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   HEMOLYTIK: A Database of Hemolytic and Non-hemolytic Peptides

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3456 details
Primary information
Hemolytik ID3456
PMID10604598
YEAR1999
SEQUENCECKLLKTFLSKWIC
LENGTH13
NAMESAC
C-ter ModificationAmidation
N-ter ModificationFree
Linear/CyclicCyclic
StereochemistryL
Modified ResiduesNone
FUNCTIONAntibacterial
ACTIVITY100% hemolysis at 5μg/ml
RBCs SOURCERat
Secondary information
PropertiesPhysico-Chemical details
STRUCTURE
Natural StructureFinal Structure
DSSP statesCCHHHHTGGGTTC
SMILESN[C@@H](CS)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c(C)c1CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CS)C(=O)O
External Links
PDB exactPDB partialSP exactSP partialTrEMBL exactTrEMBL partialIEDB exactIEDB partial
NA NA NA NA NA NA NA NA
Reference Informaiton
ARTICLEConsequences of introducing a disulfide bond into an antibacterial and hemolytic peptide.
AUTHORSKrishnakumari V,Sharadadevi A,Sitaram N
JOURNALJ Pept Res. 1999 Dec;54(6):528-35.