Entry ID |
Original Release date |
Data summary |
Entry Title |
Citation Title |
Authors |
52209 |
2024-01-06 |
Chemical Shifts: 1 set |
Chemical shifts of constitutively monomeric CXCL12 |
The acidic intrinsically disordered region of the inflammatory mediator HMGB1 mediates fuzzy interactions with CXCL12
|
Camilla Carmeno, Chiara Pastorello, Chiara Zucchelli, Federica De Leo, Francesca Caprioglio, Francesco De Marchis, Gabriele Giachin, Giacomo Quilici, Giovanna Musco, Liam Sean S Colley, Malisa Vittoria V Mantonico, Marco Emilio E Bianchi, Massimo Crippa, Michela Ghitti, Rosanna Mezzapelle, Stefano Ricagno, Tim Schulte |
18550 |
2012-09-17 |
Chemical Shifts: 1 set |
Solution-state NMR of prion protein mutant V210I at pH 7 |
Structural Rearrangements at Physiological pH: Nuclear Magnetic Resonance Insights from the V210I Human Prion Protein Mutant.
|
Gabriele Giachin, Giuseppe Legname, Gregor Ilc, Ivana Biljan, Janez Plavec |
18426 |
2012-06-18 |
Chemical Shifts: 1 set |
Solution-state NMR structure of the human prion protein |
Structural basis for the protective effect of the human prion protein carrying the dominant-negative E219K polymorphism.
|
Gabriele Giachin, Giuseppe Legname, Gregor Ilc, Igor Zhukov, Ivana Biljan, Janez Plavec |
17780 |
2012-06-25 |
Chemical Shifts: 1 set |
Human prion protein with E219K protective polymorphism |
Structural basis for the protective effect of the human prion protein carrying the dominant-negative E219K polymorphism.
|
Gabriele Giachin, Giuseppe Legname, Gregor Ilc, Igor Zhukov, Ivana Biljan, Janez Plavec |
17714 |
2011-08-19 |
Chemical Shifts: 1 set |
human prion protein mutant HuPrP(90-231, M129, V210I) |
Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation.
|
Andrea Raspadori, Gabriele Giachin, Giuseppe Legname, Gregor Ilc, Igor Zhukov, Ivana Biljan, Janez Plavec |
16743 |
2010-09-02 |
Chemical Shifts: 1 set |
Three dimensional structure of HuPrP(90-231 M129 Q212P) |
NMR structure of the human prion protein with the pathological Q212P mutation reveals unique structural features
|
Federico Benetti, Gabriele Giachin, Gregor Ilc, Guiseppe Legname, Igor Zhukov, Janez Plavec, Lukasz Jaremko, Mariusz Jaremko |