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2025

Applying a Conservation-Based Approach for Predicting Novel Phosphorylation Sites in Eukaryotes and Evaluating Their Functional Relevance.

Kalyuzhnyy, A., Eyers, P. A., Eyers, C. E., Deutsch, E. W., & Jones, A. R. (2025). Applying a Conservation-Based Approach for Predicting Novel Phosphorylation Sites in Eukaryotes and Evaluating Their Functional Relevance.. Journal of proteome research. doi:10.1021/acs.jproteome.5c00278

DOI
10.1021/acs.jproteome.5c00278
Journal article

Autophagy inhibitors block pathogenic NET release in immune-mediated inflammatory disease without impairing host defence

DOI
10.1101/2025.06.23.25330105
Preprint

Pervanadate-induced oxidation relieves autoinhibition of SRC protein tyrosine kinase

DOI
10.1101/2025.04.27.650842
Preprint

Redox regulation and dynamic control of brain-selective kinases BRSK1/2 in the AMPK family through cysteine-based mechanisms

Bendzunas, G. N., Byrne, D. P., Shrestha, S., Daly, L. A., Oswald, S. O., Katiyar, S., . . . Kannan, N. (2025). Redox regulation and dynamic control of brain-selective kinases BRSK1/2 in the AMPK family through cysteine-based mechanisms. eLife, 13. doi:10.7554/elife.92536.4

DOI
10.7554/elife.92536.4
Journal article

PSKH1 kinase activity is differentially modulated via allosteric binding of Ca<sup>2+</sup> sensor proteins.

Horne, C. R., Dite, T. A., Young, S. N., Mather, L. J., Dagley, L. F., Johnson, J. L., . . . Murphy, J. M. (2025). PSKH1 kinase activity is differentially modulated via allosteric binding of Ca<sup>2+</sup> sensor proteins.. Proceedings of the National Academy of Sciences of the United States of America, 122(8), e2420961122. doi:10.1073/pnas.2420961122

DOI
10.1073/pnas.2420961122
Journal article

Applying a conservation-based approach for predicting novel phosphorylation sites in eukaryotes and evaluating their functional relevance

DOI
10.1101/2025.01.09.632054
Preprint

2024

PSKH1 kinase activity is differentially modulated via allosteric binding of Ca<sup>2+</sup>sensor proteins

DOI
10.1101/2024.10.20.619163
Preprint

Activation loop phosphorylation of Cdk11 is restrained by PNUTS-PP1 and regulates Cdk11 activity and function

DOI
10.1101/2024.05.08.592654
Preprint

2023

Custom Workflow for the Confident Identification of Sulfotyrosine-Containing Peptides and Their Discrimination from Phosphopeptides.

Daly, L. A., Byrne, D. P., Perkins, S., Brownridge, P. J., McDonnell, E., Jones, A. R., . . . Eyers, C. E. (2023). Custom Workflow for the Confident Identification of Sulfotyrosine-Containing Peptides and Their Discrimination from Phosphopeptides.. Journal of proteome research, 22(12), 3754-3772. doi:10.1021/acs.jproteome.3c00425

DOI
10.1021/acs.jproteome.3c00425
Journal article

18P AURKB inhibition radiosensitises NSCLC by altering mitotic fate

Egerton, K., Mitchell, T. A., Gravells, P., Katse, R., Fisher, M., Muthana, M., . . . Bryant, H. E. (2023). 18P AURKB inhibition radiosensitises NSCLC by altering mitotic fate. ESMO Open, 8(1), 101664. doi:10.1016/j.esmoop.2023.101664

DOI
10.1016/j.esmoop.2023.101664
Journal article

2022

A Peroxiredoxin-P38 MAPK scaffold increases MAPK activity by MAP3K-independent mechanisms

DOI
10.1101/2022.11.15.513554
Preprint

Catalytic degradation in pseudoenzymes

Eyers, P. (2022). Catalytic degradation in pseudoenzymes. The FASEB Journal, 36(S1). doi:10.1096/fasebj.2022.36.s1.0i116

