• DRAMP ID

    • DRAMP18683
    • Peptide Name

    • Ctri9194 (Scorpions, animals)
    • Source

    • Chaerilus tricostatus (Scorpion)
    • Family

    • Belongs to the non-disulfide-bridged peptide (NDBP) superfamily. Short ant
    • Gene

    • Not found
    • Sequence

    • YIRDFITRRPPFGNI
    • Sequence Length

    • 15
    • Protein Existence

    • Not found
    • Biological Activity

    • Antimicrobial, Antiviral
    • Target Organism

    • [Ref.23415044] The HCV RNA level is screened that between 1.E+00% and 1.E+01% of control(IFNα.2a) in Huh7.5.1 cells.
    • 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

    • Not found
    • Helical Wheel Diagram

    • DRAMP18683 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP18683.
    • Formula

    • C87H133N25O21
    • Absent Amino Acids

    • ACEHKLMQSVW
    • Common Amino Acids

    • IR
    • Mass

    • 1865.17
    • PI

    • 10.74
    • Basic Residues

    • 3
    • Acidic Residues

    • 1
    • Hydrophobic Residues

    • 5
    • Net Charge

    • +2
    • Boman Index

    • -4117
    • Hydrophobicity

    • -0.467
    • Aliphatic Index

    • 78
    • Half Life

      • Mammalian:2.8 hour
      • Yeast:10 min
      • E.coli:2 min
    • Extinction Coefficient Cystines

    • 1490
    • Absorbance 280nm

    • 106.43
    • Polar Residues

    • 4

DRAMP18683

    • Function

    • Shows a low ability to inhibit hepatitis C virus (HCV) infection in Huh7.5.1 cells.
    • Tissue specificity

    • Expressed by the venom gland.
  • ·Literature 1
    • Title

    • Design of histidine-rich peptides with enhanced bioavailability and inhibitory activity against hepatitis C virus.
    • Reference

    • Biomaterials. 2013 Apr;34(13):3511-22.
    • Author

    • Hong W, Zhang R, Di Z, He Y, Zhao Z, Hu J, Wu Y, Li W, Cao Z.