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1.7.7.2: ferredoxin-nitrate reductase

This is an abbreviated version!
For detailed information about ferredoxin-nitrate reductase, go to the full flat file.

Word Map on EC 1.7.7.2

Reaction

nitrite
+
H2O
+
oxidized ferredoxin
=
nitrate
+
reduced ferredoxin
+ 2 H+

Synonyms

assimilatory ferredoxin-nitrate reductase, Assimilatory nitrate reductase, C452_13229, dissimilatory nitrate reductase, EC 1.7.99.4, Fd-dependent nitrate reductase, Fd-NAS, NaR, narB, NarGH, NAS, NasB, nitrate (ferredoxin) reductase, nitrate reductase, reductase, nitrate (ferredoxin), respiratory nitrate reductase

ECTree

     1 Oxidoreductases
         1.7 Acting on other nitrogenous compounds as donors
             1.7.7 With an iron-sulfur protein as acceptor
                1.7.7.2 ferredoxin-nitrate reductase

Inhibitors

Inhibitors on EC 1.7.7.2 - ferredoxin-nitrate reductase

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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
ammonia
-
after initial slight stimulation rapid and complete inhibition, promotes conversion of ferredoxin-nitrate reductase into its reduced inactive form, metabolic interconversion
azide
Chlorate
-
competitive inhibitor with respect to nitrate
cyanide
Dithionite
FAD
-
photoactivated FAD, irreversible inactivation
KCl
-
inhibition of nitrate reductase-ferredoxin complex formation at high ionic strength
light
-
light- and oxygen-dependent inactivation of enzyme activity in absence but not in presence of any added nitrogen source, inactivation may result from an oxidative modification of enzyme, assay in cell suspension
-
MgSO4
-
inhibition of nitrate reductase-ferredoxin complex formation at high ionic strength
N-acetylsuccinimide
-
115fold excess, loss of more than 80% and 5-10% loss of ferredoxin-dependent and methylviologen dependent activity after 1 h, respectively
NaCl
-
more than 80% inhibition above 200 mM, inhibition of nitrate reductase-ferredoxin complex formation at high ionic strength
oxygen
-
light- and oxygen-dependent inactivation of enzyme activity in absence but not in presence of any added nitrogen source, inactivation may result from an oxidative modification of enzyme, assay in cell suspension
p-hydroxymercuribenzoate
Phenylglyoxal
-
76fold excess, approx. 60% and 20% loss of ferredoxin dependent and methylviologen dependent activity after 2 h, respectively
sulfite
1 mM, 30% inhibition
thiocyanate
-
10 mM, 53% inhibition. Preincubating for 1 h does not increase the inhibition
additional information
-