General Information
-
DRAMP ID
- DRAMP29200
-
Peptide Name
- EK1-GSGSGC
-
Source
- Synthetic construct
-
Family
- Belongs to the betacoronaviruses spike protein family.
-
Gene
- S
-
Sequence
- SLDQINVTFLDLEYEMKKLEEAIKKLEESYIDLKELGSGSGC
-
Sequence Length
- 42
-
UniProt Entry
- Q8BB25
-
Protein Existence
- Hemology
-
SMILES
- CC[C@@H](C)[C@H](NC(=O)CC[C@H](NC(=O)[C@H](CCCCN)NC(=O)CC[C@H](NC(=O)[C@H](CCC(=O)N[C@@H](CCSC)C(=O)O)NC(=O)[C@H](CC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)C[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)O)[C@@H](C)O)[C@H](C)CC)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(=O)N[C@@H](CCC(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)O)C(=O)NCC(=O)NCC(=O)NCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)O)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)O)[C@H](C)CC
Activity Information
-
Biological Activity
- Antimicrobial, Antiviral(SARS-CoV-2)
-
Target Organism
-
- [Ref.33082259]Virus:
- SARS-CoV-2:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50=293±60 nM,IC90>900 nM inhibition of infection in Vero E6 cells IC50~ 41 nM - SARS-CoV-2_D614G:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50=261±136 nM,IC90=892±100 nM - SARS-CoV-2_S943P:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50=286±104 nM,IC90>1000 nM - SARS-CoV-2_S247R:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50=194±107 nM,IC90=893±77 nM - MERS-CoV:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50>1000 nM,IC90>1000 nM inhibition of infection in Vero E6 cells IC50~ 2 nM - SARS-CoV-1:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50=36±5 nM,IC90>1000 nM
-
Hemolytic Activity
-
- No hemolysis information or data found in the reference(s) presented in this entry
-
Cytotoxicity
-
- [Ref.33082259]Human embryonic kidney HEK293T cells:<5% Cytotoxicity at 10 µM;Vero E6 cells:18% Cytotoxicity at 10 µM.
-
Binding Target
- liposomes
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
-
PDB ID
- None
-
Predicted Structure
-
- Please click DRAMP29200_predicted_structure.pdb to download.
Physicochemical Information
-
Formula
- C211H341N49O72S2
Absent Amino Acids
- HPRW
Common Amino Acids
- EL
Mass
- 4780.43
PI
- 4.36
Basic Residues
- 5
Acidic Residues
- 10
Hydrophobic Residues
- 13
Net Charge
- -5
-
Boman Index
- -6573
Hydrophobicity
- -0.379
Aliphatic Index
- 102.14
Half Life
-
- Mammalian:1.9 hour
- Yeast:>20 hour
- E.coli:>10 hour
Extinction Coefficient Cystines
- 2980
Absorbance 280nm
- 72.68
Polar Residues
- 12
DRAMP29200
Comments Information
Mechanism of action
- The lipopeptide is derived from the C-terminal heptad repeat (HRC) domain of SARS-CoV-2 S that potently inhibits infection by SARS-CoV-2.
Literature Information
- ·Literature 1
-
Title
- Inhibition of Coronavirus Entry In Vitro and Ex Vivo by a Lipid-Conjugated Peptide Derived from the SARS-CoV-2 Spike Glycoprotein HRC Domain.
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Pubmed ID
- 33082259
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Reference
- mBio. 2020 Oct 20;11(5):e01935-20.
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Author
- Outlaw VK, Bovier FT, Mears MC, Cajimat MN, Zhu Y, Lin MJ, Addetia A, Lieberman NAP, Peddu V, Xie X, Shi PY, Greninger AL, Gellman SH, Bente DA, Moscona A, Porotto M.
