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EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
2.7.2.7
ATP + acetate
6% of the activity with butanoate
Clostridium acetobutylicum
ADP + acetyl phosphate
-
?
2.7.2.7
ATP + butanoate
-
Clostridium acetobutylicum
ADP + butanoyl phosphate
-
?
2.7.2.7
ATP + butanoate
-
Clostridium acetobutylicum
ADP + butanoyl phosphate
-
r
2.7.2.7
ATP + isobutanoate
54% of the activity with butanoate
Clostridium acetobutylicum
ADP + isobutanoyl phosphate
-
?
2.7.2.7
ATP + isovalerate
32% of the activity with butanoate
Clostridium acetobutylicum
ADP + isopentanoyl phosphate
-
?
2.7.2.7
ATP + propionate
43% of the activity with butanoate
Clostridium acetobutylicum
ADP + propanoyl phosphate
-
?
2.7.2.7
ATP + valerate
89% of the activity with butanoate
Clostridium acetobutylicum
ADP + pentanoyl phosphate
-
?
2.7.2.7
ATP + vinyl acetate
23% of the activity with butanoate
Clostridium acetobutylicum
ADP + vinylacetyl phosphate
-
?
2.7.2.7
more
the enzyme is not regulated by the end-product, its specific activity is constant during the fermentation
Clostridium acetobutylicum
?
-
?
2.7.2.7
more
semi-automated reverse engineering algorithm. The reconstructed metabolic network was used to create a genome-scale model that correctly characterized the butyrate kinase knock-out and the asolventogenic M5 pSOL1 megaplasmid degenerate strains. Systematic gene knock-out simulations performed to identify a set of genes encoding clostridial enzymes essential for growth in silico.
Clostridium acetobutylicum
?
-
?
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