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This page gives details of CPPsite entry with ID 2331
Primary information
CPPsite ID2331
PEPTIDE SEQUENCERQIKIWFQNRRMKWKKC
PEPTIDE NAMEPen-C-Cy5
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYCationic and amphipathic
SUB CELLULAR LOCALIZATIONNa
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONCysteine addition
UPTAKE EFFICIENCYDose dependent uptake
PROPOSED UPTAKE MECHANISMEndocytic pathway
INVITRO/INVIVOIn vitro
CELL LINEUndifferentiated malignant glioma rat (F98) cell line, CHO cells
CARGOFluorophore (Cy5)
PMID24276021
PATENTUnknown
LENGTH17
Secondary StructureCCCCSSCSCTTSCCCCC
SMILESN[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(=O)N)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](CCSC)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CS)C=O
Tertiary Structure
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  (PEPstrMOD)