What is he best known for?
The fields of study he is best known for:
His main research concerns Biochemistry, Cell biology, Stereochemistry, Genetics and Protein structure.
His work in the fields of Cell biology, such as GTPase, overlaps with other areas such as Melanosome transport, RAB27, Griscelli syndrome and Melanophilin.
His biological study spans a wide range of topics, including Epitope, Proton pump, Interleukin 15 and Binding site.
His research in Protein structure intersects with topics in Peptide sequence, Sequence alignment, Membrane and Endocytosis.
His Peptide sequence study combines topics in areas such as SH3 domain and Plasma protein binding.
His study looks at the relationship between Transfer RNA and fields such as In vivo, as well as how they intersect with chemical problems.
His most cited work include:
- Curved EFC/F-BAR-Domain Dimers Are Joined End to End into a Filament for Membrane Invagination in Endocytosis (324 citations)
- Structural genomics projects in Japan. (279 citations)
- A Novel Zinc-binding Motif Revealed by Solution Structures of DNA-binding Domains of Arabidopsis SBP-family Transcription Factors ☆ (165 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Solution structure, Crystal structure, Biochemistry, Crystallography and Stereochemistry.
His Solution structure study combines topics from a wide range of disciplines, such as RNA, Binding domain, Biophysics and Cell biology.
Takaho Terada focuses mostly in the field of Crystal structure, narrowing it down to matters related to Thermus thermophilus and, in some cases, Hypothetical protein and Ribosomal protein.
Biochemistry is represented through his Protein structure, Enzyme, Active site and Amino acid research.
His Protein structure study which covers Peptide sequence that intersects with Structural genomics.
Takaho Terada merges Stereochemistry with Terminal in his research.
He most often published in these fields:
- Solution structure (36.05%)
- Crystal structure (21.84%)
- Biochemistry (21.84%)
What were the highlights of his more recent work (between 2010-2020)?
- Biochemistry (21.84%)
- Cell biology (13.16%)
- Biophysics (16.05%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Biochemistry, Cell biology, Biophysics, Crystal structure and Stereochemistry.
His Protein biosynthesis, Protein structure, Amino acid, Protein subunit and Protease study are his primary interests in Biochemistry.
The Cell biology study combines topics in areas such as Exonic splicing enhancer and Cell adhesion.
His Biophysics research is multidisciplinary, relying on both Solution structure, ATPase, RNA, Binding domain and Beta protein.
His Crystal structure study contributes to a more complete understanding of Crystallography.
Salt bridge, Genetics, Docking, Two-dimensional nuclear magnetic resonance spectroscopy and Conserved sequence is closely connected to Peptide in his research, which is encompassed under the umbrella topic of Stereochemistry.
Between 2010 and 2020, his 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)
- Rotation mechanism of Enterococcus hirae V 1 -ATPase based on asymmetric crystal structures (88 citations)
In his most recent research, the most cited papers focused on:
Biochemistry, Cell biology, Crystallography, Stereochemistry and Enterococcus hirae are his primary areas of study.
The various areas that Takaho Terada examines in his Cell biology study include HEK 293 cells, Cell culture, Glutamine and NS3.
His Crystallography research is multidisciplinary, incorporating elements of Plasma protein binding, Molecular motor, Thermodynamics and Michaelis–Menten kinetics.
His Stereochemistry study integrates concerns from other disciplines, such as Double-stranded RNA binding, Mutation, Peptide and Enzyme.
Takaho Terada usually deals with Hydrolase and limits it to topics linked to Nucleotide and Membrane protein.
His ATP hydrolysis research integrates issues from Membrane, Helix and Eukaryotic Large Ribosomal Subunit.
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