Welcome to Entry Card of Peptide


This page gives details of CPPsite entry with ID 1323
Primary information
CPPsite ID1323
PEPTIDE SEQUENCEPRPPRLPRPRPRPLPFPRPG
PEPTIDE NAMEBac5-24
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYAntimicrobial
SUB CELLULAR LOCALIZATIONCytoplasm
N-TERMINAL MODIFICATIONConjugation with fluorescein
C-TERMINAL MODIFICATIONFree
UPTAKE EFFICIENCYLower than Tat (49-57)
PROPOSED UPTAKE MECHANISMUnknown
INVITRO/INVIVOIn vitro
CELL LINERAW 264.7
CARGOFluorophore (fluorescein)
PMID12450378
PATENTUnknown
LENGTH20
Secondary StructureCCCSCCCCSSCCSSCSCCCC
SMILESN1CCC[C@H]1C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)NCC=O
Tertiary Structure
(Technique)		View in Jmol  OR Download Structure
  (PEPstrMOD)