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Results 1 - 10 of 22 > >>
EC Number
Inhibitors
Commentary
Structure
2'-AMP
-
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2-(4-maleimidoanilino)-naphthalene-6-sulfonic acid
0.004 mM, 2 h incubation, 75% inhibition of reverse reaction catalyzed by A348C mutant enzyme, 95% inhibition of A390C mutant enzyme after 1 h, 90% inhibition of K424C mutant enzyme after 1 h, 55% inhibition of R425C mutant enzyme after 1h
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3-Aminopyridine adenine dinucleotide phosphate
competitive vs. NADP(H)
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5'-AMP
-
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acetylpyridine adenine dinucleotide
-
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Butane-2,3-dione
40 mM, almost complete inactivation of enzyme activity in chromatophores after 12 min, NAD+ and NADP+ partially protect, complete protection by a combination of NAD+ and NADP+
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Cd2+
low concentrations of Cd2+ strongly inhibit revers transhydrogenation
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N,N'-dicyclohexylcarbodiimide
NADH protects the enzyme against inhibition by N,N'-dicyclohexylcarbodiimide, while NADP+ , and to a lesser extent NADPH increase the rate of inhibition
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N,N'-dicyclohexylcarbodiimide
about 12% residual activity after 180 min at 0.5 mM
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N,N'-dicyclohexylcarbodiimide
modification of the enzyme with N,N'-dicyclohexylcarbodiimide leads to inhibition of the rate of release of NADP+ and NADPH from the enzyme, but has a much smaller effect on the binding and release of NAD+, NADH and their analogues and on the interconversion of the ternary complexes of the enzyme with its substrates
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Results 1 - 10 of 22 > >>