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This page gives details of CPPsite entry with ID 2034
Primary information
CPPsite ID2034
PEPTIDE SEQUENCEKLAKLAKKLAKLAKGRKKRRQRRRP
PEPTIDE NAMEKLA-TAT(47-57)
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
LENGTH25
Secondary StructureCHHHHHHHHHHHHHHHHHHHHCSCC
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)NCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])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](CCC(=O)N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H]
Tertiary Structure
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