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1BK4
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1bk4
CRYSTAL STRUCTURE OF RABBIT LIVER FRUCTOSE-1,6-BISPHOSPHATASE AT 2.3 ANGSTROM RESOLUTION
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE
Authors:Ghosh, D., Weeks, C.M., Erman, M., Roszak, A.W., Kaiser, R., Jornvall, H.
Deposit date:1998-07-14
Release date:1998-07-22
Modification date:2011-07-13
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Structure of rabbit liver fructose 1,6-bisphosphatase at 2.3 A resolution.
Acta Crystallogr.,Sect.D, 55, 1999
1D9Q
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1d9q
OXIDIZED PEA FRUCTOSE-1,6-BISPHOSPHATASE FORM 1
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE (E.C.3.1.3.11)
Authors:Chiadmi, M., Navaza, A., Miginiac-Maslow, M., Jacquot, J.-P., Cherfils, J.
Deposit date:1999-10-29
Release date:1999-12-03
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Redox signalling in the chloroplast: structure of oxidized pea fructose-1,6-bisphosphate phosphatase.
EMBO J., 18, 1999
1DBZ
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1dbz
C153S MUTANT OF PEA FRUCTOSE-1,6-BISPHOSPHATASE
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE (E.C.3.1.3.11) MUTANT (C153S)
Authors:Chiadmi, M., Navaza, A., Miginiac-Maslow, M., Jacquot, J.P., Cherfils, J.
Deposit date:1999-11-03
Release date:1999-12-03
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.65 Å)
Cite:Redox signalling in the chloroplast: structure of oxidized pea fructose-1,6-bisphosphate phosphatase.
EMBO J., 18, 1999
1DCU
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1dcu
REDOX SIGNALING IN THE CHLOROPLAST: STRUCTURE OF OXIDIZED PEA FRUCTOSE-1,6-BISPHOSPHATE PHOSPHATASE
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE (E.C.3.1.3.11)
Authors:Chiadmi, M., Navaza, A., Miginiac-Maslow, M., Jacquot, J.P., Cherfils, J.
Deposit date:1999-11-05
Release date:1999-12-03
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Redox signalling in the chloroplast: structure of oxidized pea fructose-1,6-bisphosphate phosphatase.
EMBO J., 18, 1999
1FRP
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1frp
CRYSTAL STRUCTURE OF FRUCTOSE-1,6-BISPHOSPHATASE COMPLEXED WITH FRUCTOSE-2,6-BISPHOSPHATE, AMP AND ZN2+ AT 2.0 ANGSTROMS RESOLUTION. ASPECTS OF SYNERGISM BETWEEN INHIBITORS
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE (D-FRUCTOSE-1,6-BISPHOSPHATE 1-PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH FRUCTOSE-2,6-BISPHOSPHATE, ADENOSINE MONOPHOSPHATE (AMP), AND ZINC
Authors:Xue, Y., Huang, S., Liang, J.-Y., Zhang, Y., Lipscomb, W.N.
Deposit date:1994-08-26
Release date:1994-11-30
Modification date:2011-07-13
Method:X-RAY DIFFRACTION (2 Å)
Cite:Crystal structure of fructose-1,6-bisphosphatase complexed with fructose 2,6-bisphosphate, AMP, and Zn2+ at 2.0-A resolution: aspects of synergism between inhibitors.
Proc.Natl.Acad.Sci.USA, 91, 1994
1FTA
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1fta
FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE, 1-PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH THE ALLOSTERIC INHIBITOR AMP
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE, ADENOSINE MONOPHOSPHATE
Authors:Zhang, Y., Liang, J.-Y., Huang, S., Lipscomb, W.N.
Deposit date:1993-09-27
Release date:1995-11-14
Modification date:2012-02-22
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:The allosteric site of human liver fructose-1,6-bisphosphatase. Analysis of six AMP site mutants based on the crystal structure.
