| DFBP ID - DFBPCYPE0001(Cytotoxic peptide) |
| DFBP ID |
DFBPCYPE0001 |
| Peptide sequence |
VAWRNRCKGTD |
| Type |
Native peptide |
| Peptide/Function name |
Cytotoxic peptide |
|
| Function-activity relationship |
| Main bioactivity |
Cytotoxic peptide activity |
| Otheir bioactivity |
Antioxidative activity [D1], Multifunctional activity [D2] |
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| Calculated physicochemical properties |
| Three-letter amino acid |
Val-Ala-Trp-Arg-Asn-Arg-Cys-Lys-Gly-Thr-Asp |
| Single-letter amino acid |
VAWRNRCKGTD |
| Peptide length |
11 |
| Peptide mass |
| Experimental mass |
Theoretical mass |
| 1306.0 Da |
1305.48 Da c |
|
| Net charge |
0.00 c |
| Isoelectric point (pI) |
10.05 c |
| IC50 |
N.D |
| pIC50 |
N.D |
| GRAVY |
-1.2182 c |
| Hydrophilic residue ratio |
36.36% c |
| Peptide calculator |
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| Peptide source & Food-borne protein(s) search |
| Classification |
Animal |
| Organism/Source |
Hen |
| Precursor protein |
Egg-white lysozyme |
| Residue position |
f(109-119)
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Precursor protein(s) search
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Link-research
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There are no literature reports on the discovery of this sequence in other food-source proteins. |
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| Biological/Functional activity & target protein |
| Cytotoxic activity |
Oxygen radical absorbance capacity-fluorescein (ORAC-FL) assay
| The peptide presented antioxidant activity with values of 1.970 ± 0.171 umol Trolox/umol peptide.
| | Thiobarbituric acid reactive substances (TBARS) in zebrafish larvae | The peptide was found to efficiently inhibit lipid perosidation (36.8 % inhibition of lipid peroxidation). | Toxicity in the Zebrafish model (Danio rerio) | The peptide was not toxic in zebrafish eggs and larvae at concentrations lower than 50 ug/ml. Concentrations higher than 50 ug/ml was toxic for both zebrafish eggs and larvae.
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| Specific target protein(s) |
N.D |
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| Taste properties & Structure |
| Bitterness |
| Literature report |
N.D |
| Bitter prediction tools |
Non-bitter taste prediction |
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| SMILES |
N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(C)C(=O)N[C@@]([H])(CC(=CN2)C1=C2C=CC=C1)C(=O)N[C@@]([H])(CCCNC(=N)N)C(=O)N[C@@]([H])(CC(=O)N)C(=O)N[C@@]([H])(CCCNC(=N)N)C(=O)N[C@@]([H])(CS)C(=O)N[C@@]([H])(CCCCN)C(=O)NCC(=O)N[C@@]([H])([C@]([H])(O)C)C(=O)N[C@@]([H])(CC(=O)O)C(=O)O |
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| Preparation method |
| Mode of preparation |
Enzymatic hydrolysis
|
| Enzyme(s)/starter culture |
Lysozyme was hydrolyzed in situ with pepsin to generate positive charged peptides. |
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| Stability & Cytotoxicity |
| Peptide stability |
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| Peptide cytotoxicity |
| Literature report: |
In the zebrafish larvae test, this peptide does not present toxicity at a concentration of 50 ug/ml for zebrafish eggs. However, concentration higher than 50 ug/ml of peptide was cytotoxic to zebrafish egg after 24 hours of incubation.
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| Prediction: |
ToxinPred |
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| Additional information |
| Additional information |
N.D |
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| Database cross-references |
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| Reference(s) |
| Primary literature |
Carrillo, W., Gómez-Ruiz, J.A., Miralles, B., Ramos, M., Barrio, D., Recio, I. Identification of antioxidant peptides of hen egg-white lysozyme and evaluation of inhibition of lipid peroxidation and cytotoxicity in the Zebrafish model. European Food Research and Technology. 2016, 242, 1777-85.
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| Other literature(s) |
N.D |
| PubDate |
2016 |
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