Welcome to Entry Card of Peptide


This page gives details of CPPsite entry with ID 1265
Primary information
CPPsite ID1265
PEPTIDE SEQUENCEIPSRWKDQFWKRWHY
PEPTIDE NAMENo.143
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYAmphipathic
SUB CELLULAR LOCALIZATIONUnknown
N-TERMINAL MODIFICATIONConjugation with fluorescein
C-TERMINAL MODIFICATIONFree
UPTAKE EFFICIENCYSimilar or greater than TAT in CHO cells, greater
PROPOSED UPTAKE MECHANISMUnknown
INVITRO/INVIVOIn vitro
CELL LINEHeLa, Jurkat and CHO
CARGOFluorophore (fluorescein)
PMID19956900
PATENTUnknown
LENGTH15
Secondary StructureCHHHHTTHHHHHTCC
SMILESN[C@@H]([C@@H](C)CC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1nc[nH]c1)C(=O)N[C@@H](Cc1ccc(O)cc1)C=O
Tertiary Structure
(Technique)
View in Jmol  OR Download Structure
 (PEPstrMOD)