Primary information |
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Hemolytik ID | 3889 |
PMID | 11318033 |
YEAR | 2001 |
SEQUENCE | QlLVDlI |
LENGTH | 7 |
NAME | Lichenysin |
C-ter Modification | Free |
N-ter Modification | Free |
Linear/Cyclic | Cyclic |
Stereochemistry | Mix (Contains both L and D amino acids) |
Modified Residues | None |
FUNCTION | Chelating agent |
ACTIVITY | 100% hemolysis at 15μM |
RBCs SOURCE | Human |
Secondary information |
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Properties | Physico-Chemical details |
STRUCTURE | |
DSSP states | CCSGGGC |
SMILES | N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)O |
External Links |
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PDB exact | PDB partial | SP exact | SP partial | TrEMBL exact | TrEMBL partial | IEDB exact | IEDB partial |
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Reference Informaiton |
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ARTICLE | Lichenysin: a more efficient cation chelator than surfactin. |
AUTHORS | Grangemard I,Wallach J,Maget-Dana R, Peypoux, ,Peypoux |
JOURNAL | Appl Biochem Biotechnol. 2001 Mar;90(3):199-210. |