Structural Characteristics, Binding Partners and Related Diseases of the Calponin Homology (CH) Domain
Structural Characteristics, Binding Partners and Related Diseases of the Calponin Homology (CH) Domain
The calponin homology (CH) domain is one of the most common modules in various actin-binding proteins and is characterized by an α-helical fold. The CH domain plays important regulatory roles in both cytoskeletal dynamics and signaling. The CH domain is required for stability and organization of the actin cytoskeleton, calcium mobilization and activation of downstream pathways. The CH domain has recently garnered increased attention due to its importance in the onset of different diseases, such as cancers and asthma. However, many roles of the CH domain in various protein functions and corresponding diseases are still unclear. Here, we review current knowledge about the structural features, interactome and related diseases of the CH domain.
- UNSW Sydney Australia
- Shanxi University of Traditional Chinese Medicine China (People's Republic of)
- Shanghai University of Traditional Chinese Medicine China (People's Republic of)
- MRC Laboratory of Molecular Biology United Kingdom
- Instituto Politécnico Nacional Mexico
tropomyosin, calmodulin, Cell and Developmental Biology, actin cytoskeleton, tubulin, CH-domain-containing proteins, QH301-705.5, Biology (General), α-helix
tropomyosin, calmodulin, Cell and Developmental Biology, actin cytoskeleton, tubulin, CH-domain-containing proteins, QH301-705.5, Biology (General), α-helix
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