Ole A. Andersen - Concepedia

Author

Ole A. Andersen

Also Known As

F.V. Rao, O Andersen, O.A. Andersen, Ole A Andersen, Ole A. Andersen, Ole Andersen, Ole Andreas Andersen, Ole A. Andersen, Øyvind M. Andersen

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

University of Dundee UiT The Arctic University of Norway University of Bergen Evotec (United Kingdom)Evotec (Germany)

About

Ole A. Andersen is an author at University of Dundee specializing in natural sciences, biochemistry, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	17	17	1K
2	Biochemistry	17	17	1K
3	Medicine	15	16	762
4	Engineering	1	1	12
5	Allergy	1	1	47

Ole A. Andersen

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Methylxanthine Drugs Are Chitinase Inhibitors: Investigation of Inhibition and Binding Modes Francesco Rao, Ole A. Andersen, Kalpit A. Vora, Chemistry & Biology Medicinal ChemistryBiochemistryBinding ModesMedicineNatural Sciences	2005	118
Crystal Structure of the Ternary Complex of the Catalytic Domain of Human Phenylalanine Hydroxylase with Tetrahydrobiopterin and 3-(2-Thienyl)-l-alanine, and its Implications for the Mechanism of Catalysis and Substrate Activation Ole A. Andersen, Torgeir Flatmark, Edward Hough Journal of Molecular Biology Crystal StructureCatalytic DomainBiochemistryNatural SciencesBiocatalysis	2002	115
High resolution crystal structures of the catalytic domain of human phenylalanine hydroxylase in its catalytically active Fe(II) form and binary complex with tetrahydrobiopterin Ole A. Andersen, Torgeir Flatmark, Edward Hough Journal of Molecular Biology Catalytic DomainBinary ComplexBiochemistryNatural SciencesBiocatalysis	2001	106
Trypsin specificity as elucidated by LIE calculations, X‐ray structures, and association constant measurements Hanna‐Kirsti S. Leiros, Bjørn Olav Brandsdal, Ole A. Andersen, Protein Science	2004	94
2.0Å Resolution Crystal Structures of the Ternary Complexes of Human Phenylalanine Hydroxylase Catalytic Domain with Tetrahydrobiopterin and 3-(2-Thienyl)-l-alanine or l-Norleucine: Substrate Specificity and Molecular Motions Related to Substrate Binding Ole A. Andersen, Anne Jorunn Stokka, Torgeir Flatmark, Journal of Molecular Biology Protein ChemistryTernary ComplexesSubstrate BindingBiochemistryNatural Sciences	2003	92
Fragment-based discovery of DNA gyrase inhibitors targeting the ATPase subunit of GyrB Michael F. Mesleh, Jason B. Cross, Jing Zhang, Bioorganic & Medicinal Chemistry Letters Atpase SubunitAldo-keto ReductaseBiochemistryNatural SciencesOligonucleotide	2016	70
Discovery and Structure–Activity Relationship of Potent and Selective Covalent Inhibitors of Transglutaminase 2 for Huntington’s Disease Michael E. Prime, Ole A. Andersen, John J. Barker, Journal of Medicinal Chemistry Structure–activity RelationshipBiochemistryG Protein-coupled ReceptorMedicineTg2 Inhibitors	2012	69
Structure-Based Dissection of the Natural Product Cyclopentapeptide Chitinase Inhibitor Argifin Ole A. Andersen, Amit Nathubhai, Mark J. Dixon, Chemistry & Biology Chitinase InhibitorsLinear PeptidesStructure-based DissectionBiochemistryMedicine	2008	66
The multiple roles of computational chemistry in fragment-based drug design Richard Law, Oliver Barker, John J. Barker, Journal of Computer-Aided Molecular Design Combinatorial ChemistryMedicinal ChemistryLigand-based Drug DesignDrug DesignDrug Discovery	2009	56
Screening-based Discovery and Structural Dissection of a Novel Family 18 Chitinase Inhibitor Alexander W. Schüttelkopf, Ole A. Andersen, Francesco Rao, Journal of Biological Chemistry Drug TargetStructural BioinformaticsBiomolecular Structure PredictionMolecular BiologyChemical Biology	2006	55

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