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Literature summary for 2.5.1.3 extracted from

  • Khare, G.; Kar, R.; Tyagi, A.K.
    Identification of inhibitors against Mycobacterium tuberculosis thiamin phosphate synthase, an important target for the development of anti-TB drugs (2011), PLoS ONE, 6, e22441.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

Cloned (Comment) Organism
expressed in Escherichia coli Mycobacterium tuberculosis

Inhibitors

Inhibitors Comment Organism Structure
3-benzylsulfanyl-phenanthro[9,10-e][1,2,4]triazine IC50 of 0.1 mg/ml Mycobacterium tuberculosis
4-[[(2-hydroxy-5-nitrophenyl)methylidene]amino]-5-methyl-2-(propan-2-yl)phenol IC50 of 0.034 mg/ml Mycobacterium tuberculosis
7-[[4-chloro-6-(diethylamino)-s-triazin-2-yl]amino]-3-phenyl-coumarin IC50 of more than 0.1 mg/ml Mycobacterium tuberculosis

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
29000
-
x * 29000, SDS-PAGE Mycobacterium tuberculosis

Organism

Organism UniProt Comment Textmining
Mycobacterium tuberculosis
-
-
-

Purification (Commentary)

Purification (Comment) Organism
strep - tactin column chromatography Mycobacterium tuberculosis

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2-methyl-4-amino-5-hydroxymethylpyrimidine diphosphate + 4-methyl-5-(2-phosphono-oxyethyl)-thiazole
-
Mycobacterium tuberculosis thiamine phosphate + diphosphate
-
?

Subunits

Subunits Comment Organism
? x * 29000, SDS-PAGE Mycobacterium tuberculosis

Synonyms

Synonyms Comment Organism
thiamin phosphate synthase
-
Mycobacterium tuberculosis
TPS
-
Mycobacterium tuberculosis