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Uroporphyrinogen III decarboxylase F006 / 9387

Uroporphyrinogen III decarboxylase F006  /  9387


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Uroporphyrinogen III decarboxylase F006 / 9387

Uroporphyrinogen III decarboxylase. Molecular model of the enzyme human uroporphyrinogen III decarboxylase (UROD). Mutations or deficiencies in this enzyme cause the disorder porphyria with a build up of porphyrins in the body

Science Photo Library features Science and Medical images including photos and illustrations

Media ID 9254419

© LAGUNA DESIGN/SCIENCE PHOTO LIBRARY

Alpha Helix Beta Sheet Enzyme Illness Inherited Proteomics Strand Tertiary Structure Biochemical Biochemistry Cutouts Disorder Molecular Molecular Model Molecular Structure Porphyria Protein


EDITORS COMMENTS
This print showcases the molecular model of Uroporphyrinogen III decarboxylase (UROD), an essential enzyme found in humans. The white background beautifully highlights the intricate structure of this protein, revealing its alpha helix and beta sheet formations that contribute to its tertiary structure. UROD plays a crucial role in our body's biochemical processes by catalyzing the conversion of uroporphyrinogen III into coproporphyrinogen III. However, mutations or deficiencies in this enzyme can lead to a disorder known as porphyria. Porphyria is characterized by an abnormal accumulation of porphyrins within the body, causing various symptoms ranging from skin sensitivity to neurological complications. This stunning illustration serves as a powerful tool for research and medicine, providing valuable insights into the molecular basis of porphyria and aiding scientists in developing effective treatments for this inherited disorder. Its detailed depiction allows researchers to study how specific mutations affect UROD's function and explore potential therapeutic interventions. The artwork not only exemplifies the beauty of biological molecules but also underscores their significance in healthcare. By unraveling the mysteries behind UROD's structure and function, we gain deeper understanding of human biochemistry and pave the way towards improved diagnosis, prevention, and treatment strategies for individuals affected by porphyria.

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