DOI
10.1096/fasebj.2022.36.s1.0i116
Journal article

Exploring the conformational landscape and stability of Aurora A using ion-mobility mass spectrometry and molecular modelling

Tomlinson, L. J., Batchelor, M., Sarsby, J., Byrne, D. P., Brownridge, P., Bayliss, R., . . . Eyers, C. E. (2022). Exploring the conformational landscape and stability of Aurora A using ion-mobility mass spectrometry and molecular modelling. Journal of the American Society for Mass Spectrometry. doi:10.1021/jasms.1c00271

DOI
10.1021/jasms.1c00271
Journal article

Analysis of human Tribbles 2 (TRIB2) pseudokinase

Harris, J. A., Fairweather, E., Byrne, D. P., & Eyers, P. A. (2022). Analysis of human Tribbles 2 (TRIB2) pseudokinase. In PSEUDOKINASES (Vol. 667, pp. 79-99). doi:10.1016/bs.mie.2022.03.025

DOI
10.1016/bs.mie.2022.03.025
Chapter

Computational tools and resources for pseudokinase research

O'Boyle, B., Shrestha, S., Kochut, K., Eyers, P. A., & Kannan, N. (2022). Computational tools and resources for pseudokinase research. In PSEUDOKINASES (Vol. 667, pp. 403-426). doi:10.1016/bs.mie.2022.03.040

DOI
10.1016/bs.mie.2022.03.040
Chapter

2021

Displacement of PKA catalytic subunit from AKAP signaling islands drives pathology in Cushing’s syndrome

DOI
10.1101/2021.10.18.464848
Preprint

Sulfated host glycan recognition by carbohydrate sulfatases of the human gut microbiota

DOI
10.1101/2021.07.23.453482
Preprint

KinOrtho: a method for mapping human kinase orthologs across the tree of life and illuminating understudied kinases

DOI
10.1101/2021.03.05.434161
Preprint

Mobility shift-based electrophoresis coupled with fluorescent detection enables real-time enzyme analysis of carbohydrate sulfatase activity (vol 478, pg 735, 2021)

Byrne, D. P., London, J. A., Eyers, P. A., Yates, E. A., & Cartmell, A. (2021). Mobility shift-based electrophoresis coupled with fluorescent detection enables real-time enzyme analysis of carbohydrate sulfatase activity (vol 478, pg 735, 2021). BIOCHEMICAL JOURNAL, 478(1), 2537-2538. doi:10.1042/BCJ20200952_COR

DOI
10.1042/BCJ20200952_COR
Journal article

A single bacterial sulfatase is required for metabolism of colonic mucin O-glycans and intestinal colonization by a symbiotic human gut bacterium

DOI
10.21203/rs.3.rs-113032/v1
Preprint

2020

A single bacterial sulfatase is required for metabolism of colonic mucin<i>O</i>-glycans and intestinal colonization by a symbiotic human gut bacterium

DOI
10.1101/2020.11.20.392076
Preprint

Marveling at the Incredible ULK4

Eyers, P. A. (2020). Marveling at the Incredible ULK4. STRUCTURE, 28(11), 1181-1183. doi:10.1016/j.str.2020.10.005

DOI
10.1016/j.str.2020.10.005
Journal article

Use of the Polo-like kinase 4 (PLK4) inhibitor centrinone to investigate intracellular signalling networks using SILAC-based phosphoproteomics

Byrne, D. P., Clarke, C. J., Brownridge, P. J., Kalyuzhnyy, A., Perkins, S., Campbell, A., . . . Eyers, C. E. (2020). Use of the Polo-like kinase 4 (PLK4) inhibitor centrinone to investigate intracellular signalling networks using SILAC-based phosphoproteomics. The Biochemical journal, 477(13), 2451-2475. doi:10.1042/bcj20200309

DOI
10.1042/bcj20200309
Journal article

Use of the Polo-like kinase 4 (PLK4) inhibitor centrinone to investigate intracellular signaling networks using SILAC-based phosphoproteomics

DOI
10.1101/2020.05.22.110767
Preprint

A novel redox-active switch in Fructosamine-3-kinases expands the regulatory repertoire of the protein kinase superfamily

