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This page gives details of CPPsite entry with ID 1543
Primary information
CPPsite ID1543
PEPTIDE SEQUENCEMGLGLHLLVLAAALQGAKKKRKV
PEPTIDE NAMEPeptide 2
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEChimeric
CATEGORYAmphipathic
SUB CELLULAR LOCALIZATIONNucleus
N-TERMINAL MODIFICATIONAcetylation
C-TERMINAL MODIFICATIONCysteamide group
UPTAKE EFFICIENCYUnknown
PROPOSED UPTAKE MECHANISMNon-endocytic pathway (direct translocation)
INVITRO/INVIVOIn vitro
CELL LINEHS-68 Cells
PMID9287160
PATENTUnknown
LENGTH23
Secondary StructureCCCSSHHHHHHHHHTTSTTTSCC
SMILESN[C@@H](CCSC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1nc[nH]c1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)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](CCC(=O)N)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C(C)C)C=O
Tertiary Structure
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