Bacterial Enzymes as Targets for Drug Discovery: Meeting the Challenges of Antibiotic Resistance addresses the gap between medical microbiology, structural biology, and genomic science in the development of new antibacterial drug development. This book consolidates detailed profiling of bacterial target enzyme families for the drug discovery process and methodologies for use and validation of the potential drug targets. The contents cover the foundations of the antibiotic drug discovery process and focus on bacterial enzymes as drug targets, building across these disciplines to provide a comprehensive resource in bacterial structural biology and genomics. This is the ideal reference for antibiotic drug discovery researchers in the pharma industry and academia. Biochemists, microbiologists, and medicinal chemists will also benefit from this books’ content.
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Part I Primer of antibiotic discovery process 1. Antibacterial drug discovery: A Silent Pandemic 2. Current scenario and future prospective of drug discovery and development against bacterial enzymes 3. Clinical diagnostics of bacterial infections and their resistance to Antibiotics — Current State and Novel Enabling Technologies Implementation Perspectives 4. An Odyssey into Phylogenetic Functional Conservation of Novel Antibacterial Targets in Human Pathogens 5. Validation of drug targets using molecular methodologies and enzymatic activity assays for validation of inhibitory potential 6. Computational tools to identify potential drug targets in bacteria 7. Antimicrobial drug resistance and bypassing strategies Part II Bacterial enzyme as drug targets 8. Designing Tomorrow's Antibiotics: Cutting-Edge Strategies and Technologies 9. Inhibiting the replication by targeting topoisomerases 10. Role of beta lactamases in antibiotic drug discovery 11. Selective vs broad spectrum inhibition of novel outer membrane targets in Gram negatives 12. Ribosomal binding antibacterial agents 13. RNA polymerase: A key target for Novel Antimicrobial Therapeutic Strategies 14. Colistin resistance and strategies against superbug, where we are? 15. Deoxythymidine pathway enzymes as an antibacterial target 16. Arresting the peptidoglycan synthesis to kill the bacteria 17. Clp protease complex as a therapeutic target for tuberculosis 18. PlaF: a bacterial Lands cycle phospholipase A mediating membrane phospholipid degradation and virulence adaptation 19. Bacterial TIR domain-containing proteins as drug targets 20. Drug Repurposing: Tackling the antibiotic resistance with existing therapeutics
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A complete overview of bacterial target enzyme families for the drug discovery process, along with the methodologies for their validation
Provides strategies and approaches to drug design aiming at overcoming antibiotic resistance. Includes most common roadblocks in identifying novel drug targets and presents the strategies to overcome. Provides potential methods to identify new drug targets by genome mining.
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Produktdetaljer

ISBN
9780443222221
Publisert
2024-11-28
Utgiver
Vendor
Academic Press Inc
Vekt
450 gr
Høyde
235 mm
Bredde
191 mm
Aldersnivå
P, 06
Språk
Product language
Engelsk
Format
Product format
Heftet
Antall sider
496

Redaktør

Om bidragsyterne

Dr. Kaur’s specialties include Bioinformatics, Structural Biology, X-ray Crystallography, and Rational Structure-Based Drug Design. Her research focuses on clinically relevant bacterial pathogens where a multidisciplinary approach is adopted to understand the antibacterial resistance mechanisms and design of novel inhibitory molecules. She has published more than 240 original publications, reviews and chapters in the field of bioinformatics, biophysical enzymatic activity and structural biology. Dr. Priyanka Sharma is a postdoctoral student with the biomedical Informatics department at the ICMR. Her work focuses on the field of computational biology involving structural bioinformatics and genomics of bacterial pathogens. She has published widely in the field of clinical bacteriology and is the author of over 30 research papers, reviews and chapters. She has work experience in field of antimicrobial resistance due to enzymatic mutations.