DOI
10.1101/2020.01.13.904870
Preprint

Analysis of 1-and 3-Phosphohistidine (pHis) Protein Modification Using Model Enzymes Expressed in Bacteria

Coldron, A. K. M. C., Byrne, D. P., & Eyers, P. A. (2020). Analysis of 1-and 3-Phosphohistidine (pHis) Protein Modification Using Model Enzymes Expressed in Bacteria. HISTIDINE PHOSPHORYLATION, 2077, 63-81. doi:10.1007/978-1-4939-9884-5_5

DOI
10.1007/978-1-4939-9884-5_5
Journal article

2019

Emerging concepts in pseudoenzyme classification, evolution, and signaling

Ribeiro, A. J. M., Das, S., Dawson, N., Zaru, R., Orchard, S., Thornton, J. M., . . . Eyers, P. A. (2019). Emerging concepts in pseudoenzyme classification, evolution, and signaling. SCIENCE SIGNALING, 12(594). doi:10.1126/scisignal.aat9797

DOI
10.1126/scisignal.aat9797
Journal article

BH3-only proteins are dispensable for apoptosis induced by pharmacological inhibition of both MCL-1 and BCL-X-L

Greaves, G., Milani, M., Butterworth, M., Carter, R. J., Byrne, D. P., Eyers, P. A., . . . Varadarajan, S. (2019). BH3-only proteins are dispensable for apoptosis induced by pharmacological inhibition of both MCL-1 and BCL-X-L. CELL DEATH AND DIFFERENTIATION, 26(6), 1037-1047. doi:10.1038/s41418-018-0183-7

DOI
10.1038/s41418-018-0183-7
Journal article

Highlights of the 2nd International Symposium on Tribbles and Diseases: tribbles tremble in therapeutics for immunity, metabolism, fundamental cell biology and cancer

Cui, B., Eyers, P. A., Dobens, L. L., Tan, N. S., Mace, P. D., Link, W. A., . . . Hu, Z. (2019). Highlights of the 2nd International Symposium on Tribbles and Diseases: tribbles tremble in therapeutics for immunity, metabolism, fundamental cell biology and cancer. ACTA PHARMACEUTICA SINICA B, 9(2), 443-454. doi:10.1016/j.apsb.2018.12.007

DOI
10.1016/j.apsb.2018.12.007
Journal article

2018

Covalent Aurora A regulation by the metabolic integrator coenzyme A

DOI
10.1101/469585
Preprint

New tools for carbohydrate sulfation analysis: heparan sulfate 2-O-sulfotransferase (HS2ST) is a target for small-molecule protein kinase inhibitors

Byrne, D. P., Li, Y., Ramakrishnan, K., Barsukov, I. L., Yates, E. A., Eyers, C. E., . . . Eyers, P. A. (2018). New tools for carbohydrate sulfation analysis: heparan sulfate 2-O-sulfotransferase (HS2ST) is a target for small-molecule protein kinase inhibitors. BIOCHEMICAL JOURNAL, 475(15), 2417-2433. doi:10.1042/BCJ20180265

DOI
10.1042/BCJ20180265
Journal article

New tools for evaluating protein tyrosine sulfation: tyrosylprotein sulfotransferases (TPSTs) are novel targets for RAF protein kinase inhibitors

Byrne, D. P., Li, Y., Ngamlert, P., Ramakrishnan, K., Eyers, C. E., Wells, C., . . . Eyers, P. A. (2018). New tools for evaluating protein tyrosine sulfation: tyrosylprotein sulfotransferases (TPSTs) are novel targets for RAF protein kinase inhibitors. BIOCHEMICAL JOURNAL, 475(15), 2435-2455. doi:10.1042/BCJ20180266

DOI
10.1042/BCJ20180266
Journal article

PO-061 BCL-2 family of proteins, BCL-XL and MCL-1, regulate apoptosis and cancer cell survival by different mechanisms

Greaves, G., Milani, M., Byrne, D., Carter, R., Butterworth, M., Luo, X., . . . Varadarajan, S. (2018). PO-061 BCL-2 family of proteins, BCL-XL and MCL-1, regulate apoptosis and cancer cell survival by different mechanisms. ESMO Open, 3, A44-A45. doi:10.1136/esmoopen-2018-eacr25.105

