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 FormulaC79H125N17O14

DescriptionStandard

        WKLFKKILKYLG
    

Molecular Weight1536.94 Da

Isoelectric Point (pI)10.18

Net Charge (pH 7.0)3.76

Net Charge (pH 7.4) 3.54

Charge Density (pH 7.0) 0.3129

GRAVY Index0.04

Hydrophobic Moment 0.81

Boman Index0.11

Instability Index-8.53

Aliphatic Index 130.00

Aromaticity 0.2500

Extinction Coeff. Reduced 6990.00

Extinction Coeff. Oxidized 6990.00

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

Amino Acid Composition

TPSA 523.52

LogP 1.98

H-bond Donors 19.0

H-bond Acceptors 18.0

Rotatable Bonds 53.0

Heavy Atoms 110.0

Ring Count 4.0

Amide Bonds 11.0

3D PDB MODEL

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2D CHEMICAL STRUCTURE

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RECORD: Rec_0029141 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_0319647 VERIFIED: YES