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TargetPantothenate synthetase
LigandBDBM50497766
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1452794 (CHEMBL3365136)
IC50>25000±n/a nM
Citation Samala, GNallangi, RDevi, PBSaxena, SYadav, RSridevi, JPYogeeswari, PSriram, D Identification and development of 2-methylimidazo[1,2-a]pyridine-3-carboxamides as Mycobacterium tuberculosis pantothenate synthetase inhibitors. Bioorg Med Chem22:4223-32 (2014) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Pantothenate synthetase
Name:Pantothenate synthetase
Synonyms:Chain A, Crystal Structure Of A Pantothenate Synthetase, Apo Enzyme In C2 Space Group | PANC_MYCTU | Pantothenate synthetase | panC
Type:n/a
Mol. Mass.:32675.10
Organism:Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv)
Description:ChEMBL_102878
Residue:309
Sequence:
MTIPAFHPGELNVYSAPGDVADVSRALRLTGRRVMLVPTMGALHEGHLALVRAAKRVPGS
VVVVSIFVNPMQFGAGEDLDAYPRTPDDDLAQLRAEGVEIAFTPTTAAMYPDGLRTTVQP
GPLAAELEGGPRPTHFAGVLTVVLKLLQIVRPDRVFFGEKDYQQLVLIRQLVADFNLDVA
VVGVPTVREADGLAMSSRNRYLDPAQRAAAVALSAALTAAAHAATAGAQAALDAARAVLD
AAPGVAVDYLELRDIGLGPMPLNGSGRLLVAARLGTTRLLDNIAIEIGTFAGTDRPDGYR
AILESHWRN
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  Blast E-value cutoff:
BDBM50497766
n/a
NameBDBM50497766
Synonyms:CHEMBL3212161
TypeSmall organic molecule
Emp. Form.C16H13N5O3
Mol. Mass.323.3061
SMILESCc1nc2ccccn2c1C(=O)N\N=C\c1ccc(cc1)[N+]([O-])=O
Structure
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