DOI
10.1136/esmoopen-2018-eacr25.105
Journal article

2017

The response of uveal melanoma (UM) cells to Bromodomain and Extra Terminal (BET) inhibitors

Bailey, F. P., Kalirai, H., Shahidipour, H., Clarke, K., Coupland, S. E., & Eyers, P. A. (2017). The response of uveal melanoma (UM) cells to Bromodomain and Extra Terminal (BET) inhibitors. In INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE Vol. 58. Retrieved from https://www.webofscience.com/

Conference Paper

2016

2015

TRIBBLES: A Twist in the Pseudokinase Tail

Eyers, P. A. (2015). TRIBBLES: A Twist in the Pseudokinase Tail. STRUCTURE, 23(11), 1974-1976. doi:10.1016/j.str.2015.10.003

DOI
10.1016/j.str.2015.10.003
Journal article

Centrin 3 is an inhibitor of centrosomal Mps1 and antagonizes centrin 2 function

Sawant, D. B., Majumder, S., Perkins, J. L., Yang, C. -H., Eyers, P. A., & Fisk, H. A. (2015). Centrin 3 is an inhibitor of centrosomal Mps1 and antagonizes centrin 2 function. MOLECULAR BIOLOGY OF THE CELL, 26(21), 3741-3753. doi:10.1091/mbc.E14-07-1248

DOI
10.1091/mbc.E14-07-1248
Journal article

Tribbles pseudokinases: novel targets for chemical biology and drug discovery?

Foulkes, D. M., Byrne, D. P., Bailey, F. P., & Eyers, P. A. (2015). Tribbles pseudokinases: novel targets for chemical biology and drug discovery?. BIOCHEMICAL SOCIETY TRANSACTIONS, 43, 1095-1103. doi:10.1042/BST20150109

DOI
10.1042/BST20150109
Journal article

TD-60 links RalA GTPase function to the CPC in mitosis

Papini, D., Langemeyer, L., Abad, M. A., Kerr, A., Samejima, I., Eyers, P. A., . . . Earnshaw, W. C. (2015). TD-60 links RalA GTPase function to the CPC in mitosis. NATURE COMMUNICATIONS, 6. doi:10.1038/ncomms8678

DOI
10.1038/ncomms8678
Journal article

The Tribbles 2 (TRB2) pseudokinase binds to ATP and autophosphorylates in a metal-independent manner

Bailey, F., Byrne, D., Oruganty, K., Eyers, C., Novotny, C. J., Shokat, K. M., . . . Eyers, P. (2015). The Tribbles 2 (TRB2) pseudokinase binds to ATP and autophosphorylates in a metal-independent manner. Biochemical Journal, 467(1), 47-62. doi:10.1042/BJ20141441

DOI
10.1042/BJ20141441
Journal article

2) Going for broke: targeting the human cancer pseudokinome.

Bailey, F. P., Byrne, D. P., McSkimming, D., Kannan, N., & Eyers, P. A. (2015). 2) Going for broke: targeting the human cancer pseudokinome.. The Biochemical journal, 466(1), 201. doi:10.1042/bj4660201v

DOI
10.1042/bj4660201v
Journal article

Going for broke: targeting the human cancer pseudokinome

Bailey, F. P., Byrne, D. P., McSkimming, D., Kannan, N., & Eyers, P. A. (2015). Going for broke: targeting the human cancer pseudokinome. BIOCHEMICAL JOURNAL, 465, 195-211. doi:10.1042/BJ20141060

DOI
10.1042/BJ20141060
Journal article

Going for broke: targeting the human cancer pseudokinome (vol 465, pg 195, 2015)

Bailey, F. P., Byrne, D. P., McSkimming, D., Kannan, N., & Eyers, P. A. (2015). Going for broke: targeting the human cancer pseudokinome (vol 465, pg 195, 2015). BIOCHEMICAL JOURNAL, 466, 201. Retrieved from https://www.webofscience.com/

Journal article

2014

DNA replication stress in CHK1-depleted tumour cells triggers premature (S-phase) mitosis through inappropriate activation of Aurora kinase B.

