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This page gives details of CPPsite entry with ID 2896
Primary information
CPPsite ID2896
PEPTIDE SEQUENCERRWRRWNRFNRRRCR
PEPTIDE NAMEP8
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYCationic
SUB CELLULAR LOCALIZATIONPunctate and diffuse cytoplasmic
N-TERMINAL MODIFICATIONConjugation with FITC
C-TERMINAL MODIFICATIONFree
CHEMICAL MODIFICATIONLinker 6-aminohexamoic acid (Ahx)
UPTAKE EFFICIENCYHigh (Comapre to Tat)
PROPOSED UPTAKE MECHANISMMacropinocytosis
INVITRO/INVIVOIn vitro
CELL LINEHeLa cells
CARGOFluorophore (FITC)
PMID25459448
PATENTUnknown
LENGTH15
Secondary StructureCCCSSSSCCCCCCCC
SMILESN[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CC(=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)N[C@@H](CS)C(=O)N[C@@H](CCCNC(=[NH2])N)C=O
Tertiary Structure
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  (PEPstrMOD)