This page gives details of CPPsite entry with ID 1036 |
| Primary information | |
|---|---|
| CPPsite ID | 1036 |
| PEPTIDE SEQUENCE | RRRRRRRRRRR |
| PEPTIDE NAME | R10 |
| CHIRALITY | L |
| LINEAR/CYCLIC | Linear |
| SOURCE | Synthetic |
| CATEGORY | Cationic |
| SUB CELLULAR LOCALIZATION | Probably cytoplasm and nucleus |
| N-TERMINAL MODIFICATION | Free |
| C-TERMINAL MODIFICATION | Conjugation with fluorescein by C-terminal Gly Cys amide |
| UPTAKE EFFICIENCY | High, less than R8 |
| PROPOSED UPTAKE MECHANISM | Non-endocytic pathway |
| INVITRO/INVIVO | In vitro |
| CELL LINE | RAW 264.7 |
| CARGO | Fluorophore (fluorescein) |
| PMID | 11084031 |
| PATENT | Unknown |
| LENGTH | 11 |
| Secondary Structure | CGGGGGGGSCC |
| SMILES | N[C@@H](CCCNC(=[NH2])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)N[C@@H](CCCNC(=[NH2])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)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) |