Zuazua-Villar, P., Rodriguez, R., Gagou, M. E., Eyers, P., & Meuth, M. (2014). DNA replication stress in CHK1-depleted tumour cells triggers premature (S-phase) mitosis through inappropriate activation of Aurora kinase B.. Cell Death and Disease, 5. doi:10.1038/cddis.2014.231

DOI
10.1038/cddis.2014.231
Journal article

A robust methodology to subclassify pseudokinases based on their nucleotide-binding properties.

Murphy, J. M., Zhang, Q., Young, S. N., Reese, M. L., Bailey, F., Eyers, P., . . . Lucet, I. S. (2014). A robust methodology to subclassify pseudokinases based on their nucleotide-binding properties.. The Biochemical Journal, 457(2), 323-334. doi:10.1042/BJ20131174

DOI
10.1042/BJ20131174
Journal article

Day of the dead: pseudokinases and pseudophosphatases in physiology and disease

Reiterer, V., Eyers, P. A., & Farhan, H. (2014). Day of the dead: pseudokinases and pseudophosphatases in physiology and disease. TRENDS IN CELL BIOLOGY, 24(9), 489-505. doi:10.1016/j.tcb.2014.03.008

DOI
10.1016/j.tcb.2014.03.008
Journal article

The Resistance Tetrad: Amino Acid Hotspots for Kinome-Wide Exploitation of Drug-Resistant Protein Kinase Alleles

Bailey, F. P., Andreev, V. I., & Eyers, P. A. (2014). The Resistance Tetrad: Amino Acid Hotspots for Kinome-Wide Exploitation of Drug-Resistant Protein Kinase Alleles. PROTEIN KINASE INHIBITORS IN RESEARCH AND MEDICINE, 548, 117-146. doi:10.1016/B978-0-12-397918-6.00005-7

DOI
10.1016/B978-0-12-397918-6.00005-7
Journal article

2013

Elucidation and Therapeutic Targeting Of The Molecular Mechanism Of TRIB2-Mediated Acute Myeloid Leukaemia

Lohan, F., Forde, C., Salome, M., O'Connor, C., Bailey, F., Cahill, M. R., . . . Keeshan, K. (2013). Elucidation and Therapeutic Targeting Of The Molecular Mechanism Of TRIB2-Mediated Acute Myeloid Leukaemia. Blood, 122(21), 3792. doi:10.1182/blood.v122.21.3792.3792

DOI
10.1182/blood.v122.21.3792.3792
Journal article

Elucidation and Therapeutic Targeting Of The Molecular Mechanism Of TRIB2-Mediated Acute Myeloid Leukaemia

Lohan, F., Forde, C., Salome, M., O'Connor, C., Bailey, F., Cahill, M. R., . . . Keeshan, K. (2013). Elucidation and Therapeutic Targeting Of The Molecular Mechanism Of TRIB2-Mediated Acute Myeloid Leukaemia. Blood, 122(21), 3799. doi:10.1182/blood.v122.21.3799.3799

DOI
10.1182/blood.v122.21.3799.3799
Journal article

Dawn of the dead: protein pseudokinases signal new adventures in cell biology.

Eyers, P. A., & Murphy, J. M. (2013). Dawn of the dead: protein pseudokinases signal new adventures in cell biology.. Biochemical Society transactions, 41(4), 969-974. doi:10.1042/bst20130115

DOI
10.1042/bst20130115
Journal article

Rheostat-ing mitosis.

Eyers, P. A. (2013). Rheostat-ing mitosis.. Chemistry & biology, 20(2), 142-143. doi:10.1016/j.chembiol.2013.02.001

DOI
10.1016/j.chembiol.2013.02.001
Journal article

A robust methodology to subclassify pseudokinases based on their nucleotide binding properties

Murphy, J. E. A. (2013). A robust methodology to subclassify pseudokinases based on their nucleotide binding properties. Biochemical Journal. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/24107129

Journal article

Getting to grips with drug-resistance in the human protein kinase superfamily

Eyers, P. A. (2013). Getting to grips with drug-resistance in the human protein kinase superfamily. European Pharmaceutical Review, 18, 49-54.

