| Entry ID | Original Release date | Data summary | Entry Title | Citation Title | Authors | 
|---|---|---|---|---|---|
| 51437 | 2024-01-12 | Chemical Shifts: 1 set | Backbone assignment of S. pombe PCNA | Checkpoint activation by Spd1: a competition-based system relying on tandem disordered PCNA binding motifs | Andreas Prestel, Antony M Carr, Birthe B Kragelund, Christian Holmberg, Gitte W Haxholm, Hossain Mohammad M Shamim, Johan G Olsen, Josefine Mortensen, Louise Lund L Rytkjar, Martin Grysbak, Noah Kassem, Olaf Nielsen, Ramon Crehuet, Riccardo Marabini, Sebastian S Broendum, Signe Simonsen | 
| 34521 | 2021-03-18 | Chemical Shifts: 1 set Spectral_peak_list: 8 sets | Ternary complex of Calmodulin bound to 2 molecules of NHE1 | Dynamic Na +/H + Exchanger 1 (NHE1):Calmodulin complexes of varying stoichiometry and structure regulate Ca 2+-dependent NHE1 activation | A Prestel, B B Kragelund, E S Pedersen, J G Olsen, L M Sjoegaard-Frich, M Severin, S F Pedersen | 
| 19959 | 2014-05-20 | Chemical Shifts: 1 set | Structural basis for binding of Pan3 to Pan2 and its function in mRNA recruitment and deadenylation | Structural basis for binding of Pan3 to Pan2 and its function in mRNA recruitment and deadenylation | B Meineke, C V Robinson, E Valkov, J Wolf, L A Passmore, Mark D Allen, M Bycroft, M Stewart, S H Mclaughlin, T M Olsen, Y Gordiyenko | 
| 18976 | 2013-07-22 | Chemical Shifts: 1 set Heteronuclear NOE Values: 2 sets | CALMODULIN, I85L, F92E, H107I, L107I, A128T, M144R MUTANT | A single mutation in a regulatory protein produces evolvable allosterically regulated catalyst of nonnatural reaction | Alissa B Olsen, Elisabeth A Raymond, Heinrich Roder, Hong Cheng, Ivan V Korendovych, Jaclyn M McLaughlin, Korrie L Mack, Krystyna Zhezherya, Olesia V Moroz, Yibing Wu, Yurii S Moroz | 
| 20072 | 2009-03-09 | Chemical Shifts: 1 set | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor Using Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri, W Seth Horne | 
| 20071 | 2009-03-09 | Chemical Shifts: 1 set | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor Using Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri, W Seth Horne | 
| 20073 | 2009-03-09 | Chemical Shifts: 1 set | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor Using Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri, W Seth Horne | 
| 20069 | 2009-02-26 | Chemical Shifts: 1 set | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
| 20064 | 2009-02-26 | Chemical Shifts: 1 set | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
| 20065 | 2009-02-26 | Chemical Shifts: 1 set | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
| 20066 | 2009-02-26 | Chemical Shifts: 1 set | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
| 20067 | 2009-02-26 | Chemical Shifts: 1 set | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
| 20068 | 2009-02-26 | Chemical Shifts: 1 set | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
| 20070 | 2009-02-26 | Chemical Shifts: 1 set | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
| 6265 | 2005-02-08 | Chemical Shifts: 1 set | Structure and Biochemical Function of a Prototypical Arabidopsis U-box Domain | Structure and Biochemical Function of a Prototypical Arabidopsis U-box Domain | A N Olsen, B B Kragelund, F H Larsen, F M Poulsen, K Skriver, N-H Chua, P Andersen |