General Information
-
DRAMP ID
- DRAMP29062
-
Peptide Name
- GHaR8R (variant of temporin-GHaR)
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Source
- Synthetic construct
-
Family
- Not found
-
Gene
- N/A
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Sequence
- FLQRIIGRLGRLF
-
Sequence Length
- 13
-
UniProt Entry
- No entry found
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Protein Existence
- Synthetic form
Activity Information
-
Biological Activity
- Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-, Antifungal
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Target Organism
-
- [Ref.33291521] Gram-positive bacteria: S. aureus(MIC / MBC = 1.6-3.1μM / 3.1μM), B. subtilis(MIC / MBC = 12.5μM / 12.5μM), S. mutans(MIC / MBC = 6.2μM / 6.2μM), MRSA(MIC / MBC = 3.1μM / 3.1μM), MRSA-1(MIC /MBC = 6.2μM / 6.2μM), MRSA-2(MIC / MBC = 3.1μM / 12.5μM), MRSA-3(MIC / MBC = 6.2μM / 12.5μM)
- Gram-negative bacteria: E. coli(MIC / MBC = 3.1μM / 3.1μM), D31(MIC /MBC = 12.5μM / 25μM), P. aeruginosa(MIC / MBC > 50μM / 50μM), PAO1(MIC / MBC = 6.2μM / 12.5μM)
- Fungi: C. albicans(MIC / MBC = 12.5μM / 12.5μM)
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Hemolytic Activity
-
- [Ref.33291521]HL50 = 160μM against human red blood cells (hRBCs)
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Cytotoxicity
-
- [Ref.33291521]GHaR6R induced a cell viability of 83%, 64% and 50% to human oral epithelial cells at 3.1μM, 6.2μM and 12.5μM.
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Binding Target
- Cell membrane
Structure Information
-
Linear/Cyclic
- Linear
-
N-terminal Modification
- Free
-
C-terminal Modification
- Free
-
Nonterminal Modifications and Unusual Amino Acids
- None
-
Stereochemistry
- L
-
Structure
- α-helical
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Structure Description
- Not found
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Helical Wheel Diagram
-
PDB ID
- None
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Predicted Structure
- There is no predicted structure for DRAMP29062.
Physicochemical Information
-
Formula
- C75H125N23O15
Absent Amino Acids
- ACDEHKMNPSTVWY
Common Amino Acids
- LR
Mass
- 1588.96
PI
- 12.3
Basic Residues
- 3
Acidic Residues
- 0
Hydrophobic Residues
- 7
Net Charge
- +3
-
Boman Index
- -1786
Hydrophobicity
- 0.631
Aliphatic Index
- 150
Half Life
-
- Mammalian:1.1 hour
- Yeast:3 min
- E.coli:2 min
Extinction Coefficient Cystines
- 0
Absorbance 280nm
- 0
Polar Residues
- 2
DRAMP29062
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