User profiles for Eva M Huber

Eva Maria Huber

Technical University of Munich
Verified email at tum.de
Cited by 1797

[HTML][HTML] Immuno-and constitutive proteasome crystal structures reveal differences in substrate and inhibitor specificity

EM Huber, M Basler, R Schwab, W Heinemeyer… - Cell, 2012 - cell.com
Constitutive proteasomes and immunoproteasomes shape the peptide repertoire presented
by major histocompatibility complex class I (MHC-I) molecules by harboring different sets of …

Structure-based design of β1i or β5i specific inhibitors of human immunoproteasomes

G de Bruin, EM Huber, BT Xin… - Journal of medicinal …, 2014 - ACS Publications
Mammalian genomes encode seven catalytic proteasome subunits, namely, β1c, β2c, β5c (assembled
into constitutive 20S proteasome core particles), β1i, β2i, β5i (incorporated into …

[HTML][HTML] A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome

EM Huber, W Heinemeyer, X Li, CS Arendt… - Nature …, 2016 - nature.com
Biogenesis of the 20S proteasome is tightly regulated. The N-terminal propeptides protecting
the active-site threonines are autocatalytically released only on completion of assembly. …

[PDF][PDF] The mammalian proteasome activator PA28 forms an asymmetric α4β3 complex

EM Huber, M Groll - Structure, 2017 - cell.com
The heptameric proteasome activator (PA) 28αβ is known to modulate class I antigen
processing by docking onto 20S proteasome core particles (CPs). The exact stoichiometry and …

[PDF][PDF] Bortezomib-resistant mutant proteasomes: structural and biochemical evaluation with carfilzomib and ONX 0914

EM Huber, W Heinemeyer, M Groll - Structure, 2015 - cell.com
Inhibition of the 20S proteasome by bortezomib (Velcade) constitutes a successfully applied
therapy for blood cancer. However, emerging resistance restricts its medicinal use. For …

[PDF][PDF] DNA minor groove sensing and widening by the CCAAT-binding complex

EM Huber, DH Scharf, P Hortschansky, M Groll… - Structure, 2012 - cell.com
The CCAAT box is a frequent element of eukaryotic promoters, and its specific recognition
by the conserved heterotrimeric CCAAT-binding complex (CBC) constitutes a key step in …

The CCAAT-binding complex (CBC) in Aspergillus species

P Hortschansky, H Haas, EM Huber, M Groll… - … et Biophysica Acta (BBA …, 2017 - Elsevier
Background The CCAAT binding complex (CBC), consisting of a heterotrimeric core structure,
is highly conserved in eukaryotes and constitutes an important general transcriptional …

Flavoenzyme‐catalyzed formation of disulfide bonds in natural products

…, C Hertweck, AA Brakhage, EM Huber - Angewandte Chemie …, 2014 - Wiley Online Library
Nature provides a rich source of compounds with diverse chemical structures and biological
activities, among them, sulfur‐containing metabolites from bacteria and fungi. Some of these …

Epipolythiodioxopiperazine‐Based Natural Products: Building Blocks, Biosynthesis and Biological Activities

EM Huber - ChemBioChem, 2022 - Wiley Online Library
Epipolythiodioxopiperazines (ETPs) are fungal secondary metabolites that share a 2,5‐diketopiperazine
scaffold built from two amino acids and bridged by a sulfide moiety. …

Systematic analyses of substrate preferences of 20S proteasomes using peptidic epoxyketone inhibitors

EM Huber, G de Bruin, W Heinemeyer… - Journal of the …, 2015 - ACS Publications
Cleavage analyses of 20S proteasomes with natural or synthetic substrates allowed to infer
the substrate specificities of the active sites and paved the way for the rational design of high-…