• DRAMP ID

    • DRAMP29138
    • Peptide Name

    • XT-7 [G4K,P5K,S15K,N16K]
    • Source

    • Synthetic construct
    • Family

    • Not found
    • Gene

    • N/A
    • Sequence

    • GLLKKLLKIAAKVGKKLL
    • Sequence Length

    • 18
    • Protein Existence

    • Protein level
    • Biological Activity

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

      • [Ref.18554256]Gram-negative bacteria:Escherichia coli ATCC 25726(MIC=12.5 µM);
      • Gram-positive bactria:Staphylococcus aureus ATCC 25923(MIC=6 µM);
      • Fungi:Candida albicans ATCC 900280(MIC=3 µM);
      • Cancer: human hepatoma‐derived cells HepG2 (LC50=6 µM).
    • Hemolytic Activity

      • [Ref.18554256]Hemolysis against human erythrocytes (LC50=25 µM).
    • Cytotoxicity

    • No cytotoxicity information found in the reference(s) presented
    • Binding Target

    • liposomes
    • Linear/Cyclic

    • Linear
    • N-terminal Modification

    • Free
    • C-terminal Modification

    • Amidation
    • Nonterminal Modifications and Unusual Amino Acids

    • None
    • Stereochemistry

    • L
    • Structure

    • Not found
    • Structure Description

    • Not found
    • Helical Wheel Diagram

    • DRAMP29138 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP29138.
    • Formula

    • C93H176N24O19
    • Absent Amino Acids

    • CDEFHMNPQRSTWY
    • Common Amino Acids

    • KL
    • Mass

    • 1934.57
    • PI

    • 10.7
    • Basic Residues

    • 6
    • Acidic Residues

    • 0
    • Hydrophobic Residues

    • 10
    • Net Charge

    • +6
    • Boman Index

    • 1068
    • Hydrophobicity

    • 0.606
    • Aliphatic Index

    • 178.89
    • Half Life

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

    • 0
    • Absorbance 280nm

    • 0
    • Polar Residues

    • 2

DRAMP29138

DRAMP29138 chydropathy plot
    • Function

    • Antibacterial activity against Gram-positive bacteria and Gram-negative bacteria.Antifungal activity against Candida albicans.
  • ·Literature 1
    • Title

    • Design of potent, non-toxic antimicrobial agents based upon the naturally occurring frog skin peptides, ascaphin-8 and peptide XT-7.
    • Reference

    • Chem Biol Drug Des. 2008 Jul;72(1):58-64.
    • Author

    • Conlon JM, Galadari S, Raza H, Condamine E.