• DRAMP ID

    • DRAMP29346
    • Peptide Name

    • LS-Cathelicidin-BF-15-a1-6
    • Sequence

    • VⓀRFKⓀFFRKFKKFV
    • Sequence Length

    • 15
    • Original Sequence

    • VKRFKKFFRKFKKFV
    • Source

    • Synthetic construct
    • Biological Activity

    • Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
    • Comments

    • Function: Antibacterial activity against Gram-positive and Gram-negative bacteria.
    • Target Organism

      • [Ref.34968054]Gram-positive bacteria:Listeria monocytogenes(MIC=8μg/mL), Staphylococcus aureus BNCC 186335(MIC=4 μg/mL), Staphylococcus aureus(MRSA)(MIC=8 μg/mL) ;
      • Gram-negative bacteria:P. aeruginosa(MIC=16 μg/mL), E. coli(MIC=4 μg/mL), Cephalosporin-resistant E. coli(MIC=16 μg/mL).
    • Hemolytic Activity

      • [Ref.34968054]MHC>128 μg/mL. The MHC is the minimum peptide concentration that caused 10% hemolysis of hRBCs.
    • Cytotoxicity

      • [Ref.34968054]Human embryonic kidney HEK293T cells: LC50=100 µg/ml.
    • Linear/Cyclic

    • Cyclic (Stapled)
    • N-terminal Modification

    • Free
    • C-terminal Modification

    • Amidation
    • Special Amino Acid and Stapling Position

    • ①The Ⓚ (position: 2 and 6) in sequence indicates Nε-o-Ns-Nα-Fmoc-lysine before stapling. ②Ⓚ (2) and Ⓚ (6) are cross-linked by a but-2-ynyl spacer employing the N-alkylation reaction.
    • Stereochemistry

    • L
    • Secondary Structure

    • No specific results about the strcture presented in the forms of tables, graphs or words
    • Structure Description

    • No other descriptive information about the structure found in the literature
    • Helical Wheel Diagram

    • DRAMP29346 helical wheel diagram
    • Predicted Structure

    • There is no predicted structure for DRAMP29346.
  • Literature 1
    • Title

    • Lysine Stapling Screening Provides Stable and Low Toxic Cationic Antimicrobial Peptides Combating Multidrug-Resistant Bacteria In Vitro and In Vivo.
    • Reference

    • J Med Chem. 2022 Jan 13;65(1):579-591. 
    • Author

    • Hu Y, Li H, Qu R, He T, Tang X, Chen W, Li L, Bai H, Li C, Wang W, Fu G, Luo G, Xia X, Zhang J.