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List of peptide properties
DFBP ID - DFBPVACO0001(Vasoconstriction peptide)
DFBP ID DFBPVACO0001
Peptide sequence ETPDCFWKYCV
Type Native peptide
Peptide/Function name Vasoconstriction peptide, Urotensin II
Function-activity relationship
Main bioactivity Vasoconstriction activity
Otheir bioactivity N.D
Calculated physicochemical properties
Three-letter amino acid Glu-Thr-Pro-Asp-Cys-Phe-Trp-Lys-Tyr-Cys-Val
Single-letter amino acid ETPDCFWKYCV
Peptide length 11
Peptide mass
Experimental mass Theoretical mass
1390.6 Da 1390.60 Da c
Net charge -1.1
Isoelectric point (pI) 4.1
IC50 N.D
pIC50 N.D
GRAVY -0.3091 c
Hydrophilic residue ratio 36.36% c
Peptide calculator
To calculate the physicochemical properties of bioactive peptide.
Peptide source & Food-borne protein(s) search
Classification Animal, Fish
Organism/Source Fish spinal cords
Precursor protein Urotensin-II (U-II)
Residue position N.D
Precursor protein(s) search
No matching precursor protein found
Link-research
There are no literature reports on the discovery of this sequence in other food-source proteins.
Biological/Functional activity & target protein
Vasoconstriction activity

The potency of vasoconstriction of U-II is an order of magnitude greater than that of endothelin-1, making human U-II the most potent mammalian vasoconstrictor identified so far. Systemic administration is associated with profound cardiovascular collapse. As human U-II-like immunoreactivity is found within cardiac and vascular tissue (including coronary atheroma), this peptide may influence cardiovascular homeostasis and pathology (for example, in ischaemic heart disease and congestive heart failure).

Specific target protein(s) N.D
Taste properties & Structure
Bitterness
Literature report N.D
Bitter prediction tools Bitter taste prediction
SMILES N[C@@]([H])(CCC(=O)O)C(=O)N[C@@]([H])([C@]([H])(O)C)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(CC(=O)O)C(=O)N[C@@]([H])(CS)C(=O)N[C@@]([H])(Cc1ccccc1)C(=O)N[C@@]([H])(CC(=CN2)C1=C2C=CC=C1)C(=O)N[C@@]([H])(CCCCN)C(=O)N[C@@]([H])(Cc1ccc(O)cc1)C(=O)N[C@@]([H])(CS)C(=O)N[C@@]([H])(C(C)C)C(=O)O
Preparation method
Mode of preparation Peptide synthesis
Enzyme(s)/starter culture Human U-II peptidyl resin was synthesized (Milipore/Biosearch 9600 synthesizer), cleaved and de-protected before purification by reverse-phase HPLC. All other peptides were from Bachem.
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] 3988, 3989
APD [D2] -
BioPepDB [D3] -
MBPDB [D4] -
Reference(s)
Primary literature Ames RS, Sarau HM, Chambers JK, Willette RN, Aiyar NV, Romanic AM, Louden CS, Foley JJ, Sauermelch CF, Coatney RW, Ao Z, Disa J, Holmes SD, Stadel JM, Martin JD, Liu WS, Glover GI, Wilson S, McNulty DE, Ellis CE, Elshourbagy NA, Shabon U, Trill JJ, Hay DW, Ohlstein EH, Bergsma DJ, Douglas SA. Human urotensin-II is a potent vasoconstrictor and agonist for the orphan receptor GPR14. Nature. 1999 Sep 16;401(6750):282-6.
PMID: 10499587
Other literature(s)

[1] Bern, H. A., Pearson, D., Larson, B. A. & Nishioka, R. S. Neurohormones from fish tails: the caudal neurosecretory system. I. ''Urophysiology'' and the caudal neurosecretory system of fishes. Recent Prog. Horm. Res. 41, 533-552 (1985).

PubDate 1999
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