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A novel allosteric site in casein kinase 2α discovered using combining bioinformatics and biochemistry methods

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/med.21317openalex-snapshot
Harnessing Allostery: A Novel Approach to Drug Discovery
inferredcites →https://doi.org/10.1002/prot.20232openalex-snapshot
Is allostery an intrinsic property of all dynamic proteins?
inferredcites →https://doi.org/10.1006/abbi.1996.0036openalex-snapshot
Protein Kinase CK2: Biphasic Kinetics with Peptide Substrates
inferredcites →https://doi.org/10.1006/bbrc.1995.1024openalex-snapshot
Mapping the Residues of Protein Kinase CK2 Implicated in Substrate Recognition: Mutagenesis of Conserved Basic Residues in the α-Subunit
inferredcites →https://doi.org/10.1006/bbrc.1995.1354openalex-snapshot
Halogenated Benzimidazoles and Benzotriazoles as Selective Inhibitors of Protein Kinases CK-I and CK-II from Saccharomyces Cerevisiae and Other Sources
inferredcites →https://doi.org/10.1007/s00018-009-9151-1openalex-snapshot
Protein Kinase CK2 in Health and Disease
inferredcites →https://doi.org/10.1007/s00018-009-9154-yopenalex-snapshot
Protein Kinase CK2 in Health and Disease
inferredcites →https://doi.org/10.1007/s11010-011-0960-9openalex-snapshot
A detailed thermodynamic profile of cyclopentyl and isopropyl derivatives binding to CK2 kinase
inferredcites →https://doi.org/10.1016/0014-5793(94)01190-7openalex-snapshot
Substrate recognition by casein kinase‐II: The role of histidine‐160
inferredcites →https://doi.org/10.1016/j.ajhg.2016.02.006openalex-snapshot
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis
inferredcites →https://doi.org/10.1016/j.ajhg.2016.09.020openalex-snapshot
Proteome-Scale Investigation of Protein Allosteric Regulation Perturbed by Somatic Mutations in 7,000 Cancer Genomes
inferredcites →https://doi.org/10.1016/j.bbapap.2007.08.017openalex-snapshot
Too much of a good thing: The role of protein kinase CK2 in tumorigenesis and prospects for therapeutic inhibition of CK2
inferredcites →https://doi.org/10.1016/j.bbapap.2009.07.018openalex-snapshot
Addiction to protein kinase CK2: A common denominator of diverse cancer cells?
inferredcites →https://doi.org/10.1016/j.ccr.2013.03.021openalex-snapshot
Gain of Interaction with IRS1 by p110α-Helical Domain Mutants Is Crucial for Their Oncogenic Functions
inferredcites →https://doi.org/10.1016/j.ccr.2014.07.027openalex-snapshot
Cancer-Selective Targeting of the NF-κB Survival Pathway with GADD45β/MKK7 Inhibitors
inferredcites →https://doi.org/10.1016/j.celrep.2013.03.027openalex-snapshot
The Protein Interaction Landscape of the Human CMGC Kinase Group
inferredcites →https://doi.org/10.1016/j.chembiol.2007.12.012openalex-snapshot
The CK2α/CK2β Interface of Human Protein Kinase CK2 Harbors a Binding Pocket for Small Molecules
inferredcites →https://doi.org/10.1016/j.drudis.2012.11.009openalex-snapshot
αC helix displacement as a general approach for allosteric modulation of protein kinases
inferredcites →https://doi.org/10.1016/j.febslet.2010.11.019openalex-snapshot
Structural basis of CX-4945 binding to human protein kinase CK2
inferredcites →https://doi.org/10.1016/j.jmb.2003.12.068openalex-snapshot
Allosteric Inhibition Through Core Disruption
inferredcites →https://doi.org/10.1016/j.jmb.2007.04.068openalex-snapshot
Evolved to Be Active: Sulfate Ions Define Substrate Recognition Sites of CK2α and Emphasise its Exceptional Role within the CMGC Family of Eukaryotic Protein Kinases
inferredcites →https://doi.org/10.1016/j.tips.2014.03.006openalex-snapshot
Unraveling structural mechanisms of allosteric drug action
inferredcites →https://doi.org/10.1016/s0026-895x(25)08527-xopenalex-snapshot
Probing of the location of the allosteric site on m1 muscarinic receptors by site-directed mutagenesis.
