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Results 1 - 10 of 11 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.101-deoxy-D-xylulose 5-phosphate + 2-iminoacetate + thiocarboxy-adenylate-[sulfur-carrier protein ThiS] - Methanocaldococcus jannaschii 2-[(2R,5Z)-2-carboxy-4-methylthiazol-5(2H)-ylidene]ethyl phosphate + [sulfur-carrier protein ThiS] + 2 H2O - ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.101-deoxy-D-xylulose 5-phosphate + 2-iminoacetate + thiocarboxy-adenylate-[sulfur-carrier protein ThiS] - Xanthomonas oryzae pv. oryzae 2-[(2R,5Z)-2-carboxy-4-methylthiazol-5(2H)-ylidene]ethyl phosphate + [sulfur-carrier protein ThiS] + 2 H2O - ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.101-deoxy-D-xylulose 5-phosphate + 2-iminoacetate + thiocarboxy-adenylate-[sulfur-carrier protein ThiS] - Bacillus subtilis 2-[(2R,5Z)-2-carboxy-4-methylthiazol-5(2H)-ylidene]ethyl phosphate + [sulfur-carrier protein ThiS] + 2 H2O - ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.101-deoxy-D-xylulose 5-phosphate + 2-iminoacetate + thiocarboxy-adenylate-[sulfur-carrier protein ThiS] - Saccharomyces cerevisiae 2-[(2R,5Z)-2-carboxy-4-methylthiazol-5(2H)-ylidene]ethyl phosphate + [sulfur-carrier protein ThiS] + 2 H2O - ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.101-deoxy-D-xylulose 5-phosphate + 2-iminoacetate + thiocarboxy-adenylate-[sulfur-carrier protein ThiS] - Methanotorris igneus 2-[(2R,5Z)-2-carboxy-4-methylthiazol-5(2H)-ylidene]ethyl phosphate + [sulfur-carrier protein ThiS] + 2 H2O - ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.101-deoxy-D-xylulose 5-phosphate + 2-iminoacetate + thiocarboxy-adenylate-[sulfur-carrier protein ThiS] - Bacillus subtilis 2-[(2R,5Z)-2-carboxy-4-methylthiazol-5(2H)-ylidene]ethyl phosphate + [sulfur-carrier protein ThiS] + 2 H2O product is a dearomatized thiazole tautomer, not thiazole phosphate ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.101-deoxy-D-xylulose 5-phosphate + 2-iminoacetate + thiocarboxy-adenylate-[sulfur-carrier protein ThiS] ThiG alone can catalyze the formation of thiazole phosphate Bacillus subtilis 2-[(2R,5Z)-2-carboxy-4-methylthiazol-5(2H)-ylidene]ethyl phosphate + [sulfur-carrier protein ThiS] + 2 H2O - ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.101-deoxy-D-xylulose 5-phosphate + 2-iminoacetate + thiocarboxy-adenylate-[sulfur-carrier protein ThiS] - Xanthomonas oryzae pv. oryzae ZJ173 2-[(2R,5Z)-2-carboxy-4-methylthiazol-5(2H)-ylidene]ethyl phosphate + [sulfur-carrier protein ThiS] + 2 H2O - ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.10more the in vitro thiazole synthase activity of cleared lysates or desalted proteins is dependent upon the addition of purified ThiG/ThiH-His complex, tyrosine, and an as yet unidentified intermediate present in the protein fraction from the cells Escherichia coli ? - ?
Show all pathways known for 2.8.1.10Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.10more the thiazole-forming activity requires four proteins isolated as heterodimers: ThiGH and ThiFS. Reconstitution of the [4Fe-4S] cluster in ThiH is essential for activity, as is the use of ThiS in the thiocarboxylate form. S-adenosylmethionine binds to the [4Fe-4S] cluster, which becomes more susceptible to reduction to the +1 state. In addition to the proteins, 1-deoxy-xylulose-5-phosphate, tyrosine, S-adenosylmethionine, and a reductant are required. 1 mol equivalent of thiazole phosphate is formed per ThiGH. For each mole of thiazole phosphate formed, 1 equivalent of S-adenosylmethionine and 1 equivalent of tyrosine are utilized, and 1 equivalent of 5-deoxyadenosine is produced. Mechanistic hypothesis suggests that S-adensylmethionine is reductively cleaved to yield a highly reactive 5-deoxyadenosyl radical. This radical abstracts the phenolic hydrogen atom from tyrosine, and the resultant substrate radical cleaves to yield dehydroglycine, which is required by ThiG for the thiazole cyclization reaction Escherichia coli ? - ?
Results 1 - 10 of 11 > >>