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Results 1 - 7 of 7
EC Number Reaction Commentary Reference
Show all pathways known for 4.2.3.1Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.1O-phospho-L-homoserine + H2O = L-threonine + phosphate analyzed crystal structure gives new insights into the catalytic mechanism of threonine synthase in general, specifically by suggesting the direct involvement of the phosphate moiety of the cofactor, rather than the inorganic phosphate product, in transferring a proton from C4 to Cgamma in the formation of the alphabeta-unsaturated aldimine -, 728848
Show all pathways known for 4.2.3.1Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.1O-phospho-L-homoserine + H2O = L-threonine + phosphate inhibitor studies concerning mechanism, model of stepwise catalytic mechanism 137559
Show all pathways known for 4.2.3.1Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.1O-phospho-L-homoserine + H2O = L-threonine + phosphate mechanism 137550, 137552, 137560, 137561
Show all pathways known for 4.2.3.1Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.1O-phospho-L-homoserine + H2O = L-threonine + phosphate mechanism of phosphohomoserine dephosphorylation/deamination activity 137546
Show all pathways known for 4.2.3.1Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.1O-phospho-L-homoserine + H2O = L-threonine + phosphate reaction proceeds via phospate removal and isomerization from primary to secondary alcohol 137544
Show all pathways known for 4.2.3.1Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.1O-phospho-L-homoserine + H2O = L-threonine + phosphate reaction proceeds via phosphate removal and isomerization from primary to secondary alcohol 663091, 665733, 666989
Show all pathways known for 4.2.3.1Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.1O-phospho-L-homoserine + H2O = L-threonine + phosphate the phosphate ion released from O-phospho-L-homoserine by gamma-elimination acts as the base catalyst for the addition of water at Cbeta of the alpha-aminocrotonate aldimine, thereby providing the basis of the reaction specificity. The phosphate ion also accelerates the protonation/deprotonation at Cgamma -, 715628
Results 1 - 7 of 7