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Results 1 - 10 of 14 > >>
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EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADH + H+ + O2 - Sinorhizobium meliloti 5,6-dimethylbenzimidazole + D-erythrose 4-phosphate + NAD+ + ? - ?
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADH + H+ + O2 - Sinorhizobium meliloti 5,6-dimethylbenzimidazole + D-erythrose 4-phosphate + NAD+ + ? 5,6-dimethylbenzimidazole is the lower axial ligand of vitamin B12, i.e. cobalamin ?
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADH + H+ + O2 BluB fragments a flavin isoalloxazine ring Sinorhizobium meliloti 5,6-dimethylbenzimidazole + D-erythrose 4-phosphate + NAD+ + ? - ?
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADH + H+ + O2 + alloxan - Sinorhizobium meliloti 5,6-dimethylbenzimidazole + D-erythrose 4-phosphate + NAD+ + dialuric acid - ?
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADH + H+ + O2 + alloxan in the first stage, BluB catalyzes the incorporation of dioxygen, and the fragmentation of the isoalloxazine ring of FMNH2 to form alloxan and the ribityl dimethylphenylenediimine. In the second stage, BluB exploits alloxan as a multifunctional cofactor, such as a proton donor, a proton acceptor, and a hydride acceptor, to catalyze the remaining no fewer than 10 steps of the reaction. The retro-aldol cleavage of the C1'-C2' bond of intermediate ribityl dimethylphenylenediimine is the rate-determining step, active site model of BluB, overview. The highly conserved residue Asp32 plays critical roles in multiple steps of the conversion by serving as a proton acceptor or a proton shuttle, and another conserved residue Ser167 plays its catalytic role mainly in the rate-determining step by stabilizing the protonated retro-aldol precursor. Formation of peroxyflavin intermediate, overview Sinorhizobium meliloti 5,6-dimethylbenzimidazole + D-erythrose 4-phosphate + NAD+ + dialuric acid - ?
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADH + H+ + O2 + H2O - Rhodospirillum rubrum 5,6-dimethylbenzimidazole + D-erythrose 4-phosphate + NAD+ + ? - ?
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADPH + H+ + O2 - Sinorhizobium meliloti 5,6-dimethylbenzimidazole + D-erythrose 4-phosphate + NADP+ + ? - r
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + O2 - Trichodesmium sp. 5,6-dimethylbenzimidazole + ? - ?
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + O2 FMNH2 reacts with oxygen to yield flavin hydroperoxide, which then undergoes a ring expansion with loss of a water molecule to produce intermediate A. This disintegrates further as a result of four hydrolysis reactions in which it is attacked by water molecules. The resulting diaminobenzene product undergoes two oxidation reactions, to form 5,6-dimethylbenzimidazole Sinorhizobium meliloti 5,6-dimethylbenzimidazole + ? - ?
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + O2 - Priestia megaterium 5,6-dimethylbenzimidazole + D-erythrose 4-phosphate + urea + ? - ?
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