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This page gives details of CPPsite entry with ID 2381
Primary information
CPPsite ID2381
PEPTIDE SEQUENCEACSGSGSGCGSGSGSCGRRRRRRRR
PEPTIDE NAMEEA1x8 L
CHIRALITYL
LINEAR/CYCLICCyclic
SOURCESynthetic
CATEGORYArginine rich
SUB CELLULAR LOCALIZATIONVesicles
N-TERMINAL MODIFICATIONExtended with Alanine and an 6-aminohexanoic acid (Ahx) spacer
C-TERMINAL MODIFICATIONAmidation
CHEMICAL MODIFICATIONAll cysteines were capped with iodoacetamide
PROPOSED UPTAKE MECHANISMEndocytic pathway
INVITRO/INVIVOIn vitro
CELL LINEHeLa
CARGOFluorophore (FITC)
PMID24697151
PATENTUnknown
LENGTH25
Secondary StructureCCCSSSBTTTBSSCGGGSTTSSSCC
SMILESN[C@@H](C)C(=O)N[C@@H](CS)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CS)C(=O)NCC(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)NCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C=O
Tertiary Structure
(Technique)
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