Unknown

Dataset Information

0

Barrier Crossing in Dihydrofolate Reductasedoes not involve a rate-promoting vibration.


ABSTRACT: We have studied atomic motions during the chemical reaction catalyzed by the enzyme dihydrofolate reductase of Escherichia coli (EcDHFR), an important enzyme for nucleic acid synthesis. In our earlier work on the enzymes human lactate dehydrogenase and purine nucleoside phosphorylase, we had identified fast sub-ps motions that are part of the reaction coordinate. We employed Transition Path Sampling (TPS) and our recently developed reaction coordinate identification methodology to investigate if such fast motions couple to the reaction in DHFR on the barrier-crossing timescale. While we identified some protein motions near the barrier crossing event, these motions do not constitute a compressive promoting vibration, and do not appear as a clearly identifiable protein component in reaction.

SUBMITTER: Dametto M 

PROVIDER: S-EPMC3430383 | biostudies-literature | 2012 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Barrier Crossing in Dihydrofolate Reductasedoes not involve a rate-promoting vibration.

Dametto Mariangela M   Antoniou Dimitri D   Schwartz Steven D SD  

Molecular physics 20120110 9-10


We have studied atomic motions during the chemical reaction catalyzed by the enzyme dihydrofolate reductase of Escherichia coli (EcDHFR), an important enzyme for nucleic acid synthesis. In our earlier work on the enzymes human lactate dehydrogenase and purine nucleoside phosphorylase, we had identified fast sub-ps motions that are part of the reaction coordinate. We employed Transition Path Sampling (TPS) and our recently developed reaction coordinate identification methodology to investigate if  ...[more]

Similar Datasets

| S-EPMC4939807 | biostudies-literature
| S-EPMC2859820 | biostudies-literature
| S-EPMC4939135 | biostudies-literature
| S-EPMC7044130 | biostudies-literature
| S-EPMC2706106 | biostudies-literature
| S-EPMC5540238 | biostudies-other
| S-EPMC6562543 | biostudies-literature
| S-EPMC3219149 | biostudies-literature
| S-EPMC10046162 | biostudies-literature
| S-EPMC2725243 | biostudies-literature