BIOPEP-UWM: Report

ID 115
Name bitter peptide
sequence
IV
Function:
(Rcaf) 0.08
 
Number of residues
2
Activity code
bi
Activity :
bitter
Chemical mass 230.3031 Monoisotopic mass 230.1625
EC50 :
0.00 µM


Bibliographic data:
Authors
Ishibashi N., Ono I., Kato K., Shigenaga T., Shinoda I., Okai H., Fukui S.
Title
Role of the hydrophobic amino acid residue in the bitterness of peptides. Agric. Biol. Chem., 52, 91-94, 1988
Year Source
1988 Journal


Additional information:
BIOPEP database of sensory peptides and amino acids


SMILES: N[C@H](C(=O)N[C@H](C(=O)O)C(C)C)[C@H](CC)C

InChI=1S/C11H22N2O3/c1-5-7(4)8(12)10(14)13-9(6(2)3)11(15)16/h6-9H,5,12H2,1-4H3,(H,13,14)(H,15,16)/t7-,8-,9-/m0/s1

InChIKey: BCXBIONYYJCSDF-CIUDSAMLSA-N


Another references concerning bitterness:

Asao M., Iwamura H., Akamatsu M., Fujita T., 1987, Quantitative structure-activity relationships of the bitter thresholds of amino acids, peptides, and their derivatives. J. Med. Chem., 30, 1873-1879

Collantes E. R., Dunn W. J., 1995, Amino acid side chain descriptors for quantitative structure-activity relationship studies of peptide analogues. J. Med. Chem., 38, 2705-2713

Glucose uptake stimulating peptide according to BIOPEP database of bioactive peptides
Activator of u-Plasminogen (EC 3.4.21.73) (MEROPS ID: S01.231) according to BRENDA database
Inhibitor of Angiotensin-converting enzyme (EC 3.4.15.1) (MEROPS ID: XM02-001) according to AHTPDB database


Database reference:
ACToR: ID 41017-96-3

AHTPDB: ID 3859; 5439; 5449

BIOPEP database of bioactive peptides: ID 8322

BRENDA: Ligand Ile-Val

ChEBI: ID 74327

ChEMBL: ID CHEMBL293266

ChemIDplus: ID 041017963

ChemSpider: ID 395950

Crystallography Open Database (COD): ID 4101260

MMDB: ID 2959

PubChem: ID 449407

ZINC: ID ZINC04899467