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The DUF1669 domain of FAM83 family proteins anchor casein kinase 1 isoforms.
- Published in:
- Science Signaling, 2018, v. 11, n. 531, p. 1, doi. 10.1126/scisignal.aao2341
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- Article
Sequence and structural variations determining the recruitment of WNK kinases to the KLHL3 E3 ligase.
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- Biochemical Journal, 2022, v. 479, n. 5, p. 661, doi. 10.1042/BCJ20220019
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- Article
Lessons from LIMK1 enzymology and their impact on inhibitor design.
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- Biochemical Journal, 2019, v. 476, n. 21, p. 3197, doi. 10.1042/BCJ20190517
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- Article
Structural complexity in the KCTD family of Cullin3-dependent E3 ubiquitin ligases.
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- Biochemical Journal, 2017, v. 474, n. 22, p. 3747, doi. 10.1042/BCJ20170527
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- Article
Structure and inhibitor specificity of the PCTAIRE-family kinase CDK16.
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- Biochemical Journal, 2017, v. 474, n. 5, p. 699, doi. 10.1042/BCJ20160941
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- Article
Structural and biochemical characterization of the KLHL3-WNK kinase interaction important in blood pressure regulation.
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- Biochemical Journal, 2014, v. 460, n. 2, p. 237, doi. 10.1042/BJ20140153
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- Article
Development of Macrocycle Kinase Inhibitors for ALK2 Using Fibrodysplasia Ossificans Progressiva‐Derived Endothelial Cells.
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- JBMR Plus, 2019, v. 3, n. 11, p. N.PAG, doi. 10.1002/jbm4.10230
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- Article
The structure of P-TEFb (CDK9/cyclin T1), its complex with flavopiridol and regulation by phosphorylation.
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- EMBO Journal, 2008, v. 27, n. 13, p. 1907, doi. 10.1038/emboj.2008.121
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- Article
New potent dual inhibitors of CK2 and Pim kinases: discovery and structural insights.
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- FASEB Journal, 2010, v. 24, n. 9, p. 3171, doi. 10.1096/fj.09-143743
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- Article
Crystal Structure-Guided Design of Bisubstrate Inhibitors and Photoluminescent Probes for Protein Kinases of the PIM Family.
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- Molecules, 2021, v. 26, n. 14, p. 4353, doi. 10.3390/molecules26144353
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- Article
Clinical Utility Gene Card for: Fibrodysplasia ossificans progressiva.
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- European Journal of Human Genetics, 2015, v. 23, n. 10, p. -1, doi. 10.1038/ejhg.2014.274
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- Article
Challenges and Opportunities for Drug Repositioning in Fibrodysplasia Ossificans Progressiva.
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- Biomedicines, 2021, v. 9, n. 2, p. 213, doi. 10.3390/biomedicines9020213
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- Article
ALK2 Receptor Kinase Association with FKBP12.6 Is Structurally Conserved with the ALK2-FKBP12 Complex.
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- Biomedicines, 2021, v. 9, n. 2, p. 129, doi. 10.3390/biomedicines9020129
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- Article
Structural consequences of BMPR2 kinase domain mutations causing pulmonary arterial hypertension.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-54830-7
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- Article
Ruthenium Half-Sandwich Complexes Bound to Protein Kinase Pim-1We gratefully acknowledge support for this work from the US National Institutes of Health through grant 1 R01 GM071695-01A1 (E.M.). The Structural Genomics Consortium is a registered charity (no. 1097737) funded by the Wellcome Trust, GlaxoSmithKline, Genome Canada, the Canadian Institutes of Health Research, the Ontario Innovation Trust, the Ontario Research and Development Challenge Fund, and the Canadian Foundation for Innovation.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 10, p. 1580, doi. 10.1002/anie.200503468
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- Article
RESCUING THE FUNCTION OF MUTANT p53.
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- Nature Reviews Cancer, 2001, v. 1, n. 1, p. 68, doi. 10.1038/35094077
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- Article
Mutations in Known Monogenic High Bone Mass Loci Only Explain a Small Proportion of High Bone Mass Cases.
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- Journal of Bone & Mineral Research, 2016, v. 31, n. 3, p. 640, doi. 10.1002/jbmr.2706
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- Article
Target highlights in CASP13: Experimental target structures through the eyes of their authors.
