Welcome to Entry Card of Peptide


This page gives details of CPPsite entry with ID 1493
Primary information
CPPsite ID1493
PEPTIDE SEQUENCETRSSRAGLQWPVGRVHRLLRKGGC
PEPTIDE NAMEBF2d
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYAntimicrobial
SUB CELLULAR LOCALIZATIONCytosol and nucleus
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONConjugation with Texas Red
UPTAKE EFFICIENCYComparable to Tat (47-57)
PROPOSED UPTAKE MECHANISMUnknown probably non endocytic pathway
INVITRO/INVIVOIn vitro
CELL LINEHeLa or TM12 cells
CARGOFluorophore (Texas Red)
PMID12417587
PATENTUnknown
LENGTH24
Secondary StructureCCCCTTTSCSCGGGGGTSHHHHCC
SMILESN[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc1nc[nH]c1)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)NCC(=O)NCC(=O)N[C@@H](CS)C=O
Tertiary Structure
(Technique)		View in Jmol  OR Download Structure
  (PEPstrMOD)