Peptide Database

Peptide NamePrecursor of hemolytic peptide

Function Ontology

Antimicrobial

Antimicrobial ▸ Antifungal

Toxicity / Safety ▸ Blood cell toxicity ▸ Hemolysis ▸ Hemolytic

Standard StatusStandard

Sequence Length12 amino acids

Chemical FormulaC70H126N16O13

DescriptionStandard

        LKLFKKILKVLG
    

Molecular Weight1399.85 Da

Isoelectric Point (pI)10.48

Net Charge (pH 7.0)3.76

Net Charge (pH 7.4) 3.55

Charge Density (pH 7.0) 0.3130

GRAVY Index0.89

Hydrophobic Moment 0.81

Boman Index0.20

Instability Index-22.68

Aliphatic Index 186.67

Aromaticity 0.0833

Extinction Coeff. Reduced 0.00

Extinction Coeff. Oxidized 0.00

The radar chart summarizes major physicochemical dimensions for quick comparison, while exact numerical values remain listed on the left.

Amino Acid Composition

TPSA 487.50

LogP 1.01

H-bond Donors 17.0

H-bond Acceptors 17.0

Rotatable Bonds 52.0

Heavy Atoms 99.0

Ring Count 1.0

Amide Bonds 11.0

3D PDB MODEL

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2D CHEMICAL STRUCTURE

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RECORD: Rec_0120649 VERIFIED: YES

Provenance & Taxonomy

Organismsynthetic construct [Synthetic]

Tax ID32630.0

Structure & Mods

Configlinear peptide [Linear]

Chiralitycanonical L-amino-acid peptide [L]

Bio-Activity Profile

Function

Hemolytic

TargetFusarium oxysporum; Penicillium expansum; Aspergillus niger; Rhizopus stolonifer

PaperBadosa E., Ferr¨¦ R., Franc¨¦s J., Bardaj¨ª E., Feliu L., Planas M., Montesinos E.. Sporicidal activity of synthetic antifungal undecapeptides and control of Penicillium rot of apples. Applied and Environmental Microbiology, 75, 5563-5569, 2009. PMID19617390 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/19617390/

RECORD: Rec_0297235 VERIFIED: YES