| ID | DRAMP29101 |
|---|---|
| Sequence | GFKDLLKGAAKALVKAVLF |
| Length | 19 |
| Name | Ascaphin-8 [T16A] |
| Source | Synthetic construct |
| Activity | Antimicrobial, Antibacterial,Anti-Gram+, Anti-Gram-, Anti-cancer, Antifungal |
| Pathogen | [Ref.18554256]Gram-negative bacteria:Escherichia coli ATCC 25726(MIC=6 µM);##Gram-positive bactria:Staphylococcus aureus ATCC 25923(MIC=3 µM);##Fungi:Candida albicans ATCC 900280(MIC=6 µM).##Cancer:human hepatoma‐derived cells HepG2 (LC50=9 µM). |
| Hemolytic Activity | [Ref.18554256]Hemolysis against human erythrocytes (LC50=22 µM). |
| Cytotoxicity | [Ref.18554256]Cytotoxicity:Mouse fibroblasts L929 (LC50=5 µM). |
| N-terminal Modification | Free |
| C-terminal Modification | Amidation |
| Linear/Cyclic/Branched | Linear |
| Uniprot | P0CJ32 |
| PDB | |
| 3D View | |
| PDB Download | Download PDB Predicted by Alphafold2 |
| PubMed ID | 18554256 |
Physicochemical Properties
| Residues | 19 |
|---|---|
| Sequence | GFKDLLKGAAKALVKAVLF |
| Molecular Weight | 1989.446 |
| Grand Average of Hydropathy | 0.868 |
| Isoelectric Point | 10.001 |
| Charge at pH 7.4 | 2.548 |
| Secondary Structure | Helix: 0.421, Turn: 0.105, Sheet: 0.421 |
| Instability Index | -13.358 |
| Aromaticity | 0.105 |
