| Structural insights and biological effects of glycogen synthase kinase 3-specific inhibitor AR-A014418 R Bhat, Y Xue, S Berg, S Hellberg, M Ormö, Y Nilsson, AC Radesäter, ... Journal of Biological Chemistry 278 (46), 45937-45945, 2003 | 627 | 2003 |
| Inhibition and catalysis of carbonic anhydrase A LILJAS, K HÅKANSSON, BH JONSSON, Y XUE European journal of biochemistry 219 (1‐2), 1-10, 1994 | 195 | 1994 |
| Exploitation of structural and regulatory diversity in glutamate racemases T Lundqvist, SL Fisher, G Kern, RHA Folmer, Y Xue, DT Newton, ... Nature 447 (7146), 817-822, 2007 | 165 | 2007 |
| Discovery of novel potent and highly selective glycogen synthase kinase-3β (GSK3β) inhibitors for Alzheimer’s disease: design, synthesis, and characterization of pyrazines S Berg, M Bergh, S Hellberg, K Högdin, Y Lo-Alfredsson, P Söderman, ... Journal of medicinal chemistry 55 (21), 9107-9119, 2012 | 151 | 2012 |
| Crystal structure of spinach plastocyanin at 1.7 Å resolution Y Xue, M Ökvist, Ö Hansson, S Young Protein science 7 (10), 2099-2105, 1998 | 131 | 1998 |
| Interfering with the inhibitory mechanism of serpins: crystal structure of a complex formed between cleaved plasminogen activator inhibitor type 1 and a reactive-centre loop … Y Xue, P Björquist, T Inghardt, M Linschoten, D Musil, L Sjölin, J Deinum Structure 6 (5), 627-636, 1998 | 124 | 1998 |
| Importance of the conserved active‐site residues Try7, Glu106 and Thr199 for the catalytic function of human carbonic anhydrase II Z LIANG, Y XUE, G BEHRAVAN, BH JONSSON, S LINDSKOG European Journal of Biochemistry 211 (3), 821-827, 1993 | 123 | 1993 |
| Crystal structure of carbonic anhydrase from Neisseria gonorrhoeae and its complex with the inhibitor acetazolamide S Huang, Y Xue, E Sauer-Eriksson, L Chirica, S Lindskog, BH Jonsson Journal of molecular biology 283 (1), 301-310, 1998 | 120 | 1998 |
| Crystallographic analysis of Thr‐200→ His human carbonic anhydrase II and its complex with the substrate, HCO3− Y Xue, J Vidgren, LA Svensson, A Liljas, BH Jonsson, S Lindskog Proteins: Structure, Function, and Bioinformatics 15 (1), 80-87, 1993 | 116 | 1993 |
| Hit-to-lead studies: the discovery of potent, orally active, thiophenecarboxamide IKK-2 inhibitors A Baxter, S Brough, A Cooper, E Floettmann, S Foster, C Harding, J Kettle, ... Bioorganic & Medicinal Chemistry Letters 14 (11), 2817-2822, 2004 | 111 | 2004 |
| Crystal structure of spinach chloroplast fructose-1, 6-bisphosphatase at 2.8. ANG. resolution V Villeret, S Huang, Y Zhang, Y Xue, WN Lipscomb Biochemistry 34 (13), 4299-4306, 1995 | 108 | 1995 |
| Crystal structure of fructose-1, 6-bisphosphatase complexed with fructose 2, 6-bisphosphate, AMP, and Zn2+ at 2.0-A resolution: aspects of synergism between inhibitors. Y Xue, S Huang, JY Liang, Y Zhang, WN Lipscomb Proceedings of the National Academy of Sciences 91 (26), 12482-12486, 1994 | 103 | 1994 |
| Structural analysis of the zinc hydroxide–Thr‐199–Glu‐106 hydrogen‐bond network in human carbonic anhydrase II Y Xue, A Liljas, BH Jonsson, S Lindskog Proteins: Structure, Function, and Bioinformatics 17 (1), 93-106, 1993 | 103 | 1993 |
| The crystal structure of allosteric chorismate mutase at 2.2-A resolution. Y Xue, WN Lipscomb, R Graf, G Schnappauf, G Braus Proceedings of the National Academy of Sciences 91 (23), 10814-10818, 1994 | 98 | 1994 |
| Structure-based ligand design to overcome CYP inhibition in drug discovery projects G Brändén, T Sjögren, V Schnecke, Y Xue Drug discovery today 19 (7), 905-911, 2014 | 93 | 2014 |
| Crystal structure of the native plasminogen reveals an activation‐resistant compact conformation Y Xue, C Bodin, K Olsson Journal of Thrombosis and Haemostasis 10 (7), 1385-1396, 2012 | 91 | 2012 |
| Clavatadine A, a natural product with selective recognition and irreversible inhibition of factor XIa MS Buchanan, AR Carroll, D Wessling, M Jobling, VM Avery, RA Davis, ... Journal of medicinal chemistry 51 (12), 3583-3587, 2008 | 88 | 2008 |
| Total synthesis and structural confirmation of chlorodysinosin A S Hanessian, JR Del Valle, Y Xue, N Blomberg Journal of the American Chemical Society 128 (32), 10491-10495, 2006 | 83 | 2006 |
| Discovery of Checkpoint Kinase Inhibitor (S)-5-(3-Fluorophenyl)-N-(piperidin-3-yl)-3-ureidothiophene-2-carboxamide (AZD7762) by Structure-Based Design and … V Oza, S Ashwell, L Almeida, P Brassil, J Breed, C Deng, T Gero, ... Journal of Medicinal Chemistry 55 (11), 5130-5142, 2012 | 79 | 2012 |
| A strategically positioned cation is crucial for efficient catalysis by chorismate mutase P Kast, C Grisostomi, IA Chen, S Li, U Krengel, Y Xue, D Hilvert Journal of Biological Chemistry 275 (47), 36832-36838, 2000 | 79 | 2000 |
