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List of peptide properties
DFBP ID - DFBPOPIO0010(Opioid peptide)
DFBP ID DFBPOPIO0010
Peptide sequence YYGY
Type Native peptide
Peptide/Function name Opioid peptide, Lactoferroxin analogues
Function-activity relationship
Main bioactivity Opioid activity
Otheir bioactivity N.D
Calculated physicochemical properties
Three-letter amino acid Tyr-Tyr-Gly-Tyr
Single-letter amino acid YYGY
Peptide length 4
Peptide mass
Experimental mass Theoretical mass
N.D 564.59 Da c
Net charge 0.00 c
Isoelectric point (pI) 5.83 c
IC50 N.D
pIC50 N.D
GRAVY -1.0750 c
Hydrophilic residue ratio 25% c
Peptide calculator
To calculate the physicochemical properties of bioactive peptide.
Peptide source & Food-borne protein(s) search
Classification Human
Organism/Source Human whey protein
Precursor protein Lactoferrin
Residue position f(537-540)
Precursor protein(s) search
Source.1: DFBPPR1485 ---- Plant proteins ---- Pheophorbide a oxygenase, chloroplastic
Source.2: DFBPPR3630 ---- Plant proteins ---- Probable anion transporter 6
Source.3: DFBPPR4149 ---- Plant proteins ---- Probable anion transporter 7
Source.4: DFBPPR5107 ---- Plant proteins ---- Cytochrome c oxidase subunit 2, mitochondrial
Source.5: DFBPPR7596 ---- Milk proteins ---- Lactotransferrin
Source.6: DFBPPR7658 ---- Milk proteins ---- Lactotransferrin
Source.7: DFBPPR7669 ---- Milk proteins ---- Lactotransferrin
Source.8: DFBPPR7683 ---- Milk proteins ---- Lactotransferrin
Source.9: DFBPPR7713 ---- Milk proteins ---- Lactotransferrin
Source.10: DFBPPR8500 ---- Milk proteins ---- Lactotransferrin
Source.11: DFBPPR16712 ---- Animal proteins ---- RNA-binding protein 47
Source.12: DFBPPR18952 ---- Animal proteins ---- Serotransferrin
Source.13: DFBPPR19309 ---- Animal proteins ---- Cadherin-related family member 1
Source.14: DFBPPR19953 ---- Animal proteins ---- Neurolysin, mitochondrial
Source.15: DFBPPR20109 ---- Animal proteins ---- Ovarian cancer G-protein coupled receptor 1
Source.16: DFBPPR20426 ---- Animal proteins ---- Thimet oligopeptidase
Source.17: DFBPPR8617 ---- Animal proteins ---- Neurolysin, mitochondrial
Source.18: DFBPPR9015 ---- Animal proteins ---- Serotransferrin
Source.19: DFBPPR9255 ---- Animal proteins ---- Thimet oligopeptidase
Source.20: DFBPPR11405 ---- Animal proteins ---- Cadherin-related family member 1
Source.21: DFBPPR12113 ---- Animal proteins ---- Protein DENND6A
Source.22: DFBPPR12251 ---- Animal proteins ---- Serotransferrin
Source.23: DFBPPR12388 ---- Animal proteins ---- Voltage-dependent L-type calcium channel subunit alpha-1S
Source.24: DFBPPR12911 ---- Animal proteins ---- Neurolysin, mitochondrial
Source.25: DFBPPR13263 ---- Animal proteins ---- Serotransferrin
Source.26: DFBPPR14003 ---- Animal proteins ---- Dihydropyridine-sensitive L-type skeletal muscle calcium channel subunit alpha-1
Source.27: DFBPPR14077 ---- Marine protein ---- Serotransferrin-1
Source.28: DFBPPR14080 ---- Marine protein ---- Serotransferrin-2
Source.29: DFBPPR14903 ---- Microorganism protein ---- Transcription elongation factor SPT6
Source.30: DFBPPR15143 ---- Microorganism protein ---- Low-affinity glucose transporter
Link-research
There are no literature reports on the discovery of this sequence in other food-source proteins.
Biological/Functional activity & target protein
Opioid activity
  • The effective bioactive sequence of the peptide is YYGY-OCH3.

  • YYGY-OCH3 have opioid activity as an antagonist peptide and had somewhat higher degrees of preference for κ-receptors than for μ-receptors. As shown in table 1.

Tabel 1 The opioid activity of peptide
Peptides
Receptor affinity (IC50, uM)
Antagonism (pA2)
μ
δ
κ
μ, GPI a
δ, MVD b
κ, RVD c
[3H]DAGO
[3H]DADLE[3H]EKCDAGO
DADLE
Dyn. A[1-13]
YYGY-OCH3
12.0
17.0
131
5.27
4.62
4.60
a Guinea pig ileum. b Mouse vas deferens. c Rabbit vas deferens.
Specific target protein(s) Specific Target Protein(s):
Kappa-type opioid receptor
Mu-type opioid receptor
Taste properties & Structure
Bitterness
Literature report N.D
Bitter prediction tools Bitter taste prediction
SMILES N[C@@]([H])(Cc1ccc(O)cc1)C(=O)N[C@@]([H])(Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@]([H])(Cc1ccc(O)cc1)C(=O)O
Preparation method
Mode of preparation

Synthesis peptide

Enzyme(s)/starter culture

The peptide was synthesized by conventional solid-phase methods with tert-butyloxy-carbonyl-Tyr (Cl2Bzl) resin as a starting material.

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] -
APD [D2] -
BioPepDB [D3] -
MBPDB [D4] -
Reference(s)
Primary literature Tani F, Iio K, Chiba H, Yoshikawa M. Isolation and characterization of opioid antagonist peptides derived from human lactoferrin. Agric Biol Chem. 1990 Jul;54(7):1803-10.
PMID: 1369293
Other literature(s) N.D
PubDate 1990
Copyright © 2020. Record / license number: Chongqing ICP No. 2000214