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orally active aminopyridines as inhibitors of tetrameric fructose 1,6- bisphosphatase[HYDROLASE]
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Orally active aminopyridines as inhibitors of tetrameric fructose 1,6- bisphosphatase[HYDROLASE]
FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE-1- PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH AN AMP SITE INHIBITOR[HYDROLASE]
FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE -1- PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH A DUAL BINDING AMP SITE INHIBITOR[HYDROLASE]
Structure of human liver FBPase complexed with potent benzoxazole allosteric inhibitiors[HYDROLASE]
Structure of human liver FBPase complexed with potent benzoxazole allosteric inhibitors[HYDROLASE]
Structure of human liver FPBase complexed with a novel benzoxazole as allosteric inhibitor[HYDROLASE]
Crystal structure of human liver FBPase in complex with tricyclic inhibitor 19a[HYDROLASE]
Crystal structure of human liver FBPase in complex with tricyclic inhibitor 10b[HYDROLASE]
Crystal structure of human liver FBPase in complex with tricyclic inhibitor 6[HYDROLASE]
Crystal structure of human liver FBPase in complex with tricyclic inhibitor[HYDROLASE]
FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE, 1-PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH THE ALLOSTERIC INHIBITOR AMP[HYDROLASE (PHOSPHORIC MONOESTER)]
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Porcine Liver Fructose-1,6-bisphosphatase cocrystallized with Fru-2,6-P2 and Zn2+, I(T)-state[HYDROLASE]
Porcine Liver Fructose-1,6-bisphosphatase cocrystallized with Fru-2,6-P2 and Mg2+, I(T)-state[HYDROLASE]
Fructose-1,6-bisphosphatase Complexed with a New Allosteric Site Inhibitor (I-State)[HYDROLASE]
Fructose-1,6-Bisphosphatase Complex With AMP, Magnesium, Fructose-6-Phosphate, Phosphate and Thallium (20 mM)[HYDROLASE]
Fructose-1,6-Bisphosphatase Complex With Magnesium, Fructose-6-Phosphate, Phosphate, EDTA and Thallium (20 mM)[HYDROLASE]
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