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Panagis Filippakopoulos

Panagis Filippakopoulos

D-Index & Metrics

Biology and Biochemistry

D-Index
63
Citations
20444
World Ranking
10013
National Ranking
343

Overview

Panagis Filippakopoulos is affiliated with the Structural Genomics Consortium in Canada. Their research primarily falls within the field of Biochemistry, Genetics and Molecular Biology, with a strong focus on Molecular Biology as a dominant subfield. Additional areas of study include Oncology, Hematology, Materials Chemistry, and Immunology.

The scientist's work addresses several main topics, notably:

  • Protein Degradation and Inhibitors
  • Ubiquitin and proteasome pathways
  • Histone Deacetylase Inhibitors Research
  • Multiple Myeloma Research and Treatments
  • Genomics and Chromatin Dynamics
  • Cancer-related gene regulation
  • Peptidase Inhibition and Analysis

Filippakopoulos has published frequently in several reputable venues. The most common publication forums include:

  • Nature Communications
  • Journal of Medicinal Chemistry
  • ChemMedChem
  • bioRxiv (Cold Spring Harbor Laboratory)
  • The Cambridge Structural Database

Some representative recent papers authored or co-authored by Filippakopoulos are:

  • "BET inhibition disrupts transcription but retains enhancer-promoter contact," 2021, Nature Communications
  • "Tuning Transcription Factor Availability through Acetylation-Mediated Genomic Redistribution," 2020, Molecular Cell
  • "BETs inhibition attenuates oxidative stress and preserves muscle integrity in Duchenne muscular dystrophy," 2020, Nature Communications
  • "Allosteric Antagonist Modulation of TRPV2 by Piperlongumine Impairs Glioblastoma Progression," 2021, ACS Central Science
  • "Dissecting the Role of BET Bromodomain Proteins BRD2 and BRD4 in Human NK Cell Function," 2021, Frontiers in Immunology

Throughout their career, Filippakopoulos has collaborated frequently with several colleagues, including:

  • S. Picaud
  • Colin R. Goding
  • Jean-Philippe Lambert
  • Philip C. Biggin
  • Pakavarin Louphrasitthiphol

Best Publications

  • Selective inhibition of BET bromodomains.

    Panagis Filippakopoulos;Jun Qi;Sarah Picaud;Yao Shen

  • Histone recognition and large-scale structural analysis of the human bromodomain family.

    Panagis Filippakopoulos;Sarah Picaud;Maria Mangos;Tracy Keates

  • Targeting bromodomains: epigenetic readers of lysine acetylation

    Panagis Filippakopoulos;Stefan Knapp

  • Large-Scale Structural Analysis of the Classical Human Protein Tyrosine Phosphatome

    Alastair J. Barr;Emilie Ugochukwu;Wen Hwa Lee;Oliver N.F. King

  • Functions of bromodomain-containing proteins and their roles in homeostasis and cancer

    Takao Fujisawa;Panagis Filippakopoulos;Panagis Filippakopoulos

  • Bromodomains as therapeutic targets.

    Susanne Muller;Panagis Filippakopoulos;Stefan Knapp

  • RVX-208, an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain.

    Sarah Picaud;Christopher Wells;Ildiko Felletar;Deborah Brotherton

  • Small-molecule inhibition of BRDT for male contraception

    Martin M. Matzuk;Michael R. McKeown;Panagis Filippakopoulos;Qinglei Li

  • The bromodomain interaction module.

    Panagis Filippakopoulos;Stefan Knapp;Stefan Knapp

  • Dual kinase-bromodomain inhibitors for rationally designed polypharmacology

    Pietro Ciceri;Susanne Müller;Alison O'Mahony;Oleg Fedorov

  • Discovery and Optimization of Small-Molecule Ligands for the CBP/p300 Bromodomains

    Duncan A Hay;Oleg Fedorov;Sarah Martin;Dean C Singleton

  • PFI-1, a Highly Selective Protein Interaction Inhibitor, Targeting BET Bromodomains

    Sarah Picaud;David Da Costa;Angeliki Thanasopoulou;Panagis Filippakopoulos

  • Small-molecule kinase inhibitors provide insight into Mps1 cell cycle function

    Nicholas Kwiatkowski;Nannette Jelluma;Panagis Filippakopoulos;Meera Soundararajan

  • Structurally Sophisticated Octahedral Metal Complexes as Highly Selective Protein Kinase Inhibitors

    Li Feng;Yann Geisselbrecht;Sebastian Blanck;Alexander Wilbuer

  • 3,5-dimethylisoxazoles act as acetyl-lysine-mimetic bromodomain ligands.

    David S. Hewings;Minghua Wang;Martin Philpott;Oleg Fedorov

  • Generation of a Selective Small Molecule Inhibitor of the CBP/p300 Bromodomain for Leukemia Therapy.

    Sarah Picaud;Sarah Picaud;Oleg Fedorov;Oleg Fedorov;Angeliki Thanasopoulou;Katharina Leonards

  • Identification of a Chemical Probe for Bromo and Extra C‑Terminal Bromodomain Inhibition through Optimization of a Fragment- Derived Hit

    Paul V. Fish;Panagis Filippakopoulos;Gerwyn Bish;Paul E. Brennan

  • Structural Coupling of SH2-Kinase Domains Links Fes and Abl Substrate Recognition and Kinase Activation

    Panagis Filippakopoulos;Michael Kofler;Oliver Hantschel;Gerald D. Gish

  • Selectivity, Cocrystal Structures, and Neuroprotective Properties of Leucettines, a Family of Protein Kinase Inhibitors Derived from the Marine Sponge Alkaloid Leucettamine B.

    Tania Tahtouh;Jonathan M. Elkins;Panagis Filippakopoulos;Meera Soundararajan

  • Abstract 5387: Dual kinase/bromodomain inhibitors for rationally designed polypharmacology

    Elizabeth R. Quinn;Pietro Ciceri;Susanne Müller-Knapp;Alison O'Mahony

Frequent Co-Authors

Stefan Knapp
Stefan Knapp Goethe University Frankfurt
Cheryl H. Arrowsmith
Cheryl H. Arrowsmith Structural Genomics Consortium
Aled M. Edwards
Aled M. Edwards Structural Genomics Consortium
Oleg Fedorov
Oleg Fedorov University of Oxford
Alex N. Bullock
Alex N. Bullock University of Oxford
Susanne Müller
Susanne Müller Structural Genomics Consortium
Paul Brennan
Paul Brennan International Agency For Research On Cancer
Udo Oppermann
Udo Oppermann University of Oxford
Opher Gileadi
Opher Gileadi Karolinska Institute
Anne-Claude Gingras
Anne-Claude Gingras Lunenfeld-Tanenbaum Research Institute

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