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   HEMOLYTIK: A Database of Hemolytic and Non-hemolytic Peptides

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1038 details
Primary information
Hemolytik ID1038
PMID10924341
YEAR2000
SEQUENCEILPWKWPWWPWRR
LENGTH13
NAMEIndolicidin
C-ter ModificationAmidation
N-ter ModificationFree
Linear/CyclicLinear
StereochemistryL
Modified ResiduesNone
FUNCTIONAntibacterial
ACTIVITY100% hemolysis at 100μg/ml
RBCs SOURCERat
Secondary information
PropertiesPhysico-Chemical details
STRUCTURE
Natural StructureFinal Structure
DSSP statesCCCCCCSSCSSCC
SMILESN[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c(C)c1CC)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c(C)c1CC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c(C)c1CC)C(=O)N[C@@H](Cc1c[nH]c(C)c1CC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c(C)c1CC)C(=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
1g89A NA NA NA NA NA NA NA
Reference Informaiton
ARTICLEAntibacterial and hemolytic activities of single tryptophan analogs of indolicidin.
AUTHORSSubbalakshmi C,Bikshapathy E,Sitaram N
JOURNALBiochem Biophys Res Commun. 2000 Aug 11;274(3):714-6.