Max-Planck-Institut für molekulare Physiologie

Key Publications 2023

Native Semisynthesis of Isopeptide-Linked Substrates for Specificity Analysis of Deubiquitinases and Ubl Proteases

Native Semisynthesis of Isopeptide-Linked Substrates for Specificity Analysis of Deubiquitinases and Ubl Proteases

Gersch Group. JACS (2023) [mehr]

Structural basis of mRNA binding by the human FERRY Rab5 effector complex

Structural basis of mRNA binding by the human FERRY Rab5 effector complex

Raunser Group. Mol Cell (2023) [mehr]

Programming inactive RNA-binding small molecules into bioactive degraders

Programming inactive RNA-binding small molecules into bioactive degraders

Waldmann Group. Nature (2023) [mehr]

Stable kinetochore-microtubule attachment requires loop-dependent Ndc80-Ndc80 binding

Stable kinetochore-microtubule attachment requires loop-dependent Ndc80-Ndc80 binding

Musacchio Group. EMBO J (2023) [mehr]

TomoTwin: generalized 3D localization of macromolecules in cryo-electron tomograms with structural data mining

TomoTwin: generalized 3D localization of macromolecules in cryo-electron tomograms with structural data mining

Raunser Group. Nature Methods (2023) [mehr]

Structural Biochemistry of Muscle Contraction

Structural Biochemistry of Muscle Contraction

Wang Z, Raunser S. Annu Rev Biochem (2023) [mehr]

The EGFR phosphatase RPTPγ is a redox-regulated suppressor of promigratory signaling.

The EGFR phosphatase RPTPγ is a redox-regulated suppressor of promigratory signaling.

Bastiaens Group. EMBO J. (2023) [mehr]

Targeting oncogenic KRasG13C with nucleotide-based covalent inhibitors

Targeting oncogenic KRasG13C with nucleotide-based covalent inhibitors

Goody Group. Elife (2023) [mehr]

The structural flexibility of MAD1 facilitates the assembly of the Mitotic Checkpoint Complex

The structural flexibility of MAD1 facilitates the assembly of the Mitotic Checkpoint Complex

Musacchio Group. Nat Commun. (2023)
[mehr]

Morphological profiling identifies the motor protein Eg5 as cellular target of spirooxindoles

Morphological profiling identifies the motor protein Eg5 as cellular target of spirooxindoles

Waldmann Group. Angew Chem Int Ed Engl. (2023) [mehr]