Matthew L Peck, Daniel Herschlag
Index: RNA 9(10) , 1180-7, (2003)
Full Text: HTML
Whereas ATPgammaS is often considered a nonhydrolyzable substrate for ATPases, we present evidence that ATPgammaS is a good substrate for the RNA-stimulated nucleotide hydrolysis and RNA unwinding activities of eIF4A. In the presence of saturating single-stranded poly(U) RNA, eIF4A hydrolyzes ATPgammaS.Mg and ATP.Mg with similar steady-state parameters (KM(NTP.Mg) = 66 and 58 microM and kcat = 1.0 and 0.97 min(-1), respectively). ATPgammaS.Mg also supports catalysis of RNA unwinding within 10-fold of the rate supported by ATP.Mg. The identical steady-state rate parameters, in comparison with the expected difference in the intrinsic rate of hydrolysis for ATP and ATPgammaS, suggest a nonchemical rate-limiting step for nucleotide hydrolysis. These results raise caution concerning the assumption that ATPgammaS is a nonhydrolyzable ATP analog and underscore the utility of thio-substituted NTPs as mechanistic probes.
| Structure | Name/CAS No. | Molecular Formula | Articles |
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Adenosine 5'-[γ-thio]triphosphate Tetralithium Salt
CAS:93839-89-5 |
C10H12Li4N5O12P3S |
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![Adenosine 5'-[γ-thio]triphosphate Tetralithium Salt Structure](https://image.chemsrc.com/caspic/206/93839-89-5.png)