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Unexpected Isomerisation of a Fragment Analogue During Fragment-Based Screening of HIV Integrase Catalytic Core Domain.
- Published in:
- Australian Journal of Chemistry, 2015, v. 68, n. 12, p. 1871, doi. 10.1071/CH15587
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- Article
Fragment Screening for the Modelling Community: SPR, ITC, and Crystallography.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1507, doi. 10.1071/CH13302
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- Article
Construction of the CSIRO Fragment Library.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1473, doi. 10.1071/CH13325
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- Article
Fragment Screening on Staphylococcus aureus HPPK - a Folate Pathway Target.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1537, doi. 10.1071/CH13298
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- Article
Development of Inhibitors of Plasmodium falciparum Apical Membrane Antigen 1 Based on Fragment Screening.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1530, doi. 10.1071/CH13266
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- Article
Analysis of Bovine Lactoferrin in Infant Formula and Adult Nutritional Products by Optical Biosensor Immunoassay: Collaborative Study, Final Action 2021.07.
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- Journal of AOAC International, 2024, v. 107, n. 5, p. 833, doi. 10.1093/jaoacint/qsae042
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- Article
Exploring the Chemical Space around 8-Mercaptoguanine as a Route to New Inhibitors of the Folate Biosynthesis Enzyme HPPK.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0059535
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- Article
Structural Model for the Interaction of a Designed Ankyrin Repeat Protein with the Human Epidermal Growth Factor Receptor 2.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059163
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- Article
Small Molecule Inhibitors of the LEDGF Site of Human Immunodeficiency Virus Integrase Identified by Fragment Screening and Structure Based Design.
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- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0040147
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- Article
Structure of S. aureus HPPK and the Discovery of a New Substrate Site Inhibitor.
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- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029444
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- Article
Structural studies of the tethered N-terminus of the Alzheimer's disease amyloid-β peptide.
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- Proteins, 2013, v. 81, n. 10, p. 1748, doi. 10.1002/prot.24312
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- Article
Isolation, kinetic analysis, and structural characterization of an antibody targeting the Bacillus anthracis major spore surface protein BclA.
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- Proteins, 2011, v. 79, n. 4, p. 1306, doi. 10.1002/prot.22971
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- Article
Shark IgNAR antibody mimotopes target a murine immunoglobulin through extended CDR3 loop structures.
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- Proteins, 2008, v. 71, n. 1, p. 119, doi. 10.1002/prot.21663
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- Article
Engineering of an anti-epidermal growth factor receptor antibody to single chain format and labeling by sortase A-mediated protein ligation.
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- Biotechnology & Bioengineering, 2012, v. 109, n. 6, p. 1461, doi. 10.1002/bit.24407
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- Article
Kinetic Characterization of a Panel of High-Affinity Monoclonal Antibodies Targeting Ricin and Recombinant Re-Formatting for Biosensor Applications.
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- Antibodies (2073-4468), 2014, v. 3, n. 2, p. 215, doi. 10.3390/antib3020215
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- Article
Shark Variable New Antigen Receptor (V<sub>NAR</sub>) Single Domain Antibody Fragments: Stability and Diagnostic Applications.
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- Antibodies (2073-4468), 2013, v. 2, n. 1, p. 66, doi. 10.3390/antib2010066
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- Article
Most clinical anti-EGFR antibodies do not neutralize both wtEGFR and EGFRvIII activation in glioma.
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- Neuro-Oncology, 2019, v. 21, n. 8, p. 1016, doi. 10.1093/neuonc/noz073
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- Article
Single-chain Fv multimers of the anti-neuraminidase antibody NC10: the residue at position 15 in the VL domain of the scFv-0 (VL−VH) molecule is primarily responsible for formation of a tetramer–trimer equilibrium.
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- Protein Engineering, 2003, v. 16, n. 1, p. 47, doi. 10.1093/proeng/gzg006
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- Article
ScFv multimers of the anti-neuraminidase antibody NC10: shortening of the linker in single-chain Fv fragment assembled in VL to VH orientation drives the formation of dimers, trimers, tetramers and higher molecular mass multimers.
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- Protein Engineering, 2000, v. 13, n. 8, p. 565, doi. 10.1093/protein/13.8.565
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- Article
8‐Mercaptoguanine Derivatives as Inhibitors of Dihydropteroate Synthase.
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- Chemistry - A European Journal, 2018, v. 24, n. 8, p. 1922, doi. 10.1002/chem.201704730
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- Article
Interrogating HIV integrase for compounds that bind- a SAMPL challenge.
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- Journal of Computer-Aided Molecular Design, 2014, v. 28, n. 4, p. 347, doi. 10.1007/s10822-014-9721-7
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- Article
The DINGO dataset: a comprehensive set of data for the SAMPL challenge.
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- Journal of Computer-Aided Molecular Design, 2012, v. 26, n. 5, p. 497, doi. 10.1007/s10822-011-9521-2
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- Article
Crystal structures of human ENPP1 in apo and bound forms.
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- Acta Crystallographica: Section D, Structural Biology, 2020, v. 76, n. 9, p. 889, doi. 10.1107/S2059798320010505
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- Article
Germline humanization of a murine Aβ antibody and crystal structure of the humanized recombinant Fab fragment.
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- Protein Science: A Publication of the Protein Society, 2010, v. 19, n. 2, p. 299, doi. 10.1002/pro.312
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- Article
Manipulating the Lewis antigen specificity of the cholesterol-dependent cytolysin lectinolysin.
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- Frontiers in Immunology, 2012, v. 3, p. 1, doi. 10.3389/fimmu.2012.00330
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- Article
Manipulating the Lewis antigen specificity of the cholesterol-dependent cytolysin lectinolysin.
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- Frontiers in Immunology, 2012, v. 3, p. 1, doi. 10.3389/fimmu.2012.00330
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- Article
A fully humanized IgG-like bispecific antibody for effective dual targeting of CXCR3 and CCR6.
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- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0184278
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- Article
Engineered antibody intervention strategies for Alzheimers disease and related dementias by targeting amyloid and toxic oligomers.
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- PEDS: Protein Engineering, Design & Selection, 2009, v. 22, n. 3, p. 199
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- Article