Related Experiment Video
Updated: Apr 17, 2026

13:35
Structural Biology and Analytical Chemistry Approaches for Characterizing C-Glycoside Metabolic Enzymes in Human Gut Microbiota
Published on: May 23, 2025
1.1K
Structural basis of sialidase in complex with geranylated flavonoids as potent natural inhibitors. Corrigendum
Youngjin Lee1, Young Bae Ryu2, Hyung Seop Youn1
1School of Life Sciences, Gwangju Institute of Science and Technology (GIST), Buk-gu, Gwangju 500-712, Republic of Korea.
Acta Crystallographica. Section D, Biological Crystallography
|February 10, 2015
Abstract:
A correction is made to the article by Lee et al. [(2014) Acta Cryst. D70, 1357-1365].
Related Concept Videos
Enzyme Inhibition
95.4K
Inhibitors are molecules that reduce enzyme activity by binding to the enzyme. In a normally functioning cell, enzymes are regulated by a variety of inhibitors. Drugs and other toxins can also inhibit enzymes. Some inhibitors bind to the enzyme’s active site, while others inhibit enzymatic activity by binding to other sites on the protein structure.
95.4K
Structure-Activity Relationships and Drug Design
2.2K
Drug design is a dynamic field that involves discovering and developing new medications based on specific biological targets. This process heavily relies on structure-activity relationships (SAR) and quantitative structure-activity relationships (QSAR) to guide the design and optimization of efficient drugs.
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
2.2K

