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This page gives details of CPPsite entry with ID 2992
Primary information
CPPsite ID2992
PEPTIDE SEQUENCEAGY(PO3)LLGKT(PO3)NLKALAALAKKIL
PEPTIDE NAMENF 3
CHIRALITYModified
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYAmphipathic
N-TERMINAL MODIFICATIONStearylation
C-TERMINAL MODIFICATIONAmidation
CHEMICAL MODIFICATIONPhosphorylation
PROPOSED UPTAKE MECHANISMEndocytosis
INVITRO/INVIVOIn vitro
CELL LINEHela pLuc 705 cells
CARGONucleic acid (SCO)
PMID0
PATENTEP 2 491 952 A1
LENGTH21
Secondary StructureCCSSSTTHHHHHHHHHHHHHC
SMILESN[C@H](C(=O)NCC(=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)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C=O)CC(C)C)[C@H](CC)C)CCCCN)CCCCN)C)CC(C)C)C)C)CC(C)C)C)CCCCN)CC(C)C)CC(=O)N)[C@H](O)C)CCCCN)CC(C)C)CC(C)C)Cc1ccc(cc1)O)C
Tertiary Structure
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  (Homology based)