J.Biol.Chem., 269, 1994
1SPI
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1spi
CRYSTAL STRUCTURE OF SPINACH CHLOROPLAST FRUCTOSE-1,6-BISPHOSPHATASE AT 2.8 ANGSTROMS RESOLUTION
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE (D-FRUCTOSE-1,6-BISPHOSPHATE 1-PHOSPHOHYDROLASE) (E.C.3.1.3.11)
Authors:Villeret, V., Huang, S., Zhang, Y., Xue, Y., Lipscomb, W.N.
Deposit date:1994-12-14
Release date:1995-02-27
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:Crystal structure of spinach chloroplast fructose-1,6-bisphosphatase at 2.8 A resolution.
Biochemistry, 34, 1995
2FHY
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2fhy
STRUCTURE OF HUMAN LIVER FPBASE COMPLEXED WITH A NOVEL BENZOXAZOLE AS ALLOSTERIC INHIBITOR
Descriptor:Fructose-1,6-bisphosphatase 1
Authors:Abad-Zapatero, C.
Deposit date:2005-12-27
Release date:2006-02-21
Modification date:2009-02-24
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
2FIE
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2fie
STRUCTURE OF HUMAN LIVER FBPASE COMPLEXED WITH POTENT BENZOXAZOLE ALLOSTERIC INHIBITORS
Descriptor:Fructose-1,6-bisphosphatase 1 (E.C.3.1.3.11)
Authors:Abad-Zapatero, C.
Deposit date:2005-12-29
Release date:2006-02-21
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.81 Å)
Cite:Benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphatase.
Bioorg.Med.Chem.Lett., 16, 2006
2FIX
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2fix
STRUCTURE OF HUMAN LIVER FBPASE COMPLEXED WITH POTENT BENZOXAZOLE ALLOSTERIC INHIBITIORS
Descriptor:Fructose-1,6-bisphosphatase 1
Authors:Abad-Zapatero, C.
Deposit date:2005-12-30
Release date:2006-02-21
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (3.5 Å)
Cite:Benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphatase.
Bioorg.Med.Chem.Lett., 16, 2006
2GQ1
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2gq1
CRYSTAL STRUCTURE OF RECOMBINANT TYPE I FRUCTOSE-1,6-BISPHOSPHATASE FROM ESCHERICHIA COLI COMPLEXED WITH SULFATE IONS
Descriptor:Fructose-1,6-bisphosphatase (E.C.3.1.3.11)
Authors:Hines, J.K., Fromm, H.J., Honzatko, R.B.
Deposit date:2006-04-19
Release date:2006-05-02
Modification date:2011-07-13
Method:X-RAY DIFFRACTION (1.45 Å)
Cite:Novel Allosteric Activation Site in Escherichia coli Fructose-1,6-bisphosphatase.
J.Biol.Chem., 281, 2006
2JJK
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2jjk
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
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE 1 (E.C.3.1.3.11)
Authors:Ruf, A., Joseph, C., Benz, J., Fol, B., Tetaz, T., Hebeisen, P.
Deposit date:2008-04-09
Release date:2008-07-22
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2 Å)
Cite:Allosteric Fbpase Inhibitors Gain 10(5) Times in Potency When Simultaneously Binding Two Neighboring AMP Sites.
Bioorg.Med.Chem.Lett., 18, 2008
2OWZ
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2owz
R-STATE, CITRATE AND FRU-6-P-BOUND ESCHERICHIA COLI FRUCTOSE-1,6-BISPHOSPHATASE
Descriptor:Fructose-1,6-bisphosphatase (E.C.3.1.3.11)
Authors:Hines, J.K., Fromm, H.J., Honzatko, R.B.
Deposit date:2007-02-17
Release date:2007-03-06
Modification date:2011-07-13
Method:X-RAY DIFFRACTION (2.18 Å)
Cite:Structures of activated fructose-1,6-bisphosphatase from Escherichia coli. Coordinate regulation of bacterial metabolism and the conservation of the R-state.
J.Biol.Chem., 282, 2007
2OX3
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2ox3
R-STATE, PEP AND FRU-6-P-BOUND, ESCHERICHIA COLI FRUCTOSE-1,6-BISPHOSPHATASE
Descriptor:Fructose-1,6-bisphosphatase (E.C.3.1.3.11)
Authors:Hines, J.K., Fromm, H.J., Honzatko, R.B.
