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Target1-acyl-sn-glycerol-3-phosphate acyltransferase beta
LigandBDBM50141287
Substrate/Competitorn/a
Meas. Tech.ChEBML_100169
IC50 60±n/a nM
Citation Gong, BHong, FKohm, CBonham, LKlein, P Synthesis and SAR of 2-arylbenzoxazoles, benzothiazoles and benzimidazoles as inhibitors of lysophosphatidic acid acyltransferase-beta. Bioorg Med Chem Lett14:1455-9 (2004) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
1-acyl-sn-glycerol-3-phosphate acyltransferase beta
Name:1-acyl-sn-glycerol-3-phosphate acyltransferase beta
Synonyms:1-acylglycerol-3-phosphate O-acyltransferase beta | AGPAT2 | PLCB_HUMAN
Type:PROTEIN
Mol. Mass.:30924.09
Organism:Homo sapiens (Human)
Description:ChEMBL_321473
Residue:278
Sequence:
MELWPCLAAALLLLLLLVQLSRAAEFYAKVALYCALCFTVSAVASLVCLLRHGGRTVENM
SIIGWFVRSFKYFYGLRFEVRDPRRLQEARPCVIVSNHQSILDMMGLMEVLPERCVQIAK
RELLFLGPVGLIMYLGGVFFINRQRSSTAMTVMADLGERMVRENLKVWIYPEGTRNDNGD
LLPFKKGAFYLAVQAQVPIVPVVYSSFSSFYNTKKKFFTSGTVTVQVLEAIPTSGLTAAD
VPALVDTCHRAMRTTFLHISKTPQENGATAGSGVQPAQ
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  Blast E-value cutoff:
BDBM50141287
n/a
NameBDBM50141287
Synonyms:5TT4A4MBLR | CHEMBL36501 | CT 32228 | CT-32228 | HE066284 | N-(4-Bromo-phenyl)-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazine-2,4-diamine
TypeSmall organic molecule
Emp. Form.C16H13BrClN5
Mol. Mass.390.665
SMILESCc1ccc(Cl)cc1-c1nc(N)nc(Nc2ccc(Br)cc2)n1
Structure
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