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T. Krojer

Researcher Next ID · RN-034273

Researcher · Chemistry

Lund University

Lund, Sweden

Accepting doctoral researchersFunding unknown
Works count
1,140
Citation count
7,035
H-index
42
i10-index
71

Research interests

Chemistry
Computer Science
Engineering
Materials Science
Enzyme Structure and Function
X-ray Diffraction in Crystallography
Computational Drug Discovery Methods
Nanoplatforms for cancer theranostics
Mass Spectrometry Techniques and Applications

Publications

  • Fragment binding to the Nsp3 macrodomain of SARS-CoV-2 identified through crystallographic screening and computational docking

    Science Advances · 2021 · 10.1126/sciadv.abf8711

  • Crystallographic and electrophilic fragment screening of the SARS-CoV-2 main protease

    Nature Communications · 2020 · https://doi.org/10.1038/s41467-020-18709-w

  • Rapid Covalent-Probe Discovery by Electrophile-Fragment Screening

    Journal of the American Chemical Society · 2019 · https://doi.org/10.1021/jacs.9b02822

  • TheXChemExplorergraphical workflow tool for routine or large-scale protein–ligand structure determination

    Acta Crystallographica Section D Structural Biology · 2017 · 10.1107/s2059798316020234

  • Gentle, fast and effective crystal soaking by acoustic dispensing

    Acta Crystallographica Section D Structural Biology · 2017 · 10.1107/s205979831700331x

  • A multi-crystal method for extracting obscured crystallographic states from conventionally uninterpretable electron density

    Nature Communications · 2017 · https://doi.org/10.1038/ncomms15123

  • Multivalent Histone and DNA Engagement by a PHD/BRD/PWWP Triple Reader Cassette Recruits ZMYND8 to K14ac-Rich Chromatin

    Cell Reports · 2016 · 10.1016/j.celrep.2016.11.014

  • 8-Substituted Pyrido[3,4- d ]pyrimidin-4(3 H )-one Derivatives As Potent, Cell Permeable, KDM4 (JMJD2) and KDM5 (JARID1) Histone Lysine Demethylase Inhibitors

    Journal of Medicinal Chemistry · 2016 · 10.1021/acs.jmedchem.5b01635

  • Structural basis of glycogen branching enzyme deficiency and pharmacologic rescue by rational peptide design

    Human Molecular Genetics · 2015 · 10.1093/hmg/ddv280

  • A poised fragment library enables rapid synthetic expansion yielding the first reported inhibitors of PHIP(2), an atypical bromodomain

    Chemical Science · 2015 · 10.1039/c5sc03115j

  • Ribosomal oxygenases are structurally conserved from prokaryotes to humans

    Nature · 2014 · 10.1038/nature13263

  • 5-Carboxy-8-hydroxyquinoline is a broad spectrum 2-oxoglutarate oxygenase inhibitor which causes iron translocation

    Chemical Science · 2013 · 10.1039/c3sc51122g

  • Structural Basis for Cul3 Protein Assembly with the BTB-Kelch Family of E3 Ubiquitin Ligases

    Journal of Biological Chemistry · 2013 · https://doi.org/10.1074/jbc.m112.437996

  • Plant Growth Regulator Daminozide Is a Selective Inhibitor of Human KDM2/7 Histone Demethylases

    Journal of Medicinal Chemistry · 2012 · 10.1021/jm300677j

  • Substrate-induced remodeling of the active site regulates human HTRA1 activity

    Nature Structural & Molecular Biology · 2011 · 10.1038/nsmb.2013

  • Crystal structures of the endoplasmic reticulum aminopeptidase-1 (ERAP1) reveal the molecular basis for N-terminal peptide trimming

    Proceedings of the National Academy of Sciences · 2011 · 10.1073/pnas.1101262108

  • HtrA proteases have a conserved activation mechanism that can be triggered by distinct molecular cues

    Nature Structural & Molecular Biology · 2010 · 10.1038/nsmb.1840

  • Crystal Structure of the 2-Oxoglutarate- and Fe(II)-Dependent Lysyl Hydroxylase JMJD6

    Journal of Molecular Biology · 2010 · 10.1016/j.jmb.2010.05.054

  • Structural and Mechanistic Studies on γ-Butyrobetaine Hydroxylase

    Chemistry & Biology · 2010 · 10.1016/j.chembiol.2010.09.016

  • Interplay of PDZ and protease domain of DegP ensures efficient elimination of misfolded proteins

    Proceedings of the National Academy of Sciences · 2008 · 10.1073/pnas.0803392105

  • Structural basis for the regulated protease and chaperone function of DegP

    Nature · 2008 · 10.1038/nature07004

  • Regulation of the σE stress response by DegS: how the PDZ domain keeps the protease inactive in the resting state and allows integration of different OMP-derived stress signals upon folding stress

    Genes & Development · 2007 · 10.1101/gad.445307

  • Crystal structure of DegP (HtrA) reveals a new protease-chaperone machine

    Nature · 2002 · 10.1038/416455a

Current projects

    No projects listed.