• DRAMP ID

    • DRAMP21372
    • Peptide Name

    • [Lys]3[Lys]7[Lys]11-VmCT1-NH2 (Derived from VmCT1)
    • Source

    • synthetic construct
    • Family

    • Not found
    • Gene

    • Not found
    • Sequence

    • FLKALWKVAKKVF
    • Sequence Length

    • 13
    • UniProt Entry

    • No entry found
    • Protein Existence

    • Synthetic form
    • Biological Activity

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

      • [Ref.31181304] Gram-positive bacteria: Micrococcus luteus A270 (MIC=0.4 μmol/L), Staphylococcus aureus ATCC 29213 (MIC=0.8 μmol/L), Bacillus megaterium ATCC 10778 (MIC=0.2 μmol/L), Staphylococcus epidermidis ATCC 12228 (MIC=3.1 μmol/L);
      • Gram-negative bacteria: Escherichia coli SBS 363 (MIC=1.6 μmol/L),Serratia marcescens ATCC 4112 (MIC=0.1μmol/L), Enterobacter cloacae β-12 (MIC=3.1 μmol/L);
      • Fungi: Candida albicans MDM8 (MIC=0.8 μmol/L), Candida tropicalis IOC 4560 (MIC=0.4μmol/L)
    • Hemolytic Activity

      • [Ref.31181304] 40% hemolysis at 12.5 μmol/L, 60% hemolysis at 25 μmol/L, 80% hemolysis at 50 μmol/L, 100% hemolysis at 100 μmol/L against human red blood cells
    • Cytotoxicity

      • [Ref.31181304] ①The cell viability of MCF-7 cells induced by [Lys3][Lys7][Lys11]-VmCT1-NH2 is 90%, 90%, 90%, 60%, 50%, 30%, 20% and 20% at peptide concentrations of 0.8, 1.6, 3.1, 12.5, 25, 50 and 100 μM. ②The cell viability of MCF-10A cells induced by [Lys3][Lys7][Lys11]-VmCT1-NH2 is 120%, 120%, 85%, 120%, 115% and 120%at peptide concentrations of 0.8, 1.6, 3.1, 6.3, 12.5 and 25 μM.
    • Binding Target

    • Not found
    • Linear/Cyclic

    • Linear
    • N-terminal Modification

    • Free
    • C-terminal Modification

    • Amidation
    • Nonterminal Modifications and Unusual Amino Acids

    • None
    • Stereochemistry

    • L
    • Structure

    • 0% Helical content in water, 3% helical content in PBS (pH7.4), 25% helical content in SDS (20 mmol/L), 23% helical content in TFE/Water (3:2, v:v), 2
    • Structure Description

    • Not found
    • Helical Wheel Diagram

    • DRAMP21372 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP21372.
    • Formula

    • C81H128N18O14
    • Absent Amino Acids

    • CDEGHIMNPQRSTY
    • Common Amino Acids

    • K
    • Mass

    • 1578.02
    • PI

    • 10.48
    • Basic Residues

    • 4
    • Acidic Residues

    • 0
    • Hydrophobic Residues

    • 9
    • Net Charge

    • +4
    • Boman Index

    • 763
    • Hydrophobicity

    • 0.669
    • Aliphatic Index

    • 120
    • Half Life

      • Mammalian:1.1 hour
      • Yeast:3 min
      • E.coli:2 min
    • Extinction Coefficient Cystines

    • 5500
    • Absorbance 280nm

    • 458.33
    • Polar Residues

    • 0

DRAMP21372

    • Function

    • Antibacterial activity against Gram-positive bacteria and Gram-negative bacteria. Antifungal activity against Candida albicans MDM8 and Candida tropicalis IOC 4560.
  • ·Literature 1
    • Title

    • The effect of lysine substitutions in the biological activities of the scorpion venom peptide VmCT1
    • Reference

    • Eur J Pharm Sci. 2019 Jun 7;136:104952. doi: 10.1016/j.ejps.2019.06.006.
    • Author

    • Pedron CN, de Oliveira CS, da Silva AF, Andrade GP, da Silva Pinhal MA, Cerchiaro G, da Silva Junior PI, da Silva FD, Torres MT, Oliveira VX