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Brenda Schulman

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Director

Max Planck Institute of Biochemistry

Germany

Research Interests

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Recent Grants

Grant: Close

Structural mechanisms underlying MYC ubiquitylation (A10)

Open Date: 2024-01-01

Close Date:

Grant: Open

Ubiquitin-Proteasome System crosstalk with Metabolism

Open Date: 2023-10-01

Close Date: 2028-09-30

Grant: Close

Conformational switching during the production of branched polyubiquitin chains (A13*)

Open Date: 2021-01-01

Close Date: 2024-12-31

Grant: Close

MECHANISMS OVERWHELMING PROTEIN AND ORGANELLE QUALITY CONTROL IN PARKINSON’S DISEASE

Open Date: 2020-09-01

Close Date: 2023-09-01

Grant: Close

Chemical Biology of the Control of Neddylation by DCN1

Open Date: 2019-07-01

Close Date: 2024-06-30

Articles (20)

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Collaborators (13)

Arno Alpi

University of Edinburgh

UNITED KINGDOM

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Jakob Farnung

Max Planck Institute of Biochemistry

GERMANY

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Benjamin G. Davis

University of Oxford

UNITED KINGDOM

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Peter Murray

Head

Max Planck Institute of Biochemistry

GERMANY

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Fleur Ferguson

UCSD

UNITED STATES

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Stefan Kubicek

Head, Molecular Discovery Platform

AUSTRIA

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Jeffrey Wade Harper

Chair

Harvard University

UNITED STATES

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Ralf Jungmann

Professor

Ludwig-Maximilians-Universität München

GERMANY

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Leo James

MRC Laboratory of Molecular Biology

UNITED KINGDOM

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Slava Ziegler

Group leader

Max Planck Institute of Molecular Physiology

GERMANY

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Leo Kiss

Junior Professor (tenure-track) of Cellular Biochemistry

Universität Duisburg-Essen

GERMANY

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Monique Mulder

Associate Professor

Leiden University Medical Center

NETHERLANDS

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Daniel Horn-Ghetko

Max-Planck-Institut für biophysikalische Chemie

GERMANY

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Brenda Schulman

Research Interests

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Recent Grants

Articles (20)

The E3 ubiquitin ligase mechanism specifying targeted microRNA degradation

Monovalent pseudo-natural products supercharge degradation of IDO1 by its native E3 KLHDC3

Metabolically regulated proteasome supramolecular organization in situ

E2 variants for probing E3 ubiquitin ligase activities

TRIP12 structures reveal HECT E3 formation of K29 linkages and branched ubiquitin chains

Imaging Ligand‐Receptor Interactions at Single‐Protein Resolution with DNA‐PAINT

C-terminal amides mark proteins for degradation via SCF–FBXO31

Thoughts for the future

UbiREAD deciphers proteasomal degradation code of homotypic and branched K48 and K63 ubiquitin chains

The many faces of the GID/CTLH E3 ligase complex

Global cellular proteo-lipidomic profiling of diverse lysosomal storage disease mutants using nMOST

Alkylamine-tethered molecules recruit FBXO22 for targeted protein degradation.

Non-canonical substrate recognition by the human WDR26-CTLH E3 ligase regulates prodrug metabolism

Skraban‐Deardorff intellectual disability syndrome‐associated mutations in WDR26 impair CTLH E3 complex assembly

Noncanonical assembly, neddylation and chimeric cullin–RING/RBR ubiquitylation by the 1.8 MDa CUL9 E3 ligase complex

Ubiquitin is a chemist’s playground

Structural basis for C-degron selectivity across KLHDCX family E3 ubiquitin ligases

Principles of paralog-specific targeted protein degradation engaging the C-degron E3 KLHDC2

Visualizing chaperone-mediated multistep assembly of the human 20S proteasome

mTORC1-CTLH E3 ligase regulates the degradation of HMG-CoA synthase 1 through the Pro/N-degron pathway

Collaborators (13)

Arno Alpi

Jakob Farnung

Benjamin G. Davis

Peter Murray

Fleur Ferguson

Stefan Kubicek

Jeffrey Wade Harper

Ralf Jungmann

Leo James

Slava Ziegler

Leo Kiss

Monique Mulder

Daniel Horn-Ghetko

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