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This page gives details of CPPsite entry with ID 2829
Primary information
CPPsite ID2829
PEPTIDE SEQUENCEYSSYSAPVSSSLSVRRSYSSSSGS
PEPTIDE NAMENFL-TBS.40-63
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONFree
CHEMICAL MODIFICATIONBiotinylation
PROPOSED UPTAKE MECHANISMEndocytic pathway
INVITRO/INVIVOIn vitro
CELL LINEGPMVs derived from U87-MG cells
CARGOFluorophore (FITC)
PMID23603097
PATENTUnknown
LENGTH24
Secondary StructureCCGGGCSSCCCSSSSCSTTTTSCC
SMILESN[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CO)C=O
Tertiary Structure
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  (PEPstrMOD)