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This page gives details of CPPsite entry with ID 2322
Primary information
CPPsite ID2322
PEPTIDE SEQUENCERKKRRQRRRGGGKLLKLLLKLLLKLLK
PEPTIDE NAMETatLK15
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEChimeric
CATEGORYCationic and Amphipathic
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONAmidation
PROPOSED UPTAKE MECHANISMEndocytic pathway
INVITRO/INVIVOIn vitro
CELL LINEHT29 and K562
CARGOFluorophore (TAMRA)
PMID24218116
PATENTUnknown
LENGTH27
Secondary StructureCGGGTCSSCCSHHHHHHHHHHHHHHCC
SMILESN[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)NCC(=O)NCC(=O)NCC(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[N
Tertiary Structure
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