General Information
-
DRAMP ID
- DRAMP20909
-
Peptide Name
- Ctry2459-H2 (Ctry2459 peptide derivative, His-rich)
-
Source
- Synthetic construct( from a scorpion venom peptide library)
-
Family
- Derived from the peptide Ctry2460
-
Gene
- Not found
-
Sequence
- FLGFLHHLF
-
Sequence Length
- 9
-
UniProt Entry
- No entry found
-
Protein Existence
- Synthetic
Activity Information
-
Biological Activity
- Antimicrobial, Antiviral
-
Target Organism
-
- [Ref.23415044] Virus: Hepatitis C virus ( EC50 = 1.08 μg/ml ).
- Cytotoxic: Huh7.5.1 cells (CC50>500 μg/ml)
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Hemolytic Activity
-
- [Ref.23415044] HC50 = 203.3 μg/ml against human red blood cells.
-
Cytotoxicity
-
- [Ref.23415044] CC50>500 μg/ml against Huh7.5.1 cells
-
Binding Target
- Not found
Structure Information
-
Linear/Cyclic
- Linear
-
N-terminal Modification
- Free
-
C-terminal Modification
- Amidation
-
Nonterminal Modifications and Unusual Amino Acids
- None
-
Stereochemistry
- L
-
Structure
- Not found
-
Structure Description
- Not found
-
Helical Wheel Diagram
-
PDB ID
- None
-
Predicted Structure
- There is no predicted structure for DRAMP20909.
Physicochemical Information
-
Formula
- C59H79N13O10
Absent Amino Acids
- ACDEIKMNPQRSTVWY
Common Amino Acids
- FL
Mass
- 1130.36
PI
- 6.92
Basic Residues
- 2
Acidic Residues
- 0
Hydrophobic Residues
- 6
Net Charge
- +2
-
Boman Index
- 1532
Hydrophobicity
- 1.444
Aliphatic Index
- 130
Half Life
-
- Mammalian:1.1 hour
- Yeast:3 min
- E.coli:2 min
Extinction Coefficient Cystines
- 0
Absorbance 280nm
- 0
Polar Residues
- 1
DRAMP20909
Comments Information
Function
- Inhibits hepatitis C virus(HCV) infection via inactivating infectious viral particle. However, it cannot suppress established infection because of the poor cellular uptake and restriction of endosomes.
Literature Information
- ·Literature 1
-
Title
- Design of histidine-rich peptides with enhanced bioavailability and inhibitory activity against hepatitis C virus.
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Pubmed ID
- 23415044
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Reference
- Biomaterials. 2013 Apr;34(13):3511-22.
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Author
- Hong W, Zhang R, Di Z, He Y, Zhao Z, Hu J, Wu Y, Li W, Cao Z.