This page gives details of CPPsite entry with ID 2493 |
Primary information | |
---|---|
CPPsite ID | 2493 |
PEPTIDE SEQUENCE | KLALKLALKALKAALKLA |
PEPTIDE NAME | MAP |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Synthetic |
CATEGORY | Amphipathic |
N-TERMINAL MODIFICATION | Conjugation with fluorescein |
C-TERMINAL MODIFICATION | Amidation |
UPTAKE EFFICIENCY | Lower uptake efficiency |
PROPOSED UPTAKE MECHANISM | Non endocytosis pathway |
INVITRO/INVIVO | In vitro |
CELL LINE | Rat basophilic leukemia RBL-2H3 cells and CHO-K1 |
CARGO | Fluorophore (Fluorescein) |
PMID | 25016968 |
PATENT | Unknown |
LENGTH | 18 |
Secondary Structure | CCHHHHHHHHHHHHTTCC |
SMILES | N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)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](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C=O |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |