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3.5.99.7: 1-aminocyclopropane-1-carboxylate deaminase

This is an abbreviated version!
For detailed information about 1-aminocyclopropane-1-carboxylate deaminase, go to the full flat file.

Word Map on EC 3.5.99.7

Reaction

1-aminocyclopropane-1-carboxylate
+
H2O
=
2-oxobutanoate
+
NH3

Synonyms

1-aminocyclopropane-1-carboxylate deaminase, 1-aminocyclopropane-1-carboxylate endolyase (deaminating), 1-aminocyclopropane-1-carboxylic acid deaminase, 1-aminocyclopropane-1-carboxylic acid-deaminase, ACC deaminase, ACC-deaminase, ACCD, ACD, AcdS, ACPC deaminase, AMETH_2787, aspB, BC_3216, DA46_1949, deaminase, 1-aminocyclopropane-1-carboxylate, EC 4.1.99.4, More, PST_1815

ECTree

     3 Hydrolases
         3.5 Acting on carbon-nitrogen bonds, other than peptide bonds
             3.5.99 In other compounds
                3.5.99.7 1-aminocyclopropane-1-carboxylate deaminase

Inhibitors

Inhibitors on EC 3.5.99.7 - 1-aminocyclopropane-1-carboxylate deaminase

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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
1-amino-2,2-difluorocyclopropane-1-carboxylic acid
-
rac-DFACC, chemical synthesis, overview. Mechanism of decomposition and inhibition of 1-aminocyclopropane-1-carboxylic acid deaminase, and Michaelis-Menten kinetics. DFACC is unstable under near-physiological conditions where it primarily decomposes via specific-base catalysis to 3-fluoro-2-oxobut-3-enoic acid. Different decomposotion mechanisms are described. Upon incubation with ACC deaminase, DFACC is a slow-dissociating inhibitor of ACC deaminase with submicromolar affinity
1-amino-2-methylenecyclopopropane-1-carboxylic acid
-
irreversible
1-aminocyclopropanephosphonate
-
-
5,5'-dithiobis(2-nitrobenzoic acid)
-
-
aminooxyacetic acid
-
0.005-1 mM, enzymatic activity is progressively inhibited as the aminooxyacetic acid concentration is increased
beta-chloro-Ala
beta-fluoro-D-Ala
-
-
cyclohexylhydrazine
-
-
D-Ser
homoserine
L-2-aminobutanoate
L-Ala
L-Ser
L-serine
-
5 mM L-serine results in at least a 50% decrease of measurable ACD activity
Monoiodoacetamide
-
-
NH2CONH-NH2
-
-
O-acetyl-D-Ser
-
-