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TargetMycothiol S-conjugate amidase
LigandBDBM50117089
Substrate/Competitorn/a
Meas. Tech.ChEBML_140808
IC50 36000±n/a nM
Citation Nicholas GMEckman LLRay SHughes ROPfefferkorn JABarluenga SNicolaou KCBewley CA Bromotyrosine-derived natural and synthetic products as inhibitors of mycothiol-S-conjugate amidase. Bioorg Med Chem Lett 12:2487-90 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Mycothiol S-conjugate amidase
Name:Mycothiol S-conjugate amidase
Synonyms:n/a
Type:PROTEIN
Mol. Mass.:32719.79
Organism:Mycobacterium tuberculosis
Description:ChEMBL_626858
Residue:288
Sequence:
MSELRLMAVHAHPDDESSKGAATLARYADEGHRVLVVTLTGGERGEILNPAMDLPDVHGR
IAEIRRDEMTKAAEILGVEHTWLGFVDSGLPKGDLPPPLPDDCFARVPLEVSTEALVRVV
REFRPHVMTTYDENGGYPHPDHIRCHQVSVAAYEAAGDFCRFPDAGEPWTVSKLYYVHGF
LRERMQMLQDEFARHGQRGPFEQWLAYWDPDHDFLTSRVTTRVECSKYFSQRDDALRAHA
TQIDPNAEFFAAPLAWQERLWPTEEFELARSRIPARPPETELFAGIEP
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  Blast E-value cutoff:
BDBM50117089
n/a
NameBDBM50117089
Synonyms:CHEMBL204484 | CHEMBL83995 | N-[2-(2-Amino-3H-imidazol-4-yl)-ethyl]-3-[4-(3-amino-propoxy)-3,5-dibromo-phenyl]-2-[(E)-hydroxyimino]-propionamide
TypeSmall organic molecule
Emp. Form.C17H22Br2N6O3
Mol. Mass.518.203
SMILESNCCCOc1c(Br)cc(CC(N=O)C(=O)NCCc2cnc(N)[nH]2)cc1Br
Structure
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