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Peptide Name
- LS-Cathelicidin-BF-15-a1-1
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Original Sequence
- VKRFKKFFRKFKKFV
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Source
- Synthetic construct
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Biological Activity
- Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
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- Function: Antibacterial activity against Gram-positive and Gram-negative bacteria.
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Target Organism
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- [Ref.34968054]Gram-positive bacteria:Listeria monocytogenes(MIC=4μg/mL), Staphylococcus aureus BNCC 186335(MIC=2 μg/mL), Staphylococcus aureus(MRSA)(MIC=2 μg/mL) ;
- Gram-negative bacteria:P. aeruginosa(MIC=16 μg/mL), E. coli(MIC=2 μg/mL), Cephalosporin-resistant E. coli(MIC=8 μg/mL).
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Hemolytic Activity
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- [Ref.34968054]MHC>128 μg/mL. The MHC is the minimum peptide concentration that caused 10% hemolysis of hRBCs.
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Cytotoxicity
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- [Ref.34968054]Human embryonic kidney HEK293T cells: LC50=64 µg/ml.
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Linear/Cyclic
- Cyclic (Stapled)
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N-terminal Modification
- Free
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C-terminal Modification
- Amidation
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Special Amino Acid and Stapling Position
- ①The Ⓚ (position: 6 and 10) in sequence indicates Nε-o-Ns-Nα-Fmoc-lysine before stapling. ②Ⓚ (6) and Ⓚ (10) are cross-linked by a (E)-but-2-enyl spacer employing the N-alkylation reaction.
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Secondary Structure
- No specific results about the strcture presented in the forms of tables, graphs or words
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Structure Description
- No other descriptive information about the structure found in the literature
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There is no predicted structure for DRAMP29341.
- Literature 1
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Title
- Lysine Stapling Screening Provides Stable and Low Toxic Cationic Antimicrobial Peptides Combating Multidrug-Resistant Bacteria In Vitro and In Vivo.
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Reference
- J Med Chem. 2022 Jan 13;65(1):579-591.
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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.