General Information
DRAVP ID DRAVPe00702
Peptide Name Indolicidin [P3,7,10A,R12,13P]
Sequence ILAWKWAWWAWPP
Sequence Length 13
UniProt ID No entry found
Source Synthetic construct(derived from Indolicidin)
Activity Information
Target Organism HIV
Assay HIV-1 integrase inhibition assay
Activity
Hemolytic Activity No hemolysis information or data found in the reference(s) presented in this entry
Cytotoxicity
Binding Target HIV Integrase
Mechanism The HIV-1 integrase plays a crucial role in the HIV-1 virus replication cycle. The peptide can inhibit the activity of integrase and thus inhibit virus replication.
Structure Information
PDB ID None
Predicted Structure Download DRAVPe00702
Linear/Cyclic Linear
N-terminal Modification Free
C-terminal Modification Amidtion
Other Modification None
Stereochemistry L
Physicochemical Information
Formula C92H115N19O14
Absent amino acids CDEFGHMNQRSTVY
Common amino acids W
Mass 1711.04
Pl 8.75
Basic residues 1
Acidic residues 0
Hydrophobic residues 10
Net charge 1
Boman Index 2137
Hydrophobicity 16.15
Aliphatic Index 83.08
Half Life
Extinction Coefficient cystines 27500
Absorbance 280nm 2291.67
Polar residues 0
Literature Information
Literature 1
Title Synthesis and HIV-1 integrase inhibitory activity of dimeric and tetrameric analogs of indolicidin.
Pubmed ID 15482931
Reference Bioorg Med Chem Lett. 2004 Nov 15;14(22):5595-8.
Author Krajewski K, Marchand C, Long YQ, Pommier Y, Roller PP.