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This page gives details of CPPsite entry with ID 3002
Primary information
CPPsite ID3002
PEPTIDE SEQUENCEAGYLLGK(Stearyl)INLKALAALAKKIL
PEPTIDE NAMEPepfect 4
CHIRALITYModified
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYAmphipathic
N-TERMINAL MODIFICATIONStearylation
C-TERMINAL MODIFICATIONAmidation
CHEMICAL MODIFICATIONOrthogonally stearylated on Lys′
PROPOSED UPTAKE MECHANISMEndocytosis
INVITRO/INVIVOIn vitro
CELL LINEHela cells
CARGONucleic acid (SCO)
PMID0
PATENTUS 2014/0140929 A1
LENGTH21
Secondary StructureCCCCCTTSCTHHHHHHHTTTC
SMILESN[C@@H](C)C(=O)NCC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C=O
Tertiary Structure
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  (PEPstrMOD)