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This page gives details of CPPsite entry with ID 2526
Primary information
CPPsite ID2526
PEPTIDE SEQUENCEKWSFRVSYRGISYRRSRGK
PEPTIDE NAMEMTpl-1
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
SUB CELLULAR LOCALIZATIONNucleus
N-TERMINAL MODIFICATIONBiotinylation
C-TERMINAL MODIFICATIONFree
UPTAKE EFFICIENCYUptake of MTpl-1 was similar to that of Tpl
PROPOSED UPTAKE MECHANISMEndocytosis-independent
INVITRO/INVIVOIn vitro
CELL LINEPlant cells, HeLa cells
CARGOProtein (?-glucuronidase enzyme, ?-galactosidase)
PMID25514997
PATENTUnknown
LENGTH19
Secondary StructureCCCCCSSSCSSSSGGGSCC
SMILESN[C@@H](CCCC[NH3])C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)NCC(=O)N[C@@H](CCCC[NH3])CO
Tertiary Structure
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