Journal article

2012

2011

Protein kinase A is central for forward transport of two-pore domain potassium channels K2P3.1 and K2P9.1.

Mant, A., Elliott, D., Eyers, P. A., & O'Kelly, I. M. (2011). Protein kinase A is central for forward transport of two-pore domain potassium channels K2P3.1 and K2P9.1.. The Journal of biological chemistry, 286(16), 14110-14119. doi:10.1074/jbc.m110.190702

DOI
10.1074/jbc.m110.190702
Journal article

Aurora A and Aurora B jointly coordinate chromosome segregation

Hegarat, N., Smith, E., Nayak, G., Takeda, S., Eyers, P. A., & Hochegger, H. (2011). Aurora A and Aurora B jointly coordinate chromosome segregation. J Cell Biol, 195, 1103-1113.

Journal article

Phosphorylation by Protein Kinase A (PKA) enables forward transport of K2P3.1 and K2P9.1, two pore domain potassium channels

Mant, A., Elliott, D., Eyers, P., & O'Kelly, I. M. (2011). Phosphorylation by Protein Kinase A (PKA) enables forward transport of K2P3.1 and K2P9.1, two pore domain potassium channels. J Biol Chem, 286, 14110-14119.

Journal article

2010

Drug-resistant aurora A mutants for cellular target validation of the small molecule kinase inhibitors MLN8054 and MLN8237.

Sloane, D. A., Trikic, M. Z., Chu, M. L. H., Lamers, M. B. A. C., Mason, C. S., Mueller, I., . . . Eyers, P. A. (2010). Drug-resistant aurora A mutants for cellular target validation of the small molecule kinase inhibitors MLN8054 and MLN8237.. ACS chemical biology, 5(6), 563-576. doi:10.1021/cb100053q

DOI
10.1021/cb100053q
Journal article

Biophysical and X-ray crystallographic analysis of Mps1 kinase inhibitor complexes.

Chu, M. L. H., Lang, Z., Chavas, L. M. G., Neres, J., Fedorova, O. S., Tabernero, L., . . . Eyers, P. A. (2010). Biophysical and X-ray crystallographic analysis of Mps1 kinase inhibitor complexes.. Biochemistry, 49(8), 1689-1701. doi:10.1021/bi901970c

DOI
10.1021/bi901970c
Journal article

2009

Rigorous determination of the stoichiometry of protein phosphorylation using mass spectrometry

Johnson, H., Eyers, C. E., Eyers, P. A., Beynon, R. J., & Gaskell, S. J. (2009). Rigorous determination of the stoichiometry of protein phosphorylation using mass spectrometry. Journal of the American Society for Mass Spectrometry, 20(12), 2211-2220. doi:10.1016/j.jasms.2009.08.009

DOI
10.1016/j.jasms.2009.08.009
Journal article

Survivin(g) phosphorylation?

Eyers, P. (2009). Survivin(g) phosphorylation?. Cell cycle (Georgetown, Tex.), 8(2), 183-184. doi:10.4161/cc.8.2.7828

DOI
10.4161/cc.8.2.7828
Journal article

Phosphoregulation of human Mps1 kinase.

Tyler, R. K., Chu, M. L. H., Johnson, H., McKenzie, E. A., Gaskell, S. J., & Eyers, P. A. (2009). Phosphoregulation of human Mps1 kinase.. The Biochemical journal, 417(1), 173-181. doi:10.1042/bj20081310

DOI
10.1042/bj20081310
Journal article

2008

Crystal structure of the catalytic domain of the mitotic checkpoint kinase Mps1 in complex with SP600125.

Chu, M. L. H., Chavas, L. M. G., Douglas, K. T., Eyers, P. A., & Tabernero, L. (2008). Crystal structure of the catalytic domain of the mitotic checkpoint kinase Mps1 in complex with SP600125.. The Journal of biological chemistry, 283(31), 21495-21500. doi:10.1074/jbc.m803026200

DOI
10.1074/jbc.m803026200
Journal article

2007

VX-680 inhibits Aurora A and Aurora B kinase activity in human cells.