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- Proteins, 2019, v. 87, n. 12, p. 1037, doi. 10.1002/prot.25805
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- Article
Protocol paper: a multi-center, double-blinded, randomized, 6-month, placebo-controlled study followed by 12-month open label extension to evaluate the safety and efficacy of Saracatinib in Fibrodysplasia Ossificans Progressiva (STOPFOP).
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- 2022
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- Publication type:
- journal article
Ruthenium Half-Sandwich Complexes Bound to Protein Kinase Pim-1We gratefully acknowledge support for this work from the US National Institutes of Health through grant 1 R01 GM071695-01A1 (E.M.). The Structural Genomics Consortium is a registered charity (no. 1097737) funded by the Wellcome Trust, GlaxoSmithKline, Genome Canada, the Canadian Institutes of Health Research, the Ontario Innovation Trust, the Ontario Research and Development Challenge Fund, and the Canadian Foundation for Innovation.
- Published in:
- Angewandte Chemie, 2006, v. 118, n. 10, p. 1610, doi. 10.1002/ange.200503468
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- Publication type:
- Article
PRMT5 inhibition shows in vitro efficacy against H3K27M-altered diffuse midline glioma, but does not extend survival in vivo.
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- Scientific Reports, 2024, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-48652-x
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- Publication type:
- Article
Suppressor of Cytokine Signaling (SOCS) 5 Utilises Distinct Domains for Regulation of JAK1 and Interaction with the Adaptor Protein Shc-1.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070536
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- Article
A New Class of Small Molecule Inhibitor of BMP Signaling.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062721
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- Publication type:
- Article
Crystal Structure of the PIM2 Kinase in Complex with an Organoruthenium Inhibitor.
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- PLoS ONE, 2009, v. 4, n. 10, p. 1, doi. 10.1371/journal.pone.0007112
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- Article
Novel Mutations in ACVR1 Result in Atypical Features in Two Fibrodysplasia Ossificans Progressiva Patients.
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- PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0005005
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- Publication type:
- Article
Discovery and characterization of a specific inhibitor of serine-threonine kinase cyclin-dependent kinase-like 5 (CDKL5) demonstrates role in hippocampal CA1 physiology.
- Published in:
- eLife, 2023, p. 1, doi. 10.7554/eLife.88206
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- Article
Synthesis of Highly Water-Soluble Adamantyl Phosphoinositide Derivatives.
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- Australian Journal of Chemistry, 2015, v. 68, n. 4, p. 543, doi. 10.1071/CH14543
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- Article
Recurrent activating ACVR1 mutations in diffuse intrinsic pontine glioma.
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- Nature Genetics, 2014, v. 46, n. 5, p. 457, doi. 10.1038/ng.2925
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- Article
Quantitative analysis of residual folding and DNA binding in mutant p53 core domain: definition of mutant states for rescue in cancer therapy.
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- Oncogene, 2000, v. 19, n. 10, p. 1245, doi. 10.1038/sj.onc.1203434
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- Article
Computational redesign of protein-protein interaction specificity.
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- Nature Structural & Molecular Biology, 2004, v. 11, n. 4, p. 371, doi. 10.1038/nsmb749
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- Article
The SGC beyond structural genomics: redefining the role of 3D structures by coupling genomic stratification with fragment-based discovery.
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- Essays in Biochemistry, 2017, v. 61, n. 5, p. 495, doi. 10.1042/EBC20170051
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- Article
Fostering open collaboration in drug development for paediatric brain tumours.
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- Biochemical Society Transactions, 2019, v. 47, n. 5, p. 1471, doi. 10.1042/BST20190315
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- Article
New strategies to inhibit KEAP1 and the Cul3-based E3 ubiquitin ligases.
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- Biochemical Society Transactions, 2014, v. 42, n. 1, p. 103, doi. 10.1042/BST20130215
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- Publication type:
- Article
Structures of the CDK12/CycK complex with AMP-PNP reveal a flexible C-terminal kinase extension important for ATP binding.
- Published in:
- Scientific Reports, 2015, p. 17122, doi. 10.1038/srep17122
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- Article
Small molecule inhibitors reveal an indispensable scaffolding role of RIPK2 in NOD2 signaling.
- Published in:
- EMBO Journal, 2018, v. 37, n. 17, p. 1, doi. 10.15252/embj.201899372
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- Article