General Information


DRAVP ID  DRAVPe00146

Peptide Name   vif 137-151

Sequence  AGHNKVGSLQYLALA

Sequence Length  15

UniProt ID  No entry found

Source  Synthetic construct(derived from HIV-1 Vif protein)



Activity Information


Target Organism  HIV

Assay  ELISA

Activity 

  • [Ref.12480936]HIV-1:inhibit vif-vif binding.

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  Vif proteins

Mechanism  Vif proteins are essential for HIV-1 replication and able to form multimer, which is critical to the biological activity of many prokaryotic and eukaryotic proteins and is a common mechanism for the functional activation/inactivation of proteins.The peptide could bind with vif proteins and block the multimerization of them,which should inhibit HIV-1 replication.



Structure Information


PDB ID  None

Predicted Structure Download  DRAVPe00146

Linear/Cyclic  Linear

N-terminal Modification  Free

C-terminal Modification  Free

Other Modification  None

Stereochemistry  L



Physicochemical Information


Formula  C69H112N20O20

Absent amino acids  CDEFIMPRTW

Common amino acids  AL

Mass  1541.77

Pl  8.64

Basic residues  2

Acidic residues  0

Hydrophobic residues  7

Net charge  2

Boman Index  18

Hydrophobicity  26.67

Aliphatic Index  117.33

Half Life 

  •     Mammalian:4.4 hour
  •     Yeast:>20 hour
  •     E.coli:>10 hour

Extinction Coefficient cystines  1490

Absorbance 280nm  106.43

Polar residues  5



Literature Information


Literature 1

Title   Potent suppression of viral infectivity by the peptides that inhibit multimerization of human immunodeficiency virus type 1 (HIV-1) Vif proteins.

Pubmed ID   12480936

Reference   J Biol Chem. 2003 Feb 21;278(8):6596-602.

Author   Yang B, Gao L, Li L, Lu Z, Fan X, Patel CA, Pomerantz RJ, DuBois GC, Zhang H.

DOI   10.1074/jbc.M210164200