This page gives details of CPPsite entry with ID 2165 |
Primary information | |
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CPPsite ID | 2165 |
PEPTIDE SEQUENCE | PKKKRKVWKLLQQFFGLM |
PEPTIDE NAME | Stearyl-NS |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Synthetic |
CATEGORY | Cationic |
SUB CELLULAR LOCALIZATION | Nucleus |
N-TERMINAL MODIFICATION | Stearylation |
C-TERMINAL MODIFICATION | Amidation |
UPTAKE EFFICIENCY | Higher Uptake |
PROPOSED UPTAKE MECHANISM | Caspase-independent pathway |
INVITRO/INVIVO | In vitro |
CELL LINE | HeLa |
CARGO | Fluorophore (FITC) |
PMID | 24958615 |
PATENT | Unknown |
LENGTH | 18 |
Secondary Structure | CGGGGGGCSGGGCTTTTC |
SMILES | N1CCC[C@H]1C(=O)N[C@@H](CCCC[NH3])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](CCCC[NH3])C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C=O |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |