4.3.2.2: adenylosuccinate lyase
This is an abbreviated version!
For detailed information about adenylosuccinate lyase, go to the full flat file.
Word Map on EC 4.3.2.2
-
4.3.2.2
-
purine
-
saicar
-
succinyladenosine
-
autistic
-
carboxamide
-
psychomotor
-
imp
-
succinylaminoimidazole
-
amylosucrase
-
ribotide
-
geothermalis
-
aminoimidazole
-
drug development
-
medicine
- 4.3.2.2
- purine
-
saicar
-
succinyladenosine
-
autistic
- carboxamide
-
psychomotor
- imp
-
succinylaminoimidazole
- amylosucrase
- ribotide
- geothermalis
-
aminoimidazole
- drug development
- medicine
Reaction
Synonyms
adenylosuccinase, adenylosuccinate lyase, ADL, ADSL, AMPS lyase, ASASE, ASL, Glutamyl-tRNA synthetase regulatory factor, lyase, adenylosuccinate, PurB, succino AMP-lyase, succino-AMP lyase
ECTree
Advanced search results
Inhibitors
Inhibitors on EC 4.3.2.2 - adenylosuccinate lyase
Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
5-aminoimidazole-4-carboxamide ribonucleoside
50% inhibition at 0.167 mM
5-aminoimidazole-4-carboxamide riboside 5'-monophosphate
-
i.e. ZMP or AICAR, product inhibition, accumulation in the brain of Lesch-Nyhan disease patients induces inhibition of mitochondrial oxidative phosphorylation and adenylosuccinate lyase activity, followed by dowregulation of ATP levels and multifocal cell death in the cerebellum
ammonium salt of N6-malonyl adenosine 5'-phosphate
-
noncompetitive inhibitor, irreversible
erythro-beta-fluoro-4-(N-succino)-5-aminoimidazole-4-carboxamide ribonucleotide
-
-
KBr
presence of increasing concentrations of KBr of 0.12.5 M disrupt electrostatic interactions leading to ASL dissociation and loss of catalytic activity
KCl
-
stimulates up to maximum concentration of 80 mM, inhibition at higher concentration
N-(5-amino-1-(beta-D-ribofuranosyl)imidazole-4-carbonyl)-L-threo-beta-methylaspartic acid 5'-phosphate
-
-
N6-(L-1-carboxy-2-methylsulfoxyethyl)-AMP
-
i.e. adenylomethylsulfoxypropionate
PO43-
-
activates at low concentration, inhibits at high concentrations above 25 mM
SO42-
-
activates at low concentrations, inhibits at concentrations above 25 mM
threo-beta-4-(N-succino)-5-aminoimidazole-4-carboxamide ribonucleotide
-
-
-
i.e. APBADP, the non-cleavable substrate analogue acts as a competitive inhibitor with respect to either substrate. ASL binds up to 4 mol of APBADP per mole of enzyme tetramer, the enzyme exhibits negative cooperativity. Binding to enzyme mutants, overview
adenosine phosphonobutyric acid, 2'(3'),5'-diphosphate
i.e. APBADP, the non-cleavable substrate analogue acts as a competitive inhibitor with respect to either substrate. ASL binds up to 4 mol of APBADP per mole of enzyme tetramer, the enzyme exhibits positive cooperativity
AMP
product inhibition competitive versus succinyladenosine monophosphate
-
10-15 µM, inhibitor reacts both with the free enzyme and the enzyme substrate complex
trans-4-hydroxy-2-nonenal
-
10-15 µM, inhibitor reacts both with the free enzyme and the enzyme substrate complex
trans-4-hydroxy-2-nonenal
-
10-15 µM, inhibitor reacts both with the free enzyme and the enzyme substrate complex
trans-4-hydroxy-2-nonenal
-
10-15 µM, inhibitor reacts both with the free enzyme and the enzyme substrate complex
-
dithiothreitol increases inhibition of trans-4-hydroxy-2-nonenal; hydroxylamine reverses inhibition of trans-4-hydroxy-2-nonenal
-
additional information
as hydrophobic interactions are weakened at 8°C and 4°C, the catalytic activity of ASL decreases strikingly and the enzyme dissociates to a mixture of monomer-dimer-trimer, with small amounts of tetramer
-
additional information
-
as hydrophobic interactions are weakened at 8°C and 4°C, the catalytic activity of ASL decreases strikingly and the enzyme dissociates to a mixture of monomer-dimer-trimer, with small amounts of tetramer
-
additional information
-
dithiothreitol increases inhibition of trans-4-hydroxy-2-nonenal; hydroxylamine reverses inhibition of trans-4-hydroxy-2-nonenal
-
additional information
-
dithiothreitol increases inhibition of trans-4-hydroxy-2-nonenal; hydroxylamine reverses inhibition of trans-4-hydroxy-2-nonenal
-
additional information
-
dithiothreitol increases inhibition of trans-4-hydroxy-2-nonenal; hydroxylamine reverses inhibition of trans-4-hydroxy-2-nonenal
-