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SCI Abstract
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Using graphlet degree vectors to predict atomic displacement parameters in protein structures
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Structural mechanism of Escherichia coli cyanase
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Neutron crystallographic refinement with REFMAC5 from the CCP4 suite
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Structural and functional characterization of the novel endo-α(1,4)-fucoidanase Mef1 from the marine bacterium Muricauda eckloniae
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Cocrystallization of ubiquitin–deubiquitinase complexes through disulfide linkage
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Atypical homodimerization revealed by the structure of the (S)-enantioselective haloalkane dehalogenase DmmarA from Mycobacterium marinum
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Domain structure and cross-linking in a giant adhesin from the Mobiluncus mulieris bacterium
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Crystal structures of the DExH-box RNA helicase DHX9
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The impact of molecular variants, crystallization conditions and the space group on ligand–protein complexes: a case study on bacterial phosphotriesterase
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Structural analysis of wild-type and Val120Thr mutant Candida boidinii formate dehydrogenase by X-ray crystallography
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Anaerobic fixed-target serial crystallography using sandwiched silicon nitride membranes
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Elucidating polymorphs of crystal structures by intensity-based hierarchical clustering analysis of multiple diffraction data sets
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Acta Crystallographica Section D-structural Biology
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Increasing the bulk of the 1TEL–target linker and retaining the 10×His tag in a 1TEL–CMG2-vWa construct improves crystal order and diffraction limits
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A user-friendly plug-and-play cyclic olefin copolymer-based microfluidic chip for room-temperature, fixed-target serial crystallography
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Crystal structures of human and mouse ketohexokinase provide a structural basis for species- and isoform-selective inhibitor design
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Structural basis for the allosteric pathway of 4-amino-4-deoxychorismate synthase
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X-ray structure of the metastable SEPT14–SEPT7 coiled coil reveals a hendecad region crucial for heterodimerization
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Predicted models and CCP4
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Correcting systematic errors in diffraction data with modern scaling algorithms
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A Python package based on robust statistical analysis for serial crystallography data processing
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Novel starting points for fragment-based drug design against mycobacterial thioredoxin reductase identified using crystallographic fragment screening
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Announcing the launch of Protein Data Bank China as an Associate Member of the Worldwide Protein Data Bank Partnership
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LifeSoaks: a tool for analyzing solvent channels in protein crystals and obstacles for soaking experiments
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Structural basis of the amidase ClbL central to the biosynthesis of the genotoxin colibactin
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Rhizobium etli has two l-asparaginases with low sequence identity but similar structure and catalytic center
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A standard descriptor for fixed-target serial crystallography
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Structural and biochemical insights into purine-based drug molecules in hBRD2 delineate a unique binding mode opening new vistas in the design of inhibitors of the BET family
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