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Introduction to Enzymes01:22

Introduction to Enzymes

30.9K
The use of enzymes by humans dates to 7000 BCE. Humans first used enzymes to ferment sugars and produce alcohol without knowing that this was an enzyme-catalyzed reaction. Wilhelm Kuhne coined the term 'enzyme' in 1877 from the Greek words ‘en’ meaning ‘in’ or ‘within’ and ‘zyme’ meaning ‘yeast.’
Most enzymes are proteins that speed up biochemical reactions without being consumed. Enzymes contain one or more active sites that...
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Enzymes02:34

Enzymes

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Inside living organisms, enzymes act as catalysts for many biochemical reactions involved in cellular metabolism. The role of enzymes is to reduce the activation energies of biochemical reactions by forming complexes with its substrates. The lowering of activation energies favor an increase in the rates of biochemical reactions.
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
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Introduction to Enzyme Kinetics01:19

Introduction to Enzyme Kinetics

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Enzyme kinetics studies the rates of biochemical reactions. Scientists monitor the reaction rates for a particular enzymatic reaction at various substrate concentrations. Additional trials with inhibitors or other molecules that affect the reaction rate may also be performed.
The experimenter can then plot the initial reaction rate or velocity (Vo) of a given trial against the substrate concentration ([S]) to obtain a graph of the reaction properties. For many enzymatic reactions involving a...
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Catalytically Perfect Enzymes01:07

Catalytically Perfect Enzymes

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The theory of catalytically perfect enzymes was first proposed by W.J. Albery and J. R. Knowles in 1976. These enzymes catalyze biochemical reactions at high-speed. Their catalytic efficiency values range from 108-109 M-1s-1. These enzymes are also called 'diffusion-controlled' as the only rate-limiting step in the catalysis is that of the substrate diffusion into the active site. Examples include triose phosphate isomerase, fumarase, and superoxide dismutase.
 
Most enzymes...
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Pharmacodynamics: Overview and Principles01:21

Pharmacodynamics: Overview and Principles

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Pharmacodynamics is a scientific field that delves into drugs' intricate biochemical, cellular, and physiological effects on the human body. The study of pharmacodynamics helps us understand how drugs interact with the body and elicit various responses.
Most drugs' effects result from their interactions with drug receptors or targets within the body. These interactions trigger specific responses at the cellular or systemic level. Drug receptors can be found on the surfaces of cells or...
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Enzyme Inhibition01:30

Enzyme Inhibition

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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.
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Related Experiment Video

Updated: Jan 4, 2026

Enzymatic Modification and Flow Cytometry Assessment of Yeast Surface Displayed Proteins
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THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Enzymes.

Stephen P H Alexander1, Doriano Fabbro2, Eamonn Kelly3

  • 1School Sciences, Nottingham Medical School, Nottingham, NG7 2UH, UK.

British Journal of Pharmacology
|November 12, 2019
PubMed
Summary

The Concise Guide to Pharmacology 2019/20 offers a comprehensive overview of 1800 human drug targets, including enzymes and receptors. This biennial publication provides essential pharmacology data and links to an extensive online knowledgebase.

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Area of Science:

  • Pharmacology
  • Drug Discovery
  • Biomedical Sciences

Background:

  • The Concise Guide to Pharmacology is a biennial publication series.
  • It serves as a reference for human drug targets and their properties.
  • The 2019/20 edition is the fourth in this series.

Purpose of the Study:

  • To provide concise overviews of nearly 1800 human drug targets.
  • To emphasize selective pharmacology and link to an open-access knowledgebase (www.guidetopharmacology.org).
  • To offer a permanent, citable record of pharmacological data.

Main Methods:

  • Compilation of data on human drug targets, categorized into six major types: G protein-coupled receptors, ion channels, nuclear hormone receptors, catalytic receptors, transporters, and enzymes.
  • Inclusion of nomenclature guidance, summary information on pharmacological tools, key references, and further reading suggestions.
  • Data collection and organization contemporary to mid-2019, superseding previous editions.

Main Results:

  • Presents key properties for approximately 1800 human drug targets.
  • Highlights selective pharmacology where available.
  • Provides links to a detailed online knowledgebase for expanded information.

Conclusions:

  • The Concise Guide to Pharmacology 2019/20 is a valuable resource for researchers and scientists.
  • It offers an official IUPHAR classification and nomenclature for human drug targets.
  • The guide facilitates comparison of related targets and serves as a reliable point-in-time reference.