This page gives details of CPPsite entry with ID 2631 |
Primary information | |
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CPPsite ID | 2631 |
PEPTIDE SEQUENCE | CGRKKRLLRQRRRPPQ |
PEPTIDE NAME | X |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Synthetic |
CATEGORY | Cationic |
SUB CELLULAR LOCALIZATION | Vesicles |
N-TERMINAL MODIFICATION | Free |
C-TERMINAL MODIFICATION | Free |
UPTAKE EFFICIENCY | Similar to TAT peptide |
PROPOSED UPTAKE MECHANISM | Endocytosis pathways |
INVITRO/INVIVO | In vitro |
CELL LINE | ARPE-19, CHO wt and CHO pgsB-618 cells |
CARGO | Fluorophore (Fluorescein) |
PMID | 22100438 |
PATENT | Unknown |
LENGTH | 16 |
Secondary Structure | CHHHHHHHHHSCSSCC |
SMILES | N[C@@H](CS)C(=O)NCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCC(=O)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)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(=O)N)C=O |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |