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This page gives details of CPPsite entry with ID 2035
Primary information
CPPsite ID2035
PEPTIDE SEQUENCEKLAKLAKKLAKLAKNYRWRCKNQN
PEPTIDE NAMEKLA-ECP(32-41)
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEChimeric
CATEGORYCationic
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONFree
INVITRO/INVIVOIn vitro and in vivo
CELL LINEBeas-2B, A549, Caco-2 and AGS
In VIVO MODELFemale Sprague-Dawley rats
CARGOPeptide (KLA)
PMID23469189
PATENTUnknown
LENGTH24
Secondary StructureCHHHHHHHHHHHSCSCSSSSSCCC
SMILESN[C@@H](CCCC[NH3])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](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](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCC[NH3])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](CC(=O)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H
Tertiary Structure
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