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2.7.7.2: FAD synthase

This is an abbreviated version!
For detailed information about FAD synthase, go to the full flat file.

Word Map on EC 2.7.7.2

Reaction

ATP
+
FMN
=
diphosphate
+
FAD

Synonyms

adenosine triphosphate-riboflavin mononucleotide transadenylase, adenosine triphosphate-riboflavine mononucleotide transadenylase, ATP-FMN adenylyltransferase, ATP:FMN adenylyl transferase, ATP:FMN adenylyltransferase, AtRibF1, AtRibF2, FAD pyrophosphorylase, FAD synthase, FAD synthetase, FAD synthetase isoform 1, FAD synthetase isoform 2, Fad1, FADS, FADS-6, FADS1, FADS2, FLAD1, flavin adenine dinucleotide synthetase, FMN adenylyltransferase, FMN pyrophosphorylase, FMN:ATP adenylyltransferase, FMNAT, lysZ, MJ1179, More, ribF, RibL, riboflavin adenine dinucleotide pyrophosphorylase, riboflavin mononucleotide adenylyltransferase, riboflavine adenine dinucleotide adenylyltransferase, SPAP_1083

ECTree

     2 Transferases
         2.7 Transferring phosphorus-containing groups
             2.7.7 Nucleotidyltransferases
                2.7.7.2 FAD synthase

Inhibitors

Inhibitors on EC 2.7.7.2 - FAD synthase

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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
(1R,2S,4aS,4bS,7R,8aR,10aS)-7-hydroxy-2,4b-dimethyl-1-[(3-oxo-3H-indol-2-yl)methyl]tetradecahydrophenanthrene-2-carboxylic acid
inhibitor of the activity of the flavin adenylyl transferase module of the FADS
1,5-Dideaza-FMN
-
-
1-deaza-FMN
-
-
2-([1-[4-(trifluoromethyl)pyrimidin-2-yl]piperidin-4-yl]carbamoyl)benzoic acid
inhibitor of the activity of the flavin adenylyl transferase module of the FADS
2-([[(9H-fluoren-9-yl)methoxy]carbonyl]amino)benzoic acid
inhibitor of the activity of the flavin adenylyl transferase module of the FADS, able to inhibit growth of Corynebacterium ammoniagenes and Mycobacterium tuberculosis
2-thio-FMN
-
-
5'-sulfo-FMN
-
-
8-hydroxy-7-methyl-FMN
-
-
D-glucose 6-phosphate
-
-
D-lyxose 5-phosphate
-
-
diphosphate
GDP
competitive inhibition
GTP
uncompetitive inhibition
hexyl 6-phosphate
-
-
KI
-
inhibits FAD hydrolysis
methyl 2-[(4-chlorophenyl)carbamoyl]-N-(3,5-dimethyl-1,2-oxazole-4-sulfonyl)hydrazine-1-carboximidothioate
56% resiudal activity at 0.25 mM, inhibitor of the activity of the flavin adenylyl transferase module of the FADS
N-(5-nitrothiophene-3-carbonyl)-2-[[4-(propan-2-yl)phenyl]carbamothioyl]hydrazine-1-carboxamide
inhibitor of the activity of the flavin adenylyl transferase module of the FADS, able to inhibit growth of Corynebacterium ammoniagenes and Mycobacterium tuberculosis
NAD+
-
inhibits FAD cleavage completely
NADH
-
inhibits FAD hydrolysis
Riboflavin 5'-diphosphate
-
weak cofactor for FAD-requiring enzymes
Urea
the enzymatic activity of isoform FADS2 decreases dramatically at increasing urea concentration, with a mid-point for activity loss at 2.1 m urea
additional information
-
no detectable inhibition with 2-[(hydroxyethyl)amino]-FMN, 2-morpholinyl-FMN, 2-(phenylamino)-FMN, 3-methyl-FMN, 3-(carboxymethyl)-FMN, 8-alpha-imidazolyl-FMN, 8-alpha-(N-methylimidazolyl)-FMN, 5'-phosphothionate, DL-glycerol 3-phosphate and propyl 3-phosphate
-