• DRAMP ID

    • DRAMP18133
    • Peptide Name

    • Peptide Ctri9819
    • Source

    • Chaerilus tricostatus (Scorpion)
    • Family

    • Not found
    • Gene

    • Not found
    • Sequence

    • NRILPTLIGPL
    • Sequence Length

    • 11
    • Protein Existence

    • Transcript level
    • Biological Activity

    • Antimicrobial, Antiviral
    • 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

    • Not found
    • Helical Wheel Diagram

    • DRAMP18133 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP18133.
    • Formula

    • C342H595N95O99S2
    • Absent Amino Acids

    • CHQWY
    • Common Amino Acids

    • LIT
    • Mass

    • 1206.49
    • PI

    • 9.75
    • Basic Residues

    • 10
    • Acidic Residues

    • 4
    • Hydrophobic Residues

    • 30
    • Net Charge

    • +6
    • Boman Index

    • -7137
    • Hydrophobicity

    • 0.459
    • Aliphatic Index

    • 127.75
    • Half Life

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

    • 0
    • Absorbance 280nm

    • 0
    • Polar Residues

    • 23

DRAMP18133

    • Function

    • Antimicrobial peptide (By similarity).##Miscellaneous
  • ·Literature 1
    • Title

    • Design of histidine-rich peptides with enhanced bioavailability andinhibitory activity against hepatitis C viruS.
    • Reference

    • Biomaterials 34:3511-3522 (2013).
    • Author

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