General Information
-
DRAMP ID
- DRAMP29060
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Peptide Name
- GHaR6R (variant of temporin-GHaR)
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Source
- Synthetic construct
-
Family
- Not found
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Gene
-
Sequence
- FLQRIRGALGRLF
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Sequence Length
- 13
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UniProt Entry
- No entry found
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Protein Existence
- Synthetic form
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SMILES
- CC[C@@H](C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)O
Activity Information
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Biological Activity
- Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-, Antifungal
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Target Organism
-
- [Ref.33291521] Gram-positive bacteria:
Target Organism Activity S. aureus MIC / MBC = 3.1μM / 12.5μM B. subtilis MIC / MBC = 25μM / 50μM S. mutans MIC / MBC = 12.5μM / 12.5μM MRSA MIC / MBC = 6.2μM / 12.5μM MRSA-1 MIC /MBC = 12.5μM / 25μM MRSA-2 MIC / MBC = 12.5μM / 25μM MRSA-3 MIC / MBC = 6.2μM / 25μM - Gram-negative bacteria:
Target Organism Activity E. coli MIC / MBC = 12.5μM / 12.5μM D31 MIC /MBC = 25μM / 50μM P. aeruginosa MIC / MBC > 50μM / 50μM PAO1 MIC / MBC = 3.1μM / 25μM - Fungi:
Target Organism Activity C. albicans MIC / MBC = 50μM / 50μM
- [Ref.33291521] Gram-positive bacteria:
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Hemolytic Activity
-
- [Ref.33291521]HL10 = 150μM against human red blood cells (hRBCs)
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Cytotoxicity
-
- [Ref.33291521]GHaR6R induced a cell viability of 98%, 95% and 83% to human oral epithelial cells at 3.1μM, 6.2μM and 12.5μM.
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Binding Target
- Cell membrane
Structure Information
Physicochemical Information
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Formula
- C72H119N23O15
Absent Amino Acids
- CDEHKMNPSTVWY
Common Amino Acids
- LR
Mass
- 1546.88
PI
- 12.3
Basic Residues
- 3
Acidic Residues
- 0
Hydrophobic Residues
- 7
Net Charge
- +3
-
Boman Index
- -2097
Hydrophobicity
- 0.423
Aliphatic Index
- 127.69
Half Life
-
- Mammalian:1.1 hour
- Yeast:3 min
- E.coli:2 min
Extinction Coefficient Cystines
- 0
Absorbance 280nm
- 0
Polar Residues
- 2
DRAMP29060
Comments Information
Comment
- GHaR6R not only exerted antimicrobial activity by destroying cell membranes of planktonic bacteria, but also exhibited anti-biofilm activity. The low-toxicity peptides of GHaR6R is expected to become promising antimicrobial candidate to develop anti-caries agents.
Literature Information
- ·Literature 1
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Title
- Temporin-Like Peptides Show Antimicrobial and Anti-Biofilm Activities against Streptococcus mutans with Reduced Hemolysis
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Pubmed ID
- 33291521
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Reference
- Molecules. 2020 Dec 4;25(23):5724. doi: 10.3390/molecules25235724.
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Author
- Wei H, Xie Z, Tan X, Guo R, Song Y, Xie X, Wang R, Li L, Wang M, Zhang Y
