Welcome to Entry Card of Peptide


This page gives details of CPPsite entry with ID 1714
Primary information
CPPsite ID1714
PEPTIDE SEQUENCEGLWRALWRGLRSLWKLKRKV
PEPTIDE NAMECADY-1d (SEQ ID No: 5)
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYUnknown
SUB CELLULAR LOCALIZATIONUnknown
N-TERMINAL MODIFICATIONAcetylation
C-TERMINAL MODIFICATIONCysteamide group
UPTAKE EFFICIENCYUnknown
PROPOSED UPTAKE MECHANISMUnknown
INVITRO/INVIVOIn vitro
CELL LINEHeLa or HS-68 cells
CARGONucleic acid (siRNA)
PMID0
PATENTUS 7943581
LENGTH20
Secondary StructureCCHHHHHHTHHHHHTTTCCC
SMILESNCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C(C)C)C=O
Tertiary Structure
(Technique)		View in Jmol  OR Download Structure
  (PEPstrMOD)