General Information
DRAVP ID DRAVPe00698
Peptide Name Indolicidin (2-13)[R12P][R13P]
Sequence LPWKWPWWPWPP
Sequence Length 12
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 DRAVPe00698
Linear/Cyclic Linear
N-terminal Modification Free
C-terminal Modification Amidtion
Other Modification None
Stereochemistry L
Physicochemical Information
Formula C92H110N18O13
Absent amino acids ACDEFGHIMNQRSTVY
Common amino acids PW
Mass 1676
Pl 8.75
Basic residues 1
Acidic residues 0
Hydrophobic residues 6
Net charge 1
Boman Index 1102
Hydrophobicity -105
Aliphatic Index 32.5
Half Life
Extinction Coefficient cystines 27500
Absorbance 280nm 2500
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.