inferredcites →https://doi.org/10.1016/s0092-8674(04)00206-5openalex-snapshot
The Protein Kinase CK2 Facilitates Repair of Chromosomal DNA Single-Strand Breaks
inferredcites →https://doi.org/10.1021/bi2008382openalex-snapshot
Unprecedented Selectivity and Structural Determinants of a New Class of Protein Kinase CK2 Inhibitors in Clinical Trials for the Treatment of Cancer
inferredcites →https://doi.org/10.1021/jm030827eopenalex-snapshot
Discovery of a Potent and Selective Protein Kinase CK2 Inhibitor by High-Throughput Docking
inferredcites →https://doi.org/10.1021/jm101251qopenalex-snapshot
Discovery and SAR of 5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-8-carboxylic Acid (CX-4945), the First Clinical Stage Inhibitor of Protein Kinase CK2 for the Treatment of Cancer
inferredcites →https://doi.org/10.1038/nature13001openalex-snapshot
The ensemble nature of allostery
inferredcites →https://doi.org/10.1038/nchembio.208openalex-snapshot
Structure and allosteric effects of low-molecular-weight activators on the protein kinase PDK1
inferredcites →https://doi.org/10.1038/sj.embor.7400115openalex-snapshot
Protein kinase CK2: a new view of an old molecular complex
inferredcites →https://doi.org/10.1038/sj.onc.1204411openalex-snapshot
Protein kinase CK2 in mammary gland tumorigenesis
inferredcites →https://doi.org/10.1042/bj20021469openalex-snapshot
Protein kinase CK2: structure, regulation and role in cellular decisions of life and death
inferredcites →https://doi.org/10.1073/pnas.1102376108openalex-snapshot
Turning a protein kinase on or off from a single allosteric site via disulfide trapping
inferredcites →https://doi.org/10.1073/pnas.1209309109openalex-snapshot
Equilibrium fluctuations of a single folded protein reveal a multitude of potential cryptic allosteric sites
inferredcites →https://doi.org/10.1073/pnas.1417811112openalex-snapshot
Discovery of multiple hidden allosteric sites by combining Markov state models and experiments
inferredcites →https://doi.org/10.1074/jbc.m001870200openalex-snapshot
The Allosteric Regulation of Pyruvate Kinase
inferredcites →https://doi.org/10.1074/jbc.m004257200openalex-snapshot
The Replacement of ATP by the Competitive Inhibitor Emodin Induces Conformational Modifications in the Catalytic Site of Protein Kinase CK2
inferredcites →https://doi.org/10.1074/mcp.m110.004390openalex-snapshot
Cyclic AMP Analog Blocks Kinase Activation by Stabilizing Inactive Conformation: Conformational Selection Highlights a New Concept in Allosteric Inhibitor Design
inferredcites →https://doi.org/10.1093/bioinformatics/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
inferredcites →https://doi.org/10.1093/bioinformatics/btt399openalex-snapshot
Allosite: a method for predicting allosteric sites
inferredcites →https://doi.org/10.1093/nar/28.1.235openalex-snapshot
The Protein Data Bank
inferredcites →https://doi.org/10.1093/nar/gkt284openalex-snapshot
MCPath: Monte Carlo path generation approach to predict likely allosteric pathways and functional residues
inferredcites →https://doi.org/10.1093/nar/gkv902openalex-snapshot
ASD v3.0: unraveling allosteric regulation with structural mechanisms and biological networks
inferredcites →https://doi.org/10.1096/fj.02-0473revopenalex-snapshot
One‐thousand‐and‐one substrates of protein kinase CK2?
