General Information

General Information

DRAVP ID DRAVPe00792

Peptide Name T2635

Sequence TTWEAWDRAIAEYAARIEALIRAAQEQQEKNEAALREL

Sequence Length 38

UniProt ID No entry found

Source Synthetic construct

Other Link DRAVPa1315

Activity Information

Target Organism HIV

Assay MAGI/cMAGI infectivity assay

Activity

[Ref.17640899]HIV IIIB:inhibition of virus infection on CEM4 cells(IC50=0.007 μg/ml);
HIV 098:inhibition of virus infection on CEM4 cells(IC50=0.018μg/ml);
HIV 098-T20:inhibition of virus infection on CEM4 cells(IC50=0.025 μg/ml);
HIV 098-T1249:inhibition of virus infection on CEM4 cells(IC50=0.015 μg/ml);
HIV 098-T651:inhibition of virus infection on CEM4 cells(IC50=0.021 μg/ml).

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 membrane

Mechanism The peptide acts by binding to the heptad repeat 1 (HR1) region of gp41 and preventing the interaction of the HR1 and HR2 domains, which is required for virus–cell fusion.

Structure Information

PDB ID None

Predicted Structure Download DRAVPe00792

Linear/Cyclic Linear

N-terminal Modification Acetylation

C-terminal Modification Amidation

Other Modification None

Stereochemistry L

Physicochemical Information

Formula C193H305N57O62

Absent amino acids CFGHMPSV

Common amino acids A

Mass 4415.89

Pl 4.64

Basic residues 5

Acidic residues 8

Hydrophobic residues 18

Net charge -3

Boman Index -9788

Hydrophobicity -67.11

Aliphatic Index 87.89

Half Life

Mammalian:7.2 hour
Yeast:>20 hour
E.coli:>10 hour

Extinction Coefficient cystines 12490

Absorbance 280nm 337.57

Polar residues 4

Literature Information

Literature 1

Title Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Pubmed ID 17640899

Reference Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12772-7.

Author Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK.

DOI 10.1073/pnas.0701478104