Deposit date:2007-02-19
Release date:2007-03-06
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.18 Å)
Cite:Structures of activated fructose-1,6-bisphosphatase from Escherichia coli. Coordinate regulation of bacterial metabolism and the conservation of the R-state.
J.Biol.Chem., 282, 2007
2Q8M
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2q8m
T-LIKE FRUCTOSE-1,6-BISPHOSPHATASE FROM ESCHERICHIA COLI WITH AMP, GLUCOSE 6-PHOSPHATE, AND FRUCTOSE 1,6-BISPHOSPHATE BOUND
Descriptor:Fructose-bisphosphatase (E.C.3.1.3.11)
Authors:Hines, J.K., Kruesel, C.E., Fromm, H.J., Honzatko, R.B.
Deposit date:2007-06-11
Release date:2007-06-19
Modification date:2011-07-13
Method:X-RAY DIFFRACTION (2.05 Å)
Cite:Structure of Inhibited Fructose-1,6-bisphosphatase from Escherichia coli: DISTINCT ALLOSTERIC INHIBITION SITES FOR AMP AND GLUCOSE 6-PHOSPHATE AND THE CHARACTERIZATION OF A GLUCONEOGENIC SWITCH.
J.Biol.Chem., 282, 2007
2QVR
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2qvr
E. COLI FRUCTOSE-1,6-BISPHOSPHATASE: CITRATE, FRU-2,6-P2, AND MG2+ BOUND
Descriptor:Fructose-1,6-bisphosphatase (E.C.3.1.3.11)
Authors:Hines, J.K., Fromm, H.J., Honzatko, R.B.
Deposit date:2007-08-08
Release date:2007-10-23
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.18 Å)
Cite:Structures of Mammalian and Bacterial Fructose-1,6-bisphosphatase Reveal the Basis for Synergism in AMP/Fructose 2,6-Bisphosphate Inhibition.
J.Biol.Chem., 282, 2007
2VT5
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2vt5
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
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE 1 (E.C.3.1.3.11)
Authors:Ruf, A., Joseph, C., Benz, J., Fol, B., Tetaz, T.
Deposit date:2008-05-09
Release date:2008-07-22
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Allosteric Fbpase Inhibitors Gain 10(5) Times in Potency When Simultaneously Binding Two Neighboring AMP Sites.
Bioorg.Med.Chem.Lett., 18, 2008
2WBB
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2wbb
FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE-1-PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH AN AMP SITE INHIBITOR
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE 1 (E.C.3.1.3.11)
Authors:Ruf, A., Joseph, C., Benz, J., Fol, B., Tetaz, T., Kitas, E., Mohr, P., Kuhn, B., Wessel, H.P., Hebeisen, P., Haap, W., Huber, W., Alvarez Sanchez, R., Paehler, A., Bernadeau, A., Gubler, M., Schott, B., Tozzo, E.
Deposit date:2009-02-26
Release date:2009-12-22
Modification date:2010-02-16
Method:X-RAY DIFFRACTION (2.22 Å)
Cite:Sulfonylureido Thiazoles as Fructose-1,6-Bisphosphatase Inhibitors for the Treatment of Type-2 Diabetes.
Bioorg.Med.Chem.Lett., 20, 2010
2WBD
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2wbd
FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE-1-PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH AN AMP SITE INHIBITOR
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE 1 (E.C.3.1.3.11)
Authors:Ruf, A., Joseph, C., Benz, J., Fol, B., Tetaz, T., Kitas, E., Mohr, P., Kuhn, B., Wessel, H.P., Hebeisen, P., Haap, W., Huber, W., Alvarez Sanchez, R., Paehler, A., Bernadeau, A., Gubler, M., Schott, B., Tozzo, E.
Deposit date:2009-02-26
Release date:2009-12-22
Modification date:2010-02-16
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Sulfonylureido Thiazoles as Fructose-1,6-Bisphosphatase Inhibitors for the Treatment of Type-2 Diabetes.
