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CRYSTAL STRUCTURE OF PORCINE FRUCTOSE-1,6-BISPHOSPHATASE COMPLEXED WITH A NOVEL ALLOSTERIC-SITE INHIBITOR[HYDROLASE]
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Mechanism of displacement of a catalytically essential loop from the active site of fructose-1,6-bisphosphatase[HYDROLASE]
orally active aminopyridines as inhibitors of tetrameric fructose 1,6- bisphosphatase[HYDROLASE]
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, EC: 3.1.3.11]
Structure of human liver FBPase complexed with potent benzoxazole allosteric inhibitiors[HYDROLASE]
Structure of human liver FBPase complexed with potent benzoxazole allosteric inhibitors[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]
Structure of human liver FPBase complexed with a novel benzoxazole as allosteric inhibitor[HYDROLASE]
R-State AMP Complex Reveals Initial Steps of the Quaternary Transition of Fructose-1,6-bisphosphatase[HYDROLASE]
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