BIOPEP-UWM: Report

ID 8
Name bitter peptide
sequence
RG
Function:
(Rcaf) 0.13
 
Number of residues
2
Activity code
bi
Activity :
bitter
Chemical mass 231.2516 Monoisotopic mass 231.1328
EC50 :
0.00 µM


Bibliographic data:
Authors
Otagiri K., Nosho Y., Shinoda I., Fukui H., Okai H.
Title
Studies on a model bitter peptides including arginine, proline and phenylalanine residues. I. Bitter taste of di- and tripeptides and bitterness increase of the model peptides by extension of the peptide chain. Agric. Biol. Chem., 49, 1019-1026, 1985
Year Source
1985 Journal


Additional information:
BIOPEP-UWM database of sensory peptides and amino acids

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

InChI=1S/C8H17N5O3/c9-5(2-1-3-12-8(10)11)7(16)13-4-6(14)15/h5H,1-4,9H2,(H,13,16)(H,14,15)(H4,10,11,12)/t5-/m0/s1

InChIKey: XUUXCWCKKCZEAW-YFKPBYRVSA-N


Inhibitor of the Leucyltransferase (EC 2.3.2.6) according to the BRENDA database
Inhibitor of the angiotensin-converting enzyme (EC 3.4.15.1) (MEROPS ID: M02-001) according to the AHTPDB database, the BIOPEP-UWM database of bioactive peptides (ID 9173), the EROP-Moscow database
Inhibitor of Dipeptidyl Peptidase IV (EC 3.4.14.5) (MEROPS ID: S09.003) according to the BIOPEP-UWM database of bioactive peptides (ID 8882)
Inhibitor of citrulline uptake in yeasts according to the ChEMBL database; the PubChem database

Salty taste enhancing peptide according to the BIOPEP database of sensory peptides and amino acids (ID 422)


Database reference:
ACToR: ID 2418-67-9

AHTPDB: ID 1479; 5433; 5448

BindingDB: ID 50188522

BioPepDB: ID biopep01186

BIOPEP-UWM database of bioactive peptides: ID 8882, 9173

BIOPEP-UWM database of sensory peptides and amino acids: ID 422

BRENDA: Ligand Arg-Gly

ChEMBL: ID CHEMBL382777

ChemIDplus: ID 002418679

ChemSpider: ID 4251526

EPA DSSTox: ID DTXCID70101376

EROP-Moscow: ID E10392

J-GLOBAL ID: 200907074614271802

Nikkaji: ID J80.480K

PubChem: CID 5074903

SATPdb: ID satpdb12415

SureChEMBL: ID SCHEMBL2117673

ZINC: ID ZINC02545093