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1.5.1.8: saccharopine dehydrogenase (NADP+, L-lysine-forming)

This is an abbreviated version!
For detailed information about saccharopine dehydrogenase (NADP+, L-lysine-forming), go to the full flat file.

Word Map on EC 1.5.1.8

Reaction

N6-(L-1,3-dicarboxypropyl)-L-lysine
+
NADP+
+
H2O
=
L-lysine
+
2-oxoglutarate
+
NADPH
+
H+

Synonyms

AasS, dehydrogenase, saccharopine (nicotinamide adenine dinucleotide phosphate, lysine-forming), L-lysine-alpha-ketoglutarate reductase, LKR, LKR/SDH, LOR, LOR-SDH, lysine 2-oxoglutarate reductase, lysine 2-oxoglutarate reductase-saccharopine dehydrogenase, lysine alpha-ketoglutarate reductase, lysine ketoglutarate reductase, lysine ketoglutarate/reductase saccharopine dehydrogenase, lysine-2-oxoglutarate reductase, lysine-alpha-ketoglutarate reductase, lysine-ketoglutarate reductase, lysine-ketoglutarate reductase/saccharopine dehydrogenase, lysine-ketoglutaric reductase, lysine:alpha-ketoglutarate:TPNH oxidoreductase (epsilon-N-[glutaryl-2]-L-lysine forming), nllkr/sdh, saccharopine (nicotinamide adenine dinucleotide phosphate, lysine-forming) dehydrogenase, saccharopine dehydrogenase, saccharopine dehydrogenase (NADP, lysine-forming), saccharopine dehydrogenase (nicotinamide adenine dinucleotide phosphate, lysine-forming)

ECTree

     1 Oxidoreductases
         1.5 Acting on the CH-NH group of donors
             1.5.1 With NAD+ or NADP+ as acceptor
                1.5.1.8 saccharopine dehydrogenase (NADP+, L-lysine-forming)

Inhibitors

Inhibitors on EC 1.5.1.8 - saccharopine dehydrogenase (NADP+, L-lysine-forming)

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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
(NH4)2SO4
-
1 mM, 71% inhibition
Alkaline phosphatase
-
CaCl2
-
3 mM, 28% loss of activity
cadaverine
-
3 mM, 26% loss of activity
Calmidazolium
-
0.04 mM, almost complete inhibition of Ca2+-dependent enhancement of enzyme activity, calmodulin antagonist
Carbamoylphosphate
-
3 mM, 25% loss of activity
CoCl2
-
1 mM, 82% loss of activity
CuSO4
-
1 mM, 87% loss of activity
detergent
-
e.g. Aerosol 22, Ultrawet 60L, deoxycholic acid, cetyltrimethyl ammonium bromide, complete inactivation
-
DL-pipecolic acid
-
6 mM, 47% loss of activity
HgCl2
-
0.01 mM, 89% loss of activity
hydroxylamine
-
3 mM, 33% loss of activity
L-Glutamic acid
-
3 mM, 40% loss of activity
L-Homocitrulline
-
3 mM, 49% loss of activity
L-Lysine-p-nitroanilide
-
inhibition noncompetitive with L-lysine, competitive with 2-oxoglutarate
L-Lysylglycine
-
3 mM, 25% loss of activity
L-ornithine
leucine
MgSO4
-
1 mM, 79% loss of activity
MnCl2
-
1 mM, 52% loss of activity
N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide
-
1.5 mM, almost complete inhibition of Ca2+-dependent enhancement of enzyme activity, calmodulin antagonist
S-2-aminoethyl-L-cysteine
saccharopine
tryptophan
-
complete inhibition of saccharopine formation
ZnCl2
-
3 mM, complete inhibition
additional information
-