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This page gives details of CPPsite entry with ID 1390
Primary information
CPPsite ID1390
PEPTIDE SEQUENCEGTKMIFVGIKKKEERADLIAYLKKA
PEPTIDE NAMECyt C 71-101
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYUnknown
SUB CELLULAR LOCALIZATIONEndoplasmic reticulum
N-TERMINAL MODIFICATIONN-terminal acylation of peptide with 6-carboxy-tetramethylrhodamine
C-TERMINAL MODIFICATIONAmidation
UPTAKE EFFICIENCYHigh (105 fold uptake)
PROPOSED UPTAKE MECHANISMUnknown
INVITRO/INVIVOIn vitro
CELL LINEU373MG cells
CARGOFluorophore (6-carboxy-tetramethylrhodamine)
PMID20659686
PATENTUnknown
LENGTH25
Secondary StructureCCSCCSCSCCCCCCCCHHHHHHHTC
SMILESNCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCSC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)
Tertiary Structure
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  (PEPstrMOD)