General Information
-
DRAMP ID
- DRAMP29199
-
Peptide Name
- MERS-CoV-HR2P-GSGSGC
-
Source
- Synthetic construct
-
Family
- Belongs to the betacoronaviruses spike protein family.
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Gene
- S
-
Sequence
- SLTQINTTLLDLTYEMLSLQQVVKALNESYIDLKELGSGSGC
-
Sequence Length
- 42
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Protein Existence
- Protein level
-
SMILES
- CC[C@@H](C)[C@H](NC(=O)[C@H](CCC(=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)NC(=O)[C@H](CCSC)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)N[C@H](C(=O)N[C@@H](CCC(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)O)C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O)C(C)C)[C@@H](C)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CO)[C@@H](C)O)[C@H](C)CC)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)O
Activity Information
-
Biological Activity
- Antimicrobial, Antiviral(SARS-CoV-2)
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Target Organism
-
- [Ref.33082259]Virus:
- SARS-CoV-2:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50>650 nM,IC90>1000 nM inhibition of infection in Vero E6 cells IC50~ 36 nM - SARS-CoV-2_D614G:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50=1000 nM,IC90>1000 nM - SARS-CoV-2_S943P:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50>1000,IC90>1000 nM - SARS-CoV-2_S247R:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50>700 nM,IC90>1000 nM - MERS-CoV:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50=417±180 nM,IC90>1000 nM inhibition of infection in Vero E6 cells IC50~ 4 nM - SARS-CoV-1:
Target Organism Activity ihibition of cell-cell fusion in 293T cells IC50=40±34 nM,IC90>700 nM
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Hemolytic Activity
-
- No hemolysis information or data found in the reference(s) presented in this entry
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Cytotoxicity
-
- [Ref.33082259]Human embryonic kidney HEK293T cells:<10% Cytotoxicity at 10 µM;Vero E6 cells:12% Cytotoxicity at 10 µM.
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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
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Structure Description
- Not found
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PDB ID
- None
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Predicted Structure
-
- Please click DRAMP29199_predicted_structure.pdb to download.
Physicochemical Information
-
Formula
- C200H331N49O69S2
Absent Amino Acids
- FHPRW
Common Amino Acids
- L
Mass
- 4590.23
PI
- 4.18
Basic Residues
- 2
Acidic Residues
- 5
Hydrophobic Residues
- 14
Net Charge
- -3
-
Boman Index
- -3597
Hydrophobicity
- 0.105
Aliphatic Index
- 118.33
Half Life
-
- Mammalian:1.9 hour
- Yeast:>20 hour
- E.coli:>10 hour
Extinction Coefficient Cystines
- 2980
Absorbance 280nm
- 72.68
Polar Residues
- 17
DRAMP29199
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.
