This page gives details of CPPsite entry with ID 2294 |
Primary information | |
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CPPsite ID | 2294 |
PEPTIDE SEQUENCE | RQIKIWFQNRRMKWKK |
PEPTIDE NAME | F(SG)4Pen |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Protein derived |
CATEGORY | Cationic and amphipathic |
N-TERMINAL MODIFICATION | Acetylation |
C-TERMINAL MODIFICATION | Amidation |
UPTAKE EFFICIENCY | Higher uptake efficiency for BSA |
PROPOSED UPTAKE MECHANISM | Endocytic pathway |
INVITRO/INVIVO | In vitro |
CELL LINE | HeLa, KG1a cells |
CARGO | Fluorophore (Alexa488), Protein (bovine serum albumin) and Nanoparticle (quantum dots) |
PMID | 25108152 |
PATENT | Unknown |
LENGTH | 16 |
Secondary Structure | CCCSSHHHHHHSSSCC |
SMILES | [NH3][C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)O)CCCC[NH3])CCCC[NH3])Cc1c[nH]c2c1cccc2)CCCC[NH3])CCSC)CCCNC(=[NH2])N)CCCNC(=[NH2])N)CC(=O)N)CCC(=O)N)Cc1ccccc1)Cc1c[nH]c2c1cccc2)[C@H](CC)C)CCCC[NH3])[C@H](CC)C)CCC(=O)N)CCCNC(=[NH2])N |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (Experimentally determined structure from PDB) |