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TargetAcetolactate synthase, chloroplastic
LigandBDBM50487162
Substrate/Competitorn/a
Meas. Tech.ChEMBL_908731 (CHEMBL3066158)
Ki 7750±n/a nM
Citation Chen, CNChen, QLiu, YCZhu, XLNiu, CWXi, ZYang, GF Syntheses and herbicidal activity of new triazolopyrimidine-2-sulfonamides as acetohydroxyacid synthase inhibitor. Bioorg Med Chem18:4897-904 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Acetolactate synthase, chloroplastic
Name:Acetolactate synthase, chloroplastic
Synonyms:AHAS | ALS | Acetolactate synthase | CSR1 | ILVB_ARATH | TZP5
Type:PROTEIN
Mol. Mass.:72585.19
Organism:Arabidopsis thaliana
Description:ChEMBL_934103
Residue:670
Sequence:
MAAATTTTTTSSSISFSTKPSPSSSKSPLPISRFSLPFSLNPNKSSSSSRRRGIKSSSPS
SISAVLNTTTNVTTTPSPTKPTKPETFISRFAPDQPRKGADILVEALERQGVETVFAYPG
GASMEIHQALTRSSSIRNVLPRHEQGGVFAAEGYARSSGKPGICIATSGPGATNLVSGLA
DALLDSVPLVAITGQVPRRMIGTDAFQETPIVEVTRSITKHNYLVMDVEDIPRIIEEAFF
LATSGRPGPVLVDVPKDIQQQLAIPNWEQAMRLPGYMSRMPKPPEDSHLEQIVRLISESK
KPVLYVGGGCLNSSDELGRFVELTGIPVASTLMGLGSYPCDDELSLHMLGMHGTVYANYA
VEHSDLLLAFGVRFDDRVTGKLEAFASRAKIVHIDIDSAEIGKNKTPHVSVCGDVKLALQ
GMNKVLENRAEELKLDFGVWRNELNVQKQKFPLSFKTFGEAIPPQYAIKVLDELTDGKAI
ISTGVGQHQMWAAQFYNYKKPRQWLSSGGLGAMGFGLPAAIGASVANPDAIVVDIDGDGS
FIMNVQELATIRVENLPVKVLLLNNQHLGMVMQWEDRFYKANRAHTFLGDPAQEDEIFPN
MLLFAAACGIPAARVTKKADLREAIQTMLDTPGPYLLDVICPHQEHVLPMIPSGGTFNDV
ITEGDGRIKY
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50487162
n/a
NameBDBM50487162
Synonyms:CHEMBL2251953
TypeSmall organic molecule
Emp. Form.C14H14ClN5O2S
Mol. Mass.351.811
SMILESCc1cc2nc(nn2c(C)n1)S(=O)(=O)Nc1cc(Cl)ccc1C
Structure
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