This page gives details of CPPsite entry with ID 1036 |
Primary information | |
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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) |