebrates, animals)
    • Source

    • Myrmecia pilosula (Jumper ant)
    • Family

    • Derived from the peptide Pilosulin-1, Belongs to the pilosulin family.
    • Gene

    • Not found
    • Sequence

    • GLGSVFGRLARILGRVIPKV
    • Sequence Length

    • 20
    • Protein Existence

    • Protein level
    • SMILES

    • Not available
    • Biological Activity

    • Antimicrobial, Antibacterial, Anti-Gram+, Anitifungal, Anti-Gram-
    • Target Organism

      • [Ref.15639237]Gram-positive bacteria:
        Target OrganismActivity
        Staphylococcus aureus 710AMIC=4 μM
        Bacillus megaterium BM11MIC=2 μM
      • Gram-negative bacteria:
        Target OrganismActivity
        Escherichia coli ML-35MIC=2 μM
        Pseudomonas aeruginosa ATCC27853MIC=8 μM
        Salmonella typhimurium ATCC14028MIC=8 μM
      • Drug resistant clinical isolates:
        Target OrganismActivity
        Staphylococcus simulans 22MIC=2 μM
        Micrococcus luteusMIC=0.5 μM
        Enterococcus spp. I-11305bMIC=2 μM
        Enterococcus spp. I-11054MIC=2 μM
        Staphylococcus haemolyticus I-10925MIC=2 μM
        Staphylococcus epidermidis LT1324MIC=2 μM
        Staphylococcus aureus 5185MIC=2 μM
        Staphylococcus aureus I-11574MIC=2 μM
        Staphylococcus aureus LT1338MIC=3 μM
        Staphylococcus aureus T1334MIC=1.5 μM
        Citrobacter freundii I-11090MIC=2 μM
        Klebsiella pneumoniae I-10910MIC=2 μM
        Escherichia coli I-11276bMIC=4 μM
        Escherichia coli O-19592MIC=2 μM
        Stenotrophomonas maltophilia O-16451MIC=2 μM
        Stenotrophomonas maltophilia I-10717MIC=2 μM
        Pseudomonas aeruginosa 4991MIC=4 μM
        Pseudomonas aeruginosa I-10968MIC=4 μM
        Candida albicans I-11301MIC=4 μM
    • Hemolytic Activity

      • [Ref.15639237]20% hemolysis at 10μM, 100% hemolysis at 100μM against human red blood cells
    • 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

    • Alpha helix
    • Structure Description

    • Not found
    • PDB ID

    • 5X3L resolved by NMR.
    • Predicted Structure

    • Formula

    • C97H170N30O22
    • Absent Amino Acids

    • CDEHMNQTWY
    • Common Amino Acids

    • G
    • Mass

    • 2108.6
    • PI

    • 12.3
    • Basic Residues

    • 4
    • Acidic Residues

    • 0
    • Hydrophobic Residues

    • 10
    • Net Charge

    • +4
    • Boman Index

    • -844
    • Hydrophobicity

    • 0.81
    • Aliphatic Index

    • 146
    • Half Life

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

    • 0
    • Absorbance 280nm

    • 0
    • Polar Residues

    • 5

DRAMP18666

    • Function

    • Has strong cytotoxic and hemolytic activities. Is more potent against mononuclear leukocytes than against granulocytes. Antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria and fungi. Adopts an alpha-helical structure.
    • Allergenic properties

    • Causes an allergic reaction in human. Binds to IgE.
  • ·Literature 1
    • Title

    • Identification and optimization of an antimicrobial peptide from the ant venom toxin pilosulin.
    • Reference

    • Arch Biochem Biophys. 2005 Feb 15;434(2):358-64.
    • Author

    • Zelezetsky I, Pag U, Antcheva N, Sahl HG, Tossi A.