General Information
DRAVP ID DRAVPe00081
Peptide Name Vpr-3 R8
Sequence LQQLLFIHFRIGRRRRRRRR
Sequence Length 20
UniProt ID No entry found
Source Synthetic construct(derived from HIV-1 gene products(Vpr))
Activity Information
Target Organism HIV
Assay Integrase assay
Activity
Hemolytic Activity No hemolysis information or data found in the reference(s) presented in this entry
Cytotoxicity
Binding Target Integrase
Mechanism IN is an essential enzyme for the stable infection of host cells because it catalyzes the insertion of viral DNA inside the pre-integration complex (PIC) into the genome of host cells in two successive reactions, designated as strand transfer and 3′-end-processing. The peptide could inhibit the activity of integrase and thus inhibit virus replication.
Structure Information
PDB ID None
Predicted Structure Download DRAVPe00081
Linear/Cyclic Linear
N-terminal Modification Acetylation
C-terminal Modification Amidation
Other Modification None
Stereochemistry L
Physicochemical Information
Formula C120H209N51O23
Absent amino acids ACDEKMNPSTVWY
Common amino acids R
Mass 2734.31
Pl 12.9
Basic residues 10
Acidic residues 0
Hydrophobic residues 7
Net charge 10
Boman Index -11852
Hydrophobicity -125.5
Aliphatic Index 97.5
Half Life
Extinction Coefficient cystines 0
Absorbance 280nm 0
Polar residues 1
Literature Information
Literature 1
Title Peptide HIV-1 integrase inhibitors from HIV-1 gene products.
Pubmed ID 20586421
Reference J Med Chem. 2010 Jul 22;53(14):5356-60.
Author Suzuki S, Urano E, Hashimoto C, Tsutsumi H, Nakahara T, Tanaka T, Nakanishi Y, Maddali K, Han Y, Hamatake M, Miyauchi K, Pommier Y, Beutler JA, Sugiura W, Fuji H, Hoshino T, Itotani K, Nomura W, Narumi T, Yamamoto N, Komano JA, Tamamura H.