Peptide Database

Peptide NameUnnamed

Function Ontology

Antimicrobial

Enzyme modulation ▸ Enzyme inhibition ▸ Inhibitor Of Cytosol Alanyl Aminopeptidase

Enzyme modulation ▸ Enzyme inhibition ▸ Tripeptidyl Peptidase II Inhibitory

Sensory / Food function ▸ Taste-active peptide ▸ Sweet peptide

Standard StatusStandard

Sequence Length3 amino acids

Chemical FormulaC9H17N3O4

DescriptionStandard

AAA

Molecular Weight231.25 Da

Isoelectric Point (pI)5.57

Net Charge (pH 7.0)-0.20

Net Charge (pH 7.4) -0.39

Charge Density (pH 7.0) -0.0680

GRAVY Index1.80

Hydrophobic Moment 0.13

Boman Index0.62

Instability Index6.67

Aliphatic Index 100.00

Aromaticity 0.0000

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 121.52

LogP -1.57

H-bond Donors 4.0

H-bond Acceptors 4.0

Rotatable Bonds 5.0

Heavy Atoms 16.0

Ring Count 0.0

Amide Bonds 2.0

3D PDB MODEL

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2D CHEMICAL STRUCTURE

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RECORD: Rec_0070556 VERIFIED: YES

Provenance & Taxonomy

Organismnot reported [other]

Structure & Mods

Configlinear peptide [Linear]

Chiralitycanonical L-amino-acid peptide [L]

Bio-Activity Profile

Function

Inhibitor Of Cytosol Alanyl Aminopeptidase

TargetCytosol alanyl aminopeptidase

RECORD: Rec_0168085 VERIFIED: YES

Provenance & Taxonomy

Organismsynthetic construct [Synthetic]

Tax ID32630

Structure & Mods

Configlinear peptide [Linear]

Chiralitycanonical L-amino-acid peptide [L]

Bio-Activity Profile

Function

Antimicrobial

RECORD: Rec_0227260 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

Tripeptidyl Peptidase II Inhibitory

TargetTripeptidyl peptidase II / CCK-8-inactivating peptidase

PaperGanellin C. R., Bishop P. B., Bambal R. B., Chan S. M., Law J. K., Marabout B., Luthra P. M., Moore A. N., Peschard O., Bourgeat P., Rose C., Vargas F.. Inhibitors of tripeptidyl peptidase II. 2. Generation of the first novel lead inhibitor of cholecystokinin-8-inactivating peptidase: a strategy for the design of peptidase inhibitors. J. Med. Chem., 43, 664-674, 2000. PMID10691692 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/10691692/

RECORD: Rec_0350634 VERIFIED: YES

Provenance & Taxonomy

Organismnot reported [other]

FamilySensory peptide

Structure & Mods

Configlinear contiguous peptide sequence [Linear]

Chiralitycanonical L-amino-acid peptide [L]

Bio-Activity Profile

Function

Sweet