General Information
-
DRAMP ID
- DRAMP31558
-
Peptide Name
- SARS-CoV S (668–679), SP-10
-
Source
- Synthetic construct
-
Family
- Coronaviridae
-
Gene
- Not found
-
Sequence
- STSQKAnti-SIVAYTM
-
Sequence Length
- 12
-
UniProt Entry
- P59594
-
Protein Existence
- Not found
Activity Information
-
Biological Activity
- Antimicrobial, Antiviral
-
Target Organism
-
- [Ref.16337697]SARS-CoV: Inhibition of pseudovirus infection in Vero cells(IC50=1.88 ± 0.52 nM).
-
Hemolytic Activity
-
- No hemolysis information or data found in the reference(s) presented in this entry
-
Cytotoxicity
-
- No cytotoxicity information or data found in the reference(s) presented in this entry
-
Binding Target
- ACE2
Structure Information
-
Linear/Cyclic
- Linear
-
N-terminal Modification
- Free
-
C-terminal Modification
- Free
-
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 DRAMP31558.
Physicochemical Information
-
Formula
- C56H94N14O20S
Absent Amino Acids
- CDEFGHLNPRW
Common Amino Acids
- S
Mass
- 1315.5
PI
- 8.31
Basic Residues
- 1
Acidic Residues
- 0
Hydrophobic Residues
- 3
Net Charge
- +1
-
Boman Index
- -1345
Hydrophobicity
- -0.008
Aliphatic Index
- 65
Half Life
-
- Mammalian:1.9 hour
- Yeast:>20 hour
- E.coli:>10 hour
Extinction Coefficient Cystines
- 1490
Absorbance 280nm
- 135.45
Polar Residues
- 6
DRAMP31558
Comments Information
Mechanism
- block the binding of S protein to ACE2.
Literature Information
- ·Literature 1
-
Title
- Design and biological activities of novel inhibitory peptides for SARS-CoV spike protein and angiotensin-converting enzyme 2 interaction.
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Pubmed ID
- 16337697
-
Reference
- Antiviral Res. 2006 Feb;69(2):70-6.
-
Author
- Ho TY, Wu SL, Chen JC, Wei YC, Cheng SE, Chang YH, Liu HJ, Hsiang CY.
