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Mechanisms and function of substrate recruitment by F-box proteins

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TLDR
The evolution of substrate recruitment by F-box proteins, the dysregulation of substrates in disease and potential avenues for F- box protein-directed disease therapies are focused on.
Abstract
S phase kinase-associated protein 1 (SKP1)-cullin 1 (CUL1)-F-box protein (SCF) ubiquitin ligase complexes use a family of F-box proteins as substrate adaptors to mediate the degradation of a large number of regulatory proteins involved in diverse processes The dysregulation of SCF complexes and their substrates contributes to multiple pathologies In the 14 years since the identification and annotation of the F-box protein family, the continued identification and characterization of novel substrates has greatly expanded our knowledge of the regulation of substrate targeting and the roles of F-box proteins in biological processes Here, we focus on the evolution of our understanding of substrate recruitment by F-box proteins, the dysregulation of substrate recruitment in disease and potential avenues for F-box protein-directed disease therapies

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Journal ArticleDOI

Affinity microfluidics enables high-throughput protein degradation analysis in cell-free extracts

TL;DR: The pDOC platform as mentioned in this paper provides a sensitive multiplex alternative to the conventional degradation assay, with relevance to biomedical and translational research associated with regulated proteolysis, and can be used for protein degradation in cell-free extracts.
Posted ContentDOI

Activity-based profiling of cullin-RING ligase networks by conformation-specific probes

TL;DR: In this article , a pipeline probing cellular networks of activated CUL1-, CUL2, CUL3- and CUL4-containing CRLs was established, revealing the CRL complexes responding to stimuli, and their baseline neddylated CRL repertoires vary, prime efficiency of targeted protein degradation, and are differentially rewired across distinct primary cell activation pathways.
Dissertation

Cooperation of p300 and iASPP in apoptosis and tumour suppression

TL;DR: The impact of the co-factor protein iASPP on p300 and TAp73 function, after treatment of tumourigenic cell lines with the chemotherapeutic drug cisplatin, is investigated and it is discovered that malignant melanoma are characterized by down-regulated iAS PP expression level.
References
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Journal ArticleDOI

The Ubiquitin System

TL;DR: This review discusses recent information on functions and mechanisms of the ubiquitin system and focuses on what the authors know, and would like to know, about the mode of action of ubi...
Journal ArticleDOI

Wnt/β-catenin signaling: components, mechanisms, and diseases

TL;DR: Some key aspects of Wnt/beta-catenin signaling in human diseases including congenital malformations, cancer, and osteoporosis are highlighted, and potential therapeutic implications are discussed.
Journal ArticleDOI

The Ubiquitin Code

TL;DR: The structure, assembly, and function of the posttranslational modification with ubiquitin, a process referred to as ubiquitylation, controls almost every process in cells.
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