PDB Search results for query - Protein Data Bank Japan

PDB: 3 results

Structure of human liver FBPase complexed with potent benzoxazole allosteric inhibitors
Descriptor:	2,5-DICHLORO-N-[5-METHOXY-7-(6-METHOXYPYRIDIN-3-YL)-1,3-BENZOXAZOL-2-YL]BENZENESULFONAMIDE, Fructose-1,6-bisphosphatase 1
Authors:	Abad-Zapatero, C.
Deposit date:	2005-12-29
Release date:	2006-02-21
Last modified:	2023-08-30
Method:	X-RAY DIFFRACTION (2.81 Å)
Cite:	Benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphatase. Bioorg.Med.Chem.Lett., 16, 2006

Structure of human liver FBPase complexed with potent benzoxazole allosteric inhibitiors
Descriptor:	Fructose-1,6-bisphosphatase 1, N-[7-(3-AMINOPHENYL)-5-METHOXY-1,3-BENZOXAZOL-2-YL]-2,5-DICHLOROBENZENESULFONAMIDE
Authors:	Abad-Zapatero, C.
Deposit date:	2005-12-30
Release date:	2006-02-21
Last modified:	2023-08-30
Method:	X-RAY DIFFRACTION (3.5 Å)
Cite:	Benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphatase. Bioorg.Med.Chem.Lett., 16, 2006

Structure of human liver FPBase complexed with a novel benzoxazole as allosteric inhibitor
Descriptor:	2,5-DICHLORO-N-(5-CHLORO-1,3-BENZOXAZOL-2-YL)BENZENESULFONAMIDE, Fructose-1,6-bisphosphatase 1, MAGNESIUM ION
Authors:	Abad-Zapatero, C.
Deposit date:	2005-12-27
Release date:	2006-02-21
Last modified:	2024-02-14
Method:	X-RAY DIFFRACTION (2.95 Å)
Cite:	Benzoxazole benzenesulfonamides are novel allosteric inhibitors of fructose-1,6-bisphosphatase with a distinct binding mode. Bioorg.Med.Chem.Lett., 16, 2006