John C. Wallace focuses on Biochemistry, Pyruvate carboxylase, Biotin, Molecular biology and Insulin-like growth factor. His Biochemistry and Biological activity, Amino acid, Binding protein, Peptide and Plasma protein binding investigations all form part of his Biochemistry research activities. His Pyruvate carboxylase research includes themes of Mutant, Gene, Saccharomyces cerevisiae, Yeast and Isozyme.
His Biotin research is multidisciplinary, incorporating perspectives in Biotin carboxylase, Cofactor, Stereochemistry and Biotinylation. His Molecular biology research incorporates elements of Growth factor, Cellular differentiation, Gene expression and Recombinant DNA. His research in Insulin-like growth factor intersects with topics in Binding domain, Potency, Signal transduction, Cell biology and Affinities.
His primary scientific interests are in Biochemistry, Pyruvate carboxylase, Molecular biology, Biotin and Enzyme. His work in Biochemistry tackles topics such as Stereochemistry which are related to areas like Binding site. His study looks at the relationship between Pyruvate carboxylase and topics such as Acetyl-CoA, which overlap with Methylcrotonyl-CoA carboxylase.
His work in Molecular biology addresses issues such as Saccharomyces cerevisiae, which are connected to fields such as Mutant. John C. Wallace interconnects Acetyl-CoA carboxylase, Biotin carboxyl carrier protein, Biotinylation and Active site in the investigation of issues within Biotin. The study incorporates disciplines such as Endocrinology and Internal medicine in addition to Amino acid.
John C. Wallace mainly investigates Biochemistry, Biotin, Pyruvate carboxylase, Molecular biology and DNA ligase. Biochemistry is frequently linked to Stereochemistry in his study. His Biotin research integrates issues from Cytoplasm, Biotin carboxyl carrier protein, Biotinylation and Fusion protein.
In Pyruvate carboxylase, John C. Wallace works on issues like Carboxylation, which are connected to Decarboxylation. His studies in Molecular biology integrate themes in fields like Proximal promoter, Gene and Transcriptional regulation. His DNA ligase study integrates concerns from other disciplines, such as Acetyl-CoA carboxylase, Repressor and Metabolic pathway.
John C. Wallace mainly focuses on Biochemistry, Biotin, DNA ligase, Pyruvate carboxylase and Ligand. Biochemistry is often connected to Stereochemistry in his work. His Biotin study combines topics in areas such as Biotin carboxyl carrier protein and Biotinylation.
His work on Biotin carboxylase is typically connected to Rhizobium etli as part of general Pyruvate carboxylase study, connecting several disciplines of science. His work deals with themes such as Ligand binding assay, Cooperative binding, Ectodomain, Wild type and Click chemistry, which intersect with Ligand. His work in Insulin-like growth factor covers topics such as Alanine scanning which are related to areas like Insulin.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Development of a Bicistronic Vector Driven by the Human Polypeptide Chain Elongation Factor 1α Promoter for Creation of Stable Mammalian Cell Lines That Express Very High Levels of Recombinant Proteins
Stephen Hobbs;Sarawut Jitrapakdee;John C. Wallace.
Biochemical and Biophysical Research Communications (1998)
Transactivation of CXCR4 by the insulin-like growth factor-1 receptor (IGF-1R) in human MDA-MB-231 breast cancer epithelial cells.
Chareeporn Akekawatchai;Jane D. Holland;Marina Kochetkova;John C. Wallace.
Journal of Biological Chemistry (2005)
Chemical and catalytic mechanisms of carboxyl transfer reactions in biotin-dependent enzymes
Paul V. Attwood;John C. Wallace.
Accounts of Chemical Research (2002)
Sequence and domain structure of yeast pyruvate carboxylase
F Lim;C P Morris;F Occhiodoro;J C Wallace.
Journal of Biological Chemistry (1988)
The biotin enzyme family: conserved structural motifs and domain rearrangements
Sarawut Jitrapakdee;John C Wallace.
Current Protein & Peptide Science (2003)
The bovine insulin-like growth factor (IGF) binding protein purified from conditioned medium requires the N-terminal tripeptide in IGF-1 for binding
Laszlo Szabo;David G. Mottershead;F.John Ballard;John C. Wallace.
Biochemical and Biophysical Research Communications (1988)
Polyadenylylated nuclear RNA contains branches
John C. Wallace;Mary Edmonds.
Proceedings of the National Academy of Sciences of the United States of America (1983)
Domain Architecture of Pyruvate Carboxylase, a Biotin-Dependent Multifunctional Enzyme
Martin St. Maurice;Martin St. Maurice;Martin St. Maurice;Laurie Reinhardt;Laurie Reinhardt;Laurie Reinhardt;Kathy H. Surinya;Kathy H. Surinya;Kathy H. Surinya;Paul V. Attwood;Paul V. Attwood;Paul V. Attwood.
Science (2007)
Natural and synthetic forms of insulin-like growth factor-1 (IGF-1) and the potent derivative, destripeptide IGF-1: biological activities and receptor binding.
F.John Ballard;Geoffrey L. Francis;Marina Ross;Christopher J. Bagley.
Biochemical and Biophysical Research Communications (1987)
Yeast pyruvate carboxylase: identification of two genes encoding isoenzymes.
Michelle E. Walker;Dale L. Val;Manfred Rohde;Rodney J. Devenish.
Biochemical and Biophysical Research Communications (1991)
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