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This page gives details of CPPsite entry with ID 1828
Primary information
CPPsite ID1828
PEPTIDE SEQUENCEKLALKLALKALKAALKLAGC
PEPTIDE NAMEMAP
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYAmphipathic
SUB CELLULAR LOCALIZATIONCytoplasm and nucleus
N-TERMINAL MODIFICATIONAcetylation
C-TERMINAL MODIFICATIONConjugation with fluorescein
UPTAKE EFFICIENCYLower than MAP (Aib)
PROPOSED UPTAKE MECHANISMUnknown
INVITRO/INVIVOIn vitro
CELL LINEA549
CARGOFluorophore (fluorescein)
PMID21875799
PATENTUnknown
LENGTH20
Secondary StructureCCHHHHHSSSGGGTSCSSCC
SMILESN[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)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](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CS)C=O
Tertiary Structure
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