This page gives details of CPPsite entry with ID 2249 |
Primary information | |
---|---|
CPPsite ID | 2249 |
PEPTIDE SEQUENCE | RKKRRQRRR |
PEPTIDE NAME | Tat-PCP |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Protein derived |
CATEGORY | Cationic |
SUB CELLULAR LOCALIZATION | Cytoplasm and Nucleus |
N-TERMINAL MODIFICATION | Acetylation |
C-TERMINAL MODIFICATION | Amidation |
CHEMICAL MODIFICATION | Φ, L-2-naphthylalanine,miniPEG, 8-amino-3,6-dioxaoctanoic acid |
UPTAKE EFFICIENCY | Lower efficiency |
PROPOSED UPTAKE MECHANISM | Endocytic pathway |
INVITRO/INVIVO | In vitro |
CELL LINE | HEK293, HeLa, MCF-7, NIH 3T3, A549, Jurkat, H1650, and H1299 cells |
CARGO | Peptide [PCP, miniPEG-DE(pCAP)LI-NH2] |
PMID | 24896852 |
PATENT | Unknown |
LENGTH | 9 |
Secondary Structure | CCCCCSCCC |
SMILES | 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](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 |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |