General Information
-
DRAMP ID
- DRAMP29201
-
Peptide Name
- SARS-CoV-2 HR1P
-
Source
- Synthetic construct
-
Family
- Belongs to the betacoronaviruses spike protein family.
-
Gene
- S
-
Sequence
- ANQFNSAIGKIQDSLSSTASALGKLQDVVNQNAQALNTLVKQ
-
Sequence Length
- 42
-
UniProt Entry
- P0DTC2
-
Protein Existence
- Protein level
Activity Information
-
Biological Activity
- Antimicrobial, Antiviral(SARS-CoV-2)
-
Target Organism
-
- [Ref.32047258]Virus:SARS-CoV-2(No inhibition of cell-cell fusion up to 40 µM in Huh-7 cells,No inhibition of infection up to 40 µM in 293T/ACE2 cells)
-
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
- 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 DRAMP29201.
Physicochemical Information
-
Formula
- C187H314N56O65
Absent Amino Acids
- CEHMPRWY
Common Amino Acids
- AQ
Mass
- 4386.89
PI
- 8.54
Basic Residues
- 3
Acidic Residues
- 2
Hydrophobic Residues
- 17
Net Charge
- +1
-
Boman Index
- -6039
Hydrophobicity
- -0.219
Aliphatic Index
- 100
Half Life
-
- Mammalian:4.4 hour
- Yeast:>20 hour
- E.coli:>10 hour
Extinction Coefficient Cystines
- 0
Absorbance 280nm
- 0
Polar Residues
- 14
DRAMP29201
Comments Information
Mechanism of action
- The peptide acted as a fusion inhibitor which against SARS-CoV-2 S protein-mediated membrane fusion and pseudovirus infection.
Literature Information
- ·Literature 1
-
Title
- Fusion mechanism of 2019-nCoV and fusion inhibitors targeting HR1 domain in spike protein.
-
Pubmed ID
- 32047258
-
Reference
- Cell Mol Immunol. 2020 Jul;17(7):765-767.
-
Author
- Xia S, Zhu Y, Liu M, Lan Q, Xu W, Wu Y, Ying T, Liu S, Shi Z, Jiang S, Lu L.