Manfred S. Weiss

Citations in supplementary material.

Crystallization and preliminary X-ray diffraction analysis of the wild-type haloalkane dehalogenase DhaA and its variant DhaA13 complexed with different ligands.

Publishing structural genomics results continued: the SSGCID special issue.

Review panel for Acta Crystallographica Section F.

Facilities for macromolecular crystallography at the Helmholtz-Zentrum Berlin.

Structure determination by multiple-wavelength anomalous dispersion (MAD) at the Pr LIII edge.

Cloning, expression, purification, crystallization and preliminary X-ray diffraction analysis of AHP2, a signal transmitter protein from Arabidopsis thaliana.

Big changes are ahead--a new format for crystallization communications in Acta Cryst. F.

Structural Sampling of Glycan Interaction Profiles Reveals Mucosal Receptors for Fimbrial Adhesins of Enterotoxigenic Escherichia coli.

Protein crystalline frameworks with controllable interpenetration directed by dual supramolecular interactions.

The times they are a-changin' - news from Acta Crystallographica Section F.

Glutamate 270 plays an essential role in K(+)-activation and domain closure of Thermus thermophilus isopropylmalate dehydrogenase.

Against the odds? De novo structure determination of a pilin with two cysteine residues by sulfur SAD.

Macromolecular crystallography and what it can contribute to antiparasite drug discovery.

Native SAD is maturing.

Combining dehydration, construct optimization and improved data collection to solve the crystal structure of a CRM1-RanGTP-SPN1-Nup214 quaternary nuclear export complex.

Dual Role of the Active Site Residues of Thermus thermophilus 3-Isopropylmalate Dehydrogenase: Chemical Catalysis and Domain Closure.

Six Biophysical Screening Methods Miss a Large Proportion of Crystallographically Discovered Fragment Hits: A Case Study.

Structures of endothiapepsin-fragment complexes from crystallographic fragment screening using a novel, diverse and affordable 96-compound fragment library.

Structure-based Epitope Mapping of Mycobacterium tuberculosis Secretary Antigen MTC28.

High-Throughput Crystallography: Reliable and Efficient Identification of Fragment Hits.

Experimental Active-Site Mapping by Fragments: Hot Spots Remote from the Catalytic Center of Endothiapepsin.

A critical examination of the recently reported crystal structures of the human SMN protein.

Active Site Mapping of an Aspartic Protease by Multiple Fragment Crystal Structures: Versatile Warheads To Address a Catalytic Dyad.

Long-Wavelength X-Ray Diffraction and Its Applications in Macromolecular Crystallography.

Substrate specificity and reaction mechanism of human prolidase.

Crystal structures of the disease-causing D444V mutant and the relevant wild type human dihydrolipoamide dehydrogenase.

Structural basis for prolidase deficiency disease mechanisms.

Elucidating the Formation and Transformation Mechanisms of the Switchable Metal-Organic Framework ELM-11 by Powder and Single-Crystal EPR Study.

MXCuBE2: the dawn of MXCuBE Collaboration.

Structure of the plastic-degrading Ideonella sakaiensis MHETase bound to a substrate.

Findable Accessible Interoperable Re-usable (FAIR) diffraction data are coming to protein crystallography.

Findable Accessible Interoperable Re-usable (FAIR) diffraction data are coming to protein crystallography.

Findable Accessible Interoperable Re-usable (FAIR) diffraction data are coming to protein crystallography.

Findable Accessible Interoperable Re-usable (FAIR) diffraction data are coming to protein crystallography.

Underlying molecular alterations in human dihydrolipoamide dehydrogenase deficiency revealed by structural analyses of disease-causing enzyme variants.

Structure-Based Screening of Tetrazolylhydrazide Inhibitors versus KDM4 Histone Demethylases.

In Situ Imine-Based Linker Formation for the Synthesis of Zirconium MOFs: A Route to CO Capture Materials and Ethylene Oligomerization Catalysts.

Regioselectivity of hyoscyamine 6β-hydroxylase-catalysed hydroxylation as revealed by high-resolution structural information and QM/MM calculations.

F2X-Universal and F2X-Entry: Structurally Diverse Compound Libraries for Crystallographic Fragment Screening.

Co-expression with chaperones can affect protein 3D structure as exemplified by loss-of-function variants of human prolidase.

The susceptibility of disulfide bonds towards radiation damage may be explained by S⋯O interactions.

Prolidase - A protein with many faces.

Insulin polymorphism induced by two polyphenols: new crystal forms and advances in macromolecular powder diffraction.

The hypothetical periplasmic protein PA1624 from Pseudomonas aeruginosa folds into a unique two-domain structure.

X-ray screening identifies active site and allosteric inhibitors of SARS-CoV-2 main protease.

Facilitated crystal handling using a simple device for evaporation reduction in microtiter plates.

Structural analysis of new compound heterozygous variants in PEPD gene identified in a patient with Prolidase Deficiency diagnosed by exome sequencing.

FragMAXapp: crystallographic fragment-screening data-analysis and project-management system.

Engineering micromechanics of soft porous crystals for negative gas adsorption.

Substrate binding modes of purine and pyrimidine nucleotides to human ecto-5'-nucleotidase (CD73) and inhibition by their bisphosphonic acid derivatives.

Frag4Lead: growing crystallographic fragment hits by catalog using fragment-guided template docking.

Enhanced Properties of a Benzimidazole Benzylpyrazole Lysine Demethylase Inhibitor: Mechanism-of-Action, Binding Site Analysis, and Activity in Cellular Models of Prostate Cancer.

Unique features of the bifunctional GH30 from Thermothelomyces thermophila revealed by structural and mutational studies.

DYW domain structures imply an unusual regulation principle in plant organellar RNA editing catalysis.