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This page gives details of CPPsite entry with ID 1826
Primary information
CPPsite ID1826
PEPTIDE SEQUENCEkcfqwqrnmrkvrgppvscikr
PEPTIDE NAMEhLF(38-59) peptide
CHIRALITYD
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYUnknown
SUB CELLULAR LOCALIZATIONMembrane bound
N-TERMINAL MODIFICATIONConjugation with fluorescein
C-TERMINAL MODIFICATIONAmidation
UPTAKE EFFICIENCYUnknown
PROPOSED UPTAKE MECHANISMUnknown
INVITRO/INVIVOIn vitro
CELL LINEHeLa
CARGOFluorophore (fluorescein)
PMID21867915
PATENTUnknown
LENGTH22
Secondary StructureCCHHHHHHHTTTTCCCTTTCCC
SMILESN[C@H](CCCC[NH3])C(=O)N[C@H](CS)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@H](CCC(=O)N)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](CCC(=O)N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CC(=O)N)C(=O)N[C@H](CCSC)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)N[C@H](CCCNC(=[NH2])N)C(=O)NCC(=O)N1CCC[C@@H]1C(=O)N1CCC[C@@H]1C(=O)N[C@H](C(C)C)C(=O)N[C@H](CO)C(=O)N[C@H](CS)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@H](CCCC[NH3])C(=O)N[C@H](CCCNC(=[NH2])N)C=O
Tertiary Structure
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  (PEPstrMOD)