This page gives details of CPPsite entry with ID 2540 |
| Primary information | |
|---|---|
| CPPsite ID | 2540 |
| PEPTIDE SEQUENCE | HHHRRRRRRRR |
| PEPTIDE NAME | MTS-(5-FAM)- H3R8 |
| CHIRALITY | L |
| LINEAR/CYCLIC | Linear |
| SOURCE | Synthetic |
| CATEGORY | Cationic |
| SUB CELLULAR LOCALIZATION | Cytosol |
| N-TERMINAL MODIFICATION | Conjugation with 5(6)-Carboxyfluorescein |
| C-TERMINAL MODIFICATION | Free |
| UPTAKE EFFICIENCY | Lower uptake efficiency |
| PROPOSED UPTAKE MECHANISM | Endocytosis |
| INVITRO/INVIVO | In vitro |
| CELL LINE | MCF-7 cells |
| CARGO | Fluorophore (5-FAM) and MTS |
| PMID | 25547808 |
| PATENT | Unknown |
| LENGTH | 11 |
| Secondary Structure | CCSTTHHHHTC |
| SMILES | N[C@@H](Cc1nc[nH]c1)C(=O)N[C@@H](Cc1nc[nH]c1)C(=O)N[C@@H](Cc1nc[nH]c1)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) |