about
Complex formation between human kallikrein 13 and serum protease inhibitorsCharacterization of the enzymatic activity of human kallikrein 6: Autoactivation, substrate specificity, and regulation by inhibitorsStructure of human ST8SiaIII sialyltransferase provides insight into cell-surface polysialylationA chemical probe selectively inhibits G9a and GLP methyltransferase activity in cellsSpecificity of Campylobacter jejuni adhesin PEB3 for phosphates and structural differences among its ligand complexesDiscovery of a 2,4-Diamino-7-aminoalkoxyquinazoline as a Potent and Selective Inhibitor of Histone Lysine Methyltransferase G9aRecognition and Specificity Determinants of the Human Cbx ChromodomainsStructural Studies of the Tandem Tudor Domains of Fragile X Mental Retardation Related Proteins FXR1 and FXR2An allosteric inhibitor of the human Cdc34 ubiquitin-conjugating enzymeCharacterization of 14-3-3 Proteins from Cryptosporidium parvumThe Cryptosporidium parvum KinomeStructure of the Mycosin-1 Protease from the Mycobacterial ESX-1 Protein Type VII Secretion SystemSequence-specific recognition of a PxLPxI/L motif by an ankyrin repeat tumbler lockAn allosteric inhibitor of protein arginine methyltransferase 3The modular structure of the inner-membrane ring component PrgK facilitates assembly of the type III secretion system basal bodyThe human kallikrein protein 5 (hK5) is enzymatically active, glycosylated and forms complexes with two protease inhibitors in ovarian cancer fluidsThe Structure of a Type 3 Secretion System (T3SS) Ruler Protein Suggests a Molecular Mechanism for Needle Length SensingChemical screening methods to identify ligands that promote protein stability, protein crystallization, and structure determination.Biophysical characterization of recombinant proteins: a key to higher structural genomics successFluorescence-based methods for screening writers and readers of histone methyl marks.Protein lysine methyltransferase G9a inhibitors: design, synthesis, and structure activity relationships of 2,4-diamino-7-aminoalkoxy-quinazolines.Structural analysis of a specialized type III secretion system peptidoglycan-cleaving enzyme.Structure and mechanism of Staphylococcus aureus TarM, the wall teichoic acid α-glycosyltransferase.Synthesis, Optimization, and Evaluation of Novel Small Molecules as Antagonists of WDR5-MLL Interaction.A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activity.Structural Insights into Inhibition of Escherichia coli Penicillin-binding Protein 1B.Small-molecule inhibition of MLL activity by disruption of its interaction with WDR5Genome-scale protein expression and structural biology of Plasmodium falciparum and related Apicomplexan organisms.Erratum: A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cellsStructural insights into the modulatory role of the accessory protein WYL1 in the Type VI-D CRISPR-Cas system.
P50
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P50
name
Gregory A Wasney
@en
type
label
Gregory A Wasney
@en
prefLabel
Gregory A Wasney
@en