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2-hydroxy-N'-((6-methyl-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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2-methyl-N'-((6-methyl-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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2-[2-(4-amino-1,2,5-oxadiazol-3-yl)-1H-indol-1-yl]-N'-[(E)-(4-methylphenyl)methylidene]acetohydrazide
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2-[2-(4-amino-1,2,5-oxadiazol-3-yl)-1H-indol-1-yl]-N'-[(E)-(5-hydroxy-2-methylphenyl)methylidene]acetohydrazide
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2-[2-(4-amino-1,2,5-oxadiazol-3-yl)-1H-indol-1-yl]-N-(2,3-dihydro-1H-inden-5-yl)acetamide
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2-[2-(4-amino-1,2,5-oxadiazol-3-yl)-1H-indol-1-yl]-N-(2,6-dimethylphenyl)acetamide
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2-[2-(4-amino-1,2,5-oxadiazol-3-yl)-1H-indol-1-yl]-N-(3-fluoro-4-methylphenyl)acetamide
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2-[2-(4-amino-1,2,5-oxadiazol-3-yl)-1H-indol-1-yl]-N-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)acetamide
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3-bromo-N'-((4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-(tert-butyl)-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-bromo-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-chloro-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-ethyl-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-fluoro-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-hydroxy-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-isopropyl-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-methyl-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-bromo-N'-((6-nitro-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-hydroxy-N'-((4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-methyl-N'-((4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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3-nitro-N'-((4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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4-bromo-N'-((6-bromo-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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4-[1-(4-chlorobenzyl)-1H-indol-2-yl]-1,2,5-oxadiazol-3-amine
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acrolein
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treatment of intact chloroplast
Cu2+
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0.1 mM, 30% inhibition
fructose 1,6-diphosphate
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at high concentrations
glycerate
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inhibits at physiological concentrations
methyl 4-([[2-(4-amino-1,2,5-oxadiazol-3-yl)-1H-indol-1-yl]acetyl]amino)benzoate
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N'-((4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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N'-((6-bromo-4-oxo-4H-chromen-3-yl)methylene)-4-(trifluoromethyl)benzohydrazide
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N'-((6-bromo-4-oxo-4H-chromen-3-yl)methylene)-4-fluorobenzohydrazide
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N'-((6-bromo-4-oxo-4H-chromen-3-yl)methylene)-4-hydroxybenzohydrazide
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N'-((6-bromo-4-oxo-4H-chromen-3-yl)methylene)-4-methylbenzohydrazide
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N'-((6-bromo-4-oxo-4H-chromen-3-yl)methylene)-4-nitrobenzohydrazide
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N'-((6-bromo-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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N'-((6-methyl-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide
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NaCl
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SBPase activity decreases at 100 mM NaCl and above
NaF
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0.01 M, 84% inhibition
oxidized thioredoxin f
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due to the formation of a stable complex between enzyme and thioredoxin
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PCMB
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0.2 mM, 35% inhibition
Ribulose 1,5-diphosphate
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inhibits at physiological concentrations
sedoheptulose-1,7-bisphosphate
AMP
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AMP
Thermosynechococcus vestitus
a regulatory inhibitor, AMP-binding loop structure analysis
Ca2+
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Ca2+
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2 mM, at pH 8.0, 83% inhibition of the thiol-treated enzyme, at pH 7.5 91% inhibition and at pH 7.0 complete inhibition
Ca2+
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0.7 mM, 50% inhibition
phosphate
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competitive
sedoheptulose-1,7-bisphosphate
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competitive
sedoheptulose-1,7-bisphosphate
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inhibits at physiological concentrations
additional information
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location of the redox-active cysteines in chloroplast sedoheptulose-1,7-bisphosphatase indicates that its allosteric regulation is similar but not identical to that of fructose 1,6-bisphosphatase
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additional information
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location of the redox-active cysteines in chloroplast sedoheptulose-1,7-bisphosphatase indicates that its allosteric regulation is similar but not identical to that of fructose 1,6-bisphosphatase
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additional information
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no substrate inhibition up to 2 mM
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additional information
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location of the redox-active cysteines in chloroplast sedoheptulose-1,7-bisphosphatase indicates that its allosteric regulation is similar but not identical to that of fructose 1,6-bisphosphatase
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