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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

Reaction

(S)-2-[5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido]succinate
=
fumarate
+
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamide

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

     4 Lyases
         4.3 Carbon-nitrogen lyases
             4.3.2 Amidine-lyases
                4.3.2.2 adenylosuccinate lyase

Inhibitors

Inhibitors on EC 4.3.2.2 - adenylosuccinate lyase

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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
2'-deoxy-AMP
4-aminopyrazolo[3,4-d]pyrimidine ribose 5'-phosphate
-
-
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
8-Aza-AMP
-
-
adenosine phosphonobutyric acid, 2'(3'),5'-diphosphate
adenosine phosphonobutyric, 2'(3'), 5'-diposphate
-
-
adenyloethylphosphonate
-
-
adenylosuccinate 2',3'-acyclic (N,N-ethyl) diamine
-
weak
adenylosuccinate 2',3'-acyclic dialcohol
-
-
adenylosuccinate 2',3'-acyclic dialdehyde
-
-
ADP
-
weak, competitive
ammonium salt of N6-malonyl adenosine 5'-phosphate
-
noncompetitive inhibitor, irreversible
arabinosyl-AMP
ATP
-
weak, competitive
CuSO4
-
complete inhibition at 0.05 mM
DL-3-phosphonoalanine
-
-
EDTA
-
above 15 mM
erythro-beta-fluoro-4-(N-succino)-5-aminoimidazole-4-carboxamide ribonucleotide
-
-
erythro-beta-fluoroadenylosuccinate
-
-
erythro-beta-fluoroaspartate
-
-
fumarate
I-
-
100-200 mM
KBr
presence of increasing concentrations of KBr of 0.1–2.5 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
mercaptopurinosuccinate
-
substrate inhibition
Mg2+
-
concentration of Mg2+ approaching that of EDTA
N-(5-amino-1-(beta-D-ribofuranosyl)imidazole-4-carbonyl)-L-threo-beta-methylaspartic acid 5'-phosphate
-
-
N6-(2-carboxyethyl)-AMP
-
i.e. adenylopropionate
N6-(D-1,2-dicarboxyethyl)-AMP
-
i.e. D-adenylosuccinate
N6-(DL-1,2-dicarboxy-threo-2-hydroxyethyl)-AMP
-
i.e. adenylomalate
N6-(DL-1-carboxy-2-phosphonoethyl)AMP
-
i.e. adenylophosphonopropionate
N6-(L-1,3-dicarboxyprop-1-yl)-AMP
-
i.e. adenyloglutarate
N6-(L-1-carboxy-2-cyanoethyl)-AMP
-
i.e. adenylocyanopropionate
N6-(L-1-carboxy-2-methylsulfoxyethyl)-AMP
-
i.e. adenylomethylsulfoxypropionate
N6-(L-1-carboxy-2-nitroethyl)-AMP
-
competitive
N6-(L-1-carboxy-2-sulfinoethyl)-AMP
-
i.e. adenylosulfinopropionate
N6-(L-1-carboxy-2-sulfoethyl)-AMP
-
i.e. adenylosulfopropionate
nitroacrylate
-
0.02 mM, 70% inactivation
NO3-
-
100-200 mM
nonenal
phosphate
-
competitive
phosphopropionoadenosine
-
-
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
-
-
threo-beta-fluoroadenylosuccinate
-
-
trans-4-hydroxy-2-nonenal
virazole 5'-phosphate
-
-
additional information
-