Date published: 2025-9-18

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MMS19 Inhibitors

MMS19 inhibitors encompass a specialized class of chemical compounds specifically formulated to target and inhibit the MMS19 protein. MMS19, also known as the cytosolic iron-sulfur assembly component 19, is a part of the intricate cellular machinery involved in the assembly and repair of iron-sulfur (Fe-S) clusters. These clusters are critical cofactors for a variety of enzymes and proteins, playing a pivotal role in numerous cellular processes, including DNA repair, replication, and metabolic reactions. MMS19 functions as a scaffold or chaperone, facilitating the insertion of Fe-S clusters into target apoproteins. Its activity is crucial for the proper functioning of these enzymes and proteins. The structure of MMS19 is complex, featuring multiple domains that are essential for its interaction with other components of the Fe-S cluster assembly machinery. The development of inhibitors targeting MMS19 focuses on these functional domains, aiming to selectively modulate the protein's activity in Fe-S cluster assembly and maintenance.

The design and synthesis of MMS19 inhibitors involve a comprehensive approach that integrates knowledge from biochemistry, molecular biology, and chemical engineering. The key to developing effective inhibitors lies in understanding the structural and functional aspects of MMS19, particularly its interaction sites with other proteins and Fe-S clusters. Advanced structural analysis techniques, such as X-ray crystallography and NMR spectroscopy, are employed to elucidate the three-dimensional structure of MMS19, providing critical insights into binding sites for inhibitors. Computational methods, including molecular docking and virtual screening, complement experimental techniques by predicting the binding affinity and specificity of inhibitors. These methods help in identifying small molecules or peptides that can effectively interact with MMS19, disrupting its role in Fe-S cluster assembly. The process of developing MMS19 inhibitors is iterative, involving the synthesis, characterization, and biological testing of various compounds. This process aims to achieve selective inhibition of MMS19 while minimizing off-target effects. The field of MMS19 inhibitors is dynamic and evolving, with ongoing research contributing to a deeper understanding of the molecular mechanisms underlying Fe-S cluster assembly and the for selective modulation of these processes.

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