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This page gives details of CPPsite entry with ID 2595
Primary information
CPPsite ID2595
PEPTIDE SEQUENCEKIAKLKAKIQKLKQKIAKLK
PEPTIDE NAMEfGeT
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
N-TERMINAL MODIFICATIONConjugation with 5(6)-Carboxyfluorescein
C-TERMINAL MODIFICATIONFree
INVITRO/INVIVOIn vitro
CELL LINEHuman dermal fibroblasts
CARGOFluorophore (Carboxyflouresein)
PMID24657280
PATENTUnknown
LENGTH20
Secondary StructureCHHHHTTHHHHHHHHHHTCC
SMILESN[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)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](C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(=O)N)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](CCC(=O)N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C=O
Tertiary Structure
(Technique)
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