This page gives details of CPPsite entry with ID 2584 |
Primary information | |
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CPPsite ID | 2584 |
PEPTIDE SEQUENCE | AYGRKKRRQRRR |
PEPTIDE NAME | DOX-TAT-LIP |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Protein derived |
CATEGORY | Cationic |
SUB CELLULAR LOCALIZATION | Cytosol and Nucleus |
N-TERMINAL MODIFICATION | Cysteine addition |
C-TERMINAL MODIFICATION | Free |
UPTAKE EFFICIENCY | Higher than those of DOX-LIP |
PROPOSED UPTAKE MECHANISM | Endocytosis |
INVITRO/INVIVO | In vitro and in vivo |
CELL LINE | C6 and bEnd.3 cells |
In VIVO MODEL | BALB/c mice |
CARGO | Nanaoparticle (Liposome), Small molecule drug (Doxorubicin) |
PMID | 24893333 |
PATENT | Unknown |
LENGTH | 12 |
Secondary Structure | CCCHHHHHTTCC |
SMILES | N[C@@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)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 |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |