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This page gives details of CPPsite entry with ID 2154
Primary information
CPPsite ID2154
PEPTIDE SEQUENCEKWFETWFTEWPKKRKGGC
PEPTIDE NAMEPep-3
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONFree
CHEMICAL MODIFICATIONLinker Di-Glycine
PROPOSED UPTAKE MECHANISMEndocytosis
INVITRO/INVIVOIn vitro
CELL LINEHT-29-luc cells
CARGOPNA
PMID25185512
PATENTUnknown
LENGTH18
Secondary StructureCCTTTTTCCCSSTTTSCC
SMILESN[C@@H](CCCC[NH3])C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCC[C@H]1C(=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)NCC(=O)NCC(=O)N[C@@H](CS)C=O
Tertiary Structure
(Technique)
View in Jmol  OR Download Structure
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