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(NH4)2SO4
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1 mM, 71% inhibition
CaCl2
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3 mM, 28% loss of activity
cadaverine
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3 mM, 26% loss of activity
Calmidazolium
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0.04 mM, almost complete inhibition of Ca2+-dependent enhancement of enzyme activity, calmodulin antagonist
Carbamoylphosphate
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3 mM, 25% loss of activity
CoCl2
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1 mM, 82% loss of activity
CuSO4
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1 mM, 87% loss of activity
detergent
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e.g. Aerosol 22, Ultrawet 60L, deoxycholic acid, cetyltrimethyl ammonium bromide, complete inactivation
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DL-pipecolic acid
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6 mM, 47% loss of activity
HgCl2
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0.01 mM, 89% loss of activity
hydroxylamine
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3 mM, 33% loss of activity
L-Glutamic acid
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3 mM, 40% loss of activity
L-Homocitrulline
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3 mM, 49% loss of activity
L-Lysine-p-nitroanilide
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inhibition noncompetitive with L-lysine, competitive with 2-oxoglutarate
L-Lysylglycine
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3 mM, 25% loss of activity
MgSO4
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1 mM, 79% loss of activity
MnCl2
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1 mM, 52% loss of activity
N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide
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1.5 mM, almost complete inhibition of Ca2+-dependent enhancement of enzyme activity, calmodulin antagonist
S-2-aminoethyl-L-cysteine
tryptophan
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complete inhibition of saccharopine formation
ZnCl2
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3 mM, complete inhibition
Alkaline phosphatase
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dephosphorylation with alkaline phosphatase significantly inhibits enzyme activity in presence of lysine, inhibitory effect is dramatically stimulated by lysine binding to LKR, which alters the conformation exposing phosphate residues to the surface
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Alkaline phosphatase
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reduces LKR activity
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EGTA
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1 mM, 21% loss of activity, addition of 1.6 mM CaCl2 increases activity by 43%
EGTA
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up to 70% inhibition, dependent on salt concentration of buffer
EGTA
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1.6 mM, 70% loss of activity in crude extract, activity can be restored by addition of 1.6 mM CaCl2
L-ornithine
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3 mM, 39% loss of activity
L-ornithine
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complete inhibition of saccharopine formation, competitive with lysine
leucine
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leucine
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complete inhibition of saccharopine formation, competitive with lysine
leucine
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slight inhibition
S-2-aminoethyl-L-cysteine
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S-2-aminoethyl-L-cysteine
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inhibits when present in assay with L-lysine, possibly competitive with L-lysine
saccharopine
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1 mM, 30% inhibition, product inhibition; competitive with 2-oxoglutarate, noncompetitive with L-lysine, uncompetitive with NADPH
saccharopine
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1 mM, 30% inhibition, product inhibition
saccharopine
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product inhibition, competitive with 2-oxoglutarate, noncompetitive with L-lysine
additional information
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not inhibited by the detergents Lubrol PX, Tween 40, saccharopine formation is not inhibited by (NH4)2SO4
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additional information
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not inhibited by 40 mM ammonium chloride, inhibition by NH4+ is probably due to contamination with glutamic dehydrogenase
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additional information
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C-hordein suppression alters the enzyme activity differentially in different developmental stages, the extent varies among the transgenic lines., overview
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additional information
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not inhibited by Triton X-100 up to 2.5 ml/l
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additional information
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not inhibited by 50 mM NH4Cl or amino-oxyacetate
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additional information
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lysine-oxoglutarate reductase shows time-dependent and protease-concentration-dependent inactivation by proteolysis followed by reactivation, saccharopine dehydrogenase-containing polypeptides obtained by prolonged digestion inhibit the activity of lysine-oxoglutarate reductase-containing polypeptides
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