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TargetPantothenate synthetase
LigandBDBM50448407
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:
BDBM50448407
n/a
NameBDBM50448407
Synonyms:CHEBI:4877 | Ethambutol
TypeSmall organic molecule
Emp. Form.C10H24N2O2
Mol. Mass.204.3098
SMILESCC[C@@H](CO)NCCN[C@@H](CC)CO |r|
Structure
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