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This page gives details of CPPsite entry with ID 2341
Primary information
CPPsite ID2341
PEPTIDE SEQUENCEGRKKRRQRRRPPQK
PEPTIDE NAMETAT
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYCationic
N-TERMINAL MODIFICATIONConjugation with 5-carboxyfluorescein via a lysine residue
C-TERMINAL MODIFICATIONFree
UPTAKE EFFICIENCYHigher uptake efficiency
INVITRO/INVIVOIn vitro and in vivo
CELL LINEWong-Kilbourne-derived human conjunctival epithelial cells (NHC)
In VIVO MODELMale SpragueDawley rats and male albino rabbits
CARGOFluorophore [5-carboxyfluorescein (FAM)]
PMID24521351
PATENTUnknown
LENGTH14
Secondary StructureCCCSCCCCCCCSCC
SMILESNCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCCC[NH3])C=O
Tertiary Structure
(Technique)		View in Jmol  OR Download Structure
  (PEPstrMOD)