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TargetGlutaminase kidney isoform, mitochondrial
LigandBDBM50400050
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1663490 (CHEMBL4013171)
IC50 81±n/a nM
Citation Yeh, TKKuo, CCLee, YZKe, YYChu, KFHsu, HYChang, HYLiu, YWSong, JSYang, CWLin, LMSun, MWu, SHKuo, PCShih, CChen, CTTsou, LKLee, SJ Design, Synthesis, and Evaluation of Thiazolidine-2,4-dione Derivatives as a Novel Class of Glutaminase Inhibitors. J Med Chem60:5599-5612 (2017) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Glutaminase kidney isoform, mitochondrial
Name:Glutaminase kidney isoform, mitochondrial
Synonyms:GLS | GLS1 | GLSK_HUMAN | Glutaminase 1 | K-glutaminase | KIAA0838 | L-glutamine amidohydrolase
Type:Protein
Mol. Mass.:73471.89
Organism:Homo sapiens (Human)
Description:O94925
Residue:669
Sequence:
MMRLRGSGMLRDLLLRSPAGVSATLRRAQPLVTLCRRPRGGGRPAAGPAAAARLHPWWGG
GGWPAEPLARGLSSSPSEILQELGKGSTHPQPGVSPPAAPAAPGPKDGPGETDAFGNSEG
KELVASGENKIKQGLLPSLEDLLFYTIAEGQEKIPVHKFITALKSTGLRTSDPRLKECMD
MLRLTLQTTSDGVMLDKDLFKKCVQSNIVLLTQAFRRKFVIPDFMSFTSHIDELYESAKK
QSGGKVADYIPQLAKFSPDLWGVSVCTVDGQRHSTGDTKVPFCLQSCVKPLKYAIAVNDL
GTEYVHRYVGKEPSGLRFNKLFLNEDDKPHNPMVNAGAIVVTSLIKQGVNNAEKFDYVMQ
FLNKMAGNEYVGFSNATFQSERESGDRNFAIGYYLKEKKCFPEGTDMVGILDFYFQLCSI
EVTCESASVMAATLANGGFCPITGERVLSPEAVRNTLSLMHSCGMYDFSGQFAFHVGLPA
KSGVAGGILLVVPNVMGMMCWSPPLDKMGNSVKGIHFCHDLVSLCNFHNYDNLRHFAKKL
DPRREGGDQRVKSVINLLFAAYTGDVSALRRFALSAMDMEQRDYDSRTALHVAAAEGHVE
VVKFLLEACKVNPFPKDRWNNTPMDEALHFGHHDVFKILQEYQVQYTPQGDSDNGKENQT
VHKNLDGLL
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50400050
n/a
NameBDBM50400050
Synonyms:CHEMBL2177757 | US10793535, Cmpd ID 1 | US11191732, Example BPTES | US8604016, 1 | US9938267, Cmpd ID 1
TypeSmall organic molecule
Emp. Form.C24H24N6O2S3
Mol. Mass.524.681
SMILESO=C(Cc1ccccc1)Nc1nnc(CCSCCc2nnc(NC(=O)Cc3ccccc3)s2)s1
Structure
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