inferredcites →https://doi.org/10.1186/2050-6511-14-36openalex-snapshot
Coumestrol from the national cancer Institute’s natural product library is a novel inhibitor of protein kinase CK2
inferredcites →https://doi.org/10.1186/2050-6511-14-s1-o37openalex-snapshot
Nitric oxide regulated cyclic di-GMP signaling

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/9780470027318.a9614openalex-snapshot
Methods Applied for the Allosteric Site Revelation
inferred← citeshttps://doi.org/10.1002/adhm.202402329openalex-snapshot
Bilayer Scaffolds Synergize Immunomodulation and Rejuvenation via Layer‐Specific Release of CK2.1 and the “Exercise Hormone” Lac‐Phe for Enhanced Osteochondral Regeneration
inferred← citeshttps://doi.org/10.1002/minf.201800089openalex-snapshot
Structure‐based Discovery of Novel CK2α‐Binding Cyclic Peptides with Anti‐cancer Activity
inferred← citeshttps://doi.org/10.1002/wcms.1585openalex-snapshot
Along the allostery stream: Recent advances in computational methods for allosteric drug discovery
inferred← citeshttps://doi.org/10.1016/b978-0-323-96121-9.00004-8openalex-snapshot
Casein kinase (CK) inhibitors
inferred← citeshttps://doi.org/10.1016/j.bcp.2026.117675openalex-snapshot
Identification and characterization of broad-spectrum cathelicidin family antimicrobial peptides from the pygmy sperm whale Kogia breviceps
inferred← citeshttps://doi.org/10.1016/j.bone.2018.03.027openalex-snapshot
Hypoxia-selective allosteric destabilization of activin receptor-like kinases: A potential therapeutic avenue for prophylaxis of heterotopic ossification
inferred← citeshttps://doi.org/10.1016/j.chembiol.2024.07.018openalex-snapshot
Chemoproteomics reveals immunogenic and tumor-associated cell surface substrates of ectokinase CK2α
inferred← citeshttps://doi.org/10.1016/j.jare.2024.11.021openalex-snapshot
Oncogenic cholesterol rewires lipid metabolism in hepatocellular carcinoma via the CSNK2A1-IGF2R Ser2484 axis
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.10.004openalex-snapshot
Negative allosteric modulator of Group Ⅰ mGluRs: Recent advances and therapeutic perspective for neuropathic pain
inferred← citeshttps://doi.org/10.1021/acs.accounts.8b00570openalex-snapshot
Allosteric Methods and Their Applications: Facilitating the Discovery of Allosteric Drugs and the Investigation of Allosteric Mechanisms
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c03783openalex-snapshot
Probing Allosteric Kinase Modulators as Next Game-Changers in Fighting Neurodegeneration
inferred← citeshttps://doi.org/10.1021/acschembio.2c00626openalex-snapshot
Identification of the Allosteric Binding Site for Thiazolopyrimidine on the C-Type Lectin Langerin
inferred← citeshttps://doi.org/10.1021/acsomega.3c10478openalex-snapshot
Recent Advances in the Discovery of CK2 Inhibitors
inferred← citeshttps://doi.org/10.1080/07391102.2021.2024449openalex-snapshot
Lead optimization, pharmacophore development and scaffold design of protein kinase CK2 inhibitors as potential COVID-19 therapeutics
inferred← citeshttps://doi.org/10.1093/nar/gky374openalex-snapshot
AlloFinder: a strategy for allosteric modulator discovery and allosterome analyses
inferred← citeshttps://doi.org/10.1136/svn-2019-000323openalex-snapshot
Big data and artificial intelligence discover novel drugs targeting proteins without 3D structure and overcome the undruggable targets
inferred← citeshttps://doi.org/10.3389/fonc.2020.00893openalex-snapshot
Protein Kinase CK2 in Cancer Energetics
inferred← citeshttps://doi.org/10.3390/ijms19010111openalex-snapshot
Insights into the Impact of Linker Flexibility and Fragment Ionization on the Design of CK2 Allosteric Inhibitors: Comparative Molecular Dynamics Simulation Studies
inferred← citeshttps://doi.org/10.3390/molecules25010237openalex-snapshot
Identification and Biological Evaluation of CK2 Allosteric Fragments through Structure-Based Virtual Screening
inferred← citeshttps://doi.org/10.3390/molecules25040870openalex-snapshot
Recent Advances in the Discovery of CK2 Allosteric Inhibitors: From Traditional Screening to Structure-Based Design
inferred← citeshttps://doi.org/10.3390/molecules29133199openalex-snapshot
Serine/Threonine Protein Kinases as Attractive Targets for Anti-Cancer Drugs—An Innovative Approach to Ligand Tuning Using Combined Quantum Chemical Calculations, Molecular Docking, Molecular Dynamic Simulations, and Network-like Similarity Graphs
inferred← citeshttps://doi.org/10.3892/etm.2021.10359openalex-snapshot
Long non‑coding RNA B3GALT5‑AS1 contributes to the progression of gastric cancer via interacting with CSNK2A1
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