Author

Selena G Burgess

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:protein folding & dynamics· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:protein structure· 1 Assay:proteomics· 1

Frequent Co-Authors

Richard Bayliss· 2 shared Arkadiusz Oleksy· 1 shared Cristina Gutiérrez-Caballero· 1 shared David Matthews· 1 shared Isabelle Vernos· 1 shared Mark W Richards· 1 shared Stephen J Royle· 1 shared Tommaso Cavazza· 1 shared

Activity by Year

2014-2016 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 18 mutual co-author links

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2 shared papersBiochemistry

Richard Bayliss

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2 papers

Recent·Most cited

BiochemistryOpen BiologyPeer-reviewedJul 1, 2016

Allosteric inhibition of Aurora-A kinase by a synthetic VNAR nanobody

Selena G Burgess, Arkadiusz Oleksy, Tommaso Cavazza…·Richard Bayliss

This paper describes the development of an allosteric inhibitor for Aurora-A kinase using a synthetic VNAR nanobody, showing it stabilizes an inactive conformation distinct from the activator TPX2.

DOI 10.1098/rsob.160089

protein structureexperimental assay

𝕏 PostBluesky

Cell BiologybioRxivNov 4, 2014

TACC3-ch-TOG track the growing tips of microtubules independently of clathrin and Aurora-A phosphorylation

Cristina Gutiérrez-Caballero, Selena G Burgess, Richard Bayliss, Stephen J Royle

This study identifies a TACC3-ch-TOG pool independent of clathrin and Aurora-A phosphorylation that tracks microtubule plus-ends, revealing distinct subcellular pools of TACC3, ch-TOG, and clathrin.

DOI 10.1242/bio.201410843

humanproteomics

𝕏 PostBluesky