| Primary information |
|---|
| Hemolytik ID | 3028 |
| PMID | 19038369 |
| YEAR | 2009 |
| SEQUENCE | ILPWKWPW*WPWRR |
| LENGTH | 13 |
| NAME | ID-W |
| C-ter Modification | Amidation |
| N-ter Modification | Free |
| Linear/Cyclic | Cyclic |
| Stereochemistry | L |
| Modified Residues | *=Reduced amide bond ψ[CH2NH] |
| FUNCTION | Antimicrobial |
| ACTIVITY | 5-10% hemolysis at 25μg/mL |
| RBCs SOURCE | Human |
| Secondary information |
|---|
| Properties | Physico-Chemical details |
| STRUCTURE | |
| DSSP states | NA |
| SMILES | NA |
| External Links |
|---|
| PDB exact | PDB partial | SP exact | SP partial | TrEMBL exact | TrEMBL partial | IEDB exact | IEDB partial |
| NA |
NA |
NA |
NA |
NA |
NA |
NA |
NA |
|
| Reference Informaiton |
|---|
| ARTICLE | Indolicidin-derived antimicrobial peptide analogs with greater bacterial selectivity and requirements for antibacterial and hemolytic activities. |
| AUTHORS | Kim SM,Kim JM,Joshi BP,Cho H |
| JOURNAL | Biochim Biophys Acta. 2009 Feb;1794(2):185-92. doi: 10.1016/j.bbapap.2008.10.009. Epub 2008 Nov 6. |
