General Information
-
DRAMP ID
- DRAMP01920
-
Peptide Name
- Brevinin-1CSa (Frogs, amphibians, animals)
-
Source
- Rana cascadae (Cascades frog)
-
Family
- Belongs to the frog skin active peptide family (Brevinin subfamily)
-
Gene
- Not found
-
Sequence
- FLPILAGLAAKIVPKLFCLATKKC
-
Sequence Length
- 24
-
UniProt Entry
- No entry found
-
Protein Existence
- Not found
Activity Information
-
Biological Activity
- Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
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Target Organism
-
- [Ref.17451843]Gram-negative bacterium: Escherichia coli (MIC=32 µM);
- Gram-positive bacterium: Staphylococcus aureus (MIC=2 µM).
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Hemolytic Activity
-
- [Ref.17451843] LD50=5 µM against human erythrocytes
-
Cytotoxicity
- No cytotoxicity information found in the reference(s) presented
-
Binding Target
- Not found
Structure Information
-
Linear/Cyclic
- Cyclic
-
N-terminal Modification
- Free
-
C-terminal Modification
- Cyclization (Cys18 and Cys24)
-
Nonterminal Modifications and Unusual Amino Acids
- Disulfide bond between Cys18 and Cys24.
-
Stereochemistry
- L
-
Structure
- Not found
-
Structure Description
- Not found
-
Helical Wheel Diagram
-
PDB ID
- None
-
Predicted Structure
- Please click DRAMP01920_predicted_structure.pdb to download.
Physicochemical Information
-
Formula
- C123H208N28O26S2
Absent Amino Acids
- DEHMNQRSWY
Common Amino Acids
- L
Mass
- 2559.3
PI
- 9.7
Basic Residues
- 4
Acidic Residues
- 0
Hydrophobic Residues
- 14
Net Charge
- +4
-
Boman Index
- 30.41
Hydrophobicity
- 1.254
Aliphatic Index
- 142.5
Half Life
-
- Mammalian:1.1 hour
- Yeast:3 min
- E.coli:2 min
Extinction Coefficient Cystines
- 125
Absorbance 280nm
- 5.43
Polar Residues
- 4
DRAMP01920
Comments Information
Brevinin-1CSa was strongly hemolytic against human erythrocytes.
Literature Information
- ·Literature 1
-
Title
- Peptide defenses of the Cascades frog Rana cascadae: implications for the evolutionary history of frogs of the Amerana species group.
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Pubmed ID
- 17451843
-
Reference
- Peptides. 2007 Jun;28(6):1268-1274.
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Author
- Conlon JM, Al-Dhaheri A, Al-Mutawa E, Al-Kharrge R, Ahmed E, Kolodziejek J, Nowotny N, Nielsen PF, Davidson C.