To the extent possible under law, the person who associated CC0 with this work has waived all copyright and related or neighboring rights to this work.
General Information
DRAVP ID DRAVPe01988
Peptide Name None
Sequence LDPAFR
Sequence Length 6
UniProt ID O92921
Source Synthetic construct
Activity Information
Target Organism HBV
Assay Scintillation count
Activity
Hemolytic Activity No hemolysis information or data found in the reference(s) presented in this entry
Cytotoxicity
Binding Target core antigen (HBcAg)(Viral assembly)
Mechanism During HBV morphogenesis, both the PreS and S domains of L-HBsAg form docking sites for the viral nucleocapsids. Thus, a compound that disrupts the interaction between the L-HBsAg and nucleocapsids could serve as a therapeutic agent against the virus based upon inhibition of morphogenesis. Peptide inhibits the association of L-HBsAg with core antigen (HBcAg).
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 C33H51N9O9
Absent amino acids CEGHIKMNQSTVWY
Common amino acids ADFLPR
Mass 717.82
Pl 5.84
Basic residues 1
Acidic residues 1
Hydrophobic residues 3
Net charge 0
Boman Index -1393
Hydrophobicity -20
Aliphatic Index 81.67
Half Life
Extinction Coefficient cystines 0
Absorbance 280nm 0
Polar residues 0
Literature Information
Literature 1
Title Inhibition of hepatitis B virus assembly with synthetic peptides derived from the viral surface and core antigens.
Pubmed ID 12469306
Reference J Gen Appl Microbiol. 2002 Apr;48(2):103-7.
Author Tan WS.
To the extent possible under law, the person who associated CC0 with this work has waived all copyright and related or neighboring rights to this work.