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This page gives details of CPPsite entry with ID 1432 |
| Primary information | |
|---|---|
| CPPsite ID | 1432 |
| PEPTIDE SEQUENCE | ALWKTLLKKVLKA |
| PEPTIDE NAME | S4(13) |
| CHIRALITY | L |
| LINEAR/CYCLIC | Linear |
| SOURCE | Protein derived |
| CATEGORY | Antimicrobial |
| SUB CELLULAR LOCALIZATION | Cytoplasm |
| N-TERMINAL MODIFICATION | Conjugation with rhodamine B |
| C-TERMINAL MODIFICATION | Amidation |
| UPTAKE EFFICIENCY | Unknown |
| PROPOSED UPTAKE MECHANISM | Non-endocytic pathway |
| INVITRO/INVIVO | In vitro |
| CELL LINE | HeLa |
| CARGO | Fluorophore (rhodamine) |
| PMID | 12119035 |
| PATENT | US 20040132970 |
| LENGTH | 13 |
| Secondary Structure | CCCTTTSSSSSCC |
| SMILES | 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@H](O)N)C)CCCC[NH3])CC(C)C)C(C)C)CCCC[NH3])CCCC[NH3])CC(C)C)CC(C)C)[C@H](O)C)CCCC[NH3])Cc1c[nH]c2c1cccc2)CC(C)C)C |
| Tertiary Structure (Technique) | View in Jmol OR Download Structure (Experimentally determined structure from PDB) |