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Peptide Name
- peptide 3 (Derived from Mag2)
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Sequence
- GIKKⓍLKSⓍKKFVKAFK
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Original Sequence
- GIGKFLHSAKKFGKAFVGEIMNS
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Source
- Synthetic construct
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SMILES
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CCC(C)[C@H](NC(=O)[C@@H2][NH3+])C(=O)N[C@H](CCCC[NH3+])C(=O)N[C@H](CCCC[NH3+])C(=O)N[C@]1(C)CCCC=CCCC[C@@](C)(C(=O)N[C@H](CCCC[NH3+])C(=O)N[C@H](CCCC[NH3+])C(=O)N[C@H](Cc2ccccc2)C(=O)N[C@@H](C(=O)N[C@H](CCCC[NH3+])C(=O)N[C@H](C)C(=O)N[C@H](Cc2ccccc2)C(=O)N[C@@H](C=O)CCCC[NH3+])C(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCC[NH3+])NC(=O)[C@H](CC(C)C)NC1=O
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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.33466998] Gram-positive bacteria: Staphylococcus aureus (MIC = 3.125 μM).
- Gram-negative bacteria: Escherichia coli (MIC = 1.56 μM), Pseudomonas aeruginosa (MIC = 3.125 μM),
multiple-drug resistant P.aeruginosa (MIC = 0.78 μM)
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Hemolytic Activity
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- [Ref.33466998] It has hemolysis against human red blood cells at 6.25 μM
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Cytotoxicity
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No cytotoxicity information found in the reference(s) presented
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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: 5 and 9) in sequence indicate (S)-4-pentenyl alanine. ②Ⓧ (5) and Ⓧ (9) are cross-linked by hydrocarbon stapling through an oct-4-enyl hydrocarbon staple.
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Secondary Structure
- α-helix in 20 mM PBS solution (pH = 7.4) with 1% SDS at peptide concentrations of 100 μM
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Structure Description
- [Ref.33466998] All peptides with side-chain stapling showed negative maxima at around 208 and 222 nm, indicating that the peptides formed a stablized helical structure.
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There is no predicted structure for DRAMP28987.
- Literature 1
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Title
- Development of Antimicrobial Stapled Peptides Based on Magainin 2 Sequence
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Reference
- Molecules. 2021 Jan 16;26(2):444. doi: 10.3390/molecules26020444.
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Author
- Motoharu Hirano, Chihiro Saito, Hidetomo Yokoo, Chihiro Goto, Ryuji Kawano, Takashi Misawa, Yosuke Demizu