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This page gives details of CPPsite entry with ID 2497
Primary information
CPPsite ID2497
PEPTIDE SEQUENCEAGYLLGKINLKALAALAKKIL
PEPTIDE NAMETP10
CHIRALITYModified
LINEAR/CYCLICLinear
SOURCEChimeric
CATEGORYAmphipathic
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONAmidation
CHEMICAL MODIFICATIONOregon Green 488 coupled to Lys7
PROPOSED UPTAKE MECHANISMNon endocytosis pathway
INVITRO/INVIVOIn vitro
CELL LINERat basophilic leukemia RBL-2H3 cells and CHO-K1
CARGOFluorophore (Fluorescein)
PMID25016968
PATENTUnknown
LENGTH21
Secondary StructureCCCCCTTSCTHHHHHHHTTTC
SMILESN[C@@H](C)C(=O)NCC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(=O)N)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](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C=O
Tertiary Structure
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