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Literature summary for 2.7.3.4 extracted from

  • Merceron, R.; Awama, A.M.; Montserret, R.; Marcillat, O.; Gouet, P.
    The substrate-free and -bound crystal structures of the duplicated taurocyamine kinase from the human parasite Schistosoma mansoni (2015), J. Biol. Chem., 290, 12951-12963.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

Cloned (Comment) Organism
recombinant overexpression of wild-type and mutant enzymes in Escherichia coli strain BL21(DE3), subcloning in Escherichia coli strain DH5alpha Schistosoma mansoni

Crystallization (Commentary)

Crystallization (Comment) Organism
purified recombinant wild-type and mutant enzymes complexed with taurocyamine or L-arginine, sitting drop vapor diffusion method, mixing of 5 mg/ml protein in 20mM Tris-HCl, pH 8.5, with reservoir solution, containing 200mM diammonium tartrate, pH 5.4, 20% w/v PEG 3350, 20% v/v ethylene glycol, in a 2:1 or 1:1 protein/solution volume ratio, 2 weeks, 20°C, X-ray diffraction structure determination and analysis at 2.2 A resolution leads to a small angle x-ray scattering model of SmTK-TSA in solution with two closed active sites, molecular replacement. The SmTK crystal is soaked with the dead end transition state analogue components taurocyamine-NO3 2-MgADP Schistosoma mansoni

Protein Variants

Protein Variants Comment Organism
C268S site-directed mutagenesis Schistosoma mansoni
C268S/C631S site-directed mutagenesis Schistosoma mansoni
C631S site-directed mutagenesis Schistosoma mansoni

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ dependent on Schistosoma mansoni

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
ATP + taurocyamine Schistosoma mansoni
-
ADP + N-phosphotaurocyamine
-
r

Organism

Organism UniProt Comment Textmining
Schistosoma mansoni P16641
-
-

Purification (Commentary)

Purification (Comment) Organism
recombinant wild-type and mutant enzymes from Escherichia coli strain BL21(DE3) by Blue Sepharose affinity and anion exchange chromatography, followed by ultrafiltration Schistosoma mansoni

Reaction

Reaction Comment Organism Reaction ID
ATP + taurocyamine = ADP + N-phosphotaurocyamine an arginine residue of the phosphagen specificity loop is crucial for substrate specificity, mechanism and structure-function relationship, overview Schistosoma mansoni

Source Tissue

Source Tissue Comment Organism Textmining

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
ATP + taurocyamine
-
Schistosoma mansoni ADP + N-phosphotaurocyamine
-
r
ATP + taurocyamine the enzyme catalyzes the reversibleMg2-dependent transfer of a phosphoryl group between ATP and taurocyamine Schistosoma mansoni ADP + N-phosphotaurocyamine
-
r

Subunits

Subunits Comment Organism
More the two unliganded lobes present a canonical open conformation and interact via their respective C- and N-terminal domains at a helix-mediated interface. The two lobes function independently Schistosoma mansoni

Cofactor

Cofactor Comment Organism Structure
ADP
-
Schistosoma mansoni
ATP
-
Schistosoma mansoni

General Information

General Information Comment Organism
evolution the enzyme belongs to the phosphagen kinase (PK) family. Schistosoma mansoni taurocyamine SmTK is derived from gene duplication, as are all known trematode taurocyamine kinases Schistosoma mansoni