Author

N. Leneva

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:cell signaling & trafficking· 1 Research Focus:protein folding & dynamics· 1 Assay:protein structure· 1 Assay:structural biology· 1 Organism:yeast· 1

Frequent Co-Authors

B. M. Collins· 2 shared K.-E. Chen· 2 shared Q. Guo· 2 shared A. K. Kendall· 1 shared A. Mayer· 1 shared B. Xie· 1 shared D. A. Stroud· 1 shared D. P. Fairlie· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersCell Biology

B. M. Collins

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2 papers

Recent·Most cited

Molecular basis for the assembly of the Vps5-Vps17 SNX-BAR proteins with Retromer

K.-E. Chen, V. A. Tillu, N. Gopaldass, S. R. Chowdhury, N. Leneva, O. Kovtun, J. Ruan, Q. Guo, N. Ariotti, A. Mayer, B. M. Collins

This study investigates how Vps5 and Vps17 SNX-BAR proteins assemble with Retromer, revealing a PL motif in Vps5 that binds Vps29 and is essential for membrane tubule association and cargo recycling.

bioRxiv · Mar 24, 2024Cell Biology

De novo macrocyclic peptides for inhibiting, stabilising and probing the function of the Retromer endosomal trafficking complex

K.-E. Chen, Q. Guo, T. A. Hill, Y. Cui, A. K. Kendall, Z. Yang, R. J. Hall, M. Healy, J. Sacharz, S. J. Norwood, S. Fonseka, B. Xie, R. C. Reid, N. Leneva, R. G. Parton, , B. M. Collins

The paper develops macrocyclic peptides that inhibit, stabilize, and probe the Retromer complex's function, showing high affinity and specificity for different subunits.

bioRxiv · Dec 3, 2020 · PreprintBiochemistry