General Information


DRAVP ID  DRAVPe01703

Peptide Name   E1P50

Sequence  PFDFWRGVISLTPLLVCV

Sequence Length  18

UniProt ID  No entry found

Source  Synthetic construct



Activity Information


Target Organism  HIV

Assay  Fluorescence resonance energy transfer (FRET) assay

Activity 

  • [Ref.26905802]HIV-1 NL4-3:inhibition of virus infection in TZM-bl cells(IC50>125 μM).

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  gp41

Mechanism  The peptide inhibits HIV-1 Env-mediated cell fusion thus inhibits virus infection.



Structure Information


PDB ID  None

Predicted Structure Download  No predicted structure available

Linear/Cyclic  Linear

N-terminal Modification  Free

C-terminal Modification  Free

Other Modification  None

Stereochemistry  L



Physicochemical Information


Formula  C100H152N22O23S

Absent amino acids  AEHKMNQY

Common amino acids  LV

Mass  2062.5

Pl  6.22

Basic residues  1

Acidic residues  1

Hydrophobic residues  10

Net charge  0

Boman Index  1270

Hydrophobicity  125.56

Aliphatic Index  135

Half Life 

  •     Mammalian:>20 hour
  •     Yeast:>20 hour
  •     E.coli:?

Extinction Coefficient cystines  5500

Absorbance 280nm  323.53

Polar residues  4



Literature Information


Literature 1

Title   Definition of an 18-mer Synthetic Peptide Derived from the GB virus C E1 Protein as a New HIV-1 Entry Inhibitor.

Pubmed ID   26905802

Reference   Biochim Biophys Acta. 2016 Jun;1860(6):1139-48.

Author   Gómara MJ, Sánchez-Merino V, Paús A, Merino-Mansilla A, Gatell JM, Yuste E, Haro I.

DOI   10.1016/j.bbagen.2016.02.008