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This page gives details of CPPsite entry with ID 1433
Primary information
CPPsite ID1433
PEPTIDE SEQUENCEALWKTLLKKVLKAPKKKRKV
PEPTIDE NAMES4(13)-PV
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEChimeric
CATEGORYKaryophilic
SUB CELLULAR LOCALIZATIONCytoplasm and nucleus
N-TERMINAL MODIFICATIONConjugation with rhodamine B
C-TERMINAL MODIFICATIONAmidation
UPTAKE EFFICIENCYUnknown
PROPOSED UPTAKE MECHANISMNon-endocytic pathway
INVITRO/INVIVOIn vitro
CELL LINEHeLa
CARGOFluorophore (rhodamine)
PMID12119035
PATENTUS 20040132970
LENGTH20
Secondary StructureCCTTTTHHHHTTSCTTTSCC
SMILESN[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)O)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](CCCC[NH3])C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=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](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C(C)C)C=O
Tertiary Structure
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