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This page gives details of CPPsite entry with ID 2641
Primary information
CPPsite ID2641
PEPTIDE SEQUENCEinlkalaalakkil
PEPTIDE NAMETAM-iMP
CHIRALITYD
LINEAR/CYCLICLinear
SOURCESynthetic
SUB CELLULAR LOCALIZATIONMembrane and cytosol
N-TERMINAL MODIFICATIONConjugation with 6-carboxytetramethyl rhodamine
UPTAKE EFFICIENCYHigh (compare to Penetratin)
PROPOSED UPTAKE MECHANISMEndocytosis
INVITRO/INVIVOIn vitro
CELL LINEU373 MG cells
CARGOFluorophore (TAMRA)
PMID22148546
PATENTUnknown
LENGTH14
Secondary StructureCCSHHHHHHHHTTC
SMILES[NH3][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)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](CC)C
Tertiary Structure
(Technique)
View in Jmol  OR Download Structure
 (Experimentally determined structure from PDB)