about
Structure of a single-chain Fv fragment of an antibody that inhibits the HIV-1 and HIV-2 proteasesDesign of HIV protease inhibitors based on inorganic polyhedral metallacarboranesA tick salivary protein targets cathepsin G and chymase and inhibits host inflammation and platelet aggregationThe crystal structure of protease Sapp1p from Candida parapsilosis in complex with the HIV protease inhibitor ritonavirStructure of the effector-binding domain of the arabinose repressor AraR fromBacillus subtilisEngineering enzyme stability and resistance to an organic cosolvent by modification of residues in the access tunnelCarborane-based carbonic anhydrase inhibitorsKinetic and structural characterization of an alternatively spliced variant of human mitochondrial 5'(3')-deoxyribonucleotidaseThermodynamic and structural analysis of HIV protease resistance to darunavir - analysis of heavily mutated patient-derived HIV-1 proteasesStructure of the effector-binding domain of deoxyribonucleoside regulator DeoR from Bacillus subtilisStructural and functional analysis of a novel haloalkane dehalogenase with two halide-binding sitesValidation and structural characterization of the LEDGF/p75-MLL interface as a new target for the treatment of MLL-dependent leukemiaConformationally constrained nucleoside phosphonic acids--potent inhibitors of human mitochondrial and cytosolic 5'(3')-nucleotidasesStructural basis for inhibition of mycobacterial and human adenosine kinase by 7-substituted 7-(Het)aryl-7-deazaadenine ribonucleosidesMultiple cellular proteins interact with LEDGF/p75 through a conserved unstructured consensus motifCarbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoformsAtomic resolution crystal structure of Sapp2p, a secreted aspartic protease from Candida parapsilosisKinetic, thermodynamic and structural analysis of tamiphosphor binding to neuraminidase of H1N1 (2009) pandemic influenza.Structure-aided design of novel inhibitors of HIV protease based on a benzodiazepine scaffold.Crystallization and diffraction analysis of β-N-acetylhexosaminidase from Aspergillus oryzae.Inhibition of HIV protease by monoclonal antibodies.Current and Novel Inhibitors of HIV ProteaseOligomeric interface modulation causes misregulation of purine 5´-nucleotidase in relapsed leukemia.Feasibility and constraints of particle targeting using the antigen-antibody interaction.Crystallographic analysis of new psychrophilic haloalkane dehalogenases: DpcA from Psychrobacter cryohalolentis K5 and DmxA from Marinobacter sp. ELB17.Triggering HIV polyprotein processing by light using rapid photodegradation of a tight-binding protease inhibitor.Crystallization and preliminary crystallographic characterization of the iron-regulated outer membrane lipoprotein FrpD from Neisseria meningitidis.Structural basis of the interaction between the putative adhesion-involved and iron-regulated FrpD and FrpC proteins of Neisseria meningitidis.Carborane-based carbonic anhydrase inhibitors: insight into CAII/CAIX specificity from a high-resolution crystal structure, modeling, and quantum chemical calculations.Identification of carbonic anhydrase I immunodominant epitopes recognized by specific autoantibodies which indicate an improved prognosis in patients with malignancy after autologous stem cell transplantation.A phenylnorstatine inhibitor binding to HIV-1 protease: geometry, protonation, and subsite-pocket interactions analyzed at atomic resolution.Crystal structure of a cross-reaction complex between an anti-HIV-1 protease antibody and an HIV-2 protease peptide.QM/MM calculations reveal the different nature of the interaction of two carborane-based sulfamide inhibitors of human carbonic anhydrase II.Ranking Power of the SQM/COSMO Scoring Function on Carbonic Anhydrase II-Inhibitor Complexes.Crystal structure of native β-N-acetylhexosaminidase isolated from Aspergillus oryzae sheds light onto its substrate specificity, high stability, and regulation by propeptide.Structures of human cytosolic and mitochondrial nucleotidases: implications for structure-based design of selective inhibitors.Kinetic, Thermodynamic, and Structural Analysis of Drug Resistance Mutations in Neuraminidase from the 2009 Pandemic Influenza VirusRegular arrangement of periodates bound to lysozymeNew techniques for membrane protein crystallization tested on photosystem II core complex of Pisum sativumPotent inhibition of drug-resistant HIV protease variants by monoclonal antibodies
P50
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P50
description
researcher ORCID ID = 0000-0001-9626-346X
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wetenschapper
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name
Pavlína Maloy Řezáčová
@ast
Pavlína Maloy Řezáčová
@br
Pavlína Maloy Řezáčová
@co
Pavlína Maloy Řezáčová
@cs
Pavlína Maloy Řezáčová
@da
Pavlína Maloy Řezáčová
@de
Pavlína Maloy Řezáčová
@en
Pavlína Maloy Řezáčová
@es
Pavlína Maloy Řezáčová
@fr
Pavlína Maloy Řezáčová
@id
type
label
Pavlína Maloy Řezáčová
@ast
Pavlína Maloy Řezáčová
@br
Pavlína Maloy Řezáčová
@co
Pavlína Maloy Řezáčová
@cs
Pavlína Maloy Řezáčová
@da
Pavlína Maloy Řezáčová
@de
Pavlína Maloy Řezáčová
@en
Pavlína Maloy Řezáčová
@es
Pavlína Maloy Řezáčová
@fr
Pavlína Maloy Řezáčová
@id
altLabel
Pavlina Rezacova
@en
Pavlína Řezáčová
@en
prefLabel
Pavlína Maloy Řezáčová
@ast
Pavlína Maloy Řezáčová
@br
Pavlína Maloy Řezáčová
@co
Pavlína Maloy Řezáčová
@cs
Pavlína Maloy Řezáčová
@da
Pavlína Maloy Řezáčová
@de
Pavlína Maloy Řezáčová
@en
Pavlína Maloy Řezáčová
@es
Pavlína Maloy Řezáčová
@fr
Pavlína Maloy Řezáčová
@id
P106
P21
P31
P496
0000-0001-9626-346X