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Biology and Biochemistry

D-Index
65
Citations
15288
World Ranking
9135
National Ranking
4057

Overview

Jeanne A. Stuckey is affiliated with the University of Michigan-Ann Arbor in the United States. Their research spans multiple fields, primarily within Biochemistry, Genetics and Molecular Biology, and Medicine.

The subfields of study most frequently associated with Jeanne A. Stuckey include Molecular Biology, Immunology, Oncology, Organic Chemistry, and Hematology. These areas reflect a diverse approach to understanding biological processes and disease mechanisms.

The main topics of their work focus heavily on protein degradation and inhibitors, peptidase inhibition and analysis, ubiquitin and proteasome pathways, cancer-related gene regulation, epigenetics and DNA methylation, PI3K/AKT/mTOR signaling in cancer, and chromatin remodeling and cancer. These topics indicate a strong emphasis on molecular mechanisms related to cancer biology and protein regulation.

Frequent co-authors working with Jeanne A. Stuckey include Krishnapriya Chinnaswamy, Shaomeng Wang, Chao-Yie Yang, Duxin Sun, and Jennifer L. Meagher, with collaboration counts ranging from 16 to 22 publications, highlighting an active network in biomedical research.

The scientist has published extensively in several academic journals. Frequent publication venues include the Journal of Medicinal Chemistry with 13 publications, ACS Medicinal Chemistry Letters with 5, Cancer Research with 4, bioRxiv (Cold Spring Harbor Laboratory) with 3, and Blood with 2 publications.

Recent papers demonstrate a focus on cancer biology, chemical biology, and immunology. Examples include:

  • A selective small-molecule STAT5 PROTAC degrader capable of achieving tumor regression in vivo (2023, Nature Chemical Biology)
  • Heteromeric three-stranded coiled coils designed using a Pb(ii)(Cys)3 template mediated strategy (2020, Nature Chemistry)
  • Lipid-based vaccine nanoparticles for induction of humoral immune responses against HIV-1 and SARS-CoV-2 (2020, Journal of Controlled Release)
  • Lisaftoclax (APG-2575) Is a Novel BCL-2 Inhibitor with Robust Antitumor Activity in Preclinical Models of Hematologic Malignancy (2022, Clinical Cancer Research)
  • SD-91 as A Potent and Selective STAT3 Degrader Capable of Achieving Complete and Long-Lasting Tumor Regression (2021, ACS Medicinal Chemistry Letters)

Best Publications

  • Structure-Based Design of Spiro-oxindoles as Potent, Specific Small-Molecule Inhibitors of the MDM2−p53 Interaction

    Ke Ding;Yipin Lu;Zaneta Nikolovska-Coleska;Guoping Wang

  • Structure-Based Design of Potent Non-Peptide MDM2 Inhibitors

    Ke Ding;Yipin Lu;Zaneta Nikolovska-Coleska;Su Qiu

  • Development and optimization of a binding assay for the XIAP BIR3 domain using fluorescence polarization

    Zaneta Nikolovska-Coleska;Renxiao Wang;Xueliang Fang;Hongguang Pan

  • A Potent and Selective Small-Molecule Degrader of STAT3 Achieves Complete Tumor Regression In Vivo

    Longchuan Bai;Haibin Zhou;Renqi Xu;Yujun Zhao

  • Crystal structure of Yersinia protein tyrosine phosphatase at 2.5 Å and the complex with tungstate

    Jeanne A. Stuckey;Heidi L. Schubert;Eric B. Fauman;Zhong Yin Zhang;Zhong Yin Zhang

  • Form and Function in Protein Dephosphorylation

    John M Denu;Jeanne A Stuckey;Mark A Saper;Jack E Dixon

  • Hydrolytic catalysis and structural stabilization in a designed metalloprotein

    Melissa L. Zastrow;Anna F. A. Peacock;Anna F. A. Peacock;Jeanne A. Stuckey;Vincent L. Pecoraro

  • Structure-based design of potent small-molecule inhibitors of anti-apoptotic Bcl-2 proteins.

    Guoping Wang;Zaneta Nikolovska-Coleska;Chao Yie Yang;Renxiao Wang

  • Discovery of ARD-69 as a Highly Potent Proteolysis Targeting Chimera (PROTAC) Degrader of Androgen Receptor (AR) for the Treatment of Prostate Cancer.

    Xin Han;Chao Wang;Chong Qin;Weiguo Xiang

  • Interaction between pyrin and the apoptotic speck protein (ASC) modulates ASC-induced apoptosis.

    Neil Richards;Philip Schaner;Arturo Diaz;Jeanne Stuckey

  • SAR405838: An optimized inhibitor of MDM2-p53 interaction that induces complete and durable tumor regression

    Shaomeng Wang;Wei Sun;Yujun Zhao;Donna McEachern

  • Discovery of QCA570 as an Exceptionally Potent and Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of the Bromodomain and Extra-Terminal (BET) Proteins Capable of Inducing Complete and Durable Tumor Regression

    Chong Qin;Yang Hu;Bing Zhou;Ester Fernandez-Salas

  • Crystal structure of a phospholipase D family member.

    Jeanne A. Stuckey;Jack E. Dixon

  • Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent Smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAP.

    Haiying Sun;Zaneta Nikolovska-Coleska;Jianfeng Lu;Jennifer L. Meagher

  • Expression, purification, and physicochemical characterization of a recombinant Yersinia protein tyrosine phosphatase.

    Zhong-Yin Zhang;J. C. Clemens;H. L. Schubert;J. A. Stuckey

  • Discovery of ERD-308 as a Highly Potent Proteolysis Targeting Chimera (PROTAC) Degrader of Estrogen Receptor (ER).

    Jiantao Hu;Biao Hu;Mingliang Wang;Fuming Xu

  • A unique carbohydrate binding domain targets the lafora disease phosphatase to glycogen.

    Jianyong Wang;Jeanne A. Stuckey;Matthew J. Wishart;Jack E. Dixon

  • SM-164: a novel, bivalent Smac mimetic that induces apoptosis and tumor regression by concurrent removal of the blockade of cIAP-1/2 and XIAP.

    Jianfeng Lu;Longchuan Bai;Haiying Sun;Zaneta Nikolovska-Coleska

  • D3R Grand Challenge 2015: Evaluation of Protein-Ligand Pose and Affinity Predictions

    Symon Gathiaka;Shuai Liu;Michael Chiu;Huanwang Yang

  • The Cys(X)5Arg Catalytic Motif in Phosphoester Hydrolysis

    Zhong Yin Zhang;Yuan Wang;Li Wu;Li Wu;Eric B. Fauman

Frequent Co-Authors

Chao Yie Yang
Chao Yie Yang University of Tennessee Health Science Center
Duxin Sun
Duxin Sun University of Michigan–Ann Arbor
Vincent L. Pecoraro
Vincent L. Pecoraro University of Michigan–Ann Arbor
Jack E. Dixon
Jack E. Dixon University of California, San Diego
Peter P. Roller
Peter P. Roller National Institutes of Health
Heather A. Carlson
Heather A. Carlson University of Michigan–Ann Arbor
Richard D. Smith
Richard D. Smith Pacific Northwest National Laboratory
Yi Sun
Yi Sun Zhejiang University
Irwin J. Goldstein
Irwin J. Goldstein University of Michigan–Ann Arbor
Zhong Yin Zhang
Zhong Yin Zhang Purdue University West Lafayette

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