Suchergebnis | Hamburg Open Science

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18 Einträge gefunden

Structural basis to repurpose boron-based proteasome inhibitors Bortezomib and Ixazomib as β-lactamase inhibitors
2022 - Forschungsinformationssystem des UKE - frei zugänglich
A Giant Extracellular Matrix Binding Protein of Staphylococcus epidermidis Binds Surface-Immobilized Fibronectin via a Novel Mechanism
2020 - Forschungsinformationssystem des UKE
Emergence of ceftazidime/avibactam non-susceptibility in an MDR Klebsiella pneumoniae isolate
2017 - Forschungsinformationssystem des UKE
Immunosuppressive Yersinia Effector YopM Binds DEAD Box Helicase DDX3 to Control Ribosomal S6 Kinase in the Nucleus of Host Cells
2016 - Forschungsinformationssystem des UKE - frei zugänglich
High resolution structures of Plasmodium falciparum GST complexes provide novel insights into the dimer-tetramer transition and a novel ligand-binding site
2015 - Forschungsinformationssystem des UKE
Isolation, identification and functional profile of excretory-secretory peptides from Onchocerca ochengi
2015 - Forschungsinformationssystem des UKE
Preliminary crystallographic analysis of a cruciferin protein from seeds of Moringa oleifera
2014 - Forschungsinformationssystem des UKE
Protective mechanisms of helminths against reactive oxygen species are highly promising drug targets.
2014 - Forschungsinformationssystem des UKE
3C protease of enterovirus 68: structure-based design of Michael acceptor inhibitors and their broad-spectrum antiviral effects against picornaviruses.
2013 - Forschungsinformationssystem des UKE
Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases.
2013 - Forschungsinformationssystem des UKE
Functional characterization and immune recognition of the extracellular superoxide dismutase from the human pathogenic parasite Onchocerca volvulus (OvEC-SOD).
2012 - Forschungsinformationssystem des UKE
Structure of the recombinant BPTI/Kunitz-type inhibitor rShPI-1A from the marine invertebrate Stichodactyla helianthus.
2012 - Forschungsinformationssystem des UKE
Structural insights into serine protease inhibition by a marine invertebrate BPTI Kunitz-type inhibitor.
2012 - Forschungsinformationssystem des UKE
Purification, crystallization and preliminary X-ray diffraction analysis of the thiaminase type II from Staphylococcus aureus.
2011 - Forschungsinformationssystem des UKE
Stage-specific excretory-secretory small heat shock proteins from the parasitic nematode Strongyloides ratti--putative links to host's intestinal mucosal defense system.
2011 - Forschungsinformationssystem des UKE
Isolation, purification, crystallization and preliminary crystallographic studies of a chitinase from Crocus vernus.
2011 - Forschungsinformationssystem des UKE
Purification, crystallization and preliminary X-ray diffraction analysis of ThiM from Staphylococcus aureus.
2011 - Forschungsinformationssystem des UKE
Isolation, crystallization and preliminary X-ray diffraction analysis of L-amino-acid oxidase from Vipera ammodytes ammodytes venom.
2008 - Forschungsinformationssystem des UKE

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Structural basis to repurpose boron-based proteasome inhibitors Bortezomib and Ixazomib as β-lactamase inhibitors

A Giant Extracellular Matrix Binding Protein of Staphylococcus epidermidis Binds Surface-Immobilized Fibronectin via a Novel Mechanism

Emergence of ceftazidime/avibactam non-susceptibility in an MDR Klebsiella pneumoniae isolate

Immunosuppressive Yersinia Effector YopM Binds DEAD Box Helicase DDX3 to Control Ribosomal S6 Kinase in the Nucleus of Host Cells

High resolution structures of Plasmodium falciparum GST complexes provide novel insights into the dimer-tetramer transition and a novel ligand-binding site

Isolation, identification and functional profile of excretory-secretory peptides from Onchocerca ochengi

Preliminary crystallographic analysis of a cruciferin protein from seeds of Moringa oleifera

Protective mechanisms of helminths against reactive oxygen species are highly promising drug targets.

3C protease of enterovirus 68: structure-based design of Michael acceptor inhibitors and their broad-spectrum antiviral effects against picornaviruses.

Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases.

Functional characterization and immune recognition of the extracellular superoxide dismutase from the human pathogenic parasite Onchocerca volvulus (OvEC-SOD).

Structure of the recombinant BPTI/Kunitz-type inhibitor rShPI-1A from the marine invertebrate Stichodactyla helianthus.

Structural insights into serine protease inhibition by a marine invertebrate BPTI Kunitz-type inhibitor.

Purification, crystallization and preliminary X-ray diffraction analysis of the thiaminase type II from Staphylococcus aureus.

Stage-specific excretory-secretory small heat shock proteins from the parasitic nematode Strongyloides ratti--putative links to host's intestinal mucosal defense system.

Isolation, purification, crystallization and preliminary crystallographic studies of a chitinase from Crocus vernus.

Purification, crystallization and preliminary X-ray diffraction analysis of ThiM from Staphylococcus aureus.

Isolation, crystallization and preliminary X-ray diffraction analysis of L-amino-acid oxidase from Vipera ammodytes ammodytes venom.