• DRAMP ID

    • DRAMP21211
    • Peptide Name

    • AmyI-1-18 (N3L, G12R) (Derived from AmyI-1-18)
    • Source

    • Synthetic construct
    • Family

    • Not found
    • Gene

    • Not found
    • Sequence

    • HLLKRVQRELIRWLDWLK
    • Sequence Length

    • 18
    • UniProt Entry

    • No entry found
    • Protein Existence

    • Synthetic form
    • Biological Activity

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

      • [Ref.27478151] Gram-negative bacteria : Porphyromonas gingivalis(IC50=2.9±0.2 μM)
    • Hemolytic Activity

      • [Ref.27478151] 14% hemolysis at 50 μM against human red blood cells
    • Cytotoxicity

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

    • Not found
    • Linear/Cyclic

    • Linear
    • N-terminal Modification

    • Free
    • C-terminal Modification

    • Free
    • Nonterminal Modifications and Unusual Amino Acids

    • None
    • Stereochemistry

    • L
    • Structure

    • Alpha helix
    • Structure Description

    • Not found
    • Helical Wheel Diagram

    • DRAMP21211 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP21211.
    • Formula

    • C113H184N34O24
    • Absent Amino Acids

    • ACFGMNPSTY
    • Common Amino Acids

    • L
    • Mass

    • 2402.92
    • PI

    • 10.9
    • Basic Residues

    • 6
    • Acidic Residues

    • 2
    • Hydrophobic Residues

    • 9
    • Net Charge

    • +4
    • Boman Index

    • -4337
    • Hydrophobicity

    • -0.506
    • Aliphatic Index

    • 146.11
    • Half Life

      • Mammalian:3.5 hour
      • Yeast:10 min
      • E.coli:>10 hour
    • Extinction Coefficient Cystines

    • 11000
    • Absorbance 280nm

    • 647.06
    • Polar Residues

    • 0

DRAMP21211

DRAMP21211 chydropathy plot
    • Function

    • Antibacterial activity against Gram-negative bacteria
  • ·Literature 1
    • Title

    • Antimicrobial activity against Porphyromonas gingivalis and mechanism of action of the cationic octadecapeptide AmyI-1-18 and its amino acid-substituted analogs.
    • Reference

    • J Biosci Bioeng. 2016 Dec;122(6):652-659. doi: 10.1016/j.jbiosc.2016.05.008.
    • Author

    • Taniguchi M, Ochiai A, Takahashi K, Nakamichi SI, Nomoto T, Saitoh E, Kato T, Tanaka T