General Information


DRAVP ID  DRAVPe00397

Peptide Name   Dermaseptin S4 (5-28)

Sequence  TLLKKVLKAAAKAALNAVLVGANA

Sequence Length  24

UniProt ID  No entry found

Taxon ID  None

Source  Synthetic construct(derived from Dermaseptin S4)

Validation   Experimentally Validated



Origin Information


Gene Name/ID  Not Available

GenBank  Not Available

Amino Acid position  Not Available

Domain Accession ID  Not Available

Nucleotide sequence ID  Not Available

Molecular Type  Not Available

Chromosomal Position  Not Available



Activity Information


Target Organism  HSV

Assay 

Activity 

  • [Ref.23161023]HSV-2 acyclovir-sensitive strain(911411):inhibition the cytopathic effect(CPE) of HSV-2 in Vero cells(EC50=27.07 μM);
  • HSV-2 acyclovir-resistant strain(ROI2):inhibition of cytopathic effet(CPE) of HSV-2 in Vero cells(EC50=25.27 μM).

Hemolytic Activity  No hemolysis information or data found in the reference(s) presented in this entry

Cytotoxicity 

  • [Ref.23161023]Vero cells:CC50=34 μM.

Binding Target  Not found

Mechanism  No machanism information found in the reference(s) presented in this entry



Structure Information


PDB ID  None

Predicted Structure Download  DRAVPe00397

Linear/Cyclic  Linear

N-terminal Modification  Free

C-terminal Modification  Free

Other Modification  None

Stereochemistry  L



Physicochemical Information


Formula  C107H194N30O28

Absent amino acids  CDEFHIMPQRSWY

Common amino acids  A

Mass  2348.9

Pl  10.48

Basic residues  4

Acidic residues  0

Hydrophobic residues  16

Net charge  4

Boman Index  1409

Hydrophobicity  92.92

Aliphatic Index  150.83

Half Life 

  •     Mammalian:7.2 hour
  •     Yeast:>20 hour
  •     E.coli:>10 hour

Extinction Coefficient cystines  0

Absorbance 280nm  0

Polar residues  4



Literature Information


Literature 1

Title    In vitro antiviral activity of dermaseptin S(4) and derivatives from amphibian skin against herpes simplex virus type 2.

Pubmed ID   23161023

Reference   J Med Virol. 2013 Feb;85(2):272-81.

Author   Bergaoui I, Zairi A, Tangy F, Aouni M, Selmi B, Hani K. 

DOI   10.1002/jmv.23450