Markus Seeliger

Assistant Professor

Stony Brook University

United States

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About

Markus Seeliger is an Assistant Professor at Stony Brook University, United States. His research focuses on protein-ligand interactions, kinase inhibition, and the structural mechanisms underlying drug-binding processes. Recent publications include studies on protein conformational dynamics, multicombination kinase inhibitor strategies, and the impact of mutations on nonreceptor tyrosine kinases.

Articles (15)

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2024

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2024

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2024

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2023

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2023

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2022

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2022

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2022

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2022

Collaborators (4)

Stefan Knapp

Goethe University Frankfurt

GERMANY

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Julie Rageul

Stony Brook University

UNITED STATES

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John R. Engen

Northeastern University

UNITED STATES

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Stella Tsirka

Distinguished Professor

Stony Brook University

UNITED STATES

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Markus Seeliger

Research Interests

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About

Articles (15)

Calculating Protein–Ligand Residence Times through State Predictive Information Bottleneck Based Enhanced Sampling

Allo-targeting of the kinase domain: Insights from in silico studies and comparison with experiments

Lucanthone, a Potential PPT1 Inhibitor, Perturbs Stemness, Reduces Tumor Microtube Formation, and Slows the Growth of Temozolomide-Resistant Gliomas In Vivo

Structural mechanism of a drug-binding process involving a large conformational change of the protein target

Biochemical Studies of Systemic Lupus Erythematosus-Associated Mutations in Nonreceptor Tyrosine Kinases Ack1 and Brk

Domain Architecture of the Nonreceptor Tyrosine Kinase Ack1

Allosteric regulation and inhibition of protein kinases

Death by a thousand cuts through kinase inhibitor combinations that maximize selectivity and enable rational multitargeting

Probing conformational dynamics to understand kinase inhibition

Extended DNA-binding interfaces beyond the canonical SAP domain contribute to the function of replication stress regulator SDE2 at DNA replication forks

Resistance to kinase inhibition through shortened target engagement

Discovery and molecular basis of subtype-selective cyclophilin inhibitors

Protein Flexibility and Dissociation Pathway Differentiation Can Explain Onset of Resistance Mutations in Kinases**

Protein Flexibility and Dissociation Pathway Differentiation Can Explain Onset of Resistance Mutations in Kinases**

Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome

Collaborators (4)

Stefan Knapp

Julie Rageul

John R. Engen

Stella Tsirka

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