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This page gives details of CPPsite entry with ID 2824
Primary information
CPPsite ID2824
PEPTIDE SEQUENCETPWWRLWTKWHHKRRDLPRKPEGC
PEPTIDE NAMEFITC-Rath
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
C-TERMINAL MODIFICATIONFree
PROPOSED UPTAKE MECHANISMEndocytosis-independent pathway
INVITRO/INVIVOIn vitro
CELL LINEU-937, HeLa cells
CARGOFluorophore (FITC)
PMID23937069
PATENTUnknown
LENGTH24
Secondary StructureCCCTTSHHHHHHCCCBSSSTTTBC
SMILESN[C@@H]([C@@H](C)O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1nc[nH]c1)C(=O)N[C@@H](Cc1nc[nH]c1)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N1CC
Tertiary Structure
(Technique)
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