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This page gives details of CPPsite entry with ID 2626
Primary information
CPPsite ID2626
PEPTIDE SEQUENCECGRKKRWWRQRWWRWWRPPQ
PEPTIDE NAMEV
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYCationic
SUB CELLULAR LOCALIZATIONVesicles
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONFree
UPTAKE EFFICIENCYSimilar to TAT peptide
PROPOSED UPTAKE MECHANISMEndocytosis pathways
INVITRO/INVIVOIn vitro
CELL LINEARPE-19, CHO wt and CHO pgsB-618 cells
CARGOFluorophore (Fluorescein)
PMID22100438
PATENTUnknown
LENGTH20
Secondary StructureCCCCSTHHHHHHHCSSSCCC
SMILESN[C@@H](CS)C(=O)NCC(=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](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)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](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)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
Tertiary Structure
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  (PEPstrMOD)