His primary scientific interests are in Biochemistry, Mycobacterium tuberculosis, Kinase, Enzyme and Cyclin-dependent kinase. His study in Cyclin-dependent kinase 2, Transferase, Venom, Binding site and Protein structure is carried out as part of his Biochemistry studies. Walter Filgueira de Azevedo works mostly in the field of Cyclin-dependent kinase 2, limiting it down to concerns involving Cyclin-dependent kinase 1 and, occasionally, Adenine derivatives, Molecular model and Cyclin-dependent kinase 5.
His study focuses on the intersection of Mycobacterium tuberculosis and fields such as Shikimate pathway with connections in the field of Whole genome sequencing, EPSP synthase and Structural bioinformatics. His research on Enzyme often connects related areas such as Herpes simplex virus. His studies deal with areas such as Cyclin T1, Stereochemistry, Protein kinase A and Cell biology as well as Cyclin-dependent kinase.
Walter Filgueira de Azevedo mainly investigates Biochemistry, Stereochemistry, Enzyme, Docking and Purine nucleoside phosphorylase. His Biochemistry study typically links adjacent topics like Mycobacterium tuberculosis. His work on Molecular model as part of his general Stereochemistry study is frequently connected to Binary complex, thereby bridging the divide between different branches of science.
His Shikimate pathway and Substrate study, which is part of a larger body of work in Enzyme, is frequently linked to Ligand, bridging the gap between disciplines. His Docking research focuses on subjects like Computational biology, which are linked to Bioinformatics and Genome. His work in Purine nucleoside phosphorylase tackles topics such as Transferase which are related to areas like Deoxyguanosine.
The scientist’s investigation covers issues in Docking, Ligand, Molecular recognition, Computational biology and Virtual screening. The concepts of his Docking study are interwoven with issues in AutoDock and Binding site. His work carried out in the field of Computational biology brings together such families of science as Cyclin-dependent kinase, Cyclin-dependent kinase 3, Kinase and Bioinformatics.
The concepts of his Virtual screening study are interwoven with issues in Protein ligand and Organic molecules. Walter Filgueira de Azevedo combines subjects such as Stereochemistry and Hydrogen bond with his study of Intermolecular force. The Enzyme study combines topics in areas such as Cancer, Gene and Mycobacterium tuberculosis.
Walter Filgueira de Azevedo spends much of his time researching Docking, Computational biology, Machine learning, Artificial intelligence and Ligand. His work on Virtual screening and Protein–ligand docking as part of general Docking study is frequently linked to Statistical analysis, bridging the gap between disciplines. He has included themes like Bioinformatics, Cyclin-dependent kinase, Function, Kinase and Cyclin in his Computational biology study.
As a part of the same scientific study, Walter Filgueira de Azevedo usually deals with the Bioinformatics, concentrating on Protease and frequently concerns with Inhibition constant. His Cyclin-dependent kinase research incorporates themes from Cyclin-dependent kinase 1, Protein target and Protein family. His Kinase research integrates issues from Molecular recognition, Cancer, Senescence and Enzyme.
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Inhibition of Cyclin‐Dependent Kinases by Purine Analogues
Walter Filgueira De Azevedo;Sophie Leclerc;Laurent Meijer;Libor Havlicek.
FEBS Journal (1994)
Molecular docking algorithms.
Raquel Dias;Walter Filgueira de Azevedo.
Current Drug Targets (2008)
4-Arylazo-3,5-diamino-1H-pyrazole CDK Inhibitors: SAR Study, Crystal Structure in Complex with CDK2, Selectivity, and Cellular Effects†
Vladimir Krystof;Petr Cankar;Iveta Frysova;Jan Slouka.
Journal of Medicinal Chemistry (2006)
Anoplin, a novel antimicrobial peptide from the venom of the solitary wasp Anoplius samariensis.
Katsuhiro Konno;Miki Hisada;Renato Fontana;Carla C.B. Lorenzi.
Biochimica et Biophysica Acta (2001)
Structural basis for inhibition of cyclin-dependent kinase 9 by flavopiridol.
Walter Filgueira de Azevedo;Fernanda Canduri;Fernanda Canduri;Nelson José Freitas da Silveira.
Biochemical and Biophysical Research Communications (2002)
How C-terminal carboxyamidation alters the biological activity of peptides from the venom of the eumenine solitary wasp.
Mauricio L. Sforca;Sérgio Oyama;Fernanda Canduri;Carla C. B. Lorenzi.
Biochemistry (2004)
Automated NMR structure determination and disulfide bond identification of the myotoxin crotamine from Crotalus durissus terrificus
Valmir Fadel;Pascal Bettendorff;Torsten Herrmann;Walter F. de Azevedo.
Toxicon (2005)
MolDock applied to structure-based virtual screening.
Walter Filgueira De Azevedo.
Current Drug Targets (2010)
Antimalarial Activity of Physalins B, D, F, and G
Matheus S. Sá;Maria N. de Menezes;Antoniana U. Krettli;Ivone M. Ribeiro.
Journal of Natural Products (2011)
Molecular model of cyclin-dependent kinase 5 complexed with roscovitine
Walter Filgueira de Azevedo;Walter Filgueira de Azevedo;Renato Tadeu Gaspar;Fernanda Canduri;Fernanda Canduri;João Carlos Camera.
Biochemical and Biophysical Research Communications (2002)
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