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The N-arylsulfonyl-indole-2-carboxamide-based inhibitors against fructose-1,6-bisphosphatase[HYDROLASE]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
Structure of human liver FBPase complexed with covalent allosteric inhibitor[HYDROLASE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
Human liver fructose-1,6-bisphosphatase 1 (fructose 1,6-bisphosphate 1-phosphatase, E.C.3.1.3.11) complexed with the allosteric inhibitor 2-[3-[(5-bromo-1,3-thiazol-2-yl)carbamoylsulfamoyl]-1-methylin...
Quadruple space group ambiguity due to rotational and translational non-crystallographic symmetry in human liver fructose-1,6-bisphosphatase[HYDROLASE]
Human liver fructose-1,6-bisphosphatase(d-fructose-1,6-bisphosphate, 1-phosphohydrolase) (e.c.3.1.3.11) complexed with the allosteric inhibitor 3[HYDROLASE/HYDROLASE INHIBITOR]
orally active aminopyridines as inhibitors of tetrameric fructose 1,6- bisphosphatase[HYDROLASE]
Orally active aminopyridines as inhibitors of tetrameric fructose 1,6- bisphosphatase[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]
FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE-1- PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH AN AMP SITE INHIBITOR[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 A Dual Binding Amp Site Inhibitor[Hydrolase, EC: 3.1.3.11]
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)]
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]
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