Bioorg.Med.Chem.Lett., 20, 2010
2Y5K
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2y5k
ORALLY ACTIVE AMINOPYRIDINES AS INHIBITORS OF TETRAMERIC FRUCTOSE 1,6-BISPHOSPHATASE
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE 1 (E.C.3.1.3.11)
Authors:Ruf, A., Hebeisen, P., Haap, W., Kuhn, B., Mohr, P., Wessel, H.P., Zutter, U., Kirchner, S., Benz, J., Joseph, C., Alvarez-Sanchez, R., Gubler, M., Schott, B., Benardeau, A., Tozzo, E., Kitas, E.
Deposit date:2011-01-14
Release date:2011-05-18
Modification date:2011-06-01
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:Orally Active Aminopyridines as Inhibitors of Tetrameric Fructose-1,6-Bisphosphatase.
Bioorg.Med.Chem.Lett., 21, 2011
2Y5L
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2y5l
ORALLY ACTIVE AMINOPYRIDINES AS INHIBITORS OF TETRAMERIC FRUCTOSE 1,6-BISPHOSPHATASE
Descriptor:FRUCTOSE-1,6-BISPHOSPHATASE 1 (E.C.3.1.3.11)
Authors:Ruf, A., Hebeisen, P., Haap, W., Kuhn, B., Mohr, P., Wessel, H.P., Zutter, U., Kirchner, S., Benz, J., Joseph, C., Alvarez-Sanchez, R., Gubler, M., Schott, B., Benardeau, A., Tozzo, E., Kitas, E.
Deposit date:2011-01-14
Release date:2011-05-18
Modification date:2011-06-01
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Orally Active Aminopyridines as Inhibitors of Tetrameric Fructose-1,6-Bisphosphatase.
Bioorg.Med.Chem.Lett., 21, 2011
3A29
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3a29
CRYSTAL STRUCTURE OF HUMAN LIVER FBPASE IN COMPLEX WITH TRICYCLIC INHIBITOR
Descriptor:Fructose-1,6-bisphosphatase 1 (E.C.3.1.3.11)
Authors:Takahashi, M., Sone, J., Hanzawa, H.
Deposit date:2009-05-08
Release date:2009-10-06
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Synthesis, SAR, and X-ray structure of tricyclic compounds as potent FBPase inhibitors
Bioorg.Med.Chem.Lett., 19, 2009
3KBZ
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3kbz
CRYSTAL STRUCTURE OF HUMAN LIVER FBPASE IN COMPLEX WITH TRICYCLIC INHIBITOR 6
Descriptor:Fructose-1,6-bisphosphatase 1 (E.C.3.1.3.11)
Authors:Takahashi, M., Sone, J., Hanzawa, H.
Deposit date:2009-10-20
Release date:2010-02-02
Method:X-RAY DIFFRACTION (2.45 Å)
Cite:Structure-based drug design of tricyclic 8H-indeno[1,2-d][1,3]thiazoles as potent FBPase inhibitors.
Bioorg.Med.Chem.Lett., 20, 2010
3KC0
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3kc0
CRYSTAL STRUCTURE OF HUMAN LIVER FBPASE IN COMPLEX WITH TRICYCLIC INHIBITOR 10B
Descriptor:Fructose-1,6-bisphosphatase 1 (E.C.3.1.3.11)
Authors:Takahashi, M., Sone, J., Hanzawa, H.
Deposit date:2009-10-20
Release date:2010-02-02
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:Structure-based drug design of tricyclic 8H-indeno[1,2-d][1,3]thiazoles as potent FBPase inhibitors.
Bioorg.Med.Chem.Lett., 20, 2010
3KC1
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3kc1
CRYSTAL STRUCTURE OF HUMAN LIVER FBPASE IN COMPLEX WITH TRICYCLIC INHIBITOR 19A
Descriptor:Fructose-1,6-bisphosphatase 1 (E.C.3.1.3.11)
Authors:Takahashi, M., Sone, J., Hanzawa, H.
Deposit date:2009-10-20
Release date:2010-02-02
Method:X-RAY DIFFRACTION (2.25 Å)
Cite:Structure-based drug design of tricyclic 8H-indeno[1,2-d][1,3]thiazoles as potent FBPase inhibitors.
Bioorg.Med.Chem.Lett., 20, 2010
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103354
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