Tyler, R. K., Shpiro, N., Marquez, R., & Eyers, P. A. (2007). VX-680 inhibits Aurora A and Aurora B kinase activity in human cells.. Cell cycle (Georgetown, Tex.), 6(22), 2846-2854. doi:10.4161/cc.6.22.4940

DOI
10.4161/cc.6.22.4940
Journal article

2006

Validating Aurora B as an anti-cancer drug target.

Girdler, F., Gascoigne, K. E., Eyers, P. A., Hartmuth, S., Crafter, C., Foote, K. M., . . . Taylor, S. S. (2006). Validating Aurora B as an anti-cancer drug target.. Journal of cell science, 119(Pt 17), 3664-3675. doi:10.1242/jcs.03145

DOI
10.1242/jcs.03145
Journal article

2005

Reduction of insulin-stimulated glucose uptake in L6 myotubes by the protein kinase inhibitor SB203580 is independent of p38MAPK activity.

Antonescu, C. N., Huang, C., Niu, W., Liu, Z., Eyers, P. A., Heidenreich, K. A., . . . Klip, A. (2005). Reduction of insulin-stimulated glucose uptake in L6 myotubes by the protein kinase inhibitor SB203580 is independent of p38MAPK activity.. Endocrinology, 146(9), 3773-3781. doi:10.1210/en.2005-0404

DOI
10.1210/en.2005-0404
Journal article

Regulation of the G(2)/M transition in Xenopus oocytes by the cAMP-dependent protein kinase.

Eyers, P. A., Liu, J., Hayashi, N. R., Lewellyn, A. L., Gautier, J., & Maller, J. L. (2005). Regulation of the G(2)/M transition in Xenopus oocytes by the cAMP-dependent protein kinase.. The Journal of biological chemistry, 280(26), 24339-24346. doi:10.1074/jbc.m412442200

DOI
10.1074/jbc.m412442200
Journal article

The Aurora A and Aurora B protein kinases: a single amino acid difference controls intrinsic activity and activation by TPX2.

Eyers, P. A., Churchill, M. E. A., & Maller, J. L. (2005). The Aurora A and Aurora B protein kinases: a single amino acid difference controls intrinsic activity and activation by TPX2.. Cell cycle (Georgetown, Tex.), 4(6), 784-789. doi:10.4161/cc.4.6.1693

DOI
10.4161/cc.4.6.1693
Journal article

2004

Regulation of Xenopus Aurora A activation by TPX2.

Eyers, P. A., & Maller, J. L. (2004). Regulation of Xenopus Aurora A activation by TPX2.. The Journal of biological chemistry, 279(10), 9008-9015. doi:10.1074/jbc.m312424200

DOI
10.1074/jbc.m312424200
Journal article

2003

Regulating the regulators: Aurora A activation and mitosis.

Eyers, P. A., & Maller, J. L. (2003). Regulating the regulators: Aurora A activation and mitosis.. Cell cycle (Georgetown, Tex.), 2(4), 287-289.

Journal article

A novel mechanism for activation of the protein kinase Aurora A.

Eyers, P. A., Erikson, E., Chen, L. G., & Maller, J. L. (2003). A novel mechanism for activation of the protein kinase Aurora A.. Current biology : CB, 13(8), 691-697. doi:10.1016/s0960-9822(03)00166-0

DOI
10.1016/s0960-9822(03)00166-0
Journal article

Identification of novel phosphorylation sites on <i>Xenopus laevis</i> aurora A and analysis of phosphopeptide enrichment by immobilized metal-affinity chromatography

Haydon, C. E., Eyers, P. A., Aveline-Wolf, L. D., Resing, K. A., Maller, J. L., & Ahn, N. G. (2003). Identification of novel phosphorylation sites on <i>Xenopus laevis</i> aurora A and analysis of phosphopeptide enrichment by immobilized metal-affinity chromatography. MOLECULAR & CELLULAR PROTEOMICS, 2(10), 1055-1067. doi:10.1074/mcp.M300054-MCP200

DOI
10.1074/mcp.M300054-MCP200
Journal article