Peptide Database

Peptide NameHPA3NT3-F8A

Function Ontology

Antimicrobial

Antimicrobial ▸ Antibacterial

Antimicrobial ▸ Antibacterial ▸ Anti-Gram-negative

Antimicrobial ▸ Antibacterial ▸ Anti-Gram-positive

Antimicrobial ▸ Antifungal

Toxicity / Safety ▸ Blood cell toxicity ▸ Hemolysis ▸ Hemolytic

Standard StatusStandard

Sequence Length15 amino acids

Chemical FormulaC98H159N27O17

DescriptionStandard

        FKRLKKLAKKIWNWK
    

Molecular Weight1987.48 Da

Isoelectric Point (pI)11.43

Net Charge (pH 7.0)6.75

Net Charge (pH 7.4) 6.54

Charge Density (pH 7.0) 0.4503

GRAVY Index-1.10

Hydrophobic Moment 0.86

Boman Index-0.36

Instability Index5.38

Aliphatic Index 84.67

Aromaticity 0.2000

Extinction Coeff. Reduced 11000.00

Extinction Coeff. Oxidized 11000.00

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

Amino Acid Composition

TPSA 763.41

LogP -1.05

H-bond Donors 28.0

H-bond Acceptors 24.0

Rotatable Bonds 71.0

Heavy Atoms 142.0

Ring Count 5.0

Amide Bonds 15.0

3D PDB MODEL

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2D CHEMICAL STRUCTURE

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RECORD: Rec_0253546 VERIFIED: YES

Provenance & Taxonomy

OrganismHelicobacter pylori [Bacterium]

Structure & Mods

Configtopology not specified [Not included yet]

Chiralitystereochemistry not specified [Other]

Bio-Activity Profile

Function

Antimicrobial Antibacterial Anti-Gram-positive Anti-Gram-negative Antifungal

TargetAspergillus awamori

Activity16 μM

MethodMIC

PaperAntimicrobial HPA3NT3 peptide analogs: placement of aromatic rings and positive charges are key determinants for cell selectivity and mechanism of action. Biochim Biophys Acta. 2013 Feb;1828(2):443-454. doi: 10.1016/j.bbamem.2012.09.005. PMID: 22982494. PMID22982494 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/22982494/

RECORD: Rec_0265492 VERIFIED: YES

Provenance & Taxonomy

OrganismHelicobacter pylori [Bacterium]

Structure & Mods

Configtopology not specified [Not included yet]

Chiralitystereochemistry not specified [Other]

Bio-Activity Profile

Function

Antimicrobial Antibacterial Anti-Gram-positive Anti-Gram-negative Antifungal

TargetCandida albicans

Activity8 μM

MethodMIC

PaperAntimicrobial HPA3NT3 peptide analogs: placement of aromatic rings and positive charges are key determinants for cell selectivity and mechanism of action. Biochim Biophys Acta. 2013 Feb;1828(2):443-454. doi: 10.1016/j.bbamem.2012.09.005. PMID: 22982494. PMID22982494 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/22982494/

RECORD: Rec_0304537 VERIFIED: YES

Provenance & Taxonomy

OrganismHelicobacter pylori [Bacterium]

Structure & Mods

Configlinear peptide [Linear]

Chiralitycanonical L-amino-acid peptide [L]

C-TermAmidation

Bio-Activity Profile

Function

Antimicrobial Antibacterial Antifungal Anti-Gram-positive Anti-Gram-negative

TargetA. awamori

Activity16 μM

MethodMIC

RECORD: Rec_0340070 VERIFIED: YES

Provenance & Taxonomy

OrganismHelicobacter pylori [Bacterium]

Structure & Mods

Configlinear peptide [Linear]

Chiralitycanonical L-amino-acid peptide [L]

C-TermAmidation

Bio-Activity Profile

Function

Antimicrobial Antibacterial Antifungal Anti-Gram-positive Anti-Gram-negative

TargetBacillus subtilis

Activity4 μM

MethodMIC

RECORD: Rec_0345559 VERIFIED: YES

Provenance & Taxonomy

OrganismHelicobacter pylori [Bacterium]

Structure & Mods

Configlinear peptide [Linear]

Chiralitycanonical L-amino-acid peptide [L]

C-TermAmidation

Bio-Activity Profile

Function

Antimicrobial Antibacterial Antifungal Anti-Gram-positive Anti-Gram-negative

TargetStaphylococcus aureus

Activity4 μM

MethodMIC

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