Author

M. Jamshad

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 Cell Biology· 2 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 5 Research Focus:chromatin & epigenetic regulation· 4 Research Focus:cell signaling & trafficking· 3 Research Focus:cancer & tumor microenvironment· 2 Organism:E. coli· 2 Organism:human· 2 Research Focus:protein folding & dynamics· 2 Assay:proteomics· 2

Frequent Co-Authors

T. Knowles· 3 shared A. S. Chauhan· 2 shared D. Huber· 2 shared J. R. Morris· 2 shared K. Starowicz· 2 shared R. M. Densham· 2 shared A. Cunningham· 1 shared A. J. Garvin· 1 shared

Activity by Year

2017-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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3 shared papersBiochemistry

T. Knowles

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

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

The deSUMOylase SENP2 coordinates homologous recombination and non-homologous end joining by independent mechanisms.

A. J. Garvin, A. K. Walker, R. M. Densham, A. S. Chauhan, H. R. Stone, H. L. MacKay, M. Jamshad, K. Starowicz, M. Daza-Martin, J. R. Morris

This study identifies SENP2 as a deSUMOylase that differentially regulates homologous recombination and non-homologous end joining through distinct mechanisms, impacting DSB repair and radioresistance.

Genes & Development · Feb 22, 2019Peer-reviewedCell Biology

PIN1 isomerisation of BRCA1 promotes replication fork protection.

M. R. Daza-Martin, M. Jamshad, K. Starowicz, A. S. Chauhan, J. F. J. Beesley, J. Coles, G. S. Stewart, R. M. Densham, J. R. Morris

This study identifies PIN1-mediated BRCA1 isomerisation as a regulator of replication fork protection through enhanced BRCA1-BARD1-RAD51 interaction, distinct from BRCA1's role in homologous recombination.

bioRxiv · Nov 28, 2018 · PreprintCell Biology

The C-terminal tail of the bacterial translocation ATPase SecA modulates its activity

M. Jamshad, T. Knowles, S. White, D. Ward, F. Mohammed, K. F. Rahman, G. W. Hughes, G. Kramer, B. Bukau, D. Huber

This study investigates how the C-terminal tail of SecA modulates its activity in cotranslational substrate protein recognition by interacting with ribosomes and substrate proteins.

bioRxiv · Aug 22, 2018Biochemistry

MCE domain proteins: conserved inner membrane lipid-binding proteins required for outer membrane homeostasis

G. Isom, N. Davies, Z.-S. Chong, J. Bryant, M. Jamshad, M. Sharif, A. Cunningham, T. Knowles, S.-S. Chng, J. Cole, I. Henderson

The paper identifies and characterizes MCE domain proteins in E. coli, showing they localize to the inner membrane and play distinct roles in maintaining outer membrane lipid asymmetry.

bioRxiv · Jul 4, 2017Microbiology