This page gives details of CPPsite entry with ID 2410 |
| Primary information | |
|---|---|
| CPPsite ID | 2410 |
| PEPTIDE SEQUENCE | GLKKLARLAHKLLKLGC |
| PEPTIDE NAME | RA |
| CHIRALITY | L |
| LINEAR/CYCLIC | Linear |
| SOURCE | Synthetic |
| CATEGORY | Amphipathic |
| N-TERMINAL MODIFICATION | Free |
| C-TERMINAL MODIFICATION | Amidation |
| UPTAKE EFFICIENCY | Higher than EA |
| PROPOSED UPTAKE MECHANISM | Endocytic pathway |
| INVITRO/INVIVO | In vitro |
| CELL LINE | HeLa, A549, PC12 and 3T3-L1 cells |
| PMID | 24867193 |
| PATENT | Unknown |
| LENGTH | 17 |
| Secondary Structure | CTTHHHHHHHHHTTCCC |
| SMILES | NCC(=O)N[C@@H](CC(C)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](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC1=CNCN1)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](CCCC[NH3])C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CS)C(=O)N |
| Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |