Sentence examples for more structural studies from inspiring English sources

Therefore, more structural studies and mutational analysis of complexes built of those domains are necessary to define the motifs and interacting residues involved.

More structural studies need to be done to further investigate this question.

More structural studies for these primosomal proteins are still necessary to elucidate the interaction between PriB and DnaT, as well as the release from the replication restart system.

In the absence of more structural studies we are unable to tell whether the least important of Holbrook and Ingram's criteria are met, but given the known structural differences this seems highly unlikely.

Recently, more extensive structural studies were carried out by White et al. [76] and it was concluded, based on room temperature PXRD and IR data, that the ionic molecules were packed as lamellar bilayer structures in a triclinic crystal system composed of fully extended all-trans hydrocarbon chains.

These results lay the foundation for more advanced structural studies and can be used to generate testable hypotheses for future structure function experiments.

The analysis of FK1TMD in DHPC micelles at 43 °C indicated a small decrease in helical content compared to that observed at 25 °C, although the significance, if any, of this observation will require more detailed structural studies.

A full understanding of the activity and mechanism of the NuRD complex will require more challenging structural studies of the intact complex and how it interacts with its chromatin substrate.

However, difficulty in securing sufficient cell wall material from the Arabidopsis ref8 mutants, which are severely stunted [ 12, 13], has limited more detailed structural studies (i.e., NMR) of the resultant lignins.

More recently, structural studies of E1 papillomavirus helicase (Enemark and Joshua-Tor, 2006) and RNA translocase Rho (Thomsen and Berger, 2009) revealed more incisive mechanistic insight into the translocation process, because the structures showed the asymmetry and different nucleotide-binding states required for a sequential-binding site change mechanism.

Our data suggest that this site may function as a priming site for S320 phosphorylation; however, more detailed structural studies are required to further investigate the role of T322 (or its analogous residue in the other Fos proteins) in tandem with S320 for Fra-2 stabilization.