This page gives details of CPPsite entry with ID 2481 |
Primary information | |
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CPPsite ID | 2481 |
PEPTIDE SEQUENCE | CGRKKRRQRRRPPQ |
PEPTIDE NAME | C16NTD |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Protein derived |
CATEGORY | Cationic |
SUB CELLULAR LOCALIZATION | Lysosome |
N-TERMINAL MODIFICATION | Palmitoylation |
C-TERMINAL MODIFICATION | Amidation |
CHEMICAL MODIFICATION | Doxorubicin is attached by a cathepsin B degradable tetrapeptide linker (-Gly-Phe-Leu-Gly-). |
UPTAKE EFFICIENCY | Showed better uptake efficiency |
PROPOSED UPTAKE MECHANISM | Endocytic pathway |
INVITRO/INVIVO | In vitro |
CELL LINE | HepG2 |
CARGO | Small molecule drug (Doxorubicin) |
PMID | 24892976 |
PATENT | Unknown |
LENGTH | 14 |
Secondary Structure | CHHHHHHHCCCSCC |
SMILES | N[C@@H](CS)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](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(=O)N)C=O |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |