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List of peptide properties
DFBP ID - DFBPAGPE0007(Alpha-gliadin peptide)
DFBP ID DFBPAGPE0007
Peptide sequence LGQQQPFPPQQPYPQPQPFPSQQPY
Type Native peptide
Peptide/Function name α-Gliadin peptide, PEPTIDE XT (31-55)
Function-activity relationship
Main bioactivity

Coeliac toxic activity

Otheir bioactivity N.D
Calculated physicochemical properties
Three-letter amino acid Leu-Gly-Gln-Gln-Gln-Pro-Phe-Pro-Pro-Gln-Gln-Pro-Tyr-Pro-Gln-Pro-Gln-Pro-Phe-Pro-Ser-Gln-Gln-Pro-Tyr
Single-letter amino acid LGQQQPFPPQQPYPQPQPFPSQQPY
Peptide length 25
Peptide mass
Experimental mass Theoretical mass
2923.2180 Da 2923.24 Da c
Net charge 0.00 c
Isoelectric point (pI) 5.87 c
IC50 N.D
pIC50 N.D
GRAVY -1.6120 c
Hydrophilic residue ratio 52% c
Peptide calculator
To calculate the physicochemical properties of bioactive peptide.
Peptide source & Food-borne protein(s) search
Classification Plant
Organism/Source Wheat gluten
Precursor protein α-Gliadin
Residue position

f(31-55) [1]

Precursor protein(s) search
Link-research
Link 1: DFBPAGPE0240----Wheat----α-Gliadin
Biological/Functional activity & target protein
Coeliac toxic activity

These peptides were tested for toxicity in celiac disease by organ culture of biopsied small intestinal tissues taken Corn patients with active celiac disease. Enterocyte height was used as a measure of peptide effect on cultured tissue. The peptide LGQQQPFPPQQPYPQPQPFPSQQPY significantly inhibited increase of enterocyte height in the cultures and were considered toxic on this basis.

Specific target protein(s) N.D
Taste properties & Structure
Bitterness
Literature report N.D
Bitter prediction tools Bitter taste prediction
SMILES N[C@@]([H])(CC(C)C)C(=O)NCC(=O)N[C@@]([H])(CCC(=O)N)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(Cc1ccccc1)C(=O)N1[C@@]([H])(CCC1)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(Cc1ccc(O)cc1)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(Cc1ccccc1)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(CO)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(Cc1ccc(O)cc1)C(=O)O
Preparation method
Mode of preparation

Enzymatic hydrolysis

Enzyme(s)/starter culture

The peptide was prepared from α-gliadin by cleavage of the protein with cyanogen bromide and chymotrypsin.

Stability & Cytotoxicity
Peptide stability
Literature report: N.D
EHP-Tool: Enzymatic Hydrolysis Prediction Tool (EHP-Tool)
Peptide cytotoxicity
Literature report: N.D
Prediction: ToxinPred
Additional information
Additional information N.D
Database cross-references
BIOPEP-UWM [D1] 3640, 7468
APD [D2] -
BioPepDB [D3] -
MBPDB [D4] -
Reference(s)
Primary literature de Ritis G, Auricchio S, Jones HW, Lew EJ, Bernardin JE, Kasarda DD. In vitro (organ culture) studies of the toxicity of specific A-gliadin peptides in celiac disease. Gastroenterology. 1988 Jan;94(1):41-9.
PMID: 3335296
Other literature(s)

[1] Kasarda D D, Okita T W, Bernardin J E, et al. Nucleic Acid (cDNA) and Amino Acid Sequences of α -Type Gliadins from Wheat (Triticum aestivum)[J]. Proceedings of the National Academy of Sciences of the United States of America, 1984, 81(15):4712-4716.

PubDate 1988
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