Listing of New BMRB NMR-STAR files
Entries released in the last month, starting from most recent release to least recent one.
The latest entries may not be immediately available here
or through the BMRB database search. They can be found in "entry lists" under "FTP access".
| Entry ID | Release Date | Title |
|---|---|---|
| 53977 | 2026-11-03 | Universal 3D Motif dynamics in RNA: The A-minor Switch |
| 53976 | 2026-11-03 | Universal 3D Motif dynamics in RNA: The A-minor Switch |
| 53975 | 2026-11-03 | Universal 3D Motif dynamics in RNA: The A-minor Switch |
| 53598 | 2026-11-03 | Structural and functional diversity of cerebrospinal fluid-derived a-synuclein fibrils in Parkinson's disease and multiple system atrophy |
| 54032 | 2026-11-03 | Cryo-EM and NMR Reveal a Membrane-Gated Doc2B-Munc13-1 Complex and a Helical Doc2B-SNARE-Binding Interface |
| 54031 | 2026-11-03 | Cryo-EM and NMR Reveal a Membrane-Gated Doc2B-Munc13-1 Complex and a Helical Doc2B-SNARE-Binding Interface |
| 53984 | 2026-11-03 | Differential histone tail citrullination by PAD Enzymes observed via NMR spectroscopy |
| 53983 | 2026-11-03 | Differential histone tail citrullination by PAD Enzymes observed via NMR spectroscopy |
| 53982 | 2026-11-03 | Differential histone tail citrullination by PAD Enzymes observed via NMR spectroscopy |
| 53981 | 2026-11-03 | Differential histone tail citrullination by PAD Enzymes observed via NMR spectroscopy |
| 53980 | 2026-11-03 | Differential histone tail citrullination by PAD Enzymes observed via NMR spectroscopy |
| 53979 | 2026-11-03 | Differential histone tail citrullination by PAD Enzymes observed via NMR spectroscopy |
| 53978 | 2026-11-03 | Differential histone tail citrullination by PAD Enzymes observed via NMR spectroscopy |
| 53605 | 2026-11-01 | Structural characterisation of the IIICS-containing region of fibronectin: Splice variants define propensity for long-range interactions |
| 53788 | 2026-11-01 | 1H, 13C, and 15N backbone resonance assignment of the N-terminal 280 amino acids of human NHERF1 protein |
| 53599 | 2026-11-01 | Structural characterisation of the IIICS-containing region of fibronectin: Splice variants define propensity for long-range interactions |
| 53603 | 2026-11-01 | Structural characterisation of the IIICS-containing region of fibronectin: Splice variants define propensity for long-range interactions |
| 54056 | 2026-10-30 | Mixed, nonclassical behavior in a classic allosteric protein. |
| 31288 | 2026-10-29 | Damping amyloid-associated conformational fluctuations in a protein by an engineered diselenide bridge |
| 31293 | 2026-10-29 | Solution structure of the surface domain of the Borrelia burgdorferi outer surface lipoprotein BBA36 |
| 31279 | 2026-10-29 | Investigating the Molecular Mechanism of Liraglutide Oligomerization |
| 31309 | 2026-10-29 | The cysteine-rich domain of SEP15, a selenoprotein co-chaperone of the ER chaperone, UDP-glucose:glycoprotein glucosyltransferase, adopts a novel fold |
| 54037 | 2026-10-27 | Conformational dynamics at the pre-miR-377 Dicer site governs selective small-molecule recognition |
| 52906 | 2026-10-26 | Chemical shift assignments for SET-9/26 PHD domain in isolation |
| 54046 | 2026-10-22 | Deamidation and isomerization to elusive isoaspartate in a computationally designed miniprotein |
| 54060 | 2026-10-22 | The disordered region 1 of Mdm2 weakens p53-binding in both its unmodified and hyperphospho-forms |
| 54045 | 2026-10-22 | Deamidation and isomerization to elusive isoaspartate in a computationally designed miniprotein |
| 53778 | 2026-10-21 | Distinct Ca2+-binding thermodynamics reveal a paralogue-specific structural response in the calmodulin-like domain of alpha-actinin-4 |
| 35045 | 2026-10-21 | Solution structure of a peptide-conjugated aggregation-induced-emission (AIE) fluorophore bound to a protein |
| 53779 | 2026-10-21 | Distinct Ca2+-binding thermodynamics reveal a paralogue-specific structural response in the calmodulin-like domain of alpha-actinin-4 |
| 54021 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54023 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54024 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54016 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54017 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54018 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54019 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54020 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54022 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 53207 | 2026-10-20 | NMR crystallography reveals active-site protonation states of Toho-1 b-lactamase in complex with avibactam |
| 53206 | 2026-10-20 | NMR crystallography reveals active-site protonation states of Toho-1 b-lactamase in complex with avibactam |
| 53885 | 2026-10-20 | Allosteric Inhibition of NDM-1 by Thanatin Preserves the Di-Zinc Center While Restricting Dynamics |
| 54026 | 2026-10-17 | The core interaction network of transcription elongation factors is broadly maintained across diverse bacteria |
| 54027 | 2026-10-17 | The core interaction network of transcription elongation factors is broadly maintained across diverse bacteria |
| 53839 | 2026-10-17 | Multisite Threonine Phosphorylation in the SPT5 C-Terminal Region 1 Enables Sequence-Dependent Regulation without Global Structural Remodeling |
| 53838 | 2026-10-17 | Multisite Threonine Phosphorylation in the SPT5 C-Terminal Region 1 Enables Sequence-Dependent Regulation without Global Structural Remodeling |
| 53820 | 2026-10-17 | 1H, 13C, and 15N backbone and side-chain resonance assignments of the Nostoc sp. H-NOX C139A variant in complex with the soluble Guanylyl Cyclase inhibitor Zinc Protoporphyrin IX |
| 54052 | 2026-10-16 | Backbone and side-chain 1H, 13C, and 15N resonance assignments of the human Sin3A PAH2 domain (residues 295-395) |
| 53884 | 2026-10-13 | Transmembrane domains of TLR1 and TLR2 tend to specific heterotypic interaction |
| 53867 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53866 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53865 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53864 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53863 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53862 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53861 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53860 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53859 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53858 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 52907 | 2026-10-11 | Chemical shift assignments of SET-9/26 PHD finger in the peptide (H3K4me3)-bound state |
| 31299 | 2026-10-11 | New insights into chemokine N-terminus dynamics by a high-resolution solution NMR ensemble of CCL11 |