General Information


DRAVP ID  DRAVPe00648

Peptide Name   LP-53

Sequence  YTSLIHSLIEESQNQQEKNEQELLEX

Sequence Length  26

UniProt ID  P03377 

Source  Synthetic construct



Activity Information


Target Organism  HIV

Assay  cell-fusion assay,single-cycle infection assay

Activity 

  • [Ref.30089693]HIV-1 HXB2:inhibition of cell-cell fusion in TZM-bl cells(IC50=2949±400 pM);
  • HIV-1 NL4-3:inhibition of pseudovirus infection in TZM-bl cells(IC50=9968±2224 pM);
  • HIV-1 JRCSF:inhibition of virus infection in TZM-bl cells(IC50=21352±1876 pM).

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

Cytotoxicity 

  • No cytotoxicity information or data found in the reference(s) presented in this entry

Binding Target  membrane

Mechanism  The peptide acts by binding to the heptad repeat 1 (HR1) region of gp41 and preventing the interaction of the HR1 and HR2 domains, which is required for virus–cell fusion.(By similar)



Structure Information


PDB ID  None

Predicted Structure Download  No predicted structure available

Linear/Cyclic  Linear

N-terminal Modification  Acetylation

C-terminal Modification  Amidation

Other Modification  The 'X' at position 26 is Lys-C16(palmitic acid)

Stereochemistry  L



Physicochemical Information


Formula  C128H202N34O48

Absent amino acids  ACDFGMPRVW

Common amino acids  E

Mass  3114.56

Pl  4.2

Basic residues  2

Acidic residues  6

Hydrophobic residues  6

Net charge  -4

Boman Index  -6990

Hydrophobicity  -112.69

Aliphatic Index  90

Half Life 

  •     Mammalian:2.8 hour
  •     Yeast:10 min
  •     E.coli:2 min

Extinction Coefficient cystines  1490

Absorbance 280nm  59.6

Polar residues  7



Literature Information


Literature 1

Title   Structural and Functional Characterization of Membrane Fusion Inhibitors with Extremely Potent Activity against Human Immunodeficiency Virus Type 1 (HIV-1), HIV-2, and Simian Immunodeficiency Virus.

Pubmed ID   30089693

Reference   J Virol. 2018 Sep 26;92(20):e01088-18.

Author   Chong H, Zhu Y, Yu D, He Y.

DOI   10.1128/JVI.01088-18