Author

M. Jeeves

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· 2 Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:protein folding & dynamics· 2 Approach:statistical model· 2 Organism:bacteria (other)· 1 Approach:biophysical modeling· 1 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

D. Huber· 2 shared I. R. Henderson· 2 shared J. A. Bryant· 2 shared M. Jamshad· 2 shared P. Sridhar· 2 shared T. Knowles· 2 shared A. Colyer· 1 shared A. Cunningham· 1 shared

Activity by Year

2018-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersBiochemistry

D. Huber

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Crosstalk between AML and stromal cells triggers acetate secretion through the metabolic rewiring of stromal cells

N. Vilaplana-Lopera, R. Almaghrabi, G. Papatzikas, V. Cuminetti, E. Gonzalez, M. Jeeves, A. Cunningham, A. Erdem, F. Schnuetgen, M. Raghavan, S. Potluri, J.-B. Cazier, J. J. Schuringa, M. A. Reed, L. Arranz, , P. Garcia

The paper identifies a metabolic crosstalk between AML and stromal cells where AML cells induce stromal cells to secrete acetate for their own energy needs.

bioRxiv · Jan 21, 2021Cell Biology

Structure-function analyses of dual-BON domain protein DolP identifies phospholipid binding as a new mechanism for protein localisation

J. A. Bryant, F. Morris, T. J. Knowles, R. Maderbocus, E. Heinz, G. Boelter, D. Alodaini, A. Colyer, P. wotherspoon, K. Staunton, M. Jeeves, D. Browning, Y. Sevastsyanovich, T. Wells, A. Rossiter, , i. henderson

This study identifies phospholipid binding as a mechanism for DolP localization, revealing its structure and function in Gram-negative bacteria.

bioRxiv · Aug 10, 2020 · PreprintBiochemistry

Iron is a ligand of SecA-like metal-binding domains in vivo

T. Cranford Smith, M. Jamshad, M. Jeeves, R. A. Chandler, J. Yule, A. Robinson, F. Alam, K. A. Dunne, E. H. Aponte Angarita, M. Alanazi, C. Carter, I. R. Henderson, J. E. Lovett, P. Winn, T. Knowles, D. Huber

This study identifies iron as a ligand for SecA-like metal-binding domains in E. coli, showing that these domains bind iron preferentially and that azide disrupts this interaction.

bioRxiv · Apr 1, 2020Biochemistry

Evidence for phospholipid export from the gram-negative inner membrane: time to rethink the Mla pathway?

G. W. Hughes, S. C. L. Hall, C. S. Laxton, P. Sridhar, A. H. Mahadi, C. Hatton, T. J. Piggot, M. Jamshad, V. Spana, I. T. Cadby, C. Harding, G. L. Isom, J. A. Bryant, R. J. Parr, Y. Yakub, , T. Knowles

The paper solves the crystal structure of MlaC and shows the Mla pathway exports phospholipids from the inner membrane to the periplasm, challenging the previous belief in retrograde transport.

bioRxiv · Aug 9, 2018 · PreprintBiophysics