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1866 details
Primary information
Hemolytik ID1866
PMID15003352
YEAR2004
SEQUENCERLRLRIGRR
LENGTH9
NAME9-Fluorenylmethoxycarbonyl (F-moc)
C-ter ModificationAmidation
N-ter ModificationFree
Linear/CyclicCyclic
StereochemistryL
Modified ResiduesNone
FUNCTIONAntimicrobial
ACTIVITY0% hemolysis at 100µg/ml (non-hemolytic)
RBCs SOURCERabbit
Secondary information
PropertiesPhysico-Chemical details
STRUCTURE
Natural StructureFinal Structure
DSSP statesCCCCCCCCC
SMILESN[C@@H](CCCN=C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CCCN=C)C(=O)O
External Links
PDB exactPDB partialSP exactSP partialTrEMBL exactTrEMBL partialIEDB exactIEDB partial
NA NA NA NA NA NA NA NA
Reference Informaiton
ARTICLEIn vitro and in vivo activity of antimicrobial peptides synthesized based on the insect defensin.
AUTHORSSaido-Sakanaka H,Ishibashi J,Momotani E,Amano F
JOURNALPeptides. 2004 Jan;25(1):19-27.