This page gives details of CPPsite entry with ID 2344 |
Primary information | |
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CPPsite ID | 2344 |
PEPTIDE SEQUENCE | VSRRRRRRGGRRRRK |
PEPTIDE NAME | Protamine |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Synthetic |
CATEGORY | Cationic |
N-TERMINAL MODIFICATION | Conjugation with 5-carboxyfluorescein via a lysine residue |
C-TERMINAL MODIFICATION | Free |
UPTAKE EFFICIENCY | Lower uptake efficiency |
INVITRO/INVIVO | In vitro and in vivo |
CELL LINE | Wong-Kilbourne-derived human conjunctival epithelial cells (NHC) |
In VIVO MODEL | Male SpragueDawley rats and male albino rabbits |
CARGO | Fluorophore [5-carboxyfluorescein (FAM)] |
PMID | 24521351 |
PATENT | Unknown |
LENGTH | 15 |
Secondary Structure | CHHHHHCCCSSTTCC |
SMILES | N[C@@H](C(C)C)C(=O)N[C@@H](CO)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)NCC(=O)NCC(=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](CCCC[NH3])CO |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |