To the extent possible under law, the person who associated CC0 with this work has waived all copyright and related or neighboring rights to this work.
General Information
DRAVP ID DRAVPe01936
Peptide Name E50,51TAT-Cd0
Sequence GREERRQRRRC
Sequence Length 11
UniProt ID No entry found
Source Synthetic construct
Activity Information
Target Organism HSV-1
Assay Antiviral assay
Activity
Hemolytic Activity No hemolysis information or data found in the reference(s) presented in this entry
Cytotoxicity
Binding Target Not found
Mechanism No mechanism information found in the reference(s).
Structure Information
PDB ID None
Predicted Structure Download No predicted structure available
Linear/Cyclic Linear
N-terminal Modification Free
C-terminal Modification Amidation
Other Modification None
Stereochemistry L
Physicochemical Information
Formula C56H104N30O17S
Absent amino acids ADFHIKLMNPSTVWY
Common amino acids R
Mass 1501.69
Pl 11.7
Basic residues 6
Acidic residues 2
Hydrophobic residues 0
Net charge 4
Boman Index -10646
Hydrophobicity -321.82
Aliphatic Index 0
Half Life
Extinction Coefficient cystines 0
Absorbance 280nm 0
Polar residues 2
Literature Information
Literature 1
Title A cationic TAT peptide inhibits Herpes simplex virus type 1 infection of human corneal epithelial cells.
Pubmed ID 21029018
Reference J Ocul Pharmacol Ther. 2010 Dec;26(6):541-7.
Author Larsen IV, Brandt CR.
To the extent possible under law, the person who associated CC0 with this work has waived all copyright and related or neighboring rights to this work.