General Information
-
DRAMP ID
- DRAMP29206
-
Peptide Name
- P7
-
Source
- Synthetic construct
-
Family
- Not found
-
Gene
- Not found
-
Sequence
- SALEEQYKTFLDKFLHELEDLLYQLALAL
-
Sequence Length
- 29
-
UniProt Entry
- No entry found
-
Protein Existence
- Not found
Activity Information
-
Biological Activity
- Antimicrobial, Antiviral(SARS-CoV-2)
-
Target Organism
-
- [Ref.33580154]Virus:SARS-CoV-2:54% inhibition of replication in Vero-E6 cells at 10 μM;inhibition of replication in Calu-3 cells(IC50>1 μM).
-
Hemolytic Activity
-
- No hemolysis information or data found in the reference(s) presented in this entry
-
Cytotoxicity
- No cytotoxicity information found in the reference(s) presented
-
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 DRAMP29206.
Physicochemical Information
-
Formula
- C162H249N35O48
Absent Amino Acids
- CGIMNPRVW
Common Amino Acids
- L
Mass
- 3454.96
PI
- 4.35
Basic Residues
- 3
Acidic Residues
- 6
Hydrophobic Residues
- 14
Net Charge
- -3
-
Boman Index
- -2210
Hydrophobicity
- 0.072
Aliphatic Index
- 131.38
Half Life
-
- Mammalian:1.9 hour
- Yeast:>20 hour
- E.coli:>10 hour
Extinction Coefficient Cystines
- 2980
Absorbance 280nm
- 106.43
Polar Residues
- 4
DRAMP29206
Comments Information
Mechanism of action
- The peptide was designed mimicking the N-terminal helix of hACE2 protein,which could prevent the SARS-CoV-2 from infecting human cells, blocking the interaction between hACE2 and the virus spike protein.
Literature Information
- ·Literature 1
-
Title
- Human ACE2 peptide-mimics block SARS-CoV-2 pulmonary cells infection.
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Pubmed ID
- 33580154
-
Reference
- Commun Biol. 2021 Feb 12;4(1):197.
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Author
- Karoyan P, Vieillard V, Gómez-Morales L, Odile E, Guihot A, Luyt CE, Denis A, Grondin P, Lequin O.