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This page gives details of CPPsite entry with ID 2334
Primary information
CPPsite ID2334
PEPTIDE SEQUENCELKRWGTIKKSKAINVLRGFRKEIGRMLNILNRRRR
PEPTIDE NAMEpepR
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYCationic
SUB CELLULAR LOCALIZATIONCytosol
N-TERMINAL MODIFICATIONConjugation with rhodamine B
C-TERMINAL MODIFICATIONFree
PROPOSED UPTAKE MECHANISMEndocytic pathway
INVITRO/INVIVOIn vitro
CELL LINEHepG2, BHK and HEK cell lineages, astrocytes and PBMC
CARGONucleic acid (ssDNA oligonucleotide labelled with Alexa-488)
PMID24286593
PATENTUnknown
LENGTH35
Secondary StructureCHHHHHSCHHHHHHHHHHHHHHHHHHHHHHHHHHC
SMILESN[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C=O)CCCNC(=N)N)CCCNC(=N)N)CCCNC(=N)N)CCCNC(=N)N)CC(=O)N)CC(C)C)[C@H](CC)C)CC(=O)N)CC(C)C)CCSC)CCCNC(
Tertiary Structure
(Technique)
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 (Homology based)