Paul A. Bates mostly deals with Cell biology, Computational biology, Protein structure, Genetics and DNA repair. His Cell biology study incorporates themes from Lateral inhibition, Cell migration, Angiogenesis and Anatomy. The study incorporates disciplines such as Protein structure prediction, Server, Homology and Protein–protein interaction in addition to Computational biology.
His research investigates the connection between Protein structure prediction and topics such as Similarity that intersect with problems in Protein secondary structure, Protein Data Bank and Crystallography. His biological study spans a wide range of topics, including Plasma protein binding, Molecular recognition, Stereochemistry, Substrate and Dissociation constant. His Genetics course of study focuses on Sequence alignment and Sequence analysis, Sequence identity and Homology modeling.
His primary areas of investigation include Crystallography, Crystal structure, Stereochemistry, Molecule and X-ray crystallography. His Crystallography research includes elements of Inorganic chemistry and Heteronuclear molecule. His work carried out in the field of Crystal structure brings together such families of science as Pyridine, Inorganic compound, Nuclear magnetic resonance spectroscopy, Hydrogen bond and Copper.
His Stereochemistry research integrates issues from Denticity, Ligand, Medicinal chemistry, Chelation and Crystal. In his research, Paul A. Bates performs multidisciplinary study on Medicinal chemistry and Enol. His Molecule research is multidisciplinary, incorporating elements of Oxidative addition, Hydrate and Ethylenediamine.
His scientific interests lie mostly in Docking, Computational biology, Cell biology, Protein protein and Protein–protein interaction. He has included themes like Genetics, Binding affinities and CASP in his Computational biology study. As a member of one scientific family, Paul A. Bates mostly works in the field of Genetics, focusing on Protein structure and, on occasion, Receptor–ligand kinetics and Cancer.
His work deals with themes such as Cell adhesion, Cytoskeleton and T-cell receptor, which intersect with Cell biology. His study in Protein–protein interaction is interdisciplinary in nature, drawing from both Space partitioning, Protein engineering, Biological system and Systems biology. The concepts of his Molecular recognition study are interwoven with issues in Crystallography and Force field.
His primary areas of study are Computational biology, Cell biology, Docking, Genetics and Molecular Docking Simulation. His research in Computational biology intersects with topics in Chromatin, CASP and Protein–protein interaction. His studies in Cell biology integrate themes in fields like Acquired immune system, Antigen and Receptor.
His work is connected to Protein protein and Macromolecular docking, as a part of Docking. His Protein protein research incorporates elements of Upload, Ligand, Molecular dynamics and Structural bioinformatics. His studies deal with areas such as Searching the conformational space for docking, Prediction algorithms, Binding affinities and Antibody antigen as well as Molecular Docking Simulation.
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Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Marco Gerlinger;Stuart Horswell;James Larkin;Andrew J Rowan.
Nature Genetics (2014)
Enhancement of protein modeling by human intervention in applying the automatic programs 3D-JIGSAW and 3D-PSSM.
Paul A. Bates;Lawrence A. Kelley;Robert M. MacCallum;Michael J.E. Sternberg.
Global topological features of cancer proteins in the human interactome
Pall F. Jonsson;Paul A. Bates.
Structure of the AAA ATPase p97.
Xiaodong Zhang;Anthony Shaw;Paul A. Bates;Richard H. Newman.
Molecular Cell (2000)
Reversal of DNA alkylation damage by two human dioxygenases
Tod Duncan;Sarah C. Trewick;Pertti Koivisto;Paul A. Bates.
Proceedings of the National Academy of Sciences of the United States of America (2002)
Repair of alkylated DNA: recent advances.
Barbara Sedgwick;Paul A Bates;Johanna Paik;Susan C Jacobs.
DNA Repair (2007)
The binding site on ICAM-1 for Plasmodium falciparum-infected erythrocytes overlaps, but is distinct from, the LFA-1-binding site.
Anthony R. Berendt;Alison McDowall;Alister G. Craig;Paul A. Bates.
Structure of an XRCC1 BRCT domain: a new protein-protein interaction module.
Xiaodong Zhang;Solange Moréra;Solange Moréra;Paul A. Bates;Philip C. Whitehead.
The EMBO Journal (1998)
Matrix geometry determines optimal cancer cell migration strategy and modulates response to interventions
Melda Tozluoğlu;Alexander L. Tournier;Robert P. Jenkins;Steven Hooper.
Nature Cell Biology (2013)
An automated classification of the structure of protein loops
Baldomero Oliva;Paul A. Bates;Enrique Querol;Francesc X. Avilés.
Journal of Molecular Biology (1997)
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