What is she best known for?
The fields of study she is best known for:
Mikako Shirouzu mainly focuses on Biochemistry, Cell biology, Stereochemistry, Genetics and Biophysics.
Her studies in Cell biology integrate themes in fields like Molecular biology, RNA polymerase II, Mutant and Transcription factor.
The various areas that Mikako Shirouzu examines in her Stereochemistry study include Proton pump, ATPase, Residue, Hydrolase and Peptide.
Her B3 domain, DNA-binding domain, Binding domain and Sequence alignment study in the realm of Genetics connects with subjects such as Prokaryotic DNA replication.
Her biological study spans a wide range of topics, including SH3 domain, Plasma protein binding, Protein structure and Cell membrane.
The study incorporates disciplines such as Crystallography, Xenopus, Bacteriorhodopsin and Protein Data Bank in addition to Biophysics.
Her most cited work include:
- Crystal Structure of the Complex of Human Epidermal Growth Factor and Receptor Extracellular Domains. (953 citations)
- A small-molecule AdipoR agonist for type 2 diabetes and short life in obesity (396 citations)
- Curved EFC/F-BAR-Domain Dimers Are Joined End to End into a Filament for Membrane Invagination in Endocytosis (324 citations)
What are the main themes of her work throughout her whole career to date?
Her main research concerns Crystal structure, Biochemistry, Solution structure, Crystallography and Stereochemistry.
In her work, Hypothetical protein, Structural genomics and Ribosomal protein is strongly intertwined with Thermus thermophilus, which is a subfield of Crystal structure.
Her study in Biochemistry focuses on Protein structure, Binding site, Transfer RNA, Amino acid and Escherichia coli.
Mikako Shirouzu interconnects RNA, Binding domain, Biophysics and Cell biology in the investigation of issues within Solution structure.
Cell biology is closely attributed to Molecular biology in her study.
Her work in Stereochemistry is not limited to one particular discipline; it also encompasses Pyrococcus horikoshii.
She most often published in these fields:
- Crystal structure (24.78%)
- Biochemistry (22.62%)
- Solution structure (21.47%)
What were the highlights of her more recent work (between 2014-2021)?
- Biochemistry (22.62%)
- Biophysics (14.70%)
- Cell biology (15.13%)
In recent papers she was focusing on the following fields of study:
Mikako Shirouzu mostly deals with Biochemistry, Biophysics, Cell biology, Crystal structure and Cancer research.
The various areas that Mikako Shirouzu examines in her Biophysics study include Extracellular, Microtubule and DNA.
Her Cell biology research includes themes of Mutation, Gene, RNA polymerase II and Nucleosome.
Her study in Crystal structure is interdisciplinary in nature, drawing from both Receptor, Adiponectin, Molecule and Stereochemistry.
Her Cancer research study combines topics from a wide range of disciplines, such as Wnt signaling pathway, Cancer cell, Cytotoxic T cell, Kinase and In vivo.
Mikako Shirouzu combines subjects such as Protein structure and Peptide sequence with her study of Binding site.
Between 2014 and 2021, her most popular works were:
- Crystal structures of the human adiponectin receptors (117 citations)
- SARS-CoV 3CL protease cleaves its C-terminal autoprocessing site by novel subsite cooperativity (98 citations)
- Structure of the complete elongation complex of RNA polymerase II with basal factors (85 citations)
In her most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Biochemistry, Biophysics, Cell biology, Protein structure and Microtubule.
Her research on Biochemistry frequently links to adjacent areas such as Column chromatography.
Her Biophysics research incorporates elements of ATP hydrolysis, Nucleotide, Crystal structure, Function and Cell adhesion.
Her Cell biology research is multidisciplinary, relying on both Protein domain, Protein subunit, Gene, RNA polymerase II and Membrane protein.
Mikako Shirouzu works mostly in the field of Protein structure, limiting it down to concerns involving Plasma protein binding and, occasionally, Ligand, HEK 293 cells, Receptor complex and Motility.
Her Microtubule research integrates issues from Microtubule nucleation, Axon and Collapsin response mediator protein family.
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