DYNAMICS OF ELECTRON TRANSFER FLAVOPROTEIN

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This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The global and local flexibility's of the L7/L12 domain are being investigated to identify the solution characterization of this protein. The results will be evaluated in terms of the position and orientation of the two L7/L12 domains in the complete ribosome. In addition, the postulant binding affinity of L10, a second ribosome protein, and elongation factor Tu with L7/L21 will be examined. This data should help further our understanding on how these proteins cooperate within the ribosome during a protein elongation.