General Information
- 
			 					
DRAMP ID
- DRAMP29227
 
 - 
			   					
Peptide Name
- IBP02V5
 
 - 
			   					
Source
- Synthetic construct
 
 - 
			   					
Family
- Not found
 
 - 
			   					
Gene
- Not found
 
 - 
			   					
Sequence
- SLTQINASVVNIQKEIDRLNEVAKNLNESLIDLQEL
 
 - 
			   					
Sequence Length
- 36
 
 - 
			   					
UniProt Entry
- No entry found
 
 - 
							
Protein Existence
- Not found
 
 
Activity Information
- 
			   					
Biological Activity
- Antimicrobial, Antiviral(SARS-CoV-2)
 
 - 
			   					
Target Organism
- 
				    					
- [Ref.34344868]Virus:
 - SARS-CoV-2:inhibition of SARS-CoV-2 S protein-mediated cell-cell fusion(IC50=2.1±0.5 nM);inhibition of SARS-CoV-2 pseudovirus infection in 293T/ACE2 cells(IC50=21 nM);inhibition of SARS-CoV-2 pseudovirus infection in Huh-7 cells(IC50=23.5 nM);
 - SARS-CoV-2 D614G:inhibition of S protein-mediated cell-cell fusion(IC50=1.3±0.1 nM);inhibition of pseudovirus infection in 293T/ACE2 cells(IC50=98.8 nM);inhibition of pseudovirus infection in Huh-7 cells(IC50=27.5 nM);
 - SARS-CoV:inhibition of pseudovirus infection in Huh-7 cells(IC50=65.9±13.2 nM);
 - MERS-CoV:inhibition of pseudovirus infection in Huh-7 cells(IC50=68.4±9.7 nM);
 - HCoV-NL63:inhibition of pseudovirus infection in Huh-7 cells(IC50=70.8±8.7 nM);
 - HCoV-229E:inhibition of pseudovirus infection in Huh-7 cells(IC50=1128.4±148.6 nM).
 
 
 - 
			   					
Hemolytic Activity
- 
				    					
- No hemolysis information or data found in the reference(s) presented in this entry
 
 
 - 
			   					
Cytotoxicity
- 
				    					
- [Ref.34344868]No significant cytotoxicity in both 293T/ACE2 and Huh-7 cells at a concentration of 10 μM.
 
 
 - 
			   					
Binding Target
- liposomes
 
 
Structure Information
- 
			   					
Linear/Cyclic
- Linear
 
 - 
			   					
N-terminal Modification
- Free
 
 - 
			   					
C-terminal Modification
- PEG8-K(Chol)
 
 - 
			   					
Nonterminal Modifications and Unusual Amino Acids
- None
 
 - 
			   					
Stereochemistry
- L
 
 - 
			   					
Structure
- 16% α-helicity in phosphate-buffered saline (PBS; pH 7.2) with a final concentration of 10 μM and incubated at 37°C
 
 - 
			   					
Structure Description
- Not found
 
 - 
								
Helical Wheel Diagram
 - 
			   					
PDB ID
- None
 
 - 
									
Predicted Structure
 - There is no predicted structure for DRAMP29227.
 
Physicochemical Information
- 
			   						
Formula
- C175H299N49O61
 
Absent Amino Acids
- CFGHMPWY
 
Common Amino Acids
- L
 
Mass
- 4065.59
 
PI
- 4.36
 
Basic Residues
- 3
 
Acidic Residues
- 6
 
Hydrophobic Residues
- 15
 
Net Charge
- -3
 
 
- 
			   						
Boman Index
- -6835
 
Hydrophobicity
- -0.206
 
Aliphatic Index
- 138.06
 
Half Life
- 
			   								
- Mammalian:1.9 hour
 - Yeast:>20 hour
 - E.coli:>10 hour
 
 
Extinction Coefficient Cystines
- 0
 
Absorbance 280nm
- 0
 
Polar Residues
- 9
 
 
DRAMP29227
					Comments Information
The peptide is a fusion inhibitor against SARS-CoV-2.
Literature Information
- ·Literature 1
 - 
			   					
Title
- SARS-CoV-2-derived fusion inhibitor lipopeptides exhibit highly potent and broad-spectrum activity against divergent human coronaviruses.
 
 - 
			   					
Pubmed ID
- 34344868
 
 - 
			   					
Reference
- Signal Transduct Target Ther. 2021 Aug 3;6(1):294.
 
 - 
			   					
Author
- Zhu Y, Yu D, Hu Y, Wu T, Chong H, He Y.
 
 
									