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FHL2 is involved in ECM-integrin receptor interaction, assembly of ECM proteins on the cell surface and bundling of focal adhesions [4], [5].
Reviewer #2: U4 and U6 small nuclear RNAs (snRNAs) undergo several conformational transitions during the spliceosome cycle, from the U4-U6 base pairing interaction, assembly into the U4/U6-U5 tri-snRNP, U4/U6-to-U6/U2 transition during splicing catalysis and U4 release, to post-spliceosomal recycling and re-assembly of the U4/U6-paired structure.
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Although lacking many proteins and interactions, the up-to-date SSU processome interaction map compiled in this study can be applied to generate new hypotheses of subcomplex interactions, assembly and function.
Therefore, ASB multimeric complexes are involved in numerous cell processes and pathways; however, their interactions, assembly, and biological roles remain poorly understood.
Protein subunit interaction and assembly in bacteria occur as the subunits are being synthesized on the ribosome.
Additionally, there are some problems with cell to cell interaction, the assembly and alignment of ECM components and the host response to scaffolds.
The seat share of the largest party, in turn, is constrained by the interaction of assembly size and electoral district magnitude in the following way.
Because FHL2 is involved in focal adhesion, ECM-cell interaction and assembly of the extracellular matrix [4], [5], a role for FHL2 in the regulation of cell mobility seems an attractive possibility.
Perhaps Impβ B3 interaction facilitates assembly of Impα Impβ MRTF-A complex.
The classical 5-stranded clade in particular appears to have given rise to several lineages that seem to function as protein interaction adapters, assembly or stability factors in very different biochemical contexts.
For the small, 30S, subunit, 21 r-proteins are structural parts of this complex; many of them interact directly with the rRNA and several are involved in protein protein interactions during assembly.
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