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Title: | Structure, regulation, and (patho-)physiological functions of the stress-induced protein kinase CK1 delta (CSNK1D) |
Authors: | Xu, P. Ianes, C. Gärtner, F. Liu, C. Burster, T. Bakulev, V. Rachidi, N. Knippschild, U. Bischof, J. |
Issue Date: | 2019 |
Publisher: | Elsevier B.V. |
Citation: | Structure, regulation, and (patho-)physiological functions of the stress-induced protein kinase CK1 delta (CSNK1D) / P. Xu, C. Ianes, F. Gärtner, et al. — DOI 10.1016/j.gene.2019.144005 // Gene. — 2019. — Vol. 715. — 144005. |
Abstract: | Members of the highly conserved pleiotropic CK1 family of serine/threonine-specific kinases are tightly regulated in the cell and play crucial regulatory roles in multiple cellular processes from protozoa to human. Since their dysregulation as well as mutations within their coding regions contribute to the development of various different pathologies, including cancer and neurodegenerative diseases, they have become interesting new drug targets within the last decade. However, to develop optimized CK1 isoform-specific therapeutics in personalized therapy concepts, a detailed knowledge of the regulation and functions of the different CK1 isoforms, their various splice variants and orthologs is mandatory. In this review we will focus on the stress-induced CK1 isoform delta (CK1δ), thereby addressing its regulation, physiological functions, the consequences of its deregulation for the development and progression of diseases, and its potential as therapeutic drug target. © 2019 Elsevier B.V. |
Keywords: | CANCER CASEIN KINASE 1 CSNK1D HEDGEHOG PATHWAY N P P53 PHOSPHORYLATION R S SITE-SPECIFIC PHOSPHORYLATION SMALL MOLECULE INHIBITOR STRESS-INDUCED KINASE WNT SIGNALING PATHWAY CASEIN KINASE IDELTA CASEIN KINASE IDELTA ISOENZYME TUMOR PROTEIN AMINO ACID SEQUENCE CARCINOGENESIS CELL CYCLE CELL STRESS CELLULAR DISTRIBUTION CIRCADIAN RHYTHM CSNK1D GENE CYTOSKELETON DISEASE COURSE DNA DAMAGE DRUG DEPENDENCE ENZYME REGULATION ENZYME STRUCTURE ENZYME SUBSTRATE GENE SEQUENCE GENETIC CODE GENETIC TRANSCRIPTION GENETIC VARIABILITY GENETIC VARIATION HEDGEHOG SIGNALING HIPPO SIGNALING HUMAN MEIOSIS METABOLIC DISORDER MITOSIS MOLECULAR RECOGNITION NONHUMAN PATHOPHYSIOLOGY POLYADENYLATION PRIORITY JOURNAL PROTEIN INTERACTION PROTEIN TARGETING REVIEW RNA FOLDING SEQUENCE ALIGNMENT STRESS TUMOR GROWTH WNT SIGNALING ANIMAL ANTAGONISTS AND INHIBITORS CHEMISTRY DRUG DELIVERY SYSTEM ENZYMOLOGY GENETICS METABOLISM NEOPLASM PATHOLOGY PROCEDURES SIGNAL TRANSDUCTION STRUCTURE ACTIVITY RELATION ANIMALS CASEIN KINASE IDELTA DRUG DELIVERY SYSTEMS HUMANS ISOENZYMES NEOPLASM PROTEINS NEOPLASMS SIGNAL TRANSDUCTION STRUCTURE-ACTIVITY RELATIONSHIP |
URI: | http://elar.urfu.ru/handle/10995/102700 |
Access: | info:eu-repo/semantics/openAccess |
SCOPUS ID: | 85070576806 |
WOS ID: | 000484876500001 |
PURE ID: | d0564cb2-17b5-4755-adf3-383631e55f12 10474048 |
ISSN: | 3781119 |
DOI: | 10.1016/j.gene.2019.144005 |
Appears in Collections: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
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